Repository: saketkc/pysradb Branch: develop Commit: 801eb8fa1f1a Files: 94 Total size: 16.8 MB Directory structure: gitextract_rf093ld_/ ├── .coveragerc ├── .editorconfig ├── .gitattributes ├── .github/ │ ├── FUNDING.yml │ ├── ISSUE_TEMPLATE/ │ │ ├── bug_report.md │ │ └── feature_request.md │ ├── ISSUE_TEMPLATE.md │ ├── dependabot.yml │ └── workflows/ │ ├── codeql-analysis.yml │ ├── publish.yml │ ├── pull_request.yml │ └── push.yml ├── .gitignore ├── AUTHORS.md ├── CITATION.cff ├── CODE_OF_CONDUCT.md ├── CONTRIBUTING.md ├── HISTORY.md ├── LICENSE ├── MANIFEST.in ├── Makefile ├── README.md ├── docs/ │ ├── Makefile │ ├── _static/ │ │ ├── copy-button.js │ │ └── custom.css │ ├── authors.md │ ├── case_studies.md │ ├── cmdline.md │ ├── commands.rst │ ├── conf.py │ ├── contributing.md │ ├── history.md │ ├── index.rst │ ├── installation.md │ ├── make.bat │ ├── modules.rst │ ├── notebooks.rst │ ├── pysradb.rst │ ├── python-api-usage.md │ └── quickstart.md ├── notebooks/ │ ├── 01.Python-API_demo.ipynb │ ├── 02.Commandline_download.ipynb │ ├── 03.ParallelDownload.ipynb │ ├── 04.SRA_to_fastq_conda.ipynb │ ├── 05.Downloading_subsets_of_a_project.ipynb │ ├── 06.Multiple_SRPs.ipynb │ ├── 07.Query_Search.ipynb │ ├── 08.PMC_DOI_Identifiers.ipynb │ ├── 09.Metadata_enrichment.ipynb │ ├── 11.Parse_Bioscience_Search.ipynb │ └── README.md ├── pyproject.toml ├── pysradb/ │ ├── __init__.py │ ├── __main__.py │ ├── cli.py │ ├── download.py │ ├── exceptions.py │ ├── filter_attrs.py │ ├── geoweb.py │ ├── metadata_enrichment.py │ ├── ontology_reference.json │ ├── search.py │ ├── sraweb.py │ ├── taxid2name.py │ └── utils.py ├── requirements.txt ├── setup.cfg └── tests/ ├── conftest.py ├── data/ │ └── test_search/ │ ├── ena_search_test1.txt │ ├── ena_test_verbosity_0.csv │ ├── ena_test_verbosity_0.json │ ├── ena_test_verbosity_1.csv │ ├── ena_test_verbosity_1.json │ ├── ena_test_verbosity_2.csv │ ├── ena_test_verbosity_2.json │ ├── ena_test_verbosity_3.csv │ ├── ena_test_verbosity_3.json │ ├── geo_search_test1.txt │ ├── sra_search_test1.txt │ ├── sra_test.xml │ ├── sra_test_2_verbosity_0.csv │ ├── sra_test_2_verbosity_1.csv │ ├── sra_test_2_verbosity_2.csv │ ├── sra_test_2_verbosity_3.csv │ ├── sra_test_ERS3331676.xml │ ├── sra_test_verbosity_0.csv │ ├── sra_test_verbosity_1.csv │ ├── sra_test_verbosity_2.csv │ ├── sra_test_verbosity_3.csv │ └── sra_uids.txt ├── test_geoweb.py ├── test_search.py ├── test_sraweb.py └── test_utils.py ================================================ FILE CONTENTS ================================================ ================================================ FILE: .coveragerc ================================================ [run] omit = pysradb/filter_attrs.py pysradb/geodb.py pysradb/sradb.py pysradb/taxid2name.py pysradb/utils.py ================================================ FILE: .editorconfig ================================================ # http://editorconfig.org root = true [*] indent_style = space indent_size = 4 trim_trailing_whitespace = true insert_final_newline = true charset = utf-8 end_of_line = lf [*.bat] indent_style = tab end_of_line = crlf [LICENSE] insert_final_newline = false [Makefile] indent_style = tab ================================================ FILE: .gitattributes ================================================ *.rst linguist-documentation *.html linguist-documentation *.ipynb linguist-language=python ================================================ FILE: .github/FUNDING.yml ================================================ # These are supported funding model platforms github: [saketkc] ================================================ FILE: .github/ISSUE_TEMPLATE/bug_report.md ================================================ --- name: Bug report about: Create a report to help us improve title: "[BUG]" labels: bug assignees: '' --- **Describe the bug** A clear and concise description of what the bug is. **To Reproduce** Steps to reproduce the behavior: `pysradb SRPxxx` **Desktop (please complete the following information):** - OS: [e.g. Ubuntu 20.04] - Python version [e.g. 3.8] **Additional context** Add any other context about the problem here. ================================================ FILE: .github/ISSUE_TEMPLATE/feature_request.md ================================================ --- name: Feature request about: Suggest an idea for this project title: "[ENH]" labels: enhancement assignees: '' --- **Is your feature request related to a problem? Please describe.** A clear and concise description of what the problem is. Ex. I'm always frustrated when [...] **Describe the solution you'd like** A clear and concise description of what you want to happen. ================================================ FILE: .github/ISSUE_TEMPLATE.md ================================================ * pysradb version: * Python version: * Operating System: ### Description Describe what you were trying to get done. Tell us what happened, what went wrong, and what you expected to happen. ### What I Did ``` Paste the command(s) you ran and the output. If there was a crash, please include the traceback here. ``` ================================================ FILE: .github/dependabot.yml ================================================ # To get started with Dependabot version updates, you'll need to specify which # package ecosystems to update and where the package manifests are located. # Please see the documentation for all configuration options: # https://help.github.com/github/administering-a-repository/configuration-options-for-dependency-updates version: 2 updates: - package-ecosystem: "pip" # See documentation for possible values directory: "/" # Location of package manifests schedule: interval: "daily" ================================================ FILE: .github/workflows/codeql-analysis.yml ================================================ # For most projects, this workflow file will not need changing; you simply need # to commit it to your repository. # # You may wish to alter this file to override the set of languages analyzed, # or to provide custom queries or build logic. # # ******** NOTE ******** # We have attempted to detect the languages in your repository. Please check # the `language` matrix defined below to confirm you have the correct set of # supported CodeQL languages. # name: "CodeQL" on: push: branches: [ master ] pull_request: # The branches below must be a subset of the branches above branches: [ master ] schedule: - cron: '35 5 * * 1' jobs: analyze: name: Analyze runs-on: ubuntu-latest permissions: actions: read contents: read security-events: write strategy: fail-fast: false matrix: language: [ 'python' ] # CodeQL supports [ 'cpp', 'csharp', 'go', 'java', 'javascript', 'python' ] # Learn more: # https://docs.github.com/en/free-pro-team@latest/github/finding-security-vulnerabilities-and-errors-in-your-code/configuring-code-scanning#changing-the-languages-that-are-analyzed steps: - name: Checkout repository uses: actions/checkout@v2 # Initializes the CodeQL tools for scanning. - name: Initialize CodeQL uses: github/codeql-action/init@v1 with: languages: ${{ matrix.language }} # If you wish to specify custom queries, you can do so here or in a config file. # By default, queries listed here will override any specified in a config file. # Prefix the list here with "+" to use these queries and those in the config file. # queries: ./path/to/local/query, your-org/your-repo/queries@main # Autobuild attempts to build any compiled languages (C/C++, C#, or Java). # If this step fails, then you should remove it and run the build manually (see below) - name: Autobuild uses: github/codeql-action/autobuild@v1 # ℹ️ Command-line programs to run using the OS shell. # 📚 https://git.io/JvXDl # ✏️ If the Autobuild fails above, remove it and uncomment the following three lines # and modify them (or add more) to build your code if your project # uses a compiled language #- run: | # make bootstrap # make release - name: Perform CodeQL Analysis uses: github/codeql-action/analyze@v1 ================================================ FILE: .github/workflows/publish.yml ================================================ name: publish on: release: types: [created] jobs: deploy: runs-on: ubuntu-latest steps: - uses: actions/checkout@v2 - name: Set up Python uses: actions/setup-python@v1 with: python-version: '3.x' - name: Install dependencies run: | python -m pip install --upgrade pip pip install setuptools wheel twine - name: Build and publish env: TWINE_USERNAME: ${{ secrets.PYPI_USERNAME }} TWINE_PASSWORD: ${{ secrets.PYPI_PASSWORD }} run: | python setup.py sdist bdist_wheel twine upload dist/* ================================================ FILE: .github/workflows/pull_request.yml ================================================ name: pull_request on: [pull_request] jobs: test: runs-on: ubuntu-latest strategy: matrix: python-version: [3.9, '3.10', '3.11', '3.12', '3.13'] steps: - uses: actions/checkout@v2 - name: Set up Python ${{ matrix.python-version }} uses: actions/setup-python@v1 with: python-version: ${{ matrix.python-version }} - name: Install dependencies run: | python -m pip install --upgrade pip pip install -U pip pip install -r requirements.txt - name: Install Ollama run: | curl -fsSL https://ollama.com/install.sh | sh # Start Ollama service in background ollama serve & # Wait for Ollama to be ready sleep 5 # Pull required models for testing ollama pull phi3 ollama pull meditron # Verify installation ollama list - name: Lint with flake8 run: | pip install -U pytest coverage pytest-cov codecov black flake8 # stop the build if there are Python syntax errors or undefined names flake8 . --count --select=E9,F63,F7,F82 --show-source --statistics # exit-zero treats all errors as warnings. The GitHub editor is 127 chars wide flake8 . --count --exit-zero --max-complexity=10 --max-line-length=127 --statistics black --check . - name: Test with pytest continue-on-error: true run: | pip install --editable ".[enrichment]" pip install pytest pytest make coverage codecov docs: runs-on: ubuntu-latest steps: - uses: actions/checkout@v2 - name: Set up Python 3.11 uses: actions/setup-python@v1 with: python-version: '3.11' - name: Install dependencies run: | python -m pip install --upgrade pip pip install -r requirements.txt pip install ".[enrichment]" pip install sphinx myst-parser sphinxcontrib-gtagjs ipython numpydoc sphinx-tabs furo nbsphinx sphinx-panels - name: Install Pandoc run: | sudo apt-get update sudo apt-get install -y pandoc - name: Build documentation run: | make docs ================================================ FILE: .github/workflows/push.yml ================================================ name: push on: [push] jobs: test: runs-on: ubuntu-latest strategy: matrix: python-version: [3.9, '3.10', '3.11', '3.12', '3.13'] steps: - uses: actions/checkout@v2 - name: Set up Python ${{ matrix.python-version }} uses: actions/setup-python@v1 with: python-version: ${{ matrix.python-version }} - name: Install dependencies run: | python -m pip install --upgrade pip pip install -U pip pip install -r requirements.txt - name: Lint with flake8 run: | pip install -U pytest coverage pytest-cov codecov black flake8 # stop the build if there are Python syntax errors or undefined names flake8 . --count --select=E9,F63,F7,F82 --show-source --statistics # exit-zero treats all errors as warnings. The GitHub editor is 127 chars wide flake8 . --count --exit-zero --max-complexity=10 --max-line-length=127 --statistics black --check . - name: Test with pytest continue-on-error: true run: | pip install --editable ".[enrichment]" pip install pytest pytest make coverage codecov docs: runs-on: ubuntu-latest steps: - uses: actions/checkout@v2 - name: Set up Python 3.11 uses: actions/setup-python@v1 with: python-version: '3.11' - name: Install dependencies run: | python -m pip install --upgrade pip pip install -r requirements.txt pip install ".[enrichment]" pip install sphinx myst-parser sphinxcontrib-gtagjs ipython numpydoc sphinx-tabs furo nbsphinx sphinx-panels - name: Install Pandoc run: | sudo apt-get update sudo apt-get install -y pandoc - name: Build documentation run: | make docs - name: Deploy uses: peaceiris/actions-gh-pages@v3 if: github.ref == 'refs/heads/develop' with: github_token: ${{ secrets.GITHUB_TOKEN }} publish_dir: ./docs/_build/html/ ================================================ FILE: .gitignore ================================================ # Byte-compiled / optimized / DLL files __pycache__/ *.py[cod] *$py.class # C extensions *.so # Distribution / packaging .Python env/ build/ develop-eggs/ dist/ downloads/ eggs/ .eggs/ lib/ lib64/ parts/ sdist/ var/ wheels/ *.egg-info/ .installed.cfg *.egg MANIFEST # PyInstaller # Usually these files are written by a python script from a template # before PyInstaller builds the exe, so as to inject date/other infos into it. *.manifest *.spec # Installer logs pip-log.txt pip-delete-this-directory.txt # Unit test / coverage reports htmlcov/ .tox/ .coverage .coverage.* .cache nosetests.xml coverage.xml *.cover .hypothesis/ .pytest_cache/ # Translations *.mo *.pot # Django stuff: *.log local_settings.py db.sqlite3 # Flask stuff: instance/ .webassets-cache # Scrapy stuff: .scrapy # Sphinx documentation docs/_build/ # PyBuilder target/ # Jupyter Notebook .ipynb_checkpoints # pyenv .python-version # celery beat schedule file celerybeat-schedule # SageMath parsed files *.sage.py # dotenv .env # Environments .env .venv env/ venv/ ENV/ env.bak/ venv.bak/ # Spyder project settings .spyderproject .spyproject # Rope project settings .ropeproject # mkdocs documentation /site # mypy .mypy_cache/ *.sqlite *.sqlite.gz geoweb_downloads/ ================================================ FILE: AUTHORS.md ================================================ # Credits ## Contributors - [Boshen Yan](https://github.com/bscrow) - [Maarten van der Sande](https://github.com/Maarten-vd-Sande) - [Dibya Gautam](https://github.com/dibyaaaaax) - [Marius van den Beek](https://github.com/mvdbeek) - [Devang Thakkar](https://github.com/DevangThakkar) ## Maintainer - Saket Choudhary \<\> ================================================ FILE: CITATION.cff ================================================ cff-version: 1.2.0 message: "If you use this software, please cite it as below." authors: - family-names: "Choudhary" given-names: "Saket" orcid: "https://orcid.org/0000-0001-5202-7633" title: "pysradb" version: 2.4.1 doi: 10.12688/f1000research.18676.1 date-released: 2025-09-28 url: "https://github.com/saketkc/pysradb" ================================================ FILE: CODE_OF_CONDUCT.md ================================================ # Contributor Covenant Code of Conduct ## Our Pledge In the interest of fostering an open and welcoming environment, we as contributors and maintainers pledge to making participation in our project and our community a harassment-free experience for everyone, regardless of age, body size, disability, ethnicity, sex characteristics, gender identity and expression, level of experience, education, socio-economic status, nationality, personal appearance, race, religion, or sexual identity and orientation. ## Our Standards Examples of behavior that contributes to creating a positive environment include: * Using welcoming and inclusive language * Being respectful of differing viewpoints and experiences * Gracefully accepting constructive criticism * Focusing on what is best for the community * Showing empathy towards other community members Examples of unacceptable behavior by participants include: * The use of sexualized language or imagery and unwelcome sexual attention or advances * Trolling, insulting/derogatory comments, and personal or political attacks * Public or private harassment * Publishing others' private information, such as a physical or electronic address, without explicit permission * Other conduct which could reasonably be considered inappropriate in a professional setting ## Our Responsibilities Project maintainers are responsible for clarifying the standards of acceptable behavior and are expected to take appropriate and fair corrective action in response to any instances of unacceptable behavior. Project maintainers have the right and responsibility to remove, edit, or reject comments, commits, code, wiki edits, issues, and other contributions that are not aligned to this Code of Conduct, or to ban temporarily or permanently any contributor for other behaviors that they deem inappropriate, threatening, offensive, or harmful. ## Scope This Code of Conduct applies both within project spaces and in public spaces when an individual is representing the project or its community. Examples of representing a project or community include using an official project e-mail address, posting via an official social media account, or acting as an appointed representative at an online or offline event. Representation of a project may be further defined and clarified by project maintainers. ## Enforcement Instances of abusive, harassing, or otherwise unacceptable behavior may be reported by contacting the project team at saketkc@gmail.com. All complaints will be reviewed and investigated and will result in a response that is deemed necessary and appropriate to the circumstances. The project team is obligated to maintain confidentiality with regard to the reporter of an incident. Further details of specific enforcement policies may be posted separately. Project maintainers who do not follow or enforce the Code of Conduct in good faith may face temporary or permanent repercussions as determined by other members of the project's leadership. ## Attribution This Code of Conduct is adapted from the [Contributor Covenant][homepage], version 1.4, available at https://www.contributor-covenant.org/version/1/4/code-of-conduct.html [homepage]: https://www.contributor-covenant.org For answers to common questions about this code of conduct, see https://www.contributor-covenant.org/faq ================================================ FILE: CONTRIBUTING.md ================================================ # Contributing Contributions are welcome, and they are greatly appreciated! Every little bit helps, and credit will always be given. You can contribute in many ways: ## Types of Contributions ### Report Bugs Report bugs at . If you are reporting a bug, please include: - Your operating system name and version. - Any details about your local setup that might be helpful in troubleshooting. - Detailed steps to reproduce the bug. ### Fix Bugs Look through the GitHub issues for bugs. Anything tagged with \"bug\" and \"help wanted\" is open to whoever wants to implement it. ### Implement Features Look through the GitHub issues for features. Anything tagged with \"enhancement\" and \"help wanted\" is open to whoever wants to implement it. ### Write Documentation pysradb could always use more documentation, whether as part of the official pysradb docs, in docstrings, or even on the web in blog posts, articles, and such. ### Submit Feedback The best way to send feedback is to file an issue at . If you are proposing a feature: - Explain in detail how it would work. - Keep the scope as narrow as possible, to make it easier to implement. - Remember that this is a volunteer-driven project, and that contributions are welcome :) ## Get Started! Ready to contribute? Here\'s how to set up [pysradb]{.title-ref} for local development. 1. Fork the [pysradb]{.title-ref} repo on GitHub. 2. Clone your fork locally: ``` shell $ git clone git@github.com:your_name_here/pysradb.git ``` 3. Install your local copy into a virtualenv. Assuming you have virtualenvwrapper installed, this is how you set up your fork for local development (If python \--version is less than 3.0, run [\$ mkvirtualenv pysradb \--python=py3]{.title-ref} instead): ``` shell $ mkvirtualenv pysradb $ cd pysradb/ $ python setup.py develop ``` 4. Create a branch for local development: ``` shell $ git checkout -b name-of-your-bugfix-or-feature ``` Now you can make your changes locally. 5. When you\'re done making changes, check that your changes pass flake8 and the tests, including testing other Python versions with tox: ``` shell $ flake8 pysradb tests $ python setup.py test or py.test $ tox ``` To get flake8 and tox, just pip install them into your virtualenv. 6. Commit your changes and push your branch to GitHub: ``` shell $ git add . $ git commit -m "Your detailed description of your changes." $ git push origin name-of-your-bugfix-or-feature ``` 7. Submit a pull request through the GitHub website. ## Pull Request Guidelines Before you submit a pull request, check that it meets these guidelines: 1. The pull request should include tests. 2. If the pull request adds functionality, the docs should be updated. Put your new functionality into a function with a docstring, and add the feature to the list in README.rst. 3. The pull request should work for Python 2.7, 3.4, 3.5 and 3.6, and for PyPy. Make sure that the tests pass for all supported Python versions. ## Tips To run a subset of tests: ``` shell $ py.test tests.test_pysradb ``` ## Deploying A reminder for the maintainers on how to deploy. Make sure all your changes are committed (including an entry in HISTORY.rst). Then run: ``` shell $ bumpversion patch # possible: major / minor / patch $ git push $ git push --tags ``` CI will then deploy to PyPI if tests pass. ================================================ FILE: HISTORY.md ================================================ # History # 3.0.0 (Unreleased) - BREAKING CHANGES ## Removal of legacy SQLite support **All local SQLite database support has been removed.** This is a major breaking change and was long overdue. - **Removed**: `SRAdb`, `GEOdb`, and `BASEdb` classes - **Removed**: `download_sradb_file()` and `download_geodb_file()` functions - **Removed**: Files: `sradb.py`, `geodb.py`, `basedb.py` - **Why**: Legacy local SQLite databases are outdated and rarely used. SRAweb (API-based) provides better, real-time data with no maintenance overhead. # 2.5.1 (2025-10-29) - Add prjna support in doi-to-identifiers [#249](https://github.com/saketkc/pysradb/pull/249) # 2.5.0 (2025-10-19) - Add pmid/doi-to-gse/srp conversion [#246](https://github.com/saketkc/pysradb/pull/246). # 2.4.1 (2025-09-27) - Add gse-to-pmid conversion [#241](https://github.com/saketkc/pysradb/pull/244). # 2.4.0 (2025-09-27) - Add sra-to-pmid conversion [#241](https://github.com/saketkc/pysradb/pull/241). Thanks [@andrewdavidsmith](https://github.com/andrewdavidsmith) for the idea. # 2.3.0 (2025-08-24) - Download logic improvements: remoted requests-ftp as requirement - Fix for handling missing metadata keys [#223](https://github.com/saketkc/pysradb/pull/223). Thanks [@andrewdavidsmith](https://github.com/andrewdavidsmith) # 2.2.2 (2024-10-03) - Fix for handling ENA urls for paired end data # 2.2.1 (2024-08-21) - Fix for handling ENA urls - Migrated to pyproject.toml # 2.2.0 (2023-09-17) - Add support for Biosamples and bioproject [#199](https://github.com/saketkc/pysradb/pull/198) - Use retmode xml for Geo search [#200](https://github.com/saketkc/pysradb/pull/200) - Documentation fixes ## 2.1.0 (2023-05-16) - Fix for [gse-to-srp] returning unrequested GSEs [#186](https://github.com/saketkc/pysradb/issues/190) - Fix for [download] using [public_urls] - Fix for [gsm-to-srx] returning false positives [#165](https://github.com/saketkc/pysradb/issues/165) - Fix for delimiter not being consistent when metadata is printed on terminal [#147](https://github.com/saketkc/pysradb/issues/147) - ENA search is currently broken because of an API change ## 2.0.2 (2023-04-09) - Fix for [gse-to-srp] to handle cases where a project is missing but SRXs are returned [#186](https://github.com/saketkc/pysradb/issues/186) - Fix gse-to-gsm [#187](https://github.com/saketkc/pysradb/issues/187) ## 2.0.1 (2023-03-18) - Fix for [pysradb download] - using [public_url] - Fix for SRX -\> SRR and related conversions [#183](https://github.com/saketkc/pysradb/pull/183) ## 2.0.0 (2023-02-23) - BREAKING change: Overhaul of how urls and associated metadata are returned (not backward compatible); all column names are lower cased by default - Fix extra space in \"organism_taxid\" column - Added support for Experiment attributes [#89](https://github.com/saketkc/pysradb/issues/89#issuecomment-1439319532) ## 1.4.2 (06-17-2022) - Fix ENA fastq fetching [#163](https://github.com/saketkc/pysradb/issues/163) ## 1.4.1 (06-04-2022) - Fix for fetching alternative URLs ## 1.4.0 (06-04-2022) - Added ability to fetch alternative URLs (GCP/AWS) for metadata [#161](https://github.com/saketkc/pysradb/issues/161) - Fix for xmldict 0.13.0 no longer defaulting to OrderedDict [#159](https://github.com/saketkc/pysradb/pull/159) - Fix for missing experiment model and description in metadata [#160](https://github.com/saketkc/pysradb/issues/160) ## 1.3.0 (02-18-2022) - Add [study_title] to [\--detailed] flag ([#152](https://github.com/saketkc/pysradb/issues/152)) - Fix [KeyError] in [metadata] where some new IDs do not have any metadata ([#151](https://github.com/saketkc/pysradb/issues/151)) ## 1.2.0 (01-10-2022) - Do not exit if a qeury returns no hits ([#149](https://github.com/saketkc/pysradb/pull/149)) ## 1.1.0 (12-12-2021) - Fixed [gsm-to-gse] failure ([#128](https://github.com/saketkc/pysradb/pull/128)) - Fixed case sensitivity bug for ENA search ([#144](https://github.com/saketkc/pysradb/pull/144)) - Fixed publication date bug for search ([#146](https://github.com/saketkc/pysradb/pull/146)) - Added support for downloading data from GEO [pysradb dowload -g GSE] ([#129](https://github.com/saketkc/pysradb/pull/129)) ## 1.0.1 (01-10-2021) - Dropped Python 3.6 since pandas 1.2 is not supported ## 1.0.0 (01-09-2021) - Retired `metadb` and `SRAdb` based search through CLI - everything defaults to `SRAweb` - `SRAweb` now supports [search](https://saket-choudhary.me/pysradb/quickstart.html#search) - [N/A] is now replaced with [pd.NA] - Two new fields in \`\--detailed\`: [instrument_model] and [instrument_model_desc] [#75](https://github.com/saketkc/pysradb/issues/75) - Updated documentation ## 0.11.1 (09-18-2020) - [library_layout] is now outputted in metadata #56 - [-detailed] unifies columns for ENA fastq links instead of appending \_x/\_y #59 - bugfix for parsing namespace in xml outputs #65 - XML errors from NCBI are now handled more gracefully #69 - Documentation and dependency updates ## 0.11.0 (09-04-2020) - [pysradb download] now supports multiple threads for paralle downloads - [pysradb download] also supports ultra fast downloads of FASTQs from ENA using aspera-client ## 0.10.3 (03-26-2020) - Added test cases for SRAweb - API limit exceeding errors are automagically handled - Bug fixes for GSE \<=\> SRR - Bug fix for metadata - supports multiple SRPs Contributors - Dibya Gautam - Marius van den Beek ## 0.10.2 (02-05-2020) - Bug fix: Handle API-rate limit exceeding =\> Retries - Enhancement: \'Alternatives\' URLs are now part of [\--detailed] ## 0.10.1 (02-04-2020) - Bug fix: Handle Python3.6 for capture_output in subprocess.run ## 0.10.0 (01-31-2020) - All the subcommands (srx-to-srr, srx-to-srs) will now print additional columns where the first two columns represent the relevant conversion - Fixed a bug where for fetching entries with single efetch record ## 0.9.9 (01-15-2020) - Major fix: some SRRs would go missing as the experiment dict was being created only once per SRR (See #15) - Features: More detailed metadata by default in the SRAweb mode - See notebook: ## 0.9.7 (01-20-2020) - Feature: instrument, run size and total spots are now printed in the metadata by default (SRAweb mode only) - Issue: Fixed an issue with srapath failing on SRP. srapath is now run on individual SRRs. ## 0.9.6 (07-20-2019) - Introduced [SRAweb] to perform queries over the web if the SQLite is missing or does not contain the relevant record. ## 0.9.0 (02-27-2019) ### Others - This release completely changes the command line interface replacing click with argparse ([#3](https://github.com/saketkc/pysradb/pull/3)) - Removed Python 2 comptaible stale code ## 0.8.0 (02-26-2019) ### New methods/functionality - \`srr-to-gsm\`: convert SRR to GSM - SRAmetadb.sqlite.gz file is deleted by default after extraction - When SRAmetadb is not found a confirmation is seeked before downloading - Confirmation option before SRA downloads ### Bugfix - download() works with wget ### Others - [\--out_dir] is now [out-dir] ## 0.7.1 (02-18-2019) Important: Python2 is no longer supported. Please consider moving to Python3. ### Bugfix - Included docs in the index whihch were missed out in the previous release ## 0.7.0 (02-08-2019) ### New methods/functionality - \`gsm-to-srr\`: convert GSM to SRR - \`gsm-to-srx\`: convert GSM to SRX - \`gsm-to-gse\`: convert GSM to GSE ### Renamed methods The following commad line options have been renamed and the changes are not compatible with 0.6.0 release: - [sra-metadata] -\> [metadata]. - [sra-search] -\> [search]. - [srametadb] -\> [metadb]. ## 0.6.0 (12-25-2018) ### Bugfix - Fixed bugs introduced in 0.5.0 with API changes where multiple redundant columns were output in [sra-metadata] ### New methods/functionality - [download] now allows piped inputs ## 0.5.0 (12-24-2018) ### New methods/functionality - Support for filtering by SRX Id for SRA downloads. - \`srr_to_srx\`: Convert SRR to SRX/SRP - \`srp_to_srx\`: Convert SRP to SRX - Stripped down [sra-metadata] to give minimal information - Added [\--assay], [\--desc], [\--detailed] flag for [sra-metadata] - Improved table printing on terminal ## 0.4.2 (12-16-2018) ### Bugfix - Fixed unicode error in tests for Python2 ## 0.4.0 (12-12-2018) ### New methods/functionality - Added a new [BASEdb] class to handle common database connections - Initial support for GEOmetadb through GEOdb class - Initial support or a command line interface: - download Download SRA project (SRPnnnn) - gse-metadata Fetch metadata for GEO ID (GSEnnnn) - gse-to-gsm Get GSM(s) for GSE - gsm-metadata Fetch metadata for GSM ID (GSMnnnn) - sra-metadata Fetch metadata for SRA project (SRPnnnn) - Added three separate notebooks for SRAdb, GEOdb, CLI usage ## 0.3.0 (12-05-2018) ### New methods/functionality - [sample_attribute] and [experiment_attribute] are now included by default in the df returned by [sra_metadata()] - [expand_sample_attribute_columns: expand metadata dataframe based on attributes in \`sample_attribute] column - New methods to guess cell/tissue/strain: [guess_cell_type()]/[guess_tissue_type()]/[guess_strain_type()] - Improved README and usage instructions ## 0.2.2 (12-03-2018) ### New methods/functionality - [search_sra()] allows full text search on SRA metadata. ## 0.2.0 (12-03-2018) ### Renamed methods The following methods have been renamed and the changes are not compatible with 0.1.0 release: - [get_query()] -\> [query()]. - [sra_convert()] -\> [sra_metadata()]. - [get_table_counts()] -\> [all_row_counts()]. ### New methods/functionality - [download_sradb_file()] makes fetching [SRAmetadb.sqlite] file easy; wget is no longer required. - [ftp] protocol is now supported besides [fsp] and hence [aspera-client] is now optional. We however, strongly recommend [aspera-client] for faster downloads. ### Bug fixes - Silenced [SettingWithCopyWarning] by excplicitly doing operations on a copy of the dataframe instead of the original. Besides these, all methods now follow a [numpydoc] compatible documentation. ## 0.1.0 (12-01-2018) - First release on PyPI. ================================================ FILE: LICENSE ================================================ BSD 3-Clause License Copyright (c) 2020-2023, Saket Choudhary All rights reserved. Redistribution and use in source and binary forms, with or without modification, are permitted provided that the following conditions are met: * Redistributions of source code must retain the above copyright notice, this list of conditions and the following disclaimer. * Redistributions in binary form must reproduce the above copyright notice, this list of conditions and the following disclaimer in the documentation and/or other materials provided with the distribution. * Neither the name of the copyright holder nor the names of its contributors may be used to endorse or promote products derived from this software without specific prior written permission. THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS "AS IS" AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE ARE DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT HOLDER OR CONTRIBUTORS BE LIABLE FOR ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, OR CONSEQUENTIAL DAMAGES (INCLUDING, BUT NOT LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR SERVICES; LOSS OF USE, DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER CAUSED AND ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY, OR TORT (INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE. ================================================ FILE: MANIFEST.in ================================================ include AUTHORS.md include CONTRIBUTING.md include HISTORY.md include LICENSE include README.md include requirements.txt recursive-include tests * recursive-exclude * __pycache__ recursive-exclude * *.py[co] recursive-exclude * *.sqlite recursive-exclude * *.sqlite.gz recursive-include docs *.md conf.py Makefile make.bat *.jpg *.png *.gif *.rst ================================================ FILE: Makefile ================================================ .PHONY: clean clean-test clean-pyc clean-build docs help .DEFAULT_GOAL := help define BROWSER_PYSCRIPT import os, webbrowser, sys try: from urllib import pathname2url except: from urllib.request import pathname2url webbrowser.open("file://" + pathname2url(os.path.abspath(sys.argv[1]))) endef export BROWSER_PYSCRIPT define PRINT_HELP_PYSCRIPT import re, sys for line in sys.stdin: match = re.match(r'^([a-zA-Z_-]+):.*?## (.*)$$', line) if match: target, help = match.groups() print("%-20s %s" % (target, help)) endef export PRINT_HELP_PYSCRIPT BROWSER := python -c "$$BROWSER_PYSCRIPT" help: @python -c "$$PRINT_HELP_PYSCRIPT" < $(MAKEFILE_LIST) clean: clean-build clean-pyc clean-test ## remove all build, test, coverage and Python artifacts clean-build: ## remove build artifacts rm -fr build/ rm -fr dist/ rm -fr .eggs/ find . -name '*.egg-info' -exec rm -fr {} + find . -name '*.egg' -exec rm -f {} + clean-pyc: ## remove Python file artifacts find . -name '*.pyc' -exec rm -f {} + find . -name '*.pyo' -exec rm -f {} + find . -name '*~' -exec rm -f {} + find . -name '__pycache__' -exec rm -fr {} + clean-test: ## remove test and coverage artifacts rm -fr .tox/ rm -f .coverage rm -fr htmlcov/ rm -fr .pytest_cache lint: ## check style with flake8 flake8 pysradb tests test: ## run tests quickly with the default Python pytest -s -v tests test-all: ## run tests on every Python version with tox tox coverage: ## check code coverage quickly with the default Python coverage run --source pysradb -m pytest coverage report -m coverage html docs: ## generate Sphinx HTML documentation, including API docs rm -f docs/pysradb.rst rm -f docs/modules.rst sphinx-apidoc -o docs/ pysradb $(MAKE) -C docs clean $(MAKE) -C docs html servedocs: docs ## compile the docs watching for changes #watchmedo shell-command -p '*.rst' -c '$(MAKE) -C docs html' -R -D . watchmedo shell-command -p '*.md|*.rst' -c '$(MAKE) -C docs html' -R -D . release: dist ## package and upload a release python -m build twine upload dist/* dist: clean ## builds source and wheel package python -m build ls -l dist install: clean ## install the package to the active Python's site-packages pip install -e . ================================================ FILE: README.md ================================================ # A Python package for retrieving metadata from SRA/ENA/GEO [![image](https://img.shields.io/pypi/v/pysradb.svg?style=flat-square)](https://pypi.python.org/pypi/pysradb) [![image](https://anaconda.org/bioconda/pysradb/badges/version.svg)](https://anaconda.org/bioconda/pysradb/badges/version.svg) [![image](https://img.shields.io/badge/install%20with-bioconda-brightgreen.svg?style=flat-square)](http://bioconda.github.io/recipes/pysradb/README.html) [![image](https://static.pepy.tech/personalized-badge/pysradb?period=month&units=international_system&left_color=black&right_color=brightgreen&left_text=Downloads/month)](https://pepy.tech/project/pysradb) [![image](https://zenodo.org/badge/159590788.svg)](https://zenodo.org/badge/latestdoi/159590788) [![image](https://github.com/saketkc/pysradb/workflows/push/badge.svg)](https://github.com/saketkc/pysradb/actions) ## Documentation ## CLI Usage `pysradb` supports command line usage. See [CLI](https://saket-choudhary.me/pysradb/cmdline.html) instructions or [quickstart guide](https://www.saket-choudhary.me/pysradb/quickstart.html). $ pysradb usage: pysradb [-h] [--version] [--citation] {metadata,download,search,gse-to-gsm,gse-to-srp,gsm-to-gse,gsm-to-srp,gsm-to-srr,gsm-to-srs,gsm-to-srx,srp-to-gse,srp-to-srr,srp-to-srs,srp-to-srx,srr-to-gsm,srr-to-srp,srr-to-srs,srr-to-srx,srs-to-gsm,srs-to-srx,srx-to-srp,srx-to-srr,srx-to-srs,geo-matrix,srp-to-pmid,gse-to-pmid,pmid-to-gse,pmid-to-srp,pmc-to-identifiers,pmid-to-identifiers,doi-to-gse,doi-to-srp,doi-to-identifiers} ... pysradb: Query NGS metadata and data from NCBI Sequence Read Archive. version: 3.0.0 Citation: 10.12688/f1000research.18676.1 options: -h, --help show this help message and exit --version show program's version number and exit --citation how to cite subcommands: {metadata,download,search,gse-to-gsm,gse-to-srp,gsm-to-gse,gsm-to-srp,gsm-to-srr,gsm-to-srs,gsm-to-srx,srp-to-gse,srp-to-srr,srp-to-srs,srp-to-srx,srr-to-gsm,srr-to-srp,srr-to-srs,srr-to-srx,srs-to-gsm,srs-to-srx,srx-to-srp,srx-to-srr,srx-to-srs,geo-matrix,srp-to-pmid,gse-to-pmid,pmid-to-gse,pmid-to-srp,pmc-to-identifiers,pmid-to-identifiers,doi-to-gse,doi-to-srp,doi-to-identifiers} metadata Fetch metadata for SRA project (SRPnnnn) download Download SRA project (SRPnnnn) search Search SRA/ENA for matching text gse-to-gsm Get GSM for a GSE gse-to-srp Get SRP for a GSE gsm-to-gse Get GSE for a GSM gsm-to-srp Get SRP for a GSM gsm-to-srr Get SRR for a GSM gsm-to-srs Get SRS for a GSM gsm-to-srx Get SRX for a GSM srp-to-gse Get GSE for a SRP srp-to-srr Get SRR for a SRP srp-to-srs Get SRS for a SRP srp-to-srx Get SRX for a SRP srr-to-gsm Get GSM for a SRR srr-to-srp Get SRP for a SRR srr-to-srs Get SRS for a SRR srr-to-srx Get SRX for a SRR srs-to-gsm Get GSM for a SRS srs-to-srx Get SRX for a SRS srx-to-srp Get SRP for a SRX srx-to-srr Get SRR for a SRX srx-to-srs Get SRS for a SRX geo-matrix Download and parse GEO Matrix files srp-to-pmid Get PMIDs for SRP accessions gse-to-pmid Get PMIDs for GSE accessions pmid-to-gse Get GSE accessions from PMIDs pmid-to-srp Get SRP accessions from PMIDs pmc-to-identifiers Extract database identifiers from PMC articles pmid-to-identifiers Extract database identifiers from PubMed articles doi-to-gse Get GSE accessions from DOIs doi-to-srp Get SRP accessions from DOIs doi-to-identifiers Extract database identifiers from articles via DOI ## Quickstart A Google Colaboratory version of most used commands are available in this [Colab Notebook](https://colab.research.google.com/drive/1C60V-jkcNZiaCra_V5iEyFs318jgVoUR) . Note that this requires only an active internet connection (no additional downloads are made). The following notebooks document all the possible features of \`pysradb\`: 1. [Python API](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/01.Python-API_demo.ipynb) 2. [Downloading datasets from SRA - command line](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/02.Commandline_download.ipynb) 3. [Parallely download multiple datasets - Python API](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/03.ParallelDownload.ipynb) 4. [Converting SRA-to-fastq - command line (requires conda)](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/04.SRA_to_fastq_conda.ipynb) 5. [Downloading subsets of a project - Python API](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/05.Downloading_subsets_of_a_project.ipynb) 6. [Metadata for multiple SRPs](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/06.Multiple_SRPs.ipynb) 7. [Searching SRA/GEO/ENA](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/07.Query_Search.ipynb) 8. [Extracting identifiers from PMC/DOI](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/08.PMC_DOI_Identifiers.ipynb) 9. [Metadata Enrichment with LLMs](https://colab.research.google.com/github/saketkc/pysradb/blob/develop/notebooks/09.Metadata_enrichment.ipynb) ## Installation To install stable version using \`pip\`: ```bash pip install pysradb ``` Alternatively, if you use conda: ```bash conda install -c bioconda pysradb ``` This step will install all the dependencies. If you have an existing environment with a lot of pre-installed packages, conda might be [slow](https://github.com/bioconda/bioconda-recipes/issues/13774). Please consider creating a new enviroment for `pysradb`: ```bash conda create -c bioconda -n pysradb PYTHON=3.13 pysradb ``` ### Dependencies pandas requests tqdm xmltodict ### Installing pysradb in development mode git clone https://github.com/saketkc/pysradb.git cd pysradb && pip install -r requirements.txt pip install -e . ## Using pysradb ### Obtaining SRA metadata $ pysradb metadata SRP000941 | head study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_strategy library_source library_selection sample_accession sample_title instrument total_spots total_size run_accession run_total_spots run_total_bases SRP000941 SRX056722 Reference Epigenome: ChIP-Seq Analysis of H3K27ac in hESC H1 Cells Reference Epigenome: ChIP-Seq Analysis of H3K27ac in hESC H1 Cells 9606 Homo sapiens ChIP-Seq GENOMIC ChIP SRS184466 Illumina HiSeq 2000 26900401 531654480 SRR179707 26900401 807012030 SRP000941 SRX027889 Reference Epigenome: ChIP-Seq Analysis of H2AK5ac in hESC Cells Reference Epigenome: ChIP-Seq Analysis of H2AK5ac in hESC Cells 9606 Homo sapiens ChIP-Seq GENOMIC ChIP SRS116481 Illumina Genome Analyzer II 37528590 779578968 SRR067978 37528590 1351029240 SRP000941 SRX027888 Reference Epigenome: ChIP-Seq Input from hESC H1 Cells Reference Epigenome: ChIP-Seq Input from hESC H1 Cells 9606 Homo sapiens ChIP-Seq GENOMIC RANDOM SRS116483 Illumina Genome Analyzer II 13603127 3232309537 SRR067977 13603127 489712572 SRP000941 SRX027887 Reference Epigenome: ChIP-Seq Input from hESC H1 Cells Reference Epigenome: ChIP-Seq Input from hESC H1 Cells 9606 Homo sapiens ChIP-Seq GENOMIC RANDOM SRS116562 Illumina Genome Analyzer II 22430523 506327844 SRR067976 22430523 807498828 SRP000941 SRX027886 Reference Epigenome: ChIP-Seq Input from hESC H1 Cells Reference Epigenome: ChIP-Seq Input from hESC H1 Cells 9606 Homo sapiens ChIP-Seq GENOMIC RANDOM SRS116560 Illumina Genome Analyzer II 15342951 301720436 SRR067975 15342951 552346236 SRP000941 SRX027885 Reference Epigenome: ChIP-Seq Input from hESC H1 Cells Reference Epigenome: ChIP-Seq Input from hESC H1 Cells 9606 Homo sapiens ChIP-Seq GENOMIC RANDOM SRS116482 Illumina Genome Analyzer II 39725232 851429082 SRR067974 39725232 1430108352 SRP000941 SRX027884 Reference Epigenome: ChIP-Seq Input from hESC H1 Cells Reference Epigenome: ChIP-Seq Input from hESC H1 Cells 9606 Homo sapiens ChIP-Seq GENOMIC RANDOM SRS116481 Illumina Genome Analyzer II 32633277 544478483 SRR067973 32633277 1174797972 SRP000941 SRX027883 Reference Epigenome: ChIP-Seq Input from hESC H1 Cells Reference Epigenome: ChIP-Seq Input from hESC H1 Cells 9606 Homo sapiens ChIP-Seq GENOMIC RANDOM SRS004118 Illumina Genome Analyzer II 22150965 3262293717 SRR067972 9357767 336879612 SRP000941 SRX027883 Reference Epigenome: ChIP-Seq Input from hESC H1 Cells Reference Epigenome: ChIP-Seq Input from hESC H1 Cells 9606 Homo sapiens ChIP-Seq GENOMIC RANDOM SRS004118 Illumina Genome Analyzer II 22150965 3262293717 SRR067971 12793198 460555128 ### Obtaining detailed SRA metadata $ pysradb metadata SRP075720 --detailed | head study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_strategy library_source library_selection sample_accession sample_title instrument total_spots total_size run_accession run_total_spots run_total_bases SRP075720 SRX1800476 GSM2177569: Kcng4_2la_H9; Mus musculus; RNA-Seq GSM2177569: Kcng4_2la_H9; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS1467643 Illumina HiSeq 2500 2547148 97658407 SRR3587912 2547148 127357400 SRP075720 SRX1800475 GSM2177568: Kcng4_2la_H8; Mus musculus; RNA-Seq GSM2177568: Kcng4_2la_H8; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS1467642 Illumina HiSeq 2500 2676053 101904264 SRR3587911 2676053 133802650 SRP075720 SRX1800474 GSM2177567: Kcng4_2la_H7; Mus musculus; RNA-Seq GSM2177567: Kcng4_2la_H7; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS1467641 Illumina HiSeq 2500 1603567 61729014 SRR3587910 1603567 80178350 SRP075720 SRX1800473 GSM2177566: Kcng4_2la_H6; Mus musculus; RNA-Seq GSM2177566: Kcng4_2la_H6; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS1467640 Illumina HiSeq 2500 2498920 94977329 SRR3587909 2498920 124946000 SRP075720 SRX1800472 GSM2177565: Kcng4_2la_H5; Mus musculus; RNA-Seq GSM2177565: Kcng4_2la_H5; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS1467639 Illumina HiSeq 2500 2226670 83473957 SRR3587908 2226670 111333500 SRP075720 SRX1800471 GSM2177564: Kcng4_2la_H4; Mus musculus; RNA-Seq GSM2177564: Kcng4_2la_H4; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS1467638 Illumina HiSeq 2500 2269546 87486278 SRR3587907 2269546 113477300 SRP075720 SRX1800470 GSM2177563: Kcng4_2la_H3; Mus musculus; RNA-Seq GSM2177563: Kcng4_2la_H3; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS1467636 Illumina HiSeq 2500 2333284 88669838 SRR3587906 2333284 116664200 SRP075720 SRX1800469 GSM2177562: Kcng4_2la_H2; Mus musculus; RNA-Seq GSM2177562: Kcng4_2la_H2; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS1467637 Illumina HiSeq 2500 2071159 79689296 SRR3587905 2071159 103557950 SRP075720 SRX1800468 GSM2177561: Kcng4_2la_H1; Mus musculus; RNA-Seq GSM2177561: Kcng4_2la_H1; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS1467635 Illumina HiSeq 2500 2321657 89307894 SRR3587904 2321657 116082850 ### Enriching metadata via CLI Enrich metadata with standardized biological attributes using biomedical-specialized LLMs through the command line: ```bash # Basic enrichment with default backend (Meditron) $ pysradb metadata GSE286254 --detailed --enrich # Using OpenBioLLM-8B (larger, trained on 500k+ biomedical entries) $ pysradb metadata GSE286254 --detailed --enrich --enrich-backend ollama/openbiollm-8b ``` Available biomedical backends: - `ollama/meditron` (default, 7B - optimized for medical text) - `ollama/openbiollm-8b` (8B - trained on 500k+ biomedical entries, superior biomedical performance) This returns the original metadata plus 9 enriched columns: - `guessed_organ` - `guessed_tissue` - `guessed_anatomical_system` - `guessed_cell_type` - `guessed_disease` - `guessed_sex` - `guessed_development_stage` - `guessed_assay` - `guessed_organism` For more details on enrichment features, prerequisites, and Python API usage, see the [Enriching metadata](#enriching-metadata) section below. ### Converting SRP to GSE $ pysradb srp-to-gse SRP075720 study_accession study_alias SRP075720 GSE81903 ### Converting GSM to SRP $ pysradb gsm-to-srp GSM2177186 experiment_alias study_accession GSM2177186 SRP075720 ### Converting GSM to GSE $ pysradb gsm-to-gse GSM2177186 experiment_alias study_alias GSM2177186 GSE81903 ### Converting GSM to SRX $ pysradb gsm-to-srx GSM2177186 experiment_alias experiment_accession GSM2177186 SRX1800089 ### Converting GSM to SRR $ pysradb gsm-to-srr GSM2177186 experiment_alias run_accession GSM2177186 SRR3587529 ### Converting SRP to PMID $ pysradb srp-to-pmid SRP045778 srp_accession bioproject pmid SRP045778 PRJNA257197 27373336 ### Converting GSE to PMID $ pysradb gse-to-pmid GSE253406 gse_accession pmid GSE253406 39528918 ### Extracting identifiers from PMC/DOI Extract database identifiers (GSE, PRJNA, SRP, etc.) from PubMed Central articles or DOIs. This feature automatically converts between GSE and SRP identifiers even when papers only mention one type! #### Get all identifiers from a PMID $ pysradb pmid-to-identifiers 39528918 pmid pmc_id gse_ids prjna_ids srp_ids 39528918 PMC10802650 GSE253406 PRJNA1058002 SRP484103 #### Get only GSE or SRP from PMID $ pysradb pmid-to-gse 39528918 pmid pmc_id gse_ids 39528918 PMC10802650 GSE253406 $ pysradb pmid-to-srp 39528918 pmid pmc_id srp_ids 39528918 PMC10802650 SRP484103 #### Extract from DOI $ pysradb doi-to-identifiers 10.12688/f1000research.18676.1 doi pmid pmc_id gse_ids srp_ids 10.12688/f1000research.18676.1 30873266 PMC6411813 GSE... SRP... #### Extract from PMC ID $ pysradb pmc-to-identifiers PMC10802650 pmc_id gse_ids prjna_ids srp_ids PMC10802650 GSE253406 PRJNA1058002 SRP484103 ### Enriching metadata Extract standardized biological metadata from SRA/GEO datasets using LLMs. #### Quickstart ```python from pysradb import SRAweb client = SRAweb() df = client.metadata("GSE286254", detailed=True, enrich=True) # Returns original + 9 enriched columns (might not always be complete): # guessed_organ, guessed_tissue, guessed_anatomical_system, # guessed_cell_type, guessed_disease, guessed_sex, # guessed_development_stage, guessed_assay, guessed_organism ``` #### Prerequisites Install Ollama: https://ollama.ai ```bash # Default backend (recommended) ollama pull meditron # Or use OpenBioLLM-8B for better biomedical performance ollama pull openbiollm-8b ``` #### Advanced Usage ```python # Use OpenBioLLM-8B backend (trained on 500k+ biomedical entries) client = SRAweb() df = client.metadata("GSE286254", detailed=True, enrich=True, enrich_backend="ollama/openbiollm-8b") # Manual enrichment with custom settings from pysradb.metadata_enrichment import create_metadata_extractor, load_ontology_reference # LLM-based extraction with default backend (meditron) extractor_llm = create_metadata_extractor(method="llm") df_enriched = extractor_llm.enrich_dataframe(df, prefix="guessed_") # LLM-based extraction with specific biomedical backend extractor_bio = create_metadata_extractor(method="llm", backend="ollama/openbiollm-8b") df_enriched = extractor_bio.enrich_dataframe(df, prefix="guessed_") # Embedding-based extraction (faster, offline) ontology_ref = load_ontology_reference() extractor_emb = create_metadata_extractor( method="embedding", model="FremyCompany/BioLORD-2023", reference_categories=ontology_ref ) df_enriched = extractor_emb.enrich_dataframe(df, prefix="guessed_") ``` See [Notebook 09](notebooks/09.Metadata_Enrichment_with_LLMs.ipynb) for detailed examples. ### Downloading supplementary files from GEO $ pysradb download -g GSE161707 ### Downloading an entire SRA/ENA project (multithreaded) `pysradb` makes it super easy to download datasets from SRA in parallel: Using 8 threads to download: $ pysradb download -y -t 8 --out-dir ./pysradb_downloads -p SRP063852 Downloads are organized by `SRP/SRX/SRR` mimicking the hierarchy of SRA projects. ## Publication > [pysradb: A Python package to query next-generation sequencing > metadata and data from NCBI Sequence Read > Archive](https://f1000research.com/articles/8-532/v1) > > Presentation slides from BOSC (ISMB-ECCB) 2019: > ## Citation Choudhary, Saket. \"pysradb: A Python Package to Query next-Generation Sequencing Metadata and Data from NCBI Sequence Read Archive.\" F1000Research, vol. 8, F1000 (Faculty of 1000 Ltd), Apr. 2019, p. 532 () @article{Choudhary2019, doi = {10.12688/f1000research.18676.1}, url = {https://doi.org/10.12688/f1000research.18676.1}, year = {2019}, month = apr, publisher = {F1000 (Faculty of 1000 Ltd)}, volume = {8}, pages = {532}, author = {Saket Choudhary}, title = {pysradb: A {P}ython package to query next-generation sequencing metadata and data from {NCBI} {S}equence {R}ead {A}rchive}, journal = {F1000Research} } Zenodo archive: Zenodo DOI: 10.5281/zenodo.2306881 ## Questions? Open an [issue](https://github.com/saketkc/pysradb/issues). ================================================ FILE: docs/Makefile ================================================ # Minimal makefile for Sphinx documentation # # You can set these variables from the command line. SPHINXOPTS = SPHINXBUILD = python -msphinx SPHINXPROJ = pysradb SOURCEDIR = . BUILDDIR = _build # Put it first so that "make" without argument is like "make help". help: @$(SPHINXBUILD) -M help "$(SOURCEDIR)" "$(BUILDDIR)" $(SPHINXOPTS) $(O) .PHONY: help Makefile # Catch-all target: route all unknown targets to Sphinx using the new # "make mode" option. $(O) is meant as a shortcut for $(SPHINXOPTS). %: Makefile @$(SPHINXBUILD) -M $@ "$(SOURCEDIR)" "$(BUILDDIR)" $(SPHINXOPTS) $(O) ================================================ FILE: docs/_static/copy-button.js ================================================ // Add copy button to code blocks document.addEventListener('DOMContentLoaded', function() { // SVG icon for clipboard const clipboardIcon = ``; // SVG icon for checkmark const checkmarkIcon = ``; // Find all code input blocks (from notebooks and regular code blocks) // Strategy: // 1. For notebooks: explicitly target pre tags inside input_area // 2. For regular docs: target all highlight divs, then filter with skip conditions let codeBlocks = document.querySelectorAll('div.input_area > div.highlight > pre'); // Also get regular documentation code blocks const docBlocks = document.querySelectorAll('div.highlight > pre'); // Combine and deduplicate codeBlocks = Array.from(codeBlocks).concat( Array.from(docBlocks).filter(block => { // Skip if already in notebook input_area if (block.closest('div.input_area')) return false; // Skip if in prompt or output if (block.closest('.prompt')) return false; if (block.closest('.nboutput')) return false; if (block.closest('.output_area')) return false; return true; }) ); codeBlocks.forEach(function(codeBlock) { // Don't add button if already present if (codeBlock.querySelector('.copy-button') || codeBlock.parentElement.querySelector('.copy-button')) { return; } // Create copy button const button = document.createElement('button'); button.className = 'copy-button'; button.innerHTML = clipboardIcon; button.title = 'Copy code to clipboard'; // Style the button button.style.cssText = ` position: absolute; top: 0.5rem; right: 0.5rem; padding: 0.4rem; background-color: rgba(0, 0, 0, 0.3); color: white; border: 1px solid rgba(255, 255, 255, 0.3); border-radius: 0.25rem; cursor: pointer; display: flex; align-items: center; justify-content: center; z-index: 1; transition: all 0.2s ease; width: 28px; height: 28px; padding: 0; `; // Add hover effect button.onmouseover = function() { this.style.backgroundColor = 'rgba(0, 0, 0, 0.5)'; }; button.onmouseout = function() { this.style.backgroundColor = 'rgba(0, 0, 0, 0.3)'; }; // Make pre block relative positioned codeBlock.style.position = 'relative'; // Add click event button.addEventListener('click', function() { const code = codeBlock.querySelector('code'); const text = code ? code.textContent : codeBlock.textContent; // Copy to clipboard navigator.clipboard.writeText(text).then(function() { // Change button icon and color temporarily const originalHTML = button.innerHTML; button.innerHTML = checkmarkIcon; button.style.backgroundColor = 'rgba(34, 197, 94, 0.7)'; setTimeout(function() { button.innerHTML = originalHTML; button.style.backgroundColor = 'rgba(0, 0, 0, 0.3)'; }, 2000); }).catch(function(err) { console.error('Failed to copy:', err); }); }); // Append button to code block codeBlock.appendChild(button); }); }); ================================================ FILE: docs/_static/custom.css ================================================ /* Override Pygments code block background color for light mode */ .highlight { background: #f5f5f5 !important; } /* Ensure code block background uses our color */ .highlight pre { background: #f5f5f5 !important; } /* Override inline code highlighting */ .highlighttable { background: #f5f5f5 !important; } .highlighttable td.linenos { background: #f5f5f5 !important; } /* Dark mode overrides */ [data-theme="dark"] .highlight { background: #1e293b !important; } [data-theme="dark"] .highlight pre { background: #1e293b !important; } [data-theme="dark"] .highlighttable { background: #1e293b !important; } [data-theme="dark"] .highlighttable td.linenos { background: #1e293b !important; } ================================================ FILE: docs/authors.md ================================================ # Credits ## Contributors - [Boshen Yan](https://github.com/bscrow) - [Maarten van der Sande](https://github.com/Maarten-vd-Sande) - [Dibya Gautam](https://github.com/dibyaaaaax) - [Marius van den Beek](https://github.com/mvdbeek) - [Devang Thakkar](https://github.com/DevangThakkar) ## Maintainer - Saket Choudhary \<\> ================================================ FILE: docs/case_studies.md ================================================ # Case Studies ## Case Study 1 Consider a scenario where somone is interested in searching for single-cell RNA-seq datasets. In particular, the interest is in studying retina: $ pysradb search --query "single-cell rna-seq retina" study_accession experiment_accession experiment_title sample_taxon_id sample_scientific_name experiment_library_strategy experiment_library_source experiment_library_selection sample_accession sample_alias experiment_instrument_model pool_member_spots run_1_size run_1_accession run_1_total_spots run_1_total_bases SRP299803 SRX9756769 GSM4995565: scATAC_Retina_WT; Mus musculus; ATAC-seq 10090 Mus musculus ATAC-seq GENOMIC other SRS7946094 GSM4995565 Illumina NovaSeq 6000 55435867 2637580797 SRR13329759 55435867 6874047508 SRP299803 SRX9756768 GSM4995564: scRNA_Retina_VSX2SEKO_Rep2; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS7946093 GSM4995564 Illumina NovaSeq 6000 96123725 4107807391 SRR13329758 96123725 12688331700 SRP299803 SRX9756767 GSM4995563: scRNA_Retina_VSX2SEKO_Rep1; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS7946092 GSM4995563 Illumina NovaSeq 6000 94345783 4056010488 SRR13329757 94345783 12453643356 SRP299803 SRX9756766 GSM4995562: scRNA_Retina_WT_Rep2; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS7946091 GSM4995562 Illumina NovaSeq 6000 99487074 4240172698 SRR13329756 99487074 13132293768 SRP299803 SRX9756765 GSM4995561: scRNA_Retina_WT_Rep1; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS7946090 GSM4995561 Illumina NovaSeq 6000 88048461 3817540828 SRR13329755 88048461 11622396852 SRP257758 SRX9537754 GSM4916438: Pou4f2-tdTomato/+ E17.5 scRNA-seq; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS7743995 GSM4916438 Illumina HiSeq 2500 364683840 8246658699 SRR13091939 364683840 32456861760 SRP257758 SRX9537753 GSM4916437: Atoh7-zsGreen/lacZ E17.5 scRNA-seq; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS7743994 GSM4916437 Illumina HiSeq 2500 530456067 11895864680 SRR13091938 530456067 47210589963 SRP257758 SRX9537752 GSM4916436: Atoh7-zsGreen/+ E17.5 scRNA-seq; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS7743993 GSM4916436 Illumina HiSeq 2500 389849416 8671923722 SRR13091937 389849416 34696598024 SRP257758 SRX9537751 GSM4916435: Atoh7-zsGreen/lacZ E14.5 scRNA-seq; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS7743992 GSM4916435 Illumina HiSeq 2500 328878355 7875737709 SRR13091936 328878355 29270173595 SRP257758 SRX9537750 GSM4916434: Atoh7-zsGreen/+ E14.5 scRNA-seq; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA SRS7743991 GSM4916434 Illumina HiSeq 2500 522040155 12760941656 SRR13091935 522040155 46461573795 ERP118072 ERX3614517 NextSeq 500 sequencing; 3' mRNA-seq of protrusions and cell bodies of BJ, PC-3M, RPE-1, U-87 and WM-266.4 cells 9606 Homo sapiens OTHER TRANSCRIPTOMIC Oligo-dT ERS3920269 SAMEA6120013 NextSeq 500 5818488 43355751 ERR3619129 1457318 109897743 ERP118072 ERX3614516 NextSeq 500 sequencing; 3' mRNA-seq of protrusions and cell bodies of BJ, PC-3M, RPE-1, U-87 and WM-266.4 cells 9606 Homo sapiens OTHER TRANSCRIPTOMIC Oligo-dT ERS3920268 SAMEA6120012 NextSeq 500 5422441 40645479 ERR3619125 1359663 102468758 SRP288715 SRX9369597 RPE1_SS119_p10 9606 Homo sapiens OTHER GENOMIC other SRS7591452 RPE1_SS119_p10.bam Illumina HiSeq 2000 5062938 88426773 SRR12904705 5062938 202517520 SRP288715 SRX9369596 RPE1_SS119_p0 9606 Homo sapiens OTHER GENOMIC other SRS7591451 RPE1_SS119_p0.bam Illumina HiSeq 2000 978835 19219630 SRR12904706 978835 39153400 SRP288715 SRX9369595 RPE1_SS111_p10 9606 Homo sapiens OTHER GENOMIC other SRS7591450 RPE1_SS111_p10.bam Illumina HiSeq 2000 6205827 108129733 SRR12904707 6205827 248233080 SRP288715 SRX9369594 RPE1_SS111_p0 9606 Homo sapiens OTHER GENOMIC other SRS7591449 RPE1_SS111_p0.bam Illumina HiSeq 2000 928703 18488436 SRR12904708 928703 37148120 SRP288715 SRX9369593 RPE1_SS51_p10 9606 Homo sapiens OTHER GENOMIC other SRS7591448 RPE1_SS51_p10.bam Illumina HiSeq 2000 6088168 106065537 SRR12904709 6088168 243526720 SRP288715 SRX9369592 RPE1_SS51_p0 9606 Homo sapiens OTHER GENOMIC other SRS7591447 RPE1_SS51_p0.bam Illumina HiSeq 2000 1624227 30610200 SRR12904710 1624227 64969080 SRP288715 SRX9369591 RPE1_SS48_p10 9606 Homo sapiens OTHER GENOMIC other SRS7591446 RPE1_SS48_p10.bam Illumina HiSeq 2000 8117881 139408135 SRR12904711 8117881 324715240 SRP288715 SRX9369590 RPE1_SS48_p0 9606 Homo sapiens OTHER GENOMIC other SRS7591445 RPE1_SS48_p0.bam Illumina HiSeq 2000 776140 15821200 SRR12904712 776140 31045600 By default search returns first 20 hits. `SRP299803` seems like a project of interest. However the information outputted by the `search` command is pretty limited. We want to look up more detailed information about this project: $ pysradb metadata SRP299803 | head study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_name library_strategy library_source library_selection library_layout sample_accession sample_title instrument instrument_model instrument_model_desc total_spots total_size run_accession run_total_spots run_total_bases SRP299803 SRX9756769 GSM4995565: scATAC_Retina_WT; Mus musculus; ATAC-seq GSM4995565: scATAC_Retina_WT; Mus musculus; ATAC-seq 10090 Mus musculus ATAC-seq GENOMIC other PAIRED SRS7946094 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 55435867 2637580797 SRR13329759 55435867 6874047508 SRP299803 SRX9756768 GSM4995564: scRNA_Retina_VSX2SEKO_Rep2; Mus musculus; RNA-Seq GSM4995564: scRNA_Retina_VSX2SEKO_Rep2; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA PAIRED SRS7946093 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 96123725 4107807391 SRR13329758 96123725 12688331700 SRP299803 SRX9756767 GSM4995563: scRNA_Retina_VSX2SEKO_Rep1; Mus musculus; RNA-Seq GSM4995563: scRNA_Retina_VSX2SEKO_Rep1; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA PAIRED SRS7946092 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 94345783 4056010488 SRR13329757 94345783 12453643356 SRP299803 SRX9756766 GSM4995562: scRNA_Retina_WT_Rep2; Mus musculus; RNA-Seq GSM4995562: scRNA_Retina_WT_Rep2; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA PAIRED SRS7946091 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 99487074 4240172698 SRR13329756 99487074 13132293768 SRP299803 SRX9756765 GSM4995561: scRNA_Retina_WT_Rep1; Mus musculus; RNA-Seq GSM4995561: scRNA_Retina_WT_Rep1; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA PAIRED SRS7946090 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 88048461 3817540828 SRR13329755 88048461 11622396852 It is also possible to get more detailed information using the `--detailed` flag: $ pysradb metadata SRP075720 --detailed run_accession study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_name library_strategy library_source library_selection library_layout sample_accession sample_title instrument instrument_model instrument_model_desc total_spots total_size run_total_spots run_total_bases run_alias sra_url experiment_alias source_name strain background genotype tissue/cell type molecule subtype ena_fastq_http ena_fastq_http_1 ena_fastq_http_2 ena_fastq_ftp ena_fastq_ftp_1 ena_fastq_ftp_2 SRR13329759 SRP299803 SRX9756769 GSM4995565: scATAC_Retina_WT; Mus musculus; ATAC-seq GSM4995565: scATAC_Retina_WT; Mus musculus; ATAC-seq 10090 Mus musculus ATAC-seq GENOMIC other PAIRED SRS7946094 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 55435867 2637580797 55435867 6874047508 GSM4995565_r1 https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/013017/SRR13329759 GSM4995565 wild type_retina C57BL/6 wild type retina http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/059/SRR13329759/SRR13329759_1.fastq.gz http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/059/SRR13329759/SRR13329759_2.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/059/SRR13329759/SRR13329759_1.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/059/SRR13329759/SRR13329759_2.fastq.gz SRR13329758 SRP299803 SRX9756768 GSM4995564: scRNA_Retina_VSX2SEKO_Rep2; Mus musculus; RNA-Seq GSM4995564: scRNA_Retina_VSX2SEKO_Rep2; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA PAIRED SRS7946093 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 96123725 4107807391 96123725 12688331700 GSM4995564_r1 https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/013017/SRR13329758 GSM4995564 Vsx2SE Δ/Δ_retina C57BL/6 Vsx2SE {delta}/{delta} retina 3' RNA http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/058/SRR13329758/SRR13329758_1.fastq.gz http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/058/SRR13329758/SRR13329758_2.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/058/SRR13329758/SRR13329758_1.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/058/SRR13329758/SRR13329758_2.fastq.gz SRR13329757 SRP299803 SRX9756767 GSM4995563: scRNA_Retina_VSX2SEKO_Rep1; Mus musculus; RNA-Seq GSM4995563: scRNA_Retina_VSX2SEKO_Rep1; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA PAIRED SRS7946092 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 94345783 4056010488 94345783 12453643356 GSM4995563_r1 https://sra-download.ncbi.nlm.nih.gov/traces/sra79/SRR/013017/SRR13329757 GSM4995563 Vsx2SE Δ/Δ_retina C57BL/6 Vsx2SE {delta}/{delta} retina 3' RNA http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/057/SRR13329757/SRR13329757_1.fastq.gz http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/057/SRR13329757/SRR13329757_2.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/057/SRR13329757/SRR13329757_1.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/057/SRR13329757/SRR13329757_2.fastq.gz SRR13329756 SRP299803 SRX9756766 GSM4995562: scRNA_Retina_WT_Rep2; Mus musculus; RNA-Seq GSM4995562: scRNA_Retina_WT_Rep2; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA PAIRED SRS7946091 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 99487074 4240172698 99487074 13132293768 GSM4995562_r1 https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/013017/SRR13329756 GSM4995562 wild type_retina C57BL/6 wild type retina 3' RNA http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/056/SRR13329756/SRR13329756_1.fastq.gz http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/056/SRR13329756/SRR13329756_2.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/056/SRR13329756/SRR13329756_1.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/056/SRR13329756/SRR13329756_2.fastq.gz SRR13329755 SRP299803 SRX9756765 GSM4995561: scRNA_Retina_WT_Rep1; Mus musculus; RNA-Seq GSM4995561: scRNA_Retina_WT_Rep1; Mus musculus; RNA-Seq 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC cDNA PAIRED SRS7946090 Illumina NovaSeq 6000 Illumina NovaSeq 6000 ILLUMINA 88048461 3817540828 88048461 11622396852 GSM4995561_r1 https://sra-download.ncbi.nlm.nih.gov/traces/sra72/SRR/013017/SRR13329755 GSM4995561 wild type_retina C57BL/6 wild type retina 3' RNA http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/055/SRR13329755/SRR13329755_1.fastq.gz http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR133/055/SRR13329755/SRR13329755_2.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/055/SRR13329755/SRR13329755_1.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR133/055/SRR13329755/SRR13329755_2.fastq.gz Having made sure this dataset is indeed of interest, we want to save some work and see if the processed dataset has been made available on GEO by the authors: $ pysradb srp-to-gse SRP299803 study_accession study_alias SRP299803 GSE164044 So indeed a GEO project exists for this SRA dataset. Notice, that the GEO information was also visible in the `metadata --detailed` operation. Assume we were in posession of the GSM id of one of the experiments to start off with, say `GSE4995565`. Starting from this GSM id, we want to get the following information: - SRP id of the project - GSE id of the project - SRX id of the experiment - SRR id(s) corresponding to the experiment Get SRP id: $ pysradb gsm-to-srp GSM4995565 experiment_alias study_accession GSM4995565 SRP299803 Get GSE id: $ pysradb gsm-to-gse GSM4995565 experiment_alias study_alias GSM4995565 GSE164044 Get SRX id: $ pysradb gsm-to-srx GSM4995565 experiment_alias experiment_accession GSM4995565 SRX9756769 Getting SRR id(s): $ pysradb gsm-to-srr GSM4995565 experiment_alias run_accession GSM4995565 SRR13329759 ## Case Study 2 Our first case study included metadata search. Next, we explore downloading datasets. We have a SRP id to start off with: `SRP000941`. We want to quickly checkout its contents: $ pysradb metadata SRP000941 --detailed| head study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_name library_strategy library_source library_selection library_layout sample_accession sample_title instrument instrument_model instrument_model_desc total_spots total_size run_accession run_total_spots run_total_bases SRP000941 SRX056722 Reference Epigenome: ChIP-Seq Analysis of H3K27ac in hESC H1 Cells Reference Epigenome: ChIP-Seq Analysis of H3K27ac in hESC H1 Cells 9606 Homo sapiens SAK270 ChIP-Seq GENOMIC ChIP SINGLE SRS184466 Illumina HiSeq 2000 Illumina HiSeq 2000 ILLUMINA 26900401 531654480 SRR179707 26900401 807012030 SRP000941 SRX027889 Reference Epigenome: ChIP-Seq Analysis of H2AK5ac in hESC Cells Reference Epigenome: ChIP-Seq Analysis of H2AK5ac in hESC Cells 9606 Homo sapiens SAK201 ChIP-Seq GENOMIC ChIP SINGLE SRS116481 Illumina Genome Analyzer II Illumina Genome Analyzer II ILLUMINA 37528590 779578968 SRR067978 37528590 1351029240 SRP000941 SRX027888 Reference Epigenome: ChIP-Seq Input from hESC H1 Cells Reference Epigenome: ChIP-Seq Input from hESC H1 Cells 9606 Homo sapiens LLH1U ChIP-Seq GENOMIC RANDOM SINGLE SRS116483 Illumina Genome Analyzer II Illumina Genome Analyzer II ILLUMINA 13603127 3232309537 SRR067977 13603127 489712572 SRP000941 SRX027887 Reference Epigenome: ChIP-Seq Input from hESC H1 Cells Reference Epigenome: ChIP-Seq Input from hESC H1 Cells 9606 Homo sapiens DM219 ChIP-Seq GENOMIC RANDOM SINGLE SRS116562 Illumina Genome Analyzer II Illumina Genome Analyzer II ILLUMINA 22430523 506327844 SRR067976 22430523 807498828 This project is a collection of multiple assays. $ pysradb metadata SRP000941 --detailed | tr -s ' ' | cut -f5 -d ' ' | sort | uniq -c 999 Bisulfite-Seq 768 ChIP-Seq 1 library_strategy 121 OTHER 353 RNA-Seq 28 WGS We want to however only download `RNA-seq` samples: $ pysradb metadata SRP000941 --detailed | grep 'study\|RNA-Seq' | pysradb download This will download all `RNA-seq` samples coming from this project using `aspera-client`, if available. Alternatively, it can also use `wget`. Downloading an entire project is easy: $ pysradb download -p SRP000941 Downloads are organized by `SRP/SRX/SRR` mimicking the hiererachy of SRA projects. ================================================ FILE: docs/cmdline.md ================================================ # CLI $ pysradb usage: pysradb [-h] [--version] [--citation] {metadata,download,search,gse-to-gsm,gse-to-srp,gsm-to-gse,gsm-to-srp,gsm-to-srr,gsm-to-srs,gsm-to-srx,srp-to-gse,srp-to-srr,srp-to-srs,srp-to-srx,srr-to-gsm,srr-to-srp,srr-to-srs,srr-to-srx,srs-to-gsm,srs-to-srx,srx-to-srp,srx-to-srr,srx-to-srs,geo-matrix,srp-to-pmid,gse-to-pmid,pmid-to-gse,pmid-to-srp,pmc-to-identifiers,pmid-to-identifiers,doi-to-gse,doi-to-srp,doi-to-identifiers} ... pysradb: Query NGS metadata and data from NCBI Sequence Read Archive. Citation: 10.12688/f1000research.18676.1 optional arguments: -h, --help show this help message and exit --version show program's version number and exit --citation how to cite subcommands: {metadata,download,search,gse-to-gsm,gse-to-srp,gsm-to-gse,gsm-to-srp,gsm-to-srr,gsm-to-srs,gsm-to-srx,srp-to-gse,srp-to-srr,srp-to-srs,srp-to-srx,srr-to-gsm,srr-to-srp,srr-to-srs,srr-to-srx,srs-to-gsm,srs-to-srx,srx-to-srp,srx-to-srr,srx-to-srs,geo-matrix,srp-to-pmid,gse-to-pmid,pmid-to-gse,pmid-to-srp,pmc-to-identifiers,pmid-to-identifiers,doi-to-gse,doi-to-srp,doi-to-identifiers} metadata Fetch metadata for SRA project (SRPnnnn) download Download SRA project (SRPnnnn) search Search SRA/ENA for matching text gse-to-gsm Get GSM for a GSE gse-to-srp Get SRP for a GSE gsm-to-gse Get GSE for a GSM gsm-to-srp Get SRP for a GSM gsm-to-srr Get SRR for a GSM gsm-to-srs Get SRS for a GSM gsm-to-srx Get SRX for a GSM srp-to-gse Get GSE for a SRP srp-to-srr Get SRR for a SRP srp-to-srs Get SRS for a SRP srp-to-srx Get SRX for a SRP srr-to-gsm Get GSM for a SRR srr-to-srp Get SRP for a SRR srr-to-srs Get SRS for a SRR srr-to-srx Get SRX for a SRR srs-to-gsm Get GSM for a SRS srs-to-srx Get SRX for a SRS srx-to-srp Get SRP for a SRX srx-to-srr Get SRR for a SRX srx-to-srs Get SRS for a SRX geo-matrix Download and parse GEO Matrix files srp-to-pmid Get PMIDs for SRP accessions gse-to-pmid Get PMIDs for GSE accessions pmid-to-gse Get GSE accessions from PMIDs pmid-to-srp Get SRP accessions from PMIDs pmc-to-identifiers Extract database identifiers from PMC articles pmid-to-identifiers Extract database identifiers from PubMed articles doi-to-gse Get GSE accessions from DOIs doi-to-srp Get SRP accessions from DOIs doi-to-identifiers Extract database identifiers from articles via DOI ## Enriching metadata Extract standardized biological metadata from SRA/GEO datasets using LLMs. ### Quickstart ```bash from pysradb import SRAweb client = SRAweb() df = client.metadata("GSE286254", detailed=True, enrich=True) # Returns original + 9 enriched columns (might not always be complete): # guessed_organ, guessed_tissue, guessed_anatomical_system, # guessed_cell_type, guessed_disease, guessed_sex, # guessed_development_stage, guessed_assay, guessed_organism ``` ### Prerequisites Install Ollama: ```bash ollama pull phi3 ``` ### Advanced Usage ```bash # Use different model df = client.metadata("GSE286254", detailed=True, enrich=True, enrich_backend="ollama/llama3.2") # Manual enrichment with custom settings from pysradb.metadata_enrichment import create_metadata_extractor, load_ontology_reference # LLM-based extraction extractor_llm = create_metadata_extractor(method="llm", backend="ollama/phi3") df_enriched = extractor_llm.enrich_dataframe(df, prefix="guessed_") # Embedding-based extraction (faster, offline) ontology_ref = load_ontology_reference() extractor_emb = create_metadata_extractor( method="embedding", model="FremyCompany/BioLORD-2023", reference_categories=ontology_ref ) df_enriched = extractor_emb.enrich_dataframe(df, prefix="guessed_") ``` See [Notebook 09](https://github.com/saketkc/pysradb/blob/develop/notebooks/09.Metadata_Enrichment_with_LLMs.ipynb) for detailed examples. ## Getting metadata for a SRA project (SRP) The most basic information associated with any SRA project is its list of experiments and run accessions. $ pysradb metadata SRP098789 study_accession experiment_accession sample_accession run_accession SRP098789 SRX2536403 SRS1956353 SRR5227288 SRP098789 SRX2536404 SRS1956354 SRR5227289 SRP098789 SRX2536405 SRS1956355 SRR5227290 SRP098789 SRX2536406 SRS1956356 SRR5227291 SRP098789 SRX2536407 SRS1956357 SRR5227292 SRP098789 SRX2536408 SRS1956358 SRR5227293 SRP098789 SRX2536409 SRS1956359 SRR5227294 Listing SRX and SRRs for a SRP is often not useful. We might want to take a quick look at the metadata associated with the samples: $ pysradb metadata SRP098789 study_accession experiment_accession sample_accession run_accession sample_attribute SRP098789 SRX2536403 SRS1956353 SRR5227288 source_name: Huh7_1.5 µM PF-067446846_10 min_ribo-seq || cell line: Huh7 || treatment time: 10 min || library type: ribo-seq SRP098789 SRX2536404 SRS1956354 SRR5227289 source_name: Huh7_1.5 µM PF-067446846_10 min_ribo-seq || cell line: Huh7 || treatment time: 10 min || library type: ribo-seq SRP098789 SRX2536405 SRS1956355 SRR5227290 source_name: Huh7_1.5 µM PF-067446846_10 min_ribo-seq || cell line: Huh7 || treatment time: 10 min || library type: ribo-seq SRP098789 SRX2536406 SRS1956356 SRR5227291 source_name: Huh7_0.3 µM PF-067446846_10 min_ribo-seq || cell line: Huh7 || treatment time: 10 min || library type: ribo-seq SRP098789 SRX2536407 SRS1956357 SRR5227292 source_name: Huh7_0.3 µM PF-067446846_10 min_ribo-seq || cell line: Huh7 || treatment time: 10 min || library type: ribo-seq SRP098789 SRX2536408 SRS1956358 SRR5227293 source_name: Huh7_0.3 µM PF-067446846_10 min_ribo-seq || cell line: Huh7 || treatment time: 10 min || library type: ribo-seq The example here came from a Ribosome profiling study and consists of a collection of both Ribo-seq and RNA-seq samples. We can filter out only the RNA-seq samples: $ pysradb metadata SRP098789 --detailed | grep 'study|RNA-Seq' SRP098789 SRX2536422 SRR5227307 RNA-Seq SINGLE - SRP098789 SRX2536424 SRR5227309 RNA-Seq SINGLE - SRP098789 SRX2536426 SRR5227311 RNA-Seq SINGLE - SRP098789 SRX2536428 SRR5227313 RNA-Seq SINGLE - A more complicated example will consist of multiple assays. For example \`SRP000941\`: $ pysradb metadata SRP000941 --detailed | tr -s ' ' | cut -f5 -d ' ' | sort | uniq -c 999 Bisulfite-Seq 768 ChIP-Seq 1 library_strategy 121 OTHER 353 RNA-Seq 28 WGS ## Enriching metadata You can enrich metadata with standardized biological attributes using biomedical-specialized LLMs through the `--enrich` flag: ### Basic enrichment (using default backend) $ pysradb metadata GSE286254 --detailed --enrich The default uses **Meditron** (7B parameters, trained on medical literature and guidelines), which is optimized for biomedical text understanding. This returns the original metadata plus 9 enriched columns: - `guessed_organ` - `guessed_tissue` - `guessed_anatomical_system` - `guessed_cell_type` - `guessed_disease` - `guessed_sex` - `guessed_development_stage` - `guessed_assay` - `guessed_organism` ### Using alternative biomedical backends $ pysradb metadata GSE286254 --detailed --enrich --enrich-backend ollama/openbiollm-8b Available biomedical backends: - `ollama/meditron` (default, 7B - optimized for medical text) - `ollama/openbiollm-8b` (8B - trained on 500k+ biomedical entries, superior biomedical performance) Both models are specialized for biomedical and clinical text understanding, making them ideal for SRA metadata enrichment. For more details on enrichment features and prerequisites, see the [Enriching metadata](#enriching-metadata) section above. ## Experiment accessions for a project (SRP =\> SRX) A frequently encountered task involves getting all the experiments (SRX) for a particular study accession (SRP). Consider project \`SRP048759\`: $ pysradb srp-to-srx SRP048759 ## Sample accessions for a project (SRP =\> SRS) Each experiment involves one or multiple biological samples (SRS), that are put through different experiments (SRX). $ pysradb srp-to-srs --detailed SRP048759 study_accession sample_accession SRP048759 SRS718878 SRP048759 SRS718879 SRP048759 SRS718880 SRP048759 SRS718881 SRP048759 SRS718882 SRP048759 SRS718883 SRP048759 SRS718884 SRP048759 SRS718885 SRP048759 SRS718886 This is very limited information. It can again be detailed out using the [\--detailed]{.title-ref} flag: $ pysradb srp-to-srs --detailed SRP048759 study_accession sample_accession experiment_accession run_accession study_alias sample_alias experiment_alias run_alias SRP048759 SRS718878 SRX729552 SRR1608490 GSE62190 GSM1521543 GSM1521543 GSM1521543_r1 SRP048759 SRS718878 SRX729552 SRR1608491 GSE62190 GSM1521543 GSM1521543 GSM1521543_r2 SRP048759 SRS718878 SRX729552 SRR1608492 GSE62190 GSM1521543 GSM1521543 GSM1521543_r3 SRP048759 SRS718878 SRX729552 SRR1608493 GSE62190 GSM1521543 GSM1521543 GSM1521543_r4 SRP048759 SRS718879 SRX729553 SRR1608494 GSE62190 GSM1521544 GSM1521544 GSM1521544_r1 SRP048759 SRS718879 SRX729553 SRR1608495 GSE62190 GSM1521544 GSM1521544 GSM1521544_r2 ## Run accessions for experiments (SRX =\> SRR) Another frequently encountered task involves fetching the run accessions (SRR) for a particular experiment (SRX). Consider experiments [SRX217956]{.title-ref} and [SRX2536403]{.title-ref}. We want to be able to resolve the run accessions for these experiments: $ pysradb srx-to-srr SRX217956 SRX2536403 --detailed experiment_accession run_accession study_accession sample_attribute SRX217956 SRR649752 SRP017942 source_name: 3T3 cells || treatment: control || cell line: 3T3 cells || assay type: Riboseq SRX2536403 SRR5227288 SRP098789 source_name: Huh7_1.5 µM PF-067446846_10 min_ribo-seq || cell line: Huh7 || treatment time: 10 min || library type: ribo-seq ## Experiment accessions for runs (SRR =\> SRX) For fetching experiment accessions (SRX) for one or multiple run accessions (SRR): $ pysradb srr-to-srx SRR5227288 SRR649752 --detailed run_accession study_accession experiment_accession sample_attribute SRR649752 SRP017942 SRX217956 source_name: 3T3 cells || treatment: control || cell line: 3T3 cells || assay type: Riboseq SRR5227288 SRP098789 SRX2536403 source_name: Huh7_1.5 µM PF-067446846_10 min_ribo-seq || cell line: Huh7 || treatment time: 10 min || library type: ribo-seq ## Downaloading entire project $ pysradb metadata --detailed SRP098789 | pysradb download ## GEO accessions for studies (SRP =\> GSE) $ pysradb srp-to-gse SRP090415 study_accession study_alias SRP090415 GSE87328 But not all SRPs will have an associated GEO id (GSE): $ pysradb srp-to-gse SRP029589 study_accession study_alias SRP029589 PRJNA218051 ## Converting GSM to SRP $ pysradb gsm-to-srp GSM2177186 experiment_alias study_accession GSM2177186 SRP075720 ## Converting GSM to GSE $ pysradb gsm-to-gse GSM2177186 experiment_alias study_alias GSM2177186 GSE81903 ## Converting GSM to SRX $ pysradb gsm-to-srx GSM2177186 experiment_alias experiment_accession GSM2177186 SRX1800089 ## Converting GSM to SRR $ pysradb gsm-to-srr GSM2177186 experiment_alias run_accession GSM2177186 SRR3587529 ## SRA accessions for GEO studies (GSE =\> SRP) $ pysradb gse-to-srp GSE87328i study_alias study_accession GSE87328 SRP090415 ## Converting SRP to PMID $ pysradb srp-to-pmid SRP045778 srp_accession bioproject pmid SRP045778 PRJNA257197 27373336 ## Converting GSE to PMID $ pysradb gse-to-pmid GSE253406 gse_accession pmid GSE253406 39528918 ## Extracting identifiers from PMC/DOI Extract database identifiers (GSE, PRJNA, SRP, etc.) from PubMed Central articles or DOIs. ### Get all identifiers from a PMID $ pysradb pmid-to-identifiers 39528918 pmid pmc_id gse_ids prjna_ids srp_ids 39528918 PMC10802650 GSE253406 PRJNA1058002 SRP484103 ### Get only GSE or SRP from PMID $ pysradb pmid-to-gse 39528918 pmid pmc_id gse_ids 39528918 PMC10802650 GSE253406 $ pysradb pmid-to-srp 39528918 pmid pmc_id srp_ids 39528918 PMC10802650 SRP484103 ### Extract from DOI $ pysradb doi-to-identifiers 10.12688/f1000research.18676.1 doi pmid pmc_id gse_ids srp_ids 10.12688/f1000research.18676.1 30873266 PMC6411813 GSE... SRP... ### Extract from PMC ID $ pysradb pmc-to-identifiers PMC10802650 pmc_id gse_ids prjna_ids srp_ids PMC10802650 GSE253406 PRJNA1058002 SRP484103 ## Downloading supplementary files from GEO $ pysradb download -g GSE161707 ## Downloading an entire SRA/ENA project (multithreaded) `pysradb` makes it super easy to download datasets from SRA in parallel: Using 8 threads to download: $ pysradb download -y -t 8 --out-dir ./pysradb_downloads -p SRP063852 Downloads are organized by `SRP/SRX/SRR` mimicking the hierarchy of SRA projects. ================================================ FILE: docs/commands.rst ================================================ API Documentation ================= See :doc:`pysradb` for the Python API reference documentation. ================================================ FILE: docs/conf.py ================================================ #!/usr/bin/env python # -*- coding: utf-8 -*- # # pysradb documentation build configuration file, created by # sphinx-quickstart on Fri Jun 9 13:47:02 2017. # # This file is execfile()d with the current directory set to its # containing dir. # # Note that not all possible configuration values are present in this # autogenerated file. # # All configuration values have a default; values that are commented out # serve to show the default. # If extensions (or modules to document with autodoc) are in another # directory, add these directories to sys.path here. If the directory is # relative to the documentation root, use os.path.abspath to make it # absolute, like shown here. # import os import sys # import guzzle_sphinx_theme import pysradb autodoc_mock_imports = ["xmltodict", "numpy", "pandas", "requests", "tqdm"] sys.path.insert(0, os.path.abspath("..")) # -- General configuration --------------------------------------------- # If your documentation needs a minimal Sphinx version, state it here. # # needs_sphinx = '1.0' # Add any Sphinx extension module names here, as strings. They can be # extensions coming with Sphinx (named 'sphinx.ext.*') or your custom ones. extensions = [ "IPython.sphinxext.ipython_directive", "IPython.sphinxext.ipython_console_highlighting", "sphinx.ext.mathjax", "sphinx.ext.autodoc", "sphinx.ext.autosummary", "sphinx.ext.doctest", "sphinx.ext.viewcode", "sphinx.ext.inheritance_diagram", "numpydoc", "sphinx_tabs.tabs", "sphinx_panels", "sphinxcontrib.gtagjs", "myst_parser", "nbsphinx", ] gtagjs_ids = [ "G-CKQZFCEENZ", ] panels_add_bootstrap_css = False # Add any paths that contain templates here, relative to this directory. templates_path = ["_templates"] # The suffix(es) of source filenames. # You can specify multiple suffix as a list of string: # source_suffix = [".rst", ".md"] # source_suffix = ".md" # The master toctree document. master_doc = "index" # General information about the project. project = "pysradb" copyright = "2023, Saket Choudhary" author = "Saket Choudhary" # The version info for the project you're documenting, acts as replacement # for |version| and |release|, also used in various other places throughout # the built documents. # # The short X.Y version. version = pysradb.__version__ # The full version, including alpha/beta/rc tags. release = pysradb.__version__ # The language for content autogenerated by Sphinx. Refer to documentation # for a list of supported languages. # # This is also used if you do content translation via gettext catalogs. # Usually you set "language" from the command line for these cases. language = "en" # List of patterns, relative to source directory, that match files and # directories to ignore when looking for source files. # This patterns also effect to html_static_path and html_extra_path exclude_patterns = ["_build", "Thumbs.db", ".DS_Store"] # The name of the Pygments (syntax highlighting) style to use. pygments_style = "sphinx" # If true, `todo` and `todoList` produce output, else they produce nothing. todo_include_todos = False # -- Options for HTML output ------------------------------------------- # The theme to use for HTML and HTML Help pages. See the documentation for # a list of builtin themes. # html_theme = "furo" # Theme options are theme-specific and customize the look and feel of a # theme further. For a list of options available for each theme, see the # documentation. # html_theme_options = { "light_css_variables": { "color-brand-primary": "#0066cc", "color-brand-content": "#0066cc", "color-code-background": "#f5f5f5", "color-inline-code-background": "#f0f0f0", }, "dark_css_variables": { "color-brand-primary": "#3b82f6", "color-brand-content": "#3b82f6", "color-code-background": "#1e293b", "color-inline-code-background": "#334155", }, } # Add any paths that contain custom static files (such as style sheets) here, # relative to this directory. They are copied after the builtin static files, # so a file named "default.css" will overwrite the builtin "default.css". html_static_path = ["_static"] # -- Options for HTMLHelp output --------------------------------------- # Output file base name for HTML help builder. htmlhelp_basename = "pysradbdoc" # -- Options for LaTeX output ------------------------------------------ latex_elements = { # The paper size ('letterpaper' or 'a4paper'). # # 'papersize': 'letterpaper', # The font size ('10pt', '11pt' or '12pt'). # # 'pointsize': '10pt', # Additional stuff for the LaTeX preamble. # # 'preamble': '', # Latex figure (float) alignment # # 'figure_align': 'htbp', } # Grouping the document tree into LaTeX files. List of tuples # (source start file, target name, title, author, documentclass # [howto, manual, or own class]). latex_documents = [ (master_doc, "pysradb.tex", "pysradb Documentation", "Saket Choudhary", "manual") ] # -- Options for manual page output ------------------------------------ # One entry per manual page. List of tuples # (source start file, name, description, authors, manual section). man_pages = [(master_doc, "pysradb", "pysradb Documentation", [author], 1)] # -- Options for Texinfo output ---------------------------------------- # Grouping the document tree into Texinfo files. List of tuples # (source start file, target name, title, author, # dir menu entry, description, category) texinfo_documents = [ ( master_doc, "pysradb", "pysradb Documentation", author, "pysradb", "One line description of project.", "Miscellaneous", ) ] numpydoc_show_class_members = False ##html_theme_path = guzzle_sphinx_theme.html_theme_path() ##html_theme = "guzzle_sphinx_theme" ## ### Register the theme as an extension to generate a sitemap.xml ##extensions.append("guzzle_sphinx_theme") ## ### Guzzle theme options (see theme.conf for more information) ##html_theme_options = { ## # Set the name of the project to appear in the sidebar ## "project_nav_name": "pysradb" ##} scv_greatest_tag = True scv_show_banner = True html_logo = "_static/pysradb_v3.png" # Load custom JavaScript for copy-to-clipboard functionality html_js_files = [ "copy-button.js", ] # Load custom CSS to override Pygments background colors html_css_files = [ "custom.css", ] # NBSphinx configuration nbsphinx_execute = "never" exclude_patterns.append("**/.ipynb_checkpoints") exclude_patterns.append("notebooks/.ipynb_checkpoints") ================================================ FILE: docs/contributing.md ================================================ # Contributing Contributions are welcome, and they are greatly appreciated! Every little bit helps, and credit will always be given. You can contribute in many ways: ## Types of Contributions ### Report Bugs Report bugs at . If you are reporting a bug, please include: - Your operating system name and version. - Any details about your local setup that might be helpful in troubleshooting. - Detailed steps to reproduce the bug. ### Fix Bugs Look through the GitHub issues for bugs. Anything tagged with \"bug\" and \"help wanted\" is open to whoever wants to implement it. ### Implement Features Look through the GitHub issues for features. Anything tagged with \"enhancement\" and \"help wanted\" is open to whoever wants to implement it. ### Write Documentation pysradb could always use more documentation, whether as part of the official pysradb docs, in docstrings, or even on the web in blog posts, articles, and such. ### Submit Feedback The best way to send feedback is to file an issue at . If you are proposing a feature: - Explain in detail how it would work. - Keep the scope as narrow as possible, to make it easier to implement. - Remember that this is a volunteer-driven project, and that contributions are welcome :) ## Get Started! Ready to contribute? Here\'s how to set up [pysradb]{.title-ref} for local development. 1. Fork the [pysradb]{.title-ref} repo on GitHub. 2. Clone your fork locally: ``` shell $ git clone git@github.com:your_name_here/pysradb.git ``` 3. Install your local copy into a virtualenv. Assuming you have virtualenvwrapper installed, this is how you set up your fork for local development (If python \--version is less than 3.0, run [\$ mkvirtualenv pysradb \--python=py3]{.title-ref} instead): ``` shell $ mkvirtualenv pysradb $ cd pysradb/ $ python setup.py develop ``` 4. Create a branch for local development: ``` shell $ git checkout -b name-of-your-bugfix-or-feature ``` Now you can make your changes locally. 5. When you\'re done making changes, check that your changes pass flake8 and the tests, including testing other Python versions with tox: ``` shell $ flake8 pysradb tests $ python setup.py test or py.test $ tox ``` To get flake8 and tox, just pip install them into your virtualenv. 6. Commit your changes and push your branch to GitHub: ``` shell $ git add . $ git commit -m "Your detailed description of your changes." $ git push origin name-of-your-bugfix-or-feature ``` 7. Submit a pull request through the GitHub website. ## Pull Request Guidelines Before you submit a pull request, check that it meets these guidelines: 1. The pull request should include tests. 2. If the pull request adds functionality, the docs should be updated. Put your new functionality into a function with a docstring, and add the feature to the list in README.rst. 3. The pull request should work for Python 2.7, 3.4, 3.5 and 3.6, and for PyPy. Make sure that the tests pass for all supported Python versions. ## Tips To run a subset of tests: ``` shell $ py.test tests.test_pysradb ``` ## Deploying A reminder for the maintainers on how to deploy. Make sure all your changes are committed (including an entry in HISTORY.rst). Then run: ``` shell $ bumpversion patch # possible: major / minor / patch $ git push $ git push --tags ``` CI will then deploy to PyPI if tests pass. ================================================ FILE: docs/history.md ================================================ # History
2.5.1 (2025-10-29) - Add prjna support in doi-to-identifiers [#249](https://github.com/saketkc/pysradb/pull/249)
2.5.0 (2025-10-19) - Add pmid/doi-to-gse/srp conversion [#246](https://github.com/saketkc/pysradb/pull/246).
2.4.1 (2025-09-27) - Add gse-to-pmid conversion [#241](https://github.com/saketkc/pysradb/pull/244).
2.4.0 (2025-09-27) - Add sra-to-pmid conversion [#241](https://github.com/saketkc/pysradb/pull/241). Thanks [@andrewdavidsmith](https://github.com/andrewdavidsmith) for the idea.
2.3.0 (2025-08-24) - Download logic improvements: remoted requests-ftp as requirement - Fix for handling missing metadata keys [#223](https://github.com/saketkc/pysradb/pull/223). Thanks [@andrewdavidsmith](https://github.com/andrewdavidsmith)
2.2.2 (2024-10-03) - Fix for handling ENA urls for paired end data
2.2.1 (2024-08-21) - Fix for handling ENA urls - Migrated to pyproject.toml
2.2.0 (2023-09-17) - Add support for Biosamples and bioproject [#199](https://github.com/saketkc/pysradb/pull/198) - Use retmode xml for Geo search [#200](https://github.com/saketkc/pysradb/pull/200) - Documentation fixes ## 2.1.0 (2023-05-16) - Fix for [gse-to-srp] returning unrequested GSEs [#186](https://github.com/saketkc/pysradb/issues/190) - Fix for [download] using [public_urls] - Fix for [gsm-to-srx] returning false positives [#165](https://github.com/saketkc/pysradb/issues/165) - Fix for delimiter not being consistent when metadata is printed on terminal [#147](https://github.com/saketkc/pysradb/issues/147) - ENA search is currently broken because of an API change ## 2.0.2 (2023-04-09) - Fix for [gse-to-srp] to handle cases where a project is missing but SRXs are returned [#186](https://github.com/saketkc/pysradb/issues/186) - Fix gse-to-gsm [#187](https://github.com/saketkc/pysradb/issues/187) ## 2.0.1 (2023-03-18) - Fix for [pysradb download] - using [public_url] - Fix for SRX -\> SRR and related conversions [#183](https://github.com/saketkc/pysradb/pull/183) ## 2.0.0 (2023-02-23) - BREAKING change: Overhaul of how urls and associated metadata are returned (not backward compatible); all column names are lower cased by default - Fix extra space in \"organism_taxid\" column - Added support for Experiment attributes [#89](https://github.com/saketkc/pysradb/issues/89#issuecomment-1439319532) ## 1.4.2 (06-17-2022) - Fix ENA fastq fetching [#163](https://github.com/saketkc/pysradb/issues/163) ## 1.4.1 (06-04-2022) - Fix for fetching alternative URLs ## 1.4.0 (06-04-2022) - Added ability to fetch alternative URLs (GCP/AWS) for metadata [#161](https://github.com/saketkc/pysradb/issues/161) - Fix for xmldict 0.13.0 no longer defaulting to OrderedDict [#159](https://github.com/saketkc/pysradb/pull/159) - Fix for missing experiment model and description in metadata [#160](https://github.com/saketkc/pysradb/issues/160) ## 1.3.0 (02-18-2022) - Add [study_title] to [\--detailed] flag ([#152](https://github.com/saketkc/pysradb/issues/152)) - Fix [KeyError] in [metadata] where some new IDs do not have any metadata ([#151](https://github.com/saketkc/pysradb/issues/151)) ## 1.2.0 (01-10-2022) - Do not exit if a qeury returns no hits ([#149](https://github.com/saketkc/pysradb/pull/149)) ## 1.1.0 (12-12-2021) - Fixed [gsm-to-gse] failure ([#128](https://github.com/saketkc/pysradb/pull/128)) - Fixed case sensitivity bug for ENA search ([#144](https://github.com/saketkc/pysradb/pull/144)) - Fixed publication date bug for search ([#146](https://github.com/saketkc/pysradb/pull/146)) - Added support for downloading data from GEO [pysradb dowload -g GSE] ([#129](https://github.com/saketkc/pysradb/pull/129)) ## 1.0.1 (01-10-2021) - Dropped Python 3.6 since pandas 1.2 is not supported ## 1.0.0 (01-09-2021) - Retired `metadb` and `SRAdb` based search through CLI - everything defaults to `SRAweb` - `SRAweb` now supports [search](https://saket-choudhary.me/pysradb/quickstart.html#search) - [N/A] is now replaced with [pd.NA] - Two new fields in \`\--detailed\`: [instrument_model] and [instrument_model_desc] [#75](https://github.com/saketkc/pysradb/issues/75) - Updated documentation ## 0.11.1 (09-18-2020) - [library_layout] is now outputted in metadata #56 - [-detailed] unifies columns for ENA fastq links instead of appending \_x/\_y #59 - bugfix for parsing namespace in xml outputs #65 - XML errors from NCBI are now handled more gracefully #69 - Documentation and dependency updates ## 0.11.0 (09-04-2020) - [pysradb download] now supports multiple threads for paralle downloads - [pysradb download] also supports ultra fast downloads of FASTQs from ENA using aspera-client ## 0.10.3 (03-26-2020) - Added test cases for SRAweb - API limit exceeding errors are automagically handled - Bug fixes for GSE \<=\> SRR - Bug fix for metadata - supports multiple SRPs Contributors - Dibya Gautam - Marius van den Beek ## 0.10.2 (02-05-2020) - Bug fix: Handle API-rate limit exceeding =\> Retries - Enhancement: \'Alternatives\' URLs are now part of [\--detailed] ## 0.10.1 (02-04-2020) - Bug fix: Handle Python3.6 for capture_output in subprocess.run ## 0.10.0 (01-31-2020) - All the subcommands (srx-to-srr, srx-to-srs) will now print additional columns where the first two columns represent the relevant conversion - Fixed a bug where for fetching entries with single efetch record ## 0.9.9 (01-15-2020) - Major fix: some SRRs would go missing as the experiment dict was being created only once per SRR (See #15) - Features: More detailed metadata by default in the SRAweb mode - See notebook: ## 0.9.7 (01-20-2020) - Feature: instrument, run size and total spots are now printed in the metadata by default (SRAweb mode only) - Issue: Fixed an issue with srapath failing on SRP. srapath is now run on individual SRRs. ## 0.9.6 (07-20-2019) - Introduced [SRAweb] to perform queries over the web if the SQLite is missing or does not contain the relevant record. ## 0.9.0 (02-27-2019) ### Others - This release completely changes the command line interface replacing click with argparse ([#3](https://github.com/saketkc/pysradb/pull/3)) - Removed Python 2 comptaible stale code ## 0.8.0 (02-26-2019) ### New methods/functionality - \`srr-to-gsm\`: convert SRR to GSM - SRAmetadb.sqlite.gz file is deleted by default after extraction - When SRAmetadb is not found a confirmation is seeked before downloading - Confirmation option before SRA downloads ### Bugfix - download() works with wget ### Others - [\--out_dir] is now [out-dir] ## 0.7.1 (02-18-2019) Important: Python2 is no longer supported. Please consider moving to Python3. ### Bugfix - Included docs in the index whihch were missed out in the previous release ## 0.7.0 (02-08-2019) ### New methods/functionality - \`gsm-to-srr\`: convert GSM to SRR - \`gsm-to-srx\`: convert GSM to SRX - \`gsm-to-gse\`: convert GSM to GSE ### Renamed methods The following commad line options have been renamed and the changes are not compatible with 0.6.0 release: - [sra-metadata] -\> [metadata]. - [sra-search] -\> [search]. - [srametadb] -\> [metadb]. ## 0.6.0 (12-25-2018) ### Bugfix - Fixed bugs introduced in 0.5.0 with API changes where multiple redundant columns were output in [sra-metadata] ### New methods/functionality - [download] now allows piped inputs ## 0.5.0 (12-24-2018) ### New methods/functionality - Support for filtering by SRX Id for SRA downloads. - \`srr_to_srx\`: Convert SRR to SRX/SRP - \`srp_to_srx\`: Convert SRP to SRX - Stripped down [sra-metadata] to give minimal information - Added [\--assay], [\--desc], [\--detailed] flag for [sra-metadata] - Improved table printing on terminal ## 0.4.2 (12-16-2018) ### Bugfix - Fixed unicode error in tests for Python2 ## 0.4.0 (12-12-2018) ### New methods/functionality - Added a new [BASEdb] class to handle common database connections - Initial support for GEOmetadb through GEOdb class - Initial support or a command line interface: - download Download SRA project (SRPnnnn) - gse-metadata Fetch metadata for GEO ID (GSEnnnn) - gse-to-gsm Get GSM(s) for GSE - gsm-metadata Fetch metadata for GSM ID (GSMnnnn) - sra-metadata Fetch metadata for SRA project (SRPnnnn) - Added three separate notebooks for SRAdb, GEOdb, CLI usage ## 0.3.0 (12-05-2018) ### New methods/functionality - [sample_attribute] and [experiment_attribute] are now included by default in the df returned by [sra_metadata()] - [expand_sample_attribute_columns: expand metadata dataframe based on attributes in \`sample_attribute] column - New methods to guess cell/tissue/strain: [guess_cell_type()]/[guess_tissue_type()]/[guess_strain_type()] - Improved README and usage instructions ## 0.2.2 (12-03-2018) ### New methods/functionality - [search_sra()] allows full text search on SRA metadata. ## 0.2.0 (12-03-2018) ### Renamed methods The following methods have been renamed and the changes are not compatible with 0.1.0 release: - [get_query()] -\> [query()]. - [sra_convert()] -\> [sra_metadata()]. - [get_table_counts()] -\> [all_row_counts()]. ### New methods/functionality - [download_sradb_file()] makes fetching [SRAmetadb.sqlite] file easy; wget is no longer required. - [ftp] protocol is now supported besides [fsp] and hence [aspera-client] is now optional. We however, strongly recommend [aspera-client] for faster downloads. ### Bug fixes - Silenced [SettingWithCopyWarning] by excplicitly doing operations on a copy of the dataframe instead of the original. Besides these, all methods now follow a [numpydoc] compatible documentation. ## 0.1.0 (12-01-2018) - First release on PyPI.
================================================ FILE: docs/index.rst ================================================ ============ Introduction ============ ``pysradb`` provides a simple method to programmatically access metadata and download sequencing data from NCBI's Sequence Read Archive (SRA) and European Bioinformatics Institute's European Nucleotide Archive (ENA). ============= Quick Example ============= To fetch metadata associated with project accession ``SRP265425`` .. code-block:: console $ pysradb metadata SRP265425 study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_name library_strategy library_source library_selection library_layout sample_accession sample_title instrument instrument_model instrument_model_desc total_spots total_size run_accession run_total_spots run_total_bases SRP265425 SRX8434255 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 63-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745319 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1311358 83306910 SRR11886735 1311358 109594216 SRP265425 SRX8434254 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 62-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745320 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2614109 204278682 SRR11886736 2614109 262305651 SRP265425 SRX8434253 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 61-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745318 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2286312 183516004 SRR11886737 2286312 263304134 SRP265425 SRX8434252 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 60-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745317 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5202567 507524965 SRR11886738 5202567 781291588 SRP265425 SRX8434251 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 38-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745315 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 3313960 356104406 SRR11886739 3313960 612430817 SRP265425 SRX8434250 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 37-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745316 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5155733 565882351 SRR11886740 5155733 954342917 SRP265425 SRX8434249 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 36-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745313 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1324589 175619046 SRR11886741 1324589 216531400 SRP265425 SRX8434248 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 35-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745314 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1639851 198973268 SRR11886742 1639851 245466005 SRP265425 SRX8434247 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 68-2020-05-07 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745312 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 3921389 210198580 SRR11886743 3921389 332935558 SRP265425 SRX8434246 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 66-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745311 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 14295475 2150005008 SRR11886744 14295475 2967829315 SRP265425 SRX8434245 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 65-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745310 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5124692 294846140 SRR11886745 5124692 431819462 SRP265425 SRX8434244 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 64-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745309 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2986306 205666872 SRR11886746 2986306 275400959 SRP265425 SRX8434243 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 34-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745308 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1182690 59471336 SRR11886747 1182690 86350631 SRP265425 SRX8434242 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 33-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745307 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 6031816 749323230 SRR11886748 6031816 928054297 To fetch detailed metadata which includes link to raw sequencing files, specify ``--detailed``: .. code-block:: console $ pysradb metadata SRP265425 --detailed run_accession study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_name library_strategy library_source library_selection library_layout sample_accession sample_title instrument instrument_model instrument_model_desc total_spots total_size run_total_spots run_total_bases run_alias sra_url_alt1 sra_url_alt2 sra_url experiment_alias isolate collected_by collection_date geo_loc_name host host_disease isolation_source lat_lon BioSampleModel sra_url_alt3 ena_fastq_http ena_fastq_http_1 ena_fastq_http_2 ena_fastq_ftp ena_fastq_ftp_1 ena_fastq_ftp_2 SRR11886735 SRP265425 SRX8434255 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 63-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745319 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1311358 83306910 1311358 109594216 IonXpress_063_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-9/SRR11886735/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886735/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/011608/SRR11886735 GC-20 NA 02-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/035/SRR11886735/SRR11886735.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/035/SRR11886735/SRR11886735.fastq.gz SRR11886736 SRP265425 SRX8434254 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 62-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745320 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2614109 204278682 2614109 262305651 IonXpress_062_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-16/SRR11886736/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRZ/011886/SRR11886736/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/011608/SRR11886736 GC-51 NA 14-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886736/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/036/SRR11886736/SRR11886736.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/036/SRR11886736/SRR11886736.fastq.gz SRR11886737 SRP265425 SRX8434253 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 61-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745318 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2286312 183516004 2286312 263304134 IonXpress_061_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-16/SRR11886737/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra29/SRZ/011886/SRR11886737/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/011608/SRR11886737 GC-24 NA 07-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886737/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/037/SRR11886737/SRR11886737.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/037/SRR11886737/SRR11886737.fastq.gz SRR11886738 SRP265425 SRX8434252 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 60-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745317 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5202567 507524965 5202567 781291588 IonXpress_060_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-15/SRR11886738/IonXpress_060_R_2020_04_22_15_56_22_user_GCEID_S5_58_SARS_CoV2_SA4.bam.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRZ/011886/SRR11886738/IonXpress_060_R_2020_04_22_15_56_22_user_GCEID_S5_58_SARS_CoV2_SA4.bam https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/011608/SRR11886738 GC-23 NA 08-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886738/IonXpress_060_R_2020_04_22_15_56_22_user_GCEID_S5_58_SARS_CoV2_SA4.bam.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/038/SRR11886738/SRR11886738.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/038/SRR11886738/SRR11886738.fastq.gz SRR11886739 SRP265425 SRX8434251 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 38-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745315 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 3313960 356104406 3313960 612430817 IonXpress_038_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-13/SRR11886739/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886739/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/011608/SRR11886739 GC-11b NA 24-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/039/SRR11886739/SRR11886739.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/039/SRR11886739/SRR11886739.fastq.gz SRR11886740 SRP265425 SRX8434250 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 37-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745316 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5155733 565882351 5155733 954342917 IonXpress_037_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-5/SRR11886740/IonXpress_037_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886740/IonXpress_037_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/011608/SRR11886740 GC-14b NA 28-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/040/SRR11886740/SRR11886740.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/040/SRR11886740/SRR11886740.fastq.gz SRR11886741 SRP265425 SRX8434249 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 36-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745313 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1324589 175619046 1324589 216531400 IonXpress_036_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-11/SRR11886741/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886741/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/011608/SRR11886741 GC-12 NA 24-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/041/SRR11886741/SRR11886741.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/041/SRR11886741/SRR11886741.fastq.gz SRR11886742 SRP265425 SRX8434248 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 35-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745314 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1639851 198973268 1639851 245466005 IonXpress_035_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-11/SRR11886742/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886742/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/011608/SRR11886742 GC-13 NA 23-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/042/SRR11886742/SRR11886742.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/042/SRR11886742/SRR11886742.fastq.gz SRR11886743 SRP265425 SRX8434247 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 68-2020-05-07 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745312 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 3921389 210198580 3921389 332935558 IonXpress_068_R_2020_05_07_11_47_51_user_GCEID-S5-60-SARS_CoV2_SA4.bam gs://sra-pub-src-17/SRR11886743/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRZ/011886/SRR11886743/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/011608/SRR11886743 GC-55 NA 24-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886743/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/043/SRR11886743/SRR11886743.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/043/SRR11886743/SRR11886743.fastq.gz SRR11886744 SRP265425 SRX8434246 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 66-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745311 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 14295475 2150005008 14295475 2967829315 IonXpress_066_R_2020_04_22_11_10_56_user_GCEID-S5-57-SARS_CoV2_SA4.fastq gs://sra-pub-src-11/SRR11886744/IonXpress_066_R_2020_04_22_11_10_56_user_GCEID-S5-57-SARS_CoV2_SA4.fastq.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886744/IonXpress_066_R_2020_04_22_11_10_56_user_GCEID-S5-57-SARS_CoV2_SA4.fastq.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/011608/SRR11886744 GC-26 NA 07-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/044/SRR11886744/SRR11886744.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/044/SRR11886744/SRR11886744.fastq.gz SRR11886745 SRP265425 SRX8434245 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 65-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745310 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5124692 294846140 5124692 431819462 IonXpress_065_R_2020_04_22_11_10_56_user_GCEID-S5-57-SARS_CoV2_SA4.bam gs://sra-pub-src-16/SRR11886745/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRZ/011886/SRR11886745/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/011608/SRR11886745 GC-25 NA 10-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886745/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/045/SRR11886745/SRR11886745.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/045/SRR11886745/SRR11886745.fastq.gz SRR11886746 SRP265425 SRX8434244 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 64-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745309 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2986306 205666872 2986306 275400959 IonXpress_064_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-17/SRR11886746/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRZ/011886/SRR11886746/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/011608/SRR11886746 GC-21 NA 03-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886746/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/046/SRR11886746/SRR11886746.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/046/SRR11886746/SRR11886746.fastq.gz SRR11886747 SRP265425 SRX8434243 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 34-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745308 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1182690 59471336 1182690 86350631 IonXpress_034_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-16/SRR11886747/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRZ/011886/SRR11886747/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/011608/SRR11886747 GC-11a NA 24-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886747/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/047/SRR11886747/SRR11886747.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/047/SRR11886747/SRR11886747.fastq.gz SRR11886748 SRP265425 SRX8434242 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 33-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745307 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 6031816 749323230 6031816 928054297 IonXpress_033_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-15/SRR11886748/IonXpress_033_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRZ/011886/SRR11886748/IonXpress_033_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/011608/SRR11886748 GC-14a NA 28-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886748/IonXpress_033_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/048/SRR11886748/SRR11886748.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/048/SRR11886748/SRR11886748.fastq.gz See :doc:`quickstart` for other examples. .. toctree:: :hidden: :maxdepth: 1 installation quickstart cmdline python-api-usage case_studies notebooks commands contributing authors history modules =========== Publication =========== `pysradb: A Python package to query next-generation sequencing metadata and data from NCBI Sequence Read Archive `_ Presentation slides from BOSC (ISMB-ECCB) 2019: https://f1000research.com/slides/8-1183 =========================================================================== ======== Citation ======== Choudhary, Saket. "pysradb: A Python Package to Query next-Generation Sequencing Metadata and Data from NCBI Sequence Read Archive." F1000Research, vol. 8, F1000 (Faculty of 1000 Ltd), Apr. 2019, p. 532 (https://f1000research.com/articles/8-532/v1) :: @article{Choudhary2019, doi = {10.12688/f1000research.18676.1}, url = {https://doi.org/10.12688/f1000research.18676.1}, year = {2019}, month = apr, publisher = {F1000 (Faculty of 1000 Ltd)}, volume = {8}, pages = {532}, author = {Saket Choudhary}, title = {pysradb: A {P}ython package to query next-generation sequencing metadata and data from {NCBI} {S}equence {R}ead {A}rchive}, journal = {F1000Research} } Zenodo archive: https://zenodo.org/badge/latestdoi/159590788 Zenodo DOI: 10.5281/zenodo.2306881 ================================================ FILE: docs/installation.md ================================================ # Installation ## Stable release To install pysradb, run this command in your terminal: ``` console $ pip install pysradb ``` This is the preferred method to install pysradb, as it will always install the most recent stable release. If you don\'t have [pip](https://pip.pypa.io) installed, this [Python installation guide](http://docs.python-guide.org/en/latest/starting/installation/) can guide you through the process. Alternatively, you may use conda: ``` bash conda install -c bioconda pysradb ``` This step will install all the dependencies except aspera-client (which is not required, but highly recommended). If you have an existing environment with a lot of pre-installed packages, conda might be [slow](https://github.com/bioconda/bioconda-recipes/issues/13774). Please consider creating a new enviroment for `pysradb`: ``` bash conda create -c bioconda -n pysradb PYTHON=3 pysradb ``` ## From sources The source files for pysradb can be downloaded from the [Github repo](https://github.com/saketkc/pysradb). You can either clone the public repository: ``` console $ git clone git://github.com/saketkc/pysradb ``` Or download the [tarball](https://github.com/saketkc/pysradb/tarball/master): ``` console $ curl -OL https://github.com/saketkc/pysradb/tarball/master ``` Once you have a copy of the source, you can install it with: ``` console $ python setup.py install ``` ================================================ FILE: docs/make.bat ================================================ @ECHO OFF pushd %~dp0 REM Command file for Sphinx documentation if "%SPHINXBUILD%" == "" ( set SPHINXBUILD=python -msphinx ) set SOURCEDIR=. set BUILDDIR=_build set SPHINXPROJ=pysradb if "%1" == "" goto help %SPHINXBUILD% >NUL 2>NUL if errorlevel 9009 ( echo. echo.The Sphinx module was not found. Make sure you have Sphinx installed, echo.then set the SPHINXBUILD environment variable to point to the full echo.path of the 'sphinx-build' executable. Alternatively you may add the echo.Sphinx directory to PATH. echo. echo.If you don't have Sphinx installed, grab it from echo.http://sphinx-doc.org/ exit /b 1 ) %SPHINXBUILD% -M %1 %SOURCEDIR% %BUILDDIR% %SPHINXOPTS% goto end :help %SPHINXBUILD% -M help %SOURCEDIR% %BUILDDIR% %SPHINXOPTS% :end popd ================================================ FILE: docs/modules.rst ================================================ pysradb ======= .. toctree:: :maxdepth: 4 pysradb ================================================ FILE: docs/notebooks.rst ================================================ Tutorials & Notebooks ===================== The following Jupyter notebooks demonstrate various features of pysradb: .. toctree:: :maxdepth: 1 :caption: notebooks/README notebooks/01.Python-API_demo.ipynb notebooks/02.Commandline_download.ipynb notebooks/03.ParallelDownload.ipynb notebooks/04.SRA_to_fastq_conda.ipynb notebooks/05.Downloading_subsets_of_a_project.ipynb notebooks/06.Multiple_SRPs.ipynb notebooks/07.Query_Search.ipynb notebooks/08.PMC_DOI_Identifiers.ipynb notebooks/09.Metadata_enrichment.ipynb You can also view the complete `notebooks directory on GitHub `_ for additional tutorials and examples. ================================================ FILE: docs/pysradb.rst ================================================ pysradb package =============== Submodules ---------- pysradb.basedb module --------------------- .. automodule:: pysradb.basedb :members: :undoc-members: :show-inheritance: pysradb.cli module ------------------ .. automodule:: pysradb.cli :members: :undoc-members: :show-inheritance: pysradb.download module ----------------------- .. automodule:: pysradb.download :members: :undoc-members: :show-inheritance: pysradb.exceptions module ------------------------- .. automodule:: pysradb.exceptions :members: :undoc-members: :show-inheritance: pysradb.filter\_attrs module ---------------------------- .. automodule:: pysradb.filter_attrs :members: :undoc-members: :show-inheritance: pysradb.geodb module -------------------- .. automodule:: pysradb.geodb :members: :undoc-members: :show-inheritance: pysradb.geoweb module --------------------- .. automodule:: pysradb.geoweb :members: :undoc-members: :show-inheritance: pysradb.metadata\_enrichment module ----------------------------------- .. automodule:: pysradb.metadata_enrichment :members: :undoc-members: :show-inheritance: pysradb.search module --------------------- .. automodule:: pysradb.search :members: :undoc-members: :show-inheritance: pysradb.sradb module -------------------- .. automodule:: pysradb.sradb :members: :undoc-members: :show-inheritance: pysradb.sraweb module --------------------- .. automodule:: pysradb.sraweb :members: :undoc-members: :show-inheritance: pysradb.taxid2name module ------------------------- .. automodule:: pysradb.taxid2name :members: :undoc-members: :show-inheritance: pysradb.utils module -------------------- .. automodule:: pysradb.utils :members: :undoc-members: :show-inheritance: Module contents --------------- .. automodule:: pysradb :members: :undoc-members: :show-inheritance: ================================================ FILE: docs/python-api-usage.md ================================================ # Python API ## Use Case 1: Fetch the metadata table (SRA-runtable) The simplest use case of [pysradb]{.title-ref} is when you know the SRA project ID (SRP) and would simply want to fetch the metadata associated with it. This is generally reflected in the [SraRunTable.txt]{.title-ref} that you get from NCBI\'s website. See an [example](https://www.ncbi.nlm.nih.gov/Traces/study/?acc=SRP098789) of a SraRunTable. ``` python from pysradb import SRAweb client = SRAweb() df = client.sra_metadata('SRP098789') df.head() ``` =============== ==================== ====================================================================== ============= ======== ================= ============== ================ ============== ============ ========== ======== ============ =============== study_accession experiment_accession experiment_title run_accession taxon_id library_selection library_layout library_strategy library_source library_name bases spots adapter_spec avg_read_length =============== ==================== ====================================================================== ============= ======== ================= ============== ================ ============== ============ ========== ======== ============ =============== SRP098789 SRX2536403 GSM2475997: 1.5 µM PF-067446846, 10 min, rep 1; Homo sapiens; OTHER SRR5227288 9606 other SINGLE - OTHER TRANSCRIPTOMIC 2104142750 42082855 50 SRP098789 SRX2536404 GSM2475998: 1.5 µM PF-067446846, 10 min, rep 2; Homo sapiens; OTHER SRR5227289 9606 other SINGLE - OTHER TRANSCRIPTOMIC 2082873050 41657461 50 SRP098789 SRX2536405 GSM2475999: 1.5 µM PF-067446846, 10 min, rep 3; Homo sapiens; OTHER SRR5227290 9606 other SINGLE - OTHER TRANSCRIPTOMIC 2023148650 40462973 50 SRP098789 SRX2536406 GSM2476000: 0.3 µM PF-067446846, 10 min, rep 1; Homo sapiens; OTHER SRR5227291 9606 other SINGLE - OTHER TRANSCRIPTOMIC 2057165950 41143319 50 SRP098789 SRX2536407 GSM2476001: 0.3 µM PF-067446846, 10 min, rep 2; Homo sapiens; OTHER SRR5227292 9606 other SINGLE - OTHER TRANSCRIPTOMIC 3027621850 60552437 50 =============== ==================== ====================================================================== ============= ======== ================= ============== ================ ============== ============ ========== ======== ============ =============== The metadata is returned as a [pandas]{.title-ref} dataframe and hence allows you to perform all regular select/query operations available through [pandas]{.title-ref}. ## Use Case 2: Downloading an entire project arranged experiment wise Once you have fetched the metadata and made sure, this is the project you were looking for, you would want to download everything at once. NCBI follows this hiererachy: [SRP =\> SRX =\> SRR]{.title-ref}. Each [SRP]{.title-ref} (project) has multiple [SRX]{.title-ref} (experiments) and each [SRX]{.title-ref} in turn has multiple [SRR]{.title-ref} (runs) inside it. We want to mimick this hiereachy in our downloads. The reason to do that is simple: in most cases you care about [SRX]{.title-ref} the most, and would want to \"merge\" your SRRs in one way or the other. Having this hierearchy ensures your downstream code can handle such cases easily, without worrying about which runs (SRR) need to be merged. We strongly recommend installing [aspera-client]{.title-ref} which uses UDP and is [designed to be faster](http://www.skullbox.net/tcpudp.php). ``` python from pysradb import SRAweb client = SRAweb() df = client.sra_metadata('SRP017942') client.download(df) ``` ## Use Case 3: Downloading a subset of experiments Often, you need to process only a smaller set of samples from a project (SRP). Consider this project which has data spanning four assays. ``` python df = client.sra_metadata('SRP000941') print(df.library_strategy.unique()) ['ChIP-Seq' 'Bisulfite-Seq' 'RNA-Seq' 'WGS' 'OTHER'] ``` But, you might be only interested in analyzing the [RNA-seq]{.title-ref} samples and would just want to download that subset. This is simple using [pysradb]{.title-ref} since the metadata can be subset just as you would subset a dataframe in pandas. ``` python df_rna = df[df.library_strategy == 'RNA-Seq'] client.download(df=df_rna, out_dir='/pysradb_downloads')() ``` ## Use Case 4: Getting cell-type/treatment information from sample_attributes Cell type/tissue informations is usually hidden in the [sample_attributes]{.title-ref} column, which can be expanded: ``` python from pysradb.filter_attrs import expand_sample_attribute_columns df = client.sra_metadata('SRP017942') expand_sample_attribute_columns(df).head() ```
study_accession experiment_accession experiment_title experiment_attribute sample_attribute run_accession taxon_id library_selection library_layout library_strategy library_source library_name bases spots adapter_spec avg_read_length assay_type cell_line source_name transfected_with treatment

SRP017942 SRP017942 SRP017942 SRP017942 SRP017942

SRX217028 SRX217029 SRX217030 SRX217031 SRX217956

GSM1063575: 293T_GFP; Homo sapiens; RNA-Seq GSM1063576: 293T_GFP_2hrs_severe_Heat_Shock; Homo sapiens; RNA-Seq GSM1063577: 293T_Hspa1a; Homo sapiens; RNA-Seq GSM1063578: 293T_Hspa1a_2hrs_severe_Heat_Shock; Homo sapiens; RNA-Seq GSM794854: 3T3-Control-Riboseq; Mus musculus; RNA-Seq

GEO Accession: GSM1063575 GEO Accession: GSM1063576 GEO Accession: GSM1063577 GEO Accession: GSM1063578 GEO Accession: GSM794854

source_name: 293T cells || cell line: 293T cells || transfected with: 3XFLAG-GFP || assay type: Riboseq source_name: 293T cells || cell line: 293T cells || transfected with: 3XFLAG-GFP || treatment: severe heat shock (44C 2 hours) || assay type: Riboseq source_name: 293T cells || cell line: 293T cells || transfected with: 3XFLAG-Hspa1a || assay type: Riboseq source_name: 293T cells || cell line: 293T cells || transfected with: 3XFLAG-Hspa1a || treatment: severe heat shock (44C 2 hours) || assay type: Riboseq source_name: 3T3 cells || treatment: control || cell line: 3T3 cells || assay type: Riboseq

SRR648667 SRR648668 SRR648669 SRR648670 SRR649752

9606 9606 9606 9606 10090

other other other other cDNA

SINGLE -SINGLE -SINGLE -SINGLE -SINGLE -

RNA-Seq RNA-Seq RNA-Seq RNA-Seq RNA-Seq

TRANSCRIPTOMIC TRANSCRIPTOMIC TRANSCRIPTOMIC TRANSCRIPTOMIC TRANSCRIPTOMIC

1806641316 3436984836 3330909216 3622123512 594945396

50184481 95471801 92525256

100614542

16526261

36 36 36 36 36

riboseq riboseq riboseq riboseq riboseq

293t cells 293t cells 293t cells 293t cells 3t3 cells

293t cells 293t cells 293t cells 293t cells 3t3 cells

3xflag-gfp 3xflag-gfp 3xflag-hspa1a 3xflag-hspa1a NaN

NaN severe heat shock (44c 2 hours) NaN severe heat shock (44c 2 hours) control

## Use Case 5: Searching for datasets Another common operation that we do on SRA is seach, plain text search. If you want to look up for all projects where [ribosome profiling]{.title-ref} appears somewhere in the description: ``` python df = client.search_sra(search_str='"ribosome profiling"') df.head() ```
study_accession experiment_accession experiment_title run_accession taxon_id library_selection library_layout library_strategy library_source library_name bases spots
DRP003075 DRX019536 Illumina Genome Analyzer IIx sequencing of SAMD00018584 DRR021383

83333

other SINGLE - OTHER TRANSCRIPTOMIC GAII05_3

978776480

12234706
DRP003075 DRX019537 Illumina Genome Analyzer IIx sequencing of SAMD00018585 DRR021384

83333

other SINGLE - OTHER TRANSCRIPTOMIC GAII05_4

894201680

11177521
DRP003075 DRX019538 Illumina Genome Analyzer IIx sequencing of SAMD00018586 DRR021385

83333

other SINGLE - OTHER TRANSCRIPTOMIC GAII05_5

931536720

11644209
DRP003075 DRX019540 Illumina Genome Analyzer IIx sequencing of SAMD00018588 DRR021387

83333

other SINGLE - OTHER TRANSCRIPTOMIC GAII07_4 2759398700 27593987
DRP003075 DRX019541 Illumina Genome Analyzer IIx sequencing of SAMD00018589 DRR021388

83333

other SINGLE - OTHER TRANSCRIPTOMIC GAII07_5 2386196500 23861965
Again, the results are available as a [pandas]{.title-ref} dataframe and hence you can perform all subset operations post your query. Your query doesn\'t need to be exact. ## Use Case 8: Finding publications (PMIDs) associated with SRA data Sometimes you have SRA accessions and want to find the publications that describe the data generation. ``` python from pysradb import SRAweb client = SRAweb() # Get PMIDs for a study accession (SRP) pmids_df = client.srp_to_pmid('SRP002605') pmids_df.head() ``` sra_accession bioproject pmid SRP002605 PRJNA129385 20703300 You can also get PMIDs for other SRA accession types: ``` python # Get PMIDs for run accessions (SRR) srr_pmids = client.srr_to_pmid('SRR057511') # Get PMIDs for experiment accessions (SRX) srx_pmids = client.srx_to_pmid('SRX021967') # Get PMIDs for sample accessions (SRS) srs_pmids = client.srs_to_pmid('SRS079386') # Get PMIDs for multiple accessions at once multi_pmids = client.sra_to_pmid(['SRP002605', 'SRP016501']) ``` You can also directly query BioProject accessions for their associated publications: ``` python # Get PMIDs directly from BioProject accessions bioproject_pmids = client.fetch_bioproject_pmids(['PRJNA257197', 'PRJNA129385']) print(bioproject_pmids) # Output: {'PRJNA257197': ['25214632'], 'PRJNA129385': ['20703300']} ``` **Note**: This functionality relies on the cross-references maintained between BioProjects and PubMed. Not all SRA datasets have associated publications, and some publications may not be properly cross-referenced in the NCBI databases. The success rate depends on: - Whether the authors included SRA/BioProject accessions in their manuscript - Whether NCBI has established the cross-references - The publication date relative to data submission ================================================ FILE: docs/quickstart.md ================================================ # Quickstart Most features in `pysradb` are accessible both from the command-line and as a python package. `pysradb` usage on the two platforms will be displayed by selecting the corresponding tab below. ```{note} If you have any questions along the way, please head over to the [Python API Usage](python-api-usage.md) or the [Command Line](cmdline.md) for more information. You may also wish to refer to the [API Documentation](commands.rst). ``` ------------------------------------------------------------------------ ## Notebooks A Google Colaboratory version of most used commands are available in this [Colab Notebook](https://colab.research.google.com/drive/1C60V-jkcNZiaCra_V5iEyFs318jgVoUR) . Colab runs Python 3.6 while `pysradb` requires Python 3.7+ and hence the notebooks no longer run on Colab, but can be downloaded and run locally. The following notebooks document all the possible features of `pysradb`: 1. [Python API](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/01.Python-API_demo.ipynb) 2. [Downloading datasets from SRA - command line](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/02.Commandline_download.ipynb) 3. [Parallely download multiple datasets - Python API](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/03.ParallelDownload.ipynb) 4. [Converting SRA-to-fastq - command line (requires conda)](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/04.SRA_to_fastq_conda.ipynb) 5. [Downloading subsets of a project - Python API](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/05.Downloading_subsets_of_a_project.ipynb) 6. [Download BAMs](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/06.Download_BAMs.ipynb) 7. [Metadata for multiple SRPs](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/07.Multiple_SRPs.ipynb) 8. [Multithreaded fastq downloads using Aspera Client](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/08.pysradb_ascp_multithreaded.ipynb) 9. [Searching SRA/GEO/ENA](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/09.Query_Search.ipynb) ## Metadata `pysradb` makes it very easy to obtain metadata from SRA/EBI: `````{tabs} ````{tab} Console ``` bash $ pysradb metadata SRP265425 ``` ```` ````{tab} Python ``` python from pysradb.sraweb import SRAweb client = SRAweb() df = client.metadata("SRP265425") df ``` ```` ````` Output: study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_name library_strategy library_source library_selection library_layout sample_accession sample_title instrument instrument_model instrument_model_desc total_spots total_size run_accession run_total_spots run_total_bases SRP265425 SRX8434255 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 63-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745319 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1311358 83306910 SRR11886735 1311358 109594216 SRP265425 SRX8434254 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 62-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745320 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2614109 204278682 SRR11886736 2614109 262305651 SRP265425 SRX8434253 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 61-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745318 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2286312 183516004 SRR11886737 2286312 263304134 SRP265425 SRX8434252 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 60-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745317 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5202567 507524965 SRR11886738 5202567 781291588 SRP265425 SRX8434251 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 38-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745315 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 3313960 356104406 SRR11886739 3313960 612430817 SRP265425 SRX8434250 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 37-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745316 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5155733 565882351 SRR11886740 5155733 954342917 SRP265425 SRX8434249 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 36-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745313 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1324589 175619046 SRR11886741 1324589 216531400 SRP265425 SRX8434248 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 35-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745314 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1639851 198973268 SRR11886742 1639851 245466005 SRP265425 SRX8434247 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 68-2020-05-07 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745312 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 3921389 210198580 SRR11886743 3921389 332935558 SRP265425 SRX8434246 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 66-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745311 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 14295475 2150005008 SRR11886744 14295475 2967829315 SRP265425 SRX8434245 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 65-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745310 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5124692 294846140 SRR11886745 5124692 431819462 SRP265425 SRX8434244 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 64-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745309 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2986306 205666872 SRR11886746 2986306 275400959 SRP265425 SRX8434243 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 34-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745308 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1182690 59471336 SRR11886747 1182690 86350631 SRP265425 SRX8434242 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 33-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745307 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 6031816 749323230 SRR11886748 6031816 928054297 Additionally to obtain locations of `.fastq/.sra` files and other metadata: `pysradb` makes it very easy to obtain metadata from SRA/EBI: `````{tabs} ````{tab} Console ``` bash $ pysradb metadata SRP265425 --detailed ``` ```` ````{tab} Python ``` python from pysradb.sraweb import SRAweb client = SRAweb() df = client.metadata("SRP265425", detailed=True) df ``` ```` ````` Output: run_accession study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_name library_strategy library_source library_selection library_layout sample_accession sample_title instrument instrument_model instrument_model_desc total_spots total_size run_total_spots run_total_bases run_alias sra_url_alt1 sra_url_alt2 sra_url experiment_alias isolate collected_by collection_date geo_loc_name host host_disease isolation_source lat_lon BioSampleModel sra_url_alt3 ena_fastq_http ena_fastq_http_1 ena_fastq_http_2 ena_fastq_ftp ena_fastq_ftp_1 ena_fastq_ftp_2 SRR11886735 SRP265425 SRX8434255 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 63-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745319 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1311358 83306910 1311358 109594216 IonXpress_063_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-9/SRR11886735/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886735/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra0/SRR/011608/SRR11886735 GC-20 NA 02-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/035/SRR11886735/SRR11886735.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/035/SRR11886735/SRR11886735.fastq.gz SRR11886736 SRP265425 SRX8434254 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 62-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745320 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2614109 204278682 2614109 262305651 IonXpress_062_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-16/SRR11886736/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra46/SRZ/011886/SRR11886736/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra50/SRR/011608/SRR11886736 GC-51 NA 14-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886736/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/036/SRR11886736/SRR11886736.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/036/SRR11886736/SRR11886736.fastq.gz SRR11886737 SRP265425 SRX8434253 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 61-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745318 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2286312 183516004 2286312 263304134 IonXpress_061_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-16/SRR11886737/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra29/SRZ/011886/SRR11886737/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra17/SRR/011608/SRR11886737 GC-24 NA 07-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886737/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/037/SRR11886737/SRR11886737.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/037/SRR11886737/SRR11886737.fastq.gz SRR11886738 SRP265425 SRX8434252 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 60-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745317 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5202567 507524965 5202567 781291588 IonXpress_060_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-15/SRR11886738/IonXpress_060_R_2020_04_22_15_56_22_user_GCEID_S5_58_SARS_CoV2_SA4.bam.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRZ/011886/SRR11886738/IonXpress_060_R_2020_04_22_15_56_22_user_GCEID_S5_58_SARS_CoV2_SA4.bam https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/011608/SRR11886738 GC-23 NA 08-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886738/IonXpress_060_R_2020_04_22_15_56_22_user_GCEID_S5_58_SARS_CoV2_SA4.bam.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/038/SRR11886738/SRR11886738.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/038/SRR11886738/SRR11886738.fastq.gz SRR11886739 SRP265425 SRX8434251 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 38-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745315 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 3313960 356104406 3313960 612430817 IonXpress_038_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-13/SRR11886739/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886739/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra24/SRR/011608/SRR11886739 GC-11b NA 24-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/039/SRR11886739/SRR11886739.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/039/SRR11886739/SRR11886739.fastq.gz SRR11886740 SRP265425 SRX8434250 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 37-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745316 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5155733 565882351 5155733 954342917 IonXpress_037_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-5/SRR11886740/IonXpress_037_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886740/IonXpress_037_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/011608/SRR11886740 GC-14b NA 28-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/040/SRR11886740/SRR11886740.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/040/SRR11886740/SRR11886740.fastq.gz SRR11886741 SRP265425 SRX8434249 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 36-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745313 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1324589 175619046 1324589 216531400 IonXpress_036_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-11/SRR11886741/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886741/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra57/SRR/011608/SRR11886741 GC-12 NA 24-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/041/SRR11886741/SRR11886741.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/041/SRR11886741/SRR11886741.fastq.gz SRR11886742 SRP265425 SRX8434248 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 35-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745314 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1639851 198973268 1639851 245466005 IonXpress_035_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-11/SRR11886742/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886742/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRR/011608/SRR11886742 GC-13 NA 23-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/042/SRR11886742/SRR11886742.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/042/SRR11886742/SRR11886742.fastq.gz SRR11886743 SRP265425 SRX8434247 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 68-2020-05-07 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745312 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 3921389 210198580 3921389 332935558 IonXpress_068_R_2020_05_07_11_47_51_user_GCEID-S5-60-SARS_CoV2_SA4.bam gs://sra-pub-src-17/SRR11886743/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra64/SRZ/011886/SRR11886743/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra54/SRR/011608/SRR11886743 GC-55 NA 24-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886743/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/043/SRR11886743/SRR11886743.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/043/SRR11886743/SRR11886743.fastq.gz SRR11886744 SRP265425 SRX8434246 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 66-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745311 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 14295475 2150005008 14295475 2967829315 IonXpress_066_R_2020_04_22_11_10_56_user_GCEID-S5-57-SARS_CoV2_SA4.fastq gs://sra-pub-src-11/SRR11886744/IonXpress_066_R_2020_04_22_11_10_56_user_GCEID-S5-57-SARS_CoV2_SA4.fastq.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886744/IonXpress_066_R_2020_04_22_11_10_56_user_GCEID-S5-57-SARS_CoV2_SA4.fastq.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/011608/SRR11886744 GC-26 NA 07-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/044/SRR11886744/SRR11886744.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/044/SRR11886744/SRR11886744.fastq.gz SRR11886745 SRP265425 SRX8434245 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 65-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745310 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 5124692 294846140 5124692 431819462 IonXpress_065_R_2020_04_22_11_10_56_user_GCEID-S5-57-SARS_CoV2_SA4.bam gs://sra-pub-src-16/SRR11886745/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra69/SRZ/011886/SRR11886745/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/011608/SRR11886745 GC-25 NA 10-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886745/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/045/SRR11886745/SRR11886745.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/045/SRR11886745/SRR11886745.fastq.gz SRR11886746 SRP265425 SRX8434244 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 64-2020-04-22 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745309 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 2986306 205666872 2986306 275400959 IonXpress_064_R_2020_04_22_15_56_22_user_GCEID-S5-58-SARS_CoV2_SA4.bam gs://sra-pub-src-17/SRR11886746/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra59/SRZ/011886/SRR11886746/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra47/SRR/011608/SRR11886746 GC-21 NA 03-Apr-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886746/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/046/SRR11886746/SRR11886746.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/046/SRR11886746/SRR11886746.fastq.gz SRR11886747 SRP265425 SRX8434243 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 34-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745308 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 1182690 59471336 1182690 86350631 IonXpress_034_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-16/SRR11886747/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRZ/011886/SRR11886747/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta https://sra-download.ncbi.nlm.nih.gov/traces/sra13/SRR/011608/SRR11886747 GC-11a NA 24-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886747/Wuhan_Hu_1_NC_045512_21500_and_subgenomics_SA4.fasta.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/047/SRR11886747/SRR11886747.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/047/SRR11886747/SRR11886747.fastq.gz SRR11886748 SRP265425 SRX8434242 Ampliseq of SARS-CoV-2 Ampliseq of SARS-CoV-2 2697049 Severe acute respiratory syndrome coronavirus 2 33-2020-04-03 AMPLICON VIRAL RNA RT-PCR SINGLE SRS6745307 Ion Torrent S5 XL Ion Torrent S5 XL ION_TORRENT 6031816 749323230 6031816 928054297 IonXpress_033_R_2020_04_03_10_09_05_user_GCEID-S5-55-SARS_CoV2_SA4.bam gs://sra-pub-src-15/SRR11886748/IonXpress_033_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam.1 https://sra-download.ncbi.nlm.nih.gov/traces/sra43/SRZ/011886/SRR11886748/IonXpress_033_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/011608/SRR11886748 GC-14a NA 28-Mar-2020 Australia: Victoria Homo sapiens COVID-19 swab NA Pathogen.cl https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR11886748/IonXpress_033_R_2020_04_03_10_09_05_user_GCEID_S5_55_SARS_CoV2_SA4.bam.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/048/SRR11886748/SRR11886748.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR118/048/SRR11886748/SRR11886748.fastq.gz ## Converting between accession numbers `pysradb` provides a suite of commands for interoperability between conversion numbers. ### Convert SRP to SRX `````{tabs} ````{tab} Console ``` bash $ pysradb srp-to-srx SRP098789 ``` ```` ````{tab} Python ``` python from pysradb.sraweb import SRAweb client = SRAweb() df = client.srp-to-srx("SRP098789") df ``` ```` ````` Output: study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_strategy library_source library_selection sample_accession sample_title instrument total_spots total_size run_accession run_total_spots run_total_bases study_accesssion SRP098789 SRX2536428 GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Homo sapiens; RNA-Seq GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Homo sapiens; RNA-Seq 9606 Homo sapiens RNA-Seq TRANSCRIPTOMIC cDNA SRS1956378 Illumina HiSeq 2500 69422931 1545681856 SRR5227313 69422931 3540569481 SRP098789 SRP098789 SRX2536427 GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-seq; Homo sapiens; OTHER GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-seq; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956377 Illumina HiSeq 2500 58065134 1302369810 SRR5227312 58065134 2961321834 SRP098789 SRP098789 SRX2536426 GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Homo sapiens; RNA-Seq GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Homo sapiens; RNA-Seq 9606 Homo sapiens RNA-Seq TRANSCRIPTOMIC cDNA SRS1956376 Illumina HiSeq 2500 63720205 1416818619 SRR5227311 63720205 3249730455 SRP098789 SRP098789 SRX2536425 GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-seq; Homo sapiens; OTHER GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-seq; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956375 Illumina HiSeq 2500 66363585 1482728577 SRR5227310 66363585 3384542835 SRP098789 SRP098789 SRX2536424 GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; Homo sapiens; RNA-Seq GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; Homo sapiens; RNA-Seq 9606 Homo sapiens RNA-Seq TRANSCRIPTOMIC cDNA SRS1956374 Illumina HiSeq 2500 40062613 904488287 SRR5227309 40062613 2043193263 SRP098789 SRP098789 SRX2536423 GSM2476017: 1.5 ?M PF-067446846, 60 min, rep 5 -riboseq; Homo sapiens; OTHER GSM2476017: 1.5 ?M PF-067446846, 60 min, rep 5 -riboseq; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956373 Illumina HiSeq 2500 65591217 1499668100 SRR5227308 65591217 3345152067 SRP098789 SRP098789 SRX2536422 GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; Homo sapiens; RNA-Seq GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; Homo sapiens; RNA-Seq 9606 Homo sapiens RNA-Seq TRANSCRIPTOMIC cDNA SRS1956372 Illumina HiSeq 2500 66480991 1564636133 SRR5227307 66480991 3390530541 SRP098789 SRP098789 SRX2536421 GSM2476015: 1.5 ?M PF-067446846, 60 min, rep 4 -riboseq; Homo sapiens; OTHER GSM2476015: 1.5 ?M PF-067446846, 60 min, rep 4 -riboseq; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956371 Illumina HiSeq 2500 57588015 1357395400 SRR5227306 57588015 2936988765 SRP098789 SRP098789 SRX2536420 GSM2476014: vehicle, 60 min rep 3; Homo sapiens; OTHER GSM2476014: vehicle, 60 min rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956370 Illumina HiSeq 2000 48405034 1530784033 SRR5227305 48405034 2420251700 SRP098789 SRP098789 SRX2536419 GSM2476013: vehicle, 60 min rep 2; Homo sapiens; OTHER GSM2476013: vehicle, 60 min rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956369 Illumina HiSeq 2000 47139057 1489018603 SRR5227304 47139057 2356952850 SRP098789 SRP098789 SRX2536418 GSM2476012: vehicle, 60 min rep 1; Homo sapiens; OTHER GSM2476012: vehicle, 60 min rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956368 Illumina HiSeq 2000 50956178 1495757884 SRR5227303 50956178 2547808900 SRP098789 SRP098789 SRX2536417 GSM2476011: 0.3 ?M PF-067446846, 60 min, rep 3; Homo sapiens; OTHER GSM2476011: 0.3 ?M PF-067446846, 60 min, rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956367 Illumina HiSeq 2000 44258180 1404548468 SRR5227302 44258180 2212909000 SRP098789 SRP098789 SRX2536416 GSM2476010: 0.3 ?M PF-067446846, 60 min, rep 2; Homo sapiens; OTHER GSM2476010: 0.3 ?M PF-067446846, 60 min, rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956366 Illumina HiSeq 2000 49129512 1536091510 SRR5227301 49129512 2456475600 SRP098789 SRP098789 SRX2536415 GSM2476009: 0.3 ?M PF-067446846, 60 min, rep 1; Homo sapiens; OTHER GSM2476009: 0.3 ?M PF-067446846, 60 min, rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956365 Illumina HiSeq 2000 30043362 903983724 SRR5227300 30043362 1502168100 SRP098789 SRP098789 SRX2536414 GSM2476008: 1.5 ?M PF-067446846, 60 min, rep 3; Homo sapiens; OTHER GSM2476008: 1.5 ?M PF-067446846, 60 min, rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956364 Illumina HiSeq 2000 48766213 1530350854 SRR5227299 48766213 2438310650 SRP098789 SRP098789 SRX2536413 GSM2476007: 1.5 ?M PF-067446846, 60 min, rep 2; Homo sapiens; OTHER GSM2476007: 1.5 ?M PF-067446846, 60 min, rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956363 Illumina HiSeq 2000 49334392 1475414353 SRR5227298 49334392 2466719600 SRP098789 SRP098789 SRX2536412 GSM2476006: 1.5 ?M PF-067446846, 60 min, rep 1; Homo sapiens; OTHER GSM2476006: 1.5 ?M PF-067446846, 60 min, rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956362 Illumina HiSeq 2000 60381365 1801283052 SRR5227297 60381365 3019068250 SRP098789 SRP098789 SRX2536411 GSM2476005: vehicle, 10 min rep 3; Homo sapiens; OTHER GSM2476005: vehicle, 10 min rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956361 Illumina HiSeq 2000 52737784 1644829192 SRR5227296 52737784 2636889200 SRP098789 SRP098789 SRX2536410 GSM2476004: vehicle, 10 min rep 2; Homo sapiens; OTHER GSM2476004: vehicle, 10 min rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956360 Illumina HiSeq 2000 46137148 1455541408 SRR5227295 46137148 2306857400 SRP098789 SRP098789 SRX2536409 GSM2476003: vehicle, 10 min rep 1; Homo sapiens; OTHER GSM2476003: vehicle, 10 min rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956359 Illumina HiSeq 2000 76002122 1552821132 SRR5227294 76002122 3800106100 SRP098789 SRP098789 SRX2536408 GSM2476002: 0.3 ?M PF-067446846, 10 min, rep 3; Homo sapiens; OTHER GSM2476002: 0.3 ?M PF-067446846, 10 min, rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956358 Illumina HiSeq 2000 42709138 1338829352 SRR5227293 42709138 2135456900 SRP098789 SRP098789 SRX2536407 GSM2476001: 0.3 ?M PF-067446846, 10 min, rep 2; Homo sapiens; OTHER GSM2476001: 0.3 ?M PF-067446846, 10 min, rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956357 Illumina HiSeq 2000 60552437 1875910244 SRR5227292 60552437 3027621850 SRP098789 SRP098789 SRX2536406 GSM2476000: 0.3 ?M PF-067446846, 10 min, rep 1; Homo sapiens; OTHER GSM2476000: 0.3 ?M PF-067446846, 10 min, rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956356 Illumina HiSeq 2000 41143319 843881081 SRR5227291 41143319 2057165950 SRP098789 SRP098789 SRX2536405 GSM2475999: 1.5 ?M PF-067446846, 10 min, rep 3; Homo sapiens; OTHER GSM2475999: 1.5 ?M PF-067446846, 10 min, rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956355 Illumina HiSeq 2000 40462973 1287284933 SRR5227290 40462973 2023148650 SRP098789 SRP098789 SRX2536404 GSM2475998: 1.5 ?M PF-067446846, 10 min, rep 2; Homo sapiens; OTHER GSM2475998: 1.5 ?M PF-067446846, 10 min, rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956354 Illumina HiSeq 2000 41657461 1360366732 SRR5227289 41657461 2082873050 SRP098789 SRP098789 SRX2536403 GSM2475997: 1.5 ?M PF-067446846, 10 min, rep 1; Homo sapiens; OTHER GSM2475997: 1.5 ?M PF-067446846, 10 min, rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956353 Illumina HiSeq 2000 42082855 916745706 SRR5227288 42082855 2104142750 SRP098789 ### Convert GSE to SRP `````{tabs} ````{tab} Console ``` bash $ pysradb srp-to-srx SRP098789 ``` ```` ````{tab} Python ``` python from pysradb.sraweb import SRAweb client = SRAweb() df = client.srp-to-srx("SRP098789") df ``` ```` ````` Output: study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_strategy library_source library_selection sample_accession sample_title instrument total_spots total_size run_accession run_total_spots run_total_bases study_accesssion SRP098789 SRX2536428 GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Homo sapiens; RNA-Seq GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Homo sapiens; RNA-Seq 9606 Homo sapiens RNA-Seq TRANSCRIPTOMIC cDNA SRS1956378 Illumina HiSeq 2500 69422931 1545681856 SRR5227313 69422931 3540569481 SRP098789 SRP098789 SRX2536427 GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-seq; Homo sapiens; OTHER GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-seq; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956377 Illumina HiSeq 2500 58065134 1302369810 SRR5227312 58065134 2961321834 SRP098789 SRP098789 SRX2536426 GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Homo sapiens; RNA-Seq GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Homo sapiens; RNA-Seq 9606 Homo sapiens RNA-Seq TRANSCRIPTOMIC cDNA SRS1956376 Illumina HiSeq 2500 63720205 1416818619 SRR5227311 63720205 3249730455 SRP098789 SRP098789 SRX2536425 GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-seq; Homo sapiens; OTHER GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-seq; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956375 Illumina HiSeq 2500 66363585 1482728577 SRR5227310 66363585 3384542835 SRP098789 SRP098789 SRX2536424 GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; Homo sapiens; RNA-Seq GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; Homo sapiens; RNA-Seq 9606 Homo sapiens RNA-Seq TRANSCRIPTOMIC cDNA SRS1956374 Illumina HiSeq 2500 40062613 904488287 SRR5227309 40062613 2043193263 SRP098789 SRP098789 SRX2536423 GSM2476017: 1.5 ?M PF-067446846, 60 min, rep 5 -riboseq; Homo sapiens; OTHER GSM2476017: 1.5 ?M PF-067446846, 60 min, rep 5 -riboseq; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956373 Illumina HiSeq 2500 65591217 1499668100 SRR5227308 65591217 3345152067 SRP098789 SRP098789 SRX2536422 GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; Homo sapiens; RNA-Seq GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; Homo sapiens; RNA-Seq 9606 Homo sapiens RNA-Seq TRANSCRIPTOMIC cDNA SRS1956372 Illumina HiSeq 2500 66480991 1564636133 SRR5227307 66480991 3390530541 SRP098789 SRP098789 SRX2536421 GSM2476015: 1.5 ?M PF-067446846, 60 min, rep 4 -riboseq; Homo sapiens; OTHER GSM2476015: 1.5 ?M PF-067446846, 60 min, rep 4 -riboseq; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956371 Illumina HiSeq 2500 57588015 1357395400 SRR5227306 57588015 2936988765 SRP098789 SRP098789 SRX2536420 GSM2476014: vehicle, 60 min rep 3; Homo sapiens; OTHER GSM2476014: vehicle, 60 min rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956370 Illumina HiSeq 2000 48405034 1530784033 SRR5227305 48405034 2420251700 SRP098789 SRP098789 SRX2536419 GSM2476013: vehicle, 60 min rep 2; Homo sapiens; OTHER GSM2476013: vehicle, 60 min rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956369 Illumina HiSeq 2000 47139057 1489018603 SRR5227304 47139057 2356952850 SRP098789 SRP098789 SRX2536418 GSM2476012: vehicle, 60 min rep 1; Homo sapiens; OTHER GSM2476012: vehicle, 60 min rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956368 Illumina HiSeq 2000 50956178 1495757884 SRR5227303 50956178 2547808900 SRP098789 SRP098789 SRX2536417 GSM2476011: 0.3 ?M PF-067446846, 60 min, rep 3; Homo sapiens; OTHER GSM2476011: 0.3 ?M PF-067446846, 60 min, rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956367 Illumina HiSeq 2000 44258180 1404548468 SRR5227302 44258180 2212909000 SRP098789 SRP098789 SRX2536416 GSM2476010: 0.3 ?M PF-067446846, 60 min, rep 2; Homo sapiens; OTHER GSM2476010: 0.3 ?M PF-067446846, 60 min, rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956366 Illumina HiSeq 2000 49129512 1536091510 SRR5227301 49129512 2456475600 SRP098789 SRP098789 SRX2536415 GSM2476009: 0.3 ?M PF-067446846, 60 min, rep 1; Homo sapiens; OTHER GSM2476009: 0.3 ?M PF-067446846, 60 min, rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956365 Illumina HiSeq 2000 30043362 903983724 SRR5227300 30043362 1502168100 SRP098789 SRP098789 SRX2536414 GSM2476008: 1.5 ?M PF-067446846, 60 min, rep 3; Homo sapiens; OTHER GSM2476008: 1.5 ?M PF-067446846, 60 min, rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956364 Illumina HiSeq 2000 48766213 1530350854 SRR5227299 48766213 2438310650 SRP098789 SRP098789 SRX2536413 GSM2476007: 1.5 ?M PF-067446846, 60 min, rep 2; Homo sapiens; OTHER GSM2476007: 1.5 ?M PF-067446846, 60 min, rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956363 Illumina HiSeq 2000 49334392 1475414353 SRR5227298 49334392 2466719600 SRP098789 SRP098789 SRX2536412 GSM2476006: 1.5 ?M PF-067446846, 60 min, rep 1; Homo sapiens; OTHER GSM2476006: 1.5 ?M PF-067446846, 60 min, rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956362 Illumina HiSeq 2000 60381365 1801283052 SRR5227297 60381365 3019068250 SRP098789 SRP098789 SRX2536411 GSM2476005: vehicle, 10 min rep 3; Homo sapiens; OTHER GSM2476005: vehicle, 10 min rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956361 Illumina HiSeq 2000 52737784 1644829192 SRR5227296 52737784 2636889200 SRP098789 SRP098789 SRX2536410 GSM2476004: vehicle, 10 min rep 2; Homo sapiens; OTHER GSM2476004: vehicle, 10 min rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956360 Illumina HiSeq 2000 46137148 1455541408 SRR5227295 46137148 2306857400 SRP098789 SRP098789 SRX2536409 GSM2476003: vehicle, 10 min rep 1; Homo sapiens; OTHER GSM2476003: vehicle, 10 min rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956359 Illumina HiSeq 2000 76002122 1552821132 SRR5227294 76002122 3800106100 SRP098789 SRP098789 SRX2536408 GSM2476002: 0.3 ?M PF-067446846, 10 min, rep 3; Homo sapiens; OTHER GSM2476002: 0.3 ?M PF-067446846, 10 min, rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956358 Illumina HiSeq 2000 42709138 1338829352 SRR5227293 42709138 2135456900 SRP098789 SRP098789 SRX2536407 GSM2476001: 0.3 ?M PF-067446846, 10 min, rep 2; Homo sapiens; OTHER GSM2476001: 0.3 ?M PF-067446846, 10 min, rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956357 Illumina HiSeq 2000 60552437 1875910244 SRR5227292 60552437 3027621850 SRP098789 SRP098789 SRX2536406 GSM2476000: 0.3 ?M PF-067446846, 10 min, rep 1; Homo sapiens; OTHER GSM2476000: 0.3 ?M PF-067446846, 10 min, rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956356 Illumina HiSeq 2000 41143319 843881081 SRR5227291 41143319 2057165950 SRP098789 SRP098789 SRX2536405 GSM2475999: 1.5 ?M PF-067446846, 10 min, rep 3; Homo sapiens; OTHER GSM2475999: 1.5 ?M PF-067446846, 10 min, rep 3; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956355 Illumina HiSeq 2000 40462973 1287284933 SRR5227290 40462973 2023148650 SRP098789 SRP098789 SRX2536404 GSM2475998: 1.5 ?M PF-067446846, 10 min, rep 2; Homo sapiens; OTHER GSM2475998: 1.5 ?M PF-067446846, 10 min, rep 2; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956354 Illumina HiSeq 2000 41657461 1360366732 SRR5227289 41657461 2082873050 SRP098789 SRP098789 SRX2536403 GSM2475997: 1.5 ?M PF-067446846, 10 min, rep 1; Homo sapiens; OTHER GSM2475997: 1.5 ?M PF-067446846, 10 min, rep 1; Homo sapiens; OTHER 9606 Homo sapiens OTHER TRANSCRIPTOMIC other SRS1956353 Illumina HiSeq 2000 42082855 916745706 SRR5227288 42082855 2104142750 SRP098789 ------------------------------------------------------------------------ ## Downloading sequencing data `pysradb` can alse be used to download either `.fastq` or `.sra` filesboth from ENA and SRA. ### Downloading via accession number `````{tabs} ````{tab} Console ``` bash $ pysradb download SRP098789 ``` ```` ````{tab} Python ``` python from pysradb.sraweb import SRAweb client = SRAweb() client.download("SRP098789") ``` ```` ````` It is also possible to pipe the dataframe from [metadata]{.title-ref} or [search]{.title-ref} to download, after filtering the dataframe entries: `````{tabs} ````{tab} Console ``` bash $ pysradb metadata SRP276671 --detailed | pysradb download ``` ```` ````{tab} Python ``` python from pysradb.sraweb import SRAweb client = SRAweb() df = client.sra_metadata('SRP016501', detailed=True) client.download(df=df) ``` ```` ````` ### Ultrafast fastq downloads With [aspera-client](https://downloads.asperasoft.com/en/downloads/8?list) installed, `pysradb` canan perform ultra fast downloads: To download all original fastqs with [aspera-client]{.title-ref} installed utilizing 8 threads: `````{tabs} ````{tab} Console ``` console $ pysradb download -t 8 --use_ascp -p SRP002605 ``` ```` ````{tab} Python ``` python from pysradb.sraweb import SRAweb client = SRAweb() client.download("SRP098789", use_ascp=True, threads=8) ``` ```` ````` Refer to the notebook for [(shallow) time benchmarks](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/08.pysradb_ascp_multithreaded.ipynb). ------------------------------------------------------------------------ ## Search ### Retrieving metadata by accession number `````{tabs} ````{tab} Console ``` bash $ pysradb metadata SRP276671 ``` ```` ````{tab} Python ``` python from pysradb.sraweb import SRAweb client = SRAweb() df = client.sra_metadata('SRP016501') df ``` ```` ````` Output: study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_strategy library_source library_selection sample_accession sample_title instrument total_spots total_size run_accession run_total_spots run_total_bases SRP276671 SRX8978626 hCov-19/Canada/ON/VIDO01/2020 (EPI ISL 413015) hCov-19/Canada/ON/VIDO01/2020 (EPI ISL 413015) 2697049 Severe acute respiratory syndrome coronavirus 2 WGS GENOMIC RT-PCR SRS7233795 MinION 96202 79690689 SRR12486810 96202 86575096 SRP276671 SRX8909137 hCoV-19/Canada/ON-VIDO-01/2020 (EPI_ISL_425177) hCoV-19/Canada/ON-VIDO-01/2020 (EPI_ISL_425177) 2697049 Severe acute respiratory syndrome coronavirus 2 WGS GENOMIC RT-PCR SRS7166526 Illumina MiSeq 866225 173474986 SRR12412952 866225 338457239 ::: note ::: title Note ::: [pysradb]{.title-ref}, when used in python, returns the retrieved metadata as a [pandas]{.title-ref} DataFrame, with all regular select/query operations available through [pandas]{.title-ref}. ::: For more detailed metadata (including download URLs), we can include the [detailed]{.title-ref} flag: `````{tabs} ````{tab} Console ``` bash $ pysradb metadata SRP276671 --detailed ``` ```` ````{tab} Python ``` python from pysradb.sraweb import SRAweb client = SRAweb() df = client.sra_metadata('SRP016501', detailed=True) df ``` ```` ````` Output: study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_strategy library_source library_selection sample_accession sample_title instrument total_spots total_size run_accession run_total_spots run_total_bases run_alias sra_url_alt sra_url experiment_alias isolate collected_by collection_date geo_loc_name host host_disease isolation_source lat_lon host_sex host_subject_id passage_history BioSampleModel sra_url_alt1 sra_url_alt2 sra_url_alt3 ena_fastq_http ena_fastq_ftp SRP276671 SRX8978626 hCov-19/Canada/ON/VIDO01/2020 (EPI ISL 413015) hCov-19/Canada/ON/VIDO01/2020 (EPI ISL 413015) 2697049 Severe acute respiratory syndrome coronavirus 2 WGS GENOMIC RT-PCR SRS7233795 N/A MinION 96202 79690689 SRR12486810 96202 86575096 VIDO-01.tar.gz https://sra-download.ncbi.nlm.nih.gov/traces/sra1/SRZ/012486/SRR12486810/VIDO-01.tar.gz https://sra-download.ncbi.nlm.nih.gov/traces/sra78/SRR/012194/SRR12486810 N/A ON-VIDO-01-P3 Public Health Ontario 2020-01-23 Canada: Ontario Homo sapiens COVID-19 missing missing male VIDO-01 Vero E6 P3 Pathogen.cl N/A N/A N/A http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR124/010/SRR12486810/SRR12486810_1.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR124/010/SRR12486810/SRR12486810_1.fastq.gz SRP276671 SRX8909137 hCoV-19/Canada/ON-VIDO-01/2020 (EPI_ISL_425177) hCoV-19/Canada/ON-VIDO-01/2020 (EPI_ISL_425177) 2697049 Severe acute respiratory syndrome coronavirus 2 WGS GENOMIC RT-PCR SRS7166526 N/A Illumina MiSeq 866225 173474986 SRR12412952 866225 338457239 SP-2_R1.fastq.gz N/A https://sra-download.ncbi.nlm.nih.gov/traces/sra48/SRR/012122/SRR12412952 N/A ON-VIDO-01-P2 Public Health Ontario 2020-01-23 Canada: Ontario Homo sapiens COVID-19 missing missing male VIDO-01 Vero E6 P2 Pathogen.cl gs://sra-pub-src-10/SRR12412952/SP-2_R2.fastq.1 s3://sra-pub-src-10/SRR12412952/SP-2_R2.fastq.1 https://sra-pub-sars-cov2.s3.amazonaws.com/sra-src/SRR12412952/SP-2_R2.fastq.1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR124/052/SRR12412952/SRR12412952.fastq.gz era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR124/052/SRR12412952/SRR12412952.fastq.gz ------------------------------------------------------------------------ ### Searching SRA/ENA databases and retrieving metadata Let\'s take for example we are interested in coronavirus sequences published on Short Reads Archive (SRA) in the first week of August 2020. `````{tabs} ````{tab} Console ``` bash $ pysradb search -q coronavirus --publication-date 01-08-2020:07-08-2020 --max 10000 ``` ```` ````{tab} Python ``` python from pysradb.search import SraSearch instance = SraSearch(return_max=10000, query="coronavirus", publication_date="01-08-2020:07-08-2020") instance.search() instance.get_df() ``` ```` ````` Output (showing only the first 10 entries): : study_accession experiment_accession experiment_title sample_taxon_id sample_scientific_name experiment_library_strategy experiment_library_source experiment_library_selection sample_accession sample_alias experiment_instrument_model pool_member_spots run_1_size run_1_accession run_1_total_spots run_1_total_bases pmid SRP270658 SRX8679965 GSM4658808: SARS-CoV-2-infected 24h 3; Chlorocebus sabaeus; Severe acute respiratory syndrome coronavirus 2; RNA-Seq 60711 Chlorocebus sabaeus RNA-Seq TRANSCRIPTOMIC cDNA SRS6959042 GSM4658808 NextSeq 500 104223040 9743267247 SRR12164500 104223040 31475358080 11295714 SRP270658 SRX8679964 GSM4658807: SARS-CoV-2-infected 24h 2; Chlorocebus sabaeus; Severe acute respiratory syndrome coronavirus 2; RNA-Seq 60711 Chlorocebus sabaeus RNA-Seq TRANSCRIPTOMIC cDNA SRS6959041 GSM4658807 NextSeq 500 92813819 8703506222 SRR12164499 92813819 28029773338 11295713 SRP253798 SRX8677889 Severe acute respiratory syndrome coronavirus 2 2697049 Severe acute respiratory syndrome coronavirus 2 AMPLICON VIRAL RNA PCR SRS6956975 hCoV-19/Australia/VIC1898/2020 NextSeq 500 456828 51422072 SRR12162149 456828 130280958 11292876 SRP253798 SRX8677888 Severe acute respiratory syndrome coronavirus 2 2697049 Severe acute respiratory syndrome coronavirus 2 AMPLICON VIRAL RNA PCR SRS6956974 hCoV-19/Australia/VIC1886/2020 NextSeq 500 268832 29923966 SRR12162150 268832 75885223 11292875 SRP253798 SRX8677887 Severe acute respiratory syndrome coronavirus 2 2697049 Severe acute respiratory syndrome coronavirus 2 AMPLICON VIRAL RNA PCR SRS6956973 hCoV-19/Australia/VIC1890/2020 NextSeq 500 483526 54629557 SRR12162151 483526 139019404 11292874 SRP253798 SRX8677886 Severe acute respiratory syndrome coronavirus 2 2697049 Severe acute respiratory syndrome coronavirus 2 AMPLICON VIRAL RNA PCR SRS6956971 hCoV-19/Australia/VIC1888/2020 NextSeq 500 473895 53675126 SRR12162152 473895 136058655 11292873 SRP253798 SRX8677885 Severe acute respiratory syndrome coronavirus 2 2697049 Severe acute respiratory syndrome coronavirus 2 AMPLICON VIRAL RNA PCR SRS6956972 hCoV-19/Australia/VIC1891/2020 NextSeq 500 482373 53331905 SRR12162153 482373 135769259 11292872 SRP253798 SRX8677884 Severe acute respiratory syndrome coronavirus 2 2697049 Severe acute respiratory syndrome coronavirus 2 AMPLICON VIRAL RNA PCR SRS6956970 hCoV-19/Australia/VIC1816/2020 NextSeq 550 357052 41111134 SRR12162154 357052 103693201 11292871 SRP253798 SRX8677883 Severe acute respiratory syndrome coronavirus 2 2697049 Severe acute respiratory syndrome coronavirus 2 AMPLICON VIRAL RNA PCR SRS6956969 hCoV-19/Australia/VIC1815/2020 NextSeq 550 307106 35306959 SRR12162155 307106 89866234 11292870 SRP253798 SRX8677882 Severe acute respiratory syndrome coronavirus 2 2697049 Severe acute respiratory syndrome coronavirus 2 AMPLICON VIRAL RNA PCR SRS6956968 hCoV-19/Australia/VIC1814/2020 NextSeq 550 353704 40652239 SRR12162156 353704 103366580 11292869 To query European Nucleotide Archive (ENA) instead: `````{tabs} ````{tab} Console ``` bash $ pysradb search --db ena -q coronavirus --publication-date 01-08-2020:07-08-2020 --max 10000 ``` ```` ````{tab} Python ``` python from pysradb.search import EnaSearch instance = EnaSearch(return_max=10000, query="coronavirus", publication_date="01-08-2020:07-08-2020") instance.search() instance.get_df() ``` ```` ````` Output (showing only the first 10 entries): : study_accession experiment_accession experiment_title description tax_id scientific_name library_strategylibrary_source library_selection sample_accession sample_title instrument_model run_accession read_count base_count PRJEB12126 ERX1264364 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus OTHER TRANSCRIPTOMIC other SAMEA3708907 Sample 1 Illumina HiSeq 2000 ERR1190989 38883498 1161289538 PRJEB12126 ERX1264365 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus OTHER TRANSCRIPTOMIC other SAMEA3708908 Sample 10 Illumina HiSeq 2000 ERR1190990 55544297 1779600908 PRJEB12126 ERX1264366 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus OTHER TRANSCRIPTOMIC other SAMEA3708909 Sample 11 Illumina HiSeq 2000 ERR1190991 54474851 1713994365 PRJEB12126 ERX1264367 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus OTHER TRANSCRIPTOMIC other SAMEA3708910 Sample 12 Illumina HiSeq 2000 ERR1190992 78497711 2489092061 PRJEB12126 ERX1264368 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC RANDOM SAMEA3708911 Sample 13 Illumina HiSeq 2000 ERR1190993 84955423 2627276298 PRJEB12126 ERX1264369 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC RANDOM SAMEA3708912 Sample 14 Illumina HiSeq 2000 ERR1190994 75097651 2293097872 PRJEB12126 ERX1264370 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC RANDOM SAMEA3708913 Sample 15 Illumina HiSeq 2000 ERR1190995 67177553 2060926619 PRJEB12126 ERX1264371 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC RANDOM SAMEA3708914 Sample 16 Illumina HiSeq 2000 ERR1190996 62940694 2061757111 PRJEB12126 ERX1264372 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC RANDOM SAMEA3708915 Sample 17 Illumina HiSeq 2000 ERR1190997 80591061 2475034240 PRJEB12126 ERX1264373 Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling 10090 Mus musculus RNA-Seq TRANSCRIPTOMIC RANDOM SAMEA3708916 Sample 18 Illumina HiSeq 2000 ERR1190998 68575621 2149386138 If the number of returned entries is large, it might be troublesome to filter through the metadata to find any information of interest. As a starting point, we can use the search feature to generate summary statistics and graphs for the search result: ### Statistics `````{tabs} ````{tab} Console ``` bash $ pysradb search --db ena --organism "Severe acute respiratory syndrome coronavirus 2" --max 10000 -s ``` ```` ````{tab} Python ``` python from pysradb.search import EnaSearch instance = EnaSearch(return_max=10000, organism="Severe acute respiratory syndrome coronavirus 2") instance.search() instance.show_result_statistics() ``` ```` ````` Output: Statistics for the search query: ================================= Number of unique studies: 7 Number of unique experiments: 10000 Number of unique runs: 10000 Number of unique samples: 9797 Mean base count of samples: 238380171.626 Median base count of samples: 164470138.000 Sample base count standard deviation: 261654776.053 Date range: 2020-04: 1299 2020-05: 2518 2020-06: 6181 2020-07: 2 Organisms: Severe acute respiratory syndrome coronavirus 2: 10000 Platform: ILLUMINA: 5175 OXFORD_NANOPORE: 4825 Library strategy: AMPLICON: 9789 RNA-Seq: 1 Targeted-Capture: 202 WGS: 8 Library source: GENOMIC: 8 METATRANSCRIPTOMIC: 1 TRANSCRIPTOMIC: 1 VIRAL RNA: 9990 Library selection: PCR: 9789 RANDOM: 9 other: 202 Library layout: PAIRED: 5059 SINGLE: 4941 ### Plotting `````{tabs} ````{tab} Console ``` bash $ pysradb search --db ena -q e --max 500000 -g ``` ```` ````{tab} Python ``` python from pysradb.search import EnaSearch instance = EnaSearch(return_max=500000, "e") instance.search() instance.visualise_results() ``` ```` ````` Output: Graphs generated will automatically be saved under [./search_plots/]{.title-ref}. Optionally, graphs can be shown in python by including the argument [show=True]{.title-ref} Here are some of the available graphs that will be generated: ![image](_static/e1.png){width="600px"} ![image](_static/e2.png){width="600px"} ![image](_static/e3.png){width="600px"} ------------------------------------------------------------------------ ## List of possible [pysradb]{.title-ref} operations $ pysradb usage: pysradb [-h] [--version] [--citation] {metadb,metadata,download,search,gse-to-gsm,gse-to-srp,gsm-to-gse,gsm-to-srp,gsm-to-srr,gsm-to-srs,gsm-to-srx,srp-to-gse,srp-to-srr,srp-to-srs,srp-to-srx,srr-to-gsm,srr-to-srp,srr-to-srs,srr-to-srx,srs-to-gsm,srs-to-srx,srx-to-srp,srx-to-srr,srx-to-srs} ... pysradb: Query NGS metadata and data from NCBI Sequence Read Archive. Citation: 10.12688/f1000research.18676.1 optional arguments: -h, --help show this help message and exit --version show program's version number and exit --citation how to cite subcommands: {metadb,metadata,download,search,gse-to-gsm,gse-to-srp,gsm-to-gse,gsm-to-srp,gsm-to-srr,gsm-to-srs,gsm-to-srx,srp-to-gse,srp-to-srr,srp-to-srs,srp-to-srx,srr-to-gsm,srr-to-srp,srr-to-srs,srr-to-srx,srs-to-gsm,srs-to-srx,srx-to-srp,srx-to-srr,srx-to-srs} metadata Fetch metadata for SRA project (SRPnnnn) download Download SRA project (SRPnnnn) search Search SRA/ENA for matching text gse-to-gsm Get GSM for a GSE gse-to-srp Get SRP for a GSE gsm-to-gse Get GSE for a GSM gsm-to-srp Get SRP for a GSM gsm-to-srr Get SRR for a GSM gsm-to-srs Get SRS for a GSM gsm-to-srx Get SRX for a GSM srp-to-gse Get GSE for a SRP srp-to-srr Get SRR for a SRP srp-to-srs Get SRS for a SRP srp-to-srx Get SRX for a SRP srr-to-gsm Get GSM for a SRR srr-to-srp Get SRP for a SRR srr-to-srs Get SRS for a SRR srr-to-srx Get SRX for a SRR srs-to-gsm Get GSM for a SRS srs-to-srx Get SRX for a SRS srx-to-srp Get SRP for a SRX srx-to-srr Get SRR for a SRX srx-to-srs Get SRS for a SRX ================================================ FILE: notebooks/01.Python-API_demo.ipynb ================================================ { "cells": [ { "cell_type": "markdown", "metadata": {}, "source": [ "[![Open In Colab](https://colab.research.google.com/assets/colab-badge.svg)](https://colab.research.google.com/github/saketkc/pysradb/blob/develop/notebooks/01.Python-API_demo.ipynb)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "# Python API Demo\n", "\n", "This notebook demonstrates the core functionality of pysradb Python API for querying SRA metadata." ] }, { "cell_type": "code", "execution_count": 1, "metadata": { "execution": { "iopub.execute_input": "2025-11-01T13:07:15.972370Z", "iopub.status.busy": "2025-11-01T13:07:15.972015Z", "iopub.status.idle": "2025-11-01T13:07:16.357927Z", "shell.execute_reply": "2025-11-01T13:07:16.356676Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "pysradb 3.0.0.dev0 is already installed\n" ] }, { "name": "stderr", "output_type": "stream", "text": [ "/data/github/pysradb/pysradb/utils.py:16: TqdmExperimentalWarning: Using `tqdm.autonotebook.tqdm` in notebook mode. Use `tqdm.tqdm` instead to force console mode (e.g. in jupyter console)\n", " from tqdm.autonotebook import tqdm\n" ] } ], "source": [ "# Install pysradb if not already installed\n", "try:\n", " import pysradb\n", "\n", " print(f\"pysradb {pysradb.__version__} is already installed\")\n", "except ImportError:\n", " print(\"Installing pysradb from GitHub...\")\n", " import sys\n", "\n", " !{sys.executable} -m pip install -q git+https://github.com/saketkc/pysradb\n", " print(\"pysradb installed successfully!\")" ] }, { "cell_type": "code", "execution_count": 2, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "execution": { "iopub.execute_input": "2025-11-01T13:07:16.423567Z", "iopub.status.busy": "2025-11-01T13:07:16.423041Z", "iopub.status.idle": "2025-11-01T13:07:16.426702Z", "shell.execute_reply": "2025-11-01T13:07:16.425713Z" }, "id": "D-CWF0xjKhxJ", "outputId": "b639c586-2a2b-4ecd-ae4a-55643c276cda" }, "outputs": [], "source": [ "# pip install git+https://github.com/saketkc/pysradb" ] }, { "cell_type": "code", "execution_count": 3, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "execution": { "iopub.execute_input": "2025-11-01T13:07:16.428767Z", "iopub.status.busy": "2025-11-01T13:07:16.428621Z", "iopub.status.idle": "2025-11-01T13:07:17.350867Z", "shell.execute_reply": "2025-11-01T13:07:17.349172Z" }, "id": "Tyd8Sjv3KpMa", "outputId": "9480b87f-a3bd-4507-fac4-c03ee2ad1c8f" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "pysradb 3.0.0.dev0\r\n" ] } ], "source": [ "!pysradb --version" ] }, { "cell_type": "code", "execution_count": 4, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "execution": { "iopub.execute_input": "2025-11-01T13:07:17.354299Z", "iopub.status.busy": "2025-11-01T13:07:17.353950Z", "iopub.status.idle": "2025-11-01T13:07:17.358832Z", "shell.execute_reply": "2025-11-01T13:07:17.357663Z" }, "id": "3h9Wlv3lKb7b", "outputId": "d3cf89f7-f059-41bd-9767-2bb2a0679dbf" }, "outputs": [], "source": [ "from pysradb.sraweb import SRAweb" ] }, { "cell_type": "code", "execution_count": 5, "metadata": { "execution": { "iopub.execute_input": "2025-11-01T13:07:17.361533Z", "iopub.status.busy": "2025-11-01T13:07:17.361250Z", "iopub.status.idle": "2025-11-01T13:07:17.365279Z", "shell.execute_reply": "2025-11-01T13:07:17.364056Z" }, "id": "0iOHm8wUKb8G" }, "outputs": [], "source": [ "db = SRAweb()" ] }, { "cell_type": "markdown", "metadata": { "id": "CDyWgOqzdn6d" }, "source": [ "## Get metadata of one project" ] }, { "cell_type": "code", "execution_count": 6, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 3152 }, "execution": { "iopub.execute_input": "2025-11-01T13:07:17.368102Z", "iopub.status.busy": "2025-11-01T13:07:17.367803Z", "iopub.status.idle": "2025-11-01T13:07:19.140051Z", "shell.execute_reply": "2025-11-01T13:07:19.139033Z" }, "id": "pXJ6WhsjKb_x", "outputId": "dfcb2624-7e85-487c-9550-0d7b7887ed68" }, "outputs": [ { "data": { "text/html": [ "
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study_accessionstudy_titleexperiment_accessionexperiment_titleexperiment_descorganism_taxidorganism_namelibrary_namelibrary_strategylibrary_source...biosamplebioprojectinstrumentinstrument_modelinstrument_model_desctotal_spotstotal_sizerun_accessionrun_total_spotsrun_total_bases
133SRP016501Evolutionary dynamics of gene and isoform regu...SRX196264GSM1020640: mouse_a_brain; Mus musculus; RNA-SeqGSM1020640: mouse_a_brain; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMIC...SAMN01766814PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA872646045927043102SRR594393872646048726460400
132SRP016501Evolutionary dynamics of gene and isoform regu...SRX196265GSM1020641: mouse_a_colon; Mus musculus; RNA-SeqGSM1020641: mouse_a_colon; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMIC...SAMN01766815PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA1018164916835402318SRR59439410181649110181649100
131SRP016501Evolutionary dynamics of gene and isoform regu...SRX196266GSM1020642: mouse_a_heart; Mus musculus; RNA-SeqGSM1020642: mouse_a_heart; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMIC...SAMN01766816PRJNA177791Illumina Genome Analyzer IIxIllumina Genome Analyzer IIxILLUMINA351759821502674440SRR594395351759822532670704
130SRP016501Evolutionary dynamics of gene and isoform regu...SRX196267GSM1020643: mouse_a_kidney; Mus musculus; RNA-SeqGSM1020643: mouse_a_kidney; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMIC...SAMN01766817PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA1192747867555854784SRR59439611927478611927478600
129SRP016501Evolutionary dynamics of gene and isoform regu...SRX196268GSM1020644: mouse_a_liver; Mus musculus; RNA-SeqGSM1020644: mouse_a_liver; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMIC...SAMN01766818PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA1162924787481554926SRR59439711629247811629247800
..................................................................
4SRP016501Evolutionary dynamics of gene and isoform regu...SRX196393GSM1020769: chicken_c_liver; Gallus gallus; RN...GSM1020769: chicken_c_liver; Gallus gallus; RN...9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766943PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA18978066562367072SRR594522189780661366420752
3SRP016501Evolutionary dynamics of gene and isoform regu...SRX196394GSM1020770: chicken_c_lung; Gallus gallus; RNA...GSM1020770: chicken_c_lung; Gallus gallus; RNA...9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766944PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA26604280931417024SRR594523266042801862299600
2SRP016501Evolutionary dynamics of gene and isoform regu...SRX196395GSM1020771: chicken_c_skm; Gallus gallus; RNA-SeqGSM1020771: chicken_c_skm; Gallus gallus; RNA-Seq9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766945PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA25606436986287075SRR594524256064361792450520
1SRP016501Evolutionary dynamics of gene and isoform regu...SRX196396GSM1020772: chicken_c_spleen; Gallus gallus; R...GSM1020772: chicken_c_spleen; Gallus gallus; R...9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766946PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA244017081201671888SRR594525244017081756922976
0SRP016501Evolutionary dynamics of gene and isoform regu...SRX196397GSM1020773: chicken_c_testes; Gallus gallus; R...GSM1020773: chicken_c_testes; Gallus gallus; R...9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766947PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA374233941980545796SRR594526374233942993871520
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134 rows × 24 columns

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" ], "text/plain": [ " study_accession study_title \\\n", "133 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "132 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "131 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "130 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "129 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", ".. ... ... \n", "4 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "3 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "2 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "1 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "0 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "\n", " experiment_accession experiment_title \\\n", "133 SRX196264 GSM1020640: mouse_a_brain; Mus musculus; RNA-Seq \n", "132 SRX196265 GSM1020641: mouse_a_colon; Mus musculus; RNA-Seq \n", "131 SRX196266 GSM1020642: mouse_a_heart; Mus musculus; RNA-Seq \n", "130 SRX196267 GSM1020643: mouse_a_kidney; Mus musculus; RNA-Seq \n", "129 SRX196268 GSM1020644: mouse_a_liver; Mus musculus; RNA-Seq \n", ".. ... ... \n", "4 SRX196393 GSM1020769: chicken_c_liver; Gallus gallus; RN... \n", "3 SRX196394 GSM1020770: chicken_c_lung; Gallus gallus; RNA... \n", "2 SRX196395 GSM1020771: chicken_c_skm; Gallus gallus; RNA-Seq \n", "1 SRX196396 GSM1020772: chicken_c_spleen; Gallus gallus; R... \n", "0 SRX196397 GSM1020773: chicken_c_testes; Gallus gallus; R... \n", "\n", " experiment_desc organism_taxid \\\n", "133 GSM1020640: mouse_a_brain; Mus musculus; RNA-Seq 10090 \n", "132 GSM1020641: mouse_a_colon; Mus musculus; RNA-Seq 10090 \n", "131 GSM1020642: mouse_a_heart; Mus musculus; RNA-Seq 10090 \n", "130 GSM1020643: mouse_a_kidney; Mus musculus; RNA-Seq 10090 \n", "129 GSM1020644: mouse_a_liver; Mus musculus; RNA-Seq 10090 \n", ".. ... ... \n", "4 GSM1020769: chicken_c_liver; Gallus gallus; RN... 9031 \n", "3 GSM1020770: chicken_c_lung; Gallus gallus; RNA... 9031 \n", "2 GSM1020771: chicken_c_skm; Gallus gallus; RNA-Seq 9031 \n", "1 GSM1020772: chicken_c_spleen; Gallus gallus; R... 9031 \n", "0 GSM1020773: chicken_c_testes; Gallus gallus; R... 9031 \n", "\n", " organism_name library_name library_strategy library_source ... \\\n", "133 Mus musculus RNA-Seq TRANSCRIPTOMIC ... \n", "132 Mus musculus RNA-Seq TRANSCRIPTOMIC ... \n", "131 Mus musculus RNA-Seq TRANSCRIPTOMIC ... \n", "130 Mus musculus RNA-Seq TRANSCRIPTOMIC ... \n", "129 Mus musculus RNA-Seq TRANSCRIPTOMIC ... \n", ".. ... ... ... ... ... \n", "4 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "3 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "2 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "1 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "0 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "\n", " biosample bioproject instrument \\\n", "133 SAMN01766814 PRJNA177791 Illumina HiSeq 2000 \n", "132 SAMN01766815 PRJNA177791 Illumina HiSeq 2000 \n", "131 SAMN01766816 PRJNA177791 Illumina Genome Analyzer IIx \n", "130 SAMN01766817 PRJNA177791 Illumina HiSeq 2000 \n", "129 SAMN01766818 PRJNA177791 Illumina HiSeq 2000 \n", ".. ... ... ... \n", "4 SAMN01766943 PRJNA177791 Illumina HiSeq 2000 \n", "3 SAMN01766944 PRJNA177791 Illumina HiSeq 2000 \n", "2 SAMN01766945 PRJNA177791 Illumina HiSeq 2000 \n", "1 SAMN01766946 PRJNA177791 Illumina HiSeq 2000 \n", "0 SAMN01766947 PRJNA177791 Illumina HiSeq 2000 \n", "\n", " instrument_model instrument_model_desc total_spots \\\n", "133 Illumina HiSeq 2000 ILLUMINA 87264604 \n", "132 Illumina HiSeq 2000 ILLUMINA 101816491 \n", "131 Illumina Genome Analyzer IIx ILLUMINA 35175982 \n", "130 Illumina HiSeq 2000 ILLUMINA 119274786 \n", "129 Illumina HiSeq 2000 ILLUMINA 116292478 \n", ".. ... ... ... \n", "4 Illumina HiSeq 2000 ILLUMINA 18978066 \n", "3 Illumina HiSeq 2000 ILLUMINA 26604280 \n", "2 Illumina HiSeq 2000 ILLUMINA 25606436 \n", "1 Illumina HiSeq 2000 ILLUMINA 24401708 \n", "0 Illumina HiSeq 2000 ILLUMINA 37423394 \n", "\n", " total_size run_accession run_total_spots run_total_bases \n", "133 5927043102 SRR594393 87264604 8726460400 \n", "132 6835402318 SRR594394 101816491 10181649100 \n", "131 1502674440 SRR594395 35175982 2532670704 \n", "130 7555854784 SRR594396 119274786 11927478600 \n", "129 7481554926 SRR594397 116292478 11629247800 \n", ".. ... ... ... ... \n", "4 562367072 SRR594522 18978066 1366420752 \n", "3 931417024 SRR594523 26604280 1862299600 \n", "2 986287075 SRR594524 25606436 1792450520 \n", "1 1201671888 SRR594525 24401708 1756922976 \n", "0 1980545796 SRR594526 37423394 2993871520 \n", "\n", "[134 rows x 24 columns]" ] }, "execution_count": 6, "metadata": {}, "output_type": "execute_result" } ], "source": [ "df = db.sra_metadata(\"SRP016501\")\n", "df" ] }, { "cell_type": "markdown", "metadata": { "id": "gl-3e2L9Kb_7" }, "source": [ "## Get detailed metadata" ] }, { "cell_type": "code", "execution_count": 7, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 1000 }, "execution": { "iopub.execute_input": "2025-11-01T13:07:19.143434Z", "iopub.status.busy": "2025-11-01T13:07:19.143150Z", "iopub.status.idle": "2025-11-01T13:07:26.352948Z", "shell.execute_reply": "2025-11-01T13:07:26.351467Z" }, "id": "JBUcbaxlKb_9", "outputId": "57afe1b5-cb98-4cdd-b452-69527cbd695d" }, "outputs": [ { "data": { "text/html": [ "
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2SRR594395SRP016501Evolutionary dynamics of gene and isoform regu...SRX196266GSM1020642: mouse_a_heart; Mus musculus; RNA-SeqGSM1020642: mouse_a_heart; Mus musculus; RNA-Seq10090Mus musculus<NA>RNA-Seq...GSM1020642_1mouse_heartheartDBA/2J<NA>http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...<NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...
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4SRR594397SRP016501Evolutionary dynamics of gene and isoform regu...SRX196268GSM1020644: mouse_a_liver; Mus musculus; RNA-SeqGSM1020644: mouse_a_liver; Mus musculus; RNA-Seq10090Mus musculus<NA>RNA-Seq...GSM1020644_1mouse_liverliverDBA/2J<NA>http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...<NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...
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129SRR594522SRP016501Evolutionary dynamics of gene and isoform regu...SRX196393GSM1020769: chicken_c_liver; Gallus gallus; RN...GSM1020769: chicken_c_liver; Gallus gallus; RN...9031Gallus gallus<NA>RNA-Seq...GSM1020769_1chicken_liverliver<NA><NA>http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...<NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...
130SRR594523SRP016501Evolutionary dynamics of gene and isoform regu...SRX196394GSM1020770: chicken_c_lung; Gallus gallus; RNA...GSM1020770: chicken_c_lung; Gallus gallus; RNA...9031Gallus gallus<NA>RNA-Seq...GSM1020770_1chicken_lunglung<NA><NA>http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...<NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...
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132SRR594525SRP016501Evolutionary dynamics of gene and isoform regu...SRX196396GSM1020772: chicken_c_spleen; Gallus gallus; R...GSM1020772: chicken_c_spleen; Gallus gallus; R...9031Gallus gallus<NA>RNA-Seq...GSM1020772_1chicken_spleenspleen<NA><NA>http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR...<NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/...
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134 rows × 53 columns

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" ], "text/plain": [ " run_accession study_accession \\\n", "0 SRR594393 SRP016501 \n", "1 SRR594394 SRP016501 \n", "2 SRR594395 SRP016501 \n", "3 SRR594396 SRP016501 \n", "4 SRR594397 SRP016501 \n", ".. ... ... \n", "129 SRR594522 SRP016501 \n", "130 SRR594523 SRP016501 \n", "131 SRR594524 SRP016501 \n", "132 SRR594525 SRP016501 \n", "133 SRR594526 SRP016501 \n", "\n", " study_title experiment_accession \\\n", "0 Evolutionary dynamics of gene and isoform regu... SRX196264 \n", "1 Evolutionary dynamics of gene and isoform regu... SRX196265 \n", "2 Evolutionary dynamics of gene and isoform regu... SRX196266 \n", "3 Evolutionary dynamics of gene and isoform regu... SRX196267 \n", "4 Evolutionary dynamics of gene and isoform regu... SRX196268 \n", ".. ... ... \n", "129 Evolutionary dynamics of gene and isoform regu... SRX196393 \n", "130 Evolutionary dynamics of gene and isoform regu... SRX196394 \n", "131 Evolutionary dynamics of gene and isoform regu... SRX196395 \n", "132 Evolutionary dynamics of gene and isoform regu... SRX196396 \n", "133 Evolutionary dynamics of gene and isoform regu... SRX196397 \n", "\n", " experiment_title \\\n", "0 GSM1020640: mouse_a_brain; Mus musculus; RNA-Seq \n", "1 GSM1020641: mouse_a_colon; Mus musculus; RNA-Seq \n", "2 GSM1020642: mouse_a_heart; Mus musculus; RNA-Seq \n", "3 GSM1020643: mouse_a_kidney; Mus musculus; RNA-Seq \n", "4 GSM1020644: mouse_a_liver; Mus musculus; RNA-Seq \n", ".. ... \n", "129 GSM1020769: chicken_c_liver; Gallus gallus; RN... \n", "130 GSM1020770: chicken_c_lung; Gallus gallus; RNA... \n", "131 GSM1020771: chicken_c_skm; Gallus gallus; RNA-Seq \n", "132 GSM1020772: chicken_c_spleen; Gallus gallus; R... \n", "133 GSM1020773: chicken_c_testes; Gallus gallus; R... \n", "\n", " experiment_desc organism_taxid \\\n", "0 GSM1020640: mouse_a_brain; Mus musculus; RNA-Seq 10090 \n", "1 GSM1020641: mouse_a_colon; Mus musculus; RNA-Seq 10090 \n", "2 GSM1020642: mouse_a_heart; Mus musculus; RNA-Seq 10090 \n", "3 GSM1020643: mouse_a_kidney; Mus musculus; RNA-Seq 10090 \n", "4 GSM1020644: mouse_a_liver; Mus musculus; RNA-Seq 10090 \n", ".. ... ... \n", "129 GSM1020769: chicken_c_liver; Gallus gallus; RN... 9031 \n", "130 GSM1020770: chicken_c_lung; Gallus gallus; RNA... 9031 \n", "131 GSM1020771: chicken_c_skm; Gallus gallus; RNA-Seq 9031 \n", "132 GSM1020772: chicken_c_spleen; Gallus gallus; R... 9031 \n", "133 GSM1020773: chicken_c_testes; Gallus gallus; R... 9031 \n", "\n", " organism_name library_name library_strategy ... experiment_alias \\\n", "0 Mus musculus RNA-Seq ... GSM1020640_1 \n", "1 Mus musculus RNA-Seq ... GSM1020641_1 \n", "2 Mus musculus RNA-Seq ... GSM1020642_1 \n", "3 Mus musculus RNA-Seq ... GSM1020643_1 \n", "4 Mus musculus RNA-Seq ... GSM1020644_1 \n", ".. ... ... ... ... ... \n", "129 Gallus gallus RNA-Seq ... GSM1020769_1 \n", "130 Gallus gallus RNA-Seq ... GSM1020770_1 \n", "131 Gallus gallus RNA-Seq ... GSM1020771_1 \n", "132 Gallus gallus RNA-Seq ... GSM1020772_1 \n", "133 Gallus gallus RNA-Seq ... GSM1020773_1 \n", "\n", " source_name tissue strain ena_fastq_http \\\n", "0 mouse_brain brain DBA/2J \n", "1 mouse_colon colon DBA/2J \n", "2 mouse_heart heart DBA/2J \n", "3 mouse_kidney kidney DBA/2J \n", "4 mouse_liver liver DBA/2J \n", ".. ... ... ... ... \n", "129 chicken_liver liver \n", "130 chicken_lung lung \n", "131 chicken_skm skeletal muscle \n", "132 chicken_spleen spleen \n", "133 chicken_testes testes \n", "\n", " ena_fastq_http_1 \\\n", "0 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "2 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "3 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "4 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", ".. ... \n", "129 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "130 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "131 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "132 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "133 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "\n", " ena_fastq_http_2 ena_fastq_ftp \\\n", "0 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "1 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "2 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "3 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "4 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", ".. ... ... \n", "129 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "130 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "131 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "132 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "133 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR594/SRR... \n", "\n", " ena_fastq_ftp_1 \\\n", "0 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "1 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "2 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "3 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "4 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", ".. ... \n", "129 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "130 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "131 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "132 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "133 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "\n", " ena_fastq_ftp_2 \n", "0 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "1 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "2 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "3 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "4 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", ".. ... \n", "129 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "130 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "131 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "132 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "133 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR594/... \n", "\n", "[134 rows x 53 columns]" ] }, "execution_count": 7, "metadata": {}, "output_type": "execute_result" } ], "source": [ "df = db.sra_metadata(\"SRP016501\", detailed=True)\n", "df" ] }, { "cell_type": "markdown", "metadata": { "id": "unVsYJARdsfL" }, "source": [ "## Get metadata of multiple projects" ] }, { "cell_type": "code", "execution_count": 8, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 1000 }, "execution": { "iopub.execute_input": "2025-11-01T13:07:26.356567Z", "iopub.status.busy": "2025-11-01T13:07:26.356317Z", "iopub.status.idle": "2025-11-01T13:07:28.115240Z", "shell.execute_reply": "2025-11-01T13:07:28.113903Z" }, "id": "YzbKfVVOdvIE", "outputId": "8333cc13-a3af-446d-ffad-54caab6fa46a" }, "outputs": [ { "data": { "text/html": [ "
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study_accessionstudy_titleexperiment_accessionexperiment_titleexperiment_descorganism_taxidorganism_namelibrary_namelibrary_strategylibrary_source...biosamplebioprojectinstrumentinstrument_modelinstrument_model_desctotal_spotstotal_sizerun_accessionrun_total_spotsrun_total_bases
25SRP098789Selective stalling of human translation throug...SRX2536403GSM2475997: 1.5 µM PF-067446846, 10 min, rep 1...GSM2475997: 1.5 µM PF-067446846, 10 min, rep 1...9606Homo sapiensOTHERTRANSCRIPTOMIC...SAMN06293487PRJNA369742Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA42082855916745706SRR5227288420828552104142750
24SRP098789Selective stalling of human translation throug...SRX2536404GSM2475998: 1.5 µM PF-067446846, 10 min, rep 2...GSM2475998: 1.5 µM PF-067446846, 10 min, rep 2...9606Homo sapiensOTHERTRANSCRIPTOMIC...SAMN06293486PRJNA369742Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA416574611360366732SRR5227289416574612082873050
23SRP098789Selective stalling of human translation throug...SRX2536405GSM2475999: 1.5 µM PF-067446846, 10 min, rep 3...GSM2475999: 1.5 µM PF-067446846, 10 min, rep 3...9606Homo sapiensOTHERTRANSCRIPTOMIC...SAMN06293485PRJNA369742Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA404629731287284933SRR5227290404629732023148650
22SRP098789Selective stalling of human translation throug...SRX2536406GSM2476000: 0.3 µM PF-067446846, 10 min, rep 1...GSM2476000: 0.3 µM PF-067446846, 10 min, rep 1...9606Homo sapiensOTHERTRANSCRIPTOMIC...SAMN06293484PRJNA369742Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA41143319843881081SRR5227291411433192057165950
21SRP098789Selective stalling of human translation throug...SRX2536407GSM2476001: 0.3 µM PF-067446846, 10 min, rep 2...GSM2476001: 0.3 µM PF-067446846, 10 min, rep 2...9606Homo sapiensOTHERTRANSCRIPTOMIC...SAMN06293483PRJNA369742Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA605524371875910244SRR5227292605524373027621850
..................................................................
30SRP016501Evolutionary dynamics of gene and isoform regu...SRX196393GSM1020769: chicken_c_liver; Gallus gallus; RN...GSM1020769: chicken_c_liver; Gallus gallus; RN...9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766943PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA18978066562367072SRR594522189780661366420752
29SRP016501Evolutionary dynamics of gene and isoform regu...SRX196394GSM1020770: chicken_c_lung; Gallus gallus; RNA...GSM1020770: chicken_c_lung; Gallus gallus; RNA...9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766944PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA26604280931417024SRR594523266042801862299600
28SRP016501Evolutionary dynamics of gene and isoform regu...SRX196395GSM1020771: chicken_c_skm; Gallus gallus; RNA-SeqGSM1020771: chicken_c_skm; Gallus gallus; RNA-Seq9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766945PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA25606436986287075SRR594524256064361792450520
27SRP016501Evolutionary dynamics of gene and isoform regu...SRX196396GSM1020772: chicken_c_spleen; Gallus gallus; R...GSM1020772: chicken_c_spleen; Gallus gallus; R...9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766946PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA244017081201671888SRR594525244017081756922976
26SRP016501Evolutionary dynamics of gene and isoform regu...SRX196397GSM1020773: chicken_c_testes; Gallus gallus; R...GSM1020773: chicken_c_testes; Gallus gallus; R...9031Gallus gallusRNA-SeqTRANSCRIPTOMIC...SAMN01766947PRJNA177791Illumina HiSeq 2000Illumina HiSeq 2000ILLUMINA374233941980545796SRR594526374233942993871520
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160 rows × 24 columns

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" ], "text/plain": [ " study_accession study_title \\\n", "25 SRP098789 Selective stalling of human translation throug... \n", "24 SRP098789 Selective stalling of human translation throug... \n", "23 SRP098789 Selective stalling of human translation throug... \n", "22 SRP098789 Selective stalling of human translation throug... \n", "21 SRP098789 Selective stalling of human translation throug... \n", ".. ... ... \n", "30 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "29 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "28 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "27 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "26 SRP016501 Evolutionary dynamics of gene and isoform regu... \n", "\n", " experiment_accession experiment_title \\\n", "25 SRX2536403 GSM2475997: 1.5 µM PF-067446846, 10 min, rep 1... \n", "24 SRX2536404 GSM2475998: 1.5 µM PF-067446846, 10 min, rep 2... \n", "23 SRX2536405 GSM2475999: 1.5 µM PF-067446846, 10 min, rep 3... \n", "22 SRX2536406 GSM2476000: 0.3 µM PF-067446846, 10 min, rep 1... \n", "21 SRX2536407 GSM2476001: 0.3 µM PF-067446846, 10 min, rep 2... \n", ".. ... ... \n", "30 SRX196393 GSM1020769: chicken_c_liver; Gallus gallus; RN... \n", "29 SRX196394 GSM1020770: chicken_c_lung; Gallus gallus; RNA... \n", "28 SRX196395 GSM1020771: chicken_c_skm; Gallus gallus; RNA-Seq \n", "27 SRX196396 GSM1020772: chicken_c_spleen; Gallus gallus; R... \n", "26 SRX196397 GSM1020773: chicken_c_testes; Gallus gallus; R... \n", "\n", " experiment_desc organism_taxid \\\n", "25 GSM2475997: 1.5 µM PF-067446846, 10 min, rep 1... 9606 \n", "24 GSM2475998: 1.5 µM PF-067446846, 10 min, rep 2... 9606 \n", "23 GSM2475999: 1.5 µM PF-067446846, 10 min, rep 3... 9606 \n", "22 GSM2476000: 0.3 µM PF-067446846, 10 min, rep 1... 9606 \n", "21 GSM2476001: 0.3 µM PF-067446846, 10 min, rep 2... 9606 \n", ".. ... ... \n", "30 GSM1020769: chicken_c_liver; Gallus gallus; RN... 9031 \n", "29 GSM1020770: chicken_c_lung; Gallus gallus; RNA... 9031 \n", "28 GSM1020771: chicken_c_skm; Gallus gallus; RNA-Seq 9031 \n", "27 GSM1020772: chicken_c_spleen; Gallus gallus; R... 9031 \n", "26 GSM1020773: chicken_c_testes; Gallus gallus; R... 9031 \n", "\n", " organism_name library_name library_strategy library_source ... \\\n", "25 Homo sapiens OTHER TRANSCRIPTOMIC ... \n", "24 Homo sapiens OTHER TRANSCRIPTOMIC ... \n", "23 Homo sapiens OTHER TRANSCRIPTOMIC ... \n", "22 Homo sapiens OTHER TRANSCRIPTOMIC ... \n", "21 Homo sapiens OTHER TRANSCRIPTOMIC ... \n", ".. ... ... ... ... ... \n", "30 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "29 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "28 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "27 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "26 Gallus gallus RNA-Seq TRANSCRIPTOMIC ... \n", "\n", " biosample bioproject instrument instrument_model \\\n", "25 SAMN06293487 PRJNA369742 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", "24 SAMN06293486 PRJNA369742 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", "23 SAMN06293485 PRJNA369742 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", "22 SAMN06293484 PRJNA369742 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", "21 SAMN06293483 PRJNA369742 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", ".. ... ... ... ... \n", "30 SAMN01766943 PRJNA177791 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", "29 SAMN01766944 PRJNA177791 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", "28 SAMN01766945 PRJNA177791 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", "27 SAMN01766946 PRJNA177791 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", "26 SAMN01766947 PRJNA177791 Illumina HiSeq 2000 Illumina HiSeq 2000 \n", "\n", " instrument_model_desc total_spots total_size run_accession \\\n", "25 ILLUMINA 42082855 916745706 SRR5227288 \n", "24 ILLUMINA 41657461 1360366732 SRR5227289 \n", "23 ILLUMINA 40462973 1287284933 SRR5227290 \n", "22 ILLUMINA 41143319 843881081 SRR5227291 \n", "21 ILLUMINA 60552437 1875910244 SRR5227292 \n", ".. ... ... ... ... \n", "30 ILLUMINA 18978066 562367072 SRR594522 \n", "29 ILLUMINA 26604280 931417024 SRR594523 \n", "28 ILLUMINA 25606436 986287075 SRR594524 \n", "27 ILLUMINA 24401708 1201671888 SRR594525 \n", "26 ILLUMINA 37423394 1980545796 SRR594526 \n", "\n", " run_total_spots run_total_bases \n", "25 42082855 2104142750 \n", "24 41657461 2082873050 \n", "23 40462973 2023148650 \n", "22 41143319 2057165950 \n", "21 60552437 3027621850 \n", ".. ... ... \n", "30 18978066 1366420752 \n", "29 26604280 1862299600 \n", "28 25606436 1792450520 \n", "27 24401708 1756922976 \n", "26 37423394 2993871520 \n", "\n", "[160 rows x 24 columns]" ] }, "execution_count": 8, "metadata": {}, "output_type": "execute_result" } ], "source": [ "df = db.sra_metadata([\"SRP016501\", \"SRP098789\"])\n", "df" ] }, { "cell_type": "markdown", "metadata": { "id": "UuKRorTWZoQQ" }, "source": [ "## Get metadata of a Run" ] }, { "cell_type": "code", "execution_count": 9, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 214 }, "execution": { "iopub.execute_input": "2025-11-01T13:07:28.118706Z", "iopub.status.busy": "2025-11-01T13:07:28.118442Z", "iopub.status.idle": "2025-11-01T13:07:32.510732Z", "shell.execute_reply": "2025-11-01T13:07:32.509474Z" }, "id": "V1bMg1W6ZqZL", "outputId": "9e6029ab-b0bf-4954-ada4-da4dc5ccb058" }, "outputs": [ { "data": { "text/html": [ "
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0SRR11085797SRP249482Bat coronavirus RaTG13 Genome sequencingSRX7724752RNA-Seq of Rhinolophus affinis:Fecal swabRNA-Seq of Rhinolophus affinis:Fecal swab694135unidentified coronavirusRaTG13RNA-Seq...not applicablefecal swabnot collectedPathogen.cl<NA>http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR110/097...http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR110/097...<NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR110/...era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR110/...
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1 rows × 60 columns

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" ], "text/plain": [ " run_accession study_accession study_title \\\n", "0 SRR11085797 SRP249482 Bat coronavirus RaTG13 Genome sequencing \n", "\n", " experiment_accession experiment_title \\\n", "0 SRX7724752 RNA-Seq of Rhinolophus affinis:Fecal swab \n", "\n", " experiment_desc organism_taxid \\\n", "0 RNA-Seq of Rhinolophus affinis:Fecal swab 694135 \n", "\n", " organism_name library_name library_strategy ... \\\n", "0 unidentified coronavirus RaTG13 RNA-Seq ... \n", "\n", " host_disease isolation_source lat_lon biosamplemodel \\\n", "0 not applicable fecal swab not collected Pathogen.cl \n", "\n", " ena_fastq_http ena_fastq_http_1 \\\n", "0 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR110/097... \n", "\n", " ena_fastq_http_2 ena_fastq_ftp \\\n", "0 http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR110/097... \n", "\n", " ena_fastq_ftp_1 \\\n", "0 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR110/... \n", "\n", " ena_fastq_ftp_2 \n", "0 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR110/... \n", "\n", "[1 rows x 60 columns]" ] }, "execution_count": 9, "metadata": {}, "output_type": "execute_result" } ], "source": [ "df = db.sra_metadata(\"SRR11085797\", detailed=True)\n", "df" ] }, { "cell_type": "markdown", "metadata": { "id": "cADqnvl0KcAn" }, "source": [ "## SRX to GSM" ] }, { "cell_type": "code", "execution_count": 10, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 80 }, "execution": { "iopub.execute_input": "2025-11-01T13:07:32.514680Z", "iopub.status.busy": "2025-11-01T13:07:32.514374Z", "iopub.status.idle": "2025-11-01T13:07:33.931846Z", "shell.execute_reply": "2025-11-01T13:07:33.930414Z" }, "id": "iCFhnY0FKcAp", "outputId": "7efff242-ca68-499a-ee9e-0ec1f1dff95a" }, "outputs": [ { "data": { "text/html": [ "
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experiment_accessionexperiment_alias
0SRX1254413GSM1887643
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" ], "text/plain": [ " experiment_accession experiment_alias\n", "0 SRX1254413 GSM1887643" ] }, "execution_count": 10, "metadata": {}, "output_type": "execute_result" } ], "source": [ "df = db.srx_to_gsm(\"SRX1254413\")\n", "df" ] } ], "metadata": { "colab": { "collapsed_sections": [], "include_colab_link": true, "name": "01.Python-API_demo.ipynb", "provenance": [] }, "kernelspec": { "display_name": "Python 3", "language": "python", "name": "python3" }, "language_info": { "codemirror_mode": { "name": "ipython", "version": 3 }, "file_extension": ".py", "mimetype": "text/x-python", "name": "python", "nbconvert_exporter": "python", "pygments_lexer": "ipython3", "version": "3.13.9" }, "widgets": { "application/vnd.jupyter.widget-state+json": { "state": {}, "version_major": 2, "version_minor": 0 } } }, "nbformat": 4, "nbformat_minor": 4 } ================================================ FILE: notebooks/02.Commandline_download.ipynb ================================================ { "cells": [ { "cell_type": "markdown", "metadata": {}, "source": [ "[![Open In Colab](https://colab.research.google.com/assets/colab-badge.svg)](https://colab.research.google.com/github/saketkc/pysradb/blob/develop/notebooks/02.Commandline_download.ipynb)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "# Command-line Download\n", "\n", "This notebook demonstrates how to use pysradb from the command line to download SRA data." ] }, { "cell_type": "code", "execution_count": null, "metadata": {}, "outputs": [], "source": [ "# Install pysradb if not already installed\n", "try:\n", " import pysradb\n", "\n", " print(f\"pysradb {pysradb.__version__} is already installed\")\n", "except ImportError:\n", " print(\"Installing pysradb from GitHub...\")\n", " import sys\n", "\n", " !{sys.executable} -m pip install -q git+https://github.com/saketkc/pysradb\n", " print(\"pysradb installed successfully!\")" ] }, { "cell_type": "code", "execution_count": 1, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 238 }, "colab_type": "code", "id": "EU_ZNQwnHJff", "outputId": "95271151-2ca0-416b-b01f-3077a1239c22" }, "outputs": [], "source": [ "# pip install -U pysradb" ] }, { "cell_type": "code", "execution_count": 2, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 34 }, "colab_type": "code", "id": "FK_PzlAUHU0b", "outputId": "a5c47c2f-f85e-4f68-fad0-8f549d0a8ea8" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "pysradb 2.4.1\n" ] } ], "source": [ "!pysradb --version" ] }, { "cell_type": "markdown", "metadata": { "colab_type": "text", "id": "wFEs7nMEHiZA" }, "source": [ "## Get metadata for SRX (SRRs/SRS etc)" ] }, { "cell_type": "code", "execution_count": 3, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 71 }, "colab_type": "code", "id": "4Krzqj3IHX6J", "outputId": "c9f0b0de-aec0-4cd1-aaae-616ae0461faa" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "experiment_accession\trun_accession\tstudy_accession\tstudy_title\texperiment_title\texperiment_desc\torganism_taxid\torganism_name\tlibrary_name\tlibrary_strategy\tlibrary_source\tlibrary_selection\tlibrary_layout\tsample_accession\tsample_title\tbiosample\tbioproject\tinstrument\tinstrument_model\tinstrument_model_desc\ttotal_spots\ttotal_size\trun_total_spots\trun_total_bases\n", "SRX4720625\tSRR7882015\tSRP162234\tTranscriptomic profile of zebrafish cardiomyocytes throughout heart development\tGSM3396533: wt_GFPpos_24hpf_rep1; Danio rerio; RNA-Seq\tGSM3396533: wt_GFPpos_24hpf_rep1; Danio rerio; RNA-Seq\t7955\tDanio rerio\t\tRNA-Seq\tTRANSCRIPTOMIC\tcDNA\tPAIRED\tSRS3805811\t\tSAMN10095723\tPRJNA492280\tNextSeq 500\tNextSeq 500\tILLUMINA\t47867961\t3470385670\t47867961\t7230485009\n" ] } ], "source": [ "!pysradb srx-to-srr SRX4720625" ] }, { "cell_type": "markdown", "metadata": { "colab_type": "text", "id": "yorftAz6HtFp" }, "source": [ "## Get detailed metadata " ] }, { "cell_type": "code", "execution_count": 4, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 71 }, "colab_type": "code", "id": "30cYmMXFHpRA", "outputId": "1ef01d12-c84c-4524-c163-e24e565b4584" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "experiment_accession\trun_accession\tstudy_accession\tstudy_title\texperiment_title\texperiment_desc\torganism_taxid\torganism_name\tlibrary_name\tlibrary_strategy\tlibrary_source\tlibrary_selection\tlibrary_layout\tsample_accession\tsample_title\tbiosample\tbioproject\tinstrument\tinstrument_model\tinstrument_model_desc\ttotal_spots\ttotal_size\trun_total_spots\trun_total_bases\trun_alias\tpublic_filename\tpublic_size\tpublic_date\tpublic_md5\tpublic_version\tpublic_semantic_name\tpublic_supertype\tpublic_sratoolkit\taws_url\taws_free_egress\taws_access_type\tpublic_url\tncbi_url\tncbi_free_egress\tncbi_access_type\tgcp_url\tgcp_free_egress\tgcp_access_type\texperiment_alias\tsource_name\ttissue\tdevelopmental stage\tgfp status\tgenetic background\tena_fastq_http\tena_fastq_http_1\tena_fastq_http_2\tena_fastq_ftp\tena_fastq_ftp_1\tena_fastq_ftp_2\n", "SRX4720625\tSRR7882015\tSRP162234\tTranscriptomic profile of zebrafish cardiomyocytes throughout heart development\tGSM3396533: wt_GFPpos_24hpf_rep1; Danio rerio; RNA-Seq\tGSM3396533: wt_GFPpos_24hpf_rep1; Danio rerio; RNA-Seq\t7955\tDanio rerio\t\tRNA-Seq\tTRANSCRIPTOMIC\tcDNA\tPAIRED\tSRS3805811\t\tSAMN10095723\tPRJNA492280\tNextSeq 500\tNextSeq 500\tILLUMINA\t47867961\t3470385670\t47867961\t7230485009\tGSM3396533_r1\tSRR7882015.sralite\t1881003321\t2020-06-14 12:02:25\t8161154ca4e9cf674e3f0e4af74c8455\t1\tSRA Lite\tPrimary ETL\t1\ts3://sra-pub-zq-8/SRR7882015/SRR7882015.sralite.1\ts3.us-east-1\taws identity\thttps://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos5/sra-pub-zq-11/SRR007/882/SRR7882015/SRR7882015.sralite.1\thttps://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos5/sra-pub-zq-11/SRR007/882/SRR7882015/SRR7882015.sralite.1\tworldwide\tanonymous\tgs://sra-pub-zq-107/SRR7882015/SRR7882015.zq.1\tgs.us-east1\tgcp identity\tGSM3396533\tFACS-sorted embryo cells\tFACS-sorted embryo cells\t24 hpf\tGFP positive\twild type\t\thttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR788/005/SRR7882015/SRR7882015_1.fastq.gz\thttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR788/005/SRR7882015/SRR7882015_2.fastq.gz\t\tera-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR788/005/SRR7882015/SRR7882015_1.fastq.gz\tera-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR788/005/SRR7882015/SRR7882015_2.fastq.gz\n" ] } ], "source": [ "!pysradb srx-to-srr SRX4720625 --detailed" ] }, { "cell_type": "markdown", "metadata": { "colab_type": "text", "id": "tTK_0p6JHyCI" }, "source": [ "## Download all runs for a particular experiment" ] }, { "cell_type": "code", "execution_count": 5, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 1000 }, "colab_type": "code", "id": "YQLxy1yzH6dQ", "outputId": "6c95ae03-f70b-4536-b461-84f8c206fa84" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Checking download URLs\n", "The following files will be downloaded: \n", "\n", "experiment_accession run_accession study_accession public_url download_url out_dir filesize\n", "SRX4720625 SRR7882015 SRP162234 https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos5/sra-pub-zq-11/SRR007/882/SRR7882015/SRR7882015.sralite.1 ftp://ftp-trace.ncbi.nlm.nih.gov/sra/sra-instant/reads/ByRun/sra/SRR/SRR788/SRR7882015/SRR7882015.sra /data/github/pysradb/notebooks/pysradb_downloads 1.9 GB \n", "\n", "\n", "Total size: 1.9 GB\n", "\n", "\n", " 0%| | 0/1 [00:00\n", " sys.exit(parse_args())\n", " File \"/data/github/pysradb/pysradb/cli.py\", line 1215, in parse_args\n", " download(\n", " File \"/data/github/pysradb/pysradb/cli.py\", line 111, in download\n", " sradb.download(\n", " File \"/data/github/pysradb/pysradb/sradb.py\", line 1543, in download\n", " if not confirm(\"Start download? \"):\n", " File \"/data/github/pysradb/pysradb/utils.py\", line 269, in confirm\n", " choice = input(\"{} [Y/n]: \".format(preceeding_text)).lower()\n", "KeyboardInterrupt\n" ] } ], "source": [ "!pysradb download -p SRP162234" ] } ], "metadata": { "colab": { "authorship_tag": "ABX9TyN0BPTWXcI8R2yJh5F/hEBk", "collapsed_sections": [], "include_colab_link": true, "name": "02.Commandline_download", "provenance": [] }, "kernelspec": { "display_name": "Python 3", "language": "python", "name": "python3" }, "language_info": { "codemirror_mode": { "name": "ipython", "version": 3 }, "file_extension": ".py", "mimetype": "text/x-python", "name": "python", "nbconvert_exporter": "python", "pygments_lexer": "ipython3", "version": "3.12.11" }, "widgets": { "application/vnd.jupyter.widget-state+json": { "state": {}, "version_major": 2, "version_minor": 0 } } }, "nbformat": 4, "nbformat_minor": 4 } ================================================ FILE: notebooks/03.ParallelDownload.ipynb ================================================ { "cells": [ { "cell_type": "markdown", "metadata": {}, "source": [ "[![Open In Colab](https://colab.research.google.com/assets/colab-badge.svg)](https://colab.research.google.com/github/saketkc/pysradb/blob/develop/notebooks/03.ParallelDownload.ipynb)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "# Parallel Download\n", "\n", "This notebook demonstrates how to download multiple SRA datasets in parallel using joblib." ] }, { "cell_type": "code", "execution_count": null, "metadata": {}, "outputs": [], "source": [ "# Install pysradb if not already installed\n", "try:\n", " import pysradb\n", "\n", " print(f\"pysradb {pysradb.__version__} is already installed\")\n", "except ImportError:\n", " print(\"Installing pysradb from GitHub...\")\n", " import sys\n", "\n", " !{sys.executable} -m pip install -q git+https://github.com/saketkc/pysradb\n", " print(\"pysradb installed successfully!\")" ] }, { "cell_type": "code", "execution_count": 1, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 664 }, "colab_type": "code", "id": "kdFGQ6S9OEeP", "outputId": "7b4ba253-c30a-43ce-b96a-6ff22b887f5a" }, "outputs": [], "source": [ "# pip install git+https://github.com/saketkc/pysradb" ] }, { "cell_type": "code", "execution_count": 2, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 34 }, "colab_type": "code", "id": "fGSXNG8LOLDI", "outputId": "4d53c90e-589f-43af-a1ad-e6d6cea9d9c7" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Requirement already satisfied: joblib in /home/saket/miniforge3/lib/python3.12/site-packages (1.5.2)\n", "Note: you may need to restart the kernel to use updated packages.\n" ] } ], "source": [ "pip install joblib" ] }, { "cell_type": "code", "execution_count": 3, "metadata": { "colab": {}, "colab_type": "code", "id": "CiEBTC4IO-pn" }, "outputs": [], "source": [ "from joblib import Parallel, delayed" ] }, { "cell_type": "code", "execution_count": 4, "metadata": { "colab": {}, "colab_type": "code", "id": "6vD2huxFOMZ_" }, "outputs": [ { "name": "stderr", "output_type": "stream", "text": [ "/home/saket/miniforge3/lib/python3.12/site-packages/pysradb/utils.py:14: TqdmExperimentalWarning: Using `tqdm.autonotebook.tqdm` in notebook mode. Use `tqdm.tqdm` instead to force console mode (e.g. in jupyter console)\n", " from tqdm.autonotebook import tqdm\n" ] } ], "source": [ "from pysradb.sraweb import SRAweb\n", "\n", "db = SRAweb()" ] }, { "cell_type": "code", "execution_count": 5, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 1000 }, "colab_type": "code", "id": "7jm1NDReOSgP", "outputId": "05ec84ac-f723-4235-a32b-5eaec0ed8462" }, "outputs": [ { "data": { "text/html": [ "
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run_accessionstudy_accessionstudy_titleexperiment_accessionexperiment_titleexperiment_descorganism_taxidorganism_namelibrary_namelibrary_strategy...source_namecell linetreatment timelibrary typeena_fastq_httpena_fastq_http_1ena_fastq_http_2ena_fastq_ftpena_fastq_ftp_1ena_fastq_ftp_2
0SRR5227288SRP098789Selective stalling of human translation throug...SRX2536403GSM2475997: 1.5 µM PF-067446846, 10 min, rep 1...GSM2475997: 1.5 µM PF-067446846, 10 min, rep 1...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
1SRR5227289SRP098789Selective stalling of human translation throug...SRX2536404GSM2475998: 1.5 µM PF-067446846, 10 min, rep 2...GSM2475998: 1.5 µM PF-067446846, 10 min, rep 2...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
2SRR5227290SRP098789Selective stalling of human translation throug...SRX2536405GSM2475999: 1.5 µM PF-067446846, 10 min, rep 3...GSM2475999: 1.5 µM PF-067446846, 10 min, rep 3...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
3SRR5227291SRP098789Selective stalling of human translation throug...SRX2536406GSM2476000: 0.3 µM PF-067446846, 10 min, rep 1...GSM2476000: 0.3 µM PF-067446846, 10 min, rep 1...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
4SRR5227292SRP098789Selective stalling of human translation throug...SRX2536407GSM2476001: 0.3 µM PF-067446846, 10 min, rep 2...GSM2476001: 0.3 µM PF-067446846, 10 min, rep 2...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
5SRR5227293SRP098789Selective stalling of human translation throug...SRX2536408GSM2476002: 0.3 µM PF-067446846, 10 min, rep 3...GSM2476002: 0.3 µM PF-067446846, 10 min, rep 3...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
6SRR5227294SRP098789Selective stalling of human translation throug...SRX2536409GSM2476003: vehicle, 10 min rep 1; Homo sapien...GSM2476003: vehicle, 10 min rep 1; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/004...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
7SRR5227295SRP098789Selective stalling of human translation throug...SRX2536410GSM2476004: vehicle, 10 min rep 2; Homo sapien...GSM2476004: vehicle, 10 min rep 2; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/005...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
8SRR5227296SRP098789Selective stalling of human translation throug...SRX2536411GSM2476005: vehicle, 10 min rep 3; Homo sapien...GSM2476005: vehicle, 10 min rep 3; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/006...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
9SRR5227297SRP098789Selective stalling of human translation throug...SRX2536412GSM2476006: 1.5 µM PF-067446846, 60 min, rep 1...GSM2476006: 1.5 µM PF-067446846, 60 min, rep 1...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/007...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
10SRR5227298SRP098789Selective stalling of human translation throug...SRX2536413GSM2476007: 1.5 µM PF-067446846, 60 min, rep 2...GSM2476007: 1.5 µM PF-067446846, 60 min, rep 2...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
11SRR5227299SRP098789Selective stalling of human translation throug...SRX2536414GSM2476008: 1.5 µM PF-067446846, 60 min, rep 3...GSM2476008: 1.5 µM PF-067446846, 60 min, rep 3...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
12SRR5227300SRP098789Selective stalling of human translation throug...SRX2536415GSM2476009: 0.3 µM PF-067446846, 60 min, rep 1...GSM2476009: 0.3 µM PF-067446846, 60 min, rep 1...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
13SRR5227301SRP098789Selective stalling of human translation throug...SRX2536416GSM2476010: 0.3 µM PF-067446846, 60 min, rep 2...GSM2476010: 0.3 µM PF-067446846, 60 min, rep 2...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
14SRR5227302SRP098789Selective stalling of human translation throug...SRX2536417GSM2476011: 0.3 µM PF-067446846, 60 min, rep 3...GSM2476011: 0.3 µM PF-067446846, 60 min, rep 3...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
15SRR5227303SRP098789Selective stalling of human translation throug...SRX2536418GSM2476012: vehicle, 60 min rep 1; Homo sapien...GSM2476012: vehicle, 60 min rep 1; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
16SRR5227304SRP098789Selective stalling of human translation throug...SRX2536419GSM2476013: vehicle, 60 min rep 2; Homo sapien...GSM2476013: vehicle, 60 min rep 2; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/004...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
17SRR5227305SRP098789Selective stalling of human translation throug...SRX2536420GSM2476014: vehicle, 60 min rep 3; Homo sapien...GSM2476014: vehicle, 60 min rep 3; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/005...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
18SRR5227306SRP098789Selective stalling of human translation throug...SRX2536421GSM2476015: 1.5 µM PF-067446846, 60 min, rep 4...GSM2476015: 1.5 µM PF-067446846, 60 min, rep 4...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/006...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
19SRR5227307SRP098789Selective stalling of human translation throug...SRX2536422GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; H...GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; H...9606Homo sapiens<NA>RNA-Seq...Huh7_Veh_60 min_Ribo-seqHuh760 minRibo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/007...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
20SRR5227308SRP098789Selective stalling of human translation throug...SRX2536423GSM2476017: 1.5 µM PF-067446846, 60 min, rep 5...GSM2476017: 1.5 µM PF-067446846, 60 min, rep 5...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
21SRR5227309SRP098789Selective stalling of human translation throug...SRX2536424GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; H...GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; H...9606Homo sapiens<NA>RNA-Seq...Huh7_vehcile_60 min_Ribo-seqHuh760 minRibo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
22SRR5227310SRP098789Selective stalling of human translation throug...SRX2536425GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-s...GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-s...9606Homo sapiens<NA>OTHER...Huh7_PF-06446846_60 min_mRNA-seqHuh760 minmRNA-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
23SRR5227311SRP098789Selective stalling of human translation throug...SRX2536426GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Ho...GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Ho...9606Homo sapiens<NA>RNA-Seq...Huh7_vehicle_60 min_RNA-seqHuh760 minpolyA-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
24SRR5227312SRP098789Selective stalling of human translation throug...SRX2536427GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-s...GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-s...9606Homo sapiens<NA>OTHER...Huh7_PF-06446846_60 min_mRNA-seqHuh760 minmRNA-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
25SRR5227313SRP098789Selective stalling of human translation throug...SRX2536428GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Ho...GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Ho...9606Homo sapiens<NA>RNA-Seq...Huh7_vehicle_60 min_RNA-seqHuh760 minpolyA-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
\n", "

26 rows × 54 columns

\n", "
" ], "text/plain": [ " run_accession study_accession \\\n", "0 SRR5227288 SRP098789 \n", "1 SRR5227289 SRP098789 \n", "2 SRR5227290 SRP098789 \n", "3 SRR5227291 SRP098789 \n", "4 SRR5227292 SRP098789 \n", "5 SRR5227293 SRP098789 \n", "6 SRR5227294 SRP098789 \n", "7 SRR5227295 SRP098789 \n", "8 SRR5227296 SRP098789 \n", "9 SRR5227297 SRP098789 \n", "10 SRR5227298 SRP098789 \n", "11 SRR5227299 SRP098789 \n", "12 SRR5227300 SRP098789 \n", "13 SRR5227301 SRP098789 \n", "14 SRR5227302 SRP098789 \n", "15 SRR5227303 SRP098789 \n", "16 SRR5227304 SRP098789 \n", "17 SRR5227305 SRP098789 \n", "18 SRR5227306 SRP098789 \n", "19 SRR5227307 SRP098789 \n", "20 SRR5227308 SRP098789 \n", "21 SRR5227309 SRP098789 \n", "22 SRR5227310 SRP098789 \n", "23 SRR5227311 SRP098789 \n", "24 SRR5227312 SRP098789 \n", "25 SRR5227313 SRP098789 \n", "\n", " study_title experiment_accession \\\n", "0 Selective stalling of human translation throug... SRX2536403 \n", "1 Selective stalling of human translation throug... SRX2536404 \n", "2 Selective stalling of human translation throug... SRX2536405 \n", "3 Selective stalling of human translation throug... SRX2536406 \n", "4 Selective stalling of human translation throug... SRX2536407 \n", "5 Selective stalling of human translation throug... SRX2536408 \n", "6 Selective stalling of human translation throug... SRX2536409 \n", "7 Selective stalling of human translation throug... SRX2536410 \n", "8 Selective stalling of human translation throug... SRX2536411 \n", "9 Selective stalling of human translation throug... SRX2536412 \n", "10 Selective stalling of human translation throug... SRX2536413 \n", "11 Selective stalling of human translation throug... SRX2536414 \n", "12 Selective stalling of human translation throug... SRX2536415 \n", "13 Selective stalling of human translation throug... SRX2536416 \n", "14 Selective stalling of human translation throug... SRX2536417 \n", "15 Selective stalling of human translation throug... SRX2536418 \n", "16 Selective stalling of human translation throug... SRX2536419 \n", "17 Selective stalling of human translation throug... SRX2536420 \n", "18 Selective stalling of human translation throug... SRX2536421 \n", "19 Selective stalling of human translation throug... SRX2536422 \n", "20 Selective stalling of human translation throug... SRX2536423 \n", "21 Selective stalling of human translation throug... SRX2536424 \n", "22 Selective stalling of human translation throug... SRX2536425 \n", "23 Selective stalling of human translation throug... SRX2536426 \n", "24 Selective stalling of human translation throug... SRX2536427 \n", "25 Selective stalling of human translation throug... SRX2536428 \n", "\n", " experiment_title \\\n", "0 GSM2475997: 1.5 µM PF-067446846, 10 min, rep 1... \n", "1 GSM2475998: 1.5 µM PF-067446846, 10 min, rep 2... \n", "2 GSM2475999: 1.5 µM PF-067446846, 10 min, rep 3... \n", "3 GSM2476000: 0.3 µM PF-067446846, 10 min, rep 1... \n", "4 GSM2476001: 0.3 µM PF-067446846, 10 min, rep 2... \n", "5 GSM2476002: 0.3 µM PF-067446846, 10 min, rep 3... \n", "6 GSM2476003: vehicle, 10 min rep 1; Homo sapien... \n", "7 GSM2476004: vehicle, 10 min rep 2; Homo sapien... \n", "8 GSM2476005: vehicle, 10 min rep 3; Homo sapien... \n", "9 GSM2476006: 1.5 µM PF-067446846, 60 min, rep 1... \n", "10 GSM2476007: 1.5 µM PF-067446846, 60 min, rep 2... \n", "11 GSM2476008: 1.5 µM PF-067446846, 60 min, rep 3... \n", "12 GSM2476009: 0.3 µM PF-067446846, 60 min, rep 1... \n", "13 GSM2476010: 0.3 µM PF-067446846, 60 min, rep 2... \n", "14 GSM2476011: 0.3 µM PF-067446846, 60 min, rep 3... \n", "15 GSM2476012: vehicle, 60 min rep 1; Homo sapien... \n", "16 GSM2476013: vehicle, 60 min rep 2; Homo sapien... \n", "17 GSM2476014: vehicle, 60 min rep 3; Homo sapien... \n", "18 GSM2476015: 1.5 µM PF-067446846, 60 min, rep 4... \n", "19 GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; H... \n", "20 GSM2476017: 1.5 µM PF-067446846, 60 min, rep 5... \n", "21 GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; H... \n", "22 GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-s... \n", "23 GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Ho... \n", "24 GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-s... \n", "25 GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Ho... \n", "\n", " experiment_desc organism_taxid \\\n", "0 GSM2475997: 1.5 µM PF-067446846, 10 min, rep 1... 9606 \n", "1 GSM2475998: 1.5 µM PF-067446846, 10 min, rep 2... 9606 \n", "2 GSM2475999: 1.5 µM PF-067446846, 10 min, rep 3... 9606 \n", "3 GSM2476000: 0.3 µM PF-067446846, 10 min, rep 1... 9606 \n", "4 GSM2476001: 0.3 µM PF-067446846, 10 min, rep 2... 9606 \n", "5 GSM2476002: 0.3 µM PF-067446846, 10 min, rep 3... 9606 \n", "6 GSM2476003: vehicle, 10 min rep 1; Homo sapien... 9606 \n", "7 GSM2476004: vehicle, 10 min rep 2; Homo sapien... 9606 \n", "8 GSM2476005: vehicle, 10 min rep 3; Homo sapien... 9606 \n", "9 GSM2476006: 1.5 µM PF-067446846, 60 min, rep 1... 9606 \n", "10 GSM2476007: 1.5 µM PF-067446846, 60 min, rep 2... 9606 \n", "11 GSM2476008: 1.5 µM PF-067446846, 60 min, rep 3... 9606 \n", "12 GSM2476009: 0.3 µM PF-067446846, 60 min, rep 1... 9606 \n", "13 GSM2476010: 0.3 µM PF-067446846, 60 min, rep 2... 9606 \n", "14 GSM2476011: 0.3 µM PF-067446846, 60 min, rep 3... 9606 \n", "15 GSM2476012: vehicle, 60 min rep 1; Homo sapien... 9606 \n", "16 GSM2476013: vehicle, 60 min rep 2; Homo sapien... 9606 \n", "17 GSM2476014: vehicle, 60 min rep 3; Homo sapien... 9606 \n", "18 GSM2476015: 1.5 µM PF-067446846, 60 min, rep 4... 9606 \n", "19 GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; H... 9606 \n", "20 GSM2476017: 1.5 µM PF-067446846, 60 min, rep 5... 9606 \n", "21 GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; H... 9606 \n", "22 GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-s... 9606 \n", "23 GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Ho... 9606 \n", "24 GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-s... 9606 \n", "25 GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Ho... 9606 \n", "\n", " organism_name library_name library_strategy ... \\\n", "0 Homo sapiens OTHER ... \n", "1 Homo sapiens OTHER ... \n", "2 Homo sapiens OTHER ... \n", "3 Homo sapiens OTHER ... \n", "4 Homo sapiens OTHER ... \n", "5 Homo sapiens OTHER ... \n", "6 Homo sapiens OTHER ... \n", "7 Homo sapiens OTHER ... \n", "8 Homo sapiens OTHER ... \n", "9 Homo sapiens OTHER ... \n", "10 Homo sapiens OTHER ... \n", "11 Homo sapiens OTHER ... \n", "12 Homo sapiens OTHER ... \n", "13 Homo sapiens OTHER ... \n", "14 Homo sapiens OTHER ... \n", "15 Homo sapiens OTHER ... \n", "16 Homo sapiens OTHER ... \n", "17 Homo sapiens OTHER ... \n", "18 Homo sapiens OTHER ... \n", "19 Homo sapiens RNA-Seq ... \n", "20 Homo sapiens OTHER ... \n", "21 Homo sapiens RNA-Seq ... \n", "22 Homo sapiens OTHER ... \n", "23 Homo sapiens RNA-Seq ... \n", "24 Homo sapiens OTHER ... \n", "25 Homo sapiens RNA-Seq ... \n", "\n", " source_name cell line treatment time \\\n", "0 Huh7_1.5 µM PF-067446846_10 min_ribo-seq Huh7 10 min \n", "1 Huh7_1.5 µM PF-067446846_10 min_ribo-seq Huh7 10 min \n", "2 Huh7_1.5 µM PF-067446846_10 min_ribo-seq Huh7 10 min \n", "3 Huh7_0.3 µM PF-067446846_10 min_ribo-seq Huh7 10 min \n", "4 Huh7_0.3 µM PF-067446846_10 min_ribo-seq Huh7 10 min \n", "5 Huh7_0.3 µM PF-067446846_10 min_ribo-seq Huh7 10 min \n", "6 Huh7_vehicle_10 min_ribo-seq Huh7 10 min \n", "7 Huh7_vehicle_10 min_ribo-seq Huh7 10 min \n", "8 Huh7_vehicle_10 min_ribo-seq Huh7 10 min \n", "9 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "10 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "11 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "12 Huh7_0.3 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "13 Huh7_0.3 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "14 Huh7_0.3 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "15 Huh7_vehicle_60 min_ribo-seq Huh7 60 min \n", "16 Huh7_vehicle_60 min_ribo-seq Huh7 60 min \n", "17 Huh7_vehicle_60 min_ribo-seq Huh7 60 min \n", "18 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "19 Huh7_Veh_60 min_Ribo-seq Huh7 60 min \n", "20 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "21 Huh7_vehcile_60 min_Ribo-seq Huh7 60 min \n", "22 Huh7_PF-06446846_60 min_mRNA-seq Huh7 60 min \n", "23 Huh7_vehicle_60 min_RNA-seq Huh7 60 min \n", "24 Huh7_PF-06446846_60 min_mRNA-seq Huh7 60 min \n", "25 Huh7_vehicle_60 min_RNA-seq Huh7 60 min \n", "\n", " library type ena_fastq_http \\\n", "0 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008... \n", "1 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009... \n", "2 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000... \n", "3 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001... \n", "4 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002... \n", "5 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003... \n", "6 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/004... \n", "7 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/005... \n", "8 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/006... \n", "9 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/007... \n", "10 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008... \n", "11 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009... \n", "12 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000... \n", "13 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001... \n", "14 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002... \n", "15 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003... \n", "16 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/004... \n", "17 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/005... \n", "18 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/006... \n", "19 Ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/007... \n", "20 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008... \n", "21 Ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009... \n", "22 mRNA-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000... \n", "23 polyA-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001... \n", "24 mRNA-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002... \n", "25 polyA-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003... \n", "\n", " ena_fastq_http_1 ena_fastq_http_2 \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", "5 \n", "6 \n", "7 \n", "8 \n", "9 \n", "10 \n", "11 \n", "12 \n", "13 \n", "14 \n", "15 \n", "16 \n", "17 \n", "18 \n", "19 \n", "20 \n", "21 \n", "22 \n", "23 \n", "24 \n", "25 \n", "\n", " ena_fastq_ftp ena_fastq_ftp_1 \\\n", "0 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "1 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "2 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "3 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "4 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "5 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "6 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "7 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "8 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "9 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "10 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "11 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "12 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "13 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "14 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "15 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "16 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "17 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "18 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "19 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "20 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "21 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "22 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "23 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "24 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "25 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "\n", " ena_fastq_ftp_2 \n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", "5 \n", "6 \n", "7 \n", "8 \n", "9 \n", "10 \n", "11 \n", "12 \n", "13 \n", "14 \n", "15 \n", "16 \n", "17 \n", "18 \n", "19 \n", "20 \n", "21 \n", "22 \n", "23 \n", "24 \n", "25 \n", "\n", "[26 rows x 54 columns]" ] }, "execution_count": 5, "metadata": {}, "output_type": "execute_result" } ], "source": [ "df = db.sra_metadata(\"SRP098789\", detailed=True)\n", "df" ] }, { "cell_type": "code", "execution_count": 6, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 1000 }, "colab_type": "code", "id": "QqjoVmskOegP", "outputId": "f8973741-bbf3-4988-aff7-ba09636a80e6" }, "outputs": [ { "data": { "text/html": [ "
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run_accessionstudy_accessionstudy_titleexperiment_accessionexperiment_titleexperiment_descorganism_taxidorganism_namelibrary_namelibrary_strategy...source_namecell linetreatment timelibrary typeena_fastq_httpena_fastq_http_1ena_fastq_http_2ena_fastq_ftpena_fastq_ftp_1ena_fastq_ftp_2
5SRR5227293SRP098789Selective stalling of human translation throug...SRX2536408GSM2476002: 0.3 µM PF-067446846, 10 min, rep 3...GSM2476002: 0.3 µM PF-067446846, 10 min, rep 3...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
6SRR5227294SRP098789Selective stalling of human translation throug...SRX2536409GSM2476003: vehicle, 10 min rep 1; Homo sapien...GSM2476003: vehicle, 10 min rep 1; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/004...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
7SRR5227295SRP098789Selective stalling of human translation throug...SRX2536410GSM2476004: vehicle, 10 min rep 2; Homo sapien...GSM2476004: vehicle, 10 min rep 2; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/005...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
8SRR5227296SRP098789Selective stalling of human translation throug...SRX2536411GSM2476005: vehicle, 10 min rep 3; Homo sapien...GSM2476005: vehicle, 10 min rep 3; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_10 min_ribo-seqHuh710 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/006...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
9SRR5227297SRP098789Selective stalling of human translation throug...SRX2536412GSM2476006: 1.5 µM PF-067446846, 60 min, rep 1...GSM2476006: 1.5 µM PF-067446846, 60 min, rep 1...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/007...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
10SRR5227298SRP098789Selective stalling of human translation throug...SRX2536413GSM2476007: 1.5 µM PF-067446846, 60 min, rep 2...GSM2476007: 1.5 µM PF-067446846, 60 min, rep 2...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
11SRR5227299SRP098789Selective stalling of human translation throug...SRX2536414GSM2476008: 1.5 µM PF-067446846, 60 min, rep 3...GSM2476008: 1.5 µM PF-067446846, 60 min, rep 3...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
12SRR5227300SRP098789Selective stalling of human translation throug...SRX2536415GSM2476009: 0.3 µM PF-067446846, 60 min, rep 1...GSM2476009: 0.3 µM PF-067446846, 60 min, rep 1...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
13SRR5227301SRP098789Selective stalling of human translation throug...SRX2536416GSM2476010: 0.3 µM PF-067446846, 60 min, rep 2...GSM2476010: 0.3 µM PF-067446846, 60 min, rep 2...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
14SRR5227302SRP098789Selective stalling of human translation throug...SRX2536417GSM2476011: 0.3 µM PF-067446846, 60 min, rep 3...GSM2476011: 0.3 µM PF-067446846, 60 min, rep 3...9606Homo sapiens<NA>OTHER...Huh7_0.3 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
15SRR5227303SRP098789Selective stalling of human translation throug...SRX2536418GSM2476012: vehicle, 60 min rep 1; Homo sapien...GSM2476012: vehicle, 60 min rep 1; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
16SRR5227304SRP098789Selective stalling of human translation throug...SRX2536419GSM2476013: vehicle, 60 min rep 2; Homo sapien...GSM2476013: vehicle, 60 min rep 2; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/004...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
17SRR5227305SRP098789Selective stalling of human translation throug...SRX2536420GSM2476014: vehicle, 60 min rep 3; Homo sapien...GSM2476014: vehicle, 60 min rep 3; Homo sapien...9606Homo sapiens<NA>OTHER...Huh7_vehicle_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/005...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
18SRR5227306SRP098789Selective stalling of human translation throug...SRX2536421GSM2476015: 1.5 µM PF-067446846, 60 min, rep 4...GSM2476015: 1.5 µM PF-067446846, 60 min, rep 4...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/006...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
19SRR5227307SRP098789Selective stalling of human translation throug...SRX2536422GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; H...GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; H...9606Homo sapiens<NA>RNA-Seq...Huh7_Veh_60 min_Ribo-seqHuh760 minRibo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/007...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
20SRR5227308SRP098789Selective stalling of human translation throug...SRX2536423GSM2476017: 1.5 µM PF-067446846, 60 min, rep 5...GSM2476017: 1.5 µM PF-067446846, 60 min, rep 5...9606Homo sapiens<NA>OTHER...Huh7_1.5 µM PF-067446846_60 min_ribo-seqHuh760 minribo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
21SRR5227309SRP098789Selective stalling of human translation throug...SRX2536424GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; H...GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; H...9606Homo sapiens<NA>RNA-Seq...Huh7_vehcile_60 min_Ribo-seqHuh760 minRibo-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
22SRR5227310SRP098789Selective stalling of human translation throug...SRX2536425GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-s...GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-s...9606Homo sapiens<NA>OTHER...Huh7_PF-06446846_60 min_mRNA-seqHuh760 minmRNA-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
23SRR5227311SRP098789Selective stalling of human translation throug...SRX2536426GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Ho...GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Ho...9606Homo sapiens<NA>RNA-Seq...Huh7_vehicle_60 min_RNA-seqHuh760 minpolyA-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
24SRR5227312SRP098789Selective stalling of human translation throug...SRX2536427GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-s...GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-s...9606Homo sapiens<NA>OTHER...Huh7_PF-06446846_60 min_mRNA-seqHuh760 minmRNA-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
25SRR5227313SRP098789Selective stalling of human translation throug...SRX2536428GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Ho...GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Ho...9606Homo sapiens<NA>RNA-Seq...Huh7_vehicle_60 min_RNA-seqHuh760 minpolyA-seqhttp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003...<NA><NA>era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/...<NA><NA>
\n", "

21 rows × 54 columns

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" ], "text/plain": [ " run_accession study_accession \\\n", "5 SRR5227293 SRP098789 \n", "6 SRR5227294 SRP098789 \n", "7 SRR5227295 SRP098789 \n", "8 SRR5227296 SRP098789 \n", "9 SRR5227297 SRP098789 \n", "10 SRR5227298 SRP098789 \n", "11 SRR5227299 SRP098789 \n", "12 SRR5227300 SRP098789 \n", "13 SRR5227301 SRP098789 \n", "14 SRR5227302 SRP098789 \n", "15 SRR5227303 SRP098789 \n", "16 SRR5227304 SRP098789 \n", "17 SRR5227305 SRP098789 \n", "18 SRR5227306 SRP098789 \n", "19 SRR5227307 SRP098789 \n", "20 SRR5227308 SRP098789 \n", "21 SRR5227309 SRP098789 \n", "22 SRR5227310 SRP098789 \n", "23 SRR5227311 SRP098789 \n", "24 SRR5227312 SRP098789 \n", "25 SRR5227313 SRP098789 \n", "\n", " study_title experiment_accession \\\n", "5 Selective stalling of human translation throug... SRX2536408 \n", "6 Selective stalling of human translation throug... SRX2536409 \n", "7 Selective stalling of human translation throug... SRX2536410 \n", "8 Selective stalling of human translation throug... SRX2536411 \n", "9 Selective stalling of human translation throug... SRX2536412 \n", "10 Selective stalling of human translation throug... SRX2536413 \n", "11 Selective stalling of human translation throug... SRX2536414 \n", "12 Selective stalling of human translation throug... SRX2536415 \n", "13 Selective stalling of human translation throug... SRX2536416 \n", "14 Selective stalling of human translation throug... SRX2536417 \n", "15 Selective stalling of human translation throug... SRX2536418 \n", "16 Selective stalling of human translation throug... SRX2536419 \n", "17 Selective stalling of human translation throug... SRX2536420 \n", "18 Selective stalling of human translation throug... SRX2536421 \n", "19 Selective stalling of human translation throug... SRX2536422 \n", "20 Selective stalling of human translation throug... SRX2536423 \n", "21 Selective stalling of human translation throug... SRX2536424 \n", "22 Selective stalling of human translation throug... SRX2536425 \n", "23 Selective stalling of human translation throug... SRX2536426 \n", "24 Selective stalling of human translation throug... SRX2536427 \n", "25 Selective stalling of human translation throug... SRX2536428 \n", "\n", " experiment_title \\\n", "5 GSM2476002: 0.3 µM PF-067446846, 10 min, rep 3... \n", "6 GSM2476003: vehicle, 10 min rep 1; Homo sapien... \n", "7 GSM2476004: vehicle, 10 min rep 2; Homo sapien... \n", "8 GSM2476005: vehicle, 10 min rep 3; Homo sapien... \n", "9 GSM2476006: 1.5 µM PF-067446846, 60 min, rep 1... \n", "10 GSM2476007: 1.5 µM PF-067446846, 60 min, rep 2... \n", "11 GSM2476008: 1.5 µM PF-067446846, 60 min, rep 3... \n", "12 GSM2476009: 0.3 µM PF-067446846, 60 min, rep 1... \n", "13 GSM2476010: 0.3 µM PF-067446846, 60 min, rep 2... \n", "14 GSM2476011: 0.3 µM PF-067446846, 60 min, rep 3... \n", "15 GSM2476012: vehicle, 60 min rep 1; Homo sapien... \n", "16 GSM2476013: vehicle, 60 min rep 2; Homo sapien... \n", "17 GSM2476014: vehicle, 60 min rep 3; Homo sapien... \n", "18 GSM2476015: 1.5 µM PF-067446846, 60 min, rep 4... \n", "19 GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; H... \n", "20 GSM2476017: 1.5 µM PF-067446846, 60 min, rep 5... \n", "21 GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; H... \n", "22 GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-s... \n", "23 GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Ho... \n", "24 GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-s... \n", "25 GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Ho... \n", "\n", " experiment_desc organism_taxid \\\n", "5 GSM2476002: 0.3 µM PF-067446846, 10 min, rep 3... 9606 \n", "6 GSM2476003: vehicle, 10 min rep 1; Homo sapien... 9606 \n", "7 GSM2476004: vehicle, 10 min rep 2; Homo sapien... 9606 \n", "8 GSM2476005: vehicle, 10 min rep 3; Homo sapien... 9606 \n", "9 GSM2476006: 1.5 µM PF-067446846, 60 min, rep 1... 9606 \n", "10 GSM2476007: 1.5 µM PF-067446846, 60 min, rep 2... 9606 \n", "11 GSM2476008: 1.5 µM PF-067446846, 60 min, rep 3... 9606 \n", "12 GSM2476009: 0.3 µM PF-067446846, 60 min, rep 1... 9606 \n", "13 GSM2476010: 0.3 µM PF-067446846, 60 min, rep 2... 9606 \n", "14 GSM2476011: 0.3 µM PF-067446846, 60 min, rep 3... 9606 \n", "15 GSM2476012: vehicle, 60 min rep 1; Homo sapien... 9606 \n", "16 GSM2476013: vehicle, 60 min rep 2; Homo sapien... 9606 \n", "17 GSM2476014: vehicle, 60 min rep 3; Homo sapien... 9606 \n", "18 GSM2476015: 1.5 µM PF-067446846, 60 min, rep 4... 9606 \n", "19 GSM2476016: Vehicle, 60 min, rep 4-ribo-seq; H... 9606 \n", "20 GSM2476017: 1.5 µM PF-067446846, 60 min, rep 5... 9606 \n", "21 GSM2476018: vehicle, 60 min, rep 5-Ribo-seq; H... 9606 \n", "22 GSM2476019: PF-06446846, 60 min, rep 4 -mRNA-s... 9606 \n", "23 GSM2476020: vehicle, 60 min, rep 4-mRNAseq; Ho... 9606 \n", "24 GSM2476021: PF-06446846, 60 min, rep 5 -mRNA-s... 9606 \n", "25 GSM2476022: vehicle, 60 min, rep 5-mRNAseq; Ho... 9606 \n", "\n", " organism_name library_name library_strategy ... \\\n", "5 Homo sapiens OTHER ... \n", "6 Homo sapiens OTHER ... \n", "7 Homo sapiens OTHER ... \n", "8 Homo sapiens OTHER ... \n", "9 Homo sapiens OTHER ... \n", "10 Homo sapiens OTHER ... \n", "11 Homo sapiens OTHER ... \n", "12 Homo sapiens OTHER ... \n", "13 Homo sapiens OTHER ... \n", "14 Homo sapiens OTHER ... \n", "15 Homo sapiens OTHER ... \n", "16 Homo sapiens OTHER ... \n", "17 Homo sapiens OTHER ... \n", "18 Homo sapiens OTHER ... \n", "19 Homo sapiens RNA-Seq ... \n", "20 Homo sapiens OTHER ... \n", "21 Homo sapiens RNA-Seq ... \n", "22 Homo sapiens OTHER ... \n", "23 Homo sapiens RNA-Seq ... \n", "24 Homo sapiens OTHER ... \n", "25 Homo sapiens RNA-Seq ... \n", "\n", " source_name cell line treatment time \\\n", "5 Huh7_0.3 µM PF-067446846_10 min_ribo-seq Huh7 10 min \n", "6 Huh7_vehicle_10 min_ribo-seq Huh7 10 min \n", "7 Huh7_vehicle_10 min_ribo-seq Huh7 10 min \n", "8 Huh7_vehicle_10 min_ribo-seq Huh7 10 min \n", "9 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "10 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "11 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "12 Huh7_0.3 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "13 Huh7_0.3 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "14 Huh7_0.3 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "15 Huh7_vehicle_60 min_ribo-seq Huh7 60 min \n", "16 Huh7_vehicle_60 min_ribo-seq Huh7 60 min \n", "17 Huh7_vehicle_60 min_ribo-seq Huh7 60 min \n", "18 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "19 Huh7_Veh_60 min_Ribo-seq Huh7 60 min \n", "20 Huh7_1.5 µM PF-067446846_60 min_ribo-seq Huh7 60 min \n", "21 Huh7_vehcile_60 min_Ribo-seq Huh7 60 min \n", "22 Huh7_PF-06446846_60 min_mRNA-seq Huh7 60 min \n", "23 Huh7_vehicle_60 min_RNA-seq Huh7 60 min \n", "24 Huh7_PF-06446846_60 min_mRNA-seq Huh7 60 min \n", "25 Huh7_vehicle_60 min_RNA-seq Huh7 60 min \n", "\n", " library type ena_fastq_http \\\n", "5 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003... \n", "6 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/004... \n", "7 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/005... \n", "8 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/006... \n", "9 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/007... \n", "10 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008... \n", "11 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009... \n", "12 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000... \n", "13 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001... \n", "14 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002... \n", "15 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003... \n", "16 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/004... \n", "17 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/005... \n", "18 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/006... \n", "19 Ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/007... \n", "20 ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/008... \n", "21 Ribo-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/009... \n", "22 mRNA-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/000... \n", "23 polyA-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/001... \n", "24 mRNA-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002... \n", "25 polyA-seq http://ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003... \n", "\n", " ena_fastq_http_1 ena_fastq_http_2 \\\n", "5 \n", "6 \n", "7 \n", "8 \n", "9 \n", "10 \n", "11 \n", "12 \n", "13 \n", "14 \n", "15 \n", "16 \n", "17 \n", "18 \n", "19 \n", "20 \n", "21 \n", "22 \n", "23 \n", "24 \n", "25 \n", "\n", " ena_fastq_ftp ena_fastq_ftp_1 \\\n", "5 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "6 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "7 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "8 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "9 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "10 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "11 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "12 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "13 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "14 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "15 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "16 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "17 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "18 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "19 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "20 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "21 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "22 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "23 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "24 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "25 era-fasp@fasp.sra.ebi.ac.uk:vol1/fastq/SRR522/... \n", "\n", " ena_fastq_ftp_2 \n", "5 \n", "6 \n", "7 \n", "8 \n", "9 \n", "10 \n", "11 \n", "12 \n", "13 \n", "14 \n", "15 \n", "16 \n", "17 \n", "18 \n", "19 \n", "20 \n", "21 \n", "22 \n", "23 \n", "24 \n", "25 \n", "\n", "[21 rows x 54 columns]" ] }, "execution_count": 6, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# randomply split into two dataframes\n", "df1, df2 = df.iloc[:5, :], df.iloc[5:, :]\n", "\n", "df2" ] }, { "cell_type": "code", "execution_count": 7, "metadata": { "colab": {}, "colab_type": "code", "id": "Wbelu2eNO4d_" }, "outputs": [], "source": [ "def single_download(df_single):\n", " db.download(df=df_single, skip_confirmation=True)" ] }, { "cell_type": "code", "execution_count": 8, "metadata": { "colab": {}, "colab_type": "code", "id": "r2TzSAZ0PSIe" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Checking download URLs\n", "Checking download URLs\n", "The following files will be downloaded: \n", "\n", "run_accession study_accession experiment_accession public_url download_url out_dir filesize\n", "SRR5227288 SRP098789 SRX2536403 https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos5/sra-pub-zq-11/SRR005/227/SRR5227288/SRR5227288.sralite.1 ftp://ftp-trace.ncbi.nlm.nih.gov/sra/sra-instant/reads/ByRun/sra/SRR/SRR522/SRR5227288/SRR5227288.sra /data/github/pysradb/notebooks/pysradb_downloads 533.5 MB\n", "SRR5227289 SRP098789 SRX2536404 https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos5/sra-pub-zq-11/SRR005/227/SRR5227289/SRR5227289.sralite.1 ftp://ftp-trace.ncbi.nlm.nih.gov/sra/sra-instant/reads/ByRun/sra/SRR/SRR522/SRR5227289/SRR5227289.sra /data/github/pysradb/notebooks/pysradb_downloads 603.2 MB\n", "SRR5227290 SRP098789 SRX2536405 https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos5/sra-pub-zq-11/SRR005/227/SRR5227290/SRR5227290.sralite.1 ftp://ftp-trace.ncbi.nlm.nih.gov/sra/sra-instant/reads/ByRun/sra/SRR/SRR522/SRR5227290/SRR5227290.sra /data/github/pysradb/notebooks/pysradb_downloads 586.1 MB\n", "SRR5227291 SRP098789 SRX2536406 https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos5/sra-pub-zq-14/SRR005/227/SRR5227291.sralite.1 ftp://ftp-trace.ncbi.nlm.nih.gov/sra/sra-instant/reads/ByRun/sra/SRR/SRR522/SRR5227291/SRR5227291.sra /data/github/pysradb/notebooks/pysradb_downloads 521.5 MB\n", "SRR5227292 SRP098789 SRX2536407 https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos5/sra-pub-zq-14/SRR005/227/SRR5227292.sralite.1 ftp://ftp-trace.ncbi.nlm.nih.gov/sra/sra-instant/reads/ByRun/sra/SRR/SRR522/SRR5227292/SRR5227292.sra /data/github/pysradb/notebooks/pysradb_downloads 871.3 MB\n", "\n", "\n", "Total size: 3.1 GB\n", "\n", "\n" ] }, { "name": "stderr", "output_type": "stream", "text": [ " 0%| | 0/5 [00:00] 551.22M 131MB/s in 4.3s \n", "\n", "2020-02-13 07:19:46 (127 MB/s) - ‘Anaconda3-5.1.0-Linux-x86_64.sh’ saved [577996269/577996269]\n", "\n", "PREFIX=/usr/local\n", "installing: python-3.6.4-hc3d631a_1 ...\n", "Python 3.6.4 :: Anaconda, Inc.\n", "installing: ca-certificates-2017.08.26-h1d4fec5_0 ...\n", "installing: conda-env-2.6.0-h36134e3_1 ...\n", "installing: intel-openmp-2018.0.0-hc7b2577_8 ...\n", "installing: libgcc-ng-7.2.0-h7cc24e2_2 ...\n", "installing: libgfortran-ng-7.2.0-h9f7466a_2 ...\n", "installing: libstdcxx-ng-7.2.0-h7a57d05_2 ...\n", "installing: bzip2-1.0.6-h9a117a8_4 ...\n", 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"installing: widgetsnbextension-3.1.0-py36_0 ...\n", "installing: anaconda-navigator-1.7.0-py36_0 ...\n", "installing: ipywidgets-7.1.1-py36_0 ...\n", "installing: jupyterlab-0.31.5-py36_0 ...\n", "installing: spyder-3.2.6-py36_0 ...\n", "installing: _ipyw_jlab_nb_ext_conf-0.1.0-py36he11e457_0 ...\n", "installing: jupyter-1.0.0-py36_4 ...\n", "installing: anaconda-5.1.0-py36_2 ...\n", "installing: conda-4.4.10-py36_0 ...\n", "installing: conda-build-3.4.1-py36_0 ...\n", "installation finished.\n", "WARNING:\n", " You currently have a PYTHONPATH environment variable set. This may cause\n", " unexpected behavior when running the Python interpreter in Anaconda3.\n", " For best results, please verify that your PYTHONPATH only points to\n", " directories of packages that are compatible with the Python interpreter\n", " in Anaconda3: /usr/local\n", "Warning: 'defaults' already in 'channels' list, moving to the top\n" ], "name": "stdout" } ] }, { "cell_type": "markdown", "metadata": { "id": "4XlnJIgobDIH", "colab_type": "text" }, "source": [ "## Install parallel-fastq-dump" ] }, { "cell_type": "code", "metadata": { "id": "XYc6vNwya_2I", "colab_type": "code", "outputId": "b96f8eef-8d05-45f0-a452-814296b6fc56", "colab": { "base_uri": "https://localhost:8080/", "height": 1000 } }, "source": [ "!conda install -y parallel-fastq-dump" ], "execution_count": 0, "outputs": [ { "output_type": "stream", "text": [ "Solving environment: - \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\b| \b\b/ \b\b- \b\b\\ \b\bdone\n", "\n", "\n", "==> WARNING: A newer version of conda exists. <==\n", " current version: 4.4.10\n", " latest version: 4.8.2\n", "\n", "Please update conda by running\n", "\n", " $ conda update -n base conda\n", "\n", "\n", "\n", "## Package Plan ##\n", "\n", " environment location: /usr/local\n", "\n", " added / updated specs: \n", " - parallel-fastq-dump\n", "\n", "\n", "The following packages will be downloaded:\n", "\n", " package | build\n", " ---------------------------|-----------------\n", " bzip2-1.0.8 | h516909a_2 396 KB conda-forge\n", " parallel-fastq-dump-0.6.6 | py_0 8 KB bioconda\n", " python-3.7.1 | h5001a0f_0 26.8 MB conda-forge\n", " ca-certificates-2019.11.28 | hecc5488_0 145 KB conda-forge\n", " _libgcc_mutex-0.1 | conda_forge 3 KB conda-forge\n", " libgcc-ng-9.2.0 | h24d8f2e_2 8.2 MB conda-forge\n", " sqlite-3.28.0 | h8b20d00_0 1.9 MB conda-forge\n", " sra-tools-2.9.1_1 | h470a237_0 38.0 MB bioconda\n", " libgomp-9.2.0 | h24d8f2e_2 816 KB conda-forge\n", " certifi-2019.11.28 | py37_0 148 KB conda-forge\n", " ncurses-6.1 | hfc679d8_2 1.3 MB conda-forge\n", " pip-20.0.2 | py_2 1.0 MB conda-forge\n", " readline-7.0 | hf8c457e_1001 391 KB conda-forge\n", " xz-5.2.4 | h14c3975_1001 366 KB conda-forge\n", " libffi-3.2.1 | hfc679d8_5 51 KB conda-forge\n", " zlib-1.2.11 | h516909a_1006 105 KB conda-forge\n", " openssl-1.0.2u | h516909a_0 3.2 MB conda-forge\n", " tk-8.6.10 | hed695b0_0 3.2 MB conda-forge\n", " setuptools-45.2.0 | py37_0 654 KB conda-forge\n", " _openmp_mutex-4.5 | 0_gnu 435 KB conda-forge\n", " wheel-0.34.2 | py_1 24 KB conda-forge\n", " ------------------------------------------------------------\n", " Total: 87.1 MB\n", "\n", "The following NEW packages will be INSTALLED:\n", "\n", " _libgcc_mutex: 0.1-conda_forge conda-forge\n", " _openmp_mutex: 4.5-0_gnu conda-forge\n", " libgomp: 9.2.0-h24d8f2e_2 conda-forge\n", " parallel-fastq-dump: 0.6.6-py_0 bioconda \n", " sra-tools: 2.9.1_1-h470a237_0 bioconda \n", "\n", "The following packages will be UPDATED:\n", "\n", " bzip2: 1.0.6-h9a117a8_4 --> 1.0.8-h516909a_2 conda-forge\n", " ca-certificates: 2017.08.26-h1d4fec5_0 --> 2019.11.28-hecc5488_0 conda-forge\n", " certifi: 2018.1.18-py36_0 --> 2019.11.28-py37_0 conda-forge\n", " libffi: 3.2.1-hd88cf55_4 --> 3.2.1-hfc679d8_5 conda-forge\n", " libgcc-ng: 7.2.0-h7cc24e2_2 --> 9.2.0-h24d8f2e_2 conda-forge\n", " ncurses: 6.0-h9df7e31_2 --> 6.1-hfc679d8_2 conda-forge\n", " openssl: 1.0.2n-hb7f436b_0 --> 1.0.2u-h516909a_0 conda-forge\n", " pip: 9.0.1-py36h6c6f9ce_4 --> 20.0.2-py_2 conda-forge\n", " python: 3.6.4-hc3d631a_1 --> 3.7.1-h5001a0f_0 conda-forge\n", " readline: 7.0-ha6073c6_4 --> 7.0-hf8c457e_1001 conda-forge\n", " setuptools: 38.4.0-py36_0 --> 45.2.0-py37_0 conda-forge\n", " sqlite: 3.22.0-h1bed415_0 --> 3.28.0-h8b20d00_0 conda-forge\n", " tk: 8.6.7-hc745277_3 --> 8.6.10-hed695b0_0 conda-forge\n", " wheel: 0.30.0-py36hfd4bba0_1 --> 0.34.2-py_1 conda-forge\n", " xz: 5.2.3-h55aa19d_2 --> 5.2.4-h14c3975_1001 conda-forge\n", " zlib: 1.2.11-ha838bed_2 --> 1.2.11-h516909a_1006 conda-forge\n", "\n", "\n", "Downloading and Extracting Packages\n", "bzip2 1.0.8: 100% 1.0/1 [00:00<00:00, 4.95it/s] \n", "parallel-fastq-dump 0.6.6: 100% 1.0/1 [00:00<00:00, 25.61it/s]\n", "python 3.7.1: 100% 1.0/1 [00:08<00:00, 8.74s/it] \n", "ca-certificates 2019.11.28: 100% 1.0/1 [00:00<00:00, 12.07it/s]\n", "_libgcc_mutex 0.1: 100% 1.0/1 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cached pandas-0.25.3-cp37-cp37m-manylinux1_x86_64.whl (10.4 MB)\n", "Collecting tqdm==4.41.1\n", " Using cached tqdm-4.41.1-py2.py3-none-any.whl (56 kB)\n", "Collecting requests==2.22.0\n", " Using cached requests-2.22.0-py2.py3-none-any.whl (57 kB)\n", "Collecting xmltodict==0.12.0\n", " Using cached xmltodict-0.12.0-py2.py3-none-any.whl (9.2 kB)\n", "Collecting python-dateutil>=2.6.1\n", " Using cached python_dateutil-2.8.1-py2.py3-none-any.whl (227 kB)\n", "Collecting numpy>=1.13.3\n", " Using cached numpy-1.18.1-cp37-cp37m-manylinux1_x86_64.whl (20.1 MB)\n", "Collecting pytz>=2017.2\n", " Using cached pytz-2019.3-py2.py3-none-any.whl (509 kB)\n", "Collecting idna<2.9,>=2.5\n", " Using cached idna-2.8-py2.py3-none-any.whl (58 kB)\n", "Collecting urllib3!=1.25.0,!=1.25.1,<1.26,>=1.21.1\n", " Using cached urllib3-1.25.8-py2.py3-none-any.whl (125 kB)\n", "Collecting chardet<3.1.0,>=3.0.2\n", " Using cached chardet-3.0.4-py2.py3-none-any.whl (133 kB)\n", "Requirement already satisfied: certifi>=2017.4.17 in /usr/local/lib/python3.7/site-packages (from requests==2.22.0->pysradb==0.10.3.dev0) (2019.11.28)\n", "Collecting six>=1.5\n", " Using cached six-1.14.0-py2.py3-none-any.whl (10 kB)\n", "Building wheels for collected packages: pysradb\n", " Building wheel for pysradb (setup.py) ... \u001b[?25l\u001b[?25hdone\n", " Created wheel for pysradb: filename=pysradb-0.10.3.dev0-py3-none-any.whl size=147407 sha256=b498f377cda436cca6ee34c470c8aabcbe9a75f5fe8af7a5e6c56796c1be9041\n", " Stored in directory: /tmp/pip-ephem-wheel-cache-a6fjccpo/wheels/3f/06/98/98805e85e0909f2d0920ce73557c06d3802e4baaa2616920e8\n", "Successfully built pysradb\n", "Installing collected packages: six, python-dateutil, numpy, pytz, pandas, tqdm, idna, urllib3, chardet, requests, xmltodict, pysradb\n", "Successfully installed chardet-3.0.4 idna-2.8 numpy-1.18.1 pandas-0.25.3 pysradb-0.10.3.dev0 python-dateutil-2.8.1 pytz-2019.3 requests-2.22.0 six-1.14.0 tqdm-4.41.1 urllib3-1.25.8 xmltodict-0.12.0\n" ], "name": "stdout" }, { "output_type": "display_data", "data": { "application/vnd.colab-display-data+json": { "pip_warning": { "packages": [ "chardet", "idna", "pandas" ] } } }, "metadata": { "tags": [] } } ] }, { "cell_type": "markdown", "metadata": { "id": "IPNGntg4bOGI", "colab_type": "text" }, "source": [ "## Get metadata" ] }, { "cell_type": "code", "metadata": { "id": "jGAxadtxbPoM", "colab_type": "code", "outputId": "dd123c11-bf3e-45a1-e260-b569ab72960c", "colab": { "base_uri": "https://localhost:8080/", "height": 71 } }, "source": [ "!pysradb metadata --detailed \tSRP063852" ], "execution_count": 0, "outputs": [ { "output_type": "stream", "text": [ "study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_strategy library_source library_selection sample_accession sample_title instrument total_spots total_size run_accession run_total_spots run_total_bases run_alias sra_url experiment_alias source_name cell line\n", "SRP063852 SRX1254413 GSM1887643: ribosome profiling; Homo sapiens; miRNA-Seq GSM1887643: ribosome profiling; Homo sapiens; miRNA-Seq 9606 Homo sapiens miRNA-Seq TRANSCRIPTOMIC size fractionation SRS1072728 N/A Illumina HiSeq 2000 31967082 626381849 SRR2433794 31967082 916773615 GSM1887643_r1 https://sra-download.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR2433794/SRR2433794.1 GSM1887643 HEK293 HEK293 \n" ], "name": "stdout" } ] }, { "cell_type": "markdown", "metadata": { "id": "7gdqjIpabSpK", "colab_type": "text" }, "source": [ "## Download data" ] }, { "cell_type": "code", "metadata": { "id": "aZOe5BSrbU3H", "colab_type": "code", "outputId": "ce236993-6074-4986-9555-cf66818abc0e", "colab": { "base_uri": "https://localhost:8080/", "height": 1000 } }, "source": [ "!pysradb download -y -p SRP063852" ], "execution_count": 0, "outputs": [ { "output_type": "stream", "text": [ "The following files will be downloaded: \n", "\n", "study_accession experiment_accession experiment_title experiment_desc organism_taxid organism_name library_strategy library_source library_selection sample_accession sample_title instrument total_spots total_size run_accession run_total_spots run_total_bases run_alias srapath_url experiment_alias source_name cell line download_url\n", " SRP063852 SRX1254413 GSM1887643: ribosome profiling; Homo sapiens; miRNA-Seq GSM1887643: ribosome profiling; Homo sapiens; miRNA-Seq 9606 Homo sapiens miRNA-Seq TRANSCRIPTOMIC size fractionation SRS1072728 N/A Illumina HiSeq 2000 31967082 626381849 SRR2433794 31967082 916773615 GSM1887643_r1 https://sra-download.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR2433794/SRR2433794.1 GSM1887643 HEK293 HEK293 \n", "\n", "\n", "Total size: 626.4 MB\n", "\n", "\n", "SRP063852/SRX1254413/SRR2433794: 0% 0/1 [00:00=2.6.1 in /usr/local/lib/python3.6/dist-packages (from pandas==0.25.3->pysradb==0.10.3.dev0) (2.6.1)\n", "Requirement already satisfied: pytz>=2017.2 in /usr/local/lib/python3.6/dist-packages (from pandas==0.25.3->pysradb==0.10.3.dev0) (2018.9)\n", "Requirement already satisfied: numpy>=1.13.3 in /usr/local/lib/python3.6/dist-packages (from pandas==0.25.3->pysradb==0.10.3.dev0) (1.17.5)\n", "Requirement already satisfied: idna<2.9,>=2.5 in /usr/local/lib/python3.6/dist-packages (from requests==2.22.0->pysradb==0.10.3.dev0) (2.8)\n", "Requirement already satisfied: urllib3!=1.25.0,!=1.25.1,<1.26,>=1.21.1 in /usr/local/lib/python3.6/dist-packages (from requests==2.22.0->pysradb==0.10.3.dev0) (1.24.3)\n", "Requirement already satisfied: certifi>=2017.4.17 in /usr/local/lib/python3.6/dist-packages (from requests==2.22.0->pysradb==0.10.3.dev0) (2019.11.28)\n", "Requirement already satisfied: chardet<3.1.0,>=3.0.2 in /usr/local/lib/python3.6/dist-packages (from requests==2.22.0->pysradb==0.10.3.dev0) (3.0.4)\n", "Requirement already satisfied: six>=1.5 in /usr/local/lib/python3.6/dist-packages (from python-dateutil>=2.6.1->pandas==0.25.3->pysradb==0.10.3.dev0) (1.12.0)\n", "Building wheels for collected packages: pysradb\n", " Building wheel for pysradb (setup.py) ... \u001b[?25l\u001b[?25hdone\n", " Created wheel for pysradb: filename=pysradb-0.10.3.dev0-cp36-none-any.whl size=147411 sha256=6ccd6874b7cde11cb10eae96cb14e86f9cdfe5f1b02b16a3c7eb20879afd6a62\n", " Stored in directory: /tmp/pip-ephem-wheel-cache-z9xalsuu/wheels/d5/24/42/81dccabc3a4aac9757e23b7175ad7270090a4b3c203cd4fc8f\n", "Successfully built pysradb\n", "\u001b[31mERROR: google-colab 1.0.0 has requirement requests~=2.21.0, but you'll have requests 2.22.0 which is incompatible.\u001b[0m\n", "\u001b[31mERROR: datascience 0.10.6 has requirement folium==0.2.1, but you'll have folium 0.8.3 which is incompatible.\u001b[0m\n", "Installing collected packages: tqdm, requests, xmltodict, pysradb\n", " Found existing installation: tqdm 4.28.1\n", " Uninstalling tqdm-4.28.1:\n", " Successfully uninstalled tqdm-4.28.1\n", " Found existing installation: requests 2.21.0\n", " Uninstalling requests-2.21.0:\n", " Successfully uninstalled requests-2.21.0\n", "Successfully installed pysradb-0.10.3.dev0 requests-2.22.0 tqdm-4.41.1 xmltodict-0.12.0\n" ], "name": "stdout" }, { "output_type": "display_data", "data": { "application/vnd.colab-display-data+json": { "pip_warning": { "packages": [ "requests", "tqdm" ] } } }, "metadata": { "tags": [] } } ] }, { "cell_type": "code", "metadata": { "id": "Dg62g5OM_qbn", "colab_type": "code", "colab": { "base_uri": "https://localhost:8080/", "height": 34 }, "outputId": "295c4af3-0a46-4f70-b695-ab395422edec" }, "source": [ "!pysradb --version" ], "execution_count": 2, "outputs": [ { "output_type": "stream", "text": [ "pysradb 0.10.3-dev0\n" ], "name": "stdout" } ] }, { "cell_type": "code", "metadata": { "id": "Vi6ELv2KF_V4", "colab_type": "code", "colab": {} }, "source": [ "from pysradb.sraweb import SRAweb\n", "\n", "db = SRAweb()" ], "execution_count": 0, "outputs": [] }, { "cell_type": "markdown", "metadata": { "id": "xLZ431sPKJcX", "colab_type": "text" }, "source": [ "## Example of a record missing \"SAMPLE_ATTRIBUES\" \n", "\n", "It also has an \"auxillary\" contig file: https://trace.ncbi.nlm.nih.gov/Traces/sra/?run=SRR5146869" ] }, { "cell_type": "code", "metadata": { "id": "x5OmbCI-GFcA", "colab_type": "code", "outputId": "8f445628-1d50-4845-b918-7a6d9dbe636d", "colab": { "base_uri": "https://localhost:8080/", "height": 966 } }, "source": [ "df = db.sra_metadata(\"SRP096127\", detailed=True)\n", "df" ], "execution_count": 4, "outputs": [ { "output_type": "execute_result", "data": { "text/html": [ "
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study_accessionexperiment_accessionexperiment_titleexperiment_descorganism_taxidorganism_namelibrary_strategylibrary_sourcelibrary_selectionsample_accessionsample_titleinstrumenttotal_spotstotal_sizerun_accessionrun_total_spotsrun_total_basesrun_aliassra_url_altsra_urlexperiment_aliassource_namecell typegroup
0SRP096127SRX2467007GSM2448483: normal.ct-970; Homo sapiens; Bisul...GSM2448483: normal.ct-970; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899466N/AIllumina HiSeq 250055954750734487SRR514905955954783216675GSM2448483_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448483blood serumblood serumhealthy control
1SRP096127SRX2467006GSM2448482: normal.ct-969; Homo sapiens; Bisul...GSM2448482: normal.ct-969; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899465N/AIllumina HiSeq 250044157740899268SRR514905844157765549383GSM2448482_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448482blood serumblood serumhealthy control
2SRP096127SRX2467005GSM2448481: normal.ct-968; Homo sapiens; Bisul...GSM2448481: normal.ct-968; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899464N/AIllumina HiSeq 250056337850951134SRR514905756337883839813GSM2448481_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448481blood serumblood serumhealthy control
3SRP096127SRX2467004GSM2448480: normal.ct-967; Homo sapiens; Bisul...GSM2448480: normal.ct-967; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899463N/AIllumina HiSeq 250042287839223860SRR514905642287862753430GSM2448480_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448480blood serumblood serumhealthy control
4SRP096127SRX2467003GSM2448479: normal.ct-966; Homo sapiens; Bisul...GSM2448479: normal.ct-966; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899461N/AIllumina HiSeq 250051725446881651SRR514905551725477004865GSM2448479_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448479blood serumblood serumhealthy control
...........................................................................
2186SRP096127SRX2464821GSM2446284: HCC.ct-5; Homo sapiens; Bisulfite-SeqGSM2446284: HCC.ct-5; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897280N/AIllumina HiSeq 2500103320483576370SRR51468731033204196635123GSM2446284_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446284blood serumblood serumhepatocellular carcinoma patient
2187SRP096127SRX2464820GSM2446283: HCC.ct-4; Homo sapiens; Bisulfite-SeqGSM2446283: HCC.ct-4; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897279N/AIllumina HiSeq 250084085368410342SRR5146872840853159822416GSM2446283_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446283blood serumblood serumhepatocellular carcinoma patient
2188SRP096127SRX2464819GSM2446282: HCC.ct-3; Homo sapiens; Bisulfite-SeqGSM2446282: HCC.ct-3; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897278N/AIllumina HiSeq 250088572471407675SRR5146871885724166270272GSM2446282_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446282blood serumblood serumhepatocellular carcinoma patient
2189SRP096127SRX2464818GSM2446281: HCC.ct-2; Homo sapiens; Bisulfite-SeqGSM2446281: HCC.ct-2; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897277N/AIllumina HiSeq 250077568462094237SRR5146870775684145671062GSM2446281_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446281blood serumblood serumhepatocellular carcinoma patient
2190SRP096127SRX2464817GSM2446280: HCC.ct-1; Homo sapiens; Bisulfite-SeqGSM2446280: HCC.ct-1; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897276N/AIllumina HiSeq 2500112403189769302SRR51468691124031212986785GSM2446280_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446280blood serumblood serumhepatocellular carcinoma patient
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2191 rows × 24 columns

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" ], "text/plain": [ " study_accession ... group\n", "0 SRP096127 ... healthy control\n", "1 SRP096127 ... healthy control\n", "2 SRP096127 ... healthy control\n", "3 SRP096127 ... healthy control\n", "4 SRP096127 ... healthy control\n", "... ... ... ...\n", "2186 SRP096127 ... hepatocellular carcinoma patient\n", "2187 SRP096127 ... hepatocellular carcinoma patient\n", "2188 SRP096127 ... hepatocellular carcinoma patient\n", "2189 SRP096127 ... hepatocellular carcinoma patient\n", "2190 SRP096127 ... hepatocellular carcinoma patient\n", "\n", "[2191 rows x 24 columns]" ] }, "metadata": { "tags": [] }, "execution_count": 4 } ] }, { "cell_type": "code", "metadata": { "id": "DDyQEQcFQCNW", "colab_type": "code", "outputId": "e7b3d325-49a2-4c97-d3c9-16b4de5fea62", "colab": { "base_uri": "https://localhost:8080/", "height": 966 } }, "source": [ "df_contig_subset = df.loc[df[\"sra_url_alt\"].str.contains(\"contig\")]\n", "df_contig_subset" ], "execution_count": 5, "outputs": [ { "output_type": "execute_result", "data": { "text/html": [ "
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study_accessionexperiment_accessionexperiment_titleexperiment_descorganism_taxidorganism_namelibrary_strategylibrary_sourcelibrary_selectionsample_accessionsample_titleinstrumenttotal_spotstotal_sizerun_accessionrun_total_spotsrun_total_basesrun_aliassra_url_altsra_urlexperiment_aliassource_namecell typegroup
0SRP096127SRX2467007GSM2448483: normal.ct-970; Homo sapiens; Bisul...GSM2448483: normal.ct-970; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899466N/AIllumina HiSeq 250055954750734487SRR514905955954783216675GSM2448483_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448483blood serumblood serumhealthy control
1SRP096127SRX2467006GSM2448482: normal.ct-969; Homo sapiens; Bisul...GSM2448482: normal.ct-969; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899465N/AIllumina HiSeq 250044157740899268SRR514905844157765549383GSM2448482_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448482blood serumblood serumhealthy control
2SRP096127SRX2467005GSM2448481: normal.ct-968; Homo sapiens; Bisul...GSM2448481: normal.ct-968; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899464N/AIllumina HiSeq 250056337850951134SRR514905756337883839813GSM2448481_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448481blood serumblood serumhealthy control
3SRP096127SRX2467004GSM2448480: normal.ct-967; Homo sapiens; Bisul...GSM2448480: normal.ct-967; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899463N/AIllumina HiSeq 250042287839223860SRR514905642287862753430GSM2448480_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448480blood serumblood serumhealthy control
4SRP096127SRX2467003GSM2448479: normal.ct-966; Homo sapiens; Bisul...GSM2448479: normal.ct-966; Homo sapiens; Bisul...9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1899461N/AIllumina HiSeq 250051725446881651SRR514905551725477004865GSM2448479_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2448479blood serumblood serumhealthy control
...........................................................................
2186SRP096127SRX2464821GSM2446284: HCC.ct-5; Homo sapiens; Bisulfite-SeqGSM2446284: HCC.ct-5; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897280N/AIllumina HiSeq 2500103320483576370SRR51468731033204196635123GSM2446284_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446284blood serumblood serumhepatocellular carcinoma patient
2187SRP096127SRX2464820GSM2446283: HCC.ct-4; Homo sapiens; Bisulfite-SeqGSM2446283: HCC.ct-4; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897279N/AIllumina HiSeq 250084085368410342SRR5146872840853159822416GSM2446283_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446283blood serumblood serumhepatocellular carcinoma patient
2188SRP096127SRX2464819GSM2446282: HCC.ct-3; Homo sapiens; Bisulfite-SeqGSM2446282: HCC.ct-3; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897278N/AIllumina HiSeq 250088572471407675SRR5146871885724166270272GSM2446282_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446282blood serumblood serumhepatocellular carcinoma patient
2189SRP096127SRX2464818GSM2446281: HCC.ct-2; Homo sapiens; Bisulfite-SeqGSM2446281: HCC.ct-2; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897277N/AIllumina HiSeq 250077568462094237SRR5146870775684145671062GSM2446281_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446281blood serumblood serumhepatocellular carcinoma patient
2190SRP096127SRX2464817GSM2446280: HCC.ct-1; Homo sapiens; Bisulfite-SeqGSM2446280: HCC.ct-1; Homo sapiens; Bisulfite-Seq9606Homo sapiensBisulfite-SeqGENOMICRANDOMSRS1897276N/AIllumina HiSeq 2500112403189769302SRR51468691124031212986785GSM2446280_r1https://sra-download.ncbi.nlm.nih.gov/traces/s...https://sra-download.st-va.ncbi.nlm.nih.gov/so...GSM2446280blood serumblood serumhepatocellular carcinoma patient
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1654 rows × 24 columns

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" ], "text/plain": [ " study_accession ... group\n", "0 SRP096127 ... healthy control\n", "1 SRP096127 ... healthy control\n", "2 SRP096127 ... healthy control\n", "3 SRP096127 ... healthy control\n", "4 SRP096127 ... healthy control\n", "... ... ... ...\n", "2186 SRP096127 ... hepatocellular carcinoma patient\n", "2187 SRP096127 ... hepatocellular carcinoma patient\n", "2188 SRP096127 ... hepatocellular carcinoma patient\n", "2189 SRP096127 ... hepatocellular carcinoma patient\n", "2190 SRP096127 ... hepatocellular carcinoma patient\n", "\n", "[1654 rows x 24 columns]" ] }, "metadata": { "tags": [] }, "execution_count": 5 } ] }, { "cell_type": "code", "metadata": { "id": "QXPobpr-PqsR", "colab_type": "code", "colab": {} }, "source": [ "db.download(df=df_contig_subset, url_col=\"sra_url_alt\")" ], "execution_count": 0, "outputs": [] }, { "cell_type": "markdown", "metadata": { "id": "Y-RVanikKONY", "colab_type": "text" }, "source": [ "## Example with a fastq file (submitted through ENA)\n", "\n", "https://trace.ncbi.nlm.nih.gov/Traces/sra/?run=ERR1520686" ] }, { "cell_type": "code", "metadata": { "id": "TwIoS6ImKEHb", "colab_type": "code", "outputId": "4e8fa031-9f88-4bb0-f994-b4bc3aae9341", "colab": { "base_uri": "https://localhost:8080/", "height": 300 } }, "source": [ "df = db.sra_metadata(\"ERP015299\", detailed=True)\n", "df" ], "execution_count": 0, "outputs": [ { "output_type": "error", "ename": "AttributeError", "evalue": "ignored", "traceback": [ "\u001b[0;31m---------------------------------------------------------------------------\u001b[0m", "\u001b[0;31mAttributeError\u001b[0m Traceback (most recent call last)", "\u001b[0;32m\u001b[0m in \u001b[0;36m\u001b[0;34m()\u001b[0m\n\u001b[0;32m----> 1\u001b[0;31m \u001b[0mdf\u001b[0m \u001b[0;34m=\u001b[0m \u001b[0mdb\u001b[0m\u001b[0;34m.\u001b[0m\u001b[0msra_metadata\u001b[0m\u001b[0;34m(\u001b[0m\u001b[0;34m'ERP015299'\u001b[0m\u001b[0;34m,\u001b[0m \u001b[0mdetailed\u001b[0m\u001b[0;34m=\u001b[0m\u001b[0;32mTrue\u001b[0m\u001b[0;34m)\u001b[0m\u001b[0;34m\u001b[0m\u001b[0;34m\u001b[0m\u001b[0m\n\u001b[0m\u001b[1;32m 2\u001b[0m \u001b[0mdf\u001b[0m\u001b[0;34m\u001b[0m\u001b[0;34m\u001b[0m\u001b[0m\n", "\u001b[0;32m/usr/local/lib/python3.6/dist-packages/pysradb/sraweb.py\u001b[0m in \u001b[0;36msra_metadata\u001b[0;34m(self, srp, sample_attribute, detailed, expand_sample_attributes, output_read_lengths, **kwargs)\u001b[0m\n\u001b[1;32m 396\u001b[0m \u001b[0;31m# detailed_record[\"run_total_spots\"] = run_set[\"@total_spots\"]\u001b[0m\u001b[0;34m\u001b[0m\u001b[0;34m\u001b[0m\u001b[0;34m\u001b[0m\u001b[0m\n\u001b[1;32m 397\u001b[0m \u001b[0;32mfor\u001b[0m \u001b[0msample_attribute\u001b[0m \u001b[0;32min\u001b[0m \u001b[0msample_attributes\u001b[0m\u001b[0;34m:\u001b[0m\u001b[0;34m\u001b[0m\u001b[0;34m\u001b[0m\u001b[0m\n\u001b[0;32m--> 398\u001b[0;31m \u001b[0mdict_values\u001b[0m \u001b[0;34m=\u001b[0m \u001b[0mlist\u001b[0m\u001b[0;34m(\u001b[0m\u001b[0msample_attribute\u001b[0m\u001b[0;34m.\u001b[0m\u001b[0mvalues\u001b[0m\u001b[0;34m(\u001b[0m\u001b[0;34m)\u001b[0m\u001b[0;34m)\u001b[0m\u001b[0;34m\u001b[0m\u001b[0;34m\u001b[0m\u001b[0m\n\u001b[0m\u001b[1;32m 399\u001b[0m \u001b[0mdetailed_record\u001b[0m\u001b[0;34m[\u001b[0m\u001b[0mdict_values\u001b[0m\u001b[0;34m[\u001b[0m\u001b[0;36m0\u001b[0m\u001b[0;34m]\u001b[0m\u001b[0;34m]\u001b[0m \u001b[0;34m=\u001b[0m \u001b[0mdict_values\u001b[0m\u001b[0;34m[\u001b[0m\u001b[0;36m1\u001b[0m\u001b[0;34m]\u001b[0m\u001b[0;34m\u001b[0m\u001b[0;34m\u001b[0m\u001b[0m\n\u001b[1;32m 400\u001b[0m \u001b[0mdetailed_records\u001b[0m\u001b[0;34m.\u001b[0m\u001b[0mappend\u001b[0m\u001b[0;34m(\u001b[0m\u001b[0mdetailed_record\u001b[0m\u001b[0;34m)\u001b[0m\u001b[0;34m\u001b[0m\u001b[0;34m\u001b[0m\u001b[0m\n", "\u001b[0;31mAttributeError\u001b[0m: 'str' object has no attribute 'values'" ] } ] } ] } ================================================ FILE: notebooks/06.Multiple_SRPs.ipynb ================================================ { "cells": [ { "cell_type": "markdown", "metadata": {}, "source": [ "[![Open In Colab](https://colab.research.google.com/assets/colab-badge.svg)](https://colab.research.google.com/github/saketkc/pysradb/blob/develop/notebooks/06.Multiple_SRPs.ipynb)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "# Querying Multiple Projects\n", "\n", "This notebook demonstrates how to query and export metadata from multiple SRA projects at once." ] }, { "cell_type": "code", "execution_count": null, "metadata": {}, "outputs": [], "source": [ "# Install pysradb if not already installed\n", "try:\n", " import pysradb\n", "\n", " print(f\"pysradb {pysradb.__version__} is already installed\")\n", "except ImportError:\n", " print(\"Installing pysradb from GitHub...\")\n", " import sys\n", "\n", " !{sys.executable} -m pip install -q git+https://github.com/saketkc/pysradb\n", " print(\"pysradb installed successfully!\")" ] }, { "cell_type": "code", "execution_count": 1, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 401 }, "colab_type": "code", "id": "kPEeKLC38WGX", "outputId": "45055cff-1f41-4b1d-f67f-0a4dc37a8333" }, "outputs": [], "source": [ "# pip install git+https://github.com/saketkc/pysradb.git" ] }, { "cell_type": "code", "execution_count": 2, "metadata": { "colab": {}, "colab_type": "code", "id": "n-lUysUE8edh" }, "outputs": [], "source": [ "SRP_list = \"\"\"ERP009675\n", "ERP007116\n", "ERP007115\n", "ERP004563\n", "ERP005660\n", "ERP001266\n", "ERP002072\n", "ERP001882\n", "ERP004883\n", "ERP004508\n", "ERP004393\n", "ERP005409\n", "ERP001464\n", "ERP004042\n", "ERP004375\n", "ERP003293\n", "ERP004689\n", "ERP001094\n", "ERP003728\n", "ERP000730\n", "ERP000411\n", "ERP000319\n", "SRP041183\n", "SRP011912\n", "SRP058392\n", "SRP044705\n", "SRP036841\n", "SRP050120\n", "ERP004116\n", "SRP030662\n", "SRP047217\n", "SRP045505\n", "ERP001556\n", "ERP000546\n", "SRP045252\n", "SRP044714\n", "DRP000524\n", "SRP044907\n", "SRP019970\n", "SRP044131\n", "SRP044042\n", "SRP043602\n", "SRP043523\n", "SRP014570\n", "SRP043067\n", "SRP042370\n", "SRP042360\n", "SRP042159\n", "SRP042085\n", "SRP042053\n", "SRP041992\n", "SRP041738\n", "SRP041679\n", "SRP041669\n", "SRP041622\n", "SRP041182\n", "SRP041377\n", "SRP021009\n", "SRP041216\n", "SRP041129\n", "SRP041119\n", "SRP041044\n", "SRP040761\n", "SRP040479\n", "SRP040072\n", "SRP040070\n", "SRP040121\n", "SRP040044\n", "SRP039841\n", "SRP039779\n", "SRP039717\n", "SRP039699\n", "SRP039672\n", "SRP039661\n", "SRP039646\n", "SRP039634\n", "SRP035451\n", "SRP039551\n", "SRP039478\n", "SRP039440\n", "SRP039448\n", "SRP030474\n", "SRP034507\n", "SRP038004\n", "SRP037780\n", "SRP037583\n", "SRP036068\n", "SRP036637\n", "SRP036632\n", "SRP035368\n", "SRP035278\n", "SRP034930\n", "SRP034844\n", "ERP004159\n", "SRP017087\n", "SRP034444\n", "SRP033229\n", "SRP033198\n", "SRP033021\n", "ERP000964\n", "ERP002429\n", "SRP032928\n", "SRP032833\n", "SRP032792\n", "SRP032766\n", "ERP003855\n", "ERP000904\n", "SRP028229\n", "SRP026361\n", "SRP023111\n", "SRP021139\n", "SRP013319\n", "SRP020006\n", "SRP019994\n", "SRP019500\n", "SRP019241\n", "SRP018672\n", "SRP018358\n", "SRP016875\n", "SRP016501\n", "SRP015460\n", "SRP015370\n", "SRP015135\n", "SRP014437\n", "SRP012378\n", "SRP012018\n", "SRP010103\n", "SRP007831\n", "SRP007412\n", "SRP007400\n", "SRP002090\n", "SRP029153\n", "SRP029445\n", "SRP029427\n", "SRP029380\n", "SRP029330\n", "SRP029333\n", "ERP000606\n", "ERP000415\n", "ERP001977\n", "ERP000373\n", "SRP029172\n", "SRP028766\n", "ERP000668\n", "ERP003627\n", "SRP017364\n", "SRP025757\n", "SRP021189\n", "SRP011154\n", "SRP014574\n", "SRP017935\n", "SRP016889\n", "SRP002016\n", "SRP018826\n", "SRP018753\n", "SRP009821\n", "SRP012925\n", "SRP012850\n", "SRP009870\n", "SRP007799\n", "SRP006748\n", "SRP000373\"\"\"\n", "SRP_list = SRP_list.split(\"\\n\")" ] }, { "cell_type": "code", "execution_count": 3, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 72 }, "colab_type": "code", "id": "1CWmd5rF8yny", "outputId": "519c91be-e3b9-48a3-fd47-fbe415bd0b2a" }, "outputs": [ { "name": "stderr", "output_type": "stream", "text": [ "/home/saket/miniforge3/lib/python3.12/site-packages/pysradb/utils.py:14: TqdmExperimentalWarning: Using `tqdm.autonotebook.tqdm` in notebook mode. Use `tqdm.tqdm` instead to force console mode (e.g. in jupyter console)\n", " from tqdm.autonotebook import tqdm\n", "Error with SRP045252\n" ] } ], "source": [ "import sys\n", "import time\n", "\n", "from pysradb import SRAweb\n", "\n", "db = SRAweb()\n", "\n", "for srp in SRP_list:\n", " try:\n", " df = db.sra_metadata(srp)\n", " df.to_csv(\"{}.tsv\".format(srp), sep=\"\\t\", index=False)\n", " except:\n", " sys.stderr.write(\"Error with {}\\n\".format(srp))\n", " time.sleep(0.5)\n", " time.sleep(0.5)" ] } ], "metadata": { "colab": { "authorship_tag": "ABX9TyMmcvA8kJPyf4bhs59mCISs", "include_colab_link": true, "mount_file_id": "1pNeuZJjjHliYFk582kGNRpGJ1Fa2h9cn", "name": "07.Multiple_SRPs", "provenance": [] }, "kernelspec": { "display_name": "Python 3", "language": "python", "name": "python3" }, "language_info": { "codemirror_mode": { "name": "ipython", "version": 3 }, "file_extension": ".py", "mimetype": "text/x-python", "name": "python", "nbconvert_exporter": "python", "pygments_lexer": "ipython3", "version": "3.12.11" }, "widgets": { "application/vnd.jupyter.widget-state+json": { "state": {}, "version_major": 2, "version_minor": 0 } } }, "nbformat": 4, "nbformat_minor": 4 } ================================================ FILE: notebooks/07.Query_Search.ipynb ================================================ { "cells": [ { "cell_type": "markdown", "metadata": {}, "source": [ "[![Open In Colab](https://colab.research.google.com/assets/colab-badge.svg)](https://colab.research.google.com/github/saketkc/pysradb/blob/develop/notebooks/07.Query_Search.ipynb)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "# Query and Search\n", "\n", "This notebook demonstrates advanced search capabilities to find SRA studies based on specific criteria." ] }, { "cell_type": "code", "execution_count": null, "metadata": {}, "outputs": [], "source": [ "# Install pysradb if not already installed\n", "try:\n", " import pysradb\n", "\n", " print(f\"pysradb {pysradb.__version__} is already installed\")\n", "except ImportError:\n", " print(\"Installing pysradb from GitHub...\")\n", " import sys\n", "\n", " !{sys.executable} -m pip install -q git+https://github.com/saketkc/pysradb\n", " print(\"pysradb installed successfully!\")" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## pysradb search\n", "##### The pysradb search module supports querying the Sequence Read Archive (SRA) and the European Nucleotide Archive (ENA) databases for sequencing data. The module also includes several built-in flags that can be used to fine-tune a search query." ] }, { "cell_type": "code", "execution_count": 1, "metadata": {}, "outputs": [ { "data": { "text/html": [ "\n" ], "text/plain": [ "" ] }, "metadata": {}, "output_type": "display_data" } ], "source": [ "%%html\n", "" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "### Terminal flags for the pysradb search module:\n", "\n", "|Flags | Explanation|\n", "|----------|------------|\n", "| -h, --help | Displays the help message |\n", "| --saveto | Saves the result in the file specified by the user.
Supported file types: txt, tsv, csv |\n", "| --db | Selects the database (SRA, ENA, or both SRA and Geo DataSets) to query. Default database is SRA. Accepted inputs: sra, ena, geo|\n", "| -v, --verbosity | This determines how much details are retrieved and shown in the search result:
0: run_accession only
1: run_accession and experiment_description only
2: (default) study_accession, experiment_accession, experiment_title, description, tax_id, scientific_name, library_strategy,
library_source, library_selection, sample_accession, sample_title, instrument_model, run_accession, read_count, base_count
3: Everything in verbosity level 2, followed by all other retrievable information from the database|\n", "| -m, --max | Maximum number of returned entries. Default number is 20.
Note: If the maximum number set is large, querying the SRA and GEO DataSets databases will take significantly longer due to API limits|\n", "| -q, --query | The main query string.
Note: if this flag is not used, at least one of the following flags must be supplied: |\n", "| --accession | A relevant study / experiment / sample / run accession number|\n", "| --organism | Scientific name of the sample organism |\n", "| --layout | Library layout. Accepted inputs: single, paired|\n", "| --mbases | Size of the sample rounded to the nearest megabase|\n", "| --publication-date | The publication date of the run in the format dd-mm-yyyy. If a date range is desired,
enter the start date, followed by end date, separated by a colon ':' in the format dd-mm-yyyy:dd-mm-yyyy
Example: 01-01-2010:31-12-2010|\n", "| --platform | Sequencing platform used for the run. Possible inputs: illumina, ion torrent, oxford nanopore |\n", "| --selection | Library selection. Possible inputs: cdna, chip, dnase, pcr, polya |\n", "| --source | Library source. Possible inputs: genomic, metagenomic, transcriptomic |\n", "| --strategy | Library Preparation strategy. Possible inputs: wgs, amplicon, rna seq |\n", "| --title | Title of the experiment associated with the run |\n", "| --geo-query | The main query string to be sent to Geo DataSets |\n", "| --geo-dataset-type | Dataset type. Possible inputs: expression profiling by array, expression profiling by high throughput sequencing, non coding rna profiling by high throughput sequencing |\n", "| --geo-entry-type | Entry type. Accepted inputs: gds, gpl, gse, gsm |" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "### Using pysradb search in python:\n", "\n", "##### pysradb search organises each search query as a instance of either the SraSearch, EnaSearch or the GeoSearch classes. These classes takes in the following parameters in their constructor: \n", "\n", "\n", "\n", "`SraSearch (verbosity=2, return_max=20, query=None, accession=None, organism=None, layout=None, mbases=None, publication_date=None, platform=None, selection=None, source=None, strategy=None, title=None, suppress_validation=False,) ` \n", "\n", "\n", "`EnaSearch (verbosity=2, return_max=20, query=None, accession=None, organism=None, layout=None, mbases=None, publication_date=None, platform=None, selection=None, source=None, strategy=None, title=None, suppress_validation=False,) ` \n", "\n", "`GeoSearch (verbosity=2, return_max=20, query=None, accession=None, organism=None, layout=None, mbases=None, publication_date=None, platform=None, selection=None, source=None, strategy=None, title=None, geo_query=None, geo_dataset_type=None, geo_entry_type=None, suppress_validation=False,) ` \n", "\n", "| Parameters | Explanations|\n", "|----------|------------|\n", "| verbosity | This determines how much details are retrieved and shown in the search result (default=2). Same as -v / --verbosity on terminal |\n", "| return_max | Maximum number of returned entries (default=20). Same as -m / --max on terminal |\n", "| suppress_validation | Defaults to False. If this is set to True, the user input format checks will be skipped. Setting this to True may cause the program to behave in unexpected ways, but allows the user to search queries that does not pass the format check.|\n", "\n", "Other parameters match the command line flags of the same name.\n", "
\n", "
\n", "\n" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "##### To query the SRA database for ribosome profiling, expecting an output of verbosity level 2, and returning at most 5 entries, we can do the following:" ] }, { "cell_type": "code", "execution_count": 2, "metadata": {}, "outputs": [ { "name": "stderr", "output_type": "stream", "text": [ "/data/github/pysradb/pysradb/utils.py:14: TqdmWarning: IProgress not found. Please update jupyter and ipywidgets. See https://ipywidgets.readthedocs.io/en/stable/user_install.html\n", " from tqdm.autonotebook import tqdm\n", "100%|████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████| 5/5 [00:00<00:00, 5.58it/s]" ] }, { "name": "stdout", "output_type": "stream", "text": [ " study_accession experiment_accession \\\n", "0 SRP630668 SRX30794203 \n", "1 SRP630668 SRX30794202 \n", "2 SRP630668 SRX30794201 \n", "3 SRP630668 SRX30794200 \n", "4 ERP179251 ERX14883219 \n", "\n", " experiment_title sample_taxon_id \\\n", "0 shRNA treated replicate 2, Ribo-seq 9606 \n", "1 shRNA treated replicate 1, Ribo-seq 9606 \n", "2 negative control replicate 2, Ribo-seq 9606 \n", "3 negative control replicate 1, Ribo-seq 9606 \n", "4 Ribosome profiling and RNA-seq of Salmonella i... 10090 \n", "\n", " sample_scientific_name experiment_library_strategy \\\n", "0 Homo sapiens Ribo-seq \n", "1 Homo sapiens Ribo-seq \n", "2 Homo sapiens Ribo-seq \n", "3 Homo sapiens Ribo-seq \n", "4 Mus musculus OTHER \n", "\n", " experiment_library_source experiment_library_selection sample_accession \\\n", "0 TRANSCRIPTOMIC size fractionation SRS26807700 \n", "1 TRANSCRIPTOMIC size fractionation SRS26807699 \n", "2 TRANSCRIPTOMIC size fractionation SRS26807698 \n", "3 TRANSCRIPTOMIC size fractionation SRS26807697 \n", "4 OTHER other ERS26530900 \n", "\n", " sample_alias experiment_instrument_model pool_member_spots run_1_size \\\n", "0 sh2_ribo Illumina NovaSeq X Plus 57288768 1354504305 \n", "1 sh1_ribo Illumina NovaSeq X Plus 61293382 1431873887 \n", "2 nc2_ribo Illumina NovaSeq X Plus 85858060 2060965292 \n", "3 nc1_ribo Illumina NovaSeq X Plus 61189912 1474261116 \n", "4 SAMEA119980013 NextSeq 2000 14962757 \n", "\n", " run_1_accession run_1_total_spots run_1_total_bases \n", "0 SRR35744894 57288768 4296657600 \n", "1 SRR35744895 61293382 4597003650 \n", "2 SRR35744896 85858060 6439354500 \n", "3 SRR35744897 61189912 4589243400 \n", "4 ERR15479323 \n" ] }, { "name": "stderr", "output_type": "stream", "text": [ "\n" ] } ], "source": [ "from pysradb.search import SraSearch\n", "\n", "instance = SraSearch(2, 5, query=\"ribosome profiling\")\n", "instance.search()\n", "df = instance.get_df()\n", "print(df)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "### Quickstart\n", "\n", "##### To query ENA instead, replace SraSearch class with the EnaSearch class:" ] }, { "cell_type": "code", "execution_count": 3, "metadata": {}, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Empty DataFrame\n", "Columns: []\n", "Index: []\n" ] } ], "source": [ "from pysradb.search import EnaSearch\n", "\n", "instance = EnaSearch(2, 5, \"ribosome profiling\")\n", "instance.search()\n", "df = instance.get_df()\n", "print(df)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "##### To query GEO DataSets instead and retrieve the metadata of linked entries in SRA:" ] }, { "cell_type": "code", "execution_count": 4, "metadata": {}, "outputs": [ { "name": "stderr", "output_type": "stream", "text": [ "100%|████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████| 5/5 [00:00<00:00, 5.53it/s]" ] }, { "name": "stdout", "output_type": "stream", "text": [ " study_accession experiment_accession \\\n", "0 SRP619527 SRX30454639 \n", "1 SRP619527 SRX30454638 \n", "2 SRP619527 SRX30454637 \n", "3 SRP619527 SRX30454636 \n", "4 SRP618293 SRX30400919 \n", "\n", " experiment_title sample_taxon_id \\\n", "0 GSM9233466: Eef1g-cKO leptotene and zygotene_r... 10090 \n", "1 GSM9233465: Eef1g-cKO leptotene and zygotene_r... 10090 \n", "2 GSM9233464: Control leptotene and zygotene_rep... 10090 \n", "3 GSM9233463: Control leptotene and zygotene_rep... 10090 \n", "4 GSM9224243: Eef1g cKO leptotene/zygotene sperm... 10090 \n", "\n", " sample_scientific_name experiment_library_strategy \\\n", "0 Mus musculus OTHER \n", "1 Mus musculus OTHER \n", "2 Mus musculus OTHER \n", "3 Mus musculus OTHER \n", "4 Mus musculus RNA-Seq \n", "\n", " experiment_library_source experiment_library_selection sample_accession \\\n", "0 TRANSCRIPTOMIC other SRS26489458 \n", "1 TRANSCRIPTOMIC other SRS26489457 \n", "2 TRANSCRIPTOMIC other SRS26489456 \n", "3 TRANSCRIPTOMIC other SRS26489455 \n", "4 TRANSCRIPTOMIC cDNA SRS26437528 \n", "\n", " sample_alias experiment_instrument_model pool_member_spots run_1_size \\\n", "0 GSM9233466 Illumina NovaSeq 6000 69632843 8660602662 \n", "1 GSM9233465 Illumina NovaSeq 6000 98921214 12243831179 \n", "2 GSM9233464 Illumina NovaSeq 6000 38336833 4708346735 \n", "3 GSM9233463 Illumina NovaSeq 6000 88212319 11000694382 \n", "4 GSM9224243 Illumina NovaSeq X 15236947 1826954111 \n", "\n", " run_1_accession run_1_total_spots run_1_total_bases \n", "0 SRR35360226 69632843 20889852900 \n", "1 SRR35360227 98921214 29676364200 \n", "2 SRR35360228 38336833 11501049900 \n", "3 SRR35360229 88212319 26463695700 \n", "4 SRR35298842 15236947 4571084100 \n" ] }, { "name": "stderr", "output_type": "stream", "text": [ "\n" ] } ], "source": [ "from pysradb.search import GeoSearch\n", "\n", "instance = GeoSearch(2, 5, geo_query=\"ribosome profiling\")\n", "instance.search()\n", "df = instance.get_df()\n", "print(df)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "##### 7. Querying GEO DataSets with publication_date filter and displaying publication dates in results:" ] }, { "cell_type": "code", "execution_count": 5, "metadata": {}, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "No results found for the following search query: \n", " SRA: {'query': 'sra gds[Filter]', 'accession': None, 'organism': None, 'layout': None, 'mbases': None, 'publication_date': '01-09-2024:30-09-2024', 'platform': None, 'selection': None, 'source': None, 'strategy': None, 'title': None}\n", "GEO DataSets: {'query': 'RNA-Seq AND gds sra[Filter]', 'dataset_type': None, 'entry_type': None, 'publication_date': '01-09-2024:30-09-2024', 'organism': None}\n", "Empty DataFrame\n", "Columns: []\n", "Index: []\n" ] } ], "source": [ "from pysradb.search import GeoSearch\n", "\n", "# Search for RNA-Seq datasets published in September 2024\n", "# Using verbosity=3 to get all available fields including publication_date\n", "instance = GeoSearch(\n", " verbosity=3,\n", " return_max=5,\n", " geo_query=\"RNA-Seq\",\n", " publication_date=\"01-09-2024:30-09-2024\",\n", ")\n", "instance.search()\n", "df = instance.get_df()\n", "\n", "# Display select columns including publication_date\n", "if not df.empty and \"publication_date\" in df.columns:\n", " cols_to_show = [\n", " \"study_accession\",\n", " \"experiment_accession\",\n", " \"sample_scientific_name\",\n", " \"experiment_library_strategy\",\n", " \"publication_date\",\n", " ]\n", " available_cols = [c for c in cols_to_show if c in df.columns]\n", " print(df[available_cols])\n", "else:\n", " print(df)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "### Error Handling\n", "\n", "##### When suppress_validation is not set to True, query fields with incorrect entries will raise IncorrectFieldException, which provides the complete list of acceptable inputs for fields such as \"selection\", etc:" ] }, { "cell_type": "code", "execution_count": 6, "metadata": {}, "outputs": [ { "ename": "IncorrectFieldException", "evalue": "Incorrect selection: Mudkip\n--selection must be one of the following: \n5-methylcytidine antibody, CAGE, ChIP, ChIP-Seq, DNase, HMPR, Hybrid Selection, \nInverse rRNA, Inverse rRNA selection, MBD2 protein methyl-CpG binding domain, \nMDA, MF, MNase, MSLL, Oligo-dT, PCR, PolyA, RACE, RANDOM, RANDOM PCR, RT-PCR, \nReduced Representation, Restriction Digest, cDNA, cDNA_oligo_dT, cDNA_randomPriming \nother, padlock probes capture method, repeat fractionation, size fractionation, \nunspecified\n\n", "output_type": "error", "traceback": [ "\u001b[0;31m---------------------------------------------------------------------------\u001b[0m", "\u001b[0;31mIncorrectFieldException\u001b[0m Traceback (most recent call last)", "Cell \u001b[0;32mIn[6], line 2\u001b[0m\n\u001b[1;32m 1\u001b[0m \u001b[38;5;66;03m# 1. Invalid query entered for \"selection\"\u001b[39;00m\n\u001b[0;32m----> 2\u001b[0m \u001b[43mSraSearch\u001b[49m\u001b[43m(\u001b[49m\u001b[43mselection\u001b[49m\u001b[38;5;241;43m=\u001b[39;49m\u001b[38;5;124;43m\"\u001b[39;49m\u001b[38;5;124;43mMudkip\u001b[39;49m\u001b[38;5;124;43m\"\u001b[39;49m\u001b[43m)\u001b[49m\n", "File \u001b[0;32m/data/github/pysradb/pysradb/search.py:735\u001b[0m, in \u001b[0;36mSraSearch.__init__\u001b[0;34m(self, verbosity, return_max, query, accession, organism, layout, mbases, publication_date, platform, selection, source, strategy, title, suppress_validation)\u001b[0m\n\u001b[1;32m 718\u001b[0m \u001b[38;5;28;01mdef\u001b[39;00m\u001b[38;5;250m \u001b[39m\u001b[38;5;21m__init__\u001b[39m(\n\u001b[1;32m 719\u001b[0m \u001b[38;5;28mself\u001b[39m,\n\u001b[1;32m 720\u001b[0m verbosity\u001b[38;5;241m=\u001b[39m\u001b[38;5;241m2\u001b[39m,\n\u001b[0;32m (...)\u001b[0m\n\u001b[1;32m 733\u001b[0m suppress_validation\u001b[38;5;241m=\u001b[39m\u001b[38;5;28;01mFalse\u001b[39;00m,\n\u001b[1;32m 734\u001b[0m ):\n\u001b[0;32m--> 735\u001b[0m \u001b[38;5;28;43msuper\u001b[39;49m\u001b[43m(\u001b[49m\u001b[43m)\u001b[49m\u001b[38;5;241;43m.\u001b[39;49m\u001b[38;5;21;43m__init__\u001b[39;49m\u001b[43m(\u001b[49m\n\u001b[1;32m 736\u001b[0m \u001b[43m \u001b[49m\u001b[43mverbosity\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 737\u001b[0m \u001b[43m \u001b[49m\u001b[43mreturn_max\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 738\u001b[0m \u001b[43m \u001b[49m\u001b[43mquery\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 739\u001b[0m \u001b[43m \u001b[49m\u001b[43maccession\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 740\u001b[0m \u001b[43m \u001b[49m\u001b[43morganism\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 741\u001b[0m \u001b[43m \u001b[49m\u001b[43mlayout\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 742\u001b[0m \u001b[43m \u001b[49m\u001b[43mmbases\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 743\u001b[0m \u001b[43m \u001b[49m\u001b[43mpublication_date\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 744\u001b[0m \u001b[43m \u001b[49m\u001b[43mplatform\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 745\u001b[0m \u001b[43m \u001b[49m\u001b[43mselection\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 746\u001b[0m \u001b[43m \u001b[49m\u001b[43msource\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 747\u001b[0m \u001b[43m \u001b[49m\u001b[43mstrategy\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 748\u001b[0m \u001b[43m \u001b[49m\u001b[43mtitle\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 749\u001b[0m \u001b[43m \u001b[49m\u001b[43msuppress_validation\u001b[49m\u001b[43m,\u001b[49m\n\u001b[1;32m 750\u001b[0m \u001b[43m \u001b[49m\u001b[43m)\u001b[49m\n\u001b[1;32m 751\u001b[0m \u001b[38;5;28mself\u001b[39m\u001b[38;5;241m.\u001b[39mentries \u001b[38;5;241m=\u001b[39m {}\n\u001b[1;32m 752\u001b[0m \u001b[38;5;28mself\u001b[39m\u001b[38;5;241m.\u001b[39mnumber_entries \u001b[38;5;241m=\u001b[39m \u001b[38;5;241m0\u001b[39m\n", "File \u001b[0;32m/data/github/pysradb/pysradb/search.py:152\u001b[0m, in \u001b[0;36mQuerySearch.__init__\u001b[0;34m(self, verbosity, return_max, query, accession, organism, layout, mbases, publication_date, platform, selection, source, strategy, title, suppress_validation)\u001b[0m\n\u001b[1;32m 150\u001b[0m \u001b[38;5;28;01mraise\u001b[39;00m MissingQueryException()\n\u001b[1;32m 151\u001b[0m \u001b[38;5;28;01mif\u001b[39;00m \u001b[38;5;129;01mnot\u001b[39;00m suppress_validation:\n\u001b[0;32m--> 152\u001b[0m \u001b[38;5;28;43mself\u001b[39;49m\u001b[38;5;241;43m.\u001b[39;49m\u001b[43m_validate_fields\u001b[49m\u001b[43m(\u001b[49m\u001b[43m)\u001b[49m\n\u001b[1;32m 153\u001b[0m \u001b[38;5;28mself\u001b[39m\u001b[38;5;241m.\u001b[39mstats \u001b[38;5;241m=\u001b[39m {\n\u001b[1;32m 154\u001b[0m \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124mstudy\u001b[39m\u001b[38;5;124m\"\u001b[39m: \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124m-\u001b[39m\u001b[38;5;124m\"\u001b[39m,\n\u001b[1;32m 155\u001b[0m \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124mexperiment\u001b[39m\u001b[38;5;124m\"\u001b[39m: \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124m-\u001b[39m\u001b[38;5;124m\"\u001b[39m,\n\u001b[0;32m (...)\u001b[0m\n\u001b[1;32m 167\u001b[0m \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124mcount_stdev\u001b[39m\u001b[38;5;124m\"\u001b[39m: \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124m-\u001b[39m\u001b[38;5;124m\"\u001b[39m,\n\u001b[1;32m 168\u001b[0m }\n\u001b[1;32m 169\u001b[0m \u001b[38;5;28mself\u001b[39m\u001b[38;5;241m.\u001b[39mplot_objects \u001b[38;5;241m=\u001b[39m {}\n", "File \u001b[0;32m/data/github/pysradb/pysradb/search.py:449\u001b[0m, in \u001b[0;36mQuerySearch._validate_fields\u001b[0;34m(self)\u001b[0m\n\u001b[1;32m 447\u001b[0m \u001b[38;5;28mself\u001b[39m\u001b[38;5;241m.\u001b[39mfields[\u001b[38;5;124m\"\u001b[39m\u001b[38;5;124mstrategy\u001b[39m\u001b[38;5;124m\"\u001b[39m] \u001b[38;5;241m=\u001b[39m output[\u001b[38;5;241m0\u001b[39m]\n\u001b[1;32m 448\u001b[0m \u001b[38;5;28;01mif\u001b[39;00m message:\n\u001b[0;32m--> 449\u001b[0m \u001b[38;5;28;01mraise\u001b[39;00m IncorrectFieldException(message)\n", "\u001b[0;31mIncorrectFieldException\u001b[0m: Incorrect selection: Mudkip\n--selection must be one of the following: \n5-methylcytidine antibody, CAGE, ChIP, ChIP-Seq, DNase, HMPR, Hybrid Selection, \nInverse rRNA, Inverse rRNA selection, MBD2 protein methyl-CpG binding domain, \nMDA, MF, MNase, MSLL, Oligo-dT, PCR, PolyA, RACE, RANDOM, RANDOM PCR, RT-PCR, \nReduced Representation, Restriction Digest, cDNA, cDNA_oligo_dT, cDNA_randomPriming \nother, padlock probes capture method, repeat fractionation, size fractionation, \nunspecified\n\n" ] } ], "source": [ "# 1. Invalid query entered for \"selection\"\n", "SraSearch(selection=\"Mudkip\")" ] }, { "cell_type": "code", "execution_count": 7, "metadata": {}, "outputs": [ { "ename": "IncorrectFieldException", "evalue": "Multiple potential matches have been identified for metagenomic viral rna :\n['METAGENOMIC', 'VIRAL RNA']\nPlease check your input.\n\n", "output_type": "error", "traceback": [ "\u001b[0;31m---------------------------------------------------------------------------\u001b[0m", "\u001b[0;31mIncorrectFieldException\u001b[0m Traceback (most recent call last)", "Cell \u001b[0;32mIn[7], line 2\u001b[0m\n\u001b[1;32m 1\u001b[0m \u001b[38;5;66;03m# 2. Ambiguous query entered for \"source\":\u001b[39;00m\n\u001b[0;32m----> 2\u001b[0m \u001b[43mEnaSearch\u001b[49m\u001b[43m(\u001b[49m\u001b[43msource\u001b[49m\u001b[38;5;241;43m=\u001b[39;49m\u001b[38;5;124;43m\"\u001b[39;49m\u001b[38;5;124;43mmetagenomic viral rna \u001b[39;49m\u001b[38;5;124;43m\"\u001b[39;49m\u001b[43m)\u001b[49m\n", "File \u001b[0;32m/data/github/pysradb/pysradb/search.py:152\u001b[0m, in \u001b[0;36mQuerySearch.__init__\u001b[0;34m(self, verbosity, return_max, query, accession, organism, layout, mbases, publication_date, platform, selection, source, strategy, title, suppress_validation)\u001b[0m\n\u001b[1;32m 150\u001b[0m \u001b[38;5;28;01mraise\u001b[39;00m MissingQueryException()\n\u001b[1;32m 151\u001b[0m \u001b[38;5;28;01mif\u001b[39;00m \u001b[38;5;129;01mnot\u001b[39;00m suppress_validation:\n\u001b[0;32m--> 152\u001b[0m \u001b[38;5;28;43mself\u001b[39;49m\u001b[38;5;241;43m.\u001b[39;49m\u001b[43m_validate_fields\u001b[49m\u001b[43m(\u001b[49m\u001b[43m)\u001b[49m\n\u001b[1;32m 153\u001b[0m \u001b[38;5;28mself\u001b[39m\u001b[38;5;241m.\u001b[39mstats \u001b[38;5;241m=\u001b[39m {\n\u001b[1;32m 154\u001b[0m \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124mstudy\u001b[39m\u001b[38;5;124m\"\u001b[39m: \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124m-\u001b[39m\u001b[38;5;124m\"\u001b[39m,\n\u001b[1;32m 155\u001b[0m \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124mexperiment\u001b[39m\u001b[38;5;124m\"\u001b[39m: \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124m-\u001b[39m\u001b[38;5;124m\"\u001b[39m,\n\u001b[0;32m (...)\u001b[0m\n\u001b[1;32m 167\u001b[0m \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124mcount_stdev\u001b[39m\u001b[38;5;124m\"\u001b[39m: \u001b[38;5;124m\"\u001b[39m\u001b[38;5;124m-\u001b[39m\u001b[38;5;124m\"\u001b[39m,\n\u001b[1;32m 168\u001b[0m }\n\u001b[1;32m 169\u001b[0m \u001b[38;5;28mself\u001b[39m\u001b[38;5;241m.\u001b[39mplot_objects \u001b[38;5;241m=\u001b[39m {}\n", "File \u001b[0;32m/data/github/pysradb/pysradb/search.py:449\u001b[0m, in \u001b[0;36mQuerySearch._validate_fields\u001b[0;34m(self)\u001b[0m\n\u001b[1;32m 447\u001b[0m \u001b[38;5;28mself\u001b[39m\u001b[38;5;241m.\u001b[39mfields[\u001b[38;5;124m\"\u001b[39m\u001b[38;5;124mstrategy\u001b[39m\u001b[38;5;124m\"\u001b[39m] \u001b[38;5;241m=\u001b[39m output[\u001b[38;5;241m0\u001b[39m]\n\u001b[1;32m 448\u001b[0m \u001b[38;5;28;01mif\u001b[39;00m message:\n\u001b[0;32m--> 449\u001b[0m \u001b[38;5;28;01mraise\u001b[39;00m IncorrectFieldException(message)\n", "\u001b[0;31mIncorrectFieldException\u001b[0m: Multiple potential matches have been identified for metagenomic viral rna :\n['METAGENOMIC', 'VIRAL RNA']\nPlease check your input.\n\n" ] } ], "source": [ "# 2. Ambiguous query entered for \"source\":\n", "EnaSearch(source=\"metagenomic viral rna \")" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "### Usage Examples:" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "##### 1. Checking the help message on terminal:" ] }, { "cell_type": "code", "execution_count": 8, "metadata": {}, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "usage: pysradb search [-h] [-o SAVETO] [-s] [-g [GRAPHS]] [-d {ena,geo,sra}]\n", " [-v {0,1,2,3}] [--run-description] [--detailed] [-m MAX]\n", " [-q QUERY [QUERY ...]] [-A ACCESSION]\n", " [-O ORGANISM [ORGANISM ...]] [-L {SINGLE,PAIRED}]\n", " [-M MBASES] [-D PUBLICATION_DATE]\n", " [-P PLATFORM [PLATFORM ...]]\n", " [-E SELECTION [SELECTION ...]] [-C SOURCE [SOURCE ...]]\n", " [-S STRATEGY [STRATEGY ...]] [-T TITLE [TITLE ...]] [-I]\n", " [-G GEO_QUERY [GEO_QUERY ...]]\n", " [-Y GEO_DATASET_TYPE [GEO_DATASET_TYPE ...]]\n", " [-Z GEO_ENTRY_TYPE [GEO_ENTRY_TYPE ...]]\n", "\n", "options:\n", " -h, --help show this help message and exit\n", " -o SAVETO, --saveto SAVETO\n", " Save search result dataframe to file\n", " -s, --stats Displays some useful statistics for the search\n", " results.\n", " -g [GRAPHS], --graphs [GRAPHS]\n", " Generates graphs to illustrate the search result. By\n", " default all graphs are generated. Alternatively,\n", " select a subset from the options below in a space-\n", " separated string: daterange, organism, source,\n", " selection, platform, basecount\n", " -d {ena,geo,sra}, --db {ena,geo,sra}\n", " Select the db API (sra, ena, or geo) to query, default\n", " = sra. Note: pysradb search works slightly differently\n", " when db = geo. Please refer to 'pysradb search --geo-\n", " info' for more details.\n", " -v {0,1,2,3}, --verbosity {0,1,2,3}\n", " Level of search result details (0, 1, 2 or 3), default\n", " = 2 0: run accession only 1: run accession and\n", " experiment title 2: accession numbers, titles and\n", " sequencing information 3: records in 2 and other\n", " information such as download url, sample attributes,\n", " etc\n", " --run-description Displays run accessions and descriptions only.\n", " Equivalent to --verbosity 1\n", " --detailed Displays detailed search results. Equivalent to\n", " --verbosity 3.\n", " -m MAX, --max MAX Maximum number of entries to return, default = 20\n", " -q QUERY [QUERY ...], --query QUERY [QUERY ...]\n", " Main query string. Note that if no query is supplied,\n", " at least one of the following flags must be present:\n", " -A ACCESSION, --accession ACCESSION\n", " Accession number\n", " -O ORGANISM [ORGANISM ...], --organism ORGANISM [ORGANISM ...]\n", " Scientific name of the sample organism\n", " -L {SINGLE,PAIRED}, --layout {SINGLE,PAIRED}\n", " Library layout. Accepts either SINGLE or PAIRED\n", " -M MBASES, --mbases MBASES\n", " Size of the sample rounded to the nearest megabase\n", " -D PUBLICATION_DATE, --publication-date PUBLICATION_DATE\n", " Publication date of the run in the format dd-mm-yyyy.\n", " If a date range is desired, enter the start date,\n", " followed by end date, separated by a colon ':'.\n", " Example: 01-01-2010:31-12-2010\n", " -P PLATFORM [PLATFORM ...], --platform PLATFORM [PLATFORM ...]\n", " Sequencing platform\n", " -E SELECTION [SELECTION ...], --selection SELECTION [SELECTION ...]\n", " Library selection\n", " -C SOURCE [SOURCE ...], --source SOURCE [SOURCE ...]\n", " Library source\n", " -S STRATEGY [STRATEGY ...], --strategy STRATEGY [STRATEGY ...]\n", " Library preparation strategy\n", " -T TITLE [TITLE ...], --title TITLE [TITLE ...]\n", " Experiment title\n", " -I, --geo-info Displays information on how to query GEO DataSets via\n", " 'pysradb search --db geo ...', including accepted\n", " inputs for -G/--geo-query, -Y/--geo-dataset-type and\n", " -Z/--geo-entry-type.\n", " -G GEO_QUERY [GEO_QUERY ...], --geo-query GEO_QUERY [GEO_QUERY ...]\n", " Main query string for GEO DataSet. This flag is only\n", " used when db is set to be geo.Please refer to 'pysradb\n", " search --geo-info' for more details.\n", " -Y GEO_DATASET_TYPE [GEO_DATASET_TYPE ...], --geo-dataset-type GEO_DATASET_TYPE [GEO_DATASET_TYPE ...]\n", " GEO DataSet Type. This flag is only used when --db is\n", " set to be geo.Please refer to 'pysradb search --geo-\n", " info' for more details.\n", " -Z GEO_ENTRY_TYPE [GEO_ENTRY_TYPE ...], --geo-entry-type GEO_ENTRY_TYPE [GEO_ENTRY_TYPE ...]\n", " GEO Entry Type. This flag is only used when --db is\n", " set to be geo.Please refer to 'pysradb search --geo-\n", " info' for more details.\n" ] } ], "source": [ "!pysradb search -h" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "##### 2. Searching for 5 illumina sequences related to the covid-19 pandemic on ENA, using the terminal:" ] }, { "cell_type": "code", "execution_count": 9, "metadata": {}, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "study_accession\texperiment_accession\texperiment_title\tdescription\ttax_id\tscientific_name\tlibrary_strategy\tlibrary_source\tlibrary_selection\tsample_accession\tsample_title\tinstrument_model\trun_accession\tread_count\tbase_count\n", "PRJEB65477\tERX11285566\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\t9606\tHomo sapiens\tRNA-Seq\tTRANSCRIPTOMIC\tInverse rRNA\tSAMEA114308724\tSample 1\tIllumina HiSeq 4000\tERR11901279\t131354572\t19834540372\n", "PRJEB65477\tERX11285567\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\t9606\tHomo sapiens\tRNA-Seq\tTRANSCRIPTOMIC\tInverse rRNA\tSAMEA114308725\tSample 10\tIllumina HiSeq 4000\tERR11901280\t95225496\t14379049896\n", "PRJEB65477\tERX11285573\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\t9606\tHomo sapiens\tRNA-Seq\tTRANSCRIPTOMIC\tInverse rRNA\tSAMEA114308731\tSample 105\tIllumina HiSeq 4000\tERR11901286\t128864216\t19458496616\n", "PRJEB65477\tERX11285574\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\t9606\tHomo sapiens\tRNA-Seq\tTRANSCRIPTOMIC\tInverse rRNA\tSAMEA114308732\tSample 106\tIllumina HiSeq 4000\tERR11901287\t123505478\t18649327178\n", "PRJEB65477\tERX11285577\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\tIllumina HiSeq 4000 sequencing: Blood RNA sequencing was performed on a cohort of adults attending the Emergency Department with suspected infection who had subsequently-confirmed viral, bacterial, COVID19 and healthy controls\t9606\tHomo sapiens\tRNA-Seq\tTRANSCRIPTOMIC\tInverse rRNA\tSAMEA114308735\tSample 109\tIllumina HiSeq 4000\tERR11901290\t120866712\t18250873512\n" ] } ], "source": [ "!pysradb search -q covid19 --platform illumina --db ena -m 5" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "##### 3. Searching for illumina sequences related to the covid-19 pandemic on ENA, using the terminal, and saving the results in a nicely formatted text file:" ] }, { "cell_type": "code", "execution_count": 10, "metadata": {}, "outputs": [], "source": [ "!pysradb search -q covid19 --db ena --saveto query.txt" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "##### 4. Searching for illumina sequences related to the covid-19 pandemic on ENA, within python: (outputs a pandas dataframe)" ] }, { "cell_type": "code", "execution_count": 11, "metadata": {}, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ " study_accession experiment_accession \\\n", "0 PRJEB65477 ERX11285566 \n", "1 PRJEB65477 ERX11285567 \n", "2 PRJEB65477 ERX11285573 \n", "3 PRJEB65477 ERX11285574 \n", "4 PRJEB65477 ERX11285577 \n", "5 PRJEB65477 ERX11285583 \n", "6 PRJEB65477 ERX11285586 \n", "7 PRJEB65477 ERX11285592 \n", "8 PRJEB65477 ERX11285595 \n", "9 PRJEB65477 ERX11285599 \n", "10 PRJEB65477 ERX11285600 \n", "11 PRJEB65477 ERX11285605 \n", "12 PRJEB65477 ERX11285607 \n", "13 PRJEB65477 ERX11285609 \n", "14 PRJEB65477 ERX11285611 \n", "15 PRJEB65477 ERX11285620 \n", "16 PRJEB65477 ERX11285623 \n", "17 PRJEB65477 ERX11285625 \n", "18 PRJEB65477 ERX11285629 \n", "19 PRJEB65477 ERX11285633 \n", "\n", " experiment_title \\\n", "0 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "1 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "2 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "3 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "4 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "5 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "6 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "7 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "8 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "9 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "10 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "11 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "12 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "13 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "14 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "15 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "16 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "17 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "18 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "19 Illumina HiSeq 4000 sequencing: Blood RNA sequ... \n", "\n", " description tax_id scientific_name \\\n", "0 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "1 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "2 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "3 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "4 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "5 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "6 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "7 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "8 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "9 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "10 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "11 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "12 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "13 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "14 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "15 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "16 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "17 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "18 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "19 Illumina HiSeq 4000 sequencing: Blood RNA sequ... 9606 Homo sapiens \n", "\n", " library_strategy library_source library_selection sample_accession \\\n", "0 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308724 \n", "1 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308725 \n", "2 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308731 \n", "3 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308732 \n", "4 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308735 \n", "5 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308741 \n", "6 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308744 \n", "7 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308750 \n", "8 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308753 \n", "9 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308757 \n", "10 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308758 \n", "11 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308763 \n", "12 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308765 \n", "13 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308767 \n", "14 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308769 \n", "15 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308778 \n", "16 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308781 \n", "17 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308783 \n", "18 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308787 \n", "19 RNA-Seq TRANSCRIPTOMIC Inverse rRNA SAMEA114308791 \n", "\n", " sample_title instrument_model run_accession read_count base_count \n", "0 Sample 1 Illumina HiSeq 4000 ERR11901279 131354572 19834540372 \n", "1 Sample 10 Illumina HiSeq 4000 ERR11901280 95225496 14379049896 \n", "2 Sample 105 Illumina HiSeq 4000 ERR11901286 128864216 19458496616 \n", "3 Sample 106 Illumina HiSeq 4000 ERR11901287 123505478 18649327178 \n", "4 Sample 109 Illumina HiSeq 4000 ERR11901290 120866712 18250873512 \n", "5 Sample 114 Illumina HiSeq 4000 ERR11901296 126581586 19113819486 \n", "6 Sample 117 Illumina HiSeq 4000 ERR11901299 126421026 19089574926 \n", "7 Sample 122 Illumina HiSeq 4000 ERR11901305 132194842 19961421142 \n", "8 Sample 125 Illumina HiSeq 4000 ERR11901308 128325648 19377172848 \n", "9 Sample 129 Illumina HiSeq 4000 ERR11901312 113973238 17209958938 \n", "10 Sample 13 Illumina HiSeq 4000 ERR11901313 103563334 15638063434 \n", "11 Sample 134 Illumina HiSeq 4000 ERR11901318 125759128 18989628328 \n", "12 Sample 15 Illumina HiSeq 4000 ERR11901320 102246922 15439285222 \n", "13 Sample 17 Illumina HiSeq 4000 ERR11901322 103868320 15684116320 \n", "14 Sample 19 Illumina HiSeq 4000 ERR11901324 102445734 15469305834 \n", "15 Sample 27 Illumina HiSeq 4000 ERR11901333 103177112 15579743912 \n", "16 Sample 3 Illumina HiSeq 4000 ERR11901336 104470270 15775010770 \n", "17 Sample 31 Illumina HiSeq 4000 ERR11901338 95555226 14428839126 \n", "18 Sample 35 Illumina HiSeq 4000 ERR11901342 104135584 15724473184 \n", "19 Sample 39 Illumina HiSeq 4000 ERR11901346 103208434 15584473534 \n" ] } ], "source": [ "from pysradb.search import EnaSearch\n", "\n", "instance = EnaSearch(2, 20, query=\"covid19\", platform=\"illumina\")\n", "instance.search()\n", "df = instance.get_df()\n", "print(df)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "##### 5. More complex example:" ] }, { "cell_type": "code", "execution_count": 13, "metadata": {}, "outputs": [ { "data": { "text/html": [ "
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study_accessionexperiment_accessionexperiment_titledescriptiontax_idscientific_namelibrary_strategylibrary_sourcelibrary_selectionsample_accession...tagtarget_genetax_lineagetaxonomic_classificationtaxonomic_identity_markertemperaturetissue_libtissue_typetransposase_protocolvariety
0PRJNA549801SRX10904916Illumina MiSeq sequencing: E. coli library mad...Illumina MiSeq sequencing: E. coli library mad...562Escherichia coliWGSGENOMICRANDOMSAMN11656391...env_tax;env_tax:freshwater;env_tax:terrestrial...<NA>1;131567;2;3379134;1224;1236;91347;543;561;562<NA><NA><NA><NA><NA><NA><NA>
1PRJNA530580SRX5658689Illumina MiSeq sequencing: Sequencing of Esche...Illumina MiSeq sequencing: Sequencing of Esche...562Escherichia coliWGSGENOMICRANDOMSAMN11319482...env_tax;env_tax:freshwater;env_tax:terrestrial...<NA>1;131567;2;3379134;1224;1236;91347;543;561;562<NA><NA><NA><NA><NA><NA><NA>
2PRJEB34285ERX3552102Illumina MiSeq paired end sequencing: Raw read...Illumina MiSeq paired end sequencing: Raw read...562Escherichia coliWGSGENOMICRANDOMSAMEA5957573...env_tax;env_tax:freshwater;env_tax:terrestrial...<NA>1;131567;2;3379134;1224;1236;91347;543;561;562<NA><NA><NA><NA><NA><NA><NA>
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3 rows × 192 columns

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" ], "text/plain": [ " study_accession experiment_accession \\\n", "0 PRJNA549801 SRX10904916 \n", "1 PRJNA530580 SRX5658689 \n", "2 PRJEB34285 ERX3552102 \n", "\n", " experiment_title \\\n", "0 Illumina MiSeq sequencing: E. coli library mad... \n", "1 Illumina MiSeq sequencing: Sequencing of Esche... \n", "2 Illumina MiSeq paired end sequencing: Raw read... \n", "\n", " description tax_id scientific_name \\\n", "0 Illumina MiSeq sequencing: E. coli library mad... 562 Escherichia coli \n", "1 Illumina MiSeq sequencing: Sequencing of Esche... 562 Escherichia coli \n", "2 Illumina MiSeq paired end sequencing: Raw read... 562 Escherichia coli \n", "\n", " library_strategy library_source library_selection sample_accession ... \\\n", "0 WGS GENOMIC RANDOM SAMN11656391 ... \n", "1 WGS GENOMIC RANDOM SAMN11319482 ... \n", "2 WGS GENOMIC RANDOM SAMEA5957573 ... \n", "\n", " tag target_gene \\\n", "0 env_tax;env_tax:freshwater;env_tax:terrestrial... \n", "1 env_tax;env_tax:freshwater;env_tax:terrestrial... \n", "2 env_tax;env_tax:freshwater;env_tax:terrestrial... \n", "\n", " tax_lineage taxonomic_classification \\\n", "0 1;131567;2;3379134;1224;1236;91347;543;561;562 \n", "1 1;131567;2;3379134;1224;1236;91347;543;561;562 \n", "2 1;131567;2;3379134;1224;1236;91347;543;561;562 \n", "\n", " taxonomic_identity_marker temperature tissue_lib tissue_type \\\n", "0 \n", "1 \n", "2 \n", "\n", " transposase_protocol variety \n", "0 \n", "1 \n", "2 \n", "\n", "[3 rows x 192 columns]" ] }, "execution_count": 13, "metadata": {}, "output_type": "execute_result" } ], "source": [ "from pysradb.search import EnaSearch\n", "\n", "instance = EnaSearch(\n", " 3,\n", " 100000,\n", " organism=\"Escherichia coli\",\n", " layout=\"Paired\",\n", " mbases=10,\n", " publication_date=\"01-01-2019:31-12-2021\",\n", " platform=\"Illumina\",\n", " selection=\"random\",\n", " source=\"Genomic\",\n", " strategy=\"WGS\",\n", ")\n", "instance.search()\n", "df = instance.get_df()\n", "df" ] }, { "cell_type": "code", "execution_count": null, "metadata": {}, "outputs": [], "source": [ "sorted(df.columns)" ] }, { "cell_type": "code", "execution_count": 16, "metadata": {}, "outputs": [ { "name": "stderr", "output_type": "stream", "text": [ "100%|████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████| 100/100 [00:02<00:00, 44.88it/s]\n" ] }, { "data": { "text/html": [ "
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study_accessionexperiment_accessionexperiment_titlesample_taxon_idsample_scientific_nameexperiment_library_strategyexperiment_library_sourceexperiment_library_selectionsample_accessionsample_alias...study_link_1_typestudy_link_1_value_1study_link_1_value_2study_study_abstractstudy_study_titlestudy_study_type_existing_study_typesubmission_accessionsubmission_aliassubmission_center_namesubmission_lab_name
0SRP531137SRX25997822GSM8501051: HEK293, Prm1 negative, Replicate 3...9606Homo sapiensHi-CGENOMICotherSRS22571584GSM8501051...<NA><NA><NA>Although the spatial organization of the genom...Large-scale manipulation of radial positioning...OtherSRA1964865SUB14711595Technion - Israel Institute of Technology<NA>
1SRP531137SRX25997821GSM8501050: HEK293, Prm1 negative, Replicate 2...9606Homo sapiensHi-CGENOMICotherSRS22571583GSM8501050...<NA><NA><NA>Although the spatial organization of the genom...Large-scale manipulation of radial positioning...OtherSRA1964865SUB14711595Technion - Israel Institute of Technology<NA>
2SRP531137SRX25997820GSM8501049: HEK293, Prm1 negative, Replicate 1...9606Homo sapiensHi-CGENOMICotherSRS22571582GSM8501049...<NA><NA><NA>Although the spatial organization of the genom...Large-scale manipulation of radial positioning...OtherSRA1964865SUB14711595Technion - Israel Institute of Technology<NA>
3SRP531137SRX25997819GSM8501048: HEK293, Prm1 positive DAPI low, Hi...9606Homo sapiensHi-CGENOMICotherSRS22571581GSM8501048...<NA><NA><NA>Although the spatial organization of the genom...Large-scale manipulation of radial positioning...OtherSRA1964865SUB14711595Technion - Israel Institute of Technology<NA>
4SRP531137SRX25997818GSM8501047: HEK293, Prm1 positive DAPI high, H...9606Homo sapiensHi-CGENOMICotherSRS22571580GSM8501047...<NA><NA><NA>Although the spatial organization of the genom...Large-scale manipulation of radial positioning...OtherSRA1964865SUB14711595Technion - Israel Institute of Technology<NA>
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95SRP530052SRX25934604GSM8493072: HSS-3; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMICcDNASRS22520997GSM8493072...XREF_LINKDB: pubmedID: 39752487Fluid shear stress (FSS) from blood flow sense...cSTAR analysis identifies endothelial cell cyc...Transcriptome AnalysisSRA1960858SUB14701816Systems Biology Ireland, University College Du...<NA>
96SRP530052SRX25934603GSM8493071: HSS-2; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMICcDNASRS22520996GSM8493071...XREF_LINKDB: pubmedID: 39752487Fluid shear stress (FSS) from blood flow sense...cSTAR analysis identifies endothelial cell cyc...Transcriptome AnalysisSRA1960858SUB14701816Systems Biology Ireland, University College Du...<NA>
97SRP530052SRX25934602GSM8493070: HSS-1; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMICcDNASRS22520995GSM8493070...XREF_LINKDB: pubmedID: 39752487Fluid shear stress (FSS) from blood flow sense...cSTAR analysis identifies endothelial cell cyc...Transcriptome AnalysisSRA1960858SUB14701816Systems Biology Ireland, University College Du...<NA>
98SRP529928SRX25928352GSM8492057: NC1 group2; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMICcDNASRS22515729GSM8492057...<NA><NA><NA>Adrenoleukodystrophy (ALD) is a rare X-linked ...Transcriptomic Analysis of Identical Twins wit...Transcriptome AnalysisSRA1960558SUB14700372Southwest Hospital, Army Medical University (T...<NA>
99SRP529928SRX25928351GSM8492056: NC1 group1; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMICcDNASRS22515728GSM8492056...<NA><NA><NA>Adrenoleukodystrophy (ALD) is a rare X-linked ...Transcriptomic Analysis of Identical Twins wit...Transcriptome AnalysisSRA1960558SUB14700372Southwest Hospital, Army Medical University (T...<NA>
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100 rows × 644 columns

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" ], "text/plain": [ " study_accession experiment_accession \\\n", "0 SRP531137 SRX25997822 \n", "1 SRP531137 SRX25997821 \n", "2 SRP531137 SRX25997820 \n", "3 SRP531137 SRX25997819 \n", "4 SRP531137 SRX25997818 \n", ".. ... ... \n", "95 SRP530052 SRX25934604 \n", "96 SRP530052 SRX25934603 \n", "97 SRP530052 SRX25934602 \n", "98 SRP529928 SRX25928352 \n", "99 SRP529928 SRX25928351 \n", "\n", " experiment_title sample_taxon_id \\\n", "0 GSM8501051: HEK293, Prm1 negative, Replicate 3... 9606 \n", "1 GSM8501050: HEK293, Prm1 negative, Replicate 2... 9606 \n", "2 GSM8501049: HEK293, Prm1 negative, Replicate 1... 9606 \n", "3 GSM8501048: HEK293, Prm1 positive DAPI low, Hi... 9606 \n", "4 GSM8501047: HEK293, Prm1 positive DAPI high, H... 9606 \n", ".. ... ... \n", "95 GSM8493072: HSS-3; Homo sapiens; RNA-Seq 9606 \n", "96 GSM8493071: HSS-2; Homo sapiens; RNA-Seq 9606 \n", "97 GSM8493070: HSS-1; Homo sapiens; RNA-Seq 9606 \n", "98 GSM8492057: NC1 group2; Homo sapiens; RNA-Seq 9606 \n", "99 GSM8492056: NC1 group1; Homo sapiens; RNA-Seq 9606 \n", "\n", " sample_scientific_name experiment_library_strategy \\\n", "0 Homo sapiens Hi-C \n", "1 Homo sapiens Hi-C \n", "2 Homo sapiens Hi-C \n", "3 Homo sapiens Hi-C \n", "4 Homo sapiens Hi-C \n", ".. ... ... \n", "95 Homo sapiens RNA-Seq \n", "96 Homo sapiens RNA-Seq \n", "97 Homo sapiens RNA-Seq \n", "98 Homo sapiens RNA-Seq \n", "99 Homo sapiens RNA-Seq \n", "\n", " experiment_library_source experiment_library_selection sample_accession \\\n", "0 GENOMIC other SRS22571584 \n", "1 GENOMIC other SRS22571583 \n", "2 GENOMIC other SRS22571582 \n", "3 GENOMIC other SRS22571581 \n", "4 GENOMIC other SRS22571580 \n", ".. ... ... ... \n", "95 TRANSCRIPTOMIC cDNA SRS22520997 \n", "96 TRANSCRIPTOMIC cDNA SRS22520996 \n", "97 TRANSCRIPTOMIC cDNA SRS22520995 \n", "98 TRANSCRIPTOMIC cDNA SRS22515729 \n", "99 TRANSCRIPTOMIC cDNA SRS22515728 \n", "\n", " sample_alias ... study_link_1_type study_link_1_value_1 \\\n", "0 GSM8501051 ... \n", "1 GSM8501050 ... \n", "2 GSM8501049 ... \n", "3 GSM8501048 ... \n", "4 GSM8501047 ... \n", ".. ... ... ... ... \n", "95 GSM8493072 ... XREF_LINK DB: pubmed \n", "96 GSM8493071 ... XREF_LINK DB: pubmed \n", "97 GSM8493070 ... XREF_LINK DB: pubmed \n", "98 GSM8492057 ... \n", "99 GSM8492056 ... \n", "\n", " study_link_1_value_2 study_study_abstract \\\n", "0 Although the spatial organization of the genom... \n", "1 Although the spatial organization of the genom... \n", "2 Although the spatial organization of the genom... \n", "3 Although the spatial organization of the genom... \n", "4 Although the spatial organization of the genom... \n", ".. ... ... \n", "95 ID: 39752487 Fluid shear stress (FSS) from blood flow sense... \n", "96 ID: 39752487 Fluid shear stress (FSS) from blood flow sense... \n", "97 ID: 39752487 Fluid shear stress (FSS) from blood flow sense... \n", "98 Adrenoleukodystrophy (ALD) is a rare X-linked ... \n", "99 Adrenoleukodystrophy (ALD) is a rare X-linked ... \n", "\n", " study_study_title \\\n", "0 Large-scale manipulation of radial positioning... \n", "1 Large-scale manipulation of radial positioning... \n", "2 Large-scale manipulation of radial positioning... \n", "3 Large-scale manipulation of radial positioning... \n", "4 Large-scale manipulation of radial positioning... \n", ".. ... \n", "95 cSTAR analysis identifies endothelial cell cyc... \n", "96 cSTAR analysis identifies endothelial cell cyc... \n", "97 cSTAR analysis identifies endothelial cell cyc... \n", "98 Transcriptomic Analysis of Identical Twins wit... \n", "99 Transcriptomic Analysis of Identical Twins wit... \n", "\n", " study_study_type_existing_study_type submission_accession submission_alias \\\n", "0 Other SRA1964865 SUB14711595 \n", "1 Other SRA1964865 SUB14711595 \n", "2 Other SRA1964865 SUB14711595 \n", "3 Other SRA1964865 SUB14711595 \n", "4 Other SRA1964865 SUB14711595 \n", ".. ... ... ... \n", "95 Transcriptome Analysis SRA1960858 SUB14701816 \n", "96 Transcriptome Analysis SRA1960858 SUB14701816 \n", "97 Transcriptome Analysis SRA1960858 SUB14701816 \n", "98 Transcriptome Analysis SRA1960558 SUB14700372 \n", "99 Transcriptome Analysis SRA1960558 SUB14700372 \n", "\n", " submission_center_name submission_lab_name \n", "0 Technion - Israel Institute of Technology \n", "1 Technion - Israel Institute of Technology \n", "2 Technion - Israel Institute of Technology \n", "3 Technion - Israel Institute of Technology \n", "4 Technion - Israel Institute of Technology \n", ".. ... ... \n", "95 Systems Biology Ireland, University College Du... \n", "96 Systems Biology Ireland, University College Du... \n", "97 Systems Biology Ireland, University College Du... \n", "98 Southwest Hospital, Army Medical University (T... \n", "99 Southwest Hospital, Army Medical University (T... \n", "\n", "[100 rows x 644 columns]" ] }, "execution_count": 16, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# https://github.com/saketkc/pysradb/issues/221\n", "instance = GeoSearch(\n", " publication_date=\"05-09-2024:06-09-2024\", return_max=100, verbosity=3\n", ")\n", "instance.search()\n", "df = instance.get_df()\n", "df" ] }, { "cell_type": "code", "execution_count": 17, "metadata": {}, "outputs": [ { "name": "stderr", "output_type": "stream", "text": [ "100%|██████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████████| 1000/1000 [00:48<00:00, 20.72it/s]\n" ] }, { "name": "stdout", "output_type": "stream", "text": [ "['GSE276554' 'GSE276553' 'GSE267301' 'GSE276379' 'GSE276473' 'GSE276365'\n", " 'GSE276447' 'GSE276438' 'GSE219269' 'GSE276372' 'GSE276338' 'GSE276337'\n", " 'GSE276206' 'GSE276309' 'GSE276304' 'GSE276245' 'GSE276204' 'GSE276185'\n", " 'GSE276195' 'GSE276192' 'GSE276153' 'GSE276130' 'GSE276122' 'GSE276065'\n", " 'GSE276058' 'GSE276038' 'GSE276037' 'GSE275962' 'GSE275896' 'GSE275863'\n", " 'GSE275777' 'GSE275778' 'GSE275571' 'GSE253407' 'GSE275211' 'GSE274586'\n", " 'GSE274408' 'GSE273907' 'GSE273844' 'GSE273813' 'GSE253145' 'GSE272793'\n", " 'GSE272635' 'GSE272394' 'GSE247707' 'GSE247706' 'GSE272252' 'GSE271996'\n", " 'GSE271746' 'GSE271667' 'GSE271653' 'GSE264193' 'GSE245033' 'GSE268837'\n", " 'GSE267343' 'GSE267342' 'GSE266976' 'GSE266471' 'GSE264212' 'GSE264012'\n", " 'GSE263804' 'GSE263798' 'GSE263549' 'GSE263414' 'GSE263441' 'GSE262699'\n", " 'GSE262282' 'GSE262272' 'GSE262127' 'GSE262125' 'GSE262126']\n" ] }, { "data": { "text/plain": [ "np.int64(0)" ] }, "execution_count": 17, "metadata": {}, "output_type": "execute_result" } ], "source": [ "instance = GeoSearch(\n", " publication_date=\"04-09-2024:06-09-2024\", return_max=1000, verbosity=3\n", ")\n", "instance.search()\n", "df = instance.get_df()\n", "print(df[\"study_alias\"].unique())" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "
\n", "\n", "##### 6. Corresponding terminal command example, with max set to 20:" ] }, { "cell_type": "code", "execution_count": null, "metadata": {}, "outputs": [], "source": [ "!pysradb search --db ena -m 20 -v 3 --organism Escherichia coli --layout Paired --mbases 100 --publication-date 01-01-2019:31-12-2019 --platform illumina --selection random --source Genomic --strategy wgs" ] }, { "cell_type": "code", "execution_count": null, "metadata": {}, "outputs": [], "source": [] } ], "metadata": { "kernelspec": { "display_name": "Python 3", "language": "python", "name": "python3" }, "language_info": { "codemirror_mode": { "name": "ipython", "version": 3 }, "file_extension": ".py", "mimetype": "text/x-python", "name": "python", "nbconvert_exporter": "python", "pygments_lexer": "ipython3", "version": "3.10.18" }, "widgets": { "application/vnd.jupyter.widget-state+json": { "state": {}, "version_major": 2, "version_minor": 0 } } }, "nbformat": 4, "nbformat_minor": 4 } ================================================ FILE: notebooks/08.PMC_DOI_Identifiers.ipynb ================================================ { "cells": [ { "cell_type": "markdown", "metadata": {}, "source": [ "[![Open In Colab](https://colab.research.google.com/assets/colab-badge.svg)](https://colab.research.google.com/github/saketkc/pysradb/blob/develop/notebooks/08.PMC_DOI_Identifiers.ipynb)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "# Extract Identifiers from PMC/DOI\n", "\n", "This notebook shows how to extract SRA identifiers from PubMed Central articles and DOI references." ] }, { "cell_type": "code", "execution_count": null, "metadata": {}, "outputs": [], "source": [ "# Install pysradb if not already installed\n", "try:\n", " import pysradb\n", "\n", " print(f\"pysradb {pysradb.__version__} is already installed\")\n", "except ImportError:\n", " print(\"Installing pysradb from GitHub...\")\n", " import sys\n", "\n", " !{sys.executable} -m pip install -q git+https://github.com/saketkc/pysradb\n", " print(\"pysradb installed successfully!\")" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Extracting Database Identifiers from Literature (PMC/DOI)\n", "\n", "This notebook demonstrates how to extract database identifiers (GSE, PRJNA, SRP, SRR, SRX, SRS) from:\n", "- PubMed Central (PMC) articles\n", "- PubMed IDs (PMIDs)\n", "- Digital Object Identifiers (DOIs)\n", "\n" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Setup\n", "\n", "First, let's import pysradb and create a connection:" ] }, { "cell_type": "code", "execution_count": 1, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:25:40.819732Z", "iopub.status.busy": "2025-10-19T11:25:40.819432Z", "iopub.status.idle": "2025-10-19T11:25:41.414646Z", "shell.execute_reply": "2025-10-19T11:25:41.414407Z", "shell.execute_reply.started": "2025-10-19T11:25:40.819709Z" } }, "outputs": [ { "name": "stderr", "output_type": "stream", "text": [ "/Users/saket/github/pysradb/pysradb/utils.py:14: TqdmExperimentalWarning: Using `tqdm.autonotebook.tqdm` in notebook mode. Use `tqdm.tqdm` instead to force console mode (e.g. in jupyter console)\n", " from tqdm.autonotebook import tqdm\n" ] } ], "source": [ "from pysradb.sraweb import SRAweb\n", "import pandas as pd\n", "\n", "db = SRAweb()" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 1: Extract Identifiers from PMID\n", "\n", "Let's extract all database identifiers from a PubMed article using its PMID:" ] }, { "cell_type": "code", "execution_count": 2, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:25:41.415030Z", "iopub.status.busy": "2025-10-19T11:25:41.414918Z", "iopub.status.idle": "2025-10-19T11:25:52.365812Z", "shell.execute_reply": "2025-10-19T11:25:52.365164Z", "shell.execute_reply.started": "2025-10-19T11:25:41.415021Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Identifiers found for PMID 39528918:\n" ] }, { "data": { "text/html": [ "
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pmidpmc_idgse_idsprjna_idssrp_idssrr_idssrx_idssrs_ids
039528918PMC11552371GSE253406NoneSRP484103NoneNoneNone
\n", "
" ], "text/plain": [ " pmid pmc_id gse_ids prjna_ids srp_ids srr_ids srx_ids \\\n", "0 39528918 PMC11552371 GSE253406 None SRP484103 None None \n", "\n", " srs_ids \n", "0 None " ] }, "execution_count": 2, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# Extract all identifiers from PMID 39528918\n", "pmid = \"39528918\"\n", "df = db.pmid_to_identifiers(pmid)\n", "\n", "print(f\"Identifiers found for PMID {pmid}:\")\n", "df" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 2: Get Only GSE IDs from PMID\n", "\n", "Sometimes you only need specific identifier types:" ] }, { "cell_type": "code", "execution_count": 3, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:25:52.367068Z", "iopub.status.busy": "2025-10-19T11:25:52.366478Z", "iopub.status.idle": "2025-10-19T11:26:02.906611Z", "shell.execute_reply": "2025-10-19T11:26:02.904561Z", "shell.execute_reply.started": "2025-10-19T11:25:52.367035Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "GSE identifiers:\n" ] }, { "data": { "text/html": [ "
\n", "\n", "\n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", "
pmidpmc_idgse_ids
039528918PMC11552371GSE253406
\n", "
" ], "text/plain": [ " pmid pmc_id gse_ids\n", "0 39528918 PMC11552371 GSE253406" ] }, "execution_count": 3, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# Get only GSE identifiers\n", "gse_df = db.pmid_to_gse(\"39528918\")\n", "print(\"GSE identifiers:\")\n", "gse_df" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 3: Get Only SRP IDs from PMID\n", "\n", "**Important:** Even if the paper only mentions GSE IDs, pysradb will automatically convert them to SRP!" ] }, { "cell_type": "code", "execution_count": 4, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:26:02.908476Z", "iopub.status.busy": "2025-10-19T11:26:02.908077Z", "iopub.status.idle": "2025-10-19T11:26:13.757381Z", "shell.execute_reply": "2025-10-19T11:26:13.756733Z", "shell.execute_reply.started": "2025-10-19T11:26:02.908448Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "SRP identifiers (auto-converted from GSE if needed):\n" ] }, { "data": { "text/html": [ "
\n", "\n", "\n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", "
pmidpmc_idsrp_ids
039528918PMC11552371SRP484103
\n", "
" ], "text/plain": [ " pmid pmc_id srp_ids\n", "0 39528918 PMC11552371 SRP484103" ] }, "execution_count": 4, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# Get only SRP identifiers\n", "# This works even if the paper only mentions GSE253406!\n", "srp_df = db.pmid_to_srp(\"39528918\")\n", "print(\"SRP identifiers (auto-converted from GSE if needed):\")\n", "srp_df" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 4: Process Multiple PMIDs\n", "\n", "You can batch process multiple PMIDs at once:" ] }, { "cell_type": "code", "execution_count": 5, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:26:13.758482Z", "iopub.status.busy": "2025-10-19T11:26:13.758266Z", "iopub.status.idle": "2025-10-19T11:26:29.005645Z", "shell.execute_reply": "2025-10-19T11:26:29.004516Z", "shell.execute_reply.started": "2025-10-19T11:26:13.758460Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Identifiers from 2 PMIDs:\n" ] }, { "data": { "text/html": [ "
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pmidpmc_idgse_idsprjna_idssrp_idssrr_idssrx_idssrs_ids
039528918PMC11552371GSE253406NoneSRP484103NoneNoneNone
127373336PMC4958508NoneNoneNoneNoneNoneNone
\n", "
" ], "text/plain": [ " pmid pmc_id gse_ids prjna_ids srp_ids srr_ids srx_ids \\\n", "0 39528918 PMC11552371 GSE253406 None SRP484103 None None \n", "1 27373336 PMC4958508 None None None None None \n", "\n", " srs_ids \n", "0 None \n", "1 None " ] }, "execution_count": 5, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# Process multiple PMIDs\n", "pmids = [\"39528918\", \"27373336\"]\n", "df_multiple = db.pmid_to_identifiers(pmids)\n", "\n", "print(f\"Identifiers from {len(pmids)} PMIDs:\")\n", "df_multiple" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 5: Extract from PMC ID\n", "\n", "If you have a PMC ID directly, you can use it:" ] }, { "cell_type": "code", "execution_count": 6, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:26:29.009263Z", "iopub.status.busy": "2025-10-19T11:26:29.008979Z", "iopub.status.idle": "2025-10-19T11:26:30.954276Z", "shell.execute_reply": "2025-10-19T11:26:30.953720Z", "shell.execute_reply.started": "2025-10-19T11:26:29.009240Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Identifiers from PMC article:\n" ] }, { "data": { "text/html": [ "
\n", "\n", "\n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", "
pmc_idgse_idsprjna_idssrp_idssrr_idssrx_idssrs_ids
0PMC10802650<NA><NA><NA><NA><NA><NA>
\n", "
" ], "text/plain": [ " pmc_id gse_ids prjna_ids srp_ids srr_ids srx_ids srs_ids\n", "0 PMC10802650 " ] }, "execution_count": 6, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# Extract from PMC ID\n", "pmc_df = db.pmc_to_identifiers(\"PMC10802650\")\n", "print(\"Identifiers from PMC article:\")\n", "pmc_df" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 6: Extract from DOI\n", "\n", "You can also extract identifiers directly from a DOI:" ] }, { "cell_type": "code", "execution_count": 7, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:26:30.955170Z", "iopub.status.busy": "2025-10-19T11:26:30.954888Z", "iopub.status.idle": "2025-10-19T11:26:37.713908Z", "shell.execute_reply": "2025-10-19T11:26:37.713227Z", "shell.execute_reply.started": "2025-10-19T11:26:30.955148Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Identifiers from DOI 10.12688/f1000research.18676.1:\n" ] }, { "data": { "text/html": [ "
\n", "\n", "\n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", "
doipmidpmc_idgse_idsprjna_idssrp_idssrr_idssrx_idssrs_ids
010.12688/f1000research.18676.131114675PMC6505635GSE100007,GSE24355,GSE25842,GSE41637NoneSRP000941,SRP003870,SRP005378,SRP010679,SRP109126SRR403882,SRR403883,SRR403884,SRR403885,SRR403...SRX118285,SRX118286,SRX118287,SRX118288,SRX118...SRS2282390,SRS2282391,SRS2282392,SRS2282393,SR...
\n", "
" ], "text/plain": [ " doi pmid pmc_id \\\n", "0 10.12688/f1000research.18676.1 31114675 PMC6505635 \n", "\n", " gse_ids prjna_ids \\\n", "0 GSE100007,GSE24355,GSE25842,GSE41637 None \n", "\n", " srp_ids \\\n", "0 SRP000941,SRP003870,SRP005378,SRP010679,SRP109126 \n", "\n", " srr_ids \\\n", "0 SRR403882,SRR403883,SRR403884,SRR403885,SRR403... \n", "\n", " srx_ids \\\n", "0 SRX118285,SRX118286,SRX118287,SRX118288,SRX118... \n", "\n", " srs_ids \n", "0 SRS2282390,SRS2282391,SRS2282392,SRS2282393,SR... " ] }, "execution_count": 7, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# Extract from DOI\n", "doi = \"10.12688/f1000research.18676.1\"\n", "doi_df = db.doi_to_identifiers(doi)\n", "\n", "print(f\"Identifiers from DOI {doi}:\")\n", "doi_df" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 7: Get GSE from DOI" ] }, { "cell_type": "code", "execution_count": 8, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:26:37.714861Z", "iopub.status.busy": "2025-10-19T11:26:37.714634Z", "iopub.status.idle": "2025-10-19T11:26:44.104644Z", "shell.execute_reply": "2025-10-19T11:26:44.104085Z", "shell.execute_reply.started": "2025-10-19T11:26:37.714839Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "GSE identifiers from DOI:\n" ] }, { "data": { "text/html": [ "
\n", "\n", "\n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", "
doipmidpmc_idgse_ids
010.12688/f1000research.18676.131114675PMC6505635GSE100007,GSE24355,GSE25842,GSE41637
\n", "
" ], "text/plain": [ " doi pmid pmc_id \\\n", "0 10.12688/f1000research.18676.1 31114675 PMC6505635 \n", "\n", " gse_ids \n", "0 GSE100007,GSE24355,GSE25842,GSE41637 " ] }, "execution_count": 8, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# Get only GSE from DOI\n", "doi_gse_df = db.doi_to_gse(\"10.12688/f1000research.18676.1\")\n", "print(\"GSE identifiers from DOI:\")\n", "doi_gse_df" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 8: Complete Workflow - DOI to Data Download\n", "\n", "Here's a complete workflow from DOI to downloading the actual data:" ] }, { "cell_type": "code", "execution_count": 9, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:26:44.105623Z", "iopub.status.busy": "2025-10-19T11:26:44.105263Z", "iopub.status.idle": "2025-10-19T11:26:51.023304Z", "shell.execute_reply": "2025-10-19T11:26:51.022717Z", "shell.execute_reply.started": "2025-10-19T11:26:44.105600Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Step 1: Extracting identifiers from DOI: 10.12688/f1000research.18676.1\n", " doi pmid pmc_id \\\n", "0 10.12688/f1000research.18676.1 31114675 PMC6505635 \n", "\n", " srp_ids \n", "0 SRP000941,SRP003870,SRP005378,SRP010679,SRP109126 \n", "\n" ] } ], "source": [ "# Step 1: Extract SRP from DOI\n", "doi = \"10.12688/f1000research.18676.1\"\n", "print(f\"Step 1: Extracting identifiers from DOI: {doi}\")\n", "doi_results = db.doi_to_srp(doi)\n", "print(doi_results)\n", "print()" ] }, { "cell_type": "code", "execution_count": 10, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:26:51.024564Z", "iopub.status.busy": "2025-10-19T11:26:51.024187Z", "iopub.status.idle": "2025-10-19T11:26:59.904233Z", "shell.execute_reply": "2025-10-19T11:26:59.903956Z", "shell.execute_reply.started": "2025-10-19T11:26:51.024535Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Step 2: Found SRP ID: SRP000941\n", "\n", "Step 3: Getting metadata for SRP000941\n", "Found 2207 samples\n", " study_accession study_title \\\n", "16 SRP000941 UCSD Human Reference Epigenome Mapping Project \n", "1055 SRP000941 UCSD Human Reference Epigenome Mapping Project \n", "1053 SRP000941 UCSD Human Reference Epigenome Mapping Project \n", "1054 SRP000941 UCSD Human Reference Epigenome Mapping Project \n", "968 SRP000941 UCSD Human Reference Epigenome Mapping Project \n", "\n", " experiment_accession experiment_title \\\n", "16 SRX027874 Reference Epigenome: ChIP-Seq Analysis of H3K9... \n", "1055 SRX006235 Reference Epigenome: ChIP-Seq Analysis of H3K3... \n", "1053 SRX006237 Reference Epigenome: ChIP-Seq Analysis of H3K4... \n", "1054 SRX006236 Reference Epigenome: ChIP-Seq Analysis of H3K4... \n", "968 SRX006240 Whole genome shotgun bisulfite sequencing of t... \n", "\n", " experiment_desc organism_taxid \\\n", "16 Reference Epigenome: ChIP-Seq Analysis of H3K9... 9606 \n", "1055 Reference Epigenome: ChIP-Seq Analysis of H3K3... 9606 \n", "1053 Reference Epigenome: ChIP-Seq Analysis of H3K4... 9606 \n", "1054 Reference Epigenome: ChIP-Seq Analysis of H3K4... 9606 \n", "968 Whole genome shotgun bisulfite sequencing of t... 9606 \n", "\n", " organism_name library_name library_strategy library_source ... \\\n", "16 Homo sapiens LL218 ChIP-Seq GENOMIC ... \n", "1055 Homo sapiens LL220 ChIP-Seq GENOMIC ... \n", "1053 Homo sapiens LL227 ChIP-Seq GENOMIC ... \n", "1054 Homo sapiens LL228 ChIP-Seq GENOMIC ... \n", "968 Homo sapiens methylC-seq_h1_r2b Bisulfite-Seq GENOMIC ... \n", "\n", " biosample bioproject instrument \\\n", "16 SAMN00004698 Illumina Genome Analyzer II \n", "1055 SAMN00004459 Illumina Genome Analyzer II \n", "1053 SAMN00004459 Illumina Genome Analyzer II \n", "1054 SAMN00004459 Illumina Genome Analyzer II \n", "968 SAMN00004462 Illumina Genome Analyzer II \n", "\n", " instrument_model instrument_model_desc total_spots \\\n", "16 Illumina Genome Analyzer II ILLUMINA 59041190 \n", "1055 Illumina Genome Analyzer II ILLUMINA 12466602 \n", "1053 Illumina Genome Analyzer II ILLUMINA 7763232 \n", "1054 Illumina Genome Analyzer II ILLUMINA 7110370 \n", "968 Illumina Genome Analyzer II ILLUMINA 544393574 \n", "\n", " total_size run_accession run_total_spots run_total_bases \n", "16 1555248627 SRR018453 11642838 419142168 \n", "1055 223017616 SRR018454 12466602 448797672 \n", "1053 204130918 SRR018455 7763232 279476352 \n", "1054 185053545 SRR018456 7110370 255973320 \n", "968 32242220269 SRR018975 16729745 1455487815 \n", "\n", "[5 rows x 24 columns]\n" ] } ], "source": [ "# Step 2: Extract SRP ID from results\n", "if not doi_results.empty and not pd.isna(doi_results.iloc[0][\"srp_ids\"]):\n", " srp_id = doi_results.iloc[0][\"srp_ids\"].split(\",\")[0] # Take first SRP if multiple\n", " print(f\"Step 2: Found SRP ID: {srp_id}\")\n", " print()\n", "\n", " # Step 3: Get metadata for this SRP\n", " print(f\"Step 3: Getting metadata for {srp_id}\")\n", " metadata = db.sra_metadata(srp_id)\n", " print(f\"Found {len(metadata)} samples\")\n", " print(metadata.head())\n", "\n", " # Optional: Download the data\n", " # db.download(df=metadata, out_dir='./downloads')\n", "else:\n", " print(\"No SRP IDs found for this DOI\")" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 9: Batch Processing Literature\n", "\n", "Process multiple papers from a literature search:" ] }, { "cell_type": "code", "execution_count": 11, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:26:59.904602Z", "iopub.status.busy": "2025-10-19T11:26:59.904525Z", "iopub.status.idle": "2025-10-19T11:27:17.447503Z", "shell.execute_reply": "2025-10-19T11:27:17.446805Z", "shell.execute_reply.started": "2025-10-19T11:26:59.904594Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Processed 3 papers\n", "Found 1 papers with SRA data\n", "\n", "Papers with SRA data:\n" ] }, { "data": { "text/html": [ "
\n", "\n", "\n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", " \n", "
pmidpmc_idgse_idsprjna_idssrp_idssrr_idssrx_idssrs_ids
039528918PMC11552371GSE253406NoneSRP484103NoneNoneNone
\n", "
" ], "text/plain": [ " pmid pmc_id gse_ids prjna_ids srp_ids srr_ids srx_ids \\\n", "0 39528918 PMC11552371 GSE253406 None SRP484103 None None \n", "\n", " srs_ids \n", "0 None " ] }, "execution_count": 11, "metadata": {}, "output_type": "execute_result" } ], "source": [ "# Simulate PMIDs from a literature search\n", "pmids_from_search = [\"39528918\", \"27373336\", \"30873266\"]\n", "\n", "# Extract identifiers from all papers\n", "results = db.pmid_to_identifiers(pmids_from_search)\n", "\n", "# Filter to papers with SRA data\n", "papers_with_sra = results[~pd.isna(results[\"srp_ids\"])]\n", "\n", "print(f\"Processed {len(pmids_from_search)} papers\")\n", "print(f\"Found {len(papers_with_sra)} papers with SRA data\")\n", "print()\n", "print(\"Papers with SRA data:\")\n", "papers_with_sra" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 10: Extract Identifiers from Custom Text\n", "\n", "You can also extract identifiers from any text:" ] }, { "cell_type": "code", "execution_count": 12, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:27:17.448365Z", "iopub.status.busy": "2025-10-19T11:27:17.448167Z", "iopub.status.idle": "2025-10-19T11:27:17.452555Z", "shell.execute_reply": "2025-10-19T11:27:17.452046Z", "shell.execute_reply.started": "2025-10-19T11:27:17.448344Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Identifiers found in text:\n", " GSE: GSE81903\n", " PRJNA: PRJNA319707\n", " SRP: SRP075720\n", " SRR: SRR3587529\n", " SRX: SRX1800089\n", " SRS: SRS1467635\n" ] } ], "source": [ "# Custom text with database identifiers\n", "text = \"\"\"\n", "This study analyzed RNA-seq data from GSE81903 and SRP075720.\n", "The BioProject accession is PRJNA319707 with representative samples \n", "SRR3587529, SRX1800089, and SRS1467635.\n", "\"\"\"\n", "\n", "identifiers = db.extract_identifiers_from_text(text)\n", "\n", "print(\"Identifiers found in text:\")\n", "for id_type, ids in identifiers.items():\n", " if ids:\n", " print(f\" {id_type.upper()}: {', '.join(ids)}\")" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Example 11: ID Conversion Utilities\n", "\n", "Convert between different identifier types:" ] }, { "cell_type": "code", "execution_count": 14, "metadata": { "execution": { "iopub.execute_input": "2025-10-19T11:28:37.588115Z", "iopub.status.busy": "2025-10-19T11:28:37.587717Z", "iopub.status.idle": "2025-10-19T11:28:40.771236Z", "shell.execute_reply": "2025-10-19T11:28:40.770044Z", "shell.execute_reply.started": "2025-10-19T11:28:37.588092Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "PMID to PMC conversion:\n", "{'27373336': 'PMC4958508'}\n", "\n", "DOI to PMID conversion:\n", "{'10.12688/f1000research.18676.1': '31114675'}\n" ] } ], "source": [ "# Convert PMID to PMC\n", "print(\"PMID to PMC conversion:\")\n", "pmid_pmc = db.pmid_to_pmc(\"27373336\")\n", "print(pmid_pmc)\n", "print()\n", "\n", "# Convert DOI to PMID\n", "print(\"DOI to PMID conversion:\")\n", "doi_pmid = db.doi_to_pmid(\"10.12688/f1000research.18676.1\")\n", "print(doi_pmid)" ] }, { "cell_type": "code", "execution_count": null, "metadata": {}, "outputs": [], "source": [] } ], "metadata": { "kernelspec": { "display_name": "Python 3", "language": "python", "name": "python3" }, "language_info": { "codemirror_mode": { "name": "ipython", "version": 3 }, "file_extension": ".py", "mimetype": "text/x-python", "name": "python", "nbconvert_exporter": "python", "pygments_lexer": "ipython3", "version": "3.11.12" } }, "nbformat": 4, "nbformat_minor": 4 } ================================================ FILE: notebooks/09.Metadata_enrichment.ipynb ================================================ { "cells": [ { "cell_type": "markdown", "metadata": { "id": "5sioFsNrTU7L" }, "source": [ "[![Open In Colab](https://colab.research.google.com/assets/colab-badge.svg)](https://colab.research.google.com/github/saketkc/pysradb/blob/develop/notebooks/09.Metadata_Enrichment_with_LLMs.ipynb)" ] }, { "cell_type": "markdown", "metadata": { "id": "QBGljXsQTU7M" }, "source": [ "# Metadata Enrichment with LLMs\n", "\n", "pysradb now helps you 'enrich' your metadata frame by leveraging recent advancements in (fast) (S)LLMs. The parsed metadata can be fed to an LLM that is 'instructed' to enrich the metadata by returning 9 ontology-based fields::\n", "`organ`, `tissue`, `anatomical_system`, `cell_type`, `disease`, `sex`, `development_stage`, `assay`, `organism`\n", "\n", "There are two approaches in which this is possible:\n", "\n", "- **LLMs** ([Requires Ollama](https://ollama.com/download) - local, no API keys)\n", "- **Embeddings** ([Using sentence-transformers](https://huggingface.co/sentence-transformers) with [BioLORD](https://arxiv.org/abs/2311.16075) embedding model)\n" ] }, { "cell_type": "code", "execution_count": 1, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "id": "RNrFmwO6TU7N", "outputId": "acb894d2-1b75-4daf-ebfa-c9508ee2da6f" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Installing pysradb from GitHub...\n", " Installing build dependencies ... \u001b[?25l\u001b[?25hdone\n", " Getting requirements to build wheel ... \u001b[?25l\u001b[?25hdone\n", " Preparing metadata (pyproject.toml) ... \u001b[?25l\u001b[?25hdone\n", " Building wheel for pysradb (pyproject.toml) ... \u001b[?25l\u001b[?25hdone\n", "pysradb installed successfully!\n" ] } ], "source": [ "# Install pysradb if not already installed\n", "try:\n", " import pysradb\n", "\n", " print(f\"pysradb {pysradb.__version__} is already installed\")\n", "except ImportError:\n", " print(\"Installing pysradb from GitHub...\")\n", " import sys\n", "\n", " !{sys.executable} -m pip install -q git+https://github.com/saketkc/pysradb\n", " print(\"pysradb installed successfully!\")" ] }, { "cell_type": "code", "execution_count": 2, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "execution": { "iopub.execute_input": "2025-10-22T16:43:39.723229Z", "iopub.status.busy": "2025-10-22T16:43:39.722983Z", "iopub.status.idle": "2025-10-22T16:43:40.469655Z", "shell.execute_reply": "2025-10-22T16:43:40.469420Z", "shell.execute_reply.started": "2025-10-22T16:43:39.723206Z" }, "id": "veB38ra_TU7N", "outputId": "e7310eaf-5a61-4106-e605-c48a28477837" }, "outputs": [ { "name": "stderr", "output_type": "stream", "text": [ "/usr/local/lib/python3.12/dist-packages/pysradb/utils.py:16: TqdmExperimentalWarning: Using `tqdm.autonotebook.tqdm` in notebook mode. Use `tqdm.tqdm` instead to force console mode (e.g. in jupyter console)\n", " from tqdm.autonotebook import tqdm\n" ] } ], "source": [ "from pysradb import SRAweb\n", "from pysradb.metadata_enrichment import create_metadata_extractor\n", "from pysradb.search import GeoSearch" ] }, { "cell_type": "markdown", "metadata": { "id": "HXBwIr21TU7O" }, "source": [ "## Quick Start\n", "\n", "One line enrichment!\n", "\n", "**Prerequisites**: Install Ollama (https://ollama.ai) and pull a model: `ollama pull phi3`\n", "\n", "The easiest way to enrich metadata is using the `enrich=True` parameter:" ] }, { "cell_type": "code", "execution_count": 3, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "id": "12mmTfSzdzgT", "outputId": "8d3999a5-e322-4c75-c90a-a61492065ce3" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Hit:1 https://developer.download.nvidia.com/compute/cuda/repos/ubuntu2204/x86_64 InRelease\n", "Get:2 https://cloud.r-project.org/bin/linux/ubuntu jammy-cran40/ InRelease [3,632 B]\n", "Hit:3 https://cli.github.com/packages stable InRelease\n", "Get:4 http://security.ubuntu.com/ubuntu jammy-security InRelease [129 kB]\n", "Get:5 https://r2u.stat.illinois.edu/ubuntu jammy InRelease [6,555 B]\n", "Hit:6 http://archive.ubuntu.com/ubuntu jammy InRelease\n", "Get:7 http://archive.ubuntu.com/ubuntu jammy-updates InRelease [128 kB]\n", "Hit:8 https://ppa.launchpadcontent.net/deadsnakes/ppa/ubuntu jammy InRelease\n", "Get:9 https://r2u.stat.illinois.edu/ubuntu jammy/main all Packages [9,413 kB]\n", "Get:10 http://security.ubuntu.com/ubuntu jammy-security/universe amd64 Packages [1,288 kB]\n", "Hit:11 https://ppa.launchpadcontent.net/graphics-drivers/ppa/ubuntu jammy InRelease\n", "Hit:12 https://ppa.launchpadcontent.net/ubuntugis/ppa/ubuntu jammy InRelease\n", "Get:13 http://security.ubuntu.com/ubuntu jammy-security/main amd64 Packages [3,479 kB]\n", "Get:14 http://archive.ubuntu.com/ubuntu jammy-backports InRelease [127 kB]\n", "Get:15 https://r2u.stat.illinois.edu/ubuntu jammy/main amd64 Packages [2,822 kB]\n", "Get:16 http://archive.ubuntu.com/ubuntu jammy-updates/universe amd64 Packages [1,594 kB]\n", "Get:17 http://archive.ubuntu.com/ubuntu jammy-updates/restricted amd64 Packages [6,148 kB]\n", "Get:18 http://archive.ubuntu.com/ubuntu jammy-updates/main amd64 Packages [3,847 kB]\n", "Fetched 29.0 MB in 3s (8,430 kB/s)\n", "Reading package lists...\n", "Building dependency tree...\n", "Reading state information...\n", "46 packages can be upgraded. Run 'apt list --upgradable' to see them.\n", "\u001b[1;33mW: \u001b[0mSkipping acquire of configured file 'main/source/Sources' as repository 'https://r2u.stat.illinois.edu/ubuntu jammy InRelease' does not seem to provide it (sources.list entry misspelt?)\u001b[0m\n", "Reading package lists...\n", "Building dependency tree...\n", "Reading state information...\n", "systemd is already the newest version (249.11-0ubuntu3.17).\n", "systemd set to manually installed.\n", "The following additional packages will be installed:\n", " libpci3 pci.ids usb.ids\n", "The following NEW packages will be installed:\n", " libpci3 lshw pci.ids pciutils usb.ids\n", "0 upgraded, 5 newly installed, 0 to remove and 46 not upgraded.\n", "Need to get 883 kB of archives.\n", "After this operation, 3,256 kB of additional disk space will be used.\n", "Get:1 http://archive.ubuntu.com/ubuntu jammy-updates/main amd64 pci.ids all 0.0~2022.01.22-1ubuntu0.1 [251 kB]\n", "Get:2 http://archive.ubuntu.com/ubuntu jammy/main amd64 libpci3 amd64 1:3.7.0-6 [28.9 kB]\n", "Get:3 http://archive.ubuntu.com/ubuntu jammy/main amd64 lshw amd64 02.19.git.2021.06.19.996aaad9c7-2build1 [321 kB]\n", "Get:4 http://archive.ubuntu.com/ubuntu jammy/main amd64 pciutils amd64 1:3.7.0-6 [63.6 kB]\n", "Get:5 http://archive.ubuntu.com/ubuntu jammy/main amd64 usb.ids all 2022.04.02-1 [219 kB]\n", "Fetched 883 kB in 1s (686 kB/s)\n", "debconf: unable to initialize frontend: Dialog\n", "debconf: (No usable dialog-like program is installed, so the dialog based frontend cannot be used. at /usr/share/perl5/Debconf/FrontEnd/Dialog.pm line 78, <> line 5.)\n", "debconf: falling back to frontend: Readline\n", "debconf: unable to initialize frontend: Readline\n", "debconf: (This frontend requires a controlling tty.)\n", "debconf: falling back to frontend: Teletype\n", "dpkg-preconfigure: unable to re-open stdin: \n", "Selecting previously unselected package pci.ids.\n", "(Reading database ... 125080 files and directories currently installed.)\n", "Preparing to unpack .../pci.ids_0.0~2022.01.22-1ubuntu0.1_all.deb ...\n", "Unpacking pci.ids (0.0~2022.01.22-1ubuntu0.1) ...\n", "Selecting previously unselected package libpci3:amd64.\n", "Preparing to unpack .../libpci3_1%3a3.7.0-6_amd64.deb ...\n", "Unpacking libpci3:amd64 (1:3.7.0-6) ...\n", "Selecting previously unselected package lshw.\n", "Preparing to unpack .../lshw_02.19.git.2021.06.19.996aaad9c7-2build1_amd64.deb ...\n", "Unpacking lshw (02.19.git.2021.06.19.996aaad9c7-2build1) ...\n", "Selecting previously unselected package pciutils.\n", "Preparing to unpack .../pciutils_1%3a3.7.0-6_amd64.deb ...\n", "Unpacking pciutils (1:3.7.0-6) ...\n", "Selecting previously unselected package usb.ids.\n", "Preparing to unpack .../usb.ids_2022.04.02-1_all.deb ...\n", "Unpacking usb.ids (2022.04.02-1) ...\n", "Setting up pci.ids (0.0~2022.01.22-1ubuntu0.1) ...\n", "Setting up lshw (02.19.git.2021.06.19.996aaad9c7-2build1) ...\n", "Setting up usb.ids (2022.04.02-1) ...\n", "Setting up libpci3:amd64 (1:3.7.0-6) ...\n", "Setting up pciutils (1:3.7.0-6) ...\n", "Processing triggers for man-db (2.10.2-1) ...\n", "Processing triggers for libc-bin (2.35-0ubuntu3.8) ...\n", "/sbin/ldconfig.real: /usr/local/lib/libumf.so.1 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libtcm.so.1 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libhwloc.so.15 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libur_loader.so.0 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libtbbbind_2_0.so.3 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libur_adapter_opencl.so.0 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libtbb.so.12 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libtbbbind_2_5.so.3 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libur_adapter_level_zero_v2.so.0 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libtbbmalloc_proxy.so.2 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libtcm_debug.so.1 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libtbbmalloc.so.2 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libur_adapter_level_zero.so.0 is not a symbolic link\n", "\n", "/sbin/ldconfig.real: /usr/local/lib/libtbbbind.so.3 is not a symbolic link\n", "\n" ] } ], "source": [ "! sudo apt update -qq && sudo apt install -qq pciutils lshw systemd" ] }, { "cell_type": "code", "execution_count": 4, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "id": "iINq3dweaUXe", "outputId": "a0b22657-6a9a-407c-a014-501eb56a4c94" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ ">>> Installing ollama to /usr/local\n", ">>> Downloading Linux amd64 bundle\n", "######################################################################## 100.0%\n", ">>> Creating ollama user...\n", ">>> Adding ollama user to video group...\n", ">>> Adding current user to ollama group...\n", ">>> Creating ollama systemd service...\n", "\u001b[1m\u001b[31mWARNING:\u001b[m systemd is not running\n", ">>> NVIDIA GPU installed.\n", ">>> The Ollama API is now available at 127.0.0.1:11434.\n", ">>> Install complete. Run \"ollama\" from the command line.\n" ] } ], "source": [ "!curl -fsSL https://ollama.com/install.sh | sh" ] }, { "cell_type": "code", "execution_count": 7, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "id": "EgCNQeDScwvX", "outputId": "9c7eb232-47f7-4ce2-abd1-27dda40519af" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ 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"NAME ID SIZE MODIFIED \n", "phi3:latest 4f2222927938 2.2 GB Less than a second ago \n" ] } ], "source": [ "!nohup ollama serve > ollama.log 2>&1 &" ] }, { "cell_type": "code", "execution_count": 8, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "id": "poMsNDr3km1l", "outputId": "9654f82b-92d8-4cdb-9441-99f80a197261" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "\u001b[?2026h\u001b[?25l\u001b[1G\u001b[?25h\u001b[?2026l\u001b[?2026h\u001b[?25l\u001b[1G\u001b[?25h\u001b[?2026l\u001b[?2026h\u001b[?25l\u001b[1G\u001b[?25h\u001b[?2026l\u001b[?2026h\u001b[?25l\u001b[1G\u001b[?25h\u001b[?2026l\u001b[?2026h\u001b[?25l\u001b[1G\u001b[?25h\u001b[?2026l\n", "NAME ID SIZE MODIFIED \n", "phi3:latest 4f2222927938 2.2 GB Less than a second ago \n" ] } ], "source": [ "!ollama pull phi3:latest && ollama list" ] }, { "cell_type": "code", "execution_count": 9, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 854, "referenced_widgets": [ "a2f7696242804d329dea1bd1d07c642a", "4df355cbf9d6499c864d55b813d5aa38", "d7be1ad3fb9d43d68ba14cc6dd95f208", "2b1c99ee25aa4f1b922782ca6240f737", "5aab185098214938a32e8b71a82fee5b", "2be83750973345c4b9e3ba357c0813f4", "827d4909df494037bd49dd50d16b16c5", "e618dba921564fd28aca140eb187bd76", "86d88cef78174f8faa2fd92c2e84e788", "951cfb8ff78b47b38146b7e062c0ed0a", "47dcd6740c84466f851e0fa1e8ee4db9" ] }, "id": "I6olFn2waePh", "outputId": "eaefb7f2-3259-4587-8ede-ee120a05554b" }, "outputs": [ { "data": { "application/vnd.jupyter.widget-view+json": { "model_id": "a2f7696242804d329dea1bd1d07c642a", "version_major": 2, "version_minor": 0 }, "text/plain": [ "Enriching metadata: 0%| | 0/24 [00:00\n", "
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sample_titlesexguessed_sextissueguessed_tissueguessed_organguessed_anatomical_systemguessed_cell_typeguessed_organguessed_tissueguessed_disease
0cov_01_RNAFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
1cov_01_antibodyFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
2cov_02_RNAFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
3cov_02_antibodyFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
4cov_03_RNAFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
5cov_03_antibodyFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
6cov_04_RNAMmale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
7cov_04_antibodyMmale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
8cov_07_RNAFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
9cov_07_antibodyFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
10cov_08_RNAFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
11cov_08_antibodyFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
12cov_09_RNAMmale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
13cov_09_antibodyMmale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
14cov_10_RNAFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
15cov_10_antibodyFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
16cov_11_RNAMmale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
17cov_11_antibodyMmale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
18cov_12_RNAFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
19cov_12_antibodyFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodcovid-19
20cov_17_RNAMmale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
21cov_17_antibodyMmale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
22cov_18_RNAFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
23cov_18_antibodyFfemale<NA>peripheral bloodbloodimmune systempbmcbloodperipheral bloodhealthy
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\n", " \n" ], "text/plain": [ " sample_title sex guessed_sex tissue guessed_tissue guessed_organ \\\n", "0 cov_01_RNA F female peripheral blood blood \n", "1 cov_01_antibody F female peripheral blood blood \n", "2 cov_02_RNA F female peripheral blood blood \n", "3 cov_02_antibody F female peripheral blood blood \n", "4 cov_03_RNA F female peripheral blood blood \n", "5 cov_03_antibody F female peripheral blood blood \n", "6 cov_04_RNA M male peripheral blood blood \n", "7 cov_04_antibody M male peripheral blood blood \n", "8 cov_07_RNA F female peripheral blood blood \n", "9 cov_07_antibody F female peripheral blood blood \n", "10 cov_08_RNA F female peripheral blood blood \n", "11 cov_08_antibody F female peripheral blood blood \n", "12 cov_09_RNA M male peripheral blood blood \n", "13 cov_09_antibody M male peripheral blood blood \n", "14 cov_10_RNA F female peripheral blood blood \n", "15 cov_10_antibody F female peripheral blood blood \n", "16 cov_11_RNA M male peripheral blood blood \n", "17 cov_11_antibody M male peripheral blood blood \n", "18 cov_12_RNA F female peripheral blood blood \n", "19 cov_12_antibody F female peripheral blood blood \n", "20 cov_17_RNA M male peripheral blood blood \n", "21 cov_17_antibody M male peripheral blood blood \n", "22 cov_18_RNA F female peripheral blood blood \n", "23 cov_18_antibody F female peripheral blood blood \n", "\n", " guessed_anatomical_system guessed_cell_type guessed_organ \\\n", "0 immune system pbmc blood \n", "1 immune system pbmc blood \n", "2 immune system pbmc blood \n", "3 immune system pbmc blood \n", "4 immune system pbmc blood \n", "5 immune system pbmc blood \n", "6 immune system pbmc blood \n", "7 immune system pbmc blood \n", "8 immune system pbmc blood \n", "9 immune system pbmc blood \n", "10 immune system pbmc blood \n", "11 immune system pbmc blood \n", "12 immune system pbmc blood \n", "13 immune system pbmc blood \n", "14 immune system pbmc blood \n", "15 immune system pbmc blood \n", "16 immune system pbmc blood \n", "17 immune system pbmc blood \n", "18 immune system pbmc blood \n", "19 immune system pbmc blood \n", "20 immune system pbmc blood \n", "21 immune system pbmc blood \n", "22 immune system pbmc blood \n", "23 immune system pbmc blood \n", "\n", " guessed_tissue guessed_disease \n", "0 peripheral blood covid-19 \n", "1 peripheral blood covid-19 \n", "2 peripheral blood covid-19 \n", "3 peripheral blood covid-19 \n", "4 peripheral blood covid-19 \n", "5 peripheral blood covid-19 \n", "6 peripheral blood covid-19 \n", "7 peripheral blood covid-19 \n", "8 peripheral blood healthy \n", "9 peripheral blood healthy \n", "10 peripheral blood healthy \n", "11 peripheral blood healthy \n", "12 peripheral blood healthy \n", "13 peripheral blood healthy \n", "14 peripheral blood covid-19 \n", "15 peripheral blood covid-19 \n", "16 peripheral blood covid-19 \n", "17 peripheral blood covid-19 \n", "18 peripheral blood covid-19 \n", "19 peripheral blood covid-19 \n", "20 peripheral blood healthy \n", "21 peripheral blood healthy \n", "22 peripheral blood healthy \n", "23 peripheral blood healthy " ] }, "metadata": {}, "output_type": "display_data" } ], "source": [ "from pysradb.sraweb import SRAweb\n", "\n", "db = SRAweb()\n", "\n", "df = db.metadata(\"GSE155673\", detailed=True, enrich=True)\n", "\n", "cols = [\n", " \"sample_title\",\n", " \"sex\",\n", " \"guessed_sex\",\n", " \"tissue\",\n", " \"guessed_tissue\",\n", " \"guessed_organ\",\n", " \"guessed_anatomical_system\",\n", " \"guessed_cell_type\",\n", " \"guessed_organ\",\n", " \"guessed_tissue\",\n", " \"guessed_disease\",\n", "]\n", "display(df[cols])" ] }, { "cell_type": "markdown", "metadata": { "id": "qa5Ch_e_TU7O" }, "source": [ "---\n", "\n", "## Manual Enrichment\n", "\n", "\n", "For more control, you can manually create extractors and enrich DataFrames:" ] }, { "cell_type": "markdown", "metadata": { "id": "1L8mU1k0TU7O" }, "source": [ "### Manual LLM-Based Enrichment\n" ] }, { "cell_type": "code", "execution_count": 10, "metadata": { "colab": { "base_uri": "https://localhost:8080/" }, "execution": { "iopub.execute_input": "2025-10-22T16:48:19.988559Z", "iopub.status.busy": "2025-10-22T16:48:19.988095Z", "iopub.status.idle": "2025-10-22T16:48:25.998632Z", "shell.execute_reply": "2025-10-22T16:48:25.997750Z", "shell.execute_reply.started": "2025-10-22T16:48:19.988525Z" }, "id": "r8zyyk6xTU7O", "outputId": "7828b9ab-4034-435b-9d7c-ba1c9d56eb8f" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Extracted metadata:\n", " organ: breast\n", " anatomical_system: digestive system\n", " cell_type: cd4+ t cell\n", " disease: cancer\n", " sex: female\n", " development_stage: adult\n", " assay: single-cell rna seq\n", " organism: homo sapiens\n" ] } ], "source": [ "# Create LLM extractor\n", "extractor_llm = create_metadata_extractor(method=\"llm\", backend=\"ollama/phi3\")\n", "\n", "# Test extraction\n", "text = (\n", " \"Single-cell RNA-seq of CD4+ T cells from breast cancer patients. sex: F. age: 55\"\n", ")\n", "result = extractor_llm.extract_metadata(text)\n", "\n", "print(\"Extracted metadata:\")\n", "for key, value in result.items():\n", " if value != \"Unknown\":\n", " print(f\" {key}: {value}\")" ] }, { "cell_type": "code", "execution_count": 11, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 195, "referenced_widgets": [ "dc19794504464b64a7ab7e46612406bb", "be2dd404c3834276abe5fa9b1ce99e44", "830cbb3b0b114c5cbd02a0c13de554bc", "56c9b305e6c84804b93a081803bdd0ec", "d7640d61db3f4e619868639a8ebd0645", "37f621bb6b5245e880eb0a68168c06f1", "2cc8a1dce49548f183960299f2bc5207", "fcb48970443f461ebec11b11a91cbb6a", "767acfa072dc4a1ea6cbc89dcbe8fe8c", "c513263cb8134f50a158028262d30dda", "f9cb0b5be77349f1a3b93adc423beb97" ] }, "execution": { "iopub.execute_input": "2025-10-22T16:48:29.277395Z", "iopub.status.busy": "2025-10-22T16:48:29.276699Z", "iopub.status.idle": "2025-10-22T16:48:45.378697Z", "shell.execute_reply": "2025-10-22T16:48:45.378199Z", "shell.execute_reply.started": "2025-10-22T16:48:29.277335Z" }, "id": "m2UKRJshTU7O", "outputId": "e9dbbcd7-6ca6-44d8-a766-b6a5b7b068fb" }, "outputs": [ { "data": { "application/vnd.jupyter.widget-view+json": { "model_id": "dc19794504464b64a7ab7e46612406bb", "version_major": 2, "version_minor": 0 }, "text/plain": [ "Enriching metadata: 0%| | 0/3 [00:00\n", "
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sample_titleguessed_organguessed_tissueguessed_anatomical_systemguessed_cell_typeguessed_diseaseguessed_sexguessed_development_stageguessed_assayguessed_organism
0cov_01_RNAbrainbrain tissuenervous systemneuronhealthyunknownadultrna-seqhomo sapiens
1cov_01_antibodyunknownunknownunknownpbmchealthyunknownadultrna-seqhomo sapiens
2cov_02_RNAbrainbrain tissuenervous systemneuronhealthyunknownadultrna-seqhomo sapiens
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\n", " \n" ], "text/plain": [ " sample_title guessed_organ guessed_tissue guessed_anatomical_system \\\n", "0 cov_01_RNA brain brain tissue nervous system \n", "1 cov_01_antibody unknown unknown unknown \n", "2 cov_02_RNA brain brain tissue nervous system \n", "\n", " guessed_cell_type guessed_disease guessed_sex guessed_development_stage \\\n", "0 neuron healthy unknown adult \n", "1 pbmc healthy unknown adult \n", "2 neuron healthy unknown adult \n", "\n", " guessed_assay guessed_organism \n", "0 rna-seq homo sapiens \n", "1 rna-seq homo sapiens \n", "2 rna-seq homo sapiens " ] }, "metadata": {}, "output_type": "display_data" } ], "source": [ "if not df.empty:\n", " df_enriched = extractor_llm.enrich_dataframe(\n", " df.head(3), text_column=\"sample_title\", prefix=\"guessed_\"\n", " )\n", "\n", " cols = [\"sample_title\"] + [\n", " c for c in df_enriched.columns if c.startswith(\"guessed_\")\n", " ]\n", " display(df_enriched[cols])" ] }, { "cell_type": "markdown", "metadata": { "id": "LpqKPbUhTU7P" }, "source": [ "### Manual Embedding-Based Enrichment\n", "\n", "Faster than LLMs, works offline. Load comprehensive ontology reference (31K+ terms):" ] }, { "cell_type": "code", "execution_count": 12, "metadata": { "colab": { "base_uri": "https://localhost:8080/", "height": 545, "referenced_widgets": [ "3e50af1eca894c3399d048aefbb845f1", "ac674fd9e2f64cfbae4a1e781a6c45bf", "dfa4e2a65fb44f238e6dc09588c545f0", "fa968cf8d2a64cf09345a87e40c4dd0e", "e8b7cb75c8b444f394671c7f2120ce40", "f765315e669d44c18c57e8e49fbc226f", "562282aa212341c48b3e1deeb9739de1", "28d0e8c7b542492398a0f79b431c761f", "61de55611634414fac9e23f7b8e515e3", "0f81ad1bb8b54f99b127b32f90bd0e69", "404fc1d6f6d047b69e318cdde29108a0", "ac3a7eb327fa4ac88391346776f3d7dc", "6d95724552fd40a6aa098d13c7e6a4fb", "af1f6c9cfce4450e806a2e00fff3ef44", "29fcf766d37c44a0a76b8faab54492a5", "9d34e6c58468477ca0e5594deaad7f1d", "b638421e5eb941009275c18da1a8017d", "f7d0e907a18c4e12a8f25c62fe17ac56", "fd80bfe57e55498e91d065dbfe6d9188", "223221f9bb0e40878e056e54c4b655bf", "15e748f4ac0848f39183cf8c1c654750", "b655ccd7cf454ff4b53621d957e790cd", "feece831475f496b97f77ac2ff53047f", "efd523b1947345cbb713ef694c37d69f", "9bd932f71d44458fae22dd7ba3195029", "f3405c9ee2c84107913fdca4224035d9", "d7c208eaca0b40f7b3c8dc1d5babc94d", "edc12ae9a28c4fe1a0340f5eebc6a2e0", "8e51c301a6d442c8b71ef060badef4f1", "5f1d696fa90f4f1eaf518d45d194a947", "8fe796d6adf84ed58ddb064ecd3c2a4c", "194897c60e2040ab900ad3d0ef0fcbe1", "be52b65723b14526b4548d4cf7b1d2e2", "6de015b4578841a8a1061350e15da8b3", "d40cecd6c2894c34b67a79df45ca9a39", "f1916e106b36449097b472a4d6d1cb91", "e37c87ef3eb448948b163a25398901cc", "9290dee1eae94d2eb43489396d269cf6", "a88b4e0cc9584d718c50ca440b7845f3", "2d075c5aa74741a3a31028fce8bd5797", "456dbcee7dcd478da6ce30f6f90a130a", "2c06260d0f2441c0bd8d968255dc10d8", "b52eb5825da446f3a376b2beaa78dd65", "7519b72c60bf438cbf95a3d003c339f7", "3f4bcc5af37b4317b2a1d4c130b5a373", "8ed6a184f6574dacaf482b9561c6fb33", "396211ba9816435f82552b95f09e07cf", "89ca287b7ee14e7188b5a33af0882670", "95a8dd57c02648ffad239a660eaae917", "584710703afb4952b8684971cb5d72a6", "1bd41f70e705403a998b8f1d13cab8f8", "245aef74caf74dd6a1c5507f3f5e4282", "3c85e4906af7437393ce44830e642fab", "3dc54a192995478e9d958dc40c23f6d0", "92e4642787eb470cbf4e4cae159fcd05", "894f6addaa1d46f89a3bfc24b11365cd", "ba758dfbb64a47d9a657d0b10650e8eb", "3853a06b132f443f906bb9816767eff3", "7711534c096545d79b3045e0551aef5b", "1aac2488bf6a46a9955a5ddb4220b6fb", "7f6b8f8f626a400795e60d672d7269ce", "0f24c00e249f4dd8a4054a4a9b7b532c", "0ccdc38cf02649b789e77de622054fdb", "efa1b78e12664fcc992c7f83fd3d93b1", "fb933752c8204395a46746b5eaf16366", "d248e27de9b043a7b6a7b78d101fb0d1", "8941e47c2fc34df0876c4924b43362c3", "552bfefdb63f41f7b64143382d491369", "dccc9017a0d44ee59b4b6105ac0b98a5", "505eb345e56d4b41aebecbac6c5f86d7", "9d6b7757dae44e5396ecf4f39cb86faa", "37592a50ec794ad09773b6c69a3c0f30", "f31ed9aa7c4f4fa5a0948d86d8d84fac", "7915e0797eaa47b9ab30ae6c0115d231", "8d43b964615b4c24beb53a95ebb5943a", "cc8cd0792bc649429358b8275dbcb56f", "40e09608ecc44d90bd8616cc8755f09b", "594fe5c3fb8d41ce827935b752501bc2", "52b67d0128d0409fb73e9d1e19185038", "9a171f788ce349ba86d73f5cb7900a3b", "17f111851229489fa0ad25d6a13db945", "caba4ab2728d48ee9b9ba432f1dcd237", "45e26b98181a4cfcbd88ee8478c8d194", "f7953c71713f4c65b378c3b5e55d3fc1", "78bf3f93860a492ea9fcc165227bd2ee", "568d84c1f8fa45418f5357b15c195553", "788a5a1fb94e4fd4a562676be589fe2d", "110984454ed444b98ff60d876935ec21", "74583c53d9104717aa07b95fd7709ec8", "f19a02904a3542c483085e8fbeea1cd2", "0dae2e3ce2ef437db14e93f1d655d951", "7ec78864c4554de49170124cd65acdd4", "fa5334659d70452e9ed95d525bd7b234", "98e0ca734a7d483cb8b1ed558e7ef2cb", "282e972be23f4ee0b8f841e0d3c75f0a", "8d11cf5627354a3fab04439e559efd5d", "c31c0f450d1f4ab984f25929f5de5be5", "8813fbaf52ec41c1b1b19522fc1db213", "ebbc6561471b44079d44f01df9ac05ec", "8f62c3240b7b40d9ab87be96b6662a3c", "31e31be7f7ed481cb9e4f6e7b838f8e0", "f7755ef9de1a4ae7be00c694e7593d50", "954d18f61d514e9ea62b72a8cd4ad36c", "0183de7c08404461baa160d61bc36243", "8a2262af2d4d4d6da4f708d9c53e2247", "d190296774fd464f8d68dedf52b116de", "8cf1c72b406145f981bfb9f26aefcde8", "347e9d0be8864fc28968ebc3e9b3590d", "43c1bcf051e041e69ea9d171b7b1b207", "5bcb11e99c624518b7d7397cdd133852", "f0ea129b00ed4cb6b5374de37e9c6639", "595012065c2f49e1987a38462fe3a59c", "7ec426bbaab8415eacc658f346143826", "6367b8afdf2f4316a6120076d0fdaedd", "780251216c5c442588fcd49dd52039d0", "f8e6e523b418444bba4fa4155d3a38dc", "71735ed3f1c0480fa309f237a3376507", "5c2b5360e7ec40f4a2b486e039b5733e", "f5ee405b832147c9b35ba2e85b805953", "69c4062e50a54903b5ec5c925ef7b4c1", "f13fb208f7a949abaf8b7c082409aa7e" ] }, "execution": { "iopub.execute_input": "2025-10-22T16:49:05.232569Z", "iopub.status.busy": "2025-10-22T16:49:05.231904Z", "iopub.status.idle": "2025-10-22T16:49:15.703066Z", "shell.execute_reply": "2025-10-22T16:49:15.702764Z", "shell.execute_reply.started": "2025-10-22T16:49:05.232516Z" }, "id": "F0iOlZ9tTU7P", "outputId": "1abe7c86-453f-4584-a61a-bbc30af03aba" }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Loaded 698 ontology terms\n" ] }, { "name": "stderr", "output_type": "stream", "text": [ "/usr/local/lib/python3.12/dist-packages/huggingface_hub/utils/_auth.py:94: UserWarning: \n", "The secret `HF_TOKEN` does not exist in your Colab secrets.\n", "To authenticate with the Hugging Face Hub, create a token in your settings tab (https://huggingface.co/settings/tokens), set it as secret in your Google Colab and restart your session.\n", "You will be able to reuse this secret in all of your notebooks.\n", "Please note that authentication is recommended but still optional to access public models or datasets.\n", " warnings.warn(\n" ] }, { "data": { "application/vnd.jupyter.widget-view+json": { "model_id": "3e50af1eca894c3399d048aefbb845f1", "version_major": 2, "version_minor": 0 }, "text/plain": [ "modules.json: 0%| | 0.00/229 [00:00= '2020-01-01']\n", "# print(f\"After date filtering (>=2020-01-01): {len(df)} entries\")" ] }, { "cell_type": "code", "execution_count": 3, "metadata": { "execution": { "iopub.execute_input": "2025-10-20T10:57:43.149760Z", "iopub.status.busy": "2025-10-20T10:57:43.149671Z", "iopub.status.idle": "2025-10-20T10:57:43.905180Z", "shell.execute_reply": "2025-10-20T10:57:43.904836Z", "shell.execute_reply.started": "2025-10-20T10:57:43.149751Z" } }, "outputs": [ { "data": { "text/html": [ "
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0SRP610621SRX30198976GSM9192063: Sublibrary 8; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMIC SINGLE CELLcDNASRS26258712GSM9192063Illumina NovaSeq 6000116620604266603478590SRR350856171166206042188925378804GSM9192063_r1<NA><NA>GSM9192063GSM9192063_r1GEOFollowing treatment, cells were dissociated into a single cell suspension, cell counts and viabi...GSM9192063<NA><NA><NA><NA>ILLUMINASRS26258712PAIREDSAMN50743878SRS26258712188925378804<NA>Homo sapiensGSM9192063Sublibrary 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lineHepaRGcell typehepatocytebatch1geo_loc_namemissingcollection_datemissing<NA><NA><NA><NA>SAMN50743878BioSampleXREF_LINKDB: bioprojectID: 1309017LABEL: PRJNA1309017Sublibrary 8GSE306046<NA><NA>GEOGSE306046PRJNA1309017BioProject<NA><NA><NA><NA><NA><NA>Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c...Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq]Transcriptome AnalysisSRA2201062SUB15557421<NA>US EPA<NA><NA>
1SRP610621SRX30198975GSM9192062: Sublibrary 7; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMIC SINGLE CELLcDNASRS26258711GSM9192062Illumina NovaSeq 6000119070374268479328404SRR350856181190703742192894006204GSM9192062_r1<NA><NA>GSM9192062GSM9192062_r1GEOFollowing treatment, cells were dissociated into a single cell suspension, cell counts and viabi...GSM9192062<NA><NA><NA><NA>ILLUMINASRS26258711PAIREDSAMN50743879SRS26258711192894006204<NA>Homo sapiensGSM9192062Sublibrary 79606<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>GSM9192062_r1<NA>5154213946744674032953471613356803343071349483067391fastqs3.us-east-1s3runs3.us-east-1s3run.zqgs.us-east1gsrun.zqs3.us-east-1s3public<Database><Table name=\"SEQUENCE\"><Statistics source=\"meta\"><Rows count=\"1190703742\" /><Elements ...1truetrue2025-08-25 00:09:09Use Cloud Data Delivery-AWSs3://sra-pub-src-3/SRR35085618/NOVA0467.Sample7_20230216_161230.L001.1.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2025-08-22 07:40:16NOVA0467.Sample7_20230216_161230.L001.1.fastq.gzfa41995fba4040ee0e309350dc5d660afastq482492506820Original<NA>1Use Cloud Data Delivery-AWSs3://sra-pub-src-3/SRR35085618/NOVA0467.Sample7_20230216_161230.L001.2.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2025-08-22 07:38:23NOVA0467.Sample7_20230216_161230.L001.2.fastq.gz0a0b687894e62ca0ac02b5404c3de7ccfastq562247718360Original<NA>1anonymousworldwideAWShttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR35085618/SRR35085618<NA><NA><NA><NA><NA><NA><NA><NA>public2025-08-22 07:52:28SRR35085618ea62d63ec7a19dc21cdb11fb0a5ec7faSRA Normalized684793306271Primary ETLhttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR35085618/SRR350856181anonymousworldwideNCBIhttps://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-zq-38/SRR035/35085/SRR35085618/SRR3508...aws identitys3.us-east-1AWSs3://sra-pub-zq-4/SRR35085618/SRR35085618.lite.1gcp identitygs.us-east1GCPgs://sra-pub-zq-106/SRR35085618/SRR35085618.lite.1public2025-08-22 08:58:57SRR35085618.lite99d6222f7b8a7e4d278b2c1bbaf43b2aSRA Lite495326780631Primary 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lineHepaRGcell typehepatocytebatch1geo_loc_namemissingcollection_datemissing<NA><NA><NA><NA>SAMN50743879BioSampleXREF_LINKDB: bioprojectID: 1309017LABEL: PRJNA1309017Sublibrary 7GSE306046<NA><NA>GEOGSE306046PRJNA1309017BioProject<NA><NA><NA><NA><NA><NA>Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c...Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq]Transcriptome AnalysisSRA2201062SUB15557421<NA>US EPA<NA><NA>
2SRP610621SRX30198974GSM9192061: Sublibrary 6; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMIC SINGLE CELLcDNASRS26258710GSM9192061Illumina NovaSeq 6000<NA><NA>SRR35085619<NA><NA>GSM9192061_r1<NA><NA>GSM9192061GSM9192061_r1GEOFollowing treatment, cells were dissociated into a single cell suspension, cell counts and viabi...GSM9192061<NA><NA><NA><NA>ILLUMINASRS26258710PAIRED<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>GSM9192061_r1<NA><NA><NA><NA><NA><NA>sources3.us-east-1s3<NA><NA><NA><NA><NA><NA><NA><NA><NA>public<NA><NA>truetrue2025-08-25 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lineHepaRGcell typehepatocytebatch1geo_loc_namemissingcollection_datemissing<NA><NA><NA><NA>SAMN50743880BioSampleXREF_LINKDB: bioprojectID: 1309017LABEL: PRJNA1309017Sublibrary 6GSE306046<NA><NA>GEOGSE306046PRJNA1309017BioProject<NA><NA><NA><NA><NA><NA>Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c...Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq]Transcriptome AnalysisSRA2201062SUB15557421<NA>US EPA<NA><NA>
3SRP610621SRX30198973GSM9192060: Sublibrary 5; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMIC SINGLE CELLcDNASRS26258709GSM9192060Illumina NovaSeq 6000<NA><NA>SRR35085620<NA><NA>GSM9192060_r1<NA><NA>GSM9192060GSM9192060_r1GEOFollowing treatment, cells were dissociated into a single cell suspension, cell counts and 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lineHepaRGcell typehepatocytebatch1geo_loc_namemissingcollection_datemissing<NA><NA><NA><NA>SAMN50743881BioSampleXREF_LINKDB: bioprojectID: 1309017LABEL: PRJNA1309017Sublibrary 5GSE306046<NA><NA>GEOGSE306046PRJNA1309017BioProject<NA><NA><NA><NA><NA><NA>Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c...Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq]Transcriptome AnalysisSRA2201062SUB15557421<NA>US EPA<NA><NA>
4SRP610621SRX30198972GSM9192059: Sublibrary 4; Homo sapiens; RNA-Seq9606Homo sapiensRNA-SeqTRANSCRIPTOMIC SINGLE CELLcDNASRS26258708GSM9192059Illumina NovaSeq 6000122199502470518842810SRR350856211221995024197963193888GSM9192059_r1<NA><NA>GSM9192059GSM9192059_r1GEOFollowing treatment, cells were dissociated into a single cell suspension, cell counts and viabi...GSM9192059<NA><NA><NA><NA>ILLUMINASRS26258708PAIREDSAMN50743882SRS26258708197963193888<NA>Homo sapiensGSM9192059Sublibrary 49606<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>GSM9192059_r1<NA>5308923365545826461230487975803743440718650215511443fastqs3.us-east-1s3runs3.us-east-1s3run.zqgs.us-east1gsrun.zqs3.us-east-1s3public<Database><Table name=\"SEQUENCE\"><Statistics source=\"meta\"><Rows count=\"1221995024\" /><Elements ...1truetrue2025-08-25 00:09:10Use Cloud Data Delivery-AWSs3://sra-pub-src-11/SRR35085621/NOVA0467.Sample4_20230216_161230.L001.1.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2025-08-22 08:17:48NOVA0467.Sample4_20230216_161230.L001.1.fastq.gz1489941887e4bfaa843b19d2c6582780fastq485601356110Original<NA>1Use Cloud Data Delivery-AWSs3://sra-pub-src-11/SRR35085621/NOVA0467.Sample4_20230216_161230.L001.2.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2025-08-22 08:21:48NOVA0467.Sample4_20230216_161230.L001.2.fastq.gz5426d657819f17b3477842223241433ffastq582378350170Original<NA>1anonymousworldwideAWShttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR35085621/SRR35085621<NA><NA><NA><NA><NA><NA><NA><NA>public2025-08-22 08:36:17SRR350856214f3ab1791f5b3a0bde6a552db1440ee1SRA Normalized705188450391Primary ETLhttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR35085621/SRR350856211anonymousworldwideNCBIhttps://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-zq-38/SRR035/35085/SRR35085621/SRR3508...aws identitys3.us-east-1AWSs3://sra-pub-zq-4/SRR35085621/SRR35085621.lite.1gcp identitygs.us-east1GCPgs://sra-pub-zq-106/SRR35085621/SRR35085621.lite.1public2025-08-22 13:44:39SRR35085621.lite4a1b64e214c8bf2cbb028eb46271ed10SRA Lite508061989351Primary 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lineHepaRGcell typehepatocytebatch1geo_loc_namemissingcollection_datemissing<NA><NA><NA><NA>SAMN50743882BioSampleXREF_LINKDB: bioprojectID: 1309017LABEL: PRJNA1309017Sublibrary 4GSE306046<NA><NA>GEOGSE306046PRJNA1309017BioProject<NA><NA><NA><NA><NA><NA>Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c...Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq]Transcriptome AnalysisSRA2201062SUB15557421<NA>US EPA<NA><NA>
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495SRP336717SRX12150014GSM5575098: db/db day 5 wound skin sodium butyrate replicate 1; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMICcDNASRS10129301GSM5575098Illumina NovaSeq 6000674437924391584473SRR158588286744379213178772204GSM5575098GEO AccessionGSM5575098GSM5575098<NA><NA>Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf...<NA>XREF_LINKDB: gdsID: 305575098LABEL: GSM5575098ILLUMINASRS10129301PAIREDSAMN21397775SRS1012930113178772204<NA>Mus musculusGSM5575098db/db day 5 wound skin sodium butyrate replicate 110090<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>GSM5575098_r1<NA>29296032283595215455369510734938324982955013674fastqs3.us-east-1s3runs3.us-east-1s3run.zqgs.us-east1gsrun.zqs3.us-east-1s3public<Database><Table name=\"SEQUENCE\"><Statistics source=\"meta\"><Rows count=\"67443792\" /><Elements co...1truetrue2021-09-16 11:09:10Use Cloud Data Delivery-AWSs3://sra-pub-src-12/SRR15858828/16-D5-SB1_S16_ME_R1.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:49:4916-D5-SB1_S16_ME_R1.fastq.gz4bbbf5b5f22cd7864dd29ca59f052598fastq35128417220Original<NA>1Use Cloud Data Delivery-AWSs3://sra-pub-src-12/SRR15858828/16-D5-SB1_S16_ME_R2.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:50:5716-D5-SB1_S16_ME_R2.fastq.gz89a1588cdb600dd5cacf920b9bab0398fastq35896851390Original<NA>1anonymousworldwideAWShttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858828/SRR15858828<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:52:56SRR15858828a84816cdd3ed30eebbd956394ff2e3e7SRA Normalized43915872721Primary ETLhttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858828/SRR158588281anonymousworldwideNCBIhttps://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-zq-38/SRR015/15858/SRR15858828/SRR1585...aws identitys3.us-east-1AWSs3://sra-pub-zq-7/SRR15858828/SRR15858828.lite.1gcp identitygs.us-east1GCPgs://sra-pub-zq-106/SRR15858828/SRR15858828.lite.1public2022-09-22 11:24:04SRR15858828.lite68a48992accba11b23dbf713cad29caaSRA Lite35188183641Primary 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skinstrainC57BL/6genotypedb/dbtissuetotal skin<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>SAMN21397775BioSampleXREF_LINKDB: bioprojectID: 762540LABEL: PRJNA762540db/db day 5 wound skin sodium butyrate replicate 1GSE183965<NA><NA>GEOGSE183965PRJNA762540BioProject<NA><NA><NA><NA><NA><NA>Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta...Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic WoundsOtherSRA1293148GEO: GSE183965GEOGEO<NA>submission brokered by GEO
496SRP336717SRX12150013GSM5575097: db/db day 5 wound skin vehicle replicate 5; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMICcDNASRS10129302GSM5575097Illumina NovaSeq 6000543953363661511279SRR158588275439533610690654836GSM5575097GEO AccessionGSM5575097GSM5575097<NA><NA>Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf...<NA>XREF_LINKDB: gdsID: 305575097LABEL: GSM5575097ILLUMINASRS10129302PAIREDSAMN21397774SRS1012930210690654836<NA>Mus musculusGSM5575097db/db day 5 wound skin vehicle replicate 510090<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>GSM5575097_r1<NA>25684795892707472034283689295148579932572952269fastqs3.us-east-1s3runs3.us-east-1s3run.zqgs.us-east1gsrun.zqs3.us-east-1s3public<Database><Table name=\"SEQUENCE\"><Statistics source=\"meta\"><Rows count=\"54395336\" /><Elements co...1truetrue2021-09-16 11:09:10Use Cloud Data Delivery-AWSs3://sra-pub-src-6/SRR15858827/15-D5-V5_S15_ME_R1.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:04:3815-D5-V5_S15_ME_R1.fastq.gz053b8b04bca99e9e4eef175f8eaa2df2fastq28779535680Original<NA>1Use Cloud Data Delivery-AWSs3://sra-pub-src-15/SRR15858827/15-D5-V5_S15_ME_R2.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:05:3115-D5-V5_S15_ME_R2.fastq.gz246213a8d92ce91f0e9813039be8128cfastq30162496460Original<NA>1anonymousworldwideAWShttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858827/SRR15858827<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:06:44SRR15858827c87c622802569752e288e715e2b1ad1dSRA Normalized36615140861Primary ETLhttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858827/SRR158588271anonymousworldwideNCBIhttps://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-zq-38/SRR015/15858/SRR15858827/SRR1585...aws identitys3.us-east-1AWSs3://sra-pub-zq-6/SRR15858827/SRR15858827.lite.1gcp identitygs.us-east1GCPgs://sra-pub-zq-104/SRR15858827/SRR15858827.lite.1public2022-09-14 17:05:21SRR15858827.liteb2a140163009df32e50c70a846e0ff0fSRA Lite28548556821Primary 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skinstrainC57BL/6genotypedb/dbtissuetotal skin<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>SAMN21397774BioSampleXREF_LINKDB: bioprojectID: 762540LABEL: PRJNA762540db/db day 5 wound skin vehicle replicate 5GSE183965<NA><NA>GEOGSE183965PRJNA762540BioProject<NA><NA><NA><NA><NA><NA>Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta...Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic WoundsOtherSRA1293148GEO: GSE183965GEOGEO<NA>submission brokered by GEO
497SRP336717SRX12150012GSM5575096: db/db day 5 wound skin vehicle replicate 4; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMICcDNASRS10129300GSM5575096Illumina NovaSeq 6000620437214091462023SRR158588266204372112241438327GSM5575096GEO AccessionGSM5575096GSM5575096<NA><NA>Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf...<NA>XREF_LINKDB: gdsID: 305575096LABEL: GSM5575096ILLUMINASRS10129300PAIREDSAMN21397773SRS1012930012241438327<NA>Mus musculusGSM5575096db/db day 5 wound skin vehicle replicate 410090<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>GSM5575096_r1<NA>27113882603302984465348294089979054912736219212fastqs3.us-east-1s3runs3.us-east-1s3run.zqgs.us-east1gsrun.zqs3.us-east-1s3public<Database><Table name=\"SEQUENCE\"><Statistics source=\"meta\"><Rows count=\"62043721\" /><Elements co...1truetrue2021-09-16 11:09:10Use Cloud Data Delivery-AWSs3://sra-pub-src-17/SRR15858826/14-D5-V4_S14_ME_R1.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:19:3014-D5-V4_S14_ME_R1.fastq.gz2c03cde0f21e108341a2f12503696b68fastq32702846880Original<NA>1Use Cloud Data Delivery-AWSs3://sra-pub-src-17/SRR15858826/14-D5-V4_S14_ME_R2.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:19:1014-D5-V4_S14_ME_R2.fastq.gzc99615c9da116c518128ddf3f0175fe8fastq33274747060Original<NA>1anonymousworldwideAWShttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858826/SRR15858826<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:20:05SRR15858826ce1036be1b68eb29040c6a3f18a8f079SRA Normalized40914648181Primary ETLhttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858826/SRR158588261anonymousworldwideNCBIhttps://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos9/sra-pub-zq-922/SRR015/15858/SRR15858826/SRR158...aws identitys3.us-east-1AWSs3://sra-pub-zq-1/SRR15858826/SRR15858826.lite.1gcp identitygs.us-east1GCPgs://sra-pub-zq-101/SRR15858826/SRR15858826.lite.1public2022-11-15 03:38:05SRR15858826.lite50ae49bf89119652fc4f2c0db770bb1bSRA Lite32619685981Primary 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skinstrainC57BL/6genotypedb/dbtissuetotal skin<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>SAMN21397773BioSampleXREF_LINKDB: bioprojectID: 762540LABEL: PRJNA762540db/db day 5 wound skin vehicle replicate 4GSE183965<NA><NA>GEOGSE183965PRJNA762540BioProject<NA><NA><NA><NA><NA><NA>Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta...Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic WoundsOtherSRA1293148GEO: GSE183965GEOGEO<NA>submission brokered by GEO
498SRP336717SRX12150011GSM5575095: db/db day 5 wound skin vehicle replicate 3; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMICcDNASRS10129299GSM5575095Illumina NovaSeq 6000659664104388118727SRR158588256596641012918706392GSM5575095GEO AccessionGSM5575095GSM5575095<NA><NA>Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf...<NA>XREF_LINKDB: gdsID: 305575095LABEL: GSM5575095ILLUMINASRS10129299PAIREDSAMN21397772SRS1012929912918706392<NA>Mus musculusGSM5575095db/db day 5 wound skin vehicle replicate 310090<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>GSM5575095_r1<NA>291313681033689807333678138268105617192947888862fastqs3.us-east-1s3runs3.us-east-1s3run.zqgs.us-east1gsrun.zqs3.us-east-1s3public<Database><Table name=\"SEQUENCE\"><Statistics source=\"meta\"><Rows count=\"65966410\" /><Elements co...1truetrue2021-09-16 11:09:10Use Cloud Data Delivery-AWSs3://sra-pub-src-6/SRR15858825/13-D5-V3_S13_ME_R1.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 17:13:2713-D5-V3_S13_ME_R1.fastq.gz4e6845c8a21031f3e269b2eec93d9bb9fastq34342662350Original<NA>1Use Cloud Data Delivery-AWSs3://sra-pub-src-6/SRR15858825/13-D5-V3_S13_ME_R2.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 17:14:3213-D5-V3_S13_ME_R2.fastq.gza2f2a9f59bff2750556946ed13492bddfastq36091439220Original<NA>1anonymousworldwideAWShttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858825/SRR15858825<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 17:16:45SRR1585882524e9c42ff70362b749fd79b2ad4d8cfcSRA Normalized43881215251Primary ETLhttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858825/SRR158588251anonymousworldwideNCBIhttps://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-zq-38/SRR015/15858/SRR15858825/SRR1585...aws identitys3.us-east-1AWSs3://sra-pub-zq-7/SRR15858825/SRR15858825.lite.1gcp identitygs.us-east1GCPgs://sra-pub-zq-109/SRR15858825/SRR15858825.lite.1public2022-09-17 14:07:40SRR15858825.lite5c04e895a40d35c76388f8736d2da1b6SRA Lite34497553691Primary 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skinstrainC57BL/6genotypedb/dbtissuetotal skin<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>SAMN21397772BioSampleXREF_LINKDB: bioprojectID: 762540LABEL: PRJNA762540db/db day 5 wound skin vehicle replicate 3GSE183965<NA><NA>GEOGSE183965PRJNA762540BioProject<NA><NA><NA><NA><NA><NA>Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta...Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic WoundsOtherSRA1293148GEO: GSE183965GEOGEO<NA>submission brokered by GEO
499SRP336717SRX12150010GSM5575094: db/db day 5 wound skin vehicle replicate 2; Mus musculus; RNA-Seq10090Mus musculusRNA-SeqTRANSCRIPTOMICcDNASRS10129298GSM5575094Illumina NovaSeq 6000655577554549420217SRR158588246555775513000066097GSM5575094GEO AccessionGSM5575094GSM5575094<NA><NA>Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf...<NA>XREF_LINKDB: gdsID: 305575094LABEL: GSM5575094ILLUMINASRS10129298PAIREDSAMN21397771SRS1012929813000066097<NA>Mus musculusGSM5575094db/db day 5 wound skin vehicle replicate 210090<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>GSM5575094_r1<NA>35595404782869481579299216716267005603572176318fastqs3.us-east-1s3runs3.us-east-1s3run.zqgs.us-east1gsrun.zqs3.us-east-1s3public<Database><Table name=\"SEQUENCE\"><Statistics source=\"meta\"><Rows count=\"65557755\" /><Elements co...1truetrue2021-09-16 11:09:10Use Cloud Data Delivery-AWSs3://sra-pub-src-3/SRR15858824/12-D5-V2_S12_ME_R1.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:15:2612-D5-V2_S12_ME_R1.fastq.gzd6285c3122f94dc490d6c2228ab13c13fastq32148000130Original<NA>1Use Cloud Data Delivery-AWSs3://sra-pub-src-3/SRR15858824/12-D5-V2_S12_ME_R2.fastq.gz.1<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:15:4512-D5-V2_S12_ME_R2.fastq.gz6b6f7202542efee92786887cd92fc5d5fastq34563931830Original<NA>1anonymousworldwideAWShttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858824/SRR15858824<NA><NA><NA><NA><NA><NA><NA><NA>public2021-09-12 15:16:26SRR158588244a9ca8f3194df802c4e366329fb77136SRA Normalized45494230181Primary ETLhttps://sra-pub-run-odp.s3.amazonaws.com/sra/SRR15858824/SRR158588241anonymousworldwideNCBIhttps://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos8/sra-pub-zq-820/SRR015/15858/SRR15858824/SRR158...aws identitys3.us-east-1AWSs3://sra-pub-zq-8/SRR15858824/SRR15858824.lite.1gcp identitygs.us-east1GCPgs://sra-pub-zq-101/SRR15858824/SRR15858824.lite.1public2022-08-05 06:04:24SRR15858824.lite43410aa709730d43955051935f830508SRA Lite34569315701Primary 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skinstrainC57BL/6genotypedb/dbtissuetotal skin<NA><NA><NA><NA><NA><NA><NA><NA><NA><NA>SAMN21397771BioSampleXREF_LINKDB: bioprojectID: 762540LABEL: PRJNA762540db/db day 5 wound skin vehicle replicate 2GSE183965<NA><NA>GEOGSE183965PRJNA762540BioProject<NA><NA><NA><NA><NA><NA>Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta...Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic WoundsOtherSRA1293148GEO: GSE183965GEOGEO<NA>submission brokered by GEO
\n", "

500 rows × 5888 columns

\n", "
" ], "text/plain": [ " study_accession experiment_accession \\\n", "0 SRP610621 SRX30198976 \n", "1 SRP610621 SRX30198975 \n", "2 SRP610621 SRX30198974 \n", "3 SRP610621 SRX30198973 \n", "4 SRP610621 SRX30198972 \n", ".. ... ... \n", "495 SRP336717 SRX12150014 \n", "496 SRP336717 SRX12150013 \n", "497 SRP336717 SRX12150012 \n", "498 SRP336717 SRX12150011 \n", "499 SRP336717 SRX12150010 \n", "\n", " experiment_title \\\n", "0 GSM9192063: Sublibrary 8; Homo sapiens; RNA-Seq \n", "1 GSM9192062: Sublibrary 7; Homo sapiens; RNA-Seq \n", "2 GSM9192061: Sublibrary 6; Homo sapiens; RNA-Seq \n", "3 GSM9192060: Sublibrary 5; Homo sapiens; RNA-Seq \n", "4 GSM9192059: Sublibrary 4; Homo sapiens; RNA-Seq \n", ".. ... \n", "495 GSM5575098: db/db day 5 wound skin sodium butyrate replicate 1; Mus musculus; RNA-Seq \n", "496 GSM5575097: db/db day 5 wound skin vehicle replicate 5; Mus musculus; RNA-Seq \n", "497 GSM5575096: db/db day 5 wound skin vehicle replicate 4; Mus musculus; RNA-Seq \n", "498 GSM5575095: db/db day 5 wound skin vehicle replicate 3; Mus musculus; RNA-Seq \n", "499 GSM5575094: db/db day 5 wound skin vehicle replicate 2; Mus musculus; RNA-Seq \n", "\n", " sample_taxon_id sample_scientific_name experiment_library_strategy \\\n", "0 9606 Homo sapiens RNA-Seq \n", "1 9606 Homo sapiens RNA-Seq \n", "2 9606 Homo sapiens RNA-Seq \n", "3 9606 Homo sapiens RNA-Seq \n", "4 9606 Homo sapiens RNA-Seq \n", ".. ... ... ... \n", "495 10090 Mus musculus RNA-Seq \n", "496 10090 Mus musculus RNA-Seq \n", "497 10090 Mus musculus RNA-Seq \n", "498 10090 Mus musculus RNA-Seq \n", "499 10090 Mus musculus RNA-Seq \n", "\n", " experiment_library_source experiment_library_selection sample_accession \\\n", "0 TRANSCRIPTOMIC SINGLE CELL cDNA SRS26258712 \n", "1 TRANSCRIPTOMIC SINGLE CELL cDNA SRS26258711 \n", "2 TRANSCRIPTOMIC SINGLE CELL cDNA SRS26258710 \n", "3 TRANSCRIPTOMIC SINGLE CELL cDNA SRS26258709 \n", "4 TRANSCRIPTOMIC SINGLE CELL cDNA SRS26258708 \n", ".. ... ... ... \n", "495 TRANSCRIPTOMIC cDNA SRS10129301 \n", "496 TRANSCRIPTOMIC cDNA SRS10129302 \n", "497 TRANSCRIPTOMIC cDNA SRS10129300 \n", "498 TRANSCRIPTOMIC cDNA SRS10129299 \n", "499 TRANSCRIPTOMIC cDNA SRS10129298 \n", "\n", " sample_alias experiment_instrument_model pool_member_spots run_1_size \\\n", "0 GSM9192063 Illumina NovaSeq 6000 1166206042 66603478590 \n", "1 GSM9192062 Illumina NovaSeq 6000 1190703742 68479328404 \n", "2 GSM9192061 Illumina NovaSeq 6000 \n", "3 GSM9192060 Illumina NovaSeq 6000 \n", "4 GSM9192059 Illumina NovaSeq 6000 1221995024 70518842810 \n", ".. ... ... ... ... \n", "495 GSM5575098 Illumina NovaSeq 6000 67443792 4391584473 \n", "496 GSM5575097 Illumina NovaSeq 6000 54395336 3661511279 \n", "497 GSM5575096 Illumina NovaSeq 6000 62043721 4091462023 \n", "498 GSM5575095 Illumina NovaSeq 6000 65966410 4388118727 \n", "499 GSM5575094 Illumina NovaSeq 6000 65557755 4549420217 \n", "\n", " run_1_accession run_1_total_spots run_1_total_bases experiment_alias \\\n", "0 SRR35085617 1166206042 188925378804 GSM9192063_r1 \n", "1 SRR35085618 1190703742 192894006204 GSM9192062_r1 \n", "2 SRR35085619 GSM9192061_r1 \n", "3 SRR35085620 GSM9192060_r1 \n", "4 SRR35085621 1221995024 197963193888 GSM9192059_r1 \n", ".. ... ... ... ... \n", "495 SRR15858828 67443792 13178772204 GSM5575098 \n", "496 SRR15858827 54395336 10690654836 GSM5575097 \n", "497 SRR15858826 62043721 12241438327 GSM5575096 \n", "498 SRR15858825 65966410 12918706392 GSM5575095 \n", "499 SRR15858824 65557755 13000066097 GSM5575094 \n", "\n", " experiment_attributes_1_tag experiment_attributes_1_value \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 GEO Accession GSM5575098 \n", "496 GEO Accession GSM5575097 \n", "497 GEO Accession GSM5575096 \n", "498 GEO Accession GSM5575095 \n", "499 GEO Accession GSM5575094 \n", "\n", " experiment_external_id experiment_external_id_1 \\\n", "0 GSM9192063 GSM9192063_r1 \n", "1 GSM9192062 GSM9192062_r1 \n", "2 GSM9192061 GSM9192061_r1 \n", "3 GSM9192060 GSM9192060_r1 \n", "4 GSM9192059 GSM9192059_r1 \n", ".. ... ... \n", "495 GSM5575098 \n", "496 GSM5575097 \n", "497 GSM5575096 \n", "498 GSM5575095 \n", "499 GSM5575094 \n", "\n", " experiment_external_id_1_namespace \\\n", "0 GEO \n", "1 GEO \n", "2 GEO \n", "3 GEO \n", "4 GEO \n", ".. ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " experiment_library_construction_protocol \\\n", "0 Following treatment, cells were dissociated into a single cell suspension, cell counts and viabi... \n", "1 Following treatment, cells were dissociated into a single cell suspension, cell counts and viabi... \n", "2 Following treatment, cells were dissociated into a single cell suspension, cell counts and viabi... \n", "3 Following treatment, cells were dissociated into a single cell suspension, cell counts and viabi... \n", "4 Following treatment, cells were dissociated into a single cell suspension, cell counts and viabi... \n", ".. ... \n", "495 Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf... \n", "496 Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf... \n", "497 Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf... \n", "498 Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf... \n", "499 Total RNA from skin and macrophages was isolated using Rneasy kit (Qiagen) rRNA removal was perf... \n", "\n", " experiment_library_name experiment_link_1_type experiment_link_1_value_1 \\\n", "0 GSM9192063 \n", "1 GSM9192062 \n", "2 GSM9192061 \n", "3 GSM9192060 \n", "4 GSM9192059 \n", ".. ... ... ... \n", "495 XREF_LINK DB: gds \n", "496 XREF_LINK DB: gds \n", "497 XREF_LINK DB: gds \n", "498 XREF_LINK DB: gds \n", "499 XREF_LINK DB: gds \n", "\n", " experiment_link_1_value_2 experiment_link_1_value_3 experiment_platform \\\n", "0 ILLUMINA \n", "1 ILLUMINA \n", "2 ILLUMINA \n", "3 ILLUMINA \n", "4 ILLUMINA \n", ".. ... ... ... \n", "495 ID: 305575098 LABEL: GSM5575098 ILLUMINA \n", "496 ID: 305575097 LABEL: GSM5575097 ILLUMINA \n", "497 ID: 305575096 LABEL: GSM5575096 ILLUMINA \n", "498 ID: 305575095 LABEL: GSM5575095 ILLUMINA \n", "499 ID: 305575094 LABEL: GSM5575094 ILLUMINA \n", "\n", " experiment_sample_descriptor_accession library_layout pool_external_id \\\n", "0 SRS26258712 PAIRED SAMN50743878 \n", "1 SRS26258711 PAIRED SAMN50743879 \n", "2 SRS26258710 PAIRED \n", "3 SRS26258709 PAIRED \n", "4 SRS26258708 PAIRED SAMN50743882 \n", ".. ... ... ... \n", "495 SRS10129301 PAIRED SAMN21397775 \n", "496 SRS10129302 PAIRED SAMN21397774 \n", "497 SRS10129300 PAIRED SAMN21397773 \n", "498 SRS10129299 PAIRED SAMN21397772 \n", "499 SRS10129298 PAIRED SAMN21397771 \n", "\n", " pool_member_accession pool_member_bases pool_member_member_name \\\n", "0 SRS26258712 188925378804 \n", "1 SRS26258711 192894006204 \n", "2 \n", "3 \n", "4 SRS26258708 197963193888 \n", ".. ... ... ... \n", "495 SRS10129301 13178772204 \n", "496 SRS10129302 10690654836 \n", "497 SRS10129300 12241438327 \n", "498 SRS10129299 12918706392 \n", "499 SRS10129298 13000066097 \n", "\n", " pool_member_organism pool_member_sample_name \\\n", "0 Homo sapiens GSM9192063 \n", "1 Homo sapiens GSM9192062 \n", "2 \n", "3 \n", "4 Homo sapiens GSM9192059 \n", ".. ... ... \n", "495 Mus musculus GSM5575098 \n", "496 Mus musculus GSM5575097 \n", "497 Mus musculus GSM5575096 \n", "498 Mus musculus GSM5575095 \n", "499 Mus musculus GSM5575094 \n", "\n", " pool_member_sample_title pool_member_tax_id \\\n", "0 Sublibrary 8 9606 \n", "1 Sublibrary 7 9606 \n", "2 \n", "3 \n", "4 Sublibrary 4 9606 \n", ".. ... ... \n", "495 db/db day 5 wound skin sodium butyrate replicate 1 10090 \n", "496 db/db day 5 wound skin vehicle replicate 5 10090 \n", "497 db/db day 5 wound skin vehicle replicate 4 10090 \n", "498 db/db day 5 wound skin vehicle replicate 3 10090 \n", "499 db/db day 5 wound skin vehicle replicate 2 10090 \n", "\n", " run_10_accession run_10_alias run_10_base_A_count run_10_base_C_count \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_base_G_count run_10_base_N_count run_10_base_T_count \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_cloudfile_1_filetype run_10_cloudfile_1_location \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_cloudfile_1_provider run_10_cloudfile_2_filetype \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_cloudfile_2_location run_10_cloudfile_2_provider \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_cloudfile_3_filetype run_10_cloudfile_3_location \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_cloudfile_3_provider run_10_cloudfile_4_filetype \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_cloudfile_4_location run_10_cloudfile_4_provider \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_cluster_name run_10_database_1 run_10_has_taxanalysis \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_is_public run_10_load_done run_10_published run_10_size \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_srafile_1_alternative_1_access_type \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... \n", "495 \n", 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... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_srafile_3_md5 run_10_srafile_3_semantic_name run_10_srafile_3_size \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_srafile_3_sratoolkit run_10_srafile_3_supertype \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_srafile_3_url run_10_srafile_3_version \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_srafile_4_alternative_1_access_type \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_srafile_4_alternative_1_free_egress \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_10_srafile_4_alternative_1_org 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run_9_total_base_cs_native run_9_total_bases \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " run_9_total_spots run_set_bases run_set_bytes run_set_runs run_set_spots \\\n", "0 188925378804 66603478590 1 1166206042 \n", "1 192894006204 68479328404 1 1190703742 \n", "2 0 0 1 0 \n", "3 0 0 1 0 \n", "4 197963193888 70518842810 1 1221995024 \n", ".. ... ... ... ... ... \n", "495 13178772204 4391584473 1 67443792 \n", "496 10690654836 3661511279 1 54395336 \n", "497 12241438327 4091462023 1 62043721 \n", "498 12918706392 4388118727 1 65966410 \n", "499 13000066097 4549420217 1 65557755 \n", "\n", " sample_attributes_10_tag sample_attributes_10_value \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " sample_attributes_11_tag sample_attributes_11_value \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " sample_attributes_12_tag sample_attributes_12_value \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " sample_attributes_1_tag sample_attributes_1_value sample_attributes_2_tag \\\n", "0 source_name liver tissue \n", "1 source_name liver tissue \n", "2 source_name liver tissue \n", "3 source_name liver tissue \n", "4 source_name liver tissue \n", ".. ... ... ... \n", "495 source_name total skin strain \n", "496 source_name total skin strain \n", "497 source_name total skin strain \n", "498 source_name total skin strain \n", "499 source_name total skin strain \n", "\n", " sample_attributes_2_value sample_attributes_3_tag \\\n", "0 liver cell line \n", "1 liver cell line \n", "2 liver cell line \n", "3 liver cell line \n", "4 liver cell line \n", ".. ... ... \n", "495 C57BL/6 genotype \n", "496 C57BL/6 genotype \n", "497 C57BL/6 genotype \n", "498 C57BL/6 genotype \n", "499 C57BL/6 genotype \n", "\n", " sample_attributes_3_value sample_attributes_4_tag \\\n", "0 HepaRG cell type \n", "1 HepaRG cell type \n", "2 HepaRG cell type \n", "3 HepaRG cell type \n", "4 HepaRG cell type \n", ".. ... ... \n", "495 db/db tissue \n", "496 db/db tissue \n", "497 db/db tissue \n", "498 db/db tissue \n", "499 db/db tissue \n", "\n", " sample_attributes_4_value sample_attributes_5_tag \\\n", "0 hepatocyte batch \n", "1 hepatocyte batch \n", "2 hepatocyte batch \n", "3 hepatocyte batch \n", "4 hepatocyte batch \n", ".. ... ... \n", "495 total skin \n", "496 total skin \n", "497 total skin \n", "498 total skin \n", "499 total skin \n", "\n", " sample_attributes_5_value sample_attributes_6_tag \\\n", "0 1 geo_loc_name \n", "1 1 geo_loc_name \n", "2 1 geo_loc_name \n", "3 1 geo_loc_name \n", "4 1 geo_loc_name \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " sample_attributes_6_value sample_attributes_7_tag \\\n", "0 missing collection_date \n", "1 missing collection_date \n", "2 missing collection_date \n", "3 missing collection_date \n", "4 missing collection_date \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " sample_attributes_7_value sample_attributes_8_tag \\\n", "0 missing \n", "1 missing \n", "2 missing \n", "3 missing \n", "4 missing \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " sample_attributes_8_value sample_attributes_9_tag \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " sample_attributes_9_value sample_external_id_1 \\\n", "0 SAMN50743878 \n", "1 SAMN50743879 \n", "2 SAMN50743880 \n", "3 SAMN50743881 \n", "4 SAMN50743882 \n", ".. ... ... \n", "495 SAMN21397775 \n", "496 SAMN21397774 \n", "497 SAMN21397773 \n", "498 SAMN21397772 \n", "499 SAMN21397771 \n", "\n", " sample_external_id_1_namespace sample_link_1_type sample_link_1_value_1 \\\n", "0 BioSample XREF_LINK DB: bioproject \n", "1 BioSample XREF_LINK DB: bioproject \n", "2 BioSample XREF_LINK DB: bioproject \n", "3 BioSample XREF_LINK DB: bioproject \n", "4 BioSample XREF_LINK DB: bioproject \n", ".. ... ... ... \n", "495 BioSample XREF_LINK DB: bioproject \n", "496 BioSample XREF_LINK DB: bioproject \n", "497 BioSample XREF_LINK DB: bioproject \n", "498 BioSample XREF_LINK DB: bioproject \n", "499 BioSample XREF_LINK DB: bioproject \n", "\n", " sample_link_1_value_2 sample_link_1_value_3 \\\n", "0 ID: 1309017 LABEL: PRJNA1309017 \n", "1 ID: 1309017 LABEL: PRJNA1309017 \n", "2 ID: 1309017 LABEL: PRJNA1309017 \n", "3 ID: 1309017 LABEL: PRJNA1309017 \n", "4 ID: 1309017 LABEL: PRJNA1309017 \n", ".. ... ... \n", "495 ID: 762540 LABEL: PRJNA762540 \n", "496 ID: 762540 LABEL: PRJNA762540 \n", "497 ID: 762540 LABEL: PRJNA762540 \n", "498 ID: 762540 LABEL: PRJNA762540 \n", "499 ID: 762540 LABEL: PRJNA762540 \n", "\n", " sample_title study_alias \\\n", "0 Sublibrary 8 GSE306046 \n", "1 Sublibrary 7 GSE306046 \n", "2 Sublibrary 6 GSE306046 \n", "3 Sublibrary 5 GSE306046 \n", "4 Sublibrary 4 GSE306046 \n", ".. ... ... \n", "495 db/db day 5 wound skin sodium butyrate replicate 1 GSE183965 \n", "496 db/db day 5 wound skin vehicle replicate 5 GSE183965 \n", "497 db/db day 5 wound skin vehicle replicate 4 GSE183965 \n", "498 db/db day 5 wound skin vehicle replicate 3 GSE183965 \n", "499 db/db day 5 wound skin vehicle replicate 2 GSE183965 \n", "\n", " study_attributes_1_tag study_attributes_1_value study_center_name \\\n", "0 GEO \n", "1 GEO \n", "2 GEO \n", "3 GEO \n", "4 GEO \n", ".. ... ... ... \n", "495 GEO \n", "496 GEO \n", "497 GEO \n", "498 GEO \n", "499 GEO \n", "\n", " study_center_project_name study_external_id_1 \\\n", "0 GSE306046 PRJNA1309017 \n", "1 GSE306046 PRJNA1309017 \n", "2 GSE306046 PRJNA1309017 \n", "3 GSE306046 PRJNA1309017 \n", "4 GSE306046 PRJNA1309017 \n", ".. ... ... \n", "495 GSE183965 PRJNA762540 \n", "496 GSE183965 PRJNA762540 \n", "497 GSE183965 PRJNA762540 \n", "498 GSE183965 PRJNA762540 \n", "499 GSE183965 PRJNA762540 \n", "\n", " study_external_id_1_namespace study_link_1_type study_link_1_value_1 \\\n", "0 BioProject \n", "1 BioProject \n", "2 BioProject \n", "3 BioProject \n", "4 BioProject \n", ".. ... ... ... \n", "495 BioProject \n", "496 BioProject \n", "497 BioProject \n", "498 BioProject \n", "499 BioProject \n", "\n", " study_link_1_value_2 study_link_2_type study_link_2_value_1 \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " study_link_2_value_2 \\\n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... \n", "495 \n", "496 \n", "497 \n", "498 \n", "499 \n", "\n", " study_study_abstract \\\n", "0 Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c... \n", "1 Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c... \n", "2 Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c... \n", "3 Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c... \n", "4 Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of c... \n", ".. ... \n", "495 Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta... \n", "496 Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta... \n", "497 Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta... \n", "498 Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta... \n", "499 Dysregulation of macrophage populations at the wound site is responsible for the non-healing sta... \n", "\n", " study_study_title \\\n", "0 Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq] \n", "1 Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq] \n", "2 Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq] \n", "3 Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq] \n", "4 Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq] \n", ".. ... \n", "495 Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic Wounds \n", "496 Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic Wounds \n", "497 Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic Wounds \n", "498 Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic Wounds \n", "499 Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic Wounds \n", "\n", " study_study_type_existing_study_type submission_accession \\\n", "0 Transcriptome Analysis SRA2201062 \n", "1 Transcriptome Analysis SRA2201062 \n", "2 Transcriptome Analysis SRA2201062 \n", "3 Transcriptome Analysis SRA2201062 \n", "4 Transcriptome Analysis SRA2201062 \n", ".. ... ... \n", "495 Other SRA1293148 \n", "496 Other SRA1293148 \n", "497 Other SRA1293148 \n", "498 Other SRA1293148 \n", "499 Other SRA1293148 \n", "\n", " submission_alias submission_broker_name submission_center_name \\\n", "0 SUB15557421 US EPA \n", "1 SUB15557421 US EPA \n", "2 SUB15557421 US EPA \n", "3 SUB15557421 US EPA \n", "4 SUB15557421 US EPA \n", ".. ... ... ... \n", "495 GEO: GSE183965 GEO GEO \n", "496 GEO: GSE183965 GEO GEO \n", "497 GEO: GSE183965 GEO GEO \n", "498 GEO: GSE183965 GEO GEO \n", "499 GEO: GSE183965 GEO GEO \n", "\n", " submission_lab_name submission_submission_comment \n", "0 \n", "1 \n", "2 \n", "3 \n", "4 \n", ".. ... ... \n", "495 submission brokered by GEO \n", "496 submission brokered by GEO \n", "497 submission brokered by GEO \n", "498 submission brokered by GEO \n", "499 submission brokered by GEO \n", "\n", "[500 rows x 5888 columns]" ] }, "execution_count": 3, "metadata": {}, "output_type": "execute_result" } ], "source": [ "df" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Filter and Explore Results\n", "\n", "Let's examine the unique studies and get an overview of the datasets:" ] }, { "cell_type": "code", "execution_count": 4, "metadata": { "execution": { "iopub.execute_input": "2025-10-20T10:57:43.905779Z", "iopub.status.busy": "2025-10-20T10:57:43.905674Z", "iopub.status.idle": "2025-10-20T10:57:43.910461Z", "shell.execute_reply": "2025-10-20T10:57:43.910215Z", "shell.execute_reply.started": "2025-10-20T10:57:43.905766Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Number of unique studies (GSE IDs): 62\n", "\n", "Unique GSE IDs:\n", "['GSE172289', 'GSE183965', 'GSE199498', 'GSE214374', 'GSE221853', 'GSE225497', 'GSE228214', 'GSE229617', 'GSE233519', 'GSE233606', 'GSE236902', 'GSE239347', 'GSE240096', 'GSE241142', 'GSE241543', 'GSE241693', 'GSE243135', 'GSE244321', 'GSE246140', 'GSE246624', 'GSE249558', 'GSE250009', 'GSE252185', 'GSE252604', 'GSE253230', 'GSE253406', 'GSE253539', 'GSE253642', 'GSE255851', 'GSE256359', 'GSE262111', 'GSE262249', 'GSE263619', 'GSE263863', 'GSE264678', 'GSE268385', 'GSE271203', 'GSE272713', 'GSE272840', 'GSE273089', 'GSE275127', 'GSE278923', 'GSE280717', 'GSE281535', 'GSE281932', 'GSE282851', 'GSE283038', 'GSE283186', 'GSE284207', 'GSE287852', 'GSE289845', 'GSE291674', 'GSE292745', 'GSE295527', 'GSE296244', 'GSE296547', 'GSE297023', 'GSE297299', 'GSE297427', 'GSE299005', 'GSE299409', 'GSE306046']\n", "\n", "================================================================================\n", "DATASET SUMMARY\n", "================================================================================\n", "Total runs: 500\n", "\n", "Organisms represented:\n", "sample_scientific_name\n", "Homo sapiens 325\n", "Mus musculus 147\n", "Gallus gallus 15\n", "Homo sapiens/Mus musculus xenograft 8\n", "Macaca nemestrina 2\n", "Rattus norvegicus 1\n", "Mustela putorius furo 1\n", "Bos taurus 1\n", "Name: count, dtype: int64\n", "\n", "Library strategies:\n", "experiment_library_strategy\n", "RNA-Seq 440\n", "Bisulfite-Seq 60\n", "Name: count, dtype: int64\n" ] } ], "source": [ "if not df.empty:\n", " # Get unique GSE IDs (study accessions)\n", " if \"study_alias\" in df.columns:\n", " unique_studies = df[\"study_alias\"].unique()\n", " print(f\"Number of unique studies (GSE IDs): {len(unique_studies)}\")\n", " print(f\"\\nUnique GSE IDs:\\n{sorted(unique_studies)}\")\n", "\n", " # Display summary information\n", " print(f\"\\n{'='*80}\")\n", " print(\"DATASET SUMMARY\")\n", " print(f\"{'='*80}\")\n", " print(f\"Total runs: {len(df)}\")\n", "\n", " if \"sample_scientific_name\" in df.columns:\n", " print(f\"\\nOrganisms represented:\")\n", " print(df[\"sample_scientific_name\"].value_counts())\n", "\n", " if \"experiment_library_strategy\" in df.columns:\n", " print(f\"\\nLibrary strategies:\")\n", " print(df[\"experiment_library_strategy\"].value_counts())\n", "else:\n", " print(\"No results found. This could mean:\")\n", " print(\"1. No Parse Bioscience datasets match the date range\")\n", " print(\"2. The search query needs adjustment\")\n", " print(\"3. Try searching with a broader query or different date range\")" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Display Key Metadata\n", "\n", "Let's create a clean summary table with the most important information:" ] }, { "cell_type": "code", "execution_count": 5, "metadata": { "execution": { "iopub.execute_input": "2025-10-20T10:57:43.910921Z", "iopub.status.busy": "2025-10-20T10:57:43.910847Z", "iopub.status.idle": "2025-10-20T10:57:43.916866Z", "shell.execute_reply": "2025-10-20T10:57:43.916635Z", "shell.execute_reply.started": "2025-10-20T10:57:43.910913Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "\n", "Parse Bioscience Dataset Summary:\n", "================================================================================\n", "\n" ] }, { "data": { "text/html": [ "
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study_accessionstudy_aliasexperiment_accessionsample_accessionsample_scientific_nameexperiment_library_strategyexperiment_titlerun_1_accession
0SRP610621GSE306046SRX30198976SRS26258712Homo sapiensRNA-SeqGSM9192063: Sublibrary 8; Homo sapiens; RNA-SeqSRR35085617
1SRP610621GSE306046SRX30198975SRS26258711Homo sapiensRNA-SeqGSM9192062: Sublibrary 7; Homo sapiens; RNA-SeqSRR35085618
2SRP610621GSE306046SRX30198974SRS26258710Homo sapiensRNA-SeqGSM9192061: Sublibrary 6; Homo sapiens; RNA-SeqSRR35085619
3SRP610621GSE306046SRX30198973SRS26258709Homo sapiensRNA-SeqGSM9192060: Sublibrary 5; Homo sapiens; RNA-SeqSRR35085620
4SRP610621GSE306046SRX30198972SRS26258708Homo sapiensRNA-SeqGSM9192059: Sublibrary 4; Homo sapiens; RNA-SeqSRR35085621
5SRP610621GSE306046SRX30198971SRS26258707Homo sapiensRNA-SeqGSM9192058: Sublibrary 3; Homo sapiens; RNA-SeqSRR35085622
6SRP610621GSE306046SRX30198970SRS26258706Homo sapiensRNA-SeqGSM9192057: Sublibrary 2; Homo sapiens; RNA-SeqSRR35085623
7SRP610621GSE306046SRX30198969SRS26258705Homo sapiensRNA-SeqGSM9192056: Sublibrary 1; Homo sapiens; RNA-SeqSRR35085624
8SRP591195GSE299409SRX29129887SRS25335612Mus musculusRNA-SeqGSM9038763: all mix sample 8; Mus musculus; RNA-SeqSRR33926227
9SRP591195GSE299409SRX29129886SRS25335611Mus musculusRNA-SeqGSM9038762: all mix sample 7; Mus musculus; RNA-SeqSRR33926228
10SRP591195GSE299409SRX29129885SRS25335610Mus musculusRNA-SeqGSM9038761: all mix sample 6; Mus musculus; RNA-SeqSRR33926229
11SRP591195GSE299409SRX29129884SRS25335609Mus musculusRNA-SeqGSM9038760: all mix sample 5; Mus musculus; RNA-SeqSRR33926230
12SRP591195GSE299409SRX29129883SRS25335608Mus musculusRNA-SeqGSM9038759: all mix sample 4; Mus musculus; RNA-SeqSRR33926231
13SRP591195GSE299409SRX29129882SRS25335607Mus musculusRNA-SeqGSM9038758: all mix sample 3; Mus musculus; RNA-SeqSRR33926232
14SRP591195GSE299409SRX29129881SRS25335606Mus musculusRNA-SeqGSM9038757: all mix sample 2; Mus musculus; RNA-SeqSRR33926233
15SRP591195GSE299409SRX29129880SRS25335605Mus musculusRNA-SeqGSM9038756: all mix sample 1; Mus musculus; RNA-SeqSRR33926234
16SRP589942GSE299005SRX29052446SRS25267580Mus musculusRNA-SeqGSM9030358: Cortical tissue, all 4 groups mixed, 6562; Mus musculus; RNA-SeqSRR33831644
17SRP589942GSE299005SRX29052445SRS25267579Mus musculusRNA-SeqGSM9030357: Cortical tissue, all 4 groups mixed, 6142; Mus musculus; RNA-SeqSRR33831645
18SRP586001GSE297427SRX28837662SRS25068573Homo sapiens/Mus musculus xenograftRNA-SeqGSM8991181: NK_CXCL10_2; Homo sapiens/Mus musculus xenograft; RNA-SeqSRR33609182
19SRP586001GSE297427SRX28837661SRS25068574Homo sapiens/Mus musculus xenograftRNA-SeqGSM8991180: NK_CXCL10_1; Homo sapiens/Mus musculus xenograft; RNA-SeqSRR33609183
\n", "" ], "text/plain": [ " study_accession study_alias experiment_accession sample_accession \\\n", "0 SRP610621 GSE306046 SRX30198976 SRS26258712 \n", "1 SRP610621 GSE306046 SRX30198975 SRS26258711 \n", "2 SRP610621 GSE306046 SRX30198974 SRS26258710 \n", "3 SRP610621 GSE306046 SRX30198973 SRS26258709 \n", "4 SRP610621 GSE306046 SRX30198972 SRS26258708 \n", "5 SRP610621 GSE306046 SRX30198971 SRS26258707 \n", "6 SRP610621 GSE306046 SRX30198970 SRS26258706 \n", "7 SRP610621 GSE306046 SRX30198969 SRS26258705 \n", "8 SRP591195 GSE299409 SRX29129887 SRS25335612 \n", "9 SRP591195 GSE299409 SRX29129886 SRS25335611 \n", "10 SRP591195 GSE299409 SRX29129885 SRS25335610 \n", "11 SRP591195 GSE299409 SRX29129884 SRS25335609 \n", "12 SRP591195 GSE299409 SRX29129883 SRS25335608 \n", "13 SRP591195 GSE299409 SRX29129882 SRS25335607 \n", "14 SRP591195 GSE299409 SRX29129881 SRS25335606 \n", "15 SRP591195 GSE299409 SRX29129880 SRS25335605 \n", "16 SRP589942 GSE299005 SRX29052446 SRS25267580 \n", "17 SRP589942 GSE299005 SRX29052445 SRS25267579 \n", "18 SRP586001 GSE297427 SRX28837662 SRS25068573 \n", "19 SRP586001 GSE297427 SRX28837661 SRS25068574 \n", "\n", " sample_scientific_name experiment_library_strategy \\\n", "0 Homo sapiens RNA-Seq \n", "1 Homo sapiens RNA-Seq \n", "2 Homo sapiens RNA-Seq \n", "3 Homo sapiens RNA-Seq \n", "4 Homo sapiens RNA-Seq \n", "5 Homo sapiens RNA-Seq \n", "6 Homo sapiens RNA-Seq \n", "7 Homo sapiens RNA-Seq \n", "8 Mus musculus RNA-Seq \n", "9 Mus musculus RNA-Seq \n", "10 Mus musculus RNA-Seq \n", "11 Mus musculus RNA-Seq \n", "12 Mus musculus RNA-Seq \n", "13 Mus musculus RNA-Seq \n", "14 Mus musculus RNA-Seq \n", "15 Mus musculus RNA-Seq \n", "16 Mus musculus RNA-Seq \n", "17 Mus musculus RNA-Seq \n", "18 Homo sapiens/Mus musculus xenograft RNA-Seq \n", "19 Homo sapiens/Mus musculus xenograft RNA-Seq \n", "\n", " experiment_title \\\n", "0 GSM9192063: Sublibrary 8; Homo sapiens; RNA-Seq \n", "1 GSM9192062: Sublibrary 7; Homo sapiens; RNA-Seq \n", "2 GSM9192061: Sublibrary 6; Homo sapiens; RNA-Seq \n", "3 GSM9192060: Sublibrary 5; Homo sapiens; RNA-Seq \n", "4 GSM9192059: Sublibrary 4; Homo sapiens; RNA-Seq \n", "5 GSM9192058: Sublibrary 3; Homo sapiens; RNA-Seq \n", "6 GSM9192057: Sublibrary 2; Homo sapiens; RNA-Seq \n", "7 GSM9192056: Sublibrary 1; Homo sapiens; RNA-Seq \n", "8 GSM9038763: all mix sample 8; Mus musculus; RNA-Seq \n", "9 GSM9038762: all mix sample 7; Mus musculus; RNA-Seq \n", "10 GSM9038761: all mix sample 6; Mus musculus; RNA-Seq \n", "11 GSM9038760: all mix sample 5; Mus musculus; RNA-Seq \n", "12 GSM9038759: all mix sample 4; Mus musculus; RNA-Seq \n", "13 GSM9038758: all mix sample 3; Mus musculus; RNA-Seq \n", "14 GSM9038757: all mix sample 2; Mus musculus; RNA-Seq \n", "15 GSM9038756: all mix sample 1; Mus musculus; RNA-Seq \n", "16 GSM9030358: Cortical tissue, all 4 groups mixed, 6562; Mus musculus; RNA-Seq \n", "17 GSM9030357: Cortical tissue, all 4 groups mixed, 6142; Mus musculus; RNA-Seq \n", "18 GSM8991181: NK_CXCL10_2; Homo sapiens/Mus musculus xenograft; RNA-Seq \n", "19 GSM8991180: NK_CXCL10_1; Homo sapiens/Mus musculus xenograft; RNA-Seq \n", "\n", " run_1_accession \n", "0 SRR35085617 \n", "1 SRR35085618 \n", "2 SRR35085619 \n", "3 SRR35085620 \n", "4 SRR35085621 \n", "5 SRR35085622 \n", "6 SRR35085623 \n", "7 SRR35085624 \n", "8 SRR33926227 \n", "9 SRR33926228 \n", "10 SRR33926229 \n", "11 SRR33926230 \n", "12 SRR33926231 \n", "13 SRR33926232 \n", "14 SRR33926233 \n", "15 SRR33926234 \n", "16 SRR33831644 \n", "17 SRR33831645 \n", "18 SRR33609182 \n", "19 SRR33609183 " ] }, "metadata": {}, "output_type": "display_data" }, { "name": "stdout", "output_type": "stream", "text": [ "\n", "... and 480 more entries\n" ] } ], "source": [ "if not df.empty:\n", " # Select key columns for display\n", " key_columns = [\n", " \"study_accession\",\n", " \"study_alias\",\n", " \"experiment_accession\",\n", " \"sample_accession\",\n", " \"sample_scientific_name\",\n", " \"experiment_library_strategy\",\n", " \"experiment_title\",\n", " \"run_1_accession\",\n", " ]\n", "\n", " # Filter to only include columns that exist\n", " available_columns = [col for col in key_columns if col in df.columns]\n", "\n", " summary_df = df[available_columns].copy()\n", "\n", " print(\"\\nParse Bioscience Dataset Summary:\")\n", " print(f\"{'='*80}\\n\")\n", " display(summary_df.head(20)) # Show first 20 entries\n", "\n", " if len(summary_df) > 20:\n", " print(f\"\\n... and {len(summary_df) - 20} more entries\")" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Organize by Study (GSE)\n", "\n", "Group the data by study to see how many samples/runs belong to each GSE:" ] }, { "cell_type": "code", "execution_count": 6, "metadata": { "execution": { "iopub.execute_input": "2025-10-20T10:57:43.918185Z", "iopub.status.busy": "2025-10-20T10:57:43.918102Z", "iopub.status.idle": "2025-10-20T10:57:43.926954Z", "shell.execute_reply": "2025-10-20T10:57:43.926738Z", "shell.execute_reply.started": "2025-10-20T10:57:43.918177Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "\n", "Study-level Summary:\n", "================================================================================\n", "\n" ] }, { "data": { "text/html": [ "
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study_aliasnum_experimentsorganismsSRP_accession
40GSE27512760Homo sapiensSRP527234
53GSE29552752Homo sapiensSRP581094
43GSE28153548Homo sapiensSRP544328
4GSE22185338Homo sapiensSRP415300
11GSE23934727Mus musculusSRP451573
...............
13GSE2411421Mus musculusSRP455769
9GSE2336061Homo sapiensSRP439840
8GSE2335191Mus musculusSRP439692
2GSE1994981Mus musculusSRP366151
31GSE2622491Mus musculusSRP497297
\n", "

62 rows × 4 columns

\n", "
" ], "text/plain": [ " study_alias num_experiments organisms SRP_accession\n", "40 GSE275127 60 Homo sapiens SRP527234\n", "53 GSE295527 52 Homo sapiens SRP581094\n", "43 GSE281535 48 Homo sapiens SRP544328\n", "4 GSE221853 38 Homo sapiens SRP415300\n", "11 GSE239347 27 Mus musculus SRP451573\n", ".. ... ... ... ...\n", "13 GSE241142 1 Mus musculus SRP455769\n", "9 GSE233606 1 Homo sapiens SRP439840\n", "8 GSE233519 1 Mus musculus SRP439692\n", "2 GSE199498 1 Mus musculus SRP366151\n", "31 GSE262249 1 Mus musculus SRP497297\n", "\n", "[62 rows x 4 columns]" ] }, "metadata": {}, "output_type": "display_data" } ], "source": [ "if not df.empty and \"study_alias\" in df.columns:\n", " # Group by study and count entries\n", " studies_summary = (\n", " df.groupby(\"study_alias\")\n", " .agg(\n", " {\n", " \"experiment_accession\": \"count\",\n", " \"sample_scientific_name\": lambda x: (\n", " \", \".join(x.unique()) if hasattr(x, \"unique\") else str(x.iloc[0])\n", " ),\n", " \"study_accession\": \"first\",\n", " }\n", " )\n", " .rename(\n", " columns={\n", " \"experiment_accession\": \"num_experiments\",\n", " \"sample_scientific_name\": \"organisms\",\n", " \"study_accession\": \"SRP_accession\",\n", " }\n", " )\n", " .reset_index()\n", " )\n", "\n", " # Sort by number of experiments (descending)\n", " studies_summary = studies_summary.sort_values(\"num_experiments\", ascending=False)\n", "\n", " print(\"\\nStudy-level Summary:\")\n", " print(f\"{'='*80}\\n\")\n", " display(studies_summary)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Get Study Titles and Descriptions\n", "\n", "Extract study titles to understand what each dataset is about:" ] }, { "cell_type": "code", "execution_count": 7, "metadata": { "execution": { "iopub.execute_input": "2025-10-20T10:57:43.927319Z", "iopub.status.busy": "2025-10-20T10:57:43.927222Z", "iopub.status.idle": "2025-10-20T10:57:43.976167Z", "shell.execute_reply": "2025-10-20T10:57:43.975771Z", "shell.execute_reply.started": "2025-10-20T10:57:43.927310Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "\n", "Study Titles and Descriptions:\n", "================================================================================\n", "\n", "GSE: GSE306046\n", "SRP: SRP610621\n", "study_study_abstract: Single-cell transcriptomics (SCTr) offers a powerful platform for decoding the complexities of cellular stress responses to chemical exposures, capturing rare and transient subpopulations that can be obscured in bulk measurements. This study employs SCTr to profile the responses of HepaRG liver cell...\n", "study_study_title: Decoding cellular stress states for toxicology using single-cell transcriptomics [scRNA-Seq]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE299409\n", "SRP: SRP591195\n", "study_study_abstract: We used single-cell RNA sequencing with the Evercode™ WT kit (Parse Biosciences) to profile kidney immune cells in a mouse model of ischemia-reperfusion injury (IRI), with or without treatment with the SYK inhibitor Entospletinib. The dataset captures immune dynamics at early and late stages of inju...\n", "study_study_title: Effect of the SYK Inhibitor Entospletinib on Renal Inflammation and the Transition from Acute Kidney Injury to Chronic Kidney Disease Induced by Ischemia-Reperfusion Injury...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE299005\n", "SRP: SRP589942\n", "study_study_abstract: Neuropsychiatric complications including depression and cognitive decline develop in the years after traumatic brain injury (TBI), negatively affecting quality of life. Microglial and type 1 interferon (IFN-I) responses are associated with the transition from acute to chronic neuroinflammation after...\n", "study_study_title: Impaired cortical neuronal homeostasis and cognition after diffuse traumatic brain injury are dependent on microglia and type I interferon responses...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE297427\n", "SRP: SRP586001\n", "study_study_abstract: Osteosarcoma (OSA) has a dismal prognosis despite surgical resection and multiagent chemotherapy. While adoptive natural killer (NK) cell therapies have been successful in hematological malignancies, the application in solid tumors is challenging due to a tumor microenvironment (TME) that impairs NK...\n", "study_study_title: CXCL10-induced chemotaxis of ex vivo-expanded natural killer cells combined with NKTR-255 enhances anti-tumor efficacy in osteosarcoma...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE297299\n", "SRP: SRP585605\n", "study_study_abstract: Despite centuries of research, metastatic cancer remains incurable due to resistance against all conventional cancer therapeutics. Alternative strategies leveraging non-proliferative vulnerabilities in cancer are required to overcome cancer recurrence. Ferroptosis is an iron dependent cell death pat...\n", "study_study_title: Mismanagement of Cellular Iron Leads to Ferroptosis Susceptibility in Cancer Cells Surviving Chemotherapy...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE297023\n", "SRP: SRP584959\n", "study_study_abstract: Most cancers are diagnosed in people over the age of sixty, but little is known about how age impacts tumorigenesis. While aging is accompanied by mutation accumulation — widely understood to contribute to cancer risk — it is also associated with numerous other cellular and molecular changes likely ...\n", "study_study_title: Aging represses oncogenic KRAS-driven lung tumorigenesis and alters tumor suppression...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE296547\n", "SRP: SRP583610\n", "study_study_abstract: Human early embryos develop under physiological hypoxia, but how hypoxia regulates human lung organogenesis remains little known. We have investigated oxygen availability effects on the human lung epithelium using organoids. We find first-trimester lung epithelial progenitors remain undifferentiated...\n", "study_study_title: Hypoxia promotes airway differentiation in the human lung epithelium [scRNAseq_hypoxia_AT2]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE296244\n", "SRP: SRP582847\n", "study_study_abstract: A novel, cost-effective nucleic acid (NA) isolation method for purifying total NA, DNA, or RNA from both two- and three-dimensional cell cultures has been developed at the Norwegian University of Science and Technology utilizing NAxtra magnetic nanoparticles. This method achieves comparable yields t...\n", "study_study_title: Rapid DNA and RNA isolation from few or single cells using low-cost NAxtra magnetic nanoparticles...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE295527\n", "SRP: SRP581094\n", "study_study_abstract: The rapid development of updated and new commercially available single-cell transcriptomics platforms is providing a range of experimental options. Cost, sensitivity, throughput, flexibility, and ease of use influence that selection. We performed a comprehensive comparison of single-cell transcrip...\n", "study_study_title: Evaluating the practical aspects and performance of commercial single-cell RNA sequencing technologies...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE292745\n", "SRP: SRP572670\n", "study_study_abstract: Cerebral hemodynamics are crucial for brain homeostasis and serve as a key proxy for brain activity. Although this process involves coordinated interaction between vessels, neurons and glial cells, its dysregulation in neuroinflammation is not well understood. We used in vivo mesoscopic functional u...\n", "study_study_title: Induction of hemodynamic traveling waves by glial-driven vasomotion in a rat model of neuroinflammation: implications for functional neuroimaging...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE291674\n", "SRP: SRP569656\n", "study_study_abstract: Loss-of-function variants of the ABCA7 gene are associated with the increased risk of Alzheimer's disease (AD). How neuronal ABCA7 contributes to AD pathogenesis is unknown. Using neuron-specific Abca7 knockout mice (nAbca7-/-) with or without 5×FAD amyloid model background and postmortem AD brains,...\n", "study_study_title: Neuronal ABCA7 deficiency aggravates mitochondrial dysfunction and neurodegeneration in Alzheimer's disease [5xFAD_snRNAseq]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE289845\n", "SRP: SRP564833\n", "study_study_abstract: We performed single cell sequencing using the Parse Biosciences WT kit to evaluate changes in dendritic cell populations following induction of experimental autoimmune encephalomyelitis. Mice in this experiment previously received CD8+ T cells from donor mice that had been immunized with PLP178-191 ...\n", "study_study_title: Myelin-reactive CD8+ T cells influence conventional dendritic cell subsets towards a mature and regulatory phenotype in experimental autoimmune encephalomyelitis...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE287852\n", "SRP: SRP559435\n", "study_study_abstract: Transcription factor (TF) screens have enabled efficient production of a few cell types; however, engineering cell types that require complex TF combinations remains challenging. Here, we report an iterative, high-throughput single-cell TF screening method that enables identification of TF combinati...\n", "study_study_title: Iterative transcription factor screening enables rapid generation of microglia-like cells from human iPSC -Single cell transcriptome timecourse analysis of TFiMGLs after SCF-MCI (SPI1, FLI1, CEBPA, CEBPB, IRF8, and Mef2C) induction....\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE284207\n", "SRP: SRP551283\n", "study_study_abstract: A longstanding barrier in genome engineering with CRISPR-Cas9 has been the inability to measure Cas9 edit outcomes at single-cell resolution. Here we present Superb-seq, a new technology for joint measurement of on-target and off-target Cas9 edits and transcriptomes by single-cell RNA sequencing. In...\n", "study_study_title: Joint single-cell profiling of Cas9 edits and transcriptomes determines on- and off-target regulatory effects...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE283186\n", "SRP: SRP548416\n", "study_study_abstract: The human nephron is a highly patterned tubular structure. Approximately 1 million nephrons form in each kidney during embryonic and fetal development and develop specialized cells that regulate bodily fluid homeostasis, blood pressure, and urine secretion throughout life. This raises the question o...\n", "study_study_title: Axial Nephron Fate Switching Demonstrates a Plastic System Tunable on Demand...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE283038\n", "SRP: SRP548062\n", "study_study_abstract: CD4? T cells are believed to be essential for effective CD8? T cell responses against hepatotropic viruses like hepatitis B virus (HBV). However, the specific locations and the cellular and molecular mechanisms through which CD4? T cells help CD8? T cells remain unclear. In this study, we generated ...\n", "study_study_title: CD4+ T cells license Kupffer cells to reverse the CD8+ T cell dysfunction induced by hepatocellular priming...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE282851\n", "SRP: SRP547691\n", "study_study_abstract: Epigenetic dysregulation is widespread in cancer. However, the specific epigenetic regulators and the processes they control to drive cancer phenotypes are poorly understood. We employed a novel, scalable and high-throughput in vivo method to perform iterative functional screens of >250 epigenetic r...\n", "study_study_title: Functional mapping of epigenomic regulators uncovers coordinated tumor suppression by the HBO1 and MLL1 complexes [scRNA-seq]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE281932\n", "SRP: SRP545300\n", "study_study_abstract: Whilst M. bovis Bacillus Calmette-Guérin (BCG) therapy remains the gold-standard for treatment of high-risk non-muscle invasive bladder cancer (BC), 30-40% of patients fail therapy, resulting in disease recurrence and progression. Loss of glutathione-S-transferase theta 2 (GSTT2) expression has been...\n", "study_study_title: Glutathione-S-transferase theta 2 (GSTT2) modulates the tumor microenvironment and the response to BCG immunotherapy in a murine orthotopic model of bladder cancer...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE281535\n", "SRP: SRP544328\n", "study_study_abstract: Midbrain dopaminergic neuron (mDA) differentiation protocols for Parkinson's disease (PD) modeling and cell replacement therapy lack comprehensive transcriptomic evaluations against in vivo references. To address this, we constructed an integrated human fetal whole brain atlas and a midbrain subatla...\n", "study_study_title: BrainSTEM: A multi-resolution fetal brain atlas to assess the fidelity of human midbrain cultures...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE280717\n", "SRP: SRP542211\n", "study_study_abstract: Obesity affects the progress of lung cancer. To understand this more, we performed single-cell RNA sequencing of dissociated tumors of four mouse lung cancer cell-lines grown subcutaneously in adult male C57BL/6 mice with and without high-fat diet-induced obesity. Overall design: Groups (n = 6-8) of...\n", "study_study_title: Gene expression profile at single cell level of mouse lung cancer cell-line tumors grown subcutaneously in adult male C57BL/6 mice with and without high-fat diet-induced obesity...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE278923\n", "SRP: SRP536902\n", "study_study_abstract: In this study, we performed single-cell RNA sequencing of E6, E7, E8 and E9 chick cerebella to analyze diversity in in Purkinje cells during development. Overall design: Single-cell suspensions of embryonic chick cerebellum were prepared following the protocols recommended by 10x Genomics. Subseque...\n", "study_study_title: Heterogeneity of Purkinje cells orchestrates cerebellar development....\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE275127\n", "SRP: SRP527234\n", "study_study_abstract: An in vitro model of human meiosis would accelerate research into this important reproductive process and development of therapies for infertility. We have developed a method to induce meiosis starting from male or female human pluripotent stem cells. We demonstrate that DNMT1 inhibition, retinoid s...\n", "study_study_title: Induction of meiosis from human pluripotent stem cells [Bisulfite-seq]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE273089\n", "SRP: SRP522182\n", "study_study_abstract: Human embryos develop under physiological hypoxia, but how hypoxia directly affects human organogenesis remains unknown. We have investigated the effects of hypoxia on human lung epithelia using organoids. First trimester lung epithelial progenitors remain undifferentiated under normoxia, but initia...\n", "study_study_title: Hypoxia promotes airway differentiation in the human lung epithelium...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE272840\n", "SRP: SRP521574\n", "study_study_abstract: In search for broad-spectrum antivirals, we discovered a small molecule inhibitor, RMC-113, that potently suppresses the replication of multiple RNA viruses including SARS-CoV-2 in human lung organoids. We demonstrated selective dual inhibition of the lipid kinases PIP4K2C and PIKfyve by RMC-113 and...\n", "study_study_title: PIP4K2C inhibition reverses autophagic flux impairment induced by SARS-CoV-2...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE272713\n", "SRP: SRP521155\n", "study_study_abstract: Abstract: The effects of immunodeficiency associated with chronic HIV infection on COVID-19 disease and viral persistence have not been directly addressed in a controlled setting. In this pilot study, we exposed two pigtail macaques (PTMs) chronically infected with SIVmac239, exhibiting from very lo...\n", "study_study_title: The Impact of SIV-Induced Immunodeficiency on SARS-CoV-2 Disease, Viral Dynamics, and Antiviral Immune Response in a Nonhuman Primate Model of Coinfection...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE271203\n", "SRP: SRP517284\n", "study_study_abstract: Pregnant women may be prescribed opioid drugs for pain or may abuse these drugs. The placenta may be key to understanding how opioids cause adverse pregnancy outcomes. Maternal oxycodone (OXY) exposure of pregnant mice leads to disturbances in the layer of invasive parietal trophoblast giant cells (...\n", "study_study_title: Transcriptome Profile of Mouse Trophoblast Giant Cells:Effects of Oxycodone on these and other Placental Lineages...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE268385\n", "SRP: SRP510112\n", "study_study_abstract: An in vitro model of human meiosis would accelerate research into this important reproductive process and development of therapies for infertility. We have developed a method to induce meiosis starting from male or female human pluripotent stem cells. We demonstrate that DNMT1 inhibition, retinoid s...\n", "study_study_title: Induction of meiosis from human pluripotent stem cells...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE264678\n", "SRP: SRP503652\n", "study_study_abstract: The kidney maintains fluid homeostasis by reabsorbing essential compounds and excreting waste. Proximal tubule cells, crucial for reabsorbing sugars, ions, and amino acids, are highly susceptible to injury, often leading to pathologies necessitating dialysis or transplants. Human pluripotent stem ce...\n", "study_study_title: Controlling proximal nephron precursor differentiation to generate proximal-biased kidney organoids with emerging maturity [scRNA-Seq]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE263863\n", "SRP: SRP501450\n", "study_study_abstract: Obesity is a global pandemic and a key risk factor for several neurodegenerative diseases including Alzheimer's disease (AD), Parkinson's disease, or dementia. The neurovascular unit (NVU), essential for blood-brain barrier (BBB) integrity and comprised of endothelial cells, glial cells (microglia a...\n", "study_study_title: Effect of obesity on the neurovascular unit transcriptome in the female mice hippocampus using single nuclei RNA seq...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE263619\n", "SRP: SRP500730\n", "study_study_abstract: Muscle stem cells (MuSCs) are specialized cells that reside in adult skeletal muscle poised to repair muscle tissue. The ability of MuSCs to regenerate damaged tissues declines markedly with aging and in diseases such as Duchenne muscular dystrophy, but the underlying causes of MuSC dysfunction rema...\n", "study_study_title: Hydrogel biomaterials that stiffen and soften on demand reveal that skeletal muscle stem cells harbor a mechanical memory...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE262249\n", "SRP: SRP497297\n", "study_study_abstract: Obesity is a global pandemic and a key risk factor for several neurodegenerative diseases including Alzheimer's disease (AD), Parkinson's disease, or dementia. The neurovascular unit (NVU), essential for blood-brain barrier (BBB) integrity and comprised of endothelial cells, glial cells (microglia a...\n", "study_study_title: Single cell transcriptomics reveals obesity-induced endothelial and neurovascular dysfunction in brain: implications for cognitive decline...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE262111\n", "SRP: SRP496942\n", "study_study_abstract: Early childhood tumours arise from transformed embryonic cells, which often carry large copy number alterations (CNA). However, it remains unclear how CNAs contribute to embryonic tumourigenesis due to a lack of suitable models. Here we employ female human embryonic stem cell (hESC) differentiation ...\n", "study_study_title: A human neural crest model reveals the developmental impact of neuroblastoma-associated chromosomal aberrations [Parse scRNA-seq]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE221853\n", "SRP: SRP415300\n", "study_study_abstract: Early childhood tumours arise from transformed embryonic cells, which often carry large copy number alterations (CNA). However, it remains unclear how CNAs contribute to embryonic tumourigenesis due to a lack of suitable models. Here we employ female human embryonic stem cell (hESC) differentiation ...\n", "study_study_title: A human neural crest model reveals the developmental impact of neuroblastoma-associated chromosomal aberrations [10x scRNA-seq]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE256359\n", "SRP: SRP491042\n", "study_study_abstract: Results: Megakaryocytes gain immune characteristics over the course of murine bone marrow failure; Megakaryocytes with immune characteristics serve as antigen-presenting cells and suppress hematopoietic stem cell function. Conclusion: Our results demonstrate the acquisition of immune functions by ma...\n", "study_study_title: Mature Megakaryocytes Acquire Immune Characteristics in a Mouse Model of Aplastic Anemia...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE255851\n", "SRP: SRP489876\n", "study_study_abstract: To determine the gene expression changes in the retina of miR-204/miR-211 RPE conditional knockout (dKO) mice, we collected retina samples from dKO and controls animals at 6 months of degeneration, generated single-cell suspensions, and created scRNA-seq libraries (Parse Biosciences), and sequened t...\n", "study_study_title: Deletion of miR-204 and miR-211 in murine retinal pigment epithelium results in slow retinal degeneration...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE228214\n", "SRP: SRP429342\n", "study_study_abstract: Due to the limitations of available in vitro systems and animal models, we lack a detailed understanding of the pathogenetic mechanisms and have minimal treatment options for liver fibrosis. To overcome this barrier, we engineered a live cell imaging system that identifies collagen producing cells i...\n", "study_study_title: Characterization of Pro-Fibrotic Signaling Pathways in Human Hepatic Organoids...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE253642\n", "SRP: SRP484595\n", "study_study_abstract: Astrocyte diversity is greatly influenced by local environmental modulation. In this study, we analyzed the impact of ciliary deficient astrocytes on astrocytes' intercellular communications and neuronal transcriptomes in the brain. Our analysis revealed a broad disturbance of astrocyte intercellula...\n", "study_study_title: Single nuclei RNAseq datasets supporting the impact of primary cilia deficiency on astrocytes' intercellular connectivity and neuronal transcriptomes in the brain....\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE253539\n", "SRP: SRP484450\n", "study_study_abstract: Osteoarthritis (OA) is a chronic, debilitating disease with no available disease-modifying drugs with end-stage surgery being the only treatment option. Biomarker identification in blood specimens of OA patients has hitherto been limited to serum proteins and bulk transcriptomics and epigenomic feat...\n", "study_study_title: Single-cell mass cytometry and transcriptomic profiling of circulating immune cells identifies an expansion of CD25hi switched memory B cells in Osteoarthritis...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE253406\n", "SRP: SRP484103\n", "study_study_abstract: Single-cell RNA sequencing experiments commonly use 10x Genomics kits due to their high-throughput capacity and standardized protocols. Recently, Parse Biosciences introduced an alternative technology that uses multiple in-situ barcoding rounds within standard 96-well plates. The Parse technology al...\n", "study_study_title: Split-pool combinatorial barcoding sequencing of murine immune cells...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE253230\n", "SRP: SRP483695\n", "study_study_abstract: Angelman syndrome is a neurodevelopmental disorder caused by (epi)genetic lesions of maternal UBE3A. Research has focused largely on the role of UBE3A in neurons due to its imprinting in that cell type. Yet, evidence suggests there may be broader neurodevelopmental impacts of UBE3A dysregulation. Hu...\n", "study_study_title: Loss of UBE3A impacts both neuronal and non-neuronal cells in human cerebral organoids....\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE252604\n", "SRP: SRP482143\n", "study_study_abstract: Systemic immune responses induced by chronic hypercholesterolemia contribute to the initiation, progression and complications of atherosclerosis. However, the consequences of an alternate high fat diet and the associated variations in plasma cholesterol levels on atherosclerosis are unknown. To addr...\n", "study_study_title: Alternate high fat diet aggravates atherosclerosis through an IL1b-dependent reprogramming of neutrophil progenitors...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE252185\n", "SRP: SRP480475\n", "study_study_abstract: Autism spectrum disorder (ASD) is characterized by a complex etiology, with genetic determinants significantly influencing its manifestation. Among these, the Scn2a gene emerges as a pivotal player, crucially involved in oligodendrocyte (OL) function. The present study elucidates the underexplored r...\n", "study_study_title: Scn2a deletion disrupts oligodendroglia function: Implication for myelination, neural circuitry, and auditory hypersensitivity in ASD....\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE250009\n", "SRP: SRP477682\n", "study_study_abstract: A major challenge to the study and treatment of neurogenetic syndromes is the difficulty in gaining access to live neurons from individuals with these disorders. Although other sources of stem cells are currently available for differentiation into neurons, these can involve invasive procedures and b...\n", "study_study_title: Single Cell Sequencing of Prader-Wlli Syndrome Dental Pulp Stem Cell-derived Neurons...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE249558\n", "SRP: SRP476292\n", "study_study_abstract: To define the regulatory role of Sox9 in intrahepatic biliary epithelium, we conducted single cell RNA-seq on biliary epithelial cells (BECs) from adult control (Sox9fl/fl) and conditional Sox9 knockout (Sox9cKO; Sox9fl/fl:Albumin-Cre) mice. Livers were dissociated to single cells and BECs isolated ...\n", "study_study_title: Single cell RNA-seq of Sox9-deficient intrahepatic biliary epithelial cells...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE172289\n", "SRP: SRP315237\n", "study_study_abstract: Our brains accommodate a largely folded cerebral cortex that associates to our advanced brain functions. Several theories have been proposed to explain the cortical folding process, reasoning the mechanical forces as neuronal tension in underlying layers, cellular expansion and glial progenitor's di...\n", "study_study_title: Gene regulatory landscape of cerebral cortex folding...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE246624\n", "SRP: SRP469371\n", "study_study_abstract: Single-cell RNA sequencing (scRNA-seq) has emerged as a powerful technique for investigating biological heterogeneity at the single-cell level in human systems and model organisms. Recent advances in scRNA-seq have enabled the pooling of cells from multiple samples into single libraries, thereby inc...\n", "study_study_title: Comparative analysis of single-cell RNA sequencing methods with and without sample multiplexing...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE246140\n", "SRP: SRP468167\n", "study_study_abstract: Multiple myeloma is a largely incurable and life-threatening malignancy of antibody-secreting plasma cells. An effective and widely available animal model that recapitulates human myeloma and related plasma cell disorders is lacking. We show that busulfan-conditioned hIL-6 transgenic NSG mice (NSG+h...\n", "study_study_title: Human IL-6 fosters long-term engraftment of human patient derived myeloma cells in immunodeficient mice...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE244321\n", "SRP: SRP463843\n", "study_study_abstract: We performed single cell RNA-sequencing (scRNA-Seq) of testes from bovine fetuses derived from either CRISPR/Cas9 NANOS3 knockout (KO; NANOS3 -/-) or wildtype control (NANOS3 +/+) embryos. The scRNA-Seq analysis showed a complete loss of primordial germ cells (PGCs) and gonocytes in NANOS3 KO fetal ...\n", "study_study_title: scRNA-Seq of bovine fetal testes derived from NANOS3 knockout and wildtype embryos...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE243135\n", "SRP: SRP460338\n", "study_study_abstract: A hallmark of idiopathic pulmonary fibrosis (IPF) and other interstitial lung diseases is dysregulated repair of the alveolar epithelium. The Hippo pathway effector transcription factors YAP and TAZ are implicated as essential for type 1 and type 2 alveolar epithelial cell (AT1 and AT2) differentiat...\n", "study_study_title: Epithelial Yap/Taz are required for functional alveolar regeneration following acute lung injury...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE241693\n", "SRP: SRP457001\n", "study_study_abstract: Type II diabetes mellitus (T2D) is a chronic metabolic disease, and a risk factor for cardiovascular disease and cerebrovascular dysfunction including vascular dementia. Sex differences in the prevalence of T2D, dementia, and global genomic changes in the brain have been observed; however, most stud...\n", "study_study_title: The global genomic profile of hippocampal endothelial cells in fefemale diabetic mice is associated with cognitive dysfunction via alterations in cell adhesion and vascular permeability....\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE241543\n", "SRP: SRP456813\n", "study_study_abstract: Organs are the ensemble of different cell types in a complex architectural milieu. It is well-known that progression through fate decisions sets up the complex cellular makeup and architecture of an organ, but how that same architecture may impact on cell fate is less clear. We sought to examine thi...\n", "study_study_title: Tissue morphology influences the temporal program of human cerebral organoids...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE241142\n", "SRP: SRP455769\n", "study_study_abstract: Diabetes (DM) increases cardiovascular and cerebrovascular disease risk. However, the mechanism of DM-associated microvascular dysfunction and neuroinflammation remain unknown. We present a global assessment of endothelial cell-specific gene expression and integrated transcriptomics directly address...\n", "study_study_title: Single nuclei transcriptomics reveals altered endothelial cell function, permeability, and cognition in diabetic mice....\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE240096\n", "SRP: SRP453503\n", "study_study_abstract: Rationale: Multiciliated cell (MCC) loss/dysfunction is common in the small airways of patients with COPD but it is unclear if this contributes to COPD lung pathology. Objectives: To determine whether loss of MCCs causes a COPD-like phenotype in mice and explore a potential role for the transcriptio...\n", "study_study_title: Loss of p73 contributes to COPD...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE239347\n", "SRP: SRP451573\n", "study_study_abstract: We wanted to transcriptomically compare single cells taken from the retinas of C57BL6/J mice, Abca4-/-Rdh8-/- (dKO) mutant mice, and Abca4PV/PVRdh8-/- (PVR) mutant mice before and at an early (24-hour post-bleach) timepoint post-bleaching, to see if the two Abca4 mutants displayed different transcri...\n", "study_study_title: Distinct mouse models of Stargardt disease display differences in pharmacological targeting of ceramides and inflammatory responses...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE236902\n", "SRP: SRP448303\n", "study_study_abstract: Ocular lens development entails epithelial to fiber cell differentiation, defects in which cause congenital cataract. We report the first single-cell multiomic atlas of lens development, leveraging snRNA-seq, snATAC-seq, and CUT&RUN-seq to discover novel mechanisms of cell fate determination and cat...\n", "study_study_title: Integrated single-cell multiomics uncovers foundational regulatory mechanisms of lens development and pathology [scRNA-seq]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE233606\n", "SRP: SRP439840\n", "study_study_abstract: This dataset describes human induced pluripotent stem cells as they differentiate into somite progenitors, and the consequences of dystrophin deficiency on the transcriptome of these single cells Overall design: hiPSCs from three cell lines (Healthy, DMD, CRISPR) were collected at Day 10 of a myogen...\n", "study_study_title: Dystrophin deficiency hampers cell state transitions during somite development...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE233519\n", "SRP: SRP439692\n", "study_study_abstract: Our parallel studies have shown that the OLIG2 inhibitor CT-179 and the TLR7/8 agonist resiquimod delivered in polyoxazoline nanoparticle (Pox-resiquimod) produce significant anti tumor effects when administered to mice with SHH medulloblastoma. To gain insight into the cellular events set in motion...\n", "study_study_title: scRNA-seq analysis of SHH medulloblastomas in Gfap-Cre/SmoM2 mice treated with CT-179 or Pox-resiquimod...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE229617\n", "SRP: SRP432473\n", "study_study_abstract: Functional precision medicine (FPM) aims to match the right patients to the right drugs by using specific features of the individual's cancer cells. Recently, FPM has been propelled by technologies that enable high throughput ex vivo drug profiling to tailor treatments for individual patients. Here,...\n", "study_study_title: Functional drug testing of pediatric acute lymphocytic leukemia cells by single-cell transcriptome sequencing for mapping cellular drug response...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE225497\n", "SRP: SRP423074\n", "study_study_abstract: Striatal neurons and striatal DA neuron fusions make up the mesolimbic pathway and respond to substances of abuse. We use scRNAseq to define the composition of our culture conditions and study their transcriptional responses to dopamine, cocaine, and morphine. Overall design: We use scRNAseq to defi...\n", "study_study_title: Gene expression profile of 2-D or 3-D neural cultures derived from an H1 hESC cell line...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE214374\n", "SRP: SRP400047\n", "study_study_abstract: Mammalian prion diseases are fatal and transmissible neurological conditions caused by the propagation of prions, self-replicating multimeric assemblies of misfolded forms of host cellular prion protein. Despite extensive studies investigating the changes in transcriptional profiles in prion disease...\n", "study_study_title: Single-cell transcriptomics of mammalian prion diseases identifies dynamic gene signatures shared between species [human_scRNAseq]...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE199498\n", "SRP: SRP366151\n", "study_study_abstract: We performed single cell RNA-sequencing of lungs from APOE knock-in mice in the absence of infection or four days post infection with SARS-CoV-2 MA10. Infected mice showed major remodeling of the cellular composition with expansion of myeloid cells and relative depletion of epithelial cells. In infe...\n", "study_study_title: scRNAseq of lungs from APOE knock-in mice with COVID-19...\n", "--------------------------------------------------------------------------------\n", "\n", "GSE: GSE183965\n", "SRP: SRP336717\n", "study_study_abstract: Dysregulation of macrophage populations at the wound site is responsible for the non-healing state of chronic wounds. The molecular mechanisms underlying macrophage dysfunction and its control in diabetes are largely unexplored on an epigenetic level. Here, we report that acetyl histone-H3 (Lys27), ...\n", "study_study_title: Acetylation State of Histone Core Defines Macrophage Dynamics in Diabetic Wounds...\n", "--------------------------------------------------------------------------------\n", "\n" ] } ], "source": [ "if not df.empty:\n", " title_cols = [\n", " col\n", " for col in df.columns\n", " if \"study_title\" in col.lower() or \"study_abstract\" in col.lower()\n", " ]\n", "\n", " if title_cols and \"study_alias\" in df.columns:\n", " # Get unique study information\n", " study_info_cols = [\"study_alias\", \"study_accession\"] + title_cols\n", " study_info_cols = [col for col in study_info_cols if col in df.columns]\n", "\n", " study_info = df[study_info_cols].drop_duplicates(subset=[\"study_alias\"])\n", "\n", " print(\"\\nStudy Titles and Descriptions:\")\n", " print(f\"{'='*80}\\n\")\n", "\n", " for idx, row in study_info.iterrows():\n", " print(f\"GSE: {row['study_alias']}\")\n", " print(f\"SRP: {row['study_accession']}\")\n", "\n", " for col in title_cols:\n", " if col in row and pd.notna(row[col]):\n", " print(f\"{col}: {row[col][:300]}...\") # Truncate long descriptions\n", " print(f\"{'-'*80}\\n\")" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Save Results\n", "\n", "Save the complete results to a file for further analysis:" ] }, { "cell_type": "code", "execution_count": 8, "metadata": { "execution": { "iopub.execute_input": "2025-10-20T10:57:43.976894Z", "iopub.status.busy": "2025-10-20T10:57:43.976787Z", "iopub.status.idle": "2025-10-20T10:57:44.516426Z", "shell.execute_reply": "2025-10-20T10:57:44.516061Z", "shell.execute_reply.started": "2025-10-20T10:57:43.976884Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Full results saved to: parse_bioscience_datasets.tsv\n", "Study summary saved to: parse_bioscience_studies_summary.tsv\n", "\n", "Total datasets found: 500\n", "Total unique studies: 62\n" ] } ], "source": [ "if not df.empty:\n", " # Save full results\n", " output_file = \"parse_bioscience_datasets.tsv\"\n", " df.to_csv(output_file, sep=\"\\t\", index=False)\n", " print(f\"Full results saved to: {output_file}\")\n", "\n", " # Also save the study-level summary\n", " if \"studies_summary\" in locals():\n", " summary_file = \"parse_bioscience_studies_summary.tsv\"\n", " studies_summary.to_csv(summary_file, sep=\"\\t\", index=False)\n", " print(f\"Study summary saved to: {summary_file}\")\n", "\n", " print(f\"\\nTotal datasets found: {len(df)}\")\n", " print(\n", " f\"Total unique studies: {len(unique_studies) if 'unique_studies' in locals() else 'N/A'}\"\n", " )" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Alternative Search Strategies\n", "\n", "Since Parse Bioscience datasets might not always explicitly mention \"Parse Bioscience\" in metadata, here are alternative search strategies:\n", "\n", "### 1. Search for SPLiT-seq (Parse's technology)\n", "Parse Biosciences uses SPLiT-seq (split-pool ligation-based transcriptome sequencing) technology." ] }, { "cell_type": "code", "execution_count": 9, "metadata": { "execution": { "iopub.execute_input": "2025-10-20T10:57:44.517202Z", "iopub.status.busy": "2025-10-20T10:57:44.517099Z", "iopub.status.idle": "2025-10-20T10:57:56.107603Z", "shell.execute_reply": "2025-10-20T10:57:56.107145Z", "shell.execute_reply.started": "2025-10-20T10:57:44.517191Z" } }, "outputs": [ { "name": "stdout", "output_type": "stream", "text": [ "Searching for SPLiT-seq / combinatorial indexing datasets...\n", "This may include Parse Bioscience and similar technologies.\n", "\n" ] }, { "name": "stderr", "output_type": "stream", "text": [ "100%|██████████████████████████████████████████████████████████████████████████| 100/100 [00:04<00:00, 20.64it/s]\n" ] }, { "name": "stdout", "output_type": "stream", "text": [ "Found 100 entries with SPLiT-seq/combinatorial indexing\n", "\n", "================================================================================\n", "Other useful search terms for Parse/single-cell datasets:\n", "- 'Parse Evercode' (Parse's platform name)\n", "- 'combinatorial barcoding'\n", "- Specific organisms: 'Parse Bioscience Homo sapiens'\n", "================================================================================\n" ] } ], "source": [ "# Search for SPLiT-seq technology\n", "print(\"Searching for SPLiT-seq / combinatorial indexing datasets...\")\n", "print(\"This may include Parse Bioscience and similar technologies.\\n\")\n", "\n", "split_seq_instance = GeoSearch(\n", " verbosity=2,\n", " return_max=100,\n", " geo_query=\"SPLiT-seq OR split-seq OR combinatorial indexing single cell\",\n", ")\n", "\n", "split_seq_instance.search()\n", "split_seq_df = split_seq_instance.get_df()\n", "\n", "if not split_seq_df.empty:\n", " print(f\"Found {len(split_seq_df)} entries with SPLiT-seq/combinatorial indexing\")\n", "\n", " if \"study_alias\" in split_seq_df.columns:\n", " split_seq_studies = split_seq_df[\"study_alias\"].unique()\n", " print(f\"Unique studies: {len(split_seq_studies)}\")\n", " print(f\"\\nGSE IDs: {sorted(split_seq_studies)}\")\n", "\n", " # Show organisms\n", " if \"sample_scientific_name\" in split_seq_df.columns:\n", " print(f\"\\nOrganisms:\")\n", " print(split_seq_df[\"sample_scientific_name\"].value_counts())\n", "else:\n", " print(\"No results found with SPLiT-seq search\")\n", "\n", "# You can also try other search terms\n", "print(\"\\n\" + \"=\" * 80)\n", "print(\"Other useful search terms for Parse/single-cell datasets:\")\n", "print(\"- 'Parse Evercode' (Parse's platform name)\")\n", "print(\"- 'combinatorial barcoding'\")\n", "print(\"- Specific organisms: 'Parse Bioscience Homo sapiens'\")\n", "print(\"=\" * 80)" ] }, { "cell_type": "markdown", "metadata": {}, "source": [ "## Command Line Usage\n", "\n", "You can also perform this search from the command line:\n", "\n", "```bash\n", "## # Basic search for Parse Bioscience datasets\n", "pysradb search --db geo \\\n", " --geo-query \"Parse Bioscience\" \\\n", " --max 500 \\\n", " --verbosity 3 \\\n", " --saveto parse_bioscience_results.tsv\n", "\n", "## # Search for SPLiT-seq technology\n", "pysradb search --db geo \\\n", " --geo-query \"SPLiT-seq OR split-seq\" \\\n", " --max 200 \\\n", " --verbosity 2 \\\n", " --saveto split_seq_results.tsv\n", "\n", "## # Search with organism filter\n", "pysradb search --db geo \\\n", " --geo-query \"Parse Bioscience\" \\\n", " --organism \"Homo sapiens\" \\\n", " --max 200 \\\n", " --saveto parse_human_results.tsv\n", "\n", "## # Note: Date filtering can be added with --publication-date flag\n", "## # but may miss some results due to how GEO indexes publication dates\n", "## # Example: --publication-date 01-01-2020:31-12-2024\n", "```" ] } ], "metadata": { "kernelspec": { "display_name": "Python 3", "language": "python", "name": "python3" }, "language_info": { "codemirror_mode": { "name": "ipython", "version": 3 }, "file_extension": ".py", "mimetype": "text/x-python", "name": "python", "nbconvert_exporter": "python", "pygments_lexer": "ipython3", "version": "3.11.12" } }, "nbformat": 4, "nbformat_minor": 4 } ================================================ FILE: notebooks/README.md ================================================ # Notebooks demonstrating functionalities of pysradb 1. [Python API](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/01.Python-API_demo.ipynb) 2. [Downloading datasets from SRA - command line](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/02.Commandline_download.ipynb) 3. [Parallely download multiple datasets - Python API](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/03.ParallelDownload.ipynb) 4. [Converting SRA-to-fastq - command line (requires conda)](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/04.SRA_to_fastq_conda.ipynb) 5. [Downloading subsets of a project - Python API](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/05.Downloading_subsets_of_a_project.ipynb) 6. [Metadata for multiple SRPs](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/06.Multiple_SRPs.ipynb) 7. [Searching SRA/GEO/ENA](https://colab.research.google.com/github/saketkc/pysradb/blob/master/notebooks/07.Query_Search.ipynb) ================================================ FILE: pyproject.toml ================================================ [build-system] requires = ["hatchling"] build-backend = "hatchling.build" [project] name = "pysradb" dynamic = ["version"] description = "A Python package for interacting with SRAdb and downloading datasets from SRA/ENA/GEO" readme = "README.md" license = {file = "LICENSE"} requires-python = ">=3.9" authors = [{ name = "Saket Choudhary", email = "saketkc@gmail.com" }] classifiers = [ "Development Status :: 5 - Production/Stable", "Intended Audience :: Science/Research", "License :: OSI Approved :: BSD License", "Programming Language :: Python :: 3", "Programming Language :: Python :: 3.9", "Programming Language :: Python :: 3.10", "Programming Language :: Python :: 3.11", "Programming Language :: Python :: 3.12", "Programming Language :: Python :: 3.13", "Topic :: Scientific/Engineering :: Bio-Informatics", ] dependencies = [ "lxml>=4.6.3", "pandas>=1.3.2", "requests>=2.26.0", "rich>=10.0.0", "tqdm>=4.62.1", "xmltodict>=0.12.0", ] [project.optional-dependencies] enrichment = ["instructor>=1.0.0", "pydantic>=2.0.0", "sentence-transformers>=2.0.0"] docs = [ "sphinx>=4.0", "furo>=2023.0.0", "sphinx-tabs>=3.4.1", "numpydoc>=1.5.0", "nbsphinx>=0.8.0", "myst-parser>=0.18.0", "ipython>=7.0", "sphinxcontrib-gtagjs>=0.2", "sphinx-panels>=0.5.2", ] all = [ "pysradb[enrichment,docs]", ] [project.scripts] pysradb = "pysradb.cli:parse_args" [project.urls] Homepage = "https://saket-choudhary.me/pysradb" [tool.hatch.version] path = "pysradb/__init__.py" ================================================ FILE: pysradb/__init__.py ================================================ # -*- coding: utf-8 -*- """Top-level package for pysradb.""" __author__ = """Saket Choudhary""" __email__ = "saketkc@gmail.com" __version__ = "3.0.0.dev0" from .filter_attrs import expand_sample_attribute_columns from .geoweb import GEOweb, download_geo_matrix, parse_geo_matrix_to_tsv from .sraweb import SRAweb ================================================ FILE: pysradb/__main__.py ================================================ import sys from .cli import parse_args if __name__ == "__main__": parse_args(sys.argv[1:]) ================================================ FILE: pysradb/cli.py ================================================ """Command line interface for pysradb""" import argparse import os import re import sys import warnings from io import StringIO from textwrap import dedent import pandas as pd from rich.columns import Columns from rich.console import Console from rich.panel import Panel from rich.table import Table from rich.text import Text from . import __version__ from .exceptions import IncorrectFieldException, MissingQueryException from .geoweb import GEOweb, download_geo_matrix, parse_geo_matrix_to_tsv from .search import EnaSearch, GeoSearch, SraSearch from .sraweb import SRAweb from .utils import confirm pd.set_option("display.max_rows", None) pd.set_option("display.max_columns", None) warnings.simplefilter(action="ignore", category=FutureWarning) console = Console() class CustomFormatterArgP( argparse.ArgumentDefaultsHelpFormatter, argparse.RawDescriptionHelpFormatter ): pass class ArgParser(argparse.ArgumentParser): def error(self, message): sys.stderr.write("error: %s\n" % message) self.print_help() sys.exit(2) def pretty_print_df(df, include_header=True): """Pretty print dataframe using rich formatting""" def format_value(v): """Convert value to string, handling None and pd.NA""" if v is None or pd.isna(v): return "[dim]-[/dim]" return str(v) if df.empty: console.print("[bright_black]No results found[/bright_black]") return try: terminal_width = console.width except: terminal_width = 80 # fallback width num_columns = len(df.columns) min_col_width = 12 # minimum width per column for readability padding = 2 # padding between columns border_space = 4 # table borders # how many columns fit max_cols_per_table = (terminal_width - border_space) // (min_col_width + padding) # chuenk if num_columns > max_cols_per_table: console.print( f"[bright_black]Displaying {num_columns} columns in chunks of {max_cols_per_table}[/bright_black]" ) console.print() for i in range(0, num_columns, max_cols_per_table): chunk_cols = df.columns[i : i + max_cols_per_table] chunk_df = df[chunk_cols] console.print( f"[bright_blue]Columns {i+1}-{min(i+max_cols_per_table, num_columns)}:[/bright_blue]" ) _create_table(chunk_df, terminal_width, include_header, format_value) console.print() else: _create_table(df, terminal_width, include_header, format_value) def _create_table(df, terminal_width, include_header, format_value): """Helper function to create a rich table with appropriate sizing""" num_columns = len(df.columns) min_col_width = 12 padding = 2 border_space = 4 available_width = terminal_width - border_space - (padding * (num_columns - 1)) col_widths = [] for column in df.columns: col_name = str(column) sample_data = df[column].head(10).astype(str) max_content_len = max( len(col_name), sample_data.str.len().max() if len(sample_data) > 0 else 0 ) col_widths.append(max_content_len) total_content_width = sum(col_widths) if total_content_width > available_width: scale_factor = available_width / total_content_width final_widths = [max(min_col_width, int(w * scale_factor)) for w in col_widths] else: final_widths = [ max(min_col_width, min(w, available_width // num_columns + 5)) for w in col_widths ] table = Table( show_header=include_header, header_style="bold bright_blue", border_style="bright_black", show_lines=True, padding=(0, 1), box=None, collapse_padding=False, width=terminal_width - 2, ) for i, column in enumerate(df.columns): table.add_column( str(column), style="dim", no_wrap=False, overflow="fold", width=final_widths[i], header_style="bold bright_blue", ) for index, row in df.iterrows(): formatted_values = [format_value(v) for v in row.tolist()] table.add_row(*formatted_values) console.print(table) def _print_save_df(df, saveto=None): """Save dataframe to file or print with rich formatting. Automatically detects format from file extension: - .csv: Comma-separated values - .tsv: Tab-separated values - .txt: Tab-separated values (text format) - .json: JSON format """ if saveto: file_ext = os.path.splitext(saveto)[1].lower() if file_ext == ".csv": df.to_csv(saveto, index=False, header=True) console.print( f"[bright_green]✓[/bright_green] Saved to CSV: [bright_blue]{saveto}[/bright_blue]" ) elif file_ext == ".json": df.to_json(saveto, orient="records", indent=2) console.print( f"[bright_green]✓[/bright_green] Saved to JSON: [bright_blue]{saveto}[/bright_blue]" ) elif file_ext in [".tsv", ".txt"]: df.to_csv(saveto, index=False, header=True, sep="\t") console.print( f"[bright_green]✓[/bright_green] Saved to TSV: [bright_blue]{saveto}[/bright_blue]" ) else: df.to_csv(saveto, index=False, header=True, sep="\t") console.print( f"[bright_green]✓[/bright_green] Saved to file: [bright_blue]{saveto}[/bright_blue]" ) else: if df is None: console.print("[bright_black]No data to display[/bright_black]") elif len(df.index): pretty_print_df(df) ###################### metadata ############################## def metadata( srp_id, assay, desc, detailed, expand, saveto, enrich=False, enrich_backend=None ): # Validate that at least one ID was provided if not srp_id: console.print( "[red]Error: No accession IDs provided. Please provide one or more SRP/GSE IDs.[/red]" ) console.print("[yellow]Usage: pysradb metadata SRP000001 [SRP000002 ...]") console.print(" pysradb metadata GSE123456[/yellow]") return client = SRAweb() srp_ids = [] gse_ids = [] for accession in srp_id: if isinstance(accession, str) and accession.upper().startswith("GSE"): gse_ids.append(accession) else: srp_ids.append(accession) metadata_frames = [] if srp_ids: srp_metadata = client.sra_metadata( srp_ids if len(srp_ids) > 1 else srp_ids[0], assay=assay, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, enrich=enrich, enrich_backend=enrich_backend if enrich_backend else "ollama/phi3", ) if srp_metadata is not None: metadata_frames.append(srp_metadata) if gse_ids: geo_metadata_df = client.geo_metadata( gse_ids if len(gse_ids) > 1 else gse_ids[0], sample_attribute=desc, detailed=detailed, enrich=enrich, enrich_backend=enrich_backend if enrich_backend else "ollama/phi3", ) if not geo_metadata_df.empty: metadata_frames.append(geo_metadata_df) if metadata_frames: df = pd.concat(metadata_frames, ignore_index=True, sort=False) else: df = pd.DataFrame() _print_save_df(df, saveto) ################################################################ ################# download ########################## def download( out_dir, srx, srp, geo, skip_confirmation, col="public_url", use_ascp=False, threads=1, ): if out_dir is None: out_dir = os.path.join(os.getcwd(), "pysradb_downloads") client = SRAweb() geoweb = GEOweb() # This block is triggered only if no -p or -g arguments are provided. # In this case, the input is taken from the pipe and assumed to be SRA, not GEO # TODO: at some point, we need to fix this if not srp and not geo: df = pd.read_csv(sys.stdin, sep="\t") client.download( df=df, out_dir=out_dir, filter_by_srx=srx, skip_confirmation=True, use_ascp=use_ascp, url_col=col, threads=threads, ) # This block is triggered for downloads using the -p argument if srp: for srp_x in srp: metadata = client.sra_metadata(srp_x, detailed=True) client.download( df=metadata, out_dir=out_dir, filter_by_srx=srx, skip_confirmation=skip_confirmation, use_ascp=use_ascp, threads=threads, ) # This block is triggered for downloads using the -g argument if geo: for geo_x in geo: links, root_url = geoweb.get_download_links(geo_x) geoweb.download(links=links, root_url=root_url, gse=geo_x, out_dir=out_dir) ######################################################### ######################### search ################################# def search(saveto, db, verbosity, return_max, fields): if fields["run_description"]: verbosity = 1 if fields["detailed"]: verbosity = 3 try: if db == "ena": instance = EnaSearch( verbosity, return_max, fields["query"], fields["accession"], fields["organism"], fields["layout"], fields["mbases"], fields["publication_date"], fields["platform"], fields["selection"], fields["source"], fields["strategy"], fields["title"], ) instance.search() elif db == "geo": instance = GeoSearch( verbosity, return_max, fields["query"], fields["accession"], fields["organism"], fields["layout"], fields["mbases"], fields["publication_date"], fields["platform"], fields["selection"], fields["source"], fields["strategy"], fields["title"], fields["geo_query"], fields["geo_dataset_type"], fields["geo_entry_type"], ) instance.search() else: instance = SraSearch( verbosity, return_max, fields["query"], fields["accession"], fields["organism"], fields["layout"], fields["mbases"], fields["publication_date"], fields["platform"], fields["selection"], fields["source"], fields["strategy"], fields["title"], ) instance.search() except (MissingQueryException, IncorrectFieldException) as e: console.print(f"[bright_red]Error:[/bright_red] {e}") return if fields["stats"]: instance.show_result_statistics() if fields["graphs"]: graph_types = tuple(fields["graphs"].split()) instance.visualise_results(graph_types, False) _print_save_df(instance.get_df(), saveto) def get_geo_search_info(): info_text = GeoSearch.info() panel = Panel( info_text, title="[bold bright_blue]GeoSearch Information[/bold bright_blue]", border_style="bright_blue", padding=(1, 2), ) console.print(panel) #################################################################### ######################### gse-to-gsm ############################### def gse_to_gsm(gse_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.gse_to_gsm( gse_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) #################################################################### ######################## gse-to-srp ################################ def gse_to_srp(gse_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.gse_to_srp( gse_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ###################################################################### ######################### gsm-to-gse ################################# def gsm_to_gse(gsm_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.gsm_to_gse( gsm_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################## ############################ gsm-to-srp ################################ def gsm_to_srp(gsm_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.gsm_to_srp( gsm_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################## ############################ gsm-to-srr ################################ def gsm_to_srr(gsm_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.gsm_to_srr( gsm_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################## ############################ gsm-to-srs ################################ def gsm_to_srs(gsm_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.gsm_to_srs( gsm_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################## ############################# gsm-to-srx ############################### def gsm_to_srx(gsm_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.gsm_to_srx( gsm_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srp-to-gse ################################## def srp_to_gse(srp_id, saveto, detailed, desc, expand): client = SRAweb() df = client.srp_to_gse( srp_id, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srp-to-srr ################################## def srp_to_srr(srp_id, saveto, detailed, desc, expand): client = SRAweb() df = client.srp_to_srr( srp_id, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srp-to-srs ################################## def srp_to_srs(srp_id, saveto, detailed, desc, expand): client = SRAweb() df = client.srp_to_srs( srp_id, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srp-to-srx ################################## def srp_to_srx(srp_id, saveto, detailed, desc, expand): client = SRAweb() df = client.srp_to_srx( srp_id, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srr-to-gsm ################################## def srr_to_gsm(srr_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.srr_to_gsm( srr_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################## ########################### srr-to-srp ################################## def srr_to_srp(srr_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.srr_to_srp( srr_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srr-to-srs ################################## def srr_to_srs(srr_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.srr_to_srs( srr_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srr-to-srx ################################## def srr_to_srx(srr_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.srr_to_srx( srr_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srs-to-gsm ################################## def srs_to_gsm(srs_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.srs_to_gsm( srs_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srs-to-srx ################################## def srs_to_srx(srs_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.srs_to_srx( srs_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srx-to-srp ################################## def srx_to_srp(srx_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.srx_to_srp( srx_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srx-to-srr ################################## def srx_to_srr(srx_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.srx_to_srr( srx_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) ######################################################################### ########################### srx-to-srs ################################## def srx_to_srs(srx_ids, saveto, detailed, desc, expand): client = SRAweb() df = client.srx_to_srs( srx_ids, detailed=detailed, sample_attribute=desc, expand_sample_attributes=expand, ) _print_save_df(df, saveto) def srp_to_pmid(srp_ids, saveto): client = SRAweb() df = client.srp_to_pmid(srp_ids) _print_save_df(df, saveto) def sra_to_pmid(sra_ids, saveto): """Backward compatibility wrapper for sra_to_pmid""" client = SRAweb() df = client.sra_to_pmid(sra_ids) _print_save_df(df, saveto) def gse_to_pmid(gse_ids, saveto): client = SRAweb() df = client.gse_to_pmid(gse_ids) _print_save_df(df, saveto) def pmid_to_gse(pmid_ids, saveto): client = SRAweb() df = client.pmid_to_gse(pmid_ids) _print_save_df(df, saveto) def pmid_to_srp(pmid_ids, saveto): client = SRAweb() df = client.pmid_to_srp(pmid_ids) _print_save_df(df, saveto) def pmc_to_identifiers(pmc_ids, saveto): client = SRAweb() df = client.pmc_to_identifiers(pmc_ids) _print_save_df(df, saveto) def pmid_to_identifiers(pmid_ids, saveto): client = SRAweb() df = client.pmid_to_identifiers(pmid_ids) _print_save_df(df, saveto) def doi_to_gse(doi_ids, saveto): client = SRAweb() df = client.doi_to_gse(doi_ids) _print_save_df(df, saveto) def doi_to_srp(doi_ids, saveto): client = SRAweb() df = client.doi_to_srp(doi_ids) _print_save_df(df, saveto) def doi_to_identifiers(doi_ids, saveto): client = SRAweb() df = client.doi_to_identifiers(doi_ids) _print_save_df(df, saveto) ######################################################################### ########################### geo-matrix ################################## def geo_matrix(accession, to_tsv, output_dir): # Download the GEO Matrix file matrix_file = download_geo_matrix(accession, output_dir=output_dir) console.print( f"[bright_green]✓[/bright_green] Downloaded GEO Matrix file to: [bright_blue]{matrix_file}[/bright_blue]" ) # If --to-tsv is specified, parse the file to TSV if to_tsv: output_tsv = os.path.join(output_dir, f"{accession}_matrix.tsv") df = parse_geo_matrix_to_tsv(matrix_file, output_tsv) console.print( f"[bright_green]✓[/bright_green] Parsed GEO Matrix file to TSV: [bright_blue]{output_tsv}[/bright_blue]" ) ######################################################################### def parse_args(args=None): """Argument parser""" parser = ArgParser( description=dedent( """\ pysradb: Query NGS metadata and data from NCBI Sequence Read Archive. version: {}. Citation: 10.12688/f1000research.18676.1""".format( __version__ ) ), formatter_class=CustomFormatterArgP, ) # pysradb subcommands subparsers = parser.add_subparsers(title="subcommands", dest="command") # pysradb --version parser.add_argument( "--version", action="version", version="%(prog)s {version}".format(version=__version__), ) # pysradb --citation parser.add_argument( "--citation", action="version", version=dedent( """ Choudhary, Saket. "pysradb: A Python Package to Query next-Generation Sequencing Metadata and Data from NCBI Sequence Read Archive." F1000Research, vol. 8, F1000 (Faculty of 1000 Ltd), Apr. 2019, p. 532 (https://f1000research.com/articles/8-532/v1) @article{Choudhary2019, doi = {10.12688/f1000research.18676.1}, url = {https://doi.org/10.12688/f1000research.18676.1}, year = {2019}, month = apr, publisher = {F1000 (Faculty of 1000 Ltd)}, volume = {8}, pages = {532}, author = {Saket Choudhary}, title = {pysradb: A {P}ython package to query next-generation sequencing metadata and data from {NCBI} {S}equence {R}ead {A}rchive}, journal = {F1000Research} } """ ), help="how to cite", ) # pysradb metadata subparser = subparsers.add_parser( "metadata", help="Fetch metadata for SRA project (SRPnnnn)" ) subparser.add_argument("--saveto", help="Save metadata dataframe to file") subparser.add_argument( "--assay", action="store_true", help="Include assay type in output" ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--detailed", action="store_true", help="Display detailed metadata table" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument( "--enrich", action="store_true", help="Enrich metadata with standardized biological attributes using LLMs", ) subparser.add_argument( "--enrich-backend", type=str, default=None, help="LLM backend for enrichment (e.g., 'ollama/phi3', 'ollama/llama3.2'). " "If not specified, uses default backend", ) subparser.add_argument("srp_id", nargs="+") subparser.set_defaults(func=metadata) # pysradb download subparser = subparsers.add_parser("download", help="Download SRA project (SRPnnnn)") subparser.add_argument("--out-dir", help="Output directory root") subparser.add_argument("--srx", "-x", help="Download only these SRX(s)", nargs="+") subparser.add_argument("--srp", "-p", help="SRP ID", nargs="+") subparser.add_argument("--geo", "-g", help="GEO ID", nargs="+") subparser.add_argument( "--skip-confirmation", "-y", action="store_true", help="Skip confirmation" ) subparser.add_argument( "--use_ascp", "-a", action="store_true", help="Use aspera instead of wget" ) subparser.add_argument( "--col", help="Specify column to download", default="public_url" ) subparser.add_argument( "--threads", "-t", help="Number of threads", default=1, type=int ) subparser.set_defaults(func=download) # pysradb search subparser = subparsers.add_parser("search", help="Search SRA/ENA for matching text") subparser.add_argument( "-o", "--saveto", help="Save search result dataframe to file" ) subparser.add_argument( "-s", "--stats", action="store_true", help="Displays some useful statistics for the search results.", ) subparser.add_argument( "-g", "--graphs", nargs="?", const="all", help=( "Generates graphs to illustrate the search result. " "By default all graphs are generated. \n" "Alternatively, select a subset from the options below in a space-separated string:\n" "daterange, organism, source, selection, platform, basecount" ), ) subparser.add_argument( "-d", "--db", choices=["ena", "geo", "sra"], default="sra", help="Select the db API (sra, ena, or geo) to query, default = sra. " "Note: pysradb search works slightly differently when db = geo. \n" "Please refer to 'pysradb search --geo-info' for more details.", ) subparser.add_argument( "-v", "--verbosity", choices=[0, 1, 2, 3], default=2, help=( "Level of search result details (0, 1, 2 or 3), default = 2\n" "0: run accession only\n" "1: run accession and experiment title\n" "2: accession numbers, titles and sequencing information\n" "3: records in 2 and other information such as download url, sample attributes, etc" ), type=int, ) subparser.add_argument( "--run-description", action="store_true", help="Displays run accessions and descriptions only. Equivalent to --verbosity 1", ) subparser.add_argument( "--detailed", action="store_true", help="Displays detailed search results. Equivalent to --verbosity 3.", ) subparser.add_argument( "-m", "--max", default=20, help="Maximum number of entries to return, default = 20", type=int, ) subparser.add_argument( "-q", "--query", nargs="+", help="Main query string. Note that if no query is supplied, at least one of the " "following flags must be present:", ) subparser.add_argument("-A", "--accession", help="Accession number") subparser.add_argument( "-O", "--organism", nargs="+", help="Scientific name of the sample organism" ) subparser.add_argument( "-L", "--layout", choices=["SINGLE", "PAIRED"], help="Library layout. Accepts either SINGLE or PAIRED", type=str.upper, ) subparser.add_argument( "-M", "--mbases", help="Size of the sample rounded to the nearest megabase", type=int, ) subparser.add_argument( "-D", "--publication-date", help="Publication date of the run in the format dd-mm-yyyy. If a date range is desired, " "enter the start date, followed by end date, separated by a colon ':'.\n " "Example: 01-01-2010:31-12-2010", ) subparser.add_argument("-P", "--platform", nargs="+", help="Sequencing platform") subparser.add_argument("-E", "--selection", nargs="+", help="Library selection") subparser.add_argument("-C", "--source", nargs="+", help="Library source") subparser.add_argument( "-S", "--strategy", nargs="+", help="Library preparation strategy" ) subparser.add_argument("-T", "--title", nargs="+", help="Experiment title") # The following arguments are for GEO DataSets only subparser.add_argument( "-I", "--geo-info", action="store_true", help="Displays information on how to query GEO DataSets via 'pysradb search --db geo ...', " "including accepted inputs for -G/--geo-query, -Y/--geo-dataset-type and -Z/--geo-entry-type. ", ) subparser.add_argument( "-G", "--geo-query", nargs="+", help="Main query string for GEO DataSet. This flag is only used when db is set to be geo." "Please refer to 'pysradb search --geo-info' for more details.", ) subparser.add_argument( "-Y", "--geo-dataset-type", nargs="+", help="GEO DataSet Type. This flag is only used when --db is set to be geo." "Please refer to 'pysradb search --geo-info' for more details.", ) subparser.add_argument( "-Z", "--geo-entry-type", nargs="+", help="GEO Entry Type. This flag is only used when --db is set to be geo." "Please refer to 'pysradb search --geo-info' for more details.", ) subparser.set_defaults(func=search) # pysradb gse-to-gsm subparser = subparsers.add_parser("gse-to-gsm", help="Get GSM for a GSE") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [sample_accession (SRS), run_accession (SRR), sample_alias (GSM), run_alias (GSM_r)]""", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("gse_ids", nargs="+") subparser.set_defaults(func=gse_to_gsm) # pysradb gse-to-srp subparser = subparsers.add_parser("gse-to-srp", help="Get SRP for a GSE") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [experiment_accession (SRX), run_accession (SRR), sample_accession (SRS), experiment_alias (GSM_), run_alias (GSM_r), sample_alias (GSM)] """, ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("gse_ids", nargs="+") subparser.set_defaults(func=gse_to_gsm) # pysradb gsm-to-gse subparser = subparsers.add_parser("gsm-to-gse", help="Get GSE for a GSM") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [sample_accession (SRS), run_accession (SRR), sample_alias (GSM), run_alias (GSM_r)]""", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("gsm_ids", nargs="+") subparser.set_defaults(func=gsm_to_gse) # pysradb gsm-to-srp subparser = subparsers.add_parser("gsm-to-srp", help="Get SRP for a GSM") subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [experiment_accession (SRX), sample_accession (SRS), run_accession (SRR), experiment_alias (GSM), sample_alias (GSM), run_alias (GSM_r), study_alias (GSE)]""", ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("gsm_ids", nargs="+") subparser.set_defaults(func=gsm_to_srp) # pysradb gsm-to-srr subparser = subparsers.add_parser("gsm-to-srr", help="Get SRR for a GSM") subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [experiment_accession (SRX), sample_accession (SRS), study_accession (SRP), run_alias (GSM_r), sample_alias (GSM), study_alias (GSE)]""", ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("gsm_ids", nargs="+") subparser.set_defaults(func=gsm_to_srr) # pysradb gsm-to-srs subparser = subparsers.add_parser("gsm-to-srs", help="Get SRS for a GSM") subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [experiment_accession (SRX), run_accession (SRR), study_accession (SRP), run_alias (GSM_r), experiment_alias (GSM), study_alias (GSE)]""", ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("gsm_ids", nargs="+") subparser.set_defaults(func=gsm_to_srs) # pysradb gsm-to-srx subparser = subparsers.add_parser("gsm-to-srx", help="Get SRX for a GSM") subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [experiment_accession (SRX), sample_accession (SRS), run_accession (SRR), experiment_alias (GSM), sample_alias (GSM), run_alias (GSM_r), study_alias (GSE)]""", ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("gsm_ids", nargs="+") subparser.set_defaults(func=gsm_to_srx) # pysradb srp-to-gse subparser = subparsers.add_parser("srp-to-gse", help="Get GSE for a SRP") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="Output additional columns: [sample_accession, run_accession]", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("srp_id") subparser.set_defaults(func=srp_to_gse) # pysradb srp-to-srr subparser = subparsers.add_parser("srp-to-srr", help="Get SRR for a SRP") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [experiment_accession (SRX), sample_accession (SRS), study_alias (GSE), experiment_alias (GSM), sample_alias (GSM_), run_alias (GSM_r)]""", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("srp_id") subparser.set_defaults(func=srp_to_srr) # pysradb srp-to-srs subparser = subparsers.add_parser("srp-to-srs", help="Get SRS for a SRP") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [run_accession (SRR), study_accession (SRP), experiment_alias (GSM), sample_alias (GSM_), run_alias (GSM_r), study_alias (GSE)]""", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("srp_id") subparser.set_defaults(func=srp_to_srs) # pysradb srp-to-srx subparser = subparsers.add_parser("srp-to-srx", help="Get SRX for a SRP") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [sample_accession (SRS), run_accession (SRR), experiment_alias (GSM), sample_alias (GSM_), run_alias (GSM_r)', study_alias (GSE)]""", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("srp_id") subparser.set_defaults(func=srp_to_srx) # pysradb srr-to-gsm subparser = subparsers.add_parser("srr-to-gsm", help="Get GSM for a SRR") subparser.add_argument( "--detailed", action="store_true", help="""'Output additional columns: [experiment_accession (SRX), study_accession (SRP), run_alias (GSM_r), sample_alias (GSM_), experiment_alias (GSM), study_alias (GSE)]""", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("srr_ids", nargs="+") subparser.set_defaults(func=srr_to_gsm) # pysradb srr-to-srp subparser = subparsers.add_parser("srr-to-srp", help="Get SRP for a SRR") subparser.add_argument( "--detailed", action="store_true", help="""'Output additional columns: [experiment_accession (SRX), sample_accession (SRS), run_alias (GSM_r), experiment_alias (GSM), sample_alias (GSM_), study_alias (GSE)]""", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("srr_ids", nargs="+") subparser.set_defaults(func=srr_to_srp) # pysradb srr-to-srs subparser = subparsers.add_parser("srr-to-srs", help="Get SRS for a SRR") subparser.add_argument( "--detailed", action="store_true", help="""'Output additional columns: [experiment_accession (SRX), study_accession (SRP), run_alias (GSM_r), sample_alias (GSM_), experiment_alias (GSM), study_alias (GSE)]""", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("srr_ids", nargs="+") subparser.set_defaults(func=srr_to_srs) # pysradb srr-to-srx subparser = subparsers.add_parser("srr-to-srx", help="Get SRX for a SRR") subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [sample_accession (SRS), study_accession (SRP), run_alias (GSM_r), experiment_alias (GSM), sample_alias (GSM_), study_alias (GSE)]""", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("srr_ids", nargs="+") subparser.set_defaults(func=srr_to_srx) # pysradb srs-to-gsm subparser = subparsers.add_parser("srs-to-gsm", help="Get GSM for a SRS") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="Output additional columns: [run_accession, study_accession]", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("srs_ids", nargs="+") subparser.set_defaults(func=srs_to_gsm) # pysradb srs-to-srx subparser = subparsers.add_parser("srs-to-srx", help="Get SRX for a SRS") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="Output additional columns: [run_accession, study_accession]", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("srs_ids", nargs="+") subparser.set_defaults(func=srs_to_srx) # pysradb srx-to-srp subparser = subparsers.add_parser("srx-to-srp", help="Get SRP for a SRX") subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--detailed", action="store_true", help="""Output additional columns: [run_accession (SRR), sample_accession (SRS), experiment_alias (GSM), run_alias (GSM_r), sample_alias (GSM), study_alias (GSE)]""", ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("srx_ids", nargs="+") subparser.set_defaults(func=srx_to_srp) # pysradb srx-to-srr subparser = subparsers.add_parser("srx-to-srr", help="Get SRR for a SRX") subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--detailed", action="store_true", help="Output additional columns: [sample_accession, study_accession]", ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("srx_ids", nargs="+") subparser.set_defaults(func=srx_to_srr) # pysradb srx-to-srs subparser = subparsers.add_parser("srx-to-srs", help="Get SRS for a SRX") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument( "--detailed", action="store_true", help="Output additional columns: [run_accession, study_accession]", ) subparser.add_argument( "--desc", action="store_true", help="Should sample_attribute be included" ) subparser.add_argument( "--expand", action="store_true", help="Should sample_attribute be expanded" ) subparser.add_argument("srx_ids", nargs="+") subparser.set_defaults(func=srx_to_srs) # pysradb geo-matrix subparser = subparsers.add_parser( "geo-matrix", help="Download and parse GEO Matrix files" ) subparser.add_argument( "--accession", required=True, help="GEO accession (e.g., GSE234190)" ) subparser.add_argument( "--to-tsv", action="store_true", help="Convert the matrix file to TSV format" ) subparser.add_argument( "--output-dir", default=".", help="Output directory (default: current directory)", ) subparser.set_defaults(func=geo_matrix) # pysradb srp-to-pmid subparser = subparsers.add_parser( "srp-to-pmid", help="Get PMIDs for SRP accessions" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("srp_ids", nargs="+", help="SRP accession(s)") subparser.set_defaults(func=srp_to_pmid) # pysradb gse-to-pmid subparser = subparsers.add_parser( "gse-to-pmid", help="Get PMIDs for GSE accessions" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("gse_ids", nargs="+", help="GSE accession(s)") subparser.set_defaults(func=gse_to_pmid) # pysradb pmid-to-gse subparser = subparsers.add_parser( "pmid-to-gse", help="Get GSE accessions from PMIDs" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("pmid_ids", nargs="+", help="PMID(s)") subparser.set_defaults(func=pmid_to_gse) # pysradb pmid-to-srp subparser = subparsers.add_parser( "pmid-to-srp", help="Get SRP accessions from PMIDs" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("pmid_ids", nargs="+", help="PMID(s)") subparser.set_defaults(func=pmid_to_srp) # pysradb pmc-to-identifiers subparser = subparsers.add_parser( "pmc-to-identifiers", help="Extract database identifiers from PMC articles" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("pmc_ids", nargs="+", help="PMC ID(s)") subparser.set_defaults(func=pmc_to_identifiers) # pysradb pmid-to-identifiers subparser = subparsers.add_parser( "pmid-to-identifiers", help="Extract database identifiers from PubMed articles" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("pmid_ids", nargs="+", help="PMID(s)") subparser.set_defaults(func=pmid_to_identifiers) # pysradb doi-to-gse subparser = subparsers.add_parser("doi-to-gse", help="Get GSE accessions from DOIs") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("doi_ids", nargs="+", help="DOI(s)") subparser.set_defaults(func=doi_to_gse) # pysradb doi-to-srp subparser = subparsers.add_parser("doi-to-srp", help="Get SRP accessions from DOIs") subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("doi_ids", nargs="+", help="DOI(s)") subparser.set_defaults(func=doi_to_srp) # pysradb doi-to-identifiers subparser = subparsers.add_parser( "doi-to-identifiers", help="Extract database identifiers from articles via DOI" ) subparser.add_argument("--saveto", help="Save output to file") subparser.add_argument("doi_ids", nargs="+", help="DOI(s)") subparser.set_defaults(func=doi_to_identifiers) args = parser.parse_args(args=None if sys.argv[1:] else ["--help"]) if args.command == "metadata": metadata( args.srp_id, args.assay, args.desc, args.detailed, args.expand, args.saveto, args.enrich, args.enrich_backend, ) elif args.command == "download": download( args.out_dir, args.srx, args.srp, args.geo, args.skip_confirmation, args.col, args.use_ascp, args.threads, ) elif args.command == "search": flags = vars(args) if flags.pop("geo_info"): get_geo_search_info() else: search( flags.pop("saveto"), flags.pop("db"), flags.pop("verbosity"), flags.pop("max"), flags, ) elif args.command == "gse-to-gsm": gse_to_gsm(args.gse_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "gse-to-srp": gse_to_srp(args.gse_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "gsm-to-gse": gsm_to_gse(args.gsm_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "gsm-to-srp": gsm_to_srp(args.gsm_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "gsm-to-srr": gsm_to_srr(args.gsm_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "gsm-to-srs": gsm_to_srs(args.gsm_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "gsm-to-srx": gsm_to_srx(args.gsm_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srp-to-gse": srp_to_gse(args.srp_id, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srp-to-srr": srp_to_srr(args.srp_id, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srp-to-srs": srp_to_srs(args.srp_id, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srp-to-srx": srp_to_srx(args.srp_id, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srr-to-gsm": srr_to_gsm(args.srr_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srr-to-srp": srr_to_srp(args.srr_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srr-to-srs": srr_to_srs(args.srr_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srr-to-srx": srr_to_srx(args.srr_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srs-to-gsm": srs_to_gsm(args.srs_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srs-to-srx": srs_to_srx(args.srs_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srx-to-srp": srx_to_srp(args.srx_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srx-to-srr": srx_to_srr(args.srx_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "srx-to-srs": srx_to_srs(args.srx_ids, args.saveto, args.detailed, args.desc, args.expand) elif args.command == "geo-matrix": geo_matrix(args.accession, args.to_tsv, args.output_dir) elif args.command == "srp-to-pmid": srp_to_pmid(args.srp_ids, args.saveto) elif args.command == "gse-to-pmid": gse_to_pmid(args.gse_ids, args.saveto) elif args.command == "pmid-to-gse": pmid_to_gse(args.pmid_ids, args.saveto) elif args.command == "pmid-to-srp": pmid_to_srp(args.pmid_ids, args.saveto) elif args.command == "pmc-to-identifiers": pmc_to_identifiers(args.pmc_ids, args.saveto) elif args.command == "pmid-to-identifiers": pmid_to_identifiers(args.pmid_ids, args.saveto) elif args.command == "doi-to-gse": doi_to_gse(args.doi_ids, args.saveto) elif args.command == "doi-to-srp": doi_to_srp(args.doi_ids, args.saveto) elif args.command == "doi-to-identifiers": doi_to_identifiers(args.doi_ids, args.saveto) if __name__ == "__main__": parse_args(sys.argv[1:]) ================================================ FILE: pysradb/download.py ================================================ """Utility function to download data""" import hashlib import math import os import shutil import sys import warnings from ftplib import FTP from urllib.parse import urlparse import numpy as np import requests from tqdm.autonotebook import tqdm from .utils import requests_3_retries warnings.simplefilter(action="ignore", category=FutureWarning) import pandas as pd tqdm.pandas() def _get_ftp_file_size(url): """Get file size from FTP server. Parameters ---------- url : str FTP URL Returns ------- size : int File size in bytes, or 0 if unable to determine """ try: parsed = urlparse(url) ftp = FTP(parsed.netloc) ftp.login() size = ftp.size(parsed.path) ftp.quit() return size if size is not None else 0 except Exception: return 0 def _download_ftp_file( url, file_path, timeout=10, block_size=1024 * 1024, show_progress=False ): """Download file from FTP server. Parameters ---------- url : str FTP URL file_path : str Local file path to store the downloaded file timeout : int Timeout in seconds block_size : int Block size for downloading show_progress : bool Show progress bar """ parsed = urlparse(url) tmp_file_path = file_path + ".part" # Check if partial file exists first_byte = os.path.getsize(tmp_file_path) if os.path.exists(tmp_file_path) else 0 file_mode = "ab" if first_byte else "wb" try: ftp = FTP(parsed.netloc, timeout=timeout) ftp.login() file_size = ftp.size(parsed.path) if file_size is None: file_size = -1 if show_progress and file_size > 0: desc = "Downloading {}".format(url.split("/")[-1]) pbar = tqdm( total=file_size, initial=first_byte, unit="B", unit_scale=True, desc=desc, ) with open(tmp_file_path, file_mode) as f: if first_byte > 0: ftp.voidcmd(f"REST {first_byte}") def callback(data): f.write(data) if show_progress and file_size > 0: pbar.update(len(data)) ftp.retrbinary(f"RETR {parsed.path}", callback, blocksize=block_size) if show_progress and file_size > 0: pbar.close() ftp.quit() if file_size == -1 or file_size == os.path.getsize(tmp_file_path): shutil.move(tmp_file_path, file_path) else: raise Exception( f"Download incomplete: expected {file_size} bytes, got {os.path.getsize(tmp_file_path)} bytes" ) except Exception as e: if show_progress and "pbar" in locals(): pbar.close() raise Exception(f"FTP download failed: {e}") def millify(n): """Convert integer to human readable format. Parameters ---------- n : int Returns ------- millidx : str Formatted integer """ millnames = ["", " KB", " MB", " GB", " TB"] # Source: http://stackoverflow.com/a/3155023/756986 n = float(n) millidx = max( 0, min( len(millnames) - 1, int(math.floor(0 if n == 0 else math.log10(abs(n)) / 3)) ), ) return "{:.1f}{}".format(n / 10 ** (3 * millidx), millnames[millidx]) def get_file_size(row, url_col): """Get size of file to be downloaded. Parameters ---------- row: pd.DataFrame row url_col: str url_column Returns ------- content_length: int """ if row[url_col] is not None: url = row[url_col] else: url = row.download_url if url is pd.NA: return 0 if not isinstance(url, str): return 0 if url.startswith("ftp."): url = "ftp://" + url if url.startswith("ftp://"): return _get_ftp_file_size(url) try: r = requests_3_retries().head(url) size = int(r.headers["content-length"]) r.raise_for_status() except requests.exceptions.Timeout: sys.exit(f"Connection to {url} has timed out. Please retry.") except requests.exceptions.HTTPError: print( f"The download URL: {url} is likely invalid.\n" f"Removing {row.run_accession} from the download list\n", flush=True, ) return np.NaN except KeyError: print("Key error for: " + url, flush=True) return 0 return size def md5_validate_file(file_path, md5_hash): """Check file containt against an MD5. Parameters ---------- file_path: string Path to file md5_hash: string Expected md5 hash Returns ------- valid: bool True if expected and observed md5 match """ observed_md5 = hashlib.md5() with open(file_path, "rb") as f: while True: # read 1MB chunk = f.read(1000 * 1000) if not chunk: break observed_md5.update(chunk) return observed_md5.hexdigest() == md5_hash def download_file( url, file_path, md5_hash=None, timeout=10, block_size=1024 * 1024, show_progress=False, ): """Resumable download. Expect the server to support byte ranges. Parameters ---------- url: string URL file_path: string Local file path to store the downloaded file md5_hash: string Expected MD5 string of downloaded file timeout: int Seconds to wait before terminating request block_size: int Chunkx of bytes to read (default: 1024 * 1024 = 1MB) show_progress: bool Show progress bar """ if url.startswith("ftp."): url = "ftp://" + url if os.path.exists(file_path) and os.path.getsize(file_path): return if url.startswith("ftp://"): _download_ftp_file(url, file_path, timeout, block_size, show_progress) # if there's a hash value, validate the file if md5_hash and not md5_validate_file(file_path, md5_hash): raise Exception("Error validating the file against its MD5 hash") return session = requests tmp_file_path = file_path + ".part" first_byte = os.path.getsize(tmp_file_path) if os.path.exists(tmp_file_path) else 0 file_mode = "ab" if first_byte else "wb" file_size = -1 try: file_size = int(session.head(url).headers["Content-length"]) headers = {"Range": "bytes=%s-" % first_byte} r = session.get(url, headers=headers, stream=True) if show_progress: desc = "Downloading {}".format(url.split("/")[-1]) pbar = tqdm( total=file_size, initial=first_byte, unit="B", unit_scale=True, desc=desc, ) with open(tmp_file_path, file_mode) as f: for chunk in r.iter_content(chunk_size=block_size): if chunk: # filter out keep-alive new chunks f.write(chunk) if show_progress: pbar.update(len(chunk)) if show_progress: pbar.close() except IOError as e: sys.stderr.write("IO Error - {}\n".format(e)) finally: # Move the temp file to desired location if os.path.exists(tmp_file_path): actual_size = os.path.getsize(tmp_file_path) if file_size == actual_size: if md5_hash and not md5_validate_file(tmp_file_path, md5_hash): raise Exception("Error validating the file against its MD5 hash") shutil.move(tmp_file_path, file_path) elif file_size == -1: # Server didn't provide Content-Length, move the file anyway shutil.move(tmp_file_path, file_path) else: print( f"Warning: File size mismatch for {url}. Expected: {file_size}, Got: {actual_size}" ) if actual_size > 0: shutil.move(tmp_file_path, file_path) ================================================ FILE: pysradb/exceptions.py ================================================ """This file contains custom Exceptions for pysradb""" class MissingQueryException(Exception): """Exception raised when the user did not supply any query fields. Attributes: message: string Error message for this Exception """ def __init__(self): self.message = ( "No valid query has been supplied. \n" "A query must be supplied to one of the following fields:\n" "[--query, --accession, --organism, --layout, --mbases, --publication-date," " --platform, --selection, --source, --strategy, --title]" ) super().__init__(self.message) class IncorrectFieldException(Exception): """Exception raised when the user enters incorrect inputs for a flag.""" pass ================================================ FILE: pysradb/filter_attrs.py ================================================ import re import warnings import numpy as np import pandas as pd def _get_sample_attr_keys(sample_attribute): if sample_attribute is None: return None, None sample_attribute_splitted = sample_attribute.split("||") split_by_colon = [ str(attr).strip().split(": ") for attr in sample_attribute_splitted ] # Iterate once more to consider first one as the key # and remaining as the value # This is because of bad annotations like in this example # Example: isolate: not applicable || organism: Mus musculus || cell_line: 17-Cl1 ||\ # infect: MHV-A59 || time point: 5: hour || compound: cycloheximide ||\ # sequencing protocol: RiboSeq || biological repeat: long read sequencing # Notice the `time: 5: hour` # sample_attribute: investigation type: metagenome || project name: Landsort Depth 20090415 transect || # sequencing method: 454 || collection date: 2009-04-15 || ammonium: 8.7: µM || chlorophyll: 0: µg/L || # dissolved oxygen: -1.33: µmol/kg || nitrate: 0.02: µM || nitrogen: 0: µM || # environmental package: water || geographic location (latitude): 58.6: DD || # geographic location (longitude): 18.2: DD || geographic location (country and/or sea,region): Baltic Sea || # environment (biome): 00002150 || environment (feature): 00002150 || environment (material): 00002150 || # depth: 400: m || Phosphate: || Total phosphorous: || Silicon: # Handle empty cases as above split_by_colon = [attr for attr in split_by_colon if len(attr) >= 2] for index, element in enumerate(split_by_colon): if len(element) > 2: key = element[0].strip() value = ":".join(element[1:]).strip() split_by_colon[index] = [key, value] try: sample_attribute_dict = dict(split_by_colon) except ValueError: print("This is most likely a bug, please report it upstream.") print(("sample_attribute: {}".format(sample_attribute))) raise sample_attribute_keys = list( map( lambda x: re.sub(r"\s+", " ", x.strip().replace(" ", "_").lower()), list(sample_attribute_dict.keys()), ) ) sample_attribute_values = list( map( lambda x: re.sub(r"\s+", " ", x.strip().lower().strip().replace(",", "__")), list(sample_attribute_dict.values()), ) ) return sample_attribute_keys, sample_attribute_values def expand_sample_attribute_columns(metadata_df): """Expand sample attribute columns to individual columns. Since the sample_attribute column content can be different for differnt rows even if coming from the same project (SRP), we explicitly iterate through the rows to first determine what additional columns need to be created. Parameters ---------- metadata_df: DataFrame Dataframe as obtained from sra_metadata or equivalent Returns ------- expanded_df: DataFrame Dataframe with additionals columns pertaining to sample_attribute appended """ additional_columns = [] metadata_df = metadata_df.copy() for idx, row in metadata_df.iterrows(): sample_attribute = row["sample_attribute"] if not sample_attribute: continue sample_attribute = sample_attribute.strip() sample_attribute_keys, _ = _get_sample_attr_keys(sample_attribute) if sample_attribute_keys: additional_columns += sample_attribute_keys additional_columns = list(sorted(set(additional_columns))) # if any of the additional column already exists # call the additional column as *_expanded additional_columns = list( map( lambda x: x if x not in metadata_df.columns.tolist() else x + "_expanded", additional_columns, ) ) additional_columns = list(sorted(additional_columns)) empty_df = pd.DataFrame(columns=additional_columns) metadata_df_expanded = pd.concat([metadata_df, empty_df], axis=1) for idx, row in metadata_df_expanded.iterrows(): sample_attribute = row["sample_attribute"] sample_attribute_keys, sample_attribute_values = _get_sample_attr_keys( sample_attribute ) if sample_attribute_keys: sample_attribute_keys = list( map( lambda x: ( x if x not in metadata_df.columns.tolist() else x + "_expanded" ), sample_attribute_keys, ) ) metadata_df_expanded.loc[idx, sample_attribute_keys] = sample_attribute_values if np.nan in metadata_df_expanded.columns.tolist(): del metadata_df_expanded[np.nan] return metadata_df_expanded def guess_cell_type(sample_attribute): """Guess possible cell line from sample_attribute data. Parameters ---------- sample_attribute: string sample_attribute string as in the metadata column Returns ------- cell_type: string Possible cell type of sample. Returns None if no match found. """ sample_attribute = str(sample_attribute) cell_type = None if "cell line:" in sample_attribute: x = re.search(r"cell line: \w+", sample_attribute) cell_type = re.sub(r"\s+", " ", x.group(0).lstrip("cell line:").lower().strip()) if "cell_line:" in sample_attribute: x = re.search(r"cell_line: \w+", sample_attribute) cell_type = re.sub(r"\s+", " ", x.group(0).lstrip("cell_line:").lower().strip()) if "cell-line:" in sample_attribute: x = re.search(r"cell-line: \w+", sample_attribute) cell_type = re.sub(r"\s+", " ", x.group(0).lstrip("cell-line:").lower().strip()) if "cell_type:" in sample_attribute: x = re.search(r"cell_type: \w+", sample_attribute) return re.sub(r"\s+", " ", x.group(0).lstrip("cell_type:").lower().strip()) if "source_name:" in sample_attribute: x = re.search(r"source_name: \w+", sample_attribute) cell_type = re.sub( r"\s+", " ", x.group(0).lstrip("source_name:").lower().strip() ) else: warnings.warn( "Couldn't parse {} for cell line".format(sample_attribute), UserWarning ) return cell_type def guess_tissue_type(sample_attribute): """Guess tissue type from sample_attribute data. Parameters ---------- sample_attribute: string sample_attribute string as in the metadata column Returns ------- tissue_type: string Possible cell type of sample. Returns None if no match found. """ sample_attribute = str(sample_attribute) tissue_type = None if "tissue: " in sample_attribute: x = re.search(r"tissue: \w+", sample_attribute) tissue_type = re.sub(r"\s+", " ", x.group(0).lstrip("tissue:").lower().strip()) else: warnings.warn( "Couldn't parse {} for tissue".format(sample_attribute), UserWarning ) return tissue_type def guess_strain_type(sample_attribute): """Guess strain type from sample_attribute data. Parameters ---------- sample_attribute: string sample_attribute string as in the metadata column Returns ------- strain_type: string Possible cell type of sample. Returns None if no match found. """ sample_attribute = str(sample_attribute) strain_type = None if "strain: " in sample_attribute: x = re.search(r"strain: \w+", sample_attribute) strain_type = re.sub(r"\s+", " ", x.group(0).lstrip("strain:").lower().strip()) else: warnings.warn( "Couldn't parse {} for strain".format(sample_attribute), UserWarning ) return strain_type ================================================ FILE: pysradb/geoweb.py ================================================ """Utilities to interact with GEO online""" import gzip import os import re import sys from io import StringIO import pandas as pd import requests from lxml import html from .download import download_file from .utils import _get_url, copyfileobj, get_gzip_uncompressed_size PY3 = True if sys.version_info[0] < 3: PY3 = False class GEOweb(object): def __init__(self): """Initialize GEOweb without any database.""" def get_download_links(self, gse): """Obtain all links from the GEO FTP page. Parameters ---------- gse: string GSE ID Returns ------- links: list List of all valid downloadable links present for a GEO ID """ prefix = gse[:-3] url = f"https://ftp.ncbi.nlm.nih.gov/geo/series/{prefix}nnn/{gse}/suppl/" link_objects = html.fromstring(requests.get(url).content).xpath("//a") links = [i.attrib["href"] for i in link_objects] # remove vulnerability link links = [ link for link in links if link != "https://www.hhs.gov/vulnerability-disclosure-policy/index.html" ] # Check if returned results are a valid page - a link to the # home page only exists where the GSE ID dow not exist if "/" in links: raise KeyError(f"The provided GEO ID {gse} does not exist.") # The list of links for a valid GSE ID also contains a link to # the parent directory - we do not want that links = [i for i in links if "geo/series/" not in i] # The links are relative, we need absolute links to download links = [i for i in links] return links, url def download(self, links, root_url, gse, verbose=False, out_dir=None): """Download GEO files. Parameters ---------- links: list List of all links valid downloadable present for a GEO ID root_url: string url for root directory for a GEO ID gse: string GEO ID verbose: bool Print file list out_dir: string Directory location for download """ if out_dir is None: out_dir = os.path.join(os.getcwd(), "pysradb_downloads") # store output in a separate directory out_dir = os.path.join(out_dir, gse) os.makedirs(out_dir, exist_ok=True) # Display files to be downloaded print("\nThe following files will be downloaded: \n") for link in links: print(link) print(os.linesep) # Check if we can access list of files in the tar file tar_list = [i for i in links if ".tar" in i] if "filelist.txt" in links: tar_file = tar_list[0] if verbose: print(f"\nThe tar file {tar_file} contains the following files:\n") file_list_contents = requests.get( root_url + "filelist.txt" ).content.decode("utf-8") print(file_list_contents) # Download files for link in links: # add a prefix to distinguish filelist.txt from different downloads prefix = "" if link == "filelist.txt": prefix = gse + "_" geo_path = os.path.join(out_dir, prefix + link) download_file(root_url + link, geo_path, show_progress=True) def download_geo_matrix(accession, output_dir="."): """ Download a GEO Matrix file for a given GEO accession ID. Args: accession (str): GEO accession ID (e.g., 'GSE234190'). output_dir (str): Directory to save the downloaded file (default: current directory). Returns: str: Path to the downloaded file. Raises: Exception: If the download fails. """ # Construct the URL for the GEO Matrix file url = f"https://ftp.ncbi.nlm.nih.gov/geo/series/{accession[:-3]}nnn/{accession}/matrix/{accession}_series_matrix.txt.gz" # Define the output file path output_file = os.path.join(output_dir, f"{accession}_series_matrix.txt.gz") # Download the file using _get_url try: _get_url(url, output_file) return output_file except Exception as e: raise Exception( f"Failed to download GEO Matrix file for {accession}. Exception: {str(e)}" ) def parse_geo_matrix_to_tsv(input_file, output_file): """ Parse a GEO Matrix file to a TSV file, extracting the expression data. Args: input_file (str): Path to the input GEO Matrix file (gzipped). output_file (str): Path to save the output TSV file. Returns: pandas.DataFrame: The parsed expression data. """ # Read the gzipped file and extract the data section data_lines = [] data_section = False with gzip.open(input_file, "rt", encoding="utf-8") as f: for line in f: line = line.strip() if line == "!series_matrix_table_begin": data_section = True continue elif line == "!series_matrix_table_end": break if data_section and line: data_lines.append(line) # Use pandas.read_csv to parse the data section df = pd.read_csv(StringIO("\n".join(data_lines)), sep="\t", comment="!") # Save to TSV df.to_csv(output_file, sep="\t", index=False) return df ================================================ FILE: pysradb/metadata_enrichment.py ================================================ """ Metadata enrichment for SRA/GEO datasets using LLMs and embeddings. """ import logging import os import subprocess import sys from abc import ABC, abstractmethod from typing import Any, Dict, List, Optional, Union import pandas as pd from pydantic import BaseModel, Field from tqdm.autonotebook import tqdm logger = logging.getLogger(__name__) def _prompt_install_enrichment_dependencies() -> bool: """ Prompt user to install enrichment dependencies. Returns: True if installation succeeded, False otherwise. """ try: response = ( input( "Enrichment requires 'instructor' and 'pydantic'. Install now? (yes/no): " ) .strip() .lower() ) except (EOFError, KeyboardInterrupt): return False if response not in ["yes", "y"]: print("Install with: pip install 'pysradb[enrichment]'") return False try: subprocess.check_call( [ sys.executable, "-m", "pip", "install", "instructor>=1.0.0", "pydantic>=2.0.0", ] ) return True except subprocess.CalledProcessError: print( "Installation failed. Install manually with: pip install 'pysradb[enrichment]'" ) return False class MetadataExtractor(ABC): """Base class for metadata extraction from experiment descriptions.""" def __init__(self): self.logger = logging.getLogger(self.__class__.__name__) @abstractmethod def extract_metadata( self, text: str, fields: Optional[List[str]] = None ) -> Dict[str, Any]: """ Extract metadata from text. Args: text: Input text (experiment description, title, etc.) fields: List of metadata fields to extract. If None, extract all. Returns: Dictionary with extracted metadata """ pass def extract_batch( self, texts: List[str], fields: Optional[List[str]] = None ) -> List[Dict[str, Any]]: """ Extract metadata from multiple texts. Args: texts: List of input texts fields: List of metadata fields to extract Returns: List of dictionaries with extracted metadata """ return [self.extract_metadata(text, fields) for text in texts] def _find_column_variant(self, df: pd.DataFrame, target_col: str) -> Optional[str]: """ Find a column that matches the target column name with flexible matching. Handles variations like: - Different casing: cell_type, Cell_Type, CELL_TYPE - Spaces vs underscores: cell_type, cell type, celltype - CamelCase: cellType, CellType Args: df: DataFrame to search target_col: Target column name (e.g., 'cell_type') Returns: Actual column name if found, None otherwise """ target_normalized = target_col.lower().replace("_", "").replace(" ", "") for col in df.columns: col_normalized = str(col).lower().replace("_", "").replace(" ", "") if col_normalized == target_normalized: return col return None def enrich_dataframe( self, df: pd.DataFrame, text_column: Optional[str] = None, fields: Optional[List[str]] = None, prefix: str = "guessed_", show_progress: bool = True, ) -> pd.DataFrame: """ Enrich a DataFrame with extracted metadata. Args: df: Input DataFrame text_column: Column containing text to analyze. If None, combines sample text columns. fields: List of metadata fields to extract prefix: Prefix for new columns show_progress: Show progress bar (default: True) Returns: DataFrame with additional metadata columns """ # If text_column not specified, combine all relevant columns if text_column is None: preferred_columns = [ "sample_title", "experiment_title", "sample_source_name", "source_name", "sample_type", "sex", "age", "tissue", "cell_type", "disease", "disease_status", "treatment", "compound", "extract_protocol", "label_protocol", "sample_summary", "description", ] exclude_columns = [ "study_title", "study_summary", "series_title", "series_summary", ] available_cols = [] for col in preferred_columns: actual_col = self._find_column_variant(df, col) if actual_col and actual_col not in exclude_columns: available_cols.append(actual_col) if not available_cols: raise ValueError( "No suitable text columns found in DataFrame. " "Please specify text_column parameter or ensure DataFrame " "contains columns like 'sample_title', 'experiment_title', etc." ) texts = [] for idx, row in df.iterrows(): parts = [] for col in available_cols: if pd.notna(row[col]): parts.append(f"{col}: {row[col]}") texts.append(". ".join(parts)) else: if text_column not in df.columns: raise ValueError(f"Column '{text_column}' not found in DataFrame") texts = df[text_column].fillna("").tolist() if show_progress: metadata_list = [ self.extract_metadata(text, fields) for text in tqdm(texts, desc="Enriching metadata", unit="row") ] else: metadata_list = self.extract_batch(texts, fields) df_enriched = df.copy() for field in metadata_list[0].keys(): df_enriched[f"{prefix}{field}"] = [m.get(field) for m in metadata_list] return df_enriched class _MetadataExtraction(BaseModel): """Model for metadata extraction aligned with CellxGene schema. Fields are designed to match CellxGene Discover metadata structure and use ontology-based terms from UBERON (anatomy), MONDO (disease), and CL (cell types). Anatomical hierarchy: anatomical_system → organ → tissue """ organ: str = Field( default="Unknown", description="High-level organ (e.g., brain, liver, heart, lung, breast)", ) tissue: str = Field( default="Unknown", description="Specific tissue within organ (UBERON-based)" ) anatomical_system: str = Field( default="Unknown", description="Body system (e.g., cardiovascular, nervous, immune)", ) cell_type: str = Field( default="Unknown", description="Specific cell type (CL ontology-based)" ) disease: str = Field( default="Unknown", description="Disease or condition (MONDO ontology-based)" ) sex: str = Field( default="Unknown", description="Biological sex (male, female, mixed, Unknown)" ) development_stage: str = Field( default="Unknown", description="Developmental stage (embryonic, fetal, adult, etc.)", ) assay: str = Field( default="Unknown", description="Experimental assay type (RNA-seq, scRNA-seq, ATAC-seq, etc.)", ) organism: str = Field( default="Unknown", description="Species (Homo sapiens, Mus musculus, etc.)" ) DEFAULT_LLM_PROVIDER = "ollama/phi3" def load_ontology_reference() -> Dict[str, List[str]]: """ Returns comprehensive reference categories from UBERON, MONDO, and CL ontologies. Returns: Dictionary with ontology terms (organs, tissues, anatomical_systems, cell_types, diseases) """ import json import os current_dir = os.path.dirname(__file__) ontology_path = os.path.join(current_dir, "ontology_reference.json") if not os.path.exists(ontology_path): raise FileNotFoundError( f"Ontology reference not found at {ontology_path}. " "Please ensure ontology_reference.json is in the pysradb package directory." ) with open(ontology_path) as f: return json.load(f) class LLMMetadataExtractor(MetadataExtractor): """Extract metadata using Large Language Models via Instructor.""" def __init__( self, backend: str = DEFAULT_LLM_PROVIDER, model: Optional[str] = None, api_key: Optional[str] = None, base_url: Optional[str] = None, temperature: float = 0.0, max_retries: int = 3, **kwargs, ): super().__init__() self.provider = backend or DEFAULT_LLM_PROVIDER self.model = model env_key = self._provider_env_key() self.api_key = api_key or (os.getenv(env_key) if env_key else None) self.base_url = base_url self.temperature = temperature self.max_retries = max_retries self.kwargs = kwargs self.client = self._initialize_client() def _provider_env_key(self) -> Optional[str]: provider_name = self.provider.split("/")[0] if provider_name.lower() == "openai": return "OPENAI_API_KEY" if provider_name.lower() == "anthropic": return "ANTHROPIC_API_KEY" if provider_name.lower() == "google": return "GOOGLE_API_KEY" if provider_name.lower() == "mistral": return "MISTRAL_API_KEY" if provider_name.lower() == "groq": return "GROQ_API_KEY" return None def _check_ollama_available(self) -> bool: """Check if ollama is installed and running.""" try: import subprocess import requests try: subprocess.run( ["ollama", "--version"], capture_output=True, check=True, timeout=10 ) except ( subprocess.CalledProcessError, FileNotFoundError, subprocess.TimeoutExpired, ): return False try: response = requests.get("http://localhost:11434/api/tags", timeout=5) return response.status_code == 200 except (requests.RequestException, requests.Timeout): return False except Exception: return False def _initialize_client(self): try: import instructor except ImportError: if _prompt_install_enrichment_dependencies(): import instructor else: raise ImportError( "instructor package required. Install with: pip install 'pysradb[enrichment]'" ) client_kwargs = self.kwargs.copy() if self.base_url: client_kwargs.setdefault("client_kwargs", {}) client_kwargs["client_kwargs"].setdefault("base_url", self.base_url) provider_name = self.provider.split("/")[0].lower() if provider_name == "ollama": if not self._check_ollama_available(): raise RuntimeError( "Ollama is not installed or not running. " "Please install ollama from https://ollama.ai/ and start it with 'ollama serve'. " "Then pull a model with 'ollama pull phi3:latest' (or another model like 'meditron-7b')." ) if provider_name in ["ollama", "local"] and "mode" not in client_kwargs: client_kwargs["mode"] = instructor.Mode.JSON return instructor.from_provider( self.provider, api_key=self.api_key, **client_kwargs, ) def _create_extraction_prompt( self, text: str, fields: Optional[List[str]] = None ) -> str: """Create prompt for metadata extraction.""" default_fields = [ "organ", "tissue", "anatomical_system", "cell_type", "disease", "sex", "development_stage", "assay", "organism", ] target_fields = fields or default_fields prompt = f"""Extract biological metadata using ontology-based terminology (UBERON, MONDO, CL). CRITICAL PRIORITY RULE: If a field is explicitly labeled in the metadata, prioritize that information. You may make reasonable generalizations (e.g., "CD19+ B cells" → "b cells", "CD4+ T cells" → "t cells"), but DO NOT over-generalize to broader categories. BULK TISSUE AND WHOLE-SAMPLE HANDLING (IMPORTANT): When the metadata contains keywords indicating bulk tissue or whole samples (bulk, PDX, xenograft, tumor, tissue, whole tissue, homogenate), the sample contains MIXED CELL TYPES. Do NOT invent specific cell types: - "bulk RNA-seq from PDX" → cell_type: "Unknown" (NOT "neuron" or any specific cell type) - "tumor tissue" → cell_type: "Unknown", organ/tissue from source if clear (NOT inferred from invented cell types) - "xenograft" → cell_type: "Unknown" (multiple cell types present) - "whole tissue" → cell_type: "Unknown" (NOT a specific cell type) RULE: If cell_type is not explicitly stated AND the sample is described as bulk/whole/tissue/tumor/PDX, return "Unknown" for cell_type. Examples of CORRECT extraction: - "cell type: CD19+ B cells" → cell_type: "b cells" or "cd19+ b cells" (NOT "pbmc" - too broad) - "cell type: CD4+ T cells" → cell_type: "t cells" or "cd4+ t cells" (NOT "lymphocyte" or "pbmc" - too broad) - "cell type: hepatocytes" → cell_type: "hepatocyte" (NOT "liver cells" - less specific) - "tissue: prefrontal cortex" → tissue: "prefrontal cortex" or "brain" (NOT "nervous tissue" - too broad) - "disease: Multiple sclerosis" → disease: "multiple sclerosis" (NOT "healthy" or "autoimmune disease") - "bulk RNA-seq from PDX" → cell_type: "Unknown" (NOT "neuron" or invented types), organ: "Unknown" if not stated - "sample_description: tumor tissue" → cell_type: "Unknown", organ: "Unknown" (do not invent) CELL TYPE INFERENCE RULES (only when NOT explicitly stated AND NOT bulk/PDX/tumor/whole tissue): - Cell types indicate their origin organ/tissue. Use this biological knowledge ONLY for purified cell populations: * Blood cells (PBMC, T cell, B cell, lymphocyte, monocyte, macrophage, NK cell) → organ: blood, tissue: peripheral blood, system: immune system * Brain cells (neuron, astrocyte, microglia, oligodendrocyte) → organ: brain, tissue: brain tissue, system: nervous system * Liver cells (hepatocyte) → organ: liver, tissue: liver parenchyma, system: digestive system * Heart cells (cardiomyocyte) → organ: heart, tissue: cardiac tissue, system: cardiovascular system * Lung cells (pneumocyte, alveolar cell) → organ: lung, tissue: lung parenchyma, system: respiratory system * Apply similar biological reasoning for OTHER PURIFIED cell types ONLY EXTRACTION RULES: 1. **cell_type**: FIRST check for "cell type:", "cell_type:", "celltype:" or "cellType:" labels. If not stated, check if sample is bulk/PDX/tumor/tissue/xenograft - if yes, return "Unknown". Otherwise, use stated value or reasonable generalization (CD19+ B cells → b cells). NEVER invent cell types. 2. **disease**: FIRST check for "disease:", "disease status:", or "condition:" labels. Use exact disease name. "Normal"/"control"/"WT"→healthy only if NO disease is stated. 3. **tissue**: FIRST check for "tissue:", "source_name:" labels. Use stated value or reasonable generalization. Otherwise infer from EXPLICITLY STATED cell_type/organ. Do NOT infer from invented cell types. 4. **organ**: Look for explicit organ name. Do NOT infer organ from invented cell types. Return "Unknown" if not stated. 5. **anatomical_system**: Derive from EXPLICIT organ/cell_type information only. Return "Unknown" if not determinable. 6. **sex**: F=female, M=male. Return: male, female, mixed, or Unknown. Lowercase. 7. **development_stage**: From age - handle 'y' for years, 'm' for months (e.g., 17m=17 months=1.4 years). Use: 0-2y=infant, 3-12y=child, 13-18y=adolescent, 19-64y=adult, 65+=aged. Convert months to years when needed. Lowercase. 8. **assay**: RNA-seq, scRNA-seq, CITE-seq, ATAC-seq, Bisulfite-Seq, etc. Lowercase. 9. **organism**: Homo sapiens, Mus musculus, or common names. Lowercase unless scientific. EXAMPLES showing CORRECT extraction with reasonable generalization: "cell type: CD19+ B cells, disease status: Multiple sclerosis" → cell_type: "b cells" (acceptable: "cd19+ b cells"), disease: "multiple sclerosis" "cell type: PBMC, tissue: peripheral blood" → cell_type: "pbmc", tissue: "peripheral blood" "cell_type: CD8+ memory T cells" → cell_type: "t cells" (acceptable: "cd8+ memory t cells", "memory t cells") "cell type: activated microglia" → cell_type: "microglia" (acceptable: "activated microglia") "sample_description: bulk RNA-seq from PDX, source: breast tumor" → cell_type: "Unknown", organ: "Unknown", disease: "Unknown" "sample_source: PDX1, sample_title: MJH1_G1M1, description: bulk RNA-seq" → cell_type: "Unknown", organ: "Unknown" (do NOT invent "neuron") Metadata: {text} Extract (use "Unknown" only if truly unclear): """ field_descriptions = { "organ": "High-level organ - use stated value only or return 'Unknown'. Do NOT invent from cell types. (lowercase)", "tissue": "Specific tissue - use stated value or reasonable generalization from EXPLICIT data only. Return 'Unknown' if not stated. (lowercase)", "anatomical_system": "Major body system - only if clearly stated or derivable from explicit organ/cell type. Return 'Unknown' otherwise. (lowercase)", "cell_type": "Cell type ONLY if explicitly stated or if bulk/PDX/tumor/tissue keywords present → return 'Unknown'. Allow generalization (CD19+ B cells → b cells) but NEVER invent specific types. (lowercase)", "disease": "Exact disease name if explicitly stated (e.g., 'multiple sclerosis'), or 'healthy' for controls. Return 'Unknown' if not stated. (lowercase)", "sex": "Biological sex: 'male', 'female', 'mixed', or 'Unknown'", "development_stage": "Life/developmental stage - from age if stated. Return 'Unknown' if age not provided. (lowercase)", "assay": "Sequencing or experimental assay type (lowercase)", "organism": "Species (scientific name preferred, or common name). Return 'Unknown' if not stated.", } for field in target_fields: if field in field_descriptions: prompt += f"- {field}: {field_descriptions[field]}\n" prompt += f""" Respond in JSON format with these exact keys: {{ "organ": "your answer", "tissue": "your answer", "anatomical_system": "your answer", "cell_type": "your answer", "disease": "your answer", "sex": "your answer", "development_stage": "your answer", "assay": "your answer", "organism": "your answer" }}""" return prompt def _call_llm(self, prompt: str) -> Dict[str, Any]: """Call the LLM backend with the prompt.""" try: create_kwargs = { "messages": [{"role": "user", "content": prompt}], "response_model": _MetadataExtraction, "temperature": self.temperature, "max_retries": self.max_retries, } if self.model is not None: create_kwargs["model"] = self.model response = self.client.chat.completions.create(**create_kwargs) return response.model_dump() except Exception as e: self.logger.error(f"LLM call failed for provider '{self.provider}': {e}") raise RuntimeError( f"LLM call failed with provider '{self.provider}': {e}" ) from e def extract_metadata( self, text: str, fields: Optional[List[str]] = None ) -> Dict[str, Any]: """ Extract metadata from text using LLM. Args: text: Input text fields: List of fields to extract Returns: Dictionary with extracted metadata """ if not text or text.strip() == "": return { "organ": "Unknown", "tissue": "Unknown", "anatomical_system": "Unknown", "cell_type": "Unknown", "disease": "Unknown", "sex": "Unknown", "development_stage": "Unknown", "assay": "Unknown", "organism": "Unknown", } prompt = self._create_extraction_prompt(text, fields) data = self._call_llm(prompt) if fields: return {field: data.get(field, "Unknown") for field in fields} return data class EmbeddingMetadataExtractor(MetadataExtractor): """Extract metadata using embedding-based similarity matching.""" def __init__( self, model_name: str = "FremyCompany/BioLORD-2023", backend: str = "sentence-transformers", reference_categories: Dict[str, List[str]] = None, **kwargs, ): """ Initialize embedding-based metadata extractor. Args: model_name: Embedding model name (default: FremyCompany/BioLORD-2023 - optimized for biomedical text) backend: Embedding backend ("sentence-transformers", "fastembed") reference_categories: Reference categories for classification (required) **kwargs: Additional parameters for embedding model Raises: ValueError: If reference_categories is not provided """ super().__init__() if reference_categories is None: raise ValueError( "reference_categories is required for embedding-based extraction. " "Please provide a dictionary mapping category names to lists of reference terms. " "Example: {'tissue': ['blood', 'brain', 'liver'], 'disease': ['healthy', 'cancer']}" ) self.model_name = model_name self.backend = backend self.kwargs = kwargs self.model = self._load_model() self.reference_categories = reference_categories self.reference_embeddings = self._compute_reference_embeddings() def _load_model(self): """Load the embedding model.""" if self.backend == "sentence-transformers": try: from sentence_transformers import SentenceTransformer return SentenceTransformer(self.model_name) except ImportError: if _prompt_install_enrichment_dependencies(): from sentence_transformers import SentenceTransformer return SentenceTransformer(self.model_name) else: raise ImportError( "sentence-transformers required. Install with: pip install sentence-transformers" ) elif self.backend == "fastembed": try: from fastembed import TextEmbedding return TextEmbedding(model_name=self.model_name) except ImportError: if _prompt_install_enrichment_dependencies(): from fastembed import TextEmbedding return TextEmbedding(model_name=self.model_name) else: raise ImportError( "fastembed required. Install with: pip install fastembed" ) else: raise ValueError(f"Unsupported backend: {self.backend}") def _get_cache_path(self) -> str: """Get path for embedding cache file.""" import hashlib import os from pathlib import Path cache_dir = Path.home() / ".cache" / "pysradb" cache_dir.mkdir(parents=True, exist_ok=True) cache_key = f"{self.model_name}_{sorted(self.reference_categories.keys())}" cache_hash = hashlib.md5(cache_key.encode()).hexdigest()[:16] return str(cache_dir / f"embeddings_{cache_hash}.npz") def _compute_reference_embeddings(self) -> Dict[str, Any]: """Compute embeddings for reference categories with caching.""" import os import numpy as np cache_path = self._get_cache_path() if os.path.exists(cache_path): try: cached = np.load(cache_path, allow_pickle=True) embeddings = {k: cached[k] for k in cached.files} self.logger.info(f"Loaded cached embeddings from {cache_path}") return embeddings except Exception as e: self.logger.warning(f"Failed to load cache: {e}") self.logger.info( f"Computing embeddings for {sum(len(v) for v in self.reference_categories.values())} terms..." ) embeddings = {} for category, terms in self.reference_categories.items(): if self.backend == "sentence-transformers": embeddings[category] = self.model.encode(terms, show_progress_bar=False) elif self.backend == "fastembed": embeddings[category] = np.array(list(self.model.embed(terms))) try: np.savez(cache_path, **embeddings) self.logger.info(f"Cached embeddings to {cache_path}") except Exception as e: self.logger.warning(f"Failed to cache embeddings: {e}") return embeddings def _find_best_match( self, text_embedding, category: str, threshold: float = 0.3 ) -> str: """Find best matching category using cosine similarity.""" import numpy as np from sklearn.metrics.pairwise import cosine_similarity if category not in self.reference_embeddings: return "Unknown" ref_embeddings = self.reference_embeddings[category] text_emb = np.array(text_embedding).reshape(1, -1) similarities = cosine_similarity(text_emb, ref_embeddings)[0] max_idx = np.argmax(similarities) max_sim = similarities[max_idx] if max_sim >= threshold: return self.reference_categories[category][max_idx] else: return "Unknown" def _parse_structured_fields(self, text: str) -> Dict[str, str]: """ Parse structured text in 'field: value' format. Args: text: Input text with potential 'field: value' patterns Returns: Dictionary of parsed field-value pairs """ import re parsed = {} # Pattern to match "field_name: value" where value extends to next field or end pattern = r"([a-z_]+):\s*([^.]+?)(?:\.|$)" matches = re.findall(pattern, text, re.IGNORECASE) for field_name, value in matches: parsed[field_name.strip().lower()] = value.strip() return parsed def _match_value_or_text( self, value: Optional[str], full_text: str, category: str ) -> str: """ Match a specific extracted value or fall back to full text matching. This method first tries to match an extracted value (e.g., "F" from "sex: F") directly against reference categories. If that fails or no value is provided, it falls back to matching the full combined text. Args: value: Extracted field value (e.g., "F" from "sex: F") full_text: Full combined text for fallback matching category: Category name to match against Returns: Best matching category value or "Unknown" """ import numpy as np if value and category in self.reference_categories: try: if self.backend == "sentence-transformers": value_embedding = self.model.encode(value) elif self.backend == "fastembed": value_embedding = np.array(list(self.model.embed([value])))[0] result = self._find_best_match(value_embedding, category) if result != "Unknown": return result except Exception: pass # Fall through to full text matching # Fall back to full text matching if category in self.reference_categories: try: if self.backend == "sentence-transformers": text_embedding = self.model.encode(full_text) elif self.backend == "fastembed": text_embedding = np.array(list(self.model.embed([full_text])))[0] return self._find_best_match(text_embedding, category) except Exception: return "Unknown" return "Unknown" def extract_metadata( self, text: str, fields: Optional[List[str]] = None ) -> Dict[str, Any]: """ Extract metadata using embedding similarity. Args: text: Input text fields: List of fields to extract Returns: Dictionary with extracted metadata """ if not text or text.strip() == "": return { "organ": "Unknown", "tissue": "Unknown", "anatomical_system": "Unknown", "cell_type": "Unknown", "disease": "Unknown", "sex": "Unknown", "development_stage": "Unknown", "assay": "Unknown", "organism": "Unknown", } structured_fields = self._parse_structured_fields(text) organ = self._match_value_or_text( structured_fields.get("organ") or structured_fields.get("source_name"), text, "organs", ) tissue = self._match_value_or_text( structured_fields.get("tissue"), text, "tissues", ) cell_type = self._match_value_or_text( structured_fields.get("cell_type"), text, "cell_types" ) disease = self._match_value_or_text( structured_fields.get("disease"), text, "diseases" ) anatomical_system = self._match_value_or_text( structured_fields.get("anatomical_system"), text, "anatomical_systems" ) sex = self._match_value_or_text(structured_fields.get("sex"), text, "sex") development_stage = self._match_value_or_text( structured_fields.get("age") or structured_fields.get("development_stage"), text, "development_stage", ) assay = self._match_value_or_text( structured_fields.get("assay") or structured_fields.get("sample_title"), text, "assay", ) organism = self._match_value_or_text( structured_fields.get("organism"), text, "organism" ) return { "organ": organ, "tissue": tissue, "anatomical_system": anatomical_system, "cell_type": cell_type, "disease": disease, "sex": sex, "development_stage": development_stage, "assay": assay, "organism": organism, } def create_metadata_extractor( method: str = "llm", backend: Optional[str] = None, model: Optional[str] = None, **kwargs, ) -> MetadataExtractor: """ Factory function to create metadata extractor. Args: method: Extraction method (``llm`` or ``embedding``) backend: Backend for the method model: Model name kwargs: Additional parameters (as keyword arguments) Returns: MetadataExtractor instance Examples: >>> # LLM-based with Instructor (default provider) >>> extractor = create_metadata_extractor(method="llm") >>> >>> # Embedding-based (default: BioLORD-2023 for biomedical text) >>> extractor = create_metadata_extractor(method="embedding") """ if method.lower() == "llm": backend = backend or DEFAULT_LLM_PROVIDER return LLMMetadataExtractor(backend=backend, model=model, **kwargs) elif method.lower() == "embedding": backend = backend or "sentence-transformers" return EmbeddingMetadataExtractor( model_name=model or "FremyCompany/BioLORD-2023", backend=backend, **kwargs, ) else: raise ValueError(f"Unknown method: {method}. Choose 'llm' or 'embedding'") def apply_dataframe_enrichment( df: pd.DataFrame, method: str = "embedding", backend: Optional[str] = None, model: Optional[str] = None, text_column: Optional[str] = None, show_progress: bool = True, prefix: str = "guessed_", ) -> pd.DataFrame: """ Utility function to apply metadata enrichment to a DataFrame. This is a convenience function that handles: - Column auto-detection - Extractor initialization - Error handling - Progress display Args: df: Input DataFrame method: Enrichment method ('llm' or 'embedding') backend: Backend for the method model: Model name text_column: Column to use (auto-detected if None) show_progress: Show progress bar prefix: Prefix for new columns Returns: Enriched DataFrame Example: >>> from pysradb.metadata_enrichment import apply_dataframe_enrichment >>> enriched_df = apply_dataframe_enrichment( ... df, ... method="embedding", ... text_column="experiment_title" ... ) """ if df is None or df.empty: return df try: extractor = create_metadata_extractor( method=method, backend=backend, model=model ) if text_column is None: candidates = [ "experiment_title", "experiment_desc", "study_title", "description", "sample_title", "source_name", "tissue", "condition", "treatment", "age", "sex", "strain", ] for candidate in candidates: if candidate in df.columns: text_column = candidate break if text_column and text_column in df.columns: return extractor.enrich_dataframe( df, text_column=text_column, prefix=prefix, show_progress=show_progress ) else: logger.warning("No suitable text column found for enrichment") return df except ImportError as e: logger.warning(f"Enrichment dependencies not installed: {e}") return df except Exception as e: logger.warning(f"Enrichment failed: {e}") return df ================================================ FILE: pysradb/ontology_reference.json ================================================ { "organs": [ "brain", "heart", "liver", "lung", "kidney", "spleen", "pancreas", "stomach", "intestine", "colon", "small intestine", "duodenum", "jejunum", "ileum", "skin", "muscle", "bone", "adipose tissue", "fat", "bone marrow", "thymus", "lymph node", "tonsil", "appendix", "eye", "retina", "cornea", "lens", "ear", "cochlea", "tongue", "tooth", "salivary gland", "esophagus", "gallbladder", "rectum", "bladder", "urinary bladder", "urethra", "ureter", "testis", "ovary", "uterus", "prostate", "mammary gland", "breast", "placenta", "adrenal gland", "pituitary gland", "thyroid gland", "parathyroid gland", "pineal gland", "trachea", "bronchus", "diaphragm", "aorta", "artery", "vein", "capillary", "nose", "nasal cavity", "sinus", "pharynx", "larynx", "cerebellum", "cerebral cortex", "hippocampus", "amygdala", "striatum", "thalamus", "hypothalamus", "spinal cord", "dorsal root ganglion", "sympathetic ganglion", "skeletal muscle", "cardiac muscle", "smooth muscle" ], "tissues": [ "blood", "plasma", "serum", "whole blood", "peripheral blood", "epithelium", "epithelial tissue", "endothelium", "mesothelium", "connective tissue", "adipose tissue", "cartilage", "bone tissue", "nervous tissue", "neural tissue", "brain tissue", "spinal cord tissue", "muscle tissue", "skeletal muscle tissue", "cardiac muscle tissue", "smooth muscle tissue", "lymphoid tissue", "myeloid tissue", "hematopoietic tissue", "skin tissue", "dermal tissue", "epidermal tissue", "vascular tissue", "blood vessel", "glandular tissue", "secretory tissue", "lung tissue", "alveolar tissue", "bronchial tissue", "liver tissue", "hepatic tissue", "kidney tissue", "renal tissue", "cortex", "medulla", "glomerulus", "heart tissue", "myocardium", "endocardium", "pericardium", "intestinal tissue", "gut tissue", "colonic tissue", "pancreatic tissue", "pancreatic islet", "thymic tissue", "splenic tissue", "bone marrow tissue", "stromal tissue", "tumor tissue", "cancerous tissue", "malignant tissue", "benign tissue", "fibrotic tissue", "scar tissue", "necrotic tissue", "embryonic tissue", "fetal tissue", "placental tissue", "stem cell niche", "germinal center", "white matter", "gray matter", "cortical tissue", "subcortical tissue" ], "anatomical_systems": [ "nervous system", "central nervous system", "peripheral nervous system", "autonomic nervous system", "cardiovascular system", "circulatory system", "vascular system", "respiratory system", "pulmonary system", "digestive system", "gastrointestinal system", "alimentary system", "urinary system", "renal system", "excretory system", "reproductive system", "genital system", "endocrine system", "hormonal system", "immune system", "lymphatic system", "hematopoietic system", "musculoskeletal system", "skeletal system", "muscular system", "integumentary system", "skin system", "sensory system", "visual system", "auditory system", "olfactory system", "gustatory system" ], "cell_types": [ "T cell", "B cell", "NK cell", "natural killer cell", "CD4 T cell", "CD8 T cell", "regulatory T cell", "Treg", "helper T cell", "cytotoxic T cell", "naive T cell", "memory T cell", "effector T cell", "activated T cell", "naive B cell", "memory B cell", "plasma cell", "plasmablast", "monocyte", "macrophage", "dendritic cell", "DC", "neutrophil", "eosinophil", "basophil", "mast cell", "erythrocyte", "red blood cell", "RBC", "platelet", "thrombocyte", "megakaryocyte", "hematopoietic stem cell", "HSC", "progenitor cell", "fibroblast", "myofibroblast", "endothelial cell", "vascular endothelial cell", "lymphatic endothelial cell", "epithelial cell", "keratinocyte", "enterocyte", "colonocyte", "neuron", "neuronal cell", "pyramidal neuron", "interneuron", "motor neuron", "sensory neuron", "astrocyte", "oligodendrocyte", "microglia", "ependymal cell", "Schwann cell", "satellite glial cell", "hepatocyte", "cholangiocyte", "Kupffer cell", "stellate cell", "cardiomyocyte", "cardiac fibroblast", "pericyte", "podocyte", "mesangial cell", "tubular epithelial cell", "pneumocyte", "type I pneumocyte", "type II pneumocyte", "alveolar macrophage", "club cell", "beta cell", "alpha cell", "delta cell", "acinar cell", "ductal cell", "adipocyte", "preadipocyte", "brown adipocyte", "white adipocyte", "osteoblast", "osteoclast", "osteocyte", "chondrocyte", "smooth muscle cell", "skeletal muscle cell", "myocyte", "stem cell", "embryonic stem cell", "ESC", "induced pluripotent stem cell", "iPSC", "mesenchymal stem cell", "MSC", "neural stem cell", "NSC", "cancer cell", "tumor cell", "malignant cell", "germ cell", "spermatocyte", "oocyte", "sperm", "egg", "Leydig cell", "Sertoli cell", "granulosa cell", "theca cell", "trophoblast", "syncytiotrophoblast", "cytotrophoblast", "photoreceptor", "rod cell", "cone cell", "retinal ganglion cell", "melanocyte", "Langerhans cell", "goblet cell", "Paneth cell", "enteroendocrine cell", "thyroid follicular cell", "parafollicular cell", "C cell" ], "diseases": [ "healthy", "normal", "control", "wild type", "WT", "cancer", "carcinoma", "sarcoma", "melanoma", "lymphoma", "leukemia", "myeloma", "tumor", "neoplasm", "malignancy", "metastasis", "lung cancer", "breast cancer", "colon cancer", "colorectal cancer", "prostate cancer", "liver cancer", "hepatocellular carcinoma", "HCC", "pancreatic cancer", "pancreatic adenocarcinoma", "brain tumor", "glioblastoma", "glioma", "astrocytoma", "melanoma", "skin cancer", "basal cell carcinoma", "squamous cell carcinoma", "ovarian cancer", "cervical cancer", "endometrial cancer", "uterine cancer", "kidney cancer", "renal cell carcinoma", "bladder cancer", "urothelial carcinoma", "gastric cancer", "stomach cancer", "acute lymphoblastic leukemia", "ALL", "acute myeloid leukemia", "AML", "chronic lymphocytic leukemia", "CLL", "chronic myeloid leukemia", "CML", "multiple myeloma", "Hodgkin lymphoma", "non-Hodgkin lymphoma", "diabetes", "diabetes mellitus", "type 1 diabetes", "T1D", "type 2 diabetes", "T2D", "obesity", "metabolic syndrome", "Alzheimer's disease", "AD", "Parkinson's disease", "PD", "multiple sclerosis", "MS", "amyotrophic lateral sclerosis", "ALS", "cardiovascular disease", "heart disease", "coronary artery disease", "CAD", "atherosclerosis", "myocardial infarction", "heart attack", "stroke", "heart failure", "cardiomyopathy", "arrhythmia", "hypertension", "high blood pressure", "hypotension", "asthma", "chronic obstructive pulmonary disease", "COPD", "emphysema", "pulmonary fibrosis", "interstitial lung disease", "inflammatory bowel disease", "IBD", "Crohn's disease", "ulcerative colitis", "rheumatoid arthritis", "RA", "osteoarthritis", "arthritis", "systemic lupus erythematosus", "SLE", "lupus", "psoriasis", "eczema", "atopic dermatitis", "dermatitis", "chronic kidney disease", "CKD", "renal failure", "kidney failure", "liver disease", "cirrhosis", "hepatitis", "fatty liver disease", "NAFLD", "infection", "bacterial infection", "viral infection", "fungal infection", "sepsis", "septic shock", "inflammation", "COVID-19", "SARS-CoV-2", "coronavirus", "influenza", "flu", "pneumonia", "HIV", "AIDS", "tuberculosis", "TB", "fibrosis", "tissue damage", "injury", "wound", "lesion", "autoimmune disease", "immunodeficiency", "allergy", "allergic reaction", "hypersensitivity", "anemia", "thrombocytopenia", "neutropenia", "congenital disorder", "genetic disorder", "inherited disease", "syndrome", "rare disease" ], "sex": [ "male", "M", "men", "man", "boy", "female", "F", "women", "woman", "girl", "mixed", "both", "male and female", "combined", "unknown", "not specified", "unspecified", "NA", "N/A" ], "development_stage": [ "embryonic", "embryo", "embryonic day", "E", "fetal", "fetus", "gestational week", "GW", "prenatal", "neonatal", "newborn", "neonate", "postnatal day", "P", "infant", "baby", "child", "childhood", "juvenile", "pediatric", "adolescent", "teenager", "pubescent", "adult", "young adult", "mature", "grown", "middle aged", "middle age", "aged", "elderly", "old", "geriatric", "senescent", "E0", "E1", "E2", "E3", "E4", "E5", "E6", "E7", "E8", "E9", "E10", "E11", "E12", "E13", "E14", "E15", "E16", "E17", "E18", "P0", "P1", "P2", "P3", "P4", "P5", "P6", "P7", "P14", "P21", "P28", "week", "weeks", "month", "months", "year", "years", "trimester", "first trimester", "second trimester", "third trimester", "stage", "developmental stage", "life stage" ], "assay": [ "RNA-seq", "RNA sequencing", "bulk RNA-seq", "total RNA-seq", "scRNA-seq", "single cell RNA-seq", "single-cell RNA sequencing", "10x", "Drop-seq", "snRNA-seq", "single nucleus RNA-seq", "single-nucleus RNA sequencing", "ChIP-seq", "ChIP sequencing", "chromatin immunoprecipitation", "ATAC-seq", "ATAC sequencing", "accessibility", "snATAC-seq", "single nucleus ATAC-seq", "scATAC-seq", "single cell ATAC-seq", "DNase-seq", "DNase hypersensitivity", "Hi-C", "chromosome conformation capture", "CITE-seq", "cellular indexing", "protein + RNA", "Perturb-seq", "CRISPR screen", "perturbation", "Spatial transcriptomics", "spatial", "Visium", "MERFISH", "seqFISH", "Bisulfite-seq", "BS-seq", "WGBS", "RRBS", "methylation", "microarray", "expression array", "Affymetrix", "Illumina array", "WGS", "whole genome sequencing", "genome sequencing", "WES", "whole exome sequencing", "exome sequencing", "targeted sequencing", "amplicon sequencing", "panel sequencing", "miRNA-seq", "microRNA sequencing", "small RNA-seq", "CUT&RUN", "CUT&Tag", "cleavage under targets", "PRO-seq", "GRO-seq", "nascent RNA", "ribosome profiling", "Ribo-seq", "translation", "long-read sequencing", "PacBio", "Nanopore", "Oxford Nanopore", "proteomics", "mass spectrometry", "LC-MS", "metabolomics", "lipidomics", "FACS", "flow cytometry", "fluorescence-activated cell sorting", "imaging", "microscopy", "immunofluorescence", "immunohistochemistry" ], "organism": [ "Homo sapiens", "human", "humans", "H. sapiens", "Mus musculus", "mouse", "mice", "M. musculus", "Rattus norvegicus", "rat", "rats", "R. norvegicus", "Danio rerio", "zebrafish", "D. rerio", "Drosophila melanogaster", "fruit fly", "Drosophila", "D. melanogaster", "Caenorhabditis elegans", "C. elegans", "nematode", "worm", "Saccharomyces cerevisiae", "yeast", "S. cerevisiae", "budding yeast", "Arabidopsis thaliana", "Arabidopsis", "A. thaliana", "Escherichia coli", "E. coli", "bacteria", "Sus scrofa", "pig", "swine", "porcine", "Bos taurus", "cow", "cattle", "bovine", "Gallus gallus", "chicken", "G. gallus", "Macaca mulatta", "rhesus macaque", "monkey", "M. mulatta", "Pan troglodytes", "chimpanzee", "chimp", "P. troglodytes", "Canis lupus familiaris", "dog", "canine", "Felis catus", "cat", "feline", "Oryctolagus cuniculus", "rabbit", "Xenopus tropicalis", "frog", "Xenopus", "X. tropicalis", "Ciona intestinalis", "sea squirt", "tunicate" ] } ================================================ FILE: pysradb/search.py ================================================ """This file contains the search classes for the search feature.""" import os import re import sys import time import urllib import xml.etree.ElementTree as Et from json import JSONDecodeError import pandas as pd import requests from tqdm.autonotebook import tqdm from .exceptions import IncorrectFieldException, MissingQueryException from .utils import requests_3_retries, scientific_name_to_taxid SEARCH_REQUEST_TIMEOUT = 20 SRA_SEARCH_GROUP_SIZE = 300 class QuerySearch: """This is the base class for the search feature. This class takes as input the user's search query, which has been tokenized by the ArgParser. The query will be sent to either SRA or ENA depending on the user's input, and the results will be returned as a pandas dataframe. Attributes ---------- self.df: Pandas DataFrame The search result belonging to this search instance Parameters ---------- verbosity : integer The level of details of the search result. return_max : int The maximum number of entries to be returned. query : str The main query string. accession : str A relevant study / experiment / sample / run accession number. organism : str Scientific name of the sample organism layout : str Library layout. Possible inputs: single, paired mbases : int Size of the sample of interest rounded to the nearest megabase. publication_date : str The publication date of the run in the format dd-mm-yyyy. If a date range is desired, input should be in the format of dd-mm-yyyy:dd-mm-yyyy platform : str Sequencing platform used for the run. Some possible inputs include: illumina, ion torrent, oxford nanopore selection : str Library selection. Some possible inputs: cdna, chip, dnase, pcr source : str Library source. Some possible inputs: genomic, metagenomic, transcriptomic strategy : str Library Preparation strategy. Some possible inputs: wgs, amplicon, rna seq title : str Title of the experiment associated with the run suppress_validation: bool Defaults to False. If this is set to True, the user input format checks will be skipped. Setting this to True may cause the program to behave in unexpected ways, but allows the user to search queries that does not pass the format check. Methods ------- get_df() Returns the dataframe storing this search result. search() Executes the search. show_result_statistics() Shows summary information about search results. visualise_results() Generate graphs that visualise the search results. get_plot_objects(): Get the plot objects for plots generated. """ def __init__( self, verbosity=2, return_max=20, query=None, accession=None, organism=None, layout=None, mbases=None, publication_date=None, platform=None, selection=None, source=None, strategy=None, title=None, suppress_validation=False, ): try: int_verbosity = int(verbosity) if int_verbosity not in range(4): raise ValueError except (TypeError, ValueError): raise IncorrectFieldException( f"Incorrect verbosity format: {verbosity}\n" "Verbosity must be an integer between 0 to 3 inclusive." ) try: int_return_max = int(return_max) if int_return_max <= 0: raise ValueError except (TypeError, ValueError): raise IncorrectFieldException( f"Incorrect return_max format: {return_max}\n" "return_max must be a positive integer." ) self.verbosity = int_verbosity self.return_max = int_return_max self.fields = { "query": query, "accession": accession, "organism": organism, "layout": layout, "mbases": mbases, "publication_date": publication_date, "platform": platform, "selection": selection, "source": source, "strategy": strategy, "title": title, } for k in self.fields: if type(self.fields[k]) == list: self.fields[k] = " ".join(self.fields[k]) self.df = pd.DataFrame() # Verify that not all query fields are empty if not any(self.fields.values()): raise MissingQueryException() if not suppress_validation: self._validate_fields() self.stats = { "study": "-", "experiment": "-", "run": "-", "sample": "-", "Date range": "-", "Organisms": "-", "Library strategy": "-", "Library source": "-", "Library selection": "-", "Library layout": "-", "Platform": "-", "count_mean": "-", "count_median": "-", "count_stdev": "-", } self.plot_objects = {} def _input_multi_regex_checker(self, regex_matcher, input_query, error_message): """Checks if the user input match exactly 1 of the possible regex. This is a helper method for _validate_fields. It takes as input a dictionary of regex expression : accepted string by API pairs, and an input string, and verifies that the input string matches exactly one of the regex expressions. Matching multiple expressions indicates the input string is ambiguous, while matching none of the expressions suggests the input will likely produce no results or an error. Once matched, this method formats the user input so that it can be accepted by the API to be queried, as ENA especially expect case-sensitive exact matches for search queries. Parameters ---------- regex_matcher : dict dictionary of regex expression : accepted string by API pairs. input_query : str input string for a particular query field. error_message : str error message to be shown if input_query does not match any of the regex expressions in regex_matcher. Returns ------- tuple tuple pair of (input_query, message). message is "" if no format error has been identified, error message otherwise. """ matched_strings = [] for regex_expression in regex_matcher: if re.match(regex_expression, input_query, re.IGNORECASE): matched_strings.append(regex_matcher[regex_expression]) if not matched_strings: return input_query, error_message elif len(matched_strings) == 1: return matched_strings[0], "" else: message = ( f"Multiple potential matches have been identified for {input_query}:\n" f"{matched_strings}\n" f"Please check your input.\n\n" ) return input_query, message def _validate_fields(self): """Verifies that user input format is correct. This helper function tries to match the input query strings from the user to the exact string that is accepted by both SRA and ENA Note: as of the implementation of this method, ENA does not have a documentation page listing the accepted values for query parameters. The list of parameters below were collected from ENA's advanced search page: https://www.ebi.ac.uk/ena/browser/advanced-search Updating new values: If any new values are accepted by ENA, it should appear under the corresponding parameter in the page. To update this method, think of a regex that captures what the user may type for the new value, and include it in the respective xxx_matcher dictionary below as a regex:value key value pair. Eg: if a new sequencing platform, Pokemon, is added to ENA, navigate to "Instrument Platform" parameter on ENA's advanced search page and copy the corresponding phrase (eg "poKe_Mon"). Then add the key value pair ".*poke.*": "poKe_Mon" to platform_matcher below. Unlike SRA, ENA requires supplied param values to be exact match to filter accordingly (eg "cDNA_oligo_dT"), which motivated this feature. Raises ------ IncorrectFieldException If the input to any query field is in the wrong format """ message = "" # verify layout if self.fields["layout"] and str(self.fields["layout"]).upper() not in [ "SINGLE", "PAIRED", ]: message += ( f"Incorrect layout field format: {self.fields['layout']}\n" "--layout must be either SINGLE or PAIRED\n\n" ) # verify mbases if self.fields["mbases"]: try: self.fields["mbases"] = int(self.fields["mbases"]) if self.fields["mbases"] <= 0: raise ValueError except (ValueError, TypeError): message += ( f"Incorrect mbases format: {self.fields['mbases']}\n" f"--mbases must be a positive integer\n\n" ) # verify publication_date date_regex = "(0[1-9]|[12][0-9]|3[01])-(0[1-9]|1[012])-(19|20)[0-9]{2}" if self.fields["publication_date"] and not re.match( f"^{date_regex}(:{date_regex})?$", self.fields["publication_date"] ): message += ( f"Incorrect publication date format: {self.fields['publication_date']}\n" f"Expected --publication-date format: dd-mm-yyyy or dd-mm-yyyy:dd-mm-yyyy, between 1900-2099\n\n" ) # verify platform platform_matcher = { ".*oxford.*|.*nanopore.*": "OXFORD_NANOPORE", ".*illumina.*": "ILLUMINA", ".*ion.*torrent.*": "ION_TORRENT", ".*capillary.*": "CAPILLARY", ".*pacbio.*|.*smrt.*": "PACBIO_SMRT", ".*abi.*solid.*": "ABI_SOLID", ".*bgi.*": "BGISEQ", ".*454.*": "LS454", ".*complete.*genomics.*": "COMPLETE_GENOMICS", ".*helicos.*": "HELICOS", } if self.fields["platform"]: error_message = ( f"Incorrect platform: {self.fields['platform']}\n" f"--platform must be one of the following: \n" f"OXFORD_NANOPORE, ILLUMINA, ION_TORRENT, \n" f"CAPILLARY, PACBIO_SMRT, ABI_SOLID, \n" f"BGISEQ, LS454, COMPLETE_GENOMICS, HELICOS\n\n" ) output = self._input_multi_regex_checker( platform_matcher, self.fields["platform"], error_message ) if output[1]: message += output[1] else: self.fields["platform"] = output[0] # verify selection selection_matcher = { ".*methylcytidine.*": "5-methylcytidine antibody", ".*cage.*": "CAGE", r".*chip\s*$": "ChIP", ".*chip.*seq.*": "ChIP-Seq", ".*dnase.*": "DNase", ".*hmpr.*": "HMPR", ".*hybrid.*": "Hybrid Selection", r".*inverse.*rrna\s*$": "Inverse rRNA", ".*inverse.*rrna.*selection.*": "Inverse rRNA selection", ".*mbd2.*protein.*methyl.*cpg.*binding.*domain.*": "MBD2 protein methyl-CpG binding domain", ".*mda.*": "MDA", ".*mf.*": "MF", ".*mnase.*": "MNase", ".*msll.*": "MSLL", r"^\s*oligo.*dt.*": "Oligo-dT", r"^\s*pcr\s*$": "PCR", ".*poly[ -_]*a.*": "PolyA", ".*race.*": "RACE", r".*random\s*$": "RANDOM", ".*random.*pcr.*": "RANDOM PCR", ".*rt[ -_]*pcr.*": "RT-PCR", ".*reduced.*representation.*": "Reduced Representation", ".*restriction.*digest.*": "Restriction Digest", r".*cdna\s*$": "cDNA", ".*cdna.*oligo.*dt": "cDNA_oligo_dT.*", # ENA only ".*cdna.*random.*priming": "cDNA_randomPriming.*", # ENA only ".*other.*": "other", ".*padlock.*probes.*capture.*method.*": "padlock probes capture method", ".*repeat.*fractionation.*": "repeat fractionation", ".*size.*fractionation.*": "size fractionation", ".*unspecified.*": "unspecified", } if self.fields["selection"]: error_message = ( f"Incorrect selection: {self.fields['selection']}\n" f"--selection must be one of the following: \n" f"5-methylcytidine antibody, CAGE, ChIP, ChIP-Seq, DNase, HMPR, Hybrid Selection, \n" f"Inverse rRNA, Inverse rRNA selection, MBD2 protein methyl-CpG binding domain, \n" f"MDA, MF, MNase, MSLL, Oligo-dT, PCR, PolyA, RACE, RANDOM, RANDOM PCR, RT-PCR, \n" f"Reduced Representation, Restriction Digest, cDNA, cDNA_oligo_dT, cDNA_randomPriming \n" f"other, padlock probes capture method, repeat fractionation, size fractionation, \n" f"unspecified\n\n" ) output = self._input_multi_regex_checker( selection_matcher, self.fields["selection"], error_message ) if output[1]: message += output[1] else: self.fields["selection"] = output[0] # verify source source_matcher = { r"^\s*genomic\s*$": "GENOMIC", ".*genomic.*single.*cell.*": "GENOMIC SINGLE CELL", ".*metagenomic.*": "METAGENOMIC", ".*metatranscriptomic.*": "METATRANSCRIPTOMIC", ".*other.*": "OTHER", ".*synthetic.*": "SYNTHETIC", r"^\s*transcriptomic\s*$": "TRANSCRIPTOMIC", ".*transcriptomic.*single.*cell.*": "TRANSCRIPTOMIC SINGLE CELL", ".*viral.*rna.*": "VIRAL RNA", } if self.fields["source"]: error_message = ( f"Incorrect source: {self.fields['source']}\n" f"--source must be one of the following: \n" f"GENOMIC, GENOMIC SINGLE CELL, METAGENOMIC, \n" f"METATRANSCRIPTOMIC, OTHER, SYNTHETIC, \n" f"TRANSCRIPTOMIC, TRANSCRIPTOMIC SINGLE CELL, VIRAL RNA\n\n" ) output = self._input_multi_regex_checker( source_matcher, self.fields["source"], error_message ) if output[1]: message += output[1] else: self.fields["source"] = output[0] # verify strategy strategy_matcher = { ".*amplicon.*": "AMPLICON", ".*atac.*": "ATAC-seq", ".*bisulfite.*": "Bisulfite-Seq", r"^\s*clone\s*$": "CLONE", ".*cloneend.*": "CLONEEND", ".*cts.*": "CTS", ".*chia.*|.*pet.*": "ChIA-PET", ".*chip.*seq.*": "ChIP-Seq", ".*dnase.*|.*hypersensitivity.*": "DNase-Hypersensitivity", r"^\s*est\s*$": "EST", ".*faire.*": "FAIRE-seq", ".*finishing.*": "FINISHING", ".*fl.*cdna.*": "FL-cDNA", ".*hi.*c.*": "Hi-C", ".*mbd.*": "MBD-Seq", ".*mnase.*": "MNase-Seq", ".*mre.*": "MRE-Seq", ".*medip.*": "MeDIP-Seq", ".*other.*": "OTHER", ".*poolclone.*": "POOLCLONE", ".*rad.*": "RAD-Seq", ".*rip.*": "RIP-Seq", r"^\s*rna.*seq": "RNA-Seq", ".*selex.*": "SELEX", ".*synthetic.*|.*long.*read.*": "Synthetic-Long-Read", ".*targeted.*capture.*": "Targeted-Capture", ".*tethered.*chromatin.*conformation.*capture.*|.*tccc.*": "Tethered Chromatin Conformation Capture", ".*tn.*": "Tn-Seq", ".*validation.*": "VALIDATION", ".*wcs.*": "WCS", ".*wga.*": "WGA", ".*wgs.*": "WGS", ".*wxs.*": "WXS", ".*mirna.*": "miRNA-Seq", ".*ncrna.*": "ncRNA-Seq", ".*ssrna.*": "ssRNA-seq", ".*gbs.*": "GBS", } if self.fields["strategy"]: error_message = ( f"Incorrect strategy: {self.fields['strategy']}\n" f"--strategy must be one of the following: \n" f"AMPLICON, ATAC-seq, Bisulfite-Seq, CLONE, CLONEEND, CTS, ChIA-PET, ChIP-Seq, \n" f"DNase-Hypersensitivity, EST, FAIRE-seq, FINISHING, FL-cDNA, Hi-C, MBD-Seq, MNase-Seq,\n" f"MRE-Seq, MeDIP-Seq, OTHER, POOLCLONE, RAD-Seq, RIP-Seq, RNA-Seq, SELEX, \n" f"Synthetic-Long-Read, Targeted-Capture, Tethered Chromatin Conformation Capture, \n" f"Tn-Seq, VALIDATION, WCS, WGA, WGS, WXS, miRNA-Seq, ncRNA-Seq, ssRNA-seq, GBS\n\n" ) output = self._input_multi_regex_checker( strategy_matcher, self.fields["strategy"], error_message ) if output[1]: message += output[1] else: self.fields["strategy"] = output[0] if message: raise IncorrectFieldException(message) def _list_stat(self, stat_header): stat = self.stats[stat_header] if type(stat) != dict: return f" {stat_header}: {stat}\n" keys = sorted(stat.keys()) stat_breakdown = "\n" for key in keys: stat_breakdown += f"\t {key}: {stat[key]}\n" return f" {stat_header}: {stat_breakdown}\n" def show_result_statistics(self): """Shows search result statistics.""" if self.df.empty: print( "No results are found for the current search query, hence no statistics can be generated." ) return stats = ( "\n Statistics for the search query:\n" + " =================================\n" + f" Number of unique studies: {self.stats['study']}\n" + f" Number of unique experiments: {self.stats['experiment']}\n" + f" Number of unique runs: {self.stats['run']}\n" + f" Number of unique samples: {self.stats['sample']}\n" + f" Mean base count of samples: {self.stats['count_mean']:.3f}\n" + f" Median base count of samples: {self.stats['count_median']:.3f}\n" + f" Sample base count standard deviation: {self.stats['count_stdev']:.3f}\n" ) # Statistics with categorical breakdowns: categorical_stats = ( "Date range", "Organisms", "Platform", "Library strategy", "Library source", "Library selection", "Library layout", ) for categorical_stat in categorical_stats: stats += self._list_stat(categorical_stat) print(stats) def visualise_results( self, graph_types=("all",), show=False, saveto="./search_plots/" ): """Generate graphs that visualise the search results. This method will only work if the optional dependency, matplotlib, is installed in the system. Parameters ---------- graph_types : tuple tuple containing strings representing types of graphs to generate. Possible strings: all, daterange, organism, source, selection, platform, basecount saveto : str directory name where the generated graphs are saved. show : bool Whether plotted graphs are immediately shown. """ if self.df.empty: print( "No results are found for the current search query, hence no graphs can be generated." ) return try: import matplotlib.pyplot as plt except ImportError: print( "The optional dependency, matplotlib, is not available on the system.\n" "matplotlib is required to generate graphs to visualise search results.\n" 'You can install matplotlib by typing "pip install matplotlib" on the command line.\n' ) return plt.rcParams["figure.autolayout"] = True if not os.path.isdir(saveto): os.mkdir(saveto) plots = [ ("Base Count",), ("Publication Date",), ("Organism",), ("Library Source",), ("Library Selection",), ("Platform",), ("Organism", "Publication Date"), ("Library Source", "Publication Date"), ("Library Selection", "Publication Date"), ("Platform", "Publication Date"), ("Library Source", "Organism"), ("Library Selection", "Organism"), ("Platform", "Organism"), ("Library Selection", "Library Source"), ("Platform", "Library Source"), ("Platform", "Library Selection"), ] plot_keys = { "daterange": "Publication Date", "organism": "Organism", "source": "Library Source", "selection": "Library Selection", "platform": "Platform", "basecount": "Base Count", } if "all" not in graph_types: selected_plots = [] for graph_type in graph_types: if graph_type not in plot_keys: continue for plot in plots: if plot_keys[graph_type] in plot and plot not in selected_plots: selected_plots.append(plot) plots = selected_plots too_many_organisms = False if self.stats["graph_raw"]["Organism"].nunique() > 30: print( "Too many types of organisms to plot (>30). Showing only top 30 organisms." ) too_many_organisms = True for plot in plots: self._plot_graph(plt, plot, show, saveto, too_many_organisms) def search(self): pass def get_df(self): """Getter for the search result dataframe.""" return self.df def get_plot_objects(self): """Get the plot objects for plots generated.""" return self.plot_objects def _plot_graph(self, plt, axes, show, savedir, too_many_organisms): """Plots a graph based on data from self.stats Parameters ---------- axes: tuple tuple containing 1 or 2 strings corresponding to the statistics to plot. 1 string: Histogram. 2 string: heat map savedir: str directory to save to show: bool whether to call plt.show """ timestamp = time.strftime("%Y-%m-%d %H-%M-%S") if ( "Publication Date" in axes and self.stats["graph_raw"]["Publication Date"].nunique() > 30 ): self.stats["graph_raw"]["Publication Date"] = self.stats["graph_raw"][ "Publication Date" ].str[:-3] if axes == ("Base Count",): count = list(self.stats["count_data"]) if len(count) == 0: return title = "Histogram of Base Count" plt.figure(figsize=(15, 10)) plt.hist(count, min(70, len(count)), color="#135c1c", log=True) plt.xlabel("Base Count", fontsize=14) plt.ylabel("Frequency", fontsize=14) plt.xticks(rotation=90) plt.title(title, fontsize=18) plt.savefig(f"{savedir}{title} {timestamp}.svg") self.plot_objects[axes] = plt elif len(axes) == 1: title = f"Histogram of {axes[0]}" data = self.stats["graph_raw"][axes[0]].value_counts() if too_many_organisms: data = data[:30] plt.figure(figsize=(15, 10)) plt.bar( range(len(data.values)), data.values, tick_label=list(data.index), color="#135c1c", ) plt.xticks(rotation=90) plt.title(title, fontsize=18) plt.xlabel(axes[0], fontsize=14) plt.ylabel("Frequency", fontsize=14) plt.savefig(f"{savedir}{title} {timestamp}.svg") self.plot_objects[axes] = plt elif len(axes) == 2: title = f"Heatmap of {axes[0]} against {axes[1]}" df = self.stats["graph_raw"][list(axes)] a = df.groupby([axes[0]]).agg({i: "value_counts" for i in df.columns[1:]}) a = a.rename(columns={axes[1]: f"{axes[1]}_count"}) b = a.reset_index(level=list(axes)) piv = ( pd.pivot_table( b, values=f"{axes[1]}_count", index=[axes[0]], columns=[axes[1]], fill_value=0, aggfunc="sum", margins=True, ) .sort_values("All", ascending=False) .drop("All", axis=1) .sort_values("All", ascending=False, axis=1) .drop("All") ) if too_many_organisms: if axes[0] == "Organism": piv = piv[:30] else: piv = piv.iloc[:, :30] fig, ax = plt.subplots(figsize=(15, 12)) im = ax.imshow(piv, cmap="Greens") fig.colorbar(im, ax=ax) ax.set_title(title, fontsize=18) ax.set_xticks(range(len(piv.columns))) ax.set_yticks(range(len(piv.index))) ax.set_xticklabels(piv.columns, rotation=90) ax.set_yticklabels(piv.index) ax.set_ylabel(axes[0], fontsize=14) ax.set_xlabel(axes[1], fontsize=14) ax.get_figure().savefig(f"{savedir}{title} {timestamp}.svg") self.plot_objects[axes] = (fig, ax) if show: plt.show() class SraSearch(QuerySearch): """Subclass of QuerySearch that implements search by querying NCBI Entrez API Methods ------- search() sends the user query via requests to NCBI Entrez API and returns search results as a pandas dataframe. show_result_statistics() Shows summary information about search results. visualise_results() Generate graphs that visualise the search results. get_plot_objects(): Get the plot objects for plots generated. get_uids(): Get NCBI uids retrieved during this search query. _format_query_string() formats the input user query into a string _format_request() formats the request payload _format_result(content) formats the search query output. See Also -------- QuerySearch: Superclass of SraSearch """ def __init__( self, verbosity=2, return_max=20, query=None, accession=None, organism=None, layout=None, mbases=None, publication_date=None, platform=None, selection=None, source=None, strategy=None, title=None, suppress_validation=False, ): super().__init__( verbosity, return_max, query, accession, organism, layout, mbases, publication_date, platform, selection, source, strategy, title, suppress_validation, ) self.entries = {} self.number_entries = 0 self.uids = [] def search(self): # Step 1: retrieves the list of uids that satisfies the input # search query payload = self._format_request() try: r = requests_3_retries().get( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi", params=payload, timeout=SEARCH_REQUEST_TIMEOUT, ) r.raise_for_status() self.uids = r.json()["esearchresult"]["idlist"] # Step 2: retrieves the detailed information for each uid # returned, in groups of SRA_SEARCH_GROUP_SIZE. if not self.uids: print( f"No results found for the following search query: \n {self.fields}" ) return # If no queries found, return nothing pbar = tqdm(total=len(self.uids)) for i in range(0, len(self.uids), SRA_SEARCH_GROUP_SIZE): current_uids = ",".join( self.uids[i : min(i + SRA_SEARCH_GROUP_SIZE, len(self.uids))] ) pbar.update(min(SRA_SEARCH_GROUP_SIZE, len(self.uids) - i)) payload2 = {"db": "sra", "retmode": "xml", "id": current_uids} r = requests_3_retries().get( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi", params=payload2, timeout=SEARCH_REQUEST_TIMEOUT, stream=True, ) r.raise_for_status() r.raw.decode_content = True self._format_response(r.raw) pbar.close() self._format_result() except requests.exceptions.Timeout: sys.exit(f"Connection to the server has timed out. Please retry.") except requests.exceptions.HTTPError: sys.exit( f"HTTPError: This is likely caused by an invalid search query: " f"\nURL queried: {r.url} \nUser query: {self.fields}" ) def get_uids(self): """Get NCBI uids retrieved during this search query. Note: There is a chance that some uids retrieved do not appear in the search result output (Refer to #88) """ return self.uids def _format_query_string(self): term = "" if self.fields["query"]: term += self.fields["query"] + " AND " if self.fields["accession"]: term += self.fields["accession"] + "[Accession] AND " if self.fields["organism"]: term += self.fields["organism"] + "[Organism] AND " if self.fields["layout"]: term += self.fields["layout"] + "[Layout] AND " if self.fields["mbases"]: term += str(self.fields["mbases"]) + "[Mbases] AND " if self.fields["publication_date"]: dates = [] for date in self.fields["publication_date"].split(":"): dates.append("/".join(date.split("-")[::-1])) term += ":".join(dates) + "[PDAT] AND " if self.fields["platform"]: term += self.fields["platform"] + "[Platform] AND " if self.fields["selection"]: term += self.fields["selection"] + "[Selection] AND " if self.fields["source"]: term += self.fields["source"] + "[Source] AND " if self.fields["strategy"]: term += self.fields["strategy"] + "[Strategy] AND " if self.fields["title"]: term += self.fields["title"] + "[Title] AND " return term[:-5] # Removing trailing " AND " def _format_request(self): payload = { "db": "sra", "term": self._format_query_string(), "retmode": "json", "retmax": self.return_max, } return payload def _format_response(self, content): field_categories = [ "EXPERIMENT", "SUBMISSION", "ORGANISATION", "STUDY", "SAMPLE", "Pool", "RUN_SET", ] for event, elem in Et.iterparse(content): if elem.tag == "EXPERIMENT_PACKAGE": self.number_entries += 1 elif elem.tag in field_categories: self._parse_entry(elem) for field in self.entries: if len(self.entries[field]) < self.number_entries: self.entries[field] += [""] * ( self.number_entries - len(self.entries[field]) ) def _format_result(self): self.df = pd.DataFrame.from_dict(self.entries).replace( r"^\s*$", pd.NA, regex=True ) self.entries.clear() if self.df.empty: return # Tabulate statistics self._update_stats() columns = list(self.df.columns) important_columns = [ "study_accession", "experiment_accession", "experiment_title", "design_description", "sample_taxon_id", "sample_scientific_name", "experiment_library_strategy", "experiment_library_source", "experiment_library_selection", "sample_accession", "sample_alias", "experiment_instrument_model", "pool_member_spots", "run_1_size", "run_1_accession", "run_1_total_spots", "run_1_total_bases", ] temp_cols = [] for col in important_columns: if col in columns: temp_cols.append(col) columns.remove(col) important_columns = temp_cols if self.verbosity <= 1: temp_dfs = [] for col in self.df.columns: if re.match("run_[0-9]+_accession", col): temp_df = self.df[[col, "experiment_title"]] temp_df = temp_df[~pd.isna(temp_df[col])].rename( columns={ col: "run_accession", "experiment_title": "experiment_title", } ) temp_dfs.append(temp_df) run_dataframe = pd.concat(temp_dfs) run_dataframe.sort_values(by=["run_accession"], kind="mergesort") self.df = run_dataframe if self.verbosity == 0: self.df = self.df[["run_accession"]] elif self.verbosity == 1: pass # df has already been formatted above elif self.verbosity == 2: self.df = self.df[important_columns] elif self.verbosity == 3: self.df = self.df[important_columns + sorted(columns)] self.df.dropna(how="all") def _parse_entry(self, entry_root): """Parses a subset of the XML tree from request stream Parameters ---------- entry_root: ElementTree.Element root element of the xml tree from requests stream """ field_header = entry_root.tag.lower() run_count = 0 # root element attributes for k, v in entry_root.attrib.items(): self._update_entry(f"{field_header}_{k}".lower(), v) for child in entry_root: # "*_REF" tags contain duplicate information that can be found # somewhere in the xml entry and are skipped if child.tag.endswith("_REF"): continue # IDENTIFIERS contain two types of children tags: # PRIMARY_ID, which repeats the accession number and # EXTERNAL_ID tags, each containing an alternative ID that is # typically used in another database (GEO, ENA etc) # IDs are numbered from 1 to differentiate between them. elif child.tag == "IDENTIFIERS": id_index = 1 for identifier in child: if identifier.tag == "EXTERNAL_ID": self._update_entry( f"{field_header}_external_id_{id_index}", identifier.text, ) self._update_entry( f"{field_header}_external_id_{id_index}_namespace", identifier.get("namespace"), ) # "*_LINKS" tags contain 0 or more "*_LINK" children tags, # each containing information (values) regarding the link # Links are numbered from 1 to differentiate between multiple # links. elif child.tag.endswith("_LINKS"): link_index = 1 for link in child: # Link type. Eg: URL_link, Xref_link self._update_entry( f"{link.tag}_{link_index}_type".lower(), link[0].tag, ) # Link values in the form of tag: value. # Eg: label: GEO sample link_value_index = 1 for link_value in link[0]: self._update_entry( f"{link.tag}_{link_index}_value_{link_value_index}".lower(), f"{link_value.tag}: {link_value.text}", ) link_value_index += 1 link_index += 1 # "*_ATTRIBUTES" tags contain tag - value pairs providing # additional information for the Experiment/Sample/Study # Attributes are numbered from 1 to differentiate between # multiple attributes. elif child.tag.endswith("_ATTRIBUTES"): attribute_index = 1 for attribute in child: for val in attribute: self._update_entry( f"{child.tag}_{attribute_index}_{val.tag}".lower(), val.text, ) attribute_index += 1 # Differentiating between sample title and experiment title. elif child.tag == "TITLE": self._update_entry(f"{field_header}_title", child.text) # Parsing platfrom information elif child.tag == "PLATFORM": platform = child[0] self._update_entry("experiment_platform", platform.tag) self._update_entry( "experiment_instrument_model", platform[0].text, ) # Parsing individual run information elif child.tag == "RUN": run_count += 1 # run attributes for k, v in child.attrib.items(): self._update_entry(f"run_{run_count}_{k}".lower(), v) for elem in child: if elem.tag == "SRAFiles": srafile_index = 1 for srafile in elem: for k, v in srafile.attrib.items(): self._update_entry( f"run_{run_count}_srafile_{srafile_index}_{k}".lower(), v, ) alternatives_index = 1 for alternatives in srafile: for k, v in alternatives.attrib.items(): self._update_entry( f"run_{run_count}_srafile_{srafile_index}_alternative_{alternatives_index}_{k}".lower(), v, ) alternatives_index += 1 srafile_index += 1 elif elem.tag == "CloudFiles": cloudfile_index = 1 for cloudfile in elem: for k, v in cloudfile.attrib.items(): self._update_entry( f"run_{run_count}_cloudfile_{cloudfile_index}_{k}".lower(), v, ) cloudfile_index += 1 elif elem.tag == "Bases": for k, v in elem.attrib.items(): self._update_entry( f"run_{run_count}_total_base_{k}".lower(), v, ) for base in elem: self._update_entry( f"run_{run_count}_base_{base.attrib['value']}_count", base.attrib["count"], ) elif elem.tag == "Databases": database_index = 1 for database in elem: self._update_entry( f"run_{run_count}_database_{database_index}".lower(), Et.tostring(database).decode(), ) database_index += 1 else: for elem in child.iter(): # Tags to ignore to avoid confusion if elem.tag in ["PRIMARY_ID", "SINGLE", "PAIRED"]: continue elif elem.text: self._update_entry( f"{field_header}_{elem.tag.lower()}", elem.text, ) elif elem.attrib: for k, v in elem.attrib.items(): self._update_entry( f"{field_header}_{elem.tag}_{k}".lower(), v, ) # Parsing library layout (single, paired) if field_header == "experiment": library_layout = child.find("./LIBRARY_DESCRIPTOR/LIBRARY_LAYOUT") if library_layout: library_layout = library_layout[0] self._update_entry(f"library_layout", library_layout.tag) # If library layout is paired, information such as nominal # standard deviation and length, etc are provided as well. if library_layout.tag == "PAIRED": for k, v in library_layout.attrib.items(): self._update_entry( f"library_layout_{k}".lower(), v, ) def _update_entry(self, field_name, field_content): """Adds information from a field into the entries dictionary This is a helper function that adds information parsed from the XML output from SRA into a dictionary of lists, for easier conversion into a Pandas dataframe later. Dictionary key is created if it doesn't exist yet. For entries that does not have information belonging to a field, the corresponding list will be padded with empty strings. Parameters ---------- field_name: str Name of the field where a value belonging to an entry is to be added field_content: str Value to be added """ if field_name not in self.entries: self.entries[field_name] = [] if len(self.entries[field_name]) > self.number_entries: return self.entries[field_name] += [""] * ( self.number_entries - len(self.entries[field_name]) ) + [field_content] def _update_stats(self): # study self.stats["study"] = self.df["study_accession"].nunique() # experiment self.stats["experiment"] = self.df["experiment_accession"].nunique() # run runs = self._merge_selected_columns(r"^run.*accession$") if not runs.empty: self.stats["run"] = runs.nunique() # sample samples = self._merge_selected_columns(r"^sample.*accession$") if not samples.empty: self.stats["sample"] = samples.nunique() # date range daterange = self._merge_selected_columns(r"^run_1_published$") if not daterange.empty: dates = pd.to_datetime(daterange).dt.to_period("M").astype(str) self.stats["Date range"] = dates.value_counts().to_dict() # organisms organisms = self._merge_selected_columns(r"^sample.*scientific_name.*") if not organisms.empty: self.stats["Organisms"] = organisms.value_counts().to_dict() # strategy if "experiment_library_strategy" in self.df.columns: self.stats["Library strategy"] = ( self.df["experiment_library_strategy"].value_counts().to_dict() ) # source if "experiment_library_source" in self.df.columns: self.stats["Library source"] = ( self.df["experiment_library_source"].value_counts().to_dict() ) # selection if "experiment_library_selection" in self.df.columns: self.stats["Library selection"] = ( self.df["experiment_library_selection"].value_counts().to_dict() ) # layout if "library_layout" in self.df.columns: self.stats["Library layout"] = ( self.df["library_layout"].value_counts().to_dict() ) # platform if "experiment_platform" in self.df.columns: self.stats["Platform"] = ( self.df["experiment_platform"].value_counts().to_dict() ) # count count = self._merge_selected_columns(r"^run_.*_total_bases$").astype("int64") self.stats["count_data"] = count self.stats["count_mean"] = count.mean() self.stats["count_median"] = count.median() self.stats["count_stdev"] = count.std() # for graphing self.stats["graph_raw"] = self.df[ [ "sample_scientific_name", "experiment_library_strategy", "experiment_library_source", "experiment_library_selection", "run_1_published", "experiment_platform", ] ].rename( columns={ "sample_scientific_name": "Organism", "experiment_library_strategy": "Library Strategy", "experiment_library_source": "Library Source", "experiment_library_selection": "Library Selection", "run_1_published": "Publication Date", "experiment_platform": "Platform", } ) self.stats["graph_raw"]["Publication Date"] = ( pd.to_datetime( self.stats["graph_raw"]["Publication Date"].replace(pd.NA, None) ) .dt.to_period("M") .astype(str) ) def _merge_selected_columns(self, regex): columns = list(self.df.filter(regex=regex, axis=1).columns) if not columns: series = pd.Series(dtype="object") elif len(columns) == 1: series = self.df[columns[0]] else: series = self.df[columns[0]] for c in columns[1:]: series = pd.concat([series, self.df[c]]) return series[~pd.isna(series)] class EnaSearch(QuerySearch): """Subclass of QuerySearch that implements search via querying ENA API Methods ------- search() sends the user query via requests to ENA API and stores search result as an instance attribute in the form of a pandas dataframe show_result_statistics() Shows summary information about search results. visualise_results() Generate graphs that visualise the search results. get_plot_objects(): Get the plot objects for plots generated. _format_query_string() formats the input user query into a string _format_request() formats the request payload _format_result(content) formats the search query output and converts it into a pandas dataframe See Also -------- QuerySearch: Superclass of EnaSearch """ def search(self): # This ensures that the spaces in the query string are not # converted to '+' by requests. payload = urllib.parse.urlencode( self._format_request(), quote_via=urllib.parse.quote ) try: r = requests_3_retries().get( "https://www.ebi.ac.uk/ena/portal/api/search", params=payload, timeout=SEARCH_REQUEST_TIMEOUT, ) r.raise_for_status() self._format_result(r.json()) except requests.exceptions.Timeout: sys.exit(f"Connection to the server has timed out. Please retry.") except requests.exceptions.HTTPError: sys.exit( f"HTTPError: This is likely caused by an invalid search query: " f"\nURL queried: {r.url} \nUser query: {self.fields}" ) except JSONDecodeError: print(f"No results found for the following search query: \n {self.fields}") return # no results found def _format_query_string(self): term = "" if self.fields["query"]: term += rf'(experiment_title="*{self.fields["query"]}*"' if not self.fields["accession"]: self.fields["query"] = self.fields["query"].upper() term += ( rf' OR study_accession="{self.fields["query"]}" OR ' rf'secondary_study_accession="{self.fields["query"]}" OR ' rf'sample_accession="{self.fields["query"]}" OR ' rf'secondary_sample_accession="{self.fields["query"]}" OR ' rf'experiment_accession="{self.fields["query"]}" OR ' rf'submission_accession="{self.fields["query"]}" OR ' rf'run_accession="{self.fields["query"]}"' ) term += ") AND " if self.fields["accession"]: self.fields["accession"] = self.fields["accession"].upper() term += ( rf'(study_accession="{self.fields["accession"]}" OR ' rf'secondary_study_accession="{self.fields["accession"]}" OR ' rf'sample_accession="{self.fields["accession"]}" OR ' rf'secondary_sample_accession="{self.fields["accession"]}" OR ' rf'experiment_accession="{self.fields["accession"]}" OR ' rf'submission_accession="{self.fields["accession"]}" OR ' rf'run_accession="{self.fields["accession"]}") AND ' ) if self.fields["organism"]: term += rf'tax_eq({scientific_name_to_taxid(self.fields["organism"])}) AND ' if self.fields["layout"]: term += rf'library_layout="{self.fields["layout"].upper()}" AND ' if self.fields["mbases"]: if type(self.fields["mbases"]) != int: raise IncorrectFieldException( f"Incorrect mbases format: {self.fields['mbases']}\n" f"--mbases must be an integer" ) upper_limit = self.fields["mbases"] * 1000000 + 500000 lower_limit = self.fields["mbases"] * 1000000 - 500000 term += rf"base_count>={lower_limit} AND base_count<{upper_limit} AND " if self.fields["publication_date"]: dates = self.fields["publication_date"].split(":") for i in range(len(dates)): dates[i] = "-".join(dates[i].split("-")[::-1]) if len(dates) == 1: term += rf"first_created={dates[0]} AND " elif len(dates) == 2: term += rf"first_created>={dates[0]} AND first_created<={dates[1]} AND " else: raise IncorrectFieldException( f"Incorrect publication date format: {self.fields['publication_date']}\n" f"Expected format: dd-mm-yyyy or dd-mm-yyyy:dd-mm-yyyy" ) if self.fields["platform"]: term += rf'instrument_platform="{self.fields["platform"]}" AND ' if self.fields["selection"]: term += rf'library_selection="{self.fields["selection"]}" AND ' if self.fields["source"]: term += rf'library_source="{self.fields["source"]}" AND ' if self.fields["strategy"]: term += rf'library_strategy="{self.fields["strategy"]}" AND ' if self.fields["title"]: term += rf'experiment_title="*{self.fields["title"]}*" AND ' return term[:-5] # Removing trailing " AND " def _format_request(self): # Note: ENA's API does not support searching a query in all fields. # Currently, if the user does not specify a query field, the query will # be matched to experiment_title (aka description), # or one of the accession fields stats_columns = () payload = { "query": self._format_query_string(), "result": "read_run", "format": "json", "limit": self.return_max, } # Selects the fields to return at different verbosity levels if self.verbosity < 3: payload["fields"] = ( "study_accession," "experiment_accession," "experiment_title," "description," "tax_id," "scientific_name," "library_strategy," "library_source," "library_selection," "sample_accession," "sample_title," "instrument_model," "run_accession," "read_count," "base_count," "first_public," "library_layout," "instrument_platform" ) elif self.verbosity == 3: payload["fields"] = "all" return payload def _format_result(self, content): if not content: return self.df = pd.DataFrame.from_dict(content).replace(r"^\s*$", pd.NA, regex=True) # Tabulate statistics self._update_stats() important_columns = [ "study_accession", "experiment_accession", "experiment_title", "description", "tax_id", "scientific_name", "library_strategy", "library_source", "library_selection", "sample_accession", "sample_title", "instrument_model", "run_accession", "read_count", "base_count", ] if self.verbosity == 0: self.df = self.df[["run_accession"]] elif self.verbosity == 1: self.df = self.df[["run_accession", "description"]] elif self.verbosity == 2: self.df = self.df[important_columns] elif self.verbosity == 3: columns = list(self.df.columns) columns = important_columns + sorted( [col for col in columns if col not in important_columns] ) self.df = self.df[columns] self.df.dropna(how="all") def _update_stats(self): # study self.stats["study"] = self.df["study_accession"].nunique() # experiment self.stats["experiment"] = self.df["experiment_accession"].nunique() # run self.stats["run"] = self.df["run_accession"].nunique() # sample self.stats["sample"] = self.df["sample_accession"].nunique() # date range daterange = self.df["first_public"] daterange = daterange[~pd.isna(daterange)] if not daterange.empty: dates = pd.to_datetime(daterange).dt.to_period("M").astype(str) self.stats["Date range"] = dates.value_counts().to_dict() # organisms organisms = self.df["scientific_name"] self.stats["Organisms"] = organisms.value_counts().to_dict() # strategy if "library_strategy" in self.df.columns: self.stats["Library strategy"] = ( self.df["library_strategy"].value_counts().to_dict() ) # source if "library_source" in self.df.columns: self.stats["Library source"] = ( self.df["library_source"].value_counts().to_dict() ) # selection if "library_selection" in self.df.columns: self.stats["Library selection"] = ( self.df["library_selection"].value_counts().to_dict() ) # layout if "library_layout" in self.df.columns: self.stats["Library layout"] = ( self.df["library_layout"].value_counts().to_dict() ) # platform if "instrument_platform" in self.df.columns: self.stats["Platform"] = ( self.df["instrument_platform"].value_counts().to_dict() ) # count count = self.df["base_count"].copy() count = count[~pd.isna(count)].astype("int64") self.stats["count_data"] = count self.stats["count_mean"] = count.mean() self.stats["count_median"] = count.median() self.stats["count_stdev"] = count.std() # For graphing self.stats["graph_raw"] = self.df[ [ "scientific_name", "library_strategy", "library_source", "library_selection", "first_public", "instrument_platform", ] ].rename( columns={ "scientific_name": "Organism", "library_strategy": "Library Strategy", "library_source": "Library Source", "library_selection": "Library Selection", "first_public": "Publication Date", "instrument_platform": "Platform", } ) self.stats["graph_raw"]["Publication Date"] = ( pd.to_datetime(self.stats["graph_raw"]["Publication Date"]) .dt.to_period("M") .astype(str) ) class GeoSearch(SraSearch): """Subclass of SraSearch that can query both GEO DataSets and SRA API. Methods ------- search() sends the user query via requests to SRA, GEO DataSets, or both depending on the search query. If query is sent to both APIs, the intersection of the two sets of query results are returned. show_result_statistics() Shows summary information about search results. visualise_results() Generate graphs that visualise the search results. get_plot_objects(): Get the plot objects for plots generated. _format_geo_query_string() formats the GEO DataSets portion of the input user query into a string. _format_geo_request() formats the GEO DataSets request payload _format_result(content) formats the search query output and converts it into a pandas dataframe See Also -------- GeoSearch.info: GeoSearch usage details SraSearch: Superclass of GeoSearch QuerySearch: Superclass of SraSearch """ def __init__( self, verbosity=2, return_max=20, query=None, accession=None, organism=None, layout=None, mbases=None, publication_date=None, platform=None, selection=None, source=None, strategy=None, title=None, geo_query=None, geo_dataset_type=None, geo_entry_type=None, suppress_validation=False, ): self.geo_fields = { "query": geo_query, "dataset_type": geo_dataset_type, "entry_type": geo_entry_type, "publication_date": publication_date, "organism": organism, } for k in self.geo_fields: if type(self.geo_fields[k]) == list: self.geo_fields[k] = " ".join(self.geo_fields[k]) self.search_sra = True self.search_geo = True self.entries = {} self.number_entries = 0 self.stats = { "study": "-", "experiment": "-", "run": "-", "sample": "-", "Date range": "-", "Organisms": "-", "Library strategy": "-", "Library source": "-", "Library selection": "-", "Library layout": "-", "Platform": "-", "count_mean": "-", "count_median": "-", "count_stdev": "-", } try: super().__init__( verbosity, return_max, query, accession, organism, layout, mbases, publication_date, platform, selection, source, strategy, title, suppress_validation, ) except MissingQueryException: self.search_sra = False if not any(self.geo_fields.values()): self.search_geo = False if not self.search_geo and not self.search_sra: raise MissingQueryException() # Narrowing down the total number of eligible uids if self.fields["query"]: self.fields["query"] += " AND sra gds[Filter]" elif self.search_sra: self.fields["query"] = "sra gds[Filter]" if self.geo_fields["query"]: self.geo_fields["query"] += " AND gds sra[Filter]" elif self.search_geo: self.geo_fields["query"] = "gds sra[Filter]" def _format_geo_query_string(self): term = "" if self.geo_fields["query"]: term += self.geo_fields["query"] + " AND " if self.geo_fields["organism"]: term += self.geo_fields["organism"] + "[Organism] AND " if self.geo_fields["publication_date"]: dates = [] for date in self.fields["publication_date"].split(":"): dates.append("/".join(date.split("-")[::-1])) term += ":".join(dates) + "[PDAT] AND " if self.geo_fields["dataset_type"]: term += self.geo_fields["dataset_type"] + "[DataSet Type] AND " if self.geo_fields["entry_type"]: term += self.geo_fields["entry_type"] + "[Entry Type] AND " return term[:-5] # Removing trailing " AND " def _format_geo_request(self): payload = { "db": "gds", "term": self._format_geo_query_string(), "retmode": "json", "retmax": self.return_max * 10, "usehistory": "y", } return payload def _format_request(self): if not self.search_geo: retmax = self.return_max else: retmax = self.return_max * 10 payload = { "db": "sra", "term": self._format_query_string(), "retmode": "json", "retmax": retmax, } return payload def search(self): """Sends the user query via requests to SRA, GEO DataSets, or both""" if not self.search_geo: super().search() else: # Step 1: retrieves the list of uids from GEO DataSets, and use # ELink to find corresponding uids in SRA geo_payload = self._format_geo_request() try: r = requests_3_retries().get( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi", params=geo_payload, timeout=SEARCH_REQUEST_TIMEOUT, ) r.raise_for_status() result = r.json()["esearchresult"] query_key = result["querykey"] web_env = result["webenv"] elink_payload = { "dbfrom": "gds", "db": "sra", "retmode": "xml", "query_key": query_key, "WebEnv": web_env, } r = requests_3_retries().get( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi", params=elink_payload, timeout=SEARCH_REQUEST_TIMEOUT, ) r.raise_for_status() try: root = Et.fromstring(r.text) uids_from_geo = [ elem.text for elem in root.findall(".//LinkSet/LinkSetDb/Link/Id") ] except (Et.ParseError, TypeError, ValueError): uids_from_geo = [] # Step 2: Retrieve list of uids from SRA and # Find the intersection of both lists of uids if self.search_sra: r = requests_3_retries().get( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi", params=self._format_request(), timeout=SEARCH_REQUEST_TIMEOUT, ) r.raise_for_status() uids_from_sra = r.json()["esearchresult"]["idlist"] else: uids_from_sra = None uids = self._combine_uids(uids_from_sra, uids_from_geo) # Ensure that only return_max number of uids are used uids = uids[: self.return_max] # Step 3: retrieves the detailed information for each uid # returned, in groups of SRA_SEARCH_GROUP_SIZE. if not uids: print( f"No results found for the following search query: \n " f"SRA: {self.fields}\nGEO DataSets: {self.geo_fields}" ) return # If no queries found, return nothing pbar = tqdm(total=len(uids)) for i in range(0, len(uids), SRA_SEARCH_GROUP_SIZE): current_uids = ",".join( uids[i : min(i + SRA_SEARCH_GROUP_SIZE, len(uids))] ) pbar.update(min(SRA_SEARCH_GROUP_SIZE, len(uids) - i)) payload2 = {"db": "sra", "retmode": "xml", "id": current_uids} r = requests_3_retries().get( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi", params=payload2, timeout=SEARCH_REQUEST_TIMEOUT, stream=True, ) r.raise_for_status() r.raw.decode_content = True self._format_response(r.raw) pbar.close() self._format_result() except requests.exceptions.Timeout: sys.exit(f"Connection to the server has timed out. Please retry.") except requests.exceptions.HTTPError: sys.exit( f"HTTPError: This is likely caused by an invalid search query: " f"\nURL queried: {r.url} \nUser query: {self.fields}" ) def _combine_uids(self, uids_from_sra, uids_from_geo): """Combine SRA and GEO uid lists while preserving ordering stability.""" if not uids_from_geo: return [] combined = [] seen = set() if uids_from_sra is not None: sra_uid_set = set(uids_from_sra) for uid in uids_from_geo: if uid in sra_uid_set and uid not in seen: combined.append(uid) seen.add(uid) else: for uid in uids_from_geo: if uid not in seen: combined.append(uid) seen.add(uid) return combined @classmethod def info(cls): """Information on how to use GeoSearch. Displays information on how to query GEO DataSets / SRA via GeoSearch, including accepted inputs for geo_query, geo_dataset_type and geo_entry_type. Returns ------- info: str Information on how to use GeoSearch. """ info = ( "General Information:\n" "--------------------\n" "GeoSearch (Or 'pysradb search --db geo ...' on the command line) \n" "is able to query both SRA and GEO DataSets, returning the subset \n" "of entries that appears within both search queries. \n\n" "Queries sent to SRA and GEO DataSets will have 'sra gds[Filter]' \n" "and 'gds sra[Filter]' appended to the search queries respectively \n" "to ensure that the entries in the search result can also be found \n" "in the other API. \n\n" "Queries sent to SRA uses the same fields as SraSearch, \n" "or 'pysradb search --db sra ...' on the command line. \n\n" "The following fields, if used, are sent as part of the GEO DataSets query: \n" "organism, publication_date, geo_query, geo_dataset_type, geo_entry_type\n\n" "Notes about GEO DataSets specific fields: \n" "----------------------------------------- \n" "geo_query: This is the free text query, similar to 'query', that \n" "is sent to GEO DataSets API. The 'query' field is the free text \n" "query sent to SRA API instead.\n\n" "geo_dataset_type: The type of GEO DataSet, which can be one of the following: \n" " expression profiling by array \n" " expression profiling by genome tiling array \n" " expression profiling by high throughput sequencing \n" " expression profiling by mpss \n" " expression profiling by rt pcr \n" " expression profiling by sage \n" " expression profiling by snp array \n" " genome binding/occupancy profiling by array \n" " genome binding/occupancy profiling by genome tiling array \n" " genome binding/occupancy profiling by high throughput sequencing \n" " genome binding/occupancy profiling by snp array \n" " genome variation profiling by array \n" " genome variation profiling by genome tiling array \n" " genome variation profiling by high throughput sequencing \n" " genome variation profiling by snp array \n" " methylation profiling by array \n" " methylation profiling by genome tiling array \n" " methylation profiling by high throughput sequencing \n" " methylation profiling by snp array \n" " non coding rna profiling by array \n" " non coding rna profiling by genome tiling array \n" " non coding rna profiling by high throughput sequencing \n" " other \n" " protein profiling by mass spec \n" " protein profiling by protein array \n" " snp genotyping by snp array \n" " third party reanalysis\n\n" "geo_dataset_type: The type of GEO entry, which can be one of the following: \n" " gds\n" " gpl\n" " gse\n" " gsm\n\n" ) return info ================================================ FILE: pysradb/sraweb.py ================================================ """Utilities to interact with SRA online""" import concurrent.futures import os import re import sys import time import warnings from collections import OrderedDict from json.decoder import JSONDecodeError from xml.parsers.expat import ExpatError import numpy as np import pandas as pd import requests import xmltodict warnings.simplefilter(action="ignore", category=FutureWarning) from xml.sax.saxutils import escape def xmlescape(data): return escape(data, entities={"'": "'", '"': """}) def _make_hashable(obj): """Convert unhashable types to hashable ones for pandas operations""" if isinstance(obj, (OrderedDict, dict)): # Extract text content from XML parsed dict/OrderedDict if "#text" in obj: return obj["#text"] # Extract the actual text content elif len(obj) == 1 and "@xmlns" in obj: return pd.NA # Handle xmlns-only dicts as missing data else: # Fallback to string representation for other dict structures return str(obj) elif isinstance(obj, list): # Convert list to tuple return tuple(_make_hashable(item) for item in obj) else: return obj def _order_first(df, column_order_list): columns = column_order_list + [ col for col in df.columns.tolist() if col not in column_order_list ] # check if all columns do exist in the dataframe if len(set(columns).intersection(df.columns)) == len(columns): df = df.loc[:, columns] df = df.mask(df.map(str).eq("[]")) # Filter out XML namespace artifacts df = df.replace(regex=r"^@xmlns.*", value=pd.NA).infer_objects(copy=False) df = df.fillna(pd.NA) return df def _retry_response(base_url, payload, key, max_retries=10): """Rerty fetching esummary if API rate limit exceeeds""" for index, _ in enumerate(range(max_retries)): try: request = requests.get(base_url, params=OrderedDict(payload)) response = request.json() results = response[key] return response except KeyError: # sleep for increasing times time.sleep(index + 1) continue raise RuntimeError("Failed to fetch esummary. API rate limit exceeded.") def get_retmax(n_records, retmax=500): """Get retstart and retmax till n_records are exhausted""" for i in range(0, n_records, retmax): yield i class SRAweb(object): def __init__(self, api_key=None): """ Initialize SRAweb for API-based access to SRA data. Parameters ---------- api_key: string API key for ncbi eutils. Optional, but recommended for higher rate limits. """ self.base_url = dict() self.base_url["esummary"] = ( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi" ) self.base_url["esearch"] = ( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi" ) self.base_url["efetch"] = ( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi" ) self.ena_fastq_search_url = "https://www.ebi.ac.uk/ena/portal/api/filereport" self.ena_params = [("result", "read_run"), ("fields", "fastq_ftp")] self.esearch_params = {} self.esearch_params["sra"] = [ ("db", "sra"), ("usehistory", "n"), ("retmode", "json"), ] self.esearch_params["geo"] = [ ("db", "gds"), ("usehistory", "n"), ("retmode", "json"), ] self.efetch_params = [ ("db", "sra"), ("usehistory", "n"), ("retmode", "runinfo"), ] if api_key is not None: self.esearch_params["sra"].append(("api_key", str(api_key))) self.esearch_params["geo"].append(("api_key", str(api_key))) self.efetch_params.append(("api_key", str(api_key))) self.sleep_time = 1 / 10 else: self.sleep_time = 1 / 3 @staticmethod def format_xml(string): """Create a fake root to make 'string' a valid xml Parameters ---------- string: str Returns -------- xml: str """ # string = unescape(string.strip()) string = string.strip() return "" + string + "" @staticmethod def xml_to_json(xml): """Convert xml to json. Parameters ---------- xml: str Input XML Returns ------- xml_dict: dict Parsed xml as dict """ try: xmldict = xmltodict.parse( xml, process_namespaces=False, dict_constructor=OrderedDict ) json = xmldict["root"] except ExpatError: raise RuntimeError("Unable to parse xml: {}".format(xml)) return json def bioproject_to_srp(self, bioproject): """Convert PRJNA BioProject ID to SRP accession Parameters ---------- bioproject: str BioProject ID (e.g., 'PRJNA810439') Returns ------- srp_accessions: list List of SRP accessions found """ if not bioproject or pd.isna(bioproject): return [] try: import re # Search SRA for records with this bioproject search_url = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi" search_params = { "db": "sra", "term": f"{bioproject}[BioProject]", "retmode": "json", "retmax": "50", } response = requests.get(search_url, params=search_params, timeout=30) result = response.json() sra_uids = result.get("esearchresult", {}).get("idlist", []) if not sra_uids: return [] # Get summaries to extract SRP accessions summary_url = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi" srp_set = set() # Process in batches to avoid too many requests for uid in sra_uids[:10]: # Limit to first 10 try: summary_params = {"db": "sra", "id": uid, "retmode": "json"} summary_response = requests.get( summary_url, params=summary_params, timeout=30 ) summary_result = summary_response.json() if uid in summary_result.get("result", {}): record = summary_result["result"][uid] expxml = record.get("expxml", "") # Extract SRP using regex from the XML srp_match = re.search(r'Study acc="(SRP\d+)"', expxml) if srp_match: srp_set.add(srp_match.group(1)) time.sleep(0.1) # Small delay between requests except Exception: continue return sorted(list(srp_set)) except Exception as e: return [] def fetch_ena_fastq(self, srp): """Fetch FASTQ records from ENA (EXPERIMENTAL) Parameters ---------- srp: string Srudy accession Returns ------- srr_url: list List of SRR fastq urls """ payload = self.ena_params.copy() payload += [("accession", srp)] request = requests.get(self.ena_fastq_search_url, params=OrderedDict(payload)) request_text = request.text.strip() urls = [] for line in request_text.split("\n"): if "fastq_ftp" in line: continue line = line.strip() line_split = line.split("\t") if len(line_split) != 2: continue url, srr = line.split("\t") # sometimes this needs to be flipped if "sra.ebi.ac.uk" in srr: url, srr = srr, url http_url = "http://{}".format(url) ftp_url = url.replace("ftp.sra.ebi.ac.uk/", "era-fasp@fasp.sra.ebi.ac.uk:") urls += [(srr, http_url, ftp_url)] # Paired end case def _handle_url_split(url_split): url1_1 = pd.NA url1_2 = pd.NA for url_temp in url_split: if "_1.fastq.gz" in url_temp: url1_1 = url_temp elif "_2.fastq.gz" in url_temp: url1_2 = url_temp return url1_1, url1_2 if ";" in request_text: urls_expanded = [] for srr, url1, url2 in urls: # strip _1, _2 srr = srr.split("_")[0] if ";" in url1: url1_split = url1.split(";") if len(url1_split) == 2: url1_1, url1_2 = url1_split else: # warnings.warn('ignoring extra urls found for paired end accession') url1_1, url1_2 = _handle_url_split(url1_split) url1_2 = "http://{}".format(url1_2) url2_split = url2.split(";") if len(url2_split) == 2: url2_1, url2_2 = url2_split else: # warnings.warn('ignoring extra urls found for paired end accession') url2_1, url2_2 = _handle_url_split(url2_split) else: url1_1 = url1 url2_1 = url2 url1_2 = "" url2_2 = "" urls_expanded.append((srr, url1_1, url1_2, url2_1, url2_2)) df = pd.DataFrame( urls_expanded, columns=[ "run_accession", "ena_fastq_http_1", "ena_fastq_http_2", "ena_fastq_ftp_1", "ena_fastq_ftp_2", ], ).sort_values(by="run_accession") return df else: return pd.DataFrame( urls, columns=["run_accession", "ena_fastq_http", "ena_fastq_ftp"] ).sort_values(by="run_accession") def create_esummary_params(self, esearchresult, db="sra"): query_key = esearchresult["querykey"] webenv = esearchresult["webenv"] retstart = esearchresult["retstart"] # TODO this should be adaptive to build # upon using the 'count' result in esearch result, # Currently only supports a max of 500 records. # retmax = esearchresult["retmax"] retmax = 500 return [ ("query_key", query_key), ("WebEnv", webenv), ("retstart", retstart), ("retmax", retmax), ] def get_esummary_response(self, db, term, usehistory="y"): assert db in ["sra", "geo"] payload = self.esearch_params[db].copy() if isinstance(term, list): term = " OR ".join(term) payload += [("term", term)] request = requests.post(self.base_url["esearch"], data=OrderedDict(payload)) try: esearch_response = request.json() except JSONDecodeError: sys.stderr.write( "Unable to parse esummary response json: {}{}. Will retry once.".format( request.text, os.linesep ) ) retry_after = request.headers.get("Retry-After", 1) time.sleep(int(retry_after)) request = requests.post(self.base_url["esearch"], data=OrderedDict(payload)) try: esearch_response = request.json() except JSONDecodeError as e: error_msg = ( "Unable to parse esummary response json: {}{}. Aborting.".format( request.text, os.linesep ) ) sys.stderr.write(error_msg) raise ValueError(error_msg) from e # retry again if "esummaryresult" in esearch_response: print("No result found") return if "error" in esearch_response: # API rate limite exceeded esearch_response = _retry_response( self.base_url["esearch"], payload, "esearchresult" ) n_records = int(esearch_response["esearchresult"]["count"]) results = {} for retstart in get_retmax(n_records): payload = self.esearch_params[db].copy() payload += self.create_esummary_params(esearch_response["esearchresult"]) payload = OrderedDict(payload) payload["retstart"] = retstart request = requests.get( self.base_url["esummary"], params=OrderedDict(payload) ) try: response = request.json() except JSONDecodeError: time.sleep(1) response = _retry_response(self.base_url["esummary"], payload, "result") if "error" in response: # API rate limite exceeded response = _retry_response(self.base_url["esummary"], payload, "result") if retstart == 0: results = response["result"] else: result = response["result"] for key, value in result.items(): if key in list(results.keys()): results[key] += value else: results[key] = value return results def get_efetch_response(self, db, term, usehistory="y"): assert db in ["sra", "geo"] payload = self.esearch_params[db].copy() if isinstance(term, list): term = " OR ".join(term) payload += [("term", term)] request = requests.get(self.base_url["esearch"], params=OrderedDict(payload)) esearch_response = request.json() if "esummaryresult" in esearch_response: print("No result found") return if "error" in esearch_response: # API rate limite exceeded esearch_response = _retry_response( self.base_url["esearch"], payload, "esearchresult" ) n_records = int(esearch_response["esearchresult"]["count"]) results = {} for retstart in get_retmax(n_records): payload = self.efetch_params.copy() payload += self.create_esummary_params(esearch_response["esearchresult"]) payload = OrderedDict(payload) payload["retstart"] = retstart request = requests.get(self.base_url["efetch"], params=OrderedDict(payload)) request_text = request.text.strip() try: request_json = request.json() except: request_json = {} # eval(request_text) if "error" in request_json: # print("Encountered: {}".format(request_json)) # print("Headers: {}".format(request.headers)) # Handle API-rate limit exceeding try: retry_after = request.headers["Retry-After"] except KeyError: if request_json["error"] == "error forwarding request": error_msg = "Encountered error while making request.\n" sys.stderr.write(error_msg) raise RuntimeError(error_msg.strip()) time.sleep(int(retry_after)) # try again request = requests.get( self.base_url["efetch"], params=OrderedDict(payload) ) request_text = request.text.strip() try: request_json = request.json() if request_json["error"] == "error forwarding request": sys.stderr.write("Encountered error while making request.\n") return except: request_json = {} # eval(request_text) try: xml_response = xmltodict.parse( request_text, process_namespaces=False, dict_constructor=OrderedDict ) exp_response = xml_response.get("EXPERIMENT_PACKAGE_SET", {}) response = exp_response.get("EXPERIMENT_PACKAGE", {}) except ExpatError as e: error_msg = "Unable to parse xml: {}{}".format(request_text, os.linesep) sys.stderr.write(error_msg) raise ValueError(error_msg.strip()) from e if not response: error_msg = "Unable to parse xml response. Received: {}{}".format( xml_response, os.linesep ) sys.stderr.write(error_msg) raise ValueError(error_msg.strip()) if retstart == 0: results = response else: result = response for value in result: results.append(value) time.sleep(self.sleep_time) return results def sra_metadata( self, srp, sample_attribute=False, detailed=False, expand_sample_attributes=False, output_read_lengths=False, include_pmids=False, enrich=False, enrich_backend="ollama/phi3", **kwargs, ): esummary_result = self.get_esummary_response("sra", srp) try: uids = esummary_result["uids"] except KeyError: return None exps_xml = OrderedDict() runs_xml = OrderedDict() exps_json = OrderedDict() runs_json = OrderedDict() for uid in uids: exps_xml[uid] = self.format_xml(esummary_result[uid]["expxml"]) runs_xml[uid] = self.format_xml(esummary_result[uid]["runs"]) for uid in uids: exps_json[uid] = self.xml_to_json(exps_xml[uid]) runs_json[uid] = self.xml_to_json(runs_xml[uid]) sra_record = [] for uid, run_json in runs_json.items(): exp_json = exps_json[uid] exp_summary = exp_json["Summary"] exp_title = exp_summary.get("Title", pd.NA) exp_platform = exp_summary.get("Platform", {}) statistics = exp_summary.get("Statistics", {}) if isinstance(exp_platform, OrderedDict): exp_platform_model = exp_platform.get("@instrument_model", pd.NA) exp_platform_desc = exp_platform.get("#text", pd.NA) else: exp_platform_model = pd.NA exp_platform_desc = pd.NA exp_total_runs = statistics.get("@total_runs", pd.NA) exp_total_spots = statistics.get("@total_spots", pd.NA) exp_total_size = statistics.get("@total_size", pd.NA) # experiment_accession exp_ID = exp_json["Experiment"]["@acc"] # experiment_title exp_name = exp_json["Experiment"]["@name"] exp_organism = exp_json.get("Organism", pd.NA) exp_organism_name = pd.NA exp_taxid = pd.NA if isinstance(exp_organism, dict): exp_organism_name = exp_organism.get("@ScientificName", pd.NA) exp_taxid = exp_organism["@taxid"] exp_instrument = list(exp_json["Instrument"].values())[0] exp_sample = exp_json["Sample"] # sample_accession exp_sample_ID = exp_sample["@acc"] # sample_title exp_sample_name = exp_sample["@name"] exp_library_descriptor = exp_json["Library_descriptor"] # library_strategy exp_library_strategy = exp_library_descriptor["LIBRARY_STRATEGY"] if isinstance(exp_library_strategy, dict): exp_library_strategy = exp_library_strategy["#text"] # library_source exp_library_source = exp_library_descriptor["LIBRARY_SOURCE"] if isinstance(exp_library_source, dict): exp_library_source = exp_library_source["#text"] # library_selection exp_library_selection = exp_library_descriptor["LIBRARY_SELECTION"] if isinstance(exp_library_selection, dict): exp_library_selection = exp_library_selection["#text"] # library_name exp_library_name = exp_library_descriptor.get("LIBRARY_NAME", "") if isinstance(exp_library_selection, dict): exp_library_name = exp_library_name["#text"] # library_layout exp_library_layout = list(exp_library_descriptor["LIBRARY_LAYOUT"].keys())[ 0 ] # biosample exp_biosample = exp_json.get("Biosample", pd.NA) # bioproject exp_bioproject = exp_json.get("Bioproject", pd.NA) experiment_record = OrderedDict() experiment_record["study_accession"] = exp_json["Study"]["@acc"] experiment_record["study_title"] = exp_json["Study"]["@name"] experiment_record["experiment_accession"] = exp_ID experiment_record["experiment_title"] = exp_name experiment_record["experiment_desc"] = exp_title experiment_record["organism_taxid"] = exp_taxid experiment_record["organism_name"] = exp_organism_name experiment_record["library_name"] = exp_library_name experiment_record["library_strategy"] = exp_library_strategy experiment_record["library_source"] = exp_library_source experiment_record["library_selection"] = exp_library_selection experiment_record["library_layout"] = exp_library_layout experiment_record["sample_accession"] = exp_sample_ID experiment_record["sample_title"] = exp_sample_name experiment_record["biosample"] = exp_biosample experiment_record["bioproject"] = exp_bioproject experiment_record["instrument"] = exp_instrument experiment_record["instrument_model"] = exp_platform_model experiment_record["instrument_model_desc"] = exp_platform_desc experiment_record["total_spots"] = exp_total_spots experiment_record["total_size"] = exp_total_size if not run_json: # Sometimes the run_accession is not populated by NCBI: # df2 = self.srx_to_srr(exp_ID) # extra_fields = set(experiment_record.keys()).difference(df2.columns.tolist()) # for idx, row in df2.iterrows(): # for field in extra_fields: # experiment_record[field] = row[field] sra_record.append(experiment_record) continue runs = run_json["Run"] if not isinstance(runs, list): runs = [runs] for run_record in runs: run_accession = run_record["@acc"] run_total_spots = run_record["@total_spots"] run_total_bases = run_record["@total_bases"] experiment_record["run_accession"] = run_accession experiment_record["run_total_spots"] = run_total_spots experiment_record["run_total_bases"] = run_total_bases sra_record.append(experiment_record.copy()) # TODO: the detailed call below does redundant operations # the code above this can be completeley done away with # Convert any unhashable types to hashable ones before creating DataFrame hashable_records = [] for record in sra_record: hashable_record = {k: _make_hashable(v) for k, v in record.items()} hashable_records.append(hashable_record) metadata_df = pd.DataFrame(hashable_records).drop_duplicates() if "run_accession" in metadata_df.columns: metadata_df = metadata_df.sort_values(by="run_accession") metadata_df.columns = [x.lower().strip() for x in metadata_df.columns] # Filter out XML namespace artifacts and replace with NA metadata_df = metadata_df.replace( regex=r"^@xmlns.*", value=pd.NA ).infer_objects(copy=False) if not detailed: return metadata_df time.sleep(self.sleep_time) efetch_result = self.get_efetch_response("sra", srp) if not isinstance(efetch_result, list): if efetch_result: efetch_result = [efetch_result] else: return None detailed_records = [] for record in efetch_result: if "SAMPLE" in record.keys() and "SAMPLE_ATTRIBUTES" in record["SAMPLE"]: sample_attributes = record["SAMPLE"]["SAMPLE_ATTRIBUTES"][ "SAMPLE_ATTRIBUTE" ] else: sample_attributes = [] if isinstance(sample_attributes, OrderedDict): sample_attributes = [sample_attributes] exp_record = record["EXPERIMENT"] exp_attributes = exp_record.get("EXPERIMENT_ATTRIBUTES", {}) run_sets = record["RUN_SET"].get("RUN", []) if not isinstance(run_sets, list): run_sets = [run_sets] for run_set in run_sets: detailed_record = OrderedDict() if not run_json: # Add experiment accession if no run info found earlier detailed_record["experiment_accession"] = exp_record["@accession"] # detailed_record["experiment_title"] = exp_record["TITLE"] for key, values in exp_attributes.items(): key = key.lower() for value_x in values: if not isinstance(value_x, dict): continue tag = value_x["TAG"].lower() value = value_x["VALUE"] if "VALUE" in value_x else None detailed_record[tag] = value lib_record = exp_record["DESIGN"]["LIBRARY_DESCRIPTOR"] for key, value in lib_record.items(): key = key.lower() if key == "library_layout": value = list(value.keys())[0] elif key == "library_construction_protocol": continue # detailed_record[key] = value detailed_record["run_accession"] = run_set["@accession"] detailed_record["run_alias"] = run_set["@alias"] sra_files = run_set.get("SRAFiles", {}) sra_files = sra_files.get("SRAFile", {}) if isinstance(sra_files, OrderedDict): # detailed_record["sra_url"] = sra_files.get("@url", pd.NA) if "Alternatives" in sra_files.keys(): alternatives = sra_files["Alternatives"] if not isinstance(alternatives, list): alternatives = [alternatives] for alternative in alternatives: org = alternative["@org"].lower() for key in alternative.keys(): if key == "@org": continue detailed_record[ "{}_{}".format(org, key.replace("@", "")) ] = alternative[key] else: for sra_file in sra_files: # Multiple download URLs # Use the one where the download filename corresponds to the SRR cluster = sra_file.get("@cluster", None).lower().strip() if cluster is None: continue for key in sra_file.keys(): if key == "@cluster": continue if key == "Alternatives": # Example: SRP184142 alternatives = sra_file["Alternatives"] if not isinstance(alternatives, list): alternatives = [alternatives] for alternative in alternatives: org = alternative["@org"].lower() for key in alternative.keys(): if key == "@org": continue detailed_record[ "{}_{}".format(org, key.replace("@", "")) ] = alternative[key] else: detailed_record[ "{}_{}".format(cluster, key.replace("@", "")) ] = sra_file[key] expt_ref = run_set["EXPERIMENT_REF"] detailed_record["experiment_alias"] = expt_ref.get("@refname", "") # detailed_record["run_total_bases"] = run_set["@total_bases"] # detailed_record["run_total_spots"] = run_set["@total_spots"] for sample_attribute in sample_attributes: dict_values = list(sample_attribute.values()) if len(dict_values) > 1: detailed_record[dict_values[0]] = dict_values[1] else: # TODO: Investigate why these fields have just the key # but no value pass detailed_records.append(detailed_record) detailed_record_df = pd.DataFrame(detailed_records).drop_duplicates() if ( "run_accession" in metadata_df.keys() and "run_accession" in detailed_record_df.keys() ): metadata_df = metadata_df.merge( detailed_record_df, on="run_accession", how="outer" ) elif "experiment_accession" in detailed_record_df.keys(): metadata_df = metadata_df.merge( detailed_record_df, on="experiment_accession", how="outer" ) metadata_df = metadata_df[metadata_df.columns.dropna()] metadata_df = metadata_df.drop_duplicates() metadata_df = metadata_df.replace(r"^\s*$", pd.NA, regex=True) ena_cols = [ "ena_fastq_http", "ena_fastq_http_1", "ena_fastq_http_2", "ena_fastq_ftp", "ena_fastq_ftp_1", "ena_fastq_ftp_2", ] empty_df = pd.DataFrame(columns=ena_cols) metadata_df = pd.concat((metadata_df, empty_df), axis=0) if "run_accession" in metadata_df.columns: metadata_df = metadata_df.set_index("run_accession") # multithreading lookup on ENA, since a lot of time is spent waiting # for its reply with concurrent.futures.ThreadPoolExecutor(max_workers=5) as executor: # load our function calls into a list of futures futures = [ executor.submit(self.fetch_ena_fastq, srp) for srp in metadata_df.study_accession.unique() ] # now proceed synchronously for future in concurrent.futures.as_completed(futures): ena_results = future.result() if ena_results.shape[0]: ena_results = ena_results.set_index("run_accession") metadata_df.update(ena_results) metadata_df = metadata_df.reset_index() metadata_df = metadata_df.fillna(pd.NA) metadata_df.columns = [x.lower().strip() for x in metadata_df.columns] # Add PMID column when detailed=True and include_pmids=True if include_pmids: try: sra_accessions = [srp] if isinstance(srp, str) else srp pmid_df = self.sra_to_pmid(sra_accessions) if pmid_df is not None and not pmid_df.empty: pmid_map = {} for _, row in pmid_df.iterrows(): study_acc = row.get("sra_accession", None) pmid = row.get("pmid") if not pd.isna(pmid): if study_acc not in pmid_map: pmid_map[study_acc] = [] pmid_map[study_acc].append(str(pmid)) metadata_df["pmid"] = metadata_df.apply( lambda row: ",".join( pmid_map.get(row.get("study_accession", ""), [""]) ), axis=1, ) metadata_df["pmid"] = metadata_df["pmid"].replace("", pd.NA) else: metadata_df["pmid"] = pd.NA except Exception as e: metadata_df["pmid"] = pd.NA # Filter out XML namespace artifacts and replace with NA metadata_df = metadata_df.replace( regex=r"^@xmlns.*", value=pd.NA ).infer_objects(copy=False) # Add GSE and GSM columns when detailed=True if detailed: try: unique_srps = metadata_df["study_accession"].dropna().unique().tolist() if unique_srps: gse_df = self.srp_to_gse(unique_srps) if gse_df is not None and not gse_df.empty: srp_to_gse_map = {} for _, row in gse_df.iterrows(): srp_acc = row.get("study_accession") gse_acc = row.get("study_alias") if not pd.isna(srp_acc) and not pd.isna(gse_acc): if srp_acc not in srp_to_gse_map: srp_to_gse_map[srp_acc] = [] srp_to_gse_map[srp_acc].append(gse_acc) metadata_df["study_geo_accession"] = metadata_df[ "study_accession" ].map( lambda x: ( ",".join(srp_to_gse_map.get(x, [])) if x in srp_to_gse_map else pd.NA ) ) metadata_df["study_geo_accession"] = metadata_df[ "study_geo_accession" ].replace("", pd.NA) else: metadata_df["study_geo_accession"] = pd.NA else: metadata_df["study_geo_accession"] = pd.NA unique_srxs = ( metadata_df["experiment_accession"].dropna().unique().tolist() ) if unique_srxs: gsm_response = self.fetch_gds_results(unique_srxs) if gsm_response is not None and not gsm_response.empty: srx_to_gsm_map = {} for _, row in gsm_response.iterrows(): if row.get("entrytype") == "GSM": gsm_acc = row.get("accession") srx_acc = row.get("SRA") if not pd.isna(srx_acc) and not pd.isna(gsm_acc): srx_to_gsm_map[srx_acc] = gsm_acc metadata_df["experiment_geo_accession"] = metadata_df[ "experiment_accession" ].map(lambda x: srx_to_gsm_map.get(x, pd.NA)) else: metadata_df["experiment_geo_accession"] = pd.NA else: metadata_df["experiment_geo_accession"] = pd.NA except Exception as e: metadata_df["study_geo_accession"] = pd.NA metadata_df["experiment_geo_accession"] = pd.NA if enrich and not metadata_df.empty: try: from pysradb.metadata_enrichment import create_metadata_extractor extractor = create_metadata_extractor( method="llm", backend=enrich_backend ) metadata_df = extractor.enrich_dataframe( metadata_df, text_column=None, prefix="guessed_" ) except Exception as e: error_msg = str(e) if "Ollama is not installed or not running" in error_msg: print(f"Error: {error_msg}") print( "Metadata enrichment requires Ollama to be installed and running." ) print( "Please install Ollama from https://ollama.ai/ and follow these steps:" ) print("1. Start Ollama server: ollama serve") print("2. Pull a model: ollama pull phi3") print("3. Try again or use a different enrichment backend") raise else: print(f"Warning: Enrichment failed: {e}") if "run_accession" in metadata_df.columns: return metadata_df.sort_values(by="run_accession") return metadata_df def fetch_gds_results(self, gse, **kwargs): result = self.get_esummary_response("geo", gse) try: uids = result["uids"] except KeyError: print("No results found for {} | Obtained result: {}".format(gse, result)) return None gse_records = [] for uid in uids: record = result[uid] del record["uid"] extrelations = record.get("extrelations") or [] if extrelations: for extrelation in extrelations: keys = list(extrelation.keys()) values = list(extrelation.values()) assert sorted(keys) == sorted( ["relationtype", "targetobject", "targetftplink"] ) assert len(values) == 3 record[extrelation["relationtype"]] = extrelation["targetobject"] del record["extrelations"] gse_records.append(record) continue # Fallback for records without extrelations (e.g., spatial transcriptomics datasets) samples = record.get("samples") or [] if samples: record["samples"] = samples gse_records.append(record) if not len(gse_records): print("No results found for {}".format(gse)) return None return pd.DataFrame(gse_records) def fetch_gsm_soft(self, gsm_ids): """ Fetch detailed GSM metadata in SOFT format. Args: gsm_ids: List of GSM accessions Returns: Dictionary mapping GSM accession to parsed SOFT metadata """ if isinstance(gsm_ids, str): gsm_ids = [gsm_ids] gsm_data = {} for gsm in gsm_ids: try: url = f"https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc={gsm}&targ=self&form=text&view=full" response = requests.get(url, timeout=30) response.raise_for_status() # Parse SOFT format soft_text = response.text metadata = {} characteristics = [] for line in soft_text.split("\n"): line = line.strip() if line.startswith("!Sample_"): if " = " in line: key, value = line.split(" = ", 1) key = key.replace("!Sample_", "").lower() # Handle characteristics specially - they can appear multiple times if "characteristics" in key: characteristics.append(value) else: # Store in metadata dict # Join multiple values with semicolon for consistency if key not in metadata: metadata[key] = value elif isinstance(metadata[key], list): metadata[key].append(value) else: # Convert to list if we have multiple values metadata[key] = [metadata[key], value] # Convert list values to semicolon-separated strings for key, value in metadata.items(): if isinstance(value, list): metadata[key] = "; ".join(str(v) for v in value) # Process characteristics into a dict char_dict = {} for char in characteristics: if ": " in char: char_key, char_val = char.split(": ", 1) char_dict[char_key.strip().lower()] = char_val.strip() metadata["characteristics"] = char_dict gsm_data[gsm] = metadata except Exception as e: print(f"Warning: Could not fetch SOFT data for {gsm}: {e}") gsm_data[gsm] = {} return gsm_data def geo_metadata( self, gse, sample_attribute=False, detailed=False, expand_sample_attributes=False, include_pmids=False, enrich=False, enrich_backend="ollama/phi3", **kwargs, ): if isinstance(gse, str): gse = [gse] if not gse: return pd.DataFrame( columns=[ "study_accession", "study_title", "study_summary", "organism_name", "platform_accession", "platform_title", "experiment_type", "bioproject", "submission_date", "supplementary_files", "series_ftp", "sample_accession", "sample_title", ] ) geo_response = self.get_esummary_response("geo", gse) if not geo_response: return pd.DataFrame( columns=[ "study_accession", "study_title", "study_summary", "organism_name", "platform_accession", "platform_title", "experiment_type", "bioproject", "submission_date", "supplementary_files", "series_ftp", "sample_accession", "sample_title", ] ) gse_records = [] sample_accessions = [] for uid in geo_response.get("uids", []): record = geo_response.get(uid, {}) if record.get("entrytype") != "GSE": continue gse_records.append(record) for sample in record.get("samples") or []: accession = sample.get("accession") if accession and accession not in sample_accessions: sample_accessions.append(accession) sample_details = {} gsm_soft_data = {} if (sample_attribute or detailed) and sample_accessions: sample_response = self.get_esummary_response("geo", sample_accessions) if sample_response: for uid in sample_response.get("uids", []): entry = sample_response.get(uid, {}) if entry.get("entrytype") == "GSM": sample_details[entry.get("accession")] = entry # Fetch full SOFT metadata when detailed=True if detailed: gsm_soft_data = self.fetch_gsm_soft(sample_accessions) # Get SRP mappings for all GSE IDs using gse_to_srp gse_to_srp_map = {} if gse and detailed: try: srp_df = self.gse_to_srp(gse) if not srp_df.empty: # Group by study_alias and join multiple SRPs with comma for gse_id in gse: srps = ( srp_df[srp_df["study_alias"] == gse_id]["study_accession"] .dropna() .tolist() ) if srps: gse_to_srp_map[gse_id] = ",".join(srps) except Exception: pass # Get SRX mappings for all GSM samples gsm_to_srx_map = {} if sample_accessions and detailed: try: # Use fetch_gds_results to get SRX from GSM entries gsm_response = self.fetch_gds_results(sample_accessions) if gsm_response is not None and not gsm_response.empty: for _, row in gsm_response.iterrows(): if row.get("entrytype") == "GSM": gsm_acc = row.get("accession") srx = row.get("SRA") if gsm_acc and srx and not pd.isna(srx): gsm_to_srx_map[gsm_acc] = srx except Exception: pass rows = [] for record in gse_records: study_accession = record.get("accession", pd.NA) platform = record.get("gpl", pd.NA) if ( isinstance(platform, str) and platform.strip() and not platform.upper().startswith("GPL") and platform.replace(" ", "").isdigit() ): platform_accession = f"GPL{platform.strip()}" else: platform_accession = platform if platform else pd.NA base_row = OrderedDict( [ ("study_accession", study_accession), ("study_title", record.get("title", pd.NA)), ("study_summary", record.get("summary", pd.NA)), ("organism_name", record.get("taxon", pd.NA)), ("platform_accession", platform_accession), ("platform_title", record.get("platformtitle", pd.NA)), ("experiment_type", record.get("gdstype", pd.NA)), ("bioproject", record.get("bioproject", pd.NA)), ("submission_date", record.get("pdat", pd.NA)), ("supplementary_files", record.get("suppfile", pd.NA)), ("series_ftp", record.get("ftplink", pd.NA)), ("sample_accession", pd.NA), ("sample_title", pd.NA), ] ) # Add SRP column when detailed=True if detailed: base_row["study_sra_accession"] = gse_to_srp_map.get( study_accession, pd.NA ) if sample_attribute: base_row["sample_summary"] = pd.NA if detailed: base_row["sample_ftp"] = pd.NA base_row["sample_supplementary"] = pd.NA base_row["sample_geo2r"] = pd.NA base_row["experiment_sra_accession"] = pd.NA # Add SOFT metadata fields base_row["sample_type"] = pd.NA base_row["sample_source_name"] = pd.NA base_row["sex"] = pd.NA base_row["age"] = pd.NA base_row["tissue"] = pd.NA base_row["cell_type"] = pd.NA base_row["disease"] = pd.NA base_row["treatment"] = pd.NA base_row["extract_protocol"] = pd.NA base_row["label_protocol"] = pd.NA samples = record.get("samples") or [] if samples: for sample in samples: row = base_row.copy() sample_acc = sample.get("accession", pd.NA) row["sample_accession"] = sample_acc row["sample_title"] = sample.get("title", pd.NA) sample_entry = sample_details.get(sample_acc, {}) if sample_attribute: row["sample_summary"] = sample_entry.get("summary", pd.NA) if detailed: row["sample_ftp"] = sample_entry.get("ftplink", pd.NA) row["sample_supplementary"] = sample_entry.get( "suppfile", pd.NA ) row["sample_geo2r"] = sample_entry.get("geo2r", pd.NA) # Add SRX from gsm_to_srx_map row["experiment_sra_accession"] = gsm_to_srx_map.get( sample_acc, pd.NA ) # Add SOFT metadata - extract ALL available fields soft_data = gsm_soft_data.get(sample_acc, {}) if soft_data: # Add all SOFT fields with sample_ prefix (characteristics handled separately) for soft_key, soft_val in soft_data.items(): if soft_key != "characteristics": col_name = f"sample_{soft_key}" row[col_name] = soft_val # Also extract commonly used fields to canonical column names for convenience row["sample_type"] = soft_data.get("type_ch1", pd.NA) row["sample_source_name"] = soft_data.get( "source_name_ch1", pd.NA ) row["extract_protocol"] = soft_data.get( "extract_protocol_ch1", pd.NA ) row["label_protocol"] = soft_data.get( "label_protocol_ch1", pd.NA ) # Process characteristics: add standard ones to canonical names, preserve all as-is chars = soft_data.get("characteristics", {}) # Standard fields with canonical names (for backward compatibility) row["sex"] = chars.get("sex", chars.get("gender", pd.NA)) row["age"] = chars.get("age", pd.NA) row["tissue"] = chars.get( "tissue", chars.get( "tissue type", chars.get("structures", chars.get("organ", pd.NA)), ), ) row["cell_type"] = chars.get( "cell type", chars.get("cell_type", chars.get("celltype", pd.NA)), ) row["disease"] = chars.get( "disease", chars.get( "disease state", chars.get( "disease_state", chars.get("disease_status", pd.NA), ), ), ) row["treatment"] = chars.get( "treatment", chars.get("compound", chars.get("drug", pd.NA)), ) # Add ALL characteristics as-is (including custom ones) for char_key, char_val in chars.items(): row[char_key] = char_val rows.append(row) else: rows.append(base_row) if not rows: return pd.DataFrame( columns=list(base_row.keys()) if "base_row" in locals() else None ) metadata_df = pd.DataFrame(rows) if include_pmids: try: pmid_df = self.gse_to_pmid(gse) except Exception: pmid_df = None if pmid_df is not None and not pmid_df.empty: pmid_map = {} for _, row in pmid_df.iterrows(): gse_acc = row.get("gse_accession") pmid = row.get("pmid") if pd.isna(pmid): continue pmid_map.setdefault(gse_acc, []).append(str(pmid)) metadata_df["pmid"] = metadata_df["study_accession"].map( lambda accession: ( ",".join(pmid_map.get(accession, [])) if accession in pmid_map else pd.NA ) ) else: metadata_df["pmid"] = pd.NA metadata_df = metadata_df.replace("", pd.NA) if "sample_accession" in metadata_df.columns: metadata_df = metadata_df.sort_values( by=["study_accession", "sample_accession"], na_position="last", ) metadata_df = metadata_df.reset_index(drop=True) if detailed and not metadata_df.empty: try: gse_bioproject_map = {} for _, row in metadata_df.iterrows(): gse_id = row.get("study_accession") bioproject = row.get("bioproject") if gse_id and str(gse_id).startswith("GSE"): if bioproject and str(bioproject).startswith("PRJNA"): gse_bioproject_map[gse_id] = bioproject gse_srp_map = {} all_fastq_data = [] for gse_id, bioproject in gse_bioproject_map.items(): try: srp_list = self.bioproject_to_srp(bioproject) if srp_list: srp = srp_list[0] # Use the first SRP found gse_srp_map[gse_id] = srp # Fetch SRA metadata and fastq URLs for this SRP try: sra_metadata_df = self.sra_metadata(srp) if not sra_metadata_df.empty: fastq_df = self.fetch_ena_fastq(srp) if not fastq_df.empty: merged_df = sra_metadata_df.merge( fastq_df, on="run_accession", how="left" ) merged_df["gse_from_bioproject"] = gse_id merged_df["srp_from_bioproject"] = srp all_fastq_data.append(merged_df) time.sleep(self.sleep_time) except Exception: pass except Exception: pass # If we found fastq data, merge it with the main metadata via GSM->SRX->SRR mapping if all_fastq_data and sample_accessions: try: # Combine all fastq data combined_fastq = pd.concat(all_fastq_data, ignore_index=True) # Map GSM to SRX for matching gsm_to_srx_map = {} for gsm_id in sample_accessions: try: srx_df = self.gsm_to_srx(gsm_id) if ( not srx_df.empty and "experiment_accession" in srx_df.columns ): srx_list = ( srx_df["experiment_accession"].dropna().tolist() ) if srx_list: gsm_to_srx_map[gsm_id] = srx_list[0] time.sleep(0.1) except Exception: pass # Add fastq columns to metadata_df fastq_cols = [ col for col in combined_fastq.columns if "fastq" in col.lower() or "ftp" in col.lower() ] for col in fastq_cols: if col not in metadata_df.columns: metadata_df[col] = pd.NA # Create a mapping from SRX->run_accession->fastq URLs srx_to_fastq_map = {} for _, row in combined_fastq.iterrows(): srx = row.get("experiment_accession", pd.NA) run_acc = row.get("run_accession", pd.NA) if not pd.isna(srx) and not pd.isna(run_acc): if srx not in srx_to_fastq_map: srx_to_fastq_map[srx] = {} srx_to_fastq_map[srx][run_acc] = row # Merge fastq URLs based on GSM->SRX->fastq mapping for col in fastq_cols: def get_fastq_url(row): gsm = row.get("sample_accession", pd.NA) if pd.isna(gsm): return pd.NA # Get SRX for this GSM srx = gsm_to_srx_map.get(gsm, pd.NA) if pd.isna(srx) or srx not in srx_to_fastq_map: return pd.NA # Get first run accession for this SRX run_accs = list(srx_to_fastq_map[srx].keys()) if run_accs: fastq_row = srx_to_fastq_map[srx][run_accs[0]] return fastq_row.get(col, pd.NA) return pd.NA metadata_df[col] = metadata_df.apply(get_fastq_url, axis=1) except Exception: pass except Exception: pass # Enrich metadata if requested if enrich and not metadata_df.empty: try: from pysradb.metadata_enrichment import create_metadata_extractor extractor = create_metadata_extractor( method="llm", backend=enrich_backend ) metadata_df = extractor.enrich_dataframe( metadata_df, text_column=None, prefix="guessed_" ) except Exception as e: error_msg = str(e) if "Ollama is not installed or not running" in error_msg: print(f"Error: {error_msg}") print( "Metadata enrichment requires Ollama to be installed and running." ) print( "Please install Ollama from https://ollama.ai/ and follow these steps:" ) print("1. Start Ollama server: ollama serve") print("2. Pull a model: ollama pull phi3") print("3. Try again or use a different enrichment backend") raise else: print(f"Warning: Enrichment failed: {e}") return metadata_df def metadata(self, accession, **kwargs): """ Unified method to fetch metadata for SRA or GEO accessions. Automatically detects accession type and calls appropriate method. Args: accession: ``SRP``/``GSE`` accession(s) - can be string or list kwargs: Additional parameters passed to ``sra_metadata()`` or ``geo_metadata()`` (e.g., ``detailed``, ``enrich``, ``enrich_backend``, ``sample_attribute``, etc.) Returns: DataFrame with metadata (enriched if enrich=True) Examples: >>> client = SRAweb() >>> df = client.metadata("GSE286254", detailed=True, enrich=True) >>> df = client.metadata("SRP253951", detailed=True, enrich=True) >>> df = client.metadata(["GSE286254", "GSE147507"], enrich=True) """ if isinstance(accession, str): accessions = [accession] else: accessions = accession if not accessions: return pd.DataFrame() # Detect accession type from first accession first_acc = accessions[0].upper() if first_acc.startswith("GSE"): return self.geo_metadata(accession, **kwargs) elif first_acc.startswith("SRP"): return self.sra_metadata(accession, **kwargs) else: raise ValueError( f"Unsupported accession type: {first_acc}. " "Supported types: GSE (GEO Series), SRP (SRA Project)" ) def gse_to_gsm(self, gse, **kwargs): if isinstance(gse, str): gse = [gse] gse_df = self.fetch_gds_results(gse, **kwargs) gse_df = gse_df.rename( columns={ "accession": "experiment_alias", "SRA": "experiment_accession", "title": "experiment_title", "summary": "sample_attribute", } ) # TODO: Fix for multiple GSEs? gse_df["study_alias"] = "" if len(gse) == 1: study_alias = gse[0] for index, row in gse_df.iterrows(): if row.entrytype == "GSE": study_alias = row["experiment_accession"] # If GSM is ecnountered, apply it the # previously encountered GSE elif row.entrytype == "GSM": gse_df.loc[index, "study_alias"] = study_alias gse_df = gse_df[gse_df.entrytype == "GSM"] if kwargs and kwargs["detailed"] == True: return gse_df return gse_df[ ["study_alias", "experiment_alias", "experiment_accession"] ].drop_duplicates() def gse_to_srp(self, gse, **kwargs): if isinstance(gse, str): gse = [gse] if not gse: # Handle empty input return pd.DataFrame(columns=["study_alias", "study_accession"]) gse_df = self.fetch_gds_results(gse, **kwargs) if gse_df is None or gse_df.empty: # Handle case where no results found return pd.DataFrame(columns=["study_alias", "study_accession"]) gse_df = gse_df.rename( columns={"accession": "study_alias", "SRA": "study_accession"} ) gse_df_subset = None if "GSE" in gse_df.entrytype.unique(): gse_df_subset = gse_df[gse_df.entrytype == "GSE"] common_gses = set(gse_df.study_alias.unique()).intersection(gse) if len(common_gses) < len(gse): gse_df_subset = None # Check if GSE entries have valid SRA accessions # If any study_accessions are NaN, fall back to extracting from GSM entries elif gse_df_subset["study_accession"].isna().any(): gse_df_subset = None if gse_df_subset is None: # sometimes SRX ids are returned instead of an entire project # see https://github.com/saketkc/pysradb/issues/186 # GSE: GSE209835; SRP =SRP388275 gse_df_subset_gse = gse_df[gse_df.entrytype == "GSE"] # Include GSEs that are missing OR have NaN study_accessions gses_without_srp = gse_df_subset_gse[ gse_df_subset_gse.study_accession.isna() ].study_alias.tolist() gse_of_interest = ( list(set(gse).difference(gse_df.study_alias.unique())) + gses_without_srp ) gse_df_subset_other = gse_df[gse_df.entrytype != "GSE"] # Filter out NaN values from study_accession before converting to SRP srx = gse_df_subset_other.study_accession.dropna().tolist() srp_df = self.srx_to_srp(srx) srp_unique = list( set(srp_df.study_accession.unique()).difference( gse_df_subset_gse.study_accession.tolist() ) ) # Handle mismatched lengths between GSEs and SRPs # Create all combinations of GSE-SRP pairs gse_srp_pairs = [] for gse_id in gse_of_interest: for srp_id in srp_unique: gse_srp_pairs.append( {"study_alias": gse_id, "study_accession": srp_id} ) if gse_srp_pairs: new_gse_df = pd.DataFrame(gse_srp_pairs) else: # If no pairs, create empty DataFrame with correct columns new_gse_df = pd.DataFrame(columns=["study_alias", "study_accession"]) # Filter out GSE entries with NaN study_accession before concatenating # as we've already created new pairs for them gse_df_subset_gse_valid = gse_df_subset_gse[ gse_df_subset_gse.study_accession.notna() ] gse_df_subset = pd.concat([gse_df_subset_gse_valid, new_gse_df]) gse_df_subset = gse_df_subset.loc[gse_df_subset.study_alias.isin(gse)] return gse_df_subset[["study_alias", "study_accession"]].drop_duplicates() def gsm_to_srp(self, gsm, **kwargs): gsm_df = self.fetch_gds_results(gsm, **kwargs) gsm_df = gsm_df[gsm_df.entrytype == "GSE"] gsm_df = gsm_df.rename( columns={"accession": "experiment_alias", "SRA": "study_accession"} ) return gsm_df[["experiment_alias", "study_accession"]].drop_duplicates() def gsm_to_srr(self, gsm, **kwargs): gsm_df = self.fetch_gds_results(gsm, **kwargs) gsm_df = gsm_df.rename( columns={ "accession": "experiment_alias", "SRA": "experiment_accession", "title": "experiment_title", "summary": "sample_attribute", } ) gsm_df = gsm_df[gsm_df.entrytype == "GSM"] srr_df = self.srx_to_srr(gsm_df.experiment_accession.tolist()) gsm_df = gsm_df.merge(srr_df, on="experiment_accession") return gsm_df[["experiment_alias", "run_accession"]] def gsm_to_srs(self, gsm, **kwargs): """Get SRS for a GSM""" gsm_df = self.fetch_gds_results(gsm, **kwargs) gsm_df = gsm_df[gsm_df.entrytype == "GSM"].rename( columns={"SRA": "experiment_accession", "accession": "experiment_alias"} ) srx = gsm_df.experiment_accession.tolist() time.sleep(self.sleep_time) srs_df = self.srx_to_srs(srx) gsm_df = srs_df.merge(gsm_df, on="experiment_accession")[ ["experiment_alias", "sample_accession"] ] return gsm_df.drop_duplicates() def gsm_to_srx(self, gsm, **kwargs): """Get SRX for a GSM""" if isinstance(gsm, str): gsm = [gsm] gsm_df = self.fetch_gds_results(gsm, **kwargs) gsm_df = gsm_df[gsm_df.entrytype == "GSM"].rename( columns={"SRA": "experiment_accession", "accession": "experiment_alias"} ) gsm_df = gsm_df.loc[gsm_df["experiment_alias"].isin(gsm)] return gsm_df[["experiment_alias", "experiment_accession"]].drop_duplicates() def gsm_to_gse(self, gsm, **kwargs): if isinstance(gsm, str): gsm = [gsm] if not gsm: # Handle empty input return pd.DataFrame(columns=["study_alias", "study_accession"]) gsm_df = self.fetch_gds_results(gsm, **kwargs) if gsm_df is None or gsm_df.empty: # Handle case where no results found return pd.DataFrame(columns=["study_alias", "study_accession"]) # For GSM queries, we need to extract GSE IDs from the 'gse' column # The entrytype will be 'GSM', not 'GSE' gsm_entries = gsm_df[gsm_df.entrytype == "GSM"] if gsm_entries.empty: return pd.DataFrame(columns=["study_alias", "study_accession"]) # Extract GSE IDs from the 'gse' column and create result rows results = [] for _, row in gsm_entries.iterrows(): gsm_id = row["accession"] gse_str = str(row.get("gse", "")) if gse_str and gse_str != "nan": # Handle multiple GSE IDs separated by semicolon gse_ids = [ gse_id.strip() for gse_id in gse_str.split(";") if gse_id.strip() ] for gse_id in gse_ids: if gse_id.isdigit(): # Add GSE prefix if it's just a number gse_id = f"GSE{gse_id}" results.append( { "study_alias": gse_id, "study_accession": row.get("SRA", pd.NA), } ) if results: result_df = pd.DataFrame(results) return result_df[["study_alias", "study_accession"]].drop_duplicates() else: return pd.DataFrame(columns=["study_alias", "study_accession"]) def srp_to_gse(self, srp, **kwargs): """Get GSE for a SRP""" srp_df = self.fetch_gds_results(srp, **kwargs) if srp_df is None: srp_df = pd.DataFrame( {"study_alias": [], "study_accession": [], "entrytype": []} ) srp_df = srp_df.rename( columns={"accession": "study_alias", "SRA": "study_accession"} ) srp_df_gse = srp_df[srp_df.entrytype == "GSE"] missing_srp = list(set(srp).difference(srp_df_gse.study_accession.tolist())) srp_df_nongse = srp_df[srp_df.entrytype != "GSE"] if srp_df_nongse.shape[0] >= 1: srp_df_nongse = pd.DataFrame( { "study_accession": missing_srp, "study_alias": [pd.NA] * len(missing_srp), "entrytpe": ["GSE"] * len(missing_srp), } ) srp_df = pd.concat([srp_df_gse, srp_df_nongse]) return srp_df[["study_accession", "study_alias"]].drop_duplicates() def srp_to_srr(self, srp, **kwargs): """Get SRR for a SRP""" srp_df = self.sra_metadata(srp, **kwargs) return _order_first(srp_df, ["study_accession", "run_accession"]) def srp_to_srs(self, srp, **kwargs): """Get SRS for a SRP""" srp_df = self.sra_metadata(srp, **kwargs) return _order_first(srp_df, ["study_accession", "sample_accession"]) def srp_to_srx(self, srp, **kwargs): """Get SRX for a SRP""" srp_df = self.sra_metadata(srp, **kwargs) srp_df["study_accesssion"] = srp return _order_first(srp_df, ["study_accession", "experiment_accession"]) def srr_to_gsm(self, srr, **kwargs): """Get GSM for a SRR""" if isinstance(srr, str): srr = [srr] srr_df = self.srr_to_srp(srr, detailed=True) # remove NAs srp = [x for x in srr_df.study_accession.tolist() if not x is pd.NA] gse_df = self.fetch_gds_results(srp, **kwargs) gse_df = gse_df[gse_df.entrytype == "GSE"].rename( columns={"SRA": "project_accession", "accession": "project_alias"} ) gsm_df = self.gse_to_gsm(gse_df.project_alias.tolist(), detailed=True) srr_cols = list( set(srr_df.columns.tolist()).difference(gsm_df.columns.tolist()) ) + ["experiment_accession"] joined_df = gsm_df.merge(srr_df[srr_cols], on="experiment_accession") df = _order_first(joined_df, ["run_accession", "experiment_alias"]) df = df.loc[df["run_accession"].isin(srr)] return df def srr_to_srp(self, srr, **kwargs): """Get SRP for a SRR""" if isinstance(srr, str): srr = [srr] srr_df = self.sra_metadata(srr, **kwargs) if kwargs and kwargs["detailed"] == True: return srr_df srr_df = srr_df.loc[srr_df["run_accession"].isin(srr)] return _order_first(srr_df, ["run_accession", "study_accession"]) def srr_to_srs(self, srr, **kwargs): """Get SRS for a SRR""" if isinstance(srr, str): srr = [srr] srr_df = self.sra_metadata(srr, **kwargs) srr_df = srr_df.loc[srr_df["run_accession"].isin(srr)] return _order_first(srr_df, ["run_accession", "sample_accession"]) def srr_to_srx(self, srr, **kwargs): """Get SRX for a SRR""" if isinstance(srr, str): srr = [srr] srr_df = self.sra_metadata(srr) srr_df = srr_df.loc[srr_df["run_accession"].isin(srr)] return _order_first(srr_df, ["run_accession", "experiment_accession"]) def srs_to_gsm(self, srs, **kwargs): """Get GSM for a SRS""" if isinstance(srs, str): srs = [srs] srx_df = self.srs_to_srx(srs) time.sleep(self.sleep_time) gsm_df = self.srx_to_gsm(srx_df.experiment_accession.tolist(), **kwargs) srs_df = srx_df.merge(gsm_df, on="experiment_accession") srs_df = srs_df.loc[srs_df["sample_accession"].isin(srs)] return _order_first(srs_df, ["sample_accession", "experiment_alias"]) def srx_to_gsm(self, srx, **kwargs): if isinstance(srx, str): srx = [srx] gsm_df = self.fetch_gds_results(srx, **kwargs) gsm_df = gsm_df[gsm_df.entrytype == "GSM"].rename( columns={"SRA": "experiment_accession", "accession": "experiment_alias"} ) gsm_df = gsm_df.loc[gsm_df["experiment_accession"].isin(srx)] return gsm_df[["experiment_accession", "experiment_alias"]].drop_duplicates() def srs_to_srx(self, srs, **kwargs): """Get SRX for a SRS""" srs_df = self.sra_metadata(srs, **kwargs) return _order_first(srs_df, ["sample_accession", "experiment_accession"]) def srx_to_srp(self, srx, **kwargs): """Get SRP for a SRX""" srx_df = self.sra_metadata(srx, **kwargs) return _order_first(srx_df, ["experiment_accession", "study_accession"]) def srx_to_srr(self, srx, **kwargs): """Get SRR for a SRX""" srx_df = self.sra_metadata(srx, **kwargs) return _order_first(srx_df, ["experiment_accession", "run_accession"]) def srx_to_srs(self, srx, **kwargs): """Get SRS for a SRX""" srx_df = self.sra_metadata(srx, **kwargs) return _order_first(srx_df, ["experiment_accession", "sample_accession"]) def search(self, *args, **kwargs): raise NotImplementedError("Search not yet implemented for Web") def fetch_bioproject_pmids(self, bioprojects): """Fetch PMIDs for given BioProject accessions Parameters ---------- bioprojects: list or str BioProject accession(s) Returns ------- bioproject_pmids: dict Mapping of BioProject to list of PMIDs """ if isinstance(bioprojects, str): bioprojects = [bioprojects] bioproject_pmids = {} for bioproject in bioprojects: if pd.isna(bioproject) or not bioproject: bioproject_pmids[bioproject] = [] continue try: payload = self.efetch_params.copy() payload = [param for param in payload if param[0] != "retmode"] payload += [ ("db", "bioproject"), ("id", bioproject), ("retmode", "xml"), ] request = requests.get( self.base_url["efetch"], params=OrderedDict(payload) ) xml_text = request.text.strip() # Parse XML to extract Publication IDs pmids = [] try: xml_dict = xmltodict.parse( xml_text, process_namespaces=False, dict_constructor=OrderedDict ) # Navigate through the XML structure if "RecordSet" in xml_dict: records = xml_dict["RecordSet"].get("DocumentSummary", []) if not isinstance(records, list): records = [records] for record in records: project_descr = record.get("Project", {}).get( "ProjectDescr", {} ) publications = project_descr.get("Publication", []) if not isinstance(publications, list): publications = [publications] for pub in publications: pub_id = pub.get("@id", "") if pub_id and pub_id.isdigit(): pmids.append(pub_id) except ExpatError: # XML parsing failed --> Look for PMID patterns in the raw text pmid_pattern = r'id="(\d+)"' matches = re.findall(pmid_pattern, xml_text) pmids = [ match for match in matches if len(match) >= 7 ] # PMIDs are typically 7+ digits # If no PMIDs found in bioproject XML, try searching PMC by bioproject ID if not pmids: pmids = self._search_pmc_by_bioproject(bioproject) bioproject_pmids[bioproject] = list(set(pmids)) # Remove duplicates time.sleep(self.sleep_time) except Exception as e: warnings.warn(f"Failed to fetch PMIDs for BioProject {bioproject}: {e}") bioproject_pmids[bioproject] = [] return bioproject_pmids def srp_to_pmid(self, srp_accessions): """Get PMIDs associated with SRP accessions Parameters ---------- srp_accessions: list or str SRP accession(s) Returns ------- srp_pmid_df: pandas.DataFrame DataFrame with SRP accessions and associated PMIDs """ if isinstance(srp_accessions, str): srp_accessions = [srp_accessions] # Get metadata to extract BioProject information metadata_df = self.sra_metadata(srp_accessions) if metadata_df is None or metadata_df.empty: return pd.DataFrame(columns=["srp_accession", "bioproject", "pmid"]) # Try to get PMIDs via BioProject first unique_bioprojects = metadata_df["bioproject"].dropna().unique().tolist() bioproject_pmids = self.fetch_bioproject_pmids(unique_bioprojects) # If no BioProject PMIDs found, try fallback search external_pmids = [] if not any(pmids for pmids in bioproject_pmids.values()): external_pmids = self._search_fallback_pmids(srp_accessions) # Build results - one row per unique SRP accession results = [] for _, row in metadata_df.iterrows(): srp_acc = self._extract_sra_accession(row) bioproject = row.get("bioproject", "") # Get PMIDs (BioProject takes priority over external) pmids = bioproject_pmids.get(bioproject, []) if not pmids and external_pmids: pmids = external_pmids # Add result with smallest PMID (if any found) smallest_pmid = self._get_smallest_pmid(pmids) if pmids else pd.NA results.append( { "srp_accession": srp_acc, "bioproject": bioproject, "pmid": smallest_pmid, } ) return pd.DataFrame(results).drop_duplicates() def _search_fallback_pmids(self, srp_accessions): """Search for PMIDs using fallback strategies (external sources + direct SRA search + GSE search)""" try: original_sleep = self.sleep_time self.sleep_time = max(0.1, self.sleep_time * 0.5) # Strategy 1: Search via external source identifiers # Example: ERP018009 detailed_metadata = self.sra_metadata( srp_accessions, detailed=True, include_pmids=False ) if detailed_metadata is not None and not detailed_metadata.empty: if external_sources := self.extract_external_sources(detailed_metadata): pmids = self.search_pmc_for_external_sources([external_sources[0]]) if pmids: return pmids # Strategy 2: Search via GSE identifiers extracted from metadata # Example: GSE253406 --> SRP484103 gse_pmids = self._search_gse_gsm_pmids( detailed_metadata, srp_accessions ) if gse_pmids: return gse_pmids # Strategy 3: Direct SRP ID search # Example: SRP047086 pmids = self.search_pmc_for_external_sources(srp_accessions) return pmids except Exception as e: return [] finally: self.sleep_time = original_sleep def _extract_sra_accession(self, row): """Extract SRA accession from metadata row""" return row.get( "study_accession", row.get( "run_accession", row.get("experiment_accession", row.get("sample_accession", "")), ), ) def _get_smallest_pmid(self, pmids): """Get the numerically smallest PMID from a list""" if not pmids: return pd.NA # Convert to integers for proper numeric sorting pmid_ints = [] for pmid in pmids: try: pmid_ints.append(int(pmid)) except ValueError: pmid_ints.append(pmid) # Keep non-numeric as-is return str(min(pmid_ints)) def extract_external_sources(self, metadata_df): """Extract external source identifiers from SRA metadata Parameters ---------- metadata_df: pandas.DataFrame DataFrame containing SRA metadata Returns ------- external_sources: list List of external source identifiers found """ external_sources = [] patterns = [ r"E-MTAB-\d+", # ArrayExpress r"GSE\d+", # GEO Series r"E-GEOD-\d+", # GEO in ArrayExpress r"E-MEXP-\d+", # MEXP in ArrayExpress r"E-TABM-\d+", # TABM in ArrayExpress ] # Fields that commonly contain external source identifiers source_fields = ["run_alias", "submitter id", "sample name", "experiment_alias"] for field in source_fields: if field in metadata_df.columns: values = metadata_df[field].dropna().unique() for value in values: value_str = str(value) for pattern in patterns: matches = re.findall(pattern, value_str) external_sources.extend( match for match in matches if match not in external_sources ) return external_sources def _search_gse_gsm_pmids(self, metadata_df, sra_accessions): """Search for PMIDs using GSE identifiers from BioProject and SRP conversion Parameters ---------- metadata_df: pandas.DataFrame Detailed metadata DataFrame sra_accessions: list List of SRA accessions being searched Returns ------- pmids: list List of PMIDs found via GSE search """ import time gse_identifiers = [] # Strategy 1: BioProject to GSE conversion via NCBI search if "bioproject" in metadata_df.columns: unique_bioprojects = metadata_df["bioproject"].dropna().unique() for bioproject in unique_bioprojects[ :3 ]: # Limit to avoid too many requests try: gse_ids = self._bioproject_to_gse(bioproject) gse_identifiers.extend(gse_ids) time.sleep(self.sleep_time) # Rate limiting except Exception: pass # Strategy 2: SRP to GSE conversion via NCBI ELink for sra_acc in sra_accessions: if sra_acc.startswith("SRP"): try: gse_ids = self._srp_to_gse_via_elink(sra_acc) gse_identifiers.extend(gse_ids) time.sleep(self.sleep_time) # Rate limiting except Exception: pass # Strategy 3: Try existing pysradb SRP to GSE conversion for sra_acc in sra_accessions: if sra_acc.startswith("SRP"): try: gse_df = self.srp_to_gse(sra_acc) if not gse_df.empty and "experiment_alias" in gse_df.columns: gse_values = gse_df["experiment_alias"].dropna().astype(str) for gse_val in gse_values: if gse_val.startswith("GSE"): gse_identifiers.append(gse_val) except Exception: pass # Remove duplicates and search PMC for GSE identifiers unique_gse_ids = list(set(gse_identifiers)) if unique_gse_ids: pmids = self.search_pmc_for_external_sources(unique_gse_ids) return pmids return [] def _bioproject_to_gse(self, bioproject): """Convert BioProject ID to GSE ID via NCBI search Parameters ---------- bioproject: str BioProject ID (e.g., 'PRJNA1065472') Returns ------- gse_ids: list List of GSE IDs found """ import requests gse_ids = [] try: search_url = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi" search_params = { "db": "gds", "term": f"{bioproject}[BioProject]", "retmode": "json", "retmax": "10", } response = requests.get(search_url, params=search_params, timeout=30) response.raise_for_status() result = response.json() geo_uids = result["esearchresult"]["idlist"] if geo_uids: # Get summary to find GSE IDs summary_url = ( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi" ) summary_params = { "db": "gds", "id": ",".join(geo_uids), "retmode": "json", } summary_response = requests.get( summary_url, params=summary_params, timeout=30 ) summary_response.raise_for_status() summary_result = summary_response.json() for uid in geo_uids: if uid in summary_result["result"]: record = summary_result["result"][uid] accession = record.get("accession", "") if accession.startswith("GSE"): gse_ids.append(accession) except Exception: pass return gse_ids def _srp_to_gse_via_elink(self, srp_id): """Convert SRP ID to GSE ID via NCBI ELink Parameters ---------- srp_id: str SRP ID (e.g., 'SRP484103') Returns ------- gse_ids: list List of GSE IDs found """ import requests gse_ids = [] try: # First, search for the SRP in SRA database to get UIDs search_url = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi" search_params = { "db": "sra", "term": srp_id, "retmode": "json", "retmax": "5", } response = requests.get(search_url, params=search_params, timeout=30) response.raise_for_status() result = response.json() sra_uids = result["esearchresult"]["idlist"] if sra_uids: # Use ELink to find related GEO records elink_url = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi" elink_params = { "dbfrom": "sra", "db": "gds", "id": sra_uids[0], # Use first UID "retmode": "json", } elink_response = requests.get( elink_url, params=elink_params, timeout=30 ) elink_response.raise_for_status() elink_result = elink_response.json() if "linksets" in elink_result: for linkset in elink_result["linksets"]: if "linksetdbs" in linkset: for linksetdb in linkset["linksetdbs"]: if linksetdb["dbto"] == "gds": geo_uids = linksetdb["links"] if geo_uids: # Get summary to find GSE IDs summary_url = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi" summary_params = { "db": "gds", "id": ",".join(geo_uids), "retmode": "json", } summary_response = requests.get( summary_url, params=summary_params, timeout=30, ) summary_response.raise_for_status() summary_result = summary_response.json() for uid in geo_uids: if uid in summary_result["result"]: record = summary_result["result"][uid] accession = record.get("accession", "") if accession.startswith("GSE"): gse_ids.append(accession) except Exception: pass return gse_ids def _search_pmc_by_bioproject(self, bioproject_id): """Search PubMed Central for PMIDs using BioProject accession ID This provides a fallback mechanism when the BioProject XML doesn't contain publication metadata but the research has been published and is cited in PMC. Parameters ---------- bioproject_id: str BioProject accession ID (e.g., PRJEB39301, PRJNA123456) Returns ------- pmids: list List of PMIDs found associated with the bioproject """ try: search_url = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi" search_params = { "db": "pmc", "term": bioproject_id, "retmode": "json", "retmax": "10", } response = requests.get(search_url, params=search_params, timeout=60) response.raise_for_status() result = response.json() pmc_ids = result.get("esearchresult", {}).get("idlist", []) if not pmc_ids: return [] # Get primary PMIDs for each PMC article summary_url = "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi" summary_params = { "db": "pmc", "id": ",".join(pmc_ids), "retmode": "json", } summary_response = requests.get( summary_url, params=summary_params, timeout=60 ) summary_result = summary_response.json() pmids = [] # Extract primary PMID for each PMC article for pmc_id in pmc_ids: if pmc_id in summary_result.get("result", {}): article = summary_result["result"][pmc_id] articleids = article.get("articleids", []) # Find the primary PMID for aid in articleids: if aid.get("idtype") == "pmid": primary_pmid = aid.get("value") if primary_pmid and primary_pmid not in pmids: pmids.append(primary_pmid) break return pmids except Exception as e: # Silently fail and return empty list for fallback mechanism return [] def search_pmc_for_external_sources(self, external_sources): """Search PubMed Central for PMIDs using external source identifiers Parameters ---------- external_sources: list List of external source identifiers Returns ------- pmids: list List of PMIDs found """ if not external_sources: return [] all_pmids = [] for source in external_sources: try: search_url = ( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esearch.fcgi" ) search_params = { "db": "pmc", "term": source, "retmode": "json", "retmax": "10", } response = requests.get(search_url, params=search_params, timeout=60) response.raise_for_status() result = response.json() pmc_ids = result["esearchresult"]["idlist"] if not pmc_ids: continue # Get primary PMIDs for each PMC article summary_url = ( "https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi" ) summary_params = { "db": "pmc", "id": ",".join(pmc_ids), "retmode": "json", } summary_response = requests.get( summary_url, params=summary_params, timeout=60 ) summary_result = summary_response.json() # Extract primary PMID for each PMC article for pmc_id in pmc_ids: if pmc_id in summary_result["result"]: article = summary_result["result"][pmc_id] articleids = article.get("articleids", []) # Find the primary PMID for aid in articleids: if aid.get("idtype") == "pmid": primary_pmid = aid.get("value") if primary_pmid and primary_pmid not in all_pmids: all_pmids.append(primary_pmid) break time.sleep(self.sleep_time) # Rate limiting except Exception as e: continue return list(set(all_pmids)) # Remove duplicates def sra_to_pmid(self, sra_accessions): """Get PMIDs for SRA accessions (backward compatibility wrapper) Parameters ---------- sra_accessions: list or str SRA accession(s) - can be SRP, SRR, SRX, or SRS Returns ------- sra_pmid_df: pandas.DataFrame DataFrame with SRA accessions and associated PMIDs """ # For SRP accessions, use the main method if isinstance(sra_accessions, str): if sra_accessions.startswith("SRP"): return self.srp_to_pmid(sra_accessions) elif isinstance(sra_accessions, list): # If all are SRP accessions, use main method if all(acc.startswith("SRP") for acc in sra_accessions): return self.srp_to_pmid(sra_accessions) # For other SRA accessions, convert to SRP first if possible # This is a simplified implementation for backward compatibility return self.srp_to_pmid(sra_accessions) def srr_to_pmid(self, srr): """Get PMIDs for Run Accessions (SRR)""" return self.sra_to_pmid(srr) def srx_to_pmid(self, srx): """Get PMIDs for Experiment Accessions (SRX)""" return self.sra_to_pmid(srx) def srs_to_pmid(self, srs): """Get PMIDs for Sample Accessions (SRS)""" return self.sra_to_pmid(srs) def gse_to_pmid(self, gse_accessions): """Get PMIDs for GSE accessions by searching PubMed Central Parameters ---------- gse_accessions: list or str GSE accession(s) Returns ------- gse_pmid_df: pandas.DataFrame DataFrame with GSE accessions and associated PMIDs """ if isinstance(gse_accessions, str): gse_accessions = [gse_accessions] results = [] for gse_acc in gse_accessions: pmids = self.search_pmc_for_external_sources([gse_acc]) smallest_pmid = self._get_smallest_pmid(pmids) if pmids else pd.NA results.append( { "gse_accession": gse_acc, "pmid": smallest_pmid, } ) return pd.DataFrame(results) def doi_to_pmid(self, dois): """Convert DOI(s) to PMID(s) Parameters ---------- dois: list or str DOI(s) Returns ------- doi_pmid_mapping: dict Mapping of DOI to PMID """ if isinstance(dois, str): dois = [dois] doi_pmid_mapping = {} for doi in dois: try: search_url = self.base_url["esearch"] search_params = { "db": "pubmed", "term": f"{doi}[DOI]", "retmode": "json", } response = requests.get(search_url, params=search_params, timeout=60) response.raise_for_status() result = response.json() id_list = result.get("esearchresult", {}).get("idlist", []) if id_list: doi_pmid_mapping[doi] = id_list[0] else: doi_pmid_mapping[doi] = None time.sleep(self.sleep_time) except requests.RequestException as e: warnings.warn(f"Network error while getting PMID for DOI {doi}: {e}") doi_pmid_mapping[doi] = None except ValueError as e: warnings.warn( f"Value error while processing response for DOI {doi}: {e}" ) doi_pmid_mapping[doi] = None return doi_pmid_mapping def pmid_to_pmc(self, pmids): """Convert PMID(s) to PMC ID(s) Parameters ---------- pmids: list or str PMID(s) Returns ------- pmid_pmc_mapping: dict Mapping of PMID to PMC ID """ if isinstance(pmids, str): pmids = [pmids] pmid_pmc_mapping = {} for pmid in pmids: try: summary_url = self.base_url["esummary"] summary_params = { "db": "pubmed", "id": pmid, "retmode": "json", } response = requests.get(summary_url, params=summary_params, timeout=60) response.raise_for_status() result = response.json() # Extract PMC ID from articleids if str(pmid) in result.get("result", {}): article = result["result"][str(pmid)] articleids = article.get("articleids", []) for aid in articleids: if aid.get("idtype") == "pmc": pmc_id = aid.get("value") pmid_pmc_mapping[pmid] = pmc_id break time.sleep(self.sleep_time) except Exception as e: warnings.warn(f"Failed to get PMC ID for PMID {pmid}: {e}") pmid_pmc_mapping[pmid] = None return pmid_pmc_mapping def fetch_pmc_fulltext(self, pmc_id): """Fetch full text from PMC article Parameters ---------- pmc_id: str PMC ID (can be with or without 'PMC' prefix) Returns ------- fulltext: str Full text of the article, or None if unavailable """ # Ensure PMC ID has the PMC prefix if not pmc_id.startswith("PMC"): pmc_id = f"PMC{pmc_id}" try: fetch_url = self.base_url["efetch"] fetch_params = {"db": "pmc", "id": pmc_id, "retmode": "xml"} response = requests.get(fetch_url, params=fetch_params, timeout=60) response.raise_for_status() time.sleep(self.sleep_time) return response.text except Exception as e: warnings.warn(f"Failed to fetch full text for {pmc_id}: {e}") return None def extract_identifiers_from_text(self, text): """Extract GSE, PRJNA, SRP, and other identifiers from text Parameters ---------- text: str Text to search for identifiers Returns ------- identifiers: dict Dictionary with lists of found identifiers by type """ if not text: return { "gse": [], "prjna": [], "srp": [], "srr": [], "srx": [], "srs": [], } # Define patterns for different identifier types patterns = { "gse": r"GSE\d+", "prjna": r"PRJNA\d+", "srp": r"SRP\d+", "srr": r"SRR\d+", "srx": r"SRX\d+", "srs": r"SRS\d+", } identifiers = {} for id_type, pattern in patterns.items(): matches = re.findall(pattern, text, re.IGNORECASE) # Convert to uppercase and remove duplicates identifiers[id_type] = sorted(list(set([m.upper() for m in matches]))) return identifiers def pmc_to_identifiers(self, pmc_ids, convert_missing=True): """Extract database identifiers from PMC articles Parameters ---------- pmc_ids: list or str PMC ID(s) (can be with or without 'PMC' prefix) convert_missing: bool If True, automatically convert GSE↔SRP when one is found but not the other Default: True Returns ------- results_df: pandas.DataFrame DataFrame with PMC IDs and extracted identifiers """ if isinstance(pmc_ids, str): pmc_ids = [pmc_ids] results = [] for pmc_id in pmc_ids: # Fetch full text fulltext = self.fetch_pmc_fulltext(pmc_id) if fulltext: # Extract identifiers identifiers = self.extract_identifiers_from_text(fulltext) if convert_missing: # If we found GSE IDs but no SRP IDs, convert GSE to SRP if identifiers["gse"] and not identifiers["srp"]: try: for gse_id in identifiers["gse"]: gse_srp_df = self.gse_to_srp(gse_id) if ( not gse_srp_df.empty and "study_accession" in gse_srp_df.columns ): srp_values = ( gse_srp_df["study_accession"].dropna().tolist() ) identifiers["srp"].extend( [str(x) for x in srp_values if not pd.isna(x)] ) identifiers["srp"] = sorted(list(set(identifiers["srp"]))) time.sleep(self.sleep_time) except Exception: pass # If we found SRP IDs but no GSE IDs, convert SRP to GSE elif identifiers["srp"] and not identifiers["gse"]: try: for srp_id in identifiers["srp"]: srp_gse_df = self.srp_to_gse(srp_id) if ( not srp_gse_df.empty and "study_alias" in srp_gse_df.columns ): gse_values = ( srp_gse_df["study_alias"].dropna().tolist() ) identifiers["gse"].extend( [str(x) for x in gse_values if not pd.isna(x)] ) identifiers["gse"] = sorted( list(set(identifiers["gse"])) ) # Remove duplicates time.sleep(self.sleep_time) except Exception: pass # If conversion fails, just keep what we found # Extract PRJNA from SRP metadata if we have SRP IDs if identifiers["srp"] and not identifiers["prjna"]: try: for srp_id in identifiers["srp"]: srp_metadata = self.sra_metadata(srp_id) if srp_metadata is not None and not srp_metadata.empty: if "bioproject" in srp_metadata.columns: bioproject_values = ( srp_metadata["bioproject"] .dropna() .unique() .tolist() ) identifiers["prjna"].extend( [ str(x) for x in bioproject_values if not pd.isna(x) ] ) identifiers["prjna"] = sorted(list(set(identifiers["prjna"]))) time.sleep(self.sleep_time) except Exception: pass results.append( { "pmc_id": ( pmc_id if pmc_id.startswith("PMC") else f"PMC{pmc_id}" ), "gse_ids": ( ",".join(identifiers["gse"]) if identifiers["gse"] else pd.NA ), "prjna_ids": ( ",".join(identifiers["prjna"]) if identifiers["prjna"] else pd.NA ), "srp_ids": ( ",".join(identifiers["srp"]) if identifiers["srp"] else pd.NA ), "srr_ids": ( ",".join(identifiers["srr"]) if identifiers["srr"] else pd.NA ), "srx_ids": ( ",".join(identifiers["srx"]) if identifiers["srx"] else pd.NA ), "srs_ids": ( ",".join(identifiers["srs"]) if identifiers["srs"] else pd.NA ), } ) else: results.append( { "pmc_id": ( pmc_id if pmc_id.startswith("PMC") else f"PMC{pmc_id}" ), "gse_ids": pd.NA, "prjna_ids": pd.NA, "srp_ids": pd.NA, "srr_ids": pd.NA, "srx_ids": pd.NA, "srs_ids": pd.NA, } ) return pd.DataFrame(results) def pmid_to_identifiers(self, pmids): """Extract database identifiers from PubMed articles via PMC Parameters ---------- pmids: list or str PMID(s) Returns ------- results_df: pandas.DataFrame DataFrame with PMIDs, PMC IDs, and extracted identifiers """ if isinstance(pmids, str): pmids = [pmids] # First convert PMIDs to PMC IDs pmid_pmc_mapping = self.pmid_to_pmc(pmids) results = [] for pmid, pmc_id in pmid_pmc_mapping.items(): if pmc_id: # Get identifiers from PMC pmc_results = self.pmc_to_identifiers([pmc_id]) if not pmc_results.empty: result = pmc_results.iloc[0].to_dict() result["pmid"] = pmid # Reorder columns to have pmid first result = { "pmid": result["pmid"], "pmc_id": result["pmc_id"], "gse_ids": result["gse_ids"], "prjna_ids": result["prjna_ids"], "srp_ids": result["srp_ids"], "srr_ids": result["srr_ids"], "srx_ids": result["srx_ids"], "srs_ids": result["srs_ids"], } results.append(result) else: results.append( { "pmid": pmid, "pmc_id": pmc_id, "gse_ids": pd.NA, "prjna_ids": pd.NA, "srp_ids": pd.NA, "srr_ids": pd.NA, "srx_ids": pd.NA, "srs_ids": pd.NA, } ) else: # No PMC ID available results.append( { "pmid": pmid, "pmc_id": pd.NA, "gse_ids": pd.NA, "prjna_ids": pd.NA, "srp_ids": pd.NA, "srr_ids": pd.NA, "srx_ids": pd.NA, "srs_ids": pd.NA, } ) return pd.DataFrame(results) def pmid_to_gse(self, pmids): """Get GSE identifiers from PMID(s) Parameters ---------- pmids: list or str PMID(s) Returns ------- results_df: pandas.DataFrame DataFrame with PMIDs and GSE identifiers """ full_results = self.pmid_to_identifiers(pmids) return full_results[["pmid", "pmc_id", "gse_ids"]] def pmid_to_srp(self, pmids): """Get SRP identifiers from PMID(s) Parameters ---------- pmids: list or str PMID(s) Returns ------- results_df: pandas.DataFrame DataFrame with PMIDs and SRP identifiers """ full_results = self.pmid_to_identifiers(pmids) return full_results[["pmid", "pmc_id", "srp_ids"]] def doi_to_identifiers(self, dois): """Extract database identifiers from articles via DOI Parameters ---------- dois: list or str DOI(s) Returns ------- results_df: pandas.DataFrame DataFrame with DOIs, PMIDs, PMC IDs, and extracted identifiers """ if isinstance(dois, str): dois = [dois] doi_pmid_mapping = self.doi_to_pmid(dois) results = [] for doi, pmid in doi_pmid_mapping.items(): if pmid: pmid_results = self.pmid_to_identifiers([pmid]) if not pmid_results.empty: result = pmid_results.iloc[0].to_dict() result["doi"] = doi result = { "doi": result["doi"], "pmid": result["pmid"], "pmc_id": result["pmc_id"], "gse_ids": result["gse_ids"], "prjna_ids": result["prjna_ids"], "srp_ids": result["srp_ids"], "srr_ids": result["srr_ids"], "srx_ids": result["srx_ids"], "srs_ids": result["srs_ids"], } results.append(result) else: results.append( { "doi": doi, "pmid": pmid, "pmc_id": pd.NA, "gse_ids": pd.NA, "prjna_ids": pd.NA, "srp_ids": pd.NA, "srr_ids": pd.NA, "srx_ids": pd.NA, "srs_ids": pd.NA, } ) else: # No PMID available results.append( { "doi": doi, "pmid": pd.NA, "pmc_id": pd.NA, "gse_ids": pd.NA, "prjna_ids": pd.NA, "srp_ids": pd.NA, "srr_ids": pd.NA, "srx_ids": pd.NA, "srs_ids": pd.NA, } ) return pd.DataFrame(results) def doi_to_gse(self, dois): """Get GSE identifiers from DOI(s) Parameters ---------- dois: list or str DOI(s) Returns ------- results_df: pandas.DataFrame DataFrame with DOIs and GSE identifiers """ full_results = self.doi_to_identifiers(dois) return full_results[["doi", "pmid", "pmc_id", "gse_ids"]] def doi_to_srp(self, dois): """Get SRP identifiers from DOI(s) Parameters ---------- dois: list or str DOI(s) Returns ------- results_df: pandas.DataFrame DataFrame with DOIs and SRP identifiers """ full_results = self.doi_to_identifiers(dois) return full_results[["doi", "pmid", "pmc_id", "srp_ids"]] ================================================ FILE: pysradb/taxid2name.py ================================================ TAXID_TO_NAME = { 0: "not_available", 1: "root", 2: "Bacteria", 6: "Azorhizobium", 7: "Azorhizobium caulinodans", 9: "Buchnera aphidicola", 10: "Cellvibrio", 11: "Cellulomonas gilvus", 13: "Dictyoglomus", 14: "Dictyoglomus thermophilum", 16: "Methylophilus", 17: "Methylophilus methylotrophus", 18: "Pelobacter", 19: "Pelobacter carbinolicus", 20: "Phenylobacterium", 21: "Phenylobacterium immobile", 22: "Shewanella", 23: "Shewanella colwelliana", 24: "Shewanella putrefaciens", 25: "Shewanella hanedai", 27: "halophilic eubacterium NRCC 41227", 28: "halophilic eubacterium", 29: "Myxococcales", 31: "Myxococcaceae", 32: "Myxococcus", 33: "Myxococcus fulvus", 34: "Myxococcus xanthus", 35: "Myxococcus macrosporus", 38: "Archangium disciforme", 39: "Archangiaceae", 40: "Stigmatella", 41: "Stigmatella aurantiaca", 42: "Cystobacter", 43: "Cystobacter fuscus", 44: "Melittangium", 45: "Melittangium lichenicola", 47: "Archangium", 48: "Archangium gephyra", 49: "Polyangiaceae", 50: "Chondromyces", 51: "Chondromyces apiculatus", 52: "Chondromyces crocatus", 53: "Nannocystis", 54: "Nannocystis exedens", 55: "Polyangium", 56: "Sorangium cellulosum", 57: "Polyangium sp.", 59: "Vitreoscilla", 60: "Vitreoscilla sp.", 61: "Vitreoscilla stercoraria", 62: "Vitreoscilla beggiatoides", 63: "Vitreoscilla filiformis", 64: "Herpetosiphon", 65: "Herpetosiphon aurantiacus", 68: "Lysobacter", 69: "Lysobacter enzymogenes", 71: "Simonsiella", 72: "Simonsiella muelleri", 75: "Caulobacter", 78: "Caulobacter sp.", 81: "Hyphomicrobium", 82: "Hyphomicrobium sp.", 83: "Hyphomicrobium vulgare", 84: "Hyphomicrobium methylovorum", 85: "Hyphomonas", 86: "Hyphomonas jannaschiana", 87: "Hyphomonas sp.", 88: "Leptothrix", 89: "Leptothrix discophora", 93: "Stella", 94: "Stella humosa", 96: "Gallionella", 97: "Gallionella ferruginea", 99: "Ancylobacter", 100: "Ancylobacter aquaticus", 101: "Flectobacillus", 102: "Polaribacter glomeratus", 103: "Flectobacillus major", 104: "Cyclobacterium marinum", 105: "Runella", 106: "Runella slithyformis", 107: "Spirosoma", 108: "Spirosoma linguale", 109: "Blastobacter", 110: "Xanthobacter viscosus", 112: "Planctomycetales", 113: "Gemmata", 114: "Gemmata obscuriglobus", 117: "Pirellula sp.", 118: "Planctomyces", 119: "Rubinisphaera brasiliensis", 120: "Planctopirus limnophila", 122: "Gimesia maris", 123: "Pirellula", 124: "Blastopirellula marina", 125: "Pirellula staleyi", 126: "Planctomycetaceae", 127: "Isosphaera", 128: "Isosphaera pallida", 131: "Tuberoidobacter", 132: "Tuberoidobacter mutans", 133: "Methylocystis", 134: "Methylocystis parvus", 136: "Spirochaetales", 137: "Spirochaetaceae", 138: "Borrelia", 139: "Borreliella burgdorferi", 140: "Borrelia hermsii", 141: "Borrelia parkeri", 142: "Borrelia turicatae", 143: "Borrelia anserina", 144: "Borrelia coriaceae", 145: "Borrelia sp.", 146: "Spirochaeta", 147: "Spirochaeta aurantia", 148: "Sediminispirochaeta bajacaliforniensis", 149: "Spirochaeta halophila", 150: "Spirochaeta isovalerica", 151: "Oceanispirochaeta litoralis", 152: "Treponema stenostreptum", 154: "Spirochaeta thermophila", 156: "Treponema zuelzerae", 157: "Treponema", 158: "Treponema denticola", 159: "Brachyspira hyodysenteriae", 160: "Treponema pallidum", 161: "Treponema pallidum subsp. pallidum", 162: "Treponema phagedenis", 163: "Treponema bryantii", 164: "Treponema pectinovorum", 165: "Treponema saccharophilum", 166: "Treponema sp.", 167: "Treponema succinifaciens", 168: "Treponema pallidum subsp. pertenue", 170: "Leptospiraceae", 171: "Leptospira", 172: "Leptospira biflexa", 173: "Leptospira interrogans", 174: "Leptospira borgpetersenii", 176: "Leptospira interrogans serovar Hardjo", 178: "Leptospira sp.", 179: "Leptospirillum", 180: "Leptospirillum ferrooxidans", 181: "Leptospirillum sp.", 183: "Leptonema illini", 185: "wall-less spirochete", 187: "Aquaspirillum", 188: "Magnetospirillum magnetotacticum", 189: "Novispirillum itersonii", 190: "Aquaspirillum serpens", 191: "Azospirillum", 192: "Azospirillum brasilense", 193: "Azospirillum lipoferum", 194: "Campylobacter", 195: "Campylobacter coli", 196: "Campylobacter fetus", 197: "Campylobacter jejuni", 198: "Campylobacter hyointestinalis", 199: "Campylobacter concisus", 200: "Campylobacter curvus", 201: "Campylobacter lari", 202: "Campylobacter mucosalis", 203: "Campylobacter rectus", 204: "Campylobacter showae", 205: "Campylobacter sp.", 206: "Campylobacter sputorum", 207: "Campylobacter jejuni-like bacterium", 209: "Helicobacter", 210: "Helicobacter pylori", 211: "Helicobacter sp. CLO-3", 212: "Helicobacter acinonychis", 213: "Helicobacter cinaedi", 214: "Helicobacter felis", 215: "Helicobacter fennelliae", 216: "Helicobacter muridarum", 217: "Helicobacter mustelae", 218: "Helicobacter sp.", 222: "Achromobacter", 223: "Achromobacter cycloclastes", 224: "Achromobacter lyticus", 226: "Alteromonas", 227: "Pseudoalteromonas carrageenovora", 228: "Pseudoalteromonas haloplanktis", 232: "Alteromonas sp.", 234: "Brucella", 235: "Brucella abortus", 236: "Brucella ovis", 237: "Flavobacterium", 238: "Elizabethkingia meningoseptica", 239: "Flavobacterium sp.", 240: "Flavobacterium sp. 141-8", 241: "Flavobacterium sp. SC12154", 242: "Flavobacterium sp. U-188", 244: "Planomicrobium okeanokoites", 245: "Flavobacterium aquatile", 246: "Chryseobacterium balustinum", 247: "Empedobacter brevis", 249: "Terrimonas ferruginea", 250: "Chryseobacterium gleum", 251: "Psychroflexus gondwanensis", 252: "Halomonas halmophila", 253: "Chryseobacterium indologenes", 254: "Chryseobacterium indoltheticum", 255: "[Flavobacterium] lutescens", 256: "Myroides odoratus", 258: "Sphingobacterium spiritivorum", 259: "Sphingobacterium thalpophilum", 261: "Flavobacterium sp. K172", 262: "Francisella", 263: "Francisella tularensis", 264: "Francisella tularensis subsp. novicida", 265: "Paracoccus", 266: "Paracoccus denitrificans", 267: "Paracoccus sp.", 270: "Thermus", 271: "Thermus aquaticus", 272: "Thermus caldophilus", 274: "Thermus thermophilus", 275: "Thermus sp.", 276: "Thermus filiformis", 277: "Meiothermus ruber", 279: "Xanthobacter", 280: "Xanthobacter autotrophicus", 281: "Xanthobacter flavus", 283: "Comamonas", 285: "Comamonas testosteroni", 286: "Pseudomonas", 287: "Pseudomonas aeruginosa", 288: "Pseudoalteromonas atlantica", 290: "Pseudomonas carboxydohydrogena", 292: "Burkholderia cepacia", 293: "Brevundimonas diminuta", 294: "Pseudomonas fluorescens", 296: "Pseudomonas fragi", 297: "Hydrogenophilus thermoluteolus", 298: "Pseudomonas marginalis", 300: "Pseudomonas mendocina", 301: "Pseudomonas oleovorans", 303: "Pseudomonas putida", 304: "Pelomonas saccharophila", 305: "Ralstonia solanacearum", 306: "Pseudomonas sp.", 307: "Pseudomonas sp. KKS102", 308: "Pseudomonas sp. PG2982", 309: "Pseudomonas sp. SE83", 311: "Pseudomonas sp. KWI-56", 312: "Pseudomonas sp. RS-16", 313: "Pseudomonas sp. ATCC29598", 314: "Pseudomonas sp. NK87", 315: "Pseudomonas sp. ATCC19151", 316: "Pseudomonas stutzeri", 317: "Pseudomonas syringae", 318: "Pseudomonas savastanoi pv. glycinea", 319: "Pseudomonas savastanoi pv. phaseolicola", 321: "Pseudomonas syringae pv. syringae", 322: "Pseudomonas amygdali pv. tabaci", 323: "Pseudomonas syringae pv. tomato", 329: "Ralstonia pickettii", 333: "Pseudomonas chlororaphis subsp. chlororaphis", 335: "Pseudomonas fluorescens bv. C", 337: "Burkholderia glumae", 338: "Xanthomonas", 339: "Xanthomonas campestris", 340: "Xanthomonas campestris pv. campestris", 343: "Xanthomonas translucens", 346: "Xanthomonas citri", 347: "Xanthomonas oryzae", 349: "Zoogloea", 350: "Zoogloea ramigera", 351: "Azotobacter group", 352: "Azotobacter", 353: "Azotobacter chroococcum", 354: "Azotobacter vinelandii", 355: "Azotobacter chroococcum (strain mcd 1)", 356: "Rhizobiales", 357: "Agrobacterium", 358: "Agrobacterium tumefaciens", 359: "Agrobacterium rhizogenes", 361: "Agrobacterium sp.", 370: "Agrobacterium tumefaciens (strain apple 185)", 371: "Agrobacterium tumefaciens (strain B2A)", 372: "Agrobacterium tumefaciens (strain II CHRYS)", 373: "Agrobacterium vitis", 374: "Bradyrhizobium", 375: "Bradyrhizobium japonicum", 376: "Bradyrhizobium sp.", 377: "Bradyrhizobium sp. ANU 289", 378: "Bradyrhizobium sp. RP501", 379: "Rhizobium", 380: "Sinorhizobium fredii", 381: "Mesorhizobium loti", 382: "Sinorhizobium meliloti", 384: "Rhizobium leguminosarum", 385: "Rhizobium leguminosarum bv. phaseoli", 386: "Rhizobium leguminosarum bv. trifolii", 387: "Rhizobium leguminosarum bv. viciae", 391: "Rhizobium sp.", 393: "Rhizobium sp. MPIK3030", 394: "Sinorhizobium fredii NGR234", 396: "Rhizobium phaseoli", 398: "Rhizobium tropici", 399: "Neorhizobium galegae", 400: "Rhizobium sp. IRc78", 403: "Methylococcaceae", 404: "Methylobacillus", 405: "Methylobacillus flagellatus", 406: "Methylobacillus glycogenes", 407: "Methylobacterium", 408: "Methylorubrum extorquens", 409: "Methylobacterium sp.", 410: "Methylobacterium organophilum", 411: "Methylobacterium specialis", 413: "Methylococcus", 414: "Methylococcus capsulatus", 415: "Methylobacter luteus", 416: "Methylomonas", 417: "Methylomonas clara", 418: "Methylomonas sp.", 421: "Methylomonas methanica", 423: "Methylomonas methylovora", 424: "Methylomonas rubra", 425: "Methylosinus", 426: "Methylosinus trichosporium", 427: "Methylosinus sp.", 428: "Methylosinus sporium", 429: "Methylobacter", 430: "Methylobacter capsulatus", 433: "Acetobacteraceae", 434: "Acetobacter", 435: "Acetobacter aceti", 436: "Komagataeibacter hansenii", 437: "Acidomonas methanolica", 438: "Acetobacter pasteurianus", 439: "Gluconacetobacter polyoxogenes", 440: "Acetobacter sp.", 441: "Gluconobacter", 442: "Gluconobacter oxydans", 444: "Legionellaceae", 445: "Legionella", 446: "Legionella pneumophila", 447: "Fluoribacter bozemanae", 448: "Legionella erythra", 449: "Legionella hackeliae", 450: "Legionella longbeachae", 451: "Tatlockia micdadei", 452: "Legionella spiritensis", 453: "Legionella feeleii", 454: "Legionella israelensis", 455: "Legionella jamestowniensis", 456: "Legionella jordanis", 458: "Legionella rubrilucens", 459: "Legionella sp.", 460: "Legionella steigerwaltii", 461: "Fluoribacter", 463: "Fluoribacter dumoffii", 464: "Fluoribacter gormanii", 465: "Tatlockia", 466: "Legionella maceachernii", 468: "Moraxellaceae", 469: "Acinetobacter", 470: "Acinetobacter baumannii", 471: "Acinetobacter calcoaceticus", 472: "Acinetobacter sp.", 474: "Acinetobacter glutaminasificans", 475: "Moraxella", 476: "Moraxella bovis", 477: "Moraxella lacunata", 478: "Moraxella nonliquefaciens", 479: "Moraxella sp.", 480: "Moraxella catarrhalis", 481: "Neisseriaceae", 482: "Neisseria", 483: "Neisseria cinerea", 484: "Neisseria flavescens", 485: "Neisseria gonorrhoeae", 486: "Neisseria lactamica", 487: "Neisseria meningitidis", 488: "Neisseria mucosa", 489: "Neisseria polysaccharea", 490: "Neisseria sicca", 491: "Neisseria meningitidis serogroup B", 492: "Neisseria animalis", 493: "Neisseria canis", 494: "Bergeriella denitrificans", 495: "Neisseria elongata", 496: "Neisseria macacae", 497: "Psychrobacter", 498: "Psychrobacter immobilis", 499: "Thermomicrobium", 500: "Thermomicrobium roseum", 502: "Kingella denitrificans", 504: "Kingella kingae", 505: "Kingella oralis", 506: "Alcaligenaceae", 507: "Alcaligenes", 511: "Alcaligenes faecalis", 512: "Alcaligenes sp.", 516: "Alcaligenes hydrogenophilus", 517: "Bordetella", 518: "Bordetella bronchiseptica", 519: "Bordetella parapertussis", 520: "Bordetella pertussis", 521: "Bordetella avium", 522: "Acidiphilium", 523: "Acidiphilium angustum", 524: "Acidiphilium cryptum", 525: "Acidocella facilis", 526: "Acidiphilium rubrum", 527: "Acidiphilium sp.", 528: "Ochrobactrum", 529: "Ochrobactrum anthropi", 531: "Polaribacter irgensii", 532: "Beijerinckia", 533: "Beijerinckia indica", 535: "Chromobacterium", 536: "Chromobacterium violaceum", 537: "Iodobacter fluviatilis", 538: "Eikenella", 539: "Eikenella corrodens", 540: "Eikenella sp.", 541: "Zymomonas", 542: "Zymomonas mobilis", 543: "Enterobacteriaceae", 544: "Citrobacter", 545: "Citrobacter koseri", 546: "Citrobacter freundii", 547: "Enterobacter", 548: "Klebsiella aerogenes", 549: "Pantoea agglomerans", 550: "Enterobacter cloacae", 551: "Erwinia", 552: "Erwinia amylovora", 553: "Pantoea ananatis", 554: "Pectobacterium carotovorum", 555: "Pectobacterium carotovorum subsp. carotovorum", 556: "Dickeya chrysanthemi", 558: "Erwinia sp.", 561: "Escherichia", 562: "Escherichia coli", 563: "Shimwellia blattae", 564: "Escherichia fergusonii", 565: "Atlantibacter hermannii", 566: "Pseudescherichia vulneris", 568: "Hafnia", 569: "Hafnia alvei", 570: "Klebsiella", 571: "Klebsiella oxytoca", 573: "Klebsiella pneumoniae", 574: "Klebsiella pneumoniae subsp. ozaenae", 575: "Raoultella planticola", 576: "Klebsiella sp.", 577: "Raoultella terrigena", 579: "Kluyvera", 580: "Kluyvera cryocrescens", 581: "Morganella", 582: "Morganella morganii", 583: "Proteus", 584: "Proteus mirabilis", 585: "Proteus vulgaris", 586: "Providencia", 587: "Providencia rettgeri", 588: "Providencia stuartii", 589: "Providencia sp.", 590: "Salmonella", 594: "Salmonella enterica subsp. enterica serovar Gallinarum", 595: "Salmonella enterica subsp. enterica serovar Infantis", 596: "Salmonella enterica subsp. enterica serovar Muenchen", 597: "Salmonella enterica subsp. enterica serovar Potsdam", 598: "Salmonella enterica subsp. enterica serovar Rubislaw", 599: "Salmonella sp.", 600: "Salmonella enterica subsp. enterica serovar Thompson", 604: "Salmonella enterica subsp. enterica serovar Gallinarum/pullorum", 605: "Salmonella enterica subsp. enterica serovar Pullorum", 607: "Salmonella enterica subsp. enterica serovar Abortusequi", 610: "Salmonella enterica subsp. enterica serovar Abortus", 611: "Salmonella enterica subsp. enterica serovar Heidelberg", 612: "Salmonella enterica subsp. enterica serovar Ordonez", 613: "Serratia", 614: "Serratia liquefaciens", 615: "Serratia marcescens", 616: "Serratia sp.", 617: "Serratia sp. E-15", 618: "Serratia odorifera", 620: "Shigella", 621: "Shigella boydii", 622: "Shigella dysenteriae", 623: "Shigella flexneri", 624: "Shigella sonnei", 625: "Shigella sp.", 626: "Xenorhabdus", 628: "Xenorhabdus nematophila", 629: "Yersinia", 630: "Yersinia enterocolitica", 631: "Yersinia intermedia", 632: "Yersinia pestis", 633: "Yersinia pseudotuberculosis", 634: "Yersinia bercovieri", 635: "Edwardsiella", 636: "Edwardsiella tarda", 637: "Arsenophonus", 638: "Arsenophonus nasoniae", 641: "Vibrionaceae", 642: "Aeromonas", 644: "Aeromonas hydrophila", 645: "Aeromonas salmonicida", 646: "Aeromonas sobria", 647: "Aeromonas sp.", 648: "Aeromonas caviae", 649: "Aeromonas eucrenophila", 650: "Aeromonas jandaei", 651: "Aeromonas media", 652: "Aeromonas schubertii", 654: "Aeromonas veronii", 656: "Aeromonas allosaccharophila", 657: "Photobacterium", 658: "Photobacterium leiognathi subsp. leiognathi", 659: "Photobacterium phosphoreum", 660: "Photobacterium sp.", 661: "Photobacterium angustum", 662: "Vibrio", 663: "Vibrio alginolyticus", 664: "Vibrio alginolyticus chemovar iophagus", 666: "Vibrio cholerae", 668: "Aliivibrio fischeri", 669: "Vibrio harveyi", 670: "Vibrio parahaemolyticus", 671: "Vibrio proteolyticus", 672: "Vibrio vulnificus", 673: "Grimontia hollisae", 674: "Vibrio mimicus", 675: "Vibrio cincinnatiensis", 676: "Vibrio fluvialis", 678: "Vibrio sp.", 679: "Vibrio adaptatus", 680: "Vibrio campbellii", 683: "Vibrio cyclosites", 685: "Vibrio diazotrophicus", 686: "Vibrio cholerae O1 biovar El Tor", 687: "Vibrio gazogenes", 688: "Aliivibrio logei", 689: "Vibrio mediterranei", 691: "Vibrio natriegens", 693: "Vibrio nereis", 701: "magnetite-containing magnetic coccus", 702: "Plesiomonas", 703: "Plesiomonas shigelloides", 704: "Cryptosaras couesi symbiont", 709: "Melanocetus johnsoni symbiont", 712: "Pasteurellaceae", 713: "Actinobacillus", 714: "Aggregatibacter actinomycetemcomitans", 715: "Actinobacillus pleuropneumoniae", 716: "Actinobacillus suis", 717: "Actinobacillus capsulatus", 718: "Actinobacillus equuli", 719: "Actinobacillus hominis", 720: "Actinobacillus lignieresii", 721: "Actinobacillus salpingitidis", 722: "Actinobacillus seminis", 723: "Actinobacillus ureae", 724: "Haemophilus", 725: "Haemophilus influenzae biotype aegyptius", 726: "Haemophilus haemolyticus", 727: "Haemophilus influenzae", 728: "Avibacterium paragallinarum", 729: "Haemophilus parainfluenzae", 730: "[Haemophilus] ducreyi", 731: "Histophilus somni", 732: "Aggregatibacter aphrophilus", 733: "Haemophilus haemoglobinophilus", 734: "Haemophilus paracuniculus", 735: "Haemophilus parahaemolyticus", 736: "Haemophilus paraphrohaemolyticus", 738: "Glaesserella parasuis", 739: "Aggregatibacter segnis", 740: "Haemophilus sp.", 741: "Haemophilus taxon C", 745: "Pasteurella", 747: "Pasteurella multocida", 749: "[Pasteurella] aerogenes", 750: "Gallibacterium anatis", 751: "Avibacterium avium", 752: "Pasteurella bettyae", 753: "Pasteurella canis", 754: "Pasteurella dagmatis", 755: "Avibacterium gallinarum", 756: "Pasteurella langaaensis", 757: "[Pasteurella] mairii", 758: "Rodentibacter pneumotropicus", 759: "Pasteurella sp.", 760: "Pasteurella stomatis", 761: "Pasteurella testudinis", 762: "Avibacterium volantium", 766: "Rickettsiales", 768: "Anaplasma", 769: "Anaplasma centrale", 770: "Anaplasma marginale", 772: "Bartonellaceae", 773: "Bartonella", 774: "Bartonella bacilliformis", 775: "Rickettsiaceae", 776: "Coxiella", 777: "Coxiella burnetii", 779: "Ehrlichia ruminantium", 780: "Rickettsia", 781: "Rickettsia conorii", 782: "Rickettsia prowazekii", 783: "Rickettsia rickettsii", 784: "Orientia tsutsugamushi", 785: "Rickettsia typhi", 786: "Rickettsia akari", 787: "Rickettsia australis", 788: "Rickettsia canadensis", 789: "Rickettsia sp.", 801: "BEV proteobacterium", 803: "Bartonella quintana", 807: "Bartonella elizabethae", 809: "Chlamydiaceae", 810: "Chlamydia", 813: "Chlamydia trachomatis", 815: "Bacteroidaceae", 816: "Bacteroides", 817: "Bacteroides fragilis", 818: "Bacteroides thetaiotaomicron", 820: "Bacteroides uniformis", 821: "Bacteroides vulgatus", 823: "Parabacteroides distasonis", 824: "Campylobacter gracilis", 826: "Sebaldella termitidis", 827: "Campylobacter ureolyticus", 830: "Butyrivibrio", 831: "Butyrivibrio fibrisolvens", 832: "Fibrobacter", 833: "Fibrobacter succinogenes", 834: "Fibrobacter succinogenes subsp. succinogenes", 836: "Porphyromonas", 837: "Porphyromonas gingivalis", 838: "Prevotella", 839: "Prevotella ruminicola", 840: "Prevotella loescheii", 841: "Roseburia", 842: "Roseburia cecicola", 843: "Wolinella", 844: "Wolinella succinogenes", 846: "Oxalobacter", 847: "Oxalobacter formigenes", 848: "Fusobacterium", 849: "Fusobacterium gonidiaformans", 850: "Fusobacterium mortiferum", 851: "Fusobacterium nucleatum", 852: "Fusobacterium perfoetens", 853: "Faecalibacterium prausnitzii", 854: "Fusobacterium russii", 855: "Fusobacterium simiae", 856: "Fusobacterium varium", 858: "Fusobacterium necrogenes", 859: "Fusobacterium necrophorum", 860: "Fusobacterium periodonticum", 861: "Fusobacterium ulcerans", 862: "Syntrophomonas", 863: "Syntrophomonas wolfei", 864: "Pectinatus", 865: "Pectinatus frisingensis", 866: "Ruminobacter", 867: "Ruminobacter amylophilus", 868: "Cardiobacteriaceae", 869: "Dichelobacter", 870: "Dichelobacter nodosus", 872: "Desulfovibrio", 873: "Desulfocurvibacter africanus", 876: "Desulfovibrio desulfuricans", 878: "Desulfovibrio fructosivorans", 879: "Desulfovibrio gigas", 880: "Desulfovibrio salexigens", 881: "Desulfovibrio vulgaris", 882: "Desulfovibrio vulgaris str. Hildenborough", 883: "Desulfovibrio vulgaris str. 'Miyazaki F'", 884: "Desulfovibrio oxamicus (strain Monticello)", 885: "Desulfovibrio sp.", 886: "Thermodesulfobacterium thermophilum", 888: "Desulfobotulus sapovorans", 889: "Desulfovibrio longus", 890: "Desulfuromonas", 891: "Desulfuromonas acetoxidans", 892: "Desulfuromonas sp.", 893: "Desulfobulbus", 894: "Desulfobulbus propionicus", 895: "Desulfobulbus sp.", 896: "Desulfococcus", 897: "Desulfococcus multivorans", 898: "Desulfomicrobium", 899: "Desulfomicrobium baculatum", 901: "Desulfovibrio piger", 904: "Acidaminococcus", 905: "Acidaminococcus fermentans", 906: "Megasphaera", 907: "Megasphaera elsdenii", 911: "Nitrobacter", 912: "Nitrobacter hamburgensis", 913: "Nitrobacter winogradskyi", 914: "Nitrosomonas", 915: "Nitrosomonas europaea", 916: "Nitrosomonas eutropha", 917: "Nitrosomonas marina", 919: "Thiobacillus", 920: "Acidithiobacillus ferrooxidans", 921: "Starkeya novella", 923: "Guyparkeria hydrothermalis", 924: "Thiobacillus sp.", 926: "Thiomonas intermedia", 927: "Halothiobacillus neapolitanus", 928: "Thiomonas perometabolis", 929: "Thermithiobacillus tepidarius", 930: "Acidithiobacillus thiooxidans", 931: "Thiobacillus thioparus", 932: "Thiomicrospira thyasirae", 933: "Thiomicrospira", 934: "Thiomicrospira pelophila", 935: "Thiomicrospira sp.", 936: "Thiovulum", 937: "Thiovulum sp.", 939: "Hydrogenobacter", 940: "Hydrogenobacter thermophilus", 942: "Anaplasmataceae", 943: "Ehrlichia", 944: "Ehrlichia canis", 945: "Ehrlichia chaffeensis", 947: "Ehrlichia ewingii", 948: "Anaplasma phagocytophilum", 949: "Anaplasma platys", 950: "Neorickettsia risticii", 951: "Neorickettsia sennetsu", 952: "Wolbachieae", 953: "Wolbachia", 954: "Francisella persica", 955: "Wolbachia pipientis", 956: "Wolbachia sp.", 958: "Bdellovibrio", 959: "Bdellovibrio bacteriovorus", 960: "Bacteriovorax stolpii", 962: "Campylobacter-like bacterium", 963: "Herbaspirillum", 964: "Herbaspirillum seropedicae", 965: "Oceanospirillum", 966: "Oceanospirillum linum", 967: "Spirillum", 968: "Spirillum volutans", 970: "Selenomonas", 971: "Selenomonas ruminantium", 972: "Halanaerobiaceae", 973: "Sporohalobacter", 974: "Sporohalobacter lortetii", 976: "Bacteroidetes", 978: "Cytophaga", 979: "Cellulophaga lytica", 981: "Persicobacter diffluens", 982: "Saccharicrinis fermentans", 983: "Flavobacterium flevense", 984: "Pedobacter heparinus", 985: "Cytophaga hutchinsonii", 986: "Flavobacterium johnsoniae", 987: "Aquimarina latercula", 988: "Leeuwenhoekiella marinoflava", 989: "Marinilabilia salmonicolor", 990: "Cytophaga xylanolytica", 991: "Flavobacterium hydatis", 992: "Flexibacter", 995: "Solitalea canadensis", 996: "Flavobacterium columnare", 997: "Eisenibacter elegans", 998: "Flexibacter flexilis", 999: "Bernardetia litoralis", 1001: "Garritya polymorpha", 1002: "Hugenholtzia roseola", 1003: "Thermoflexibacter ruber", 1004: "Chitinophaga sancti", 1005: "Flexibacter sp.", 1006: "Marivirga tractuosa", 1007: "Saprospira", 1008: "Saprospira grandis", 1010: "Sphingobacterium mizutaii", 1011: "Sporocytophaga", 1012: "Sporocytophaga cauliformis", 1013: "Weeksella", 1014: "Weeksella virosa", 1015: "Bergeyella zoohelcum", 1016: "Capnocytophaga", 1017: "Capnocytophaga gingivalis", 1018: "Capnocytophaga ochracea", 1019: "Capnocytophaga sputigena", 1021: "Beggiatoa", 1022: "Beggiatoa alba", 1023: "Microscilla", 1025: "Flammeovirga arenaria", 1026: "Marinoscillum furvescens", 1027: "Microscilla marina", 1028: "Marivirga sericea", 1030: "Thiothrix", 1031: "Thiothrix nivea", 1032: "Thiothrix sp.", 1033: "Afipia", 1034: "Afipia clevelandensis", 1035: "Afipia felis", 1037: "Barophile WHB 46", 1041: "Erythrobacter", 1042: "Erythrobacter sp.", 1044: "Erythrobacter longus", 1046: "Chromatiaceae", 1047: "Chromatium", 1048: "Marichromatium gracile", 1049: "Allochromatium vinosum", 1050: "Thermochromatium tepidum", 1051: "Ectothiorhodospira", 1052: "Halorhodospira halochloris", 1053: "Halorhodospira halophila", 1054: "Ectothiorhodospira shaposhnikovii", 1056: "Thiocapsa", 1057: "Thiococcus pfennigii", 1058: "Thiocapsa roseopersicina", 1060: "Rhodobacter", 1061: "Rhodobacter capsulatus", 1062: "Rhodobacter sp.", 1063: "Rhodobacter sphaeroides", 1064: "Rhodocyclus", 1066: "Rhodocyclus tenuis", 1067: "Rhodocyclus purpureus", 1068: "Rhodomicrobium", 1069: "Rhodomicrobium vannielii", 1070: "Rhodopila", 1071: "Rhodopila globiformis", 1073: "Rhodopseudomonas", 1074: "Rhodoblastus acidophilus", 1075: "Rhodobacter blasticus", 1076: "Rhodopseudomonas palustris", 1078: "Rhodopseudomonas sp.", 1079: "Blastochloris viridis", 1080: "Afifella marina", 1081: "Rhodospirillum", 1082: "Phaeospirillum fulvum", 1083: "Phaeospirillum molischianum", 1084: "Pararhodospirillum photometricum", 1085: "Rhodospirillum rubrum", 1086: "Rhodothalassium salexigens", 1087: "Rhodovibrio salinarum", 1088: "Rhodovibrio sodomensis", 1090: "Chlorobi", 1091: "Chlorobium", 1092: "Chlorobium limicola", 1094: "Chlorobium phaeovibrioides", 1095: "Chlorobium sp.", 1096: "Chlorobium phaeobacteroides", 1097: "Chlorobaculum tepidum", 1098: "Prosthecochloris vibrioformis", 1099: "Pelodictyon", 1100: "Pelodictyon luteolum", 1101: "Prosthecochloris", 1102: "Prosthecochloris aestuarii", 1103: "Clathrochloris", 1104: "Clathrochloris sulfurica", 1106: "Chloroflexaceae", 1107: "Chloroflexus", 1108: "Chloroflexus aurantiacus", 1109: "Heliothrix", 1110: "Heliothrix oregonensis", 1111: "Porphyrobacter", 1112: "Porphyrobacter neustonensis", 1113: "Porphyrobacter sp.", 1117: "Cyanobacteria", 1118: "Chroococcales", 1119: "Aphanocapsa", 1121: "Aphanothece", 1122: "Aphanothece sacrum", 1123: "Chlorogloeopsis", 1124: "Chlorogloeopsis fritschii", 1125: "Microcystis", 1126: "Microcystis aeruginosa", 1127: "Microcystis sp.", 1128: "Microcystis sp. 'BC 84/1'", 1129: "Synechococcus", 1131: "Synechococcus sp.", 1140: "Synechococcus elongatus PCC 7942", 1142: "Synechocystis", 1143: "Synechocystis sp.", 1144: "Synechocystis sp. PCC 6701", 1147: "Synechocystis sp. PCC 6714", 1148: "Synechocystis sp. PCC 6803", 1150: "Oscillatoriales", 1151: "Oscillatoriales cyanobacterium", 1152: "Pseudanabaena", 1153: "Pseudanabaena sp.", 1154: "Spirulina", 1157: "Spirulina sp.", 1158: "Oscillatoria", 1159: "Oscillatoria sp.", 1160: "Planktothrix agardhii", 1161: "Nostocales", 1162: "Nostocaceae", 1163: "Anabaena", 1164: "Trichormus azollae", 1165: "Anabaena cylindrica", 1166: "Dolichospermum flos-aquae", 1167: "Anabaena sp.", 1168: "Nostoc sp. PCC 7119", 1173: "Anabaena oscillarioides", 1175: "Aphanizomenon", 1176: "Aphanizomenon flos-aquae", 1177: "Nostoc", 1178: "Nostoc commune", 1179: "Desmonostoc muscorum", 1180: "Nostoc sp.", 1181: "Desmonostoc sp. PCC 7906", 1182: "Scytonemataceae", 1183: "Plectonema", 1184: "Leptolyngbya boryana", 1185: "Rivulariaceae", 1186: "Calothrix", 1187: "Calothrix sp.", 1188: "Tolypothrix sp. PCC 7601", 1189: "Stigonemataceae", 1190: "Fischerella", 1191: "Fischerella sp.", 1197: "Microchaete diplosiphon", 1198: "Phormidium", 1199: "Phormidium sp.", 1200: "Phormidium minutum", 1202: "Leptolyngbya ectocarpi", 1203: "Scytonema", 1204: "Scytonema sp.", 1205: "Trichodesmium", 1206: "Trichodesmium erythraeum", 1207: "Trichodesmium sp.", 1208: "Trichodesmium thiebautii", 1211: "uncultured cyanobacterium", 1213: "Prochloraceae", 1214: "Prochloron", 1215: "Prochloron sp.", 1216: "Prochloron didemni", 1218: "Prochlorococcus", 1219: "Prochlorococcus marinus", 1220: "Prochlorococcus sp.", 1222: "Prochlorothrix", 1223: "Prochlorothrix hollandica", 1224: "Proteobacteria", 1227: "Nitrosococcus", 1229: "Nitrosococcus oceani", 1231: "Nitrosospira multiformis", 1232: "Nitrosovibrio", 1233: "Nitrosovibrio tenuis", 1234: "Nitrospira", 1236: "Gammaproteobacteria", 1237: "Piscirickettsia", 1238: "Piscirickettsia salmonis", 1239: "Firmicutes", 1243: "Leuconostoc", 1244: "Leuconostoc gelidum", 1245: "Leuconostoc mesenteroides", 1246: "Leuconostoc lactis", 1247: "Oenococcus oeni", 1249: "Weissella paramesenteroides", 1251: "Leuconostoc fallax", 1252: "Leuconostoc carnosum", 1253: "Pediococcus", 1254: "Pediococcus acidilactici", 1255: "Pediococcus pentosaceus", 1257: "Peptostreptococcus", 1258: "Peptoniphilus asaccharolyticus", 1259: "Peptostreptococcus glycinophilus", 1260: "Finegoldia magna", 1261: "Peptostreptococcus anaerobius", 1262: "Peptostreptococcus sp.", 1263: "Ruminococcus", 1264: "Ruminococcus albus", 1265: "Ruminococcus flavefaciens", 1266: "Sarcina", 1267: "Clostridium ventriculi", 1268: "Micrococcaceae", 1269: "Micrococcus", 1270: "Micrococcus luteus", 1271: "Micrococcus sp.", 1272: "Kocuria varians", 1273: "Micrococcus lylae", 1274: "Dermacoccus nishinomiyaensis", 1275: "Kocuria rosea", 1276: "Kytococcus sedentarius", 1279: "Staphylococcus", 1280: "Staphylococcus aureus", 1281: "Staphylococcus carnosus", 1282: "Staphylococcus epidermidis", 1283: "Staphylococcus haemolyticus", 1284: "Staphylococcus hyicus", 1285: "Staphylococcus intermedius", 1286: "Staphylococcus simulans", 1287: "Staphylococcus simulans bv. staphylolyticus", 1288: "Staphylococcus xylosus", 1290: "Staphylococcus hominis", 1292: "Staphylococcus warneri", 1293: "Staphylococcus gallinarum", 1294: "Staphylococcus muscae", 1295: "Staphylococcus schleiferi", 1296: "Staphylococcus sciuri", 1297: "Deinococcus-Thermus", 1298: "Deinococcus", 1299: "Deinococcus radiodurans", 1300: "Streptococcaceae", 1301: "Streptococcus", 1302: "Streptococcus gordonii", 1303: "Streptococcus oralis", 1304: "Streptococcus salivarius", 1305: "Streptococcus sanguinis", 1306: "Streptococcus sp.", 1307: "Streptococcus suis", 1308: "Streptococcus thermophilus", 1309: "Streptococcus mutans", 1310: "Streptococcus sobrinus", 1311: "Streptococcus agalactiae", 1313: "Streptococcus pneumoniae", 1314: "Streptococcus pyogenes", 1317: "Streptococcus downei", 1318: "Streptococcus parasanguinis", 1319: "Streptococcus sp. 'group B'", 1320: "Streptococcus sp. 'group G'", 1322: "Blautia hansenii", 1323: "Faecalicoccus pleomorphus", 1324: "Streptococcus sp. G148", 1325: "Streptococcus sp. GX7805", 1326: "Streptococcus acidominimus", 1327: "Streptococcus alactolytiens", 1328: "Streptococcus anginosus", 1329: "Streptococcus canis", 1332: "Streptococcus criae", 1333: "Streptococcus criceti", 1334: "Streptococcus dysgalactiae", 1335: "Streptococcus equinus", 1336: "Streptococcus equi", 1337: "Streptococcus hyointestinalis", 1338: "Streptococcus intermedius", 1339: "Streptococcus macacae", 1340: "Streptococcus porcinus", 1341: "Streptococcus ratti", 1343: "Streptococcus vestibularis", 1345: "Streptococcus ferus", 1346: "Streptococcus iniae", 1348: "Streptococcus parauberis", 1349: "Streptococcus uberis", 1350: "Enterococcus", 1351: "Enterococcus faecalis", 1352: "Enterococcus faecium", 1353: "Enterococcus gallinarum", 1354: "Enterococcus hirae", 1355: "Enterococcus columbae", 1356: "Enterococcus sulfureus", 1357: "Lactococcus", 1358: "Lactococcus lactis", 1359: "Lactococcus lactis subsp. cremoris", 1360: "Lactococcus lactis subsp. lactis", 1363: "Lactococcus garvieae", 1364: "Lactococcus piscium", 1365: "Lactococcus plantarum", 1366: "Lactococcus raffinolactis", 1370: "Marinococcus", 1371: "Marinococcus halophilus", 1372: "Planococcus", 1373: "Planococcus citreus", 1374: "Planococcus kocurii", 1375: "Aerococcus", 1376: "Aerococcus urinae", 1377: "Aerococcus viridans", 1378: "Gemella", 1379: "Gemella haemolysans", 1380: "Atopobium", 1381: "Atopobium minutum", 1382: "Atopobium parvulum", 1383: "Atopobium rimae", 1385: "Bacillales", 1386: "Bacillus", 1388: "Alicyclobacillus acidocaldarius subsp. acidocaldarius", 1390: "Bacillus amyloliquefaciens", 1391: "Aneurinibacillus aneurinilyticus", 1392: "Bacillus anthracis", 1393: "Brevibacillus brevis", 1394: "[Bacillus] caldolyticus", 1395: "[Bacillus] caldotenax", 1396: "Bacillus cereus", 1397: "Bacillus circulans", 1398: "Bacillus coagulans", 1399: "Bacillus firmus", 1400: "Bacillus intermedius", 1401: "Paenibacillus lautus", 1402: "Bacillus licheniformis", 1404: "Bacillus megaterium", 1405: "Bacillus mycoides", 1406: "Paenibacillus polymyxa", 1407: "Bacillus psychrosaccharolyticus", 1408: "Bacillus pumilus", 1409: "Bacillus sp. (in: Bacteria)", 1410: "Bacillus sp. 1011", 1411: "Bacillus akibai", 1412: "Bacillus sp. 38-2", 1413: "Bacillus cellulosilyticus", 1415: "Bacillus sp. KSM-635", 1416: "Bacillus sp. 707", 1417: "Bacillus sp. B1018", 1418: "Bacillus mannanilyticus", 1419: "Bacillus sp. NS-129", 1420: "Bacillus sp. RC607", 1421: "Lysinibacillus sphaericus", 1422: "Geobacillus stearothermophilus", 1423: "Bacillus subtilis", 1424: "Bacillus subtilis strain DY", 1425: "Bacillus thermoamyloliquefaciens", 1426: "Parageobacillus thermoglucosidasius", 1427: "Bacillus thermoproteolyticus", 1428: "Bacillus thuringiensis", 1430: "Bacillus thuringiensis serovar israelensis", 1432: "Bacillus thuringiensis serovar thuringiensis", 1433: "Bacillus thuringiensis serovar aizawai", 1434: "Bacillus thuringiensis serovar berliner", 1435: "Bacillus thuringiensis serovar san diego", 1436: "Bacillus thuringiensis serovar entomocidus", 1440: "Bacillus thuringiensis serovar alesti", 1441: "Bacillus thuringiensis serovar morrisoni", 1442: "Bacillus thuringiensis serovar tolworthi", 1444: "Bacillus thuringiensis serovar tenebrionis", 1445: "Bacillus alcalophilus", 1447: "Bacillus sp. Q", 1449: "Amphibacillus xylanus", 1450: "Alicyclobacillus acidoterrestris", 1451: "Paenibacillus amylolyticus", 1452: "Bacillus atrophaeus", 1454: "Bacillus azotoformans", 1455: "Bacillus badius", 1456: "Bacillus benzoevorans", 1457: "Alicyclobacillus cycloheptanicus", 1458: "Bacillus fastidiosus", 1459: "Sporosarcina globispora", 1461: "Psychrobacillus insolitus", 1462: "Geobacillus kaustophilus", 1464: "Paenibacillus larvae", 1465: "Brevibacillus laterosporus", 1467: "Bacillus lentus", 1468: "Paenibacillus macquariensis subsp. macquariensis", 1471: "Bacillus methanolicus", 1472: "Paenibacillus pabuli", 1473: "Virgibacillus pantothenticus", 1474: "Sporosarcina pasteurii", 1476: "Sporosarcina psychrophila", 1477: "Paenibacillus larvae subsp. pulvifaciens", 1478: "Bacillus simplex", 1479: "Bacillus smithii", 1481: "Bacillus ohbensis", 1482: "Virgibacillus halodenitrificans", 1483: "Bacillus subtilis subsp. amylosacchariticus", 1484: "Hydrogenibacillus schlegelii", 1485: "Clostridium", 1487: "[Butyribacterium] methylotrophicum", 1488: "Clostridium acetobutylicum", 1490: "Paraclostridium bifermentans", 1491: "Clostridium botulinum", 1492: "Clostridium butyricum", 1493: "Clostridium cellulovorans", 1494: "Clostridium cochlearium", 1495: "Clostridium cylindrosporum", 1496: "Clostridioides difficile", 1497: "Clostridium formicaceticum", 1498: "Hathewaya histolytica", 1499: "Ruminiclostridium josui", 1501: "Clostridium pasteurianum", 1502: "Clostridium perfringens", 1503: "Gottschalkia purinilytica", 1504: "Clostridium septicum", 1505: "Paeniclostridium sordellii", 1506: "Clostridium sp.", 1507: "Clostridium sp. ATCC 29733", 1508: "Clostridium sp. F1", 1509: "Clostridium sporogenes", 1510: "Thermoclostridium stercorarium", 1511: "Acetoanaerobium sticklandii", 1512: "[Clostridium] symbiosum", 1513: "Clostridium tetani", 1515: "Hungateiclostridium thermocellum", 1516: "Thermoanaerobacter thermohydrosulfuricus", 1517: "Thermoanaerobacterium thermosaccharolyticum", 1519: "Clostridium tyrobutyricum", 1520: "Clostridium beijerinckii", 1521: "Ruminiclostridium cellulolyticum", 1522: "[Clostridium] innocuum", 1523: "Clostridium longisporum", 1524: "[Clostridium] piliforme", 1525: "Moorella thermoacetica", 1526: "[Clostridium] aminophilum", 1527: "Anaerocolumna aminovalerica", 1528: "Eubacterium barkeri", 1529: "Clostridium cadaveris", 1530: "Clostridium carnis", 1531: "[Clostridium] clostridioforme", 1532: "Blautia coccoides", 1533: "Clostridium fallax", 1534: "Clostridium kluyveri", 1535: "[Clostridium] leptum", 1536: "Hathewaya limosa", 1537: "Romboutsia lituseburensis", 1538: "Clostridium ljungdahlii", 1539: "Clostridium malenominatum", 1540: "Clostridioides mangenotii", 1541: "Terrisporobacter mayombei", 1542: "Clostridium novyi", 1543: "Clostridium oceanicum", 1544: "Faecalicatena orotica", 1547: "Erysipelatoclostridium ramosum", 1548: "Clostridium scatologenes", 1549: "[Clostridium] sporosphaeroides", 1550: "Clostridium subterminale", 1551: "Clostridium aurantibutyricum", 1552: "Clostridium estertheticum subsp. estertheticum", 1553: "Clostridium tetanomorphum", 1556: "Gottschalkia acidurici", 1557: "Peptoclostridium litorale", 1559: "Clostridium tertium", 1560: "Moorella thermoautotrophica", 1561: "Clostridium baratii", 1562: "Desulfotomaculum", 1563: "Desulfosporosinus orientis", 1564: "Desulfotomaculum ruminis", 1565: "Desulfotomaculum nigrificans", 1566: "Desulfofundulus australicus", 1567: "Quinella", 1568: "Quinella ovalis", 1569: "Sporosarcina", 1570: "Halobacillus halophilus", 1571: "Sporosarcina ureae", 1573: "Clavibacter", 1575: "Leifsonia xyli", 1578: "Lactobacillus", 1579: "Lactobacillus acidophilus", 1580: "Lactobacillus brevis", 1581: "Lactobacillus buchneri", 1582: "Lactobacillus casei", 1583: "Weissella confusa", 1584: "Lactobacillus delbrueckii", 1585: "Lactobacillus delbrueckii subsp. bulgaricus", 1587: "Lactobacillus helveticus", 1588: "Lactobacillus hilgardii", 1589: "Lactobacillus pentosus", 1590: "Lactobacillus plantarum", 1591: "Lactobacillus sp.", 1593: "Lactobacillus sp. 30A", 1596: "Lactobacillus gasseri", 1597: "Lactobacillus paracasei", 1598: "Lactobacillus reuteri", 1599: "Lactobacillus sakei", 1600: "Lactobacillus acetotolerans", 1601: "Lactobacillus agilis", 1602: "Lactobacillus alimentarius", 1603: "Lactobacillus amylophilus", 1604: "Lactobacillus amylovorus", 1605: "Lactobacillus animalis", 1606: "Lactobacillus aviarius", 1607: "Lactobacillus bifermentans", 1610: "Lactobacillus coryniformis", 1612: "Lactobacillus farciminis", 1613: "Lactobacillus fermentum", 1614: "Lactobacillus fructivorans", 1615: "Weissella halotolerans", 1616: "Weissella kandleri", 1618: "Lactobacillus mali", 1620: "Weissella minor", 1622: "Lactobacillus murinus", 1623: "Lactobacillus ruminis", 1624: "Lactobacillus salivarius", 1625: "Lactobacillus sanfranciscensis", 1626: "Lactobacillus sharpeae", 1627: "Lactobacillus thermophilus", 1628: "Lactobacillus vermiforme", 1629: "Weissella viridescens", 1630: "Kandleria vitulina", 1631: "Fructobacillus fructosus", 1632: "Lactobacillus oris", 1633: "Lactobacillus vaginalis", 1634: "Lactobacillus sakei L45", 1637: "Listeria", 1638: "Listeria ivanovii", 1639: "Listeria monocytogenes", 1640: "Listeria seeligeri", 1641: "Listeria grayi", 1642: "Listeria innocua", 1643: "Listeria welshimeri", 1645: "Renibacterium", 1646: "Renibacterium salmoninarum", 1647: "Erysipelothrix", 1648: "Erysipelothrix rhusiopathiae", 1649: "Kurthia", 1650: "Kurthia zopfii", 1651: "Alloiococcus", 1652: "Alloiococcus otitis", 1653: "Corynebacteriaceae", 1654: "Actinomyces", 1655: "Actinomyces naeslundii", 1656: "Actinomyces viscosus", 1657: "Actinobaculum suis", 1658: "Actinomyces bovis", 1659: "Actinomyces israelii", 1660: "Schaalia odontolytica", 1661: "Trueperella pyogenes", 1663: "Arthrobacter", 1664: "Arthrobacter glacialis", 1665: "Arthrobacter globiformis", 1667: "Arthrobacter sp.", 1669: "Arthrobacter sp. NRRL B3728", 1670: "Arthrobacter citreus", 1671: "Pseudarthrobacter oxydans", 1672: "Arthrobacter ramosus", 1673: "Rhizobium viscosum", 1676: "Pseudarthrobacter polychromogenes", 1677: "Arthrobacter pascens", 1678: "Bifidobacterium", 1679: "Bifidobacterium longum subsp. longum", 1680: "Bifidobacterium adolescentis", 1681: "Bifidobacterium bifidum", 1682: "Bifidobacterium longum subsp. infantis", 1683: "Bifidobacterium angulatum", 1684: "Bifidobacterium asteroides", 1685: "Bifidobacterium breve", 1686: "Bifidobacterium catenulatum", 1687: "Bifidobacterium coryneforme", 1688: "Bifidobacterium cuniculi", 1689: "Bifidobacterium dentium", 1690: "Bifidobacterium pseudolongum subsp. globosum", 1691: "Bifidobacterium indicum", 1692: "Bifidobacterium magnum", 1693: "Bifidobacterium minimum", 1694: "Bifidobacterium pseudolongum", 1695: "Bifidobacterium longum subsp. suis", 1696: "Brevibacterium", 1697: "Corynebacterium ammoniagenes", 1698: "Brevibacterium epidermidis", 1701: "Brevibacterium sp.", 1702: "Brevibacterium sterolicum", 1703: "Brevibacterium linens", 1704: "Brevibacterium helvolum", 1705: "Corynebacterium stationis", 1707: "Cellulomonas", 1708: "Cellulomonas fimi", 1709: "Cellulomonas biazotea", 1710: "Cellulosimicrobium cellulans", 1711: "Cellulomonas flavigena", 1712: "Cellulomonas gelida", 1713: "Oerskovia turbata", 1714: "Cellulomonas uda", 1716: "Corynebacterium", 1717: "Corynebacterium diphtheriae", 1718: "Corynebacterium glutamicum", 1719: "Corynebacterium pseudotuberculosis", 1720: "Corynebacterium sp.", 1721: "Corynebacterium callunae", 1722: "Corynebacterium nephridii", 1724: "Corynebacterium renale", 1725: "Corynebacterium xerosis", 1727: "Corynebacterium variabile", 1728: "coryneform bacterium", 1730: "Eubacterium", 1731: "Peptoclostridium acidaminophilum", 1732: "Eubacterium oxidoreducens", 1733: "uncultured bacterium 'eubacterium sp.'", 1735: "Holdemanella biformis", 1736: "Eubacterium limosum", 1737: "[Eubacterium] tenue", 1740: "Thermodesulfobacterium", 1741: "Thermodesulfobacterium commune", 1743: "Propionibacterium", 1744: "Propionibacterium freudenreichii", 1747: "Cutibacterium acnes", 1748: "Acidipropionibacterium acidipropionici", 1749: "Acidipropionibacterium jensenii", 1750: "Pseudopropionibacterium propionicum", 1751: "Acidipropionibacterium thoenii", 1752: "Propionibacterium freudenreichii subsp. shermanii", 1753: "Propioniferax innocua", 1754: "Thermoanaerobacter", 1755: "Thermoanaerobacter sp.", 1757: "Thermoanaerobacter ethanolicus", 1760: "Actinobacteria", 1762: "Mycobacteriaceae", 1763: "Mycobacterium", 1764: "Mycobacterium avium", 1765: "Mycobacterium tuberculosis variant bovis", 1766: "Mycolicibacterium fortuitum", 1767: "Mycobacterium intracellulare", 1768: "Mycobacterium kansasii", 1769: "Mycobacterium leprae", 1770: "Mycobacterium avium subsp. paratuberculosis", 1771: "Mycolicibacterium phlei", 1772: "Mycolicibacterium smegmatis", 1773: "Mycobacterium tuberculosis", 1774: "Mycobacteroides chelonae", 1775: "Mycobacterium cookii", 1776: "Mycolicibacterium flavescens", 1777: "Mycobacterium gastri", 1778: "Mycobacterium gordonae", 1779: "Mycolicibacterium komossense", 1780: "Mycobacterium malmoense", 1781: "Mycobacterium marinum", 1782: "Mycolicibacter nonchromogenicus", 1783: "Mycobacterium scrofulaceum", 1784: "Mycobacterium simiae", 1785: "Mycobacterium sp.", 1786: "Mycolicibacterium sphagni", 1787: "Mycobacterium szulgai", 1788: "Mycolicibacter terrae", 1789: "Mycobacterium xenopi", 1790: "Mycobacterium asiaticum", 1791: "Mycolicibacterium aurum", 1792: "Mycolicibacterium chitae", 1793: "Mycolicibacterium fallax", 1794: "Mycolicibacterium gadium", 1795: "Mycolicibacterium neoaurum", 1796: "Mycolicibacterium senegalense", 1797: "Mycolicibacterium thermoresistibile", 1798: "Mycolicibacillus trivialis", 1799: "Mycolicibacterium aichiense", 1800: "Mycolicibacterium chubuense", 1801: "Mycolicibacterium diernhoferi", 1802: "Mycolicibacterium farcinogenes", 1804: "Mycolicibacterium gilvum", 1806: "Mycobacterium tuberculosis variant microti", 1807: "Mycolicibacterium obuense", 1809: "Mycobacterium ulcerans", 1810: "Mycolicibacterium vaccae", 1811: "Mycobacterium hyorhinis", 1813: "Amycolatopsis", 1814: "Amycolatopsis methanolica", 1816: "Actinokineospora fastidiosa", 1817: "Nocardia", 1818: "Nocardia globerula", 1821: "Nocardia sp.", 1822: "Nocardia vaccinii", 1823: "Nocardia otitidiscaviarum", 1824: "Nocardia asteroides", 1827: "Rhodococcus", 1828: "Rhodococcus fascians", 1829: "Rhodococcus rhodochrous", 1830: "Rhodococcus ruber", 1831: "Rhodococcus sp.", 1833: "Rhodococcus erythropolis", 1835: "Saccharopolyspora", 1836: "Saccharopolyspora erythraea", 1837: "Saccharopolyspora hirsuta", 1838: "Saccharopolyspora hordei", 1839: "Nocardioides", 1841: "Nocardioides albus", 1843: "Nocardioides jensenii", 1844: "Nocardioides luteus", 1847: "Pseudonocardia", 1848: "Pseudonocardia thermophila", 1849: "Actinopolyspora", 1850: "Actinopolyspora halophila", 1851: "Saccharomonospora", 1852: "Saccharomonospora viridis", 1854: "Frankia", 1855: "Frankia sp.", 1856: "Frankia torreyi", 1857: "Frankia sp. FaC1", 1858: "Frankia sp. ArI3", 1859: "Frankia alni", 1860: "Geodermatophilus", 1861: "Geodermatophilus obscurus", 1862: "Dermatophilus", 1863: "Dermatophilus congolensis", 1865: "Actinoplanes", 1866: "Actinoplanes missouriensis", 1867: "Actinoplanes teichomyceticus", 1868: "Actinoplanes digitatis", 1869: "Actinoplanes utahensis", 1871: "Actinoplanes sp.", 1872: "Actinoplanes sp. ATCC 31351", 1873: "Micromonospora", 1874: "Micromonospora chalcea", 1876: "Micromonospora sp.", 1877: "Micromonospora echinospora", 1878: "Micromonospora rosea", 1879: "Micromonospora zionensis", 1880: "Micromonospora olivasterospora", 1881: "Micromonospora viridifaciens", 1883: "Streptomyces", 1884: "Streptomyces acrimycini", 1885: "Streptomyces actuosus", 1886: "Streptomyces albidoflavus", 1887: "Streptomyces albogriseolus", 1888: "Streptomyces albus", 1889: "Streptomyces ambofaciens", 1890: "Streptomyces antibioticus", 1891: "Streptomyces antifibrinolyticus", 1892: "Streptomyces anulatus", 1893: "Streptomyces atratus", 1894: "Kitasatospora aureofaciens", 1895: "Streptomyces avidinii", 1896: "Streptomyces bikiniensis", 1897: "Streptomyces carzinostaticus", 1898: "Streptomyces cacaoi", 1900: "Streptomyces cinnamonensis", 1901: "Streptomyces clavuligerus", 1902: "Streptomyces coelicolor", 1903: "Streptomyces corchorusii", 1904: "Streptomyces cyaneus", 1905: "Streptomyces exfoliatus", 1906: "Streptomyces fradiae", 1907: "Streptomyces glaucescens", 1908: "Streptomyces globisporus", 1909: "Streptomyces griseolus", 1910: "Streptomyces griseosporeus", 1911: "Streptomyces griseus", 1912: "Streptomyces hygroscopicus", 1913: "Amycolatopsis lactamdurans", 1914: "Streptomyces lavendulae", 1915: "Streptomyces lincolnensis", 1916: "Streptomyces lividans", 1917: "Streptomyces macromomyceticus", 1918: "Streptomyces malayensis", 1919: "Streptomyces microflavus", 1920: "Streptomyces nigrescens", 1921: "Streptomyces olivaceoviridis", 1922: "Streptomyces plicatus", 1923: "Streptomyces phaeochromogenes", 1924: "Streptomyces purpurascens", 1925: "Streptomyces ramocissimus", 1926: "Streptomyces reticuli", 1927: "Streptomyces rimosus", 1928: "Streptomyces rochei", 1929: "Streptomyces rubiginosus", 1930: "Streptomyces scabiei", 1931: "Streptomyces sp.", 1932: "Streptomyces tendae", 1933: "Streptoalloteichus tenebrarius", 1934: "Streptomyces thermovulgaris", 1935: "Streptomyces violaceoruber", 1936: "Streptomyces violaceus", 1938: "Streptomyces viridochromogenes", 1940: "Streptomyces albireticuli", 1941: "Streptomyces badius", 1942: "Streptomyces goshikiensis", 1943: "Streptomyces griseoruber", 1944: "Streptomyces halstedii", 1945: "Streptomyces jumonjinensis", 1946: "Streptomyces kasugaensis", 1947: "Streptomyces limosus", 1948: "Streptomyces longisporus", 1949: "Streptomyces mycarofaciens", 1950: "Streptomyces peucetius", 1951: "Streptomyces purpureus", 1952: "Streptomyces thermoviolaceus", 1954: "Streptomyces brasiliensis", 1955: "Streptomyces cinereus", 1956: "Streptomyces diastaticus", 1957: "Streptomyces sclerotialus", 1958: "Streptomyces sp. K15", 1960: "Streptomyces vinaceus", 1961: "Streptomyces virginiae", 1962: "Streptomyces albus G", 1963: "Streptomyces olivochromogenes", 1965: "Streptomyces espinosus", 1967: "Streptomyces kanamyceticus", 1968: "Streptomyces cellulosae", 1969: "Streptomyces chartreusis", 1970: "Streptomyces morookaense", 1971: "Streptomyces noursei", 1972: "Streptomyces roseiscleroticus", 1988: "Actinomadura", 1989: "Actinomadura sp.", 1990: "Actinomadura atramentaria", 1991: "Actinomadura cremea", 1992: "Actinomadura echinospora", 1993: "Actinomadura madurae", 1994: "Actinomadura rugatobispora", 1995: "Microtetraspora", 1996: "Microtetraspora glauca", 1997: "Microtetraspora fusca", 1998: "Planomonospora", 1999: "Planomonospora venezuelensis", 2000: "Streptosporangium", 2001: "Streptosporangium roseum", 2002: "Streptosporangium amethystogenes", 2004: "Streptosporangiaceae", 2005: "Microbispora", 2006: "Thermobispora bispora", 2012: "Thermomonosporaceae", 2013: "Nocardiopsis", 2014: "Nocardiopsis dassonvillei", 2015: "Nocardiopsis prasina", 2016: "Streptoalloteichus", 2017: "Streptoalloteichus hindustanus", 2019: "Thermomonospora", 2020: "Thermomonospora curvata", 2021: "Thermobifida fusca", 2023: "Thermoactinomyces", 2024: "Thermoactinomyces intermedius", 2025: "Thermoactinomyces sp.", 2026: "Thermoactinomyces vulgaris", 2029: "Kibdelosporangium", 2030: "Kibdelosporangium aridum", 2033: "Microbacterium testaceum", 2034: "Curtobacterium", 2035: "Curtobacterium flaccumfaciens", 2036: "Curtobacterium citreum", 2037: "Actinomycetales", 2038: "Tropheryma", 2039: "Tropheryma whipplei", 2040: "Aeromicrobium", 2041: "Aeromicrobium erythreum", 2044: "Pimelobacter", 2045: "Pimelobacter simplex", 2047: "Rothia dentocariosa", 2049: "Actinomycetaceae", 2050: "Mobiluncus", 2051: "Mobiluncus curtisii", 2052: "Mobiluncus mulieris", 2053: "Gordonia", 2054: "Gordonia bronchialis", 2055: "Gordonia terrae", 2056: "Sphaerobacter", 2057: "Sphaerobacter thermophilus", 2060: "Tsukamurella", 2061: "Tsukamurella paurometabola", 2062: "Streptomycetaceae", 2063: "Kitasatospora", 2064: "Kitasatospora griseola", 2065: "Kitasatospora phosalacinea", 2066: "Kitasatospora setae", 2070: "Pseudonocardiaceae", 2071: "Saccharothrix", 2072: "Saccharothrix australiensis", 2074: "Pseudonocardia autotrophica", 2075: "Pseudonocardia nitrificans", 2077: "Sporolactobacillus", 2078: "Sporolactobacillus inulinus", 2080: "Sporolactobacillus laevus", 2082: "Syntrophomonas bryantii", 2085: "Mycoplasmatales", 2086: "Anaeroplasma", 2087: "Anaeroplasma abactoclasticum", 2088: "Anaeroplasma bactoclasticum", 2089: "Anaeroplasma varium", 2090: "Anaeroplasma intermedium", 2092: "Mycoplasmataceae", 2093: "Mycoplasma", 2094: "Mycoplasma arginini", 2095: "Mycoplasma capricolum", 2096: "Mycoplasma gallisepticum", 2097: "Mycoplasma genitalium", 2098: "Mycoplasma hominis", 2099: "Mycoplasma hyopneumoniae", 2100: "Mycoplasma hyorhinis", 2101: "Mycoplasma incognitus", 2102: "Mycoplasma mycoides", 2103: "Mycoplasma mycoides subsp. mycoides", 2104: "Mycoplasma pneumoniae", 2105: "Mycoplasma leachii", 2106: "Mycoplasma corogypsi", 2107: "Mycoplasma pulmonis", 2108: "Mycoplasma sp.", 2109: "Mycoplasma synoviae", 2110: "Mycoplasma agalactiae", 2111: "Mycoplasma arthritidis", 2112: "Mycoplasma bovigenitalium", 2113: "Mycoplasma californicum", 2114: "Entomoplasma ellychniae", 2115: "Mycoplasma fermentans", 2116: "Mycoplasma iowae", 2117: "Mycoplasma lipophilum", 2118: "Mycoplasma mobile", 2119: "Mycoplasma muris", 2120: "Mycoplasma neurolyticum", 2121: "Mycoplasma orale", 2122: "Mycoplasma pirum", 2123: "Mycoplasma putrefaciens", 2124: "Mycoplasma salivarium", 2125: "Mycoplasma sualvi", 2127: "Mycoplasma collis", 2128: "Mycoplasma flocculare", 2129: "Ureaplasma", 2130: "Ureaplasma urealyticum", 2131: "Spiroplasmataceae", 2132: "Spiroplasma", 2133: "Spiroplasma citri", 2134: "Spiroplasma melliferum", 2135: "Spiroplasma sp.", 2136: "Spiroplasma monobiae", 2137: "Spiroplasma apis", 2138: "Spiroplasma poulsonii", 2139: "Spiroplasma clarkii", 2141: "Spiroplasma ixodetis", 2142: "Spiroplasma diabroticae", 2143: "Spiroplasma gladiatoris", 2144: "Spiroplasma mirum", 2145: "Spiroplasma taiwanense", 2146: "Acholeplasmataceae", 2147: "Acholeplasma", 2148: "Acholeplasma laidlawii", 2149: "Mesoplasma entomophilum", 2150: "Acholeplasma modicum", 2151: "Mesoplasma florum", 2152: "Asteroleplasma", 2153: "Asteroleplasma anaerobium", 2155: "Candidatus Phytoplasma sp.", 2157: "Archaea", 2158: "Methanobacteriales", 2159: "Methanobacteriaceae", 2160: "Methanobacterium", 2161: "Methanobacterium bryantii", 2162: "Methanobacterium formicicum", 2163: "Methanobacterium ivanovii", 2164: "Methanobacterium sp.", 2171: "Methanobacterium palustre", 2172: "Methanobrevibacter", 2173: "Methanobrevibacter smithii", 2174: "Metopus palaeformis endosymbiont", 2175: "Methanohalophilus", 2176: "Methanohalophilus mahii", 2177: "Methanohalophilus halophilus", 2178: "Methanothermaceae", 2179: "Methanothermus", 2180: "Methanothermus fervidus", 2181: "Methanothermus sociabilis", 2182: "Methanococcales", 2183: "Methanococcaceae", 2184: "Methanococcus", 2186: "Methanothermococcus thermolithotrophicus", 2187: "Methanococcus vannielii", 2188: "Methanococcus voltae", 2189: "Methanotorris igneus", 2190: "Methanocaldococcus jannaschii", 2191: "Methanomicrobiales", 2192: "Methanocorpusculum", 2193: "Methanocorpusculum parvum", 2194: "Methanomicrobiaceae", 2195: "Methanogenium", 2196: "Methanogenium sp.", 2197: "Methanogenium cariaci", 2198: "Methanoculleus marisnigri", 2199: "Methanogenium organophilum", 2200: "Methanoculleus thermophilus", 2201: "Methanofollis liminatans", 2202: "Methanospirillum", 2203: "Methanospirillum hungatei", 2204: "Methanomicrobium", 2205: "Methanomicrobium mobile", 2206: "Methanosarcinaceae", 2207: "Methanosarcina", 2208: "Methanosarcina barkeri", 2209: "Methanosarcina mazei", 2210: "Methanosarcina thermophila", 2213: "Methanosarcina sp.", 2214: "Methanosarcina acetivorans", 2215: "Methanosarcina vacuolata", 2220: "Methanolobus", 2221: "Methanolobus tindarius", 2222: "Methanothrix", 2223: "Methanothrix soehngenii", 2224: "Methanothrix thermoacetophila", 2225: "Methanococcoides", 2226: "Methanococcoides methylutens", 2231: "Archaeoglobales", 2232: "Archaeoglobaceae", 2233: "Archaeoglobus", 2234: "Archaeoglobus fulgidus", 2235: "Halobacteriales", 2236: "Halobacteriaceae", 2237: "Haloarcula", 2238: "Haloarcula marismortui", 2239: "Halobacterium", 2242: "Halobacterium salinarum", 2243: "Halobacterium sp.", 2246: "Haloferax volcanii", 2247: "Halorubrum lacusprofundi", 2248: "Halorubrum saccharovorum", 2249: "Halococcus", 2250: "Halococcus morrhuae", 2251: "Haloferax", 2252: "Haloferax mediterranei", 2253: "Haloferax sp.", 2254: "Haloferax lucentense", 2256: "Natronobacterium", 2257: "Natronomonas pharaonis", 2258: "Thermococcales", 2259: "Thermococcaceae", 2260: "Pyrococcus", 2261: "Pyrococcus furiosus", 2262: "Pyrococcus woesei", 2263: "Thermococcus", 2264: "Thermococcus celer", 2265: "Thermococcus litoralis", 2266: "Thermoproteales", 2267: "Thermoproteaceae", 2268: "Thermofilum", 2269: "Thermofilum pendens", 2270: "Thermoproteus", 2271: "Thermoproteus tenax", 2272: "Desulfurococcaceae", 2273: "Desulfurococcus", 2275: "Desulfurococcus mucosus", 2276: "Pyrobaculum", 2277: "Pyrobaculum islandicum", 2278: "Pyrobaculum organotrophum", 2279: "Staphylothermus", 2280: "Staphylothermus marinus", 2281: "Sulfolobales", 2283: "Acidianus ambivalens", 2284: "Sulfolobus", 2285: "Sulfolobus acidocaldarius", 2286: "Saccharolobus shibatae", 2287: "Saccharolobus solfataricus", 2288: "Sulfolobus sp.", 2289: "Desulfobacter", 2290: "Desulfobacter curvatus", 2291: "Desulfobacter hydrogenophilus", 2292: "Desulfobacter latus", 2293: "Desulfobacter postgatei", 2294: "Desulfobacter sp.", 2295: "Desulfobacterium", 2296: "Desulfobacterium autotrophicum", 2297: "Desulfobacterium niacini", 2298: "Desulfobacterium vacuolatum", 2299: "Desulfosarcina", 2300: "Desulfosarcina variabilis", 2301: "Thermoplasmatales", 2302: "Thermoplasma", 2303: "Thermoplasma acidophilum", 2306: "archaeal group 2", 2307: "Pyrodictiaceae", 2308: "Pyrodictium", 2309: "Pyrodictium occultum", 2312: "Trimyema sp. archaeal symbiont", 2314: "Methanoplanus", 2315: "Methanoplanus limicola", 2316: "Methanosphaera", 2317: "Methanosphaera stadtmanae", 2319: "Methanopyrus", 2320: "Methanopyrus kandleri", 2321: "Methanohalobium", 2322: "Methanohalobium evestigatum", 2323: "unclassified Bacteria", 2325: "Thermoanaerobacter kivui", 2326: "Alvinoconcha hessleri symbiotic bacterium", 2327: "Methylophilus methylotrophus W3A1", 2330: "Halanaerobium", 2331: "Halanaerobium praevalens", 2332: "Propionigenium", 2333: "Propionigenium modestum", 2334: "Bacillus sp. PS3", 2335: "Thermotoga", 2336: "Thermotoga maritima", 2337: "Thermotoga neapolitana", 2339: "Thyasira flexuosa gill symbiont", 2340: "Solemya velum gill symbiont", 2341: "primary endosymbiont of Sitophilus zeamais", 2342: "Candidatus Sodalis pierantonius str. SOPE", 2343: "endosymbiont of Rhinocyllus conicus", 2344: "Methylosporovibrio", 2345: "Methylosporovibrio methanica", 2347: "Iron sulfide-containing magnetotactic bacterium", 2349: "Haliscomenobacter", 2350: "Haliscomenobacter hydrossis", 2351: "Flexistipes", 2352: "Flexistipes sinusarabici", 2353: "Flexispira", 2354: "Flexispira rappini", 2355: "unidentified bacterial endosymbiont", 2357: "Desulfomonile", 2358: "Desulfomonile tiedjei", 2360: "Bathymodiolus thermophilus thioautotrophic gill symbiont", 2361: "Calyptogena magnifica symbiont", 2362: "Codakia orbicularis gill symbiont", 2363: "Lucinoma aequizonata gill symbiont", 2364: "Lucinoma annulata gill symbiont", 2365: "Riftia pachyptila trophosome symbiont", 2366: "endosymbiont of Bangasternus orientalis", 2368: "Arhodomonas", 2369: "Arhodomonas aquaeolei", 2370: "Xylella", 2371: "Xylella fastidiosa", 2373: "Acetonema", 2374: "Acetonema longum", 2375: "Sporomusa", 2376: "Sporomusa paucivorans", 2377: "Sporomusa termitida", 2378: "Sporomusa ovata", 2382: "Acetitomaculum ruminis", 2383: "Epulopiscium", 2384: "Epulopiscium sp.", 2387: "transposons", 2388: "Transposon Tn-cam204", 2389: "Transposon Tn10", 2390: "Transposon Tn1331", 2391: "Transposon Tn1525", 2392: "Transposon Tn1681", 2393: "Transposon Tn1696", 2394: "Transposon Tn1721", 2395: "Transposon Tn21", 2396: "Transposon Tn2426", 2397: "Transposon Tn2501", 2398: "Transposon Tn2680", 2399: "Transposon Tn2921", 2400: "Transposon Tn3411", 2401: "Transposon Tn3", 2402: "Transposon Tn431", 2403: "Transposon Tn4351", 2404: "Transposon Tn4521", 2405: "Transposon Tn4551", 2406: "Transposon Tn4556", 2407: "Transposon Tn501", 2408: "Transposon Tn5053", 2409: "Transposon Tn5393", 2410: "Transposon Tn554", 2411: "Transposon Tn5", 2412: "Transposon Tn602", 2413: "Transposon Tn7", 2414: "Transposon Tn903", 2415: "Transposon Tn916", 2416: "Transposon Tn917", 2417: "Transposon Tn9", 2418: "Transposon gamma-delta", 2419: "Thermotogales", 2420: "Thermosipho", 2421: "Thermosipho africanus", 2422: "Fervidobacterium", 2423: "Fervidobacterium islandicum", 2424: "Fervidobacterium nodosum", 2425: "Teredinibacter", 2426: "Teredinibacter turnerae", 2428: "TOL plasmid", 2429: "Solemya reidi gill symbiont", 2433: "Roseobacter", 2434: "Roseobacter denitrificans", 2436: "Plasmid CloDF13", 2437: "Plasmid ColA-CA31", 2438: "Plasmid ColA", 2439: "Plasmid ColB2", 2440: "Plasmid ColB4", 2441: "Plasmid ColBM-Cl139", 2442: "Plasmid ColD", 2443: "Plasmid ColE1", 2446: "Plasmid ColE2", 2447: "Plasmid ColE3-CA38", 2448: "Plasmid ColE5-099", 2449: "Plasmid ColE6-CT14", 2450: "Plasmid ColE7", 2451: "Plasmid ColE8", 2452: "Plasmid ColE9", 2453: "Plasmid ColIa", 2454: "Plasmid ColIb-P9", 2455: "Plasmid ColIb", 2456: "Plasmid ColK", 2457: "Plasmid ColV-K30", 2458: "Plasmid ColV2-K94", 2459: "Plasmid ColV3-K30", 2460: "Plasmid ColVBtrp", 2461: "Plasmid ColV", 2462: "Plasmid ENTR", 2463: "Plasmid ENT", 2464: "Plasmid EWD 299", 2465: "Plasmid F", 2466: "Plasmid NAH7", 2467: "Plasmid NR1", 2468: "Plasmid NR79", 2469: "Plasmid NTP16", 2470: "Plasmid P15a", 2471: "Plasmid P1", 2472: "Plasmid P307", 2473: "Plasmid P6", 2474: "Plasmid PDS075", 2476: "Plasmid R1-19", 2477: "Plasmid R1033", 2478: "Plasmid R1162", 2479: "Plasmid R124", 2480: "Plasmid R144", 2481: "Plasmid R1767", 2482: "Plasmid R1", 2483: "Plasmid R26", 2484: "Plasmid R27", 2485: "Plasmid R386", 2486: "Plasmid R387", 2487: "Plasmid R401", 2488: "Plasmid R46", 2489: "Plasmid R483", 2490: "Plasmid R485", 2491: "Plasmid R538", 2492: "Plasmid R64", 2493: "Plasmid R65", 2494: "Plasmid R67", 2495: "Plasmid R6K", 2496: "Plasmid R751", 2497: "Plasmid R773", 2498: "Plasmid R974", 2499: "Plasmid RGN238", 2500: "Plasmid RI13", 2501: "Plasmid RK2Te-r", 2502: "Plasmid RK2", 2503: "Plasmid RP4", 2504: "Plasmid RSF1010", 2505: "Plasmid RSF1030", 2506: "Plasmid Ri", 2507: "Plasmid Rts1", 2508: "Plasmid R", 2509: "Plasmid SCP1", 2510: "Plasmid SLP1", 2511: "Plasmid SYM", 2512: "Plasmid Ti", 2513: "Plasmid incB", 2514: "Plasmid incI-1", 2515: "Plasmid incI-gamma", 2516: "Plasmid p42d", 2517: "Sequencing vector pAA3.7X", 2518: "Plasmid pAC27", 2520: "Plasmid pAD1", 2522: "Plasmid pAL5000", 2523: "Plasmid pAM-beta-1", 2524: "Plasmid pAM77", 2525: "Plasmid pAZ1", 2526: "Plasmid pBAA1", 2527: "Plasmid pBC16", 2528: "Plasmid pBC1", 2530: "Plasmid pBP60-1", 2531: "Plasmid pBS2", 2532: "Plasmid pBWH77", 2534: "Plasmid pC194", 2535: "Plasmid pC30il", 2536: "Plasmid pCD1", 2538: "Plasmid pCHL1", 2540: "Plasmid pCMS1", 2541: "Plasmid pCN2", 2542: "Plasmid pCN3", 2543: "Plasmid pCU1", 2544: "Plasmid pColBM-C1139", 2546: "Plasmid pDK1", 2547: "Plasmid pDU1358", 2548: "Plasmid pDU1", 2549: "Plasmid pE194", 2550: "Plasmid pEA3", 2551: "Plasmid pED208", 2552: "Plasmid pEP2", 2553: "Plasmid pEST1226", 2554: "Plasmid pEX102", 2555: "Plasmid pF166", 2556: "Plasmid pFA3", 2557: "Plasmid pGS05", 2558: "Plasmid pHG1", 2560: "Plasmid pHH502", 2561: "Plasmid pHH507", 2562: "Plasmid pHV2", 2564: "Plasmid pI258", 2565: "Plasmid pIB485", 2566: "Plasmid pIE545", 2567: "Plasmid pIJ101", 2568: "Plasmid pIM13", 2570: "Plasmid pIP1433", 2571: "Plasmid pIP1527", 2573: "Plasmid pIP404", 2574: "Plasmid pIP501", 2575: "Plasmid pIP630", 2576: "Plasmid pIP816", 2577: "Plasmid pJD1", 2578: "Plasmid pJHC-MW1", 2580: "Plasmid pJP4", 2581: "Plasmid pJR225", 2582: "Plasmid pJS37", 2584: "Plasmid pKLH104", 2585: "Plasmid pKLH1", 2586: "Plasmid pKLH202", 2588: "Plasmid pKM101", 2589: "Plasmid pKY1", 2590: "Plasmid pKYM", 2591: "Plasmid pLAB1000", 2592: "Plasmid pLB1", 2593: "Plasmid pLP1", 2594: "Plasmid pLS11", 2595: "Plasmid pLS1", 2596: "Plasmid pME2001", 2597: "Plasmid pMEA100", 2598: "Plasmid pMK157", 2599: "Plasmid pMM110", 2600: "Plasmid pMM237", 2601: "Recombinant plasmid pMM25-3", 2602: "Recombinant plasmid pMM5-3", 2603: "Recombinant plasmid pMM5-5", 2604: "Plasmid pMON234", 2605: "Plasmid pMU707", 2606: "Plasmid pMV158", 2607: "Plasmid pMYSH6000", 2608: "Plasmid pNE131", 2609: "Plasmid pNG2", 2611: "Plasmid pNRC100", 2612: "Plasmid pNS1981", 2613: "Plasmid pNS1", 2616: "Plasmid pRA1", 2618: "Plasmid pRE-I", 2619: "Plasmid pRJF1", 2620: "Plasmid pSA209", 2621: "Plasmid pSA2100", 2622: "Plasmid pSAM2", 2623: "Plasmid pSB24.2", 2624: "Plasmid pSBK203", 2625: "Plasmid pSC101", 2626: "Plasmid pSE211", 2627: "Plasmid pSG1", 2628: "Plasmid pSK11L", 2629: "Plasmid pSL1", 2630: "Plasmid pSL2", 2631: "Plasmid pSLP124", 2632: "Plasmid pSM32", 2633: "Plasmid pSMB74", 2636: "Plasmid pSX267", 2637: "Plasmid pSa", 2638: "Plasmid pT181", 2639: "Plasmid pT48", 2641: "Plasmid pTB913", 2642: "Plasmid pTD1", 2643: "Plasmid pTF-FC2", 2645: "Plasmid pTiA6", 2646: "Plasmid pTiAB3", 2647: "Plasmid pTiAch5", 2648: "Plasmid pTiAg162", 2649: "Plasmid pTiAg57", 2650: "Plasmid pTiB6S3", 2651: "Plasmid pTiC58", 2652: "Plasmid pTiS4", 2653: "Plasmid pUB110cop1", 2655: "Plasmid pUB110", 2656: "Plasmid pUH1", 2657: "Plasmid pUR400", 2658: "Plasmid pVA380-1", 2659: "Plasmid pVI150", 2660: "Plasmid pWM5", 2661: "Plasmid pWR100", 2662: "Plasmid pWR60", 2663: "Plasmid pWW0", 2664: "Plasmid pWW53", 2665: "Plasmid pYV03", 2666: "Plasmid pYVe439-80", 2670: "Plasmid RP1", 2671: "integrons", 2673: "insertion sequences", 2678: "Insertion sequence IS2", 2681: "Insertion sequence IS407", 2684: "Insertion sequence IS4", 2693: "Incompatibility symbiont of Nasonia vitripennis", 2694: "Incompatibility symbiont of Nasonia longicornis", 2695: "Incompatibility symbiont of Nasonia giraulti", 2697: "Heliobacterium", 2698: "Heliobacterium chlorum", 2699: "Heliobacterium gestii", 2701: "Gardnerella", 2702: "Gardnerella vaginalis", 2704: "Thermoanaerobacter acetoethylicus", 2706: "Citrus", 2707: "Citrus greening disease-associated bacterium", 2708: "Citrus limon", 2709: "Citrus cavaleriei", 2711: "Citrus sinensis", 2713: "Aquifex", 2714: "Aquifex pyrophilus", 2717: "Cardiobacterium", 2718: "Cardiobacterium hominis", 2722: "unidentified proteobacterium", 2723: "Hirschia", 2724: "Hirschia baltica", 2725: "unidentified prokaryotic organism", 2728: "Candidatus Legionella jeonii", 2733: "Symbiobacterium", 2734: "Symbiobacterium thermophilum", 2735: "Verrucomicrobium", 2736: "Verrucomicrobium spinosum", 2737: "Vagococcus", 2738: "Vagococcus fluvialis", 2739: "Vagococcus salmoninarum", 2740: "Peptococcus", 2741: "Peptococcus niger", 2742: "Marinobacter", 2743: "Marinobacter hydrocarbonoclasticus", 2745: "Halomonas", 2746: "Halomonas elongata", 2747: "Carnobacterium", 2748: "Carnobacterium divergens", 2749: "Carnobacterium gallinarum", 2750: "Carnobacterium mobile", 2751: "Carnobacterium maltaromaticum", 2752: "Carnobacterium funditum", 2753: "Synergistes", 2754: "Synergistes jonesii", 2755: "Brochothrix", 2756: "Brochothrix thermosphacta", 2757: "Brochothrix campestris", 2759: "Eukaryota", 2761: "Cyanophora", 2762: "Cyanophora paradoxa", 2763: "Rhodophyta", 2764: "Aglaothamnion", 2765: "Aglaothamnion neglectum", 2766: "Antithamnion", 2767: "Antithamnion sp.", 2768: "Chondrus", 2769: "Chondrus crispus", 2770: "Cyanidium", 2771: "Cyanidium caldarium", 2772: "Gastroclonium", 2773: "Gastroclonium coulteri", 2774: "Gracilaria", 2777: "Gracilaria gracilis", 2779: "Gracilaria tikvahiae", 2781: "Gracilariopsis", 2782: "Gracilariopsis lemaneiformis", 2783: "Gracilariopsis sp.", 2784: "Porphyra", 2785: "Pyropia tenera", 2786: "Porphyra umbilicalis", 2787: "Porphyra purpurea", 2788: "Pyropia yezoensis", 2790: "Porphyra sp.", 2791: "Porphyridium", 2792: "Porphyridium aerugineum", 2794: "Rhodymenia", 2797: "Bangiophyceae", 2798: "Porphyridiales", 2799: "Porphyridiaceae", 2800: "Rhodella", 2801: "Rhodella violacea", 2802: "Ceramiales", 2803: "Rhodomelaceae", 2804: "Polysiphonia", 2805: "Polysiphonia boldii", 2806: "Florideophyceae", 2807: "Nemaliales", 2808: "Gelidiaceae", 2809: "Batrachospermum", 2810: "Batrachospermum ectocarpum", 2811: "Gelidium", 2812: "Gelidium amansii", 2814: "Endocladiaceae", 2815: "Carpopeltis", 2816: "Grateloupia crispata", 2819: "Palmariales", 2820: "Palmariaceae", 2821: "Palmaria", 2822: "Palmaria palmata", 2823: "Gloiopeltis", 2824: "Gloiopeltis complanata", 2825: "Chrysophyceae", 2828: "Heterosigma", 2829: "Heterosigma akashiwo", 2830: "Haptophyta", 2831: "Pavlova", 2832: "Pavlova lutheri", 2833: "Xanthophyceae", 2834: "Bumilleriopsis", 2835: "Bumilleriopsis filiformis", 2836: "Bacillariophyta", 2838: "Odontella", 2842: "Skeletonema", 2843: "Skeletonema costatum", 2849: "Phaeodactylum", 2850: "Phaeodactylum tricornutum", 2852: "Cylindrotheca", 2853: "Cylindrotheca fusiformis", 2854: "Cylindrotheca sp.", 2855: "Cylindrotheca sp. (STRAIN N1)", 2856: "Cylindrotheca closterium", 2857: "Nitzschia", 2858: "Nitzschia alba", 2862: "Diatoma", 2864: "Dinophyceae", 2865: "Crypthecodinium", 2866: "Crypthecodinium cohnii", 2867: "Peridinium", 2868: "Peridinium bipes", 2869: "Peridinium foliaceum", 2870: "Phaeophyceae", 2871: "Costaria", 2872: "Costaria costata", 2873: "Dictyotales", 2874: "Dictyotaceae", 2875: "Dictyota", 2876: "Dictyota dichotoma", 2877: "Ectocarpales", 2878: "Ectocarpaceae", 2879: "Ectocarpus", 2880: "Ectocarpus siliculosus", 2881: "Ectocarpus variabilis", 2882: "Pylaiella", 2885: "Pylaiella littoralis", 2886: "Laminariales", 2887: "Alariaceae", 2888: "Alaria", 2889: "Alaria esculenta", 2891: "Scytosiphonaceae", 2892: "Petalonia", 2893: "Petalonia fascia", 2896: "Cryptomonadaceae", 2897: "Chilomonas", 2898: "Cryptomonas paramecium", 2902: "Emiliania", 2903: "Emiliania huxleyi", 2905: "Ochrosphaera", 2907: "Ochrosphaera sp. 181", 2910: "Peridiniales", 2912: "Gonyaulax", 2915: "Ceratium", 2916: "Tripos fusus", 2918: "Heterocapsa", 2919: "Heterocapsa illdefina", 2920: "Heterocapsa niei", 2922: "Thoracosphaera", 2923: "Thoracosphaera heimii", 2924: "Alexandrium", 2925: "Alexandrium catenella", 2926: "Alexandrium tamarense", 2928: "Alexandrium cohorticula", 2929: "Alexandrium concavum", 2932: "Alexandrium fundyense", 2935: "Alexandrium insuetum", 2936: "Alexandrium kutnerae", 2937: "Alexandrium leei", 2938: "Alexandrium lusitanicum", 2939: "Alexandrium tropicale", 2940: "Cachonina", 2942: "Prorocentrales", 2943: "Prorocentraceae", 2944: "Prorocentrum", 2945: "Prorocentrum micans", 2946: "Prorocentrum mariae-labouriae", 2949: "Symbiodinium", 2950: "Symbiodinium sp.", 2951: "Symbiodinium microadriaticum", 2952: "Symbiodinium pilosum", 2953: "Gymnodiniales", 2955: "Gymnodinium", 2957: "Protodinium simplex", 2958: "Gymnodinium varians", 2959: "Gymnodinium sp.", 2960: "Amphidinium", 2961: "Amphidinium carterae", 2962: "Woloszynskia", 2964: "Noctilucales", 2965: "Noctiluca", 2966: "Noctiluca scintillans", 2968: "Oxyrrhis", 2969: "Oxyrrhis marina", 2970: "Pyrocystales", 2971: "Pyrocystis", 2972: "Pyrocystis lunula", 2974: "Vaucheriales", 2975: "Vaucheriaceae", 2976: "Vaucheria", 2977: "Vaucheria bursata", 2978: "Tribonematales", 2979: "Tribonemataceae", 2980: "Tribonema", 2981: "Tribonema aequale", 2985: "Ochromonas", 2986: "Ochromonas danica", 2988: "Mallomonas", 2989: "Mallomonas papillosa", 2990: "Mallomonas striata", 2991: "Synura", 2992: "Synura spinosa", 2995: "Hydrurus", 2996: "Hydrurus foetidus", 2997: "Chromulina", 2998: "Chromulina chionophila", 2999: "Hibberdia", 3000: "Hibberdia magna", 3002: "Bacillaria", 3003: "Bacillaria paxillifer", 3004: "Rhizosolenia", 3005: "Rhizosolenia setigera", 3006: "Stephanopyxis", 3009: "Fucales", 3010: "Fucaceae", 3011: "Fucus", 3012: "Fucus distichus", 3013: "Fucus gardneri", 3014: "Sargassaceae", 3015: "Sargassum", 3016: "Sargassum fulvellum", 3017: "Acinetospora", 3018: "Acinetospora crinita", 3021: "Akkesiphycus", 3022: "Akkesiphycus lubricum", 3024: "Chordaceae", 3025: "Chordaria", 3026: "Chordaria flagelliformis", 3027: "Cryptophyta", 3028: "Chroomonas", 3029: "Chroomonas sp.", 3030: "Cryptomonas", 3031: "Cryptomonas sp.", 3032: "Hanusia phi", 3033: "Pyrenomonas", 3034: "Pyrenomonas salina", 3035: "Euglenida", 3036: "Astasia", 3037: "Euglena longa", 3038: "Euglena", 3039: "Euglena gracilis", 3040: "Euglena viridis", 3041: "Chlorophyta", 3042: "Chlamydomonadales", 3043: "Dunaliellaceae", 3044: "Dunaliella", 3046: "Dunaliella salina", 3047: "Dunaliella tertiolecta", 3048: "Dunaliella parva", 3049: "Polytomella", 3050: "Polytomella agilis", 3051: "Chlamydomonadaceae", 3052: "Chlamydomonas", 3054: "Chlamydomonas moewusii", 3055: "Chlamydomonas reinhardtii", 3056: "Chlamydomonas sp. TK-1983", 3057: "Chlamydomonas sp. WXM", 3059: "Chlamydomonas gelatinosa", 3061: "Chlamydomonas pitschmannii", 3062: "Spondylomoraceae", 3063: "Pyrobotrys", 3064: "Pyrobotrys stellata", 3065: "Volvocaceae", 3066: "Volvox", 3067: "Volvox carteri", 3068: "Volvox carteri f. nagariensis", 3070: "Oocystaceae", 3071: "Chlorella", 3072: "Pseudochlorella pringsheimii", 3073: "[Chlorella] fusca", 3074: "Parachlorella kessleri", 3075: "Auxenochlorella protothecoides", 3076: "Chlorella sorokiniana", 3077: "Chlorella vulgaris", 3078: "Auxenochlorella pyrenoidosa", 3079: "Chlorella sp.", 3080: "Lobosphaeropsis lobophora", 3081: "Neodesmus pupukensis", 3082: "Chloroidium saccharophilum", 3083: "Edaphochlorella mirabilis", 3084: "green alga KS3/2", 3086: "Scenedesmaceae", 3087: "Scenedesmus", 3088: "Tetradesmus obliquus", 3089: "Scenedesmus quadricauda", 3090: "Chlorococcaceae", 3091: "Characium", 3092: "Characiopodium hindakii", 3093: "Characium perforatum", 3094: "Characium saccatum", 3095: "Chlamydopodium vacuolatum", 3097: "Ettlia minuta", 3098: "Neochloris", 3099: "Neochloris aquatica", 3100: "Neochloris vigensis", 3101: "Parietochloris", 3102: "Ettlia pseudoalveolaris", 3103: "Hydrodictyaceae", 3104: "Pediastrum", 3105: "Pediastrum duplex", 3106: "Hydrodictyon", 3107: "Hydrodictyon reticulatum", 3108: "Ankistrodesmus", 3109: "Ankistrodesmus stipitatus", 3110: "Prototheca", 3111: "Prototheca wickerhamii", 3112: "Prototheca zopfii", 3113: "Ulvales", 3114: "Ulvaceae", 3116: "Ulva intestinalis", 3117: "Ulva prolifera", 3118: "Ulva", 3119: "Ulva arasakii", 3120: "Ulva pertusa", 3122: "Coleochaetaceae", 3123: "Coleochaete", 3124: "Coleochaete orbicularis", 3125: "Coleochaete scutata", 3127: "Bryopsidaceae", 3128: "Bryopsis", 3129: "Bryopsis maxima", 3130: "Bryopsis plumosa", 3131: "Codiaceae", 3132: "Codium", 3133: "Codium fragile", 3134: "Dasycladales", 3135: "Dasycladaceae", 3136: "Acetabularia", 3139: "Batophora", 3140: "Batophora oerstedii", 3142: "Chlorokybaceae", 3143: "Chlorokybus", 3144: "Chlorokybus atmophyticus", 3146: "Characeae", 3148: "Nitella", 3149: "Nitella sp.", 3150: "Nitella flexilis", 3151: "Nitella axillaris", 3155: "Asteromonas", 3156: "Asteromonas gracilis", 3158: "Pedinomonas", 3159: "Pedinomonas minor", 3160: "Platymonas", 3161: "Tetraselmis subcordiformis", 3162: "Prasinocladus", 3163: "Prasinocladus sp. UTEX732", 3164: "Tetraselmis", 3165: "Tetraselmis striata", 3166: "Chlorophyceae", 3168: "Chlorella-like algae", 3170: "Friedmannia", 3171: "Myrmecia israeliensis", 3172: "Klebsormidiales", 3173: "Klebsormidiaceae", 3174: "Klebsormidium", 3175: "Klebsormidium flaccidum", 3176: "Zygnematales", 3178: "Zygnemataceae", 3179: "Spirogyra", 3180: "Spirogyra maxima", 3181: "Spirogyra sp.", 3182: "Spirogyra grevilleana", 3183: "Cladophorales", 3185: "Chaetomorpha", 3186: "Chaetomorpha moniligera", 3187: "Nannochloris", 3188: "Picochlorum eukaryotum sensu Mainz 1", 3189: "Scherffelia", 3190: "Scherffelia dubia", 3191: "Spermatozopsis", 3192: "Spermatozopsis similis", 3193: "Embryophyta", 3195: "Marchantiophyta", 3196: "Marchantia", 3197: "Marchantia polymorpha", 3199: "Jungermanniales", 3200: "Jungermanniineae", 3201: "Jungermanniaceae", 3202: "Jungermannia", 3204: "Lophocoleineae", 3206: "Lophocolea", 3207: "Lophocolea heterophylla", 3208: "Bryophyta", 3210: "Polytrichales", 3211: "Polytrichaceae", 3212: "Polytrichum", 3213: "Polytrichum commune", 3214: "Bryopsida", 3215: "Funariales", 3216: "Funariaceae", 3217: "Physcomitrella", 3218: "Physcomitrella patens", 3219: "Dicranales", 3220: "Dicranaceae", 3221: "Dicranum", 3222: "Dicranum scoparium", 3223: "Ditrichaceae", 3224: "Ceratodon", 3225: "Ceratodon purpureus", 3226: "Bryales", 3227: "Mniaceae", 3228: "Mnium", 3229: "Mnium rugicum", 3230: "Plagiomnium", 3231: "Plagiomnium trichomanes", 3233: "Anthoceros", 3234: "Anthoceros punctatus", 3236: "Psilotopsida", 3237: "Psilotales", 3238: "Psilotaceae", 3239: "Psilotum", 3240: "Psilotum nudum", 3244: "Selaginellales", 3245: "Selaginellaceae", 3246: "Selaginella", 3247: "Selaginella martensii", 3249: "Lycopodiales", 3250: "Lycopodiaceae", 3251: "Lycopodium", 3252: "Lycopodium clavatum", 3255: "Equisetales", 3256: "Equisetaceae", 3257: "Equisetum", 3258: "Equisetum arvense", 3259: "Equisetum giganteum", 3260: "Equisetum telmateia", 3261: "Equisetum scirpoides", 3262: "Equisetum hyemale", 3264: "Marattiales", 3265: "Marattiaceae", 3266: "Angiopteris", 3267: "Angiopteris lygodiifolia", 3268: "Polypodiales", 3269: "Dicksoniaceae", 3270: "Dicksonia", 3271: "Dicksonia antarctica", 3272: "Gleicheniaceae", 3273: "Gleichenia", 3274: "Gleichenia japonica", 3275: "Polypodiaceae", 3276: "Matteuccia", 3277: "Matteuccia struthiopteris", 3278: "Polystichum", 3279: "Polystichum munitum", 3280: "Onoclea", 3281: "Onoclea sensibilis", 3282: "Osmundaceae", 3283: "Osmunda", 3284: "Osmundastrum cinnamomeum", 3285: "Osmunda regalis", 3287: "Dryopteris", 3288: "Dryopteris acuminata", 3289: "Dryopteris filix-mas", 3296: "Cycadopsida", 3297: "Cycadales", 3298: "Zamiaceae", 3299: "Encephalartos", 3300: "Encephalartos altensteinii", 3301: "Encephalartos ferox", 3302: "Encephalartos arenarius", 3303: "Zamia", 3304: "Zamia pumila", 3305: "Zamia integrifolia", 3306: "Zamia pygmaea", 3307: "Zamia inermis", 3308: "Ginkgoales", 3309: "Ginkgoaceae", 3310: "Ginkgo", 3311: "Ginkgo biloba", 3313: "Pinidae", 3315: "Thuja", 3316: "Thuja plicata", 3317: "Thuja occidentalis", 3318: "Pinaceae", 3319: "Abies", 3320: "Abies magnifica", 3321: "Cedrus", 3322: "Cedrus deodara", 3323: "Keteleeria", 3324: "Keteleeria davidiana", 3325: "Larix", 3326: "Larix laricina", 3327: "Larix occidentalis", 3328: "Picea", 3329: "Picea abies", 3330: "Picea glauca", 3331: "Picea pungens", 3332: "Picea sitchensis", 3333: "Picea rubens", 3334: "Picea engelmannii", 3335: "Picea mariana", 3336: "Picea omorika", 3337: "Pinus", 3338: "Pinus balfouriana", 3339: "Pinus contorta", 3340: "Pinus edulis", 3341: "Pinus wallichiana", 3342: "Pinus krempfii", 3343: "Pinus lambertiana", 3344: "Pinus longaeva", 3345: "Pinus monticola", 3346: "Pinus pinea", 3347: "Pinus radiata", 3348: "Pinus strobus", 3349: "Pinus sylvestris", 3350: "Pinus thunbergii", 3351: "Pinus coulteri", 3352: "Pinus taeda", 3353: "Pinus banksiana", 3354: "Pseudolarix", 3355: "Pseudolarix amabilis", 3356: "Pseudotsuga", 3357: "Pseudotsuga menziesii", 3358: "Tsuga", 3359: "Tsuga heterophylla", 3362: "Podocarpaceae", 3363: "Podocarpus", 3366: "Podocarpus henkelii", 3367: "Cupressaceae", 3368: "Cryptomeria", 3369: "Cryptomeria japonica", 3370: "Metasequoia", 3371: "Metasequoia glyptostroboides", 3372: "Gnetopsida", 3374: "Welwitschiales", 3375: "Welwitschiaceae", 3376: "Welwitschia", 3377: "Welwitschia mirabilis", 3378: "Gnetales", 3379: "Gnetaceae", 3380: "Gnetum", 3381: "Gnetum montanum", 3382: "Gnetum gnemon", 3383: "Gnetum ula", 3385: "Ephedrales", 3386: "Ephedraceae", 3387: "Ephedra", 3388: "Ephedra kokanica", 3389: "Ephedra distachya", 3390: "Ephedra tweediana", 3391: "Ephedra altissima", 3394: "Cycadaceae", 3395: "Cycas", 3396: "Cycas revoluta", 3397: "Cycas circinalis", 3398: "Magnoliopsida", 3400: "Magnoliales", 3401: "Magnoliaceae", 3402: "Magnolia", 3403: "Magnolia liliiflora", 3404: "Magnolia acuminata", 3406: "Magnolia grandiflora", 3407: "Magnolia x soulangeana", 3408: "Magnolia hypoleuca", 3409: "Magnolia latahensis", 3410: "Magnolia macrophylla", 3411: "Magnolia salicifolia", 3412: "Magnolia virginiana", 3413: "Liriodendron", 3414: "Liriodendron chinense", 3415: "Liriodendron tulipifera", 3417: "Winteraceae", 3418: "Drimys", 3419: "Drimys winteri", 3420: "Tasmannia lanceolata", 3421: "Tasmannia", 3422: "Tasmannia insipida", 3423: "Tasmannia purpurascens", 3424: "Canellaceae", 3425: "Canella", 3426: "Canella winterana", 3427: "Calycanthaceae", 3428: "Calycanthus", 3429: "Calycanthus floridus", 3430: "Calycanthus occidentalis", 3431: "Calycanthus chinensis", 3432: "Laurales", 3433: "Lauraceae", 3434: "Persea", 3435: "Persea americana", 3436: "Persea borbonia", 3437: "Umbellularia", 3438: "Umbellularia californica", 3440: "Ranunculaceae", 3441: "Coptis", 3442: "Coptis japonica", 3443: "Nigella", 3444: "Nigella damascena", 3445: "Ranunculus", 3447: "Ranunculus acris", 3448: "Caltha", 3449: "Caltha palustris", 3450: "Aquilegia", 3451: "Aquilegia vulgaris", 3452: "Clematis", 3453: "Clematis rehderiana", 3454: "Clematis ligusticifolia", 3455: "Menispermaceae", 3456: "Dioscoreophyllum", 3457: "Dioscoreophyllum cumminsii", 3458: "Coriariaceae", 3459: "Coriaria", 3460: "Coriaria myrtifolia", 3462: "Fumarioideae", 3463: "Corydalis", 3464: "Capnoides sempervirens", 3465: "Papaveraceae", 3466: "Eschscholzia", 3467: "Eschscholzia californica", 3468: "Papaver", 3469: "Papaver somniferum", 3471: "Sanguinaria", 3472: "Sanguinaria canadensis", 3474: "Ulmaceae", 3475: "Parasponia", 3476: "Parasponia andersonii", 3477: "Parasponia rigida", 3478: "Rhizobium sp. ANU289", 3479: "Trema", 3480: "Trema tomentosum", 3481: "Cannabaceae", 3482: "Cannabis", 3483: "Cannabis sativa", 3484: "Humulus", 3485: "Humulus japonicus", 3486: "Humulus lupulus", 3487: "Moraceae", 3488: "Artocarpus", 3489: "Artocarpus heterophyllus", 3490: "Artocarpus integer", 3492: "Artocarpus tonkinensis", 3493: "Ficus", 3494: "Ficus carica", 3495: "Maclura", 3496: "Maclura pomifera", 3497: "Morus", 3498: "Morus alba", 3499: "Urticaceae", 3500: "Urtica", 3501: "Urtica dioica", 3502: "Fagales", 3503: "Fagaceae", 3504: "Betula", 3505: "Betula pendula", 3507: "Betula papyrifera", 3508: "Betula nigra", 3509: "Myrica", 3510: "Morella cerifera", 3511: "Quercus", 3512: "Quercus rubra", 3513: "Quercus alba", 3514: "Betulaceae", 3515: "Alnus", 3516: "Alnus incana", 3517: "Alnus glutinosa", 3518: "Alnus alnobetula subsp. crispa", 3520: "Casuarinaceae", 3521: "Casuarina", 3522: "Casuarina glauca", 3523: "Casuarina equisetifolia", 3524: "Caryophyllales", 3525: "Phytolaccaceae", 3526: "Phytolacca", 3527: "Phytolacca americana", 3528: "Phytolacca acinosa", 3529: "Gisekia", 3530: "Gisekia pharnaceoides", 3531: "Rivineae", 3532: "Rivina", 3533: "Rivina humilis", 3534: "Stegnosperma", 3535: "Stegnosperma halimifolium", 3536: "Nyctaginaceae", 3537: "Mirabilis", 3538: "Mirabilis jalapa", 3540: "Bougainvillea", 3541: "Bougainvillea glabra", 3542: "Aizoaceae", 3543: "Mesembryanthemum", 3544: "Mesembryanthemum crystallinum", 3545: "Lithops", 3546: "Lithops sp.", 3547: "Trianthema", 3548: "Trianthema portulacastrum", 3550: "Atriplex", 3551: "Atriplex patula", 3552: "Atriplex rosea", 3553: "Atriplex nummularia", 3554: "Beta", 3555: "Beta vulgaris subsp. vulgaris", 3557: "Patellifolia patellaris", 3558: "Chenopodium", 3559: "Chenopodium album", 3560: "Oxybasis rubra", 3561: "Spinacia", 3562: "Spinacia oleracea", 3563: "Amaranthaceae", 3564: "Amaranthus", 3565: "Amaranthus hybridus", 3567: "Amaranthus caudatus", 3568: "Caryophyllaceae", 3569: "Dianthus", 3570: "Dianthus caryophyllus", 3571: "Saponaria", 3572: "Saponaria officinalis", 3573: "Silene", 3575: "Silene gallica", 3577: "Arenaria", 3578: "Arenaria drummondii", 3579: "Cerastium", 3580: "Cerastium glomeratum", 3581: "Portulacaceae", 3582: "Portulaca", 3583: "Portulaca grandiflora", 3584: "Didiereaceae", 3585: "Alluaudia", 3586: "Alluaudia procera", 3587: "Basellaceae", 3588: "Basella", 3589: "Basella alba", 3590: "Molluginaceae", 3591: "Mollugo", 3592: "Mollugo verticillata", 3593: "Cactaceae", 3594: "Schlumbergera", 3595: "Schlumbergera truncata", 3596: "Pereskia", 3597: "Pereskia aculeata", 3599: "Phaulothamnus", 3600: "Phaulothamnus spinescens", 3602: "Vitaceae", 3603: "Vitis", 3604: "Vitis sp.", 3605: "Vitis aestivalis", 3606: "Parthenocissus", 3607: "Parthenocissus quinquefolia", 3608: "Rhamnaceae", 3609: "Rhamnus", 3610: "Rhamnus cathartica", 3612: "Colletia", 3613: "Colletia armata", 3615: "Polygonaceae", 3616: "Fagopyrum", 3617: "Fagopyrum esculentum", 3618: "Rumex", 3619: "Rumex obtusifolius", 3620: "Rheum", 3621: "Rheum rhabarbarum", 3623: "Actinidiaceae", 3624: "Actinidia", 3625: "Actinidia chinensis", 3627: "Actinidia deliciosa", 3629: "Malvaceae", 3630: "Abutilon", 3631: "Abutilon theophrasti", 3633: "Gossypium", 3634: "Gossypium barbadense", 3635: "Gossypium hirsutum", 3636: "Gossypium robinsonii", 3637: "Thespesia", 3638: "Thespesia populnea", 3640: "Theobroma", 3641: "Theobroma cacao", 3642: "Lecythidaceae", 3644: "Bertholletia", 3645: "Bertholletia excelsa", 3646: "Malpighiales", 3647: "Caricaceae", 3648: "Carica", 3649: "Carica papaya", 3650: "Cucurbitaceae", 3651: "Bryonia", 3652: "Bryonia dioica", 3653: "Citrullus", 3654: "Citrullus lanatus", 3655: "Cucumis", 3656: "Cucumis melo", 3657: "Cucumis melo var. conomon", 3658: "Cucumis melo var. cantalupo", 3659: "Cucumis sativus", 3660: "Cucurbita", 3661: "Cucurbita maxima", 3662: "Cucurbita moschata", 3663: "Cucurbita pepo", 3664: "Cucurbita pepo subsp. pepo", 3665: "Cucurbita pepo var. melopepo", 3667: "Lagenaria", 3668: "Lagenaria siceraria", 3669: "Luffa", 3670: "Luffa aegyptiaca", 3671: "Momordica", 3672: "Momordica balsamina", 3673: "Momordica charantia", 3674: "Momordica cochinchinensis", 3675: "Momordica repens", 3676: "Trichosanthes", 3677: "Trichosanthes kirilowii", 3678: "Ecballium", 3679: "Ecballium elaterium", 3680: "Begoniaceae", 3681: "Begonia", 3682: "Begonia metallica x Begonia sanguinea", 3683: "Passifloraceae", 3684: "Passiflora", 3685: "Passiflora quadrangularis", 3688: "Salicaceae", 3689: "Populus", 3690: "Populus x canadensis", 3691: "Populus nigra", 3693: "Populus tremuloides", 3694: "Populus trichocarpa", 3695: "Populus trichocarpa x Populus deltoides", 3696: "Populus deltoides", 3697: "Populus sp.", 3699: "Brassicales", 3700: "Brassicaceae", 3701: "Arabidopsis", 3702: "Arabidopsis thaliana", 3703: "Armoracia", 3704: "Armoracia rusticana", 3705: "Brassica", 3707: "Brassica juncea", 3708: "Brassica napus", 3709: "Brassica napus subsp. rapifera", 3710: "Brassica nigra", 3711: "Brassica rapa", 3712: "Brassica oleracea", 3713: "Brassica oleracea var. viridis", 3714: "Brassica oleracea var. alboglabra", 3715: "Brassica oleracea var. botrytis", 3716: "Brassica oleracea var. capitata", 3717: "Brassica sp.", 3718: "Capsella", 3719: "Capsella bursa-pastoris", 3720: "Crambe", 3721: "Crambe hispanica subsp. abyssinica", 3722: "Crambe crambe", 3723: "Matthiola", 3724: "Matthiola incana", 3725: "Raphanus", 3726: "Raphanus sativus", 3727: "Sinapis", 3728: "Sinapis alba", 3729: "Sisymbrium", 3730: "Sisymbrium irio", 3731: "Diplotaxis", 3732: "Diplotaxis erucoides", 3733: "Moringaceae", 3734: "Moringa", 3735: "Moringa oleifera", 3737: "Sapotaceae", 3740: "Manilkara", 3741: "Manilkara zapota", 3743: "Synsepalum dulcificum", 3744: "Rosales", 3745: "Rosaceae", 3746: "Fragaria", 3747: "Fragaria x ananassa", 3749: "Malus", 3750: "Malus domestica", 3751: "Malus sp.", 3752: "Malus sylvestris", 3754: "Prunus", 3755: "Prunus dulcis", 3756: "Prunus dulcis var. amara", 3758: "Prunus domestica", 3759: "Prunus yedoensis", 3760: "Prunus persica", 3761: "Geum", 3762: "Geum chiloense", 3763: "Geum borisii", 3764: "Rosa", 3765: "Rosa x damascena", 3766: "Pyrus", 3767: "Pyrus pyrifolia", 3769: "Byblis", 3770: "Byblis liniflora", 3771: "Roridula", 3772: "Roridula gorgonias", 3773: "Cephalotaceae", 3774: "Cephalotus", 3775: "Cephalotus follicularis", 3776: "Cunoniaceae", 3777: "Ceratopetalum", 3778: "Ceratopetalum gummiferum", 3779: "Weinmannia", 3780: "Weinmannia silvicola", 3781: "Crassulaceae", 3782: "Crassula", 3784: "Sedum", 3785: "Sedum rubrotinctum", 3786: "Pachyphytum", 3790: "Eucryphia", 3791: "Eucryphia lucida", 3792: "Saxifragaceae", 3794: "Heuchera", 3795: "Heuchera micrantha", 3796: "Parnassia", 3797: "Parnassia fimbriata", 3798: "Saxifraga", 3799: "Micranthes integrifolia", 3801: "Ribes", 3802: "Ribes americanum", 3803: "Fabaceae", 3804: "Caesalpinioideae", 3805: "Bauhinia", 3806: "Bauhinia purpurea", 3807: "mimosoid clade", 3808: "Acacia", 3809: "Acacia confusa", 3810: "Adenanthera", 3811: "Adenanthera pavonina", 3812: "Albizia", 3813: "Albizia julibrissin", 3814: "Papilionoideae", 3815: "Abrus", 3816: "Abrus precatorius", 3817: "Arachis", 3818: "Arachis hypogaea", 3820: "Cajanus", 3821: "Cajanus cajan", 3822: "Canavalia", 3823: "Canavalia ensiformis", 3824: "Canavalia gladiata", 3825: "Canavalia rosea", 3826: "Cicer", 3827: "Cicer arietinum", 3828: "Crotalaria", 3829: "Crotalaria juncea", 3830: "Crotalaria pallida", 3831: "Cyamopsis", 3832: "Cyamopsis tetragonoloba", 3833: "Cytisus", 3834: "Cytisophyllum sessilifolium", 3835: "Cytisus scoparius", 3836: "Dioclea", 3837: "Dioclea grandiflora", 3838: "Dioclea lehmannii", 3839: "Dolichos", 3840: "Vigna unguiculata subsp. cylindrica", 3841: "Erythrina", 3842: "Erythrina caffra", 3843: "Erythrina corallodendron", 3844: "Erythrina latissima", 3845: "Erythrina variegata", 3846: "Glycine", 3847: "Glycine max", 3848: "Glycine soja", 3849: "Griffonia", 3850: "Griffonia simplicifolia", 3851: "Laburnum", 3852: "Laburnum alpinum", 3853: "Lathyrus", 3854: "Lathyrus aphaca", 3855: "Lathyrus clymenum", 3856: "Lathyrus cicera", 3857: "Lathyrus hirsutus", 3858: "Lathyrus ochrus", 3859: "Lathyrus odoratus", 3860: "Lathyrus sativus", 3861: "Lathyrus sphaericus", 3862: "Lathyrus tingitanus", 3863: "Lens", 3864: "Lens culinaris", 3865: "Leucaena", 3866: "Leucaena leucocephala", 3867: "Lotus", 3868: "Lotus tetragonolobus", 3869: "Lupinus", 3870: "Lupinus albus", 3871: "Lupinus angustifolius", 3872: "Lupinus arboreus", 3873: "Lupinus luteus", 3874: "Lupinus polyphyllus", 3875: "Macrotyloma", 3876: "Macrotyloma axillare", 3877: "Medicago", 3878: "Medicago falcata", 3879: "Medicago sativa", 3880: "Medicago truncatula", 3881: "Onobrychis", 3882: "Onobrychis viciifolia", 3883: "Phaseolus", 3884: "Phaseolus lunatus", 3885: "Phaseolus vulgaris", 3886: "Phaseolus coccineus", 3887: "Pisum", 3888: "Pisum sativum", 3889: "Psophocarpus", 3890: "Psophocarpus scandens", 3891: "Psophocarpus tetragonolobus", 3892: "Pueraria", 3893: "Pueraria montana var. lobata", 3894: "Sesbania", 3895: "Sesbania rostrata", 3896: "Sophora", 3897: "Styphnolobium japonicum", 3898: "Trifolium", 3899: "Trifolium repens", 3900: "Trifolium subterraneum", 3901: "Ulex", 3902: "Ulex europaeus", 3904: "Vicia", 3905: "Vicia cracca", 3906: "Vicia faba", 3907: "Vicia faba var. minor", 3908: "Vicia sativa", 3909: "Vicia sativa subsp. nigra", 3910: "Vicia hirsuta", 3911: "Vicia villosa", 3912: "Vicia narbonensis", 3913: "Vigna", 3914: "Vigna angularis", 3915: "Vigna mungo", 3916: "Vigna radiata var. radiata", 3917: "Vigna unguiculata", 3918: "Vigna aconitifolia", 3920: "Vigna unguiculata subsp. unguiculata", 3921: "Wisteria", 3922: "Wisteria floribunda", 3925: "Lonchocarpus", 3926: "Philenoptera violacea", 3928: "Lythraceae", 3929: "Cuphea", 3930: "Cuphea lanceolata", 3931: "Myrtaceae", 3932: "Eucalyptus", 3933: "Eucalyptus gunnii", 3934: "Onagraceae", 3935: "Clarkia", 3936: "Clarkia lewisii", 3937: "Clarkia unguiculata", 3938: "Clarkia xantiana", 3939: "Oenothera", 3940: "Oenothera argillicola", 3941: "Oenothera villaricae", 3942: "Oenothera biennis", 3945: "Oenothera organensis", 3946: "Oenothera picensis", 3947: "Oenothera picensis subsp. picensis", 3948: "Oenothera sp.", 3949: "Oenothera ammophila", 3950: "Oenothera berteroana", 3951: "Oenothera odorata", 3953: "Oenothera speciosa", 3954: "Combretaceae", 3955: "Quisqualis", 3956: "Combretum indicum", 3958: "Santalaceae", 3959: "Pyrularia", 3960: "Pyrularia pubera", 3961: "Buckleya", 3962: "Buckleya distichophylla", 3963: "Loranthaceae", 3964: "Dendrophthora", 3965: "Dendrophthora clavata", 3966: "Dendrophthora domingensis", 3967: "Phoradendron", 3968: "Phoradendron liga", 3969: "Phoradendron leucarpum subsp. tomentosum", 3970: "Phoradendron leucarpum", 3971: "Viscum", 3972: "Viscum album", 3973: "Olacaceae", 3974: "Schoepfia", 3975: "Schoepfia arenaria", 3977: "Euphorbiaceae", 3978: "Gelonium", 3979: "Suregada multiflora", 3980: "Hevea", 3981: "Hevea brasiliensis", 3982: "Manihot", 3983: "Manihot esculenta", 3984: "Mercurialis", 3985: "Mercurialis perennis", 3986: "Mercurialis annua", 3987: "Ricinus", 3988: "Ricinus communis", 3990: "Euphorbia", 3991: "Euphorbia characias", 3992: "Euphorbia dulcis", 3993: "Euphorbia esula", 3994: "Euphorbia polychroma", 3995: "Jatropha", 3996: "Jatropha multifida", 3997: "Simmondsiaceae", 3998: "Simmondsia", 3999: "Simmondsia chinensis", 4000: "Buxaceae", 4001: "Buxus", 4002: "Buxus sempervirens", 4004: "Linaceae", 4005: "Linum", 4006: "Linum usitatissimum", 4007: "Humiriaceae", 4008: "Humiria", 4009: "Humiria balsamifera", 4011: "Anacardiaceae", 4012: "Rhus", 4013: "Toxicodendron vernicifluum", 4014: "Burseraceae", 4015: "Bursera", 4016: "Bursera inaguensis", 4018: "Tropaeolaceae", 4019: "Tropaeolum", 4020: "Tropaeolum majus", 4022: "Acer", 4023: "Acer negundo", 4024: "Acer saccharum", 4025: "Acer platanoides", 4026: "Acer pseudoplatanus", 4027: "Geraniaceae", 4028: "Geranium", 4029: "Pelargonium grandiflorum", 4030: "Pelargonium", 4031: "Pelargonium x hortorum", 4032: "Pelargonium zonale", 4033: "Oxalidaceae", 4034: "Oxalis", 4035: "Oxalis dillenii", 4036: "Apiales", 4037: "Apiaceae", 4038: "Daucus", 4039: "Daucus carota", 4040: "Pastinaca", 4041: "Pastinaca sativa", 4042: "Petroselinum", 4043: "Petroselinum crispum", 4044: "Apium", 4045: "Apium graveolens", 4046: "Coriandrum", 4047: "Coriandrum sativum", 4048: "Hydrocotyle", 4049: "Hydrocotyle sibthorpioides", 4050: "Araliaceae", 4051: "Hedera", 4052: "Hedera helix", 4053: "Panax", 4054: "Panax ginseng", 4055: "Gentianales", 4056: "Apocynaceae", 4057: "Catharanthus", 4058: "Catharanthus roseus", 4059: "Rauvolfia", 4060: "Rauvolfia serpentina", 4062: "Rauvolfia mannii", 4065: "Calotropis", 4066: "Calotropis gigantea", 4067: "Gymnema", 4068: "Gymnema sylvestre", 4069: "Solanales", 4070: "Solanaceae", 4071: "Capsicum", 4072: "Capsicum annuum", 4073: "Capsicum frutescens", 4074: "Datura", 4075: "Datura inoxia", 4076: "Datura stramonium", 4078: "Hyoscyamus", 4079: "Hyoscyamus niger", 4081: "Solanum lycopersicum", 4082: "Solanum peruvianum", 4083: "Solanum chilense", 4084: "Solanum pimpinellifolium", 4085: "Nicotiana", 4086: "Nicotiana acuminata", 4087: "Nicotiana alata", 4088: "Nicotiana quadrivalvis var. bigelovii", 4089: "Nicotiana debneyi", 4090: "Nicotiana glauca", 4091: "Nicotiana otophora", 4092: "Nicotiana plumbaginifolia", 4093: "Nicotiana rustica", 4094: "Nicotiana sp.", 4096: "Nicotiana sylvestris", 4097: "Nicotiana tabacum", 4098: "Nicotiana tomentosiformis", 4100: "Nicotiana benthamiana", 4101: "Petunia", 4102: "Petunia x hybrida", 4103: "Petunia integrifolia", 4104: "Petunia sp.", 4107: "Solanum", 4108: "Solanum chacoense", 4109: "Solanum commersonii", 4110: "Solanum crispum", 4111: "Solanum melongena", 4112: "Solanum nigrum", 4113: "Solanum tuberosum", 4114: "Solanum aviculare", 4115: "Solanum palustre", 4116: "Solanum petrophilum", 4118: "Convolvulaceae", 4119: "Ipomoea", 4120: "Ipomoea batatas", 4121: "Ipomoea purpurea", 4122: "Convolvulus", 4123: "Convolvulus arvensis", 4124: "Convolvulus tricolor", 4128: "Cuscuta", 4129: "Cuscuta reflexa", 4130: "Hydrophyllaceae", 4131: "Eriodictyon", 4132: "Eriodictyon californicum", 4133: "Hydrophyllum", 4134: "Hydrophyllum virginianum", 4136: "Lamiaceae", 4137: "Leonurus", 4138: "Leonurus japonicus", 4139: "Scutellaria", 4142: "Plectranthus scutellarioides", 4143: "Lamiales", 4144: "Oleaceae", 4145: "Olea", 4146: "Olea europaea", 4147: "Jasminum", 4148: "Jasminum simplicifolium subsp. suavissimum", 4149: "Scrophulariaceae", 4150: "Antirrhinum", 4151: "Antirrhinum majus", 4152: "Craterostigma", 4153: "Craterostigma plantagineum", 4154: "Mimulus", 4155: "Erythranthe guttata", 4156: "Erythranthe laciniata", 4157: "Erythranthe arvensis", 4158: "Erythranthe nasuta", 4159: "Erythranthe nudata", 4160: "Erythranthe microphylla", 4161: "Erythranthe tilingii", 4162: "Erythranthe glaucescens", 4163: "Digitalis", 4164: "Digitalis purpurea", 4165: "Cymbalaria", 4166: "Cymbalaria muralis", 4167: "Lamourouxia", 4168: "Lamourouxia sp. UCB", 4169: "Striga", 4170: "Striga asiatica", 4172: "Agalinis auriculata", 4173: "Veronica", 4174: "Veronica pilosa", 4176: "Epifagus", 4177: "Epifagus virginiana", 4178: "Conopholis", 4179: "Conopholis americana", 4180: "Pedaliaceae", 4181: "Sesamum", 4182: "Sesamum indicum", 4183: "Harpagophytum", 4184: "Uncarina grandidieri", 4185: "Acanthaceae", 4186: "Aphelandra", 4187: "Aphelandra sinclairiana", 4188: "Barleria", 4189: "Barleria prionitis", 4190: "Justicia", 4191: "Justicia odora", 4192: "Nelsonia", 4193: "Nelsonia campestris", 4194: "Ruttya", 4195: "Ruttya fruticosa", 4196: "Lentibulariaceae", 4197: "Pinguicula", 4198: "Pinguicula caerulea", 4199: "Dipsacales", 4200: "Caprifoliaceae", 4201: "Sambucus", 4202: "Sambucus nigra", 4203: "Sambucus racemosa", 4204: "Viburnum", 4205: "Viburnum acerifolium", 4206: "Adoxaceae", 4207: "Adoxa", 4208: "Adoxa moschatellina", 4209: "Asterales", 4210: "Asteraceae", 4211: "Ambrosia", 4212: "Ambrosia artemisiifolia", 4214: "Ambrosia trifida", 4215: "Ambrosia artemisiifolia var. elatior", 4216: "Arctium", 4217: "Arctium lappa", 4218: "Arctium tomentosum", 4219: "Artemisia", 4220: "Artemisia vulgaris", 4221: "Carthamus", 4222: "Carthamus tinctorius", 4223: "Flaveria", 4224: "Flaveria bidentis", 4225: "Flaveria linearis", 4226: "Flaveria pringlei", 4227: "Flaveria trinervia", 4228: "Flaveria chlorifolia", 4229: "Guizotia", 4230: "Guizotia abyssinica", 4231: "Helianthus", 4232: "Helianthus annuus", 4233: "Helianthus tuberosus", 4234: "Helianthus petiolaris", 4235: "Lactuca", 4236: "Lactuca sativa", 4237: "Barnadesia", 4238: "Barnadesia caryophylla", 4239: "Ligularia", 4240: "Ligularia calthifolia", 4242: "Adenothamnus", 4243: "Adenothamnus validus", 4244: "Argyroxiphium", 4245: "Argyroxiphium caliginis", 4246: "Arnica", 4247: "Arnica mollis", 4248: "Dubautia", 4249: "Dubautia arborea", 4250: "Dubautia menziesii", 4251: "Hulsea", 4252: "Hulsea algida", 4253: "Madia", 4254: "Kyhosia bolanderi", 4255: "Madia elegans", 4256: "Harmonia stebbinsii", 4257: "Raillardella", 4258: "Raillardella pringlei", 4260: "Carlquistia muirii", 4261: "Anisocarpus scabridus", 4262: "Wilkesia", 4263: "Wilkesia gymnoxiphium", 4264: "Cynara", 4265: "Cynara cardunculus", 4268: "Malpighiaceae", 4269: "Byrsonima", 4270: "Byrsonima crassifolia", 4272: "Platytheca", 4273: "Platytheca verticillata", 4274: "Polygalaceae", 4275: "Polygala", 4276: "Polygala cruciata", 4277: "Securidaca", 4278: "Securidaca diversifolia", 4280: "Cornoideae", 4281: "Cornus", 4282: "Cornus canadensis", 4283: "Cornus florida", 4284: "Cornus racemosa", 4285: "Cornus mas", 4286: "Garryaceae", 4287: "Garrya", 4288: "Garrya elliptica", 4289: "Nyssaceae", 4290: "Nyssa", 4292: "Nyssa sylvatica", 4294: "Aquifoliaceae", 4295: "Ilex", 4296: "Ilex crenata", 4297: "Ilex vomitoria", 4298: "Ilex aquifolium", 4299: "Ilex ciliospinosa", 4300: "Ilex pernyi", 4301: "Nemopanthus", 4302: "Nemopanthus mucronatus", 4303: "Phelline", 4304: "Phelline comosa", 4305: "Celastraceae", 4306: "Euonymus", 4307: "Euonymus alatus", 4309: "Euonymus maackii", 4310: "Corynocarpaceae", 4311: "Corynocarpus", 4312: "Corynocarpus laevigatus", 4313: "Dichapetalaceae", 4314: "Dichapetalum", 4315: "Dichapetalum crassifolium", 4317: "Hippocratea", 4318: "Hippocratea richardiana", 4319: "Salacia", 4320: "Salacia pallescens", 4321: "Icacinaceae", 4322: "Icacina", 4323: "Icacina mannii", 4324: "Salvadoraceae", 4325: "Salvadora", 4326: "Salvadora persica", 4328: "Proteaceae", 4329: "Macadamia", 4330: "Macadamia ternifolia", 4331: "Protea", 4332: "Protea repens", 4335: "Primulaceae", 4336: "Anagallis", 4337: "Anagallis arvensis", 4339: "Cyrillaceae", 4340: "Cyrilla", 4341: "Cyrilla racemiflora", 4343: "Epacris", 4344: "Epacris sp.", 4345: "Ericaceae", 4346: "Rhododendron", 4347: "Rhododendron hippophaeoides", 4348: "Pterospora", 4349: "Pterospora andromedea", 4350: "Sarcodes", 4351: "Sarcodes sanguinea", 4353: "Sarraceniaceae", 4354: "Darlingtonia", 4355: "Darlingtonia californica", 4356: "Heliamphora", 4357: "Heliamphora nutans", 4358: "Sarracenia", 4359: "Sarracenia flava", 4360: "Droseraceae", 4361: "Dionaea", 4362: "Dionaea muscipula", 4363: "Drosera", 4364: "Drosera binata", 4365: "Drosera burmannii", 4366: "Drosera capensis", 4367: "Drosera dichrosepala", 4368: "Drosera filiformis", 4369: "Drosera peltata", 4370: "Drosera petiolaris", 4371: "Drosera regia", 4372: "Drosophyllum", 4373: "Drosophyllum lusitanicum", 4374: "Nepenthaceae", 4375: "Nepenthes", 4376: "Nepenthes alata", 4377: "Dillenia", 4378: "Dillenia indica", 4381: "Campanulaceae", 4382: "Lobelia", 4383: "Lobelia sp.", 4386: "Daphniphyllaceae", 4387: "Daphniphyllum", 4388: "Daphniphyllum sp.", 4390: "Eucommiaceae", 4391: "Eucommia", 4392: "Eucommia ulmoides", 4395: "Hamamelis", 4396: "Hamamelis mollis", 4397: "Hamamelis virginiana", 4398: "Liquidambar", 4400: "Liquidambar styraciflua", 4401: "Platanaceae", 4402: "Platanus", 4403: "Platanus occidentalis", 4405: "Trochodendraceae", 4406: "Trochodendron", 4407: "Trochodendron aralioides", 4410: "Nymphaeaceae", 4411: "Barclaya", 4412: "Barclaya longifolia", 4413: "Euryale", 4414: "Euryale ferox", 4415: "Nuphar", 4416: "Nuphar variegata", 4418: "Nymphaea", 4419: "Nymphaea odorata", 4420: "Victoria", 4421: "Victoria cruziana", 4422: "Cabombaceae", 4423: "Brasenia", 4424: "Brasenia schreberi", 4425: "Cabomba", 4426: "Cabomba caroliniana", 4427: "Ceratophyllum", 4428: "Ceratophyllum demersum", 4429: "Nelumbonaceae", 4430: "Nelumbo", 4431: "Nelumbo lutea", 4432: "Nelumbo nucifera", 4434: "Bataceae", 4435: "Batis", 4436: "Batis maritima", 4437: "Plumbaginaceae", 4439: "Plumbago", 4441: "Camellia", 4442: "Camellia sinensis", 4443: "Camellia japonica", 4447: "Liliopsida", 4449: "Alismataceae", 4450: "Sagittaria", 4451: "Sagittaria sagittifolia", 4452: "Sagittaria lancifolia", 4454: "Araceae", 4455: "Alocasia", 4456: "Alocasia macrorrhizos", 4457: "Arum", 4458: "Arum maculatum", 4459: "Colocasia", 4460: "Colocasia esculenta", 4462: "Sauromatum", 4463: "Sauromatum venosum", 4464: "Acorus", 4465: "Acorus calamus", 4466: "Gymnostachys", 4467: "Gymnostachys anceps", 4469: "Lemna", 4470: "Lemna gibba", 4472: "Lemna minor", 4473: "Spirodela", 4476: "Pistia", 4477: "Pistia stratiotes", 4479: "Poaceae", 4480: "Aegilops", 4481: "Aegilops crassa", 4483: "Aegilops bicornis", 4485: "Aegilops comosa", 4486: "Aegilops longissima", 4487: "Aegilops searsii", 4491: "Aegilops umbellulata", 4492: "Aegilops uniaristata", 4493: "Aegilops columnaris", 4494: "Aegilops markgrafii", 4496: "Avena", 4497: "Avena nuda", 4498: "Avena sativa", 4499: "Avena fatua", 4500: "Avena longiglumis", 4501: "Bromus", 4502: "Bromus secalinus", 4504: "Coix", 4505: "Coix lacryma-jobi", 4508: "Dactylis", 4509: "Dactylis glomerata", 4510: "Eleusine", 4511: "Eleusine coracana", 4512: "Hordeum", 4513: "Hordeum vulgare", 4515: "Hordeum bogdanii", 4516: "Hordeum bulbosum", 4517: "Hordeum jubatum", 4519: "Hordeum marinum", 4520: "Lolium", 4521: "Lolium multiflorum", 4522: "Lolium perenne", 4523: "Neurachne", 4524: "Neurachne munroi", 4525: "Neurachne tenuifolia", 4527: "Oryza", 4528: "Oryza longistaminata", 4529: "Oryza rufipogon", 4530: "Oryza sativa", 4532: "Oryza australiensis", 4533: "Oryza brachyantha", 4534: "Oryza latifolia", 4535: "Oryza officinalis", 4536: "Oryza sativa f. spontanea", 4537: "Oryza punctata", 4538: "Oryza glaberrima", 4539: "Panicum", 4540: "Panicum miliaceum", 4541: "Pennisetum", 4543: "Cenchrus americanus", 4544: "Poa", 4545: "Poa pratensis", 4546: "Saccharum", 4547: "Saccharum officinarum", 4549: "Secale", 4550: "Secale cereale", 4551: "Secale montanum", 4552: "Secale sylvestre", 4553: "Secale cereale subsp. vavilovii", 4554: "Setaria", 4555: "Setaria italica", 4556: "Setaria viridis", 4557: "Sorghum", 4558: "Sorghum bicolor", 4560: "Sorghum halepense", 4562: "Tripsacum", 4563: "Tripsacum dactyloides", 4564: "Triticum", 4565: "Triticum aestivum", 4566: "Triticum aestivum x Triticum timopheevi", 4567: "Triticum turgidum subsp. durum", 4568: "Triticum monococcum", 4569: "Triticum sp.", 4570: "Triticum timopheevii", 4571: "Triticum turgidum", 4572: "Triticum urartu", 4573: "Aegilops speltoides", 4575: "Zea", 4576: "Zea diploperennis", 4577: "Zea mays", 4579: "Zea mays subsp. mexicana", 4580: "Zea perennis", 4581: "Bambusa", 4582: "Bambusa multiplex", 4583: "Cenchrus", 4584: "Cenchrus setiger", 4585: "Psathyrostachys", 4586: "Psathyrostachys juncea", 4587: "Thinopyrum", 4588: "Thinopyrum elongatum", 4589: "Thinopyrum ponticum", 4590: "Arundinaria", 4591: "Arundinaria gigantea", 4592: "Agropyron", 4593: "Agropyron cristatum", 4594: "Amblyopyrum", 4595: "Amblyopyrum muticum", 4596: "Australopyrum", 4597: "Australopyrum retrofractum", 4601: "Thinopyrum bessarabicum", 4603: "Thinopyrum junceum", 4604: "Pseudoroegneria spicata", 4605: "Festuca", 4606: "Festuca arundinacea", 4607: "Festuca arizonica", 4608: "Festuca pratensis", 4609: "Cyperaceae", 4610: "Cyperus", 4611: "Cyperus alternifolius", 4613: "Bromeliaceae", 4614: "Ananas", 4615: "Ananas comosus", 4616: "Bromelia", 4617: "Bromelia plumieri", 4618: "Zingiberales", 4619: "Marantaceae", 4620: "Thaumatococcus", 4621: "Thaumatococcus daniellii", 4622: "Calathea", 4623: "Goeppertia loeseneri", 4624: "Marantochloa", 4625: "Marantochloa purpurea", 4626: "Cannaceae", 4627: "Canna", 4628: "Canna indica", 4629: "Canna tuerckheimii", 4630: "Costaceae", 4631: "Costus", 4632: "Costus barbatus", 4633: "Monocostus", 4634: "Monocostus uniflorus", 4635: "Tapeinochilos", 4636: "Tapeinochilos ananassae", 4637: "Musaceae", 4638: "Ensete", 4639: "Ensete ventricosum", 4640: "Musa", 4641: "Musa acuminata", 4642: "Zingiberaceae", 4643: "Globba", 4644: "Globba curtisii", 4645: "Hedychium", 4646: "Hedychium flavum", 4647: "Hedychium gardnerianum", 4648: "Riedelia", 4649: "Riedelia aff. wrayii SBG 83-203", 4650: "Zingiber", 4651: "Zingiber gramineum", 4652: "Heliconiaceae", 4653: "Heliconia", 4654: "Heliconia latispatha", 4655: "Heliconia paka", 4656: "Lowiaceae", 4657: "Orchidantha", 4658: "Orchidantha fimbriata", 4660: "Strelitziaceae", 4661: "Phenakospermum", 4662: "Phenakospermum guyannense", 4663: "Ravenala", 4664: "Ravenala madagascariensis", 4665: "Strelitzia", 4666: "Strelitzia nicolai", 4667: "Liliales", 4668: "Amaryllidaceae", 4669: "Galanthus", 4670: "Galanthus nivalis", 4671: "Dioscoreaceae", 4672: "Dioscorea", 4673: "Dioscorea japonica", 4674: "Hypoxidaceae", 4675: "Curculigo", 4676: "Molineria latifolia", 4677: "Liliaceae", 4678: "Allium", 4679: "Allium cepa", 4681: "Allium ampeloprasum", 4682: "Allium sativum", 4683: "Allium tuberosum", 4684: "Allium ursinum", 4685: "Asparagus", 4686: "Asparagus officinalis", 4688: "Lilium", 4689: "Lilium henryi", 4690: "Lilium longiflorum", 4691: "Lilium speciosum", 4692: "Lilium superbum", 4693: "Medeola", 4694: "Medeola virginiana", 4695: "Hippeastrum", 4696: "Hippeastrum sp.", 4697: "Narcissus", 4698: "Narcissus hybrid cultivar", 4699: "Uvularia", 4700: "Uvularia sessilifolia", 4701: "Scilla", 4702: "Scilla siberica", 4703: "Smilacaceae", 4704: "Geitonoplesium", 4705: "Geitonoplesium cymosum", 4706: "Lapageria", 4707: "Lapageria rosea", 4710: "Arecaceae", 4711: "Calamus", 4712: "Calamus usitatus", 4713: "Caryota", 4714: "Caryota mitis", 4715: "Drymophloeus", 4716: "Drymophloeus subdistichus", 4717: "Nypa", 4718: "Nypa fruticans", 4719: "Phoenix", 4720: "Phoenix reclinata", 4721: "Serenoa", 4722: "Serenoa repens", 4724: "Pandanaceae", 4725: "Pandanus", 4726: "Pandanus tectorius", 4729: "Sparganium", 4731: "Typhaceae", 4732: "Typha", 4733: "Typha latifolia", 4734: "commelinids", 4736: "Joinvilleaceae", 4737: "Joinvillea", 4738: "Joinvillea plicata", 4739: "Commelinales", 4740: "Commelinaceae", 4741: "Tradescantia", 4742: "Tradescantia soconuscana", 4743: "Commelina", 4744: "Commelina communis", 4747: "Orchidaceae", 4748: "x Doritaenopsis", 4749: "x Doritaenopsis sp.", 4751: "Fungi", 4753: "Pneumocystis", 4754: "Pneumocystis carinii", 4756: "Neocallimastix", 4757: "Neocallimastix frontalis", 4758: "Neocallimastix patriciarum", 4760: "Neocallimastix joyonii", 4761: "Chytridiomycota", 4762: "Oomycetes", 4763: "Saprolegniales", 4764: "Saprolegniaceae", 4765: "Achlya", 4766: "Achlya bisexualis", 4767: "Achlya klebsiana", 4768: "Achlya ambisexualis", 4769: "Saprolegnia", 4770: "Saprolegnia ferax", 4772: "Schizochytrium", 4773: "Schizochytrium aggregatum", 4774: "Thraustochytrium", 4775: "Thraustochytrium visurgense", 4776: "Peronosporales", 4777: "Peronosporaceae", 4778: "Bremia", 4779: "Bremia lactucae", 4780: "Plasmopara", 4781: "Plasmopara halstedii", 4782: "Pythiaceae", 4783: "Phytophthora", 4784: "Phytophthora capsici", 4785: "Phytophthora cinnamomi", 4786: "Phytophthora cryptogea", 4787: "Phytophthora infestans", 4788: "Phytophthora megasperma", 4790: "Phytophthora nicotianae", 4791: "Phytophthora nicotianae var. parasitica", 4792: "Phytophthora parasitica", 4793: "Phytophthora citrophthora", 4794: "Phytophthora drechsleri", 4795: "Phytophthora megakarya", 4796: "Phytophthora palmivora", 4797: "Pythium", 4798: "Pythium hydnosporum", 4799: "Pythium torulosum", 4800: "Lagenidiales", 4801: "Lagenidiaceae", 4802: "Lagenidium", 4803: "Lagenidium giganteum", 4805: "Blastocladiales", 4806: "Blastocladiaceae", 4807: "Blastocladiella", 4808: "Blastocladiella emersonii", 4809: "Blastocladiella simplex", 4810: "Chytridiales", 4812: "Chytridiaceae", 4813: "Chytridium", 4814: "Chytriomyces hyalinus", 4815: "Spizellomyces", 4816: "Spizellomyces acuminatus", 4819: "Phlyctochytrium", 4820: "Phlyctochytrium irregulare", 4821: "Piromyces", 4822: "Piromyces communis", 4823: "Caecomyces", 4824: "Caecomyces communis", 4827: "Mucorales", 4828: "Absidia", 4829: "Absidia glauca", 4830: "Mucor", 4836: "Phycomyces", 4837: "Phycomyces blakesleeanus", 4838: "Rhizomucor", 4839: "Rhizomucor miehei", 4840: "Rhizomucor pusillus", 4841: "Mucor racemosus", 4842: "Rhizopus", 4843: "Rhizopus microsporus var. chinensis", 4844: "Rhizopus niveus", 4846: "Rhizopus stolonifer", 4847: "Rhizopus microsporus var. oligosporus", 4849: "Blakeslea", 4850: "Blakeslea trispora", 4851: "Cunninghamellaceae", 4852: "Cunninghamella", 4853: "Cunninghamella elegans", 4854: "Mortierellaceae", 4855: "Mortierella", 4856: "Mortierella formosensis", 4857: "Entomophthorales", 4858: "Basidiobolaceae", 4859: "Basidiobolus", 4860: "Basidiobolus magnus", 4861: "Kickxellales", 4862: "Kickxellaceae", 4863: "Coemansia", 4864: "Coemansia mojavensis", 4865: "Dipsacomyces", 4866: "Dipsacomyces acuminosporus", 4867: "Linderina", 4868: "Linderina macrospora", 4869: "Endogonales", 4870: "Endogonaceae", 4871: "Endogone", 4872: "Endogone pisiformis", 4873: "Gigaspora", 4874: "Gigaspora margarita", 4875: "Glomus", 4876: "Rhizophagus intraradices", 4880: "Amoebidium", 4881: "Amoebidium parasiticum", 4883: "Legeriomycetaceae", 4884: "Capniomyces", 4885: "Capniomyces stellatus", 4886: "Genistelloides", 4887: "Genistelloides hibernus", 4888: "Smittium", 4890: "Ascomycota", 4891: "Saccharomycetes", 4892: "Saccharomycetales", 4893: "Saccharomycetaceae", 4894: "Schizosaccharomycetaceae", 4895: "Schizosaccharomyces", 4896: "Schizosaccharomyces pombe", 4897: "Schizosaccharomyces japonicus", 4899: "Schizosaccharomyces octosporus", 4903: "Cyberlindnera jadinii", 4908: "Issatchenkia", 4909: "Pichia kudriavzevii", 4910: "Kluyveromyces", 4911: "Kluyveromyces marxianus", 4914: "Lachancea waltii", 4917: "Pachysolen", 4918: "Pachysolen tannophilus", 4919: "Pichia", 4920: "Millerozyma farinosa", 4921: "Pichia norvegensis", 4922: "Komagataella pastoris", 4923: "Ogataea pini", 4924: "Scheffersomyces stipitis", 4925: "Pichia sp.", 4926: "Pichia membranifaciens", 4927: "Wickerhamomyces anomalus", 4929: "Meyerozyma guilliermondii", 4930: "Saccharomyces", 4931: "Saccharomyces bayanus", 4932: "Saccharomyces cerevisiae", 4934: "Lachancea kluyveri", 4935: "Saccharomyces sp.", 4943: "Saccharomycopsis", 4944: "Saccharomycopsis fibuligera", 4947: "Schwanniomyces occidentalis var. occidentalis", 4948: "Torulaspora", 4950: "Torulaspora delbrueckii", 4951: "Yarrowia", 4952: "Yarrowia lipolytica", 4953: "Zygosaccharomyces", 4954: "Zygosaccharomyces bailii", 4955: "Lachancea fermentati", 4956: "Zygosaccharomyces rouxii", 4957: "Zygosaccharomyces bisporus", 4958: "Debaryomyces", 4959: "Debaryomyces hansenii", 4962: "Williopsis", 4967: "Eremascus", 4968: "Eremascus albus", 4970: "Bullera", 4972: "Dioszegia hungarica", 4973: "Dioszegia aurantiaca", 4974: "Dioszegia crocea", 4975: "Kwoniella dendrophila", 4976: "Vishniacozyma globospora", 4978: "Sugitazyma miyagiana", 4979: "Hannaella oryzae", 4981: "Papiliotrema pseudoalba", 4983: "Hannaella sinensis", 4986: "Ruinenia rubra", 4987: "Ballistosporomyces xanthus", 4988: "Bensingtonia", 4989: "Bensingtonia ciliata", 4990: "Pseudobensingtonia ingoldii", 4992: "Kondoa miscanthi", 4993: "Bensingtonia naganoensis", 4995: "Kondoa subrosea", 4996: "Bannozyma yamatoana", 4997: "Kondoa yuccicola", 4998: "Kockovaella", 4999: "Kockovaella imperatae", 5000: "Kockovaella thailandica", 5001: "Sporidiobolus", 5002: "Sporobolomyces johnsonii", 5003: "Sporidiobolus pararoseus", 5004: "Rhodosporidiobolus ruineniae", 5005: "Sporidiobolus salmonicolor", 5007: "Brettanomyces bruxellensis", 5008: "Taphrinales", 5009: "Taphrinaceae", 5010: "Taphrina", 5011: "Taphrina deformans", 5012: "Taphrina wiesneri", 5014: "Dothideales", 5015: "Cochliobolus", 5016: "Bipolaris maydis", 5017: "Bipolaris zeicola", 5020: "Phaeosphaeriaceae", 5021: "Leptosphaeria", 5022: "Leptosphaeria maculans", 5023: "Venturiaceae", 5024: "Venturia", 5025: "Venturia inaequalis", 5027: "Pyrenophora", 5028: "Pyrenophora graminea", 5032: "Microstroma", 5033: "Pseudomicrostroma juglandis", 5036: "Histoplasma", 5037: "Histoplasma capsulatum", 5039: "Blastomyces dermatitidis", 5040: "Malbranchea", 5041: "Malbranchea cinnamomea", 5042: "Eurotiales", 5043: "Acremonium", 5044: "Acremonium chrysogenum", 5045: "Acremonium sp. (in: Ascomycota)", 5046: "Sarocladium strictum", 5047: "Epichloe coenophiala", 5050: "Epichloe uncinata", 5051: "Acremonium persicinum", 5052: "Aspergillus", 5053: "Aspergillus aculeatus", 5054: "Aspergillus amstelodami", 5057: "Aspergillus clavatus", 5058: "Aspergillus ficuum", 5059: "Aspergillus flavus", 5060: "Aspergillus giganteus", 5061: "Aspergillus niger", 5062: "Aspergillus oryzae", 5063: "Aspergillus phoenicis", 5064: "Aspergillus restrictus", 5065: "Aspergillus sp.", 5066: "Aspergillus wentii", 5067: "Aspergillus parasiticus", 5068: "Aspergillus tubingensis", 5070: "Aspergillus shirousami", 5071: "Emericella", 5073: "Penicillium", 5074: "Penicillium brevicompactum", 5075: "Penicillium camemberti", 5076: "Penicillium chrysogenum", 5077: "Penicillium citrinum", 5078: "Penicillium griseofulvum", 5079: "Penicillium janthinellum", 5081: "Penicillium sp.", 5082: "Penicillium roqueforti", 5083: "Penicillium canescens", 5086: "Thermoascus", 5087: "Thermoascus aurantiacus", 5088: "Thermoascus crustaceus", 5092: "Byssochlamys", 5093: "Byssochlamys nivea", 5094: "Talaromyces", 5095: "Talaromyces flavus", 5097: "Monascus", 5098: "Monascus purpureus", 5100: "Amorphotheca", 5101: "Amorphotheca resinae", 5103: "Ascosphaeraceae", 5104: "Ascosphaera", 5105: "Ascosphaera apis", 5106: "Verticillium", 5107: "Verticillium sp. (in: Hypocreales)", 5110: "Claviceps", 5111: "Claviceps purpurea", 5112: "Epichloe", 5113: "Epichloe typhina", 5114: "Diaporthales", 5115: "Cryphonectria", 5116: "Cryphonectria parasitica", 5117: "Valsaceae", 5118: "Leucostoma", 5120: "Erysiphales", 5121: "Erysiphe", 5125: "Hypocreales", 5127: "Fusarium fujikuroi", 5128: "Fusarium sambucinum", 5129: "Hypocreaceae", 5130: "Hypomyces", 5131: "Hypomyces chrysospermus", 5132: "Hypomyces rosellus", 5133: "Nectria", 5135: "Phyllachorales", 5136: "Phyllachoraceae", 5139: "Sordariales", 5140: "Neurospora", 5141: "Neurospora crassa", 5142: "Neurospora intermedia", 5143: "Neurospora africana", 5144: "Podospora", 5146: "Sordaria", 5147: "Sordaria macrospora", 5148: "Sordariaceae", 5149: "Chaetomium", 5150: "Chaetomium elatum", 5151: "Ophiostomatales", 5152: "Ophiostomataceae", 5153: "Ceratocystiopsis", 5154: "Ceratocystiopsis alba", 5155: "Cornuvesica falcata", 5157: "Ceratocystis", 5158: "Ceratocystis fimbriata", 5159: "Ophiostoma", 5160: "Ceratocystiopsis collifera", 5161: "Grosmannia crassivaginata", 5162: "Ophiostoma fasciatum", 5163: "Ophiostoma ips", 5164: "Ophiostoma longisporum", 5168: "Ceratocystiopsis parva", 5169: "Ceratocystiopsis ranaculosa", 5170: "Ophiostoma retusum", 5171: "Ophiostoma sp. UM855", 5173: "Sporothrix stenoceras", 5174: "Ophiostoma ulmi", 5175: "Sphaeronaemella", 5176: "Sphaeronaemella fimicola", 5178: "Helotiales", 5179: "Sclerotinia", 5180: "Sclerotinia sclerotiorum", 5181: "Helotiaceae", 5182: "Hymenoscyphus", 5184: "Hymenoscyphus monotropae", 5185: "Pezizales", 5186: "Pezizaceae", 5187: "Aleuria", 5188: "Aleuria aurantia", 5189: "Ascobolaceae", 5190: "Ascobolus", 5191: "Ascobolus immersus", 5192: "Morchellaceae", 5193: "Morchella", 5194: "Morchella conica", 5197: "Lecanorales", 5198: "Cladoniaceae", 5199: "Cladonia", 5200: "Cladonia merochlorophaea", 5201: "Cladonia chlorophaea", 5204: "Basidiomycota", 5206: "Cryptococcus", 5207: "Cryptococcus neoformans", 5208: "Cryptococcus depauperatus", 5209: "Filobasidium", 5210: "Filobasidium floriforme", 5211: "Piskurozyma capsuligena", 5212: "Filobasidium uniguttulatum", 5215: "Tremellaceae", 5217: "Tremella mesenterica", 5218: "Exidia", 5219: "Exidia glandulosa", 5220: "Trimorphomyces", 5221: "Trimorphomyces papilionaceus", 5222: "Phleogenaceae", 5223: "Phleogena", 5224: "Phleogena faginea", 5226: "Auriculariales", 5227: "Auriculariaceae", 5228: "Atractiella", 5229: "Atractiella solani", 5230: "Auricularia", 5233: "Colacogloea peniophorae", 5234: "Tremellales", 5235: "Efibulobasidium", 5236: "Efibulobasidium albescens", 5237: "Tulasnellaceae", 5238: "Thanatephorus", 5240: "Tulasnella", 5241: "Tulasnella violea", 5242: "Uthatobasidium", 5244: "Septobasidiales", 5245: "Septobasidiaceae", 5246: "Septobasidium", 5247: "Septobasidium carestianum", 5250: "Ceratobasidiaceae", 5251: "Ceratobasidium", 5252: "Ceratobasidium cornigerum", 5254: "Dacrymycetaceae", 5255: "Dacrymyces", 5256: "Dacrymyces deliquescens", 5257: "Ustilaginomycetes", 5258: "Pucciniales", 5259: "Melampsoraceae", 5260: "Melampsora", 5261: "Melampsora lini", 5262: "Pucciniaceae", 5263: "Uromyces", 5264: "Uromyces appendiculatus", 5265: "Gymnosporangium", 5266: "Gymnosporangium clavariiforme", 5267: "Ustilaginales", 5268: "Ustilaginaceae", 5269: "Ustilago", 5270: "Ustilago maydis", 5271: "Ustilago sphaerogena", 5272: "Microbotryum violaceum", 5274: "Graphiolaceae", 5275: "Graphiola", 5276: "Graphiola phoenicis", 5277: "Leucosporidium", 5278: "Leucosporidium scottii", 5279: "Tilletiaceae", 5280: "Tilletiaria", 5281: "Tilletiaria anomala", 5286: "Rhodotorula toruloides", 5288: "Rhodotorula diobovata", 5296: "Puccinia", 5297: "Puccinia graminis", 5298: "Puccinia poarum", 5300: "Coleosporium", 5301: "Coleosporium tussilaginis", 5302: "Agaricomycotina", 5303: "Polyporales", 5304: "Corticiaceae", 5305: "Phanerochaete", 5306: "Phanerochaete chrysosporium", 5307: "Phlebia", 5308: "Phlebia radiata", 5309: "Athelia", 5310: "Athelia bombacina", 5314: "Ganoderma", 5315: "Ganoderma lucidum", 5317: "Polyporaceae", 5318: "Irpex", 5319: "Irpex lacteus", 5320: "Pleurotus", 5321: "Pleurotus cornucopiae", 5322: "Pleurotus ostreatus", 5323: "Pleurotus eryngii", 5324: "Trametes", 5325: "Trametes versicolor", 5326: "Coriolus", 5327: "Trametes hirsuta", 5328: "Spongipellis", 5329: "Spongipellis unicolor", 5330: "Bjerkandera", 5331: "Bjerkandera adusta", 5332: "Schizophyllaceae", 5333: "Schizophyllum", 5334: "Schizophyllum commune", 5335: "Schizophyllum sp.", 5336: "Endophyllum", 5337: "Endophyllum sempervivi", 5338: "Agaricales", 5339: "Agaricaceae", 5340: "Agaricus", 5341: "Agaricus bisporus", 5342: "Agaricus edulis", 5343: "Agaricus bitorquis", 5345: "Coprinus", 5346: "Coprinopsis cinerea", 5347: "Coprinellus congregatus", 5350: "Coprinopsis radiata", 5351: "Tricholomataceae", 5352: "Lentinula", 5353: "Lentinula edodes", 5354: "Lentinellus", 5355: "Lentinellus montanus", 5356: "Lentinellus omphalodes", 5357: "Lentinus", 5358: "Lentinus crinitus", 5360: "Neolentinus kauffmanii", 5362: "Neolentinus ponderosus", 5363: "Lentinus strigosus", 5364: "Heliocybe sulcata", 5365: "Lentinus tigrinus", 5367: "Lentinus velutinus", 5368: "Boletaceae", 5369: "Boletus", 5370: "Rubroboletus satanas", 5371: "Paragyrodon", 5372: "Paragyrodon sphaerosporus", 5373: "Phylloporus", 5374: "Phylloporus rhodoxanthus", 5375: "Rhizopogon", 5376: "Rhizopogon subcaerulescens", 5377: "Rhizopogon ochraceorubens", 5379: "Suillus", 5380: "Suillus cavipes", 5381: "Suillus sinuspaulianus", 5382: "Suillus grevillei", 5383: "Suillus spraguei", 5384: "Suillus luteus", 5385: "Xerocomus", 5387: "Gastrosuillus", 5388: "Gastrosuillus luricinus", 5389: "Gomphidiaceae", 5390: "Chroogomphus", 5391: "Chroogomphus vinicolor", 5392: "Gomphidius", 5393: "Gomphidius glutinosus", 5394: "Paxillaceae", 5395: "Paxillus", 5398: "Bolbitiaceae", 5399: "Agrocybe", 5400: "Agrocybe aegerita", 5401: "Russulaceae", 5402: "Russula", 5403: "Russula cyanoxantha", 5404: "Exobasidiales", 5405: "Exobasidiaceae", 5406: "Exobasidium", 5407: "Exobasidium vaccinii", 5408: "Filobasidiaceae", 5410: "Cystofilobasidium", 5411: "Cystofilobasidium bisporidii", 5412: "Cystofilobasidium capitatum", 5413: "Erythrobasidium", 5414: "Erythrobasidium hasegawianum", 5416: "Saitozyma flava", 5417: "Vanrija humicola", 5418: "Papiliotrema laurentii", 5421: "Xanthophyllomyces dendrorhous", 5422: "Kabatiella", 5423: "Kabatiella microsticta", 5426: "Lycoperdaceae", 5427: "Lycoperdon", 5428: "Lycoperdon pyriforme", 5429: "Sporobolomyces", 5432: "Erythrobasidium elongatum", 5433: "Colacogloea falcata", 5434: "Symmetrospora foliicola", 5435: "Symmetrospora gracilis", 5436: "Chrysozyma griseoflava", 5438: "Fellozyma inositophila", 5439: "Buckleyzyma kluyveri-nielii", 5440: "Cystobasidiopsis lactophilus", 5441: "[Sporobolomyces] oryzicola", 5442: "Buckleyzyma phyllomatis", 5443: "Buckleyzyma salicina", 5444: "Ballistosporomyces sasicola", 5445: "Hamamotoa singularis", 5446: "Phyllozyma subbrunnea", 5447: "Slooffia tsugae", 5450: "Arthromyces", 5451: "Agaricales sp. 'Arthromyces ramosus'", 5453: "Ascochyta", 5454: "Ascochyta rabiei", 5455: "Colletotrichum", 5456: "Colletotrichum capsici", 5460: "Colletotrichum caudatum", 5461: "Colletotrichum fuscum", 5462: "Colletotrichum lagenaria", 5463: "Colletotrichum malvarum", 5464: "Colletotrichum musae", 5465: "Colletotrichum orbiculare", 5466: "Colletotrichum trifolii", 5467: "Colletotrichum truncatum", 5468: "Robillarda", 5470: "Robillarda sp.", 5473: "Leptoxyphium", 5474: "Leptoxyphium fumago", 5475: "Candida", 5476: "Candida albicans", 5477: "[Candida] boidinii", 5478: "[Candida] glabrata", 5479: "Candida maltosa", 5480: "Candida parapsilosis", 5481: "Diutina rugosa", 5482: "Candida tropicalis", 5483: "Pseudozyma tsukubaensis", 5486: "Candida viswanathii", 5488: "Wickerhamiella azyma", 5489: "Saturnispora diversa", 5490: "Starmerella magnoliae", 5491: "Candida melibiosica", 5492: "[Candida] rugopelliculosa", 5493: "[Candida] zeylanoides", 5495: "[Candida] nitratophila", 5498: "Cladosporium", 5499: "Passalora fulva", 5500: "Coccidioides", 5501: "Coccidioides immitis", 5502: "Curvularia", 5503: "Curvularia lunata", 5506: "Fusarium", 5507: "Fusarium oxysporum", 5508: "Fusarium oxysporum f. sp. cucumerinum", 5514: "Fusarium sporotrichioides", 5515: "Fusarium acuminatum", 5516: "Fusarium culmorum", 5518: "Fusarium graminearum", 5520: "Microdochium nivale", 5523: "Fusarium lateritium", 5526: "Humicola", 5528: "Humicola grisea var. thermoidea", 5529: "Metarhizium", 5530: "Metarhizium anisopliae", 5531: "Myrothecium", 5533: "Rhodotorula", 5535: "Rhodotorula glutinis", 5537: "Rhodotorula mucilaginosa", 5538: "Scytalidium", 5539: "Scytalidium lignicola", 5540: "Thermomyces", 5541: "Thermomyces lanuginosus", 5543: "Trichoderma", 5544: "Trichoderma harzianum", 5547: "Trichoderma viride", 5548: "Trichoderma longibrachiatum", 5549: "Trichoderma saturnisporum", 5550: "Trichophyton", 5551: "Trichophyton rubrum", 5552: "Trichosporon", 5553: "Trichosporon beigelii", 5554: "Cutaneotrichosporon cutaneum", 5562: "Gloeocercospora", 5566: "Sclerotium hydrophilum", 5569: "Cenococcum", 5570: "Cenococcum geophilum", 5574: "Helicobasidium purpureum", 5575: "Tricharina hiemalis", 5579: "Aureobasidium", 5580: "Aureobasidium pullulans", 5581: "Beauveria", 5583: "Exophiala", 5584: "Exophiala jeanselmei", 5585: "Phaeococcus", 5586: "Phaeococcus exophiales", 5587: "Rhinocladiella", 5588: "Rhinocladiella atrovirens", 5589: "Xylohypha", 5592: "Microascales", 5593: "Microascaceae", 5594: "Microascus", 5595: "Microascus cirrosus", 5596: "Pseudallescheria", 5597: "Scedosporium boydii", 5598: "Alternaria", 5599: "Alternaria alternata", 5600: "Phialophora", 5601: "Phialophora americana", 5605: "Saitoella", 5606: "Saitoella complicata", 5607: "Fellomyces", 5609: "Kockovaella fuzhouensis", 5610: "Fellomyces penicillatus", 5611: "Fellomyces polyborus", 5612: "Kurtzmanomyces", 5613: "Kurtzmanomyces nectairei", 5615: "Sterigmatomyces", 5616: "Sterigmatomyces elviae", 5617: "Sterigmatomyces halophilus", 5618: "Tsuchiyaea", 5619: "Cryptococcus wingfieldii", 5620: "Zygoascus", 5621: "Zygoascus hellenicus", 5624: "Collybia", 5625: "Collybia earleae", 5626: "Grifola", 5627: "Grifola frondosa", 5629: "Laetiporus", 5630: "Laetiporus sulphureus", 5631: "Lenzites", 5632: "Lenzites betulinus", 5633: "Ossicaulis", 5634: "Ossicaulis lignatilis", 5635: "Panellus", 5636: "Panellus stipticus", 5637: "Polyporus", 5639: "Polyporus arcularius", 5640: "Polyporus squamosus", 5641: "Polyporus squamulosus", 5642: "Pycnoporus", 5643: "Trametes cinnabarina", 5644: "Stereum", 5645: "Stereum complicatum", 5647: "Sterigmatosporidium polymorphum", 5653: "Kinetoplastida", 5654: "Trypanosomatidae", 5655: "Crithidia", 5656: "Crithidia fasciculata", 5657: "Strigomonas oncopelti", 5658: "Leishmania", 5659: "Leishmania amazonensis", 5660: "Leishmania braziliensis", 5661: "Leishmania donovani", 5663: "Leishmania enriettii", 5664: "Leishmania major", 5665: "Leishmania mexicana", 5666: "Leishmania tropica", 5667: "Leishmania aethiopica", 5670: "Leishmania guyanensis", 5671: "Leishmania infantum", 5674: "Leishmania adleri", 5677: "Leishmania lainsoni", 5678: "Leishmania naiffi", 5679: "Leishmania panamensis", 5680: "Leishmania shawi", 5681: "Leishmania peruviana", 5682: "Leishmania pifanoi", 5683: "Leptomonas", 5684: "Leptomonas seymouri", 5685: "Leptomonas sp.", 5688: "lizard Leishmania", 5689: "Leishmania tarentolae", 5690: "Trypanosoma", 5691: "Trypanosoma brucei", 5692: "Trypanosoma congolense", 5693: "Trypanosoma cruzi", 5694: "Trypanosoma equiperdum", 5695: "Trypanosoma lewisi", 5696: "Trypanosoma sp.", 5697: "Trypanosoma evansi", 5698: "Trypanosoma rangeli", 5699: "Trypanosoma vivax", 5701: "Trypanosoma simiae", 5702: "Trypanosoma brucei brucei", 5703: "Endotrypanum", 5704: "Endotrypanum schaudinni", 5705: "Endotrypanum monterogeii", 5706: "Phytomonas", 5707: "Phytomonas serpens", 5708: "Bodonidae", 5709: "Trypanoplasma", 5710: "Trypanoplasma borreli", 5712: "Bodo", 5714: "Herpetomonas", 5715: "Herpetomonas samuelpessoai", 5717: "Herpetomonas megaseliae", 5718: "Herpetomonas muscarum", 5719: "Parabasalia", 5721: "Trichomonas", 5722: "Trichomonas vaginalis", 5723: "Tritrichomonas", 5725: "Tritrichomonas augusta", 5726: "Tritrichomonas muris", 5727: "Pentatrichomonas", 5728: "Pentatrichomonas hominis", 5729: "Tetratrichomonas", 5730: "Tetratrichomonas gallinarum", 5731: "Trichomitus", 5732: "Trichomitus batrachorum", 5734: "Hypotrichomonas", 5735: "Hypotrichomonas acosta", 5736: "Monocercomonas", 5737: "Monocercomonas sp.", 5738: "Diplomonadida", 5739: "Hexamitidae", 5740: "Giardia", 5741: "Giardia intestinalis", 5742: "Giardia muris", 5743: "Giardia ardeae", 5744: "Giardia sp.", 5747: "Eustigmatophyceae", 5748: "Nannochloropsis", 5752: "Heterolobosea", 5754: "Acanthamoeba", 5755: "Acanthamoeba castellanii", 5756: "Acanthamoeba sp.", 5757: "Acanthamoeba polyphaga", 5758: "Entamoeba", 5759: "Entamoeba histolytica", 5761: "Naegleria", 5762: "Naegleria gruberi", 5763: "Naegleria fowleri", 5764: "Naegleria andersoni", 5765: "Vahlkampfiidae", 5768: "Tetramitus", 5769: "Tetramitus rostratus", 5770: "Vahlkampfia", 5771: "Vahlkampfia lobospinosa", 5774: "Amoeba", 5775: "Amoeba proteus", 5776: "Hartmannellidae", 5777: "Hartmannella", 5778: "Vermamoeba vermiformis", 5782: "Dictyostelium", 5784: "Dictyostelium sp.", 5785: "Dictyostelium sp. (STRAIN GA11)", 5786: "Dictyostelium purpureum", 5787: "Dictyostelium giganteum", 5789: "Physariida", 5790: "Physarum", 5791: "Physarum polycephalum", 5792: "Didymium", 5793: "Didymium iridis", 5794: "Apicomplexa", 5796: "Coccidia", 5799: "Eimeriidae", 5800: "Eimeria", 5801: "Eimeria acervulina", 5802: "Eimeria tenella", 5803: "Eimeria bovis", 5804: "Eimeria maxima", 5806: "Cryptosporidium", 5807: "Cryptosporidium parvum", 5808: "Cryptosporidium muris", 5809: "Sarcocystidae", 5810: "Toxoplasma", 5811: "Toxoplasma gondii", 5812: "Sarcocystis", 5813: "Sarcocystis muris", 5814: "Sarcocystis gigantea", 5815: "Sarcocystis arieticanis", 5816: "Sarcocystis capracanis", 5817: "Sarcocystis cruzi", 5818: "Sarcocystis tenella", 5819: "Haemosporida", 5820: "Plasmodium", 5821: "Plasmodium berghei", 5823: "Plasmodium berghei ANKA", 5824: "Plasmodium brasilianum", 5825: "Plasmodium chabaudi", 5826: "Plasmodium chabaudi adami", 5827: "Plasmodium cynomolgi", 5828: "Plasmodium cynomolgi strain Berok", 5829: "Plasmodium cynomolgi strain Ceylon", 5830: "Plasmodium cynomolgi strain Gombak", 5831: "Plasmodium cynomolgi strain London", 5832: "Plasmodium cynomolgi strain Mulligan/NIH", 5833: "Plasmodium falciparum", 5834: "Plasmodium falciparum RO-33", 5835: "Plasmodium falciparum CAMP/Malaysia", 5836: "Plasmodium falciparum CDC/Honduras", 5837: "Plasmodium falciparum FC27/Papua New Guinea", 5838: "Plasmodium falciparum FCR-3/Gambia", 5839: "Plasmodium falciparum K1", 5840: "Plasmodium falciparum LE5", 5841: "Plasmodium falciparum Mad20/Papua New Guinea", 5842: "Plasmodium falciparum NF7/Ghana", 5843: "Plasmodium falciparum NF54", 5845: "Plasmodium falciparum FCM17/Senegal", 5846: "Plasmodium falciparum T4/Thailand", 5847: "Plasmodium falciparum V1", 5848: "Plasmodium falciparum isolate WELLCOME", 5849: "Plasmodium gallinaceum", 5850: "Plasmodium knowlesi", 5851: "Plasmodium knowlesi strain H", 5852: "Plasmodium knowlesi strain Nuri", 5853: "Plasmodium lophurae", 5854: "Plasmodium reichenowi", 5855: "Plasmodium vivax", 5857: "Plasmodium fragile", 5858: "Plasmodium malariae", 5859: "Plasmodium simium", 5860: "Plasmodium vinckei", 5861: "Plasmodium yoelii", 5862: "Plasmodium berghei yoelii", 5863: "Piroplasmida", 5864: "Babesia", 5865: "Babesia bovis", 5866: "Babesia bigemina", 5867: "Babesia canis", 5868: "Babesia microti", 5869: "Babesia ovis", 5870: "Babesia rodhaini", 5871: "Babesia caballi", 5872: "Theileria equi", 5873: "Theileria", 5874: "Theileria annulata", 5875: "Theileria parva", 5876: "Theileria buffeli", 5877: "Theileria sergenti", 5878: "Ciliophora", 5882: "Glaucoma", 5883: "Glaucoma chattoni", 5884: "Paramecium", 5885: "Paramecium caudatum", 5886: "Paramecium primaurelia", 5887: "Paramecium sp.", 5888: "Paramecium tetraurelia", 5889: "Paramecium aurelia", 5890: "Tetrahymena", 5891: "Tetrahymena americanis", 5892: "Tetrahymena australis", 5893: "Tetrahymena borealis", 5894: "Tetrahymena canadensis", 5895: "Tetrahymena capricornis", 5896: "Tetrahymena caudata", 5897: "Tetrahymena elliotti", 5898: "Tetrahymena furgasoni", 5899: "Tetrahymena hyperangularis", 5900: "Tetrahymena leucophrys", 5901: "Tetrahymena malaccensis", 5902: "Tetrahymena mimbres", 5903: "Tetrahymena nanneyi", 5905: "Tetrahymena paravorax", 5906: "Tetrahymena patula", 5907: "Tetrahymena pigmentosa", 5908: "Tetrahymena pyriformis", 5909: "Tetrahymena rostrata", 5910: "Tetrahymena sonneborni", 5911: "Tetrahymena thermophila", 5912: "Tetrahymena tropicalis", 5913: "Tetrahymena asiatica", 5914: "Tetrahymena corlissi", 5916: "Tetrahymena limacis", 5917: "Tetrahymena setosa", 5918: "Tetrahymena silvana", 5919: "Tetrahymena vorax", 5921: "Tetrahymena cosmopolitanis", 5922: "Tetrahymena nipissingi", 5923: "Tetrahymena hegewischi", 5926: "Colpidium", 5927: "Dexiostoma campyla", 5928: "Colpidium colpoda", 5931: "Ichthyophthirius", 5932: "Ichthyophthirius multifiliis", 5934: "Hypotrichia", 5935: "Euplotes", 5936: "Moneuplotes crassus", 5938: "Euplotes raikovi", 5939: "Euplotes vannus", 5940: "Euplotes aediculatus", 5941: "Euplotes eurystomus", 5942: "Euplotes woodruffi", 5943: "Oxytricha", 5944: "Oxytricha fallax", 5947: "Oxytricha granulifera", 5948: "Stylonychia", 5949: "Stylonychia lemnae", 5950: "Stylonychia mytilus", 5955: "Uronychia", 5956: "Uronychia sp.", 5957: "Heterotrichida", 5959: "Blepharisma", 5960: "Blepharisma americanum", 5961: "Blepharisma japonicum", 5962: "Stentor", 5963: "Stentor coeruleus", 5964: "Metopus", 5965: "Heterometopus palaeformis", 5970: "Exophiala dermatitidis", 5972: "Halteriidae", 5973: "Halteria", 5974: "Halteria grandinella", 5977: "Colpodea", 5978: "Colpodidae", 5979: "Colpoda", 5980: "Colpoda inflata", 5981: "Bresslaua", 5982: "Bresslaua vorax", 5985: "Isotrichidae", 5986: "Isotricha", 5987: "Isotricha prostoma", 5988: "Litostomatea", 5989: "Haptorida", 5991: "Chaenea", 5992: "Chaenea vorax", 5993: "Enchelys", 5994: "Enchelys pelucida", 5996: "Didinium", 5997: "Didinium nasutum", 6000: "Prostomatea", 6001: "Prorodontida", 6002: "Colepidae", 6003: "Coleps", 6004: "Coleps sp.", 6008: "Loxodes", 6009: "Loxodes striatus", 6013: "Paraurostyla", 6014: "Paraurostyla sp.", 6015: "Nassophorea", 6018: "Pseudomicrothorax", 6019: "Pseudomicrothorax sp.", 6020: "Oligohymenophorea", 6021: "Peritrichia", 6025: "Opisthonecta", 6026: "Opisthonecta henneguyi", 6027: "Onychodromus", 6028: "Onychodromus quadricornutus", 6029: "Microsporidia", 6032: "Apansporoblastina", 6033: "Encephalitozoon", 6035: "Encephalitozoon cuniculi", 6036: "Pansporoblastina", 6037: "Burenellidae", 6038: "Vairimorpha", 6039: "Vairimorpha necatrix", 6040: "Porifera", 6042: "Demospongiae", 6045: "Geodiidae", 6046: "Geodia", 6047: "Geodia cydonium", 6049: "Haplosclerida", 6050: "Spongillidae", 6051: "Ephydatia", 6052: "Ephydatia muelleri", 6054: "Spongilla", 6055: "Spongilla lacustris", 6056: "Chalinidae", 6057: "Haliclona", 6058: "Haliclona oculata", 6060: "Halichondriidae", 6061: "Halichondria", 6062: "Halichondria japonica", 6063: "Halichondria panicea", 6065: "Hymeniacidon", 6068: "Dictyonella", 6069: "Dictyonella incisa", 6070: "Spongosorites", 6071: "Spongosorites genitrix", 6072: "Eumetazoa", 6073: "Cnidaria", 6074: "Hydrozoa", 6077: "Corynidae", 6078: "Sarsia", 6079: "Sarsia sp.", 6080: "Hydridae", 6082: "Hydra viridissima", 6083: "Hydra", 6086: "Hydra sp.", 6087: "Hydra vulgaris", 6088: "Hydra oligactis", 6089: "Polyorchidae", 6090: "Polyorchis", 6091: "Polyorchis penicillatus", 6092: "Spirocodon", 6093: "Spirocodon saltatrix", 6094: "Hydractiniidae", 6095: "Podocoryna", 6096: "Podocoryna carnea", 6098: "Campanulinidae", 6099: "Aequorea", 6100: "Aequorea victoria", 6101: "Anthozoa", 6102: "Hexacorallia", 6103: "Actiniaria", 6104: "Actinia", 6105: "Actinia tenebrosa", 6106: "Actinia equina", 6107: "Anemonia", 6108: "Anemonia sulcata", 6109: "Anthopleura", 6110: "Anthopleura elegantissima", 6111: "Anthopleura fuscoviridis", 6112: "Anthopleura xanthogrammica", 6113: "Calliactis", 6114: "Calliactis parasitica", 6115: "Metridium", 6116: "Metridium senile", 6118: "Entacmaea quadricolor", 6120: "Heteractis sp.", 6122: "Stichodactyla", 6123: "Stichodactyla helianthus", 6124: "Stichodactyla sp.", 6125: "Scleractinia", 6126: "Acroporidae", 6127: "Acropora", 6129: "Acropora latistella", 6130: "Acropora cervicornis", 6131: "Acropora palmata", 6132: "Octocorallia", 6133: "Pennatulacea", 6134: "Renilla", 6135: "Renilla koellikeri", 6136: "Renilla reniformis", 6137: "Cubozoa", 6139: "Carybdeidae", 6140: "Tripedalia", 6141: "Tripedalia cystophora", 6142: "Scyphozoa", 6143: "Semaeostomeae", 6144: "Aurelia", 6145: "Aurelia aurita", 6146: "Pelagiidae", 6147: "Chrysaora", 6148: "Chrysaora quinquecirrha", 6149: "Nemopsis", 6150: "Nemopsis dofleini", 6151: "Eunicella", 6152: "Eunicella stricta", 6153: "Forskalia", 6154: "Forskalia edwardsi", 6157: "Platyhelminthes", 6159: "Tricladida", 6160: "Dugesia", 6161: "Dugesia japonica", 6162: "Girardia tigrina", 6163: "Polycladida", 6166: "Planoceridae", 6167: "Planocera", 6168: "Planocera reticulata", 6169: "Lecithoepitheliata", 6170: "Prorhynchidae", 6171: "Geocentrophora", 6172: "Geocentrophora baltica", 6173: "Geocentrophora incognita", 6174: "Geocentrophora intersticialis", 6175: "Geocentrophora porfirievae", 6176: "Geocentrophora sphyrocephala", 6177: "Geocentrophora wasiliewi", 6178: "Trematoda", 6179: "Digenea", 6180: "Strigeidida", 6181: "Schistosoma", 6182: "Schistosoma japonicum", 6183: "Schistosoma mansoni", 6184: "Schistosoma bovis", 6185: "Schistosoma haematobium", 6186: "Schistosoma curassoni", 6187: "Schistosoma intercalatum", 6188: "Schistosoma rodhaini", 6189: "Schistosoma spindale", 6191: "Fasciola", 6192: "Fasciola hepatica", 6193: "Opisthorchiida", 6194: "Opisthorchiata", 6196: "Opisthorchiidae", 6197: "Opisthorchis", 6198: "Opisthorchis viverrini", 6199: "Cestoda", 6200: "Eucestoda", 6201: "Cyclophyllidea", 6202: "Taenia", 6203: "Taenia ovis", 6204: "Taenia solium", 6205: "Hydatigera taeniaeformis", 6206: "Taenia saginata", 6207: "Taenia crassiceps", 6208: "Taeniidae", 6209: "Echinococcus", 6210: "Echinococcus granulosus", 6211: "Echinococcus multilocularis", 6212: "Echinococcus oligarthrus", 6213: "Echinococcus vogeli", 6214: "Hymenolepididae", 6215: "Hymenolepis", 6216: "Hymenolepis diminuta", 6217: "Nemertea", 6218: "Pilidiophora", 6219: "Heteronemertea", 6220: "Cerebratulus", 6221: "Cerebratulus lacteus", 6222: "Lineidae", 6223: "Lineus", 6225: "Enopla", 6226: "Hoplonemertea", 6227: "Monostilifera", 6228: "Emplectonematidae", 6229: "Emplectonema", 6230: "Emplectonema gracile", 6231: "Nematoda", 6232: "Panagrellus", 6233: "Panagrellus redivivus", 6234: "Panagrellus silusiae", 6236: "Rhabditida", 6237: "Caenorhabditis", 6238: "Caenorhabditis briggsae", 6239: "Caenorhabditis elegans", 6243: "Rhabditidae", 6244: "Rhabditis", 6245: "Rhabditis tokai", 6246: "Strongyloididae", 6247: "Strongyloides", 6248: "Strongyloides stercoralis", 6249: "Ascaridomorpha", 6250: "Ascarididae", 6251: "Ascaris", 6252: "Ascaris lumbricoides", 6253: "Ascaris suum", 6254: "Parascaris", 6255: "Parascaris sp.", 6256: "Parascaris equorum", 6257: "Parascaris univalens", 6258: "Baylisascaris", 6259: "Baylisascaris procyonis", 6260: "Baylisascaris transfuga", 6261: "Heterocheilus", 6262: "Heterocheilus tunicatus", 6264: "Toxocara", 6265: "Toxocara canis", 6266: "Toxocara cati", 6267: "Anisakidae", 6268: "Anisakis", 6269: "Anisakis simplex", 6270: "Pseudoterranova", 6271: "Pseudoterranova decipiens", 6272: "Terranova", 6273: "Terranova caballeroi", 6274: "Spirurina", 6276: "Acanthocheilonema", 6277: "Acanthocheilonema viteae", 6278: "Brugia", 6279: "Brugia malayi", 6280: "Brugia pahangi", 6281: "Onchocerca", 6282: "Onchocerca volvulus", 6283: "Onchocerca gutturosa", 6284: "Onchocerca gibsoni", 6285: "Onchocerca microfilariae", 6286: "Dirofilaria", 6287: "Dirofilaria immitis", 6288: "Haemonchus", 6289: "Haemonchus contortus", 6290: "Haemonchus placei", 6291: "Haemonchus similis", 6292: "Wuchereria", 6293: "Wuchereria bancrofti", 6295: "Filarioidea", 6296: "Onchocercidae", 6298: "Litomosoides", 6299: "Litomosoides carinii", 6300: "Tylenchina", 6301: "Heteroderidae", 6303: "Meloidogyne javanica", 6304: "Meloidogyne arenaria", 6305: "Meloidogyne hapla", 6306: "Meloidogyne incognita", 6308: "Strongylida", 6310: "Metastrongyloidea", 6312: "Angiostrongylus", 6313: "Angiostrongylus cantonensis", 6314: "Trichostrongyloidea", 6315: "Trichostrongylidae", 6316: "Ostertagia", 6317: "Ostertagia ostertagi", 6318: "Trichostrongylus", 6319: "Trichostrongylus colubriformis", 6324: "Bursaphelenchus", 6325: "Bursaphelenchus mucronatus", 6326: "Bursaphelenchus xylophilus", 6329: "Trichinellida", 6332: "Trichinellidae", 6333: "Trichinella", 6334: "Trichinella spiralis", 6335: "Trichinella nativa", 6336: "Trichinella nelsoni", 6337: "Trichinella pseudospiralis", 6338: "Heligmosomoides", 6339: "Heligmosomoides polygyrus", 6340: "Annelida", 6341: "Polychaeta", 6342: "Capitellida", 6343: "Arenicola", 6344: "Arenicola marina", 6346: "Owenia", 6347: "Owenia fusiformis", 6348: "Phyllodocida", 6349: "Glycera", 6350: "Glycera dibranchiata", 6351: "Nereis", 6354: "Perinereis", 6355: "Perinereis vancaurica", 6356: "Perinereis brevicirris", 6357: "Perinereis vancaurica tetradentata", 6358: "Platynereis", 6359: "Platynereis dumerilii", 6360: "Tylorrhynchus", 6361: "Tylorrhynchus heterochaetus", 6362: "Sabellida", 6363: "Eudistylia", 6364: "Eudistylia vancouveri", 6366: "Sabellidae", 6367: "Sabellastarte", 6368: "Sabellastarte japonica", 6373: "Terebellida", 6374: "Ampharetidae", 6375: "Alvinella", 6376: "Alvinella pompejana", 6378: "Chaetopteridae", 6379: "Chaetopterus", 6380: "Chaetopterus sp. 1 Woods Hole MA", 6381: "Oligochaeta", 6382: "Haplotaxida", 6383: "Tubificina", 6385: "Tubifex", 6386: "Tubifex tubifex", 6388: "Enchytraeidae", 6389: "Enchytraeus", 6390: "Enchytraeus albidus", 6391: "Lumbricina", 6392: "Lumbricidae", 6393: "Eisenia", 6395: "Eisenia bicyclis", 6396: "Eisenia fetida", 6397: "Lumbricus", 6398: "Lumbricus terrestris", 6399: "Lumbricus sp.", 6400: "Megascolecidae", 6401: "Pheretima", 6404: "Macrobdella", 6405: "Macrobdella decora", 6406: "Rhynchobdellida", 6407: "Glossiphoniidae", 6408: "Haementeria", 6409: "Haementeria ghilianii", 6410: "Haementeria officinalis", 6411: "Helobdella", 6412: "Helobdella robusta", 6413: "Helobdella triserialis", 6414: "Placobdella", 6415: "Placobdella ornata", 6416: "Hirudiniformes", 6417: "Hirudinidae", 6418: "Hirudinaria", 6420: "Hirudo", 6421: "Hirudo medicinalis", 6423: "Lamellibrachia", 6424: "Lamellibrachia sp.", 6425: "Riftia", 6426: "Riftia pachyptila", 6427: "Echiura", 6428: "Xenopneusta", 6429: "Urechidae", 6430: "Urechis", 6431: "Urechis caupo", 6432: "Urechis unicinctus", 6433: "Sipuncula", 6434: "Golfingiidae", 6435: "Themiste", 6436: "Themiste dyscritum", 6438: "Golfingia", 6440: "Sipunculidae", 6441: "Phascolopsis", 6442: "Phascolopsis gouldii", 6443: "Siphonosoma", 6444: "Siphonosoma cumanense", 6445: "Sipunculus", 6446: "Sipunculus nudus", 6447: "Mollusca", 6448: "Gastropoda", 6451: "Haliotidae", 6452: "Haliotis", 6453: "Haliotis corrugata", 6454: "Haliotis rufescens", 6455: "Haliotis cracherodii", 6456: "Haliotis fulgens", 6457: "Haliotis kamtschatkana", 6458: "Haliotis sorenseni", 6459: "Haliotis walallensis", 6462: "Patellidae", 6463: "Patella", 6465: "Patella vulgata", 6466: "Trochidae", 6467: "Tegula", 6470: "Potamididae", 6471: "Cerithidea", 6472: "Cerithidea rhizophorarum", 6475: "Ampullarioidea", 6476: "Bithyniidae", 6477: "Bithynia", 6478: "Bithynia tentaculata", 6479: "Neogastropoda", 6480: "Melongenidae", 6481: "Busycon", 6483: "Nassariidae", 6484: "Nassarius", 6486: "Fasciolariidae", 6487: "Fusinus", 6488: "Fusinus ferrugineus", 6489: "Conidae", 6490: "Conus", 6491: "Conus geographus", 6492: "Conus magus", 6493: "Conus striatus", 6494: "Conus textile", 6495: "Conus tulipa", 6496: "Euopisthobranchia", 6497: "Aplysiida", 6498: "Aplysiidae", 6499: "Aplysia", 6500: "Aplysia californica", 6501: "Aplysia kurodai", 6502: "Aplysia limacina", 6503: "Aplysia parvula", 6504: "Aplysia sp.", 6506: "Aplysia juliana", 6507: "Bursatella", 6508: "Bursatella leachii", 6510: "Dolabella", 6511: "Dolabella auricularia", 6512: "Gymnosomata", 6514: "Eudoridoidea", 6515: "Discodorididae", 6521: "Lymnaeidae", 6522: "Lymnaea", 6523: "Lymnaea stagnalis", 6524: "Planorbidae", 6525: "Biomphalaria", 6526: "Biomphalaria glabrata", 6527: "Stylommatophora", 6528: "Achatinidae", 6529: "Achatina", 6530: "Achatina fulica", 6531: "Limicolaria", 6532: "Limicolaria kambeul", 6533: "Helicidae", 6534: "Helix", 6535: "Helix aspersa", 6536: "Helix pomatia", 6540: "Arionidae", 6542: "Arion", 6543: "Arion rufus", 6544: "Bivalvia", 6545: "Pteriomorphia", 6546: "Mytiloida", 6547: "Mytilidae", 6548: "Mytilus", 6549: "Mytilus californianus", 6550: "Mytilus edulis", 6551: "Mytilus trossulus", 6552: "Arcoida", 6553: "Arcidae", 6554: "Anadara", 6556: "Anadara trapezia", 6557: "Barbatia", 6558: "Barbatia reeveana", 6559: "Barbatia virescens", 6560: "Scapharca", 6561: "Scapharca inaequivalvis", 6562: "Ostreoida", 6563: "Ostreidae", 6564: "Crassostrea", 6565: "Crassostrea virginica", 6566: "Pectinidae", 6569: "Chlamys", 6570: "Chlamys nipponensis", 6571: "Chlamys nipponensis akazara", 6572: "Patinopecten", 6573: "Mizuhopecten yessoensis", 6574: "Patinopecten sp.", 6576: "Placopecten", 6577: "Placopecten magellanicus", 6578: "Pecten", 6579: "Pecten maximus", 6580: "Veneroida", 6581: "Mactridae", 6582: "Spisula", 6584: "Spisula solidissima", 6585: "Solenidae", 6586: "Ensis", 6587: "Ensis minor", 6588: "Vesicomyidae", 6589: "Calyptogena", 6591: "Calyptogena magnifica", 6592: "Veneridae", 6593: "Macrocallista", 6594: "Macrocallista nimbosa", 6595: "Mercenaria", 6596: "Mercenaria mercenaria", 6598: "unidentified clam", 6599: "Heterodonta", 6601: "Myoidea", 6602: "Myidae", 6603: "Mya", 6604: "Mya arenaria", 6605: "Cephalopoda", 6606: "Coleoidea", 6608: "Sepiidae", 6609: "Sepia", 6610: "Sepia officinalis", 6612: "Euprymna", 6613: "Euprymna scolopes", 6615: "Loliginidae", 6616: "Loligo", 6618: "Loligo forbesii", 6622: "Loligo vulgaris", 6623: "Enoploteuthidae", 6624: "Watasenia", 6625: "Watasenia scintillans", 6626: "Ommastrephidae", 6627: "Illex", 6628: "Illex argentinus", 6629: "Illex illecebrosus", 6630: "Nototodarus", 6631: "Nototodarus gouldi", 6632: "Ommastrephes", 6636: "Todarodes", 6637: "Todarodes pacificus", 6638: "Octopoda", 6639: "Eledone", 6641: "Eledone moschata", 6643: "Octopus", 6645: "Octopus vulgaris", 6646: "Incirrata", 6647: "Octopodidae", 6650: "Polyplacophora", 6651: "Neoloricata", 6652: "Chitonida", 6653: "Acanthochitonidae", 6654: "Cryptochiton", 6655: "Cryptochiton stelleri", 6656: "Arthropoda", 6657: "Crustacea", 6658: "Branchiopoda", 6659: "Anostraca", 6660: "Artemia", 6661: "Artemia franciscana", 6662: "Artemia sp.", 6663: "Artemia parthenogenetica", 6665: "Cladocera", 6668: "Daphnia", 6669: "Daphnia pulex", 6670: "Ostracoda", 6671: "Myodocopa", 6672: "Cypridinidae", 6673: "Vargula", 6674: "Vargula hilgendorfii", 6675: "Cirripedia", 6676: "Thoracica", 6677: "Balanus", 6678: "Balanus nubilus", 6679: "Megabalanus", 6680: "Megabalanus rosa", 6681: "Malacostraca", 6682: "Eucarida", 6683: "Decapoda", 6684: "Dendrobranchiata", 6685: "Penaeidae", 6687: "Penaeus monodon", 6688: "Penaeus sp.", 6689: "Penaeus vannamei", 6690: "Penaeus aztecus", 6692: "Pleocyemata", 6693: "lobster", 6694: "Caridea", 6695: "Palaemonidae", 6696: "Macrobrachium", 6697: "Macrobrachium malcolmsonii", 6700: "Palaemon kadiakensis", 6701: "Pandalidae", 6702: "Pandalus", 6703: "Pandalus borealis", 6704: "Nephropidae", 6705: "Homarus", 6706: "Homarus americanus", 6707: "Homarus gammarus", 6709: "Procarididae", 6710: "Procaris", 6711: "Procaris ascensionis", 6712: "Astacidea", 6713: "Astacidae", 6714: "Astacus", 6715: "Astacus astacus", 6717: "Astacus leptodactylus", 6719: "Pacifastacus", 6720: "Pacifastacus leniusculus", 6722: "Cherax", 6723: "Cherax destructor", 6724: "Astacoidea", 6725: "Cambaridae", 6726: "Procambarus", 6727: "Procambarus leonensis", 6728: "Procambarus clarkii", 6729: "Procambarus bouvieri", 6730: "Achelata", 6731: "Palinuridae", 6732: "Palinurus", 6733: "Palinurus vulgaris", 6734: "Panulirus", 6735: "Panulirus interruptus", 6736: "Panulirus japonicus", 6737: "Panulirus argus", 6738: "Anomura", 6739: "Lithodidae", 6740: "Paralithodes", 6741: "Paralithodes camtschaticus", 6742: "Oedignathus", 6743: "Oedignathus inermis", 6744: "Paguroidea", 6745: "Paguridae", 6746: "Pagurus", 6747: "Pagurus pollicaris", 6749: "Diogenidae", 6750: "Clibanarius", 6751: "Clibanarius vittatus", 6752: "Brachyura", 6753: "Cancridae", 6754: "Cancer", 6755: "Cancer pagurus", 6756: "Cancer irroratus", 6757: "Portunidae", 6758: "Carcinus", 6759: "Carcinus maenas", 6760: "Scylla", 6761: "Scylla serrata", 6762: "Callinectes", 6763: "Callinectes sapidus", 6764: "Gecarcinidae", 6765: "Cardisoma", 6766: "Cardisoma carnifex", 6767: "Cardisoma guanhumi", 6768: "Gecarcinus", 6769: "Gecarcinus lateralis", 6770: "Ocypodidae", 6771: "Leptuca", 6772: "Leptuca pugilator", 6774: "Portunoidea", 6775: "Geryonidae", 6776: "Geryon", 6778: "Xanthoidea", 6779: "Xanthidae", 6780: "Menippe", 6781: "Menippe mercenaria", 6782: "Dromiacea", 6783: "Dromioidea", 6784: "Dromiidae", 6785: "Dromidia", 6786: "Dromidia antillensis", 6787: "Hypoconcha", 6788: "Hypoconcha arcuata", 6789: "Raninoidea", 6790: "Raninidae", 6791: "Ranilia", 6792: "Ranilia muricata", 6793: "Raninoides", 6794: "Raninoides louisianensis", 6796: "Leucosioidea", 6797: "Calappidae", 6798: "Hepatus", 6799: "Hepatus epheliticus", 6800: "Leucosiidae", 6801: "Iliacantha", 6802: "Iliacantha subglobosa", 6804: "Majoidea", 6805: "Majidae", 6806: "Libinia", 6807: "Libinia emarginata", 6808: "Parthenopoidea", 6809: "Parthenopidae", 6810: "Parthenope", 6811: "Parthenope serrata", 6812: "Stenopodidea", 6813: "Stenopodidae", 6814: "Stenopus", 6815: "Stenopus hispidus", 6816: "Euphausiacea", 6817: "Euphausiidae", 6818: "Euphausia", 6819: "Euphausia superba", 6820: "Peracarida", 6821: "Amphipoda", 6825: "Parascelidae", 6826: "Euscelis", 6827: "Euscelis plebejus", 6828: "Nephrops", 6829: "Nephrops norvegicus", 6830: "Copepoda", 6831: "Tigriopus", 6832: "Tigriopus californicus", 6833: "Calanoida", 6835: "Calanidae", 6836: "Calanus", 6837: "Calanus finmarchicus", 6838: "Branchiura", 6839: "Arguloida", 6840: "Argulidae", 6842: "Argulus nobilis", 6843: "Chelicerata", 6844: "Merostomata", 6845: "Xiphosura", 6846: "Limulidae", 6847: "Carcinoscorpius", 6848: "Carcinoscorpius rotundicauda", 6849: "Limulus", 6850: "Limulus polyphemus", 6851: "Tachypleus", 6852: "Tachypleus gigas", 6853: "Tachypleus tridentatus", 6854: "Arachnida", 6855: "Scorpiones", 6856: "Buthidae", 6857: "Androctonus", 6858: "Androctonus australis", 6859: "Androctonus mauritanicus", 6860: "Androctonus mauritanicus mauritanicus", 6862: "Hottentotta", 6863: "Hottentotta judaicus", 6865: "Buthus", 6868: "Buthus occitanus", 6869: "Buthus occitanus mardochei", 6870: "Buthus occitanus occitanus", 6871: "Buthus occitanus tunetanus", 6875: "Centruroides", 6876: "Centruroides limpidus", 6878: "Centruroides noxius", 6879: "Centruroides exilicauda", 6880: "Centruroides suffusus", 6881: "Centruroides suffusus suffusus", 6882: "Leiurus", 6883: "Leiurus quinquestriatus", 6884: "Leiurus quinquestriatus hebraeus", 6885: "Leiurus quinquestriatus quinquestriatus", 6886: "Tityus", 6887: "Tityus serrulatus", 6888: "Scorpionidae", 6889: "Urodacus", 6890: "Urodacus hoplurus", 6891: "Orthochirus", 6892: "Orthochirus scrobiculosus", 6893: "Araneae", 6894: "Mygalomorphae", 6895: "Theraphosidae", 6896: "Aphonopelma", 6899: "Aphonopelma chalcodes", 6901: "Hexathelidae", 6902: "Atrax", 6903: "Atrax robustus", 6904: "Hadronyche versuta", 6905: "Araneomorphae", 6906: "Agelenidae", 6907: "Agelenopsis", 6908: "Agelenopsis aperta", 6909: "Hololena", 6910: "Hololena curta", 6913: "Araneidae", 6914: "Nephila", 6916: "Ctenidae", 6917: "Phoneutria", 6918: "Phoneutria nigriventer", 6919: "Sicariidae", 6920: "Loxosceles", 6921: "Loxosceles reclusa", 6923: "Latrodectus", 6924: "Latrodectus mactans", 6925: "Latrodectus tredecimguttatus", 6927: "Cupiennius", 6928: "Cupiennius salei", 6930: "Pholcidae", 6931: "Pholcus", 6932: "Pholcus phalangioides", 6933: "Acari", 6934: "Parasitiformes", 6935: "Ixodida", 6936: "Argasidae", 6937: "Ornithodoros", 6938: "Ornithodoros moubata", 6939: "Ixodidae", 6940: "Boophilus", 6941: "Rhipicephalus microplus", 6942: "Amblyomma", 6943: "Amblyomma americanum", 6944: "Ixodes", 6945: "Ixodes scapularis", 6946: "Acariformes", 6947: "Prostigmata", 6948: "Pyemotidae", 6949: "Pyemotes", 6950: "Pyemotes tritici", 6951: "Astigmata", 6952: "Pyroglyphidae", 6953: "Dermatophagoides", 6954: "Dermatophagoides farinae", 6955: "Dermatophagoides microceras", 6956: "Dermatophagoides pteronyssinus", 6957: "Euroglyphus", 6958: "Euroglyphus maynei", 6960: "Hexapoda", 6961: "Odonata", 6962: "Anisoptera", 6964: "Libellulidae", 6965: "Libellula", 6966: "Libellula auripennis", 6967: "Libellula pulchella", 6968: "Sympetrum", 6969: "Sympetrum striolatum", 6970: "Dictyoptera", 6972: "Blattella", 6973: "Blattella germanica", 6974: "Blattidae", 6975: "Blatta", 6976: "Blatta orientalis", 6977: "Periplaneta", 6978: "Periplaneta americana", 6979: "Blaberidae", 6980: "Blaberus", 6981: "Blaberus discoidalis", 6982: "Blaberus craniifer", 6983: "Diploptera", 6984: "Diploptera punctata", 6989: "Nauphoeta", 6990: "Nauphoeta cinerea", 6993: "Orthoptera", 6994: "Ensifera", 6995: "Gryllidae", 6996: "Acheta", 6997: "Acheta domesticus", 6998: "Gryllus", 6999: "Gryllus bimaculatus", 7000: "Gryllus firmus", 7001: "Caelifera", 7002: "Acrididae", 7003: "Locusta", 7004: "Locusta migratoria", 7005: "Locusta migratoria migratorioides", 7006: "Romalea", 7007: "Romalea microptera", 7008: "Schistocerca", 7009: "Schistocerca americana", 7010: "Schistocerca gregaria", 7011: "Schistocerca nitens", 7013: "Caledia", 7014: "Caledia captiva", 7018: "Stauroderus", 7019: "Stauroderus scalaris", 7020: "Phasmatodea", 7021: "Carausius", 7022: "Carausius morosus", 7023: "Extatosoma", 7024: "Extatosoma tiaratum", 7028: "Acyrthosiphon", 7029: "Acyrthosiphon pisum", 7030: "Acyrthosiphon magnoliae", 7033: "Cicadidae", 7034: "Tibicen", 7035: "Tibicen sp. JLJ-1991", 7036: "Aleyrodidae", 7037: "Bemisia", 7038: "Bemisia tabaci", 7039: "Siphoninus", 7040: "Siphoninus phillyreae", 7041: "Coleoptera", 7042: "Curculionidae", 7043: "Anthonomus", 7044: "Anthonomus grandis", 7045: "Sitophilus", 7046: "Sitophilus granarius", 7047: "Sitophilus zeamais", 7048: "Sitophilus oryzae", 7049: "Lampyridae", 7050: "Luciola", 7051: "Luciola cruciata", 7052: "Aquatica lateralis", 7053: "Photinus", 7054: "Photinus pyralis", 7055: "Scarabaeidae", 7056: "Cetoniinae", 7057: "Pachnoda", 7058: "Pachnoda marginata", 7059: "Melolonthinae", 7060: "Melolontha", 7061: "Melolontha melolontha", 7062: "Rutelinae", 7063: "Popillia", 7064: "Popillia japonica", 7065: "Tenebrionidae", 7066: "Tenebrio", 7067: "Tenebrio molitor", 7069: "Tribolium", 7070: "Tribolium castaneum", 7071: "Tribolium confusum", 7072: "Tribolium freemani", 7073: "Zophobas", 7074: "Zophobas atratus", 7076: "Palorus", 7077: "Palorus ratzeburgii", 7080: "Coccinellidae", 7081: "Coccinellinae", 7083: "Adalia", 7084: "Adalia bipunctata", 7085: "Polyphaga aegyptiaca", 7086: "Geotrupes", 7088: "Lepidoptera", 7089: "Bombycidae", 7090: "Bombyx", 7091: "Bombyx mori", 7092: "Bombyx mandarina", 7096: "Lasiocampidae", 7097: "Malacosoma", 7098: "Malacosoma neustria", 7099: "Malacosoma americanum", 7100: "Noctuidae", 7101: "Heliothis", 7102: "Heliothis virescens", 7106: "Spodoptera", 7107: "Spodoptera exigua", 7108: "Spodoptera frugiperda", 7109: "Spodoptera littoralis", 7110: "Trichoplusia", 7111: "Trichoplusia ni", 7112: "Helicoverpa", 7113: "Helicoverpa zea", 7114: "Pieridae", 7115: "Pieris", 7116: "Pieris brassicae", 7117: "Saturniidae", 7118: "Antheraea", 7119: "Antheraea pernyi", 7120: "Antheraea polyphemus", 7121: "Antheraea yamamai", 7122: "Hyalophora", 7123: "Hyalophora cecropia", 7124: "Lonomia", 7125: "Lonomia achelous", 7126: "Samia", 7127: "Samia cynthia", 7128: "Sphingidae", 7129: "Manduca", 7130: "Manduca sexta", 7135: "Pyralidae", 7136: "Galleria", 7137: "Galleria mellonella", 7139: "Tortricidae", 7140: "Choristoneura", 7141: "Choristoneura fumiferana", 7143: "Papilionidae", 7145: "Papilio", 7146: "Papilio polyxenes", 7147: "Diptera", 7148: "Nematocera", 7149: "Chironomidae", 7150: "Chironomus", 7151: "Chironomus pallidivittatus", 7152: "Chironomus sp.", 7153: "Chironomus tentans", 7154: "Chironomus thummi", 7155: "Chironomus thummi thummi", 7156: "Chironomus piger", 7157: "Culicidae", 7158: "Aedes", 7159: "Aedes aegypti", 7160: "Aedes albopictus", 7161: "Aedes simpsoni", 7162: "Ochlerotatus triseriatus", 7163: "Aedes vexans", 7164: "Anopheles", 7165: "Anopheles gambiae", 7166: "Anopheles quadrimaculatus", 7167: "Anopheles albimanus", 7168: "Anopheles dirus", 7170: "Anopheles freeborni", 7171: "Anopheles hermsi", 7172: "Anopheles occidentalis", 7173: "Anopheles arabiensis", 7174: "Culex", 7175: "Culex pipiens", 7176: "Culex quinquefasciatus", 7177: "Culex tarsalis", 7178: "Culex tritaeniorhynchus", 7180: "Haemagogus", 7181: "Haemagogus mesodentatus", 7182: "Psorophora", 7183: "Psorophora ferox", 7184: "Sciaridae", 7185: "Rhynchosciara", 7186: "Rhynchosciara americana", 7190: "Simuliidae", 7191: "Simulium", 7192: "Simulium vittatum", 7193: "Simulium decorum", 7194: "Simulium venustum", 7197: "Psychodidae", 7198: "Phlebotominae", 7199: "Lutzomyia", 7200: "Lutzomyia longipalpis", 7201: "Psychoda", 7202: "Psychoda cinerea", 7203: "Brachycera", 7205: "Tabanidae", 7206: "Tabanus", 7207: "Tabanus atratus", 7208: "Loa", 7209: "Loa loa", 7211: "Tephritidae", 7212: "Ceratitis", 7213: "Ceratitis capitata", 7214: "Drosophilidae", 7215: "Drosophila", 7216: "Drosophila ambigua", 7217: "Drosophila ananassae", 7218: "Drosophila bifasciata", 7219: "Drosophila differens", 7220: "Drosophila erecta", 7221: "Drosophila funebris", 7222: "Drosophila grimshawi", 7224: "Drosophila hydei", 7225: "Scaptodrosophila lebanonensis", 7226: "Drosophila mauritiana", 7227: "Drosophila melanogaster", 7228: "Drosophila mettleri", 7229: "Drosophila miranda", 7230: "Drosophila mojavensis", 7231: "Drosophila mulleri", 7232: "Drosophila navojoa", 7233: "Drosophila orena", 7234: "Drosophila persimilis", 7235: "Drosophila picticornis", 7236: "Drosophila planitibia", 7237: "Drosophila pseudoobscura", 7238: "Drosophila sechellia", 7239: "Drosophila subsilvestris", 7240: "Drosophila simulans", 7241: "Drosophila subobscura", 7242: "Drosophila sp. (in: Insecta)", 7243: "Drosophila teissieri", 7244: "Drosophila virilis", 7245: "Drosophila yakuba", 7246: "Drosophila affinis", 7247: "Drosophila algonquin", 7248: "Drosophila athabasca", 7249: "Drosophila azteca", 7250: "Drosophila immigrans", 7251: "Drosophila lowei", 7252: "Drosophila melanica", 7253: "Drosophila mercatorum", 7254: "Drosophila narragansett", 7255: "Hirtodrosophila pictiventris", 7256: "Drosophila pinicola", 7257: "Drosophila robusta", 7258: "Drosophila stonei", 7259: "Drosophila tolteca", 7260: "Drosophila willistoni", 7261: "Drosophila adiastola", 7262: "Drosophila affinidisjuncta", 7263: "Drosophila arizonae", 7264: "Drosophila buzzatii", 7266: "Drosophila guanche", 7267: "Drosophila gymnobasis", 7268: "Drosophila mayaguana", 7269: "Drosophila mediostriata", 7270: "Drosophila mimica", 7271: "Drosophila nebulosa", 7272: "Drosophila nigra", 7273: "Drosophila saltans", 7274: "Drosophila serrata", 7275: "Drosophila silvarentis", 7277: "Drosophila wheeleri", 7278: "Drosophila bromeliae", 7279: "Drosophila falleni", 7280: "Drosophila kitumensis", 7281: "Drosophila microlabis", 7282: "Drosophila obscura", 7283: "Drosophila phalerata", 7284: "Drosophila tristis", 7287: "Drosophila cilifemorata", 7289: "Drosophila sproati", 7290: "Drosophila stigma", 7291: "Drosophila albomicans", 7292: "Chymomyza", 7293: "Chymomyza amoena", 7294: "Liodrosophila", 7295: "Liodrosophila aerea", 7296: "Zaprionus", 7297: "Zaprionus tuberculatus", 7298: "Scaptomyza", 7299: "Scaptomyza albovittata", 7300: "Scaptomyza pallida", 7301: "Scaptomyza exigua", 7324: "Hirtodrosophila", 7329: "Leucophenga", 7331: "Lordiphosa", 7337: "Mulgravea", 7338: "Mycodrosophila", 7340: "Neotanygastrella", 7343: "Paraliodrosophila", 7344: "Paramycodrosophila", 7346: "Phorticella", 7353: "Samoaia", 7354: "Scaptodrosophila", 7356: "Sphaerogastrella", 7359: "Styloptera", 7361: "Titanochaeta", 7366: "Muscidae", 7367: "Haematobia", 7368: "Haematobia irritans", 7369: "Musca", 7370: "Musca domestica", 7371: "Calliphoridae", 7372: "Calliphora", 7373: "Calliphora vicina", 7374: "Lucilia", 7375: "Lucilia cuprina", 7376: "Lucilia illustris", 7377: "Phormia", 7380: "Phormia regina", 7381: "Sarcophagidae", 7382: "Boettcherisca", 7384: "Sarcophaga", 7385: "Sarcophaga bullata", 7386: "Sarcophaga peregrina", 7387: "Oestridae", 7388: "Hypoderma", 7389: "Hypoderma lineatum", 7392: "Glossinidae", 7393: "Glossina", 7394: "Glossina morsitans", 7395: "Glossina austeni", 7396: "Glossina fuscipes", 7397: "Glossina palpalis", 7398: "Glossina pallidipes", 7399: "Hymenoptera", 7400: "Apocrita", 7401: "Ichneumonoidea", 7402: "Braconidae", 7403: "Apanteles", 7405: "Chelonus", 7406: "Chelonus sp.", 7407: "Chelonus sp. 'Jones et al.'", 7408: "Ichneumonidae", 7411: "Exeristes", 7412: "Exeristes roborator", 7415: "Campoletis", 7416: "Campoletis sonorensis", 7419: "Diadromus", 7420: "Diadromus pulchellus", 7421: "Diadromus collaris", 7422: "Chalcidoidea", 7423: "Pteromalidae", 7424: "Nasonia", 7425: "Nasonia vitripennis", 7426: "Nasonia giraulti", 7427: "Nasonia longicornis", 7428: "Muscidifurax", 7429: "Muscidifurax uniraptor", 7430: "Eupelmidae", 7431: "Eupelmus", 7432: "Eupelmus vuilleti", 7433: "Eupelmus orientalis", 7434: "Aculeata", 7435: "Scoliidae", 7436: "Megascolia", 7437: "Megascolia flavifrons", 7438: "Vespidae", 7439: "Vespinae", 7440: "Dolichovespula", 7441: "Dolichovespula maculata", 7442: "Dolichovespula arenaria", 7443: "Vespa", 7444: "Vespa basalis", 7445: "Vespa crabro", 7446: "Vespa mandarinia", 7447: "Vespa orientalis", 7448: "Vespa simillima xanthoptera", 7449: "Vespa analis", 7450: "Vespa tropica", 7451: "Vespula", 7452: "Vespula lewisii", 7453: "Vespula maculifrons", 7454: "Vespula vulgaris", 7455: "Polistinae", 7456: "Polistes", 7458: "Apidae", 7459: "Apis", 7460: "Apis mellifera", 7461: "Apis cerana", 7462: "Apis dorsata", 7463: "Apis florea", 7464: "Apis andreniformis", 7468: "Apis koschevnikovi", 7469: "Apis mellifera ligustica", 7474: "Anthophorinae", 7476: "Xylocopa", 7477: "Xylocopa sp.", 7479: "Formicinae", 7482: "Lasius", 7483: "Lasius sp. HL-1992", 7485: "Sphecidae", 7486: "Sphecius", 7487: "Sphecius speciosus", 7489: "Trichogrammatidae", 7490: "Trichogramma", 7491: "Trichogramma cordubensis", 7492: "Trichogramma deion", 7493: "Trichogramma pretiosum", 7494: "Icaria", 7495: "Icaria sp.", 7496: "Pterygota", 7501: "Termopsidae", 7502: "Zootermopsis", 7503: "Zootermopsis angusticollis", 7504: "Mantodea", 7505: "Mantidae", 7506: "Mantis", 7507: "Mantis religiosa", 7509: "Siphonaptera", 7511: "Pulicidae", 7514: "Ctenocephalides", 7515: "Ctenocephalides felis", 7516: "Neuroptera", 7520: "Chrysopidae", 7521: "Chrysoperla", 7522: "Chrysoperla plorabunda", 7524: "Hemiptera", 7527: "Urostylididae", 7529: "Urostyla sp. ABT-1992", 7533: "Lygaeidae", 7535: "Oncopeltus", 7536: "Oncopeltus fasciatus", 7538: "Leptinotarsa", 7539: "Leptinotarsa decemlineata", 7540: "Chilopoda", 7543: "Cryptopidae", 7544: "Cryptops", 7548: "Lithobiidae", 7551: "Lithobius", 7552: "Lithobius forficatus", 7553: "Diplopoda", 7558: "Spirobolidae", 7559: "Spirobolus", 7560: "Spirobolus marginatus", 7561: "Pentastomida", 7563: "Porocephalida", 7565: "Porocephalidae", 7566: "Porocephalus", 7567: "Porocephalus crotali", 7568: "Brachiopoda", 7570: "Lingulida", 7571: "Lingula", 7574: "Lingula anatina", 7575: "Lingula reevii", 7578: "Terebratulida", 7579: "Terebratulina", 7580: "Terebratulina retusa", 7581: "Comatulida", 7583: "Mariametridae", 7584: "Lamprometra", 7585: "Lamprometra palmata", 7586: "Echinodermata", 7587: "Asterozoa", 7588: "Asteroidea", 7589: "Dermasterias", 7590: "Dermasterias imbricata", 7591: "Velatida", 7592: "Asterinidae", 7593: "Asterina", 7594: "Patiria pectinifera", 7596: "Solasteridae", 7597: "Solaster", 7598: "Solaster stimpsoni", 7599: "Forcipulatida", 7600: "Asteriidae", 7601: "Asterias", 7602: "Asterias amurensis", 7603: "Asterias forbesi", 7604: "Asterias rubens", 7608: "Marthasterias", 7609: "Marthasterias glacialis", 7610: "Pisaster", 7611: "Pisaster brevispinus", 7612: "Pisaster ochraceus", 7613: "Pycnopodia", 7614: "Pycnopodia helianthoides", 7615: "Evasterias", 7616: "Evasterias troschelii", 7618: "Ophiuroidea", 7619: "Ophiurida", 7620: "Chilophiurina", 7621: "Ophiocomidae", 7622: "Ophiocoma", 7623: "Ophiocoma wendtii", 7624: "Echinozoa", 7625: "Echinoidea", 7626: "Perischoechinoidea", 7627: "Cidaroida", 7630: "Cidaridae", 7631: "Eucidaris", 7632: "Eucidaris tribuloides", 7633: "Heliocidaris", 7634: "Heliocidaris erythrogramma", 7635: "Heliocidaris tuberculata", 7638: "Euechinoidea", 7639: "Arbacia", 7640: "Arbacia lixula", 7641: "Arbacia punctulata", 7642: "Arbacia sp.", 7643: "Clypeaster", 7644: "Clypeaster japonicus", 7645: "Echinolampas", 7646: "Echinolampas crassa", 7647: "Echinus", 7648: "Echinus esculentus", 7649: "Hemicentrotus", 7650: "Hemicentrotus pulcherrimus", 7651: "Hemicentrotus sp.", 7652: "Lytechinus", 7653: "Lytechinus pictus", 7654: "Lytechinus variegatus", 7655: "Paracentrotus", 7656: "Paracentrotus lividus", 7657: "Parechinus", 7658: "Parechinus angulosus", 7659: "Psammechinus", 7660: "Psammechinus miliaris", 7661: "Stomopneustes", 7663: "Stomopneustes variolaris", 7664: "Strongylocentrotus", 7666: "Mesocentrotus nudus", 7667: "Strongylocentrotus intermedius", 7668: "Strongylocentrotus purpuratus", 7670: "Strongylocentrotus pallidus", 7671: "Strongylocentrotus droebachiensis", 7672: "Tripneustes", 7673: "Tripneustes gratilla", 7674: "Echinacea", 7675: "Echinoida", 7676: "Echinidae", 7677: "Pseudocentrotus", 7678: "Pseudocentrotus depressus", 7679: "unidentified sea urchin", 7681: "Aspidochirotacea", 7682: "Aspidochirotida", 7683: "Holothuriidae", 7684: "Holothuria", 7685: "Holothuria tubulosa", 7687: "Stichopodidae", 7688: "Parastichopus", 7691: "Stichopus", 7693: "Stichopus oshimae", 7694: "Apodacea", 7695: "Molpadida", 7696: "Caudinidae", 7697: "Caudina", 7698: "Molpadia arenicola", 7699: "Paracaudina", 7700: "Paracaudina chilensis", 7701: "Apodida", 7702: "Synaptidae", 7703: "Leptosynapta", 7704: "Leptosynapta inhaerens", 7705: "Holothuroidea", 7706: "Dendrochirotacea", 7707: "Dendrochirotida", 7709: "Sclerodactyla", 7710: "Sclerodactyla briareus", 7711: "Chordata", 7712: "Tunicata", 7713: "Ascidiacea", 7716: "Phlebobranchia", 7717: "Cionidae", 7718: "Ciona", 7719: "Ciona intestinalis", 7720: "Stolidobranchia", 7721: "Styelidae", 7722: "Polyandrocarpa", 7723: "Polyandrocarpa misakiensis", 7724: "Styela", 7725: "Styela clava", 7726: "Styela plicata", 7727: "Pyuridae", 7728: "Halocynthia", 7729: "Halocynthia roretzi", 7730: "Pyura", 7731: "Pyura stolonifera", 7732: "Herdmania", 7733: "Herdmania momus", 7734: "Pyuridae gen. sp.", 7735: "Cephalochordata", 7736: "Branchiostomidae", 7737: "Branchiostoma", 7738: "Branchiostoma californiense", 7739: "Branchiostoma floridae", 7740: "Branchiostoma lanceolatum", 7741: "Branchiostoma belcheri", 7742: "Vertebrata", 7745: "Petromyzontiformes", 7746: "Petromyzontidae", 7748: "Lampetra fluviatilis", 7750: "Lampetra planeri", 7752: "Lampetra aepyptera", 7753: "Lethenteron reissneri", 7754: "Mordacia", 7755: "Mordacia mordax", 7756: "Petromyzon", 7757: "Petromyzon marinus", 7758: "Petromyzontidae gen. sp.", 7761: "Myxiniformes", 7762: "Myxinidae", 7763: "Eptatretus", 7764: "Eptatretus burgeri", 7765: "Eptatretus stoutii", 7767: "Eptatretus okinoseanus", 7769: "Myxine glutinosa", 7772: "Ichthyomyzon", 7776: "Gnathostomata", 7777: "Chondrichthyes", 7778: "Elasmobranchii", 7780: "Raja", 7781: "Raja clavata", 7782: "Leucoraja erinacea", 7784: "Discopyge", 7786: "Torpedo", 7787: "Tetronarce californica", 7788: "Torpedo marmorata", 7790: "Heterodontidae", 7791: "Heterodontus", 7792: "Heterodontus francisci", 7793: "Heterodontus portusjacksoni", 7796: "Squalus", 7797: "Squalus acanthias", 7798: "Squalus suckleyi", 7800: "Ginglymostoma", 7801: "Ginglymostoma cirratum", 7802: "Odontaspididae", 7805: "Carcharhinidae", 7806: "Carcharhinus", 7807: "Carcharhinus obscurus", 7808: "Carcharhinus plumbeus", 7810: "Carcharhinus porosus", 7811: "Mustelus", 7812: "Mustelus canis", 7813: "Mustelus antarcticus", 7814: "Prionace", 7815: "Prionace glauca", 7816: "Scoliodon", 7818: "Galeocerdo", 7819: "Galeocerdo cuvier", 7820: "Negaprion", 7821: "Negaprion brevirostris", 7822: "Sphyrna", 7823: "Sphyrna lewini", 7824: "Sphyrna tiburo", 7825: "Sphyrna tiburo vespertina", 7826: "Scyliorhinidae", 7827: "Poroderma", 7829: "Scyliorhinus", 7830: "Scyliorhinus canicula", 7832: "Echinorhinidae", 7833: "Echinorhinus", 7834: "Echinorhinus cookei", 7839: "Triakidae", 7840: "Triakis", 7844: "Lamninae", 7845: "Isurus", 7847: "Isurus paucus", 7848: "Lamna", 7849: "Lamna nasus", 7850: "Alopiidae", 7851: "Alopias", 7852: "Alopias vulpinus", 7855: "Hexanchidae", 7856: "Notorynchus", 7857: "Notorynchus cepedianus", 7858: "Rajiformes", 7860: "Rhinobatidae", 7861: "Rhinobatos", 7862: "Pseudobatos lentiginosus", 7863: "Holocephali", 7864: "Chimaeriformes", 7865: "Callorhinchidae", 7866: "Callorhinchus", 7867: "Callorhinchus callorynchus", 7868: "Callorhinchus milii", 7869: "Chimaeridae", 7870: "Chimaera", 7871: "Chimaera monstrosa", 7872: "Hydrolagus", 7873: "Hydrolagus colliei", 7874: "Galeorhinus", 7878: "Dipnoi", 7879: "Lepidosireniformes", 7880: "Lepidosirenidae", 7881: "Lepidosiren", 7883: "Lepidosiren paradoxa", 7884: "Protopteridae", 7885: "Protopterus", 7886: "Protopterus aethiopicus", 7887: "Protopterus sp.", 7888: "Protopterus annectens", 7889: "Ceratodontidae", 7890: "Neoceratodus", 7892: "Neoceratodus forsteri", 7894: "Coelacanthiformes", 7895: "Coelacanthidae", 7896: "Latimeria", 7897: "Latimeria chalumnae", 7898: "Actinopterygii", 7899: "Acipenseriformes", 7900: "Acipenseridae", 7901: "Acipenser", 7902: "Acipenser gueldenstaedtii", 7903: "Acipenser stellatus", 7904: "Acipenser transmontanus", 7906: "Acipenser ruthenus", 7907: "Acipenser brevirostrum", 7908: "Acipenser medirostris", 7909: "Scaphirhynchus", 7910: "Scaphirhynchus platorynchus", 7911: "Polyodontidae", 7912: "Polyodon", 7913: "Polyodon spathula", 7914: "Semionotiformes", 7915: "Lepisosteidae", 7916: "Lepisosteus", 7917: "Atractosteus spatula", 7918: "Lepisosteus oculatus", 7921: "Amiiformes", 7922: "Amiidae", 7923: "Amia", 7924: "Amia calva", 7925: "Elopiformes", 7926: "Elopidae", 7927: "Elops", 7928: "Elops saurus", 7930: "Megalopidae", 7931: "Megalops", 7932: "Megalops atlanticus", 7933: "Anguilliformes", 7934: "Anguillidae", 7935: "Anguilla", 7936: "Anguilla anguilla", 7937: "Anguilla japonica", 7938: "Anguilla rostrata", 7939: "Anguilla marmorata", 7940: "Anguilla australis", 7941: "Congridae", 7942: "Conger", 7943: "Conger myriaster", 7944: "Muraenesocidae", 7945: "Muraenesox", 7946: "Muraenesox cinereus", 7948: "Clupeinae", 7949: "Clupea", 7950: "Clupea harengus", 7952: "Cypriniformes", 7953: "Cyprinidae", 7954: "Danio", 7955: "Danio rerio", 7956: "Carassius", 7957: "Carassius auratus", 7958: "Ctenopharyngodon", 7959: "Ctenopharyngodon idella", 7961: "Cyprinus", 7962: "Cyprinus carpio", 7963: "Hypophthalmichthys", 7965: "Hypophthalmichthys nobilis", 7966: "Lythrurus", 7967: "Lythrurus roseipinnis", 7968: "Catostomidae", 7969: "Catostomus", 7970: "Catostomus clarkii", 7971: "Catostomus commersonii", 7972: "Ictiobus", 7973: "Ictiobus bubalus", 7979: "Formosania", 7980: "Formosania lacustris", 7982: "Cobitidae", 7983: "Misgurnus", 7984: "Misgurnus fossilis", 7986: "Anostomidae", 7987: "Leporinus", 7988: "Megaleporinus elongatus", 7991: "Characiformes", 7992: "Characidae", 7993: "Astyanax", 7994: "Astyanax mexicanus", 7995: "Siluriformes", 7996: "Ictaluridae", 7997: "Ictalurus", 7998: "Ictalurus punctatus", 7999: "Pangasiidae", 8000: "Pangasius", 8001: "Pangasius pangasius", 8002: "Gymnotiformes", 8004: "Electrophorus", 8005: "Electrophorus electricus", 8006: "Salmoniformes", 8007: "Esociformes", 8008: "Esocidae", 8009: "Esox", 8010: "Esox lucius", 8012: "Osmeridae", 8013: "Osmerus", 8014: "Osmerus mordax", 8015: "Salmonidae", 8016: "Oncorhynchus", 8017: "Oncorhynchus gorbuscha", 8018: "Oncorhynchus keta", 8019: "Oncorhynchus kisutch", 8020: "Oncorhynchus masou", 8021: "Oncorhynchus masou ishikawae", 8022: "Oncorhynchus mykiss", 8023: "Oncorhynchus nerka", 8025: "Oncorhynchus sp.", 8028: "Salmo", 8030: "Salmo salar", 8031: "Salmo sp.", 8032: "Salmo trutta", 8033: "Salvelinus", 8034: "Salvelinus leucomaenis", 8035: "Salvelinus leucomaenis pluvius", 8036: "Salvelinus alpinus", 8037: "Salvelinus confluentus", 8038: "Salvelinus fontinalis", 8039: "Salvelinus malma", 8040: "Salvelinus namaycush", 8041: "Hucho", 8042: "Parahucho perryi", 8043: "Gadiformes", 8045: "Gadidae", 8046: "Eleginus", 8047: "Eleginus gracilis", 8048: "Gadus", 8049: "Gadus morhua", 8051: "Gadus sp.", 8052: "Gadus ogac", 8053: "Gadus morhua callarias", 8055: "Melanogrammus", 8056: "Melanogrammus aeglefinus", 8057: "Merlangius", 8058: "Merlangius merlangus", 8059: "Pollachius", 8060: "Pollachius virens", 8061: "Merlucciidae", 8062: "Merluccius", 8063: "Merluccius merluccius", 8064: "Batrachoidiformes", 8065: "Batrachoididae", 8066: "Batrachoididae gen. sp.", 8067: "Opsanus", 8068: "Opsanus tau", 8070: "Lophiiformes", 8071: "Lophiidae", 8072: "Lophius", 8073: "Lophius americanus", 8074: "Lophius piscatorius", 8075: "Atheriniformes", 8076: "Cyprinodontidae", 8077: "Fundulus", 8078: "Fundulus heteroclitus", 8079: "Poeciliidae", 8080: "Poecilia", 8081: "Poecilia reticulata", 8082: "Xiphophorus", 8083: "Xiphophorus maculatus", 8084: "Xiphophorus hellerii", 8085: "Xiphophorus sp.", 8086: "Xiphophorus xiphidium", 8087: "Cyprinodontoidei", 8088: "Oryziinae", 8089: "Oryzias", 8090: "Oryzias latipes", 8092: "Cottidae", 8093: "Hemitripterus", 8094: "Hemitripterus americanus", 8095: "Myoxocephalus", 8096: "Myoxocephalus aenaeus", 8097: "Myoxocephalus scorpius", 8098: "Cottus", 8099: "Leocottus kesslerii", 8100: "Cottioidei", 8101: "Cyclopteridae", 8102: "Cyclopterus", 8103: "Cyclopterus lumpus", 8107: "Scorpaenoidei", 8108: "Scorpaenidae", 8109: "Sebastolobus", 8110: "Sebastolobus altivelis", 8111: "Perciformes", 8112: "Percoidei", 8113: "Cichlidae", 8114: "Cichlasoma", 8117: "Herichthys cyanoguttatus", 8121: "Haplochromis", 8124: "Julidochromis", 8125: "Julidochromis regani", 8126: "Tilapia", 8127: "Oreochromis mossambicus", 8128: "Oreochromis niloticus", 8129: "Coptodon rendalli", 8130: "Coptodon zillii", 8139: "Oreochromis", 8141: "Oreochromis placidus", 8142: "Oreochromis tanganicae", 8143: "Sarotherodon", 8144: "Sarotherodon galilaeus", 8145: "Tropheus", 8146: "Tropheus annectens", 8147: "Tropheus brichardi", 8148: "Tropheus duboisi", 8149: "Tropheus kasabae", 8150: "Tropheus moorii", 8151: "Tropheus polli", 8152: "Astatotilapia", 8153: "Haplochromis burtoni", 8154: "Astatotilapia calliptera", 8155: "Simochromis", 8156: "Pseudosimochromis babaulti", 8157: "Carangidae", 8158: "Caranx", 8160: "Seriola", 8161: "Seriola quinqueradiata", 8162: "Percichthyidae", 8163: "Lateolabrax", 8164: "Lateolabrax japonicus", 8165: "Percidae", 8166: "Perca", 8167: "Perca flavescens", 8168: "Perca fluviatilis", 8169: "Sparidae", 8172: "Pagrus", 8173: "Pagrus pagrus", 8174: "Sparus", 8175: "Sparus aurata", 8176: "Acanthopagrus", 8177: "Acanthopagrus latus", 8179: "Acanthopagrus butcheri", 8180: "Centrarchidae", 8181: "Pomoxis", 8182: "Pomoxis nigromaculatus", 8184: "Centropomidae", 8186: "Lates", 8187: "Lates calcarifer", 8189: "Mugilidae", 8190: "Mugil", 8192: "Zoarcales", 8193: "Zoarcidae", 8196: "Lycodes", 8197: "Lycodes polaris", 8199: "Zoarces americanus", 8200: "Lycodichthys", 8201: "Lycodichthys dearborni", 8202: "Anarhichadidae", 8203: "Anarhichas", 8204: "Anarhichas lupus", 8205: "Notothenioidei", 8206: "Nototheniidae", 8207: "Notothenia", 8208: "Notothenia coriiceps", 8210: "Notothenia angustata", 8211: "Pagothenia", 8213: "Pagothenia borchgrevinki", 8214: "Bathydraconidae", 8215: "Cygnodraco", 8216: "Cygnodraco mawsoni", 8217: "Gymnodraco", 8218: "Gymnodraco acuticeps", 8219: "Gobioidei", 8220: "Gobiidae", 8221: "Gillichthys", 8222: "Gillichthys mirabilis", 8224: "Scombridae", 8225: "Euthynnus", 8226: "Katsuwonus pelamis", 8227: "Euthynnus affinis", 8228: "Euthynnus alletteratus", 8229: "Sarda", 8230: "Sarda orientalis", 8231: "Sarda chiliensis", 8232: "Sarda sarda", 8233: "Scombridae gen. sp.", 8234: "Thunnus", 8235: "Thunnus alalunga", 8236: "Thunnus albacares", 8237: "Thunnus thynnus", 8238: "Thunnus orientalis", 8239: "Thunnus sp.", 8240: "Thunnus maccoyii", 8241: "Thunnus obesus", 8242: "Thunnus thynnus thynnus", 8243: "Xiphiidae", 8244: "Xiphias", 8245: "Xiphias gladius", 8247: "Labridae", 8248: "Gomphosus", 8249: "Gomphosus varius", 8252: "Pleuronectiformes", 8253: "Bothidae", 8254: "Paralichthys", 8255: "Paralichthys olivaceus", 8256: "Pleuronectidae", 8257: "Limanda", 8258: "Myzopsetta ferruginea", 8259: "Platichthys", 8260: "Platichthys flesus", 8261: "Pleuronectes", 8262: "Pleuronectes platessa", 8264: "Pseudopleuronectes", 8265: "Pseudopleuronectes americanus", 8266: "Hippoglossus", 8267: "Hippoglossus hippoglossus", 8274: "Pantodontidae", 8275: "Pantodon", 8276: "Pantodon buchholzi", 8277: "Beryciformes", 8279: "Anomalopidae", 8283: "Leuciscus", 8284: "Squalius cephalus", 8285: "Pardachirus", 8286: "Pardachirus pavoninus", 8287: "Sarcopterygii", 8288: "Polypteriformes", 8289: "Polypteridae", 8290: "Polypterus", 8291: "Polypterus sp.", 8292: "Amphibia", 8293: "Caudata", 8294: "Ambystomatidae", 8295: "Ambystoma", 8296: "Ambystoma mexicanum", 8297: "Ambystoma jeffersonianum", 8298: "Ambystoma laterale", 8299: "Ambystoma laterale x Ambystoma jeffersonianum", 8304: "Ambystoma texanum", 8305: "Ambystoma tigrinum", 8306: "Ambystoma talpoideum", 8307: "Ambystoma 'unisexual hybrid'", 8310: "Amphiumidae", 8311: "Amphiuma", 8312: "Amphiuma means", 8313: "Amphiuma tridactylum", 8314: "Salamandridae", 8315: "Notophthalmus", 8316: "Notophthalmus viridescens", 8317: "Pleurodeles", 8319: "Pleurodeles waltl", 8320: "Taricha", 8321: "Taricha granulosa", 8322: "Triturus", 8323: "Triturus cristatus", 8324: "Lissotriton vulgaris", 8325: "Triturus karelinii", 8326: "Triturus carnifex", 8327: "Triturus dobrogicus", 8328: "Triturus marmoratus", 8329: "Cynops", 8330: "Cynops pyrrhogaster", 8332: "Plethodontidae", 8333: "Bolitoglossa", 8334: "Bolitoglossa subpalmata", 8335: "Plethodon", 8336: "Plethodon jordani", 8337: "Plethodon yonahlossee", 8339: "Sirenidae", 8340: "Siren", 8341: "Siren intermedia", 8342: "Anura", 8343: "Alytidae", 8344: "Bombina", 8345: "Bombina bombina", 8346: "Bombina orientalis", 8348: "Bombina variegata", 8349: "Bombina sp.", 8350: "Discoglossus", 8351: "Discoglossus pictus", 8352: "Pipidae", 8353: "Xenopus", 8354: "Xenopus borealis", 8355: "Xenopus laevis", 8356: "Xenopus sp.", 8358: "Xenopus clivii", 8359: "Xenopus laevis/gilli", 8360: "Xenopodinae", 8361: "Hymenochirus", 8362: "Hymenochirus curtipes", 8363: "Silurana", 8364: "Xenopus tropicalis", 8365: "Myobatrachidae", 8366: "Uperoleia", 8367: "Uperoleia marmorata", 8368: "Uperoleia rugosa", 8370: "Litoria", 8371: "Litoria aurea", 8372: "Leptodactylidae", 8373: "Crinia", 8374: "Crinia georgiana", 8375: "Lepidobatrachus", 8376: "Lepidobatrachus laevis", 8377: "Physalaemus", 8378: "Physalaemus fuscomaculatus", 8380: "Eleutherodactylus", 8381: "Eleutherodactylus cuneatus", 8382: "Bufonidae", 8383: "Bufo", 8384: "Bufo bufo", 8386: "Rhinella marina", 8387: "Bufo japonicus", 8388: "Incilius valliceps", 8389: "Anaxyrus americanus", 8392: "Phyllomedusa", 8393: "Phyllomedusa bicolor", 8394: "Pithecopus rohdei", 8395: "Phyllomedusa sauvagii", 8397: "Ranidae", 8398: "Ranidae gen. sp.", 8399: "Rana", 8400: "Lithobates catesbeianus", 8401: "Pelophylax esculentus", 8402: "Rana japonica", 8403: "Pelophylax perezi", 8404: "Rana pipiens", 8406: "Pelophylax ridibundus", 8407: "Rana temporaria", 8409: "Pelophylax nigromaculatus", 8410: "Rugosa rugosa", 8412: "Hyperoliidae", 8413: "Kassina", 8414: "Kassina maculata", 8415: "Kassina senegalensis", 8416: "Neobatrachia", 8417: "Hyloidea", 8418: "Hylidae", 8419: "Gastrotheca", 8420: "Gastrotheca riobambae", 8421: "Hyla", 8422: "Dryophytes cinereus", 8423: "Sooglossidae", 8425: "Sooglossus thomasseti", 8426: "Microhyloidea", 8427: "Microhylidae", 8428: "Gastrophryne", 8429: "Gastrophryne carolinensis", 8431: "Pelobatoidea", 8432: "Pelobatidae", 8434: "Scaphiopus", 8435: "Scaphiopus holbrookii", 8438: "Ascaphus", 8439: "Ascaphus truei", 8441: "Rana sp.", 8442: "Alytes", 8443: "Alytes obstetricans", 8445: "Gymnophiona", 8446: "Caeciliidae", 8447: "Grandisonia", 8448: "Grandisonia alternans", 8449: "Hypogeophis", 8450: "Hypogeophis rostratus", 8451: "Ichthyophiidae", 8452: "Ichthyophis", 8453: "Ichthyophis bannanicus", 8454: "Typhlonectidae", 8455: "Typhlonectes", 8456: "Typhlonectes natans", 8457: "Sauropsida", 8459: "Testudines", 8460: "Pleurodira", 8461: "Chelidae", 8462: "Phrynops", 8463: "Phrynops hilarii", 8464: "Cryptodira", 8465: "Cheloniidae", 8466: "Caretta", 8467: "Caretta caretta", 8468: "Chelonia", 8469: "Chelonia mydas", 8471: "Lepidochelys", 8472: "Lepidochelys kempii", 8473: "Chelydridae", 8474: "Chelydra", 8475: "Chelydra serpentina", 8476: "Emydidae", 8477: "Chrysemys", 8478: "Chrysemys picta bellii", 8479: "Chrysemys picta", 8480: "Graptemys", 8481: "Graptemys geographica", 8484: "Malaclemys", 8485: "Malaclemys terrapin", 8486: "Testudinoidea", 8487: "Testudinidae", 8488: "Chinemys", 8492: "Archosauria", 8493: "Crocodylidae", 8495: "Alligator", 8496: "Alligator mississippiensis", 8497: "Caiman", 8499: "Caiman crocodilus", 8500: "Crocodylus", 8501: "Crocodylus niloticus", 8502: "Crocodylus porosus", 8503: "Crocodylus novaeguineae", 8504: "Lepidosauria", 8505: "Sphenodontia", 8506: "Sphenodontidae", 8507: "Sphenodon", 8508: "Sphenodon punctatus", 8509: "Squamata", 8511: "Iguania", 8515: "Iguanidae", 8516: "Iguana", 8517: "Iguana iguana", 8518: "Sceloporus", 8519: "Sceloporus occidentalis", 8520: "Sceloporus undulatus", 8522: "Lacertidae", 8523: "Lacerta", 8524: "Zootoca vivipara", 8526: "Tiliqua", 8527: "Tiliqua rugosa", 8528: "Eumeces", 8530: "Teiidae", 8531: "Tupinambis", 8532: "Tupinambis teguixin", 8533: "Ameiva", 8534: "Pholidoscelis auberi", 8535: "Ameiva ameiva", 8536: "Xantusiidae", 8537: "Cricosaurinae", 8538: "Cricosaura", 8539: "Cricosaura typica", 8540: "Xantusiinae", 8541: "Lepidophyma", 8542: "Lepidophyma smithii", 8543: "Xantusia", 8544: "Xantusia bolsonae", 8545: "Xantusia henshawi", 8546: "Xantusia riversiana", 8547: "Xantusia vigilis", 8548: "Anguimorpha", 8549: "Helodermatidae", 8550: "Heloderma", 8551: "Heloderma horridum", 8552: "Heloderma horridum horridum", 8553: "Heloderma sp.", 8554: "Heloderma suspectum", 8555: "Varanidae", 8556: "Varanus", 8557: "Varanus exanthematicus", 8558: "Varanus albigularis", 8559: "Varanus varius", 8560: "Gekkota", 8561: "Gekkonidae", 8565: "Gekko", 8568: "Tarentola", 8569: "Tarentola mauritanica", 8570: "Serpentes", 8572: "Boidae", 8573: "Boa", 8574: "Boa constrictor", 8575: "Epicrates", 8576: "Chilabothrus subflavus", 8578: "Colubridae", 8579: "Elaphe", 8582: "Erythrolamprus miliaris", 8583: "Natrix", 8584: "Natrix tessellata", 8585: "Natrix maura", 8587: "Ptyas dhumnades", 8589: "Coluber", 8590: "Coluber constrictor", 8591: "Nerodia", 8592: "Nerodia sipedon", 8594: "Pituophis", 8595: "Pituophis melanoleucus", 8596: "Heterodon", 8597: "Heterodon platirhinos", 8598: "Atractaspidinae", 8599: "Atractaspis", 8600: "Atractaspis andersonii", 8602: "Elapidae", 8604: "Acanthophis", 8605: "Acanthophis antarcticus", 8606: "Aspidelaps", 8607: "Aspidelaps scutatus", 8608: "Boulengerina", 8609: "Naja annulata", 8610: "Naja annulata annulata", 8611: "Naja christyi", 8612: "Bungarus", 8613: "Bungarus fasciatus", 8614: "Bungarus flaviceps", 8615: "Bungarus flaviceps flaviceps", 8616: "Bungarus multicinctus", 8617: "Dendroaspis", 8618: "Dendroaspis angusticeps", 8619: "Dendroaspis jamesoni kaimosae", 8620: "Dendroaspis polylepis polylepis", 8621: "Dendroaspis viridis", 8623: "Dendroaspis jamesoni", 8624: "Dendroaspis polylepis", 8625: "Hemachatus", 8626: "Hemachatus haemachatus", 8627: "Laticauda", 8628: "Laticauda colubrina", 8629: "Laticauda crockeri", 8630: "Laticauda laticaudata", 8631: "Laticauda semifasciata", 8633: "Calliophis bivirgatus", 8634: "Micrurus", 8635: "Micrurus nigrocinctus", 8636: "Micrurus tener microgalbineus", 8637: "Micrurus fulvius", 8638: "Naja", 8639: "Naja haje", 8642: "Naja haje haje", 8643: "Naja melanoleuca", 8644: "Naja mossambica", 8649: "Naja kaouthia", 8654: "Naja nigricollis", 8655: "Naja nivea", 8656: "Naja atra", 8657: "Naja oxiana", 8658: "Naja pallida", 8659: "Naja philippinensis", 8660: "Naja samarensis", 8661: "Notechis", 8663: "Notechis scutatus", 8664: "Ophiophagus", 8665: "Ophiophagus hannah", 8666: "Oxyuranus", 8667: "Oxyuranus scutellatus scutellatus", 8668: "Oxyuranus scutellatus", 8669: "Pseudechis", 8670: "Pseudechis australis", 8671: "Pseudechis porphyriacus", 8672: "Pseudonaja", 8673: "Pseudonaja textilis", 8675: "Acalyptophis", 8676: "Hydrophis peronii", 8677: "Aipysurus", 8678: "Aipysurus laevis", 8679: "Astrotia", 8682: "Hydrophis schistosus", 8683: "Hydrophis", 8684: "Hydrophis lapemoides", 8685: "Hydrophis ornatus", 8686: "Hydrophis cyanocinctus", 8687: "Pelamis", 8688: "Hydrophis platurus", 8689: "Viperidae", 8690: "Viperinae", 8691: "Bitis", 8692: "Bitis arietans", 8693: "Bitis caudalis", 8694: "Bitis gabonica", 8695: "Bitis nasicornis", 8696: "Cerastes", 8697: "Cerastes cerastes", 8698: "Cerastes vipera", 8699: "Echis", 8700: "Echis pyramidum", 8703: "Vipera", 8704: "Vipera ammodytes", 8705: "Vipera ammodytes ammodytes", 8706: "Vipera aspis", 8707: "Daboia russelii", 8709: "Macrovipera lebetina", 8710: "Crotalinae", 8711: "Agkistrodon", 8713: "Agkistrodon contortrix contortrix", 8714: "Gloydius halys", 8715: "Agkistrodon piscivorus", 8716: "Agkistrodon piscivorus piscivorus", 8717: "Calloselasma rhodostoma", 8718: "Agkistrodon bilineatus", 8719: "Gloydius halys halys", 8720: "Agkistrodon contortrix", 8721: "Bothrops", 8722: "Bothrops asper", 8723: "Bothrops insularis", 8724: "Bothrops jararaca", 8725: "Bothrops atrox", 8726: "Bothrops jararacussu", 8727: "Bothrops cotiara", 8728: "Crotalus", 8729: "Crotalus adamanteus", 8730: "Crotalus atrox", 8731: "Crotalus durissus", 8732: "Crotalus durissus terrificus", 8733: "Crotalus molossus", 8734: "Crotalus molossus nigrescens", 8735: "Crotalus ruber", 8736: "Crotalus ruber ruber", 8737: "Crotalus scutulatus", 8738: "Crotalus scutulatus scutulatus", 8739: "Crotalus viridis", 8740: "Crotalus oreganus concolor", 8741: "Crotalus oreganus helleri", 8742: "Crotalus viridis viridis", 8743: "Crotalus aquilus", 8744: "Crotalus basiliscus", 8746: "Crotalus cerastes", 8747: "Crotalus horridus horridus", 8748: "Crotalus pricei pricei", 8749: "Crotalus triseriatus triseriatus", 8751: "Lachesis", 8752: "Lachesis muta", 8753: "Lachesis muta muta", 8755: "Sistrurus", 8756: "Sistrurus catenatus", 8757: "Sistrurus tergeminus", 8758: "Sistrurus miliarius", 8759: "Sistrurus miliarius barbouri", 8762: "Sistrurus catenatus edwardsi", 8764: "Trimeresurus", 8765: "Trimeresurus albolabris", 8767: "Trimeresurus gramineus", 8769: "Ovophis okinavensis", 8770: "Tropidolaemus wagleri", 8772: "Azemiops", 8773: "Azemiops feae", 8774: "Calloselasma", 8781: "Hydrophis hardwickii", 8782: "Aves", 8783: "Palaeognathae", 8784: "Casuariiformes", 8785: "Casuariidae", 8786: "Casuarius", 8787: "Casuarius casuarius", 8788: "Dromaiidae", 8789: "Dromaius", 8790: "Dromaius novaehollandiae", 8792: "Rheiformes", 8793: "Rheidae", 8794: "Pterocnemia", 8795: "Pterocnemia pennata", 8796: "Rhea", 8797: "Rhea americana", 8798: "Struthioniformes", 8799: "Struthionidae", 8800: "Struthio", 8801: "Struthio camelus", 8802: "Tinamiformes", 8803: "Tinamidae", 8804: "Eudromia", 8805: "Eudromia elegans", 8806: "Nothoprocta", 8807: "Nothoprocta cinerascens", 8808: "Dinornithiformes", 8809: "Emeidae", 8810: "Anomalopteryx", 8811: "Anomalopteryx didiformis", 8812: "Megalapteryx", 8813: "Megalapteryx didinus", 8814: "Pachyornis", 8815: "Pachyornis elephantopus", 8816: "Dinornithidae", 8817: "Dinornis", 8818: "Dinornis novaezealandiae", 8819: "Apterygiformes", 8820: "Apterygidae", 8821: "Apteryx", 8822: "Apteryx australis", 8823: "Apteryx haastii", 8824: "Apteryx owenii", 8825: "Neognathae", 8826: "Anseriformes", 8827: "Anhimidae", 8828: "Chauna", 8829: "Chauna chavaria", 8830: "Anatidae", 8831: "Aix", 8832: "Aix galericulata", 8833: "Aix sponsa", 8834: "Aix sp.", 8835: "Anas", 8837: "Anas capensis", 8838: "Mareca penelope", 8839: "Anas platyrhynchos", 8840: "Anas platyrhynchos platyrhynchos", 8841: "Anas platyrhynchos x Cairina moschata", 8842: "Anser", 8843: "Anser anser", 8844: "Anser anser anser", 8845: "Anser cygnoides", 8846: "Anser indicus", 8847: "Anser sp.", 8848: "Anser anser domesticus", 8849: "Anser caerulescens", 8850: "Anseranas", 8851: "Anseranas semipalmata", 8852: "Branta", 8853: "Branta canadensis", 8854: "Cairina", 8855: "Cairina moschata", 8856: "Cairina sp.", 8857: "Cereopsis", 8858: "Cereopsis novaehollandiae", 8859: "Chloephaga", 8860: "Chloephaga melanoptera", 8861: "Chloephaga picta", 8862: "Coscoroba", 8863: "Coscoroba coscoroba", 8864: "Cyanochen", 8865: "Cyanochen cyanopterus", 8867: "Cygnus", 8868: "Cygnus atratus", 8869: "Cygnus olor", 8870: "Dendrocygna", 8871: "Dendrocygna arborea", 8872: "Dendrocygna arcuata", 8873: "Dendrocygna autumnalis", 8874: "Dendrocygna bicolor", 8875: "Dendrocygna eytoni", 8876: "Dendrocygna viduata", 8877: "Mergus", 8879: "Mergus serrator", 8880: "Mergus merganser", 8881: "Neochen", 8882: "Neochen jubata", 8883: "Oxyura", 8884: "Oxyura jamaicensis", 8885: "Oxyura vittata", 8886: "Sarkidiornis", 8887: "Sarkidiornis melanotos", 8888: "Tadorna", 8889: "Tadorna radjah", 8892: "Apodiformes", 8893: "Apodidae", 8894: "Apus", 8895: "Apus apus", 8896: "Chaetura", 8897: "Chaetura pelagica", 8899: "Ardeidae", 8900: "Nycticorax", 8901: "Nycticorax nycticorax", 8902: "Caprimulgiformes", 8903: "Podargidae", 8904: "Podargus", 8905: "Podargus strigoides", 8906: "Charadriiformes", 8907: "Charadriidae", 8908: "Hoplopterus", 8909: "Hoplopterus spinosus", 8910: "Laridae", 8911: "Larus", 8912: "Larus marinus", 8915: "Larus fuscus", 8917: "Scolopacidae", 8918: "Calidris", 8919: "Calidris alpina", 8920: "Ciconiiformes", 8922: "Cathartidae", 8923: "Vultur", 8924: "Vultur gryphus", 8926: "Ciconiidae", 8927: "Ciconia", 8928: "Ciconia ciconia", 8929: "Columbiformes", 8930: "Columbidae", 8931: "Columba", 8932: "Columba livia", 8933: "Columba sp.", 8934: "Columba palumbus", 8936: "Coraciiformes", 8937: "Alcedinidae", 8938: "Dacelo", 8939: "Dacelo novaeguineae", 8940: "Cuculiformes", 8941: "Cuculidae", 8942: "Carpococcyx", 8943: "Carpococcyx renauldi", 8944: "Eudynamys", 8945: "Eudynamys scolopaceus", 8946: "Geococcyx", 8947: "Geococcyx californianus", 8948: "Falconiformes", 8949: "Falconidae", 8951: "Caracara plancus", 8952: "Falco", 8953: "Falco columbarius", 8954: "Falco peregrinus", 8955: "Accipitrinae", 8956: "Accipiter", 8957: "Accipiter gentilis", 8958: "Aegypius", 8959: "Aegypius monachus", 8960: "Aquila", 8961: "Aquila audax", 8962: "Aquila chrysaetos", 8963: "Circus", 8964: "Circus aeruginosus", 8965: "Gyps", 8966: "Gyps coprotheres", 8967: "Gyps rueppellii", 8968: "Haliaeetus", 8969: "Haliaeetus albicilla", 8970: "Haliastur", 8971: "Haliastur indus", 8972: "Polyboroides", 8973: "Polyboroides radiatus", 8974: "Trigonoceps", 8975: "Trigonoceps occipitalis", 8976: "Galliformes", 8977: "Megapodiidae", 8978: "Megapodius", 8979: "Megapodius freycinet", 8980: "Leipoa", 8981: "Leipoa ocellata", 8982: "Cracidae", 8983: "Ortalis", 8984: "Ortalis vetula", 8985: "Penelope", 8986: "Penelope jacucaca", 8987: "Penelope superciliaris", 8988: "Aburria", 8990: "Numididae", 8991: "Acryllium", 8992: "Acryllium vulturinum", 8993: "Guttera", 8994: "Guttera pucherani", 8995: "Numida", 8996: "Numida meleagris", 8999: "Bonasa", 9000: "Bonasa umbellus", 9001: "Centrocercus", 9002: "Centrocercus urophasianus", 9003: "Tympanuchus", 9004: "Tympanuchus cupido", 9005: "Phasianidae", 9006: "Phasianidae gen. sp.", 9008: "Callipepla", 9009: "Callipepla squamata", 9010: "Callipepla squamata castanogastris", 9011: "Callipepla squamata pallida", 9013: "Colinus", 9014: "Colinus virginianus", 9016: "Cyrtonyx", 9017: "Cyrtonyx montezumae", 9018: "Francolinus", 9019: "Francolinus pondicerianus", 9020: "Francolinus afer", 9021: "Francolinus coqui", 9022: "Francolinus erckelii", 9023: "Francolinus francolinus", 9027: "Oreortyx", 9029: "Oreortyx pictus", 9030: "Gallus", 9031: "Gallus gallus", 9032: "Gallus lafayetii", 9033: "Gallus sonneratii", 9034: "Gallus varius", 9036: "Gallus sp.", 9039: "Lophophorus", 9040: "Lophophorus impejanus", 9041: "Lophura", 9042: "Lophura bulweri", 9043: "Lophura edwardsi", 9044: "Lophura ignita", 9046: "Lophura nycthemera", 9048: "Pavo", 9049: "Pavo cristatus", 9050: "Pavo muticus", 9051: "Perdix", 9052: "Perdix perdix", 9053: "Phasianus", 9054: "Phasianus colchicus", 9055: "Phasianus versicolor", 9056: "Phasianus sp.", 9057: "Phasianus colchicus colchicus", 9058: "Polyplectron", 9059: "Polyplectron bicalcaratum", 9060: "Pucrasia", 9061: "Pucrasia macrolopha", 9062: "Syrmaticus", 9063: "Syrmaticus ellioti", 9064: "Syrmaticus humiae", 9065: "Syrmaticus mikado", 9066: "Syrmaticus reevesii", 9067: "Syrmaticus soemmerringii", 9069: "Tragopan", 9070: "Tragopan satyra", 9071: "Tragopan temminckii", 9072: "Phasianinae", 9075: "Afropavo", 9076: "Afropavo congensis", 9077: "Alectoris", 9078: "Alectoris chukar", 9079: "Alectoris rufa", 9080: "Argusianus", 9081: "Argusianus argus", 9082: "Bambusicola", 9083: "Bambusicola thoracicus", 9084: "Catreus", 9085: "Catreus wallichii", 9087: "Chrysolophus", 9088: "Chrysolophus amherstiae", 9089: "Chrysolophus pictus", 9090: "Coturnix", 9091: "Coturnix coturnix", 9093: "Coturnix delegorguei", 9095: "Crossoptilon", 9096: "Crossoptilon auritum", 9097: "Crossoptilon mantchuricum", 9100: "Agriocharis", 9101: "Meleagris ocellata", 9102: "Meleagris", 9103: "Meleagris gallopavo", 9104: "Arborophila", 9105: "Arborophila torqueola", 9108: "Gruiformes", 9109: "Gruidae", 9111: "Anthropoides virgo", 9114: "Grus", 9115: "Grus vipio", 9116: "Grus antigone", 9117: "Grus americana", 9118: "Grus carunculatus", 9119: "Rallidae", 9120: "Fulica", 9121: "Fulica atra", 9122: "Gallinula", 9123: "Gallinula chloropus", 9124: "Gallirallus", 9125: "Gallirallus australis", 9126: "Passeriformes", 9127: "Cotingidae", 9128: "Ampelion", 9131: "Gymnorhina", 9132: "Gymnorhina tibicen", 9133: "Fringillidae", 9134: "Serinus", 9135: "Serinus canaria", 9136: "Furnariidae", 9137: "Asthenes", 9138: "Asthenes dorbignyi", 9140: "Thripophaga", 9143: "Corcoracidae", 9144: "Corcorax", 9145: "Corcorax melanorhamphos", 9146: "Meliphagidae", 9147: "Ptiloprora", 9148: "Ptiloprora plumbea", 9149: "Paradisaeidae", 9150: "Epimachus", 9151: "Epimachus albertisi", 9153: "Paridae", 9154: "Parus", 9157: "Parus major", 9158: "Passeridae", 9159: "Passer", 9160: "Passer montanus", 9161: "Pittidae", 9162: "Pitta", 9163: "Pitta sordida", 9164: "Ptilonorhynchidae", 9165: "Amblyornis", 9166: "Amblyornis macgregoriae", 9167: "Rhinocryptidae", 9168: "Scytalopus", 9169: "Scytalopus magellanicus", 9170: "Sturnidae", 9171: "Sturnus", 9172: "Sturnus vulgaris", 9173: "Timaliidae", 9174: "Pomatostomus", 9175: "Pomatostomus isidorei", 9176: "Pomatostomus ruficeps", 9177: "Pomatostomus superciliosus", 9178: "Pomatostomus temporalis", 9180: "Pomatostomus halli", 9181: "Phylloscopus", 9182: "Phylloscopus trochilus", 9183: "Turdidae", 9184: "Catharus", 9185: "Catharus guttatus", 9186: "Turdus", 9187: "Turdus merula", 9188: "Turdus migratorius", 9190: "Agelaius", 9191: "Agelaius tricolor", 9193: "Laniidae", 9194: "Laniarius", 9195: "Laniarius aethiopicus", 9196: "Laniarius barbarus", 9198: "Laniarius luehderi", 9199: "Laniarius ruficeps rufinuchalis", 9200: "Laniarius turatii", 9201: "Laniarius ruficeps", 9202: "Telophorus", 9204: "Telophorus bocagei", 9205: "Pelecaniformes", 9206: "Phalacrocoracidae", 9207: "Phalacrocorax", 9208: "Leucocarbo albiventer", 9209: "Phalacrocorax carbo", 9210: "Phalacrocorax sulcirostris", 9211: "Anhingidae", 9212: "Anhinga", 9213: "Anhinga novaehollandiae", 9214: "Phoenicopteriformes", 9215: "Phoenicopteridae", 9216: "Phoenicopterus", 9217: "Phoenicopterus ruber", 9218: "Phoenicopterus ruber ruber", 9219: "Piciformes", 9220: "Picidae", 9221: "Colaptes", 9222: "Colaptes rupicola", 9223: "Psittaciformes", 9224: "Psittacidae", 9225: "Ara", 9226: "Ara ararauna", 9227: "Psittacula", 9228: "Psittacula krameri", 9230: "Sphenisciformes", 9231: "Spheniscidae", 9232: "Aptenodytes", 9233: "Aptenodytes forsteri", 9234: "Aptenodytes patagonicus", 9235: "Eudyptes", 9237: "Pygoscelis", 9238: "Pygoscelis adeliae", 9239: "Spheniscus", 9240: "Spheniscus humboldti", 9242: "Trochilidae", 9243: "Calypte", 9244: "Calypte anna", 9246: "Turnicidae", 9247: "Turnix", 9248: "Turnix sylvaticus", 9251: "Podilymbus", 9252: "Podilymbus podiceps", 9254: "Prototheria", 9255: "Monotremata", 9256: "Ornithorhynchidae", 9257: "Ornithorhynchus", 9258: "Ornithorhynchus anatinus", 9259: "Tachyglossidae", 9260: "Tachyglossus", 9261: "Tachyglossus aculeatus", 9263: "Metatheria", 9265: "Didelphidae", 9266: "Didelphis", 9267: "Didelphis virginiana", 9268: "Didelphis marsupialis", 9269: "Marmosa", 9271: "Philander", 9272: "Philander opossum", 9273: "Thylacinidae", 9274: "Thylacinus", 9275: "Thylacinus cynocephalus", 9277: "Dasyuridae", 9278: "Dasyurus", 9279: "Dasyurus viverrinus", 9280: "Dasyurus hallucatus", 9281: "Dasyurus maculatus", 9282: "Antechinus", 9283: "Antechinus stuartii", 9284: "Antechinus swainsonii", 9286: "Dasykaluta", 9288: "Murexia", 9290: "Parantechinus", 9291: "Parantechinus apicalis", 9292: "Phascogale", 9293: "Phascogale tapoatafa", 9294: "Phascolosorex", 9295: "Phascolosorex dorsalis", 9296: "Planigale", 9297: "Planigale maculata", 9298: "Pseudantechinus", 9299: "Pseudantechinus macdonnellensis", 9300: "Sminthopsis", 9301: "Sminthopsis crassicaudata", 9302: "Sminthopsis macroura", 9304: "Sarcophilus", 9305: "Sarcophilus harrisii", 9307: "Macropodidae", 9309: "Potorous", 9310: "Potorous tridactylus", 9312: "Macropus", 9313: "Notamacropus agilis", 9314: "Osphranter antilopinus", 9315: "Notamacropus eugenii", 9316: "Macropus fuliginosus", 9317: "Macropus giganteus", 9318: "Notamacropus parryi", 9319: "Osphranter robustus", 9321: "Osphranter rufus", 9322: "Macropus sp.", 9323: "Osphranter bernardus", 9324: "Petrogale", 9325: "Petrogale xanthopus", 9326: "Thylogale", 9327: "Thylogale billardierii", 9328: "Thylogale stigmatica", 9329: "Wallabia", 9330: "Wallabia bicolor", 9331: "Petauridae", 9332: "Pseudocheirus", 9333: "Pseudocheirus peregrinus", 9335: "Phalangeridae", 9336: "Trichosurus", 9337: "Trichosurus vulpecula", 9338: "Vombatidae", 9342: "Peramelidae", 9343: "Perameles", 9344: "Perameles nasuta", 9347: "Eutheria", 9348: "Xenarthra", 9349: "Myrmecophagidae", 9350: "Tamandua", 9351: "Tamandua mexicana", 9352: "Bradypodidae", 9353: "Bradypus", 9354: "Bradypus tridactylus", 9355: "Bradypus variegatus", 9357: "Choloepus", 9358: "Choloepus hoffmanni", 9359: "Dasypodidae", 9360: "Dasypus", 9361: "Dasypus novemcinctus", 9362: "Eulipotyphla", 9363: "Erinaceidae", 9364: "Erinaceus", 9365: "Erinaceus europaeus", 9366: "Galericinae", 9367: "Atelerix", 9368: "Atelerix albiventris", 9369: "Tenrecidae", 9370: "Echinops", 9371: "Echinops telfairi", 9372: "Echinops exaltatus", 9373: "Talpidae", 9374: "Talpa", 9375: "Talpa europaea", 9376: "Soricidae", 9377: "Suncus", 9378: "Suncus murinus", 9379: "Sorex", 9380: "Sorex cinereus acadicus", 9381: "Sorex cinereus cinereus", 9382: "Sorex cinereus miscix", 9383: "Sorex haydeni", 9384: "Sorex hoyi", 9386: "Blarina", 9387: "Blarina brevicauda", 9389: "Chrysochloridae", 9390: "Amblysomus", 9391: "Amblysomus hottentotus", 9392: "Scandentia", 9393: "Tupaiidae", 9394: "Tupaia", 9395: "Tupaia glis", 9397: "Chiroptera", 9398: "Pteropodidae", 9399: "Cynopterus", 9400: "Cynopterus sphinx", 9401: "Pteropus", 9402: "Pteropus alecto", 9403: "Pteropus poliocephalus", 9404: "Pteropus temminckii", 9405: "Pteropus hypomelanus", 9406: "Rousettus", 9407: "Rousettus aegyptiacus", 9408: "Rousettus leschenaultii", 9409: "Megadermatidae", 9410: "Macroderma", 9411: "Macroderma gigas", 9412: "Megaderma", 9413: "Megaderma lyra", 9414: "Megaderma spasma", 9415: "Phyllostomidae", 9416: "Artibeus", 9417: "Artibeus jamaicensis", 9418: "Macrotus", 9419: "Macrotus californicus", 9420: "Brachyphylla", 9421: "Brachyphylla cavernarum", 9422: "Phyllostomus", 9423: "Phyllostomus hastatus", 9425: "Tonatia", 9426: "Tonatia bidens", 9429: "Desmodus", 9430: "Desmodus rotundus", 9431: "Vespertilionidae", 9432: "Miniopterus", 9433: "Miniopterus schreibersii", 9434: "Myotis", 9435: "Myotis velifer", 9436: "Molossidae", 9437: "Tadarida", 9438: "Tadarida brasiliensis", 9439: "Antrozous", 9440: "Antrozous pallidus", 9443: "Primates", 9445: "Lemuridae", 9446: "Lemur", 9447: "Lemur catta", 9452: "Lepilemur", 9453: "Lepilemur mustelinus", 9454: "Varecia", 9455: "Varecia variegata", 9456: "Cynocephalus", 9459: "Cheirogaleus", 9460: "Cheirogaleus medius", 9461: "Lorisidae", 9462: "Galago", 9463: "Otolemur crassicaudatus", 9464: "Galago sp.", 9465: "Galago senegalensis", 9467: "Loris", 9468: "Loris tardigradus", 9469: "Nycticebus", 9470: "Nycticebus coucang", 9471: "Perodicticus", 9472: "Perodicticus potto", 9473: "Perodicticus potto edwarsi", 9475: "Tarsiidae", 9476: "Tarsius", 9477: "Cephalopachus bancanus", 9479: "Platyrrhini", 9480: "Callitrichinae", 9481: "Callithrix", 9482: "Mico argentatus", 9483: "Callithrix jacchus", 9485: "Callithrix sp.", 9486: "Saguinus", 9487: "Leontocebus fuscicollis", 9488: "Saguinus mystax", 9489: "Leontocebus nigricollis", 9490: "Saguinus oedipus", 9491: "Saguinus imperator", 9493: "Callithrix pygmaea", 9494: "Callimico", 9495: "Callimico goeldii", 9498: "Cebidae", 9499: "Alouatta", 9502: "Alouatta caraya", 9503: "Alouatta seniculus", 9504: "Aotus", 9505: "Aotus trivirgatus", 9506: "Ateles", 9507: "Ateles belzebuth", 9508: "Ateles fusciceps", 9509: "Ateles geoffroyi", 9510: "Ateles paniscus", 9511: "Ateles sp.", 9513: "Cebus", 9514: "Cebus albifrons", 9515: "Sapajus apella", 9516: "Cebus capucinus", 9517: "Cebus sp.", 9518: "Lagothrix", 9519: "Lagothrix lagotricha", 9520: "Saimiri", 9521: "Saimiri sciureus", 9522: "Callicebus", 9523: "Plecturocebus moloch", 9524: "Chiropotes", 9525: "Chiropotes satanas", 9526: "Catarrhini", 9527: "Cercopithecidae", 9528: "Cercopithecinae", 9529: "Cercocebus", 9530: "Cercocebus torquatus", 9531: "Cercocebus atys", 9532: "Cercocebus galeritus", 9533: "Cercopithecus", 9534: "Chlorocebus aethiops", 9535: "Cercopithecus cephus", 9536: "Cercopithecus hamlyni", 9537: "Erythrocebus", 9538: "Erythrocebus patas", 9539: "Macaca", 9540: "Macaca arctoides", 9541: "Macaca fascicularis", 9542: "Macaca fuscata", 9543: "Macaca fuscata fuscata", 9544: "Macaca mulatta", 9545: "Macaca nemestrina", 9546: "Macaca sylvanus", 9548: "Macaca radiata", 9549: "Macaca sp.", 9551: "Macaca assamensis", 9552: "Macaca sinica", 9553: "Macaca speciosa", 9554: "Papio", 9555: "Papio anubis", 9556: "Papio cynocephalus", 9557: "Papio hamadryas", 9561: "Mandrillus sphinx", 9562: "Papio hamadryas hamadryas", 9564: "Theropithecus", 9565: "Theropithecus gelada", 9567: "Mandrillus", 9568: "Mandrillus leucophaeus", 9569: "Colobinae", 9570: "Colobus", 9572: "Colobus polykomos", 9573: "Presbytis", 9576: "Cercopithecidae gen. sp.", 9577: "Hylobatidae", 9578: "Hylobates", 9579: "Hylobates agilis", 9580: "Hylobates lar", 9581: "Hylobates sp.", 9583: "Hylobates agilis unko", 9586: "Nomascus siki", 9587: "Hylobates klossii", 9588: "Hylobates muelleri", 9589: "Hylobates pileatus", 9590: "Symphalangus syndactylus", 9592: "Gorilla", 9593: "Gorilla gorilla", 9595: "Gorilla gorilla gorilla", 9596: "Pan", 9597: "Pan paniscus", 9598: "Pan troglodytes", 9599: "Pongo", 9600: "Pongo pygmaeus", 9601: "Pongo abelii", 9602: "Pongo pygmaeus pygmaeus", 9603: "Pongo sp.", 9604: "Hominidae", 9605: "Homo", 9606: "Homo sapiens", 9608: "Canidae", 9611: "Canis", 9612: "Canis lupus", 9614: "Canis latrans", 9615: "Canis lupus familiaris", 9616: "Canis sp.", 9619: "Dusicyon", 9620: "Cerdocyon thous", 9621: "Lycaon", 9622: "Lycaon pictus", 9623: "Otocyon", 9624: "Otocyon megalotis", 9625: "Vulpes", 9626: "Vulpes chama", 9627: "Vulpes vulpes", 9629: "Vulpes corsac", 9630: "Vulpes macrotis", 9631: "Vulpes velox", 9632: "Ursidae", 9633: "Helarctos", 9634: "Helarctos malayanus", 9635: "Melursus", 9636: "Melursus ursinus", 9637: "Tremarctos", 9638: "Tremarctos ornatus", 9639: "Ursus", 9641: "Ursus sp.", 9642: "Ursus thibetanus", 9643: "Ursus americanus", 9644: "Ursus arctos", 9645: "Ailuropoda", 9646: "Ailuropoda melanoleuca", 9647: "Procyonidae", 9648: "Ailurus", 9649: "Ailurus fulgens", 9650: "Nasua", 9651: "Nasua nasua", 9652: "Nasua nasua rufa", 9653: "Procyon", 9654: "Procyon lotor", 9655: "Mustelidae", 9656: "Lutra", 9657: "Lutra lutra", 9658: "Martes", 9659: "Martes foina", 9660: "Martes americana", 9661: "Meles", 9662: "Meles meles", 9663: "Mellivora", 9664: "Mellivora capensis", 9665: "Mustela", 9666: "Mustela lutreola", 9668: "Mustela putorius", 9669: "Mustela putorius furo", 9671: "Pteronura", 9672: "Pteronura brasiliensis", 9673: "Viverridae", 9674: "Paguma", 9675: "Paguma larvata", 9676: "Hyaenidae", 9677: "Crocuta", 9678: "Crocuta crocuta", 9679: "Proteles", 9680: "Proteles cristata", 9681: "Felidae", 9682: "Felis", 9683: "Felis silvestris", 9685: "Felis catus", 9687: "Felis sp.", 9688: "Panthera", 9689: "Panthera leo", 9690: "Panthera onca", 9691: "Panthera pardus", 9692: "Panthera pardus orientalis", 9693: "Panthera pardus saxicolor", 9694: "Panthera tigris", 9695: "Panthera tigris sumatrae", 9696: "Puma concolor", 9697: "Herpestidae", 9699: "Herpestes", 9700: "Herpestes ichneumon", 9702: "Otariidae", 9703: "Zalophus", 9704: "Zalophus californianus", 9705: "Odobenidae", 9706: "Odobenus", 9707: "Odobenus rosmarus", 9708: "Odobenus rosmarus divergens", 9709: "Phocidae", 9710: "Halichoerus", 9711: "Halichoerus grypus", 9712: "Leptonychotes", 9713: "Leptonychotes weddellii", 9714: "Mirounga", 9715: "Mirounga leonina", 9716: "Mirounga angustirostris", 9717: "Phoca", 9718: "Pusa hispida", 9719: "Pusa sibirica", 9720: "Phoca vitulina", 9721: "Cetacea", 9722: "Odontoceti", 9723: "Platanistidae", 9724: "Inia", 9725: "Inia geoffrensis", 9726: "Delphinidae", 9727: "Delphinus", 9728: "Delphinus delphis", 9729: "Globicephala", 9731: "Globicephala melas", 9732: "Orcinus", 9733: "Orcinus orca", 9734: "Stenella", 9735: "Stenella attenuata", 9736: "Stenella longirostris", 9737: "Stenella coeruleoalba", 9738: "Tursiops", 9739: "Tursiops truncatus", 9740: "Phocoenidae", 9741: "Phocoena", 9742: "Phocoena phocoena", 9743: "Phocoenoides", 9744: "Phocoenoides dalli", 9745: "Phocoenoides dalli dalli", 9747: "Monodontidae", 9748: "Delphinapterus", 9749: "Delphinapterus leucas", 9750: "Physeteridae", 9751: "Kogia", 9752: "Kogia sima", 9753: "Physeter", 9755: "Physeter catodon", 9756: "Ziphiidae", 9757: "Mesoplodon", 9758: "Mesoplodon carlhubbsi", 9759: "Ziphius", 9760: "Ziphius cavirostris", 9761: "Mysticeti", 9762: "Eschrichtiidae", 9763: "Eschrichtius", 9764: "Eschrichtius robustus", 9765: "Balaenopteridae", 9766: "Balaenoptera", 9767: "Balaenoptera acutorostrata", 9768: "Balaenoptera borealis", 9769: "Balaenoptera edeni", 9770: "Balaenoptera physalus", 9771: "Balaenoptera musculus", 9772: "Megaptera", 9773: "Megaptera novaeangliae", 9774: "Sirenia", 9775: "Trichechidae", 9776: "Trichechus", 9777: "Trichechus inunguis", 9778: "Trichechus manatus", 9779: "Proboscidea", 9780: "Elephantidae", 9781: "Elephantidae gen. sp.", 9782: "Elephas", 9783: "Elephas maximus", 9784: "Loxodonta", 9785: "Loxodonta africana", 9786: "Proboscidea louisiana", 9787: "Perissodactyla", 9788: "Equidae", 9789: "Equus", 9790: "Equus burchellii", 9791: "Equus zebra", 9792: "Equus grevyi", 9793: "Equus asinus", 9794: "Equus hemionus", 9796: "Equus caballus", 9798: "Equus przewalskii", 9799: "Tapiridae", 9800: "Tapirus", 9801: "Tapirus terrestris", 9802: "Tapirus indicus", 9803: "Rhinocerotidae", 9804: "Diceros", 9805: "Diceros bicornis", 9806: "Ceratotherium", 9807: "Ceratotherium simum", 9808: "Rhinoceros", 9809: "Rhinoceros unicornis", 9810: "Hyracoidea", 9811: "Procaviidae", 9812: "Procavia", 9813: "Procavia capensis", 9814: "Procavia capensis habessinica", 9815: "Tubulidentata", 9816: "Orycteropodidae", 9817: "Orycteropus", 9818: "Orycteropus afer", 9821: "Suidae", 9822: "Sus", 9823: "Sus scrofa", 9825: "Sus scrofa domesticus", 9826: "Sus sp.", 9827: "Tayassuidae", 9828: "Tayassu", 9829: "Pecari tajacu", 9831: "Hippopotamidae", 9832: "Hippopotamus", 9833: "Hippopotamus amphibius", 9834: "Tylopoda", 9835: "Camelidae", 9836: "Camelus", 9837: "Camelus bactrianus", 9838: "Camelus dromedarius", 9839: "Lama", 9840: "Lama guanicoe", 9843: "Vicugna vicugna", 9844: "Lama glama", 9845: "Ruminantia", 9846: "Tragulidae", 9847: "Tragulus", 9848: "Tragulus napu", 9849: "Tragulus javanicus", 9850: "Cervidae", 9851: "Alces", 9852: "Alces alces", 9853: "Alces alces alces", 9855: "Axis", 9857: "Capreolus", 9858: "Capreolus capreolus", 9859: "Cervus", 9860: "Cervus elaphus", 9861: "Cervus canadensis canadensis", 9863: "Cervus nippon", 9864: "Cervus canadensis nelsoni", 9865: "Cervus elaphus xanthopygus", 9867: "Dama", 9869: "Rangifer", 9870: "Rangifer tarandus", 9871: "Odocoileus", 9872: "Odocoileus hemionus", 9873: "Odocoileus hemionus columbianus", 9874: "Odocoileus virginianus", 9875: "Odocoileus virginianus virginianus", 9876: "Odocoileus hemionus crooki", 9877: "Odocoileus hemionus hemionus", 9878: "Odocoileus hemionus sitkensis", 9879: "Odocoileus virginianus dakotensis", 9880: "Odocoileus virginianus texanus", 9881: "Odocoileinae", 9882: "Hydropotes", 9883: "Hydropotes inermis", 9885: "Muntiacus", 9886: "Muntiacus reevesi", 9887: "Muntiacus vaginalis", 9888: "Muntiacus muntjak", 9889: "Antilocapridae", 9890: "Antilocapra", 9891: "Antilocapra americana", 9892: "Giraffidae", 9893: "Giraffa", 9894: "Giraffa camelopardalis", 9895: "Bovidae", 9896: "Aepyceros", 9897: "Aepyceros melampus", 9898: "Ammotragus", 9899: "Ammotragus lervia", 9900: "Bison", 9901: "Bison bison", 9902: "Bison bonasus", 9903: "Bos", 9904: "Bos gaurus", 9906: "Bos javanicus", 9909: "Bos primigenius", 9913: "Bos taurus", 9915: "Bos indicus", 9916: "Boselaphus", 9917: "Boselaphus tragocamelus", 9918: "Bubalus", 9922: "Capra", 9923: "Capra aegagrus", 9925: "Capra hircus", 9926: "Connochaetes", 9927: "Connochaetes taurinus", 9928: "Damaliscus", 9929: "Damaliscus lunatus", 9930: "Damaliscus lunatus korrigum", 9931: "Damaliscus pygargus", 9933: "Gazella", 9935: "Ovis", 9938: "Ovis aries musimon", 9939: "Ovis sp.", 9940: "Ovis aries", 9943: "Ovis dalli", 9944: "Tragelaphus", 9945: "Tragelaphus oryx", 9946: "Tragelaphus strepsiceros", 9947: "Tragelaphus imberbis", 9948: "Antilopinae", 9950: "Madoqua", 9952: "Cephalophinae", 9954: "Cephalophus", 9957: "Oryx", 9958: "Oryx gazella", 9959: "Hippotraginae", 9961: "Kobus", 9962: "Kobus ellipsiprymnus", 9963: "Caprinae", 9965: "Capricornis", 9966: "Capricornis crispus", 9969: "Syncerus", 9970: "Syncerus caffer", 9971: "Pholidota", 9972: "Manidae", 9973: "Manis", 9974: "Manis javanica", 9975: "Lagomorpha", 9976: "Ochotonidae", 9977: "Ochotona", 9978: "Ochotona princeps", 9979: "Leporidae", 9980: "Lepus", 9981: "Lepus capensis", 9983: "Lepus europaeus", 9984: "Oryctolagus", 9986: "Oryctolagus cuniculus", 9987: "Sylvilagus", 9988: "Sylvilagus floridanus", 9989: "Rodentia", 9991: "Sciurinae", 9992: "Marmota", 9993: "Marmota marmota", 9994: "Marmota marmota marmota", 9995: "Marmota monax", 9996: "Spermophilus", 9997: "Spermophilus citellus", 9999: "Urocitellus parryii", 10001: "Sciurus", 10002: "Sciurus aberti aberti", 10003: "Sciurus aberti barberi", 10004: "Sciurus aberti chuscensis", 10005: "Sciurus aberti ferreus", 10006: "Sciurus aberti kaibabensis", 10007: "Sciurus aberti", 10008: "Tamiasciurus", 10009: "Tamiasciurus hudsonicus", 10010: "Geomyidae", 10011: "Thomomys", 10012: "Thomomys townsendii", 10013: "Thomomys bottae", 10015: "Heteromyidae", 10016: "Dipodomys", 10017: "Dipodomys californicus", 10018: "Dipodomys heermanni", 10019: "Dipodomys panamintinus", 10020: "Dipodomys ordii", 10021: "Pedetidae", 10022: "Pedetes", 10023: "Pedetes capensis", 10026: "Cricetinae", 10028: "Cricetulus", 10029: "Cricetulus griseus", 10030: "Cricetulus longicaudatus", 10031: "Cricetulus sp.", 10032: "Cricetulus migratorius", 10033: "Cricetus", 10034: "Cricetus cricetus", 10035: "Mesocricetus", 10036: "Mesocricetus auratus", 10037: "Mesocricetus brandti", 10038: "Mesocricetus sp.", 10040: "Peromyscus", 10041: "Peromyscus leucopus", 10042: "Peromyscus maniculatus", 10043: "Phodopus", 10044: "Phodopus sungorus", 10045: "Gerbillinae", 10046: "Meriones", 10047: "Meriones unguiculatus", 10049: "Arvicola", 10053: "Microtus", 10054: "Microtus xanthognathus", 10055: "Microtus chrotorrhinus", 10058: "Microtus pennsylvanicus", 10059: "Ondatra", 10060: "Ondatra zibethicus", 10061: "Spalacinae", 10062: "Spalax", 10066: "Muridae", 10067: "Acomys", 10068: "Acomys cahirinus", 10069: "Akodon", 10070: "Akodon aerosus", 10072: "Akodon boliviensis", 10073: "Akodon juninensis", 10074: "Akodon kofordi", 10075: "Akodon mollis", 10076: "Akodon lutescens puer", 10077: "Akodon subfuscus", 10078: "Akodon torques", 10080: "Bolomys", 10081: "Bolomys amoenus", 10084: "Cricetomys", 10085: "Cricetomys gambianus", 10087: "Akodon mimus", 10088: "Mus", 10089: "Mus caroli", 10090: "Mus musculus", 10091: "Mus musculus castaneus", 10092: "Mus musculus domesticus", 10093: "Mus pahari", 10094: "Mus saxicola", 10095: "Mus sp.", 10096: "Mus spretus", 10097: "Mus cervicolor", 10098: "Mus cookii", 10100: "Mus macedonicus", 10101: "Mus platythrix", 10102: "Mus setulosus", 10103: "Mus spicilegus", 10105: "Mus minutoides", 10108: "Mus abbotti", 10111: "Praomys", 10112: "Mastomys natalensis", 10113: "Praomys daltoni", 10114: "Rattus", 10115: "Rattus leucopus", 10116: "Rattus norvegicus", 10117: "Rattus rattus", 10118: "Rattus sp.", 10119: "Rattus fuscipes", 10120: "Rattus sordidus", 10121: "Rattus tunneyi", 10122: "Rattus villosissimus", 10126: "Conilurus", 10127: "Conilurus penicillatus", 10128: "Apodemus", 10129: "Apodemus sylvaticus", 10132: "Calomyscus", 10133: "Calomyscus sp.", 10135: "Hystricidae", 10136: "Hystrix", 10137: "Hystrix cristata", 10138: "Hystrix africaeaustralis", 10139: "Caviidae", 10140: "Cavia", 10141: "Cavia porcellus", 10143: "Cavia sp.", 10144: "Cavia cutleri", 10145: "Galea", 10146: "Galea musteloides", 10147: "Hydrochaeridae", 10148: "Hydrochoerus", 10149: "Hydrochoerus hydrochaeris", 10150: "Chinchillidae", 10151: "Chinchilla", 10152: "Chinchilla chinchilla", 10153: "Lagostomus", 10154: "Lagostomus maximus", 10155: "Myocastoridae", 10156: "Myocastor", 10157: "Myocastor coypus", 10158: "Octodontidae", 10159: "Octodon", 10160: "Octodon degus", 10161: "Echimyidae", 10162: "Proechimys", 10163: "Proechimys guairae", 10164: "Ctenodactylidae", 10165: "Ctenodactylus", 10166: "Ctenodactylus gundi", 10167: "Bathyergidae", 10168: "Thryonomys", 10169: "Thryonomys swinderianus", 10170: "Bathyergus", 10171: "Bathyergus janetta", 10172: "Bathyergus suillus", 10173: "Cryptomys", 10175: "Cryptomys hottentotus", 10176: "Georychus", 10177: "Georychus capensis", 10178: "Heliophobius", 10179: "Heliophobius argenteocinereus", 10180: "Heterocephalus", 10181: "Heterocephalus glaber", 10182: "Petromus", 10183: "Petromus typicus", 10184: "Castor", 10185: "Castor fiber", 10186: "Gerbillus", 10187: "Gerbillus sp.", 10190: "Rotifera", 10191: "Monogononta", 10193: "Brachionidae", 10194: "Brachionus", 10195: "Brachionus plicatilis", 10197: "Ctenophora", 10199: "Beroe", 10200: "Beroe mitrata", 10201: "Beroe ovata", 10205: "Bryozoa", 10206: "Gymnolaemata", 10207: "Cheilostomatida", 10210: "Bugulidae", 10211: "Bugula", 10212: "Bugula neritina", 10213: "Mesozoa", 10214: "Rhombozoa", 10215: "Dicyemida", 10216: "Dicyemidae", 10217: "Dicyema", 10218: "Dicyema misakiense", 10219: "Hemichordata", 10220: "Enteropneusta", 10221: "Harrimaniidae", 10222: "Saccoglossus", 10224: "Saccoglossus kowalevskii", 10226: "Placozoa", 10227: "Trichoplax", 10228: "Trichoplax adhaerens", 10229: "Chaetognatha", 10230: "Sagitta", 10231: "Sagitta elegans", 10232: "Acanthocephala", 10233: "Archiacanthocephala", 10234: "Moniliformida", 10235: "Moniliformidae", 10236: "Moniliformis", 10237: "Moniliformis moniliformis", 10239: "Viruses", 10240: "Poxviridae", 10241: "Chordopoxvirinae", 10242: "Orthopoxvirus", 10243: "Cowpox virus", 10244: "Monkeypox virus", 10245: "Vaccinia virus", 10246: "Vaccinia virus LC16MO", 10247: "Vaccinia virus WR 65-16", 10248: "Vaccinia virus LC16M8", 10249: "Vaccinia virus Copenhagen", 10250: "Vaccinia virus Dairen I", 10251: "Vaccinia virus IHD-J", 10252: "Vaccinia virus Lister", 10253: "Vaccinia virus Tian Tan", 10254: "Vaccinia virus WR", 10255: "Variola virus", 10256: "Raccoonpox virus", 10257: "Parapoxvirus", 10258: "Orf virus", 10259: "Orf virus (strain NZ2)", 10260: "Avipoxvirus", 10261: "Fowlpox virus", 10263: "Fowlpox virus isolate HP-438/Munich", 10264: "Pigeonpox virus", 10265: "Capripoxvirus", 10266: "Sheeppox virus", 10268: "Sheeppox virus INS-1", 10269: "Sheeppox virus KS-1", 10270: "Leporipoxvirus", 10271: "Rabbit fibroma virus", 10272: "Rabbit fibroma virus (strain Kasza)", 10273: "Myxoma virus", 10274: "Malignant rabbit fibroma virus", 10275: "Suipoxvirus", 10276: "Swinepox virus", 10277: "Swinepox virus (STRAIN KASZA)", 10278: "Molluscipoxvirus", 10279: "Molluscum contagiosum virus", 10280: "Molluscum contagiosum virus subtype 1", 10281: "Molluscum contagiosum virus subtype 2", 10282: "Yatapoxvirus", 10283: "unidentified poxvirus", 10284: "Entomopoxvirinae", 10286: "Betaentomopoxvirus", 10288: "Choristoneura biennis entomopoxvirus", 10290: "Heliothis armigera entomopoxvirus", 10291: "unidentified entomopoxvirus", 10292: "Herpesviridae", 10293: "Alphaherpesvirinae", 10294: "Simplexvirus", 10295: "Bovine alphaherpesvirus 2", 10296: "Bovine herpesvirus type 2 (strain BMV)", 10297: "Bovine herpesvirus type 2 (strain BHM-1)", 10298: "Human alphaherpesvirus 1", 10299: "Human alphaherpesvirus 1 strain 17", 10300: "Human alphaherpesvirus 1 strain A44", 10301: "Human alphaherpesvirus 1 strain Angelotti", 10302: "Human alphaherpesvirus 1 strain CL101", 10303: "Human alphaherpesvirus 1 strain HFEM", 10304: "Human alphaherpesvirus 1 strain F", 10305: "Human alphaherpesvirus 1 strain HZT", 10306: "Human alphaherpesvirus 1 strain KOS", 10307: "Human alphaherpesvirus 1 strain MP", 10308: "Human alphaherpesvirus 1 strain Patton", 10309: "Human alphaherpesvirus 1 strain SC16", 10310: "Human alphaherpesvirus 2", 10312: "Human herpesvirus 2 strain 186", 10313: "Human herpesvirus 2 strain 333", 10314: "Human herpesvirus 2 strain G", 10315: "Human herpesvirus 2 strain HG52", 10316: "Human herpesvirus 2 strain SA8", 10317: "Cercopithecine alphaherpesvirus 2", 10319: "Varicellovirus", 10320: "Bovine alphaherpesvirus 1", 10321: "Bovine herpesvirus type 1.2 strain Q3932", 10322: "Bovine herpesvirus type 1 strain 6660", 10323: "Bovine herpesvirus type 1.1 (strain Cooper)", 10324: "Bovine herpesvirus type 1.1 (strain P8-2)", 10325: "Macacine alphaherpesvirus 1", 10326: "Equid alphaherpesvirus 1", 10327: "Equine herpesvirus type 1 (isolate HSV25A)", 10328: "Equine herpesvirus type 1 (strain AB1)", 10329: "Equine herpesvirus type 1 (strain Kentucky A)", 10330: "Equine herpesvirus type 1 (strain Kentucky D)", 10331: "Equid alphaherpesvirus 4", 10333: "Equine herpesvirus type 4 (strain 1942)", 10334: "Felid alphaherpesvirus 1", 10335: "Human alphaherpesvirus 3", 10338: "Human herpesvirus 3 strain Dumas", 10343: "Infectious laryngotracheitis virus (strain SA-2)", 10344: "Infectious laryngotracheitis virus (strain Thorne V882)", 10345: "Suid alphaherpesvirus 1", 10346: "Suid herpesvirus 1 strain Becker", 10349: "Suid herpesvirus 1 (strain NIA-3)", 10350: "Suid herpesvirus 1 (strain Rice)", 10353: "Saimiriine alphaherpesvirus 1", 10355: "Bovine herpesvirus 4 (isolate DN-599)", 10357: "Betaherpesvirinae", 10358: "Cytomegalovirus", 10359: "Human betaherpesvirus 5", 10360: "Human herpesvirus 5 strain AD169", 10361: "Human herpesvirus 5 strain Colburn", 10362: "Human herpesvirus 5 strain Eisenhardt", 10363: "Human herpesvirus 5 strain Towne", 10364: "Simian cytomegalovirus", 10365: "Muromegalovirus", 10366: "Murid betaherpesvirus 1", 10367: "Murine cytomegalovirus (strain Smith)", 10368: "Human betaherpesvirus 6", 10369: "Human herpesvirus 6 (strain GS)", 10370: "Human herpesvirus 6 (strain Uganda-1102)", 10371: "Equid gammaherpesvirus 5", 10372: "Human betaherpesvirus 7", 10373: "Macaca mulatta cytomegalovirus", 10374: "Gammaherpesvirinae", 10375: "Lymphocryptovirus", 10376: "Human gammaherpesvirus 4", 10377: "Human herpesvirus 4 strain B95-8", 10378: "Human herpesvirus 4 strain RAJI", 10379: "Rhadinovirus", 10380: "Ateline gammaherpesvirus 2", 10381: "Saimiriine gammaherpesvirus 2", 10382: "Herpesvirus saimiri (strain 484-77)", 10383: "Herpesvirus saimiri (strain 11)", 10384: "Herpesvirus saimiri (strain 488)", 10385: "Bovine gammaherpesvirus 4", 10386: "Gallid alphaherpesvirus 1", 10387: "Marek's disease herpesvirus type 1 strain BC-1", 10388: "Marek's disease herpesvirus strain GA", 10389: "Marek's disease herpesvirus type 1 strain MD5", 10390: "Gallid alphaherpesvirus 2", 10391: "Gallid herpesvirus 2 strain FC126", 10392: "Gallid herpesvirus 2 strain H2", 10395: "Herpesvirus sylvilagus", 10397: "Tupaiid betaherpesvirus 1", 10398: "Ovine gammaherpesvirus 2", 10401: "Ictalurid herpesvirus 1", 10404: "Hepadnaviridae", 10405: "Orthohepadnavirus", 10406: "Ground squirrel hepatitis virus", 10407: "Hepatitis B virus", 10408: "Hepatitis B virus subtype adw2", 10409: "Hepatitis B virus adr4", 10410: "Hepatitis B virus adw/991", 10411: "Hepatitis B virus alpha1", 10412: "Hepatitis B virus adw/Indonesia/PIDW420", 10413: "Hepatitis B virus adw/Japan/PJDW233", 10414: "Hepatitis B virus LSH/chimpanzee", 10415: "Hepatitis B virus adw/Okinawa/PODW282", 10418: "Hepatitis B virus subtype ayw", 10419: "Hepatitis B virus subtype adyw", 10421: "Hepatitis delta virus (ISOLATE 7/18/83)", 10422: "Hepatitis delta virus (ISOLATE AMERICAN)", 10423: "Hepatitis delta virus (ISOLATE ITALIAN)", 10424: "Hepatitis delta virus (ISOLATE JAPANESE M-1)", 10425: "Hepatitis delta virus (ISOLATE JAPANESE M-2)", 10426: "Hepatitis delta virus (ISOLATE NAURU)", 10427: "Hepatitis delta virus (ISOLATE JAPANESE S-1)", 10428: "Hepatitis delta virus (ISOLATE JAPANESE S-2)", 10430: "Woodchuck hepatitis virus 1", 10431: "Woodchuck hepatitis virus 59", 10432: "Woodchuck hepatitis virus 7", 10433: "Woodchuck hepatitis virus 8", 10436: "Woodchuck hepatitis virus w64 (ISOLATE PWS23)", 10437: "Avihepadnavirus", 10439: "Duck hepatitis B virus brown Shanghai duck/S5", 10440: "Duck hepatitis B virus white Shanghai duck/S31", 10442: "Baculoviridae", 10449: "Lymantria dispar multiple nucleopolyhedrovirus", 10450: "Orgyia pseudotsugata single capsid nuclopolyhedrovirus", 10453: "Panolis flammea nucleopolyhedrovirus", 10454: "Spodoptera exigua multiple nucleopolyhedrovirus", 10455: "Spodoptera frugiperda multiple nucleopolyhedrovirus", 10456: "Spodoptera littoralis nucleopolyhedrovirus", 10462: "Trichoplusia ni granulovirus", 10463: "unidentified granulovirus", 10464: "Agrotis segetum granulovirus", 10465: "Pieris brassicae granulovirus", 10468: "Helicoverpa zea single nucleopolyhedrovirus", 10469: "unidentified baculovirus", 10471: "unidentified nuclear polyhedrosis viruses", 10472: "Plasmaviridae", 10473: "Plasmavirus", 10474: "Fuselloviridae", 10475: "Alphafusellovirus", 10477: "Lipothrixviridae", 10479: "Thermoproteus tenax virus 1", 10480: "Thermoproteus tenax virus 1 (STRAIN KRA1)", 10481: "Thermoproteus tenax virus 1 (STRAIN VT3)", 10482: "Polydnaviridae", 10483: "Ichnovirus", 10484: "Campoletis sonorensis ichnovirus", 10485: "Bracovirus", 10486: "Iridoviridae", 10487: "Iridovirus", 10489: "Simulium sp. iridescent virus", 10490: "Tipula iridescent virus", 10491: "Chloriridovirus", 10492: "Ranavirus", 10493: "Frog virus 3", 10494: "Lymphocystivirus", 10497: "African swine fever virus", 10498: "African swine fever virus BA71V", 10499: "African swine fever virus LIS57", 10500: "African swine fever virus Malawi LIL 20/1", 10501: "Phycodnaviridae", 10506: "Paramecium bursaria Chlorella virus 1", 10507: "Chlorella virus", 10508: "Adenoviridae", 10509: "Mastadenovirus", 10510: "Bovine adenovirus 3", 10511: "Bovine adenovirus 7", 10512: "Canine adenovirus 1", 10513: "Canine adenovirus 1 strain Glaxo", 10514: "Canine adenovirus 2", 10515: "Human adenovirus 2", 10519: "Human adenovirus 7", 10521: "Human adenovirus 14", 10522: "Human adenovirus 35", 10524: "Human adenovirus 41", 10527: "Human adenovirus D9", 10528: "Human adenovirus 18", 10529: "Human adenovirus 31", 10530: "Murine adenovirus 1", 10532: "Simian adenovirus 7", 10533: "Human adenovirus 1", 10534: "Human adenovirus 6", 10535: "unidentified adenovirus", 10537: "Canine mastadenovirus A", 10541: "Human adenovirus 11", 10546: "Bovine adenovirus 1", 10547: "Fowl aviadenovirus 10", 10548: "Human adenovirus 34", 10552: "Aviadenovirus", 10553: "Fowl aviadenovirus 1", 10556: "Rhizidiovirus", 10560: "Bovine papillomavirus type 2", 10561: "Xipapillomavirus 1", 10562: "Bovine papillomavirus type 4", 10563: "Bovine papillomavirus type 6", 10564: "Deltapapillomavirus 2", 10565: "Deltapapillomavirus 1", 10566: "Human papillomavirus", 10567: "Iotapapillomavirus 1", 10568: "Micromys minutus papillomavirus 1", 10569: "Reindeer papillomavirus", 10570: "Alphapapillomavirus 12", 10571: "Bovine papillomavirus", 10572: "Hamster papovavirus", 10573: "Human papillomavirus type 13", 10574: "Monkey B-lymphotropic papovavirus", 10576: "Pygmy chimpanzee papillomavirus type 1", 10577: "Chaffinch papillomavirus", 10579: "Human papillomavirus type 8", 10580: "Human papillomavirus type 11", 10583: "Human papillomavirus type 1a", 10584: "Human papillomavirus type 2a", 10585: "Human papillomavirus type 31", 10586: "Human papillomavirus type 33", 10587: "Human papillomavirus type 35", 10588: "Human papillomavirus type 39", 10589: "Human papillomavirus type 41", 10590: "Human papillomavirus type 42", 10591: "Human papillomavirus type 43", 10592: "Human papillomavirus type 44", 10593: "Human papillomavirus type 45", 10594: "Human papillomavirus type 47", 10595: "Human papillomavirus type 51", 10596: "Human papillomavirus type 56", 10598: "Human papillomavirus type 58", 10599: "Human papillomavirus type 5b", 10600: "Human papillomavirus type 6b", 10601: "Human papillomavirus type 6c", 10602: "Human papillomavirus type me180", 10604: "Human papillomavirus type 12", 10605: "Human papillomavirus type 14", 10606: "Human papillomavirus 15", 10607: "Human papillomavirus 17", 10608: "Human papillomavirus 19", 10609: "Human papillomavirus type 25", 10610: "Human papillomavirus type 2c", 10611: "Human papillomavirus type 30", 10614: "Human papillomavirus 3", 10615: "Human papillomavirus type 40", 10616: "Human papillomavirus type 49", 10617: "Human papillomavirus 4", 10618: "Human papillomavirus type 52", 10620: "Human papillomavirus type 7", 10621: "Human papillomavirus 9", 10622: "Monkey papillomavirus", 10623: "Kappapapillomavirus 2", 10630: "BK virus strain GS", 10631: "BK virus strain AS", 10632: "JC polyomavirus", 10636: "Murine polyomavirus strain A2", 10637: "Mouse polyomavirus (strain Crawford small-plaque)", 10638: "Kilham polyomavirus", 10639: "Caulimovirus", 10640: "Carnation etched ring virus", 10641: "Cauliflower mosaic virus", 10642: "Cauliflower mosaic virus (STRAIN D4)", 10643: "Cauliflower mosaic virus (STRAIN BARI 1)", 10644: "Cauliflower mosaic virus (STRAIN CM-1841)", 10645: "Cauliflower mosaic virus (STRAIN D/H)", 10646: "Cauliflower mosaic virus (STRAIN S-JAPAN)", 10647: "Cauliflower mosaic virus (STRAIN PV147)", 10648: "Cauliflower mosaic virus (STRAIN STRASBOURG)", 10649: "Figwort mosaic virus", 10650: "Figwort mosaic virus (STRAIN DXS)", 10651: "Soybean chlorotic mottle virus", 10652: "Badnavirus", 10653: "Commelina yellow mottle virus", 10654: "Rice tungro bacilliform virus", 10655: "Rice tungro bacilliform virus (isolate Philippines)", 10656: "Tectiviridae", 10658: "Enterobacteria phage PRD1", 10659: "Corticoviridae", 10660: "Corticovirus", 10661: "Pseudoalteromonas virus PM2", 10662: "Myoviridae", 10663: "Tequatrovirus", 10664: "Enterobacteria phage T2", 10665: "Escherichia virus T4", 10666: "Enterobacteria phage T6", 10667: "Bacillus phage PBSX", 10674: "Enterobacteria phage K3", 10676: "Enterobacteria phage M1", 10677: "Escherichia virus Mu", 10678: "Escherichia virus P1", 10679: "Escherichia virus P2", 10680: "Enterobacteria phage P4", 10681: "Enterobacteria phage phiR73", 10682: "Enterobacteria phage P7", 10683: "Bacillus virus PBS1", 10684: "Bacillus phage PBS2", 10685: "Bacillus virus SPO1", 10686: "Enterobacteria phage TuIa", 10687: "Enterobacteria phage TuIb", 10689: "Vibrio phage CP-T1", 10690: "Haemophilus virus HP1", 10691: "Enterobacteria phage Ox2", 10692: "Enterobacteria phage RB18", 10693: "Enterobacteria phage RB51", 10696: "Bacillus phage SP82", 10699: "Siphoviridae", 10701: "Actinophage RP3", 10702: "Streptomyces phage VWB", 10703: "Corynephage beta", 10704: "Rhizobium phage 16-3", 10705: "Enterobacteria phage 82", 10707: "Escherichia virus BF23", 10708: "Pseudomonas virus D3112", 10710: "Escherichia virus Lambda", 10711: "Enterobacteria phage P21", 10712: "Phage 434", 10713: "Enterobacteria phage phi80", 10714: "Corynephage omega", 10715: "Staphylococcus phage 42D.m", 10717: "Bacillus phage phi105", 10719: "Streptomyces virus phiC31", 10721: "Staphylococcus phage S phi-C", 10723: "Bacillus phage SPO2", 10724: "Bacillus phage SPP1", 10725: "Bacillus phage SPR", 10726: "Escherichia virus T5", 10727: "Staphylococcus phage L54a", 10728: "Streptococcus pneumoniae phage HB-3", 10730: "Escherichia phage 933W", 10732: "Streptomyces phage R4", 10733: "Corynebacterium phage gamma", 10735: "Bacillus phage rho11s", 10736: "Bacillus phage phi3T", 10737: "Enterobacteria phage phi21", 10738: "Enterobacteria phage PA-2", 10742: "Escherichia virus HK022", 10743: "Phage 21", 10744: "Podoviridae", 10746: "Lactococcus phage phi-vML3", 10747: "Streptococcus phage Cp1", 10748: "Streptococcus phage CP-7", 10749: "Streptococcus phage CP-9", 10750: "Enterobacteria phage LP7", 10752: "Escherichia virus N4", 10753: "Bacillus phage Nf", 10754: "Salmonella virus P22", 10755: "Phage phi-15", 10756: "Bacillus virus phi29", 10757: "Bacillus phage PZA", 10759: "Enterobacteria phage T3", 10760: "Escherichia phage T7", 10761: "Shigella virus Sf6", 10765: "Bacillus phage H1", 10766: "Enterobacteria phage K11", 10773: "Bacillus phage SF6", 10778: "Bacillus virus B103", 10779: "Bacillus phage BS32", 10780: "Parvoviridae", 10783: "Aleutian mink disease parvovirus (STRAIN G)", 10784: "Bovine parvovirus", 10785: "Feline parvovirus", 10786: "Feline panleukopenia virus", 10787: "Feline panleukopenia virus (strain 193)", 10788: "Canine parvovirus", 10789: "Canine parvovirus strain 780929", 10790: "Canine parvovirus strain CPV-D CORNELL 320", 10791: "Canine parvovirus strain N", 10792: "Mink enteritis virus", 10793: "Mink enteritis virus strain Abashiri", 10794: "Minute virus of mice", 10795: "Murine minute virus (STRAIN MVMI)", 10796: "Porcine parvovirus", 10797: "Porcine parvovirus NADL-2", 10798: "Human parvovirus B19", 10799: "H-1 parvovirus", 10800: "Parvovirus H3", 10801: "Parvovirus R1", 10802: "Raccoon parvovirus", 10803: "Dependoparvovirus", 10804: "Adeno-associated virus - 2", 10805: "Adeno-associated virus 2H", 10806: "Ambidensovirus", 10808: "Aedes densonucleosis virus (STRAIN GKV 002 002)", 10809: "Bombyx mori densovirus", 10811: "Geminiviridae", 10812: "Mastrevirus", 10813: "Curtovirus", 10814: "Begomovirus", 10815: "Abutilon mosaic virus", 10816: "Abutilon mosaic virus - [WEST INDIA]", 10817: "African cassava mosaic virus", 10818: "African cassava mosaic virus - [West Kenya 844]", 10820: "Chloris striate mosaic virus", 10821: "Maize streak virus", 10822: "Maize streak virus - [Kenya]", 10823: "Maize streak virus - [Nigeria]", 10824: "Maize streak virus - [South Africa]", 10825: "Miscanthus streak virus", 10826: "Panicum streak virus", 10827: "Potato yellow mosaic virus", 10829: "Squash leaf curl virus", 10830: "Tobacco yellow dwarf virus", 10831: "Tomato golden mosaic virus", 10832: "Tomato yellow leaf curl virus", 10834: "Wheat dwarf virus", 10835: "Tomato mottle virus", 10836: "Sugarcane streak virus", 10837: "Digitaria streak virus", 10838: "Bean dwarf mosaic virus", 10839: "Bean golden mosaic virus", 10840: "Beet curly top virus", 10841: "Microviridae", 10842: "Microvirus", 10843: "Escherichia phage G4", 10844: "Enterobacteria phage S13", 10845: "Escherichia phage St-1", 10847: "Escherichia virus phiX174", 10848: "Escherichia virus phiK", 10849: "Escherichia phage alpha3", 10850: "Enterobacteria phage G14", 10851: "Enterobacteria phage U3", 10852: "Spiromicrovirus", 10854: "Spiroplasma phage 1-R8A2B", 10855: "Spiroplasma virus SpV4", 10856: "Bdellomicrovirus", 10860: "Inoviridae", 10861: "Inovirus", 10862: "Xanthomonas virus Cf1c", 10863: "Enterobacteria phage f1", 10864: "Enterobacteria phage fd", 10866: "Enterobacteria phage ZJ/2", 10867: "Enterobacteria phage Ike", 10868: "Enterobacteria phage If1", 10869: "Escherichia virus I22", 10872: "Pseudomonas phage Pf3", 10874: "Shigella phage SfX", 10875: "Plectrovirus", 10877: "Cystoviridae", 10878: "Cystovirus", 10879: "Pseudomonas virus phi6", 10880: "Reoviridae", 10882: "Orthoreovirus", 10884: "Mammalian orthoreovirus 1 Lang", 10885: "Mammalian orthoreovirus 2 D5/Jones", 10886: "Mammalian orthoreovirus 3 Dearing", 10891: "Reovirus sp.", 10892: "Orbivirus", 10893: "Broadhaven virus", 10894: "Tick and insect-borne orbivirus", 10895: "Australian bluetongue virus", 10897: "African horse sickness virus 9", 10900: "Bluetongue virus (serotype 10 / American isolate)", 10903: "Bluetongue virus 17", 10904: "Bluetongue virus (serotype 1 / isolate Australia)", 10905: "Bluetongue virus (serotype 1 / isolate South Africa)", 10906: "Bluetongue virus 10", 10907: "Bluetongue virus (serotype 2 / isolate USA)", 10910: "Epizootic hemorrhagic disease virus (serotype 2 / strain Alberta)", 10911: "Coltivirus", 10912: "Rotavirus", 10913: "Porcine rotavirus", 10915: "Porcine rotavirus serotype 5/strain OSU", 10916: "Porcine rotavirus C strain Cowden", 10917: "Porcine rotavirus strain Gottfried", 10918: "Porcine rotavirus strain K", 10919: "Porcine rotavirus strain YM", 10921: "Feline rotavirus", 10922: "Simian rotavirus", 10923: "Simian rotavirus A/SA11", 10925: "Simian rotavirus A/SA11-FEM", 10926: "Simian rotavirus A/SA11-SEM", 10927: "Bovine rotavirus", 10928: "Bovine rotavirus strain B641/G6", 10929: "Bovine rotavirus (serotype 6 / STRAIN 61A)", 10931: "Bovine rotavirus C486", 10933: "Bovine rotavirus strain RF", 10934: "Bovine rotavirus strain UK/G6", 10935: "Bovine rotavirus (strain VMRI)", 10937: "Equine rotavirus", 10939: "Equine rotavirus strain H-2", 10941: "Human rotavirus A", 10942: "Human rotavirus B", 10943: "Human rotavirus C", 10944: "Human rotavirus serotype 1 / strain 1076", 10946: "Human rotavirus (STRAIN RV5)", 10947: "Human rotavirus serotype 1 / strain 69M", 10948: "Human rotavirus (SEROTYPE 2 / STRAIN HU5)", 10949: "Human rotavirus (SEROTYPE G / STRAIN B37)", 10950: "Human rotavirus (SEROTYPE 2 / STRAIN DS1)", 10951: "Human rotavirus (SEROTYPE 2 / STRAIN HN126)", 10952: "Human rotavirus strain KU", 10953: "Human rotavirus (STRAIN L26)", 10954: "Human rotavirus serotype 1 / strain M37", 10955: "Human rotavirus strain MCN13", 10956: "Human rotavirus serotype 1 / strain MO", 10957: "Human rotavirus strain P", 10958: "Human rotavirus strain RRV", 10959: "Human rotavirus (SEROTYPE 2 / STRAIN S2)", 10960: "Human rotavirus G4 strain St. Thomas 3", 10961: "Human rotavirus G4 strain VA70", 10962: "Human rotavirus strain WA", 10963: "Rabbit rotavirus", 10967: "Porcine rotavirus A", 10968: "Porcine rotavirus C", 10970: "Rotavirus sp.", 10971: "Rotavirus subgroup 2", 10978: "Rotavirus subgroup 1", 10979: "Aquareovirus", 10981: "Cypovirus", 10983: "Euxoa scandens cypovirus 5", 10985: "Phytoreovirus", 10986: "Rice gall dwarf virus", 10987: "Wound tumor virus", 10988: "Fijivirus", 10989: "Maize rough dwarf virus", 10990: "Rice black streaked dwarf virus", 10991: "Rice dwarf virus", 10992: "Oryzavirus", 10993: "Birnaviridae", 10995: "Infectious bursal disease virus", 10996: "Infectious bursal disease virus 52/70", 10997: "Infectious bursal disease virus 002-73/AUS", 10998: "Infectious bursal disease virus CU-1", 10999: "Infectious bursal disease virus OH", 11000: "Infectious bursal disease virus PBG-98", 11001: "Infectious bursal disease virus STC", 11002: "Infectious pancreatic necrosis virus", 11003: "Infectious pancreatic necrosis virus - Jasper", 11004: "Infectious pancreatic necrosis virus - N1", 11005: "Infectious pancreatic necrosis virus - Sp", 11006: "Totiviridae", 11007: "Totivirus", 11008: "Saccharomyces cerevisiae virus L-A", 11009: "Ustilago maydis virus P4", 11010: "Ustilago maydis virus P6", 11011: "Giardiavirus", 11012: "Partitiviridae", 11014: "Chrysovirus", 11018: "Togaviridae", 11019: "Alphavirus", 11020: "Barmah Forest virus", 11021: "Eastern equine encephalitis virus", 11022: "Eastern equine encephalitis virus (STRAIN VA33[TEN BROECK])", 11023: "Middelburg virus", 11024: "Highlands J virus", 11028: "O'nyong-nyong virus strain Gulu", 11029: "Ross River virus", 11030: "Ross river virus (STRAIN 213970)", 11031: "Ross river virus (STRAIN NB5092)", 11032: "Ross river virus (STRAIN T48)", 11033: "Semliki Forest virus", 11034: "Sindbis virus", 11036: "Venezuelan equine encephalitis virus", 11037: "Venezuelan equine encephalitis virus (strain TC-83)", 11038: "Venezuelan equine encephalitis virus (strain Trinidad donkey)", 11039: "Western equine encephalitis virus", 11040: "Rubivirus", 11041: "Rubella virus", 11043: "Rubella virus strain M33", 11044: "Rubella virus vaccine strain RA27/3", 11045: "Rubella virus strain Therien", 11047: "Equine arteritis virus", 11048: "Lactate dehydrogenase-elevating virus", 11049: "Lelystad virus", 11050: "Flaviviridae", 11051: "Flavivirus", 11052: "Dengue virus group", 11053: "Dengue virus 1", 11057: "Dengue virus 1 Thailand/AHF 82-80/1980", 11058: "Dengue virus 1 Jamaica/CV1636/1977", 11059: "Dengue virus 1 Nauru/West Pac/1974", 11060: "Dengue virus 2", 11062: "Dengue virus 2 Malaysia M2", 11063: "Dengue virus 2 Malaysia M3", 11064: "Dengue virus 2 Jamaica/1409/1983", 11065: "Dengue virus 2 Thailand/NGS-C/1944", 11066: "Dengue virus 2 Puerto Rico/PR159-S1/1969", 11067: "Dengue virus 2 Tonga/EKB194/1974", 11068: "Dengue virus 2 Thailand/PUO-218/1980", 11069: "Dengue virus 3", 11070: "Dengue virus 4", 11071: "Japanese encephalitis virus group", 11072: "Japanese encephalitis virus", 11073: "Japanese encephalitis virus strain SA-14", 11074: "Japanese encephalitis virus strain SA(V)", 11075: "Japanese encephalitis virus strain JAOARS982", 11076: "Japanese encephalitis virus strain Nakayama", 11077: "Kunjin virus", 11078: "Kunjin virus (STRAIN MRM61C)", 11079: "Murray Valley encephalitis virus", 11080: "Saint Louis encephalitis virus", 11081: "St. Louis encephalitis virus (strain MS1-7)", 11082: "West Nile virus", 11083: "Powassan virus", 11084: "Tick-borne encephalitis virus", 11085: "Langat virus", 11086: "Louping ill virus", 11087: "Tick-borne encephalitis virus (STRAIN SOFJIN)", 11088: "Tick-borne encephalitis virus (WESTERN SUBTYPE)", 11089: "Yellow fever virus", 11090: "Yellow fever virus 17D", 11092: "Kumlinge virus", 11093: "Flavivirus sp.", 11094: "Negishi virus", 11095: "Pestivirus", 11096: "Classical swine fever virus", 11097: "Hog cholera virus (strain Alfort)", 11098: "Classical swine fever virus - Brescia", 11099: "Bovine viral diarrhea virus 1", 11100: "Bovine viral diarrhea virus 1-NADL", 11101: "Pestivirus type 3", 11102: "Hepacivirus", 11103: "Hepacivirus C", 11104: "Hepatitis C virus (isolate 1)", 11105: "Hepatitis C virus (isolate BK)", 11106: "Hepatitis C virus (isolate EC10)", 11107: "Hepatitis C virus (isolate EC1)", 11108: "Hepatitis C virus (isolate H)", 11109: "Hepatitis C virus HCT27", 11110: "Hepatitis C virus HCT18", 11111: "Hepatitis C virus HC-J2", 11112: "Hepatitis C virus HC-J5", 11113: "Hepatitis C virus isolate HC-J6", 11114: "Hepatitis C virus HC-J7", 11115: "Hepatitis C virus isolate HC-J8", 11116: "Hepatitis C virus (isolate Japanese)", 11117: "Hepatitis C virus (isolate TH)", 11118: "Coronaviridae", 11120: "Infectious bronchitis virus", 11121: "Avian infectious bronchitis virus (strain 6/82)", 11122: "Avian infectious bronchitis virus (strain Beaudette)", 11123: "Avian infectious bronchitis virus (strain Beaudette M42)", 11124: "Avian infectious bronchitis virus (strain D274)", 11125: "Avian infectious bronchitis virus (strain D3896)", 11126: "Avian infectious bronchitis virus (strain KB8523)", 11127: "Avian infectious bronchitis virus (strain M41)", 11128: "Bovine coronavirus", 11129: "Bovine coronavirus strain F15", 11130: "Bovine coronavirus strain L9", 11131: "Bovine coronavirus LY-138", 11132: "Bovine coronavirus Mebus", 11133: "Bovine coronavirus strain Quebec", 11134: "Bovine coronavirus strain vaccine", 11135: "Feline infectious peritonitis virus", 11137: "Human coronavirus 229E", 11138: "Murine hepatitis virus", 11139: "Murine hepatitis virus strain 1", 11140: "Murine hepatitis virus strain 3", 11142: "Murine hepatitis virus strain A59", 11143: "Murine hepatitis virus strain defective JHM", 11144: "Murine hepatitis virus strain JHM", 11145: "Murine hepatitis virus strain S", 11146: "Porcine respiratory coronavirus", 11148: "Porcine respiratory coronavirus (STRAIN RM4)", 11149: "Transmissible gastroenteritis virus", 11150: "Porcine transmissible gastroenteritis coronavirus strain FS772/70", 11151: "Porcine transmissible gastroenteritis coronavirus strain Purdue", 11152: "Turkey coronavirus", 11153: "Canine coronavirus", 11155: "Torovirus", 11156: "Berne virus", 11157: "Mononegavirales", 11158: "Paramyxoviridae", 11159: "Paramyxovirinae", 11162: "Mumps virus strain Edinburgh 2", 11163: "Mumps virus strain Edinburgh 4", 11164: "Mumps virus strain Edinburgh 6", 11165: "Mumps virus strain Matsuyama", 11166: "Mumps virus strain Belfast", 11167: "Mumps virus strain Enders", 11168: "Mumps virus strain Jeryl Lynn", 11169: "Mumps virus strain Kilham", 11170: "Mumps virus Bristol 1", 11171: "Mumps virus Miyahara vaccine", 11172: "Mumps virus strain RW", 11173: "Mumps virus strain SBL-1", 11174: "Mumps virus strain Takahashi", 11175: "Mumps virus strain Urabe vaccine AM9", 11176: "Avian avulavirus 1", 11177: "Newcastle disease virus (STRAIN AUSTRALIA-VICTORIA/32)", 11178: "Newcastle disease virus strain Beaudette C/45", 11179: "Newcastle disease virus CHI/85", 11180: "Newcastle disease virus strain D26/76", 11181: "Newcastle disease virus (STRAIN B1-HITCHNER/47)", 11182: "Newcastle disease virus strain Italien/45", 11183: "Newcastle disease virus (STRAIN IBA/85)", 11184: "Newcastle disease virus (STRAIN LAS/46)", 11185: "Newcastle disease virus Miyadera/51", 11186: "Newcastle disease virus strain Queensland/66", 11187: "Newcastle disease virus strain HER/33", 11188: "Newcastle disease virus (STRAIN TEXAS)", 11189: "Newcastle disease virus (STRAIN TEXAS G.B./48)", 11190: "Newcastle disease virus Ulster/67", 11191: "Murine respirovirus", 11193: "Sendai virus (strain 6/94)", 11194: "Sendai virus (strain Enders)", 11195: "Sendai virus (strain Fushimi)", 11196: "Sendai virus (strain Harris)", 11198: "Sendai virus (Z)", 11208: "Simian virus 5 (strain W3)", 11210: "Human parainfluenza virus 1 (C39)", 11211: "HPIV-1 (human/Washington/1957)", 11213: "Human parainfluenza virus 2 (strain Greer)", 11214: "Human parainfluenza virus 2 (strain Toshiba)", 11215: "Bovine respirovirus 3", 11216: "Human respirovirus 3", 11217: "Human parainfluenza 3 virus (strain NIH 47885)", 11218: "Human parainfluenza 3 virus (strain AUS/124854/74)", 11219: "Human parainfluenza 3 virus (strain TEX/545/80)", 11220: "Human parainfluenza 3 virus (strain TEX/9305/82)", 11221: "Human parainfluenza 3 virus (strain TEX/12677/83)", 11222: "Human parainfluenza 3 virus (strain WASH/641/79)", 11223: "Human parainfluenza 3 virus (strain WASH/1511/73)", 11224: "Human parainfluenza virus 4a", 11225: "Human parainfluenza virus 4a (strain Toshiba)", 11226: "Human parainfluenza virus 4b", 11227: "Human parainfluenza virus 4b (strain 68-333)", 11229: "Morbillivirus", 11232: "Canine morbillivirus", 11233: "Canine distemper virus strain Onderstepoort", 11234: "Measles morbillivirus", 11235: "Measles virus strain Edmonston", 11236: "Measles virus strain Halle", 11237: "Measles virus strain IP-3-CA", 11238: "Measles virus strain HU2", 11239: "Measles virus strain Yamagata-1", 11240: "Phocine morbillivirus", 11241: "Rinderpest morbillivirus", 11242: "Rinderpest virus (strain Kabete O)", 11243: "Rinderpest virus (strain L)", 11244: "Pneumoviridae", 11245: "Pneumovirus", 11246: "Bovine orthopneumovirus", 11247: "Bovine respiratory syncytial virus ATCC51908", 11248: "Bovine respiratory syncytial virus (strain Copenhagen)", 11249: "Bovine respiratory syncytial virus (strain RB94)", 11250: "Human orthopneumovirus", 11251: "Human respiratory syncytial virus (subgroup B / strain 18537)", 11252: "Human respiratory syncytial virus (strain RSB642)", 11253: "Human respiratory syncytial virus (strain RSB1734)", 11254: "Human respiratory syncytial virus (strain RSB5857)", 11255: "Human respiratory syncytial virus (strain RSB6190)", 11256: "Human respiratory syncytial virus (strain RSB6256)", 11257: "Human respiratory syncytial virus (strain RSB6614)", 11258: "Human respiratory syncytial virus (subgroup B / strain 8/60)", 11259: "Human respiratory syncytial virus A2", 11260: "Human respiratory syncytial virus A strain Long", 11261: "Human respiratory syncytial virus strain RSS-2", 11263: "Murine orthopneumovirus", 11264: "Turkey rhinotracheitis virus", 11266: "Filoviridae", 11269: "Marburg marburgvirus", 11270: "Rhabdoviridae", 11271: "Vesiculovirus", 11272: "Chandipura virus", 11273: "Chandipura virus I653514", 11274: "Piry virus", 11276: "Vesicular stomatitis virus", 11277: "Vesicular stomatitis Indiana virus", 11278: "Vesicular stomatitis Indiana virus strain Glasgow", 11279: "Vesicular stomatitis Indiana virus strain Mudd-Summers", 11280: "Vesicular stomatitis New Jersey virus", 11281: "Vesicular stomatitis virus (serotype New Jersey / strain Hazelhurst)", 11282: "Vesicular stomatitis virus (serotype New Jersey / strain Missouri)", 11283: "Vesicular stomatitis virus (serotype New Jersey / strain Ogden)", 11284: "Vesicular stomatitis Indiana virus strain Orsay", 11285: "Vesicular stomatitis Indiana virus strain San Juan", 11286: "Lyssavirus", 11287: "Viral hemorrhagic septicemia virus", 11288: "Viral hemorrhagic septicemia virus 07-71", 11289: "Viral hemorrhagic septicemia virus strain MAKAH", 11290: "Infectious hematopoietic necrosis virus", 11291: "Infectious hematopoietic necrosis virus - round butte", 11292: "Rabies lyssavirus", 11293: "Rabies virus AVO1", 11294: "Rabies virus CVS-11", 11295: "Rabies virus ERA", 11296: "Rabies virus HEP-FLURY", 11297: "Rabies virus PM", 11298: "Rabies virus Nishigahara RCEH", 11300: "Rabies virus SAD B19", 11301: "Sigma virus", 11303: "Bovine ephemeral fever virus", 11305: "Cytorhabdovirus", 11306: "Nucleorhabdovirus", 11307: "Sonchus yellow net nucleorhabdovirus", 11308: "Orthomyxoviridae", 11309: "unidentified influenza virus", 11313: "Fowl plague virus", 11318: "Dhori thogotovirus", 11319: "Dhori virus (strain Indian/1313/61)", 11320: "Influenza A virus", 11338: "Influenza A virus (A/chicken/Alabama/1/75(H4))", 11339: "Influenza A virus (STRAIN A/CHICKEN/GERMANY/N/49)", 11340: "Influenza A virus (A/chicken/Japan/24(H7N7))", 11357: "Influenza A virus (STRAIN A/DUCK/HOKKAIDO/5/77)", 11359: "Influenza A virus (A/duck/Hokkaido/33/80(H3))", 11360: "Influenza A virus (A/duck/Hokkaido/7/82(H3))", 11361: "Influenza A virus (A/duck/Hokkaido/21/82(H3))", 11362: "Influenza A virus (A/duck/Hokkaido/9/85(H3))", 11363: "Influenza A virus (A/duck/Hokkaido/10/85(H3))", 11369: "Influenza A virus (STRAIN A/DUCK/NEW YORK/12/78)", 11375: "Influenza A virus (A/Dunedin/4/73(H3N2))", 11384: "Influenza A virus (A/chicken/FPV/Weybridge(H7N7))", 11397: "Influenza A virus (A/equine/Cornell/16/74(H7N7))", 11408: "Influenza A virus (STRAIN A/EQUINE/NEW MARKET/76)", 11414: "Influenza A virus (A/equine/Santiago/1/1985(H3N8))", 11418: "Influenza A virus (STRAIN A/EQUINE/TOKYO/71)", 11430: "Influenza A virus (A/mallard/Alberta/88/76(H3N8))", 11432: "Influenza A virus (STRAIN A/MALLARD/ALBERTA/827/78)", 11433: "Influenza A virus (A/mallard/Astrakhan/244/1982(H14N6))", 11444: "Influenza A virus (STRAIN A/MYNAH/HANEDA-THAI/76)", 11448: "Influenza A virus (A/parrot/Ulster/73(H7N1))", 11450: "Influenza A virus (STRAIN A/PINTAIL/ALBERTA/121/79)", 11451: "Influenza A virus (STRAIN A/PINTAIL/ALBERTA/268/78)", 11452: "Influenza A virus (STRAIN A/PINTAIL/ALBERTA/358/79)", 11462: "Influenza A virus (STRAIN A/SHEARWATER/AUSTRALIA/75)", 11482: "Influenza A virus (STRAIN A/VICTORIA/5/68)", 11484: "Influenza A virus (A/whale/Maine/1/84(H13N9))", 11486: "Influenza A virus (STRAIN A/WHALE/PACIFIC OCEAN/19/76)", 11495: "Influenza A virus (STRAIN A/SWINE/GERMANY/2/81)", 11520: "Influenza B virus", 11521: "Influenza B virus (B/Ann Arbor/1/1986)", 11522: "Influenza B virus (B/Ann Arbor/1/1966 [cold-adapted])", 11523: "Influenza B virus (B/Ann Arbor/1/1966 [wild- type])", 11524: "Influenza B virus (B/BA/78)", 11525: "Influenza B virus (STRAIN B/BEIJING/1/87)", 11527: "Influenza B virus (STRAIN B/ENGLAND/222/82)", 11528: "Influenza B virus (B/FUKUOKA/80/81)", 11529: "Influenza B virus (B/GA/86)", 11530: "Influenza B virus (STRAIN B/GL/54)", 11532: "Influenza B virus (STRAIN B/HT/84)", 11534: "Influenza B virus (STRAIN B/ID/86)", 11536: "Influenza B virus (STRAIN B/LENINGRAD/179/86)", 11537: "Influenza B virus (STRAIN B/MARYLAND/59)", 11538: "Influenza B virus (STRAIN B/MEMPHIS/6/86)", 11540: "Influenza B virus (STRAIN B/NAGASAKI/1/87)", 11541: "Influenza B virus (B/Oregon/5/80)", 11542: "Influenza B virus (STRAIN B/PA/79)", 11543: "Influenza B virus (STRAIN B/RU/69)", 11545: "Influenza B virus (STRAIN B/SINGAPORE/64)", 11547: "Influenza B virus (STRAIN B/VICTORIA/3/85)", 11548: "Influenza B virus (STRAIN B/VICTORIA/87)", 11550: "Influenza B virus (B/Yamagata/1/73)", 11552: "Influenza C virus", 11553: "Influenza C virus (C/Ann Arbor/1/50)", 11554: "Influenza C virus (C/Berlin/1/85)", 11556: "Influenza C virus (C/England/892/1983)", 11557: "Influenza C virus (C/Great Lakes/1167/1954)", 11560: "Influenza C virus (C/JJ/1950)", 11564: "Influenza C virus (C/pig/Beijing/10/1981)", 11566: "Influenza C virus (C/PIG/Beijing/439/1982)", 11567: "Influenza C virus (C/Taylor/1233/1947)", 11568: "Influenza C virus (C/Yamagata/10/1981)", 11569: "Thogoto thogotovirus", 11572: "Orthobunyavirus", 11574: "Germiston virus", 11575: "Maguari virus", 11577: "La Crosse virus", 11578: "La Crosse virus L74", 11580: "Snowshoe hare virus", 11582: "Aino virus", 11583: "HoJo virus", 11584: "Phlebovirus", 11587: "Punta Toro virus", 11588: "Rift Valley fever virus", 11589: "Rift valley fever virus (STRAIN ZH-548 M12)", 11590: "Toscana virus", 11591: "Uukuniemi virus", 11594: "Crimean-Congo hemorrhagic fever virus (isolate C68031)", 11596: "Hazara virus", 11597: "Hazara virus (isolate JC280)", 11601: "Hantaan virus Lee", 11602: "Hantaan virus 76-118", 11605: "Puumala virus Hallnas B1", 11606: "Puumala virus - Sotkamo", 11607: "Sapporo rat virus", 11610: "Seoul virus SR11", 11612: "Impatiens necrotic spot virus", 11615: "Tomato spotted wilt virus (Hawaiian isolate)", 11617: "Arenaviridae", 11618: "Arenavirus", 11620: "Lassa mammarenavirus", 11621: "Lassa virus GA391", 11622: "Lassa virus Josiah", 11623: "Lymphocytic choriomeningitis mammarenavirus", 11624: "Lymphocytic choriomeningitis virus (strain Armstrong)", 11625: "Lymphocytic choriomeningitis virus (strain Pasteur)", 11626: "Lymphocytic choriomeningitis virus (strain Traub)", 11627: "Lymphocytic choriomeningitis virus (strain WE)", 11628: "Machupo mammarenavirus", 11629: "Mopeia mammarenavirus", 11631: "Tacaribe mammarenavirus", 11632: "Retroviridae", 11636: "Reticuloendotheliosis virus", 11640: "Spumavirus", 11641: "Human foamy virus", 11642: "Simian foamy virus", 11644: "Simian foamy virus (TYPE 3 / STRAIN LK3)", 11646: "Lentivirus", 11648: "Panther lentivirus", 11652: "Primate lentivirus group", 11653: "Ovine/caprine lentivirus group", 11654: "Equine lentivirus group", 11655: "Feline lentivirus group", 11656: "Bovine lentivirus group", 11657: "Bovine immunodeficiency virus", 11659: "BIV R29-127", 11660: "Caprine arthritis encephalitis virus", 11661: "Caprine arthritis encephalitis virus strain Cork", 11662: "Caprine arthritis encephalitis virus G63", 11663: "Ovine lentivirus", 11664: "Ovine lentivirus (strain SA-OMVV)", 11665: "Equine infectious anemia virus", 11666: "Equine infectious anemia virus (CLONE P3.2-1)", 11667: "Equine infectious anemia virus (CLONE P3.2-2)", 11668: "Equine infectious anemia virus (CLONE P3.2-3)", 11669: "Equine infectious anemia virus (CLONE P3.2-5)", 11670: "Equine infectious anemia virus (CLONE 1369)", 11671: "Equine infectious anemia virus (STRAIN WSU5)", 11672: "Equine infectious anemia virus (ISOLATE WYOMING)", 11673: "Feline immunodeficiency virus", 11674: "Feline immunodeficiency virus (isolate Petaluma)", 11675: "Feline immunodeficiency virus (isolate San Diego)", 11676: "Human immunodeficiency virus 1", 11678: "Human immunodeficiency virus type 1 BH10", 11679: "Human immunodeficiency virus type 1 (CLONE 12)", 11680: "Human immunodeficiency virus type 1 (ZAIRE 3 ISOLATE)", 11681: "Human immunodeficiency virus type 1 (Z-84 ISOLATE)", 11682: "Human immunodeficiency virus type 1 (BH5 ISOLATE)", 11683: "Human immunodeficiency virus type 1 (Z2/CDC-Z34 ISOLATE)", 11684: "Human immunodeficiency virus type 1 (BH8 ISOLATE)", 11685: "HIV-1 M:B_ARV2/SF2", 11686: "Human immunodeficiency virus type 1 (BRU ISOLATE)", 11687: "Human immunodeficiency virus type 1 (CDC-451 ISOLATE)", 11688: "Human immunodeficiency virus type 1 (JRCSF ISOLATE)", 11689: "Human immunodeficiency virus type 1 (ELI ISOLATE)", 11690: "Human immunodeficiency virus type 1 (SF33 ISOLATE)", 11691: "Human immunodeficiency virus type 1 (SF162 ISOLATE)", 11692: "Human immunodeficiency virus type 1 (ZAIRE HZ321 ISOLATE)", 11693: "Human immunodeficiency virus type 1 (BRAIN ISOLATE)", 11694: "Human immunodeficiency virus type 1 (JH3 ISOLATE)", 11695: "Human immunodeficiency virus type 1 (NDK ISOLATE)", 11696: "HIV-1 M:B_MN", 11697: "Human immunodeficiency virus type 1 (MAL ISOLATE)", 11698: "Human immunodeficiency virus type 1 (NEW YORK-5 ISOLATE)", 11699: "Human immunodeficiency virus type 1 (OYI ISOLATE)", 11701: "Human immunodeficiency virus type 1 (RF/HAT ISOLATE)", 11702: "Human immunodeficiency virus type 1 (SC ISOLATE)", 11703: "Human immunodeficiency virus type 1 (STRAIN UGANDAN / ISOLATE U455)", 11704: "Human immunodeficiency virus type 1 (MFA ISOLATE)", 11705: "Human immunodeficiency virus type 1 (WMJ2 ISOLATE)", 11706: "HIV-1 M:B_HXB2R", 11707: "Human immunodeficiency virus type 1 (HXB3 ISOLATE)", 11708: "Human immunodeficiency virus type 1 (ZAIRE 6 ISOLATE)", 11709: "Human immunodeficiency virus 2", 11711: "Simian immunodeficiency virus - mac", 11712: "Simian immunodeficiency virus - sm", 11713: "Human immunodeficiency virus type 2 (ISOLATE D194)", 11714: "Human immunodeficiency virus type 2 (ISOLATE BEN)", 11715: "Human immunodeficiency virus type 2 (ISOLATE CAM2)", 11716: "Human immunodeficiency virus type 2 (ISOLATE D205,7)", 11717: "Human immunodeficiency virus type 2 (ISOLATE GHANA-1)", 11718: "Human immunodeficiency virus type 2 (ISOLATE SBLISY)", 11719: "Human immunodeficiency virus type 2 (ISOLATE NIH-Z)", 11720: "Human immunodeficiency virus type 2 (ISOLATE ROD)", 11721: "Human immunodeficiency virus type 2 (ISOLATE ST)", 11723: "Simian immunodeficiency virus", 11725: "Human T-cell lymphotropic virus type 4", 11726: "Simian immunodeficiency virus - agm", 11727: "Simian immunodeficiency virus (AGM155 ISOLATE)", 11728: "Simian immunodeficiency virus (AGM266 ISOLATE)", 11729: "Simian immunodeficiency virus (AGM385 ISOLATE)", 11730: "Simian immunodeficiency virus (AGM3 ISOLATE)", 11731: "Simian immunodeficiency virus (TYO-1 ISOLATE)", 11732: "Simian immunodeficiency virus (ISOLATE GB1)", 11733: "Simian immunodeficiency virus (MM142-83 ISOLATE)", 11734: "Simian immunodeficiency virus (MM251 ISOLATE)", 11735: "Simian immunodeficiency virus - mac K6W", 11736: "Simian immunodeficiency virus (K78 ISOLATE)", 11737: "Simian immunodeficiency virus (F236/SMH4 ISOLATE) (SOOTY MANGABEY)", 11738: "Simian immunodeficiency virus (PBJ/BC13 ISOLATE) (SOOTY MANGABEY)", 11742: "Visna lentivirus (strain 1514)", 11743: "Visna lentivirus (strain 1514 / clone LV1-1KS1)", 11744: "Visna lentivirus (strain 1514 / clone LV1-1KS2)", 11745: "Human endogenous retrovirus ERV-9", 11746: "Jaagsiekte sheep retrovirus", 11749: "Intracisternal A-particles", 11750: "Chinese hamster Intracisternal A-particle", 11751: "Chinese hamster Intracisternal A-particle CHIAP34", 11752: "Golden hamster intracisternal A-particle H18", 11753: "Mouse intracisternal A-particle MIA14", 11754: "Mouse intracisternal A-particle MIAIL3", 11757: "Mouse mammary tumor virus", 11758: "Mouse mammary tumor virus (STRAIN BR6)", 11759: "Mouse mammary tumor virus (STRAIN C3H)", 11760: "Mouse mammary tumor virus (STRAIN GR)", 11764: "Baboon endogenous virus strain M7", 11765: "Feline endogenous virus", 11766: "Feline endogenous virus ECE1", 11767: "Feline endogenous virus RD114", 11768: "Feline leukemia virus", 11769: "Feline leukemia virus strain A/Glasgow-1", 11772: "Feline sarcoma virus", 11774: "Gardner-Arnstein feline sarcoma virus", 11775: "Feline sarcoma virus (STRAIN GARDNER-RASHEED)", 11776: "Feline sarcoma virus (STRAIN HARDY-ZUCKERMAN 2)", 11777: "Feline sarcoma virus (STRAIN HARDY-ZUCKERMAN 4)", 11778: "Feline sarcoma virus (STRAIN MCDONOUGH)", 11779: "Feline sarcoma virus (STRAIN SM)", 11780: "Snyder-Theilen feline sarcoma virus", 11783: "Friend mink cell focus-forming virus", 11784: "Rauscher mink cell focus-forming virus", 11785: "Mink cell focus-forming virus", 11786: "Murine leukemia virus", 11787: "Radiation murine leukemia virus", 11788: "Abelson murine leukemia virus", 11790: "AKT8 murine leukemia virus", 11791: "AKR (endogenous) murine leukemia virus", 11792: "Cas-Br-E murine leukemia virus", 11793: "Cas NS-1 murine leukemia virus", 11794: "Duplan murine leukemia virus", 11795: "Friend murine leukemia virus", 11796: "Friend murine leukemia virus (ISOLATE 57)", 11797: "Friend murine leukemia virus (ISOLATE FB29)", 11798: "Friend murine leukemia virus (ISOLATE PVC-211)", 11799: "HoMuLV murine leukemia virus", 11800: "Kirsten murine leukemia virus", 11801: "Moloney murine leukemia virus", 11803: "BALB murine sarcoma virus", 11804: "Cas-NS-1 murine sarcoma virus", 11805: "FBJ murine osteosarcoma virus", 11807: "Harvey murine sarcoma virus", 11808: "Kirsten murine sarcoma virus", 11809: "Moloney murine sarcoma virus", 11810: "Moloney murine sarcoma virus (STRAIN HT-1)", 11811: "Moloney murine sarcoma virus (STRAIN M1)", 11812: "Murine sarcoma virus 3611", 11813: "Myeloproliferative sarcoma virus", 11814: "Myeloproliferative sarcoma virus (CLONE TS159)", 11815: "NS.C58 murine sarcoma virus", 11816: "Rasheed rat sarcoma virus", 11818: "Simian sarcoma-associated virus", 11819: "Spleen focus-forming virus", 11820: "Friend spleen focus-forming virus", 11821: "Rauscher spleen focus-forming virus", 11823: "GR mouse mammary tumor virus", 11824: "Gardner-Arnstein feline leukemia oncovirus B", 11827: "Human endogenous retrovirus", 11829: "Macaca mulatta type C retrovirus", 11830: "Murine osteosarcoma virus", 11832: "Murine retrovirus SL3-3", 11833: "N-tropic ecotropic endogenous retrovirus", 11834: "RD114 retrovirus", 11836: "Spleen necrosis virus", 11837: "Xenotropic murine leukemia virus", 11838: "Chimpanzee type C endogenous retrovirus", 11840: "Gibbon ape leukemia virus", 11841: "Gross passage A murine leukemia virus", 11843: "Macaca endogenous retrovirus", 11845: "Mouse RFV endogenous retrovirus", 11846: "Murine non-leukeminogenic retrovirus", 11847: "Murine retrovirus SL3-2", 11848: "Rat sarcoma virus", 11849: "Soule murine leukemia virus", 11850: "Tikaut murine leukemia virus", 11854: "Thymotropic retrovirus type B", 11855: "Mason-Pfizer monkey virus", 11856: "Squirrel monkey retrovirus", 11857: "Squirrel monkey retrovirus-H", 11859: "Avian endogenous virus ev-1", 11861: "Avian erythroblastosis virus", 11862: "Avian erythroblastosis virus (strain Sloan-Kettering)", 11863: "Avian erythroblastosis virus (strain S13)", 11864: "Avian leukosis virus", 11865: "Rous-associated virus", 11866: "Avian myeloblastosis virus", 11867: "Avian myelocytomatosis virus", 11868: "Avian myelocytomatosis virus 29", 11869: "Avian myelocytomatosis virus CMII", 11870: "Avian carcinoma Mill Hill virus 2", 11871: "Avian myelocytomatosis virus OK10", 11873: "Avian musculoaponeurotic fibrosarcoma virus AS42", 11874: "Avian retrovirus IC10", 11875: "Avian retrovirus NK24", 11876: "Avian sarcoma virus", 11877: "Avian sarcoma virus 17", 11878: "Avian sarcoma virus CT10", 11879: "Avian sarcoma virus PR2257", 11880: "Avian sarcoma virus PRCII", 11881: "Avian sarcoma virus S1", 11882: "Avian sarcoma virus S2", 11884: "Y73 sarcoma virus", 11885: "Fujinami sarcoma virus", 11886: "Rous sarcoma virus", 11887: "Rous sarcoma virus (strain H-19)", 11888: "Rous sarcoma virus - Prague C", 11889: "Rous sarcoma virus (strain Schmidt-Ruppin)", 11894: "Avian sarcoma virus RASV1441", 11899: "Avian spleen necrosis virus", 11901: "Bovine leukemia virus", 11902: "Bovine leukemia virus (AMERICAN ISOLATE FLK)", 11903: "Bovine leukemia virus (AUSTRALIAN ISOLATE)", 11904: "Bovine leukemia virus (AMERICAN ISOLATE VDM)", 11905: "Bovine leukemia virus (BELGIUM ISOLATE LB285)", 11906: "Bovine leukemia virus (BELGIUM ISOLATE LB59)", 11907: "Bovine leukemia virus (JAPANESE ISOLATE BLV-1)", 11908: "Human T-cell leukemia virus type I", 11909: "Human T-lymphotropic virus 2", 11913: "Avian leukemia virus e26", 11915: "Avian myelocytomatosis virus hbi", 11916: "Avian retrovirus mh2e21", 11921: "Feline leukemia provirus (clone CFE-16)", 11922: "Feline leukemia provirus (clone CFE-6)", 11923: "Feline leukemia provirus ftt", 11926: "Human T-cell lymphotrophic virus type 1 (strain ATK)", 11927: "Human T-cell lymphotrophic virus type 1 (Caribbean isolate)", 11928: "Human T-cell lymphotrophic virus type 1 (isolate MT-2)", 11932: "Mouse Intracisternal A-particle", 11935: "Mink cell focus-forming murine leukemia virus", 11936: "Mink cell focus-forming murine leukemia virus (ISOLATE CI-3)", 11938: "Rauscher murine leukemia virus", 11942: "Simian retrovirus 1", 11945: "Avian endogenous virus", 11946: "Avian leukemia virus", 11948: "Rous-associated virus type 2", 11949: "Rous-associated virus type 0", 11950: "Rous-associated virus type 1", 11955: "Avian retrovirus", 11957: "Avian sarcoma virus 1", 11958: "Avian carcinoma virus", 11960: "Avian myeloblastosis-associated virus", 11961: "Lymphoproliferative disease virus", 11963: "Human spumaretrovirus", 11965: "Simian foamy virus 3", 11966: "Aids-associated retrovirus", 11968: "IAP H10", 11970: "Woolly monkey sarcoma virus", 11971: "Avian hemangioma-inducing virus", 11973: "Myeloproliferative leukemia virus", 11974: "Caliciviridae", 11976: "Rabbit hemorrhagic disease virus", 11977: "Rabbit hemorrhagic disease virus-V351", 11978: "Feline calicivirus", 11979: "Feline calicivirus strain CFI/68 FIV", 11980: "Feline calicivirus strain Japanese F4", 11981: "Feline calicivirus strain F9", 11982: "San Miguel sea lion virus", 11983: "Norwalk virus", 11984: "Southampton virus", 11985: "Carmovirus", 11986: "Carnation mottle virus", 11987: "Melon necrotic spot virus", 11988: "Turnip crinkle virus", 11989: "Leviviridae", 11990: "Levivirus", 12008: "Allolevivirus", 12014: "Enterobacteria phage BO1", 12015: "Enterobacteria phage isolate BZ13", 12016: "Enterobacteria phage f2", 12017: "Enterobacteria phage fr", 12018: "Enterobacteria phage GA", 12019: "Enterobacteria phage JP34", 12020: "Enterobacteria phage JP501", 12021: "Enterobacteria phage KU1", 12022: "Enterobacteria phage MS2", 12023: "Pseudomonas phage PP7", 12024: "Pseudomonas phage PRR1", 12026: "Enterobacteria phage R17", 12027: "Enterobacteria phage SP", 12029: "Enterobacteria phage TH1", 12030: "Enterobacteria phage TW19", 12031: "Enterobacteria phage TW28", 12032: "Enterobacteria phage VK", 12034: "Enterobacteria phage fr1", 12036: "Luteovirus", 12037: "Barley yellow dwarf virus", 12039: "Barley yellow dwarf virus (ISOLATE NY-RPV)", 12041: "Bean leafroll virus", 12042: "Beet western yellows virus", 12043: "Beet western yellows virus-FL1", 12044: "Beet western yellows virus (ISOLATE GB1)", 12045: "Potato leafroll virus", 12046: "Potato leafroll virus (STRAIN 1)", 12047: "Potato leafroll virus (STRAIN ROWHANI)", 12048: "Potato leafroll virus (STRAIN WAGENINGEN)", 12049: "Soybean dwarf virus", 12050: "Waikavirus", 12051: "Marafivirus", 12054: "unidentified tobacco necrosis virus", 12055: "Tobacco necrosis virus A", 12056: "Tobacco necrosis virus D", 12057: "Sequivirus", 12058: "Picornaviridae", 12059: "Enterovirus", 12060: "Echovirus E9", 12062: "Echovirus E6", 12063: "Human parechovirus 1", 12064: "Enterovirus E", 12065: "Bovine enterovirus strain VG-5-27", 12066: "Coxsackievirus", 12067: "Coxsackievirus A9", 12068: "Human coxsackievirus A9 (strain Griggs)", 12069: "Coxsackievirus A21", 12070: "Human coxsackievirus A21 Coe", 12071: "Coxsackievirus B1", 12072: "Coxsackievirus B3", 12073: "Coxsackievirus B4", 12074: "Coxsackievirus B5", 12075: "Swine vesicular disease virus", 12076: "Swine vesicular disease virus (STRAIN H/3 '76)", 12077: "Swine vesicular disease virus (STRAIN UKG/27/72)", 12078: "Echovirus E11", 12079: "unidentified poliovirus", 12080: "Human poliovirus 1", 12081: "Human poliovirus 1 Mahoney", 12082: "Human poliovirus 1 strain Sabin", 12083: "Human poliovirus 2", 12084: "Poliovirus type 2 strain Lansing", 12085: "Poliovirus type 2 strain W-2", 12086: "Human poliovirus 3", 12087: "Poliovirus type 3 (strain 23127)", 12088: "Poliovirus type 3 (strains P3/LEON/37 AND P3/LEON 12A[1]B)", 12089: "Coxsackievirus A24", 12090: "Human enterovirus 70", 12091: "Hepatovirus", 12092: "Hepatovirus A", 12093: "Human hepatitis A virus Shanghai/LCDC-1/1984", 12097: "Human hepatitis A virus Hu/Costa Rica/CR326/1960", 12098: "Human hepatitis A virus Hu/Australia/HM175/1976", 12099: "Human hepatitis A virus Hu/Los Angelos/LA/1975", 12100: "Human hepatitis A virus Hu/Northern Africa/MBB/1978", 12101: "Simian hepatitis A virus", 12102: "Simian hepatitis A virus Cercopithecus/Kenya/AGM-27/1985", 12103: "Cardiovirus", 12104: "Encephalomyocarditis virus", 12105: "Encephalomyocarditis virus strain emc-b nondiabetogenic", 12106: "Encephalomyocarditis virus strain emc-d diabetogenic", 12107: "Mengo virus", 12109: "Aphthovirus", 12110: "Foot-and-mouth disease virus", 12111: "Foot-and-mouth disease virus - type A", 12112: "Foot-and-mouth disease virus (strain A10-61)", 12113: "Foot-and-mouth disease virus (strain A5)", 12114: "Foot-and-mouth disease virus (strain A12)", 12115: "Foot-and-mouth disease virus (strain A24 Cruzeiro)", 12116: "Foot-and-mouth disease virus - type C", 12117: "Foot-and-mouth disease virus (strain C3 Indaial)", 12118: "Foot-and-mouth disease virus - type O", 12120: "Foot-and-mouth disease virus (strain C1-Santa Pau)", 12121: "Foot-and-mouth disease virus C1", 12122: "Foot-and-mouth disease virus - type SAT 1", 12123: "Foot-and-mouth disease virus - type SAT 3", 12124: "Theiler's encephalomyelitis virus", 12125: "Theiler's encephalomyelitis virus (STRAIN BEAN 8386)", 12126: "Theiler's encephalomyelitis virus (STRAIN DA)", 12127: "Theiler's murine encephalomyeltits virus GDVII", 12129: "Human rhinovirus 1B", 12130: "Human rhinovirus A2", 12131: "Rhinovirus B14", 12132: "Human rhinovirus A89", 12134: "Human rhinovirus 1A", 12135: "Human rhinovirus A23", 12136: "Cricket paralysis virus", 12137: "Sobemovirus", 12138: "Maize chlorotic mottle virus", 12139: "Southern bean mosaic virus", 12141: "Tombusvirus", 12142: "Artichoke mottled crinkle virus", 12143: "Cucumber necrosis virus", 12144: "Cymbidium ringspot virus", 12145: "Tomato bushy stunt virus", 12146: "Tomato bushy stunt virus (STRAIN BS-3)", 12147: "Tomato bushy stunt virus (STRAIN CHERRY)", 12148: "Tymovirus", 12149: "Belladonna mottle virus", 12150: "Cacao yellow mosaic virus", 12151: "Eggplant mosaic virus", 12152: "Erysimum latent virus", 12153: "Ononis yellow mosaic virus", 12154: "Turnip yellow mosaic virus", 12155: "Turnip yellow mosaic virus (Australian isolate)", 12157: "Clitoria yellow vein virus", 12158: "Kennedya yellow mosaic virus", 12160: "Closterovirus", 12161: "Beet yellows virus", 12162: "Citrus tristeza virus", 12163: "Carlavirus", 12164: "Carnation latent virus", 12165: "Chrysanthemum virus B", 12166: "Poplar mosaic virus", 12167: "Potato virus M", 12168: "Potato virus M (strain Russian)", 12169: "Potato virus S", 12170: "Potato virus S (strain Peruvian)", 12171: "Helenium virus S", 12172: "Shallot latent virus", 12173: "Lily symptomless virus", 12174: "Capillovirus", 12175: "Apple chlorotic leaf spot virus", 12176: "Potexvirus", 12177: "Clover yellow mosaic virus", 12178: "Cymbidium mosaic virus", 12179: "Foxtail mosaic virus", 12180: "Narcissus mosaic virus", 12181: "Papaya mosaic virus", 12182: "Potato aucuba mosaic virus", 12183: "Potato virus X", 12184: "Potato virus X (strain CP)", 12185: "Potato virus X (strain X3)", 12186: "Potato virus X (strain XC)", 12187: "Strawberry mild yellow edge virus", 12188: "White clover mosaic virus", 12189: "White clover mosaic virus (strain M)", 12190: "White clover mosaic virus (strain O)", 12194: "Lily virus X", 12195: "Potyvirus", 12196: "Bean common mosaic virus", 12197: "Bean yellow mosaic virus", 12198: "Clover yellow vein virus", 12199: "Cowpea aphid-borne mosaic virus", 12200: "Garlic mosaic virus", 12201: "Gloriosa stripe mosaic virus", 12202: "Lettuce mosaic virus", 12203: "Maize dwarf mosaic virus", 12204: "Ornithogalum mosaic virus", 12205: "Papaya ringspot virus", 12206: "Papaya ringspot virus P", 12207: "Papaya ringspot virus W", 12208: "Pea seed-borne mosaic virus", 12209: "Pepper mottle virus", 12210: "Pepper severe mosaic virus", 12211: "Plum pox virus", 12212: "Plum pox virus D", 12213: "Plum pox virus isolate NAT", 12214: "Plum pox virus strain Rankovic", 12215: "Potato virus A", 12216: "Potato virus Y", 12217: "Potato virus Y strain C", 12218: "Potato virus Y strain Chinese isolate", 12219: "Potato virus Y strain N", 12220: "Potato virus Y strain O", 12221: "Potato virus Y strain YO", 12222: "Soybean mosaic virus", 12223: "Soybean mosaic virus N", 12224: "Sugarcane mosaic virus", 12225: "Sugarcane mosaic virus SC", 12226: "Tamarillo mosaic virus", 12227: "Tobacco etch virus", 12228: "Tobacco vein mottling virus", 12229: "Tulip breaking virus", 12230: "Turnip mosaic virus", 12232: "Zucchini yellow mosaic virus", 12233: "South African passiflora virus", 12234: "Tobamovirus", 12235: "Cucumber green mottle mosaic virus", 12236: "Cucumber green mottle mosaic virus (watermelon strain SH)", 12237: "Cucumber green mottle mosaic virus (watermelon strain W)", 12238: "Odontoglossum ringspot virus", 12239: "Pepper mild mottle virus", 12240: "Sunn-hemp mosaic virus", 12241: "Tobacco mild green mosaic virus", 12242: "Tobacco mosaic virus", 12243: "Tobacco mosaic virus (vulgare)", 12244: "Tobacco mosaic virus strain 06", 12246: "Tobacco mosaic virus strain Dahlemense", 12247: "Tobacco mosaic virus strain ER", 12248: "Tobacco mosaic virus strain HR", 12249: "Tobacco mosaic virus strain Kokubu", 12250: "Tobacco mosaic virus (strain O)", 12251: "Tobacco mosaic virus strain OM", 12252: "Tobacco mosaic virus strain tomato/L", 12253: "Tomato mosaic virus", 12256: "Beet necrotic yellow vein mosaic virus F2", 12257: "Beet necrotic yellow vein mosaic virus G1", 12258: "Comovirus", 12259: "Andean potato mottle virus", 12260: "Bean pod mottle virus", 12261: "Cowpea severe mosaic virus", 12262: "Red clover mottle virus", 12263: "Squash mosaic virus", 12264: "Cowpea mosaic virus", 12266: "Dianthovirus", 12267: "Red clover necrotic mosaic virus", 12268: "Carnation ringspot virus", 12269: "Fabavirus", 12270: "Nepovirus", 12271: "Arabis mosaic virus", 12273: "Grapevine chrome mosaic virus", 12274: "Grapevine fanleaf virus", 12275: "Tomato black ring virus", 12276: "Tomato black ring virus (STRAIN C)", 12277: "Tomato black ring virus (STRAIN E)", 12278: "Tomato black ring virus (STRAIN L)", 12280: "Tomato ringspot virus", 12281: "Tomato ringspot virus (isolate raspberry)", 12282: "Tobacco ringspot virus", 12283: "Nodaviridae", 12285: "Black beetle virus", 12286: "Boolarra virus", 12287: "Flock House virus", 12288: "Nodamura virus", 12289: "Enamovirus", 12291: "Furovirus", 12292: "Nicotiana velutina mosaic virus", 12293: "Tobravirus", 12294: "Pea early-browning virus", 12295: "Tobacco rattle virus", 12296: "Tobacco rattle virus-CAM", 12297: "Tobacco rattle virus-PSG", 12298: "Tobacco rattle virus-SYM", 12299: "Tobacco rattle virus-TCM", 12300: "Bromovirus", 12301: "Broad bean mottle virus", 12302: "Brome mosaic virus", 12303: "Cowpea chlorotic mottle virus", 12304: "Cucumovirus", 12305: "Cucumber mosaic virus", 12306: "Cucumber mosaic virus (strain C)", 12307: "Cucumber mosaic virus (strain FNY)", 12308: "Cucumber mosaic virus (strain I17F)", 12309: "Cucumber mosaic virus (strain O)", 12310: "Cucumber mosaic virus (strain Q)", 12311: "Cucumber mosaic virus (strain WL)", 12312: "Cucumber mosaic virus (strain Y)", 12313: "Peanut stunt virus", 12314: "Peanut stunt virus (strain J)", 12315: "Tomato aspermy virus", 12316: "Ilarvirus", 12317: "Tobacco streak virus", 12318: "Tobacco streak virus (strain WC)", 12319: "Apple mosaic virus", 12320: "Alfamovirus", 12321: "Alfalfa mosaic virus", 12322: "Alfalfa mosaic virus (strain 425 / isolate Leiden)", 12323: "Alfalfa mosaic virus (strain 425 / isolate Madison)", 12324: "Alfalfa mosaic virus (strain Strasbourg)", 12325: "Alfalfa mosaic virus (strain YSMV)", 12326: "Hordeivirus", 12327: "Barley stripe mosaic virus", 12328: "Poa semilatent virus", 12329: "Tenuivirus", 12330: "Maize stripe tenuivirus", 12331: "Rice stripe tenuivirus", 12332: "Rice hoja blanca tenuivirus", 12333: "unclassified bacterial viruses", 12335: "Nocardia phage NJL", 12336: "Clostridium phage c-st", 12340: "Enterobacteria phage 933J", 12342: "Xanthomonas phage Cf16", 12344: "Streptococcus phage Cp-5", 12345: "Bacillus virus GA1", 12347: "Actinophage JHJ-1", 12348: "Lactobacillus phage LL-H", 12349: "Phage M13mp7", 12350: "Phage M13mp8", 12352: "Bacillus phage M2Y", 12353: "Escherichia phage RB69", 12354: "Enterobacteria phage ST", 12356: "Lactococcus phage phiUS3", 12357: "Bacillus phage Z", 12360: "Staphylococcus virus 11", 12366: "Streptococcus pyogenes phage H4489A", 12371: "Phage h30", 12374: "Lactococcus phage", 12375: "Lactococcus phage (ISOLATE 7-9)", 12381: "Klebsiella phage No. 11", 12386: "Lactococcus phage mi7-9", 12387: "Lactococcus phage F4-1", 12388: "Mycobacterium phage FRAT1", 12390: "Lactococcus phage phiLC3", 12392: "Lactobacillus phage mv4", 12397: "Bacillus phage H2", 12402: "Streptococcus phage EJ-1", 12403: "Leuconostoc phage P32", 12404: "Leuconostoc phage P37", 12405: "Leuconostoc phage P54", 12406: "Leuconostocphage PAt5-12", 12407: "Salmonella virus PsP3", 12408: "Leuconostoc phage PZt11-15", 12409: "Clostridium phage d-16 phi", 12412: "Staphylococcus phage phi-42", 12413: "Lactococcusphage phi7-9", 12417: "Lactobacillus phage phiadh", 12420: "Filamentous phage", 12424: "Phage 13", 12425: "Phage 16", 12426: "Salmonella phage 5", 12427: "Lactococcus lactis phage phi 197", 12428: "Retronphage phi R73", 12429: "unclassified viruses", 12430: "Garlic virus D", 12431: "Garlic virus C", 12432: "Garlic virus B", 12433: "Garlic virus A", 12435: "Sugarcane bacilliform virus", 12436: "Cucumber mosaic virus satellite RNA", 12438: "AKT8 retrovirus", 12439: "20S RNA replicon", 12440: "Non-A, non-B hepatitis virus", 12441: "Kilham rat virus", 12444: "Satellite tobacco necrosis virus 2", 12445: "Satellite tobacco necrosis virus 1", 12450: "Saccharomyces cerevisiae killer virus M1", 12451: "Raspberry bushy dwarf virus", 12452: "Flame chlorosis virus-like agent", 12455: "Borna disease virus", 12456: "Human astrovirus 1", 12458: "Garlic latent virus", 12461: "Hepatitis E virus", 12465: "Barley yellow mosaic virus", 12466: "Barley mild mosaic virus", 12468: "Maus-Elberfeld virus", 12470: "Lucerne transient streak virus", 12471: "Solanum nodiflorum mottle virus", 12472: "Subterranean clover mottle virus", 12473: "Velvet tobacco mottle virus", 12474: "Coconut foliar decay virus", 12475: "Hepatitis delta virus", 12477: "Killer virus of S.cerevisiae", 12478: "Cryphonectria hypovirus 1-EP713", 12480: "African green monkey polyomavirus", 12499: "Chorella virus", 12509: "Human herpesvirus 4 type 2", 12513: "Hepatitis B virus 2", 12519: "Intracisternal A-type particle IAP", 12521: "JDV virus", 12524: "Junonia coenia densovirus", 12530: "Leishmania RNA virus 1 - 4", 12538: "Mokola lyssavirus", 12541: "Nudaurelia capensis omega virus", 12542: "Omsk hemorrhagic fever virus", 12557: "Seoul virus 80-39", 12558: "Sesbania mosaic virus", 12571: "Vilyuisk human encephalomyelitis virus", 12578: "Rotavirus str. I321", 12583: "Avian retrovirus FH3", 12584: "Avian rotavirus Ty-1", 12585: "Banana bunchy top virus", 12615: "Cherry leaf roll virus", 12618: "Chicken anemia virus", 12627: "Cowpea mottle virus", 12637: "Dengue virus", 12639: "Duck hepatitis B virus", 12643: "Ectromelia virus", 12645: "Avian endogenous virus ev-21", 12647: "Epizootic hemorrhagic disease of deer virus", 12657: "Equid gammaherpesvirus 2", 12663: "Feline coronavirus", 12672: "Frog erythrocytic virus", 12675: "Groundnut ringspot virus", 12701: "Human astrovirus 2", 12705: "Adult diarrheal rotavirus", 12721: "Human immunodeficiency virus", 12730: "Human respirovirus 1", 12733: "Human endogenous retrovirus 1", 12742: "Infectious flacherie virus", 12750: "Visna/maedi virus EV1", 12760: "Murine hepatitis virus strain 4", 12777: "Parsnip yellow fleck virus", 12783: "Pear blister canker viroid", 12795: "Porcine pestivirus", 12804: "Puma lentivirus", 12809: "Raspberry ringspot virus", 12811: "Reovirus S4", 12814: "Respiratory syncytial virus", 12830: "Simian immunodeficiency virus - mnd", 12844: "Sweet potato feathery mottle virus", 12845: "Swine influenza virus", 12851: "Tomato chlorotic spot virus", 12870: "Variola major virus", 12877: "Satellites", 12881: "Satellite tobacco mosaic virus", 12885: "Tomato apical stunt viroid", 12886: "Dapple plum and peach fruit disease viroid", 12887: "Dapple peach fruit disease viroid", 12888: "Tomato planta macho viroid", 12889: "Coconut tinangaja viroid", 12890: "Citrus exocortis viroid", 12892: "Potato spindle tuber viroid", 12893: "Hop stunt viroid", 12894: "Peach latent mosaic viroid", 12895: "Apple scar skin viroid", 12896: "Avocado sunblotch viroid", 12897: "Chrysanthemum stunt viroid", 12898: "Citrus bark cracking viroid", 12899: "Coleus blumei viroid", 12901: "Columnea latent viroid", 12902: "Hop stunt viroid - cucumber", 12903: "Grapevine viroid", 12904: "Grapevine yellow speckle viroid 1", 12905: "Grapevine yellow speckle viroid", 12906: "Citrus bent leaf viroid", 12907: "Hop latent viroid", 12908: "unclassified sequences", 12912: "Acanthurus", 12913: "Acanthurus nigrofuscus", 12914: "Acidianus", 12915: "Acidianus infernus", 12916: "Acidovorax", 12917: "Acidovorax facilis", 12920: "Aeshna", 12921: "Aeshna cyanea", 12922: "Aiptasia", 12924: "Aiptasia pulchella", 12927: "Alviniconcha", 12928: "Alviniconcha hessleri", 12929: "Amazona", 12930: "Amazona aestiva", 12934: "Thiocapsa pendens", 12939: "Anemia", 12940: "Anemia phyllitidis", 12941: "Aphanocladium", 12942: "Aphanocladium album", 12943: "Aptostichus", 12944: "Apomastus schlingeri", 12945: "Aratinga", 12946: "Psittacara erythrogenys", 12947: "Aristolochia", 12948: "Aristolochia gigantea", 12949: "Aristolochia macrophylla", 12952: "Asimina", 12953: "Asimina triloba", 12956: "Atta", 12957: "Atta cephalotes", 12958: "Axinella", 12959: "Axinella polypoides", 12960: "Azoarcus", 12963: "Bathydraco", 12964: "Bathydraco marri", 12965: "Bathymodiolus", 12966: "Bathymodiolus thermophilus", 12967: "Blastocystis", 12968: "Blastocystis hominis", 12979: "Butea", 12981: "Cacatua", 12983: "Cacatua goffiniana", 12984: "Cadra", 12985: "Cadra cautella", 12989: "Carpinus", 12990: "Carpinus betulus", 12991: "Carpinus caroliniana", 12992: "Cassiopea", 12993: "Cassiopea xamachana", 12996: "Cestum", 12997: "Cestum veneris", 12998: "Chaitophorus", 12999: "Chaitophorus viminalis", 13000: "Chalara", 13001: "Thielaviopsis paradoxa", 13005: "Chloranthus", 13006: "Chloranthus spicatus", 13007: "Chloranthus japonicus", 13008: "Chorthippus", 13010: "Circaea", 13011: "Circaea cordata", 13012: "Clarias", 13013: "Clarias gariepinus", 13015: "Codakia", 13016: "Codakia orbicularis", 13020: "Creatonotos", 13021: "Creatonotos transiens", 13022: "Culcita", 13023: "Calochlaena dubia", 13024: "Curculio", 13025: "Curculio caryae", 13028: "Cynoscion", 13029: "Cynoscion nebulosus", 13034: "Dactylococcopsis", 13035: "Dactylococcopsis salina PCC 8305", 13036: "Danaus", 13037: "Danaus plexippus", 13038: "Daubentonia", 13039: "Diaprepes", 13040: "Diaprepes abbreviatus", 13043: "Duchesnea", 13044: "Potentilla indica", 13047: "Echinodorus", 13048: "Echinodorus cordifolius", 13049: "Eleutheria", 13050: "Eleutheria dichotoma", 13052: "Engiscaptomyza", 13053: "Scaptomyza crassifemur", 13054: "Epilobium", 13055: "Chamaenerion angustifolium", 13063: "Euscelidius", 13064: "Euscelidius variegatus", 13067: "Forficula", 13068: "Forficula auricularia", 13069: "Fuchsia", 13070: "Fuchsia triphylla", 13073: "Geophagus", 13074: "Geophagus steindachneri", 13075: "Globicatella", 13076: "Globicatella sanguinis", 13077: "Halodule", 13078: "Halodule wrightii", 13080: "Hauya", 13081: "Hauya elegans", 13082: "Hedycarya", 13083: "Hedycarya arborea", 13084: "Heteronotia", 13085: "Heteronotia binoei", 13090: "Hosta", 13091: "Hosta lancifolia", 13092: "Hydractinia", 13093: "Hydractinia symbiolongicarpus", 13095: "Hypophthalmichthys molitrix", 13097: "Illicium", 13098: "Illicium floridanum", 13099: "Illicium parviflorum", 13100: "Juniperus", 13101: "Juniperus ashei", 13102: "Juniperus rigida var. conferta", 13103: "Lampetra", 13105: "Lepomis", 13106: "Lepomis macrochirus", 13107: "Leuckartiara", 13108: "Leuckartiara octona", 13109: "Lissoclinum", 13110: "Lissoclinum patella", 13111: "Lopezia", 13112: "Lopezia hirsuta", 13113: "Lorius", 13114: "Lorius garrulus", 13115: "Lucinoma", 13116: "Lucinoma aequizonata", 13117: "Lucinoma annulata", 13118: "Ludwigia", 13119: "Ludwigia peploides", 13122: "Lymantria", 13123: "Lymantria dispar", 13124: "Lynx", 13125: "Lynx lynx", 13128: "Lythrum", 13129: "Lythrum salicaria", 13130: "Macrosiphum", 13131: "Macrosiphum euphorbiae", 13134: "Magnetospirillum", 13136: "unidentified marine bacterioplankton", 13138: "Mastotermes", 13139: "Mastotermes darwiniensis", 13140: "Mastotermes electrodominicus", 13141: "Melaphis", 13142: "Melaphis rhois", 13145: "Melopsittacus", 13146: "Melopsittacus undulatus", 13149: "Microcebus", 13150: "Micromys", 13151: "Micromys minutus", 13152: "Mindarus", 13153: "Mindarus kinseyi", 13157: "Mougeotia", 13158: "Mougeotia scalaris", 13159: "Mycoplana", 13160: "Brevundimonas bullata", 13163: "Myzus", 13164: "Myzus persicae", 13165: "Najas", 13166: "Najas guadaliensis", 13169: "Nematanthus", 13170: "Nematanthus wettsteinii", 13171: "Neobellieria", 13173: "Neothyris", 13174: "Neothyris lenticularis", 13179: "Nymphicus", 13180: "Nymphicus hollandicus", 13186: "Parietaria", 13187: "Parietaria officinalis", 13190: "Pectinophora", 13191: "Pectinophora gossypiella", 13192: "Pemphigus", 13193: "Pemphigus betae", 13196: "Peperomia", 13197: "Peperomia sp. Qiu 91047", 13201: "Phaeococcomyces", 13202: "Exophiala exophialae", 13203: "Phlebotomus", 13204: "Phlebotomus perniciosus", 13205: "Pholiota", 13206: "Pholiota aurivella", 13207: "Phragmatopoma", 13208: "Phragmatopoma californica", 13213: "Pionus", 13214: "Pionus menstruus", 13215: "Piper", 13216: "Piper nigrum", 13217: "Piper betle", 13220: "Pleurochrysis", 13221: "Chrysotila carterae", 13224: "Pomatoschistus", 13225: "Pomatoschistus minutus", 13228: "Potamogeton", 13230: "Prosopis juliflora", 13231: "Pseudococcus", 13232: "Pseudococcus affinis", 13233: "Pseudococcus longispinus", 13234: "Pseudococcus maritimus", 13239: "Psittacus", 13242: "Rarobacter", 13243: "Rarobacter faecitabidus", 13244: "Regulus", 13245: "Regulus satrapa", 13248: "Rhodnius", 13249: "Rhodnius prolixus", 13253: "Sabal", 13257: "Saruma", 13258: "Saruma henryi", 13259: "Saururus", 13260: "Saururus cernuus", 13261: "Schizaphis", 13262: "Schizaphis graminum", 13264: "Brachyspira innocens", 13265: "Smilodon", 13266: "Smilodon fatalis", 13267: "Solemya", 13268: "Solemya velum", 13273: "Stellaria", 13274: "Stellaria media", 13275: "Suttonella", 13276: "Suttonella indologenes", 13278: "Synanceia", 13279: "Synanceia horrida", 13280: "Taphozous", 13281: "Taphozous georgianus", 13282: "Taxodium", 13283: "Terebratella", 13284: "Terebratella sanguinea", 13285: "Theromyzon", 13286: "Theromyzon tessulatum", 13287: "Thlaspi", 13288: "Thlaspi arvense", 13289: "Tilletia", 13290: "Tilletia caries", 13291: "Tilletia controversa", 13305: "Tulipa", 13306: "Tulipa gesneriana", 13322: "Acanthocybium", 13323: "Acanthocybium solandri", 13324: "Acanthoproctus", 13326: "Acanthus", 13327: "Acanthus montanus", 13328: "Achillea", 13329: "Achillea millefolium", 13330: "Akebia", 13331: "Akebia quinata", 13332: "Amborella", 13333: "Amborella trichopoda", 13334: "Anaerobiospirillum", 13335: "Anaerobiospirillum succiniciproducens", 13336: "Annona", 13337: "Annona muricata", 13338: "Apocynum", 13339: "Apocynum cannabinum", 13340: "Aralia", 13341: "Aralia spinosa", 13342: "Arbutus", 13343: "Arbutus canariensis", 13344: "Ardisia", 13345: "Ardisia crenata", 13346: "Armadillidium", 13347: "Armadillidium vulgare", 13348: "Arthrobotrys", 13349: "Arthrobotrys oligospora", 13350: "Austrobaileya", 13351: "Austrobaileya scandens", 13352: "Auxis", 13353: "Auxis thazard", 13356: "Zygogynum", 13357: "Zygogynum sp. Qiu 90024", 13358: "Blennosperma", 13359: "Blennosperma nanum", 13360: "Boopis", 13361: "Boopis anthemoides", 13362: "Borago", 13363: "Borago officinalis", 13364: "Bowenia", 13365: "Bowenia serrulata", 13366: "Brettanomyces", 13368: "Brettanomyces custersianus", 13370: "Brettanomyces naardenensis", 13373: "Burkholderia mallei", 13376: "Cacosmia", 13377: "Cacosmia rugosa", 13378: "Callistephus", 13379: "Callistephus chinensis", 13380: "Callitriche", 13381: "Callitriche heterophylla", 13382: "Callitris", 13383: "Callitris rhomboidea", 13384: "Calluna", 13385: "Calluna vulgaris", 13386: "Calocedrus", 13387: "Calocedrus decurrens", 13390: "Camponotus", 13391: "Camponotus festinatus", 13392: "Cananga", 13393: "Cananga odorata", 13394: "Capparis", 13395: "Capparis masaikai", 13396: "Carcharodon", 13397: "Carcharodon carcharias", 13398: "Carex", 13399: "Carex hostiana", 13402: "Carya", 13403: "Carya glabra", 13404: "Cassiope", 13405: "Cassiope mertensiana", 13406: "Catalpa", 13407: "Catalpa sp. Olmstead 92-99", 13408: "Celtis", 13409: "Celtis yunnanensis", 13410: "Ceratiola", 13411: "Ceratiola ericoides", 13412: "Cercidiphyllum", 13413: "Cercidiphyllum japonicum", 13414: "Chamaecyparis", 13415: "Chamaecyparis obtusa", 13416: "Chamaedaphne", 13417: "Chamaedaphne calyculata", 13418: "Chimonanthus", 13419: "Chimonanthus praecox", 13420: "Chromolaena", 13421: "Chromolaena sp. Dillon 4105", 13422: "Chrysanthemum", 13423: "Leucanthemum maximum", 13424: "Chrysophyllum", 13425: "Chrysophyllum oliviforme", 13426: "Cichorium", 13427: "Cichorium intybus", 13428: "Cinnamomum", 13429: "Cinnamomum camphora", 13430: "Clavija", 13431: "Clavija eggersiana", 13432: "Clerodendrum", 13433: "Clerodendrum fragrans", 13434: "Clethra", 13435: "Clethra alnifolia", 13436: "Clytia", 13438: "Cnephia", 13439: "Cnephia dacotensis", 13440: "Cocculus", 13441: "Cocculus trilobus", 13442: "Coffea", 13443: "Coffea arabica", 13444: "Colchicum", 13445: "Colchicum speciosum", 13446: "Conium", 13447: "Conium maculatum", 13448: "Coreopsis", 13449: "Coreopsis grandiflora", 13450: "Corylus", 13451: "Corylus avellana", 13452: "Corylus cornuta", 13453: "Coryphaena", 13454: "Coryphaena equiselis", 13456: "Cratogeomys castanops castanops", 13457: "Cratogeomys castanops tamaulipensis", 13458: "Cratogeomys fumosus", 13459: "Cratogeomys goldmani goldmani", 13461: "Cratogeomys gymnurus", 13462: "Cratogeomys merriami", 13463: "Cratogeomys tylorhinus", 13464: "Crepis", 13465: "Crepis capillaris", 13466: "Cupaniopsis", 13467: "Cupaniopsis anacardioides", 13468: "Cupressus", 13469: "Cupressus sempervirens", 13470: "Cyathea", 13471: "Cyathea crinita", 13472: "Styphelia", 13473: "Acrothamnus colensoi", 13474: "Cylindrocarpon", 13476: "Cyprinella", 13477: "Cyprinella spiloptera", 13478: "Daboecia", 13479: "Daboecia cantabrica", 13480: "Dasyphyllum", 13481: "Dasyphyllum diacanthoides", 13482: "Degeneria", 13483: "Degeneria vitiensis", 13484: "Dianella", 13485: "Dianella ensifolia", 13486: "Diapensia", 13487: "Diapensia lapponica", 13488: "Dicentrarchus", 13489: "Dicentrarchus labrax", 13490: "Dimorphotheca", 13491: "Dimorphotheca pluvialis", 13492: "Diospyros", 13493: "Diospyros virginiana", 13496: "Diselma", 13497: "Diselma archeri", 13498: "Dolichosaccus", 13499: "Dracophyllum", 13500: "Dracophyllum longifolium", 13502: "Brettanomyces nanus", 13503: "Elegia", 13504: "Elegia sp. Chase 209", 13505: "Elliottia", 13506: "Elliottia racemosa", 13507: "Enkianthus", 13508: "Enkianthus campanulatus", 13509: "Erica", 13510: "Erica australis", 13511: "Erythroxylum", 13512: "Erythroxylum confusum", 13513: "Eulemur", 13514: "Eulemur coronatus", 13515: "Eulemur fulvus", 13516: "Eupatorium", 13517: "Eupatorium atrorubens", 13518: "Eupolymnia", 13519: "Eupolymnia nebulosa", 13520: "Eupomatia", 13521: "Eupomatia bennettii", 13522: "Euptelea", 13523: "Euptelea polyandra", 13524: "Exacum", 13525: "Exacum affine", 13526: "Felicia", 13527: "Felicia bergeriana", 13528: "Flagellaria", 13529: "Flagellaria indica", 13530: "Floerkea", 13531: "Floerkea proserpinacoides", 13532: "Fouquieria", 13533: "Fouquieria splendens", 13534: "Galbulimima", 13535: "Galbulimima belgraveana", 13536: "Gasterochisma", 13537: "Gasterochisma melampus", 13538: "Gaultheria", 13539: "Gaultheria eriophylla", 13540: "Gazania", 13541: "Gazania splendens", 13542: "Gempylus", 13543: "Gempylus serpens", 13544: "Geomys", 13546: "Gerbera", 13547: "Gerbera jamesonii", 13548: "Glomerella", 13550: "Gryllodes", 13551: "Gryllodes sigillatus", 13552: "Gyrocarpus", 13553: "Gyrocarpus sp. Chase 317", 13554: "Haemadipsa", 13555: "Haemadipsa sylvestris", 13556: "Hapalemur", 13557: "Hapalemur griseus", 13558: "Hedyosmum", 13559: "Hedyosmum arborescens", 13560: "Hernandia", 13561: "Hernandia ovigera", 13562: "Heterobasidion", 13563: "Heterobasidion annosum", 13564: "Heterobasidion araucariae", 13565: "Hetrodes", 13567: "Hexamita", 13568: "Hydrastis", 13569: "Hydrastis canadensis", 13570: "Hypoestes", 13571: "Hypoestes forskaolii", 13572: "Idiospermum", 13573: "Idiospermum australiense", 13574: "Istiophorus", 13575: "Istiophorus platypterus", 13576: "Jalmenus", 13577: "Jalmenus evagoras", 13578: "Juncus", 13579: "Juncus effusus", 13580: "Katsuwonus", 13582: "Knema", 13583: "Knema latericia", 13585: "Kalmia buxifolia", 13586: "Lepidocybium", 13587: "Lepidocybium flavobrunneum", 13588: "Lepidagathis", 13589: "Lepidagathis villosa", 13590: "Leucopogon", 13591: "Leucopogon fraseri", 13592: "Libanasidus", 13593: "Libanasidus vittatus", 13594: "Libocedrus", 13595: "Libocedrus plumosa", 13596: "Ligustrum", 13597: "Ligustrum vulgare", 13598: "Liolophura", 13599: "Liolophura japonica", 13601: "Berberis bealei", 13602: "Makaira", 13603: "Istiompax indica", 13604: "Makaira nigricans", 13605: "Manglietia", 13606: "Magnolia fordiana", 13607: "Mantoniella", 13608: "Mantoniella squamata", 13609: "Maoricolpus", 13610: "Maoricolpus roseus", 13611: "Michelia", 13612: "Magnolia figo", 13613: "Microbiota", 13614: "Microbiota decussata", 13615: "Monodelphis", 13616: "Monodelphis domestica", 13617: "Myrmecia", 13618: "Myrmecia pilosula", 13621: "Ostrya", 13622: "Ostrya virginiana", 13623: "Oxychloe", 13624: "Oxychloe andina", 13625: "Paeonia", 13626: "Paeonia tenuifolia", 13627: "Cratogeomys", 13628: "Pappogeomys bulleri", 13629: "Pentachondra", 13630: "Pentachondra pumila", 13632: "Lucilia sericata", 13633: "Phalera", 13634: "Phalera flavescens", 13635: "Piptocarpha", 13636: "Piptocarpha axillaris", 13637: "Platycladus", 13639: "Polemonium", 13640: "Polemonium reptans", 13641: "Polysphondylium", 13642: "Heterostelium pallidum", 13643: "Prionium", 13644: "Prionium serratum", 13645: "Prosimulium", 13646: "Prosimulium fuscum", 13647: "Prosimulium magnum", 13648: "Puccinellia", 13649: "Puccinellia distans", 13650: "Pyrola", 13651: "Pyrola rotundifolia", 13653: "Reinwardtia", 13654: "Reinwardtia indica", 13656: "Rhizorhapis suberifaciens", 13657: "Romanomermis", 13658: "Romanomermis culicivorax", 13659: "Ruellia", 13660: "Ruellia brevifolia", 13661: "Ruvettus", 13662: "Ruvettus pretiosus", 13663: "Sabia", 13664: "Sabia sp. Qiu 91025", 13665: "Sanicula", 13666: "Sanicula gregaria", 13667: "Sansevieria", 13668: "Sansevieria cylindrica", 13669: "Sarcandra", 13670: "Sarcandra grandifolia", 13673: "Schisandra", 13674: "Schisandra sphenanthera", 13675: "Scomber", 13676: "Scomber japonicus", 13677: "Scomber scombrus", 13678: "Scomberomorus", 13679: "Scomberomorus cavalla", 13684: "Parastagonospora nodorum", 13685: "Solenopsis", 13686: "Solenopsis invicta", 13687: "Sphingomonas", 13688: "Novosphingobium capsulatum", 13689: "Sphingomonas paucimobilis", 13690: "Sphingobium yanoikuyae", 13691: "Sphyraena", 13692: "Sphyraena sphyraena", 13693: "Stegopterna", 13694: "Stegopterna mutata", 13695: "Stokesia", 13696: "Stokesia laevis", 13697: "Strymon", 13698: "Strymon melinus", 13699: "Styrax", 13700: "Styrax americanus", 13701: "Symphoricarpos", 13702: "Symphoricarpos albus", 13705: "Syncephalastrum", 13706: "Syncephalastrum racemosum", 13707: "Tagetes", 13708: "Tagetes erecta", 13711: "Magnolia singapurensis", 13712: "Tamias", 13714: "Tetracentron", 13715: "Tetracentron sinense", 13716: "Tetraclinis", 13717: "Tetraclinis articulata", 13718: "Tetrapturus", 13719: "Kajikia albida", 13720: "Tetrapturus angustirostris", 13721: "Kajikia audax", 13722: "Tetrapturus belone", 13723: "Tetrapturus pfluegeri", 13724: "Thiocystis", 13725: "Thiocystis violacea", 13726: "Thujopsis", 13727: "Thujopsis dolabrata", 13728: "Thunbergia", 13729: "Thunbergia usambarica", 13730: "Tragopogon", 13731: "Tragopogon porrifolius", 13732: "Trichiurus", 13733: "Trichiurus lepturus", 13734: "Trionyx", 13735: "Pelodiscus sinensis", 13736: "Turritella", 13737: "Turritella acropora", 13738: "Turritella anactor", 13739: "Turritella communis", 13740: "Turritella exoleta", 13741: "Turritella gonostoma", 13742: "Turritella leucostoma", 13743: "Turritella nodulosa", 13744: "Turritella terebra", 13745: "Uria", 13746: "Uria aalge", 13747: "Utricularia", 13748: "Utricularia gibba", 13749: "Vaccinium", 13750: "Vaccinium macrocarpon", 13751: "Vermicularia", 13752: "Vermicularia knorri", 13753: "Vernonia", 13754: "Gymnanthemum mespilifolium", 13755: "Villarsia", 13756: "Villarsia calthifolia", 13757: "Viola", 13758: "Viola sororia", 13759: "Widdringtonia", 13760: "Widdringtonia cedarbergensis", 13761: "Xanthorhiza", 13762: "Xanthorhiza simplicissima", 13763: "Xyrichtys", 13764: "Xyrichtys martinicensis", 13765: "Xyrichtys novacula", 13766: "Xyrichtys splendens", 13767: "Zenobia", 13768: "Zenobia pulverulenta", 13769: "Natrialba magadii", 13773: "Pyrobaculum aerophilum", 13774: "Metopus contortus archaeal symbiont", 13776: "unidentified archaeon", 13777: "Nitella translucens", 13778: "Chara", 13779: "Chara connivens", 13780: "Chara foetida", 13781: "Klebsormidium sp.", 13782: "Sirogonium", 13783: "Sirogonium melanosporum", 13786: "Trebouxia", 13787: "Trebouxia asymmetrica", 13788: "Trebouxia impressa", 13789: "Asterochloris magna", 13790: "Dunaliella bioculata", 13792: "Mamiellales", 13794: "Andreaeales", 13795: "Andreaeaceae", 13796: "Andreaea", 13797: "Andreaea rupestris", 13798: "Hypnales", 13799: "Sematophyllaceae", 13800: "Brotherella", 13801: "Brotherella recurvans", 13802: "Sphagnales", 13803: "Sphagnaceae", 13804: "Sphagnum", 13805: "Sphagnum palustre", 13806: "Lepidoziaceae", 13807: "Bazzania", 13808: "Bazzania trilobata", 13809: "Anthocerotophyta", 13810: "Anthocerotales", 13811: "Anthocerotaceae", 13812: "Megaceros", 13813: "Nothoceros aenigmaticus", 13814: "Marsileaceae", 13815: "Marsilea", 13816: "Marsilea quadrifolia", 13817: "Adiantum", 13818: "Adiantum capillus-veneris", 13819: "Pteridaceae", 13820: "Pteris", 13821: "Pteris vittata", 13822: "Schizaeaceae", 13823: "Lygodium", 13824: "Lygodium japonicum", 13825: "Angiopteris evecta", 13827: "Ophioglossales", 13828: "Ophioglossaceae", 13829: "Botrychium", 13830: "Sceptridium biternatum", 13832: "Botrypus strictus", 13833: "Ophioglossum", 13834: "Ophioglossum engelmannii", 13836: "Isoetales", 13837: "Isoetaceae", 13838: "Isoetes", 13839: "Isoetes melanopoda", 13840: "Spinulum annotinum", 13841: "Diphasiastrum digitatum", 13893: "Cocos", 13894: "Cocos nucifera", 14009: "Rhapis", 14026: "Trachycarpus", 14027: "Trachycarpus fortunei", 14081: "Rapateaceae", 14097: "Stegolepis", 14101: "Juncaceae", 14107: "Restionaceae", 14146: "Flagellariaceae", 14366: "Cymbidium", 14457: "Epipactis", 14605: "Listera", 14999: "Alisma", 395: "Azorhizobium caulinodans", 229: "Shewanella colwelliana", 230: "Shewanella putrefaciens", 30: "Myxococcales", 46: "Archangiaceae", 37: "Cystobacter", 129: "Ancylobacter", 121: "Pirellula staleyi", 177: "Leptonema illini", 219: "Helicobacter pylori", 273: "Thermus thermophilus", 330: "Pseudomonas oleovorans", 369: "Agrobacterium tumefaciens", 360: "Agrobacterium rhizogenes", 383: "Sinorhizobium meliloti", 397: "Rhizobium leguminosarum", 2610: "Sinorhizobium fredii NGR234", 401: "Rhizobium sp. IRc78", 412: "Methylobacterium organophilum", 443: "Gluconobacter oxydans", 457: "Legionella maceachernii", 514: "Bordetella bronchiseptica", 557: "Pantoea agglomerans", 560: "Pantoea ananatis", 643: "Aeromonas caviae", 710: "Photobacterium", 711: "Photobacterium sp.", 705: "Vibrio", 681: "Vibrio harveyi", 737: "Aggregatibacter aphrophilus", 802: "Bartonella", 804: "Bartonella elizabethae", 2081: "Syntrophomonas", 900: "Desulfovibrio", 874: "Desulfomicrobium baculatum", 778: "Ehrlichia", 946: "Anaplasma phagocytophilum", 994: "Flavobacterium johnsoniae", 1055: "Ectothiorhodospira shaposhnikovii", 12933: "Thiocapsa", 1077: "Rhodopseudomonas palustris", 1217: "Prochloraceae", 1278: "Kocuria rosea", 1291: "Staphylococcus simulans bv. staphylolyticus", 1289: "Streptococcus mutans", 1315: "Streptococcus equinus", 1469: "Bacillus simplex", 1594: "Lactobacillus delbrueckii subsp. bulgaricus", 1644: "Listeria grayi", 1825: "Cellulomonas", 1826: "Cellulosimicrobium cellulans", 1746: "Propionibacterium freudenreichii subsp. shermanii", 2324: "Thermoanaerobacter", 1845: "Saccharopolyspora", 2073: "Pseudonocardia", 1870: "Actinoplanes", 1875: "Micromonospora echinospora", 1973: "Streptomyces", 1899: "Streptomyces anulatus", 1344: "Streptomyces coelicolor", 1939: "Streptomyces microflavus", 1975: "Streptomyces sp.", 1986: "Streptomyces purpureus", 2069: "Streptomyces morookaense", 1840: "Pimelobacter simplex", 2091: "Mycoplasmatales", 2521: "Mycoplasma mycoides", 2140: "Spiroplasma monobiae", 2154: "Candidatus Phytoplasma sp.", 13770: "Methanobacterium bryantii", 2185: "Methanobacterium ivanovii", 2227: "Methanohalophilus", 2170: "Methanothermus fervidus", 2169: "Methanothermococcus thermolithotrophicus", 2212: "Methanosarcina mazei", 2241: "Halobacterium salinarum", 2274: "Desulfurococcus mucosus", 2732: "Bacillus sp. PS3", 1619: "Carnobacterium maltaromaticum", 2778: "Gracilariopsis lemaneiformis", 2795: "Palmaria palmata", 2827: "Pavlova lutheri", 2884: "Pylaiella", 2883: "Pylaiella littoralis", 2906: "Ochrosphaera sp. 181", 2941: "Heterocapsa niei", 2895: "Cryptophyta", 3069: "Chlamydomonadales", 3045: "Dunaliella salina", 3053: "Chlamydomonas moewusii", 3058: "Chlamydomonas reinhardtii", 3115: "Ulva", 3194: "Bryophyta", 3235: "Psilotopsida", 3241: "Psilotum nudum", 3361: "Keteleeria davidiana", 3314: "Cupressaceae", 4408: "Magnoliales", 13709: "Magnolia", 3416: "Liriodendron chinense", 3461: "Papaveraceae", 3491: "Artocarpus integer", 3519: "Fagales", 4352: "Caryophyllales", 3556: "Beta vulgaris subsp. vulgaris", 3549: "Amaranthaceae", 3611: "Rhamnus cathartica", 3639: "Malvaceae", 3643: "Lecythidaceae", 4385: "Malpighiales", 3692: "Populus nigra", 3706: "Brassica rapa", 4266: "Rosales", 3748: "Fragaria x ananassa", 3757: "Prunus dulcis", 3789: "Cunoniaceae", 3903: "Ulex europaeus", 3919: "Vigna angularis", 3952: "Oenothera berteroana", 4064: "Apocynaceae", 4061: "Rauvolfia", 4063: "Rauvolfia serpentina", 4105: "Petunia x hybrida", 4080: "Solanum", 4117: "Solanum nigrum", 4175: "Scrophulariaceae", 3768: "Lentibulariaceae", 4380: "Asterales", 4213: "Ambrosia artemisiifolia", 4316: "Celastraceae", 4308: "Euonymus maackii", 4342: "Ericaceae", 4438: "Plumbaginaceae", 4468: "Araceae", 4461: "Colocasia esculenta", 4484: "Aegilops markgrafii", 4531: "Oryza officinalis", 4542: "Cenchrus americanus", 4574: "Triticum aestivum x Triticum timopheevi", 4489: "Aegilops speltoides", 4578: "Zea mays", 4600: "Thinopyrum", 4602: "Thinopyrum elongatum", 4495: "Amblyopyrum muticum", 4728: "Typhaceae", 4804: "Chytridiomycota", 4961: "Cyberlindnera jadinii", 4945: "Debaryomyces", 5437: "Sporobolomyces johnsonii", 13369: "Brettanomyces bruxellensis", 5080: "Penicillium chrysogenum", 5049: "Epichloe typhina", 5521: "Fusarium sambucinum", 5561: "Hypomyces rosellus", 5415: "Cryptococcus", 5316: "Ganoderma lucidum", 5313: "Polyporaceae", 5425: "Agaricales", 5344: "Agaricaceae", 5348: "Coprinopsis cinerea", 5126: "Fusarium", 5285: "Rhodotorula", 5534: "Rhodotorula mucilaginosa", 5662: "Leishmania infantum", 5766: "Tetramitus", 5920: "Tetrahymena americanis", 5952: "Stylonychia mytilus", 6031: "Microsporidia", 6048: "Demospongiae", 6064: "Halichondriidae", 6081: "Hydra", 6085: "Hydra vulgaris", 6121: "Heteractis sp.", 6294: "Spirurina", 6297: "Onchocercidae", 6331: "Trichinellida", 6439: "Phascolopsis gouldii", 6460: "Haliotis", 13619: "Nassarius", 6509: "Aplysiidae", 6634: "Todarodes pacificus", 6748: "Paguroidea", 6963: "Anisoptera", 13009: "Stauroderus scalaris", 7075: "Zophobas atratus", 7103: "Helicoverpa zea", 7326: "Drosophila", 13631: "Lucilia", 13172: "Sarcophaga bullata", 7383: "Sarcophaga peregrina", 7418: "Ichneumonidae", 7510: "Siphonaptera", 7517: "Neuroptera", 7562: "Pentastomida", 7572: "Lingula anatina", 7605: "Asterias rubens", 7628: "Heliocidaris", 8091: "Perciformes", 8122: "Haplochromis burtoni", 8123: "Astatotilapia calliptera", 8170: "Pagrus", 8263: "Pseudopleuronectes americanus", 8470: "Chelonia mydas", 8494: "Crocodylidae", 13294: "Tiliqua rugosa", 8588: "Ptyas dhumnades", 8645: "Naja mossambica", 8648: "Naja atra", 8662: "Notechis scutatus", 8780: "Hydrophis", 8775: "Calloselasma rhodostoma", 8761: "Sistrurus tergeminus", 8760: "Sistrurus miliarius barbouri", 8791: "Dromaius novaehollandiae", 8890: "Anser", 8891: "Anser caerulescens", 9241: "Apodiformes", 9245: "Charadriiformes", 9099: "Phasianidae", 9024: "Callipepla", 9028: "Oreortyx pictus", 9073: "Arborophila", 9074: "Arborophila torqueola", 9110: "Grus", 9113: "Grus carunculatus", 9141: "Asthenes dorbignyi", 9492: "Callithrix", 9484: "Callithrix jacchus", 9563: "Papio anubis", 9560: "Papio hamadryas", 9609: "Vulpes", 9628: "Vulpes vulpes", 9698: "Herpestidae", 9797: "Equus asinus", 9795: "Equus hemionus", 9936: "Ovis aries", 9985: "Oryctolagus cuniculus", 10109: "Mus spicilegus", 10202: "Ctenophora", 12871: "Variola virus", 12738: "Bovine alphaherpesvirus 1", 12829: "Macacine alphaherpesvirus 1", 10396: "Saimiriine alphaherpesvirus 1", 10354: "Bovine gammaherpesvirus 4", 12743: "Gallid alphaherpesvirus 1", 12614: "Ictalurid herpesvirus 1", 10502: "Phycodnaviridae", 12592: "Bovine adenovirus 3", 12607: "Canine adenovirus 1", 12757: "Murine adenovirus 1", 10554: "Fowl aviadenovirus 1", 10657: "Tectiviridae", 12398: "Bacillus virus SPO1", 12422: "Phage 434", 12339: "Staphylococcus phage 42D.m", 12414: "Streptomyces virus phiC31", 12028: "Bacillus phage SPR", 12373: "Staphylococcus phage L54a", 12346: "Streptococcus pneumoniae phage HB-3", 12334: "Streptomyces phage R4", 12380: "Bacillus phage rho11s", 10716: "Enterobacteria phage PA-2", 12419: "Escherichia virus HK022", 12377: "Lactococcus phage phi-vML3", 10741: "Enterobacteria phage LP7", 10675: "Enterobacteria phage K11", 10810: "Bombyx mori densovirus", 10858: "Escherichia virus phiK", 10706: "Escherichia phage alpha3", 10853: "Spiroplasma phage 1-R8A2B", 10890: "Mammalian orthoreovirus 1 Lang", 10889: "Mammalian orthoreovirus 2 D5/Jones", 10888: "Mammalian orthoreovirus 3 Dearing", 10920: "Porcine rotavirus strain Gottfried", 10924: "Simian rotavirus A/SA11", 12706: "Human rotavirus C", 10972: "Human rotavirus G4 strain St. Thomas 3", 12794: "Porcine rotavirus C", 12740: "Infectious bursal disease virus", 12744: "Infectious pancreatic necrosis virus", 12525: "Saccharomyces cerevisiae virus L-A", 12625: "Classical swine fever virus", 12859: "Transmissible gastroenteritis virus", 11197: "Sendai virus (Z)", 11202: "Human respirovirus 3", 11204: "Human parainfluenza virus 4a", 11205: "Human parainfluenza virus 4b", 11230: "Measles morbillivirus", 12604: "Bovine orthopneumovirus", 11267: "Filoviridae", 12872: "Vesicular stomatitis virus", 12874: "Viral hemorrhagic septicemia virus", 12826: "Sigma virus", 12565: "Thogoto thogotovirus", 11600: "HoJo virus", 12748: "Lymphocytic choriomeningitis mammarenavirus", 11872: "Reticuloendotheliosis virus", 11647: "Bovine immunodeficiency virus", 12610: "Caprine arthritis encephalitis virus", 11722: "Human immunodeficiency virus type 1 (ZAIRE 6 ISOLATE)", 11740: "Simian immunodeficiency virus", 12704: "Human endogenous retrovirus ERV-9", 12746: "Jaagsiekte sheep retrovirus", 11969: "Golden hamster intracisternal A-particle H18", 11933: "Mouse intracisternal A-particle MIA14", 11934: "Mouse intracisternal A-particle MIAIL3", 11920: "Feline leukemia virus", 11773: "Gardner-Arnstein feline sarcoma virus", 11825: "Feline sarcoma virus (STRAIN HARDY-ZUCKERMAN 4)", 12763: "Murine leukemia virus", 11831: "AKR (endogenous) murine leukemia virus", 11972: "Cas NS-1 murine leukemia virus", 11802: "Moloney murine sarcoma virus", 12767: "Myeloproliferative sarcoma virus", 11940: "NS.C58 murine sarcoma virus", 11939: "Mason-Pfizer monkey virus", 12562: "Squirrel monkey retrovirus-H", 12581: "Avian myeloblastosis virus", 11952: "Avian myelocytomatosis virus", 11917: "Avian carcinoma Mill Hill virus 2", 11918: "Avian myelocytomatosis virus OK10", 11959: "Avian musculoaponeurotic fibrosarcoma virus AS42", 11890: "Avian sarcoma virus 17", 11892: "Avian sarcoma virus CT10", 11891: "Avian sarcoma virus PR2257", 11893: "Avian sarcoma virus PRCII", 11895: "Avian sarcoma virus S1", 11896: "Avian sarcoma virus S2", 11898: "Y73 sarcoma virus", 11755: "Mouse Intracisternal A-particle", 11852: "Simian retrovirus 1", 11953: "Rous-associated virus type 0", 11954: "Rous-associated virus type 1", 12766: "Avian myeloblastosis-associated virus", 12749: "Lymphoproliferative disease virus", 11817: "Woolly monkey sarcoma virus", 12806: "Rabbit hemorrhagic disease virus", 11991: "Enterobacteria phage BO1", 11992: "Enterobacteria phage isolate BZ13", 11994: "Enterobacteria phage f2", 11995: "Enterobacteria phage fr", 11997: "Enterobacteria phage GA", 11998: "Enterobacteria phage JP34", 11999: "Enterobacteria phage JP501", 12000: "Enterobacteria phage KU1", 12001: "Enterobacteria phage MS2", 12011: "Pseudomonas phage PP7", 12012: "Pseudomonas phage PRR1", 12002: "Enterobacteria phage R17", 12010: "Enterobacteria phage SP", 12004: "Enterobacteria phage TH1", 12006: "Enterobacteria phage TW28", 12007: "Enterobacteria phage VK", 11996: "Enterobacteria phage fr1", 12128: "Enterovirus", 12630: "Coxsackievirus B3", 12564: "Theiler's encephalomyelitis virus", 12469: "Sobemovirus", 12547: "Belladonna mottle virus", 12156: "Eggplant mosaic virus", 12840: "Strawberry mild yellow edge virus", 12863: "Turnip mosaic virus", 12265: "Bean pod mottle virus", 12792: "Poa semilatent virus", 12448: "Clostridium phage c-st", 12003: "Enterobacteria phage ST", 12411: "Staphylococcus virus 11", 12372: "Streptococcus pyogenes phage H4489A", 12364: "Lactococcus phage (ISOLATE 7-9)", 12369: "Lactococcus phage F4-1", 12418: "Lactococcus phage phiLC3", 10698: "Salmonella virus PsP3", 12358: "Lactobacillus phage phiadh", 12572: "AKT8 retrovirus", 12646: "Non-A, non-B hepatitis virus", 12682: "Hepatitis delta virus", 12616: "Cryphonectria hypovirus 1-EP713", 10628: "African green monkey polyomavirus", 11609: "Seoul virus 80-39", 10975: "Adult diarrheal rotavirus", 11209: "Human respirovirus 1", 11141: "Murine hepatitis virus strain 4", 12869: "Variola major virus", 12254: "Satellite tobacco mosaic virus", 2282: "Acidianus", 10204: "Cestum veneris", 5496: "Chalara", 6155: "Leuckartiara", 6156: "Leuckartiara octona", 13671: "Saruma", 13672: "Saruma henryi", 13501: "Brettanomyces", 13655: "Sphingomonas", 13831: "Botrychium", 3243: "Isoetales", 4708: "Alismatales", 13600: "Berberis", 4021: "Sapindaceae", 4271: "Elaeocarpaceae", 4946: "Schwanniomyces occidentalis", 7015: "Oedipodinae", 13437: "Clytia gregaria", 1846: "Saccharopolyspora rectivirgula", 1864: "Micromonosporaceae", 825: "Prevotella intermedia", 706: "Vibrio aestuarianus", 707: "Vibrio ordalii", 13137: "unidentified marine eubacterium", 12485: "Amsacta moorei entomopoxvirus", 12865: "Human type D retrovirus", 12796: "Porcine reproductive and respiratory syndrome virus", 10973: "Rotavirus A", 10974: "Rotavirus B", 12741: "IDIR agent", 1756: "Thermoanaerobacterium saccharolyticum", 591: "Salmonella enterica", 12379: "Clostridium botulinum D phage", 1734: "[Clostridium] scindens", 1617: "Lactobacillus delbrueckii subsp. lactis", 348: "Xanthomonas campestris pv. cyanopsidis", 627: "Photorhabdus luminescens", 653: "Aeromonas enteropelogenes", 708: "Vibrio tubiashii", 13263: "Brachyspira", 3286: "Dryopteridaceae", 6897: "Aphonopelma sp.", 7773: "Ichthyomyzon unicuspis", 8003: "Gymnotidae", 6568: "Argopecten irradians", 12880: "Satellite maize white line mosaic virus", 10695: "Escherichia phage RB3", 10945: "Human rotavirus 1 strain RV4", 12613: "Cell fusing agent virus", 12551: "Avian retrovirus RPL30", 12831: "Simian immunodeficiency virus - mac1A11", 11025: "Ockelbo virus", 12255: "Beet necrotic yellow vein virus", 12341: "Lactococcus phage BK5-T", 12376: "Mycobacterium virus L5", 5459: "Colletotrichum graminicola", 692: "Comamonas terrigena", 67: "Xanthomonadaceae", 1141: "Synechococcus elongatus", 805: "Bartonella vinsonii", 3126: "Bryopsidales", 5102: "Onygenales", 10024: "Sciuromorpha", 10348: "Suid herpesvirus 1 strain Kaplan", 11147: "Porcine respiratory coronavirus (strain 86/137004 / British isolate)", 12629: "Coxsackievirus A2", 12385: "Lactobacillus phage mv1", 2032: "Microbacterium", 1820: "Amycolatopsis mediterranei", 1250: "Leuconostoc citreum", 922: "Paracoccus versutus", 90: "Sphaerotilus", 91: "Sphaerotilus natans", 3698: "Populus sieboldii x Populus grandidentata", 4936: "Kazachstania exigua", 5122: "Blumeria graminis", 7817: "Rhizoprionodon acutus", 8521: "Scinciformata", 12688: "Ateline alphaherpesvirus 1", 12593: "Bovine alphaherpesvirus 5", 12835: "Cercopithecine alphaherpesvirus 9", 10429: "Woodchuck hepatitis virus", 12784: "Pelargonium leaf curl virus", 11573: "Bunyamwera virus", 11581: "Simbu orthobunyavirus", 12378: "Streptococcus phage T12", 3184: "Cladophoraceae", 1982: "Streptomyces mobaraensis", 8650: "Naja naja", 2921: "Heterocapsa pygmaea", 2793: "Porphyridium purpureum", 3060: "Chlamydomonas applanata", 1230: "Nitrosospira", 3138: "Acetabularia acetabulum", 3137: "Acetabularia peniculus", 6461: "Haliotis diversicolor", 8195: "Pachycara brachycephalum", 12410: "Enterobacteria phage phi50", 10505: "Paramecium bursaria Chlorella virus CV-XZ6E", 10624: "Polyomavirus sp.", 10495: "Lymphocystis disease virus 1", 10977: "Rotavirus C", 10966: "Bovine rotavirus strain NCDV/G6", 10940: "Equine rotavirus L338/G13", 10938: "Equine rotavirus (serotype 14 / strain FI-14)", 12891: "Coconut cadang-cadang viroid", 10027: "Cricetinae gen. sp.", 5497: "Chalara sp.", 2435: "plasmids", 12842: "Subterranean clover stunt virus", 1803: "Mycobacterium genavense", 1815: "Amycolatopsis azurea", 5484: "Clavispora lusitaniae", 6985: "Gromphadorhina", 6986: "Gromphadorhina portentosa", 6987: "Rhyparobia", 6988: "Rhyparobia maderae", 6991: "Schultesia", 6992: "Schultesia lampyridiformis", 9941: "Ovibos moschatus", 7016: "Dissosteira", 7017: "Dissosteira carolina", 2076: "Pseudonocardia petroleophila", 8105: "Batrachocottus", 8106: "Batrachocottus baicalensis", 9396: "Tupaia belangeri", 2027: "Laceyella sacchari", 3574: "Silene latifolia", 13367: "Brettanomyces anomalus", 4482: "Aegilops tauschii", 1819: "Rhodococcus opacus", 1700: "Glutamicibacter nicotianae", 13460: "Cratogeomys goldmani rubellus", 5558: "Parengyodontium album", 12361: "unidentified phage", 806: "Bartonella henselae", 2519: "Cloning vector pACYC184", 4727: "Poales", 11853: "Simian retrovirus 2", 13835: "Selaginella apoda", 2228: "Methanohalophilus portucalensis", 419: "Methylomicrobium agile", 420: "Methylomicrobium album", 12009: "Escherichia virus Qbeta", 11993: "Escherichia virus FI", 12365: "Lactococcus phage 936", 10896: "African horse sickness virus", 12591: "Bluetongue virus", 10908: "Epizootic hemorrhagic disease virus", 291: "Oligotropha carboxidovorans", 345: "Stenotrophomonas maltophilia", 4723: "Pandanales", 4709: "Arecales", 8212: "Trematomus bernacchii", 1706: "Exiguobacterium acetylicum", 910: "Bradyrhizobiaceae", 6422: "Siboglinidae", 3439: "Ranunculales", 4279: "Cornales", 4010: "Sapindales", 3628: "Malvales", 4017: "Geraniales", 3927: "Myrtales", 4338: "Ericales", 4393: "Saxifragales", 3957: "Santalales", 1342: "Enterococcus saccharolyticus", 3576: "Silene vulgaris", 4394: "Hamamelidaceae", 7708: "Sclerodactylidae", 6872: "Mesobuthus tamulus sindicus", 4977: "Udeniomyces megalosporus", 4982: "Udeniomyces puniceus", 4980: "Udeniomyces pyricola", 9270: "Micoureus regina", 1834: "Rhodococcus hoagii", 2328: "Caldicellulosiruptor", 2329: "Caldicellulosiruptor saccharolyticus", 1330: "Enterococcus cecorum", 1463: "Bacillus thuringiensis serovar kyushuensis", 1389: "Paenibacillus alvei", 1453: "Paenibacillus durus", 1403: "Paenibacillus macerans", 1460: "Paenibacillus validus", 5669: "Leishmania chagasi", 748: "Pasteurella multocida subsp. multocida", 3783: "Crassula marnierana", 4440: "Plumbago auriculata", 12511: "Human endogenous retrovirus K", 13584: "Kalmia", 10446: "Autographa californica nucleopolyhedrovirus", 10504: "Paramecium bursaria Chlorella virus NC1A", 12619: "Paramecium bursaria Chlorella virus NY2A", 289: "Hydrogenophaga pseudoflava", 10531: "Tree shrew adenovirus 1", 2003: "Kutzneria viridogrisea", 8191: "Mugil cephalus", 8198: "Zoarces", 5137: "Pyricularia", 4474: "Landoltia punctata", 334: "Pseudomonas fluorescens bv. B", 1980: "Streptomyces griseocarneus", 667: "Salinivibrio costicola", 5546: "Trichoderma reesei", 1256: "Tetragenococcus halophilus", 877: "Desulfomicrobium norvegicum", 1842: "Aeromicrobium fastidiosum", 530: "Polaribacter", 11262: "Porcine rubulavirus", 2058: "Terrabacter", 1979: "Streptomyces cinnamoneus", 4140: "Scutellaria bolanderi", 3405: "Magnolia kobus", 13703: "Symplocos", 13704: "Symplocos paniculata", 665: "Vibrio anguillarum", 6403: "Hirudinea", 4106: "Petunia axillaris subsp. parodii", 12980: "Butea monosperma", 13475: "Neonectria galligena", 5724: "Tritrichomonas suis", 3365: "Afrocarpus falcatus", 5517: "Fusarium decemcellulare", 5519: "Fusarium striatum", 13240: "Psittacus erithacus", 5844: "Plasmodium falciparum Palo Alto/Uganda", 6482: "Busycotypus canaliculatus", 7846: "Isurus oxyrinchus", 13638: "Platycladus orientalis", 2009: "Microbispora rosea subsp. rosea", 4488: "Aegilops sharonensis", 603: "Salmonella enterica subsp. arizonae", 5366: "Panus conchatus", 2059: "Terrabacter tumescens", 5522: "Fusarium equiseti", 8601: "Atractaspis bibronii", 8120: "Cryptoheros spilurus", 8116: "Amphilophus citrinellus", 8118: "Amphilophus labiatus", 9584: "Nomascus gabriellae", 9585: "Nomascus leucogenys", 9189: "Emberizinae", 5123: "Blumeria graminis f. sp. hordei", 8115: "Archocentrus centrarchus", 4845: "Rhizopus oryzae", 13713: "Tamias sibiricus", 1959: "Actinoalloteichus cyanogriseus", 559: "Pantoea stewartii subsp. stewartii", 1978: "Streptomyces roseoverticillatus", 9951: "Madoqua kirkii", 567: "Citrobacter intermedius", 10722: "Bacillus virus SPbeta", 4789: "Phytophthora sojae", 9025: "Callipepla californica", 9026: "Callipepla gambelii", 13313: "Calloria", 13314: "Calloria inconspicua", 1974: "Streptomyces griseoverticillatus", 1983: "Streptomyces olivoreticuli", 1953: "Streptomyces violaceusniger", 2703: "Coprothermobacter", 7169: "Anopheles farauti", 11710: "HIV-2.D205", 9934: "Eudorcas thomsonii", 12950: "Artioposthia", 10731: "Enterobacteria phage H-19B", 3205: "Geocalycaceae", 1024: "Flexithrix dorotheae", 3399: "eudicotyledons", 9907: "Bos mutus", 5396: "Tapinella atrotomentosa", 4745: "Asparagales", 5048: "Epichloe festucae var. lolii", 12: "Photobacterium profundum", 77: "Brevundimonas bacteroides", 79: "Brevundimonas subvibrioides", 3291: "Salviniales", 8026: "Oncorhynchus tshawytscha", 8836: "Lophonetta specularioides", 746: "Mannheimia haemolytica", 925: "Acidiphilium acidophilum", 4518: "Hordeum vulgare subsp. spontaneum", 4417: "Nuphar lutea", 2338: "uncultured bacterium", 1475: "Paenibacillus popilliae", 1466: "Paenibacillus lentimorbus", 10452: "Mamestra brassicae multiple nucleopolyhedrovirus", 9236: "Eudyptes chrysocome", 284: "Delftia acidovorans", 6583: "Pseudocardium sachalinense", 6468: "Omphalius pfeifferi", 812: "Chlamydia psittaci", 811: "Chlamydia pneumoniae", 10192: "Ploima", 5555: "Moesziomyces antarcticus", 1761: "Corynebacteriales", 1882: "Streptomycetales", 684: "Photobacterium damselae subsp. damselae", 3944: "Oenothera elata subsp. hookeri", 515: "Achromobacter xylosoxidans", 1414: "Bacillus halodurans", 6464: "Cymbula granatina", 9574: "Semnopithecus entellus", 8771: "Protobothrops elegans", 8766: "Protobothrops flavoviridis", 8411: "Pelophylax porosus brevipodus", 10071: "Abrothrix andinus", 977: "Cytophagaceae", 9919: "Bubalus bubalis", 5590: "Cladophialophora bantiana", 601: "Salmonella enterica subsp. enterica serovar Typhi", 602: "Salmonella enterica subsp. enterica serovar Typhimurium", 677: "Moritella marina", 4612: "commelinids incertae sedis", 4293: "fabids", 4379: "campanulids", 5946: "Sterkiella histriomuscorum", 5359: "Neolentinus dactyloides", 8563: "Eublepharis", 8641: "Naja annulifera", 1977: "Streptomyces abikoensis", 1984: "Streptomyces salmonis", 593: "Salmonella enterica subsp. enterica serovar Dublin", 11539: "Influenza B virus (B/Memphis/3/89)", 7978: "Balitoridae", 7975: "Nemacheilus", 13680: "Scomberomorus maculatus", 9998: "Urocitellus townsendii", 11559: "Influenza C virus (C/Johannesburg/1/66)", 14098: "Epidryos allenii", 4848: "Choanephoraceae", 10964: "Rabbit rotavirus strain Alabama", 4659: "Orchidantha siamensis", 6642: "Eledone cirrhosa", 1174: "Nostoc sp. PCC 7120", 7104: "Mythimna", 11770: "Feline leukemia virus strain B/lambda-B1", 11771: "Feline leukemia virus strain C/Sarma", 11299: "Rabies virus strain Pasteur vaccin", 8768: "Protobothrops mucrosquamatus", 5055: "Aspergillus awamori", 4994: "Kondoa phyllada", 5287: "Sakaguchia dacryoidea", 10394: "Papiine gammaherpesvirus 1", 510: "Cupriavidus necator", 10416: "Hepatitis B virus subtype adr", 10417: "Hepatitis B virus subtype adw", 1000: "Tenacibaculum maritimum", 11533: "Influenza B virus (B/Ibaraki/2/85)", 11544: "Influenza B virus (B/Singapore/222/79)", 5420: "Phaffia", 473: "Acinetobacter calcoaceticus subsp. anitratus", 5239: "Thanatephorus cucumeris", 5565: "Sclerotium", 8701: "Eristicophis", 8702: "Eristicophis macmahoni", 10745: "Teseptimavirus", 7768: "Myxininae", 10982: "Bombyx mori cypovirus 1", 4514: "Hordeum vulgare subsp. vulgare", 4730: "Sparganium americanum", 3209: "Polytrichopsida", 4991: "Leucosporidium intermedium", 6795: "Eubrachyura", 6803: "Heterotremata", 6699: "Palaemon", 2729: "Buchnera aphidicola (Acyrthosiphon pisum)", 1156: "Arthrospira platensis", 1312: "Streptococcus dysgalactiae subsp. equisimilis", 5273: "Ustilago hordei", 8581: "Erythrolamprus", 6352: "Hediste diversicolor", 6128: "Acropora formosa", 5856: "Plasmodium vivax Sal-1", 1155: "Limnospira maxima", 10538: "Duck adenovirus 1", 8119: "Hypsophrys nicaraguensis", 12951: "Arthurdendyus triangulatus", 11489: "Influenza A virus (A/X-31(H3N2))", 1020: "Thiotrichaceae", 7976: "Barbatula barbatula", 5510: "[Nectria] haematococca", 9045: "Lophura leucomelanos", 9047: "Lophura swinhoii", 12982: "Cacatua galerita", 9155: "Baeolophus inornatus", 257: "Salegentibacter salegens", 260: "Zobellia uliginosa", 8171: "Pagrus major", 857: "Filifactor alocis", 1723: "Leifsonia aquatica", 6505: "Aplysia fasciata", 2167: "Methanothermobacter wolfeii", 2166: "Methanothermobacter thermautotrophicus", 12231: "Watermelon mosaic virus", 1546: "Dendrosporobacter quercicolus", 2011: "Microbispora rosea subsp. aerata", 5096: "Elaphomycetaceae", 5138: "Pyricularia grisea", 6555: "Scapharca broughtonii", 592: "Salmonella enterica subsp. enterica serovar Enteritidis", 13710: "Magnolia ovata", 11639: "Alpharetrovirus", 11762: "Gammaretrovirus", 12879: "Panicum mosaic satellite virus", 80: "Caulobacter vibrioides", 9156: "Cyanistes caeruleus", 4971: "Bullera alba", 10635: "Murine polyomavirus strain A3", 5646: "Sterigmatosporidium", 2913: "Lingulodinium polyedra", 4471: "Lemna minuta", 8140: "Oreochromis urolepis hornorum", 10460: "Antheraea pernyi nucleopolyhedrovirus", 5072: "Aspergillus nidulans", 9571: "Piliocolobus badius", 4985: "Sporobolomyces", 4259: "Anisocarpus", 5767: "Tetramitus jugosus", 12133: "Human rhinovirus sp.", 12415: "Halobacterium phage phiH", 3666: "Cucurbita hybrid cultivar", 2780: "Gracilaria bursa-pastoris", 5582: "Beauveria bassiana", 10488: "Invertebrate iridescent virus 6", 6066: "Hymeniacidon perlevis", 7404: "Cotesia kariyai", 9500: "Alouatta guariba", 36: "Corallococcus coralloides", 10777: "Staphylococcus virus 13", 10807: "Aedes aegypti densovirus", 11512: "Influenza A virus (A/swine/New Jersey/11/1976(H1N1))", 10700: "Lambdavirus", 1196: "Microchaete", 6517: "Diaulula", 12279: "Beet ringspot virus", 12290: "Pea enation mosaic virus 1", 6777: "Chaceon quinquedens", 5945: "Sterkiella nova", 5951: "Stylonychia pustulata", 8580: "Coelognathus radiatus", 8209: "Notothenia neglecta", 11555: "Influenza C virus (C/California/78)", 11558: "Influenza C virus (C/Hyogo/1/83)", 11562: "Influenza C virus (C/Mississippi/80)", 11565: "Influenza C virus (C/pig/Beijing/115/81)", 11563: "Influenza C virus (C/Nara/82)", 11561: "Influenza C virus (C/Kyoto/41/82)", 11268: "Ebola virus sp.", 10448: "Choristoneura fumiferana multiple nucleopolyhedrovirus", 5971: "Oligotrichia", 11455: "Influenza A virus (A/Puerto Rico/8/1934(H1N1))", 8989: "Pipile pipile", 6635: "Nototodarus sloanii", 11478: "Influenza A virus (A/Texas/1/68(H2N2))", 11415: "Influenza A virus (A/equine/Sao Paulo/1/76(H7N7))", 11416: "Influenza A virus (A/equine/Switzerland/137/72(H7N7))", 11409: "Influenza A virus (A/equine/Newmarket/1/77(H7N7))", 11398: "Influenza A virus (A/equine/Detroit/1/64(H7N7))", 11395: "Influenza A virus (A/equine/Cambridge/1/73(H7N7))", 11396: "Influenza A virus (A/equine/C.Detroit/1/64(H7N7))", 11394: "Influenza A virus (A/equine/Cambridge/1/63(H7N7))", 11456: "Influenza A virus (A/Queensland/7/70(H3N2))", 10819: "African cassava mosaic virus - [Nigeria]", 10828: "Potato yellow mosaic virus - [Venezuela]", 130: "Ancylobacter vacuolatus", 9007: "Odontophoridae", 11526: "Influenza B virus (B/Bonn/43)", 11546: "Influenza B virus (B/USSR/100/83)", 5289: "Sporidiobolales", 9229: "Psittacula eupatria", 10079: "Abrothrix jelskii", 3290: "Polypodiopsida", 12563: "Sulfolobus spindle-shaped virus 1", 7751: "Lampetra tridentata", 10110: "Mus terricolor", 7457: "Polistes jokahamae", 13545: "Geomys jugossicularis jugossicularis", 7087: "Anoplotrupes stercorosus", 8489: "Mauremys reevesii", 12393: "Enterobacteria phage PR772", 9427: "Lophostoma silvicolum", 8640: "Naja anchietae", 1172: "Trichormus variabilis", 6649: "Enteroctopus dofleini", 1139: "Synechococcus elongatus PCC 6301", 10458: "Bombyx mori nucleopolyhedrovirus", 7105: "Mythimna separata", 8878: "Lophodytes cucullatus", 5458: "Colletotrichum lindemuthianum", 4127: "Cuscuteae", 7809: "Carcharhinus perezii", 10447: "Galleria mellonella MNPV", 7692: "Apostichopus japonicus", 11471: "Influenza A virus (A/turkey/Ontario/6118/1968(H8N4))", 12396: "Enterobacteria phage L17", 12395: "Enterobacteria phage PR4", 12394: "Enterobacteria phage PR5", 2963: "Tovellia coronata", 111: "Bradyrhizobium denitrificans", 8935: "Streptopelia risoria", 10751: "Bacillus phage M2", 8750: "Crotalus oreganus lutosus", 12033: "Enterobacteria phage ZR", 10597: "Human papillomavirus type 57", 10603: "Human papillomavirus type 10", 10581: "Human papillomavirus type 16", 10582: "Human papillomavirus type 18", 10612: "Human papillomavirus type 32", 10613: "Human papillomavirus type 34", 10619: "Human papillomavirus type 53", 10578: "Human papillomavirus 5", 2244: "Halorubrum chaoviator", 10559: "Deltapapillomavirus 4", 11964: "Macaque simian foamy virus", 8708: "Daboia siamensis", 12391: "Enterobacteria phage K1F", 8159: "Pseudocaranx dentex", 11231: "Measles virus strain Biken", 5713: "Parabodo caudatus", 11349: "Influenza A virus (A/mallard/Alberta/35/1976(H1N1))", 11364: "Influenza A virus (A/duck/Hong Kong/7/1975(H3N2))", 11434: "Influenza A virus (A/mallard/Astrakhan/263/1982(H14N5))", 11806: "Finkel-Biskis-Jinkins murine sarcoma virus", 11897: "UR2 sarcoma virus", 8680: "Hydrophis stokesii", 8424: "Sooglossus", 10865: "Xanthomonas phage Xf", 5166: "Ceratocystiopsis minuta-bicolor", 5167: "Ceratocystiopsis minuta", 5165: "Ceratocystiopsis minima", 6437: "Themiste hennahi", 9444: "Strepsirrhini", 11445: "Influenza A virus (A/New Jersey/8/1976(H1N1))", 11465: "Influenza A virus (A/Taiwan/1/1986(H1N1))", 11380: "Influenza A virus (A/Fort Monmouth/1/1947-mouse adapted(H1N1))", 11467: "Influenza A virus (A/turkey/Ireland/1378/1983(H5N8))", 11470: "Influenza A virus (A/turkey/Ontario/7732/1966(H5N9))", 11412: "Influenza A virus (A/equine/Prague/1/1956(H7N7))", 11417: "Influenza A virus (A/equine/Tennessee/5/1986(H3N8))", 11406: "Influenza A virus (A/equine/London/1416/1973(H7N7))", 11503: "Influenza A virus (A/swine/Iowa/17672/1988(H1N1))", 11500: "Influenza A virus (A/swine/Iowa/15/1930(H1N1))", 11458: "Influenza A virus (A/ruddy turnstone/New Jersey/47/1985(H4N6))", 11488: "Influenza A virus (A/Wisconsin/3523/1988(H1N1))", 11511: "Influenza A virus (A/swine/Netherlands/12/1985(H1N1))", 11469: "Influenza A virus (A/turkey/Minnesota/1661/1981(H1N1))", 11474: "Influenza A virus (A/Tokyo/3/1967(H2N2))", 11427: "Influenza A virus (A/Leningrad/134/47/1957(H2N2))", 11337: "Influenza A virus (A/Chile/1/1983(H1N1))", 4916: "Lachancea thermotolerans", 9129: "Zaratornis stresemanni", 11481: "Influenza A virus (A/USSR/90/1977(H1N1))", 11480: "Influenza A virus (A/Udorn/307/1972(H3N2))", 11487: "Influenza A virus (A/Wilson-Smith/1933(H1N1))", 11463: "Influenza A virus (A/Singapore/1/1957(H2N2))", 11457: "Influenza A virus (A/RI/5-/1957(H2N2))", 11356: "Influenza A virus (A/chicken/Germany/N/1949(H10N7))", 11442: "Influenza A virus (A/mink/Sweden/1984(H10N4))", 11490: "Influenza A virus (A/swine/29/1937(H1N1))", 11492: "Influenza A virus (A/swine/Cambridge/1/1935(H1N1))", 11494: "Influenza A virus (A/swine/Dandong/9/1983(H3N2))", 11498: "Influenza A virus (A/swine/Hong Kong/126/1982(H3N2))", 11508: "Influenza A virus (A/swine/Italy/839/1989(H1N1))", 11507: "Influenza A virus (A/swine/Italy/141/1981(H1N1))", 11506: "Influenza A virus (A/swine/Italy/2/1979(H1N1))", 11505: "Influenza A virus (A/swine/Italy/437/1976(H1N1))", 11519: "Influenza A virus (A/swine/Wisconsin/1/1961(H1N1))", 11518: "Influenza A virus (A/swine/Wisconsin/1/1957(H1N1))", 11510: "Influenza A virus (A/swine/May/1954(H1N1))", 11491: "Influenza A virus (A/swine/41/1949(H1N1))", 11502: "Influenza A virus (A/swine/Iowa/1946(H1N1))", 11509: "Influenza A virus (A/swine/Jamesburg/1942(H1N1))", 11513: "Influenza A virus (A/swine/Ohio/23/1935(H1N1))", 11376: "Influenza A virus (A/England/19/1955(H1N1))", 11400: "Influenza A virus (A/Hickox/1940(H1N1))", 11466: "Influenza A virus (A/teal/Iceland/29/1980(H7N7))", 11350: "Influenza A virus (A/duck/Australia/749/1980(H1N1))", 11352: "Influenza A virus (A/duck/Beijing/1/1978(H3N6))", 11355: "Influenza A virus (A/duck/england/1/1962(H4N6))", 11354: "Influenza A virus (A/duck/England/1/1956(H11N6))", 11382: "Influenza A virus (A/fowl/Dobson/'Dutch'/1927(H7N7))", 11386: "Influenza A virus (A/gull/Maryland/5/1977(H11N9))", 11367: "Influenza A virus (A/duck/Memphis/928/1974(H3N8))", 11371: "Influenza A virus (A/duck/Pennsylvania/1/1969(H6N1))", 11368: "Influenza A virus (A/duck/Manitoba/1/1953(H10N7))", 11440: "Influenza A virus (A/Memphis/6/1986(H3N2))", 11438: "Influenza A virus (A/Memphis/1/1971(H3N2))", 11441: "Influenza A virus (A/Memphis/8/1988(H3N2))", 11323: "Influenza A virus (A/Anas acuta/Primorje/695/1976(H2N3))", 11461: "Influenza A virus (A/shearwater/Australia/1/1972(H6N5))", 11516: "Influenza A virus (A/swine/Tennessee/26/1977(H1N1))", 11501: "Influenza A virus (A/swine/Iowa/1976/1931(H1N1))", 11499: "Influenza A virus (A/swine/Hong Kong/127/1982(H3N2))", 11497: "Influenza A virus (A/swine/Hong Kong/81/1978(H3N2))", 11496: "Influenza A virus (A/swine/Hong Kong/6/1976(H3N2))", 11504: "Influenza A virus (A/Swine/Indiana/1726/1988(H1N1))", 11429: "Influenza A virus (A/Loyang/4/1957(H1N1))", 11477: "Influenza A virus (A/tern/Turkmenia/18/1972(H3N3))", 11459: "Influenza A virus (A/seal/Mass/1/1980(H7N7))", 11422: "Influenza A virus (A/Kiev/59/1979(H1N1))", 11324: "Influenza A virus (A/Ann Arbor/6/1960(H2N2))", 11387: "Influenza A virus (A/gull/Maryland/704/1977(H13N6))", 11327: "Influenza A virus (A/Beijing/11/1956(H1N1))", 11514: "Influenza A virus (A/swine/Ontario/2/1981(H1N1))", 11435: "Influenza A virus (A/mallard/New York/6750/1978(H2N2))", 11449: "Influenza A virus (A/pintail/Alberta/119/1979(H4N6))", 11446: "Influenza A virus (A/nt/60/1968(H3N2))", 11475: "Influenza A virus (A/tern/Australia/G70C/1975(H11N9))", 11476: "Influenza A virus (A/tern/South Africa/1961(H5N3))", 11436: "Influenza A virus (A/mallard/New York/6874/1978(H3N2))", 11381: "Influenza A virus (A/Fort Warren/1/1950(H1N1))", 11335: "Influenza A virus (A/canberra grammar/1977(H3N2))", 11328: "Influenza A virus (A/Berkeley/1/1968(H2N2))", 11322: "Influenza A virus (A/Alaska/6/1977(H3N2))", 11374: "Influenza A virus (A/duck/Ukraine/1/1963(H3N8))", 11347: "Influenza A virus (A/duck/Alberta/60/1976(H12N5))", 11401: "Influenza A virus (A/equine/Jilin/1/1989(H3N8))", 11341: "Influenza A virus (A/chicken/Pennsylvania/1/1983(H5N2))", 11332: "Influenza A virus (A/budgerigar/Hokkaido/1/1977(H4N6))", 11373: "Influenza A virus (A/duck/Ukraine/2/1960(H11N8))", 11353: "Influenza A virus (A/duck/Czechoslovakia/1956(H4N6))", 11370: "Influenza A virus (A/duck/New Zealand/31/1976(H4N6))", 11485: "Influenza A virus (A/whale/Maine/328/1984(H13N2))", 11447: "Influenza A virus (A/Ohio/4/1983(H1N1))", 11392: "Influenza A virus (A/gull/Minnesota/945/1980(H13N6))", 11389: "Influenza A virus (A/gull/Maryland/1815/1979(H13N6))", 11388: "Influenza A virus (A/gull/Maryland/1824/1978(H13N9))", 11390: "Influenza A virus (A/gull/Astrakhan/227/1984(H13N6))", 11403: "Influenza A virus (A/equine/Kentucky/2/1986(H3N8))", 11515: "Influenza A virus (A/swine/Tennessee/24/1977(H1N1))", 11342: "Influenza A virus (A/chicken/Pennsylvania/1370/1983(H5N2))", 11343: "Influenza A virus (A/chicken/Pennsylvania/8125/1983(H5N2))", 11473: "Influenza A virus (A/turkey/Wisconsin/1/1966(H9N2))", 11454: "Influenza A virus (A/Port Chalmers/1/1973(H3N2))", 11391: "Influenza A virus (A/gull/Massachusetts/26/1980(H13N6))", 11329: "Influenza A virus (A/bh/1935(H1N1))", 11325: "Influenza A virus (A/Bangkok/1/1979(H3N2))", 11431: "Influenza A virus (A/mallard/Alberta/283/1977(H8N4))", 11330: "Influenza A virus (A/blue-winged teal/604/1978(H2N3))", 11472: "Influenza A virus (A/turkey/Oregon/1971(H7N3))", 11326: "Influenza A virus (A/black duck/Australia/702/1978(H3N8))", 11346: "Influenza A virus (A/duck/Alberta/28/1976(H4N6))", 11439: "Influenza A virus (A/Memphis/102/1972(H3N2))", 11517: "Influenza A virus (A/swine/Ukkel/1/1984(H3N2))", 11493: "Influenza A virus (A/swine/Colorado/1/1977(H3N2))", 11348: "Influenza A virus (A/duck/Alberta/78/1976(H3N2))", 11321: "Influenza A virus (A/Aichi/2/1968(H3N2))", 11377: "Influenza A virus (A/England/878/1969(H3N2))", 11411: "Influenza A virus (A/Hong Kong/5/1983(H3N2))", 11421: "Influenza A virus (A/Japan/305/1957(H2N2))", 11425: "Influenza A virus (A/Leningrad/134/1957(H2N2))", 11336: "Influenza A virus (A/camel/Mongolia/1982(H1N1))", 11351: "Influenza A virus (A/duck/Bavaria/2/1977(H1N1))", 11358: "Influenza A virus (A/duck/Hokkaido/8/1980(H3N8))", 11365: "Influenza A virus (A/duck/Ireland/113/1983(H5N8))", 11366: "Influenza A virus (A/duck/memphis/546/1976(H11N9))", 11372: "Influenza A virus (A/duck/ukraine/1/1960(H11N))", 11393: "Influenza A virus (A/equine/Algiers/1972(H3N8))", 11399: "Influenza A virus (A/equine/Fontainebleau/1976(H3N8))", 11404: "Influenza A virus (A/equine/Kentucky/1/1987(H3N8))", 11407: "Influenza A virus (A/equine/Miami/1/1963(H3N8))", 11413: "Influenza A virus (A/equine/Romania/1980(H3N8))", 11419: "Influenza A virus (A/equine/Uruguay/1/1963(H3N8))", 11460: "Influenza A virus (A/seal/Massachussetts/133/1982(H4N5))", 11483: "Influenza A virus (A/Victoria/3/1975(H3N2))", 11383: "Influenza A virus (A/chicken/Rostock/8/1934(H7N1))", 11428: "Influenza A virus (A/Leningrad/1954/1(H1N1))", 11331: "Influenza A virus (A/Brazil/11/1978(H1N1))", 11420: "Influenza A virus (A/India/6263/1980(H1N1))", 11378: "Influenza A virus (A/England/321/1977(H3N2))", 11385: "Influenza A virus (A/gray teal/Australia/2/1979(H4N4))", 11345: "Influenza A virus (A/chicken/Victoria/1985(H7N7))", 11464: "Influenza A virus (A/starling/Victoria/5156/1985(H7N7))", 11344: "Influenza A virus (A/chicken/Scotland/1959(H5N1))", 6076: "Anthoathecata", 2956: "Karlodinium veneficum", 10550: "Simian adenovirus 8", 10536: "unclassified Simian adenoviruses", 11551: "Influenza B virus (B/Yamagata/16/1988)", 6224: "Notospermus geniculatus", 11333: "Influenza A virus (A/California/10/1978(H1N1))", 2863: "Diatoma tenuis", 11531: "Influenza B virus (B/Hong Kong/8/1973)", 10969: "Simian rotavirus A strain RRV", 11479: "Influenza A virus (A/Texas/1/1977(H3N2))", 13014: "Myodes", 9667: "Neovison vison", 887: "Desulfarculus baarsii", 341: "Xanthomonas euvesicatoria", 8529: "Plestiodon skiltonianus", 3203: "Liochlaena subulata", 8998: "Tetraoninae", 5805: "Eimeria stiedai", 5457: "Colletotrichum gloeosporioides", 11402: "Influenza A virus (A/equine/Kentucky/1/1981(H3N8))", 11405: "Influenza A virus (A/equine/Lexington/1/1966(H7N7))", 8564: "Eublepharis macularius", 9457: "Galeopterus variegatus", 11423: "Influenza A virus (A/Korea/426/1968(H2N2))", 9610: "Vulpes lagopus", 9594: "Gorilla beringei", 6097: "Leptothecata", 11410: "Influenza A virus (A/Hong Kong/1/1968(H3N2))", 6402: "Metaphire sieboldi", 5311: "Syzygospora", 11535: "Influenza B virus (B/Lee/1940)", 6607: "Sepiida", 10461: "Betabaculovirus", 10208: "Flustrina", 3096: "Ettlia", 6518: "Peltodoris nobilis", 4928: "Wickerhamomyces pijperi", 6138: "Carybdeida", 9862: "Rusa unicolor", 10671: "Escherichia phage D108", 3787: "Pachyphytum oviferum", 11275: "Carp sprivivirus", 9582: "Hylobates albibarbis", 5085: "Aspergillus fumigatus", 4905: "Ogataea angusta", 6353: "Alitta virens", 2126: "Mycoplasma leachii PG50", 10174: "Fukomys damarensis", 4906: "Cyberlindnera saturnus", 9955: "Philantomba maxwellii", 7749: "Lethenteron camtschaticum", 8763: "Crotalus ravus", 9854: "Alces americanus", 2859: "Tryblionella apiculata", 4963: "Cyberlindnera mrakii", 6877: "Centruroides tecomanus", 5312: "Syzygospora pallida", 7629: "Heliocidaris crassispina", 10050: "Arvicola amphibius", 6971: "Ectobiidae", 6621: "Doryteuthis pealeii", 7686: "Holothuria poli", 11549: "Influenza B virus (B/Victoria/2/1987)", 6474: "Cerithideopsis scalariformis", 4907: "Wickerhamomyces canadensis", 8914: "Chroicocephalus ridibundus", 5419: "Hannaella luteola", 4889: "Zancudomyces culisetae", 5156: "Knoxdaviesia proteae", 5119: "Cytospora leucostoma", 12702: "Mamastrovirus 1", 5638: "Neofavolus alveolaris", 6590: "Phreagena soyoae", 5573: "Rhizoctonia", 7665: "Mesocentrotus franciscanus", 6419: "Poecilobdella manillensis", 5386: "Xerocomellus chrysenteron", 4984: "Bulleribasidium variabile", 7545: "Cryptops anomalans", 6617: "Heterololigo bleekeri", 10223: "Saccoglossus ruber", 8223: "Scombriformes", 8188: "Mugilomorphae", 8246: "Labriformes", 5545: "Trichoderma ceramicum", 10781: "Protoparvovirus", 11017: "Betapartitivirus", 2839: "Trieres chinensis", 13826: "Ophioglossidae", 3254: "Equisetidae", 3248: "Lycopodiopsida", 5602: "Gaeumannomyces radicicola", 5563: "Microdochium sorghi", 12923: "Exaiptasia pallida", 5183: "Pezoloma ericae", 6044: "Astrophorina", 10930: "Rotavirus A RVA/Cow-tc/USA/B223/1983/G10P[11]", 5532: "Albifimbria verrucaria", 9478: "Carlito syrichta", 7785: "Diplobatis ommata", 1221: "Pseudanabaenaceae", 10626: "Mesocricetus auratus polyomavirus 1", 10634: "Mus musculus polyomavirus 1", 10625: "Aves polyomavirus 1", 10627: "Bos taurus polyomavirus 1", 10629: "Human polyomavirus 1", 10633: "Macaca mulatta polyomavirus 1", 5556: "Cutaneotrichosporon moniliiforme", 7690: "Apostichopus parvimensis", 5686: "Wallacemonas collosoma", 9197: "Laniarius nigerrimus", 7499: "Termitoidae", 12355: "Escherichia virus T1", 11613: "Tomato spotted wilt tospovirus", 13620: "Tritia mutabilis", 6485: "Tritia reticulata", 9320: "Notamacropus", 5716: "Lafontella mariadeanei", 10870: "Escherichia virus M13", 10876: "Acholeplasma virus MV-L51", 8390: "Sclerophrys regularis", 11212: "Human rubulavirus 2", 11203: "Human rubulavirus 4", 12837: "Mammalian rubulavirus 5", 11161: "Mumps rubulavirus", 11228: "Simian rubulavirus", 11571: "Peribunyaviridae", 11598: "Orthohantavirus", 12506: "Dobrava-Belgrade orthohantavirus", 11599: "Hantaan orthohantavirus", 11603: "Prospect Hill orthohantavirus", 11604: "Puumala orthohantavirus", 11608: "Seoul orthohantavirus", 11592: "Orthonairovirus", 11593: "Crimean-Congo hemorrhagic fever orthonairovirus", 11595: "Dugbe orthonairovirus", 12367: "Chlamydia virus Chp1", 12382: "Mycobacterium virus I3", 10871: "Pseudomonas virus Pf1", 7689: "Apostichopus californicus", 6384: "Naididae", 9130: "Artamidae", 11027: "Onyong-nyong virus", 11741: "Visna-maedi virus", 12038: "Barley yellow dwarf virus MAV", 12040: "Barley yellow dwarf virus PAV", 11619: "Argentinian mammarenavirus", 11630: "Cali mammarenavirus", 5937: "Euplotoides octocarinatus", 2775: "Agarophyton chilense", 2776: "Agarophyton tenuistipitatum", 5749: "Microchloropsis salina", 8916: "Chroicocephalus novaehollandiae", 11611: "Orthotospovirus", 5527: "Trichocladium griseum", 6915: "Trichonephila clavipes", 5145: "Podospora anserina", 5243: "Rhizoctonia fusispora", 2930: "Alexandrium fraterculus", } ================================================ FILE: pysradb/utils.py ================================================ import errno import gzip import io import ntpath import os import shlex import subprocess import urllib.request as urllib_request import warnings import requests from requests.adapters import HTTPAdapter from requests.packages.urllib3.util.retry import Retry warnings.filterwarnings("ignore", category=UserWarning, module="tqdm") from tqdm.autonotebook import tqdm from .exceptions import IncorrectFieldException warnings.simplefilter(action="ignore", category=FutureWarning) tqdm.pandas() def path_leaf(path): """Get path's tail from a filepath. Parameters ---------- path: string Filepath Returns ------- tail: string Filename """ head, tail = ntpath.split(path) return tail or ntpath.basename(head) def requests_3_retries(): """Generates a requests session object that allows 3 retries. Returns ------- session: requests.Session requests session object that allows 3 retries for server-side errors. """ session = requests.Session() retry = Retry( total=3, backoff_factor=0.5, status_forcelist=[500, 502, 503, 504], ) adapter = HTTPAdapter(max_retries=retry) session.mount("http://", adapter) session.mount("https://", adapter) return session def scientific_name_to_taxid(name): """Converts a scientific name to its corresponding taxonomy ID. Parameters ---------- name: str Scientific name of interest. Returns ------- taxid: str Taxonomy Id of the Scientific name. Raises ------ IncorrectFieldException If the scientific name cannot be found. """ session = requests_3_retries() r = session.get( "https://www.ebi.ac.uk/ena/taxonomy/rest/scientific-name/" + name, timeout=10, ) if r.status_code == 404: raise IncorrectFieldException(f"Unknown scientific name: {name}") r.raise_for_status() try: data = r.json() except requests.exceptions.JSONDecodeError as e: raise IncorrectFieldException( f"Failed to parse taxonomy response for '{name}'. " f"API returned status {r.status_code} but invalid JSON. " f"Response: {r.text[:200]}" ) from e if not data or not isinstance(data, list) or len(data) == 0: raise IncorrectFieldException( f"No taxonomy data found for scientific name: {name}" ) return data[0]["taxId"] def unique(sequence): """Get unique elements from a list maintaining the order. Parameters ---------- input_list: list Returns ------- unique_list: list List with unique elements maintaining the order """ visited = set() return [x for x in sequence if not (x in visited or visited.add(x))] class TqdmUpTo(tqdm): """Alternative Class-based version of the above. Provides `update_to(n)` which uses `tqdm.update(delta_n)`. Inspired by [twine#242](https://github.com/pypa/twine/pull/242), [here](https://github.com/pypa/twine/commit/42e55e06). Credits: https://github.com/tqdm/tqdm/blob/69326b718905816bb827e0e66c5508c9c04bc06c/examples/tqdm_wget.py """ def update_to(self, b=1, bsize=1, tsize=None): """ b : int, optional Number of blocks transferred so far [default: 1]. bsize : int, optional Size of each block (in tqdm units) [default: 1]. tsize : int, optional Total size (in tqdm units). If [default: None] remains unchanged. """ if tsize is not None: self.total = tsize self.update(b * bsize - self.n) # will also set self.n = b * bsize def _extract_first_field(data): """Extract first field from a list of fields.""" return list(next(iter(zip(*data)))) def _find_aspera_keypath(aspera_dir=None): """Locate aspera key. Parameters ---------- aspera_dir: string Location to aspera directory (optional) Returns ------- aspera_keypath: string Location to aspera key """ if aspera_dir is None: aspera_dir = os.path.join(os.path.expanduser("~"), ".aspera") aspera_keypath = os.path.join( aspera_dir, "connect", "etc", "asperaweb_id_dsa.openssh" ) if os.path.isfile(aspera_keypath): return aspera_keypath def mkdir_p(path): """Python version mkdir -p Parameters ---------- path : string Path to directory to create """ if path: try: os.makedirs(path) except OSError as exc: # Python >2.5 if exc.errno == errno.EEXIST and os.path.isdir(path): pass else: raise def order_dataframe(df, columns): """Order a dataframe Order a dataframe by moving the `columns` in the front Parameters ---------- df: Dataframe Dataframe columns: list List of columns that need to be put in front """ remaining_columns = [w for w in df.columns if w not in columns] df = df[columns + remaining_columns] return df def _get_url(url, download_to, show_progress=True): """Download anything at a given url. Parameters ---------- url: string http/https/ftp url download_to: string File location to write the downloaded file to show_progress: bool Set to True by default to print progress bar """ desc_file = "Downloading {}".format(url.split("/")[-1]) mkdir_p(os.path.dirname(download_to)) if show_progress: with TqdmUpTo( unit="B", unit_scale=True, unit_divisor=1024, miniters=1, desc=desc_file ) as t: urllib_request.urlretrieve( url, download_to, reporthook=t.update_to, data=None ) else: urllib_request.urlretrieve(url, download_to) def run_command(command, verbose=False): """Run a shell command""" process = subprocess.Popen( shlex.split(command), stdout=subprocess.PIPE, stderr=subprocess.STDOUT ) while True: output = process.stdout.readline().strip() output = output.decode("utf-8") if output == "" and process.poll() is not None: break if output: if verbose: print((str(output.strip()))) rc = process.poll() return rc def get_gzip_uncompressed_size(filepath): """Get uncompressed size of a .gz file Parameters ---------- filepath: string Path to input file Returns ------- filesize: int Uncompressed file size """ with gzip.open(filepath, "rb") as file_obj: return file_obj.seek(0, io.SEEK_END) def confirm(preceeding_text): """Confirm user input. Parameters ---------- preceeding_text: str Text to print Returns ------- response: bool """ print(os.linesep, flush=True) notification_str = "Please respond with 'y' or 'n'" while True: choice = input("{} [Y/n]: ".format(preceeding_text)).lower() if choice in ["yes", "y"] or not choice: return True if choice in ["no", "n"]: return False print(notification_str, flush=True) def copyfileobj(fsrc, fdst, bufsize=16384, filesize=None, desc=""): """Copy file object with a progress bar. Parameters ---------- fsrc: filehandle Input file handle fdst: filehandle Output file handle bufsize: int Length of output buffer filesize: int Input file file size desc: string Description for tqdm status """ with tqdm( total=filesize, unit="B", unit_scale=True, miniters=1, unit_divisor=1024, desc=desc, ) as pbar: while True: buf = fsrc.read(bufsize) if not buf: break fdst.write(buf) pbar.update(len(buf)) ================================================ FILE: requirements.txt ================================================ lxml>=4.6.3 pandas>=1.3.2 requests>=2.26.0 tqdm>=4.62.1 xmltodict>=0.12.0 ================================================ FILE: setup.cfg ================================================ [bumpversion] current_version = 2.4.1 commit = True tag = False parse = (?P\d+)\.(?P\d+)\.(?P\d+)(\-(?P[a-z]+)(?P\d+))? serialize = {major}.{minor}.{patch}-{release}{build} {major}.{minor}.{patch} [bumpversion:part:release] optional_value = prod first_value = dev values = dev prod [bumpversion:part:build] [bumpversion:file:setup.py] search = version="{current_version}" replace = version="{new_version}" [bumpversion:file:pysradb/__init__.py] search = __version__ = "{current_version}" replace = __version__ = "{new_version}" [flake8] exclude = docs [aliases] test = pytest [tool:pytest] collect_ignore = ["setup.py"] ================================================ FILE: tests/conftest.py ================================================ # contents of conftest.py import pytest # Test fixtures will be added here as needed for SRAweb and GEOweb tests ================================================ FILE: tests/data/test_search/ena_search_test1.txt ================================================ run_accession SRR492850 SRR500270 SRR609956 SRR609957 SRR609958 SRR609959 SRR609960 SRR609961 SRR609962 SRR609963 SRR609964 SRR609965 SRR609966 SRR609967 SRR609968 SRR609969 SRR609970 SRR609971 SRR609972 SRR609973 SRR609974 SRR609975 SRR609976 SRR609977 SRR609978 SRR609979 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Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719521,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719522,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719523,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719524,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719525,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719526,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719527,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719528,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719529,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719530,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719531,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719532,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719533,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling ERR1719534,Illumina HiSeq 2000 sequencing; 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ERR1797530,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant. ERR1797531,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant. ERR1797532,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant. ERR1802070,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1802071,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1802072,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1802073,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1802074,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1802075,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1802076,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1802077,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1802078,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1802079,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing ERR1856693,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling ERR1856694,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling ERR1856695,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling ERR1994959,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994960,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994961,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994962,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994963,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994964,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994965,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994966,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994967,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994968,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994969,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994970,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994971,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994972,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994973,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR1994974,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe ERR2003518,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003519,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003520,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003521,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003522,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003523,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003524,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003525,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003526,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003527,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003528,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003529,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003530,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003531,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003532,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003533,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003534,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003535,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003536,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003537,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003538,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003539,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003540,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003541,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003542,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003543,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003544,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003545,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003546,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003547,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003548,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003549,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003550,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003551,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003552,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003553,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2003554,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation ERR2093966,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells. ERR2093967,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells. ERR2093968,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells. ERR2093969,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells. ERR2193146,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193147,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193148,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193149,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193150,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193151,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193152,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193153,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193154,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193155,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193156,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193157,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193158,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2193159,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples ERR2201443,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus ERR2201444,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus ERR2201445,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus ERR2201446,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus ERR2201447,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus ERR2201448,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus ERR2201449,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus ERR2201450,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus ERR2201451,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus ERR2528907,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2528908,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2528909,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2528910,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2528911,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2528912,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2528913,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2528914,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2528915,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2528916,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain." ERR2660262,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions ERR2660263,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions ERR2660264,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions ERR2660265,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions ERR2660266,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions ERR2660267,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions ERR2660269,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions ERR2660271,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions ERR2681846,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681847,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681848,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681849,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681850,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681851,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681852,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681853,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681854,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681855,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681856,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2681857,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae ERR2812328,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812329,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812330,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812331,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812332,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812333,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812334,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812335,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812336,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812337,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812338,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812339,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812340,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812341,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812342,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812343,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812344,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812345,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812346,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812347,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812348,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812349,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812350,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812351,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812352,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812353,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812354,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812355,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812356,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812357,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812358,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812359,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812360,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812361,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812362,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812363,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812364,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812365,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812366,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812367,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812368,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812369,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812370,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812371,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812372,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812373,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812374,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812375,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812376,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812377,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812378,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812379,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812380,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812381,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812382,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812383,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812384,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812385,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812386,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812387,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812388,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812389,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812390,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812391,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812392,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812393,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812394,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812395,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812396,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812397,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812398,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812399,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812400,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812401,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812402,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812403,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812404,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812405,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812406,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812407,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812408,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812409,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812410,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812411,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812412,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812413,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812414,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812415,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812416,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812417,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812418,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812419,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812420,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812421,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812422,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812423,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812424,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812425,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812426,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812427,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812428,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812429,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812430,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812431,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812432,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812433,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812434,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812435,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812436,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812437,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812438,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812439,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812440,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812441,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812442,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2812443,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers ERR2976734,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976735,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976736,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976737,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976738,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976739,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976740,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976741,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976742,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976743,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976744,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR2976745,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B ERR3218426,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218427,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218428,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218429,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218430,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218431,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218432,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218433,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218434,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218435,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218436,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218437,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218438,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218439,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218440,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3218441,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C. ERR3276516,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276517,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276518,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276519,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276520,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276521,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276522,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276523,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276524,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276525,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276526,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3276527,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus ERR3366404,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells ERR3366405,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells ERR3366406,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells ERR3366407,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells ERR3771179,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771180,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771181,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771182,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771183,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771184,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771185,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771186,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771187,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771188,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771189,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771190,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771191,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771192,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771193,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR3771194,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs ERR419248,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt ERR419249,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt ERR419250,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt ERR419251,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt ERR419252,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt ERR466122,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI ERR466123,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI ERR466124,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI ERR466125,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI ERR599189,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis ERR599190,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis ERR599191,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis ERR599192,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis ERR601607,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse ERR601608,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse ERR601609,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse ERR601610,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse ERR605044,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling. ERR605045,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling. ERR605046,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling. ERR618768,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli ERR618769,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli ERR618770,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli ERR618771,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli ERR618772,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli ERR618773,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli ERR618774,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli ERR618775,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli SRR10100140,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 3 SRR10100141,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 2 SRR10100142,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 1 SRR10174361,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte SRR10174368,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo SRR10174369,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo SRR10174370,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo SRR10174375,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte SRR10174376,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte SRR10174377,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte SRR10174378,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte SRR10174379,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte SRR10174380,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte SRR10174381,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte SRR10174382,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte SRR10294592,Illumina HiSeq 2500 sequencing; GSM4125802: Replicate 1 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER SRR10294593,Illumina HiSeq 2500 sequencing; GSM4125803: Replicate 2 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER SRR10294594,Illumina HiSeq 2500 sequencing; GSM4125804: Replicate 1 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER SRR10294595,Illumina HiSeq 2500 sequencing; GSM4125805: Replicate 2 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER SRR10294596,Illumina HiSeq 2500 sequencing; GSM4125806: Flash freeze harvesting with anisomycin ribosome profiling; Haloferax volcanii DS2; OTHER SRR10294597,Illumina HiSeq 2500 sequencing; GSM4125807: Flash freeze harvesting with harringtonine ribosome profiling; Haloferax volcanii DS2; OTHER SRR10294598,Illumina HiSeq 2500 sequencing; GSM4125808: Flash freeze harvesting with serine hydroxamate ribosome profiling; Haloferax volcanii DS2; OTHER SRR10294600,Illumina HiSeq 2500 sequencing; GSM4125810: Total RNA treated with MNase ribosome profiling; Haloferax volcanii DS2; OTHER SRR1040263,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 1 SRR1040415,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome footprint fraction replicate 1 SRR1040423,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 1 SRR1040427,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 2 SRR1042900,Illumina Genome Analyzer II sequencing; GSM1279707: Ribosome Profiling with Control siRNA; Homo sapiens; OTHER SRR1042901,Illumina Genome Analyzer II sequencing; GSM1279708: Ribosome Profiling with AUF1 siRNA; Homo sapiens; OTHER SRR1042902,Illumina Genome Analyzer II sequencing; GSM1279709: Ribosome Profiling with HuR siRNA; Homo sapiens; OTHER SRR1067765,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER SRR1067766,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER SRR1067767,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER SRR1067768,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER SRR1067769,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER SRR1067770,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER SRR1067771,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER SRR1067772,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER SRR10959087,NextSeq 500 sequencing; GSM4282352: Ribosome profiling_sgABCE1-1; Homo sapiens; OTHER SRR10959088,NextSeq 500 sequencing; GSM4282353: Ribosome profiling_sgABCE1-2; Homo sapiens; OTHER SRR10959089,NextSeq 500 sequencing; GSM4282354: Ribosome profiling_sgNT1; Homo sapiens; OTHER SRR10959090,NextSeq 500 sequencing; GSM4282355: Ribosome profiling_sgNT2; Homo sapiens; OTHER SRR11217089,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82 SRR11217090,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82 SRR1167750,Illumina HiSeq 2000 sequencing; GSM1326110: M2G Ribosome profiling; Caulobacter vibrioides NA1000; OTHER SRR1167751,Illumina HiSeq 2000 sequencing; GSM1326111: PYE Ribosome profiling; Caulobacter vibrioides NA1000; OTHER SRR11794832,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells SRR11794833,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells SRR11794834,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells SRR11794835,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells SRR11794836,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells SRR11794837,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells SRR11794840,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells SRR11794841,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells SRR11794842,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells SRR11794843,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells SRR11794844,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KOWT cells SRR11794845,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells SRR11794846,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KO cells SRR11794847,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells SRR11794848,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells SRR11794849,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells SRR11836448,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs SRR11836450,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs SRR11836452,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs SRR11836454,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs SRR11837742,Illumina NovaSeq 6000 sequencing; GSM4567011: Gcn2 WT +AA - Ribosome profiling; Mus musculus; OTHER SRR11837743,Illumina NovaSeq 6000 sequencing; GSM4567012: Gcn2 WT -Leu - Ribosome profiling; Mus musculus; OTHER SRR11837744,Illumina NovaSeq 6000 sequencing; GSM4567013: Gcn2 KO +AA - Ribosome profiling; Mus musculus; OTHER SRR11837745,Illumina NovaSeq 6000 sequencing; GSM4567014: Gcn2 KO -Leu - Ribosome profiling; Mus musculus; OTHER SRR12164922,"Illumina HiSeq 2500 sequencing; GSM4658960: Ribosome profiling from untreated cells, rep 1; Saccharomyces cerevisiae; OTHER" SRR12164924,"Illumina HiSeq 2500 sequencing; GSM4658962: Ribosome profiling from untreated cells, rep 2; Saccharomyces cerevisiae; OTHER" SRR12164926,"Illumina HiSeq 2500 sequencing; GSM4658964: Ribosome profiling from untreated cells, rep 3; Saccharomyces cerevisiae; OTHER" SRR12164928,"Illumina HiSeq 2500 sequencing; GSM4658966: Ribosome profiling from radicicol cells, rep 1; Saccharomyces cerevisiae; OTHER" SRR12164930,"Illumina HiSeq 2500 sequencing; GSM4658968: Ribosome profiling from radicicol cells, rep 2; Saccharomyces cerevisiae; OTHER" SRR12164932,"Illumina HiSeq 2500 sequencing; GSM4658970: Ribosome profiling from radicicol cells, rep 3; Saccharomyces cerevisiae; OTHER" SRR12185464,"Illumina HiSeq 2500 sequencing; GSM4663991: control mouse brain, SMN-specific ribosome profiling, P5, rep 1; Mus musculus; OTHER" SRR12185465,"Illumina HiSeq 2500 sequencing; GSM4663992: control mouse brain, SMN-specific ribosome profiling, P5, rep 2; Mus musculus; OTHER" SRR12185466,"Illumina HiSeq 2500 sequencing; GSM4663993: control mouse brain, SMN-specific ribosome profiling, P5, rep 3; Mus musculus; OTHER" SRR12185467,"Illumina HiSeq 2500 sequencing; GSM4663994: control mouse brain, IgG control ribosome profiling, P5, rep 1; Mus musculus; OTHER" SRR1258539,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 1 of 2" SRR1258540,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 2 of 2" SRR1258541,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 1 of 2" SRR1258542,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 2 of 2" SRR1258543,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, fragmented control" SRR1258544,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, fragmented control" SRR1425203,Illumina HiSeq 2000 sequencing; GSM1415871: ribosome profiling MicL t0; Escherichia coli; RNA-Seq SRR1425204,Illumina HiSeq 2000 sequencing; GSM1415872: ribosome profiling MicL t20; Escherichia coli; RNA-Seq SRR1583082,Illumina HiSeq 2000 sequencing; GSM1509451: Ribosome profiling data of untreated E. coli cells; Escherichia coli BW25113; RNA-Seq SRR1583083,Illumina HiSeq 2000 sequencing; GSM1509452: Ribosome profiling data of E. coli cells treated with the antibiotic erythromycin; Escherichia coli BW25113; RNA-Seq SRR1583084,Illumina HiSeq 2000 sequencing; GSM1509453: Ribosome profiling data of E. coli cells treated with the antibiotic telithromycin; Escherichia coli BW25113; RNA-Seq SRR1598971,Illumina Genome Analyzer II sequencing; GSM1248735: mock-transfected ribosome profiling; Homo sapiens; RNA-Seq SRR1598975,Illumina HiSeq 2000 sequencing; GSM1248729: miR-1-transfected ribosome profiling; Homo sapiens; RNA-Seq SRR1598981,Illumina Genome Analyzer II sequencing; GSM1248732: miR-155-transfected ribosome profiling; Homo sapiens; RNA-Seq SRR1660328,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq SRR1660329,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq SRR1660330,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq SRR1660331,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq SRR1660332,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq SRR1660333,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq SRR1660334,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq SRR1660335,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq SRR1661491,Illumina HiSeq 2000 sequencing; GSM1553248: Ribosome profiling rep1-SiControl-RPF; Homo sapiens; OTHER SRR1661492,Illumina HiSeq 2000 sequencing; GSM1553249: Ribosome profiling rep1-SiControl-input-ribominus; Homo sapiens; OTHER SRR1661493,Illumina HiSeq 2000 sequencing; GSM1553250: Ribosome profiling rep1-SiYTHDF1_1-RPF; Homo sapiens; OTHER SRR1661494,Illumina HiSeq 2000 sequencing; GSM1553251: Ribosome profiling rep1-SiYTHDF1_1-input-ribominus; Homo sapiens; OTHER SRR1661495,Illumina HiSeq 2000 sequencing; GSM1553252: Ribosome profiling rep2-SiControl-RPF; Homo sapiens; OTHER SRR1661496,Illumina HiSeq 2000 sequencing; GSM1553253: Ribosome profiling rep2-SiControl-input-ribominus; Homo sapiens; OTHER SRR1661497,Illumina HiSeq 2000 sequencing; GSM1553254: Ribosome profiling rep2-SiYTHDF1_8-RPF; Homo sapiens; OTHER SRR1661498,Illumina HiSeq 2000 sequencing; GSM1553255: Ribosome profiling rep2-SiYTHDF1_8-input-ribominus; Homo sapiens; OTHER SRR1763106,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate1 SRR1763107,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate2 SRR1765340,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate1 SRR1765360,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate2 SRR1840399,Illumina HiSeq 2000 sequencing; GSM1625823: Cotyledon (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq SRR1840401,Illumina HiSeq 2000 sequencing; GSM1625825: Cotyledon (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq SRR1840403,Illumina HiSeq 2000 sequencing; GSM1625827: Seed Coat (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq SRR1840405,Illumina HiSeq 2000 sequencing; GSM1625829: Seed Coat (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq SRR1840407,Illumina HiSeq 2000 sequencing; GSM1625831: Cotyledon (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq SRR1840409,Illumina HiSeq 2000 sequencing; GSM1625833: Cotyledon (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq SRR1840411,Illumina HiSeq 2000 sequencing; GSM1625835: Seed Coat (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq SRR1840413,Illumina HiSeq 2000 sequencing; GSM1625837: Seed Coat (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq SRR1840415,Illumina HiSeq 2000 sequencing; GSM1625839: Cotyledon (300-400 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq SRR1840417,Illumina HiSeq 2000 sequencing; GSM1625841: Cotyledon (300-400 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq SRR1964306,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER SRR1964307,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER SRR1964308,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER SRR1964309,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER SRR1964310,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER SRR1964311,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER SRR1964312,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER SRR1964313,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER SRR1964314,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER SRR1964315,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER SRR1964316,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER SRR1964317,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER SRR1964318,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER SRR1964319,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER SRR1964320,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER SRR1964321,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER SRR1964322,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER SRR1964323,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER SRR1964324,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER SRR1964325,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER SRR1964326,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER SRR1964327,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER SRR1964328,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER SRR1964329,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER SRR1991275,Illumina HiSeq 2000 sequencing; GSM1665594: swarmer M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq SRR1991276,Illumina HiSeq 2000 sequencing; GSM1665595: early stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq SRR1991277,Illumina HiSeq 2000 sequencing; GSM1665596: late stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq SRR1991278,Illumina HiSeq 2000 sequencing; GSM1665597: early prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq SRR1991279,Illumina HiSeq 2000 sequencing; GSM1665598: late prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq SRR1991280,Illumina HiSeq 2000 sequencing; GSM1665599: post division M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq SRR2007064,"Illumina HiSeq 2500 sequencing; GSM1666805: ATF4-/- ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER" SRR2007065,"Illumina HiSeq 2500 sequencing; GSM1666806: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER" SRR2007066,"Illumina HiSeq 2500 sequencing; GSM1666807: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER" SRR2007067,"Illumina HiSeq 2500 sequencing; GSM1666808: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER" SRR2007068,"Illumina HiSeq 2500 sequencing; GSM1666809: ATF4-/- ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER" SRR2007069,"Illumina HiSeq 2500 sequencing; GSM1666810: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER" SRR2007070,"Illumina HiSeq 2500 sequencing; GSM1666811: ATF4-/- ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER" SRR2007071,"Illumina HiSeq 2500 sequencing; GSM1666812: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER" SRR2007072,"Illumina HiSeq 2500 sequencing; GSM1666813: ATF4-/- ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER" SRR2007073,"Illumina HiSeq 2500 sequencing; GSM1666814: ATF4-/- cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER" SRR2007074,"Illumina HiSeq 2500 sequencing; GSM1666815: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER" SRR2007075,"Illumina HiSeq 2500 sequencing; GSM1666816: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER" SRR2007076,"Illumina HiSeq 2500 sequencing; GSM1666817: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER" SRR2007077,"Illumina HiSeq 2500 sequencing; GSM1666818: ATF4-/- ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER" SRR2007078,"Illumina HiSeq 2500 sequencing; GSM1666819: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER" SRR2007079,"Illumina HiSeq 2500 sequencing; GSM1666820: ATF4-/- ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER" SRR2007080,"Illumina HiSeq 2500 sequencing; GSM1666821: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER" SRR2007081,"Illumina HiSeq 2500 sequencing; GSM1666822: ATF4-/- ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER" SRR2007082,"Illumina HiSeq 2500 sequencing; GSM1666823: ATF4-/- cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER" SRR2007083,"Illumina HiSeq 2500 sequencing; GSM1666824: ATF4-/- ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER" SRR2007084,"Illumina HiSeq 2500 sequencing; GSM1666825: eIF2A S51A ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER" SRR2007085,"Illumina HiSeq 2500 sequencing; GSM1666826: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER" SRR2007086,"Illumina HiSeq 2500 sequencing; GSM1666827: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER" SRR2007087,"Illumina HiSeq 2500 sequencing; GSM1666828: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER" SRR2007088,"Illumina HiSeq 2500 sequencing; GSM1666829: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER" SRR2007089,"Illumina HiSeq 2500 sequencing; GSM1666830: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER" SRR2007090,"Illumina HiSeq 2500 sequencing; GSM1666831: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER" SRR2007091,"Illumina HiSeq 2500 sequencing; GSM1666832: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER" SRR2007092,"Illumina HiSeq 2500 sequencing; GSM1666833: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER" SRR2007093,"Illumina HiSeq 2500 sequencing; GSM1666834: eIF2A S51A cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER" SRR2007094,"Illumina HiSeq 2500 sequencing; GSM1666835: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER" SRR2007095,"Illumina HiSeq 2500 sequencing; GSM1666836: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER" SRR2007096,"Illumina HiSeq 2500 sequencing; GSM1666837: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER" SRR2007097,"Illumina HiSeq 2500 sequencing; GSM1666838: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER" SRR2007098,"Illumina HiSeq 2500 sequencing; GSM1666839: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER" SRR2007099,"Illumina HiSeq 2500 sequencing; GSM1666840: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER" SRR2007100,"Illumina HiSeq 2500 sequencing; GSM1666841: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER" SRR2007101,"Illumina HiSeq 2500 sequencing; GSM1666842: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER" SRR2007102,"Illumina HiSeq 2500 sequencing; GSM1666843: eIF2A S51A cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER" SRR2007103,"Illumina HiSeq 2500 sequencing; GSM1666844: eIF2A S51A ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER" SRR2007769,"Illumina HiSeq 2500 sequencing; GSM1674110: WT cytosol ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER" SRR2007770,"Illumina HiSeq 2500 sequencing; GSM1674111: WT cytosol ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER" SRR2007771,"Illumina HiSeq 2500 sequencing; GSM1674112: WT ER ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER" SRR2007772,"Illumina HiSeq 2500 sequencing; GSM1674113: WT ER ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER" SRR2007773,"Illumina HiSeq 2500 sequencing; GSM1674114: WT cytosol ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER" SRR2007774,"Illumina HiSeq 2500 sequencing; GSM1674115: WT cytosol ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER" SRR2007775,"Illumina HiSeq 2500 sequencing; GSM1674116: WT ER ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER" SRR2007776,"Illumina HiSeq 2500 sequencing; GSM1674117: WT ER ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER" SRR2007777,"Illumina HiSeq 2500 sequencing; GSM1674118: WT cytosol ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER" SRR2007778,"Illumina HiSeq 2500 sequencing; GSM1674119: WT cytosol ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER" SRR2007779,"Illumina HiSeq 2500 sequencing; GSM1674120: WT ER ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER" SRR2007780,"Illumina HiSeq 2500 sequencing; GSM1674121: WT ER ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER" SRR2007781,"Illumina HiSeq 2500 sequencing; GSM1674122: WT cytosol ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER" SRR2007782,"Illumina HiSeq 2500 sequencing; GSM1674123: WT cytosol ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER" SRR2007783,"Illumina HiSeq 2500 sequencing; GSM1674124: WT ER ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER" SRR2007784,"Illumina HiSeq 2500 sequencing; GSM1674125: WT ER ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER" SRR2007785,"Illumina HiSeq 2500 sequencing; GSM1674126: WT cytosol ribosome profiling, no Tg (rep1); Mus musculus; OTHER" SRR2007786,"Illumina HiSeq 2500 sequencing; GSM1674127: WT cytosol ribosome profiling, no Tg (rep2); Mus musculus; OTHER" SRR2007787,"Illumina HiSeq 2500 sequencing; GSM1674128: WT ER ribosome profiling, no Tg (rep1); Mus musculus; OTHER" SRR2007788,"Illumina HiSeq 2500 sequencing; GSM1674129: WT ER ribosome profiling, no Tg (rep2); Mus musculus; OTHER" SRR2047225,Illumina HiSeq 2000 paired end sequencing; Shield Stage Embryos matched to Ribosome Profiling SRR2052911,Illumina HiSeq 2500 sequencing; GSM1704503: 6 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052912,Illumina HiSeq 2500 sequencing; GSM1704504: 6 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052913,Illumina HiSeq 2500 sequencing; GSM1704505: 12 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052914,Illumina HiSeq 2500 sequencing; GSM1704506: 12 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052915,Illumina HiSeq 2500 sequencing; GSM1704507: 24 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052916,Illumina HiSeq 2500 sequencing; GSM1704508: 24 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052917,Illumina HiSeq 2500 sequencing; GSM1704509: 40 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052918,Illumina HiSeq 2500 sequencing; GSM1704510: 40 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052919,Illumina HiSeq 2500 sequencing; GSM1704511: Interferon treatment cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052920,Illumina HiSeq 2500 sequencing; GSM1704512: Interferon treatment ER ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052921,Illumina HiSeq 2500 sequencing; GSM1704513: Uninfected cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052922,Illumina HiSeq 2500 sequencing; GSM1704514: Uninfected ER ribosome profiling (Rep 1); Homo sapiens; OTHER SRR2052923,Illumina HiSeq 2500 sequencing; GSM1704515: 6 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052924,Illumina HiSeq 2500 sequencing; GSM1704516: 6 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052925,Illumina HiSeq 2500 sequencing; GSM1704517: 12 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052926,Illumina HiSeq 2500 sequencing; GSM1704518: 12 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052927,Illumina HiSeq 2500 sequencing; GSM1704519: 24 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052928,Illumina HiSeq 2500 sequencing; GSM1704520: 24 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052929,Illumina HiSeq 2500 sequencing; GSM1704521: 40 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052930,Illumina HiSeq 2500 sequencing; GSM1704522: 40 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052931,Illumina HiSeq 2500 sequencing; GSM1704523: Interferon treatment cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052932,Illumina HiSeq 2500 sequencing; GSM1704524: Interferon treatment ER ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052933,Illumina HiSeq 2500 sequencing; GSM1704525: Uninfected cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052934,Illumina HiSeq 2500 sequencing; GSM1704526: Uninfected ER ribosome profiling (Rep 2); Homo sapiens; OTHER SRR2052935,Illumina HiSeq 2500 sequencing; GSM1704527: 6 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052936,Illumina HiSeq 2500 sequencing; GSM1704528: 6 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052937,Illumina HiSeq 2500 sequencing; GSM1704529: 12 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052938,Illumina HiSeq 2500 sequencing; GSM1704530: 12 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052939,Illumina HiSeq 2500 sequencing; GSM1704531: 24 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052940,Illumina HiSeq 2500 sequencing; GSM1704532: 24 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052941,Illumina HiSeq 2500 sequencing; GSM1704533: 40 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052942,Illumina HiSeq 2500 sequencing; GSM1704534: 40 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052943,Illumina HiSeq 2500 sequencing; GSM1704535: Interferon treatment cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052944,Illumina HiSeq 2500 sequencing; GSM1704536: Interferon treatment ER ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052945,Illumina HiSeq 2500 sequencing; GSM1704537: Uninfected cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052946,Illumina HiSeq 2500 sequencing; GSM1704538: Uninfected ER ribosome profiling (Rep 3); Homo sapiens; OTHER SRR2052947,Illumina HiSeq 2500 sequencing; GSM1704539: 6 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052948,Illumina HiSeq 2500 sequencing; GSM1704540: 6 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052949,Illumina HiSeq 2500 sequencing; GSM1704541: 12 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052950,Illumina HiSeq 2500 sequencing; GSM1704542: 12 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052951,Illumina HiSeq 2500 sequencing; GSM1704543: 24 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052952,Illumina HiSeq 2500 sequencing; GSM1704544: 24 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052953,Illumina HiSeq 2500 sequencing; GSM1704545: 40 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052954,Illumina HiSeq 2500 sequencing; GSM1704546: 40 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052955,Illumina HiSeq 2500 sequencing; GSM1704547: Interferon treatment cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052956,Illumina HiSeq 2500 sequencing; GSM1704548: Interferon treatment ER ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052957,Illumina HiSeq 2500 sequencing; GSM1704549: Uninfected cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052958,Illumina HiSeq 2500 sequencing; GSM1704550: Uninfected ER ribosome profiling (Rep 4); Homo sapiens; OTHER SRR2052983,Illumina HiSeq 2500 sequencing; GSM1704575: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052984,Illumina HiSeq 2500 sequencing; GSM1704576: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052985,Illumina HiSeq 2500 sequencing; GSM1704577: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052986,Illumina HiSeq 2500 sequencing; GSM1704578: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052987,Illumina HiSeq 2500 sequencing; GSM1704579: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052988,Illumina HiSeq 2500 sequencing; GSM1704580: Uninfected Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052989,Illumina HiSeq 2500 sequencing; GSM1704581: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2052990,Illumina HiSeq 2500 sequencing; GSM1704582: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2052991,Illumina HiSeq 2500 sequencing; GSM1704583: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2052992,Illumina HiSeq 2500 sequencing; GSM1704584: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2052993,Illumina HiSeq 2500 sequencing; GSM1704585: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2052994,Illumina HiSeq 2500 sequencing; GSM1704586: Uninfected Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2052995,Illumina HiSeq 2500 sequencing; GSM1704587: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052996,Illumina HiSeq 2500 sequencing; GSM1704588: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052997,Illumina HiSeq 2500 sequencing; GSM1704589: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052998,Illumina HiSeq 2500 sequencing; GSM1704590: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2052999,Illumina HiSeq 2500 sequencing; GSM1704591: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER SRR2053000,Illumina HiSeq 2500 sequencing; GSM1704592: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2053001,Illumina HiSeq 2500 sequencing; GSM1704593: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2053002,Illumina HiSeq 2500 sequencing; GSM1704594: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2053003,Illumina HiSeq 2500 sequencing; GSM1704595: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2053004,Illumina HiSeq 2500 sequencing; GSM1704596: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER SRR2057646,Ion Torrent PGM sequencing; GSM1707652: Ribosome profiling no exercise rep1; Mus musculus; RNA-Seq SRR2057647,Ion Torrent PGM sequencing; GSM1707653: Ribosome profiling no exercise rep2; Mus musculus; RNA-Seq SRR2057648,Ion Torrent PGM sequencing; GSM1707654: Ribosome profiling exercise rep1; Mus musculus; RNA-Seq SRR2057649,Ion Torrent PGM sequencing; GSM1707655: Ribosome profiling exercise rep2; Mus musculus; RNA-Seq SRR2060674,Illumina HiSeq 2500 sequencing; GSM1709012: ER Ribosome profiling Untreated 1; Mus musculus; OTHER SRR2060675,Illumina HiSeq 2500 sequencing; GSM1709013: ER Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER SRR2060676,Illumina HiSeq 2500 sequencing; GSM1709014: ER Ribosome profiling 1 h Tg 1; Mus musculus; OTHER SRR2060677,Illumina HiSeq 2500 sequencing; GSM1709015: ER Ribosome profiling 2 h Tg 1; Mus musculus; OTHER SRR2060678,Illumina HiSeq 2500 sequencing; GSM1709016: ER Ribosome profiling 4 h Tg 1; Mus musculus; OTHER SRR2060679,Illumina HiSeq 2500 sequencing; GSM1709017: ER Ribosome profiling Untreated 2; Mus musculus; OTHER SRR2060680,Illumina HiSeq 2500 sequencing; GSM1709018: ER Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER SRR2060681,Illumina HiSeq 2500 sequencing; GSM1709019: ER Ribosome profiling 1 h Tg 2; Mus musculus; OTHER SRR2060682,Illumina HiSeq 2500 sequencing; GSM1709020: ER Ribosome profiling 2 h Tg 2; Mus musculus; OTHER SRR2060683,Illumina HiSeq 2500 sequencing; GSM1709021: ER Ribosome profiling 4 h Tg 2; Mus musculus; OTHER SRR2060684,Illumina HiSeq 2500 sequencing; GSM1709022: Cytosol Ribosome profiling Untreated 1; Mus musculus; OTHER SRR2060685,Illumina HiSeq 2500 sequencing; GSM1709023: Cytosol Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER SRR2060686,Illumina HiSeq 2500 sequencing; GSM1709024: Cytosol Ribosome profiling 1 h Tg 1; Mus musculus; OTHER SRR2060687,Illumina HiSeq 2500 sequencing; GSM1709025: Cytosol Ribosome profiling 2 h Tg 1; Mus musculus; OTHER SRR2060688,Illumina HiSeq 2500 sequencing; GSM1709026: Cytosol Ribosome profiling 4 h Tg 1; Mus musculus; OTHER SRR2060689,Illumina HiSeq 2500 sequencing; GSM1709027: Cytosol Ribosome profiling Untreated 2; Mus musculus; OTHER SRR2060690,Illumina HiSeq 2500 sequencing; GSM1709028: Cytosol Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER SRR2060691,Illumina HiSeq 2500 sequencing; GSM1709029: Cytosol Ribosome profiling 1 h Tg 2; Mus musculus; OTHER SRR2060692,Illumina HiSeq 2500 sequencing; GSM1709030: Cytosol Ribosome profiling 2 h Tg 2; Mus musculus; OTHER SRR2060693,Illumina HiSeq 2500 sequencing; GSM1709031: Cytosol Ribosome profiling 4 h Tg 2; Mus musculus; OTHER SRR2075417,Illumina HiSeq 2000 sequencing; GSM1717890: Ribosome profiling SiControl-RPF; Homo sapiens; OTHER SRR2075418,Illumina HiSeq 2000 sequencing; GSM1717891: Ribosome profiling SiControl-input-poly(A); Homo sapiens; OTHER SRR2075419,Illumina HiSeq 2000 sequencing; GSM1717892: Ribosome profiling SiMETTL3-RPF; Homo sapiens; OTHER SRR2075420,Illumina HiSeq 2000 sequencing; GSM1717893: Ribosome profiling SiMETTL3-input-poly(A); Homo sapiens; OTHER SRR2096964,Illumina HiSeq 2500 sequencing; GSM1819217: Rluc control ribosome profiling rep1; Homo sapiens; OTHER SRR2096965,Illumina HiSeq 2500 sequencing; GSM1819218: DDX3 WT ribosome profiling rep1; Homo sapiens; OTHER SRR2096966,Illumina HiSeq 2500 sequencing; GSM1819219: DDX3 R534H ribosome profiling rep1; Homo sapiens; OTHER SRR2096967,Illumina HiSeq 2500 sequencing; GSM1819220: Rluc control ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER SRR2096968,Illumina HiSeq 2500 sequencing; GSM1819221: DDX3 WT ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER SRR2096969,Illumina HiSeq 2500 sequencing; GSM1819222: DDX3 R534H ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER SRR2096970,Illumina HiSeq 2500 sequencing; GSM1819223: Rluc control ribosome profiling rep2; Homo sapiens; OTHER SRR2096971,Illumina HiSeq 2500 sequencing; GSM1819224: DDX3 WT ribosome profiling rep2; Homo sapiens; OTHER SRR2096972,Illumina HiSeq 2500 sequencing; GSM1819225: DDX3 R534H ribosome profiling rep2; Homo sapiens; OTHER SRR2096973,Illumina HiSeq 2500 sequencing; GSM1819226: Rluc control ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER SRR2096974,Illumina HiSeq 2500 sequencing; GSM1819227: DDX3 WT ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER SRR2096975,Illumina HiSeq 2500 sequencing; GSM1819228: DDX3 R534H ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER SRR2433794,Illumina HiSeq 2000 sequencing; GSM1887643: ribosome profiling; Homo sapiens; miRNA-Seq SRR2732970,NextSeq 500 sequencing; Ribosome profiling of lactimidomycin treated Jurkat cells SRR2733100,NextSeq 500 sequencing; Ribosome profiling of cycloheximide treated Jurkat cells SRR3147100,Illumina HiSeq 2000 sequencing; GSM2055244: ribosome profiling 37°C in WT; Escherichia coli; OTHER SRR3208296,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells SRR3208406,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells SRR3208450,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with WT 18S rRNA SRR3208452,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with mutant 18S rRNA SRR3286543,Illumina HiSeq 2500 sequencing; GSM2097522: HBE cells ribosome profiling; Homo sapiens; RNA-Seq SRR3286544,Illumina HiSeq 2500 sequencing; GSM2097523: A549 cells ribosome profiling; Homo sapiens; RNA-Seq SRR3286545,Illumina HiSeq 2500 sequencing; GSM2097524: H1299 cells ribosome profiling; Homo sapiens; RNA-Seq SRR3306583,Illumina HiSeq 2000 sequencing; GSM2100596: S phase ribosome profiling replicate 1; Homo sapiens; OTHER SRR3306584,Illumina HiSeq 2000 sequencing; GSM2100597: S phase ribosome profiling replicate 2; Homo sapiens; OTHER SRR3306585,Illumina HiSeq 2000 sequencing; GSM2100598: M phase ribosome profiling replicate 1; Homo sapiens; OTHER SRR3306586,Illumina HiSeq 2000 sequencing; GSM2100599: M phase ribosome profiling replicate 2; Homo sapiens; OTHER SRR3306587,Illumina HiSeq 2000 sequencing; GSM2100600: M phase ribosome profiling synchronized by shake off; Homo sapiens; OTHER SRR3306588,Illumina HiSeq 2000 sequencing; GSM2100601: Asynchronous cell ribosome profiling 1; Homo sapiens; OTHER SRR3306589,Illumina HiSeq 2000 sequencing; GSM2100602: Asynchronous cell ribosome profiling 2; Homo sapiens; OTHER SRR3392126,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells SRR3392899,Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Control for Methionine Starvation) SRR3398188,Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Methionine Starvation) SRR4293693,NextSeq 500 sequencing; GSM2327825: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with lactimidomycin; Homo sapiens; OTHER SRR4293694,NextSeq 500 sequencing; GSM2327826: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with cycloheximide; Homo sapiens; OTHER SRR4293695,NextSeq 500 sequencing; GSM2327827: Ribosome profiling of control HCT116 cells treated with lactimidomycin; Homo sapiens; OTHER SRR4293696,NextSeq 500 sequencing; GSM2327828: Ribosome profiling of control HCT116 cells treated with cycloheximide; Homo sapiens; OTHER SRR4424237,Illumina HiSeq 2000 sequencing; GSM2346474: Ribosome profiling of wild-type ecotype Landsberg erecta treated with lactimidomycin; Arabidopsis thaliana; OTHER SRR4424238,Illumina HiSeq 2000 sequencing; GSM2346475: Ribosome profiling of wild-type ecotype Landsberg erecta treated with cycloheximide; Arabidopsis thaliana; OTHER SRR458756,Illumina Genome Analyzer II sequencing; GSM910953: A3-1 Ribosome profiling - siLuc; Mus musculus; OTHER SRR458757,Illumina Genome Analyzer II sequencing; GSM910954: A3-1 Ribosome profiling - siLin28a; Mus musculus; OTHER SRR5026356,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026359,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026589,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026592,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026603,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026637,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5090708,NextSeq 500 sequencing; GSM2420418: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 monosomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq SRR5090709,NextSeq 500 sequencing; GSM2420419: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 polysomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq SRR5099275,Illumina HiSeq 4000 sequencing; GSM2424851: Ribosome profiling-siControl-RPF; Homo sapiens; OTHER SRR5099276,Illumina HiSeq 4000 sequencing; GSM2424852: Ribosome profiling-siControl-input; Homo sapiens; OTHER SRR5099277,Illumina HiSeq 4000 sequencing; GSM2424853: Ribosome profiling-rep1-siYTHDF3-RPF; Homo sapiens; OTHER SRR5099278,Illumina HiSeq 4000 sequencing; GSM2424854: Ribosome profiling-rep1-siYTHDF3-input; Homo sapiens; OTHER SRR5099279,Illumina HiSeq 4000 sequencing; GSM2424855: Ribosome profiling-rep2-siYTHDF3-RPF; Homo sapiens; OTHER SRR5099280,Illumina HiSeq 4000 sequencing; GSM2424856: Ribosome profiling-rep2-siYTHDF3-input; Homo sapiens; OTHER SRR5186136,Illumina HiSeq 4000 sequencing; GSM2462933: ribosome profiling 37°C in WT with control plasmid; Escherichia coli; OTHER SRR5186137,Illumina HiSeq 4000 sequencing; GSM2462934: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUA; Escherichia coli; OTHER SRR5186138,Illumina HiSeq 4000 sequencing; GSM2462935: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUG; Escherichia coli; OTHER SRR5223162,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with harringtonine SRR5223163,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with cycloheximide SRR5239050,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER SRR5239051,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER SRR5239052,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER SRR5239053,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER SRR5239054,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER SRR5239055,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER SRR5239056,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER SRR5239057,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER SRR5239058,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER SRR5239059,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER SRR5239060,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER SRR5239061,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER SRR5239062,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER SRR5239063,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER SRR5239064,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER SRR5239065,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER SRR5239066,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER SRR5239067,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER SRR5239068,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER SRR5239069,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER SRR5239070,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER SRR5239071,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER SRR5239072,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER SRR5239073,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER SRR5239074,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER SRR5239075,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER SRR5239076,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER SRR5239077,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER SRR5239078,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER SRR5239079,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER SRR5239080,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER SRR5239081,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER SRR5239082,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER SRR5239083,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER SRR5239084,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER SRR5239085,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER SRR5356885,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in n-alkanes SRR5356887,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in n-alkanes SRR5356889,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in n-alkanes SRR5356891,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in Glycerol SRR5356893,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in Glycerol SRR5356895,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in Glycerol SRR5356897,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in n-alkanes SRR5356899,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in n-alkanes SRR5356901,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in n-alkanes SRR5356903,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in Glycerol SRR5356905,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in Glycerol SRR5356907,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in Glycerol SRR5483532,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant SRR5483533,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant rep2 SRR5483534,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep1 SRR5483539,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep2 SRR5667267,NextSeq 500 sequencing; GSM2664256: wild type ribosome profiling replicate 1; Drosophila melanogaster; OTHER SRR5667268,NextSeq 500 sequencing; GSM2664257: wild type ribosome profiling replicate 2; Drosophila melanogaster; OTHER SRR5667269,NextSeq 500 sequencing; GSM2664258: wild type ribosome profiling replicate 3; Drosophila melanogaster; OTHER SRR5667276,NextSeq 500 sequencing; GSM2664265: GluRIIA ribosome profiling replicate 1; Drosophila melanogaster; OTHER SRR5667277,NextSeq 500 sequencing; GSM2664266: GluRIIA ribosome profiling replicate 2; Drosophila melanogaster; OTHER SRR5667278,NextSeq 500 sequencing; GSM2664267: GluRIIA ribosome profiling replicate 3; Drosophila melanogaster; OTHER SRR5667282,NextSeq 500 sequencing; GSM2664271: Tor-OE ribosome profiling replicate 1; Drosophila melanogaster; OTHER SRR5667283,NextSeq 500 sequencing; GSM2664272: Tor-OE ribosome profiling replicate 2; Drosophila melanogaster; OTHER SRR5667284,NextSeq 500 sequencing; GSM2664273: Tor-OE ribosome profiling replicate 3; Drosophila melanogaster; OTHER SRR5735992,"Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq" SRR5735993,"Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq" SRR5735994,"Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq" SRR5735995,"Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq" SRR5735996,"Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq" SRR5735997,"Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq" SRR5735998,"Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq" SRR5735999,"Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq" SRR5736000,"Illumina HiSeq 2000 sequencing; GSM2678053: WT Ribosome Profiling, rep1; Mus musculus; RNA-Seq" SRR5736001,"Illumina HiSeq 2000 sequencing; GSM2678054: WT Ribosome Profiling, rep2; Mus musculus; RNA-Seq" SRR5736002,"Illumina HiSeq 2000 sequencing; GSM2678055: KO Ribosome Profiling, rep1; Mus musculus; RNA-Seq" SRR5736003,"Illumina HiSeq 2000 sequencing; GSM2678056: KO Ribosome Profiling, rep2; Mus musculus; RNA-Seq" SRR5799562,Illumina HiSeq 4000 sequencing; GSM2692350: ribosome profiling 0h; Mus musculus; OTHER SRR5799563,Illumina HiSeq 4000 sequencing; GSM2692351: ribosome profiling 12h; Mus musculus; OTHER SRR5952328,Illumina HiSeq 2000 sequencing; GSM2747838: Ribosome Profiling H19:H391; Mus musculus; OTHER SRR5952329,Illumina HiSeq 2000 sequencing; GSM2747839: Ribosome Profiling SECIS1 deletion2; Mus musculus; OTHER SRR5952330,Illumina HiSeq 2000 sequencing; GSM2747840: Ribosome Profiling SECIS1 deletion3; Mus musculus; OTHER SRR5952331,Illumina HiSeq 2000 sequencing; GSM2747841: Ribosome Profiling SECIS1 WT1; Mus musculus; OTHER SRR5952332,Illumina HiSeq 2000 sequencing; GSM2747842: Ribosome Profiling SECIS1 WT2; Mus musculus; OTHER SRR5952333,Illumina HiSeq 2000 sequencing; GSM2747843: Ribosome Profiling SECIS1 WT3; Mus musculus; OTHER SRR5952340,Illumina HiSeq 2000 sequencing; GSM2747850: Ribosome Profiling SECIS2 WT1; Mus musculus; OTHER SRR5952341,Illumina HiSeq 2000 sequencing; GSM2747851: Ribosome Profiling SECIS2 WT2; Mus musculus; OTHER SRR5952342,Illumina HiSeq 2000 sequencing; GSM2747852: Ribosome Profiling SECIS2 WT3; Mus musculus; OTHER SRR5952343,Illumina HiSeq 2000 sequencing; GSM2747853: Ribosome Profiling SECIS2 deletion1; Mus musculus; OTHER SRR5952344,Illumina HiSeq 2000 sequencing; GSM2747854: Ribosome Profiling SECIS2 deletion2; Mus musculus; OTHER SRR5952345,Illumina HiSeq 2000 sequencing; GSM2747855: Ribosome Profiling SECIS2 deletion3; Mus musculus; OTHER SRR6001737,Illumina Genome Analyzer II sequencing; GSM2770989: Ribosome profiling at 37°C in WT cells_1; Escherichia coli; RNA-Seq SRR6001738,Illumina Genome Analyzer II sequencing; GSM2770990: Ribosome profiling 10 min after shift to 10°C in WT cells_1; Escherichia coli; RNA-Seq SRR6001739,Illumina Genome Analyzer II sequencing; GSM2770991: Ribosome profiling 30 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq SRR6001740,Illumina Genome Analyzer II sequencing; GSM2770992: Ribosome profiling 2 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq SRR6001741,Illumina Genome Analyzer II sequencing; GSM2770993: Ribosome profiling 3 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq SRR6001742,Illumina Genome Analyzer II sequencing; GSM2770994: Ribosome profiling 4 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq SRR6001743,Illumina Genome Analyzer II sequencing; GSM2770995: Ribosome profiling 6 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq SRR6001744,Illumina HiSeq 2000 sequencing; GSM2770996: Ribosome profiling 5 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq SRR6001745,Illumina HiSeq 2000 sequencing; GSM2770997: Ribosome profiling 10 min after shift to 10°C in WT cells_2; Escherichia coli; RNA-Seq SRR6001746,Illumina HiSeq 2000 sequencing; GSM2770998: Ribosome profiling 15 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq SRR6001747,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq SRR6001748,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq SRR6001749,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq SRR6001750,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq SRR6001751,Illumina HiSeq 2000 sequencing; GSM2771001: Ribosome profiling at 37°C in WT cells_2; Escherichia coli; RNA-Seq SRR6001752,Illumina HiSeq 2000 sequencing; GSM2771002: Ribosome profiling at 37°C in ∆cspABCEG cells; Escherichia coli; RNA-Seq SRR618770,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #1" SRR618771,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #2" SRR618772,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #1" SRR618773,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #2" SRR618774,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with cycloheximide SRR618775,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with lactimidomycin SRR619082,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 1 SRR619083,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 2 SRR619084,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 1 SRR619085,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 2 SRR619086,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC only SRR619087,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with MG132 only SRR619088,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO SRR619089,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO SRR619090,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER SRR619091,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER SRR619092,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES SRR619093,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES SRR619094,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA SRR619095,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA SRR619096,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells no treatment SRR619097,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells treated with rapalog SRR619098,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells NOT expressing K71M SRR619099,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 1 SRR619100,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 2 SRR6252013,NextSeq 500 sequencing; GSM2838830: Dengue 1 ribosome profiling mRNA REP1; Homo sapiens; OTHER SRR6252014,NextSeq 500 sequencing; GSM2838831: Dengue 1 ribosome profiling footprint REP1; Homo sapiens; OTHER SRR6252015,NextSeq 500 sequencing; GSM2838832: Dengue 1 ribosome profiling mRNA REP2; Homo sapiens; OTHER SRR6252016,NextSeq 500 sequencing; GSM2838833: Dengue 1 ribosome profiling footprint REP2; Homo sapiens; OTHER SRR6286686,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii SRR6286687,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii SRR6286690,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii SRR6286691,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii SRR6286692,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii SRR6286693,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii SRR6315847,Illumina HiSeq 2000 sequencing; Hip1 total hippocampus Ribosome profiling SRR6395814,Illumina HiSeq 2500 sequencing; GSM2895436: KO-ribosome profiling; Mus musculus; OTHER SRR6395815,Illumina HiSeq 2500 sequencing; GSM2895437: KO-ribosome profiling input; Mus musculus; OTHER SRR6395816,Illumina HiSeq 2500 sequencing; GSM2895438: WT-ribosome profiling; Mus musculus; OTHER SRR6395817,Illumina HiSeq 2500 sequencing; GSM2895439: WT-ribosome profiling input; Mus musculus; OTHER SRR7123172,Illumina HiSeq 2500 sequencing; GSM3131863: WT-ribosome profiling replicate 2; Mus musculus; OTHER SRR7123173,Illumina HiSeq 3000 sequencing; GSM3131864: WT-ribosome profiling input replicate 2; Mus musculus; OTHER SRR7123174,Illumina HiSeq 2500 sequencing; GSM3131865: KO-ribosome profiling replicate 2; Mus musculus; OTHER SRR7123175,Illumina HiSeq 3000 sequencing; GSM3131866: KO-ribosome profiling input replicate 2; Mus musculus; OTHER SRR7132277,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #4 SRR7132286,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #2 SRR7132287,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #3 SRR7132288,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #3 SRR7132289,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #4 SRR7132290,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:control replicate #1 SRR7132291,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #2 SRR7132292,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #3 SRR7132293,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #1 SRR7132294,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #1 SRR7132295,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #2 SRR7241910,Illumina HiSeq 2500 sequencing; GSM3168387: MDA-MB-231 ribosome profiling; Homo sapiens; RNA-Seq SRR7241911,Illumina HiSeq 2500 sequencing; GSM3168388: C. elegans embryos ribosome profiling; Caenorhabditis elegans; RNA-Seq SRR7241912,Illumina HiSeq 2500 sequencing; GSM3168389: HeLa ribosome profiling 1; Homo sapiens; RNA-Seq SRR7241913,Illumina HiSeq 2500 sequencing; GSM3168390: HeLa ribosome profiling 2; Homo sapiens; RNA-Seq SRR7517655,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells SRR7517656,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells SRR7517657,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells SRR7517658,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells SRR8040412,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type plus radicicol SRR8040414,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type SRR8040416,NextSeq 500 sequencing; Ribosome profiling of L. donovani HSP90rr plus radicicol SRR8258332,Illumina MiSeq sequencing; GSM3048762: ΔrrnIcomp - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq SRR8258333,Illumina MiSeq sequencing; GSM3048763: ΔrrnI - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq SRR8258336,Illumina MiSeq sequencing; GSM3048766: ΔrrnIcomp - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq SRR8258337,Illumina MiSeq sequencing; GSM3048767: ΔrrnI - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq SRR8445000,"Illumina HiSeq 4000 sequencing; GSM3563711: HEK 293 cells, ribosome profiling, ctrl, Replicate 1; Homo sapiens; OTHER" SRR8445001,"Illumina HiSeq 4000 sequencing; GSM3563712: HEK 293 cells, ribosome profiling, ctrl, Replicate 2; Homo sapiens; OTHER" SRR8445002,"Illumina HiSeq 4000 sequencing; GSM3563713: HEK 293 cells, ribosome profiling, siDDX3, Replicate 1; Homo sapiens; OTHER" SRR8445003,"Illumina HiSeq 4000 sequencing; GSM3563714: HEK 293 cells, ribosome profiling, siDDX3, Replicate 2; Homo sapiens; OTHER" SRR870722,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER SRR870723,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER SRR870724,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER SRR870725,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870726,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870727,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870728,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870729,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870730,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870731,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870732,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870733,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870734,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER SRR870735,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER SRR870736,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER SRR870737,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870738,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870739,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870740,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870741,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870742,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870743,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870744,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870745,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR870746,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER SRR8732200,Illumina HiSeq 2500 sequencing; GSM3671680: ribosome profiling wt_1; Homo sapiens; RNA-Seq SRR8732201,Illumina HiSeq 2500 sequencing; GSM3671681: ribosome profiling wt_2; Homo sapiens; RNA-Seq SRR8732202,Illumina HiSeq 2500 sequencing; GSM3671682: ribosome profiling wt_3; Homo sapiens; RNA-Seq SRR8732203,Illumina HiSeq 2500 sequencing; GSM3671683: ribosome profiling APP_1; Homo sapiens; RNA-Seq SRR8732204,Illumina HiSeq 2500 sequencing; GSM3671684: ribosome profiling APP_2; Homo sapiens; RNA-Seq SRR8732205,Illumina HiSeq 2500 sequencing; GSM3671685: ribosome profiling APP_3; Homo sapiens; RNA-Seq SRR8732206,Illumina HiSeq 2500 sequencing; GSM3671686: ribosome profiling PSEN_1; Homo sapiens; RNA-Seq SRR8732207,Illumina HiSeq 2500 sequencing; GSM3671687: ribosome profiling PSEN_2; Homo sapiens; RNA-Seq SRR8732208,Illumina HiSeq 2500 sequencing; GSM3671688: ribosome profiling PSEN_3; Homo sapiens; RNA-Seq SRR8732209,Illumina HiSeq 2500 sequencing; GSM3671689: ribosome profiling APP/PSEN1_1; Homo sapiens; RNA-Seq SRR8732210,Illumina HiSeq 2500 sequencing; GSM3671690: ribosome profiling APP/PSEN1_2; Homo sapiens; RNA-Seq SRR8732211,Illumina HiSeq 2500 sequencing; GSM3671691: ribosome profiling APP/PSEN1_3; Homo sapiens; RNA-Seq SRR9113062,"Illumina HiSeq 4000 sequencing; GSM3791723: iPSC ribosome profiling, harringtonine-treated; Homo sapiens; OTHER" SRR9113063,"Illumina HiSeq 4000 sequencing; GSM3791724: Cardiomyocyte ribosome profiling, harringtonine-treated; Homo sapiens; OTHER" SRR9113064,"Illumina HiSeq 4000 sequencing; GSM3791725: iPSC ribosome profiling, no drug treatment, replicate 1; Homo sapiens; OTHER" SRR9113065,"Illumina HiSeq 4000 sequencing; GSM3791726: iPSC ribosome profiling, no drug treatment, replicate 2; Homo sapiens; OTHER" SRR9113066,"Illumina HiSeq 4000 sequencing; GSM3791727: iPSC ribosome profiling, no drug treatment, replicate 3; Homo sapiens; OTHER" SRR9113067,"Illumina HiSeq 4000 sequencing; GSM3791728: Cardiomyocyte ribosome profiling, no drug treatment, replicate 1; Homo sapiens; OTHER" SRR9113068,"Illumina HiSeq 4000 sequencing; GSM3791729: Cardiomyocyte ribosome profiling, no drug treatment, replicate 2; Homo sapiens; OTHER" SRR9113069,"Illumina HiSeq 4000 sequencing; GSM3791730: Cardiomyocyte ribosome profiling, no drug treatment, replicate 3; Homo sapiens; OTHER" SRR9265420,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 42C SRR9265421,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 42C SRR9265422,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C SRR9265423,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C SRR9265424,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C SRR9265425,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C SRR9265426,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample SRR9265427,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample SRR9265429,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample SRR9265438,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 42C SRR9265440,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 42C SRR944653,Illumina HiSeq 2000 sequencing; GSM1197612: Ribosome profiling rep1-SiControl-RPF C1; Homo sapiens; OTHER SRR944654,Illumina HiSeq 2000 sequencing; GSM1197613: Ribosome profiling rep1-SiControl-input-polyA C2; Homo sapiens; RNA-Seq SRR944655,Illumina HiSeq 2000 sequencing; GSM1197614: Ribosome profiling rep1-SiYTHDF2-RPF C3; Homo sapiens; OTHER ================================================ FILE: tests/data/test_search/ena_test_verbosity_1.json ================================================ [{"study_accession": "PRJEB12126", "experiment_accession": "ERX1264364", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708907", "sample_title": "Sample 1", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190989", "read_count": "38883498", "base_count": "1161289538", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264365", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708908", "sample_title": "Sample 10", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190990", "read_count": "55544297", "base_count": "1779600908", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264366", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708909", "sample_title": "Sample 11", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190991", "read_count": "54474851", "base_count": "1713994365", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264367", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708910", "sample_title": "Sample 12", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190992", "read_count": "78497711", "base_count": "2489092061", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264368", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "RNA-Seq", "library_source": "TRANSCRIPTOMIC", "library_selection": "RANDOM", "sample_accession": "SAMEA3708911", "sample_title": "Sample 13", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190993", "read_count": "84955423", "base_count": "2627276298", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264369", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "RNA-Seq", "library_source": "TRANSCRIPTOMIC", "library_selection": "RANDOM", "sample_accession": "SAMEA3708912", "sample_title": "Sample 14", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190994", "read_count": "75097651", "base_count": "2293097872", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264370", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "RNA-Seq", "library_source": "TRANSCRIPTOMIC", "library_selection": "RANDOM", "sample_accession": "SAMEA3708913", "sample_title": "Sample 15", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190995", "read_count": "67177553", "base_count": "2060926619", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264371", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "RNA-Seq", "library_source": "TRANSCRIPTOMIC", "library_selection": "RANDOM", "sample_accession": "SAMEA3708914", "sample_title": "Sample 16", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190996", "read_count": "62940694", "base_count": "2061757111", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264372", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "RNA-Seq", "library_source": "TRANSCRIPTOMIC", "library_selection": "RANDOM", "sample_accession": "SAMEA3708915", "sample_title": "Sample 17", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190997", "read_count": "80591061", "base_count": "2475034240", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264373", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "RNA-Seq", "library_source": "TRANSCRIPTOMIC", "library_selection": "RANDOM", "sample_accession": "SAMEA3708916", "sample_title": "Sample 18", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190998", "read_count": "68575621", "base_count": "2149386138", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264374", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708917", "sample_title": "Sample 19", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1190999", "read_count": "59543450", "base_count": "1840946911", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264375", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708918", "sample_title": "Sample 2", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1191000", "read_count": "48420348", "base_count": "1429402558", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264376", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708919", "sample_title": "Sample 20", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1191001", "read_count": "39413642", "base_count": "1197490271", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264377", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708920", "sample_title": "Sample 21", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1191002", "read_count": "43109202", "base_count": "1310217152", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264378", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708921", "sample_title": "Sample 22", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1191003", "read_count": "48048678", "base_count": "1464094378", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264379", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708922", "sample_title": "Sample 23", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1191004", "read_count": "55458988", "base_count": "1762359654", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264380", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708923", "sample_title": "Sample 24", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1191005", "read_count": "47426381", "base_count": "1463185679", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264381", "experiment_title": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "description": "Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling", "tax_id": "10090", "scientific_name": "Mus musculus", "library_strategy": "OTHER", "library_source": "TRANSCRIPTOMIC", "library_selection": "other", "sample_accession": "SAMEA3708924", "sample_title": "Sample 25", "instrument_model": "Illumina HiSeq 2000", "run_accession": "ERR1191006", "read_count": "53368431", "base_count": "1671809961", "first_public": "2016-02-08", "library_layout": "SINGLE", "instrument_platform": "ILLUMINA"}, {"study_accession": "PRJEB12126", "experiment_accession": "ERX1264382", "experiment_title": "Illumina HiSeq 2000 sequencing; 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Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708925,Sample 26,Illumina HiSeq 2000,ERR1191007,63008359,1879252598 PRJEB12126,ERX1264383,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708926,Sample 27,Illumina HiSeq 2000,ERR1191008,54398154,1665685103 PRJEB12126,ERX1264384,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708927,Sample 28,Illumina HiSeq 2000,ERR1191009,60588893,1898719877 PRJEB12126,ERX1264385,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708928,Sample 29,Illumina HiSeq 2000,ERR1191010,51322850,1636915300 PRJEB12126,ERX1264386,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708929,Sample 3,Illumina HiSeq 2000,ERR1191011,51075405,1550469279 PRJEB12126,ERX1264387,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708930,Sample 30,Illumina HiSeq 2000,ERR1191012,68573681,2176015649 PRJEB12126,ERX1264388,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708931,Sample 31,Illumina HiSeq 2000,ERR1191013,67660607,2053109515 PRJEB12126,ERX1264389,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708932,Sample 32,Illumina HiSeq 2000,ERR1191014,79400383,2502665973 PRJEB12126,ERX1264390,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708933,Sample 33,Illumina HiSeq 2000,ERR1191015,65832767,2077595830 PRJEB12126,ERX1264391,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708934,Sample 34,Illumina HiSeq 2000,ERR1191016,65880576,2068785301 PRJEB12126,ERX1264392,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708935,Sample 35,Illumina HiSeq 2000,ERR1191017,45934156,1461586536 PRJEB12126,ERX1264393,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708936,Sample 36,Illumina HiSeq 2000,ERR1191018,62115857,1934185771 PRJEB12126,ERX1264394,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708937,Sample 37,Illumina HiSeq 2000,ERR1191019,56038006,1696854260 PRJEB12126,ERX1264395,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708938,Sample 38,Illumina HiSeq 2000,ERR1191020,50038369,1585387757 PRJEB12126,ERX1264396,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708939,Sample 39,Illumina HiSeq 2000,ERR1191021,82282313,2638880669 PRJEB12126,ERX1264397,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708940,Sample 4,Illumina HiSeq 2000,ERR1191022,63170089,2044068461 PRJEB12126,ERX1264398,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708941,Sample 40,Illumina HiSeq 2000,ERR1191023,76077975,3120456466 PRJEB12126,ERX1264399,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708942,Sample 5,Illumina HiSeq 2000,ERR1191024,38540171,1192143682 PRJEB12126,ERX1264400,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708943,Sample 6,Illumina HiSeq 2000,ERR1191025,27122370,839903135 PRJEB12126,ERX1264401,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708944,Sample 7,Illumina HiSeq 2000,ERR1191026,52888637,1629947931 PRJEB12126,ERX1264402,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708945,Sample 8,Illumina HiSeq 2000,ERR1191027,47240129,1457468497 PRJEB12126,ERX1264403,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708946,Sample 9,Illumina HiSeq 2000,ERR1191028,58914298,1823035475 PRJEB17636,ERX1789731,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534046,Sample 1,Illumina HiSeq 2000,ERR1719518,41599973,1375854749 PRJEB17636,ERX1789732,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534047,Sample 10,NextSeq 500,ERR1719519,23069695,740677911 PRJEB17636,ERX1789733,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534048,Sample 11,NextSeq 500,ERR1719520,29010875,922672397 PRJEB17636,ERX1789734,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534049,Sample 12,NextSeq 500,ERR1719521,30202884,976358769 PRJEB17636,ERX1789735,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534050,Sample 13,NextSeq 500,ERR1719522,19815295,629646715 PRJEB17636,ERX1789736,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534051,Sample 14,NextSeq 500,ERR1719523,37199064,1177627544 PRJEB17636,ERX1789737,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534052,Sample 15,NextSeq 500,ERR1719524,26965806,866250047 PRJEB17636,ERX1789738,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534053,Sample 16,NextSeq 500,ERR1719525,31150940,974286119 PRJEB17636,ERX1789739,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534054,Sample 17,NextSeq 500,ERR1719526,31786494,975436074 PRJEB17636,ERX1789740,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534055,Sample 18,NextSeq 500,ERR1719527,31291402,1004598571 PRJEB17636,ERX1789741,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534056,Sample 19,NextSeq 500,ERR1719528,28466729,885092147 PRJEB17636,ERX1789742,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534057,Sample 2,Illumina HiSeq 2000,ERR1719529,43631646,1380630106 PRJEB17636,ERX1789743,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534058,Sample 20,NextSeq 500,ERR1719530,33738268,1059476203 PRJEB17636,ERX1789744,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534059,Sample 3,Illumina HiSeq 2000,ERR1719531,40726173,1283483477 PRJEB17636,ERX1789745,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534060,Sample 4,Illumina HiSeq 2000,ERR1719532,39825021,1261053649 PRJEB17636,ERX1789746,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534061,Sample 5,Illumina HiSeq 2000,ERR1719533,50368881,1646355648 PRJEB17636,ERX1789747,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534062,Sample 6,Illumina HiSeq 2000,ERR1719534,47535077,1522019700 PRJEB17636,ERX1789748,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534063,Sample 7,Illumina HiSeq 2000,ERR1719535,49746314,1603492330 PRJEB17636,ERX1789749,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534064,Sample 8,Illumina HiSeq 2000,ERR1719536,48745145,1548939461 PRJEB17636,ERX1789750,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534065,Sample 9,NextSeq 500,ERR1719537,24213954,761912205 PRJEB19014,ERX1861079,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,294,Pseudomonas fluorescens,MNase-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA50540668,hfq1,Illumina HiSeq 2000,ERR1797529,37747215,1025325032 PRJEB19014,ERX1861080,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,294,Pseudomonas fluorescens,MNase-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA50541418,hfq2,Illumina HiSeq 2000,ERR1797530,27730412,742041285 PRJEB19014,ERX1861081,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,294,Pseudomonas fluorescens,MNase-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA50542168,wt1,Illumina HiSeq 2000,ERR1797531,13719271,374602064 PRJEB19014,ERX1861082,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,294,Pseudomonas fluorescens,MNase-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA50542918,wt2,Illumina HiSeq 2000,ERR1797532,24135343,663303116 PRJEB19102,ERX1865801,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,60711,Chlorocebus sabaeus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52778668,Sample 1,NextSeq 500,ERR1802070,32991341,1030531389 PRJEB19102,ERX1865802,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52779418,Sample 10,NextSeq 500,ERR1802071,32655516,1036495741 PRJEB19102,ERX1865803,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,60711,Chlorocebus sabaeus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52780168,Sample 2,NextSeq 500,ERR1802072,37859333,1233151851 PRJEB19102,ERX1865804,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,60711,Chlorocebus sabaeus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52780918,Sample 3,NextSeq 500,ERR1802073,23378265,748417766 PRJEB19102,ERX1865805,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,60711,Chlorocebus sabaeus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52781668,Sample 4,NextSeq 500,ERR1802074,19273387,614792063 PRJEB19102,ERX1865806,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52782418,Sample 5,NextSeq 500,ERR1802075,30830839,1009143241 PRJEB19102,ERX1865807,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52783168,Sample 6,NextSeq 500,ERR1802076,26929369,882916179 PRJEB19102,ERX1865808,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52783918,Sample 7,NextSeq 500,ERR1802077,12627212,397075719 PRJEB19102,ERX1865809,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52784668,Sample 8,NextSeq 500,ERR1802078,17629538,542405945 PRJEB19102,ERX1865810,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52785418,Sample 9,NextSeq 500,ERR1802079,40647908,1316636689 PRJEB19678,ERX1918552,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA100849168,Sample 1,NextSeq 500,ERR1856693,111880423,3793356586 PRJEB19678,ERX1918553,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA100849918,Sample 2,NextSeq 500,ERR1856694,58039284,1693191518 PRJEB19678,ERX1918554,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA100850668,Sample 3,NextSeq 500,ERR1856695,54983210,1222852079 PRJEB21099,ERX2054828,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106710,wt.N.CHX.mrna.1,Illumina HiSeq 2000,ERR1994959,26425976,1321298800 PRJEB21099,ERX2054829,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106711,wt.N.CHX.mrna.3,Illumina HiSeq 2000,ERR1994960,36240950,1812047500 PRJEB21099,ERX2054830,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106712,wt.N.CHX.ribo.1,NextSeq 550,ERR1994961,63059496,3152974800 PRJEB21099,ERX2054831,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106713,wt.N.CHX.ribo.3,Illumina HiSeq 2000,ERR1994962,26742065,1337103250 PRJEB21099,ERX2054832,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106714,wt.N.noCHX.mrna.1,Illumina HiSeq 2000,ERR1994963,16170457,808522850 PRJEB21099,ERX2054833,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106715,wt.N.noCHX.mrna.3,Illumina HiSeq 2000,ERR1994964,23972947,1198647350 PRJEB21099,ERX2054834,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106716,wt.N.noCHX.ribo.1,Illumina HiSeq 2000,ERR1994965,40531552,2026577600 PRJEB21099,ERX2054835,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106717,wt.N.noCHX.ribo.3,Illumina HiSeq 2000,ERR1994966,32968604,1648430200 PRJEB21099,ERX2054836,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106718,wt.noN.CHX.mrna.1,Illumina HiSeq 2000,ERR1994967,21546857,1077342850 PRJEB21099,ERX2054837,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106719,wt.noN.CHX.mrna.3,Illumina HiSeq 2000,ERR1994968,33734733,1686736650 PRJEB21099,ERX2054838,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106720,wt.noN.CHX.ribo.1,NextSeq 550,ERR1994969,83235717,4161785850 PRJEB21099,ERX2054839,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106721,wt.noN.CHX.ribo.3,Illumina HiSeq 2000,ERR1994970,31175890,1558794500 PRJEB21099,ERX2054840,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106722,wt.noN.noCHX.mrna.1,Illumina HiSeq 2000,ERR1994971,18195992,909799600 PRJEB21099,ERX2054841,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106723,wt.noN.noCHX.mrna.3,Illumina HiSeq 2000,ERR1994972,23231253,1161562650 PRJEB21099,ERX2054842,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106724,wt.noN.noCHX.ribo.1,Illumina HiSeq 2000,ERR1994973,40848270,2042413500 PRJEB21099,ERX2054843,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106725,wt.noN.noCHX.ribo.3,Illumina HiSeq 2000,ERR1994974,31871091,1593554550 PRJEB21224,ERX2063387,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118808,gcn2.AT.mrna.3,NextSeq 550,ERR2003518,37068610,2804773487 PRJEB21224,ERX2063388,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118809,gcn2.AT.mrna.4,NextSeq 550,ERR2003519,32243483,2439588430 PRJEB21224,ERX2063389,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118810,gcn2.AT.ribo.3,NextSeq 550,ERR2003520,31434722,1571736100 PRJEB21224,ERX2063390,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118811,gcn2.AT.ribo.4,NextSeq 550,ERR2003521,56596125,2829806250 PRJEB21224,ERX2063391,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118812,gcn2.noAT.mrna.3,NextSeq 550,ERR2003522,16204245,1226035737 PRJEB21224,ERX2063392,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118813,gcn2.noAT.mrna.4,NextSeq 550,ERR2003523,33797257,2557225027 PRJEB21224,ERX2063393,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118814,gcn2.noAT.ribo.3,NextSeq 550,ERR2003524,31214960,1560748000 PRJEB21224,ERX2063394,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118815,gcn2.noAT.ribo.4,NextSeq 550,ERR2003525,106865118,5343255900 PRJEB21224,ERX2063395,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118816,wt.AT.CHX.mrna.11,NextSeq 550,ERR2003526,52513972,2625698600 PRJEB21224,ERX2063396,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118817,wt.AT.CHX.mrna.13,NextSeq 550,ERR2003527,35611500,1780575000 PRJEB21224,ERX2063397,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118818,wt.AT.CHX.ribo.11,NextSeq 550,ERR2003528,62968779,3148438950 PRJEB21224,ERX2063398,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118819,wt.AT.CHX.ribo.13,NextSeq 550,ERR2003529,28486176,1424308800 PRJEB21224,ERX2063399,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118820,wt.AT.mrna.2B,NextSeq 550,ERR2003530,39443224,2984603676 PRJEB21224,ERX2063400,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118821,wt.AT.mrna.3,NextSeq 550,ERR2003531,14151645,1070787968 PRJEB21224,ERX2063401,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118822,wt.AT.mrna.4,NextSeq 550,ERR2003532,39994820,3026173391 PRJEB21224,ERX2063402,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118823,wt.AT.noCHX.mrna.11,NextSeq 550,ERR2003533,18348290,917414500 PRJEB21224,ERX2063403,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118824,wt.AT.noCHX.mrna.13,NextSeq 550,ERR2003534,27306569,1365328450 PRJEB21224,ERX2063404,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118825,wt.AT.noCHX.ribo.11,NextSeq 550,ERR2003535,119503388,5975169400 PRJEB21224,ERX2063405,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118826,wt.AT.noCHX.ribo.13,NextSeq 550,ERR2003536,31631553,1581577650 PRJEB21224,ERX2063406,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118827,wt.AT.ribo.2-1,NextSeq 550,ERR2003537,17283910,881479182 PRJEB21224,ERX2063407,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118828,wt.AT.ribo.2-2,NextSeq 550,ERR2003538,60683650,3034182500 PRJEB21224,ERX2063408,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118829,wt.AT.ribo.3,NextSeq 550,ERR2003539,37185178,1859258900 PRJEB21224,ERX2063409,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118830,wt.AT.ribo.4,NextSeq 550,ERR2003540,68616943,3430847150 PRJEB21224,ERX2063410,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118831,wt.noAT.CHX.mrna.11,NextSeq 550,ERR2003541,4368155,218407750 PRJEB21224,ERX2063411,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118832,wt.noAT.CHX.mrna.13,NextSeq 550,ERR2003542,36240950,1812047500 PRJEB21224,ERX2063412,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118833,wt.noAT.CHX.ribo.11,NextSeq 550,ERR2003543,32008211,1600410550 PRJEB21224,ERX2063413,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118834,wt.noAT.CHX.ribo.13,NextSeq 550,ERR2003544,26742065,1337103250 PRJEB21224,ERX2063414,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118835,wt.noAT.mrna.2B,NextSeq 550,ERR2003545,24001975,1816117196 PRJEB21224,ERX2063415,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118836,wt.noAT.mrna.3,NextSeq 550,ERR2003546,15509062,1173469392 PRJEB21224,ERX2063416,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118837,wt.noAT.mrna.4,NextSeq 550,ERR2003547,23729256,1795439617 PRJEB21224,ERX2063417,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118838,wt.noAT.noCHX.mrna.11,NextSeq 550,ERR2003548,19274273,963713650 PRJEB21224,ERX2063418,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118839,wt.noAT.noCHX.mrna.13,NextSeq 550,ERR2003549,23972947,1198647350 PRJEB21224,ERX2063419,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118840,wt.noAT.noCHX.ribo.11,NextSeq 550,ERR2003550,26638047,1331902350 PRJEB21224,ERX2063420,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118841,wt.noAT.noCHX.ribo.13,NextSeq 550,ERR2003551,32968604,1648430200 PRJEB21224,ERX2063421,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118842,wt.noAT.ribo.2,NextSeq 550,ERR2003552,3359956,171357719 PRJEB21224,ERX2063422,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118843,wt.noAT.ribo.3,NextSeq 550,ERR2003553,30905560,1545278000 PRJEB21224,ERX2063423,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118844,wt.noAT.ribo.4,NextSeq 550,ERR2003554,47605239,2380261950 PRJEB22128,ERX2151380,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,9606,Homo sapiens,RIP-Seq,TRANSCRIPTOMIC,other,SAMEA104209704,Riboseq CHX pool,Illumina HiSeq 2000,ERR2093966,5129748,512974800 PRJEB22128,ERX2151381,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA104209705,RNA-seq CHX 1,Illumina HiSeq 2000,ERR2093967,81139076,8113907600 PRJEB22128,ERX2151382,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA104209706,RNA-seq CHX 2,Illumina HiSeq 2000,ERR2093968,80937413,8093741300 PRJEB22128,ERX2151383,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA104209707,RNA-seq CHX 3,Illumina HiSeq 2000,ERR2093969,75600500,7560050000 PRJEB23398,ERX2249169,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375964,ID18RPF,Illumina HiSeq 2500,ERR2193146,29058055,2934863555 PRJEB23398,ERX2249170,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375965,ID18WT,Illumina HiSeq 2500,ERR2193147,45096290,4554725290 PRJEB23398,ERX2249171,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375966,ID22RPF,Illumina HiSeq 2500,ERR2193148,43451260,4388577260 PRJEB23398,ERX2249172,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375967,ID22WT,Illumina HiSeq 2500,ERR2193149,46404718,4686876518 PRJEB23398,ERX2249173,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375968,ID25RPF,Illumina HiSeq 2500,ERR2193150,52071822,5259254022 PRJEB23398,ERX2249174,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375969,ID25WT,Illumina HiSeq 2500,ERR2193151,33735834,3407319234 PRJEB23398,ERX2249175,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375970,ID28RPF,Illumina HiSeq 2500,ERR2193152,47060340,4753094340 PRJEB23398,ERX2249176,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375971,ID28WT,Illumina HiSeq 2500,ERR2193153,34725379,3507263279 PRJEB23398,ERX2249177,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375972,ID29RPF,Illumina HiSeq 2500,ERR2193154,36753828,3712136628 PRJEB23398,ERX2249178,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375973,ID29WT,Illumina HiSeq 2500,ERR2193155,37389224,3776311624 PRJEB23398,ERX2249179,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375974,ID30RPF,Illumina HiSeq 2500,ERR2193156,58732724,5932005124 PRJEB23398,ERX2249180,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375975,ID30WT,Illumina HiSeq 2500,ERR2193157,27507989,2778306889 PRJEB23398,ERX2249181,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375976,ID31RPF,Illumina HiSeq 2500,ERR2193158,38200240,3858224240 PRJEB23398,ERX2249182,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375977,ID31WT,Illumina HiSeq 2500,ERR2193159,31139926,3145132526 PRJEB23562,ERX2256431,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104395996,Mock-RiboSeq-CHX-1,Illumina HiSeq 2000,ERR2201443,43087035,1347230056 PRJEB23562,ERX2256432,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104395999,Mock-RNASeq-1,Illumina HiSeq 2000,ERR2201444,34760070,1082072656 PRJEB23562,ERX2256433,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396001,Mock-RiboSeq-CHX-2,NextSeq 500,ERR2201445,7925554,229108181 PRJEB23562,ERX2256434,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396002,Mock-RNASeq-2,NextSeq 500,ERR2201446,17904218,536508323 PRJEB23562,ERX2256435,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396003,RiboSeq-CHX-1,Illumina HiSeq 2000,ERR2201447,62327174,1889305290 PRJEB23562,ERX2256436,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396004,RiboSeq-HAR,Illumina HiSeq 2000,ERR2201448,29880691,918985348 PRJEB23562,ERX2256437,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396005,RNASeq-1,Illumina HiSeq 2000,ERR2201449,99428786,3052553985 PRJEB23562,ERX2256438,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396006,RiboSeq-CHX-2,NextSeq 500,ERR2201450,11326057,306768073 PRJEB23562,ERX2256439,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396007,RNASeq-2,NextSeq 500,ERR2201451,17348527,519625143 PRJEB26279,ERX2547744,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590062,Sample 10,NextSeq 500,ERR2528907,14307741,1087388316 PRJEB26279,ERX2547745,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590063,Sample 1,NextSeq 500,ERR2528908,32539697,2473016956 PRJEB26279,ERX2547746,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590064,Sample 2,NextSeq 500,ERR2528909,32365237,2459757997 PRJEB26279,ERX2547747,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590065,Sample 3,NextSeq 500,ERR2528910,27720458,2106754808 PRJEB26279,ERX2547748,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590066,Sample 4,NextSeq 500,ERR2528911,27618945,2099039820 PRJEB26279,ERX2547749,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4590067,Sample 5,NextSeq 500,ERR2528912,29429175,2236617172 PRJEB26279,ERX2547750,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4590068,Sample 6,NextSeq 500,ERR2528913,53891222,4095732642 PRJEB26279,ERX2547751,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4590069,Sample 7,NextSeq 500,ERR2528914,25078726,1905983073 PRJEB26279,ERX2547752,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4590070,Sample 8,NextSeq 500,ERR2528915,33016656,2509265722 PRJEB26279,ERX2547753,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590071,Sample 9,NextSeq 500,ERR2528916,13436449,1021170124 PRJEB27418,ERX2676640,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4753492,S1_eEF3_normal_rep1,Illumina HiSeq 2500,ERR2660262,143636526,7325462826 PRJEB27418,ERX2676641,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4753493,S3_eEF3_normal_rep2,Illumina HiSeq 2500,ERR2660263,133848724,6826284924 PRJEB27418,ERX2676642,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4753495,S5_eEF3_normal_rep1,Illumina HiSeq 2500,ERR2660264,87339001,4454289051 PRJEB27418,ERX2676643,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4753496,S7_eEF3_normal_rep2,Illumina HiSeq 2500,ERR2660265,81861785,4174951035 PRJEB27418,ERX2676644,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4753498,S2_eEF3_depleted_rep1,Illumina HiSeq 2500,ERR2660266,140684593,7174914243 PRJEB27418,ERX2676645,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4753500,S4_eEF3_depleted_rep2,Illumina HiSeq 2500,ERR2660267,132564691,6760799241 PRJEB27418,ERX2676646,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4753503,S6_eEF3_depleted_rep1,Illumina HiSeq 2500,ERR2660269,78528010,4004928510 PRJEB27418,ERX2676647,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4753504,S8_eEF3_depleted_rep2,Illumina HiSeq 2500,ERR2660271,79828450,4071250950 PRJEB27604,ERX2696677,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776570,new1_KO_riboseq_S2,Illumina HiSeq 2500,ERR2681846,67361162,3435419262 PRJEB27604,ERX2696678,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776571,new1_KO_riboseq_S4,Illumina HiSeq 2500,ERR2681847,80946528,4128272928 PRJEB27604,ERX2696679,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776572,new1_KO_riboseq_S6,Illumina HiSeq 2500,ERR2681848,69690799,3554230749 PRJEB27604,ERX2696680,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776573,WT_riboseq_S1,Illumina HiSeq 2500,ERR2681849,68722759,3504860709 PRJEB27604,ERX2696681,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776574,WT_riboseq_S3,Illumina HiSeq 2500,ERR2681850,85579580,4364558580 PRJEB27604,ERX2696682,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776575,WT_riboseq_S5,Illumina HiSeq 2500,ERR2681851,83078459,4237001409 PRJEB27604,ERX2696683,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776576,new1_KO_RNAseq_S10,Illumina HiSeq 2500,ERR2681852,24694922,1259441022 PRJEB27604,ERX2696684,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776577,new1_KO_RNAseq_S12,Illumina HiSeq 2500,ERR2681853,27198724,1387134924 PRJEB27604,ERX2696685,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776578,new1_KO_RNAseq_S8,Illumina HiSeq 2500,ERR2681854,42548074,2169951774 PRJEB27604,ERX2696686,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776579,WT_RNAseq_S11,Illumina HiSeq 2500,ERR2681855,22479763,1146467913 PRJEB27604,ERX2696687,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776580,WT_RNAseq_S7,Illumina HiSeq 2500,ERR2681856,25728303,1312143453 PRJEB27604,ERX2696688,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776581,WT_RNAseq_S9,Illumina HiSeq 2500,ERR2681857,24022337,1225139187 PRJEB28810,ERX2819159,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939567,chicken_brain_ribo_1,Illumina HiSeq 2500,ERR2812328,89507736,9040281336 PRJEB28810,ERX2819160,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939568,chicken_brain_ribo_2,Illumina HiSeq 2500,ERR2812329,, PRJEB28810,ERX2819161,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939569,chicken_brain_ribo_3,Illumina HiSeq 2500,ERR2812330,, PRJEB28810,ERX2819162,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939570,chicken_brain_rna_1,Illumina HiSeq 2500,ERR2812331,78156882,3986000982 PRJEB28810,ERX2819163,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939571,chicken_brain_rna_2,Illumina HiSeq 2500,ERR2812332,, PRJEB28810,ERX2819164,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939572,chicken_brain_rna_3,Illumina HiSeq 2500,ERR2812333,, PRJEB28810,ERX2819165,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939573,chicken_liver_ribo_1,Illumina HiSeq 2500,ERR2812334,50822663,2591955813 PRJEB28810,ERX2819166,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939574,chicken_liver_ribo_2,Illumina HiSeq 2500,ERR2812335,, PRJEB28810,ERX2819167,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939575,chicken_liver_ribo_3,Illumina HiSeq 2500,ERR2812336,, PRJEB28810,ERX2819168,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939576,chicken_liver_rna_1,Illumina HiSeq 2500,ERR2812337,102696548,5237523948 PRJEB28810,ERX2819169,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939577,chicken_liver_rna_2,Illumina HiSeq 2500,ERR2812338,, PRJEB28810,ERX2819170,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939578,chicken_liver_rna_3,Illumina HiSeq 2500,ERR2812339,, PRJEB28810,ERX2819171,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939579,chicken_testis_ribo_1,Illumina HiSeq 2500,ERR2812340,176588839,9006030789 PRJEB28810,ERX2819172,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939580,chicken_testis_ribo_2,Illumina HiSeq 2500,ERR2812341,, PRJEB28810,ERX2819173,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939581,chicken_testis_ribo_3,Illumina HiSeq 2500,ERR2812342,, PRJEB28810,ERX2819174,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939582,chicken_testis_rna_1,Illumina HiSeq 2500,ERR2812343,69052194,3521661894 PRJEB28810,ERX2819175,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939583,chicken_testis_rna_2,Illumina HiSeq 2500,ERR2812344,, PRJEB28810,ERX2819176,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939584,chicken_testis_rna_3,Illumina HiSeq 2500,ERR2812345,, PRJEB28810,ERX2819177,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939585,human_brain_ribo_1,Illumina HiSeq 2500,ERR2812346,, PRJEB28810,ERX2819178,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939586,human_brain_ribo_2,Illumina HiSeq 2500,ERR2812347,, PRJEB28810,ERX2819179,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939587,human_brain_ribo_3,Illumina HiSeq 2500,ERR2812348,, PRJEB28810,ERX2819180,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939588,human_brain_rna_1,Illumina HiSeq 2500,ERR2812349,, PRJEB28810,ERX2819181,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939589,human_brain_rna_2,Illumina HiSeq 2500,ERR2812350,, PRJEB28810,ERX2819182,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939590,human_brain_rna_3,Illumina HiSeq 2500,ERR2812351,, PRJEB28810,ERX2819183,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939591,human_liver_ribo_1,Illumina HiSeq 2500,ERR2812352,, PRJEB28810,ERX2819184,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939592,human_liver_ribo_2,Illumina HiSeq 2500,ERR2812353,, PRJEB28810,ERX2819185,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939593,human_liver_ribo_3,Illumina HiSeq 2500,ERR2812354,, PRJEB28810,ERX2819186,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939594,human_liver_rna_1,Illumina HiSeq 2500,ERR2812355,, PRJEB28810,ERX2819187,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939595,human_liver_rna_2,Illumina HiSeq 2500,ERR2812356,, PRJEB28810,ERX2819188,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939596,human_liver_rna_3,Illumina HiSeq 2500,ERR2812357,, PRJEB28810,ERX2819189,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939597,human_testis_ribo_1,Illumina HiSeq 2500,ERR2812358,, PRJEB28810,ERX2819190,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939598,human_testis_ribo_2,Illumina HiSeq 2500,ERR2812359,, PRJEB28810,ERX2819191,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939599,human_testis_ribo_3,Illumina HiSeq 2500,ERR2812360,, PRJEB28810,ERX2819192,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939600,human_testis_rna_1,Illumina HiSeq 2500,ERR2812361,, PRJEB28810,ERX2819193,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939601,human_testis_rna_2,Illumina HiSeq 2500,ERR2812362,, PRJEB28810,ERX2819194,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939602,human_testis_rna_3,Illumina HiSeq 2500,ERR2812363,, PRJEB28810,ERX2819195,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939603,macaque_brain_ribo_1,Illumina HiSeq 2500,ERR2812364,, PRJEB28810,ERX2819196,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939604,macaque_brain_ribo_2,Illumina HiSeq 2500,ERR2812365,, PRJEB28810,ERX2819197,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939605,macaque_brain_ribo_3,Illumina HiSeq 2500,ERR2812366,, PRJEB28810,ERX2819198,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939606,macaque_brain_rna_1,Illumina HiSeq 2500,ERR2812367,, PRJEB28810,ERX2819199,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939607,macaque_brain_rna_2,Illumina HiSeq 2500,ERR2812368,, PRJEB28810,ERX2819200,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939608,macaque_brain_rna_3,Illumina HiSeq 2500,ERR2812369,, PRJEB28810,ERX2819201,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939609,macaque_liver_ribo_1,Illumina HiSeq 2500,ERR2812370,, PRJEB28810,ERX2819202,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939610,macaque_liver_ribo_2,Illumina HiSeq 2500,ERR2812371,, PRJEB28810,ERX2819203,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939611,macaque_liver_ribo_3,Illumina HiSeq 2500,ERR2812372,, PRJEB28810,ERX2819204,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939612,macaque_liver_rna_1,Illumina HiSeq 2500,ERR2812373,, PRJEB28810,ERX2819205,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939613,macaque_liver_rna_2,Illumina HiSeq 2500,ERR2812374,, PRJEB28810,ERX2819206,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939614,macaque_liver_rna_3,Illumina HiSeq 2500,ERR2812375,, PRJEB28810,ERX2819207,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939615,macaque_testis_ribo_1,Illumina HiSeq 2500,ERR2812376,, PRJEB28810,ERX2819208,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939616,macaque_testis_ribo_2,Illumina HiSeq 2500,ERR2812377,, PRJEB28810,ERX2819209,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939617,macaque_testis_ribo_3,Illumina HiSeq 2500,ERR2812378,, PRJEB28810,ERX2819210,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939618,macaque_testis_rna_1,Illumina HiSeq 2500,ERR2812379,, PRJEB28810,ERX2819211,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939619,macaque_testis_rna_2,Illumina HiSeq 2500,ERR2812380,, PRJEB28810,ERX2819212,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939620,macaque_testis_rna_3,Illumina HiSeq 2500,ERR2812381,, PRJEB28810,ERX2819213,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939621,mouse_brain_ribo_1,Illumina HiSeq 2500,ERR2812382,125913653,12717278953 PRJEB28810,ERX2819214,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939622,mouse_brain_ribo_2,Illumina HiSeq 2500,ERR2812383,, PRJEB28810,ERX2819215,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939623,mouse_brain_ribo_3,Illumina HiSeq 2500,ERR2812384,, PRJEB28810,ERX2819216,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939624,mouse_brain_rna_1,Illumina HiSeq 2500,ERR2812385,59718135,6031531635 PRJEB28810,ERX2819217,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939625,mouse_brain_rna_2,Illumina HiSeq 2500,ERR2812386,, PRJEB28810,ERX2819218,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939626,mouse_brain_rna_3,Illumina HiSeq 2500,ERR2812387,, PRJEB28810,ERX2819219,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939627,mouse_liver_ribo_1,Illumina HiSeq 2500,ERR2812388,133782505,11314315655 PRJEB28810,ERX2819220,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939628,mouse_liver_ribo_2,Illumina HiSeq 2500,ERR2812389,, PRJEB28810,ERX2819221,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939629,mouse_liver_ribo_3,Illumina HiSeq 2500,ERR2812390,, PRJEB28810,ERX2819222,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939630,mouse_liver_rna_1,Illumina HiSeq 2500,ERR2812391,56370619,5693432519 PRJEB28810,ERX2819223,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939631,mouse_liver_rna_2,Illumina HiSeq 2500,ERR2812392,, PRJEB28810,ERX2819224,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939632,mouse_liver_rna_3,Illumina HiSeq 2500,ERR2812393,, PRJEB28810,ERX2819225,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939633,mouse_testis_ribo_1,Illumina HiSeq 2500,ERR2812394,117238132,11841051332 PRJEB28810,ERX2819226,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939634,mouse_testis_ribo_2,Illumina HiSeq 2500,ERR2812395,, PRJEB28810,ERX2819227,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939635,mouse_testis_ribo_3,Illumina HiSeq 2500,ERR2812396,, PRJEB28810,ERX2819228,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939636,mouse_testis_rna_1,Illumina HiSeq 2500,ERR2812397,60491740,6109665740 PRJEB28810,ERX2819229,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939637,mouse_testis_rna_2,Illumina HiSeq 2500,ERR2812398,, PRJEB28810,ERX2819230,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939638,mouse_testis_rna_3,Illumina HiSeq 2500,ERR2812399,, PRJEB28810,ERX2819231,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939639,opossum_brain_ribo_1,Illumina HiSeq 2500,ERR2812400,99962696,5098097496 PRJEB28810,ERX2819232,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939640,opossum_brain_ribo_2,Illumina HiSeq 2500,ERR2812401,, PRJEB28810,ERX2819233,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939641,opossum_brain_ribo_3,Illumina HiSeq 2500,ERR2812402,, PRJEB28810,ERX2819234,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939642,opossum_brain_rna_1,Illumina HiSeq 2500,ERR2812403,118076072,6021879672 PRJEB28810,ERX2819235,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939643,opossum_brain_rna_2,Illumina HiSeq 2500,ERR2812404,, PRJEB28810,ERX2819236,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939644,opossum_brain_rna_3,Illumina HiSeq 2500,ERR2812405,, PRJEB28810,ERX2819237,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939645,opossum_liver_ribo_1,Illumina HiSeq 2500,ERR2812406,102073266,7960719316 PRJEB28810,ERX2819238,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939646,opossum_liver_ribo_2,Illumina HiSeq 2500,ERR2812407,, PRJEB28810,ERX2819239,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939647,opossum_liver_ribo_3,Illumina HiSeq 2500,ERR2812408,, PRJEB28810,ERX2819240,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939648,opossum_liver_rna_1,Illumina HiSeq 2500,ERR2812409,122985784,8335560284 PRJEB28810,ERX2819241,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939649,opossum_liver_rna_2,Illumina HiSeq 2500,ERR2812410,, PRJEB28810,ERX2819242,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939650,opossum_liver_rna_3,Illumina HiSeq 2500,ERR2812411,, PRJEB28810,ERX2819243,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939651,opossum_testis_ribo_1,Illumina HiSeq 2500,ERR2812412,372136872,18978980472 PRJEB28810,ERX2819244,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939652,opossum_testis_ribo_2,Illumina HiSeq 2500,ERR2812413,, PRJEB28810,ERX2819245,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939653,opossum_testis_ribo_3,Illumina HiSeq 2500,ERR2812414,, PRJEB28810,ERX2819246,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939654,opossum_testis_rna_1,Illumina HiSeq 2500,ERR2812415,91675215,4675435965 PRJEB28810,ERX2819247,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939655,opossum_testis_rna_2,Illumina HiSeq 2500,ERR2812416,, PRJEB28810,ERX2819248,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939656,opossum_testis_rna_3,Illumina HiSeq 2500,ERR2812417,, PRJEB28810,ERX2819249,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939657,platypus_brain_ribo_1,Illumina HiSeq 2500,ERR2812418,524355445,33524134145 PRJEB28810,ERX2819250,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939658,platypus_brain_ribo_2,Illumina HiSeq 2500,ERR2812419,, PRJEB28810,ERX2819251,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939659,platypus_brain_ribo_3,Illumina HiSeq 2500,ERR2812420,, PRJEB28810,ERX2819252,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939660,platypus_brain_rna_1,Illumina HiSeq 2500,ERR2812421,88501433,4513573083 PRJEB28810,ERX2819253,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939661,platypus_brain_rna_2,Illumina HiSeq 2500,ERR2812422,, PRJEB28810,ERX2819254,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939662,platypus_brain_rna_3,Illumina HiSeq 2500,ERR2812423,, PRJEB28810,ERX2819255,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939663,platypus_liver_ribo_1,Illumina HiSeq 2500,ERR2812424,205764142,10493971242 PRJEB28810,ERX2819256,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939664,platypus_liver_ribo_2,Illumina HiSeq 2500,ERR2812425,, PRJEB28810,ERX2819257,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939665,platypus_liver_ribo_3,Illumina HiSeq 2500,ERR2812426,, PRJEB28810,ERX2819258,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939666,platypus_liver_rna_1,Illumina HiSeq 2500,ERR2812427,107403200,5477563200 PRJEB28810,ERX2819259,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939667,platypus_liver_rna_2,Illumina HiSeq 2500,ERR2812428,, PRJEB28810,ERX2819260,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939668,platypus_liver_rna_3,Illumina HiSeq 2500,ERR2812429,, PRJEB28810,ERX2819261,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939669,platypus_testis_ribo_1,Illumina HiSeq 2500,ERR2812430,, PRJEB28810,ERX2819262,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939670,platypus_testis_ribo_2,Illumina HiSeq 2500,ERR2812431,, PRJEB28810,ERX2819263,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939671,platypus_testis_ribo_3,Illumina HiSeq 2500,ERR2812432,, PRJEB28810,ERX2819264,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939672,platypus_testis_rna_1,Illumina HiSeq 2500,ERR2812433,, PRJEB28810,ERX2819265,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939673,platypus_testis_rna_2,Illumina HiSeq 2500,ERR2812434,, PRJEB28810,ERX2819266,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939674,platypus_testis_rna_3,Illumina HiSeq 2500,ERR2812435,, PRJEB28810,ERX2819267,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939675,chicken_liver_ribo_4,Illumina HiSeq 2500,ERR2812436,, PRJEB28810,ERX2819268,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939676,chicken_liver_ribo_5,Illumina HiSeq 2500,ERR2812437,, PRJEB28810,ERX2819269,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939677,chicken_liver_rna_4,Illumina HiSeq 2500,ERR2812438,, PRJEB28810,ERX2819270,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939678,chicken_liver_rna_5,Illumina HiSeq 2500,ERR2812439,, PRJEB28810,ERX2819271,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939679,mouse_liver_ribo_4,Illumina HiSeq 2500,ERR2812440,, PRJEB28810,ERX2819272,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939680,mouse_liver_ribo_5,Illumina HiSeq 2500,ERR2812441,, PRJEB28810,ERX2819273,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939681,mouse_liver_rna_4,Illumina HiSeq 2500,ERR2812442,, PRJEB28810,ERX2819274,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939682,mouse_liver_rna_5,Illumina HiSeq 2500,ERR2812443,, PRJEB30076,ERX2979492,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147536,RPF_0h_n1,Illumina HiSeq 2500,ERR2976734,14287455,409427591 PRJEB30076,ERX2979493,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147537,RPF_0h_n2,Illumina HiSeq 2500,ERR2976735,5520862,154466485 PRJEB30076,ERX2979494,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147538,RPF_0h_n3,Illumina HiSeq 2500,ERR2976736,5499258,155393274 PRJEB30076,ERX2979495,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147539,RPF_3h_n1,Illumina HiSeq 2500,ERR2976737,13926097,391986840 PRJEB30076,ERX2979496,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147540,RPF_3h_n2,Illumina HiSeq 2500,ERR2976738,14126686,422171925 PRJEB30076,ERX2979497,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147541,RPF_3h_n3,Illumina HiSeq 2500,ERR2976739,14499877,434534946 PRJEB30076,ERX2979498,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147542,TotalRNA_0h_n1,Illumina HiSeq 2500,ERR2976740,27907935,866451536 PRJEB30076,ERX2979499,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147543,TotalRNA_0h_n2,Illumina HiSeq 2500,ERR2976741,13444837,351478756 PRJEB30076,ERX2979500,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147544,TotalRNA_0h_n3,Illumina HiSeq 2500,ERR2976742,23418108,620300138 PRJEB30076,ERX2979501,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147545,TotalRNA_3h_n1,Illumina HiSeq 2500,ERR2976743,3499361,112009663 PRJEB30076,ERX2979502,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147546,TotalRNA_3h_n2,Illumina HiSeq 2500,ERR2976744,11299566,305079262 PRJEB30076,ERX2979503,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147547,TotalRNA_3h_n3,Illumina HiSeq 2500,ERR2976745,7169019,210001916 PRJEB31666,ERX3245944,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417311,new1_KO_20C_riboseq_S6,Illumina HiSeq 2500,ERR3218426,42524298,2168739198 PRJEB31666,ERX3245945,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417312,new1_KO_20C_riboseq_S8,Illumina HiSeq 2500,ERR3218427,47049069,2399502519 PRJEB31666,ERX3245946,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417313,new1_KO_20C_rnaseq_S26,Illumina HiSeq 2500,ERR3218428,19253626,981934926 PRJEB31666,ERX3245947,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417314,new1_KO_20C_rnaseq_S28,Illumina HiSeq 2500,ERR3218429,17912055,913514805 PRJEB31666,ERX3245948,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417315,new1_KO_30C_riboseq_S2,Illumina HiSeq 2500,ERR3218430,41003606,2091183906 PRJEB31666,ERX3245949,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417316,new1_KO_30C_riboseq_S4,Illumina HiSeq 2500,ERR3218431,46314080,2362018080 PRJEB31666,ERX3245950,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417317,new1_KO_30C_rnaseq_S22,Illumina HiSeq 2500,ERR3218432,16606183,846915333 PRJEB31666,ERX3245951,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417318,new1_KO_30C_rnaseq_S24,Illumina HiSeq 2500,ERR3218433,20180603,1029210753 PRJEB31666,ERX3245952,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417319,WT_20C_riboseq_S5,Illumina HiSeq 2500,ERR3218434,36716398,1872536298 PRJEB31666,ERX3245953,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417320,WT_20C_riboseq_S7,Illumina HiSeq 2500,ERR3218435,39097639,1993979589 PRJEB31666,ERX3245954,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417321,WT_20C_rnaseq_S25,Illumina HiSeq 2500,ERR3218436,20712520,1056338520 PRJEB31666,ERX3245955,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417322,WT_20C_rnaseq_S27,Illumina HiSeq 2500,ERR3218437,17927270,914290770 PRJEB31666,ERX3245956,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417323,WT_30C_riboseq_S1,Illumina HiSeq 2500,ERR3218438,42073144,2145730344 PRJEB31666,ERX3245957,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417324,WT_30C_riboseq_S3,Illumina HiSeq 2500,ERR3218439,44105472,2249379072 PRJEB31666,ERX3245958,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417325,WT_30C_rnaseq_S21,Illumina HiSeq 2500,ERR3218440,32260678,1645294578 PRJEB31666,ERX3245959,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417326,WT_30C_rnaseq_S23,Illumina HiSeq 2500,ERR3218441,28075810,1431866310 PRJEB32121,ERX3303389,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563290,Sample 10,NextSeq 500,ERR3276516,55053803,2331547026 PRJEB32121,ERX3303390,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563291,Sample 5,NextSeq 500,ERR3276517,26947157,1513258341 PRJEB32121,ERX3303391,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563292,Sample 6,NextSeq 500,ERR3276518,55020617,2287339126 PRJEB32121,ERX3303392,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563293,Sample 9,NextSeq 500,ERR3276519,26710399,1628290372 PRJEB32121,ERX3303393,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563294,Sample 1,NextSeq 500,ERR3276520,24759896,1470848970 PRJEB32121,ERX3303394,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563295,Sample 11,NextSeq 500,ERR3276521,40743255,720199228 PRJEB32121,ERX3303395,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563296,Sample 12,NextSeq 500,ERR3276522,51225481,2179088593 PRJEB32121,ERX3303396,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563297,Sample 2,NextSeq 500,ERR3276523,46244710,1870162578 PRJEB32121,ERX3303397,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563298,Sample 3,NextSeq 500,ERR3276524,24691642,1389875907 PRJEB32121,ERX3303398,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563299,Sample 4,NextSeq 500,ERR3276525,45214219,1852094222 PRJEB32121,ERX3303399,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563300,Sample 7,NextSeq 500,ERR3276526,25782829,1431543565 PRJEB32121,ERX3303400,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563301,Sample 8,NextSeq 500,ERR3276527,56002673,2257682429 PRJEB32969,ERX3390678,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMEA5703368,Sample 1,NextSeq 500,ERR3366404,33896631,1214976883 PRJEB32969,ERX3390679,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMEA5703369,Sample 2,NextSeq 500,ERR3366405,41162069,1528126888 PRJEB32969,ERX3390680,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMEA5703370,Sample 3,NextSeq 500,ERR3366406,11238470,457167576 PRJEB32969,ERX3390681,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMEA5703371,Sample 4,NextSeq 500,ERR3366407,12881017,487714175 PRJEB28810,ERX3772928,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426174,mouse_elongatingSpermatids_ribo_1,Illumina HiSeq 2500,ERR3771179,, PRJEB28810,ERX3772929,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426175,mouse_elongatingSpermatids_ribo_2,Illumina HiSeq 2500,ERR3771180,, PRJEB28810,ERX3772930,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426176,mouse_elongatingSpermatids_rna_1,Illumina HiSeq 2500,ERR3771181,, PRJEB28810,ERX3772931,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426177,mouse_elongatingSpermatids_rna_2,Illumina HiSeq 2500,ERR3771182,, PRJEB28810,ERX3772932,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426178,mouse_roundSpermatids_ribo_1,Illumina HiSeq 2500,ERR3771183,219656784,22185335184 PRJEB28810,ERX3772933,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426179,mouse_roundSpermatids_ribo_2,Illumina HiSeq 2500,ERR3771184,, PRJEB28810,ERX3772934,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426180,mouse_roundSpermatids_rna_1,Illumina HiSeq 2500,ERR3771185,97775962,9875372162 PRJEB28810,ERX3772935,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426181,mouse_roundSpermatids_rna_2,Illumina HiSeq 2500,ERR3771186,, PRJEB28810,ERX3772936,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426182,mouse_spermatocytes_ribo_1,Illumina HiSeq 2500,ERR3771187,224389341,22663323441 PRJEB28810,ERX3772937,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426183,mouse_spermatocytes_ribo_2,Illumina HiSeq 2500,ERR3771188,, PRJEB28810,ERX3772938,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426184,mouse_spermatocytes_rna_1,Illumina HiSeq 2500,ERR3771189,89103148,8999417948 PRJEB28810,ERX3772939,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426185,mouse_spermatocytes_rna_2,Illumina HiSeq 2500,ERR3771190,, PRJEB28810,ERX3772940,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426186,mouse_spermatozoa_ribo_1,Illumina HiSeq 2500,ERR3771191,294527983,15020927133 PRJEB28810,ERX3772941,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426187,mouse_spermatozoa_ribo_2,Illumina HiSeq 2500,ERR3771192,, PRJEB28810,ERX3772942,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426188,mouse_spermatozoa_rna_1,Illumina HiSeq 2500,ERR3771193,70036428,3571857828 PRJEB28810,ERX3772943,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426189,mouse_spermatozoa_rna_2,Illumina HiSeq 2500,ERR3771194,, PRJEB5285,ERX385549,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341082,HeLa_Unk+Gfp_overexpression_replicate_1,Illumina HiSeq 2000,ERR419248,21602660,1101735660 PRJEB5285,ERX385547,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341080,HeLa_Gfp_expression_control_replicate_1,Illumina HiSeq 2000,ERR419249,26065903,1329361053 PRJEB5285,ERX385548,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341081,HeLa_Unk+Gfp_overexpression_replicate_3,Illumina HiSeq 2000,ERR419250,21264420,1084485420 PRJEB5285,ERX385545,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341078,HeLa_Unk+Gfp_overexpression_replicate_2,Illumina HiSeq 2000,ERR419251,21619019,1102569969 PRJEB5285,ERX385546,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341079,HeLa_Gfp_expression_control_replicate_2,Illumina HiSeq 2000,ERR419252,21819011,1112769561 PRJEB5938,ERX432361,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,7227,Drosophila melanogaster,OTHER,OTHER,other,SAMEA2421582,Kc167_RNaseI,Illumina Genome Analyzer IIx,ERR466122,54573979,2279364497 PRJEB5938,ERX432358,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,7227,Drosophila melanogaster,OTHER,OTHER,other,SAMEA2421579,Kc167_MN,Illumina Genome Analyzer IIx,ERR466123,45195752,1873531552 PRJEB5938,ERX432359,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,9606,Homo sapiens,OTHER,OTHER,other,SAMEA2421580,U2OS_MN,Illumina Genome Analyzer IIx,ERR466124,44727293,1852579997 PRJEB5938,ERX432360,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,9606,Homo sapiens,OTHER,OTHER,other,SAMEA2421581,U2OS_RNaseI,Illumina Genome Analyzer IIx,ERR466125,41623326,1799245747 PRJEB7261,ERX556151,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,246196,Mycolicibacterium smegmatis MC2 155,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2766082,smeg RNA-seq rep1,Illumina HiSeq 2500,ERR599189,89004821,4539245871 PRJEB7261,ERX556152,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,246196,Mycolicibacterium smegmatis MC2 155,OTHER,TRANSCRIPTOMIC,size fractionation,SAMEA2766083,smeg Ribo-seq rep1,Illumina HiSeq 2500,ERR599190,99829689,5091314139 PRJEB7261,ERX556153,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,246196,Mycolicibacterium smegmatis MC2 155,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2766084,smeg RNA-seq rep2,Illumina HiSeq 2500,ERR599191,100542696,5127677496 PRJEB7261,ERX556154,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,246196,Mycolicibacterium smegmatis MC2 155,OTHER,TRANSCRIPTOMIC,size fractionation,SAMEA2766085,smeg Ribo-seq rep2,Illumina HiSeq 2500,ERR599192,80612378,4111231278 PRJEB7276,ERX558436,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,3055,Chlamydomonas reinhardtii,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2769884,Chlamy-RNASeq-WT-2,Illumina HiSeq 2000,ERR601607,55247955,2707149795 PRJEB7276,ERX558438,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,3055,Chlamydomonas reinhardtii,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2769886,Chlamy-RiboSeq-WT-2,Illumina HiSeq 2000,ERR601608,26028360,1275389640 PRJEB7276,ERX558437,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2769885,MusMus-RNASeq,Illumina HiSeq 2000,ERR601609,80602120,4110708120 PRJEB7276,ERX558439,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2769887,MusMus-RiboSeq,Illumina HiSeq 2000,ERR601610,38543800,1965733800 PRJEB7282,ERX561998,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,cDNA,SAMEA2770197,Ribosome_profiling_LUs19,Illumina HiSeq 2500,ERR605044,187831868,9391593400 PRJEB7282,ERX561999,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,cDNA,SAMEA2770198,Ribosome_profiling_LUs18,Illumina HiSeq 2500,ERR605045,125136641,6256832050 PRJEB7282,ERX562000,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,cDNA,SAMEA2770199,Ribosome_profiling_LUs20,Illumina HiSeq 2500,ERR605046,169888632,8494431600 PRJEB7301,ERX575541,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130362,RyhB RNA-seq rep2,Illumina HiSeq 2500,ERR618768,204609482,5115237050 PRJEB7301,ERX575542,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130357,RyhB RNA-seq rep1,Illumina HiSeq 2500,ERR618769,66334068,3383037468 PRJEB7301,ERX575546,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130355,RyhB Ribo-seq rep2,Illumina HiSeq 2500,ERR618770,194819312,4870482800 PRJEB7301,ERX575545,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130358,control Ribo-seq rep2,Illumina HiSeq 2500,ERR618771,161912593,4047814825 PRJEB7301,ERX575543,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130361,RyhB Ribo-seq rep1,Illumina HiSeq 2500,ERR618772,69520696,3545555496 PRJEB7301,ERX575540,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130359,control RNA-seq rep1,Illumina HiSeq 2500,ERR618773,94444604,4816674804 PRJEB7301,ERX575544,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130360,control RNA-seq rep2,Illumina HiSeq 2500,ERR618774,188584261,4714606525 PRJEB7301,ERX575539,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130356,control Ribo-seq rep1,Illumina HiSeq 2500,ERR618775,48903913,2494099563 PRJNA564991,SRX6832089,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 3,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 3,376686,Flavobacterium johnsoniae UW101,OTHER,TRANSCRIPTOMIC,other,SAMN12730772,F johnsoniae culture 2016 replicate 3,Illumina HiSeq 2500,SRR10100140,19043505,440593520 PRJNA564991,SRX6832088,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 2,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 2,376686,Flavobacterium johnsoniae UW101,OTHER,TRANSCRIPTOMIC,other,SAMN12730771,F johnsoniae culture 2016 replicate 2,Illumina HiSeq 2500,SRR10100141,14410982,335664145 PRJNA564991,SRX6832087,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 1,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 1,986,Flavobacterium johnsoniae,OTHER,TRANSCRIPTOMIC,other,SAMN12730770,F johnsoniae culture 2016 replicate 1,Illumina HiSeq 2500,SRR10100142,26216828,637267461 PRJNA573922,SRX6895802,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831194,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174361,43426278,3256970850 PRJNA573922,SRX6895795,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831208,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174368,26966897,2022517275 PRJNA573922,SRX6895794,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831207,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174369,39112396,2933429700 PRJNA573922,SRX6895793,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831206,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174370,26837661,2012824575 PRJNA573922,SRX6895788,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831202,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174375,63692380,4776928500 PRJNA573922,SRX6895787,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831201,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174376,41691393,3126854475 PRJNA573922,SRX6895786,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831200,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174377,49155765,3686682375 PRJNA573922,SRX6895785,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831199,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174378,83368394,6252629550 PRJNA573922,SRX6895784,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831198,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174379,83683932,6276294900 PRJNA573922,SRX6895783,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831197,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174380,37912988,2843474100 PRJNA573922,SRX6895782,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831196,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174381,, PRJNA573922,SRX6895781,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831195,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174382,57951230,4346342250 PRJNA577942,SRX7007420,Illumina HiSeq 2500 sequencing; GSM4125802: Replicate 1 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125802: Replicate 1 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041939,Replicate 1 centrifugation harvesting ribosome profiling,Illumina HiSeq 2500,SRR10294592,24325319,1629796373 PRJNA577942,SRX7007421,Illumina HiSeq 2500 sequencing; GSM4125803: Replicate 2 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125803: Replicate 2 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041938,Replicate 2 centrifugation harvesting ribosome profiling,Illumina HiSeq 2500,SRR10294593,108269604,7037524260 PRJNA577942,SRX7007422,Illumina HiSeq 2500 sequencing; GSM4125804: Replicate 1 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125804: Replicate 1 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041936,Replicate 1 flash freeze harvesting no drugs ribosome profiling,Illumina HiSeq 2500,SRR10294594,4480382,448038200 PRJNA577942,SRX7007423,Illumina HiSeq 2500 sequencing; GSM4125805: Replicate 2 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125805: Replicate 2 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041934,Replicate 2 flash freeze harvesting no drugs ribosome profiling,Illumina HiSeq 2500,SRR10294595,8990526,449526300 PRJNA577942,SRX7007424,Illumina HiSeq 2500 sequencing; GSM4125806: Flash freeze harvesting with anisomycin ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125806: Flash freeze harvesting with anisomycin ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041933,Flash freeze harvesting with anisomycin ribosome profiling,Illumina HiSeq 2500,SRR10294596,9421109,471055450 PRJNA577942,SRX7007425,Illumina HiSeq 2500 sequencing; GSM4125807: Flash freeze harvesting with harringtonine ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125807: Flash freeze harvesting with harringtonine ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041930,Flash freeze harvesting with harringtonine ribosome profiling,Illumina HiSeq 2500,SRR10294597,16070885,1607088500 PRJNA577942,SRX7007426,Illumina HiSeq 2500 sequencing; GSM4125808: Flash freeze harvesting with serine hydroxamate ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125808: Flash freeze harvesting with serine hydroxamate ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041929,Flash freeze harvesting with serine hydroxamate ribosome profiling,Illumina HiSeq 2500,SRR10294598,15432004,1543200400 PRJNA577942,SRX7007428,Illumina HiSeq 2500 sequencing; GSM4125810: Total RNA treated with MNase ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125810: Total RNA treated with MNase ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041923,Total RNA treated with MNase ribosome profiling,Illumina HiSeq 2500,SRR10294600,8365069,418253450 PRJNA214730,SRX384923,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 1,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 1,1306155,mixed culture,OTHER,TRANSCRIPTOMIC,unspecified,SAMN02401351,Mixed parental selected mRNA fragments,Illumina HiSeq 2000,SRR1040263,112580832,4052909952 PRJNA214730,SRX385099,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome footprint fraction replicate 1,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome footprint fraction replicate 1,1306155,mixed culture,OTHER,TRANSCRIPTOMIC,unspecified,SAMN02401352,Mixed parental ribosome protected fragments replicate 1,Illumina HiSeq 2000,SRR1040415,140321514,5051574504 PRJNA214730,SRX385185,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 1,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 1,1306155,mixed culture,OTHER,TRANSCRIPTOMIC,unspecified,SAMN02401353,Mixed parental ribosome protected fragments replicate 2 lane 1,Illumina HiSeq 2000,SRR1040423,130172032,4686193152 PRJNA214730,SRX385187,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 2,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 2,1306155,mixed culture,OTHER,TRANSCRIPTOMIC,unspecified,SAMN02401354,Mixed parental ribosome protected fragments replicate 2 lane 2,Illumina HiSeq 2000,SRR1040427,171400626,6170422536 PRJNA230610,SRX387034,Illumina Genome Analyzer II sequencing; GSM1279707: Ribosome Profiling with Control siRNA; Homo sapiens; OTHER,Illumina Genome Analyzer II sequencing; GSM1279707: Ribosome Profiling with Control siRNA; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN02435722,Ribosome Profiling with Control siRNA,Illumina Genome Analyzer II,SRR1042900,21277427,893651934 PRJNA230610,SRX387035,Illumina Genome Analyzer II sequencing; GSM1279708: Ribosome Profiling with AUF1 siRNA; Homo sapiens; OTHER,Illumina Genome Analyzer II sequencing; GSM1279708: Ribosome Profiling with AUF1 siRNA; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN02435724,Ribosome Profiling with AUF1 siRNA,Illumina Genome Analyzer II,SRR1042901,22678915,952514430 PRJNA230610,SRX387036,Illumina Genome Analyzer II sequencing; GSM1279709: Ribosome Profiling with HuR siRNA; Homo sapiens; OTHER,Illumina Genome Analyzer II sequencing; GSM1279709: Ribosome Profiling with HuR siRNA; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN02435723,Ribosome Profiling with HuR siRNA,Illumina Genome Analyzer II,SRR1042902,3818427,160373934 PRJNA232843,SRX403935,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566834,ribosome profiling in rich defined media,Illumina HiSeq 2000,SRR1067765,30562326,1528116300 PRJNA232843,SRX403935,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566834,ribosome profiling in rich defined media,Illumina HiSeq 2000,SRR1067766,163797786,8353687086 PRJNA232843,SRX403935,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566834,ribosome profiling in rich defined media,Illumina HiSeq 2000,SRR1067767,60601845,3090694095 PRJNA232843,SRX403935,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566834,ribosome profiling in rich defined media,Illumina HiSeq 2000,SRR1067768,141202340,7201319340 PRJNA232843,SRX403936,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566832,ribosome profiling in minimal media 1,Illumina HiSeq 2500,SRR1067769,88792279,4528406229 PRJNA232843,SRX403936,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566832,ribosome profiling in minimal media 1,Illumina HiSeq 2500,SRR1067770,41605070,2121858570 PRJNA232843,SRX403937,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566833,ribosome profiling in minimal media 2,Illumina HiSeq 2500,SRR1067771,65430349,3336947799 PRJNA232843,SRX403937,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566833,ribosome profiling in minimal media 2,Illumina HiSeq 2500,SRR1067772,70786149,3610093599 PRJNA602917,SRX7625186,NextSeq 500 sequencing; GSM4282352: Ribosome profiling_sgABCE1-1; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM4282352: Ribosome profiling_sgABCE1-1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN13910616,Ribosome profiling_sgABCE1-1,NextSeq 500,SRR10959087,63652500,4901242500 PRJNA602917,SRX7625187,NextSeq 500 sequencing; GSM4282353: Ribosome profiling_sgABCE1-2; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM4282353: Ribosome profiling_sgABCE1-2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN13910615,Ribosome profiling_sgABCE1-2,NextSeq 500,SRR10959088,67271269,5179887713 PRJNA602917,SRX7625188,NextSeq 500 sequencing; GSM4282354: Ribosome profiling_sgNT1; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM4282354: Ribosome profiling_sgNT1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN13910614,Ribosome profiling_sgNT1,NextSeq 500,SRR10959089,91168220,7019952940 PRJNA602917,SRX7625189,NextSeq 500 sequencing; GSM4282355: Ribosome profiling_sgNT2; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM4282355: Ribosome profiling_sgNT2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN13910613,Ribosome profiling_sgNT2,NextSeq 500,SRR10959090,104512107,8047432239 PRJNA609842,SRX7829328,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82,591946,Escherichia coli LF82,RNA-Seq,OTHER,other,SAMN14260632,LF82-anaerobic,Illumina HiSeq 2500,SRR11217089,450754,10867843 PRJNA609842,SRX7829327,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82,591946,Escherichia coli LF82,RNA-Seq,OTHER,other,SAMN14260632,LF82-anaerobic,Illumina HiSeq 2500,SRR11217090,89211,1982957 PRJNA237963,SRX469443,Illumina HiSeq 2000 sequencing; GSM1326110: M2G Ribosome profiling; Caulobacter vibrioides NA1000; OTHER,Illumina HiSeq 2000 sequencing; GSM1326110: M2G Ribosome profiling; Caulobacter vibrioides NA1000; OTHER,565050,Caulobacter vibrioides NA1000,OTHER,TRANSCRIPTOMIC,other,SAMN02640191,M2G Ribosome profiling,Illumina HiSeq 2000,SRR1167750,2656902,84987700 PRJNA237963,SRX469444,Illumina HiSeq 2000 sequencing; GSM1326111: PYE Ribosome profiling; Caulobacter vibrioides NA1000; OTHER,Illumina HiSeq 2000 sequencing; GSM1326111: PYE Ribosome profiling; Caulobacter vibrioides NA1000; OTHER,565050,Caulobacter vibrioides NA1000,OTHER,TRANSCRIPTOMIC,other,SAMN02640188,PYE Ribosome profiling,Illumina HiSeq 2000,SRR1167751,4274091,130370413 PRJNA633047,SRX8346823,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931307,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794832,10913971,818547825 PRJNA633047,SRX8346822,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931307,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794833,13852845,1038963375 PRJNA633047,SRX8346821,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931306,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794834,8940111,670508325 PRJNA633047,SRX8346820,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931306,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794835,15366865,1152514875 PRJNA633047,SRX8346819,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931305,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794836,11605004,870375300 PRJNA633047,SRX8346818,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931305,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794837,23196621,1739746575 PRJNA633047,SRX8346815,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931312,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794840,9198727,689904525 PRJNA633047,SRX8346814,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931312,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794841,17944493,1345836975 PRJNA633047,SRX8346813,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931311,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794842,8435062,632629650 PRJNA633047,SRX8346812,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931311,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794843,21767715,1632578625 PRJNA633047,SRX8346811,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KOWT cells,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KOWT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931310,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794844,11905053,892878975 PRJNA633047,SRX8346810,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931310,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794845,20046166,1503462450 PRJNA633047,SRX8346809,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931309,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794846,7457075,559280625 PRJNA633047,SRX8346808,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931309,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794847,17374979,1303123425 PRJNA633047,SRX8346807,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931308,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794848,10427687,782076525 PRJNA633047,SRX8346806,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931308,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794849,19019697,1426477275 PRJNA634689,SRX8386869,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15005046,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,Illumina HiSeq 2000,SRR11836448,145591529,7279576450 PRJNA634689,SRX8386867,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15005045,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,Illumina HiSeq 2000,SRR11836450,140445387,7022269350 PRJNA634689,SRX8386865,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15005044,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,Illumina HiSeq 2000,SRR11836452,105289031,5264451550 PRJNA634689,SRX8386863,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15005043,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,Illumina HiSeq 2000,SRR11836454,220484500,11024225000 PRJNA634769,SRX8388156,Illumina NovaSeq 6000 sequencing; GSM4567011: Gcn2 WT +AA - Ribosome profiling; Mus musculus; OTHER,Illumina NovaSeq 6000 sequencing; GSM4567011: Gcn2 WT +AA - Ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15006898,Gcn2 WT +AA - Ribosome profiling,Illumina NovaSeq 6000,SRR11837742,25517300,959270048 PRJNA634769,SRX8388157,Illumina NovaSeq 6000 sequencing; GSM4567012: Gcn2 WT -Leu - Ribosome profiling; Mus musculus; OTHER,Illumina NovaSeq 6000 sequencing; GSM4567012: Gcn2 WT -Leu - Ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15006897,Gcn2 WT -Leu - Ribosome profiling,Illumina NovaSeq 6000,SRR11837743,9333359,363034141 PRJNA634769,SRX8388158,Illumina NovaSeq 6000 sequencing; GSM4567013: Gcn2 KO +AA - Ribosome profiling; Mus musculus; OTHER,Illumina NovaSeq 6000 sequencing; GSM4567013: Gcn2 KO +AA - Ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15006896,Gcn2 KO +AA - Ribosome profiling,Illumina NovaSeq 6000,SRR11837744,19672326,749452566 PRJNA634769,SRX8388159,Illumina NovaSeq 6000 sequencing; GSM4567014: Gcn2 KO -Leu - Ribosome profiling; Mus musculus; OTHER,Illumina NovaSeq 6000 sequencing; GSM4567014: Gcn2 KO -Leu - Ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15006895,Gcn2 KO -Leu - Ribosome profiling,Illumina NovaSeq 6000,SRR11837745,15327574,596032744 PRJNA644594,SRX8680381,"Illumina HiSeq 2500 sequencing; GSM4658960: Ribosome profiling from untreated cells, rep 1; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658960: Ribosome profiling from untreated cells, rep 1; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464693,"Ribosome profiling from untreated cells, rep 1",Illumina HiSeq 2500,SRR12164922,12957040,647852000 PRJNA644594,SRX8680383,"Illumina HiSeq 2500 sequencing; GSM4658962: Ribosome profiling from untreated cells, rep 2; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658962: Ribosome profiling from untreated cells, rep 2; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464691,"Ribosome profiling from untreated cells, rep 2",Illumina HiSeq 2500,SRR12164924,13572040,678602000 PRJNA644594,SRX8680385,"Illumina HiSeq 2500 sequencing; GSM4658964: Ribosome profiling from untreated cells, rep 3; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658964: Ribosome profiling from untreated cells, rep 3; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464689,"Ribosome profiling from untreated cells, rep 3",Illumina HiSeq 2500,SRR12164926,13747244,687362200 PRJNA644594,SRX8680387,"Illumina HiSeq 2500 sequencing; GSM4658966: Ribosome profiling from radicicol cells, rep 1; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658966: Ribosome profiling from radicicol cells, rep 1; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464687,"Ribosome profiling from radicicol cells, rep 1",Illumina HiSeq 2500,SRR12164928,16942016,847100800 PRJNA644594,SRX8680389,"Illumina HiSeq 2500 sequencing; GSM4658968: Ribosome profiling from radicicol cells, rep 2; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658968: Ribosome profiling from radicicol cells, rep 2; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464684,"Ribosome profiling from radicicol cells, rep 2",Illumina HiSeq 2500,SRR12164930,19204213,960210650 PRJNA644594,SRX8680391,"Illumina HiSeq 2500 sequencing; GSM4658970: Ribosome profiling from radicicol cells, rep 3; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658970: Ribosome profiling from radicicol cells, rep 3; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464682,"Ribosome profiling from radicicol cells, rep 3",Illumina HiSeq 2500,SRR12164932,18470726,923536300 PRJNA645135,SRX8699982,"Illumina HiSeq 2500 sequencing; GSM4663991: control mouse brain, SMN-specific ribosome profiling, P5, rep 1; Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM4663991: control mouse brain, SMN-specific ribosome profiling, P5, rep 1; Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15493455,"control mouse brain, SMN-specific ribosome profiling, P5, rep 1",Illumina HiSeq 2500,SRR12185464,49288500,2464425000 PRJNA645135,SRX8699983,"Illumina HiSeq 2500 sequencing; GSM4663992: control mouse brain, SMN-specific ribosome profiling, P5, rep 2; Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM4663992: control mouse brain, SMN-specific ribosome profiling, P5, rep 2; Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15493454,"control mouse brain, SMN-specific ribosome profiling, P5, rep 2",Illumina HiSeq 2500,SRR12185465,33474442,1673722100 PRJNA645135,SRX8699984,"Illumina HiSeq 2500 sequencing; GSM4663993: control mouse brain, SMN-specific ribosome profiling, P5, rep 3; Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM4663993: control mouse brain, SMN-specific ribosome profiling, P5, rep 3; Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15493464,"control mouse brain, SMN-specific ribosome profiling, P5, rep 3",Illumina HiSeq 2500,SRR12185466,85414030,4270701500 PRJNA645135,SRX8699985,"Illumina HiSeq 2500 sequencing; GSM4663994: control mouse brain, IgG control ribosome profiling, P5, rep 1; Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM4663994: control mouse brain, IgG control ribosome profiling, P5, rep 1; Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15493463,"control mouse brain, IgG control ribosome profiling, P5, rep 1",Illumina HiSeq 2500,SRR12185467,116656582,5832829100 PRJNA245106,SRX523430,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 1 of 2","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 1 of 2",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN02731565,Saccharomyces cerevisiae Ribosome profiling Wild-type,Illumina HiSeq 2500,SRR1258539,28404464,1448627664 PRJNA245106,SRX523431,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 2 of 2","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 2 of 2",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN02731565,Saccharomyces cerevisiae Ribosome profiling Wild-type,Illumina HiSeq 2500,SRR1258540,22793695,1162478445 PRJNA245106,SRX523432,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 1 of 2","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 1 of 2",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN02731566,Saccharomyces cerevisiae Ribosome profiling upf1,Illumina HiSeq 2500,SRR1258541,21727393,1108097043 PRJNA245106,SRX523433,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 2 of 2","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 2 of 2",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN02731566,Saccharomyces cerevisiae Ribosome profiling upf1,Illumina HiSeq 2500,SRR1258542,23351093,1190905743 PRJNA245106,SRX523434,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, fragmented control","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, fragmented control",4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMN02731567,"Saccharomyces cerevisiae Ribosome profiling Wild-type, fragmented control",Illumina HiSeq 2500,SRR1258543,7341479,374415429 PRJNA245106,SRX523435,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, fragmented control","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, fragmented control",4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMN02731568,"Saccharomyces cerevisiae Ribosome profiling upf1, fragmented control",Illumina HiSeq 2500,SRR1258544,7912713,403548363 PRJNA253056,SRX610794,Illumina HiSeq 2000 sequencing; GSM1415871: ribosome profiling MicL t0; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1415871: ribosome profiling MicL t0; Escherichia coli; RNA-Seq,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02866373,ribosome profiling MicL t0,Illumina HiSeq 2000,SRR1425203,18782455,595176034 PRJNA253056,SRX610795,Illumina HiSeq 2000 sequencing; GSM1415872: ribosome profiling MicL t20; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1415872: ribosome profiling MicL t20; Escherichia coli; RNA-Seq,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02866371,ribosome profiling MicL t20,Illumina HiSeq 2000,SRR1425204,28587329,869137845 PRJNA261698,SRX708004,Illumina HiSeq 2000 sequencing; GSM1509451: Ribosome profiling data of untreated E. coli cells; Escherichia coli BW25113; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1509451: Ribosome profiling data of untreated E. coli cells; Escherichia coli BW25113; RNA-Seq,679895,Escherichia coli BW25113,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03075507,Ribosome profiling data of untreated E. coli cells,Illumina HiSeq 2000,SRR1583082,22259168,1135217568 PRJNA261698,SRX708005,Illumina HiSeq 2000 sequencing; GSM1509452: Ribosome profiling data of E. coli cells treated with the antibiotic erythromycin; Escherichia coli BW25113; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1509452: Ribosome profiling data of E. coli cells treated with the antibiotic erythromycin; Escherichia coli BW25113; RNA-Seq,679895,Escherichia coli BW25113,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03075508,Ribosome profiling data of E. coli cells treated with the antibiotic erythromycin,Illumina HiSeq 2000,SRR1583083,26096770,1330935270 PRJNA261698,SRX708006,Illumina HiSeq 2000 sequencing; GSM1509453: Ribosome profiling data of E. coli cells treated with the antibiotic telithromycin; Escherichia coli BW25113; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1509453: Ribosome profiling data of E. coli cells treated with the antibiotic telithromycin; Escherichia coli BW25113; RNA-Seq,679895,Escherichia coli BW25113,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03075509,Ribosome profiling data of E. coli cells treated with the antibiotic telithromycin,Illumina HiSeq 2000,SRR1583084,23465502,1196740602 PRJNA223608,SRX367006,Illumina Genome Analyzer II sequencing; GSM1248735: mock-transfected ribosome profiling; Homo sapiens; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM1248735: mock-transfected ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02380977,mock-transfected ribosome profiling,Illumina Genome Analyzer II,SRR1598971,28443731,1023974316 PRJNA223608,SRX367000,Illumina HiSeq 2000 sequencing; GSM1248729: miR-1-transfected ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1248729: miR-1-transfected ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02380975,miR-1-transfected ribosome profiling,Illumina HiSeq 2000,SRR1598975,92575736,4628786800 PRJNA223608,SRX367003,Illumina Genome Analyzer II sequencing; GSM1248732: miR-155-transfected ribosome profiling; Homo sapiens; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM1248732: miR-155-transfected ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02380973,miR-155-transfected ribosome profiling,Illumina Genome Analyzer II,SRR1598981,29613617,1066090212 PRJNA268222,SRX765941,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216854,Rec-OE NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660328,30964025,2322301875 PRJNA268222,SRX765941,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216854,Rec-OE NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660329,39632893,2972466975 PRJNA268222,SRX765941,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216854,Rec-OE NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660330,43632403,3272430225 PRJNA268222,SRX765941,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216854,Rec-OE NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660331,38175907,2863193025 PRJNA268222,SRX765942,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216852,WT control NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660332,61772582,4632943650 PRJNA268222,SRX765942,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216852,WT control NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660333,21771791,661735742 PRJNA268222,SRX765942,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216852,WT control NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660334,30106441,2257983075 PRJNA268222,SRX765942,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216852,WT control NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660335,44297155,3322286625 PRJNA268354,SRX767133,Illumina HiSeq 2000 sequencing; GSM1553248: Ribosome profiling rep1-SiControl-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553248: Ribosome profiling rep1-SiControl-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218424,Ribosome profiling rep1-SiControl-RPF,Illumina HiSeq 2000,SRR1661491,23525682,855434980 PRJNA268354,SRX767134,Illumina HiSeq 2000 sequencing; GSM1553249: Ribosome profiling rep1-SiControl-input-ribominus; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553249: Ribosome profiling rep1-SiControl-input-ribominus; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218421,Ribosome profiling rep1-SiControl-input-ribominus,Illumina HiSeq 2000,SRR1661492,21062618,958344392 PRJNA268354,SRX767135,Illumina HiSeq 2000 sequencing; GSM1553250: Ribosome profiling rep1-SiYTHDF1_1-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553250: Ribosome profiling rep1-SiYTHDF1_1-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218422,Ribosome profiling rep1-SiYTHDF1_1-RPF,Illumina HiSeq 2000,SRR1661493,36490823,1257840702 PRJNA268354,SRX767136,Illumina HiSeq 2000 sequencing; GSM1553251: Ribosome profiling rep1-SiYTHDF1_1-input-ribominus; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553251: Ribosome profiling rep1-SiYTHDF1_1-input-ribominus; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218419,Ribosome profiling rep1-SiYTHDF1_1-input-ribominus,Illumina HiSeq 2000,SRR1661494,22039846,991227095 PRJNA268354,SRX767137,Illumina HiSeq 2000 sequencing; GSM1553252: Ribosome profiling rep2-SiControl-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553252: Ribosome profiling rep2-SiControl-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218420,Ribosome profiling rep2-SiControl-RPF,Illumina HiSeq 2000,SRR1661495,26427579,966115970 PRJNA268354,SRX767138,Illumina HiSeq 2000 sequencing; GSM1553253: Ribosome profiling rep2-SiControl-input-ribominus; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553253: Ribosome profiling rep2-SiControl-input-ribominus; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218426,Ribosome profiling rep2-SiControl-input-ribominus,Illumina HiSeq 2000,SRR1661496,26388944,1086043707 PRJNA268354,SRX767139,Illumina HiSeq 2000 sequencing; GSM1553254: Ribosome profiling rep2-SiYTHDF1_8-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553254: Ribosome profiling rep2-SiYTHDF1_8-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218425,Ribosome profiling rep2-SiYTHDF1_8-RPF,Illumina HiSeq 2000,SRR1661497,26197590,927371837 PRJNA268354,SRX767140,Illumina HiSeq 2000 sequencing; GSM1553255: Ribosome profiling rep2-SiYTHDF1_8-input-ribominus; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553255: Ribosome profiling rep2-SiYTHDF1_8-input-ribominus; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218427,Ribosome profiling rep2-SiYTHDF1_8-input-ribominus,Illumina HiSeq 2000,SRR1661498,29088381,1229624248 PRJNA272662,SRX845439,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate1,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate1,4577,Zea mays,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03284755,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,Illumina HiSeq 2500,SRR1763106,110961112,5548055600 PRJNA272662,SRX845455,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate2,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate2,4577,Zea mays,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03284755,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,Illumina HiSeq 2500,SRR1763107,132900577,6645028850 PRJNA272662,SRX847139,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate1,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate1,4577,Zea mays,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03284757,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,Illumina HiSeq 2500,SRR1765340,71262874,3563143700 PRJNA272662,SRX847143,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate2,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate2,4577,Zea mays,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03284757,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,Illumina HiSeq 2500,SRR1765360,78615417,3930770850 PRJNA277363,SRX902511,Illumina HiSeq 2000 sequencing; GSM1625823: Cotyledon (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625823: Cotyledon (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389597,Cotyledon (25-50 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840399,51640489,2582024450 PRJNA277363,SRX902513,Illumina HiSeq 2000 sequencing; GSM1625825: Cotyledon (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625825: Cotyledon (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389589,Cotyledon (25-50 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840401,77525914,7752591400 PRJNA277363,SRX902515,Illumina HiSeq 2000 sequencing; GSM1625827: Seed Coat (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625827: Seed Coat (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389599,Seed Coat (25-50 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840403,50150107,2507505350 PRJNA277363,SRX902517,Illumina HiSeq 2000 sequencing; GSM1625829: Seed Coat (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625829: Seed Coat (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389600,Seed Coat (25-50 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840405,58241888,2912094400 PRJNA277363,SRX902519,Illumina HiSeq 2000 sequencing; GSM1625831: Cotyledon (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625831: Cotyledon (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389590,Cotyledon (100-200 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840407,86277212,4313860600 PRJNA277363,SRX902521,Illumina HiSeq 2000 sequencing; GSM1625833: Cotyledon (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625833: Cotyledon (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389603,Cotyledon (100-200 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840409,100907777,10090777700 PRJNA277363,SRX902523,Illumina HiSeq 2000 sequencing; GSM1625835: Seed Coat (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625835: Seed Coat (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389594,Seed Coat (100-200 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840411,57960236,2898011800 PRJNA277363,SRX902525,Illumina HiSeq 2000 sequencing; GSM1625837: Seed Coat (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625837: Seed Coat (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389593,Seed Coat (100-200 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840413,72276634,3613831700 PRJNA277363,SRX902527,Illumina HiSeq 2000 sequencing; GSM1625839: Cotyledon (300-400 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625839: Cotyledon (300-400 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389601,Cotyledon (300-400 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840415,82331167,4116558350 PRJNA277363,SRX902529,Illumina HiSeq 2000 sequencing; GSM1625841: Cotyledon (300-400 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625841: Cotyledon (300-400 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389595,Cotyledon (300-400 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840417,66026031,3301301550 PRJNA280809,SRX986365,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470223,Ribosome Profiling control replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964306,39082700,1954135000 PRJNA280809,SRX986365,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470223,Ribosome Profiling control replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964307,52274080,2613704000 PRJNA280809,SRX986365,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470223,Ribosome Profiling control replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964308,29216820,1460841000 PRJNA280809,SRX986366,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470224,Ribosome Profiling control replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964309,46953344,2347667200 PRJNA280809,SRX986366,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470224,Ribosome Profiling control replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964310,67731496,3386574800 PRJNA280809,SRX986366,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470224,Ribosome Profiling control replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964311,22651281,1132564050 PRJNA280809,SRX986367,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470225,Ribosome Profiling harringtonine replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964312,46189851,2309492550 PRJNA280809,SRX986367,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470225,Ribosome Profiling harringtonine replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964313,65269559,3263477950 PRJNA280809,SRX986367,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470225,Ribosome Profiling harringtonine replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964314,21259213,1062960650 PRJNA280809,SRX986368,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470226,Ribosome Profiling harringtonine replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964315,43321863,2166093150 PRJNA280809,SRX986368,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470226,Ribosome Profiling harringtonine replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964316,56929421,2846471050 PRJNA280809,SRX986368,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470226,Ribosome Profiling harringtonine replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964317,22068321,1103416050 PRJNA280809,SRX986369,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470227,Ribosome Profiling pateamineA replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964318,44125437,2206271850 PRJNA280809,SRX986369,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470227,Ribosome Profiling pateamineA replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964319,61197424,3059871200 PRJNA280809,SRX986369,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470227,Ribosome Profiling pateamineA replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964320,30423239,1521161950 PRJNA280809,SRX986370,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470228,Ribosome Profiling pateamineA replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964321,50476436,2523821800 PRJNA280809,SRX986370,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470228,Ribosome Profiling pateamineA replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964322,72527646,3626382300 PRJNA280809,SRX986370,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470228,Ribosome Profiling pateamineA replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964323,25168492,1258424600 PRJNA280809,SRX986371,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470229,Ribosome Profiling puromycin replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964324,35262036,1763101800 PRJNA280809,SRX986371,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470229,Ribosome Profiling puromycin replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964325,24502833,1225141650 PRJNA280809,SRX986371,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470229,Ribosome Profiling puromycin replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964326,27538483,1376924150 PRJNA280809,SRX986372,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470230,Ribosome Profiling puromycin replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964327,34155138,1707756900 PRJNA280809,SRX986372,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470230,Ribosome Profiling puromycin replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964328,23825786,1191289300 PRJNA280809,SRX986372,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470230,Ribosome Profiling puromycin replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964329,23506757,1175337850 PRJNA282016,SRX1006950,Illumina HiSeq 2000 sequencing; GSM1665594: swarmer M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665594: swarmer M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565828,swarmer M2G ribosome profiling,Illumina HiSeq 2000,SRR1991275,20703090,660389778 PRJNA282016,SRX1006951,Illumina HiSeq 2000 sequencing; GSM1665595: early stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665595: early stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565829,early stalk M2G ribosome profiling,Illumina HiSeq 2000,SRR1991276,80717688,2400826270 PRJNA282016,SRX1006952,Illumina HiSeq 2000 sequencing; GSM1665596: late stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665596: late stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565830,late stalk M2G ribosome profiling,Illumina HiSeq 2000,SRR1991277,22993484,674619628 PRJNA282016,SRX1006953,Illumina HiSeq 2000 sequencing; GSM1665597: early prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665597: early prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565832,early prediv M2G ribosome profiling,Illumina HiSeq 2000,SRR1991278,17278060,518095336 PRJNA282016,SRX1006954,Illumina HiSeq 2000 sequencing; GSM1665598: late prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665598: late prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565831,late prediv M2G ribosome profiling,Illumina HiSeq 2000,SRR1991279,20443469,604238206 PRJNA282016,SRX1006955,Illumina HiSeq 2000 sequencing; GSM1665599: post division M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665599: post division M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565833,post division M2G ribosome profiling,Illumina HiSeq 2000,SRR1991280,13538820,382410272 PRJNA282960,SRX1017035,"Illumina HiSeq 2500 sequencing; GSM1666805: ATF4-/- ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666805: ATF4-/- ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581119,"ATF4-/- ER ribosome profiling, untreated (rep 1)",Illumina HiSeq 2500,SRR2007064,19223712,980409312 PRJNA282960,SRX1017036,"Illumina HiSeq 2500 sequencing; GSM1666806: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666806: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581120,"ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007065,20859677,1063843527 PRJNA282960,SRX1017037,"Illumina HiSeq 2500 sequencing; GSM1666807: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666807: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581117,"ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007066,22014222,1122725322 PRJNA282960,SRX1017038,"Illumina HiSeq 2500 sequencing; GSM1666808: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666808: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581118,"ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007067,21063979,1074262929 PRJNA282960,SRX1017039,"Illumina HiSeq 2500 sequencing; GSM1666809: ATF4-/- ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666809: ATF4-/- ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581121,"ATF4-/- ER ribosome profiling, 1 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007068,22870593,1166400243 PRJNA282960,SRX1017040,"Illumina HiSeq 2500 sequencing; GSM1666810: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666810: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581122,"ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007069,21153634,1078835334 PRJNA282960,SRX1017041,"Illumina HiSeq 2500 sequencing; GSM1666811: ATF4-/- ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666811: ATF4-/- ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581123,"ATF4-/- ER ribosome profiling, 2 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007070,23215960,1184013960 PRJNA282960,SRX1017042,"Illumina HiSeq 2500 sequencing; GSM1666812: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666812: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581124,"ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007071,22260855,1135303605 PRJNA282960,SRX1017043,"Illumina HiSeq 2500 sequencing; GSM1666813: ATF4-/- ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666813: ATF4-/- ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581125,"ATF4-/- ER ribosome profiling, 4 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007072,23138057,1180040907 PRJNA282960,SRX1017044,"Illumina HiSeq 2500 sequencing; GSM1666814: ATF4-/- cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666814: ATF4-/- cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581126,"ATF4-/- cytosol ribosome profiling, untreated (rep 1)",Illumina HiSeq 2500,SRR2007073,22787710,1162173210 PRJNA282960,SRX1017045,"Illumina HiSeq 2500 sequencing; GSM1666815: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666815: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581127,"ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007074,20343583,1037522733 PRJNA282960,SRX1017046,"Illumina HiSeq 2500 sequencing; GSM1666816: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666816: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581128,"ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007075,20132638,1026764538 PRJNA282960,SRX1017047,"Illumina HiSeq 2500 sequencing; GSM1666817: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666817: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581129,"ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007076,20134079,1026838029 PRJNA282960,SRX1017048,"Illumina HiSeq 2500 sequencing; GSM1666818: ATF4-/- ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666818: ATF4-/- ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581130,"ATF4-/- ER ribosome profiling, 1 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007077,22615405,1153385655 PRJNA282960,SRX1017049,"Illumina HiSeq 2500 sequencing; GSM1666819: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666819: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581131,"ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007078,20873353,1064541003 PRJNA282960,SRX1017050,"Illumina HiSeq 2500 sequencing; GSM1666820: ATF4-/- ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666820: ATF4-/- ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581132,"ATF4-/- ER ribosome profiling, 2 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007079,21371573,1089950223 PRJNA282960,SRX1017051,"Illumina HiSeq 2500 sequencing; GSM1666821: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666821: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581133,"ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007080,21983441,1121155491 PRJNA282960,SRX1017052,"Illumina HiSeq 2500 sequencing; GSM1666822: ATF4-/- ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666822: ATF4-/- ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581134,"ATF4-/- ER ribosome profiling, 4 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007081,22835371,1164603921 PRJNA282960,SRX1017053,"Illumina HiSeq 2500 sequencing; GSM1666823: ATF4-/- cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666823: ATF4-/- cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581135,"ATF4-/- cytosol ribosome profiling, untreated (rep 2)",Illumina HiSeq 2500,SRR2007082,20677901,1054572951 PRJNA282960,SRX1017054,"Illumina HiSeq 2500 sequencing; GSM1666824: ATF4-/- ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666824: ATF4-/- ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581057,"ATF4-/- ER ribosome profiling, untreated (rep 2)",Illumina HiSeq 2500,SRR2007083,21128656,1077561456 PRJNA282960,SRX1017055,"Illumina HiSeq 2500 sequencing; GSM1666825: eIF2A S51A ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666825: eIF2A S51A ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581058,"eIF2A S51A ER ribosome profiling, untreated (rep 1)",Illumina HiSeq 2500,SRR2007084,16251551,828829101 PRJNA282960,SRX1017056,"Illumina HiSeq 2500 sequencing; GSM1666826: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666826: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581059,"eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007085,18983118,968139018 PRJNA282960,SRX1017057,"Illumina HiSeq 2500 sequencing; GSM1666827: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666827: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581060,"eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007086,15833217,807494067 PRJNA282960,SRX1017058,"Illumina HiSeq 2500 sequencing; GSM1666828: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666828: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581061,"eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007087,17567181,895926231 PRJNA282960,SRX1017059,"Illumina HiSeq 2500 sequencing; GSM1666829: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666829: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581062,"eIF2A S51A ER ribosome profiling, 1 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007088,19935281,1016699331 PRJNA282960,SRX1017060,"Illumina HiSeq 2500 sequencing; GSM1666830: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666830: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581063,"eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007089,15247010,777597510 PRJNA282960,SRX1017061,"Illumina HiSeq 2500 sequencing; GSM1666831: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666831: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581064,"eIF2A S51A ER ribosome profiling, 2 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007090,13881251,707943801 PRJNA282960,SRX1017062,"Illumina HiSeq 2500 sequencing; GSM1666832: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666832: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581065,"eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007091,17489985,891989235 PRJNA282960,SRX1017063,"Illumina HiSeq 2500 sequencing; GSM1666833: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666833: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581066,"eIF2A S51A ER ribosome profiling, 4 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007092,15210074,775713774 PRJNA282960,SRX1017064,"Illumina HiSeq 2500 sequencing; GSM1666834: eIF2A S51A cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666834: eIF2A S51A cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581067,"eIF2A S51A cytosol ribosome profiling, untreated (rep 1)",Illumina HiSeq 2500,SRR2007093,17142687,874277037 PRJNA282960,SRX1017065,"Illumina HiSeq 2500 sequencing; GSM1666835: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666835: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581068,"eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007094,20026160,1021334160 PRJNA282960,SRX1017066,"Illumina HiSeq 2500 sequencing; GSM1666836: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666836: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581069,"eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007095,18703857,953896707 PRJNA282960,SRX1017067,"Illumina HiSeq 2500 sequencing; GSM1666837: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666837: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581070,"eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007096,23577690,1202462190 PRJNA282960,SRX1017068,"Illumina HiSeq 2500 sequencing; GSM1666838: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666838: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581071,"eIF2A S51A ER ribosome profiling, 1 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007097,24731497,1261306347 PRJNA282960,SRX1017069,"Illumina HiSeq 2500 sequencing; GSM1666839: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666839: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581072,"eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007098,21716584,1107545784 PRJNA282960,SRX1017070,"Illumina HiSeq 2500 sequencing; GSM1666840: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666840: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581073,"eIF2A S51A ER ribosome profiling, 2 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007099,23696982,1208546082 PRJNA282960,SRX1017071,"Illumina HiSeq 2500 sequencing; GSM1666841: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666841: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581074,"eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007100,24517717,1250403567 PRJNA282960,SRX1017072,"Illumina HiSeq 2500 sequencing; GSM1666842: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666842: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581075,"eIF2A S51A ER ribosome profiling, 4 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007101,20573167,1049231517 PRJNA282960,SRX1017073,"Illumina HiSeq 2500 sequencing; GSM1666843: eIF2A S51A cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666843: eIF2A S51A cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581076,"eIF2A S51A cytosol ribosome profiling, untreated (rep 2)",Illumina HiSeq 2500,SRR2007102,20689853,1055182503 PRJNA282960,SRX1017074,"Illumina HiSeq 2500 sequencing; GSM1666844: eIF2A S51A ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666844: eIF2A S51A ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581077,"eIF2A S51A ER ribosome profiling, untreated (rep 2)",Illumina HiSeq 2500,SRR2007103,20314148,1036021548 PRJNA282960,SRX1017479,"Illumina HiSeq 2500 sequencing; GSM1674110: WT cytosol ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674110: WT cytosol ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581028,"WT cytosol ribosome profiling, 0.5 h Tg (rep1)",Illumina HiSeq 2500,SRR2007769,17607850,898000350 PRJNA282960,SRX1017480,"Illumina HiSeq 2500 sequencing; GSM1674111: WT cytosol ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674111: WT cytosol ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581029,"WT cytosol ribosome profiling, 0.5 h Tg (rep2)",Illumina HiSeq 2500,SRR2007770,8004515,408230265 PRJNA282960,SRX1017481,"Illumina HiSeq 2500 sequencing; GSM1674112: WT ER ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674112: WT ER ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581030,"WT ER ribosome profiling, 0.5 h Tg (rep1)",Illumina HiSeq 2500,SRR2007771,34274786,1748014086 PRJNA282960,SRX1017482,"Illumina HiSeq 2500 sequencing; GSM1674113: WT ER ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674113: WT ER ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581031,"WT ER ribosome profiling, 0.5 h Tg (rep2)",Illumina HiSeq 2500,SRR2007772,44962240,2293074240 PRJNA282960,SRX1017483,"Illumina HiSeq 2500 sequencing; GSM1674114: WT cytosol ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674114: WT cytosol ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581032,"WT cytosol ribosome profiling, 1 h Tg (rep1)",Illumina HiSeq 2500,SRR2007773,60458951,3083406501 PRJNA282960,SRX1017484,"Illumina HiSeq 2500 sequencing; GSM1674115: WT cytosol ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674115: WT cytosol ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581033,"WT cytosol ribosome profiling, 1 h Tg (rep2)",Illumina HiSeq 2500,SRR2007774,5600537,285627387 PRJNA282960,SRX1017485,"Illumina HiSeq 2500 sequencing; GSM1674116: WT ER ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674116: WT ER ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581034,"WT ER ribosome profiling, 1 h Tg (rep1)",Illumina HiSeq 2500,SRR2007775,29433660,1501116660 PRJNA282960,SRX1017486,"Illumina HiSeq 2500 sequencing; GSM1674117: WT ER ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674117: WT ER ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581035,"WT ER ribosome profiling, 1 h Tg (rep2)",Illumina HiSeq 2500,SRR2007776,27741791,1414831341 PRJNA282960,SRX1017487,"Illumina HiSeq 2500 sequencing; GSM1674118: WT cytosol ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674118: WT cytosol ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581036,"WT cytosol ribosome profiling, 2 h Tg (rep1)",Illumina HiSeq 2500,SRR2007777,20792693,1060427343 PRJNA282960,SRX1017488,"Illumina HiSeq 2500 sequencing; GSM1674119: WT cytosol ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674119: WT cytosol ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581037,"WT cytosol ribosome profiling, 2 h Tg (rep2)",Illumina HiSeq 2500,SRR2007778,7300567,372328917 PRJNA282960,SRX1017489,"Illumina HiSeq 2500 sequencing; GSM1674120: WT ER ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674120: WT ER ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581038,"WT ER ribosome profiling, 2 h Tg (rep1)",Illumina HiSeq 2500,SRR2007779,17578993,896528643 PRJNA282960,SRX1017490,"Illumina HiSeq 2500 sequencing; GSM1674121: WT ER ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674121: WT ER ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581039,"WT ER ribosome profiling, 2 h Tg (rep2)",Illumina HiSeq 2500,SRR2007780,16585777,845874627 PRJNA282960,SRX1017491,"Illumina HiSeq 2500 sequencing; GSM1674122: WT cytosol ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674122: WT cytosol ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581040,"WT cytosol ribosome profiling, 4 h Tg (rep1)",Illumina HiSeq 2500,SRR2007781,20561299,1048626249 PRJNA282960,SRX1017492,"Illumina HiSeq 2500 sequencing; GSM1674123: WT cytosol ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674123: WT cytosol ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581041,"WT cytosol ribosome profiling, 4 h Tg (rep2)",Illumina HiSeq 2500,SRR2007782,15876938,809723838 PRJNA282960,SRX1017493,"Illumina HiSeq 2500 sequencing; GSM1674124: WT ER ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674124: WT ER ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581042,"WT ER ribosome profiling, 4 h Tg (rep1)",Illumina HiSeq 2500,SRR2007783,8558520,436484520 PRJNA282960,SRX1017494,"Illumina HiSeq 2500 sequencing; GSM1674125: WT ER ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674125: WT ER ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581043,"WT ER ribosome profiling, 4 h Tg (rep2)",Illumina HiSeq 2500,SRR2007784,35387962,1804786062 PRJNA282960,SRX1017495,"Illumina HiSeq 2500 sequencing; GSM1674126: WT cytosol ribosome profiling, no Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674126: WT cytosol ribosome profiling, no Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581044,"WT cytosol ribosome profiling, no Tg (rep1)",Illumina HiSeq 2500,SRR2007785,11957757,609845607 PRJNA282960,SRX1017496,"Illumina HiSeq 2500 sequencing; GSM1674127: WT cytosol ribosome profiling, no Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674127: WT cytosol ribosome profiling, no Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581045,"WT cytosol ribosome profiling, no Tg (rep2)",Illumina HiSeq 2500,SRR2007786,14492687,739127037 PRJNA282960,SRX1017497,"Illumina HiSeq 2500 sequencing; GSM1674128: WT ER ribosome profiling, no Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674128: WT ER ribosome profiling, no Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581046,"WT ER ribosome profiling, no Tg (rep1)",Illumina HiSeq 2500,SRR2007787,20017242,1020879342 PRJNA282960,SRX1017498,"Illumina HiSeq 2500 sequencing; GSM1674129: WT ER ribosome profiling, no Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674129: WT ER ribosome profiling, no Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581047,"WT ER ribosome profiling, no Tg (rep2)",Illumina HiSeq 2500,SRR2007788,14374170,733082670 PRJNA285515,SRX1045363,Illumina HiSeq 2000 paired end sequencing; Shield Stage Embryos matched to Ribosome Profiling,Illumina HiSeq 2000 paired end sequencing; Shield Stage Embryos matched to Ribosome Profiling,7955,Danio rerio,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03754651,Danio rerio Shield Stage Embryos RNA-Seq,Illumina HiSeq 2000,SRR2047225,48328189,7345884728 PRJNA285961,SRX1050328,Illumina HiSeq 2500 sequencing; GSM1704503: 6 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704503: 6 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763400,6 h infection cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052911,16250647,828782997 PRJNA285961,SRX1050329,Illumina HiSeq 2500 sequencing; GSM1704504: 6 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704504: 6 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763401,6 h infection ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052912,18073831,921765381 PRJNA285961,SRX1050330,Illumina HiSeq 2500 sequencing; GSM1704505: 12 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704505: 12 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763402,12 h infection cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052913,18948536,966375336 PRJNA285961,SRX1050331,Illumina HiSeq 2500 sequencing; GSM1704506: 12 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704506: 12 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763403,12 h infection ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052914,26865068,1370118468 PRJNA285961,SRX1050332,Illumina HiSeq 2500 sequencing; GSM1704507: 24 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704507: 24 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763404,24 h infection cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052915,26423896,1347618696 PRJNA285961,SRX1050333,Illumina HiSeq 2500 sequencing; GSM1704508: 24 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704508: 24 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763405,24 h infection ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052916,13129805,669620055 PRJNA285961,SRX1050334,Illumina HiSeq 2500 sequencing; GSM1704509: 40 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704509: 40 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763406,40 h infection cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052917,31892235,1626503985 PRJNA285961,SRX1050335,Illumina HiSeq 2500 sequencing; GSM1704510: 40 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704510: 40 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763407,40 h infection ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052918,34039497,1736014347 PRJNA285961,SRX1050336,Illumina HiSeq 2500 sequencing; GSM1704511: Interferon treatment cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704511: Interferon treatment cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763408,Interferon treatment cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052919,11895393,606665043 PRJNA285961,SRX1050337,Illumina HiSeq 2500 sequencing; GSM1704512: Interferon treatment ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704512: Interferon treatment ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763409,Interferon treatment ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052920,7444252,379656852 PRJNA285961,SRX1050338,Illumina HiSeq 2500 sequencing; GSM1704513: Uninfected cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704513: Uninfected cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763410,Uninfected cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052921,14469150,737926650 PRJNA285961,SRX1050339,Illumina HiSeq 2500 sequencing; GSM1704514: Uninfected ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704514: Uninfected ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763411,Uninfected ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052922,14972823,763613973 PRJNA285961,SRX1050340,Illumina HiSeq 2500 sequencing; GSM1704515: 6 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704515: 6 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763412,6 h infection cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052923,3399547,173376897 PRJNA285961,SRX1050341,Illumina HiSeq 2500 sequencing; GSM1704516: 6 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704516: 6 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763413,6 h infection ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052924,6698199,341608149 PRJNA285961,SRX1050342,Illumina HiSeq 2500 sequencing; GSM1704517: 12 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704517: 12 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763414,12 h infection cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052925,751226,38312526 PRJNA285961,SRX1050343,Illumina HiSeq 2500 sequencing; GSM1704518: 12 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704518: 12 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763415,12 h infection ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052926,6988731,356425281 PRJNA285961,SRX1050344,Illumina HiSeq 2500 sequencing; GSM1704519: 24 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704519: 24 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763416,24 h infection cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052927,6813487,347487837 PRJNA285961,SRX1050345,Illumina HiSeq 2500 sequencing; GSM1704520: 24 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704520: 24 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763417,24 h infection ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052928,6242440,318364440 PRJNA285961,SRX1050346,Illumina HiSeq 2500 sequencing; GSM1704521: 40 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704521: 40 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763418,40 h infection cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052929,3488237,177900087 PRJNA285961,SRX1050347,Illumina HiSeq 2500 sequencing; GSM1704522: 40 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704522: 40 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763419,40 h infection ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052930,5860692,298895292 PRJNA285961,SRX1050348,Illumina HiSeq 2500 sequencing; GSM1704523: Interferon treatment cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704523: Interferon treatment cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763420,Interferon treatment cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052931,4934701,251669751 PRJNA285961,SRX1050349,Illumina HiSeq 2500 sequencing; GSM1704524: Interferon treatment ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704524: Interferon treatment ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763423,Interferon treatment ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052932,2421308,123486708 PRJNA285961,SRX1050350,Illumina HiSeq 2500 sequencing; GSM1704525: Uninfected cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704525: Uninfected cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763424,Uninfected cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052933,4141321,211207371 PRJNA285961,SRX1050351,Illumina HiSeq 2500 sequencing; GSM1704526: Uninfected ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704526: Uninfected ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763425,Uninfected ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052934,8749582,446228682 PRJNA285961,SRX1050352,Illumina HiSeq 2500 sequencing; GSM1704527: 6 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704527: 6 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763426,6 h infection cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052935,17150043,874652193 PRJNA285961,SRX1050353,Illumina HiSeq 2500 sequencing; GSM1704528: 6 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704528: 6 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763427,6 h infection ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052936,16165711,824451261 PRJNA285961,SRX1050354,Illumina HiSeq 2500 sequencing; GSM1704529: 12 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704529: 12 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763428,12 h infection cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052937,17650994,900200694 PRJNA285961,SRX1050355,Illumina HiSeq 2500 sequencing; GSM1704530: 12 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704530: 12 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763421,12 h infection ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052938,18658813,951599463 PRJNA285961,SRX1050356,Illumina HiSeq 2500 sequencing; GSM1704531: 24 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704531: 24 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763422,24 h infection cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052939,16313320,831979320 PRJNA285961,SRX1050357,Illumina HiSeq 2500 sequencing; GSM1704532: 24 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704532: 24 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763429,24 h infection ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052940,15616355,796434105 PRJNA285961,SRX1050358,Illumina HiSeq 2500 sequencing; GSM1704533: 40 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704533: 40 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763370,40 h infection cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052941,12189412,621660012 PRJNA285961,SRX1050359,Illumina HiSeq 2500 sequencing; GSM1704534: 40 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704534: 40 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763371,40 h infection ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052942,15349821,782840871 PRJNA285961,SRX1050360,Illumina HiSeq 2500 sequencing; GSM1704535: Interferon treatment cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704535: Interferon treatment cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763372,Interferon treatment cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052943,12076928,615923328 PRJNA285961,SRX1050361,Illumina HiSeq 2500 sequencing; GSM1704536: Interferon treatment ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704536: Interferon treatment ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763373,Interferon treatment ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052944,12808901,653253951 PRJNA285961,SRX1050362,Illumina HiSeq 2500 sequencing; GSM1704537: Uninfected cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704537: Uninfected cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763374,Uninfected cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052945,19895121,1014651171 PRJNA285961,SRX1050363,Illumina HiSeq 2500 sequencing; GSM1704538: Uninfected ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704538: Uninfected ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763375,Uninfected ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052946,22208615,1132639365 PRJNA285961,SRX1050364,Illumina HiSeq 2500 sequencing; GSM1704539: 6 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704539: 6 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763376,6 h infection cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052947,2910736,148447536 PRJNA285961,SRX1050365,Illumina HiSeq 2500 sequencing; GSM1704540: 6 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704540: 6 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763377,6 h infection ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052948,2339594,119319294 PRJNA285961,SRX1050366,Illumina HiSeq 2500 sequencing; GSM1704541: 12 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704541: 12 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763378,12 h infection cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052949,3846689,196181139 PRJNA285961,SRX1050367,Illumina HiSeq 2500 sequencing; GSM1704542: 12 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704542: 12 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763379,12 h infection ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052950,2870385,146389635 PRJNA285961,SRX1050368,Illumina HiSeq 2500 sequencing; GSM1704543: 24 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704543: 24 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763380,24 h infection cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052951,2087976,106486776 PRJNA285961,SRX1050369,Illumina HiSeq 2500 sequencing; GSM1704544: 24 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704544: 24 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763381,24 h infection ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052952,2291662,116874762 PRJNA285961,SRX1050370,Illumina HiSeq 2500 sequencing; GSM1704545: 40 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704545: 40 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763382,40 h infection cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052953,8358678,426292578 PRJNA285961,SRX1050371,Illumina HiSeq 2500 sequencing; GSM1704546: 40 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704546: 40 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763383,40 h infection ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052954,2257987,115157337 PRJNA285961,SRX1050372,Illumina HiSeq 2500 sequencing; GSM1704547: Interferon treatment cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704547: Interferon treatment cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763384,Interferon treatment cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052955,15968518,814394418 PRJNA285961,SRX1050373,Illumina HiSeq 2500 sequencing; GSM1704548: Interferon treatment ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704548: Interferon treatment ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763385,Interferon treatment ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052956,3080222,157091322 PRJNA285961,SRX1050374,Illumina HiSeq 2500 sequencing; GSM1704549: Uninfected cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704549: Uninfected cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763386,Uninfected cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052957,2543624,129724824 PRJNA285961,SRX1050375,Illumina HiSeq 2500 sequencing; GSM1704550: Uninfected ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704550: Uninfected ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763387,Uninfected ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052958,2587866,131981166 PRJNA285961,SRX1050400,Illumina HiSeq 2500 sequencing; GSM1704575: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704575: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763467,12 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052983,50720722,2586756822 PRJNA285961,SRX1050401,Illumina HiSeq 2500 sequencing; GSM1704576: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704576: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763468,24 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052984,32000428,1632021828 PRJNA285961,SRX1050402,Illumina HiSeq 2500 sequencing; GSM1704577: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704577: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763469,48 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052985,29304738,1494541638 PRJNA285961,SRX1050403,Illumina HiSeq 2500 sequencing; GSM1704578: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704578: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763470,6 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052986,31483076,1605636876 PRJNA285961,SRX1050404,Illumina HiSeq 2500 sequencing; GSM1704579: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704579: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763471,72 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052987,31451899,1604046849 PRJNA285961,SRX1050405,Illumina HiSeq 2500 sequencing; GSM1704580: Uninfected Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704580: Uninfected Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763472,Uninfected Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052988,30257426,1543128726 PRJNA285961,SRX1050406,Illumina HiSeq 2500 sequencing; GSM1704581: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704581: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763473,12 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052989,50837419,2592708369 PRJNA285961,SRX1050407,Illumina HiSeq 2500 sequencing; GSM1704582: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704582: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763474,24 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052990,35106005,1790406255 PRJNA285961,SRX1050408,Illumina HiSeq 2500 sequencing; GSM1704583: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704583: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763475,48 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052991,35561514,1813637214 PRJNA285961,SRX1050409,Illumina HiSeq 2500 sequencing; GSM1704584: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704584: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763476,6 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052992,34060969,1737109419 PRJNA285961,SRX1050410,Illumina HiSeq 2500 sequencing; GSM1704585: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704585: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763477,72 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052993,35772157,1824380007 PRJNA285961,SRX1050411,Illumina HiSeq 2500 sequencing; GSM1704586: Uninfected Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704586: Uninfected Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763478,Uninfected Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052994,32219386,1643188686 PRJNA285961,SRX1050412,Illumina HiSeq 2500 sequencing; GSM1704587: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704587: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763479,12 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052995,29483113,1503638763 PRJNA285961,SRX1050413,Illumina HiSeq 2500 sequencing; GSM1704588: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704588: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763480,24 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052996,27309344,1392776544 PRJNA285961,SRX1050414,Illumina HiSeq 2500 sequencing; GSM1704589: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704589: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763481,48 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052997,36128791,1842568341 PRJNA285961,SRX1050415,Illumina HiSeq 2500 sequencing; GSM1704590: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704590: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763482,6 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052998,29795235,1519556985 PRJNA285961,SRX1050416,Illumina HiSeq 2500 sequencing; GSM1704591: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704591: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763483,72 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052999,46793485,2386467735 PRJNA285961,SRX1050417,Illumina HiSeq 2500 sequencing; GSM1704592: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704592: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763484,12 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053000,33921101,1729976151 PRJNA285961,SRX1050418,Illumina HiSeq 2500 sequencing; GSM1704593: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704593: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763485,24 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053001,35278187,1799187537 PRJNA285961,SRX1050419,Illumina HiSeq 2500 sequencing; GSM1704594: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704594: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763430,48 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053002,32317528,1648193928 PRJNA285961,SRX1050420,Illumina HiSeq 2500 sequencing; GSM1704595: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704595: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763431,6 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053003,34457090,1757311590 PRJNA285961,SRX1050421,Illumina HiSeq 2500 sequencing; GSM1704596: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704596: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763432,72 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053004,40495001,2065245051 PRJNA286218,SRX1054425,Ion Torrent PGM sequencing; GSM1707652: Ribosome profiling no exercise rep1; Mus musculus; RNA-Seq,Ion Torrent PGM sequencing; GSM1707652: Ribosome profiling no exercise rep1; Mus musculus; RNA-Seq,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03766237,Ribosome profiling no exercise rep1,Ion Torrent PGM,SRR2057646,2743301,82639361 PRJNA286218,SRX1054426,Ion Torrent PGM sequencing; GSM1707653: Ribosome profiling no exercise rep2; Mus musculus; RNA-Seq,Ion Torrent PGM sequencing; GSM1707653: Ribosome profiling no exercise rep2; Mus musculus; RNA-Seq,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03766238,Ribosome profiling no exercise rep2,Ion Torrent PGM,SRR2057647,3049697,92492307 PRJNA286218,SRX1054427,Ion Torrent PGM sequencing; GSM1707654: Ribosome profiling exercise rep1; Mus musculus; RNA-Seq,Ion Torrent PGM sequencing; GSM1707654: Ribosome profiling exercise rep1; Mus musculus; RNA-Seq,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03766239,Ribosome profiling exercise rep1,Ion Torrent PGM,SRR2057648,3565792,104708331 PRJNA286218,SRX1054428,Ion Torrent PGM sequencing; GSM1707655: Ribosome profiling exercise rep2; Mus musculus; RNA-Seq,Ion Torrent PGM sequencing; GSM1707655: Ribosome profiling exercise rep2; Mus musculus; RNA-Seq,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03766240,Ribosome profiling exercise rep2,Ion Torrent PGM,SRR2057649,2673445,83153884 PRJNA286792,SRX1056749,Illumina HiSeq 2500 sequencing; GSM1709012: ER Ribosome profiling Untreated 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709012: ER Ribosome profiling Untreated 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770657,ER Ribosome profiling Untreated 1,Illumina HiSeq 2500,SRR2060674,78647403,4011017553 PRJNA286792,SRX1056750,Illumina HiSeq 2500 sequencing; GSM1709013: ER Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709013: ER Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770658,ER Ribosome profiling 0.5 h Tg 1,Illumina HiSeq 2500,SRR2060675,10680002,544680102 PRJNA286792,SRX1056751,Illumina HiSeq 2500 sequencing; GSM1709014: ER Ribosome profiling 1 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709014: ER Ribosome profiling 1 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770659,ER Ribosome profiling 1 h Tg 1,Illumina HiSeq 2500,SRR2060676,10272599,523902549 PRJNA286792,SRX1056752,Illumina HiSeq 2500 sequencing; GSM1709015: ER Ribosome profiling 2 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709015: ER Ribosome profiling 2 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770660,ER Ribosome profiling 2 h Tg 1,Illumina HiSeq 2500,SRR2060677,9291951,473889501 PRJNA286792,SRX1056753,Illumina HiSeq 2500 sequencing; GSM1709016: ER Ribosome profiling 4 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709016: ER Ribosome profiling 4 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770661,ER Ribosome profiling 4 h Tg 1,Illumina HiSeq 2500,SRR2060678,7836885,399681135 PRJNA286792,SRX1056754,Illumina HiSeq 2500 sequencing; GSM1709017: ER Ribosome profiling Untreated 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709017: ER Ribosome profiling Untreated 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770662,ER Ribosome profiling Untreated 2,Illumina HiSeq 2500,SRR2060679,12238357,624156207 PRJNA286792,SRX1056755,Illumina HiSeq 2500 sequencing; GSM1709018: ER Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709018: ER Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770663,ER Ribosome profiling 0.5 h Tg 2,Illumina HiSeq 2500,SRR2060680,27383252,1396545852 PRJNA286792,SRX1056756,Illumina HiSeq 2500 sequencing; GSM1709019: ER Ribosome profiling 1 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709019: ER Ribosome profiling 1 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770664,ER Ribosome profiling 1 h Tg 2,Illumina HiSeq 2500,SRR2060681,8062047,411164397 PRJNA286792,SRX1056757,Illumina HiSeq 2500 sequencing; GSM1709020: ER Ribosome profiling 2 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709020: ER Ribosome profiling 2 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770665,ER Ribosome profiling 2 h Tg 2,Illumina HiSeq 2500,SRR2060682,18856341,961673391 PRJNA286792,SRX1056758,Illumina HiSeq 2500 sequencing; GSM1709021: ER Ribosome profiling 4 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709021: ER Ribosome profiling 4 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770666,ER Ribosome profiling 4 h Tg 2,Illumina HiSeq 2500,SRR2060683,8565355,436833105 PRJNA286792,SRX1056759,Illumina HiSeq 2500 sequencing; GSM1709022: Cytosol Ribosome profiling Untreated 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709022: Cytosol Ribosome profiling Untreated 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770667,Cytosol Ribosome profiling Untreated 1,Illumina HiSeq 2500,SRR2060684,4063729,207250179 PRJNA286792,SRX1056760,Illumina HiSeq 2500 sequencing; GSM1709023: Cytosol Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709023: Cytosol Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770668,Cytosol Ribosome profiling 0.5 h Tg 1,Illumina HiSeq 2500,SRR2060685,29053643,1481735793 PRJNA286792,SRX1056761,Illumina HiSeq 2500 sequencing; GSM1709024: Cytosol Ribosome profiling 1 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709024: Cytosol Ribosome profiling 1 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770669,Cytosol Ribosome profiling 1 h Tg 1,Illumina HiSeq 2500,SRR2060686,64964205,3313174455 PRJNA286792,SRX1056762,Illumina HiSeq 2500 sequencing; GSM1709025: Cytosol Ribosome profiling 2 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709025: Cytosol Ribosome profiling 2 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770670,Cytosol Ribosome profiling 2 h Tg 1,Illumina HiSeq 2500,SRR2060687,21767084,1110121284 PRJNA286792,SRX1056763,Illumina HiSeq 2500 sequencing; GSM1709026: Cytosol Ribosome profiling 4 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709026: Cytosol Ribosome profiling 4 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770671,Cytosol Ribosome profiling 4 h Tg 1,Illumina HiSeq 2500,SRR2060688,24180440,1233202440 PRJNA286792,SRX1056764,Illumina HiSeq 2500 sequencing; GSM1709027: Cytosol Ribosome profiling Untreated 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709027: Cytosol Ribosome profiling Untreated 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770672,Cytosol Ribosome profiling Untreated 2,Illumina HiSeq 2500,SRR2060689,10236103,522041253 PRJNA286792,SRX1056765,Illumina HiSeq 2500 sequencing; GSM1709028: Cytosol Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709028: Cytosol Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770673,Cytosol Ribosome profiling 0.5 h Tg 2,Illumina HiSeq 2500,SRR2060690,16977612,865858212 PRJNA286792,SRX1056766,Illumina HiSeq 2500 sequencing; GSM1709029: Cytosol Ribosome profiling 1 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709029: Cytosol Ribosome profiling 1 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770674,Cytosol Ribosome profiling 1 h Tg 2,Illumina HiSeq 2500,SRR2060691,19996790,1019836290 PRJNA286792,SRX1056767,Illumina HiSeq 2500 sequencing; GSM1709030: Cytosol Ribosome profiling 2 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709030: Cytosol Ribosome profiling 2 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770675,Cytosol Ribosome profiling 2 h Tg 2,Illumina HiSeq 2500,SRR2060692,10192777,519831627 PRJNA286792,SRX1056768,Illumina HiSeq 2500 sequencing; GSM1709031: Cytosol Ribosome profiling 4 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709031: Cytosol Ribosome profiling 4 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770676,Cytosol Ribosome profiling 4 h Tg 2,Illumina HiSeq 2500,SRR2060693,24131402,1230701502 PRJNA268354,SRX1070446,Illumina HiSeq 2000 sequencing; GSM1717890: Ribosome profiling SiControl-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1717890: Ribosome profiling SiControl-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03787322,Ribosome profiling SiControl-RPF,Illumina HiSeq 2000,SRR2075417,29365657,996912114 PRJNA268354,SRX1070447,Illumina HiSeq 2000 sequencing; GSM1717891: Ribosome profiling SiControl-input-poly(A); Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1717891: Ribosome profiling SiControl-input-poly(A); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03787323,Ribosome profiling SiControl-input-poly(A),Illumina HiSeq 2000,SRR2075418,62485200,2952569004 PRJNA268354,SRX1070448,Illumina HiSeq 2000 sequencing; GSM1717892: Ribosome profiling SiMETTL3-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1717892: Ribosome profiling SiMETTL3-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03787324,Ribosome profiling SiMETTL3-RPF,Illumina HiSeq 2000,SRR2075419,25609568,1012594286 PRJNA268354,SRX1070449,Illumina HiSeq 2000 sequencing; GSM1717893: Ribosome profiling SiMETTL3-input-poly(A); Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1717893: Ribosome profiling SiMETTL3-input-poly(A); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03787325,Ribosome profiling SiMETTL3-input-poly(A),Illumina HiSeq 2000,SRR2075420,44646468,4412410928 PRJNA289569,SRX1092012,Illumina HiSeq 2500 sequencing; GSM1819217: Rluc control ribosome profiling rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819217: Rluc control ribosome profiling rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855826,Rluc control ribosome profiling rep1,Illumina HiSeq 2500,SRR2096964,40053175,2002658750 PRJNA289569,SRX1092013,Illumina HiSeq 2500 sequencing; GSM1819218: DDX3 WT ribosome profiling rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819218: DDX3 WT ribosome profiling rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855827,DDX3 WT ribosome profiling rep1,Illumina HiSeq 2500,SRR2096965,27500547,1375027350 PRJNA289569,SRX1092014,Illumina HiSeq 2500 sequencing; GSM1819219: DDX3 R534H ribosome profiling rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819219: DDX3 R534H ribosome profiling rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855828,DDX3 R534H ribosome profiling rep1,Illumina HiSeq 2500,SRR2096966,25807053,1290352650 PRJNA289569,SRX1092015,Illumina HiSeq 2500 sequencing; GSM1819220: Rluc control ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819220: Rluc control ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855829,Rluc control ribosome profiling with sodium arsenite rep1,Illumina HiSeq 2500,SRR2096967,27874521,1393726050 PRJNA289569,SRX1092016,Illumina HiSeq 2500 sequencing; GSM1819221: DDX3 WT ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819221: DDX3 WT ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855830,DDX3 WT ribosome profiling with sodium arsenite rep1,Illumina HiSeq 2500,SRR2096968,19408923,970446150 PRJNA289569,SRX1092017,Illumina HiSeq 2500 sequencing; GSM1819222: DDX3 R534H ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819222: DDX3 R534H ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855831,DDX3 R534H ribosome profiling with sodium arsenite rep1,Illumina HiSeq 2500,SRR2096969,26932125,1346606250 PRJNA289569,SRX1092018,Illumina HiSeq 2500 sequencing; GSM1819223: Rluc control ribosome profiling rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819223: Rluc control ribosome profiling rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855832,Rluc control ribosome profiling rep2,Illumina HiSeq 2500,SRR2096970,32077723,1603886150 PRJNA289569,SRX1092019,Illumina HiSeq 2500 sequencing; GSM1819224: DDX3 WT ribosome profiling rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819224: DDX3 WT ribosome profiling rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855833,DDX3 WT ribosome profiling rep2,Illumina HiSeq 2500,SRR2096971,26066702,1303335100 PRJNA289569,SRX1092020,Illumina HiSeq 2500 sequencing; GSM1819225: DDX3 R534H ribosome profiling rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819225: DDX3 R534H ribosome profiling rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855834,DDX3 R534H ribosome profiling rep2,Illumina HiSeq 2500,SRR2096972,20450140,1022507000 PRJNA289569,SRX1092021,Illumina HiSeq 2500 sequencing; GSM1819226: Rluc control ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819226: Rluc control ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855835,Rluc control ribosome profiling with sodium arsenite rep2,Illumina HiSeq 2500,SRR2096973,20927350,1046367500 PRJNA289569,SRX1092022,Illumina HiSeq 2500 sequencing; GSM1819227: DDX3 WT ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819227: DDX3 WT ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855836,DDX3 WT ribosome profiling with sodium arsenite rep2,Illumina HiSeq 2500,SRR2096974,27176847,1358842350 PRJNA289569,SRX1092023,Illumina HiSeq 2500 sequencing; GSM1819228: DDX3 R534H ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819228: DDX3 R534H ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855837,DDX3 R534H ribosome profiling with sodium arsenite rep2,Illumina HiSeq 2500,SRR2096975,28797113,1439855650 PRJNA296059,SRX1254413,Illumina HiSeq 2000 sequencing; GSM1887643: ribosome profiling; Homo sapiens; miRNA-Seq,Illumina HiSeq 2000 sequencing; GSM1887643: ribosome profiling; Homo sapiens; miRNA-Seq,9606,Homo sapiens,miRNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN04093818,ribosome profiling,Illumina HiSeq 2000,SRR2433794,31967082,916773615 PRJNA299254,SRX1356474,NextSeq 500 sequencing; Ribosome profiling of lactimidomycin treated Jurkat cells,NextSeq 500 sequencing; Ribosome profiling of lactimidomycin treated Jurkat cells,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMN04195657,Lactimidomycin treated Jurkat cells,NextSeq 500,SRR2732970,378053973,28732101948 PRJNA299254,SRX1356478,NextSeq 500 sequencing; Ribosome profiling of cycloheximide treated Jurkat cells,NextSeq 500 sequencing; Ribosome profiling of cycloheximide treated Jurkat cells,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMN04195655,Cycloheximide treated Jurkat cells,NextSeq 500,SRR2733100,388812515,29549751140 PRJNA311041,SRX1562724,Illumina HiSeq 2000 sequencing; GSM2055244: ribosome profiling 37°C in WT; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM2055244: ribosome profiling 37°C in WT; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN04457972,ribosome profiling 37°C in WT,Illumina HiSeq 2000,SRR3147100,61258516,3124184316 PRJNA314248,SRX1616307,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04531072,Ribosome profiling of HEK293 cells,Illumina HiSeq 2000,SRR3208296,44716778,1265915396 PRJNA314248,SRX1616308,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN04531073,Ribosome profiling of MEF cells,Illumina HiSeq 2000,SRR3208406,23534216,729844417 PRJNA314248,SRX1616309,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with WT 18S rRNA,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with WT 18S rRNA,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN04531074,Ribosome profiling of MEF cells transfected with WT 18S rRNA,Illumina HiSeq 2000,SRR3208450,27696228,850735689 PRJNA314248,SRX1616310,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with mutant 18S rRNA,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with mutant 18S rRNA,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN04531075,Ribosome profiling of MEF cells transfected with mutant 18S rRNA,Illumina HiSeq 2000,SRR3208452,59116544,1698553234 PRJNA316125,SRX1657158,Illumina HiSeq 2500 sequencing; GSM2097522: HBE cells ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM2097522: HBE cells ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN04576208,HBE cells ribosome profiling,Illumina HiSeq 2500,SRR3286543,110777954,5538897700 PRJNA316125,SRX1657159,Illumina HiSeq 2500 sequencing; GSM2097523: A549 cells ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM2097523: A549 cells ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN04576209,A549 cells ribosome profiling,Illumina HiSeq 2500,SRR3286544,95891656,4794582800 PRJNA316125,SRX1657160,Illumina HiSeq 2500 sequencing; GSM2097524: H1299 cells ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM2097524: H1299 cells ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN04576210,H1299 cells ribosome profiling,Illumina HiSeq 2500,SRR3286545,111526324,5576316200 PRJNA316618,SRX1667364,Illumina HiSeq 2000 sequencing; GSM2100596: S phase ribosome profiling replicate 1; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100596: S phase ribosome profiling replicate 1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588783,S phase ribosome profiling replicate 1,Illumina HiSeq 2000,SRR3306583,178511892,9104106492 PRJNA316618,SRX1667365,Illumina HiSeq 2000 sequencing; GSM2100597: S phase ribosome profiling replicate 2; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100597: S phase ribosome profiling replicate 2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588784,S phase ribosome profiling replicate 2,Illumina HiSeq 2000,SRR3306584,242256008,12355056408 PRJNA316618,SRX1667366,Illumina HiSeq 2000 sequencing; GSM2100598: M phase ribosome profiling replicate 1; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100598: M phase ribosome profiling replicate 1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588785,M phase ribosome profiling replicate 1,Illumina HiSeq 2000,SRR3306585,116546351,5943863901 PRJNA316618,SRX1667367,Illumina HiSeq 2000 sequencing; GSM2100599: M phase ribosome profiling replicate 2; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100599: M phase ribosome profiling replicate 2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588786,M phase ribosome profiling replicate 2,Illumina HiSeq 2000,SRR3306586,239897608,12234778008 PRJNA316618,SRX1667368,Illumina HiSeq 2000 sequencing; GSM2100600: M phase ribosome profiling synchronized by shake off; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100600: M phase ribosome profiling synchronized by shake off; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588787,M phase ribosome profiling synchronized by shake off,Illumina HiSeq 2000,SRR3306587,242516177,12368325027 PRJNA316618,SRX1667369,Illumina HiSeq 2000 sequencing; GSM2100601: Asynchronous cell ribosome profiling 1; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100601: Asynchronous cell ribosome profiling 1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588788,Asynchronous cell ribosome profiling 1,Illumina HiSeq 2000,SRR3306588,173946221,8871257271 PRJNA316618,SRX1667370,Illumina HiSeq 2000 sequencing; GSM2100602: Asynchronous cell ribosome profiling 2; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100602: Asynchronous cell ribosome profiling 2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588789,Asynchronous cell ribosome profiling 2,Illumina HiSeq 2000,SRR3306589,242417925,12363314175 PRJNA314248,SRX1616308,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN04531073,Ribosome profiling of MEF cells,Illumina HiSeq 2000,SRR3392126,60694250,1876859442 PRJNA314248,SRX1704872,Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Control for Methionine Starvation),Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Control for Methionine Starvation),9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04625643,HEK293T cells for Ribosome profiling (Control for Methionine Starvation),Illumina HiSeq 2000,SRR3392899,38333571,1136913910 PRJNA314248,SRX1704873,Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Methionine Starvation),Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Methionine Starvation),9606,Homo sapiens,OTHER,OTHER,other,SAMN04625644,HEK293T cells for Ribosome profiling (Methionine Starvation),Illumina HiSeq 2000,SRR3398188,38629161,1141710659 PRJNA344393,SRX2189156,NextSeq 500 sequencing; GSM2327825: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with lactimidomycin; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2327825: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with lactimidomycin; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN05821926,Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with lactimidomycin,NextSeq 500,SRR4293693,178964457,13601298732 PRJNA344393,SRX2189157,NextSeq 500 sequencing; GSM2327826: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with cycloheximide; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2327826: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with cycloheximide; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN05821925,Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with cycloheximide,NextSeq 500,SRR4293694,184823119,14046557044 PRJNA344393,SRX2189158,NextSeq 500 sequencing; GSM2327827: Ribosome profiling of control HCT116 cells treated with lactimidomycin; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2327827: Ribosome profiling of control HCT116 cells treated with lactimidomycin; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN05821924,Ribosome profiling of control HCT116 cells treated with lactimidomycin,NextSeq 500,SRR4293695,199563521,15166827596 PRJNA344393,SRX2189159,NextSeq 500 sequencing; GSM2327828: Ribosome profiling of control HCT116 cells treated with cycloheximide; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2327828: Ribosome profiling of control HCT116 cells treated with cycloheximide; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN05821923,Ribosome profiling of control HCT116 cells treated with cycloheximide,NextSeq 500,SRR4293696,225042166,17103204616 PRJNA348553,SRX2246398,Illumina HiSeq 2000 sequencing; GSM2346474: Ribosome profiling of wild-type ecotype Landsberg erecta treated with lactimidomycin; Arabidopsis thaliana; OTHER,Illumina HiSeq 2000 sequencing; GSM2346474: Ribosome profiling of wild-type ecotype Landsberg erecta treated with lactimidomycin; Arabidopsis thaliana; OTHER,3702,Arabidopsis thaliana,OTHER,TRANSCRIPTOMIC,other,SAMN05912771,Ribosome profiling of wild-type ecotype Landsberg erecta treated with lactimidomycin,Illumina HiSeq 2000,SRR4424237,104721382,5340790482 PRJNA348553,SRX2246399,Illumina HiSeq 2000 sequencing; GSM2346475: Ribosome profiling of wild-type ecotype Landsberg erecta treated with cycloheximide; Arabidopsis thaliana; OTHER,Illumina HiSeq 2000 sequencing; GSM2346475: Ribosome profiling of wild-type ecotype Landsberg erecta treated with cycloheximide; Arabidopsis thaliana; OTHER,3702,Arabidopsis thaliana,OTHER,TRANSCRIPTOMIC,other,SAMN05912770,Ribosome profiling of wild-type ecotype Landsberg erecta treated with cycloheximide,Illumina HiSeq 2000,SRR4424238,99524632,5075756232 PRJNA158351,SRX137370,Illumina Genome Analyzer II sequencing; GSM910953: A3-1 Ribosome profiling - siLuc; Mus musculus; OTHER,Illumina Genome Analyzer II sequencing; GSM910953: A3-1 Ribosome profiling - siLuc; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN00854339,A3-1 Ribosome profiling - siLuc,Illumina Genome Analyzer II,SRR458756,21824511,785682396 PRJNA158351,SRX137371,Illumina Genome Analyzer II sequencing; GSM910954: A3-1 Ribosome profiling - siLin28a; Mus musculus; OTHER,Illumina Genome Analyzer II sequencing; GSM910954: A3-1 Ribosome profiling - siLin28a; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN00854340,A3-1 Ribosome profiling - siLin28a,Illumina Genome Analyzer II,SRR458757,18520372,666733392 PRJNA353604,SRX2349147,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026356,335001052,16750052600 PRJNA353604,SRX2352572,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026359,66094062,3304703100 PRJNA353604,SRX2352779,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026589,125934593,6296729650 PRJNA353604,SRX2352796,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026592,109643569,5482178450 PRJNA353604,SRX2352801,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026603,139378431,6968921550 PRJNA353604,SRX2352818,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026637,138903638,6945181900 PRJNA356772,SRX2407647,NextSeq 500 sequencing; GSM2420418: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 monosomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq,NextSeq 500 sequencing; GSM2420418: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 monosomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq,216597,Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN06127036,Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 monosomes,NextSeq 500,SRR5090708,191796596,14576541296 PRJNA356772,SRX2407648,NextSeq 500 sequencing; GSM2420419: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 polysomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq,NextSeq 500 sequencing; GSM2420419: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 polysomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq,216597,Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN06127035,Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 polysomes,NextSeq 500,SRR5090709,174834326,13287408776 PRJNA340948,SRX2416031,Illumina HiSeq 4000 sequencing; GSM2424851: Ribosome profiling-siControl-RPF; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424851: Ribosome profiling-siControl-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131999,Ribosome profiling-siControl-RPF,Illumina HiSeq 4000,SRR5099275,48648149,2432407450 PRJNA340948,SRX2416032,Illumina HiSeq 4000 sequencing; GSM2424852: Ribosome profiling-siControl-input; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424852: Ribosome profiling-siControl-input; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131998,Ribosome profiling-siControl-input,Illumina HiSeq 4000,SRR5099276,46915311,2345765550 PRJNA340948,SRX2416033,Illumina HiSeq 4000 sequencing; GSM2424853: Ribosome profiling-rep1-siYTHDF3-RPF; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424853: Ribosome profiling-rep1-siYTHDF3-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131997,Ribosome profiling-rep1-siYTHDF3-RPF,Illumina HiSeq 4000,SRR5099277,41072030,2053601500 PRJNA340948,SRX2416034,Illumina HiSeq 4000 sequencing; GSM2424854: Ribosome profiling-rep1-siYTHDF3-input; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424854: Ribosome profiling-rep1-siYTHDF3-input; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131996,Ribosome profiling-rep1-siYTHDF3-input,Illumina HiSeq 4000,SRR5099278,39819574,1990978700 PRJNA340948,SRX2416035,Illumina HiSeq 4000 sequencing; GSM2424855: Ribosome profiling-rep2-siYTHDF3-RPF; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424855: Ribosome profiling-rep2-siYTHDF3-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131995,Ribosome profiling-rep2-siYTHDF3-RPF,Illumina HiSeq 4000,SRR5099279,48158932,2407946600 PRJNA340948,SRX2416036,Illumina HiSeq 4000 sequencing; GSM2424856: Ribosome profiling-rep2-siYTHDF3-input; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424856: Ribosome profiling-rep2-siYTHDF3-input; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131994,Ribosome profiling-rep2-siYTHDF3-input,Illumina HiSeq 4000,SRR5099280,54048791,2702439550 PRJNA311041,SRX2502104,Illumina HiSeq 4000 sequencing; GSM2462933: ribosome profiling 37°C in WT with control plasmid; Escherichia coli; OTHER,Illumina HiSeq 4000 sequencing; GSM2462933: ribosome profiling 37°C in WT with control plasmid; Escherichia coli; OTHER,562,Escherichia coli,OTHER,TRANSCRIPTOMIC,other,SAMN06240270,ribosome profiling 37°C in WT with control plasmid,Illumina HiSeq 4000,SRR5186136,61670104,3145175304 PRJNA311041,SRX2502105,Illumina HiSeq 4000 sequencing; GSM2462934: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUA; Escherichia coli; OTHER,Illumina HiSeq 4000 sequencing; GSM2462934: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUA; Escherichia coli; OTHER,562,Escherichia coli,OTHER,TRANSCRIPTOMIC,other,SAMN06240269,ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUA,Illumina HiSeq 4000,SRR5186137,68702208,3503812608 PRJNA311041,SRX2502106,Illumina HiSeq 4000 sequencing; GSM2462935: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUG; Escherichia coli; OTHER,Illumina HiSeq 4000 sequencing; GSM2462935: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUG; Escherichia coli; OTHER,562,Escherichia coli,OTHER,TRANSCRIPTOMIC,other,SAMN06240268,ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUG,Illumina HiSeq 4000,SRR5186138,43070262,2196583362 PRJNA369552,SRX2532339,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with harringtonine,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with harringtonine,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06289120,This sample has been submitted by pda|zhpn1024 on 2018-03-02; Homo sapiens,Illumina HiSeq 2500,SRR5223162,31545576,1608824376 PRJNA369552,SRX2532340,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with cycloheximide,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with cycloheximide,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06289120,This sample has been submitted by pda|zhpn1024 on 2018-03-02; Homo sapiens,Illumina HiSeq 2500,SRR5223163,28042962,1430191062 PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239050,8854232,451565832 PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239051,8867186,452226486 PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239052,7927705,404312955 PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239053,7894562,402622662 PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239054,9216208,470026608 PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239055,9218352,470135952 PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239056,15501047,790553397 PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239057,15538226,792449526 PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239058,12487833,636879483 PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239059,12480350,636497850 PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239060,13840587,705869937 PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239061,13903399,709073349 PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239062,10734719,547470669 PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239063,10757923,548654073 PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239064,9189103,468644253 PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239065,9168761,467606811 PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239066,10490820,535031820 PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239067,10510772,536049372 PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239068,15528375,791947125 PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239069,15552791,793192341 PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239070,12819970,653818470 PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239071,12805289,653069739 PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239072,14501119,739557069 PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239073,14557524,742433724 PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239074,10128748,516566148 PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239075,10149979,517648929 PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239076,8844053,451046703 PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239077,8826385,450145635 PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239078,10169123,518625273 PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239079,10199333,520165983 PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239080,13771867,702365217 PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239081,13769712,702255312 PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239082,12473768,636162168 PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239083,12393265,632056515 PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239084,14602972,744751572 PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239085,14574634,743306334 PRJNA379630,SRX2652914,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in n-alkanes,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617379,Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in n-alkanes,Illumina HiSeq 2500,SRR5356885,92012581,4600629050 PRJNA379630,SRX2652916,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in n-alkanes,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617378,Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in n-alkanes,Illumina HiSeq 2500,SRR5356887,62093655,3104682750 PRJNA379630,SRX2652918,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in n-alkanes,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617377,Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in n-alkanes,Illumina HiSeq 2500,SRR5356889,100563944,5028197200 PRJNA379630,SRX2652920,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in Glycerol,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617376,Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in Glycerol,Illumina HiSeq 2500,SRR5356891,83809807,4190490350 PRJNA379630,SRX2652922,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in Glycerol,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617375,Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in Glycerol,Illumina HiSeq 2500,SRR5356893,90928652,4546432600 PRJNA379630,SRX2652924,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in Glycerol,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617374,Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in Glycerol,Illumina HiSeq 2500,SRR5356895,106331232,5316561600 PRJNA379630,SRX2652926,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in n-alkanes,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617373,Pseudomonas aeruginosa PAO1 replicate 3 grown in n-alkanes,Illumina HiSeq 2500,SRR5356897,101520011,5076000550 PRJNA379630,SRX2652928,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in n-alkanes,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617372,Pseudomonas aeruginosa PAO1 replicate 2 grown in n-alkanes,Illumina HiSeq 2500,SRR5356899,83560401,4178020050 PRJNA379630,SRX2652930,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in n-alkanes,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617371,Pseudomonas aeruginosa PAO1 replicate 1 grown in n-alkanes,Illumina HiSeq 2500,SRR5356901,94948217,4747410850 PRJNA379630,SRX2652932,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in Glycerol,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617370,Pseudomonas aeruginosa PAO1 replicate 3 grown in Glycerol,Illumina HiSeq 2500,SRR5356903,71767127,3588356350 PRJNA379630,SRX2652934,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in Glycerol,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617369,Pseudomonas aeruginosa PAO1 replicate 2 grown in Glycerol,Illumina HiSeq 2500,SRR5356905,90030430,4501521500 PRJNA379630,SRX2652936,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in Glycerol,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617368,Pseudomonas aeruginosa PAO1 replicate 1 grown in Glycerol,Illumina HiSeq 2500,SRR5356907,73952429,3697621450 PRJNA384569,SRX2766861,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant,4932,Saccharomyces cerevisiae,miRNA-Seq,TRANSCRIPTOMIC,PCR,SAMN06841405,RFP for puf3 ko mutant replicate 1,Illumina HiSeq 2000,SRR5483532,31667620,1583381000 PRJNA384569,SRX2766864,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant rep2,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant rep2,4932,Saccharomyces cerevisiae,miRNA-Seq,TRANSCRIPTOMIC,PCR,SAMN06841406,RFP for puf3 ko mutant replicate 2,Illumina HiSeq 2000,SRR5483533,33068533,1653426650 PRJNA384569,SRX2766865,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep1,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep1,4932,Saccharomyces cerevisiae,miRNA-Seq,TRANSCRIPTOMIC,PCR,SAMN06841407,RFP for WT replicate 1,Illumina HiSeq 2000,SRR5483534,24523690,1226184500 PRJNA384569,SRX2766866,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep2,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep2,4932,Saccharomyces cerevisiae,miRNA-Seq,TRANSCRIPTOMIC,PCR,SAMN06841408,RFP for WT replicate 2,Illumina HiSeq 2000,SRR5483539,16691481,834574050 PRJNA390134,SRX2902855,NextSeq 500 sequencing; GSM2664256: wild type ribosome profiling replicate 1; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664256: wild type ribosome profiling replicate 1; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220960,wild type ribosome profiling replicate 1,NextSeq 500,SRR5667267,46651854,1621851282 PRJNA390134,SRX2902856,NextSeq 500 sequencing; GSM2664257: wild type ribosome profiling replicate 2; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664257: wild type ribosome profiling replicate 2; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220959,wild type ribosome profiling replicate 2,NextSeq 500,SRR5667268,122734505,4216803822 PRJNA390134,SRX2902857,NextSeq 500 sequencing; GSM2664258: wild type ribosome profiling replicate 3; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664258: wild type ribosome profiling replicate 3; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220958,wild type ribosome profiling replicate 3,NextSeq 500,SRR5667269,45156367,1539402070 PRJNA390134,SRX2902864,NextSeq 500 sequencing; GSM2664265: GluRIIA ribosome profiling replicate 1; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664265: GluRIIA ribosome profiling replicate 1; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220951,GluRIIA ribosome profiling replicate 1,NextSeq 500,SRR5667276,35199688,1194135764 PRJNA390134,SRX2902865,NextSeq 500 sequencing; GSM2664266: GluRIIA ribosome profiling replicate 2; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664266: GluRIIA ribosome profiling replicate 2; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220950,GluRIIA ribosome profiling replicate 2,NextSeq 500,SRR5667277,78959629,2610438767 PRJNA390134,SRX2902866,NextSeq 500 sequencing; GSM2664267: GluRIIA ribosome profiling replicate 3; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664267: GluRIIA ribosome profiling replicate 3; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220949,GluRIIA ribosome profiling replicate 3,NextSeq 500,SRR5667278,20752434,676573468 PRJNA390134,SRX2902870,NextSeq 500 sequencing; GSM2664271: Tor-OE ribosome profiling replicate 1; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664271: Tor-OE ribosome profiling replicate 1; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220945,Tor-OE ribosome profiling replicate 1,NextSeq 500,SRR5667282,56343352,1940386794 PRJNA390134,SRX2902871,NextSeq 500 sequencing; GSM2664272: Tor-OE ribosome profiling replicate 2; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664272: Tor-OE ribosome profiling replicate 2; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220944,Tor-OE ribosome profiling replicate 2,NextSeq 500,SRR5667283,32872272,1104998701 PRJNA390134,SRX2902872,NextSeq 500 sequencing; GSM2664273: Tor-OE ribosome profiling replicate 3; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664273: Tor-OE ribosome profiling replicate 3; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220943,Tor-OE ribosome profiling replicate 3,NextSeq 500,SRR5667284,69053087,2392506309 PRJNA391352,SRX2943745,"Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266693,"Ribosome Profiling Input for WT, rep1",Illumina HiSeq 2000,SRR5735992,16800285,2553643320 PRJNA391352,SRX2943745,"Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266693,"Ribosome Profiling Input for WT, rep1",Illumina HiSeq 2000,SRR5735993,8361509,1270949368 PRJNA391352,SRX2943746,"Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266700,"Ribosome Profiling Input for WT, rep2",Illumina HiSeq 2000,SRR5735994,15807404,2402725408 PRJNA391352,SRX2943746,"Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266700,"Ribosome Profiling Input for WT, rep2",Illumina HiSeq 2000,SRR5735995,7892805,1199706360 PRJNA391352,SRX2943747,"Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266699,"Ribosome Profiling Input for KO, rep1",Illumina HiSeq 2000,SRR5735996,17287993,2627774936 PRJNA391352,SRX2943747,"Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266699,"Ribosome Profiling Input for KO, rep1",Illumina HiSeq 2000,SRR5735997,8808526,1338895952 PRJNA391352,SRX2943748,"Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266698,"Ribosome Profiling Input for KO, rep2",Illumina HiSeq 2000,SRR5735998,16011015,2433674280 PRJNA391352,SRX2943748,"Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266698,"Ribosome Profiling Input for KO, rep2",Illumina HiSeq 2000,SRR5735999,8221919,1249731688 PRJNA391352,SRX2943749,"Illumina HiSeq 2000 sequencing; GSM2678053: WT Ribosome Profiling, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678053: WT Ribosome Profiling, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266697,"WT Ribosome Profiling, rep1",Illumina HiSeq 2000,SRR5736000,49930735,3794735860 PRJNA391352,SRX2943750,"Illumina HiSeq 2000 sequencing; GSM2678054: WT Ribosome Profiling, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678054: WT Ribosome Profiling, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266696,"WT Ribosome Profiling, rep2",Illumina HiSeq 2000,SRR5736001,72687482,5524248632 PRJNA391352,SRX2943751,"Illumina HiSeq 2000 sequencing; GSM2678055: KO Ribosome Profiling, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678055: KO Ribosome Profiling, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266695,"KO Ribosome Profiling, rep1",Illumina HiSeq 2000,SRR5736002,64000307,4864023332 PRJNA391352,SRX2943752,"Illumina HiSeq 2000 sequencing; GSM2678056: KO Ribosome Profiling, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678056: KO Ribosome Profiling, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266694,"KO Ribosome Profiling, rep2",Illumina HiSeq 2000,SRR5736003,64705916,4917649616 PRJNA392904,SRX2979029,Illumina HiSeq 4000 sequencing; GSM2692350: ribosome profiling 0h; Mus musculus; OTHER,Illumina HiSeq 4000 sequencing; GSM2692350: ribosome profiling 0h; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07312004,ribosome profiling 0h,Illumina HiSeq 4000,SRR5799562,64408917,1800217292 PRJNA392904,SRX2979030,Illumina HiSeq 4000 sequencing; GSM2692351: ribosome profiling 12h; Mus musculus; OTHER,Illumina HiSeq 4000 sequencing; GSM2692351: ribosome profiling 12h; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07312003,ribosome profiling 12h,Illumina HiSeq 4000,SRR5799563,142369751,4133742550 PRJNA399166,SRX3110787,Illumina HiSeq 2000 sequencing; GSM2747838: Ribosome Profiling H19:H391; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747838: Ribosome Profiling H19:H391; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525042,Ribosome Profiling H19:H391,Illumina HiSeq 2000,SRR5952328,202796598,10139829900 PRJNA399166,SRX3110788,Illumina HiSeq 2000 sequencing; GSM2747839: Ribosome Profiling SECIS1 deletion2; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747839: Ribosome Profiling SECIS1 deletion2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525041,Ribosome Profiling SECIS1 deletion2,Illumina HiSeq 2000,SRR5952329,202925674,10146283700 PRJNA399166,SRX3110789,Illumina HiSeq 2000 sequencing; GSM2747840: Ribosome Profiling SECIS1 deletion3; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747840: Ribosome Profiling SECIS1 deletion3; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525040,Ribosome Profiling SECIS1 deletion3,Illumina HiSeq 2000,SRR5952330,196597095,9829854750 PRJNA399166,SRX3110790,Illumina HiSeq 2000 sequencing; GSM2747841: Ribosome Profiling SECIS1 WT1; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747841: Ribosome Profiling SECIS1 WT1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525039,Ribosome Profiling SECIS1 WT1,Illumina HiSeq 2000,SRR5952331,202636712,10131835600 PRJNA399166,SRX3110791,Illumina HiSeq 2000 sequencing; GSM2747842: Ribosome Profiling SECIS1 WT2; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747842: Ribosome Profiling SECIS1 WT2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525038,Ribosome Profiling SECIS1 WT2,Illumina HiSeq 2000,SRR5952332,189180961,9459048050 PRJNA399166,SRX3110792,Illumina HiSeq 2000 sequencing; GSM2747843: Ribosome Profiling SECIS1 WT3; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747843: Ribosome Profiling SECIS1 WT3; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525037,Ribosome Profiling SECIS1 WT3,Illumina HiSeq 2000,SRR5952333,175785634,8789281700 PRJNA399166,SRX3110799,Illumina HiSeq 2000 sequencing; GSM2747850: Ribosome Profiling SECIS2 WT1; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747850: Ribosome Profiling SECIS2 WT1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525028,Ribosome Profiling SECIS2 WT1,Illumina HiSeq 2000,SRR5952340,228456278,11422813900 PRJNA399166,SRX3110800,Illumina HiSeq 2000 sequencing; GSM2747851: Ribosome Profiling SECIS2 WT2; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747851: Ribosome Profiling SECIS2 WT2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525032,Ribosome Profiling SECIS2 WT2,Illumina HiSeq 2000,SRR5952341,188204162,9410208100 PRJNA399166,SRX3110801,Illumina HiSeq 2000 sequencing; GSM2747852: Ribosome Profiling SECIS2 WT3; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747852: Ribosome Profiling SECIS2 WT3; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525031,Ribosome Profiling SECIS2 WT3,Illumina HiSeq 2000,SRR5952342,203369022,10168451100 PRJNA399166,SRX3110802,Illumina HiSeq 2000 sequencing; GSM2747853: Ribosome Profiling SECIS2 deletion1; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747853: Ribosome Profiling SECIS2 deletion1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525030,Ribosome Profiling SECIS2 deletion1,Illumina HiSeq 2000,SRR5952343,202822349,10141117450 PRJNA399166,SRX3110803,Illumina HiSeq 2000 sequencing; GSM2747854: Ribosome Profiling SECIS2 deletion2; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747854: Ribosome Profiling SECIS2 deletion2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525019,Ribosome Profiling SECIS2 deletion2,Illumina HiSeq 2000,SRR5952344,226331185,11316559250 PRJNA399166,SRX3110804,Illumina HiSeq 2000 sequencing; GSM2747855: Ribosome Profiling SECIS2 deletion3; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747855: Ribosome Profiling SECIS2 deletion3; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525027,Ribosome Profiling SECIS2 deletion3,Illumina HiSeq 2000,SRR5952345,197895247,9894762350 PRJNA401857,SRX3157107,Illumina Genome Analyzer II sequencing; GSM2770989: Ribosome profiling at 37°C in WT cells_1; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770989: Ribosome profiling at 37°C in WT cells_1; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602624,Ribosome profiling at 37°C in WT cells_1,Illumina Genome Analyzer II,SRR6001737,20671753,614302032 PRJNA401857,SRX3157108,Illumina Genome Analyzer II sequencing; GSM2770990: Ribosome profiling 10 min after shift to 10°C in WT cells_1; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770990: Ribosome profiling 10 min after shift to 10°C in WT cells_1; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602623,Ribosome profiling 10 min after shift to 10°C in WT cells_1,Illumina Genome Analyzer II,SRR6001738,16625543,487122180 PRJNA401857,SRX3157109,Illumina Genome Analyzer II sequencing; GSM2770991: Ribosome profiling 30 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770991: Ribosome profiling 30 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602622,Ribosome profiling 30 min after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001739,8816443,253931666 PRJNA401857,SRX3157110,Illumina Genome Analyzer II sequencing; GSM2770992: Ribosome profiling 2 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770992: Ribosome profiling 2 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602621,Ribosome profiling 2 hr after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001740,7472980,210323047 PRJNA401857,SRX3157111,Illumina Genome Analyzer II sequencing; GSM2770993: Ribosome profiling 3 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770993: Ribosome profiling 3 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602620,Ribosome profiling 3 hr after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001741,16047781,463280196 PRJNA401857,SRX3157112,Illumina Genome Analyzer II sequencing; GSM2770994: Ribosome profiling 4 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770994: Ribosome profiling 4 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602619,Ribosome profiling 4 hr after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001742,5968378,168325033 PRJNA401857,SRX3157113,Illumina Genome Analyzer II sequencing; GSM2770995: Ribosome profiling 6 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770995: Ribosome profiling 6 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602618,Ribosome profiling 6 hr after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001743,6838687,194508545 PRJNA401857,SRX3157114,Illumina HiSeq 2000 sequencing; GSM2770996: Ribosome profiling 5 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770996: Ribosome profiling 5 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602617,Ribosome profiling 5 min after shift to 10°C in WT cells,Illumina HiSeq 2000,SRR6001744,38289935,1914496750 PRJNA401857,SRX3157115,Illumina HiSeq 2000 sequencing; GSM2770997: Ribosome profiling 10 min after shift to 10°C in WT cells_2; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770997: Ribosome profiling 10 min after shift to 10°C in WT cells_2; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602616,Ribosome profiling 10 min after shift to 10°C in WT cells_2,Illumina HiSeq 2000,SRR6001745,11745422,587271100 PRJNA401857,SRX3157116,Illumina HiSeq 2000 sequencing; GSM2770998: Ribosome profiling 15 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770998: Ribosome profiling 15 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602615,Ribosome profiling 15 min after shift to 10°C in WT cells,Illumina HiSeq 2000,SRR6001746,16428973,821448650 PRJNA401857,SRX3157117,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602614,Ribosome profiling 8 hr after shift to 10°C in WT cells,Illumina HiSeq 2000,SRR6001747,11769741,600256791 PRJNA401857,SRX3157117,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602614,Ribosome profiling 8 hr after shift to 10°C in WT cells,Illumina HiSeq 2000,SRR6001748,11622124,592728324 PRJNA401857,SRX3157118,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602613,Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells,Illumina HiSeq 2000,SRR6001749,12537556,639415356 PRJNA401857,SRX3157118,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602613,Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells,Illumina HiSeq 2000,SRR6001750,12383731,631570281 PRJNA401857,SRX3157119,Illumina HiSeq 2000 sequencing; GSM2771001: Ribosome profiling at 37°C in WT cells_2; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2771001: Ribosome profiling at 37°C in WT cells_2; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602612,Ribosome profiling at 37°C in WT cells_2,Illumina HiSeq 2000,SRR6001751,61258516,3124184316 PRJNA401857,SRX3157120,Illumina HiSeq 2000 sequencing; GSM2771002: Ribosome profiling at 37°C in ∆cspABCEG cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2771002: Ribosome profiling at 37°C in ∆cspABCEG cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602611,Ribosome profiling at 37°C in ∆cspABCEG cells,Illumina HiSeq 2000,SRR6001752,59003587,3009182937 PRJNA171327,SRX172315,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #1","Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #1",9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01093931,"Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #1",Illumina HiSeq 2000,SRR618770,9742062,467618976 PRJNA171327,SRX172361,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #2","Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #2",9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01093932,"Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #2",Illumina HiSeq 2000,SRR618771,44827310,2151710880 PRJNA171327,SRX172360,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #1","Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #1",9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01093933,"Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #1",Illumina HiSeq 2000,SRR618772,15628782,750181536 PRJNA171327,SRX172392,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #2","Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #2",9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01093934,"Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #2",Illumina HiSeq 2000,SRR618773,28457106,1365941088 PRJNA171327,SRX172393,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with cycloheximide,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with cycloheximide,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01094235,Ribosome profiling of MEF cells treated with cycloheximide,Illumina HiSeq 2000,SRR618774,25957180,1245944640 PRJNA171327,SRX172394,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with lactimidomycin,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with lactimidomycin,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01094236,Ribosome profiling of MEF cells treated with lactimidomycin,Illumina HiSeq 2000,SRR618775,43068755,2067300240 PRJNA181016,SRX205658,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 1,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 1,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816428,HEK293_CON_Rep1,Illumina Genome Analyzer II,SRR619082,10167363,416861883 PRJNA181016,SRX205661,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 2,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 2,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816429,HEK293_CON_Rep2,Illumina HiSeq 2000,SRR619083,48902334,2347312032 PRJNA181016,SRX205662,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 1,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 1,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816430,HEK293_AZC+MG132_Rep1,Illumina Genome Analyzer II,SRR619084,10921343,447775063 PRJNA181016,SRX205663,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 2,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 2,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816431,HEK293_AZC+MG132_Rep2,Illumina HiSeq 2000,SRR619085,42857031,2057137488 PRJNA181016,SRX205664,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC only,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC only,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816432,HEK293_AZC,Illumina Genome Analyzer II,SRR619086,5553281,227684521 PRJNA181016,SRX205665,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with MG132 only,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with MG132 only,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816433,HEK293_MG132,Illumina Genome Analyzer II,SRR619087,10922721,447831561 PRJNA181016,SRX205666,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816434,HEK293_DMSO,Illumina HiSeq 2000,SRR619088,10086263,484140624 PRJNA181016,SRX205666,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816434,HEK293_DMSO,Illumina HiSeq 2000,SRR619089,4286560,205754880 PRJNA181016,SRX205667,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816435,HEK293_VER,Illumina HiSeq 2000,SRR619090,8919827,428151696 PRJNA181016,SRX205667,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816435,HEK293_VER,Illumina HiSeq 2000,SRR619091,3924183,188360784 PRJNA181016,SRX205668,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816436,HEK293_PES,Illumina HiSeq 2000,SRR619092,8469084,406516032 PRJNA181016,SRX205668,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816436,HEK293_PES,Illumina HiSeq 2000,SRR619093,3737571,179403408 PRJNA181016,SRX205669,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816437,HEK293_GA,Illumina HiSeq 2000,SRR619094,9294787,446149776 PRJNA181016,SRX205669,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816437,HEK293_GA,Illumina HiSeq 2000,SRR619095,4044711,194146128 PRJNA181016,SRX205670,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells no treatment,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells no treatment,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816438,FRB-FKBP-Rapalog,Illumina Genome Analyzer II,SRR619096,19318730,1062530150 PRJNA181016,SRX205671,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells treated with rapalog,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells treated with rapalog,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816439,FRB-FKBP+Rapalog,Illumina Genome Analyzer II,SRR619097,24771678,1362442290 PRJNA181016,SRX205672,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells NOT expressing K71M,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells NOT expressing K71M,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816440,Hela_K71M+Dox,Illumina HiSeq 2000,SRR619098,24593755,1180500240 PRJNA181016,SRX205673,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 1,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 1,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816441,Hela_K71M-Dox_Rep1,Illumina HiSeq 2000,SRR619099,22424972,1076398656 PRJNA181016,SRX205675,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 2,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 2,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816442,Hela_K71M-Dox_Rep2,Illumina HiSeq 2000,SRR619100,46612873,2237417904 PRJNA417011,SRX3358946,NextSeq 500 sequencing; GSM2838830: Dengue 1 ribosome profiling mRNA REP1; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2838830: Dengue 1 ribosome profiling mRNA REP1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN07974487,Dengue 1 ribosome profiling mRNA REP1,NextSeq 500,SRR6252013,127084864,9531364800 PRJNA417011,SRX3358947,NextSeq 500 sequencing; GSM2838831: Dengue 1 ribosome profiling footprint REP1; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2838831: Dengue 1 ribosome profiling footprint REP1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN07974486,Dengue 1 ribosome profiling footprint REP1,NextSeq 500,SRR6252014,127716843,9578763225 PRJNA417011,SRX3358948,NextSeq 500 sequencing; GSM2838832: Dengue 1 ribosome profiling mRNA REP2; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2838832: Dengue 1 ribosome profiling mRNA REP2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN07974437,Dengue 1 ribosome profiling mRNA REP2,NextSeq 500,SRR6252015,115517289,8663796675 PRJNA417011,SRX3358949,NextSeq 500 sequencing; GSM2838833: Dengue 1 ribosome profiling footprint REP2; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2838833: Dengue 1 ribosome profiling footprint REP2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN07974489,Dengue 1 ribosome profiling footprint REP2,NextSeq 500,SRR6252016,128141714,9610628550 PRJNA418190,SRX3388077,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022097,Ribo_HF_rep2,Illumina HiSeq 4000,SRR6286686,31815773,3181577300 PRJNA418190,SRX3388076,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022096,Ribo_HF_rep1,Illumina HiSeq 4000,SRR6286687,31226831,3122683100 PRJNA418190,SRX3388073,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022093,Ribo_CO_rep2,Illumina HiSeq 4000,SRR6286690,95785654,2709048603 PRJNA418190,SRX3388072,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022092,Ribo_CO_rep1,Illumina HiSeq 4000,SRR6286691,74932501,2100103575 PRJNA418190,SRX3388071,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022095,Ribo_H2CO2_rep2,Illumina HiSeq 4000,SRR6286692,44431801,4443180100 PRJNA418190,SRX3388070,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022094,Ribo_H2CO2_rep1,Illumina HiSeq 4000,SRR6286693,50618624,5061862400 PRJNA418997,SRX3415715,Illumina HiSeq 2000 sequencing; Hip1 total hippocampus Ribosome profiling,Illumina HiSeq 2000 sequencing; Hip1 total hippocampus Ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08040363,Hip1 total hippocampus Ribosome profiling,Illumina HiSeq 2000,SRR6315847,6628200,180389814 PRJNA423188,SRX3489120,Illumina HiSeq 2500 sequencing; GSM2895436: KO-ribosome profiling; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM2895436: KO-ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08213272,KO-ribosome profiling,Illumina HiSeq 2500,SRR6395814,31806217,1590310850 PRJNA423188,SRX3489121,Illumina HiSeq 2500 sequencing; GSM2895437: KO-ribosome profiling input; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM2895437: KO-ribosome profiling input; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08213281,KO-ribosome profiling input,Illumina HiSeq 2500,SRR6395815,43112301,2155615050 PRJNA423188,SRX3489122,Illumina HiSeq 2500 sequencing; GSM2895438: WT-ribosome profiling; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM2895438: WT-ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08213280,WT-ribosome profiling,Illumina HiSeq 2500,SRR6395816,40248624,2012431200 PRJNA423188,SRX3489123,Illumina HiSeq 2500 sequencing; GSM2895439: WT-ribosome profiling input; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM2895439: WT-ribosome profiling input; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08213279,WT-ribosome profiling input,Illumina HiSeq 2500,SRR6395817,33585015,1679250750 PRJNA423188,SRX4044241,Illumina HiSeq 2500 sequencing; GSM3131863: WT-ribosome profiling replicate 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM3131863: WT-ribosome profiling replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN09076541,WT-ribosome profiling replicate 2,Illumina HiSeq 2500,SRR7123172,43725854,2186292700 PRJNA423188,SRX4044242,Illumina HiSeq 3000 sequencing; GSM3131864: WT-ribosome profiling input replicate 2; Mus musculus; OTHER,Illumina HiSeq 3000 sequencing; GSM3131864: WT-ribosome profiling input replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN09076736,WT-ribosome profiling input replicate 2,Illumina HiSeq 3000,SRR7123173,26771648,8031494400 PRJNA423188,SRX4044243,Illumina HiSeq 2500 sequencing; GSM3131865: KO-ribosome profiling replicate 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM3131865: KO-ribosome profiling replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN09076734,KO-ribosome profiling replicate 2,Illumina HiSeq 2500,SRR7123174,32054335,1602716750 PRJNA423188,SRX4044244,Illumina HiSeq 3000 sequencing; GSM3131866: KO-ribosome profiling input replicate 2; Mus musculus; OTHER,Illumina HiSeq 3000 sequencing; GSM3131866: KO-ribosome profiling input replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN09076731,KO-ribosome profiling input replicate 2,Illumina HiSeq 3000,SRR7123175,24239197,7271759100 PRJNA466150,SRX4053284,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #4,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #4,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091234,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132277,53840664,4038049800 PRJNA466150,SRX4053275,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #2,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #2,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091232,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132286,96147759,7211081925 PRJNA466150,SRX4053274,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #3,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #3,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091233,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132287,49283336,3696250200 PRJNA466150,SRX4053273,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #3,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #3,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091226,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132288,78056300,5854222500 PRJNA466150,SRX4053272,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #4,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #4,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091227,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132289,44947356,3371051700 PRJNA466150,SRX4053271,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:control replicate #1,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:control replicate #1,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091224,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,Illumina HiSeq 2000,SRR7132290,64927827,3246391350 PRJNA466150,SRX4053270,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #2,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #2,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091225,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132291,89912857,6743464275 PRJNA466150,SRX4053269,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #3,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #3,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091230,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132292,69602339,5220175425 PRJNA466150,SRX4053268,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #1,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #1,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091231,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132293,57310413,2865520650 PRJNA466150,SRX4053267,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #1,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #1,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091228,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,Illumina HiSeq 2000,SRR7132294,106961271,8022095325 PRJNA466150,SRX4053266,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #2,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #2,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091229,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132295,43401129,3255084675 PRJNA473989,SRX4147683,Illumina HiSeq 2500 sequencing; GSM3168387: MDA-MB-231 ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3168387: MDA-MB-231 ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN09288723,MDA-MB-231 ribosome profiling,Illumina HiSeq 2500,SRR7241910,27002674,1350133700 PRJNA473989,SRX4147684,Illumina HiSeq 2500 sequencing; GSM3168388: C. elegans embryos ribosome profiling; Caenorhabditis elegans; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3168388: C. elegans embryos ribosome profiling; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN09288722,C. elegans embryos ribosome profiling,Illumina HiSeq 2500,SRR7241911,76408239,3820411950 PRJNA473989,SRX4147685,Illumina HiSeq 2500 sequencing; GSM3168389: HeLa ribosome profiling 1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3168389: HeLa ribosome profiling 1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN09288721,HeLa ribosome profiling 1,Illumina HiSeq 2500,SRR7241912,53902947,2695147350 PRJNA473989,SRX4147686,Illumina HiSeq 2500 sequencing; GSM3168390: HeLa ribosome profiling 2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3168390: HeLa ribosome profiling 2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN09288720,HeLa ribosome profiling 2,Illumina HiSeq 2500,SRR7241913,45242293,2262114650 PRJNA480953,SRX4387664,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,other,SAMN09652702,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,NextSeq 500,SRR7517655,227390056,11369502800 PRJNA480953,SRX4387663,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,other,SAMN09652704,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,NextSeq 500,SRR7517656,287250155,14362507750 PRJNA480953,SRX4387662,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,Oligo-dT,SAMN09652701,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,NextSeq 500,SRR7517657,162626902,8131345100 PRJNA480953,SRX4387661,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,Oligo-dT,SAMN09652703,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,NextSeq 500,SRR7517658,146674049,7333702450 PRJNA495919,SRX4870934,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type plus radicicol,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type plus radicicol,5661,Leishmania donovani,OTHER,TRANSCRIPTOMIC,RANDOM,SAMN10234888,wild type plus RAD,NextSeq 500,SRR8040412,45205841,3435643916 PRJNA495919,SRX4870932,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type,5661,Leishmania donovani,OTHER,TRANSCRIPTOMIC,RANDOM,SAMN10234887,wild type minus RAD,NextSeq 500,SRR8040414,24741340,1880341840 PRJNA495919,SRX4870930,NextSeq 500 sequencing; Ribosome profiling of L. donovani HSP90rr plus radicicol,NextSeq 500 sequencing; Ribosome profiling of L. donovani HSP90rr plus radicicol,5661,Leishmania donovani,OTHER,TRANSCRIPTOMIC,RANDOM,SAMN10234889,HSP90rr plus RAD,NextSeq 500,SRR8040416,28476385,2164205260 PRJNA438895,SRX5075516,Illumina MiSeq sequencing; GSM3048762: ΔrrnIcomp - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq,Illumina MiSeq sequencing; GSM3048762: ΔrrnIcomp - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq,216895,Vibrio vulnificus CMCP6,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN08731684,ΔrrnIcomp - ribosome profiling data rep1,Illumina MiSeq,SRR8258332,5105532,183799152 PRJNA438895,SRX5075517,Illumina MiSeq sequencing; GSM3048763: ΔrrnI - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq,Illumina MiSeq sequencing; GSM3048763: ΔrrnI - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq,216895,Vibrio vulnificus CMCP6,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN08731683,ΔrrnI - ribosome profiling data rep1,Illumina MiSeq,SRR8258333,5834528,210043008 PRJNA438895,SRX5075520,Illumina MiSeq sequencing; GSM3048766: ΔrrnIcomp - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq,Illumina MiSeq sequencing; GSM3048766: ΔrrnIcomp - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq,216895,Vibrio vulnificus CMCP6,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN08731680,ΔrrnIcomp - ribosome profiling data rep2,Illumina MiSeq,SRR8258336,20039467,1022012817 PRJNA438895,SRX5075521,Illumina MiSeq sequencing; GSM3048767: ΔrrnI - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq,Illumina MiSeq sequencing; GSM3048767: ΔrrnI - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq,216895,Vibrio vulnificus CMCP6,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN08731687,ΔrrnI - ribosome profiling data rep2,Illumina MiSeq,SRR8258337,26587915,1355983665 PRJNA515289,SRX5252133,"Illumina HiSeq 4000 sequencing; GSM3563711: HEK 293 cells, ribosome profiling, ctrl, Replicate 1; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3563711: HEK 293 cells, ribosome profiling, ctrl, Replicate 1; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN10752247,"HEK 293 cells, ribosome profiling, ctrl, Replicate 1",Illumina HiSeq 4000,SRR8445000,101076288,5154890688 PRJNA515289,SRX5252134,"Illumina HiSeq 4000 sequencing; GSM3563712: HEK 293 cells, ribosome profiling, ctrl, Replicate 2; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3563712: HEK 293 cells, ribosome profiling, ctrl, Replicate 2; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN10752246,"HEK 293 cells, ribosome profiling, ctrl, Replicate 2",Illumina HiSeq 4000,SRR8445001,96501939,4921598889 PRJNA515289,SRX5252135,"Illumina HiSeq 4000 sequencing; GSM3563713: HEK 293 cells, ribosome profiling, siDDX3, Replicate 1; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3563713: HEK 293 cells, ribosome profiling, siDDX3, Replicate 1; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN10752245,"HEK 293 cells, ribosome profiling, siDDX3, Replicate 1",Illumina HiSeq 4000,SRR8445002,92758439,4730680389 PRJNA515289,SRX5252136,"Illumina HiSeq 4000 sequencing; GSM3563714: HEK 293 cells, ribosome profiling, siDDX3, Replicate 2; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3563714: HEK 293 cells, ribosome profiling, siDDX3, Replicate 2; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN10752244,"HEK 293 cells, ribosome profiling, siDDX3, Replicate 2",Illumina HiSeq 4000,SRR8445003,92190382,4701709482 PRJNA206070,SRX288474,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183598,WT input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870722,4000000,304000000 PRJNA206070,SRX288474,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183598,WT input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870723,3768017,286369292 PRJNA206070,SRX288474,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183598,WT input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870724,4000000,304000000 PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870725,4000000,304000000 PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870726,4000000,304000000 PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870727,4000000,304000000 PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870728,3877037,294654812 PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870729,4000000,304000000 PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870730,4000000,304000000 PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870731,4000000,304000000 PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870732,4000000,304000000 PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870733,4000000,304000000 PRJNA206070,SRX288476,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183600,Nanog + SoxB1 MO input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870734,4000000,304000000 PRJNA206070,SRX288476,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183600,Nanog + SoxB1 MO input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870735,4000000,304000000 PRJNA206070,SRX288476,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183600,Nanog + SoxB1 MO input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870736,2117060,160896560 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870737,4000000,304000000 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870738,4000000,304000000 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870739,4000000,304000000 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870740,4000000,304000000 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870741,4000000,304000000 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870742,4000000,304000000 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870743,4000000,304000000 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870744,4000000,304000000 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870745,2436469,185171644 PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870746,4000000,304000000 PRJNA527204,SRX5525062,Illumina HiSeq 2500 sequencing; GSM3671680: ribosome profiling wt_1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671680: ribosome profiling wt_1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130407,ribosome profiling wt_1,Illumina HiSeq 2500,SRR8732200,18661991,933099550 PRJNA527204,SRX5525063,Illumina HiSeq 2500 sequencing; GSM3671681: ribosome profiling wt_2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671681: ribosome profiling wt_2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130406,ribosome profiling wt_2,Illumina HiSeq 2500,SRR8732201,17636110,881805500 PRJNA527204,SRX5525064,Illumina HiSeq 2500 sequencing; GSM3671682: ribosome profiling wt_3; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671682: ribosome profiling wt_3; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130405,ribosome profiling wt_3,Illumina HiSeq 2500,SRR8732202,23560878,1178043900 PRJNA527204,SRX5525065,Illumina HiSeq 2500 sequencing; GSM3671683: ribosome profiling APP_1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671683: ribosome profiling APP_1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130404,ribosome profiling APP_1,Illumina HiSeq 2500,SRR8732203,22107235,1105361750 PRJNA527204,SRX5525066,Illumina HiSeq 2500 sequencing; GSM3671684: ribosome profiling APP_2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671684: ribosome profiling APP_2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130403,ribosome profiling APP_2,Illumina HiSeq 2500,SRR8732204,18895655,944782750 PRJNA527204,SRX5525067,Illumina HiSeq 2500 sequencing; GSM3671685: ribosome profiling APP_3; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671685: ribosome profiling APP_3; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130402,ribosome profiling APP_3,Illumina HiSeq 2500,SRR8732205,20817886,1040894300 PRJNA527204,SRX5525068,Illumina HiSeq 2500 sequencing; GSM3671686: ribosome profiling PSEN_1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671686: ribosome profiling PSEN_1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130401,ribosome profiling PSEN_1,Illumina HiSeq 2500,SRR8732206,20629961,1031498050 PRJNA527204,SRX5525069,Illumina HiSeq 2500 sequencing; GSM3671687: ribosome profiling PSEN_2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671687: ribosome profiling PSEN_2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130400,ribosome profiling PSEN_2,Illumina HiSeq 2500,SRR8732207,20358650,1017932500 PRJNA527204,SRX5525070,Illumina HiSeq 2500 sequencing; GSM3671688: ribosome profiling PSEN_3; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671688: ribosome profiling PSEN_3; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130427,ribosome profiling PSEN_3,Illumina HiSeq 2500,SRR8732208,20652398,1032619900 PRJNA527204,SRX5525071,Illumina HiSeq 2500 sequencing; GSM3671689: ribosome profiling APP/PSEN1_1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671689: ribosome profiling APP/PSEN1_1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130426,ribosome profiling APP/PSEN1_1,Illumina HiSeq 2500,SRR8732209,21629538,1081476900 PRJNA527204,SRX5525072,Illumina HiSeq 2500 sequencing; GSM3671690: ribosome profiling APP/PSEN1_2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671690: ribosome profiling APP/PSEN1_2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130425,ribosome profiling APP/PSEN1_2,Illumina HiSeq 2500,SRR8732210,22115725,1105786250 PRJNA527204,SRX5525073,Illumina HiSeq 2500 sequencing; GSM3671691: ribosome profiling APP/PSEN1_3; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671691: ribosome profiling APP/PSEN1_3; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130424,ribosome profiling APP/PSEN1_3,Illumina HiSeq 2500,SRR8732211,26892978,1344648900 PRJNA544411,SRX5887326,"Illumina HiSeq 4000 sequencing; GSM3791723: iPSC ribosome profiling, harringtonine-treated; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791723: iPSC ribosome profiling, harringtonine-treated; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835522,"iPSC ribosome profiling, harringtonine-treated",Illumina HiSeq 4000,SRR9113062,131541396,3743828156 PRJNA544411,SRX5887327,"Illumina HiSeq 4000 sequencing; GSM3791724: Cardiomyocyte ribosome profiling, harringtonine-treated; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791724: Cardiomyocyte ribosome profiling, harringtonine-treated; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835521,"Cardiomyocyte ribosome profiling, harringtonine-treated",Illumina HiSeq 4000,SRR9113063,105449435,2785265458 PRJNA544411,SRX5887328,"Illumina HiSeq 4000 sequencing; GSM3791725: iPSC ribosome profiling, no drug treatment, replicate 1; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791725: iPSC ribosome profiling, no drug treatment, replicate 1; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835520,"iPSC ribosome profiling, no drug treatment, replicate 1",Illumina HiSeq 4000,SRR9113064,52479474,1453634111 PRJNA544411,SRX5887329,"Illumina HiSeq 4000 sequencing; GSM3791726: iPSC ribosome profiling, no drug treatment, replicate 2; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791726: iPSC ribosome profiling, no drug treatment, replicate 2; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835519,"iPSC ribosome profiling, no drug treatment, replicate 2",Illumina HiSeq 4000,SRR9113065,51856183,1508584022 PRJNA544411,SRX5887330,"Illumina HiSeq 4000 sequencing; GSM3791727: iPSC ribosome profiling, no drug treatment, replicate 3; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791727: iPSC ribosome profiling, no drug treatment, replicate 3; 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Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265422,49583723,1502676985 PRJNA548255,SRX6035775,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265423,58906924,1740811245 PRJNA548255,SRX6035774,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265424,45951630,1310462981 PRJNA548255,SRX6035773,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265425,47383970,1423177661 PRJNA548255,SRX6035772,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265426,42590657,1193803088 PRJNA548255,SRX6035771,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265427,66588117,2042292918 PRJNA548255,SRX6035769,Illumina HiSeq 1500 sequencing; 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Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016057,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/000/ERR1190990,1388161294,ftp.sra.ebi.ac.uk/vol1/err/ERR119/000/ERR1190990,ftp.sra.ebi.ac.uk/vol1/err/ERR119/000/ERR1190990,7b5e3a268df65bf04e953ebe7879d235,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190990/sample_10.fq.gz,1392173132,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190990/sample_10.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190990/sample_10.fq.gz,,d46272984dec850c41c06498903a225b,,,,,,,, PRJEB12126,ERX1264366,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708909,Sample 11,Illumina HiSeq 2000,ERR1190991,54474851,1713994365,SAMEA3708909,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 11,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/001/ERR1190991/ERR1190991.fastq.gz,1591009111,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/001/ERR1190991/ERR1190991.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/001/ERR1190991/ERR1190991.fastq.gz,3614cc1ddb4f166e9fd1e584d546938f,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 11,,,,,,,,,E-MTAB-4111:Sample 11,,E-MTAB-4111:Sample 11,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016058,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/001/ERR1190991,1332847226,ftp.sra.ebi.ac.uk/vol1/err/ERR119/001/ERR1190991,ftp.sra.ebi.ac.uk/vol1/err/ERR119/001/ERR1190991,98df90accff50e575b2bb2431f109512,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190991/sample_11.fq.gz,1427842939,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190991/sample_11.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190991/sample_11.fq.gz,,fa614ffc148689a0e8266afd4320192e,,,,,,,, PRJEB12126,ERX1264367,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708910,Sample 12,Illumina HiSeq 2000,ERR1190992,78497711,2489092061,SAMEA3708910,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 12,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/002/ERR1190992/ERR1190992.fastq.gz,2220963756,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/002/ERR1190992/ERR1190992.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/002/ERR1190992/ERR1190992.fastq.gz,2edb49df7be0c15b785e89f4c41ddcf2,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 12,,,,,,,,,E-MTAB-4111:Sample 12,,E-MTAB-4111:Sample 12,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016059,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/002/ERR1190992,1909616007,ftp.sra.ebi.ac.uk/vol1/err/ERR119/002/ERR1190992,ftp.sra.ebi.ac.uk/vol1/err/ERR119/002/ERR1190992,f4f3f8acfc07a286f47710ebd8d8faa3,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190992/sample_12.fq.gz,1984919544,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190992/sample_12.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190992/sample_12.fq.gz,,023d007cd36eca91bf65fb940666fb48,,,,,,,, PRJEB12126,ERX1264368,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708911,Sample 13,Illumina HiSeq 2000,ERR1190993,84955423,2627276298,SAMEA3708911,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 13,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/003/ERR1190993/ERR1190993.fastq.gz,2552783402,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/003/ERR1190993/ERR1190993.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/003/ERR1190993/ERR1190993.fastq.gz,4c9b92304199100be89710b362a059d4,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 13,,,,,,,,,E-MTAB-4111:Sample 13,,E-MTAB-4111:Sample 13,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016060,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/003/ERR1190993,2041075242,ftp.sra.ebi.ac.uk/vol1/err/ERR119/003/ERR1190993,ftp.sra.ebi.ac.uk/vol1/err/ERR119/003/ERR1190993,11a8ad15b7b301bd54cbc22b6dda19b5,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190993/sample_13.fq.gz,2295593342,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190993/sample_13.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190993/sample_13.fq.gz,,b50b57061d2f520a458de1f95c61753a,,,,,,,, PRJEB12126,ERX1264369,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708912,Sample 14,Illumina HiSeq 2000,ERR1190994,75097651,2293097872,SAMEA3708912,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 14,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/004/ERR1190994/ERR1190994.fastq.gz,2253968208,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/004/ERR1190994/ERR1190994.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/004/ERR1190994/ERR1190994.fastq.gz,6d050a4b42639848a784a3e21c49248b,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 14,,,,,,,,,E-MTAB-4111:Sample 14,,E-MTAB-4111:Sample 14,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016061,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/004/ERR1190994,1790148639,ftp.sra.ebi.ac.uk/vol1/err/ERR119/004/ERR1190994,ftp.sra.ebi.ac.uk/vol1/err/ERR119/004/ERR1190994,abd24ffc6ebb0dbf086de7af272239cd,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190994/sample_14.fq.gz,2025533568,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190994/sample_14.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190994/sample_14.fq.gz,,66e310243e5c0a8b507de4d74a1a7ae3,,,,,,,, PRJEB12126,ERX1264370,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708913,Sample 15,Illumina HiSeq 2000,ERR1190995,67177553,2060926619,SAMEA3708913,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 15,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/005/ERR1190995/ERR1190995.fastq.gz,2104874167,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/005/ERR1190995/ERR1190995.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/005/ERR1190995/ERR1190995.fastq.gz,125b6677cddeb17960f81f7af310b057,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 15,,,,,,,,,E-MTAB-4111:Sample 15,,E-MTAB-4111:Sample 15,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016062,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/005/ERR1190995,1631544238,ftp.sra.ebi.ac.uk/vol1/err/ERR119/005/ERR1190995,ftp.sra.ebi.ac.uk/vol1/err/ERR119/005/ERR1190995,8bc88ec81d681e8061e66fd4159f6cf6,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190995/sample_15.fq.gz,1899642594,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190995/sample_15.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190995/sample_15.fq.gz,,3a3e9867381f2ea48d1d05e893653b94,,,,,,,, PRJEB12126,ERX1264371,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708914,Sample 16,Illumina HiSeq 2000,ERR1190996,62940694,2061757111,SAMEA3708914,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 16,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/006/ERR1190996/ERR1190996.fastq.gz,2082203724,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/006/ERR1190996/ERR1190996.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/006/ERR1190996/ERR1190996.fastq.gz,1ee18cd6e209d1bdb7b642a120881f3f,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 16,,,,,,,,,E-MTAB-4111:Sample 16,,E-MTAB-4111:Sample 16,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016063,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/006/ERR1190996,1610743957,ftp.sra.ebi.ac.uk/vol1/err/ERR119/006/ERR1190996,ftp.sra.ebi.ac.uk/vol1/err/ERR119/006/ERR1190996,6e13c879e603fd67b09e36c739c27087,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190996/sample_16.fq.gz,1890642373,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190996/sample_16.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190996/sample_16.fq.gz,,9221dd53a73c1fcdbde047950278aad7,,,,,,,, PRJEB12126,ERX1264372,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708915,Sample 17,Illumina HiSeq 2000,ERR1190997,80591061,2475034240,SAMEA3708915,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 17,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/007/ERR1190997/ERR1190997.fastq.gz,2406895127,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/007/ERR1190997/ERR1190997.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/007/ERR1190997/ERR1190997.fastq.gz,8cb8ae554f44ba1d78613f273f397021,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 17,,,,,,,,,E-MTAB-4111:Sample 17,,E-MTAB-4111:Sample 17,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016064,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/007/ERR1190997,1908102168,ftp.sra.ebi.ac.uk/vol1/err/ERR119/007/ERR1190997,ftp.sra.ebi.ac.uk/vol1/err/ERR119/007/ERR1190997,c4f1bb4a2fa95e6b34f5bb061d4e85b8,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190997/sample_17.fq.gz,2162207875,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190997/sample_17.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190997/sample_17.fq.gz,,75acec50d70831728043119b9da063ad,,,,,,,, PRJEB12126,ERX1264373,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708916,Sample 18,Illumina HiSeq 2000,ERR1190998,68575621,2149386138,SAMEA3708916,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 18,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/008/ERR1190998/ERR1190998.fastq.gz,2105063166,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/008/ERR1190998/ERR1190998.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/008/ERR1190998/ERR1190998.fastq.gz,67aeca982e478564bd253865fc7a766c,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 18,,,,,,,,,E-MTAB-4111:Sample 18,,E-MTAB-4111:Sample 18,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016065,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/008/ERR1190998,1673112882,ftp.sra.ebi.ac.uk/vol1/err/ERR119/008/ERR1190998,ftp.sra.ebi.ac.uk/vol1/err/ERR119/008/ERR1190998,9c855553edd8015483826226f0e454df,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190998/sample_18.fq.gz,1896924035,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190998/sample_18.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190998/sample_18.fq.gz,,b2b559e0b4440f9c0bf6876f1b98428d,,,,,,,, PRJEB12126,ERX1264374,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708917,Sample 19,Illumina HiSeq 2000,ERR1190999,59543450,1840946911,SAMEA3708917,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 19,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/009/ERR1190999/ERR1190999.fastq.gz,1849353625,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/009/ERR1190999/ERR1190999.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/009/ERR1190999/ERR1190999.fastq.gz,b882b08b070548aeda29798236ae9748,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 19,,,,,,,,,E-MTAB-4111:Sample 19,,E-MTAB-4111:Sample 19,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016066,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/009/ERR1190999,2502027026,ftp.sra.ebi.ac.uk/vol1/err/ERR119/009/ERR1190999,ftp.sra.ebi.ac.uk/vol1/err/ERR119/009/ERR1190999,a37fd463a68c6e684a37082e9a50764e,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1190999/sample_19.fq.gz,1642503565,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190999/sample_19.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1190999/sample_19.fq.gz,,40b79160ef0e73cb5b9259e6ce9cdbf6,,,,,,,, PRJEB12126,ERX1264375,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708918,Sample 2,Illumina HiSeq 2000,ERR1191000,48420348,1429402558,SAMEA3708918,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/000/ERR1191000/ERR1191000.fastq.gz,1486205806,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/000/ERR1191000/ERR1191000.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/000/ERR1191000/ERR1191000.fastq.gz,cc362c5676dd6906ee40a18e191a3f6e,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 2,,,,,,,,,E-MTAB-4111:Sample 2,,E-MTAB-4111:Sample 2,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016067,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/000/ERR1191000,1126300261,ftp.sra.ebi.ac.uk/vol1/err/ERR119/000/ERR1191000,ftp.sra.ebi.ac.uk/vol1/err/ERR119/000/ERR1191000,2a5d2bd5e5f7025ee9ca6f84623ffeb4,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191000/sample_2.fq.gz,1339301011,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191000/sample_2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191000/sample_2.fq.gz,,7b69d69117d5183d3dc09efb4c94f3b4,,,,,,,, PRJEB12126,ERX1264376,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708919,Sample 20,Illumina HiSeq 2000,ERR1191001,39413642,1197490271,SAMEA3708919,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 20,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/001/ERR1191001/ERR1191001.fastq.gz,1141288041,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/001/ERR1191001/ERR1191001.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/001/ERR1191001/ERR1191001.fastq.gz,787ad729d733f2a27ac88b294831886f,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 20,,,,,,,,,E-MTAB-4111:Sample 20,,E-MTAB-4111:Sample 20,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016068,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/001/ERR1191001,1605804992,ftp.sra.ebi.ac.uk/vol1/err/ERR119/001/ERR1191001,ftp.sra.ebi.ac.uk/vol1/err/ERR119/001/ERR1191001,bee621a67c007d8c973fe4ee913834df,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191001/sample_20.fq.gz,1007509886,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191001/sample_20.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191001/sample_20.fq.gz,,83ef3dda9bcfe546ad1ad337a7324b24,,,,,,,, PRJEB12126,ERX1264377,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708920,Sample 21,Illumina HiSeq 2000,ERR1191002,43109202,1310217152,SAMEA3708920,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 21,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/002/ERR1191002/ERR1191002.fastq.gz,1239735906,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/002/ERR1191002/ERR1191002.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/002/ERR1191002/ERR1191002.fastq.gz,6f4f6a9287936464f800713018cd20d6,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 21,,,,,,,,,E-MTAB-4111:Sample 21,,E-MTAB-4111:Sample 21,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016069,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/002/ERR1191002,1739389406,ftp.sra.ebi.ac.uk/vol1/err/ERR119/002/ERR1191002,ftp.sra.ebi.ac.uk/vol1/err/ERR119/002/ERR1191002,4df6f3214d933fbd18381d4918bce059,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191002/sample_21.fq.gz,1092021312,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191002/sample_21.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191002/sample_21.fq.gz,,86273e2401b4193dd9e044528da23737,,,,,,,, PRJEB12126,ERX1264378,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708921,Sample 22,Illumina HiSeq 2000,ERR1191003,48048678,1464094378,SAMEA3708921,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 22,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/003/ERR1191003/ERR1191003.fastq.gz,1357313096,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/003/ERR1191003/ERR1191003.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/003/ERR1191003/ERR1191003.fastq.gz,cef8cd38a28ac5472337fdd7d954670f,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 22,,,,,,,,,E-MTAB-4111:Sample 22,,E-MTAB-4111:Sample 22,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016070,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/003/ERR1191003,1962593928,ftp.sra.ebi.ac.uk/vol1/err/ERR119/003/ERR1191003,ftp.sra.ebi.ac.uk/vol1/err/ERR119/003/ERR1191003,29faace51726dedcc4cfe90d24ac57b8,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191003/sample_22.fq.gz,1193034122,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191003/sample_22.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191003/sample_22.fq.gz,,da5cbe40b5f33f4ea7be71dfd6517939,,,,,,,, PRJEB12126,ERX1264379,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708922,Sample 23,Illumina HiSeq 2000,ERR1191004,55458988,1762359654,SAMEA3708922,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 23,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/004/ERR1191004/ERR1191004.fastq.gz,1582844288,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/004/ERR1191004/ERR1191004.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/004/ERR1191004/ERR1191004.fastq.gz,9e6e4bf2a2fefee8a950da6c45b5d56e,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 23,,,,,,,,,E-MTAB-4111:Sample 23,,E-MTAB-4111:Sample 23,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016071,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/004/ERR1191004,2308370862,ftp.sra.ebi.ac.uk/vol1/err/ERR119/004/ERR1191004,ftp.sra.ebi.ac.uk/vol1/err/ERR119/004/ERR1191004,f45389510ca23ad73806c9df445ca1dc,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191004/sample_23.fq.gz,1391504392,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191004/sample_23.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191004/sample_23.fq.gz,,bc935a775c9af96f365a07cc2a50272e,,,,,,,, PRJEB12126,ERX1264380,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708923,Sample 24,Illumina HiSeq 2000,ERR1191005,47426381,1463185679,SAMEA3708923,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 24,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/005/ERR1191005/ERR1191005.fastq.gz,1447507751,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/005/ERR1191005/ERR1191005.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/005/ERR1191005/ERR1191005.fastq.gz,c8eb21287506e80e971947e50fdd6090,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 24,,,,,,,,,E-MTAB-4111:Sample 24,,E-MTAB-4111:Sample 24,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016072,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/005/ERR1191005,1945207335,ftp.sra.ebi.ac.uk/vol1/err/ERR119/005/ERR1191005,ftp.sra.ebi.ac.uk/vol1/err/ERR119/005/ERR1191005,fb668c85ce592f96208c6f6c2d5f59a1,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191005/sample_24.fq.gz,1284098890,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191005/sample_24.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191005/sample_24.fq.gz,,c743b40f8d67881847f75110a2054be1,,,,,,,, PRJEB12126,ERX1264381,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708924,Sample 25,Illumina HiSeq 2000,ERR1191006,53368431,1671809961,SAMEA3708924,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 25,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/006/ERR1191006/ERR1191006.fastq.gz,1602355593,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/006/ERR1191006/ERR1191006.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/006/ERR1191006/ERR1191006.fastq.gz,d12cc91b5aaea781d3826471df591fd7,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 25,,,,,,,,,E-MTAB-4111:Sample 25,,E-MTAB-4111:Sample 25,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016073,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/006/ERR1191006,2251645247,ftp.sra.ebi.ac.uk/vol1/err/ERR119/006/ERR1191006,ftp.sra.ebi.ac.uk/vol1/err/ERR119/006/ERR1191006,dd25784a85ba684ae712269c45f1a825,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191006/sample_25.fq.gz,1419230073,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191006/sample_25.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191006/sample_25.fq.gz,,45be74f821d5feebd3884f206e88fff0,,,,,,,, PRJEB12126,ERX1264382,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708925,Sample 26,Illumina HiSeq 2000,ERR1191007,63008359,1879252598,SAMEA3708925,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 26,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/007/ERR1191007/ERR1191007.fastq.gz,1777894174,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/007/ERR1191007/ERR1191007.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/007/ERR1191007/ERR1191007.fastq.gz,5890bccd90637255bb7f74b5007a8b2a,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 26,,,,,,,,,E-MTAB-4111:Sample 26,,E-MTAB-4111:Sample 26,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016074,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/007/ERR1191007,2545066040,ftp.sra.ebi.ac.uk/vol1/err/ERR119/007/ERR1191007,ftp.sra.ebi.ac.uk/vol1/err/ERR119/007/ERR1191007,6a6152aa872fd53ca33cc659e4ce8b40,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191007/sample_26.fq.gz,1563700433,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191007/sample_26.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191007/sample_26.fq.gz,,47b17b647455ce2719134860b2850738,,,,,,,, PRJEB12126,ERX1264383,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708926,Sample 27,Illumina HiSeq 2000,ERR1191008,54398154,1665685103,SAMEA3708926,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 27,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/008/ERR1191008/ERR1191008.fastq.gz,1522964619,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/008/ERR1191008/ERR1191008.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/008/ERR1191008/ERR1191008.fastq.gz,8272c34e6eaf0ef3237f6bbd4db5ea00,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 27,,,,,,,,,E-MTAB-4111:Sample 27,,E-MTAB-4111:Sample 27,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016075,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/008/ERR1191008,2186751978,ftp.sra.ebi.ac.uk/vol1/err/ERR119/008/ERR1191008,ftp.sra.ebi.ac.uk/vol1/err/ERR119/008/ERR1191008,3a466c0cd79c8b2d210cd884ff0fbdd7,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191008/sample_27.fq.gz,1337240873,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191008/sample_27.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191008/sample_27.fq.gz,,7a3ac0c73cf7965f5f923913e8fe9bac,,,,,,,, PRJEB12126,ERX1264384,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708927,Sample 28,Illumina HiSeq 2000,ERR1191009,60588893,1898719877,SAMEA3708927,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 28,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/009/ERR1191009/ERR1191009.fastq.gz,1753873588,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/009/ERR1191009/ERR1191009.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/009/ERR1191009/ERR1191009.fastq.gz,39bcbd18c110cfc9ffec625fb6e686a2,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 28,,,,,,,,,E-MTAB-4111:Sample 28,,E-MTAB-4111:Sample 28,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016076,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/009/ERR1191009,2488581123,ftp.sra.ebi.ac.uk/vol1/err/ERR119/009/ERR1191009,ftp.sra.ebi.ac.uk/vol1/err/ERR119/009/ERR1191009,48361580974064dad2ae0ec9d114be07,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191009/sample_28.fq.gz,1543882466,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191009/sample_28.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191009/sample_28.fq.gz,,db51ab8f81a223a5cb508f5b30cf54cd,,,,,,,, PRJEB12126,ERX1264385,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708928,Sample 29,Illumina HiSeq 2000,ERR1191010,51322850,1636915300,SAMEA3708928,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 29,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/000/ERR1191010/ERR1191010.fastq.gz,1486538345,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/000/ERR1191010/ERR1191010.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/000/ERR1191010/ERR1191010.fastq.gz,eb3069fd56f66c306bc2cc691566f913,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 29,,,,,,,,,E-MTAB-4111:Sample 29,,E-MTAB-4111:Sample 29,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016077,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/000/ERR1191010,2130483818,ftp.sra.ebi.ac.uk/vol1/err/ERR119/000/ERR1191010,ftp.sra.ebi.ac.uk/vol1/err/ERR119/000/ERR1191010,b00ddc4df80690f60bb938f77d537fe5,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191010/sample_29.fq.gz,1308219057,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191010/sample_29.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191010/sample_29.fq.gz,,da28d91910441e2346dc66138bef13d9,,,,,,,, PRJEB12126,ERX1264386,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708929,Sample 3,Illumina HiSeq 2000,ERR1191011,51075405,1550469279,SAMEA3708929,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 3,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/001/ERR1191011/ERR1191011.fastq.gz,1590752820,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/001/ERR1191011/ERR1191011.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/001/ERR1191011/ERR1191011.fastq.gz,af410b9267ab7d486027d74de292c082,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 3,,,,,,,,,E-MTAB-4111:Sample 3,,E-MTAB-4111:Sample 3,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016078,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/001/ERR1191011,1238674308,ftp.sra.ebi.ac.uk/vol1/err/ERR119/001/ERR1191011,ftp.sra.ebi.ac.uk/vol1/err/ERR119/001/ERR1191011,cc132945ba293515e8faa5a81969024d,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191011/sample_3.fq.gz,1436625037,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191011/sample_3.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191011/sample_3.fq.gz,,0349e1e38f4fcd0ead4cbccde82cc83c,,,,,,,, PRJEB12126,ERX1264387,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708930,Sample 30,Illumina HiSeq 2000,ERR1191012,68573681,2176015649,SAMEA3708930,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 30,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/002/ERR1191012/ERR1191012.fastq.gz,2027489100,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/002/ERR1191012/ERR1191012.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/002/ERR1191012/ERR1191012.fastq.gz,79afb9440724de715d1469f78f456131,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 30,,,,,,,,,E-MTAB-4111:Sample 30,,E-MTAB-4111:Sample 30,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016079,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/002/ERR1191012,2830391998,ftp.sra.ebi.ac.uk/vol1/err/ERR119/002/ERR1191012,ftp.sra.ebi.ac.uk/vol1/err/ERR119/002/ERR1191012,a6b4a2e7c8b94eb67755d21a611eb2a4,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191012/sample_30.fq.gz,1790233662,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191012/sample_30.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191012/sample_30.fq.gz,,5525b842763c6363457bec6de5b27d3f,,,,,,,, PRJEB12126,ERX1264388,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708931,Sample 31,Illumina HiSeq 2000,ERR1191013,67660607,2053109515,SAMEA3708931,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 31,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/003/ERR1191013/ERR1191013.fastq.gz,2012242869,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/003/ERR1191013/ERR1191013.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/003/ERR1191013/ERR1191013.fastq.gz,c62be9cb3dfba3da0d97581f5b3c5892,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 31,,,,,,,,,E-MTAB-4111:Sample 31,,E-MTAB-4111:Sample 31,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016080,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/003/ERR1191013,2805301114,ftp.sra.ebi.ac.uk/vol1/err/ERR119/003/ERR1191013,ftp.sra.ebi.ac.uk/vol1/err/ERR119/003/ERR1191013,e26e3534a6895a612c62adc2fc0c33f1,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191013/sample_31.fq.gz,1781942533,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191013/sample_31.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191013/sample_31.fq.gz,,83b0e4910698bf1e56805fdf3b1fc096,,,,,,,, PRJEB12126,ERX1264389,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708932,Sample 32,Illumina HiSeq 2000,ERR1191014,79400383,2502665973,SAMEA3708932,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 32,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/004/ERR1191014/ERR1191014.fastq.gz,2431896210,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/004/ERR1191014/ERR1191014.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/004/ERR1191014/ERR1191014.fastq.gz,6334994ef89af6e331dcd8d6ad465085,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 32,,,,,,,,,E-MTAB-4111:Sample 32,,E-MTAB-4111:Sample 32,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016081,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/004/ERR1191014,3257300205,ftp.sra.ebi.ac.uk/vol1/err/ERR119/004/ERR1191014,ftp.sra.ebi.ac.uk/vol1/err/ERR119/004/ERR1191014,881976478b1b30fe14d9ab0d1e7bbee8,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191014/sample_32.fq.gz,2160091413,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191014/sample_32.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191014/sample_32.fq.gz,,15012bb2b07a0aee12516719e259c25b,,,,,,,, PRJEB12126,ERX1264390,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708933,Sample 33,Illumina HiSeq 2000,ERR1191015,65832767,2077595830,SAMEA3708933,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 33,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/005/ERR1191015/ERR1191015.fastq.gz,2070910806,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/005/ERR1191015/ERR1191015.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/005/ERR1191015/ERR1191015.fastq.gz,6f2a68b4d7dcd0a32fbb5bef07c08bbd,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 33,,,,,,,,,E-MTAB-4111:Sample 33,,E-MTAB-4111:Sample 33,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016082,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/005/ERR1191015,2659209451,ftp.sra.ebi.ac.uk/vol1/err/ERR119/005/ERR1191015,ftp.sra.ebi.ac.uk/vol1/err/ERR119/005/ERR1191015,5ee490d45864065bd0c0ec0dbae21cec,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191015/sample_33.fq.gz,1843275407,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191015/sample_33.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191015/sample_33.fq.gz,,87d67939ec0ac27d90f1298b6ba2245e,,,,,,,, PRJEB12126,ERX1264391,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708934,Sample 34,Illumina HiSeq 2000,ERR1191016,65880576,2068785301,SAMEA3708934,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 34,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/006/ERR1191016/ERR1191016.fastq.gz,2120284424,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/006/ERR1191016/ERR1191016.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/006/ERR1191016/ERR1191016.fastq.gz,80a690f7967284ffac227b2637d3b6ed,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 34,,,,,,,,,E-MTAB-4111:Sample 34,,E-MTAB-4111:Sample 34,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016083,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/006/ERR1191016,2696199926,ftp.sra.ebi.ac.uk/vol1/err/ERR119/006/ERR1191016,ftp.sra.ebi.ac.uk/vol1/err/ERR119/006/ERR1191016,9a2660f7d60b07cd5fa9b1dc3900fb3c,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191016/sample_34.fq.gz,1892977218,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191016/sample_34.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191016/sample_34.fq.gz,,ae7a1f86ea12281b74aec3fdb38fa395,,,,,,,, PRJEB12126,ERX1264392,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708935,Sample 35,Illumina HiSeq 2000,ERR1191017,45934156,1461586536,SAMEA3708935,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 35,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/007/ERR1191017/ERR1191017.fastq.gz,1353976017,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/007/ERR1191017/ERR1191017.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/007/ERR1191017/ERR1191017.fastq.gz,9585abc09fdaf0f4bd1bf157326967eb,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 35,,,,,,,,,E-MTAB-4111:Sample 35,,E-MTAB-4111:Sample 35,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016084,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/007/ERR1191017,1896513293,ftp.sra.ebi.ac.uk/vol1/err/ERR119/007/ERR1191017,ftp.sra.ebi.ac.uk/vol1/err/ERR119/007/ERR1191017,8fda104bcbe4de59ab89ad5407169f57,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191017/sample_35.fq.gz,1197236441,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191017/sample_35.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191017/sample_35.fq.gz,,b17f71f7bf6a6e5c5a5769547aabc661,,,,,,,, PRJEB12126,ERX1264393,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708936,Sample 36,Illumina HiSeq 2000,ERR1191018,62115857,1934185771,SAMEA3708936,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 36,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/008/ERR1191018/ERR1191018.fastq.gz,1857288901,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/008/ERR1191018/ERR1191018.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/008/ERR1191018/ERR1191018.fastq.gz,ad00da99b68a6ee63d49af56b792e7c7,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 36,,,,,,,,,E-MTAB-4111:Sample 36,,E-MTAB-4111:Sample 36,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016085,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/008/ERR1191018,2520416726,ftp.sra.ebi.ac.uk/vol1/err/ERR119/008/ERR1191018,ftp.sra.ebi.ac.uk/vol1/err/ERR119/008/ERR1191018,97afafedc5da93fdbbbb7654b4ef82c3,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191018/sample_36.fq.gz,1644311147,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191018/sample_36.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191018/sample_36.fq.gz,,17414093b819e27c0ce20b202427e6cc,,,,,,,, PRJEB12126,ERX1264394,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708937,Sample 37,Illumina HiSeq 2000,ERR1191019,56038006,1696854260,SAMEA3708937,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 37,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/009/ERR1191019/ERR1191019.fastq.gz,1755886457,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/009/ERR1191019/ERR1191019.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/009/ERR1191019/ERR1191019.fastq.gz,be79206b59e20c9a25857fefcde8dbb3,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 37,,,,,,,,,E-MTAB-4111:Sample 37,,E-MTAB-4111:Sample 37,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016086,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/009/ERR1191019,2324169926,ftp.sra.ebi.ac.uk/vol1/err/ERR119/009/ERR1191019,ftp.sra.ebi.ac.uk/vol1/err/ERR119/009/ERR1191019,f9a345535a5fa855ae6d7095402e3970,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191019/sample_37.fq.gz,1564888687,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191019/sample_37.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191019/sample_37.fq.gz,,f7ca496d49e5cff15b940d108753fd7f,,,,,,,, PRJEB12126,ERX1264395,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708938,Sample 38,Illumina HiSeq 2000,ERR1191020,50038369,1585387757,SAMEA3708938,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 38,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/000/ERR1191020/ERR1191020.fastq.gz,1509235624,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/000/ERR1191020/ERR1191020.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/000/ERR1191020/ERR1191020.fastq.gz,355dd641e453e5ca871646ad77efcea3,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 38,,,,,,,,,E-MTAB-4111:Sample 38,,E-MTAB-4111:Sample 38,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016087,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/000/ERR1191020,2115107355,ftp.sra.ebi.ac.uk/vol1/err/ERR119/000/ERR1191020,ftp.sra.ebi.ac.uk/vol1/err/ERR119/000/ERR1191020,3855e4dd818fa217bf5cb5a7bf6b0b9a,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191020/sample_38.fq.gz,1337496712,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191020/sample_38.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191020/sample_38.fq.gz,,8b5b9fc0caae885ffd5d09e48c7fecd4,,,,,,,, PRJEB12126,ERX1264396,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA3708939,Sample 39,Illumina HiSeq 2000,ERR1191021,82282313,2638880669,SAMEA3708939,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 39,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/001/ERR1191021/ERR1191021.fastq.gz,2540452181,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/001/ERR1191021/ERR1191021.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/001/ERR1191021/ERR1191021.fastq.gz,bda5b21fff30a47b6929f2f2023425e2,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 39,,,,,,,,,E-MTAB-4111:Sample 39,,E-MTAB-4111:Sample 39,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016088,ERP013565,RNASeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/001/ERR1191021,3394960101,ftp.sra.ebi.ac.uk/vol1/err/ERR119/001/ERR1191021,ftp.sra.ebi.ac.uk/vol1/err/ERR119/001/ERR1191021,d51343ffb1cef4dbb459cdb33082e598,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191021/sample_39.fq.gz,2258671903,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191021/sample_39.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191021/sample_39.fq.gz,,6fed3e69c73767a36bdb02c3407254cf,,,,,,,, PRJEB12126,ERX1264397,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708940,Sample 4,Illumina HiSeq 2000,ERR1191022,63170089,2044068461,SAMEA3708940,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 4,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/002/ERR1191022/ERR1191022.fastq.gz,1821948135,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/002/ERR1191022/ERR1191022.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/002/ERR1191022/ERR1191022.fastq.gz,41aa148a1806adabdea66f2596872b8b,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 4,,,,,,,,,E-MTAB-4111:Sample 4,,E-MTAB-4111:Sample 4,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016089,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/002/ERR1191022,1601578940,ftp.sra.ebi.ac.uk/vol1/err/ERR119/002/ERR1191022,ftp.sra.ebi.ac.uk/vol1/err/ERR119/002/ERR1191022,e128180afc489283025692bdfdfb445a,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191022/sample_4.fq.gz,1637538599,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191022/sample_4.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191022/sample_4.fq.gz,,a227f514c1cd0f5233cae18945ba73f0,,,,,,,, PRJEB12126,ERX1264398,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708941,Sample 40,Illumina HiSeq 2000,ERR1191023,76077975,3120456466,SAMEA3708941,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 40,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/003/ERR1191023/ERR1191023.fastq.gz,2651414559,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/003/ERR1191023/ERR1191023.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/003/ERR1191023/ERR1191023.fastq.gz,de907d29d9197af82b0e202c1d2e88db,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 40,,,,,,,,,E-MTAB-4111:Sample 40,,E-MTAB-4111:Sample 40,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016090,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/003/ERR1191023,3756169072,ftp.sra.ebi.ac.uk/vol1/err/ERR119/003/ERR1191023,ftp.sra.ebi.ac.uk/vol1/err/ERR119/003/ERR1191023,d42fd900183d840b865863e124305edd,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191023/sample_40.fq.gz,2388267629,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191023/sample_40.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191023/sample_40.fq.gz,,4532c47d9a0510c643863a5ae417a5b2,,,,,,,, PRJEB12126,ERX1264399,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708942,Sample 5,Illumina HiSeq 2000,ERR1191024,38540171,1192143682,SAMEA3708942,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 5,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/004/ERR1191024/ERR1191024.fastq.gz,1192911261,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/004/ERR1191024/ERR1191024.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/004/ERR1191024/ERR1191024.fastq.gz,1d7574ce44c781a4c868dacbfb841893,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 5,,,,,,,,,E-MTAB-4111:Sample 5,,E-MTAB-4111:Sample 5,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016091,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/004/ERR1191024,930675946,ftp.sra.ebi.ac.uk/vol1/err/ERR119/004/ERR1191024,ftp.sra.ebi.ac.uk/vol1/err/ERR119/004/ERR1191024,5b569950e11b3c769c5b087da44f4b3f,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191024/sample_5.fq.gz,1078055632,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191024/sample_5.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191024/sample_5.fq.gz,,4dc16b0f6a8c84a17fe38e0386e80dbe,,,,,,,, PRJEB12126,ERX1264400,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708943,Sample 6,Illumina HiSeq 2000,ERR1191025,27122370,839903135,SAMEA3708943,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 6,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/005/ERR1191025/ERR1191025.fastq.gz,864566366,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/005/ERR1191025/ERR1191025.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/005/ERR1191025/ERR1191025.fastq.gz,5b88a3746732c352f9b668d26be0b0c2,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 6,,,,,,,,,E-MTAB-4111:Sample 6,,E-MTAB-4111:Sample 6,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016092,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/005/ERR1191025,661628933,ftp.sra.ebi.ac.uk/vol1/err/ERR119/005/ERR1191025,ftp.sra.ebi.ac.uk/vol1/err/ERR119/005/ERR1191025,fd1bc249a76fcea9e7df10b2c759832c,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191025/sample_6.fq.gz,783523472,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191025/sample_6.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191025/sample_6.fq.gz,,671d6907041a3b8c39d29af063fbc0d5,,,,,,,, PRJEB12126,ERX1264401,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708944,Sample 7,Illumina HiSeq 2000,ERR1191026,52888637,1629947931,SAMEA3708944,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 7,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/006/ERR1191026/ERR1191026.fastq.gz,1628603632,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/006/ERR1191026/ERR1191026.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/006/ERR1191026/ERR1191026.fastq.gz,8445cf7dfee54be87fcffa6c449f5a20,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 7,,,,,,,,,E-MTAB-4111:Sample 7,,E-MTAB-4111:Sample 7,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016093,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/006/ERR1191026,1288626489,ftp.sra.ebi.ac.uk/vol1/err/ERR119/006/ERR1191026,ftp.sra.ebi.ac.uk/vol1/err/ERR119/006/ERR1191026,11cba143ba3b6bd6810ab95984c9f827,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191026/sample_7.fq.gz,1467714303,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191026/sample_7.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191026/sample_7.fq.gz,,899744746c051635a5532981d60abd1d,,,,,,,, PRJEB12126,ERX1264402,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708945,Sample 8,Illumina HiSeq 2000,ERR1191027,47240129,1457468497,SAMEA3708945,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 8,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/007/ERR1191027/ERR1191027.fastq.gz,1464475125,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/007/ERR1191027/ERR1191027.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/007/ERR1191027/ERR1191027.fastq.gz,3b737aded7057f76f036867773cf6f15,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 8,,,,,,,,,E-MTAB-4111:Sample 8,,E-MTAB-4111:Sample 8,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016094,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/007/ERR1191027,1148039809,ftp.sra.ebi.ac.uk/vol1/err/ERR119/007/ERR1191027,ftp.sra.ebi.ac.uk/vol1/err/ERR119/007/ERR1191027,62e6e13e173547cac37908435a906aa2,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191027/sample_8.fq.gz,1319898533,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191027/sample_8.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191027/sample_8.fq.gz,,759076aeedba29d5122490011fa4481f,,,,,,,, PRJEB12126,ERX1264403,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA3708946,Sample 9,Illumina HiSeq 2000,ERR1191028,58914298,1823035475,SAMEA3708946,,,,,,ArrayExpress,17-Cl1,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-4111:Sample 9,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR119/008/ERR1191028/ERR1191028.fastq.gz,1799861171,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/008/ERR1191028/ERR1191028.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR119/008/ERR1191028/ERR1191028.fastq.gz,a782b1d1fa098137d2e4af3f9af7bfeb,2015-12-14,2016-02-08,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 9,,,,,,,,,E-MTAB-4111:Sample 9,,E-MTAB-4111:Sample 9,,"Protocols: Murine 17 clone 1 (17Cl-1) (Sturman and Takemoto, 1972) and BHK-21 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum (FCS). Recombinant MHV strain A59 (MHV-A59) was derived as previously described (Coley et al., 2005). 17Cl-1 cells (10^7) were plated in 10 cm dishes and, upon reaching 70-80% confluence, were infected with MHV-A59 at a multiplicity of infection (MOI) of 10 PFU/cell (or 200 PFU/cell in the High MOI experiment - samples 37-39) in Hanks balanced salt solution (HBSS) containing 50 mg/ml DEAE-dextran and 0.2% bovine serum albumin (BSA). After 45 min at 37 oC, the inoculum was removed and the cells were incubated in DMEM containing 10% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 oC until harvest. At the appropriate time point, cells were treated with CHX (Sigma-Aldrich; to 100 g/ml; 2 min), or HAR (LKT laboratories; 2 g/ml, 3 min) then CHX (to 100 g/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 g/ml cycloheximide and 25 U/ml TURBOTM DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 oC, the supernatants recovered and sto",,,,,ERS1016095,ERP013565,RiboSeq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR119/008/ERR1191028,1442864149,ftp.sra.ebi.ac.uk/vol1/err/ERR119/008/ERR1191028,ftp.sra.ebi.ac.uk/vol1/err/ERR119/008/ERR1191028,2e50dd4483885797c3d040fe85a76d4c,,E-MTAB-4111,Analysis of coronavirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA542783,fasp.sra.ebi.ac.uk:/vol1/run/ERR119/ERR1191028/sample_9.fq.gz,1619624159,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191028/sample_9.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR119/ERR1191028/sample_9.fq.gz,,bd7614dfcbdda387485a1ba2adc411e1,,,,,,,, PRJEB17636,ERX1789731,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534046,Sample 1,Illumina HiSeq 2000,ERR1719518,41599973,1375854749,SAMEA4534046,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/008/ERR1719518/ERR1719518.fastq.gz,1008609000,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/008/ERR1719518/ERR1719518.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/008/ERR1719518/ERR1719518.fastq.gz,25387b8619161645bb17d6b304dcc570,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 1_s,,,,,,,,,E-MTAB-5206:Sample 1,,E-MTAB-5206:Sample 1,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433225,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/008/ERR1719518,1721608527,ftp.sra.ebi.ac.uk/vol1/err/ERR171/008/ERR1719518,ftp.sra.ebi.ac.uk/vol1/err/ERR171/008/ERR1719518,296c9fe5aefbbdfb5a67f03e702df3c6,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719518/sample_1.fq.gz,872679569,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719518/sample_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719518/sample_1.fq.gz,,8277c093b80adbd0514b7cd6edaa0b6d,,,,,,,, PRJEB17636,ERX1789732,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534047,Sample 10,NextSeq 500,ERR1719519,23069695,740677911,SAMEA4534047,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 10_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/009/ERR1719519/ERR1719519.fastq.gz,458231375,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/009/ERR1719519/ERR1719519.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/009/ERR1719519/ERR1719519.fastq.gz,d37bb2c302934b7b25e204821ec15ecd,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 10_s,,,,,,,,,E-MTAB-5206:Sample 10,,E-MTAB-5206:Sample 10,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433226,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/009/ERR1719519,410162104,ftp.sra.ebi.ac.uk/vol1/err/ERR171/009/ERR1719519,ftp.sra.ebi.ac.uk/vol1/err/ERR171/009/ERR1719519,4927259a6f290ce6dfb902d462e2d17e,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719519/sample_10.fq.gz,394444293,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719519/sample_10.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719519/sample_10.fq.gz,,2c7274a10e255b56cdb0422573e795d5,,,,,,,, PRJEB17636,ERX1789733,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534048,Sample 11,NextSeq 500,ERR1719520,29010875,922672397,SAMEA4534048,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/000/ERR1719520/ERR1719520.fastq.gz,571720642,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/000/ERR1719520/ERR1719520.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/000/ERR1719520/ERR1719520.fastq.gz,3e4b34c0fa86510d02fc2c715dd7cd34,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 11_s,,,,,,,,,E-MTAB-5206:Sample 11,,E-MTAB-5206:Sample 11,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433227,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/000/ERR1719520,511639505,ftp.sra.ebi.ac.uk/vol1/err/ERR171/000/ERR1719520,ftp.sra.ebi.ac.uk/vol1/err/ERR171/000/ERR1719520,2b413b2772d7646eeb6e2179efab7627,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719520/sample_11.fq.gz,491194232,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719520/sample_11.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719520/sample_11.fq.gz,,70102d6e6894193ae62bd8b041547498,,,,,,,, PRJEB17636,ERX1789734,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534049,Sample 12,NextSeq 500,ERR1719521,30202884,976358769,SAMEA4534049,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 12_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/001/ERR1719521/ERR1719521.fastq.gz,610917361,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/001/ERR1719521/ERR1719521.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/001/ERR1719521/ERR1719521.fastq.gz,be245f1204beb717807d43116c5172ea,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 12_s,,,,,,,,,E-MTAB-5206:Sample 12,,E-MTAB-5206:Sample 12,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433228,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/001/ERR1719521,537625182,ftp.sra.ebi.ac.uk/vol1/err/ERR171/001/ERR1719521,ftp.sra.ebi.ac.uk/vol1/err/ERR171/001/ERR1719521,d94e73606808be9fe2a048f2a664f611,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719521/sample_12.fq.gz,527204938,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719521/sample_12.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719521/sample_12.fq.gz,,5974f783c47ad69a0b2fdf52bc89a213,,,,,,,, PRJEB17636,ERX1789735,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534050,Sample 13,NextSeq 500,ERR1719522,19815295,629646715,SAMEA4534050,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 13_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/002/ERR1719522/ERR1719522.fastq.gz,406709306,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/002/ERR1719522/ERR1719522.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/002/ERR1719522/ERR1719522.fastq.gz,b2521d97a5aeabe6a7de5bc9b549c959,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 13_s,,,,,,,,,E-MTAB-5206:Sample 13,,E-MTAB-5206:Sample 13,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433229,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/002/ERR1719522,356680454,ftp.sra.ebi.ac.uk/vol1/err/ERR171/002/ERR1719522,ftp.sra.ebi.ac.uk/vol1/err/ERR171/002/ERR1719522,30f278013c0d9fe683aaca6ac27d393d,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719522/sample_13.fq.gz,351825253,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719522/sample_13.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719522/sample_13.fq.gz,,a2195232b0d14f3c63cd1941979679c1,,,,,,,, PRJEB17636,ERX1789736,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534051,Sample 14,NextSeq 500,ERR1719523,37199064,1177627544,SAMEA4534051,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 14_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/003/ERR1719523/ERR1719523.fastq.gz,731365330,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/003/ERR1719523/ERR1719523.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/003/ERR1719523/ERR1719523.fastq.gz,6405c3025eda517feca5c7c9dcb6a895,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 14_s,,,,,,,,,E-MTAB-5206:Sample 14,,E-MTAB-5206:Sample 14,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433230,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/003/ERR1719523,645254517,ftp.sra.ebi.ac.uk/vol1/err/ERR171/003/ERR1719523,ftp.sra.ebi.ac.uk/vol1/err/ERR171/003/ERR1719523,87a514676c98b93bb5a7580bc7ffa536,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719523/sample_14.fq.gz,628202566,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719523/sample_14.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719523/sample_14.fq.gz,,81ae3916a7ab5a0b72bc9487911b9e9b,,,,,,,, PRJEB17636,ERX1789737,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534052,Sample 15,NextSeq 500,ERR1719524,26965806,866250047,SAMEA4534052,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 15_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/004/ERR1719524/ERR1719524.fastq.gz,691925041,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/004/ERR1719524/ERR1719524.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/004/ERR1719524/ERR1719524.fastq.gz,7120a589d29cf5af0d95f0cc75590353,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 15_s,,,,,,,,,E-MTAB-5206:Sample 15,,E-MTAB-5206:Sample 15,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433231,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/004/ERR1719524,483815391,ftp.sra.ebi.ac.uk/vol1/err/ERR171/004/ERR1719524,ftp.sra.ebi.ac.uk/vol1/err/ERR171/004/ERR1719524,11a30fb40150e5fbf5c9f98b678d7409,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719524/sample_15.fq.gz,617403660,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719524/sample_15.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719524/sample_15.fq.gz,,97dc0f41171d0cffe108fb19f8e4d16c,,,,,,,, PRJEB17636,ERX1789738,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534053,Sample 16,NextSeq 500,ERR1719525,31150940,974286119,SAMEA4534053,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 16_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/005/ERR1719525/ERR1719525.fastq.gz,787670275,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/005/ERR1719525/ERR1719525.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/005/ERR1719525/ERR1719525.fastq.gz,f44deb3c552f152312a7f01ac487b55d,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 16_s,,,,,,,,,E-MTAB-5206:Sample 16,,E-MTAB-5206:Sample 16,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433232,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/005/ERR1719525,547142349,ftp.sra.ebi.ac.uk/vol1/err/ERR171/005/ERR1719525,ftp.sra.ebi.ac.uk/vol1/err/ERR171/005/ERR1719525,2d3de60835a6f81ea66500a92dc85e3a,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719525/sample_16.fq.gz,701764361,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719525/sample_16.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719525/sample_16.fq.gz,,038984beeae23ce4366d8517982d5063,,,,,,,, PRJEB17636,ERX1789739,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534054,Sample 17,NextSeq 500,ERR1719526,31786494,975436074,SAMEA4534054,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 17_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/006/ERR1719526/ERR1719526.fastq.gz,818879202,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/006/ERR1719526/ERR1719526.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/006/ERR1719526/ERR1719526.fastq.gz,f311a48da57a11dd008c79b99ae797a2,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 17_s,,,,,,,,,E-MTAB-5206:Sample 17,,E-MTAB-5206:Sample 17,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433233,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/006/ERR1719526,560198194,ftp.sra.ebi.ac.uk/vol1/err/ERR171/006/ERR1719526,ftp.sra.ebi.ac.uk/vol1/err/ERR171/006/ERR1719526,acfd31db42ee761f560e87aec204c79d,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719526/sample_17.fq.gz,730894352,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719526/sample_17.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719526/sample_17.fq.gz,,8373d6ecf7acfba3e7c80e3cafd2a803,,,,,,,, PRJEB17636,ERX1789740,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534055,Sample 18,NextSeq 500,ERR1719527,31291402,1004598571,SAMEA4534055,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 18_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/007/ERR1719527/ERR1719527.fastq.gz,840918222,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/007/ERR1719527/ERR1719527.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/007/ERR1719527/ERR1719527.fastq.gz,fc5578f9ee78ffce0611454452d44692,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 18_s,,,,,,,,,E-MTAB-5206:Sample 18,,E-MTAB-5206:Sample 18,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433234,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/007/ERR1719527,577945834,ftp.sra.ebi.ac.uk/vol1/err/ERR171/007/ERR1719527,ftp.sra.ebi.ac.uk/vol1/err/ERR171/007/ERR1719527,e03d750bdaa793342db431d8515c6260,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719527/sample_18.fq.gz,754086134,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719527/sample_18.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719527/sample_18.fq.gz,,3bb78f549702f3cf5dc47a3ecf1e0e6d,,,,,,,, PRJEB17636,ERX1789741,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534056,Sample 19,NextSeq 500,ERR1719528,28466729,885092147,SAMEA4534056,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 19_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/008/ERR1719528/ERR1719528.fastq.gz,707716702,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/008/ERR1719528/ERR1719528.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/008/ERR1719528/ERR1719528.fastq.gz,f7be09cca41578cfd0908e06148290f7,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 19_s,,,,,,,,,E-MTAB-5206:Sample 19,,E-MTAB-5206:Sample 19,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433235,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/008/ERR1719528,499453371,ftp.sra.ebi.ac.uk/vol1/err/ERR171/008/ERR1719528,ftp.sra.ebi.ac.uk/vol1/err/ERR171/008/ERR1719528,73be180fce0f4d9ae632eee911bb0624,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719528/sample_19.fq.gz,629200707,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719528/sample_19.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719528/sample_19.fq.gz,,b3feded98fd6881e634e5ab5ac95dc7e,,,,,,,, PRJEB17636,ERX1789742,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534057,Sample 2,Illumina HiSeq 2000,ERR1719529,43631646,1380630106,SAMEA4534057,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/009/ERR1719529/ERR1719529.fastq.gz,1058683503,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/009/ERR1719529/ERR1719529.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/009/ERR1719529/ERR1719529.fastq.gz,916a578e64e43a04947e992454349e72,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 2_s,,,,,,,,,E-MTAB-5206:Sample 2,,E-MTAB-5206:Sample 2,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433236,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/009/ERR1719529,1763202120,ftp.sra.ebi.ac.uk/vol1/err/ERR171/009/ERR1719529,ftp.sra.ebi.ac.uk/vol1/err/ERR171/009/ERR1719529,9353c4ada0cd817671006ffc1d2dda4e,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719529/sample_2.fq.gz,916473158,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719529/sample_2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719529/sample_2.fq.gz,,e2a8904246130772f761be27b5ec82ce,,,,,,,, PRJEB17636,ERX1789743,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4534058,Sample 20,NextSeq 500,ERR1719530,33738268,1059476203,SAMEA4534058,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 20_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/000/ERR1719530/ERR1719530.fastq.gz,882666039,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/000/ERR1719530/ERR1719530.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/000/ERR1719530/ERR1719530.fastq.gz,52d572f1d91de492383c42e3142d34e1,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 20_s,,,,,,,,,E-MTAB-5206:Sample 20,,E-MTAB-5206:Sample 20,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433237,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/000/ERR1719530,610179466,ftp.sra.ebi.ac.uk/vol1/err/ERR171/000/ERR1719530,ftp.sra.ebi.ac.uk/vol1/err/ERR171/000/ERR1719530,e3119cc6c92f9d585f88797583367ddb,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719530/sample_20.fq.gz,788657456,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719530/sample_20.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719530/sample_20.fq.gz,,20abd963290b6f20ad4792b0b371076b,,,,,,,, PRJEB17636,ERX1789744,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534059,Sample 3,Illumina HiSeq 2000,ERR1719531,40726173,1283483477,SAMEA4534059,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/001/ERR1719531/ERR1719531.fastq.gz,1019672098,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/001/ERR1719531/ERR1719531.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/001/ERR1719531/ERR1719531.fastq.gz,48d63305141197c7e59df7132e8bf73e,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 3_s,,,,,,,,,E-MTAB-5206:Sample 3,,E-MTAB-5206:Sample 3,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433238,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/001/ERR1719531,1662489502,ftp.sra.ebi.ac.uk/vol1/err/ERR171/001/ERR1719531,ftp.sra.ebi.ac.uk/vol1/err/ERR171/001/ERR1719531,f52b777f26dd5cc122df62feb35688f1,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719531/sample_3.fq.gz,886717805,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719531/sample_3.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719531/sample_3.fq.gz,,bd5fcc9547df90643208ec3c1d330814,,,,,,,, PRJEB17636,ERX1789745,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534060,Sample 4,Illumina HiSeq 2000,ERR1719532,39825021,1261053649,SAMEA4534060,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/002/ERR1719532/ERR1719532.fastq.gz,990700184,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/002/ERR1719532/ERR1719532.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/002/ERR1719532/ERR1719532.fastq.gz,10d73df1a9d525e440a5e9a47cd4ac82,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 4_s,,,,,,,,,E-MTAB-5206:Sample 4,,E-MTAB-5206:Sample 4,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433239,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/002/ERR1719532,1626909751,ftp.sra.ebi.ac.uk/vol1/err/ERR171/002/ERR1719532,ftp.sra.ebi.ac.uk/vol1/err/ERR171/002/ERR1719532,48a2a2d1974ba5dec6797a51f6aa2c13,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719532/sample_4.fq.gz,860845392,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719532/sample_4.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719532/sample_4.fq.gz,,4c13293dd35556619b6ffe7c97b0d709,,,,,,,, PRJEB17636,ERX1789746,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534061,Sample 5,Illumina HiSeq 2000,ERR1719533,50368881,1646355648,SAMEA4534061,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 5_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/003/ERR1719533/ERR1719533.fastq.gz,1172357066,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/003/ERR1719533/ERR1719533.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/003/ERR1719533/ERR1719533.fastq.gz,a15ff1ac533b37496d33be390a6dd81f,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 5_s,,,,,,,,,E-MTAB-5206:Sample 5,,E-MTAB-5206:Sample 5,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433240,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/003/ERR1719533,2032983145,ftp.sra.ebi.ac.uk/vol1/err/ERR171/003/ERR1719533,ftp.sra.ebi.ac.uk/vol1/err/ERR171/003/ERR1719533,9df3e1afe9b16ea46f4fabb4a4a34b41,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719533/sample_5.fq.gz,1007432317,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719533/sample_5.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719533/sample_5.fq.gz,,5d272240ba617f84ab649dbbfc48e6de,,,,,,,, PRJEB17636,ERX1789747,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534062,Sample 6,Illumina HiSeq 2000,ERR1719534,47535077,1522019700,SAMEA4534062,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 6_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/004/ERR1719534/ERR1719534.fastq.gz,1123174355,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/004/ERR1719534/ERR1719534.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/004/ERR1719534/ERR1719534.fastq.gz,50881946a7b7ec6afeab6dd1274b92b6,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 6_s,,,,,,,,,E-MTAB-5206:Sample 6,,E-MTAB-5206:Sample 6,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433241,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/004/ERR1719534,1907435873,ftp.sra.ebi.ac.uk/vol1/err/ERR171/004/ERR1719534,ftp.sra.ebi.ac.uk/vol1/err/ERR171/004/ERR1719534,26481ec08a46592003763de5e1baafa9,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719534/sample_6.fq.gz,967566566,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719534/sample_6.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719534/sample_6.fq.gz,,3d95e695d24547022d48cc14462b80e1,,,,,,,, PRJEB17636,ERX1789748,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534063,Sample 7,Illumina HiSeq 2000,ERR1719535,49746314,1603492330,SAMEA4534063,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 7_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/005/ERR1719535/ERR1719535.fastq.gz,1175924373,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/005/ERR1719535/ERR1719535.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/005/ERR1719535/ERR1719535.fastq.gz,b5270b79d2ef0fb543cc4e601b5bb8f5,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 7_s,,,,,,,,,E-MTAB-5206:Sample 7,,E-MTAB-5206:Sample 7,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433242,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/005/ERR1719535,2013088184,ftp.sra.ebi.ac.uk/vol1/err/ERR171/005/ERR1719535,ftp.sra.ebi.ac.uk/vol1/err/ERR171/005/ERR1719535,f84395c1b2022dc4e8a3a6728f78ac45,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719535/sample_7.fq.gz,1012794146,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719535/sample_7.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719535/sample_7.fq.gz,,bc03d5e87c560ec1fa0e736923c233f8,,,,,,,, PRJEB17636,ERX1789749,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,Illumina HiSeq 2000 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534064,Sample 8,Illumina HiSeq 2000,ERR1719536,48745145,1548939461,SAMEA4534064,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 8_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/006/ERR1719536/ERR1719536.fastq.gz,1114980042,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/006/ERR1719536/ERR1719536.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/006/ERR1719536/ERR1719536.fastq.gz,1e7cede29d7563266d0886ab3ba026d4,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 8_s,,,,,,,,,E-MTAB-5206:Sample 8,,E-MTAB-5206:Sample 8,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433243,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/006/ERR1719536,1928974188,ftp.sra.ebi.ac.uk/vol1/err/ERR171/006/ERR1719536,ftp.sra.ebi.ac.uk/vol1/err/ERR171/006/ERR1719536,693dc8ef726eb7b3bb10cbb312f20da1,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719536/sample_8.fq.gz,956004832,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719536/sample_8.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719536/sample_8.fq.gz,,a73001fde95a00d362b8c3128611c2a6,,,,,,,, PRJEB17636,ERX1789750,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,NextSeq 500 sequencing; Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMEA4534065,Sample 9,NextSeq 500,ERR1719537,24213954,761912205,SAMEA4534065,,,,,,ArrayExpress,L929,fibroblast,"Department of Pathology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5206:Sample 9_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR171/007/ERR1719537/ERR1719537.fastq.gz,491156447,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/007/ERR1719537/ERR1719537.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR171/007/ERR1719537/ERR1719537.fastq.gz,4baec9c7efd0f98ed355e96ed8b0c5eb,2016-11-03,2017-06-02,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 9_s,,,,,,,,,E-MTAB-5206:Sample 9,,E-MTAB-5206:Sample 9,,"Protocols: L929 cells in 60-mm dishes were infected at an MOI of 10 in an initial volume of 1.5 ml DMEM with 1% FBS. After 1 h adsorption at 37 °C an additional 3.5 ml was added and incubation continued. At the appropriate time points, cells were treated with cycloheximide (Sigma-Aldrich; to 100 μg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 μl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 μg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to Ribo-Seq and RNA-Seq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina smallRNA v2 to allow multiplexing, as described previously (Chung et al., 2015).",,,,,ERS1433244,ERP019506,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR171/007/ERR1719537,428529750,ftp.sra.ebi.ac.uk/vol1/err/ERR171/007/ERR1719537,ftp.sra.ebi.ac.uk/vol1/err/ERR171/007/ERR1719537,8c4a9ed9734a79388e4d42da7a73b75d,,E-MTAB-5206,Analysis of cardiovirus and infected host-cell gene expression through RNA sequencing and ribosome profiling,,,ERA745198,fasp.sra.ebi.ac.uk:/vol1/run/ERR171/ERR1719537/sample_9.fq.gz,424063048,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719537/sample_9.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR171/ERR1719537/sample_9.fq.gz,,fd6eb0c69ba313efc69e684433686a31,,,,,,,, PRJEB19014,ERX1861079,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,294,Pseudomonas fluorescens,MNase-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA50540668,hfq1,Illumina HiSeq 2000,ERR1797529,37747215,1025325032,SAMEA50540668,,,,,,ArrayExpress,,,Department of Molecular Microbiology John Innes Centre,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5408:hfq1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR179/009/ERR1797529/ERR1797529.fastq.gz,948526016,ftp.sra.ebi.ac.uk/vol1/fastq/ERR179/009/ERR1797529/ERR1797529.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR179/009/ERR1797529/ERR1797529.fastq.gz,e4dfbe06a856fe49927470a37c3736b6,2017-01-16,2017-08-24,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,hfq1_s,,,,,,,,,E-MTAB-5408:hfq1,,E-MTAB-5408:hfq1,,"Protocols: SBW25 WT and Δhfq cultures were grown at 28°C in M9 medium supplemented with 0.4% pyruvate and 0.4% casamino acids to the late exponential phase. Cells were harvested by rapid filtration as described in Oh et al. (2011) Cell 147(6):1295-1308. Collected cells were flash frozen in liquid nitrogen and cryogenically pulverized by mixer milling (Retsch). Pulverized cells were thawed and clarified by centrifugation. Resulting lysates were digested with MNase, quenched with EGTA and resolved by sucrose density gradient ultracentrifugation. Ribosome-protected mRNA footprints were processed as previously described in Becker et al.(2013) Nat Protoc 8(11):2212-2239. Sequencing library was prepared as described in Oh et al. (2011) Cell 147(6):1295-1308. Briefly, RNA extracted from monosome fractions was size selected for 28 to 42 nucleotides by running on a 15% TBE-urea gel using a 10 bp ladder as the standard. The 3′ ends of RNA were dephosphorylated by T4 PNK and then ligated to the linker 5′_App/CTGTAGGCACCATCAAT/3 ddC_3′. The ligated products were size selected for 45 to 60 nucleotides and reverse transcribed with no more than five molar excess of 5′_5phosCAAGCAGAAGACGGCATACGAATTGATGGTGCCTACAG_3′. The reverse transcribed cDNA was size selected for 125 to 150 bp and circularised. The circDNA was PCR amplified with 5′_AATGATACGGCGACCACCGA_3′ and 5′_CAAGCAGAAGACGGCATACGA_3′ for 7 to 10 cycles and the amplicons were resolved on an 8% polyacrylamide gel i...",,,,,ERS1505502,ERP020995,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR179/009/ERR1797529,802201547,ftp.sra.ebi.ac.uk/vol1/err/ERR179/009/ERR1797529,ftp.sra.ebi.ac.uk/vol1/err/ERR179/009/ERR1797529,fe15d6e453b6e73be3e498edce65ab3f,,E-MTAB-5408,Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,,,ERA789570,fasp.sra.ebi.ac.uk:/vol1/run/ERR179/ERR1797529/hfq1.fq.gz,838072192,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR179/ERR1797529/hfq1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR179/ERR1797529/hfq1.fq.gz,,78706f2559c01ce0fccf6f48fe3250e8,,,,,,,, PRJEB19014,ERX1861080,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,294,Pseudomonas fluorescens,MNase-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA50541418,hfq2,Illumina HiSeq 2000,ERR1797530,27730412,742041285,SAMEA50541418,,,,,,ArrayExpress,,,Department of Molecular Microbiology John Innes Centre,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5408:hfq2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR179/000/ERR1797530/ERR1797530.fastq.gz,692039537,ftp.sra.ebi.ac.uk/vol1/fastq/ERR179/000/ERR1797530/ERR1797530.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR179/000/ERR1797530/ERR1797530.fastq.gz,40a07583c5292f0dd0a8109ec25e375b,2017-01-16,2017-08-24,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,hfq2_s,,,,,,,,,E-MTAB-5408:hfq2,,E-MTAB-5408:hfq2,,"Protocols: SBW25 WT and Δhfq cultures were grown at 28°C in M9 medium supplemented with 0.4% pyruvate and 0.4% casamino acids to the late exponential phase. Cells were harvested by rapid filtration as described in Oh et al. (2011) Cell 147(6):1295-1308. Collected cells were flash frozen in liquid nitrogen and cryogenically pulverized by mixer milling (Retsch). Pulverized cells were thawed and clarified by centrifugation. Resulting lysates were digested with MNase, quenched with EGTA and resolved by sucrose density gradient ultracentrifugation. Ribosome-protected mRNA footprints were processed as previously described in Becker et al.(2013) Nat Protoc 8(11):2212-2239. Sequencing library was prepared as described in Oh et al. (2011) Cell 147(6):1295-1308. Briefly, RNA extracted from monosome fractions was size selected for 28 to 42 nucleotides by running on a 15% TBE-urea gel using a 10 bp ladder as the standard. The 3′ ends of RNA were dephosphorylated by T4 PNK and then ligated to the linker 5′_App/CTGTAGGCACCATCAAT/3 ddC_3′. The ligated products were size selected for 45 to 60 nucleotides and reverse transcribed with no more than five molar excess of 5′_5phosCAAGCAGAAGACGGCATACGAATTGATGGTGCCTACAG_3′. The reverse transcribed cDNA was size selected for 125 to 150 bp and circularised. The circDNA was PCR amplified with 5′_AATGATACGGCGACCACCGA_3′ and 5′_CAAGCAGAAGACGGCATACGA_3′ for 7 to 10 cycles and the amplicons were resolved on an 8% polyacrylamide gel i...",,,,,ERS1505503,ERP020995,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR179/000/ERR1797530,586053596,ftp.sra.ebi.ac.uk/vol1/err/ERR179/000/ERR1797530,ftp.sra.ebi.ac.uk/vol1/err/ERR179/000/ERR1797530,bcc230a0385c0388f391eca368c17afb,,E-MTAB-5408,Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,,,ERA789570,fasp.sra.ebi.ac.uk:/vol1/run/ERR179/ERR1797530/hfq2.fq.gz,611634904,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR179/ERR1797530/hfq2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR179/ERR1797530/hfq2.fq.gz,,0620a248cbfdcca0cd00b646f2642e04,,,,,,,, PRJEB19014,ERX1861081,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,294,Pseudomonas fluorescens,MNase-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA50542168,wt1,Illumina HiSeq 2000,ERR1797531,13719271,374602064,SAMEA50542168,,,,,,ArrayExpress,,,Department of Molecular Microbiology John Innes Centre,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5408:wt1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR179/001/ERR1797531/ERR1797531.fastq.gz,362855921,ftp.sra.ebi.ac.uk/vol1/fastq/ERR179/001/ERR1797531/ERR1797531.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR179/001/ERR1797531/ERR1797531.fastq.gz,cf07c48dd63c1ab727d086ba9550b16c,2017-01-16,2017-08-24,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt1_s,,,,,,,,,E-MTAB-5408:wt1,,E-MTAB-5408:wt1,,"Protocols: SBW25 WT and Δhfq cultures were grown at 28°C in M9 medium supplemented with 0.4% pyruvate and 0.4% casamino acids to the late exponential phase. Cells were harvested by rapid filtration as described in Oh et al. (2011) Cell 147(6):1295-1308. Collected cells were flash frozen in liquid nitrogen and cryogenically pulverized by mixer milling (Retsch). Pulverized cells were thawed and clarified by centrifugation. Resulting lysates were digested with MNase, quenched with EGTA and resolved by sucrose density gradient ultracentrifugation. Ribosome-protected mRNA footprints were processed as previously described in Becker et al.(2013) Nat Protoc 8(11):2212-2239. Sequencing library was prepared as described in Oh et al. (2011) Cell 147(6):1295-1308. Briefly, RNA extracted from monosome fractions was size selected for 28 to 42 nucleotides by running on a 15% TBE-urea gel using a 10 bp ladder as the standard. The 3′ ends of RNA were dephosphorylated by T4 PNK and then ligated to the linker 5′_App/CTGTAGGCACCATCAAT/3 ddC_3′. The ligated products were size selected for 45 to 60 nucleotides and reverse transcribed with no more than five molar excess of 5′_5phosCAAGCAGAAGACGGCATACGAATTGATGGTGCCTACAG_3′. The reverse transcribed cDNA was size selected for 125 to 150 bp and circularised. The circDNA was PCR amplified with 5′_AATGATACGGCGACCACCGA_3′ and 5′_CAAGCAGAAGACGGCATACGA_3′ for 7 to 10 cycles and the amplicons were resolved on an 8% polyacrylamide gel i...",,,,,ERS1505504,ERP020995,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR179/001/ERR1797531,300467121,ftp.sra.ebi.ac.uk/vol1/err/ERR179/001/ERR1797531,ftp.sra.ebi.ac.uk/vol1/err/ERR179/001/ERR1797531,739f2a5645bb845f3f85e93ebb5a948f,,E-MTAB-5408,Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,,,ERA789570,fasp.sra.ebi.ac.uk:/vol1/run/ERR179/ERR1797531/wt1.fq.gz,324671862,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR179/ERR1797531/wt1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR179/ERR1797531/wt1.fq.gz,,136f34db14a59e479c1e8c0e7dd5007d,,,,,,,, PRJEB19014,ERX1861082,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,Illumina HiSeq 2000 sequencing; Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,294,Pseudomonas fluorescens,MNase-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA50542918,wt2,Illumina HiSeq 2000,ERR1797532,24135343,663303116,SAMEA50542918,,,,,,ArrayExpress,,,Department of Molecular Microbiology John Innes Centre,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5408:wt2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR179/002/ERR1797532/ERR1797532.fastq.gz,653795293,ftp.sra.ebi.ac.uk/vol1/fastq/ERR179/002/ERR1797532/ERR1797532.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR179/002/ERR1797532/ERR1797532.fastq.gz,6f7228a4e98039f4b9a94a4843b2aae6,2017-01-16,2017-08-24,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt2_s,,,,,,,,,E-MTAB-5408:wt2,,E-MTAB-5408:wt2,,"Protocols: SBW25 WT and Δhfq cultures were grown at 28°C in M9 medium supplemented with 0.4% pyruvate and 0.4% casamino acids to the late exponential phase. Cells were harvested by rapid filtration as described in Oh et al. (2011) Cell 147(6):1295-1308. Collected cells were flash frozen in liquid nitrogen and cryogenically pulverized by mixer milling (Retsch). Pulverized cells were thawed and clarified by centrifugation. Resulting lysates were digested with MNase, quenched with EGTA and resolved by sucrose density gradient ultracentrifugation. Ribosome-protected mRNA footprints were processed as previously described in Becker et al.(2013) Nat Protoc 8(11):2212-2239. Sequencing library was prepared as described in Oh et al. (2011) Cell 147(6):1295-1308. Briefly, RNA extracted from monosome fractions was size selected for 28 to 42 nucleotides by running on a 15% TBE-urea gel using a 10 bp ladder as the standard. The 3′ ends of RNA were dephosphorylated by T4 PNK and then ligated to the linker 5′_App/CTGTAGGCACCATCAAT/3 ddC_3′. The ligated products were size selected for 45 to 60 nucleotides and reverse transcribed with no more than five molar excess of 5′_5phosCAAGCAGAAGACGGCATACGAATTGATGGTGCCTACAG_3′. The reverse transcribed cDNA was size selected for 125 to 150 bp and circularised. The circDNA was PCR amplified with 5′_AATGATACGGCGACCACCGA_3′ and 5′_CAAGCAGAAGACGGCATACGA_3′ for 7 to 10 cycles and the amplicons were resolved on an 8% polyacrylamide gel i...",,,,,ERS1505505,ERP020995,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR179/002/ERR1797532,526683309,ftp.sra.ebi.ac.uk/vol1/err/ERR179/002/ERR1797532,ftp.sra.ebi.ac.uk/vol1/err/ERR179/002/ERR1797532,ac58b97cc46257413a5535c08e625e3b,,E-MTAB-5408,Ribosome profiling of Pseudomonas fluorescens SBW25 and its hfq deletion mutant.,,,ERA789570,fasp.sra.ebi.ac.uk:/vol1/run/ERR179/ERR1797532/wt2.fq.gz,584238401,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR179/ERR1797532/wt2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR179/ERR1797532/wt2.fq.gz,,82525737b32cebd8d6321c5fba4968ec,,,,,,,, PRJEB19102,ERX1865801,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,60711,Chlorocebus sabaeus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52778668,Sample 1,NextSeq 500,ERR1802070,32991341,1030531389,SAMEA52778668,,,,,,ArrayExpress,Vero E6,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/000/ERR1802070/ERR1802070.fastq.gz,610134012,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/000/ERR1802070/ERR1802070.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/000/ERR1802070/ERR1802070.fastq.gz,da72039586c0cbe142650842bcdc81af,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 1_s,,,,,,,,,E-MTAB-5418:Sample 1,,E-MTAB-5418:Sample 1,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508486,ERP021092,Ribo-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/000/ERR1802070,491183459,ftp.sra.ebi.ac.uk/vol1/err/ERR180/000/ERR1802070,ftp.sra.ebi.ac.uk/vol1/err/ERR180/000/ERR1802070,5965f6f3df65edfd47d8285f9cf1688d,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802070/Sample1.fastq.gz,526689778,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802070/Sample1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802070/Sample1.fastq.gz,,380346adff941ebb9f939a6392834b91,,,,,,,, PRJEB19102,ERX1865802,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52779418,Sample 10,NextSeq 500,ERR1802071,32655516,1036495741,SAMEA52779418,,,,,,ArrayExpress,C6/36,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 10_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/001/ERR1802071/ERR1802071.fastq.gz,702011605,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/001/ERR1802071/ERR1802071.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/001/ERR1802071/ERR1802071.fastq.gz,ef0088fd6a144e3e5575aaefae96f255,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 10_s,,,,,,,,,E-MTAB-5418:Sample 10,,E-MTAB-5418:Sample 10,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508487,ERP021092,RNA-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/001/ERR1802071,510390485,ftp.sra.ebi.ac.uk/vol1/err/ERR180/001/ERR1802071,ftp.sra.ebi.ac.uk/vol1/err/ERR180/001/ERR1802071,d7201eef6ab91963cdcd491850ff8bb3,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802071/Sample10.fastq.gz,619825846,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802071/Sample10.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802071/Sample10.fastq.gz,,94ca5667be23a76e456feff537560c43,,,,,,,, PRJEB19102,ERX1865803,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,60711,Chlorocebus sabaeus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52780168,Sample 2,NextSeq 500,ERR1802072,37859333,1233151851,SAMEA52780168,,,,,,ArrayExpress,Vero E6,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/002/ERR1802072/ERR1802072.fastq.gz,621052293,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/002/ERR1802072/ERR1802072.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/002/ERR1802072/ERR1802072.fastq.gz,ec3d0980fe015cef38affb1e25d2e96c,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 2_s,,,,,,,,,E-MTAB-5418:Sample 2,,E-MTAB-5418:Sample 2,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508488,ERP021092,Ribo-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/002/ERR1802072,563597198,ftp.sra.ebi.ac.uk/vol1/err/ERR180/002/ERR1802072,ftp.sra.ebi.ac.uk/vol1/err/ERR180/002/ERR1802072,7e0fdf8de58a8cd1aed739fa006b6ade,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802072/Sample2.fastq.gz,527347450,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802072/Sample2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802072/Sample2.fastq.gz,,2041ed192547aa96423a498aa34f1a89,,,,,,,, PRJEB19102,ERX1865804,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,60711,Chlorocebus sabaeus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52780918,Sample 3,NextSeq 500,ERR1802073,23378265,748417766,SAMEA52780918,,,,,,ArrayExpress,Vero E6,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/003/ERR1802073/ERR1802073.fastq.gz,453818663,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/003/ERR1802073/ERR1802073.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/003/ERR1802073/ERR1802073.fastq.gz,f9afcc4af8960ab6a992d0fd3808fdfb,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 3_s,,,,,,,,,E-MTAB-5418:Sample 3,,E-MTAB-5418:Sample 3,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508489,ERP021092,RNA-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/003/ERR1802073,350560539,ftp.sra.ebi.ac.uk/vol1/err/ERR180/003/ERR1802073,ftp.sra.ebi.ac.uk/vol1/err/ERR180/003/ERR1802073,3d01009fca7104387156ac9e698c8c1a,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802073/Sample3.fastq.gz,395747699,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802073/Sample3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802073/Sample3.fastq.gz,,94fcabb57b33bbf149d16b9d347c4fcb,,,,,,,, PRJEB19102,ERX1865805,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,60711,Chlorocebus sabaeus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52781668,Sample 4,NextSeq 500,ERR1802074,19273387,614792063,SAMEA52781668,,,,,,ArrayExpress,Vero E6,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/004/ERR1802074/ERR1802074.fastq.gz,379620437,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/004/ERR1802074/ERR1802074.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/004/ERR1802074/ERR1802074.fastq.gz,5cf2010390bc8783e2f03c1317f59319,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 4_s,,,,,,,,,E-MTAB-5418:Sample 4,,E-MTAB-5418:Sample 4,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508490,ERP021092,RNA-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/004/ERR1802074,288983413,ftp.sra.ebi.ac.uk/vol1/err/ERR180/004/ERR1802074,ftp.sra.ebi.ac.uk/vol1/err/ERR180/004/ERR1802074,681f6a80b91b68c5300e99cc784bb2d0,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802074/Sample4.fastq.gz,331470220,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802074/Sample4.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802074/Sample4.fastq.gz,,f1a79e4ba3f3727333b10e85d698d8c5,,,,,,,, PRJEB19102,ERX1865806,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52782418,Sample 5,NextSeq 500,ERR1802075,30830839,1009143241,SAMEA52782418,,,,,,ArrayExpress,C6/36,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 5_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/005/ERR1802075/ERR1802075.fastq.gz,486016098,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/005/ERR1802075/ERR1802075.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/005/ERR1802075/ERR1802075.fastq.gz,ee15beed9076b95222305329bfb634cf,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 5_s,,,,,,,,,E-MTAB-5418:Sample 5,,E-MTAB-5418:Sample 5,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508491,ERP021092,Ribo-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/005/ERR1802075,469454317,ftp.sra.ebi.ac.uk/vol1/err/ERR180/005/ERR1802075,ftp.sra.ebi.ac.uk/vol1/err/ERR180/005/ERR1802075,070e3a2b42ca59f7bae480daecf17d47,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802075/Sample5.fastq.gz,411393311,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802075/Sample5.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802075/Sample5.fastq.gz,,dc68c1c1b602a1cd15c25c6268323a4f,,,,,,,, PRJEB19102,ERX1865807,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52783168,Sample 6,NextSeq 500,ERR1802076,26929369,882916179,SAMEA52783168,,,,,,ArrayExpress,C6/36,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 6_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/006/ERR1802076/ERR1802076.fastq.gz,431341702,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/006/ERR1802076/ERR1802076.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/006/ERR1802076/ERR1802076.fastq.gz,fa4d73057913f6bb8e9d0729fa81d1fb,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 6_s,,,,,,,,,E-MTAB-5418:Sample 6,,E-MTAB-5418:Sample 6,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508492,ERP021092,Ribo-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/006/ERR1802076,415790072,ftp.sra.ebi.ac.uk/vol1/err/ERR180/006/ERR1802076,ftp.sra.ebi.ac.uk/vol1/err/ERR180/006/ERR1802076,b2a8290fd209cfe8b5a2af80f7168a9b,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802076/Sample6.fastq.gz,366269719,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802076/Sample6.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802076/Sample6.fastq.gz,,8c4df8abdb860b9ae181490f359e444f,,,,,,,, PRJEB19102,ERX1865808,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52783918,Sample 7,NextSeq 500,ERR1802077,12627212,397075719,SAMEA52783918,,,,,,ArrayExpress,C6/36,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 7_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/007/ERR1802077/ERR1802077.fastq.gz,294559013,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/007/ERR1802077/ERR1802077.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/007/ERR1802077/ERR1802077.fastq.gz,63606bb96bac868c1752ff776502bc15,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 7_s,,,,,,,,,E-MTAB-5418:Sample 7,,E-MTAB-5418:Sample 7,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508493,ERP021092,Ribo-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/007/ERR1802077,216350595,ftp.sra.ebi.ac.uk/vol1/err/ERR180/007/ERR1802077,ftp.sra.ebi.ac.uk/vol1/err/ERR180/007/ERR1802077,f9e1224f5b6b84b07d557747ee84b6f3,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802077/Sample7.fastq.gz,263810595,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802077/Sample7.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802077/Sample7.fastq.gz,,b57cfd282eb198f81d91c22946e3591d,,,,,,,, PRJEB19102,ERX1865809,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52784668,Sample 8,NextSeq 500,ERR1802078,17629538,542405945,SAMEA52784668,,,,,,ArrayExpress,C6/36,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 8_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/008/ERR1802078/ERR1802078.fastq.gz,369946531,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/008/ERR1802078/ERR1802078.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/008/ERR1802078/ERR1802078.fastq.gz,af713240f690d78b61635dc31648ddb6,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 8_s,,,,,,,,,E-MTAB-5418:Sample 8,,E-MTAB-5418:Sample 8,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508494,ERP021092,Ribo-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/008/ERR1802078,296553517,ftp.sra.ebi.ac.uk/vol1/err/ERR180/008/ERR1802078,ftp.sra.ebi.ac.uk/vol1/err/ERR180/008/ERR1802078,640145932bbb3ef5ea2850294d6de9e9,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802078/Sample8.fastq.gz,327537302,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802078/Sample8.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802078/Sample8.fastq.gz,,953d343b979e1bbd230bc1f4c9827732,,,,,,,, PRJEB19102,ERX1865810,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,NextSeq 500 sequencing; Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,7160,Aedes albopictus,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA52785418,Sample 9,NextSeq 500,ERR1802079,40647908,1316636689,SAMEA52785418,,,,,,ArrayExpress,C6/36,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5418:Sample 9_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR180/009/ERR1802079/ERR1802079.fastq.gz,883547645,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/009/ERR1802079/ERR1802079.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR180/009/ERR1802079/ERR1802079.fastq.gz,499237736f390bf7827d5d48311dfba4,2017-01-19,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 9_s,,,,,,,,,E-MTAB-5418:Sample 9,,E-MTAB-5418:Sample 9,,"Protocols: Vero E6 cells and C6/36 cells were maintained in Dulbecco’s modification of Eagle’s medium supplemented with 10% (vol/vol) fetal calf serum (FCS). ZIKV strain Pe243 (ZIKV-PE243) was derived as previously described (Donald et al., 2016). At 24 h p.i., cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia et al., 2009; Ingolia et al., 2012), except ribosomal RNA contamination was removed by treatment with duplex-specific nuclease (DSN) for Samples 7 and 8, and library amplicons were constructed using a small RNA cloning strategy (Guo et al., 2010) adapted to Illumina small RNA v2 to allow multiplexing. The methods used were as described by Irigoyen et al. (2016).",,,,,ERS1508495,ERP021092,RNA-Seq,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR180/009/ERR1802079,641885480,ftp.sra.ebi.ac.uk/vol1/err/ERR180/009/ERR1802079,ftp.sra.ebi.ac.uk/vol1/err/ERR180/009/ERR1802079,01f7bd2ff313f8ebc998e2e080f7aace,,E-MTAB-5418,Analysis of Zika Virus gene expression by Ribosome profiling and RNA sequencing,,,ERA789926,fasp.sra.ebi.ac.uk:/vol1/run/ERR180/ERR1802079/Sample9.fastq.gz,780157423,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802079/Sample9.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR180/ERR1802079/Sample9.fastq.gz,,1c908808c5c2a0629d0972fdaf647e39,,,,,,,, PRJEB19678,ERX1918552,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA100849168,Sample 1,NextSeq 500,ERR1856693,111880423,3793356586,SAMEA100849168,,,,,,ArrayExpress,HEK293,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5519:Sample 1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR185/003/ERR1856693/ERR1856693.fastq.gz,1574781621,ftp.sra.ebi.ac.uk/vol1/fastq/ERR185/003/ERR1856693/ERR1856693.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR185/003/ERR1856693/ERR1856693.fastq.gz,933d015121139cb65f059cd94cc2879c,2017-02-27,2017-07-25,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 1_s,,,,,,,,,E-MTAB-5519:Sample 1,,E-MTAB-5519:Sample 1,,"Protocols: For Ribo-Seq, parental HEK293 and PDE12-/- cells were treated with 100 μg/ml chloramphenicol and 100 μg/mL cycloheximide for 5 min. Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and transferred to dry ice. Cells were lysed in 400 μl of lysis buffer (20 mM Tris-HCl (pH 7.5), 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1 % Triton X-100, 100 μg/ml chloramphenicol and cycloheximide). Cells were scraped and lysates clarified by centrifugation for 20 min at 13,000 g at 4°C. 200 μl aliquots of cell lysates were treated with 7.5 μl RNase 1 (100 units/μl) at 28°C. The reaction was layered onto a 10-30 % sucrose gradient [2ml 10-30% (v/v)] in 50mM Tris-HCl (pH7.2), 20mM Mg(OAc)2, 80mM NH4Cl, 0.1M KCl, 1mM PMSF and centrifuged for 2h 15min at 100,000 gmax at 4°C (39,000 rpm, Beckman Coulter TLS-55 rotor) and fractions collected. Subsequently, all fractions containing mitochondrial monosomes, ascertained by western blotting, were pooled and digested with proteinase K (200 μg/ml) for 30 min at 42°C. RPFs were recovered by extracting twice with pre-warmed (65°C) acidic phenol:chloroform and once with chloroform (1:1, v/v, buffered with 10 mM Tris pH 7.5, 0.1 mM EDTA) followed by ethanol precipitation. RPFs (1 μg) were separated on 15 % denaturing polyacrylamide gels and RNA species migrating between 25 and 35 nt were harvested. RNA was eluted from the gel slices and ethanol precipitated. The RNA samples ...",,,,,ERS1572580,ERP021735,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR185/003/ERR1856693,1703931232,ftp.sra.ebi.ac.uk/vol1/err/ERR185/003/ERR1856693,ftp.sra.ebi.ac.uk/vol1/err/ERR185/003/ERR1856693,912d6dfd0e558ff0d5ecae201894647a,,E-MTAB-5519,Analysis of mitochondrial gene expression with Ribosome Profiling,,,ERA827970,fasp.sra.ebi.ac.uk:/vol1/run/ERR185/ERR1856693/sample_1.fq.gz,1297850069,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR185/ERR1856693/sample_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR185/ERR1856693/sample_1.fq.gz,,be77b26802183d016e9a09b954fa9eb9,,,,,,,, PRJEB19678,ERX1918553,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA100849918,Sample 2,NextSeq 500,ERR1856694,58039284,1693191518,SAMEA100849918,,,,,,ArrayExpress,HEK293 PDE12-/-,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5519:Sample 2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR185/004/ERR1856694/ERR1856694.fastq.gz,858424316,ftp.sra.ebi.ac.uk/vol1/fastq/ERR185/004/ERR1856694/ERR1856694.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR185/004/ERR1856694/ERR1856694.fastq.gz,56ac8f6c0af130c4c23e5f0f59b1ae8b,2017-02-27,2017-07-25,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 2_s,,,,,,,,,E-MTAB-5519:Sample 2,,E-MTAB-5519:Sample 2,,"Protocols: For Ribo-Seq, parental HEK293 and PDE12-/- cells were treated with 100 μg/ml chloramphenicol and 100 μg/mL cycloheximide for 5 min. Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and transferred to dry ice. Cells were lysed in 400 μl of lysis buffer (20 mM Tris-HCl (pH 7.5), 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1 % Triton X-100, 100 μg/ml chloramphenicol and cycloheximide). Cells were scraped and lysates clarified by centrifugation for 20 min at 13,000 g at 4°C. 200 μl aliquots of cell lysates were treated with 7.5 μl RNase 1 (100 units/μl) at 28°C. The reaction was layered onto a 10-30 % sucrose gradient [2ml 10-30% (v/v)] in 50mM Tris-HCl (pH7.2), 20mM Mg(OAc)2, 80mM NH4Cl, 0.1M KCl, 1mM PMSF and centrifuged for 2h 15min at 100,000 gmax at 4°C (39,000 rpm, Beckman Coulter TLS-55 rotor) and fractions collected. Subsequently, all fractions containing mitochondrial monosomes, ascertained by western blotting, were pooled and digested with proteinase K (200 μg/ml) for 30 min at 42°C. RPFs were recovered by extracting twice with pre-warmed (65°C) acidic phenol:chloroform and once with chloroform (1:1, v/v, buffered with 10 mM Tris pH 7.5, 0.1 mM EDTA) followed by ethanol precipitation. RPFs (1 μg) were separated on 15 % denaturing polyacrylamide gels and RNA species migrating between 25 and 35 nt were harvested. RNA was eluted from the gel slices and ethanol precipitated. The RNA samples ...",,,,,ERS1572581,ERP021735,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR185/004/ERR1856694,831078268,ftp.sra.ebi.ac.uk/vol1/err/ERR185/004/ERR1856694,ftp.sra.ebi.ac.uk/vol1/err/ERR185/004/ERR1856694,61c1d55cd716a7969ea1a981efe55fd5,,E-MTAB-5519,Analysis of mitochondrial gene expression with Ribosome Profiling,,,ERA827970,fasp.sra.ebi.ac.uk:/vol1/run/ERR185/ERR1856694/sample_2.fq.gz,706733223,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR185/ERR1856694/sample_2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR185/ERR1856694/sample_2.fq.gz,,ef9aa0bcfbec535ff24d8e5fd039b064,,,,,,,, PRJEB19678,ERX1918554,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,NextSeq 500 sequencing; Analysis of mitochondrial gene expression with Ribosome Profiling,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA100850668,Sample 3,NextSeq 500,ERR1856695,54983210,1222852079,SAMEA100850668,,,,,,ArrayExpress,deltaFLP 143B cybrid,,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5519:Sample 3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR185/005/ERR1856695/ERR1856695.fastq.gz,767654136,ftp.sra.ebi.ac.uk/vol1/fastq/ERR185/005/ERR1856695/ERR1856695.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR185/005/ERR1856695/ERR1856695.fastq.gz,c35c92172d2b9f554b4de63c2304ba2f,2017-02-27,2017-07-25,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 3_s,,,,,,,,,E-MTAB-5519:Sample 3,,E-MTAB-5519:Sample 3,,"Protocols: For Ribo-Seq, parental HEK293 and PDE12-/- cells were treated with 100 μg/ml chloramphenicol and 100 μg/mL cycloheximide for 5 min. Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and transferred to dry ice. Cells were lysed in 400 μl of lysis buffer (20 mM Tris-HCl (pH 7.5), 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1 % Triton X-100, 100 μg/ml chloramphenicol and cycloheximide). Cells were scraped and lysates clarified by centrifugation for 20 min at 13,000 g at 4°C. 200 μl aliquots of cell lysates were treated with 7.5 μl RNase 1 (100 units/μl) at 28°C. The reaction was layered onto a 10-30 % sucrose gradient [2ml 10-30% (v/v)] in 50mM Tris-HCl (pH7.2), 20mM Mg(OAc)2, 80mM NH4Cl, 0.1M KCl, 1mM PMSF and centrifuged for 2h 15min at 100,000 gmax at 4°C (39,000 rpm, Beckman Coulter TLS-55 rotor) and fractions collected. Subsequently, all fractions containing mitochondrial monosomes, ascertained by western blotting, were pooled and digested with proteinase K (200 μg/ml) for 30 min at 42°C. RPFs were recovered by extracting twice with pre-warmed (65°C) acidic phenol:chloroform and once with chloroform (1:1, v/v, buffered with 10 mM Tris pH 7.5, 0.1 mM EDTA) followed by ethanol precipitation. RPFs (1 μg) were separated on 15 % denaturing polyacrylamide gels and RNA species migrating between 25 and 35 nt were harvested. RNA was eluted from the gel slices and ethanol precipitated. The RNA samples ...",,,,,ERS1572582,ERP021735,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR185/005/ERR1856695,652346364,ftp.sra.ebi.ac.uk/vol1/err/ERR185/005/ERR1856695,ftp.sra.ebi.ac.uk/vol1/err/ERR185/005/ERR1856695,c55c732aa688fae7b85f86928020617d,,E-MTAB-5519,Analysis of mitochondrial gene expression with Ribosome Profiling,,,ERA827970,fasp.sra.ebi.ac.uk:/vol1/run/ERR185/ERR1856695/sample_3.fq.gz,629809812,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR185/ERR1856695/sample_3.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR185/ERR1856695/sample_3.fq.gz,,2113d8303e17bf756a6891ecbbaa480b,,,,,,,, PRJEB21099,ERX2054828,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106710,wt.N.CHX.mrna.1,Illumina HiSeq 2000,ERR1994959,26425976,1321298800,SAMEA104106710,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.N.CHX.mrna.1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/009/ERR1994959/ERR1994959.fastq.gz,995033263,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/009/ERR1994959/ERR1994959.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/009/ERR1994959/ERR1994959.fastq.gz,b7f9c8e11e2e4e763df74a45cd98c5e8,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.N.CHX.mrna.1_s,,,,,,,,,E-MTAB-5794:wt.N.CHX.mrna.1,,E-MTAB-5794:wt.N.CHX.mrna.1,,Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source Cells were grown in the presence of CHX at 100 ug/ml for 5 minutes before colletion Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1770603,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/009/ERR1994959,632849503,ftp.sra.ebi.ac.uk/vol1/err/ERR199/009/ERR1994959,ftp.sra.ebi.ac.uk/vol1/err/ERR199/009/ERR1994959,4f73d68c5790826e57b5b0e7b8d4909e,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994959/wt_N_CHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT014_TCTCGGTT.fq.gz,926190374,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994959/wt_N_CHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT014_TCTCGGTT.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994959/wt_N_CHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT014_TCTCGGTT.fq.gz,,35a1e4be3db8cc591d065c11f47d3f9c,,,,,,,, PRJEB21099,ERX2054829,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106711,wt.N.CHX.mrna.3,Illumina HiSeq 2000,ERR1994960,36240950,1812047500,SAMEA104106711,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.N.CHX.mrna.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/000/ERR1994960/ERR1994960.fastq.gz,1300749872,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/000/ERR1994960/ERR1994960.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/000/ERR1994960/ERR1994960.fastq.gz,e8f9ba45a15606dac9e652ab818d21fa,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.N.CHX.mrna.3_s,,,,,,,,,E-MTAB-5794:wt.N.CHX.mrna.3,,E-MTAB-5794:wt.N.CHX.mrna.3,,Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source Cells were grown in the presence of CHX at 100 ug/ml for 5 minutes before colletion Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1770604,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/000/ERR1994960,806658360,ftp.sra.ebi.ac.uk/vol1/err/ERR199/000/ERR1994960,ftp.sra.ebi.ac.uk/vol1/err/ERR199/000/ERR1994960,338ea494b74e528931dd790bf8ad1cba,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994960/mrna_mAT_pN_pCHX_exp26_SLX-13147_RPI_GAGGTGCT.fq.gz,1225381442,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994960/mrna_mAT_pN_pCHX_exp26_SLX-13147_RPI_GAGGTGCT.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994960/mrna_mAT_pN_pCHX_exp26_SLX-13147_RPI_GAGGTGCT.fq.gz,,cdf5e357aca1a3ba53528fa99a8a76ae,,,,,,,, PRJEB21099,ERX2054830,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106712,wt.N.CHX.ribo.1,NextSeq 550,ERR1994961,63059496,3152974800,SAMEA104106712,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.N.CHX.ribo.1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/001/ERR1994961/ERR1994961.fastq.gz,2134700561,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/001/ERR1994961/ERR1994961.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/001/ERR1994961/ERR1994961.fastq.gz,d73c2e9ef299c80e12f6e4a540a021bd,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.N.CHX.ribo.1_s,,,,,,,,,E-MTAB-5794:wt.N.CHX.ribo.1,,E-MTAB-5794:wt.N.CHX.ribo.1,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source Cells were grown in the presence of CHX at 100 ug/ml for 5 minutes before colletion Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 u",,,,,ERS1770605,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/001/ERR1994961,1527179953,ftp.sra.ebi.ac.uk/vol1/err/ERR199/001/ERR1994961,ftp.sra.ebi.ac.uk/vol1/err/ERR199/001/ERR1994961,cb9d26b9069bc646127c61b13bde847c,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994961/wt_N_NH4_CHX_fastfreeze_exp05_ribo_11848X2_150923_D00294_0200_BC7V3HANXX_3.txt.gz,1947828885,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994961/wt_N_NH4_CHX_fastfreeze_exp05_ribo_11848X2_150923_D00294_0200_BC7V3HANXX_3.txt.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994961/wt_N_NH4_CHX_fastfreeze_exp05_ribo_11848X2_150923_D00294_0200_BC7V3HANXX_3.txt.gz,,efeaba3dc538ae90859e916fe41fe088,,,,,,,, PRJEB21099,ERX2054831,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106713,wt.N.CHX.ribo.3,Illumina HiSeq 2000,ERR1994962,26742065,1337103250,SAMEA104106713,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.N.CHX.ribo.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/002/ERR1994962/ERR1994962.fastq.gz,635225493,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/002/ERR1994962/ERR1994962.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/002/ERR1994962/ERR1994962.fastq.gz,6a7c0c961264caaad13cfdcb77a99a96,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.N.CHX.ribo.3_s,,,,,,,,,E-MTAB-5794:wt.N.CHX.ribo.3,,E-MTAB-5794:wt.N.CHX.ribo.3,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source Cells were grown in the presence of CHX at 100 ug/ml for 5 minutes before colletion Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 u",,,,,ERS1770606,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/002/ERR1994962,457766401,ftp.sra.ebi.ac.uk/vol1/err/ERR199/002/ERR1994962,ftp.sra.ebi.ac.uk/vol1/err/ERR199/002/ERR1994962,2897f2ab1b2663fc0cf0f7967e2e34e1,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994962/mono_mAT_pN_pCHX_exp26_SLX-13145.RPI22.HJM3GBBXX.s_4.r_1.fq.gz,558194785,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994962/mono_mAT_pN_pCHX_exp26_SLX-13145.RPI22.HJM3GBBXX.s_4.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994962/mono_mAT_pN_pCHX_exp26_SLX-13145.RPI22.HJM3GBBXX.s_4.r_1.fq.gz,,ef4ec4280601e2884d421aadb1ab7425,,,,,,,, PRJEB21099,ERX2054832,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106714,wt.N.noCHX.mrna.1,Illumina HiSeq 2000,ERR1994963,16170457,808522850,SAMEA104106714,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.N.noCHX.mrna.1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/003/ERR1994963/ERR1994963.fastq.gz,607730223,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/003/ERR1994963/ERR1994963.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/003/ERR1994963/ERR1994963.fastq.gz,19af49409b3eec0e8431270bf065831b,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.N.noCHX.mrna.1_s,,,,,,,,,E-MTAB-5794:wt.N.noCHX.mrna.1,,E-MTAB-5794:wt.N.noCHX.mrna.1,,Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1770607,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/003/ERR1994963,386844062,ftp.sra.ebi.ac.uk/vol1/err/ERR199/003/ERR1994963,ftp.sra.ebi.ac.uk/vol1/err/ERR199/003/ERR1994963,211e384f7d2a778db4c767ebcd91cc15,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994963/wt_N_noCHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT047_TAGTCTTG.fq.gz,565567145,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994963/wt_N_noCHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT047_TAGTCTTG.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994963/wt_N_noCHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT047_TAGTCTTG.fq.gz,,d89c8102a993ce07077206a583c1e7f3,,,,,,,, PRJEB21099,ERX2054833,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106715,wt.N.noCHX.mrna.3,Illumina HiSeq 2000,ERR1994964,23972947,1198647350,SAMEA104106715,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.N.noCHX.mrna.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/004/ERR1994964/ERR1994964.fastq.gz,862604448,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/004/ERR1994964/ERR1994964.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/004/ERR1994964/ERR1994964.fastq.gz,c2892a4144768ae6a4b3737dfeb15800,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.N.noCHX.mrna.3_s,,,,,,,,,E-MTAB-5794:wt.N.noCHX.mrna.3,,E-MTAB-5794:wt.N.noCHX.mrna.3,,Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1770608,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/004/ERR1994964,537673923,ftp.sra.ebi.ac.uk/vol1/err/ERR199/004/ERR1994964,ftp.sra.ebi.ac.uk/vol1/err/ERR199/004/ERR1994964,361b4ef11f71fee64cf67f02e5a89913,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994964/mrna_mAT_pN_mCHX_exp26_SLX-13147_RPI_TATGTGGC.fq.gz,812213937,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994964/mrna_mAT_pN_mCHX_exp26_SLX-13147_RPI_TATGTGGC.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994964/mrna_mAT_pN_mCHX_exp26_SLX-13147_RPI_TATGTGGC.fq.gz,,9fe61461eeb189b43ea05180b3d86f6a,,,,,,,, PRJEB21099,ERX2054834,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106716,wt.N.noCHX.ribo.1,Illumina HiSeq 2000,ERR1994965,40531552,2026577600,SAMEA104106716,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.N.noCHX.ribo.1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/005/ERR1994965/ERR1994965.fastq.gz,1186671453,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/005/ERR1994965/ERR1994965.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/005/ERR1994965/ERR1994965.fastq.gz,4e14966124f7211f96fda37c50d38db9,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.N.noCHX.ribo.1_s,,,,,,,,,E-MTAB-5794:wt.N.noCHX.ribo.1,,E-MTAB-5794:wt.N.noCHX.ribo.1,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris pH 7, 50 mM DTT, 100",,,,,ERS1770609,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/005/ERR1994965,892395507,ftp.sra.ebi.ac.uk/vol1/err/ERR199/005/ERR1994965,ftp.sra.ebi.ac.uk/vol1/err/ERR199/005/ERR1994965,0fa361486319cef90bba643e4ab359d4,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994965/h-_N_noCHX_exp05_24530671-23_merged.fastq.gz,1083575475,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994965/h-_N_noCHX_exp05_24530671-23_merged.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994965/h-_N_noCHX_exp05_24530671-23_merged.fastq.gz,,3e7703e2d9bead9b3c2aa5e6bfd4b7da,,,,,,,, PRJEB21099,ERX2054835,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106717,wt.N.noCHX.ribo.3,Illumina HiSeq 2000,ERR1994966,32968604,1648430200,SAMEA104106717,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.N.noCHX.ribo.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/006/ERR1994966/ERR1994966.fastq.gz,708584838,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/006/ERR1994966/ERR1994966.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/006/ERR1994966/ERR1994966.fastq.gz,7a946a2a13f7722ed5182215193407d3,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.N.noCHX.ribo.3_s,,,,,,,,,E-MTAB-5794:wt.N.noCHX.ribo.3,,E-MTAB-5794:wt.N.noCHX.ribo.3,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris pH 7, 50 mM DTT, 100",,,,,ERS1770610,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/006/ERR1994966,549410966,ftp.sra.ebi.ac.uk/vol1/err/ERR199/006/ERR1994966,ftp.sra.ebi.ac.uk/vol1/err/ERR199/006/ERR1994966,aa28000c05057d38442fa44bcd29a311,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994966/mono_mAT_pN_mCHX_exp26_SLX-13145.RPI21.HJM3GBBXX.s_4.r_1.fq.gz,614854275,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994966/mono_mAT_pN_mCHX_exp26_SLX-13145.RPI21.HJM3GBBXX.s_4.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994966/mono_mAT_pN_mCHX_exp26_SLX-13145.RPI21.HJM3GBBXX.s_4.r_1.fq.gz,,16a064d8c45d9eb04890f741fc2f6a5e,,,,,,,, PRJEB21099,ERX2054836,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106718,wt.noN.CHX.mrna.1,Illumina HiSeq 2000,ERR1994967,21546857,1077342850,SAMEA104106718,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.noN.CHX.mrna.1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/007/ERR1994967/ERR1994967.fastq.gz,806586598,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/007/ERR1994967/ERR1994967.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/007/ERR1994967/ERR1994967.fastq.gz,08431fd32793730f9681f3fea0743324,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noN.CHX.mrna.1_s,,,,,,,,,E-MTAB-5794:wt.noN.CHX.mrna.1,,E-MTAB-5794:wt.noN.CHX.mrna.1,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source. Cells were washed with EMM containing no NH4Cl (EMM-N), resuspended in EMM-N, and grown at 32C for 60 minutes. Cells were grown in the presence of CHX at 100 ug/ml for 5 minutes before colletion Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).",,,,,ERS1770611,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/007/ERR1994967,513308843,ftp.sra.ebi.ac.uk/vol1/err/ERR199/007/ERR1994967,ftp.sra.ebi.ac.uk/vol1/err/ERR199/007/ERR1994967,e1665cc3b0151e7c1f484e1cf4d64f09,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994967/wt_noN_CHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT083_GCTCCTTG.fq.gz,750304102,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994967/wt_noN_CHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT083_GCTCCTTG.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994967/wt_noN_CHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT083_GCTCCTTG.fq.gz,,34dca6e9e68ca958c8cc92e70593cfc9,,,,,,,, PRJEB21099,ERX2054837,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106719,wt.noN.CHX.mrna.3,Illumina HiSeq 2000,ERR1994968,33734733,1686736650,SAMEA104106719,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.noN.CHX.mrna.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/008/ERR1994968/ERR1994968.fastq.gz,1210607260,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/008/ERR1994968/ERR1994968.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/008/ERR1994968/ERR1994968.fastq.gz,eafabf6e43e1ef29b94acb5fa031e00f,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noN.CHX.mrna.3_s,,,,,,,,,E-MTAB-5794:wt.noN.CHX.mrna.3,,E-MTAB-5794:wt.noN.CHX.mrna.3,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source. Cells were washed with EMM containing no NH4Cl (EMM-N), resuspended in EMM-N, and grown at 32C for 60 minutes. Cells were grown in the presence of CHX at 100 ug/ml for 5 minutes before colletion Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).",,,,,ERS1770612,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/008/ERR1994968,750146237,ftp.sra.ebi.ac.uk/vol1/err/ERR199/008/ERR1994968,ftp.sra.ebi.ac.uk/vol1/err/ERR199/008/ERR1994968,e5aca9222f168e1071f1af5bd73d180d,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994968/mrna_mN_pCHX_exp26_SLX-13147_RPI_TAGTGACT.fq.gz,1145597785,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994968/mrna_mN_pCHX_exp26_SLX-13147_RPI_TAGTGACT.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994968/mrna_mN_pCHX_exp26_SLX-13147_RPI_TAGTGACT.fq.gz,,1f51017df36590a5ec4fc8a950627b23,,,,,,,, PRJEB21099,ERX2054838,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,NextSeq 550 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106720,wt.noN.CHX.ribo.1,NextSeq 550,ERR1994969,83235717,4161785850,SAMEA104106720,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.noN.CHX.ribo.1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/009/ERR1994969/ERR1994969.fastq.gz,2976594762,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/009/ERR1994969/ERR1994969.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/009/ERR1994969/ERR1994969.fastq.gz,cf6a8a5f98b413b5cdcf6f556c1006fd,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noN.CHX.ribo.1_s,,,,,,,,,E-MTAB-5794:wt.noN.CHX.ribo.1,,E-MTAB-5794:wt.noN.CHX.ribo.1,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source. Cells were washed with EMM containing no NH4Cl (EMM-N), resuspended in EMM-N, and grown at 32C for 60 minutes. Cells were grown in the presence of CHX at 100 ug/ml for 5 minutes before colletion Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). F",,,,,ERS1770613,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/009/ERR1994969,2232558012,ftp.sra.ebi.ac.uk/vol1/err/ERR199/009/ERR1994969,ftp.sra.ebi.ac.uk/vol1/err/ERR199/009/ERR1994969,9844a6537f22f7eccfb17bba7e51245f,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994969/wt_noN_NH4_CHX_fastfreeze_exp05_ribo_11847X4_150923_D00294_0200_BC7V3HANXX_7.txt.gz,2729772383,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994969/wt_noN_NH4_CHX_fastfreeze_exp05_ribo_11847X4_150923_D00294_0200_BC7V3HANXX_7.txt.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994969/wt_noN_NH4_CHX_fastfreeze_exp05_ribo_11847X4_150923_D00294_0200_BC7V3HANXX_7.txt.gz,,09f4c60319275fcf7ea113e157ec31b8,,,,,,,, PRJEB21099,ERX2054839,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106721,wt.noN.CHX.ribo.3,Illumina HiSeq 2000,ERR1994970,31175890,1558794500,SAMEA104106721,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.noN.CHX.ribo.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/000/ERR1994970/ERR1994970.fastq.gz,690408708,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/000/ERR1994970/ERR1994970.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/000/ERR1994970/ERR1994970.fastq.gz,304b7defcf34e505f6d947207dbc8011,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noN.CHX.ribo.3_s,,,,,,,,,E-MTAB-5794:wt.noN.CHX.ribo.3,,E-MTAB-5794:wt.noN.CHX.ribo.3,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source. Cells were washed with EMM containing no NH4Cl (EMM-N), resuspended in EMM-N, and grown at 32C for 60 minutes. Cells were grown in the presence of CHX at 100 ug/ml for 5 minutes before colletion Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). F",,,,,ERS1770614,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/000/ERR1994970,528601857,ftp.sra.ebi.ac.uk/vol1/err/ERR199/000/ERR1994970,ftp.sra.ebi.ac.uk/vol1/err/ERR199/000/ERR1994970,3d98d6f5d394de5217e2d4e730860c26,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994970/mono_mN_pCHX_exp26_SLX-13144.RPI24.HJM3GBBXX.s_3.r_1.fq.gz,601679718,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994970/mono_mN_pCHX_exp26_SLX-13144.RPI24.HJM3GBBXX.s_3.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994970/mono_mN_pCHX_exp26_SLX-13144.RPI24.HJM3GBBXX.s_3.r_1.fq.gz,,6a08e3bcfe02c4cc9d8a0129c2107d10,,,,,,,, PRJEB21099,ERX2054840,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106722,wt.noN.noCHX.mrna.1,Illumina HiSeq 2000,ERR1994971,18195992,909799600,SAMEA104106722,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.noN.noCHX.mrna.1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/001/ERR1994971/ERR1994971.fastq.gz,684190038,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/001/ERR1994971/ERR1994971.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/001/ERR1994971/ERR1994971.fastq.gz,bbfb54c543b493b60d789904399363ae,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noN.noCHX.mrna.1_s,,,,,,,,,E-MTAB-5794:wt.noN.noCHX.mrna.1,,E-MTAB-5794:wt.noN.noCHX.mrna.1,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source. Cells were washed with EMM containing no NH4Cl (EMM-N), resuspended in EMM-N, and grown at 32C for 60 minutes. Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).",,,,,ERS1770615,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/001/ERR1994971,436393081,ftp.sra.ebi.ac.uk/vol1/err/ERR199/001/ERR1994971,ftp.sra.ebi.ac.uk/vol1/err/ERR199/001/ERR1994971,053e99117f28b90f87fae18f8a8e1d76,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994971/wt_noN_noCHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT070_GATCTCTT.fq.gz,636700835,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994971/wt_noN_noCHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT070_GATCTCTT.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994971/wt_noN_noCHX_fastfreeze_mrna_exp_05_SLX-9971_NXHT070_GATCTCTT.fq.gz,,1f1340c21e4df8afd8454dab3bb49822,,,,,,,, PRJEB21099,ERX2054841,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106723,wt.noN.noCHX.mrna.3,Illumina HiSeq 2000,ERR1994972,23231253,1161562650,SAMEA104106723,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.noN.noCHX.mrna.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/002/ERR1994972/ERR1994972.fastq.gz,841393565,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/002/ERR1994972/ERR1994972.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/002/ERR1994972/ERR1994972.fastq.gz,b868b04a82cafc2f51b81beef5114d9b,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noN.noCHX.mrna.3_s,,,,,,,,,E-MTAB-5794:wt.noN.noCHX.mrna.3,,E-MTAB-5794:wt.noN.noCHX.mrna.3,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source. Cells were washed with EMM containing no NH4Cl (EMM-N), resuspended in EMM-N, and grown at 32C for 60 minutes. Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).",,,,,ERS1770616,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/002/ERR1994972,521879358,ftp.sra.ebi.ac.uk/vol1/err/ERR199/002/ERR1994972,ftp.sra.ebi.ac.uk/vol1/err/ERR199/002/ERR1994972,97498d30bfe65d90f747760949f40c59,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994972/mrna_mN_mCHX_exp26_SLX-13147_RPI_TCGTTAGC.fq.gz,794564416,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994972/mrna_mN_mCHX_exp26_SLX-13147_RPI_TCGTTAGC.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994972/mrna_mN_mCHX_exp26_SLX-13147_RPI_TCGTTAGC.fq.gz,,025b5818871045ddac77844186f3279a,,,,,,,, PRJEB21099,ERX2054842,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106724,wt.noN.noCHX.ribo.1,Illumina HiSeq 2000,ERR1994973,40848270,2042413500,SAMEA104106724,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.noN.noCHX.ribo.1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/003/ERR1994973/ERR1994973.fastq.gz,1162167018,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/003/ERR1994973/ERR1994973.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/003/ERR1994973/ERR1994973.fastq.gz,97bfcbbc1587ee4e9cdef5901a96c6ad,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noN.noCHX.ribo.1_s,,,,,,,,,E-MTAB-5794:wt.noN.noCHX.ribo.1,,E-MTAB-5794:wt.noN.noCHX.ribo.1,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source. Cells were washed with EMM containing no NH4Cl (EMM-N), resuspended in EMM-N, and grown at 32C for 60 minutes. Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fra",,,,,ERS1770617,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/003/ERR1994973,906144237,ftp.sra.ebi.ac.uk/vol1/err/ERR199/003/ERR1994973,ftp.sra.ebi.ac.uk/vol1/err/ERR199/003/ERR1994973,ac246f805ab758cd857c95880c9938f6,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994973/h-_noN_noCHX_exp05_24530674-24_merged.fastq.gz,1058842485,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994973/h-_noN_noCHX_exp05_24530674-24_merged.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994973/h-_noN_noCHX_exp05_24530674-24_merged.fastq.gz,,7138d88b1bb3bd4be532927a75478fc3,,,,,,,, PRJEB21099,ERX2054843,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,Illumina HiSeq 2000 sequencing; Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA104106725,wt.noN.noCHX.ribo.3,Illumina HiSeq 2000,ERR1994974,31871091,1593554550,SAMEA104106725,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5794:wt.noN.noCHX.ribo.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR199/004/ERR1994974/ERR1994974.fastq.gz,693940038,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/004/ERR1994974/ERR1994974.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR199/004/ERR1994974/ERR1994974.fastq.gz,3ad51405942aaecd04f6618422ccd4dd,2017-05-31,2017-09-05,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noN.noCHX.ribo.3_s,,,,,,,,,E-MTAB-5794:wt.noN.noCHX.ribo.3,,E-MTAB-5794:wt.noN.noCHX.ribo.3,,"Protocols: Cells were grown at a temperature of 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795) containing NH4Cl as a nitrogen source. Cells were washed with EMM containing no NH4Cl (EMM-N), resuspended in EMM-N, and grown at 32C for 60 minutes. Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fra",,,,,ERS1770618,ERP023328,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR199/004/ERR1994974,538080074,ftp.sra.ebi.ac.uk/vol1/err/ERR199/004/ERR1994974,ftp.sra.ebi.ac.uk/vol1/err/ERR199/004/ERR1994974,d5eff10fa646e8cf5c217d9548269efa,,E-MTAB-5794,Effects of cycloheximide (CHX) on ribosome profiling experiments in Schizosaccharomyces pombe,,,ERA947782,fasp.sra.ebi.ac.uk:/vol1/run/ERR199/ERR1994974/mono_mN_mCHX_exp26_SLX-13144.RPI23.HJM3GBBXX.s_3.r_1.fq.gz,603833538,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994974/mono_mN_mCHX_exp26_SLX-13144.RPI23.HJM3GBBXX.s_3.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR199/ERR1994974/mono_mN_mCHX_exp26_SLX-13144.RPI23.HJM3GBBXX.s_3.r_1.fq.gz,,0bca2c2637e94d4be54215a4d2c4106d,,,,,,,, PRJEB21224,ERX2063387,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118808,gcn2.AT.mrna.3,NextSeq 550,ERR2003518,37068610,2804773487,SAMEA104118808,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:gcn2.AT.mrna.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/008/ERR2003518/ERR2003518.fastq.gz,1893968511,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/008/ERR2003518/ERR2003518.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/008/ERR2003518/ERR2003518.fastq.gz,2b550100b972d70287e65d615443dfaa,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,gcn2.AT.mrna.3_s,,,,,,,,,E-MTAB-5810:gcn2.AT.mrna.3,,E-MTAB-5810:gcn2.AT.mrna.3,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782701,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/008/ERR2003518,1296680135,ftp.sra.ebi.ac.uk/vol1/err/ERR200/008/ERR2003518,ftp.sra.ebi.ac.uk/vol1/err/ERR200/008/ERR2003518,05c3e57987ddc9ce8c662182c0451ef4,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003518/gcn2_3AT_07_mRNA-230315-3_S7.fastq.gz,1794478551,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003518/gcn2_3AT_07_mRNA-230315-3_S7.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003518/gcn2_3AT_07_mRNA-230315-3_S7.fastq.gz,,ce22d1f5b16b9330845dca2a52314ef4,,,,,,,, PRJEB21224,ERX2063388,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118809,gcn2.AT.mrna.4,NextSeq 550,ERR2003519,32243483,2439588430,SAMEA104118809,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:gcn2.AT.mrna.4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/009/ERR2003519/ERR2003519.fastq.gz,1431433687,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/009/ERR2003519/ERR2003519.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/009/ERR2003519/ERR2003519.fastq.gz,e2c0a6e6559c0d9b1f519df8f98392c9,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,gcn2.AT.mrna.4_s,,,,,,,,,E-MTAB-5810:gcn2.AT.mrna.4,,E-MTAB-5810:gcn2.AT.mrna.4,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782702,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/009/ERR2003519,976729722,ftp.sra.ebi.ac.uk/vol1/err/ERR200/009/ERR2003519,ftp.sra.ebi.ac.uk/vol1/err/ERR200/009/ERR2003519,eb054ec6ff766dbd8b4b4c29029711a1,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003519/gcn2-3AT_16_mRNA-050615-18_S18.fastq.gz,1347495524,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003519/gcn2-3AT_16_mRNA-050615-18_S18.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003519/gcn2-3AT_16_mRNA-050615-18_S18.fastq.gz,,595135a2e69a7b32a01d93c9226693b9,,,,,,,, PRJEB21224,ERX2063389,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118810,gcn2.AT.ribo.3,NextSeq 550,ERR2003520,31434722,1571736100,SAMEA104118810,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:gcn2.AT.ribo.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/000/ERR2003520/ERR2003520.fastq.gz,952761440,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/000/ERR2003520/ERR2003520.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/000/ERR2003520/ERR2003520.fastq.gz,1a398e3601a225d9bc0d817b5220fbab,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,gcn2.AT.ribo.3_s,,,,,,,,,E-MTAB-5810:gcn2.AT.ribo.3,,E-MTAB-5810:gcn2.AT.ribo.3,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments",,,,,ERS1782703,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/000/ERR2003520,693153509,ftp.sra.ebi.ac.uk/vol1/err/ERR200/000/ERR2003520,ftp.sra.ebi.ac.uk/vol1/err/ERR200/000/ERR2003520,16d8165f05ae6b51473d1063ca89f631,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003520/gcn2_3AT_exp07_24530672-16_merged.fastq.gz,872386677,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003520/gcn2_3AT_exp07_24530672-16_merged.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003520/gcn2_3AT_exp07_24530672-16_merged.fastq.gz,,b3f5937c547123c93b45789e6fa63d9a,,,,,,,, PRJEB21224,ERX2063390,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118811,gcn2.AT.ribo.4,NextSeq 550,ERR2003521,56596125,2829806250,SAMEA104118811,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:gcn2.AT.ribo.4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/001/ERR2003521/ERR2003521.fastq.gz,2075087720,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/001/ERR2003521/ERR2003521.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/001/ERR2003521/ERR2003521.fastq.gz,668380c066c3e628525f58053e69d539,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,gcn2.AT.ribo.4_s,,,,,,,,,E-MTAB-5810:gcn2.AT.ribo.4,,E-MTAB-5810:gcn2.AT.ribo.4,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments",,,,,ERS1782704,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/001/ERR2003521,1519052633,ftp.sra.ebi.ac.uk/vol1/err/ERR200/001/ERR2003521,ftp.sra.ebi.ac.uk/vol1/err/ERR200/001/ERR2003521,b42a8bc4f5d248a44d3185b76cef4822,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003521/gcn2_3AT_exp16_ribo_11847X2_150923_D00294_0200_BC7V3HANXX_7.txt.gz,1904816558,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003521/gcn2_3AT_exp16_ribo_11847X2_150923_D00294_0200_BC7V3HANXX_7.txt.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003521/gcn2_3AT_exp16_ribo_11847X2_150923_D00294_0200_BC7V3HANXX_7.txt.gz,,947ac9403e3ae4b2262626768f5efbe5,,,,,,,, PRJEB21224,ERX2063391,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118812,gcn2.noAT.mrna.3,NextSeq 550,ERR2003522,16204245,1226035737,SAMEA104118812,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:gcn2.noAT.mrna.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/002/ERR2003522/ERR2003522.fastq.gz,833872893,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/002/ERR2003522/ERR2003522.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/002/ERR2003522/ERR2003522.fastq.gz,570a362ba4857754da0011c10ff05b34,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,gcn2.noAT.mrna.3_s,,,,,,,,,E-MTAB-5810:gcn2.noAT.mrna.3,,E-MTAB-5810:gcn2.noAT.mrna.3,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782705,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/002/ERR2003522,569859294,ftp.sra.ebi.ac.uk/vol1/err/ERR200/002/ERR2003522,ftp.sra.ebi.ac.uk/vol1/err/ERR200/002/ERR2003522,2b093eaee2aaf8c9287c949eda1203fe,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003522/gcn2_no3AT_07_mRNA-230315-12_S17.fastq.gz,790954260,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003522/gcn2_no3AT_07_mRNA-230315-12_S17.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003522/gcn2_no3AT_07_mRNA-230315-12_S17.fastq.gz,,d350bf2756fb19d68cec31dbb782947c,,,,,,,, PRJEB21224,ERX2063392,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118813,gcn2.noAT.mrna.4,NextSeq 550,ERR2003523,33797257,2557225027,SAMEA104118813,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:gcn2.noAT.mrna.4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/003/ERR2003523/ERR2003523.fastq.gz,1505516244,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/003/ERR2003523/ERR2003523.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/003/ERR2003523/ERR2003523.fastq.gz,19563b6ddb5d9704879d3cb999ec0907,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,gcn2.noAT.mrna.4_s,,,,,,,,,E-MTAB-5810:gcn2.noAT.mrna.4,,E-MTAB-5810:gcn2.noAT.mrna.4,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782706,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/003/ERR2003523,1025536797,ftp.sra.ebi.ac.uk/vol1/err/ERR200/003/ERR2003523,ftp.sra.ebi.ac.uk/vol1/err/ERR200/003/ERR2003523,cfb4a9dbe479d7d8102772f93aff19bd,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003523/gcn2-no3AT_16_mRNA-050615-17_S9.fastq.gz,1416163883,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003523/gcn2-no3AT_16_mRNA-050615-17_S9.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003523/gcn2-no3AT_16_mRNA-050615-17_S9.fastq.gz,,0e5c65014fa3658348761bb7330e44dc,,,,,,,, PRJEB21224,ERX2063393,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118814,gcn2.noAT.ribo.3,NextSeq 550,ERR2003524,31214960,1560748000,SAMEA104118814,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:gcn2.noAT.ribo.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/004/ERR2003524/ERR2003524.fastq.gz,959974227,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/004/ERR2003524/ERR2003524.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/004/ERR2003524/ERR2003524.fastq.gz,f04a4787d1fcd21a7da8c72db1540286,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,gcn2.noAT.ribo.3_s,,,,,,,,,E-MTAB-5810:gcn2.noAT.ribo.3,,E-MTAB-5810:gcn2.noAT.ribo.3,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris p",,,,,ERS1782707,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/004/ERR2003524,684675507,ftp.sra.ebi.ac.uk/vol1/err/ERR200/004/ERR2003524,ftp.sra.ebi.ac.uk/vol1/err/ERR200/004/ERR2003524,94d256c35d704958a4f8eebeccbe3df9,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003524/gcn2_no3AT_exp07_24530667-17_merged.fastq.gz,880833027,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003524/gcn2_no3AT_exp07_24530667-17_merged.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003524/gcn2_no3AT_exp07_24530667-17_merged.fastq.gz,,0fdb3caac64c84b5abad76cb8c81d1b3,,,,,,,, PRJEB21224,ERX2063394,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118815,gcn2.noAT.ribo.4,NextSeq 550,ERR2003525,106865118,5343255900,SAMEA104118815,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:gcn2.noAT.ribo.4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/005/ERR2003525/ERR2003525.fastq.gz,3862724769,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/005/ERR2003525/ERR2003525.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/005/ERR2003525/ERR2003525.fastq.gz,a1685d1f1ebc6099feebe9909ed7f8a6,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,gcn2.noAT.ribo.4_s,,,,,,,,,E-MTAB-5810:gcn2.noAT.ribo.4,,E-MTAB-5810:gcn2.noAT.ribo.4,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris p",,,,,ERS1782708,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/005/ERR2003525,2868222256,ftp.sra.ebi.ac.uk/vol1/err/ERR200/005/ERR2003525,ftp.sra.ebi.ac.uk/vol1/err/ERR200/005/ERR2003525,df7074e5be6140a00d9d02de58afca65,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003525/gcn2_no3AT_exp16_ribo_11847X1_150923_D00294_0200_BC7V3HANXX_7.txt.gz,3549142331,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003525/gcn2_no3AT_exp16_ribo_11847X1_150923_D00294_0200_BC7V3HANXX_7.txt.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003525/gcn2_no3AT_exp16_ribo_11847X1_150923_D00294_0200_BC7V3HANXX_7.txt.gz,,7812b70f1a7633621aec21bbc8d967ea,,,,,,,, PRJEB21224,ERX2063395,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118816,wt.AT.CHX.mrna.11,NextSeq 550,ERR2003526,52513972,2625698600,SAMEA104118816,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.CHX.mrna.11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/006/ERR2003526/ERR2003526.fastq.gz,1177305229,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/006/ERR2003526/ERR2003526.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/006/ERR2003526/ERR2003526.fastq.gz,7ee6488a9803eb2136fbcda0a0d21569,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.CHX.mrna.11_s,,,,,,,,,E-MTAB-5810:wt.AT.CHX.mrna.11,,E-MTAB-5810:wt.AT.CHX.mrna.11,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782709,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/006/ERR2003526,1040367179,ftp.sra.ebi.ac.uk/vol1/err/ERR200/006/ERR2003526,ftp.sra.ebi.ac.uk/vol1/err/ERR200/006/ERR2003526,b3f7a3a6022ce2c39d7ed76bbf6ad02d,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003526/mRNApCpATe23_SLX-12423_NXHT005_ACAGTGGT.fq.gz,1023550001,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003526/mRNApCpATe23_SLX-12423_NXHT005_ACAGTGGT.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003526/mRNApCpATe23_SLX-12423_NXHT005_ACAGTGGT.fq.gz,,cff16eedab8eaa3fe661551e4f93f031,,,,,,,, PRJEB21224,ERX2063396,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118817,wt.AT.CHX.mrna.13,NextSeq 550,ERR2003527,35611500,1780575000,SAMEA104118817,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.CHX.mrna.13_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/007/ERR2003527/ERR2003527.fastq.gz,1275555809,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/007/ERR2003527/ERR2003527.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/007/ERR2003527/ERR2003527.fastq.gz,8581ac36ff6f90577e477a5e02f430a9,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.CHX.mrna.13_s,,,,,,,,,E-MTAB-5810:wt.AT.CHX.mrna.13,,E-MTAB-5810:wt.AT.CHX.mrna.13,,Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782710,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/007/ERR2003527,788706819,ftp.sra.ebi.ac.uk/vol1/err/ERR200/007/ERR2003527,ftp.sra.ebi.ac.uk/vol1/err/ERR200/007/ERR2003527,7df1c844552de47347aedd99041c304f,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003527/mrna_pAT_pCHX_exp26_SLX-13147_RPI_TTCAGCTC.fq.gz,1199379761,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003527/mrna_pAT_pCHX_exp26_SLX-13147_RPI_TTCAGCTC.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003527/mrna_pAT_pCHX_exp26_SLX-13147_RPI_TTCAGCTC.fq.gz,,cfcfabfb6363f650210f470476b089a8,,,,,,,, PRJEB21224,ERX2063397,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118818,wt.AT.CHX.ribo.11,NextSeq 550,ERR2003528,62968779,3148438950,SAMEA104118818,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.CHX.ribo.11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/008/ERR2003528/ERR2003528.fastq.gz,1666209345,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/008/ERR2003528/ERR2003528.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/008/ERR2003528/ERR2003528.fastq.gz,9fd70e70e139a875dbe57f2c06a55e4f,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.CHX.ribo.11_s,,,,,,,,,E-MTAB-5810:wt.AT.CHX.ribo.11,,E-MTAB-5810:wt.AT.CHX.ribo.11,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris p",,,,,ERS1782711,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/008/ERR2003528,1222310242,ftp.sra.ebi.ac.uk/vol1/err/ERR200/008/ERR2003528,ftp.sra.ebi.ac.uk/vol1/err/ERR200/008/ERR2003528,d27e5494bbdf710a5b5cc7cde51f42f4,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003528/RPFpCpATe23_SLX-12983.RPI29.HGLNNBBXX.s_8.r_1.fq.gz,1462489095,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003528/RPFpCpATe23_SLX-12983.RPI29.HGLNNBBXX.s_8.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003528/RPFpCpATe23_SLX-12983.RPI29.HGLNNBBXX.s_8.r_1.fq.gz,,1a4a395ae1f9fb2cecbe9f114649ab0e,,,,,,,, PRJEB21224,ERX2063398,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118819,wt.AT.CHX.ribo.13,NextSeq 550,ERR2003529,28486176,1424308800,SAMEA104118819,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.CHX.ribo.13_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/009/ERR2003529/ERR2003529.fastq.gz,660781571,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/009/ERR2003529/ERR2003529.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/009/ERR2003529/ERR2003529.fastq.gz,0d08431c8d52085ce32156c330612a5f,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.CHX.ribo.13_s,,,,,,,,,E-MTAB-5810:wt.AT.CHX.ribo.13,,E-MTAB-5810:wt.AT.CHX.ribo.13,,"Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris pH 7, 50 mM DTT, 100 mM MgCl2) for 30 min at 37C. ATP and buffer A (Thermo",,,,,ERS1782712,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/009/ERR2003529,472720418,ftp.sra.ebi.ac.uk/vol1/err/ERR200/009/ERR2003529,ftp.sra.ebi.ac.uk/vol1/err/ERR200/009/ERR2003529,a3782428ea352caddb8bd41f79909ed2,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003529/mono_pAT_pCHX_exp26_SLX-13146.RPI20.HJM3GBBXX.s_5.r_1.fq.gz,579227971,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003529/mono_pAT_pCHX_exp26_SLX-13146.RPI20.HJM3GBBXX.s_5.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003529/mono_pAT_pCHX_exp26_SLX-13146.RPI20.HJM3GBBXX.s_5.r_1.fq.gz,,d8c0b57c3a9c40b46463d64105ae401b,,,,,,,, PRJEB21224,ERX2063399,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118820,wt.AT.mrna.2B,NextSeq 550,ERR2003530,39443224,2984603676,SAMEA104118820,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.mrna.2B_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/000/ERR2003530/ERR2003530.fastq.gz,1743412044,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/000/ERR2003530/ERR2003530.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/000/ERR2003530/ERR2003530.fastq.gz,1a5548885934e5433503f169752a7e74,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.mrna.2B_s,,,,,,,,,E-MTAB-5810:wt.AT.mrna.2B,,E-MTAB-5810:wt.AT.mrna.2B,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782713,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/000/ERR2003530,1181846323,ftp.sra.ebi.ac.uk/vol1/err/ERR200/000/ERR2003530,ftp.sra.ebi.ac.uk/vol1/err/ERR200/000/ERR2003530,a843e005dbb8781d73c22202a79c50e0,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003530/h90-3AT_18_mRNA-050615-22_S15.fastq.gz,1640096403,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003530/h90-3AT_18_mRNA-050615-22_S15.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003530/h90-3AT_18_mRNA-050615-22_S15.fastq.gz,,ba46722c4e80b2096d71843ff4853b40,,,,,,,, PRJEB21224,ERX2063400,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118821,wt.AT.mrna.3,NextSeq 550,ERR2003531,14151645,1070787968,SAMEA104118821,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.mrna.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/001/ERR2003531/ERR2003531.fastq.gz,732779452,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/001/ERR2003531/ERR2003531.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/001/ERR2003531/ERR2003531.fastq.gz,18f29a7fbe2aa2e264d75c0024f9a715,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.mrna.3_s,,,,,,,,,E-MTAB-5810:wt.AT.mrna.3,,E-MTAB-5810:wt.AT.mrna.3,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782714,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/001/ERR2003531,497998964,ftp.sra.ebi.ac.uk/vol1/err/ERR200/001/ERR2003531,ftp.sra.ebi.ac.uk/vol1/err/ERR200/001/ERR2003531,057fc17c8b972d80b503dce5b1f75381,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003531/h90_3AT_07_mRNA-230315-10_S19.fastq.gz,695485993,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003531/h90_3AT_07_mRNA-230315-10_S19.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003531/h90_3AT_07_mRNA-230315-10_S19.fastq.gz,,9c72a16c05123dad6b0abda521b3dc63,,,,,,,, PRJEB21224,ERX2063401,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118822,wt.AT.mrna.4,NextSeq 550,ERR2003532,39994820,3026173391,SAMEA104118822,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.mrna.4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/002/ERR2003532/ERR2003532.fastq.gz,1755221335,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/002/ERR2003532/ERR2003532.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/002/ERR2003532/ERR2003532.fastq.gz,ea2439c76183c1c13778cd649904800a,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.mrna.4_s,,,,,,,,,E-MTAB-5810:wt.AT.mrna.4,,E-MTAB-5810:wt.AT.mrna.4,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782715,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/002/ERR2003532,1190387316,ftp.sra.ebi.ac.uk/vol1/err/ERR200/002/ERR2003532,ftp.sra.ebi.ac.uk/vol1/err/ERR200/002/ERR2003532,337be00db2bcf2a4d6f39a2af6347baa,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003532/h90-3AT_16_mRNA-050615-20_S14.fastq.gz,1650311357,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003532/h90-3AT_16_mRNA-050615-20_S14.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003532/h90-3AT_16_mRNA-050615-20_S14.fastq.gz,,597196db20e6ed8243e6e544cc93dc9e,,,,,,,, PRJEB21224,ERX2063402,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118823,wt.AT.noCHX.mrna.11,NextSeq 550,ERR2003533,18348290,917414500,SAMEA104118823,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.noCHX.mrna.11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/003/ERR2003533/ERR2003533.fastq.gz,557797042,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/003/ERR2003533/ERR2003533.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/003/ERR2003533/ERR2003533.fastq.gz,72d626dc55ffe8a99a45b0fce9e9de1a,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.noCHX.mrna.11_s,,,,,,,,,E-MTAB-5810:wt.AT.noCHX.mrna.11,,E-MTAB-5810:wt.AT.noCHX.mrna.11,,Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782716,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/003/ERR2003533,371473051,ftp.sra.ebi.ac.uk/vol1/err/ERR200/003/ERR2003533,ftp.sra.ebi.ac.uk/vol1/err/ERR200/003/ERR2003533,9f5750bd2a6ecb3f75ed5629e97425f4,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003533/mRNAmCpAe23_SLX-12423_NXHT028_TACAGGAT.fq.gz,504798817,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003533/mRNAmCpAe23_SLX-12423_NXHT028_TACAGGAT.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003533/mRNAmCpAe23_SLX-12423_NXHT028_TACAGGAT.fq.gz,,332d3d0d200fe86838b2670ce40ea5f9,,,,,,,, PRJEB21224,ERX2063403,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118824,wt.AT.noCHX.mrna.13,NextSeq 550,ERR2003534,27306569,1365328450,SAMEA104118824,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.noCHX.mrna.13_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/004/ERR2003534/ERR2003534.fastq.gz,985937947,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/004/ERR2003534/ERR2003534.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/004/ERR2003534/ERR2003534.fastq.gz,0cc70783f4f8898040cff08095e2acb0,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.noCHX.mrna.13_s,,,,,,,,,E-MTAB-5810:wt.AT.noCHX.mrna.13,,E-MTAB-5810:wt.AT.noCHX.mrna.13,,Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782717,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/004/ERR2003534,612489209,ftp.sra.ebi.ac.uk/vol1/err/ERR200/004/ERR2003534,ftp.sra.ebi.ac.uk/vol1/err/ERR200/004/ERR2003534,2640c7ef78636539ac882aa5f02e322a,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003534/mrna_pAT_mCHX_exp26_SLX-13147_RPI_GTAAGGTG.fq.gz,931904188,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003534/mrna_pAT_mCHX_exp26_SLX-13147_RPI_GTAAGGTG.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003534/mrna_pAT_mCHX_exp26_SLX-13147_RPI_GTAAGGTG.fq.gz,,ea2dcf642b3f3321cf4b35251399c051,,,,,,,, PRJEB21224,ERX2063404,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118825,wt.AT.noCHX.ribo.11,NextSeq 550,ERR2003535,119503388,5975169400,SAMEA104118825,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.noCHX.ribo.11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/005/ERR2003535/ERR2003535.fastq.gz,3043126397,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/005/ERR2003535/ERR2003535.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/005/ERR2003535/ERR2003535.fastq.gz,402f77beac3bc9923185ed7fcd2acf59,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.noCHX.ribo.11_s,,,,,,,,,E-MTAB-5810:wt.AT.noCHX.ribo.11,,E-MTAB-5810:wt.AT.noCHX.ribo.11,,"Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris pH 7, 50 mM DTT, 100 mM MgCl2) for 30 min at 37C. ATP and buffer A (Thermo",,,,,ERS1782718,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/005/ERR2003535,2287012468,ftp.sra.ebi.ac.uk/vol1/err/ERR200/005/ERR2003535,ftp.sra.ebi.ac.uk/vol1/err/ERR200/005/ERR2003535,0dbe31c34a7870da7d0de1f343064e77,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003535/RPFmCpATe23_SLX-12983.RPI27.HGLNNBBXX.s_8.r_1.fq.gz,2667502124,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003535/RPFmCpATe23_SLX-12983.RPI27.HGLNNBBXX.s_8.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003535/RPFmCpATe23_SLX-12983.RPI27.HGLNNBBXX.s_8.r_1.fq.gz,,27966036d32945f3c6da7f60a43951fd,,,,,,,, PRJEB21224,ERX2063405,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118826,wt.AT.noCHX.ribo.13,NextSeq 550,ERR2003536,31631553,1581577650,SAMEA104118826,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.noCHX.ribo.13_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/006/ERR2003536/ERR2003536.fastq.gz,699606031,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/006/ERR2003536/ERR2003536.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/006/ERR2003536/ERR2003536.fastq.gz,499bbf1aa42ba38f52798403a5660183,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.noCHX.ribo.13_s,,,,,,,,,E-MTAB-5810:wt.AT.noCHX.ribo.13,,E-MTAB-5810:wt.AT.noCHX.ribo.13,,"Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris pH 7, 50 mM DTT, 100 mM MgCl2) for 30 min at 37C. ATP and buffer A (Thermo",,,,,ERS1782719,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/006/ERR2003536,524549808,ftp.sra.ebi.ac.uk/vol1/err/ERR200/006/ERR2003536,ftp.sra.ebi.ac.uk/vol1/err/ERR200/006/ERR2003536,63e2d7b8f92dcf1508d715b73d9df6d7,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003536/mono_pAT_mCHX_exp26_SLX-13146.RPI19.HJM3GBBXX.s_5.r_1.fq.gz,609988153,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003536/mono_pAT_mCHX_exp26_SLX-13146.RPI19.HJM3GBBXX.s_5.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003536/mono_pAT_mCHX_exp26_SLX-13146.RPI19.HJM3GBBXX.s_5.r_1.fq.gz,,565632529106cc7c21a6aad361553481,,,,,,,, PRJEB21224,ERX2063406,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118827,wt.AT.ribo.2-1,NextSeq 550,ERR2003537,17283910,881479182,SAMEA104118827,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.ribo.2-1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/007/ERR2003537/ERR2003537.fastq.gz,589659698,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/007/ERR2003537/ERR2003537.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/007/ERR2003537/ERR2003537.fastq.gz,73241f735dd4c2b4f99c2d793c3f49c5,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.ribo.2-1_s,,,,,,,,,E-MTAB-5810:wt.AT.ribo.2-1,,E-MTAB-5810:wt.AT.ribo.2-1,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments",,,,,ERS1782720,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/007/ERR2003537,445091210,ftp.sra.ebi.ac.uk/vol1/err/ERR200/007/ERR2003537,ftp.sra.ebi.ac.uk/vol1/err/ERR200/007/ERR2003537,a1d701d5691c10fc8a97a3628754fa8d,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003537/CD-RiboSeq-7.fastq.ACG.fq.gz,540425982,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003537/CD-RiboSeq-7.fastq.ACG.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003537/CD-RiboSeq-7.fastq.ACG.fq.gz,,16ddef4ee3fc7c5e45206f424b15904f,,,,,,,, PRJEB21224,ERX2063407,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118828,wt.AT.ribo.2-2,NextSeq 550,ERR2003538,60683650,3034182500,SAMEA104118828,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.ribo.2-2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/008/ERR2003538/ERR2003538.fastq.gz,1857856864,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/008/ERR2003538/ERR2003538.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/008/ERR2003538/ERR2003538.fastq.gz,1ab488c931419ed2fc80d283d0e54f00,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.ribo.2-2_s,,,,,,,,,E-MTAB-5810:wt.AT.ribo.2-2,,E-MTAB-5810:wt.AT.ribo.2-2,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris p",,,,,ERS1782721,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/008/ERR2003538,1437803587,ftp.sra.ebi.ac.uk/vol1/err/ERR200/008/ERR2003538,ftp.sra.ebi.ac.uk/vol1/err/ERR200/008/ERR2003538,2a6f89145bf6d5c69ad1623f75e5c3a6,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003538/11201X1_141113_D00294_0141_BC5U3MANXX_8.ACG.fq.gz,1660794933,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003538/11201X1_141113_D00294_0141_BC5U3MANXX_8.ACG.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003538/11201X1_141113_D00294_0141_BC5U3MANXX_8.ACG.fq.gz,,39e2a0c5a2dd927544728d3307c9d9b7,,,,,,,, PRJEB21224,ERX2063408,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118829,wt.AT.ribo.3,NextSeq 550,ERR2003539,37185178,1859258900,SAMEA104118829,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.ribo.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/009/ERR2003539/ERR2003539.fastq.gz,1098948044,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/009/ERR2003539/ERR2003539.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/009/ERR2003539/ERR2003539.fastq.gz,467ddb35049f6a2337e4118c83d9c826,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.ribo.3_s,,,,,,,,,E-MTAB-5810:wt.AT.ribo.3,,E-MTAB-5810:wt.AT.ribo.3,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments",,,,,ERS1782722,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/009/ERR2003539,818878229,ftp.sra.ebi.ac.uk/vol1/err/ERR200/009/ERR2003539,ftp.sra.ebi.ac.uk/vol1/err/ERR200/009/ERR2003539,df041f31a79e9aeeed3ca46813de2a54,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003539/h90_3AT_exp07_24530669-14_merged.fastq.gz,1004387847,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003539/h90_3AT_exp07_24530669-14_merged.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003539/h90_3AT_exp07_24530669-14_merged.fastq.gz,,3f6594a2c9eef2cd20c51dbf324062c0,,,,,,,, PRJEB21224,ERX2063409,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118830,wt.AT.ribo.4,NextSeq 550,ERR2003540,68616943,3430847150,SAMEA104118830,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.AT.ribo.4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/000/ERR2003540/ERR2003540.fastq.gz,2500974085,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/000/ERR2003540/ERR2003540.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/000/ERR2003540/ERR2003540.fastq.gz,7bf449c3ff4638fa6a317e4ad17a2a7d,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.AT.ribo.4_s,,,,,,,,,E-MTAB-5810:wt.AT.ribo.4,,E-MTAB-5810:wt.AT.ribo.4,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Cells were grown in EMM2 (Moreno et al. Methods Enzymology 194: 795) in the presence of 10 mM 3-AT for 60 minutes at 32C. This treatment mimics histidine starvation. Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments",,,,,ERS1782723,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/000/ERR2003540,1843866405,ftp.sra.ebi.ac.uk/vol1/err/ERR200/000/ERR2003540,ftp.sra.ebi.ac.uk/vol1/err/ERR200/000/ERR2003540,48c3c61d387817c018f69aeee09089c8,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003540/wt_3AT_exp16_ribo_11847X3_150923_D00294_0200_BC7V3HANXX_7.txt.gz,2294020723,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003540/wt_3AT_exp16_ribo_11847X3_150923_D00294_0200_BC7V3HANXX_7.txt.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003540/wt_3AT_exp16_ribo_11847X3_150923_D00294_0200_BC7V3HANXX_7.txt.gz,,57b4ef83c61df64e06901c9d9a859c6d,,,,,,,, PRJEB21224,ERX2063410,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118831,wt.noAT.CHX.mrna.11,NextSeq 550,ERR2003541,4368155,218407750,SAMEA104118831,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.CHX.mrna.11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/001/ERR2003541/ERR2003541.fastq.gz,130062464,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/001/ERR2003541/ERR2003541.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/001/ERR2003541/ERR2003541.fastq.gz,655097cad43649361b15b68be9decd5b,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.CHX.mrna.11_s,,,,,,,,,E-MTAB-5810:wt.noAT.CHX.mrna.11,,E-MTAB-5810:wt.noAT.CHX.mrna.11,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782724,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/001/ERR2003541,90380475,ftp.sra.ebi.ac.uk/vol1/err/ERR200/001/ERR2003541,ftp.sra.ebi.ac.uk/vol1/err/ERR200/001/ERR2003541,0e012cb5e21877200e421b273bf9ec6e,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003541/mRNApCmATe23_SLX-12423_NXHT003_TTAGGCAT.fq.gz,118154679,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003541/mRNApCmATe23_SLX-12423_NXHT003_TTAGGCAT.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003541/mRNApCmATe23_SLX-12423_NXHT003_TTAGGCAT.fq.gz,,e259265a6862a9cad732fc6c89cb89aa,,,,,,,, PRJEB21224,ERX2063411,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118832,wt.noAT.CHX.mrna.13,NextSeq 550,ERR2003542,36240950,1812047500,SAMEA104118832,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.CHX.mrna.13_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/002/ERR2003542/ERR2003542.fastq.gz,1300747744,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/002/ERR2003542/ERR2003542.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/002/ERR2003542/ERR2003542.fastq.gz,064d7e59cb7f24e8faf93890ccafa828,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.CHX.mrna.13_s,,,,,,,,,E-MTAB-5810:wt.noAT.CHX.mrna.13,,E-MTAB-5810:wt.noAT.CHX.mrna.13,,Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782725,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/002/ERR2003542,806658368,ftp.sra.ebi.ac.uk/vol1/err/ERR200/002/ERR2003542,ftp.sra.ebi.ac.uk/vol1/err/ERR200/002/ERR2003542,b7ff110b8ec1b68705c23321ffc1c384,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003542/mrna_mAT_pN_pCHX_exp26_SLX-13147_RPI_GAGGTGCT.fq.gz,1225381442,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003542/mrna_mAT_pN_pCHX_exp26_SLX-13147_RPI_GAGGTGCT.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003542/mrna_mAT_pN_pCHX_exp26_SLX-13147_RPI_GAGGTGCT.fq.gz,,cdf5e357aca1a3ba53528fa99a8a76ae,,,,,,,, PRJEB21224,ERX2063412,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118833,wt.noAT.CHX.ribo.11,NextSeq 550,ERR2003543,32008211,1600410550,SAMEA104118833,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.CHX.ribo.11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/003/ERR2003543/ERR2003543.fastq.gz,848061258,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/003/ERR2003543/ERR2003543.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/003/ERR2003543/ERR2003543.fastq.gz,1525219220ef1170f37680d6a3f7d590,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.CHX.ribo.11_s,,,,,,,,,E-MTAB-5810:wt.noAT.CHX.ribo.11,,E-MTAB-5810:wt.noAT.CHX.ribo.11,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris p",,,,,ERS1782726,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/003/ERR2003543,624070632,ftp.sra.ebi.ac.uk/vol1/err/ERR200/003/ERR2003543,ftp.sra.ebi.ac.uk/vol1/err/ERR200/003/ERR2003543,312299d9c8dd7633a6b39cb89768b35e,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003543/RPFpCmATe23_SLX-12983.RPI28.HGLNNBBXX.s_8.r_1.fq.gz,752023572,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003543/RPFpCmATe23_SLX-12983.RPI28.HGLNNBBXX.s_8.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003543/RPFpCmATe23_SLX-12983.RPI28.HGLNNBBXX.s_8.r_1.fq.gz,,c602c03e9f371082e570cddfa969c589,,,,,,,, PRJEB21224,ERX2063413,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118834,wt.noAT.CHX.ribo.13,NextSeq 550,ERR2003544,26742065,1337103250,SAMEA104118834,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.CHX.ribo.13_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/004/ERR2003544/ERR2003544.fastq.gz,635231766,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/004/ERR2003544/ERR2003544.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/004/ERR2003544/ERR2003544.fastq.gz,e4d53be20e3954cc312ee278e50f83e3,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.CHX.ribo.13_s,,,,,,,,,E-MTAB-5810:wt.noAT.CHX.ribo.13,,E-MTAB-5810:wt.noAT.CHX.ribo.13,,"Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris pH 7, 50 mM DTT, 100 mM MgCl2) for 30 min at 37C. ATP and buffer A (Thermo",,,,,ERS1782727,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/004/ERR2003544,457766341,ftp.sra.ebi.ac.uk/vol1/err/ERR200/004/ERR2003544,ftp.sra.ebi.ac.uk/vol1/err/ERR200/004/ERR2003544,ca5121a2da40e795d052155dfa9df1aa,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003544/mono_mAT_pN_pCHX_exp26_SLX-13145.RPI22.HJM3GBBXX.s_4.r_1.fq.gz,558194785,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003544/mono_mAT_pN_pCHX_exp26_SLX-13145.RPI22.HJM3GBBXX.s_4.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003544/mono_mAT_pN_pCHX_exp26_SLX-13145.RPI22.HJM3GBBXX.s_4.r_1.fq.gz,,ef4ec4280601e2884d421aadb1ab7425,,,,,,,, PRJEB21224,ERX2063414,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118835,wt.noAT.mrna.2B,NextSeq 550,ERR2003545,24001975,1816117196,SAMEA104118835,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.mrna.2B_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/005/ERR2003545/ERR2003545.fastq.gz,1060397446,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/005/ERR2003545/ERR2003545.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/005/ERR2003545/ERR2003545.fastq.gz,06959834055ca25ab1ecbe11f21d0801,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.mrna.2B_s,,,,,,,,,E-MTAB-5810:wt.noAT.mrna.2B,,E-MTAB-5810:wt.noAT.mrna.2B,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782728,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/005/ERR2003545,720112602,ftp.sra.ebi.ac.uk/vol1/err/ERR200/005/ERR2003545,ftp.sra.ebi.ac.uk/vol1/err/ERR200/005/ERR2003545,e27fe92fb580c9ff4bf3e588a7282b8f,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003545/h90-no3AT_18_mRNA-050615-23_S19.fastq.gz,997311595,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003545/h90-no3AT_18_mRNA-050615-23_S19.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003545/h90-no3AT_18_mRNA-050615-23_S19.fastq.gz,,34a9115e73844b6e9e39053e2c94081e,,,,,,,, PRJEB21224,ERX2063415,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118836,wt.noAT.mrna.3,NextSeq 550,ERR2003546,15509062,1173469392,SAMEA104118836,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.mrna.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/006/ERR2003546/ERR2003546.fastq.gz,803924922,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/006/ERR2003546/ERR2003546.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/006/ERR2003546/ERR2003546.fastq.gz,dac054247d9664db1a04a01c0085205d,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.mrna.3_s,,,,,,,,,E-MTAB-5810:wt.noAT.mrna.3,,E-MTAB-5810:wt.noAT.mrna.3,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782729,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/006/ERR2003546,549215848,ftp.sra.ebi.ac.uk/vol1/err/ERR200/006/ERR2003546,ftp.sra.ebi.ac.uk/vol1/err/ERR200/006/ERR2003546,759823058aa253b0e0962b3a9cc6cdca,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003546/h90_no3AT_07_mRNA-230315-1_S20.fastq.gz,762817160,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003546/h90_no3AT_07_mRNA-230315-1_S20.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003546/h90_no3AT_07_mRNA-230315-1_S20.fastq.gz,,5636a268bb7e916d7d9baa534cbfe73d,,,,,,,, PRJEB21224,ERX2063416,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118837,wt.noAT.mrna.4,NextSeq 550,ERR2003547,23729256,1795439617,SAMEA104118837,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.mrna.4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/007/ERR2003547/ERR2003547.fastq.gz,1072582617,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/007/ERR2003547/ERR2003547.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/007/ERR2003547/ERR2003547.fastq.gz,0280cc7a0523d8627476ef6531490bef,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.mrna.4_s,,,,,,,,,E-MTAB-5810:wt.noAT.mrna.4,,E-MTAB-5810:wt.noAT.mrna.4,,Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Total RNA was extracted using a hot phenol extraction method as described in Lyne et al. (2003) BMC Genomics 4:27. Clean up and DNase treatment were performed on with Purelink RNA microcolumns (Life Technologies) following the manufacturer’s instructions. Samples were ribo-depleted using Ribo-Zero Gold rRNA Removal Kit Yeast (Illumina) with a 4 ug input. 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782730,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/007/ERR2003547,729745793,ftp.sra.ebi.ac.uk/vol1/err/ERR200/007/ERR2003547,ftp.sra.ebi.ac.uk/vol1/err/ERR200/007/ERR2003547,e45bbe6c77200db5c1ff08f40bcb53ae,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003547/h90-no3AT_16_mRNA-050615-19_S13.fastq.gz,1010233555,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003547/h90-no3AT_16_mRNA-050615-19_S13.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003547/h90-no3AT_16_mRNA-050615-19_S13.fastq.gz,,dcbfb9373b46c3156dba72d53b76c9e6,,,,,,,, PRJEB21224,ERX2063417,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118838,wt.noAT.noCHX.mrna.11,NextSeq 550,ERR2003548,19274273,963713650,SAMEA104118838,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.noCHX.mrna.11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/008/ERR2003548/ERR2003548.fastq.gz,532713519,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/008/ERR2003548/ERR2003548.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/008/ERR2003548/ERR2003548.fastq.gz,e40e326a746971ea5e3126e3192ca877,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.noCHX.mrna.11_s,,,,,,,,,E-MTAB-5810:wt.noAT.noCHX.mrna.11,,E-MTAB-5810:wt.noAT.noCHX.mrna.11,,Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782731,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/008/ERR2003548,390252964,ftp.sra.ebi.ac.uk/vol1/err/ERR200/008/ERR2003548,ftp.sra.ebi.ac.uk/vol1/err/ERR200/008/ERR2003548,3546b7720323b82f3bcdc0462f7977c5,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003548/mRNAmCmAe23_SLX-12423_NXHT046_TCAGATTC.fq.gz,476585944,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003548/mRNAmCmAe23_SLX-12423_NXHT046_TCAGATTC.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003548/mRNAmCmAe23_SLX-12423_NXHT046_TCAGATTC.fq.gz,,770137c407471e576d8d48a20eec17a9,,,,,,,, PRJEB21224,ERX2063418,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,RNA-Seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA104118839,wt.noAT.noCHX.mrna.13,NextSeq 550,ERR2003549,23972947,1198647350,SAMEA104118839,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.noCHX.mrna.13_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/009/ERR2003549/ERR2003549.fastq.gz,862599495,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/009/ERR2003549/ERR2003549.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/009/ERR2003549/ERR2003549.fastq.gz,f69e5f34a2d3cf8df1ed883b5c9966a6,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.noCHX.mrna.13_s,,,,,,,,,E-MTAB-5810:wt.noAT.noCHX.mrna.13,,E-MTAB-5810:wt.noAT.noCHX.mrna.13,,Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). 30 ng of ribo-depleted RNA was used as starting material for the NEXTflex Rapid Directional qRNA-Seq Kit (Bioo Scientific).,,,,,ERS1782732,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/009/ERR2003549,537673923,ftp.sra.ebi.ac.uk/vol1/err/ERR200/009/ERR2003549,ftp.sra.ebi.ac.uk/vol1/err/ERR200/009/ERR2003549,bc636800872c6ec3d306bcfdcc831766,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003549/mrna_mAT_pN_mCHX_exp26_SLX-13147_RPI_TATGTGGC.fq.gz,812213937,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003549/mrna_mAT_pN_mCHX_exp26_SLX-13147_RPI_TATGTGGC.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003549/mrna_mAT_pN_mCHX_exp26_SLX-13147_RPI_TATGTGGC.fq.gz,,9fe61461eeb189b43ea05180b3d86f6a,,,,,,,, PRJEB21224,ERX2063419,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118840,wt.noAT.noCHX.ribo.11,NextSeq 550,ERR2003550,26638047,1331902350,SAMEA104118840,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.noCHX.ribo.11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/000/ERR2003550/ERR2003550.fastq.gz,719510214,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/000/ERR2003550/ERR2003550.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/000/ERR2003550/ERR2003550.fastq.gz,5287ef3126158842fcce22607376e4ab,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.noCHX.ribo.11_s,,,,,,,,,E-MTAB-5810:wt.noAT.noCHX.ribo.11,,E-MTAB-5810:wt.noAT.noCHX.ribo.11,,"Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris pH 7, 50 mM DTT, 100 mM MgCl2) for 30 min at 37C. ATP and buffer A (Thermo",,,,,ERS1782733,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/000/ERR2003550,528958135,ftp.sra.ebi.ac.uk/vol1/err/ERR200/000/ERR2003550,ftp.sra.ebi.ac.uk/vol1/err/ERR200/000/ERR2003550,c9b8a3f906a5326616ae8bf09712c3c3,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003550/RPFmCmATe23_SLX-12983.RPI26.HGLNNBBXX.s_8.r_1.fq.gz,637943365,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003550/RPFmCmATe23_SLX-12983.RPI26.HGLNNBBXX.s_8.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003550/RPFmCmATe23_SLX-12983.RPI26.HGLNNBBXX.s_8.r_1.fq.gz,,98f9160d85f357335c9dc52b9841f8cc,,,,,,,, PRJEB21224,ERX2063420,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118841,wt.noAT.noCHX.ribo.13,NextSeq 550,ERR2003551,32968604,1648430200,SAMEA104118841,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.noCHX.ribo.13_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/001/ERR2003551/ERR2003551.fastq.gz,708592113,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/001/ERR2003551/ERR2003551.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/001/ERR2003551/ERR2003551.fastq.gz,8fbff505aabe627b3d946913530748fe,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.noCHX.ribo.13_s,,,,,,,,,E-MTAB-5810:wt.noAT.noCHX.ribo.13,,E-MTAB-5810:wt.noAT.noCHX.ribo.13,,"Protocols: Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris pH 7, 50 mM DTT, 100 mM MgCl2) for 30 min at 37C. ATP and buffer A (Thermo",,,,,ERS1782734,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/001/ERR2003551,549410930,ftp.sra.ebi.ac.uk/vol1/err/ERR200/001/ERR2003551,ftp.sra.ebi.ac.uk/vol1/err/ERR200/001/ERR2003551,0ef540e339cf96d5cb12df142c71fd06,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003551/mono_mAT_pN_mCHX_exp26_SLX-13145.RPI21.HJM3GBBXX.s_4.r_1.fq.gz,614854275,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003551/mono_mAT_pN_mCHX_exp26_SLX-13145.RPI21.HJM3GBBXX.s_4.r_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003551/mono_mAT_pN_mCHX_exp26_SLX-13145.RPI21.HJM3GBBXX.s_4.r_1.fq.gz,,16a064d8c45d9eb04890f741fc2f6a5e,,,,,,,, PRJEB21224,ERX2063421,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118842,wt.noAT.ribo.2,NextSeq 550,ERR2003552,3359956,171357719,SAMEA104118842,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.ribo.2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/002/ERR2003552/ERR2003552.fastq.gz,136192939,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/002/ERR2003552/ERR2003552.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/002/ERR2003552/ERR2003552.fastq.gz,6e3f10c17d0a5e171a66f17beee5c6af,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.ribo.2_s,,,,,,,,,E-MTAB-5810:wt.noAT.ribo.2,,E-MTAB-5810:wt.noAT.ribo.2,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. RNA samples were purified using Purelink RNA microcolumns (Life Technologies) as described by the manufacturer, e",,,,,ERS1782735,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/002/ERR2003552,87007481,ftp.sra.ebi.ac.uk/vol1/err/ERR200/002/ERR2003552,ftp.sra.ebi.ac.uk/vol1/err/ERR200/002/ERR2003552,5b1fcdf4dfb101f97fe5fa710bf5266c,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003552/CD-RiboSeq-5.fastq.ACG.fq.gz,126534954,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003552/CD-RiboSeq-5.fastq.ACG.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003552/CD-RiboSeq-5.fastq.ACG.fq.gz,,28b6ed3e7aacd7f6f74cd6740ede2d87,,,,,,,, PRJEB21224,ERX2063422,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118843,wt.noAT.ribo.3,NextSeq 550,ERR2003553,30905560,1545278000,SAMEA104118843,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.ribo.3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/003/ERR2003553/ERR2003553.fastq.gz,919281065,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/003/ERR2003553/ERR2003553.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/003/ERR2003553/ERR2003553.fastq.gz,b035d4b3fccf176993f1c6c2d64af63f,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.ribo.3_s,,,,,,,,,E-MTAB-5810:wt.noAT.ribo.3,,E-MTAB-5810:wt.noAT.ribo.3,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris p",,,,,ERS1782736,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/003/ERR2003553,682389112,ftp.sra.ebi.ac.uk/vol1/err/ERR200/003/ERR2003553,ftp.sra.ebi.ac.uk/vol1/err/ERR200/003/ERR2003553,365d62ae914902987a9a50c61d7fc5da,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003553/h90_no3AT_exp07_24530670-1_merged.fastq.gz,839893104,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003553/h90_no3AT_exp07_24530670-1_merged.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003553/h90_no3AT_exp07_24530670-1_merged.fastq.gz,,243c79d740a9f42e6cf01aac1382d678,,,,,,,, PRJEB21224,ERX2063423,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,NextSeq 550 sequencing; Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,4896,Schizosaccharomyces pombe,OTHER,TRANSCRIPTOMIC,unspecified,SAMEA104118844,wt.noAT.ribo.4,NextSeq 550,ERR2003554,47605239,2380261950,SAMEA104118844,,,,,,ArrayExpress,,,Department of Biochemistry University of Cambridge UK,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5810:wt.noAT.ribo.4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR200/004/ERR2003554/ERR2003554.fastq.gz,1561204140,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/004/ERR2003554/ERR2003554.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR200/004/ERR2003554/ERR2003554.fastq.gz,76cedea84235f1ea0d5aeb8f8cc7334e,2017-06-09,2018-02-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,wt.noAT.ribo.4_s,,,,,,,,,E-MTAB-5810:wt.noAT.ribo.4,,E-MTAB-5810:wt.noAT.ribo.4,,"Protocols: Cells were incubated with CHX at 100 ug/ul for 5 minutes before collection Cells were grown at 32C in EMM2 (Moreno et al. Methods Enzymology 194: 795). Between 3x10E8 and 12x10E8 cells were resuspended in 100 ul of lysis buffer (20 mM Tris-HCl pH 8.0, 140 mM KCl, 5 mM Mg2Cl, 1 % Triton X-100, 100 ug/ml cycloheximide) with 1 g of chilled glass beads (Biospec) and lysed using a Fastprep 24 bead-beater (MP Biomedicals) at level 6 for 13 seconds. The extract was diluted with 400 ul of lysis buffer and cleared by centrifugation in two steps at 4 degrees C at 16,000 g (5 minutes followed by 15 minutes). 600 A260 units of cell extract were digested with 750 units of RNase I (Life Technologies) for 45 minutes. Reactions were quenched with 600 units of SUPERaseIn (Life Technologies). Digested extracts in 500 ul were loaded onto a 14 ml linear 10-50% (w/v) sucrose gradient prepared with a Gradient Master (Biocomp), and separated by centrifugation for 160 min at 35,000 rpm in a SW 40Ti rotor (Beckman). The gradients were then fractionated by upward displacement with 55% (w/v) sucrose, and fractions containing monosomes selected for further processing. RNAs were then purified by phenol extraction, passed through amicon ultra 100 kDa columns (Millipore), and run on 15% TBE-urea gels (Life Technologies). Fragments of around 28 nucleotides were extracted from the gel. Gel purified RNA fragments were treated with 10 units of T4 PNK (Thermo Fisher) in a low pH buffer (700 mM Tris p",,,,,ERS1782737,ERP023462,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR200/004/ERR2003554,1172398652,ftp.sra.ebi.ac.uk/vol1/err/ERR200/004/ERR2003554,ftp.sra.ebi.ac.uk/vol1/err/ERR200/004/ERR2003554,2df3955cc43fc1c7ce49095bf5f44fda,,E-MTAB-5810,Ribosome profiling and parallel RNA-seq of S. pombe cells subject to amino acid starvation,,,ERA955947,fasp.sra.ebi.ac.uk:/vol1/run/ERR200/ERR2003554/wt_no3AT_exp16_ribo_11848X1_150923_D00294_0200_BC7V3HANXX_3.txt.gz,1421560841,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003554/wt_no3AT_exp16_ribo_11848X1_150923_D00294_0200_BC7V3HANXX_3.txt.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR200/ERR2003554/wt_no3AT_exp16_ribo_11848X1_150923_D00294_0200_BC7V3HANXX_3.txt.gz,,d081fb12f6f36fc00466234d3d3bf462,,,,,,,, PRJEB22128,ERX2151380,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,9606,Homo sapiens,RIP-Seq,TRANSCRIPTOMIC,other,SAMEA104209704,Riboseq CHX pool,Illumina HiSeq 2000,ERR2093966,5129748,512974800,SAMEA104209704,,,,,,ArrayExpress,,T-helper 1 cell,"INGM, National Institute of Molecular Genetics, “Romeo ed Enrica Invernizzi”, Milan, Italy",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5961:Riboseq CHX pool_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR209/006/ERR2093966/ERR2093966.fastq.gz,214688909,ftp.sra.ebi.ac.uk/vol1/fastq/ERR209/006/ERR2093966/ERR2093966.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR209/006/ERR2093966/ERR2093966.fastq.gz,71582570bd22aa93035d1d4e7197c61a,2017-08-10,2020-04-14,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Riboseq CHX pool_s,,,,,,,,,E-MTAB-5961:Riboseq CHX pool,,E-MTAB-5961:Riboseq CHX pool,,"Protocols: Naive CD4+ T cells purified from the blood of healthy donors were polarized in vitro to TH1 in RPMI media with 10% FBS, 0.1% Penicillin/Streptomycin 0.1 % nonessential amino acids and 0,1% Sodium Pyruvate at 37°C and 5% CO2. For Riboseq samples, RNA footprints were extracted according to Ingolia et al., 2012 DOI : 10.1038/nprot.2012.086. Libraries for Riboseq were prepared according to Ingolia et al., 2012 DOI :10.1038/nprot.2012.086.",,,,,ERS1868722,ERP024464,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR209/006/ERR2093966,229799063,ftp.sra.ebi.ac.uk/vol1/err/ERR209/006/ERR2093966,ftp.sra.ebi.ac.uk/vol1/err/ERR209/006/ERR2093966,154085cb25014a690039b3c47d40aeff,,E-MTAB-5961,Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,,,ERA986360,fasp.sra.ebi.ac.uk:/vol1/run/ERR209/ERR2093966/Sample_A_R1.fastq.gz,200358957,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR209/ERR2093966/Sample_A_R1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR209/ERR2093966/Sample_A_R1.fastq.gz,,f20b4b4169217cf66ca94775fe2f1dd7,,,,,,,, PRJEB22128,ERX2151381,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA104209705,RNA-seq CHX 1,Illumina HiSeq 2000,ERR2093967,81139076,8113907600,SAMEA104209705,,,,,,ArrayExpress,,T-helper 1 cell,"INGM, National Institute of Molecular Genetics, “Romeo ed Enrica Invernizzi”, Milan, Italy",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5961:RNA-seq CHX 1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR209/007/ERR2093967/ERR2093967.fastq.gz,4201953300,ftp.sra.ebi.ac.uk/vol1/fastq/ERR209/007/ERR2093967/ERR2093967.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR209/007/ERR2093967/ERR2093967.fastq.gz,69e70a483e6e41626d6d37183986e5b1,2017-08-10,2020-04-14,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RNA-seq CHX 1_s,,,,,,,,,E-MTAB-5961:RNA-seq CHX 1,,E-MTAB-5961:RNA-seq CHX 1,,"Protocols: Naive CD4+ T cells purified from the blood of healthy donors were polarized in vitro to TH1 in RPMI media with 10% FBS, 0.1% Penicillin/Streptomycin 0.1 % nonessential amino acids and 0,1% Sodium Pyruvate at 37°C and 5% CO2. For RNAseq samples, RNA was extracted using the mirVana isolation kit according to manufacturer's instructions (mirVana ThermoFisher #AM 1560) Libraries for RNAseq were prepared using Illumina TruSeq Stranded Total RNA Library Prep Kit",,,,,ERS1868723,ERP024464,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR209/007/ERR2093967,3847920527,ftp.sra.ebi.ac.uk/vol1/err/ERR209/007/ERR2093967,ftp.sra.ebi.ac.uk/vol1/err/ERR209/007/ERR2093967,6453a85e4bdeb5949f741a7a8b4e48b4,,E-MTAB-5961,Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,,,ERA986360,fasp.sra.ebi.ac.uk:/vol1/run/ERR209/ERR2093967/Sample_L_R1.fastq.gz,3947447338,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR209/ERR2093967/Sample_L_R1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR209/ERR2093967/Sample_L_R1.fastq.gz,,8d7a9c63ed04ece9e3fed868d5dec207,,,,,,,, PRJEB22128,ERX2151382,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA104209706,RNA-seq CHX 2,Illumina HiSeq 2000,ERR2093968,80937413,8093741300,SAMEA104209706,,,,,,ArrayExpress,,T-helper 1 cell,"INGM, National Institute of Molecular Genetics, “Romeo ed Enrica Invernizzi”, Milan, Italy",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5961:RNA-seq CHX 2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR209/008/ERR2093968/ERR2093968.fastq.gz,4226944443,ftp.sra.ebi.ac.uk/vol1/fastq/ERR209/008/ERR2093968/ERR2093968.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR209/008/ERR2093968/ERR2093968.fastq.gz,63a1e7bfb1c07cf75025fd00118c454c,2017-08-10,2020-04-14,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RNA-seq CHX 2_s,,,,,,,,,E-MTAB-5961:RNA-seq CHX 2,,E-MTAB-5961:RNA-seq CHX 2,,"Protocols: Naive CD4+ T cells purified from the blood of healthy donors were polarized in vitro to TH1 in RPMI media with 10% FBS, 0.1% Penicillin/Streptomycin 0.1 % nonessential amino acids and 0,1% Sodium Pyruvate at 37°C and 5% CO2. For RNAseq samples, RNA was extracted using the mirVana isolation kit according to manufacturer's instructions (mirVana ThermoFisher #AM 1560) Libraries for RNAseq were prepared using Illumina TruSeq Stranded Total RNA Library Prep Kit",,,,,ERS1868724,ERP024464,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR209/008/ERR2093968,3824195041,ftp.sra.ebi.ac.uk/vol1/err/ERR209/008/ERR2093968,ftp.sra.ebi.ac.uk/vol1/err/ERR209/008/ERR2093968,b45edbf8d050efb3ba93ff55dcafb810,,E-MTAB-5961,Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,,,ERA986360,fasp.sra.ebi.ac.uk:/vol1/run/ERR209/ERR2093968/Sample_M_R1.fastq.gz,3974164189,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR209/ERR2093968/Sample_M_R1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR209/ERR2093968/Sample_M_R1.fastq.gz,,3af0b8702704f13c6cd09c165e3a43e5,,,,,,,, PRJEB22128,ERX2151383,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,Illumina HiSeq 2000 sequencing; Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA104209707,RNA-seq CHX 3,Illumina HiSeq 2000,ERR2093969,75600500,7560050000,SAMEA104209707,,,,,,ArrayExpress,,T-helper 1 cell,"INGM, National Institute of Molecular Genetics, “Romeo ed Enrica Invernizzi”, Milan, Italy",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-5961:RNA-seq CHX 3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR209/009/ERR2093969/ERR2093969.fastq.gz,4116057628,ftp.sra.ebi.ac.uk/vol1/fastq/ERR209/009/ERR2093969/ERR2093969.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR209/009/ERR2093969/ERR2093969.fastq.gz,f2cfc9500a6823c3095293971f64614e,2017-08-10,2020-04-14,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RNA-seq CHX 3_s,,,,,,,,,E-MTAB-5961:RNA-seq CHX 3,,E-MTAB-5961:RNA-seq CHX 3,,"Protocols: Naive CD4+ T cells purified from the blood of healthy donors were polarized in vitro to TH1 in RPMI media with 10% FBS, 0.1% Penicillin/Streptomycin 0.1 % nonessential amino acids and 0,1% Sodium Pyruvate at 37°C and 5% CO2. For RNAseq samples, RNA was extracted using the mirVana isolation kit according to manufacturer's instructions (mirVana ThermoFisher #AM 1560) Libraries for RNAseq were prepared using Illumina TruSeq Stranded Total RNA Library Prep Kit",,,,,ERS1868725,ERP024464,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR209/009/ERR2093969,3582427727,ftp.sra.ebi.ac.uk/vol1/err/ERR209/009/ERR2093969,ftp.sra.ebi.ac.uk/vol1/err/ERR209/009/ERR2093969,b87351c635843228450bfc634654d65e,,E-MTAB-5961,Ribosome profiling and RNA-seq of in vitro differentiated human CD4+ Th1 cells.,,,ERA986360,fasp.sra.ebi.ac.uk:/vol1/run/ERR209/ERR2093969/Sample_N_R1.fastq.gz,3876651292,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR209/ERR2093969/Sample_N_R1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR209/ERR2093969/Sample_N_R1.fastq.gz,,375115f1d361debf98b508ba622cf1f1,,,,,,,, PRJEB23398,ERX2249169,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375964,ID18RPF,Illumina HiSeq 2500,ERR2193146,29058055,2934863555,SAMEA104375964,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID18RPF_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/006/ERR2193146/ERR2193146.fastq.gz,1573561416,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/006/ERR2193146/ERR2193146.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/006/ERR2193146/ERR2193146.fastq.gz,b93e33eaf78fd3fb52bf5d5bbee7a673,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID18RPF_s,,,,,,,,,E-MTAB-6196:ID18RPF,,E-MTAB-6196:ID18RPF,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. RNase I (0.5 U/µl) was added to lysates for 30 minutes at room temperature with gentle rotation. Lysates were then layered on sucrose gradients and centrifuged at 38000 rpm, 4deg C for 2 hours in a Sorvall centrifuge with settings acceleration 9 and deceleration 6 with a SW-41 Ti rotor. Samples were fractionated using FoxyR1 Fractionation System and RPF UV traces were compared (plus/minus RNAse I) to determine those fractions (typically 9 to 11) that contained riboso...",,,,,ERS2000942,ERP105150,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/006/ERR2193146,1803068210,ftp.sra.ebi.ac.uk/vol1/err/ERR219/006/ERR2193146,ftp.sra.ebi.ac.uk/vol1/err/ERR219/006/ERR2193146,9fdaf581f04c65383a64bac84bea3b67,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193146/ID18RPF.fastq.gz,1488986518,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193146/ID18RPF.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193146/ID18RPF.fastq.gz,,8e404bc8f441966394e1f0baa18d7bf4,female,,,,,,, PRJEB23398,ERX2249170,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375965,ID18WT,Illumina HiSeq 2500,ERR2193147,45096290,4554725290,SAMEA104375965,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID18WT_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/007/ERR2193147/ERR2193147.fastq.gz,3410807017,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/007/ERR2193147/ERR2193147.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/007/ERR2193147/ERR2193147.fastq.gz,8d20cf1107d1cff3168f63039a44223c,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID18WT_s,,,,,,,,,E-MTAB-6196:ID18WT,,E-MTAB-6196:ID18WT,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. Trizol LS (1.4 ml) was added to the fractions, mixed, and allowed to stand for 5 minutes at room temperature to dissociate the nucleoprotein complexes. Bromochloropropane (BCP) (200 µl) was added and samples were shaken for 15 seconds to mix and allowed to settle for 5 to 10 minutes prior to centrifugation in a refrigerated centrifuge for 15 minutes at 4deg C. The aqueous layer was carefully removed and isopropanol (1 ml) and GlycoBlue (1 µl) were added. Following...",,,,,ERS2000943,ERP105150,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/007/ERR2193147,2640553524,ftp.sra.ebi.ac.uk/vol1/err/ERR219/007/ERR2193147,ftp.sra.ebi.ac.uk/vol1/err/ERR219/007/ERR2193147,d8c0b1f15e2c2493b61ed64c4833002f,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193147/ID18WT.fastq.gz,3263121909,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193147/ID18WT.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193147/ID18WT.fastq.gz,,8530f0e8418cc9b7b1d692193b8d308b,female,,,,,,, PRJEB23398,ERX2249171,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375966,ID22RPF,Illumina HiSeq 2500,ERR2193148,43451260,4388577260,SAMEA104375966,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID22RPF_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/008/ERR2193148/ERR2193148.fastq.gz,2329793550,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/008/ERR2193148/ERR2193148.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/008/ERR2193148/ERR2193148.fastq.gz,2f30064fc1110498fada7e78e06c034b,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID22RPF_s,,,,,,,,,E-MTAB-6196:ID22RPF,,E-MTAB-6196:ID22RPF,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. RNase I (0.5 U/µl) was added to lysates for 30 minutes at room temperature with gentle rotation. Lysates were then layered on sucrose gradients and centrifuged at 38000 rpm, 4deg C for 2 hours in a Sorvall centrifuge with settings acceleration 9 and deceleration 6 with a SW-41 Ti rotor. Samples were fractionated using FoxyR1 Fractionation System and RPF UV traces were compared (plus/minus RNAse I) to determine those fractions (typically 9 to 11) that contained riboso...",,,,,ERS2000944,ERP105150,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/008/ERR2193148,2600015573,ftp.sra.ebi.ac.uk/vol1/err/ERR219/008/ERR2193148,ftp.sra.ebi.ac.uk/vol1/err/ERR219/008/ERR2193148,e335d7936291862112c808fd8e050d06,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193148/ID22RPF.fastq.gz,2200828788,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193148/ID22RPF.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193148/ID22RPF.fastq.gz,,8ad02a697da0c38556bc54385776e7ab,male,,,,,,, PRJEB23398,ERX2249172,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375967,ID22WT,Illumina HiSeq 2500,ERR2193149,46404718,4686876518,SAMEA104375967,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID22WT_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/009/ERR2193149/ERR2193149.fastq.gz,3527929924,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/009/ERR2193149/ERR2193149.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/009/ERR2193149/ERR2193149.fastq.gz,c6acac12bf732e2d9ebdf840ad0cf0ea,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID22WT_s,,,,,,,,,E-MTAB-6196:ID22WT,,E-MTAB-6196:ID22WT,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. Trizol LS (1.4 ml) was added to the fractions, mixed, and allowed to stand for 5 minutes at room temperature to dissociate the nucleoprotein complexes. Bromochloropropane (BCP) (200 µl) was added and samples were shaken for 15 seconds to mix and allowed to settle for 5 to 10 minutes prior to centrifugation in a refrigerated centrifuge for 15 minutes at 4deg C. The aqueous layer was carefully removed and isopropanol (1 ml) and GlycoBlue (1 µl) were added. Following...",,,,,ERS2000945,ERP105150,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/009/ERR2193149,2721704196,ftp.sra.ebi.ac.uk/vol1/err/ERR219/009/ERR2193149,ftp.sra.ebi.ac.uk/vol1/err/ERR219/009/ERR2193149,375c276d971f778730c8d16fca1ec72f,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193149/ID22WT.fastq.gz,3376570447,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193149/ID22WT.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193149/ID22WT.fastq.gz,,72fc072ba90c099fad43b3607bc010c1,male,,,,,,, PRJEB23398,ERX2249173,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375968,ID25RPF,Illumina HiSeq 2500,ERR2193150,52071822,5259254022,SAMEA104375968,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID25RPF_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/000/ERR2193150/ERR2193150.fastq.gz,2600448486,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/000/ERR2193150/ERR2193150.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/000/ERR2193150/ERR2193150.fastq.gz,42100fc47a60aa28e75c181e58cadc43,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID25RPF_s,,,,,,,,,E-MTAB-6196:ID25RPF,,E-MTAB-6196:ID25RPF,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. RNase I (0.5 U/µl) was added to lysates for 30 minutes at room temperature with gentle rotation. Lysates were then layered on sucrose gradients and centrifuged at 38000 rpm, 4deg C for 2 hours in a Sorvall centrifuge with settings acceleration 9 and deceleration 6 with a SW-41 Ti rotor. Samples were fractionated using FoxyR1 Fractionation System and RPF UV traces were compared (plus/minus RNAse I) to determine those fractions (typically 9 to 11) that contained riboso...",,,,,ERS2000946,ERP105150,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/000/ERR2193150,3078601047,ftp.sra.ebi.ac.uk/vol1/err/ERR219/000/ERR2193150,ftp.sra.ebi.ac.uk/vol1/err/ERR219/000/ERR2193150,4f3a1e170f87a613b3f123d64e7f50a8,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193150/ID25RPF.fastq.gz,2447853100,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193150/ID25RPF.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193150/ID25RPF.fastq.gz,,4fc3a227b0b1c11b67df4c48ea364c58,female,,,,,,, PRJEB23398,ERX2249174,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375969,ID25WT,Illumina HiSeq 2500,ERR2193151,33735834,3407319234,SAMEA104375969,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID25WT_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/001/ERR2193151/ERR2193151.fastq.gz,2572225460,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/001/ERR2193151/ERR2193151.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/001/ERR2193151/ERR2193151.fastq.gz,f14f936f9d2a89482e1ecf2af585db51,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID25WT_s,,,,,,,,,E-MTAB-6196:ID25WT,,E-MTAB-6196:ID25WT,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. Trizol LS (1.4 ml) was added to the fractions, mixed, and allowed to stand for 5 minutes at room temperature to dissociate the nucleoprotein complexes. Bromochloropropane (BCP) (200 µl) was added and samples were shaken for 15 seconds to mix and allowed to settle for 5 to 10 minutes prior to centrifugation in a refrigerated centrifuge for 15 minutes at 4deg C. The aqueous layer was carefully removed and isopropanol (1 ml) and GlycoBlue (1 µl) were added. Following...",,,,,ERS2000947,ERP105150,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/001/ERR2193151,1977627436,ftp.sra.ebi.ac.uk/vol1/err/ERR219/001/ERR2193151,ftp.sra.ebi.ac.uk/vol1/err/ERR219/001/ERR2193151,15fba7dff57518c07b7f375ef72d04c0,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193151/ID25WT.fastq.gz,2462336890,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193151/ID25WT.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193151/ID25WT.fastq.gz,,af5da609cf911cd49cfa7b297c5f31b2,female,,,,,,, PRJEB23398,ERX2249175,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375970,ID28RPF,Illumina HiSeq 2500,ERR2193152,47060340,4753094340,SAMEA104375970,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID28RPF_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/002/ERR2193152/ERR2193152.fastq.gz,2527284516,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/002/ERR2193152/ERR2193152.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/002/ERR2193152/ERR2193152.fastq.gz,81606e9543683e996c5fae8cbc6bacd3,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID28RPF_s,,,,,,,,,E-MTAB-6196:ID28RPF,,E-MTAB-6196:ID28RPF,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. RNase I (0.5 U/µl) was added to lysates for 30 minutes at room temperature with gentle rotation. Lysates were then layered on sucrose gradients and centrifuged at 38000 rpm, 4deg C for 2 hours in a Sorvall centrifuge with settings acceleration 9 and deceleration 6 with a SW-41 Ti rotor. Samples were fractionated using FoxyR1 Fractionation System and RPF UV traces were compared (plus/minus RNAse I) to determine those fractions (typically 9 to 11) that contained riboso...",,,,,ERS2000948,ERP105150,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/002/ERR2193152,2895713619,ftp.sra.ebi.ac.uk/vol1/err/ERR219/002/ERR2193152,ftp.sra.ebi.ac.uk/vol1/err/ERR219/002/ERR2193152,9dfec7fbd0a210703d0678ccd62ef87d,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193152/ID28RPF.fastq.gz,2388811054,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193152/ID28RPF.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193152/ID28RPF.fastq.gz,,25dc4d1bdc9849cee2c52fc766e28085,male,,,,,,, PRJEB23398,ERX2249176,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375971,ID28WT,Illumina HiSeq 2500,ERR2193153,34725379,3507263279,SAMEA104375971,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID28WT_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/003/ERR2193153/ERR2193153.fastq.gz,2616433457,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/003/ERR2193153/ERR2193153.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/003/ERR2193153/ERR2193153.fastq.gz,d820271d27ecf099ec3c7ce2d1c9caa4,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID28WT_s,,,,,,,,,E-MTAB-6196:ID28WT,,E-MTAB-6196:ID28WT,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. Trizol LS (1.4 ml) was added to the fractions, mixed, and allowed to stand for 5 minutes at room temperature to dissociate the nucleoprotein complexes. Bromochloropropane (BCP) (200 µl) was added and samples were shaken for 15 seconds to mix and allowed to settle for 5 to 10 minutes prior to centrifugation in a refrigerated centrifuge for 15 minutes at 4deg C. The aqueous layer was carefully removed and isopropanol (1 ml) and GlycoBlue (1 µl) were added. Following...",,,,,ERS2000949,ERP105150,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/003/ERR2193153,2026367968,ftp.sra.ebi.ac.uk/vol1/err/ERR219/003/ERR2193153,ftp.sra.ebi.ac.uk/vol1/err/ERR219/003/ERR2193153,34253a78dd7bfe8371d13e7eac32ad77,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193153/ID28WT.fastq.gz,2503494073,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193153/ID28WT.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193153/ID28WT.fastq.gz,,02df98486e57c33b3f43430d7d51e089,male,,,,,,, PRJEB23398,ERX2249177,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375972,ID29RPF,Illumina HiSeq 2500,ERR2193154,36753828,3712136628,SAMEA104375972,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID29RPF_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/004/ERR2193154/ERR2193154.fastq.gz,1776551378,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/004/ERR2193154/ERR2193154.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/004/ERR2193154/ERR2193154.fastq.gz,9001e61596a39a0fa4a26d72586d0aaf,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID29RPF_s,,,,,,,,,E-MTAB-6196:ID29RPF,,E-MTAB-6196:ID29RPF,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. RNase I (0.5 U/µl) was added to lysates for 30 minutes at room temperature with gentle rotation. Lysates were then layered on sucrose gradients and centrifuged at 38000 rpm, 4deg C for 2 hours in a Sorvall centrifuge with settings acceleration 9 and deceleration 6 with a SW-41 Ti rotor. Samples were fractionated using FoxyR1 Fractionation System and RPF UV traces were compared (plus/minus RNAse I) to determine those fractions (typically 9 to 11) that contained riboso...",,,,,ERS2000950,ERP105150,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/004/ERR2193154,2128088521,ftp.sra.ebi.ac.uk/vol1/err/ERR219/004/ERR2193154,ftp.sra.ebi.ac.uk/vol1/err/ERR219/004/ERR2193154,192e3cee139e1481625b3c3d2eb2b794,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193154/ID29RPF.fastq.gz,1671170019,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193154/ID29RPF.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193154/ID29RPF.fastq.gz,,4de4ae51f5391c8c755efdc673db1328,male,,,,,,, PRJEB23398,ERX2249178,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375973,ID29WT,Illumina HiSeq 2500,ERR2193155,37389224,3776311624,SAMEA104375973,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID29WT_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/005/ERR2193155/ERR2193155.fastq.gz,2817496407,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/005/ERR2193155/ERR2193155.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/005/ERR2193155/ERR2193155.fastq.gz,fe6b2f014b201569b7956732b278bde7,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID29WT_s,,,,,,,,,E-MTAB-6196:ID29WT,,E-MTAB-6196:ID29WT,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. Trizol LS (1.4 ml) was added to the fractions, mixed, and allowed to stand for 5 minutes at room temperature to dissociate the nucleoprotein complexes. Bromochloropropane (BCP) (200 µl) was added and samples were shaken for 15 seconds to mix and allowed to settle for 5 to 10 minutes prior to centrifugation in a refrigerated centrifuge for 15 minutes at 4deg C. The aqueous layer was carefully removed and isopropanol (1 ml) and GlycoBlue (1 µl) were added. Following...",,,,,ERS2000951,ERP105150,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/005/ERR2193155,2181262948,ftp.sra.ebi.ac.uk/vol1/err/ERR219/005/ERR2193155,ftp.sra.ebi.ac.uk/vol1/err/ERR219/005/ERR2193155,1f8add82d6c39cf91ef9d621fd57b1ab,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193155/ID29WT.fastq.gz,2695716796,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193155/ID29WT.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193155/ID29WT.fastq.gz,,3685ab83da03380a7f8ed8900ab19b56,male,,,,,,, PRJEB23398,ERX2249179,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375974,ID30RPF,Illumina HiSeq 2500,ERR2193156,58732724,5932005124,SAMEA104375974,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID30RPF_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/006/ERR2193156/ERR2193156.fastq.gz,3099589720,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/006/ERR2193156/ERR2193156.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/006/ERR2193156/ERR2193156.fastq.gz,6dfb36e0da335ab347c7f6468c104c78,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID30RPF_s,,,,,,,,,E-MTAB-6196:ID30RPF,,E-MTAB-6196:ID30RPF,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. RNase I (0.5 U/µl) was added to lysates for 30 minutes at room temperature with gentle rotation. Lysates were then layered on sucrose gradients and centrifuged at 38000 rpm, 4deg C for 2 hours in a Sorvall centrifuge with settings acceleration 9 and deceleration 6 with a SW-41 Ti rotor. Samples were fractionated using FoxyR1 Fractionation System and RPF UV traces were compared (plus/minus RNAse I) to determine those fractions (typically 9 to 11) that contained riboso...",,,,,ERS2000952,ERP105150,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/006/ERR2193156,3559384666,ftp.sra.ebi.ac.uk/vol1/err/ERR219/006/ERR2193156,ftp.sra.ebi.ac.uk/vol1/err/ERR219/006/ERR2193156,525f81894f2d78167a63992a19e8d0b7,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193156/ID30RPF.fastq.gz,2925285861,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193156/ID30RPF.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193156/ID30RPF.fastq.gz,,5f27217987a6bca8d43d498fc43fb322,male,,,,,,, PRJEB23398,ERX2249180,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375975,ID30WT,Illumina HiSeq 2500,ERR2193157,27507989,2778306889,SAMEA104375975,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID30WT_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/007/ERR2193157/ERR2193157.fastq.gz,2082475331,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/007/ERR2193157/ERR2193157.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/007/ERR2193157/ERR2193157.fastq.gz,2701a003d9d30c1593a3de50a369d074,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID30WT_s,,,,,,,,,E-MTAB-6196:ID30WT,,E-MTAB-6196:ID30WT,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. Trizol LS (1.4 ml) was added to the fractions, mixed, and allowed to stand for 5 minutes at room temperature to dissociate the nucleoprotein complexes. Bromochloropropane (BCP) (200 µl) was added and samples were shaken for 15 seconds to mix and allowed to settle for 5 to 10 minutes prior to centrifugation in a refrigerated centrifuge for 15 minutes at 4deg C. The aqueous layer was carefully removed and isopropanol (1 ml) and GlycoBlue (1 µl) were added. Following...",,,,,ERS2000953,ERP105150,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/007/ERR2193157,1608619337,ftp.sra.ebi.ac.uk/vol1/err/ERR219/007/ERR2193157,ftp.sra.ebi.ac.uk/vol1/err/ERR219/007/ERR2193157,ff38a3c520b181a0872c86fe67fb5436,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193157/ID30WT.fastq.gz,1994160495,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193157/ID30WT.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193157/ID30WT.fastq.gz,,d70b88ec1cb7f739840721d76c2d273a,male,,,,,,, PRJEB23398,ERX2249181,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA104375976,ID31RPF,Illumina HiSeq 2500,ERR2193158,38200240,3858224240,SAMEA104375976,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID31RPF_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/008/ERR2193158/ERR2193158.fastq.gz,1997019291,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/008/ERR2193158/ERR2193158.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/008/ERR2193158/ERR2193158.fastq.gz,6559878dabef5b7e3025ab970761560d,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID31RPF_s,,,,,,,,,E-MTAB-6196:ID31RPF,,E-MTAB-6196:ID31RPF,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. RNase I (0.5 U/µl) was added to lysates for 30 minutes at room temperature with gentle rotation. Lysates were then layered on sucrose gradients and centrifuged at 38000 rpm, 4deg C for 2 hours in a Sorvall centrifuge with settings acceleration 9 and deceleration 6 with a SW-41 Ti rotor. Samples were fractionated using FoxyR1 Fractionation System and RPF UV traces were compared (plus/minus RNAse I) to determine those fractions (typically 9 to 11) that contained riboso...",,,,,ERS2000954,ERP105150,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/008/ERR2193158,2273662566,ftp.sra.ebi.ac.uk/vol1/err/ERR219/008/ERR2193158,ftp.sra.ebi.ac.uk/vol1/err/ERR219/008/ERR2193158,fec58f46177791ab56b2ba3f190bdcad,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193158/ID31RPF.fastq.gz,1884322505,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193158/ID31RPF.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193158/ID31RPF.fastq.gz,,b6e3b9583153f29eb5fb2486b523d3a9,female,,,,,,, PRJEB23398,ERX2249182,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,Illumina HiSeq 2500 sequencing; Ribosome profiling of CLL patient samples,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMEA104375977,ID31WT,Illumina HiSeq 2500,ERR2193159,31139926,3145132526,SAMEA104375977,,,,,,ArrayExpress,,lymphocyte of B lineage,MRC Toxicology Unit,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6196:ID31WT_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR219/009/ERR2193159/ERR2193159.fastq.gz,2354464727,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/009/ERR2193159/ERR2193159.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR219/009/ERR2193159/ERR2193159.fastq.gz,66a78bb17955bfa674db58d4c156057c,2017-11-09,2018-08-07,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,ID31WT_s,,,,,,,,,E-MTAB-6196:ID31WT,,E-MTAB-6196:ID31WT,,"Protocols: Cycloheximide (100 µg/ml) was added to the wells for 5 min at 37deg to stop translation and, working at 4deg C, CLL cells were removed from the plates by pipetting and transferred to 15 ml Falcon tubes on ice prior to centrifugation at 300g, 4deg C for 3 minutes. The pellet was resuspended in 5 ml of ice cold PBS with cycloheximide (100 µg/ml) and centrifuged again at 300g, 4deg C for 3 minutes. Following the addition of 0.5 ml lysis buffer (3M NaCl, 150mM MgCl2, 150mM Tris-HCl (pH7.5), 20mM DTT, cycloheximide (1mg/ml), 1% Triton X-100 and RNasin (12.4µl/ml), lysates were centrifuged at 3000 rpm, 4deg C for 5 minutes before being snap frozen in liquid nitrogen and stored at -80deg C. Fibroblasts expressing CD40L were irradiated (35 Gy for 15 minutes) and placed on a 6-well plate so as to produce an ~80% confluent culture. 1 day following irradiation CLL cells at 3x106 cell/ml were added to this feeder layer with IL-4 (10 ng/ml). CLL cells were cultured for 72 hours before harvesting. Trizol LS (1.4 ml) was added to the fractions, mixed, and allowed to stand for 5 minutes at room temperature to dissociate the nucleoprotein complexes. Bromochloropropane (BCP) (200 µl) was added and samples were shaken for 15 seconds to mix and allowed to settle for 5 to 10 minutes prior to centrifugation in a refrigerated centrifuge for 15 minutes at 4deg C. The aqueous layer was carefully removed and isopropanol (1 ml) and GlycoBlue (1 µl) were added. Following...",,,,,ERS2000955,ERP105150,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR219/009/ERR2193159,1818113941,ftp.sra.ebi.ac.uk/vol1/err/ERR219/009/ERR2193159,ftp.sra.ebi.ac.uk/vol1/err/ERR219/009/ERR2193159,a71b556b0ba4c4426b7deadf538ddff9,,E-MTAB-6196,Ribosome profiling of CLL patient samples,,,ERA1131598,fasp.sra.ebi.ac.uk:/vol1/run/ERR219/ERR2193159/ID31WT.fastq.gz,2253851597,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193159/ID31WT.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR219/ERR2193159/ID31WT.fastq.gz,,1c8345672021b7ae07a4ecfe2eef09fe,female,,,,,,, PRJEB23562,ERX2256431,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104395996,Mock-RiboSeq-CHX-1,Illumina HiSeq 2000,ERR2201443,43087035,1347230056,SAMEA104395996,,,,,,ArrayExpress,Rat2,fibroblast,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6231:Mock-RiboSeq-CHX-1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR220/003/ERR2201443/ERR2201443.fastq.gz,1487540430,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/003/ERR2201443/ERR2201443.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/003/ERR2201443/ERR2201443.fastq.gz,f89b5d8e1d49929a35f30da4cc9c1ef9,2017-11-22,2018-01-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Mock-RiboSeq-CHX-1_s,,,,,,,,,E-MTAB-6231:Mock-RiboSeq-CHX-1,,E-MTAB-6231:Mock-RiboSeq-CHX-1,,"Protocols: In order to produce infectious virions, the full-length MuLV Moloney strain proviral clone pNCA (Colicelli J and Goff SP 1988, a kind gift of S.P. Goff, Columbia University) (GenBank accession number: NC_001501) was transfected to 293T monolayers at 40% confluence. Cells were harvested at 72 h post-transfection and tissue culture supernatant was used to infect in duplicate fresh Rat2 (Rattus norvegicus) monolayers at 10% confluence. At 96 h p.i. cells were treated with cyclohexamide [CHX] (Sigma-Aldrich; to 100 mg/ml; 2 min), or harringtonine HAR (LKT laboratories; 2 mg/ml, 3 min) then CHX (to 100 mg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and then transferred to dry ice and 400 ml of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 mg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. Cells were scraped, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4ºC. Cell lysates were subjected to RiboSeq and RNASeq as described in (Chung 2015). The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia 2009 and Ingolia 2012), except ribosomal RNA contamination removed by treatment with duplex-specific nuclease (DSN) and library amplicons were constructed using a small RNA cloning strategy adapted to",,,,,ERS2013938,ERP105321,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR220/003/ERR2201443,2093153699,ftp.sra.ebi.ac.uk/vol1/err/ERR220/003/ERR2201443,ftp.sra.ebi.ac.uk/vol1/err/ERR220/003/ERR2201443,7b66c7a6e8b1dbd717096d32a499a29e,,E-MTAB-6231,Ribosome profiling of the retrovirus murine leukemia virus,,,ERA1138911,fasp.sra.ebi.ac.uk:/vol1/run/ERR220/ERR2201443/Mock-RiboSeq-CHX-1.fq.gz,1342208811,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201443/Mock-RiboSeq-CHX-1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201443/Mock-RiboSeq-CHX-1.fq.gz,,6768ca10681a69c85d040feca1dfab29,,,,,,,, PRJEB23562,ERX2256432,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104395999,Mock-RNASeq-1,Illumina HiSeq 2000,ERR2201444,34760070,1082072656,SAMEA104395999,,,,,,ArrayExpress,Rat2,fibroblast,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6231:Mock-RNASeq-1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR220/004/ERR2201444/ERR2201444.fastq.gz,1183296606,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/004/ERR2201444/ERR2201444.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/004/ERR2201444/ERR2201444.fastq.gz,0f255eeedf21bad5723c3499474ca8b6,2017-11-22,2018-01-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Mock-RNASeq-1_s,,,,,,,,,E-MTAB-6231:Mock-RNASeq-1,,E-MTAB-6231:Mock-RNASeq-1,,"Protocols: In order to produce infectious virions, the full-length MuLV Moloney strain proviral clone pNCA (Colicelli J and Goff SP 1988, a kind gift of S.P. Goff, Columbia University) (GenBank accession number: NC_001501) was transfected to 293T monolayers at 40% confluence. Cells were harvested at 72 h post-transfection and tissue culture supernatant was used to infect in duplicate fresh Rat2 (Rattus norvegicus) monolayers at 10% confluence. At 96 h p.i. cells were treated with cyclohexamide [CHX] (Sigma-Aldrich; to 100 mg/ml; 2 min), or harringtonine HAR (LKT laboratories; 2 mg/ml, 3 min) then CHX (to 100 mg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and then transferred to dry ice and 400 ml of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 mg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. Cells were scraped, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4ºC. Cell lysates were subjected to RiboSeq and RNASeq as described in (Chung 2015). The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia 2009 and Ingolia 2012), except ribosomal RNA contamination removed by treatment with duplex-specific nuclease (DSN) and library amplicons were constructed using a small RNA cloning strategy adapted to",,,,,ERS2013941,ERP105321,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR220/004/ERR2201444,1665438452,ftp.sra.ebi.ac.uk/vol1/err/ERR220/004/ERR2201444,ftp.sra.ebi.ac.uk/vol1/err/ERR220/004/ERR2201444,8a10fec42620fe779a92febcb81215e1,,E-MTAB-6231,Ribosome profiling of the retrovirus murine leukemia virus,,,ERA1138911,fasp.sra.ebi.ac.uk:/vol1/run/ERR220/ERR2201444/Mock-RNASeq-1.fq.gz,1067468058,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201444/Mock-RNASeq-1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201444/Mock-RNASeq-1.fq.gz,,005a7b53065d351da301a07dfc8b6056,,,,,,,, PRJEB23562,ERX2256433,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396001,Mock-RiboSeq-CHX-2,NextSeq 500,ERR2201445,7925554,229108181,SAMEA104396001,,,,,,ArrayExpress,Rat2,fibroblast,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6231:Mock-RiboSeq-CHX-2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR220/005/ERR2201445/ERR2201445.fastq.gz,158330738,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/005/ERR2201445/ERR2201445.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/005/ERR2201445/ERR2201445.fastq.gz,a8c85d2b0273b3b672a31f144cc38c74,2017-11-22,2018-01-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Mock-RiboSeq-CHX-2_s,,,,,,,,,E-MTAB-6231:Mock-RiboSeq-CHX-2,,E-MTAB-6231:Mock-RiboSeq-CHX-2,,"Protocols: In order to produce infectious virions, the full-length MuLV Moloney strain proviral clone pNCA (Colicelli J and Goff SP 1988, a kind gift of S.P. Goff, Columbia University) (GenBank accession number: NC_001501) was transfected to 293T monolayers at 40% confluence. Cells were harvested at 72 h post-transfection and tissue culture supernatant was used to infect in duplicate fresh Rat2 (Rattus norvegicus) monolayers at 10% confluence. At 96 h p.i. cells were treated with cyclohexamide [CHX] (Sigma-Aldrich; to 100 mg/ml; 2 min), or harringtonine HAR (LKT laboratories; 2 mg/ml, 3 min) then CHX (to 100 mg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and then transferred to dry ice and 400 ml of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 mg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. Cells were scraped, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4ºC. Cell lysates were subjected to RiboSeq and RNASeq as described in (Chung 2015). The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia 2009 and Ingolia 2012), except ribosomal RNA contamination removed by treatment with duplex-specific nuclease (DSN) and library amplicons were constructed using a small RNA cloning strategy adapted to",,,,,ERS2013943,ERP105321,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR220/005/ERR2201445,120612133,ftp.sra.ebi.ac.uk/vol1/err/ERR220/005/ERR2201445,ftp.sra.ebi.ac.uk/vol1/err/ERR220/005/ERR2201445,97acbbb7b55fc8e382d874f51c4fcfa7,,E-MTAB-6231,Ribosome profiling of the retrovirus murine leukemia virus,,,ERA1138911,fasp.sra.ebi.ac.uk:/vol1/run/ERR220/ERR2201445/Mock-RiboSeq-CHX-2.fq.gz,138990959,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201445/Mock-RiboSeq-CHX-2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201445/Mock-RiboSeq-CHX-2.fq.gz,,cc117ae5a4c1e535b96341b8be71ef78,,,,,,,, PRJEB23562,ERX2256434,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396002,Mock-RNASeq-2,NextSeq 500,ERR2201446,17904218,536508323,SAMEA104396002,,,,,,ArrayExpress,Rat2,fibroblast,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6231:Mock-RNASeq-2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR220/006/ERR2201446/ERR2201446.fastq.gz,366079923,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/006/ERR2201446/ERR2201446.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/006/ERR2201446/ERR2201446.fastq.gz,069be68332a9ba6d5eb6773e1d61fcac,2017-11-22,2018-01-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Mock-RNASeq-2_s,,,,,,,,,E-MTAB-6231:Mock-RNASeq-2,,E-MTAB-6231:Mock-RNASeq-2,,"Protocols: In order to produce infectious virions, the full-length MuLV Moloney strain proviral clone pNCA (Colicelli J and Goff SP 1988, a kind gift of S.P. Goff, Columbia University) (GenBank accession number: NC_001501) was transfected to 293T monolayers at 40% confluence. Cells were harvested at 72 h post-transfection and tissue culture supernatant was used to infect in duplicate fresh Rat2 (Rattus norvegicus) monolayers at 10% confluence. At 96 h p.i. cells were treated with cyclohexamide [CHX] (Sigma-Aldrich; to 100 mg/ml; 2 min), or harringtonine HAR (LKT laboratories; 2 mg/ml, 3 min) then CHX (to 100 mg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and then transferred to dry ice and 400 ml of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 mg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. Cells were scraped, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4ºC. Cell lysates were subjected to RiboSeq and RNASeq as described in (Chung 2015). The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia 2009 and Ingolia 2012), except ribosomal RNA contamination removed by treatment with duplex-specific nuclease (DSN) and library amplicons were constructed using a small RNA cloning strategy adapted to",,,,,ERS2013944,ERP105321,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR220/006/ERR2201446,270906636,ftp.sra.ebi.ac.uk/vol1/err/ERR220/006/ERR2201446,ftp.sra.ebi.ac.uk/vol1/err/ERR220/006/ERR2201446,5d2d45f5e1d7fa7540f74abfa8f5bd38,,E-MTAB-6231,Ribosome profiling of the retrovirus murine leukemia virus,,,ERA1138911,fasp.sra.ebi.ac.uk:/vol1/run/ERR220/ERR2201446/Mock-RNASeq-2.fq.gz,320961522,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201446/Mock-RNASeq-2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201446/Mock-RNASeq-2.fq.gz,,a494e5cc7597375dd88815bdd76a4d61,,,,,,,, PRJEB23562,ERX2256435,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396003,RiboSeq-CHX-1,Illumina HiSeq 2000,ERR2201447,62327174,1889305290,SAMEA104396003,,,,,,ArrayExpress,Rat2,fibroblast,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6231:RiboSeq-CHX-1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR220/007/ERR2201447/ERR2201447.fastq.gz,1262052941,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/007/ERR2201447/ERR2201447.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/007/ERR2201447/ERR2201447.fastq.gz,e8c2b19037cc77891ea0732d415adf63,2017-11-22,2018-01-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RiboSeq-CHX-1_s,,,,,,,,,E-MTAB-6231:RiboSeq-CHX-1,,E-MTAB-6231:RiboSeq-CHX-1,,"Protocols: In order to produce infectious virions, the full-length MuLV Moloney strain proviral clone pNCA (Colicelli J and Goff SP 1988, a kind gift of S.P. Goff, Columbia University) (GenBank accession number: NC_001501) was transfected to 293T monolayers at 40% confluence. Cells were harvested at 72 h post-transfection and tissue culture supernatant was used to infect in duplicate fresh Rat2 (Rattus norvegicus) monolayers at 10% confluence. At 96 h p.i. cells were treated with cyclohexamide [CHX] (Sigma-Aldrich; to 100 mg/ml; 2 min), or harringtonine HAR (LKT laboratories; 2 mg/ml, 3 min) then CHX (to 100 mg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and then transferred to dry ice and 400 ml of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 mg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. Cells were scraped, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4ºC. Cell lysates were subjected to RiboSeq and RNASeq as described in (Chung 2015). The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia 2009 and Ingolia 2012), except ribosomal RNA contamination removed by treatment with duplex-specific nuclease (DSN) and library amplicons were constructed using a small RNA cloning strategy adapted to",,,,,ERS2013945,ERP105321,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR220/007/ERR2201447,2081463537,ftp.sra.ebi.ac.uk/vol1/err/ERR220/007/ERR2201447,ftp.sra.ebi.ac.uk/vol1/err/ERR220/007/ERR2201447,e9860953d8ef520055fef75be6159281,,E-MTAB-6231,Ribosome profiling of the retrovirus murine leukemia virus,,,ERA1138911,fasp.sra.ebi.ac.uk:/vol1/run/ERR220/ERR2201447/RiboSeq-CHX-1.fq.gz,1065765178,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201447/RiboSeq-CHX-1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201447/RiboSeq-CHX-1.fq.gz,,e2749972a1244b85e6e43671fe00d1a7,,,,,,,, PRJEB23562,ERX2256436,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396004,RiboSeq-HAR,Illumina HiSeq 2000,ERR2201448,29880691,918985348,SAMEA104396004,,,,,,ArrayExpress,Rat2,fibroblast,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6231:RiboSeq-HAR_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR220/008/ERR2201448/ERR2201448.fastq.gz,628850450,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/008/ERR2201448/ERR2201448.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/008/ERR2201448/ERR2201448.fastq.gz,c3315dd32b4e48931a8dcee839c534e7,2017-11-22,2018-01-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RiboSeq-HAR_s,,,,,,,,,E-MTAB-6231:RiboSeq-HAR,,E-MTAB-6231:RiboSeq-HAR,,"Protocols: In order to produce infectious virions, the full-length MuLV Moloney strain proviral clone pNCA (Colicelli J and Goff SP 1988, a kind gift of S.P. Goff, Columbia University) (GenBank accession number: NC_001501) was transfected to 293T monolayers at 40% confluence. Cells were harvested at 72 h post-transfection and tissue culture supernatant was used to infect in duplicate fresh Rat2 (Rattus norvegicus) monolayers at 10% confluence. At 96 h p.i. cells were treated with cyclohexamide [CHX] (Sigma-Aldrich; to 100 mg/ml; 2 min), or harringtonine HAR (LKT laboratories; 2 mg/ml, 3 min) then CHX (to 100 mg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and then transferred to dry ice and 400 ml of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 mg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. Cells were scraped, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4ºC. Cell lysates were subjected to RiboSeq and RNASeq as described in (Chung 2015). The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia 2009 and Ingolia 2012), except ribosomal RNA contamination removed by treatment with duplex-specific nuclease (DSN) and library amplicons were constructed using a small RNA cloning strategy adapted to",,,,,ERS2013946,ERP105321,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR220/008/ERR2201448,1017895659,ftp.sra.ebi.ac.uk/vol1/err/ERR220/008/ERR2201448,ftp.sra.ebi.ac.uk/vol1/err/ERR220/008/ERR2201448,920f8432aed0b0d23c74b512ee685d37,,E-MTAB-6231,Ribosome profiling of the retrovirus murine leukemia virus,,,ERA1138911,fasp.sra.ebi.ac.uk:/vol1/run/ERR220/ERR2201448/RiboSeq-HAR.fq.gz,537553833,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201448/RiboSeq-HAR.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201448/RiboSeq-HAR.fq.gz,,8c148d22038b4f5d63593c1e4da770c1,,,,,,,, PRJEB23562,ERX2256437,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,Illumina HiSeq 2000 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396005,RNASeq-1,Illumina HiSeq 2000,ERR2201449,99428786,3052553985,SAMEA104396005,,,,,,ArrayExpress,Rat2,fibroblast,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6231:RNASeq-1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR220/009/ERR2201449/ERR2201449.fastq.gz,1878340635,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/009/ERR2201449/ERR2201449.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/009/ERR2201449/ERR2201449.fastq.gz,a09f25a5d3a5e19997bc15fb50ccb689,2017-11-22,2018-01-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RNASeq-1_s,,,,,,,,,E-MTAB-6231:RNASeq-1,,E-MTAB-6231:RNASeq-1,,"Protocols: In order to produce infectious virions, the full-length MuLV Moloney strain proviral clone pNCA (Colicelli J and Goff SP 1988, a kind gift of S.P. Goff, Columbia University) (GenBank accession number: NC_001501) was transfected to 293T monolayers at 40% confluence. Cells were harvested at 72 h post-transfection and tissue culture supernatant was used to infect in duplicate fresh Rat2 (Rattus norvegicus) monolayers at 10% confluence. At 96 h p.i. cells were treated with cyclohexamide [CHX] (Sigma-Aldrich; to 100 mg/ml; 2 min), or harringtonine HAR (LKT laboratories; 2 mg/ml, 3 min) then CHX (to 100 mg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and then transferred to dry ice and 400 ml of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 mg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. Cells were scraped, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4ºC. Cell lysates were subjected to RiboSeq and RNASeq as described in (Chung 2015). The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia 2009 and Ingolia 2012), except ribosomal RNA contamination removed by treatment with duplex-specific nuclease (DSN) and library amplicons were constructed using a small RNA cloning strategy adapted to",,,,,ERS2013947,ERP105321,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR220/009/ERR2201449,3311032252,ftp.sra.ebi.ac.uk/vol1/err/ERR220/009/ERR2201449,ftp.sra.ebi.ac.uk/vol1/err/ERR220/009/ERR2201449,64ec3edfe6585a7d269b291b1551109c,,E-MTAB-6231,Ribosome profiling of the retrovirus murine leukemia virus,,,ERA1138911,fasp.sra.ebi.ac.uk:/vol1/run/ERR220/ERR2201449/RNASeq-1.fq.gz,1550349695,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201449/RNASeq-1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201449/RNASeq-1.fq.gz,,5e36fdad8feef96fa52f48f20f1f3717,,,,,,,, PRJEB23562,ERX2256438,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396006,RiboSeq-CHX-2,NextSeq 500,ERR2201450,11326057,306768073,SAMEA104396006,,,,,,ArrayExpress,Rat2,fibroblast,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6231:RiboSeq-CHX-2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR220/000/ERR2201450/ERR2201450.fastq.gz,232252130,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/000/ERR2201450/ERR2201450.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/000/ERR2201450/ERR2201450.fastq.gz,d69579d55bf5f3911a33e80f27046cd3,2017-11-22,2018-01-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RiboSeq-CHX-2_s,,,,,,,,,E-MTAB-6231:RiboSeq-CHX-2,,E-MTAB-6231:RiboSeq-CHX-2,,"Protocols: In order to produce infectious virions, the full-length MuLV Moloney strain proviral clone pNCA (Colicelli J and Goff SP 1988, a kind gift of S.P. Goff, Columbia University) (GenBank accession number: NC_001501) was transfected to 293T monolayers at 40% confluence. Cells were harvested at 72 h post-transfection and tissue culture supernatant was used to infect in duplicate fresh Rat2 (Rattus norvegicus) monolayers at 10% confluence. At 96 h p.i. cells were treated with cyclohexamide [CHX] (Sigma-Aldrich; to 100 mg/ml; 2 min), or harringtonine HAR (LKT laboratories; 2 mg/ml, 3 min) then CHX (to 100 mg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and then transferred to dry ice and 400 ml of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 mg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. Cells were scraped, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4ºC. Cell lysates were subjected to RiboSeq and RNASeq as described in (Chung 2015). The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia 2009 and Ingolia 2012), except ribosomal RNA contamination removed by treatment with duplex-specific nuclease (DSN) and library amplicons were constructed using a small RNA cloning strategy adapted to",,,,,ERS2013948,ERP105321,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR220/000/ERR2201450,166574209,ftp.sra.ebi.ac.uk/vol1/err/ERR220/000/ERR2201450,ftp.sra.ebi.ac.uk/vol1/err/ERR220/000/ERR2201450,486d66ea1f3cbac2b59b14fc7e0db54a,,E-MTAB-6231,Ribosome profiling of the retrovirus murine leukemia virus,,,ERA1138911,fasp.sra.ebi.ac.uk:/vol1/run/ERR220/ERR2201450/RiboSeq-CHX-2.fq.gz,204138283,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201450/RiboSeq-CHX-2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201450/RiboSeq-CHX-2.fq.gz,,299440c24e68309f5b4a94bdfcafe951,,,,,,,, PRJEB23562,ERX2256439,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,NextSeq 500 sequencing; Ribosome profiling of the retrovirus murine leukemia virus,10116,Rattus norvegicus,OTHER,TRANSCRIPTOMIC,other,SAMEA104396007,RNASeq-2,NextSeq 500,ERR2201451,17348527,519625143,SAMEA104396007,,,,,,ArrayExpress,Rat2,fibroblast,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6231:RNASeq-2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR220/001/ERR2201451/ERR2201451.fastq.gz,348615230,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/001/ERR2201451/ERR2201451.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR220/001/ERR2201451/ERR2201451.fastq.gz,28a78a6637fb61d85af1bb62bc0aab78,2017-11-22,2018-01-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RNASeq-2_s,,,,,,,,,E-MTAB-6231:RNASeq-2,,E-MTAB-6231:RNASeq-2,,"Protocols: In order to produce infectious virions, the full-length MuLV Moloney strain proviral clone pNCA (Colicelli J and Goff SP 1988, a kind gift of S.P. Goff, Columbia University) (GenBank accession number: NC_001501) was transfected to 293T monolayers at 40% confluence. Cells were harvested at 72 h post-transfection and tissue culture supernatant was used to infect in duplicate fresh Rat2 (Rattus norvegicus) monolayers at 10% confluence. At 96 h p.i. cells were treated with cyclohexamide [CHX] (Sigma-Aldrich; to 100 mg/ml; 2 min), or harringtonine HAR (LKT laboratories; 2 mg/ml, 3 min) then CHX (to 100 mg/ml; 2 min). Cells were rinsed with 5 ml of ice-cold PBS, the dishes were submerged in a reservoir of liquid nitrogen for 10 s and then transferred to dry ice and 400 ml of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 mg/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies)] dripped onto the cells. Cells were scraped, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4ºC. Cell lysates were subjected to RiboSeq and RNASeq as described in (Chung 2015). The methodologies employed were based on the original protocols of Ingolia and colleagues (Ingolia 2009 and Ingolia 2012), except ribosomal RNA contamination removed by treatment with duplex-specific nuclease (DSN) and library amplicons were constructed using a small RNA cloning strategy adapted to",,,,,ERS2013949,ERP105321,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR220/001/ERR2201451,262185848,ftp.sra.ebi.ac.uk/vol1/err/ERR220/001/ERR2201451,ftp.sra.ebi.ac.uk/vol1/err/ERR220/001/ERR2201451,62396a19c7a5ea7b8fd0f260baa1861a,,E-MTAB-6231,Ribosome profiling of the retrovirus murine leukemia virus,,,ERA1138911,fasp.sra.ebi.ac.uk:/vol1/run/ERR220/ERR2201451/RNASeq-2.fq.gz,304945440,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201451/RNASeq-2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR220/ERR2201451/RNASeq-2.fq.gz,,92cb0153a063bdf4da26da81556c0f78,,,,,,,, PRJEB26279,ERX2547744,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590062,Sample 10,NextSeq 500,ERR2528907,14307741,1087388316,SAMEA4590062,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 10_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/007/ERR2528907/ERR2528907.fastq.gz,444017467,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/007/ERR2528907/ERR2528907.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/007/ERR2528907/ERR2528907.fastq.gz,c419e9207baa9df9af2fd476bb6e916a,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 10_s,,,,,,,,,E-MTAB-6656:Sample 10,,E-MTAB-6656:Sample 10,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410782,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/007/ERR2528907,449216423,ftp.sra.ebi.ac.uk/vol1/err/ERR252/007/ERR2528907,ftp.sra.ebi.ac.uk/vol1/err/ERR252/007/ERR2528907,20693e2d694875b4172cb28be3953f40,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528907/Sample10.fq.gz,407111835,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528907/Sample10.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528907/Sample10.fq.gz,,91ead2d2fc134ce5fb4e5527559f0bb5,,,,,,,, PRJEB26279,ERX2547745,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590063,Sample 1,NextSeq 500,ERR2528908,32539697,2473016956,SAMEA4590063,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/008/ERR2528908/ERR2528908.fastq.gz,916434933,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/008/ERR2528908/ERR2528908.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/008/ERR2528908/ERR2528908.fastq.gz,03a7e33bfe6097bef42704e0fe8c4202,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 1_s,,,,,,,,,E-MTAB-6656:Sample 1,,E-MTAB-6656:Sample 1,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410783,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/008/ERR2528908,950264915,ftp.sra.ebi.ac.uk/vol1/err/ERR252/008/ERR2528908,ftp.sra.ebi.ac.uk/vol1/err/ERR252/008/ERR2528908,6306f5c16d60d02c94683af865936e20,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528908/Sample1.fq.gz,835523432,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528908/Sample1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528908/Sample1.fq.gz,,c731bd5d853cf1a40311c44d7d038fd6,,,,,,,, PRJEB26279,ERX2547746,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590064,Sample 2,NextSeq 500,ERR2528909,32365237,2459757997,SAMEA4590064,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/009/ERR2528909/ERR2528909.fastq.gz,914663689,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/009/ERR2528909/ERR2528909.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/009/ERR2528909/ERR2528909.fastq.gz,dee4f9de28c1932b034f491a4ae05fd5,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 2_s,,,,,,,,,E-MTAB-6656:Sample 2,,E-MTAB-6656:Sample 2,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410784,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/009/ERR2528909,962946491,ftp.sra.ebi.ac.uk/vol1/err/ERR252/009/ERR2528909,ftp.sra.ebi.ac.uk/vol1/err/ERR252/009/ERR2528909,91540e3027473d51b8eaa8594e674309,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528909/Sample2.fq.gz,834943257,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528909/Sample2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528909/Sample2.fq.gz,,98d10b01225b317532e3040ebc936613,,,,,,,, PRJEB26279,ERX2547747,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590065,Sample 3,NextSeq 500,ERR2528910,27720458,2106754808,SAMEA4590065,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/000/ERR2528910/ERR2528910.fastq.gz,990930953,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/000/ERR2528910/ERR2528910.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/000/ERR2528910/ERR2528910.fastq.gz,4f4928a411abdf7240adf05ddbe59c7a,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 3_s,,,,,,,,,E-MTAB-6656:Sample 3,,E-MTAB-6656:Sample 3,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410785,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/000/ERR2528910,937401010,ftp.sra.ebi.ac.uk/vol1/err/ERR252/000/ERR2528910,ftp.sra.ebi.ac.uk/vol1/err/ERR252/000/ERR2528910,2dc2bfd9bb01e17176a867d20364ab16,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528910/Sample3.fq.gz,918475255,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528910/Sample3.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528910/Sample3.fq.gz,,401c905924e664c8b7b1ae75c48af73b,,,,,,,, PRJEB26279,ERX2547748,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590066,Sample 4,NextSeq 500,ERR2528911,27618945,2099039820,SAMEA4590066,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/001/ERR2528911/ERR2528911.fastq.gz,988561450,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/001/ERR2528911/ERR2528911.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/001/ERR2528911/ERR2528911.fastq.gz,a573090ebe54ddf657332e7b3bc734e2,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 4_s,,,,,,,,,E-MTAB-6656:Sample 4,,E-MTAB-6656:Sample 4,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410786,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/001/ERR2528911,928545753,ftp.sra.ebi.ac.uk/vol1/err/ERR252/001/ERR2528911,ftp.sra.ebi.ac.uk/vol1/err/ERR252/001/ERR2528911,bbddb69e41d452803e50087816f3280c,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528911/Sample4.fq.gz,915972022,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528911/Sample4.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528911/Sample4.fq.gz,,810821af12e35047dca314b41197e420,,,,,,,, PRJEB26279,ERX2547749,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4590067,Sample 5,NextSeq 500,ERR2528912,29429175,2236617172,SAMEA4590067,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 5_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/002/ERR2528912/ERR2528912.fastq.gz,916124892,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/002/ERR2528912/ERR2528912.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/002/ERR2528912/ERR2528912.fastq.gz,7acbbe11e371b91cbeb76fe3532747cb,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 5_s,,,,,,,,,E-MTAB-6656:Sample 5,,E-MTAB-6656:Sample 5,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410787,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/002/ERR2528912,866487587,ftp.sra.ebi.ac.uk/vol1/err/ERR252/002/ERR2528912,ftp.sra.ebi.ac.uk/vol1/err/ERR252/002/ERR2528912,0222cdceac13a1352bdea7b70a745681,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528912/Sample5.fq.gz,843749179,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528912/Sample5.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528912/Sample5.fq.gz,,fed2a839b1d380c2ec9dca54ed64c110,,,,,,,, PRJEB26279,ERX2547750,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4590068,Sample 6,NextSeq 500,ERR2528913,53891222,4095732642,SAMEA4590068,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 6_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/003/ERR2528913/ERR2528913.fastq.gz,1644265971,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/003/ERR2528913/ERR2528913.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/003/ERR2528913/ERR2528913.fastq.gz,0ae3fcd1746bf279554fc773b30324af,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 6_s,,,,,,,,,E-MTAB-6656:Sample 6,,E-MTAB-6656:Sample 6,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410788,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/003/ERR2528913,1578942597,ftp.sra.ebi.ac.uk/vol1/err/ERR252/003/ERR2528913,ftp.sra.ebi.ac.uk/vol1/err/ERR252/003/ERR2528913,6110f2bed0261fa4eefbb5a8141397e1,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528913/Sample6.fq.gz,1508771857,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528913/Sample6.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528913/Sample6.fq.gz,,8e7b647e7b2fbc5977f33e6ee6c4b58e,,,,,,,, PRJEB26279,ERX2547751,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4590069,Sample 7,NextSeq 500,ERR2528914,25078726,1905983073,SAMEA4590069,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 7_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/004/ERR2528914/ERR2528914.fastq.gz,810600718,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/004/ERR2528914/ERR2528914.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/004/ERR2528914/ERR2528914.fastq.gz,815cc5109e118340a2caadc186a9e6c3,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 7_s,,,,,,,,,E-MTAB-6656:Sample 7,,E-MTAB-6656:Sample 7,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410789,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/004/ERR2528914,758579618,ftp.sra.ebi.ac.uk/vol1/err/ERR252/004/ERR2528914,ftp.sra.ebi.ac.uk/vol1/err/ERR252/004/ERR2528914,682d1000a9d1e15f4994057472258300,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528914/Sample7.fq.gz,748344398,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528914/Sample7.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528914/Sample7.fq.gz,,a09d788eeaadead730d854b48abb4957,,,,,,,, PRJEB26279,ERX2547752,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,RNA-Seq,TRANSCRIPTOMIC,RANDOM,SAMEA4590070,Sample 8,NextSeq 500,ERR2528915,33016656,2509265722,SAMEA4590070,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 8_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/005/ERR2528915/ERR2528915.fastq.gz,1077815750,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/005/ERR2528915/ERR2528915.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/005/ERR2528915/ERR2528915.fastq.gz,66f2ad23d98025d98a84e7c880f8916c,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 8_s,,,,,,,,,E-MTAB-6656:Sample 8,,E-MTAB-6656:Sample 8,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410790,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/005/ERR2528915,995571542,ftp.sra.ebi.ac.uk/vol1/err/ERR252/005/ERR2528915,ftp.sra.ebi.ac.uk/vol1/err/ERR252/005/ERR2528915,47ffad2543f34bfe03d1335358487ff8,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528915/Sample8.fq.gz,995006551,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528915/Sample8.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528915/Sample8.fq.gz,,7da408272dd24b22a4ac5cf2679d4c26,,,,,,,, PRJEB26279,ERX2547753,"NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.","NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",9796,Equus caballus,OTHER,TRANSCRIPTOMIC,other,SAMEA4590071,Sample 9,NextSeq 500,ERR2528916,13436449,1021170124,SAMEA4590071,,,,,,ArrayExpress,E. Derm (NBL-6),fibroblast of dermis,University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6656:Sample 9_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR252/006/ERR2528916/ERR2528916.fastq.gz,427773647,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/006/ERR2528916/ERR2528916.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR252/006/ERR2528916/ERR2528916.fastq.gz,6d5e4881545abbbb326bdd84c472b04e,2018-04-17,2018-05-15,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Sample 9_s,,,,,,,,,E-MTAB-6656:Sample 9,,E-MTAB-6656:Sample 9,,"Protocols: Equine dermal fibroblast (ED) cells were maintained in Dulbecco’s modification of Eagle’s medium (DMEM) supplemented with 10% (vol/vol) fetal calf serum (FCS). Equine torovirus (EToV, Berne strain) was passaged as previously described (Smits et al., 2005). ED cells were plated in 15 cm dishes and, upon reaching 80% confluence, were infected with EToV at a multiplicity of infection (MOI) of 1 PFU/cell in serum-free DMEM. After 1 hour at 37 ºC, the inoculum was removed and the cells were incubated in DMEM containing 2% FCS, 100 U/ml penicillin and 100 mg/ml streptomycin at 37 ºC until 10 hours post-infection. Where specified, cells were treated with CHX (Sigma-Aldrich; to 100 µg/ml; 2 min), or HAR (LKT laboratories; 2 µg/ml, 3 min) then CHX (to 100 µg/ml; 2 min), prior to harvest. Cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 s, transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to RiboSeq and RNASeq. The methodologies employed were based on the original protocols of Ingolia and ...",,,,,ERS2410791,ERP108253,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR252/006/ERR2528916,428025826,ftp.sra.ebi.ac.uk/vol1/err/ERR252/006/ERR2528916,ftp.sra.ebi.ac.uk/vol1/err/ERR252/006/ERR2528916,b83e90220f03940b23cc5f39dfe5d96d,,E-MTAB-6656,"Ribosome profiling and RNA sequencing of ED fibroblast cells in response to infection by equine torovirus, Berne strain.",,,ERA1318702,fasp.sra.ebi.ac.uk:/vol1/run/ERR252/ERR2528916/Sample9.fq.gz,393226943,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528916/Sample9.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR252/ERR2528916/Sample9.fq.gz,,3c68e374d90dfb57819f3d416585c4a9,,,,,,,, PRJEB27418,ERX2676640,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4753492,S1_eEF3_normal_rep1,Illumina HiSeq 2500,ERR2660262,143636526,7325462826,SAMEA4753492,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6938:S1_eEF3_normal_rep1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR266/002/ERR2660262/ERR2660262.fastq.gz,5008576668,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/002/ERR2660262/ERR2660262.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/002/ERR2660262/ERR2660262.fastq.gz,7fb5e61b8b148257ec9572de907c445d,2018-06-22,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,S1_eEF3_normal_rep1_s,,,,,,,,,E-MTAB-6938:S1_eEF3_normal_rep1,,E-MTAB-6938:S1_eEF3_normal_rep1,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen and cryogenic milling. Cultured at 30 degrees Celsius in 700 ml of synthetic drop-out SC -met-cys medium supplemented with or without 0.5 mM of methionine. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2573591,ERP109495,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR266/002/ERR2660262,3987351904,ftp.sra.ebi.ac.uk/vol1/err/ERR266/002/ERR2660262,ftp.sra.ebi.ac.uk/vol1/err/ERR266/002/ERR2660262,ba8cc141ec3ce86a071aac9d9ed3e48f,,E-MTAB-6938,Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,,,ERA1523062,fasp.sra.ebi.ac.uk:/vol1/run/ERR266/ERR2660262/new_all_S1.fastq.gz,4583895503,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660262/new_all_S1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660262/new_all_S1.fastq.gz,,f883c4bffa8c249f1c2f8d69e5bc0b81,,,,,,,, PRJEB27418,ERX2676641,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4753493,S3_eEF3_normal_rep2,Illumina HiSeq 2500,ERR2660263,133848724,6826284924,SAMEA4753493,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6938:S3_eEF3_normal_rep2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR266/003/ERR2660263/ERR2660263.fastq.gz,4609066086,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/003/ERR2660263/ERR2660263.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/003/ERR2660263/ERR2660263.fastq.gz,c0aec93a1a105fab85a7fcd4f5b78ecc,2018-06-22,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,S3_eEF3_normal_rep2_s,,,,,,,,,E-MTAB-6938:S3_eEF3_normal_rep2,,E-MTAB-6938:S3_eEF3_normal_rep2,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen and cryogenic milling. Cultured at 30 degrees Celsius in 700 ml of synthetic drop-out SC -met-cys medium supplemented with or without 0.5 mM of methionine. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2573592,ERP109495,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR266/003/ERR2660263,3713112909,ftp.sra.ebi.ac.uk/vol1/err/ERR266/003/ERR2660263,ftp.sra.ebi.ac.uk/vol1/err/ERR266/003/ERR2660263,eb202737ceb1bcf43bd8b257608dd07a,,E-MTAB-6938,Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,,,ERA1523062,fasp.sra.ebi.ac.uk:/vol1/run/ERR266/ERR2660263/new_all_S3.fastq.gz,4208506878,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660263/new_all_S3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660263/new_all_S3.fastq.gz,,61a3dcfc5bf584f490ff87726f5cf2bc,,,,,,,, PRJEB27418,ERX2676642,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4753495,S5_eEF3_normal_rep1,Illumina HiSeq 2500,ERR2660264,87339001,4454289051,SAMEA4753495,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6938:S5_eEF3_normal_rep1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR266/004/ERR2660264/ERR2660264.fastq.gz,3630024840,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/004/ERR2660264/ERR2660264.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/004/ERR2660264/ERR2660264.fastq.gz,2931101c22d52aec3027c6197a4752d7,2018-06-22,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,S5_eEF3_normal_rep1_s,,,,,,,,,E-MTAB-6938:S5_eEF3_normal_rep1,,E-MTAB-6938:S5_eEF3_normal_rep1,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen and cryogenic milling. Cultured at 30 degrees Celsius in 700 ml of synthetic drop-out SC -met-cys medium supplemented with or without 0.5 mM of methionine. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2573594,ERP109495,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR266/004/ERR2660264,2373451645,ftp.sra.ebi.ac.uk/vol1/err/ERR266/004/ERR2660264,ftp.sra.ebi.ac.uk/vol1/err/ERR266/004/ERR2660264,bd952284f04706f19a1f78b2bfa1ffa1,,E-MTAB-6938,Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,,,ERA1523062,fasp.sra.ebi.ac.uk:/vol1/run/ERR266/ERR2660264/new_all_S5.fastq.gz,3363162869,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660264/new_all_S5.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660264/new_all_S5.fastq.gz,,5d426ed4a1d665799e8361c2fb919040,,,,,,,, PRJEB27418,ERX2676643,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4753496,S7_eEF3_normal_rep2,Illumina HiSeq 2500,ERR2660265,81861785,4174951035,SAMEA4753496,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6938:S7_eEF3_normal_rep2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR266/005/ERR2660265/ERR2660265.fastq.gz,3390445107,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/005/ERR2660265/ERR2660265.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/005/ERR2660265/ERR2660265.fastq.gz,285303664b8e23920873215f949fb21e,2018-06-22,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,S7_eEF3_normal_rep2_s,,,,,,,,,E-MTAB-6938:S7_eEF3_normal_rep2,,E-MTAB-6938:S7_eEF3_normal_rep2,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen and cryogenic milling. Cultured at 30 degrees Celsius in 700 ml of synthetic drop-out SC -met-cys medium supplemented with or without 0.5 mM of methionine. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2573595,ERP109495,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR266/005/ERR2660265,2214633655,ftp.sra.ebi.ac.uk/vol1/err/ERR266/005/ERR2660265,ftp.sra.ebi.ac.uk/vol1/err/ERR266/005/ERR2660265,031394711c8e3e44d39d380996a09407,,E-MTAB-6938,Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,,,ERA1523062,fasp.sra.ebi.ac.uk:/vol1/run/ERR266/ERR2660265/new_all_S7.fastq.gz,3253384454,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660265/new_all_S7.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660265/new_all_S7.fastq.gz,,9fe6224e776eebaa0cb64472b1850e2c,,,,,,,, PRJEB27418,ERX2676644,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4753498,S2_eEF3_depleted_rep1,Illumina HiSeq 2500,ERR2660266,140684593,7174914243,SAMEA4753498,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6938:S2_eEF3_depleted_rep1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR266/006/ERR2660266/ERR2660266.fastq.gz,5102748453,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/006/ERR2660266/ERR2660266.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/006/ERR2660266/ERR2660266.fastq.gz,2fa5ac4cdb38901166076a7dae3e5c0a,2018-06-22,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,S2_eEF3_depleted_rep1_s,,,,,,,,,E-MTAB-6938:S2_eEF3_depleted_rep1,,E-MTAB-6938:S2_eEF3_depleted_rep1,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen and cryogenic milling. Cultured at 30 degrees Celsius in 700 ml of synthetic drop-out SC -met-cys medium supplemented with or without 0.5 mM of methionine. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2573597,ERP109495,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR266/006/ERR2660266,3896483815,ftp.sra.ebi.ac.uk/vol1/err/ERR266/006/ERR2660266,ftp.sra.ebi.ac.uk/vol1/err/ERR266/006/ERR2660266,df08c7cff4f9fabd701de012c82e9415,,E-MTAB-6938,Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,,,ERA1523062,fasp.sra.ebi.ac.uk:/vol1/run/ERR266/ERR2660266/new_all_S2.fastq.gz,4682534363,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660266/new_all_S2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660266/new_all_S2.fastq.gz,,7431f15153ffc8af41b3339eed306416,,,,,,,, PRJEB27418,ERX2676645,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4753500,S4_eEF3_depleted_rep2,Illumina HiSeq 2500,ERR2660267,132564691,6760799241,SAMEA4753500,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6938:S4_eEF3_depleted_rep2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR266/007/ERR2660267/ERR2660267.fastq.gz,4714773891,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/007/ERR2660267/ERR2660267.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/007/ERR2660267/ERR2660267.fastq.gz,97a27385c4f857084a7dfe86cc0f341d,2018-06-22,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,S4_eEF3_depleted_rep2_s,,,,,,,,,E-MTAB-6938:S4_eEF3_depleted_rep2,,E-MTAB-6938:S4_eEF3_depleted_rep2,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen and cryogenic milling. Cultured at 30 degrees Celsius in 700 ml of synthetic drop-out SC -met-cys medium supplemented with or without 0.5 mM of methionine. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2573599,ERP109495,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR266/007/ERR2660267,3704745912,ftp.sra.ebi.ac.uk/vol1/err/ERR266/007/ERR2660267,ftp.sra.ebi.ac.uk/vol1/err/ERR266/007/ERR2660267,bc30fe7efd165e15593eeb0e5568eb67,,E-MTAB-6938,Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,,,ERA1523062,fasp.sra.ebi.ac.uk:/vol1/run/ERR266/ERR2660267/new_all_S4.fastq.gz,4316956123,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660267/new_all_S4.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660267/new_all_S4.fastq.gz,,887d5b8b8c686bee8951acce9503738c,,,,,,,, PRJEB27418,ERX2676646,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4753503,S6_eEF3_depleted_rep1,Illumina HiSeq 2500,ERR2660269,78528010,4004928510,SAMEA4753503,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6938:S6_eEF3_depleted_rep1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR266/009/ERR2660269/ERR2660269.fastq.gz,3217716316,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/009/ERR2660269/ERR2660269.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/009/ERR2660269/ERR2660269.fastq.gz,ff4ae569584311f5d5bb63aa8d99d914,2018-06-22,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,S6_eEF3_depleted_rep1_s,,,,,,,,,E-MTAB-6938:S6_eEF3_depleted_rep1,,E-MTAB-6938:S6_eEF3_depleted_rep1,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen and cryogenic milling. Cultured at 30 degrees Celsius in 700 ml of synthetic drop-out SC -met-cys medium supplemented with or without 0.5 mM of methionine. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2573602,ERP109495,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR266/009/ERR2660269,2124455511,ftp.sra.ebi.ac.uk/vol1/err/ERR266/009/ERR2660269,ftp.sra.ebi.ac.uk/vol1/err/ERR266/009/ERR2660269,c67395967094ad09c325df08067dafea,,E-MTAB-6938,Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,,,ERA1523062,fasp.sra.ebi.ac.uk:/vol1/run/ERR266/ERR2660269/new_all_S6.fastq.gz,3087882051,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660269/new_all_S6.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660269/new_all_S6.fastq.gz,,944f6769aad888576199c543789b7441,,,,,,,, PRJEB27418,ERX2676647,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,Illumina HiSeq 2500 sequencing; Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4753504,S8_eEF3_depleted_rep2,Illumina HiSeq 2500,ERR2660271,79828450,4071250950,SAMEA4753504,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6938:S8_eEF3_depleted_rep2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR266/001/ERR2660271/ERR2660271.fastq.gz,3279968501,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/001/ERR2660271/ERR2660271.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR266/001/ERR2660271/ERR2660271.fastq.gz,f201954ecb82b2b9bc68f47c324dcc44,2018-06-22,2018-06-30,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,S8_eEF3_depleted_rep2_s,,,,,,,,,E-MTAB-6938:S8_eEF3_depleted_rep2,,E-MTAB-6938:S8_eEF3_depleted_rep2,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen and cryogenic milling. Cultured at 30 degrees Celsius in 700 ml of synthetic drop-out SC -met-cys medium supplemented with or without 0.5 mM of methionine. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2573603,ERP109495,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR266/001/ERR2660271,2152297917,ftp.sra.ebi.ac.uk/vol1/err/ERR266/001/ERR2660271,ftp.sra.ebi.ac.uk/vol1/err/ERR266/001/ERR2660271,c19e48d69ec829364434a7edef987f55,,E-MTAB-6938,Ribosome profiling of budding yeast Saccharomyces cerevisiae in eEF3 depleted conditions,,,ERA1523062,fasp.sra.ebi.ac.uk:/vol1/run/ERR266/ERR2660271/new_all_S8.fastq.gz,3034473219,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660271/new_all_S8.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR266/ERR2660271/new_all_S8.fastq.gz,,4eac56e9394c8c213accecd24020c1bd,,,,,,,, PRJEB27604,ERX2696677,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776570,new1_KO_riboseq_S2,Illumina HiSeq 2500,ERR2681846,67361162,3435419262,SAMEA4776570,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:new1_KO_riboseq_S2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/006/ERR2681846/ERR2681846.fastq.gz,2558486376,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/006/ERR2681846/ERR2681846.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/006/ERR2681846/ERR2681846.fastq.gz,3fa09a7375d1e27d54f129fb1f72501a,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,new1_KO_riboseq_S2_s,,,,,,,,,E-MTAB-6963:new1_KO_riboseq_S2,,E-MTAB-6963:new1_KO_riboseq_S2,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596519,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/006/ERR2681846,1953473929,ftp.sra.ebi.ac.uk/vol1/err/ERR268/006/ERR2681846,ftp.sra.ebi.ac.uk/vol1/err/ERR268/006/ERR2681846,5162b220c5ea3fb0515b2884fd1e48c1,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681846/new1_S2_pooled_rep3.fastq.gz,2726900690,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681846/new1_S2_pooled_rep3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681846/new1_S2_pooled_rep3.fastq.gz,,d3ffeeaad35047845d09d7f391686dec,,,,,,,, PRJEB27604,ERX2696678,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776571,new1_KO_riboseq_S4,Illumina HiSeq 2500,ERR2681847,80946528,4128272928,SAMEA4776571,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:new1_KO_riboseq_S4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/007/ERR2681847/ERR2681847.fastq.gz,3034391046,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/007/ERR2681847/ERR2681847.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/007/ERR2681847/ERR2681847.fastq.gz,b5cf20abdb8c715973eb828d08cb7045,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,new1_KO_riboseq_S4_s,,,,,,,,,E-MTAB-6963:new1_KO_riboseq_S4,,E-MTAB-6963:new1_KO_riboseq_S4,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596520,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/007/ERR2681847,2337537910,ftp.sra.ebi.ac.uk/vol1/err/ERR268/007/ERR2681847,ftp.sra.ebi.ac.uk/vol1/err/ERR268/007/ERR2681847,c43d9c2e78639b5ceb220b4d3bca5697,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681847/new1_S4_pooled_rep2.fastq.gz,3244176828,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681847/new1_S4_pooled_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681847/new1_S4_pooled_rep2.fastq.gz,,3bd8903d0e25a3e25b380748662dbf0f,,,,,,,, PRJEB27604,ERX2696679,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776572,new1_KO_riboseq_S6,Illumina HiSeq 2500,ERR2681848,69690799,3554230749,SAMEA4776572,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:new1_KO_riboseq_S6_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/008/ERR2681848/ERR2681848.fastq.gz,2655322678,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/008/ERR2681848/ERR2681848.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/008/ERR2681848/ERR2681848.fastq.gz,990cf0eaa18875ddef564b8b13fb795c,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,new1_KO_riboseq_S6_s,,,,,,,,,E-MTAB-6963:new1_KO_riboseq_S6,,E-MTAB-6963:new1_KO_riboseq_S6,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596521,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/008/ERR2681848,2018432977,ftp.sra.ebi.ac.uk/vol1/err/ERR268/008/ERR2681848,ftp.sra.ebi.ac.uk/vol1/err/ERR268/008/ERR2681848,5ea2fb2f47a93351cc7118b16c8c4ec7,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681848/new1_S6_pooled_rep1.fastq.gz,2830291377,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681848/new1_S6_pooled_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681848/new1_S6_pooled_rep1.fastq.gz,,d8578998890b8ae6c5506220f8a86fe4,,,,,,,, PRJEB27604,ERX2696680,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776573,WT_riboseq_S1,Illumina HiSeq 2500,ERR2681849,68722759,3504860709,SAMEA4776573,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:WT_riboseq_S1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/009/ERR2681849/ERR2681849.fastq.gz,2484685042,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/009/ERR2681849/ERR2681849.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/009/ERR2681849/ERR2681849.fastq.gz,0eb0818f9e87e75d26caad3759a76422,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,WT_riboseq_S1_s,,,,,,,,,E-MTAB-6963:WT_riboseq_S1,,E-MTAB-6963:WT_riboseq_S1,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596522,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/009/ERR2681849,1979371599,ftp.sra.ebi.ac.uk/vol1/err/ERR268/009/ERR2681849,ftp.sra.ebi.ac.uk/vol1/err/ERR268/009/ERR2681849,6b39689ae1cca8721dbdbd0de32c99b5,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681849/WT_S1_pooled_rep3.fastq.gz,2608812582,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681849/WT_S1_pooled_rep3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681849/WT_S1_pooled_rep3.fastq.gz,,fd0496024d50ab2d4d5eb69485bf5ce4,,,,,,,, PRJEB27604,ERX2696681,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776574,WT_riboseq_S3,Illumina HiSeq 2500,ERR2681850,85579580,4364558580,SAMEA4776574,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:WT_riboseq_S3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/000/ERR2681850/ERR2681850.fastq.gz,3162706951,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/000/ERR2681850/ERR2681850.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/000/ERR2681850/ERR2681850.fastq.gz,d582109fb6f8a2d40c288d38c4009d09,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,WT_riboseq_S3_s,,,,,,,,,E-MTAB-6963:WT_riboseq_S3,,E-MTAB-6963:WT_riboseq_S3,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596523,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/000/ERR2681850,2479134898,ftp.sra.ebi.ac.uk/vol1/err/ERR268/000/ERR2681850,ftp.sra.ebi.ac.uk/vol1/err/ERR268/000/ERR2681850,dbce1e5d889b22eece9096c2a863e5c2,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681850/WT_S3_pooled_rep2.fastq.gz,3361010119,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681850/WT_S3_pooled_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681850/WT_S3_pooled_rep2.fastq.gz,,261e5d6b114732be751063b7f3af2f5b,,,,,,,, PRJEB27604,ERX2696682,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA4776575,WT_riboseq_S5,Illumina HiSeq 2500,ERR2681851,83078459,4237001409,SAMEA4776575,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:WT_riboseq_S5_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/001/ERR2681851/ERR2681851.fastq.gz,3036098300,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/001/ERR2681851/ERR2681851.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/001/ERR2681851/ERR2681851.fastq.gz,17b9077bdf197eedb342df0c5ba9c770,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,WT_riboseq_S5_s,,,,,,,,,E-MTAB-6963:WT_riboseq_S5,,E-MTAB-6963:WT_riboseq_S5,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596524,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/001/ERR2681851,2392558687,ftp.sra.ebi.ac.uk/vol1/err/ERR268/001/ERR2681851,ftp.sra.ebi.ac.uk/vol1/err/ERR268/001/ERR2681851,996031ac6aff8ac3aebbd7083094da34,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681851/WT_S5_pooled_rep1.fastq.gz,3216091543,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681851/WT_S5_pooled_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681851/WT_S5_pooled_rep1.fastq.gz,,cee721b47ce7cd35a46bb25dd68fdec0,,,,,,,, PRJEB27604,ERX2696683,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776576,new1_KO_RNAseq_S10,Illumina HiSeq 2500,ERR2681852,24694922,1259441022,SAMEA4776576,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:new1_KO_RNAseq_S10_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/002/ERR2681852/ERR2681852.fastq.gz,1033258951,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/002/ERR2681852/ERR2681852.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/002/ERR2681852/ERR2681852.fastq.gz,f75ce03956f3f6d8a4a9ff0656b94ff5,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,new1_KO_RNAseq_S10_s,,,,,,,,,E-MTAB-6963:new1_KO_RNAseq_S10,,E-MTAB-6963:new1_KO_RNAseq_S10,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596525,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/002/ERR2681852,683742840,ftp.sra.ebi.ac.uk/vol1/err/ERR268/002/ERR2681852,ftp.sra.ebi.ac.uk/vol1/err/ERR268/002/ERR2681852,afcdc30caa9ee49d0dd41fdf991711e4,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681852/new1_S10_RNAseq_pooled_rep2.fastq.gz,1060872597,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681852/new1_S10_RNAseq_pooled_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681852/new1_S10_RNAseq_pooled_rep2.fastq.gz,,85d31209ffff2a56b70a3c061d70011a,,,,,,,, PRJEB27604,ERX2696684,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776577,new1_KO_RNAseq_S12,Illumina HiSeq 2500,ERR2681853,27198724,1387134924,SAMEA4776577,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:new1_KO_RNAseq_S12_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/003/ERR2681853/ERR2681853.fastq.gz,1128301390,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/003/ERR2681853/ERR2681853.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/003/ERR2681853/ERR2681853.fastq.gz,afee742ca15b4c6f3504141343c23b4f,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,new1_KO_RNAseq_S12_s,,,,,,,,,E-MTAB-6963:new1_KO_RNAseq_S12,,E-MTAB-6963:new1_KO_RNAseq_S12,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596526,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/003/ERR2681853,751153191,ftp.sra.ebi.ac.uk/vol1/err/ERR268/003/ERR2681853,ftp.sra.ebi.ac.uk/vol1/err/ERR268/003/ERR2681853,9c3671efba0128a0f72160aec17c5a11,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681853/new1_S12_RNAseq_pooled_rep1.fastq.gz,1157286286,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681853/new1_S12_RNAseq_pooled_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681853/new1_S12_RNAseq_pooled_rep1.fastq.gz,,44c7ae553ed700e612093d5d092884e4,,,,,,,, PRJEB27604,ERX2696685,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776578,new1_KO_RNAseq_S8,Illumina HiSeq 2500,ERR2681854,42548074,2169951774,SAMEA4776578,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:new1_KO_RNAseq_S8_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/004/ERR2681854/ERR2681854.fastq.gz,1813112363,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/004/ERR2681854/ERR2681854.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/004/ERR2681854/ERR2681854.fastq.gz,de7540d312a6797fd9f01de26cf46ac6,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,new1_KO_RNAseq_S8_s,,,,,,,,,E-MTAB-6963:new1_KO_RNAseq_S8,,E-MTAB-6963:new1_KO_RNAseq_S8,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596527,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/004/ERR2681854,1195812994,ftp.sra.ebi.ac.uk/vol1/err/ERR268/004/ERR2681854,ftp.sra.ebi.ac.uk/vol1/err/ERR268/004/ERR2681854,22c01e7aebd72ea0f4973c7a522e61e9,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681854/new1_S8_RNAseq_pooled_rep3.fastq.gz,1865874682,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681854/new1_S8_RNAseq_pooled_rep3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681854/new1_S8_RNAseq_pooled_rep3.fastq.gz,,9a8778c2192f61f02b5e63f084714b0e,,,,,,,, PRJEB27604,ERX2696686,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776579,WT_RNAseq_S11,Illumina HiSeq 2500,ERR2681855,22479763,1146467913,SAMEA4776579,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:WT_RNAseq_S11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/005/ERR2681855/ERR2681855.fastq.gz,933992443,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/005/ERR2681855/ERR2681855.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/005/ERR2681855/ERR2681855.fastq.gz,83ce786c432bd4e635303461e0a00e24,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,WT_RNAseq_S11_s,,,,,,,,,E-MTAB-6963:WT_RNAseq_S11,,E-MTAB-6963:WT_RNAseq_S11,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596528,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/005/ERR2681855,622879062,ftp.sra.ebi.ac.uk/vol1/err/ERR268/005/ERR2681855,ftp.sra.ebi.ac.uk/vol1/err/ERR268/005/ERR2681855,1084f5bf407e2d2b81b1581303a53849,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681855/WT_S11_RNAseq_pooled_rep1.fastq.gz,962423438,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681855/WT_S11_RNAseq_pooled_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681855/WT_S11_RNAseq_pooled_rep1.fastq.gz,,de8c65c6622fc600ec9049a07ea7cc59,,,,,,,, PRJEB27604,ERX2696687,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776580,WT_RNAseq_S7,Illumina HiSeq 2500,ERR2681856,25728303,1312143453,SAMEA4776580,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:WT_RNAseq_S7_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/006/ERR2681856/ERR2681856.fastq.gz,1088797156,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/006/ERR2681856/ERR2681856.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/006/ERR2681856/ERR2681856.fastq.gz,15054d89aa85d6562759fd8e1b2b825a,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,WT_RNAseq_S7_s,,,,,,,,,E-MTAB-6963:WT_RNAseq_S7,,E-MTAB-6963:WT_RNAseq_S7,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596529,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/006/ERR2681856,712153234,ftp.sra.ebi.ac.uk/vol1/err/ERR268/006/ERR2681856,ftp.sra.ebi.ac.uk/vol1/err/ERR268/006/ERR2681856,ff9f7e86f9ccf2584b9aaddd9abfb327,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681856/WT_S7_RNAseq_pooled_rep3.fastq.gz,1115503475,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681856/WT_S7_RNAseq_pooled_rep3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681856/WT_S7_RNAseq_pooled_rep3.fastq.gz,,597e2414433df519e770bf95dbe86c7f,,,,,,,, PRJEB27604,ERX2696688,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA4776581,WT_RNAseq_S9,Illumina HiSeq 2500,ERR2681857,24022337,1225139187,SAMEA4776581,,,,,,ArrayExpress,,,Postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-6963:WT_RNAseq_S9_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR268/007/ERR2681857/ERR2681857.fastq.gz,1001738705,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/007/ERR2681857/ERR2681857.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR268/007/ERR2681857/ERR2681857.fastq.gz,704304b6e6320ef9964709015da42a64,2018-07-04,2018-11-10,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,WT_RNAseq_S9_s,,,,,,,,,E-MTAB-6963:WT_RNAseq_S9,,E-MTAB-6963:WT_RNAseq_S9,,"Protocols: Cells were collected by rapid vacuum filtration and subsequent flash-freezing in liquid nitrogen. Frozen cell pellets were lysed using cryogenic milling. Cultured at 20 degrees Celsius in 750 ml of synthetic complete medium up to OD600 of 0.6. TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS2596530,ERP109708,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR268/007/ERR2681857,666400945,ftp.sra.ebi.ac.uk/vol1/err/ERR268/007/ERR2681857,ftp.sra.ebi.ac.uk/vol1/err/ERR268/007/ERR2681857,8e7f86bd54332b6b34fae60b7ba4e3d9,,E-MTAB-6963,Ribosome profiling of NEW1 knock-out of budding yeast Saccharomyces cerevisiae,,,ERA1534224,fasp.sra.ebi.ac.uk:/vol1/run/ERR268/ERR2681857/WT_S9_RNAseq_pooled_rep2.fastq.gz,1030179917,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681857/WT_S9_RNAseq_pooled_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR268/ERR2681857/WT_S9_RNAseq_pooled_rep2.fastq.gz,,47b2b32ec67d463091272ce5d6ae9b21,,,,,,,, PRJEB28810,ERX2819159,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939567,chicken_brain_ribo_1,Illumina HiSeq 2500,ERR2812328,89507736,9040281336,SAMEA4939567,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_brain_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/008/ERR2812328/ERR2812328.fastq.gz,2753287851,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/008/ERR2812328/ERR2812328.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/008/ERR2812328/ERR2812328.fastq.gz,d99405145c5a293b9dc8861ea4d042b4,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_brain_ribo_1_s,,,,,,,,,E-MTAB-7247:chicken_brain_ribo_1,,E-MTAB-7247:chicken_brain_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758350,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/008/ERR2812328,3208902588,ftp.sra.ebi.ac.uk/vol1/err/ERR281/008/ERR2812328,ftp.sra.ebi.ac.uk/vol1/err/ERR281/008/ERR2812328,2b34760db78a0093c6035e821b969ebe,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812328/chicken_brain_ribo_1.fastq.gz,2507104144,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812328/chicken_brain_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812328/chicken_brain_ribo_1.fastq.gz,,7c3f3611b0b6072acc6346ee06362515,male,,,,,,, PRJEB28810,ERX2819160,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939568,chicken_brain_ribo_2,Illumina HiSeq 2500,ERR2812329,,,SAMEA4939568,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_brain_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_brain_ribo_2_s,,,,,,,,,E-MTAB-7247:chicken_brain_ribo_2,,E-MTAB-7247:chicken_brain_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758351,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812329/chicken_brain_ribo_2.fastq.gz,2658456358,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812329/chicken_brain_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812329/chicken_brain_ribo_2.fastq.gz,,18ee7a0f021cf94ac7f4ed394647beae,male,,,,,,, PRJEB28810,ERX2819161,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939569,chicken_brain_ribo_3,Illumina HiSeq 2500,ERR2812330,,,SAMEA4939569,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_brain_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_brain_ribo_3_s,,,,,,,,,E-MTAB-7247:chicken_brain_ribo_3,,E-MTAB-7247:chicken_brain_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758352,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812330/chicken_brain_ribo_3.fastq.gz,3644754614,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812330/chicken_brain_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812330/chicken_brain_ribo_3.fastq.gz,,da20800aa9ecba82388b7a3e1f8de365,male,,,,,,, PRJEB28810,ERX2819162,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939570,chicken_brain_rna_1,Illumina HiSeq 2500,ERR2812331,78156882,3986000982,SAMEA4939570,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_brain_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/001/ERR2812331/ERR2812331.fastq.gz,2652776437,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/001/ERR2812331/ERR2812331.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/001/ERR2812331/ERR2812331.fastq.gz,9af99479261025085ffe761639e62642,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_brain_rna_1_s,,,,,,,,,E-MTAB-7247:chicken_brain_rna_1,,E-MTAB-7247:chicken_brain_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758353,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/001/ERR2812331,1741233075,ftp.sra.ebi.ac.uk/vol1/err/ERR281/001/ERR2812331,ftp.sra.ebi.ac.uk/vol1/err/ERR281/001/ERR2812331,d4c94b96012e37ecdc428ca8d0c2d18b,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812331/chicken_brain_rna_1.fastq.gz,2438877920,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812331/chicken_brain_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812331/chicken_brain_rna_1.fastq.gz,,10c5a98aa07c89b4340a01bbdaa09ce1,male,,,,,,, PRJEB28810,ERX2819163,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939571,chicken_brain_rna_2,Illumina HiSeq 2500,ERR2812332,,,SAMEA4939571,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_brain_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_brain_rna_2_s,,,,,,,,,E-MTAB-7247:chicken_brain_rna_2,,E-MTAB-7247:chicken_brain_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758354,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812332/chicken_brain_rna_2.fastq.gz,2748702300,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812332/chicken_brain_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812332/chicken_brain_rna_2.fastq.gz,,ece46e4fb0c1f26316e1190e0f039896,male,,,,,,, PRJEB28810,ERX2819164,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939572,chicken_brain_rna_3,Illumina HiSeq 2500,ERR2812333,,,SAMEA4939572,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_brain_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_brain_rna_3_s,,,,,,,,,E-MTAB-7247:chicken_brain_rna_3,,E-MTAB-7247:chicken_brain_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758355,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812333/chicken_brain_rna_3.fastq.gz,2390768468,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812333/chicken_brain_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812333/chicken_brain_rna_3.fastq.gz,,41909d0ff65f49c611554067043568d4,male,,,,,,, PRJEB28810,ERX2819165,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939573,chicken_liver_ribo_1,Illumina HiSeq 2500,ERR2812334,50822663,2591955813,SAMEA4939573,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/004/ERR2812334/ERR2812334.fastq.gz,1312823495,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/004/ERR2812334/ERR2812334.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/004/ERR2812334/ERR2812334.fastq.gz,ce07e246dd54fbf09ff55d86ad9f205a,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_ribo_1_s,,,,,,,,,E-MTAB-7247:chicken_liver_ribo_1,,E-MTAB-7247:chicken_liver_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758356,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/004/ERR2812334,1046624318,ftp.sra.ebi.ac.uk/vol1/err/ERR281/004/ERR2812334,ftp.sra.ebi.ac.uk/vol1/err/ERR281/004/ERR2812334,397dc7dcca4656d9674fc0d19ba6079e,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812334/chicken_liver_ribo_1.fastq.gz,1177240004,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812334/chicken_liver_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812334/chicken_liver_ribo_1.fastq.gz,,bf7fdb40ef324efae0ba58c2c4396581,male,,,,,,, PRJEB28810,ERX2819166,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939574,chicken_liver_ribo_2,Illumina HiSeq 2500,ERR2812335,,,SAMEA4939574,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_ribo_2_s,,,,,,,,,E-MTAB-7247:chicken_liver_ribo_2,,E-MTAB-7247:chicken_liver_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758357,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812335/chicken_liver_ribo_2.fastq.gz,1896247202,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812335/chicken_liver_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812335/chicken_liver_ribo_2.fastq.gz,,ddd2c5286a334f5d5dc91aab87dd3c5a,male,,,,,,, PRJEB28810,ERX2819167,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939575,chicken_liver_ribo_3,Illumina HiSeq 2500,ERR2812336,,,SAMEA4939575,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_ribo_3_s,,,,,,,,,E-MTAB-7247:chicken_liver_ribo_3,,E-MTAB-7247:chicken_liver_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758358,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812336/chicken_liver_ribo_3.fastq.gz,5166486900,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812336/chicken_liver_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812336/chicken_liver_ribo_3.fastq.gz,,fed3691fd2c796c0bf48af5895c13371,male,,,,,,, PRJEB28810,ERX2819168,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939576,chicken_liver_rna_1,Illumina HiSeq 2500,ERR2812337,102696548,5237523948,SAMEA4939576,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/007/ERR2812337/ERR2812337.fastq.gz,2958121986,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/007/ERR2812337/ERR2812337.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/007/ERR2812337/ERR2812337.fastq.gz,2447190aacfb941cee320f12ce1a6e43,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_rna_1_s,,,,,,,,,E-MTAB-7247:chicken_liver_rna_1,,E-MTAB-7247:chicken_liver_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758359,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/007/ERR2812337,2201620960,ftp.sra.ebi.ac.uk/vol1/err/ERR281/007/ERR2812337,ftp.sra.ebi.ac.uk/vol1/err/ERR281/007/ERR2812337,cdf080d1b58b4e50c2df76fdfc02b5f3,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812337/chicken_liver_rna_1.fastq.gz,2678000769,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812337/chicken_liver_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812337/chicken_liver_rna_1.fastq.gz,,6aee14e5a4a41dbdf15b90c40a66afe0,male,,,,,,, PRJEB28810,ERX2819169,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939577,chicken_liver_rna_2,Illumina HiSeq 2500,ERR2812338,,,SAMEA4939577,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_rna_2_s,,,,,,,,,E-MTAB-7247:chicken_liver_rna_2,,E-MTAB-7247:chicken_liver_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758360,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812338/chicken_liver_rna_2.fastq.gz,4788127159,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812338/chicken_liver_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812338/chicken_liver_rna_2.fastq.gz,,e5a61276d9336ebf8a826388ff1da8e2,male,,,,,,, PRJEB28810,ERX2819170,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939578,chicken_liver_rna_3,Illumina HiSeq 2500,ERR2812339,,,SAMEA4939578,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_rna_3_s,,,,,,,,,E-MTAB-7247:chicken_liver_rna_3,,E-MTAB-7247:chicken_liver_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758361,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812339/chicken_liver_rna_3.fastq.gz,5661008289,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812339/chicken_liver_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812339/chicken_liver_rna_3.fastq.gz,,b11fb5c6ddcdd86e98ec5cd6df542303,male,,,,,,, PRJEB28810,ERX2819171,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939579,chicken_testis_ribo_1,Illumina HiSeq 2500,ERR2812340,176588839,9006030789,SAMEA4939579,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_testis_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/000/ERR2812340/ERR2812340.fastq.gz,4778699566,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/000/ERR2812340/ERR2812340.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/000/ERR2812340/ERR2812340.fastq.gz,eeda42d3c6b84f08ee63f02681351689,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_testis_ribo_1_s,,,,,,,,,E-MTAB-7247:chicken_testis_ribo_1,,E-MTAB-7247:chicken_testis_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758362,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/000/ERR2812340,3866865953,ftp.sra.ebi.ac.uk/vol1/err/ERR281/000/ERR2812340,ftp.sra.ebi.ac.uk/vol1/err/ERR281/000/ERR2812340,1ffdf77ed979d88a6d171adfe42784e9,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812340/chicken_testis_ribo_1.fastq.gz,4330023930,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812340/chicken_testis_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812340/chicken_testis_ribo_1.fastq.gz,,ce27f54856f3da8b07d80f06e8749ca9,male,,,,,,, PRJEB28810,ERX2819172,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939580,chicken_testis_ribo_2,Illumina HiSeq 2500,ERR2812341,,,SAMEA4939580,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_testis_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_testis_ribo_2_s,,,,,,,,,E-MTAB-7247:chicken_testis_ribo_2,,E-MTAB-7247:chicken_testis_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758363,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812341/chicken_testis_ribo_2.fastq.gz,2675433665,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812341/chicken_testis_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812341/chicken_testis_ribo_2.fastq.gz,,ebe921efe57639961063143d7f7bfad4,male,,,,,,, PRJEB28810,ERX2819173,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939581,chicken_testis_ribo_3,Illumina HiSeq 2500,ERR2812342,,,SAMEA4939581,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_testis_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_testis_ribo_3_s,,,,,,,,,E-MTAB-7247:chicken_testis_ribo_3,,E-MTAB-7247:chicken_testis_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758364,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812342/chicken_testis_ribo_3.fastq.gz,4283027459,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812342/chicken_testis_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812342/chicken_testis_ribo_3.fastq.gz,,ca83889829f2d3747c8b57a5337bf9cd,male,,,,,,, PRJEB28810,ERX2819174,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939582,chicken_testis_rna_1,Illumina HiSeq 2500,ERR2812343,69052194,3521661894,SAMEA4939582,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_testis_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/003/ERR2812343/ERR2812343.fastq.gz,2274304876,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/003/ERR2812343/ERR2812343.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/003/ERR2812343/ERR2812343.fastq.gz,d873545c97d1b3a5c8a4a58060102959,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_testis_rna_1_s,,,,,,,,,E-MTAB-7247:chicken_testis_rna_1,,E-MTAB-7247:chicken_testis_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758365,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/003/ERR2812343,1473342757,ftp.sra.ebi.ac.uk/vol1/err/ERR281/003/ERR2812343,ftp.sra.ebi.ac.uk/vol1/err/ERR281/003/ERR2812343,a011cc24a662ceabc1e902c410d9158f,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812343/chicken_testis_rna_1.fastq.gz,2085284218,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812343/chicken_testis_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812343/chicken_testis_rna_1.fastq.gz,,a4a48fea8031cdb278402ee587a6e03d,male,,,,,,, PRJEB28810,ERX2819175,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939583,chicken_testis_rna_2,Illumina HiSeq 2500,ERR2812344,,,SAMEA4939583,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_testis_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_testis_rna_2_s,,,,,,,,,E-MTAB-7247:chicken_testis_rna_2,,E-MTAB-7247:chicken_testis_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758366,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812344/chicken_testis_rna_2.fastq.gz,2397183306,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812344/chicken_testis_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812344/chicken_testis_rna_2.fastq.gz,,ac0ff7868293955592f39fc0bf728333,male,,,,,,, PRJEB28810,ERX2819176,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939584,chicken_testis_rna_3,Illumina HiSeq 2500,ERR2812345,,,SAMEA4939584,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_testis_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_testis_rna_3_s,,,,,,,,,E-MTAB-7247:chicken_testis_rna_3,,E-MTAB-7247:chicken_testis_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758367,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812345/chicken_testis_rna_3.fastq.gz,3304972131,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812345/chicken_testis_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812345/chicken_testis_rna_3.fastq.gz,,cac0a9de52b09dae17b40ce3f5ea7bcf,male,,,,,,, PRJEB28810,ERX2819177,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939585,human_brain_ribo_1,Illumina HiSeq 2500,ERR2812346,,,SAMEA4939585,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_brain_ribo_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_brain_ribo_1_s,,,,,,,,,E-MTAB-7247:human_brain_ribo_1,,E-MTAB-7247:human_brain_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758368,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812346/human_brain_ribo_1.fastq.gz,3178570176,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812346/human_brain_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812346/human_brain_ribo_1.fastq.gz,,c09d7a3e32afc5148df5f9cfcb437b7e,male,,,,,,, PRJEB28810,ERX2819178,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939586,human_brain_ribo_2,Illumina HiSeq 2500,ERR2812347,,,SAMEA4939586,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_brain_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_brain_ribo_2_s,,,,,,,,,E-MTAB-7247:human_brain_ribo_2,,E-MTAB-7247:human_brain_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758369,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812347/human_brain_ribo_2.fastq.gz,3570312065,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812347/human_brain_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812347/human_brain_ribo_2.fastq.gz,,17bca2a5f61b881069d68a9cee9e42c2,male,,,,,,, PRJEB28810,ERX2819179,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939587,human_brain_ribo_3,Illumina HiSeq 2500,ERR2812348,,,SAMEA4939587,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_brain_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_brain_ribo_3_s,,,,,,,,,E-MTAB-7247:human_brain_ribo_3,,E-MTAB-7247:human_brain_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758370,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812348/human_brain_ribo_3.fastq.gz,2884466964,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812348/human_brain_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812348/human_brain_ribo_3.fastq.gz,,eaaac9d14663b57b3470a3fa0ab3f8be,male,,,,,,, PRJEB28810,ERX2819180,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939588,human_brain_rna_1,Illumina HiSeq 2500,ERR2812349,,,SAMEA4939588,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_brain_rna_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_brain_rna_1_s,,,,,,,,,E-MTAB-7247:human_brain_rna_1,,E-MTAB-7247:human_brain_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758371,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812349/human_brain_rna_1.fastq.gz,4721884572,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812349/human_brain_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812349/human_brain_rna_1.fastq.gz,,8d599b2223fc1095bd750c810bd95576,male,,,,,,, PRJEB28810,ERX2819181,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939589,human_brain_rna_2,Illumina HiSeq 2500,ERR2812350,,,SAMEA4939589,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_brain_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_brain_rna_2_s,,,,,,,,,E-MTAB-7247:human_brain_rna_2,,E-MTAB-7247:human_brain_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758372,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812350/human_brain_rna_2.fastq.gz,6561145490,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812350/human_brain_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812350/human_brain_rna_2.fastq.gz,,4f4fd329cdbfbf70612be93369865674,male,,,,,,, PRJEB28810,ERX2819182,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939590,human_brain_rna_3,Illumina HiSeq 2500,ERR2812351,,,SAMEA4939590,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_brain_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_brain_rna_3_s,,,,,,,,,E-MTAB-7247:human_brain_rna_3,,E-MTAB-7247:human_brain_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758373,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812351/human_brain_rna_3.fastq.gz,6741967887,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812351/human_brain_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812351/human_brain_rna_3.fastq.gz,,4bcbea53a6d3911f9ba22d7d505241ca,male,,,,,,, PRJEB28810,ERX2819183,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939591,human_liver_ribo_1,Illumina HiSeq 2500,ERR2812352,,,SAMEA4939591,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_liver_ribo_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_liver_ribo_1_s,,,,,,,,,E-MTAB-7247:human_liver_ribo_1,,E-MTAB-7247:human_liver_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758374,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812352/human_liver_ribo_1.fastq.gz,1868149033,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812352/human_liver_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812352/human_liver_ribo_1.fastq.gz,,2e8522bb5952ff42279ad028d4e2dc41,male,,,,,,, PRJEB28810,ERX2819184,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939592,human_liver_ribo_2,Illumina HiSeq 2500,ERR2812353,,,SAMEA4939592,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_liver_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_liver_ribo_2_s,,,,,,,,,E-MTAB-7247:human_liver_ribo_2,,E-MTAB-7247:human_liver_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758375,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812353/human_liver_ribo_2.fastq.gz,3264470178,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812353/human_liver_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812353/human_liver_ribo_2.fastq.gz,,fc90d8777eebbed01a41c7ea7f982302,male,,,,,,, PRJEB28810,ERX2819185,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939593,human_liver_ribo_3,Illumina HiSeq 2500,ERR2812354,,,SAMEA4939593,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_liver_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_liver_ribo_3_s,,,,,,,,,E-MTAB-7247:human_liver_ribo_3,,E-MTAB-7247:human_liver_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758376,ERP111066,,,,female,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812354/human_liver_ribo_3.fastq.gz,5276013267,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812354/human_liver_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812354/human_liver_ribo_3.fastq.gz,,ceb77d5ff75ea57ba00cea639dce920c,female,,,,,,, PRJEB28810,ERX2819186,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939594,human_liver_rna_1,Illumina HiSeq 2500,ERR2812355,,,SAMEA4939594,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_liver_rna_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_liver_rna_1_s,,,,,,,,,E-MTAB-7247:human_liver_rna_1,,E-MTAB-7247:human_liver_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758377,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812355/human_liver_rna_1.fastq.gz,7369874634,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812355/human_liver_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812355/human_liver_rna_1.fastq.gz,,aaaa91705bf59abba98d59bff4780403,male,,,,,,, PRJEB28810,ERX2819187,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939595,human_liver_rna_2,Illumina HiSeq 2500,ERR2812356,,,SAMEA4939595,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_liver_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_liver_rna_2_s,,,,,,,,,E-MTAB-7247:human_liver_rna_2,,E-MTAB-7247:human_liver_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758378,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812356/human_liver_rna_2.fastq.gz,6853412150,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812356/human_liver_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812356/human_liver_rna_2.fastq.gz,,8fcdcc6b40a0e34d8d947a53ce4e9499,male,,,,,,, PRJEB28810,ERX2819188,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939596,human_liver_rna_3,Illumina HiSeq 2500,ERR2812357,,,SAMEA4939596,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_liver_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_liver_rna_3_s,,,,,,,,,E-MTAB-7247:human_liver_rna_3,,E-MTAB-7247:human_liver_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758379,ERP111066,,,,female,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812357/human_liver_rna_3.fastq.gz,5259012589,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812357/human_liver_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812357/human_liver_rna_3.fastq.gz,,9ab36f8211b18b238f45b523325035c2,female,,,,,,, PRJEB28810,ERX2819189,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939597,human_testis_ribo_1,Illumina HiSeq 2500,ERR2812358,,,SAMEA4939597,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_testis_ribo_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_testis_ribo_1_s,,,,,,,,,E-MTAB-7247:human_testis_ribo_1,,E-MTAB-7247:human_testis_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758380,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812358/human_testis_ribo_1.fastq.gz,4667214891,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812358/human_testis_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812358/human_testis_ribo_1.fastq.gz,,b087df97b018689a2110898cfd1b7d33,male,,,,,,, PRJEB28810,ERX2819190,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939598,human_testis_ribo_2,Illumina HiSeq 2500,ERR2812359,,,SAMEA4939598,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_testis_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_testis_ribo_2_s,,,,,,,,,E-MTAB-7247:human_testis_ribo_2,,E-MTAB-7247:human_testis_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758381,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812359/human_testis_ribo_2.fastq.gz,3347099828,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812359/human_testis_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812359/human_testis_ribo_2.fastq.gz,,32ca5adcbb4640a4daab2130c6087785,male,,,,,,, PRJEB28810,ERX2819191,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939599,human_testis_ribo_3,Illumina HiSeq 2500,ERR2812360,,,SAMEA4939599,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_testis_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_testis_ribo_3_s,,,,,,,,,E-MTAB-7247:human_testis_ribo_3,,E-MTAB-7247:human_testis_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758382,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812360/human_testis_ribo_3.fastq.gz,5917939009,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812360/human_testis_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812360/human_testis_ribo_3.fastq.gz,,589e94f25f6f844e4a41e99c36f42684,male,,,,,,, PRJEB28810,ERX2819192,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939600,human_testis_rna_1,Illumina HiSeq 2500,ERR2812361,,,SAMEA4939600,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_testis_rna_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_testis_rna_1_s,,,,,,,,,E-MTAB-7247:human_testis_rna_1,,E-MTAB-7247:human_testis_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758383,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812361/human_testis_rna_1.fastq.gz,2247251094,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812361/human_testis_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812361/human_testis_rna_1.fastq.gz,,1ab7f2e9de9d3abba340c7ed43ab6b50,male,,,,,,, PRJEB28810,ERX2819193,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939601,human_testis_rna_2,Illumina HiSeq 2500,ERR2812362,,,SAMEA4939601,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_testis_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_testis_rna_2_s,,,,,,,,,E-MTAB-7247:human_testis_rna_2,,E-MTAB-7247:human_testis_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758384,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812362/human_testis_rna_2.fastq.gz,8308614348,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812362/human_testis_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812362/human_testis_rna_2.fastq.gz,,afbcc7d1264a969e9fe19aae93d005c5,male,,,,,,, PRJEB28810,ERX2819194,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9606,Homo sapiens,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939602,human_testis_rna_3,Illumina HiSeq 2500,ERR2812363,,,SAMEA4939602,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:human_testis_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,human_testis_rna_3_s,,,,,,,,,E-MTAB-7247:human_testis_rna_3,,E-MTAB-7247:human_testis_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758385,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812363/human_testis_rna_3.fastq.gz,6436821091,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812363/human_testis_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812363/human_testis_rna_3.fastq.gz,,39186c63fdcef5f6d680369d55f0da65,male,,,,,,, PRJEB28810,ERX2819195,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939603,macaque_brain_ribo_1,Illumina HiSeq 2500,ERR2812364,,,SAMEA4939603,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_brain_ribo_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_brain_ribo_1_s,,,,,,,,,E-MTAB-7247:macaque_brain_ribo_1,,E-MTAB-7247:macaque_brain_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758386,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812364/macaque_brain_ribo_1.fastq.gz,2011776255,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812364/macaque_brain_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812364/macaque_brain_ribo_1.fastq.gz,,a5d4cd58192a9f2d63778f09a430c3fd,male,,,,,,, PRJEB28810,ERX2819196,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939604,macaque_brain_ribo_2,Illumina HiSeq 2500,ERR2812365,,,SAMEA4939604,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_brain_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_brain_ribo_2_s,,,,,,,,,E-MTAB-7247:macaque_brain_ribo_2,,E-MTAB-7247:macaque_brain_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758387,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812365/macaque_brain_ribo_2.fastq.gz,1811989107,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812365/macaque_brain_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812365/macaque_brain_ribo_2.fastq.gz,,40061c21dae7ec6b454b9fb70de595e6,male,,,,,,, PRJEB28810,ERX2819197,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939605,macaque_brain_ribo_3,Illumina HiSeq 2500,ERR2812366,,,SAMEA4939605,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_brain_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_brain_ribo_3_s,,,,,,,,,E-MTAB-7247:macaque_brain_ribo_3,,E-MTAB-7247:macaque_brain_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758388,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812366/macaque_brain_ribo_3.fastq.gz,1457293319,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812366/macaque_brain_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812366/macaque_brain_ribo_3.fastq.gz,,09cfcf5ce35d1a7a599a201f2ef87b9e,male,,,,,,, PRJEB28810,ERX2819198,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939606,macaque_brain_rna_1,Illumina HiSeq 2500,ERR2812367,,,SAMEA4939606,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_brain_rna_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_brain_rna_1_s,,,,,,,,,E-MTAB-7247:macaque_brain_rna_1,,E-MTAB-7247:macaque_brain_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758389,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812367/macaque_brain_rna_1.fastq.gz,4177020682,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812367/macaque_brain_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812367/macaque_brain_rna_1.fastq.gz,,78b971c44621208b5ffe3a9ba8187960,male,,,,,,, PRJEB28810,ERX2819199,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939607,macaque_brain_rna_2,Illumina HiSeq 2500,ERR2812368,,,SAMEA4939607,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_brain_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_brain_rna_2_s,,,,,,,,,E-MTAB-7247:macaque_brain_rna_2,,E-MTAB-7247:macaque_brain_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758390,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812368/macaque_brain_rna_2.fastq.gz,3480059130,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812368/macaque_brain_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812368/macaque_brain_rna_2.fastq.gz,,c58679acb470ddebeaca55b27266c0c9,male,,,,,,, PRJEB28810,ERX2819200,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939608,macaque_brain_rna_3,Illumina HiSeq 2500,ERR2812369,,,SAMEA4939608,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_brain_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_brain_rna_3_s,,,,,,,,,E-MTAB-7247:macaque_brain_rna_3,,E-MTAB-7247:macaque_brain_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758391,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812369/macaque_brain_rna_3.fastq.gz,5377995284,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812369/macaque_brain_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812369/macaque_brain_rna_3.fastq.gz,,6c1c0432d7a4407b1fad3fc450f1cace,male,,,,,,, PRJEB28810,ERX2819201,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939609,macaque_liver_ribo_1,Illumina HiSeq 2500,ERR2812370,,,SAMEA4939609,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_liver_ribo_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_liver_ribo_1_s,,,,,,,,,E-MTAB-7247:macaque_liver_ribo_1,,E-MTAB-7247:macaque_liver_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758392,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812370/macaque_liver_ribo_1.fastq.gz,1516435228,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812370/macaque_liver_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812370/macaque_liver_ribo_1.fastq.gz,,0c202649daa808f1fa5121d33eb82586,male,,,,,,, PRJEB28810,ERX2819202,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939610,macaque_liver_ribo_2,Illumina HiSeq 2500,ERR2812371,,,SAMEA4939610,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_liver_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_liver_ribo_2_s,,,,,,,,,E-MTAB-7247:macaque_liver_ribo_2,,E-MTAB-7247:macaque_liver_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758393,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812371/macaque_liver_ribo_2.fastq.gz,4387128178,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812371/macaque_liver_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812371/macaque_liver_ribo_2.fastq.gz,,dc13d21ab0d2da8bb6421183ea940cc8,male,,,,,,, PRJEB28810,ERX2819203,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939611,macaque_liver_ribo_3,Illumina HiSeq 2500,ERR2812372,,,SAMEA4939611,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_liver_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_liver_ribo_3_s,,,,,,,,,E-MTAB-7247:macaque_liver_ribo_3,,E-MTAB-7247:macaque_liver_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758394,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812372/macaque_liver_ribo_3.fastq.gz,1781413198,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812372/macaque_liver_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812372/macaque_liver_ribo_3.fastq.gz,,7e3f4bc0d47d5ec49db234fd1497ff78,male,,,,,,, PRJEB28810,ERX2819204,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939612,macaque_liver_rna_1,Illumina HiSeq 2500,ERR2812373,,,SAMEA4939612,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_liver_rna_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_liver_rna_1_s,,,,,,,,,E-MTAB-7247:macaque_liver_rna_1,,E-MTAB-7247:macaque_liver_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758395,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812373/macaque_liver_rna_1.fastq.gz,3222326391,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812373/macaque_liver_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812373/macaque_liver_rna_1.fastq.gz,,49f5c704344ca8284a05a933f12e8955,male,,,,,,, PRJEB28810,ERX2819205,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939613,macaque_liver_rna_2,Illumina HiSeq 2500,ERR2812374,,,SAMEA4939613,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_liver_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_liver_rna_2_s,,,,,,,,,E-MTAB-7247:macaque_liver_rna_2,,E-MTAB-7247:macaque_liver_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758396,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812374/macaque_liver_rna_2.fastq.gz,4425994878,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812374/macaque_liver_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812374/macaque_liver_rna_2.fastq.gz,,c4f65cf62f5b9728fa7f68f78f9ae8bc,male,,,,,,, PRJEB28810,ERX2819206,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939614,macaque_liver_rna_3,Illumina HiSeq 2500,ERR2812375,,,SAMEA4939614,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_liver_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_liver_rna_3_s,,,,,,,,,E-MTAB-7247:macaque_liver_rna_3,,E-MTAB-7247:macaque_liver_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758397,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812375/macaque_liver_rna_3.fastq.gz,5410031650,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812375/macaque_liver_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812375/macaque_liver_rna_3.fastq.gz,,c42f6231de35259ebe5e4186440d60e2,male,,,,,,, PRJEB28810,ERX2819207,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939615,macaque_testis_ribo_1,Illumina HiSeq 2500,ERR2812376,,,SAMEA4939615,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_testis_ribo_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_testis_ribo_1_s,,,,,,,,,E-MTAB-7247:macaque_testis_ribo_1,,E-MTAB-7247:macaque_testis_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758398,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812376/macaque_testis_ribo_1.fastq.gz,3581301244,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812376/macaque_testis_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812376/macaque_testis_ribo_1.fastq.gz,,803e8058e13b4099b977fe8a93622b1c,male,,,,,,, PRJEB28810,ERX2819208,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939616,macaque_testis_ribo_2,Illumina HiSeq 2500,ERR2812377,,,SAMEA4939616,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_testis_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_testis_ribo_2_s,,,,,,,,,E-MTAB-7247:macaque_testis_ribo_2,,E-MTAB-7247:macaque_testis_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758399,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812377/macaque_testis_ribo_2.fastq.gz,1894421321,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812377/macaque_testis_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812377/macaque_testis_ribo_2.fastq.gz,,a60d6a26765570160840e000e5e0d9d8,male,,,,,,, PRJEB28810,ERX2819209,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939617,macaque_testis_ribo_3,Illumina HiSeq 2500,ERR2812378,,,SAMEA4939617,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_testis_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_testis_ribo_3_s,,,,,,,,,E-MTAB-7247:macaque_testis_ribo_3,,E-MTAB-7247:macaque_testis_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758400,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812378/macaque_testis_ribo_3.fastq.gz,3972316269,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812378/macaque_testis_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812378/macaque_testis_ribo_3.fastq.gz,,f74594f0722d4cb387f98f5760e54dee,male,,,,,,, PRJEB28810,ERX2819210,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939618,macaque_testis_rna_1,Illumina HiSeq 2500,ERR2812379,,,SAMEA4939618,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_testis_rna_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_testis_rna_1_s,,,,,,,,,E-MTAB-7247:macaque_testis_rna_1,,E-MTAB-7247:macaque_testis_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758401,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812379/macaque_testis_rna_1.fastq.gz,1691666019,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812379/macaque_testis_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812379/macaque_testis_rna_1.fastq.gz,,f22c403a21df510348e7b6b0a07a69bd,male,,,,,,, PRJEB28810,ERX2819211,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939619,macaque_testis_rna_2,Illumina HiSeq 2500,ERR2812380,,,SAMEA4939619,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_testis_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_testis_rna_2_s,,,,,,,,,E-MTAB-7247:macaque_testis_rna_2,,E-MTAB-7247:macaque_testis_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758402,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812380/macaque_testis_rna_2.fastq.gz,2350440132,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812380/macaque_testis_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812380/macaque_testis_rna_2.fastq.gz,,194e8209b559d614a81e9c37d7f0b94a,male,,,,,,, PRJEB28810,ERX2819212,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9544,Macaca mulatta,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939620,macaque_testis_rna_3,Illumina HiSeq 2500,ERR2812381,,,SAMEA4939620,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:macaque_testis_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,macaque_testis_rna_3_s,,,,,,,,,E-MTAB-7247:macaque_testis_rna_3,,E-MTAB-7247:macaque_testis_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758403,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812381/macaque_testis_rna_3.fastq.gz,1670149927,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812381/macaque_testis_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812381/macaque_testis_rna_3.fastq.gz,,3951de9e0a7c3736837243b496c5b266,male,,,,,,, PRJEB28810,ERX2819213,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939621,mouse_brain_ribo_1,Illumina HiSeq 2500,ERR2812382,125913653,12717278953,SAMEA4939621,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_brain_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/002/ERR2812382/ERR2812382.fastq.gz,4268499466,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/002/ERR2812382/ERR2812382.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/002/ERR2812382/ERR2812382.fastq.gz,9e240fddeb85c06efd560a31377516a5,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_brain_ribo_1_s,,,,,,,,,E-MTAB-7247:mouse_brain_ribo_1,,E-MTAB-7247:mouse_brain_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758404,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/002/ERR2812382,4776213072,ftp.sra.ebi.ac.uk/vol1/err/ERR281/002/ERR2812382,ftp.sra.ebi.ac.uk/vol1/err/ERR281/002/ERR2812382,7a75f5b6eccdf2f3971b018bbfe49720,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812382/mouse_brain_ribo_1.fastq.gz,3932289156,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812382/mouse_brain_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812382/mouse_brain_ribo_1.fastq.gz,,11f1ccbf68fc9d2fd7f6c803c183523a,male,,,,,,, PRJEB28810,ERX2819214,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939622,mouse_brain_ribo_2,Illumina HiSeq 2500,ERR2812383,,,SAMEA4939622,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_brain_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_brain_ribo_2_s,,,,,,,,,E-MTAB-7247:mouse_brain_ribo_2,,E-MTAB-7247:mouse_brain_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758405,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812383/mouse_brain_ribo_2.fastq.gz,1929836249,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812383/mouse_brain_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812383/mouse_brain_ribo_2.fastq.gz,,cda902fbd2e67b3fd842b29e5df92b25,male,,,,,,, PRJEB28810,ERX2819215,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939623,mouse_brain_ribo_3,Illumina HiSeq 2500,ERR2812384,,,SAMEA4939623,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_brain_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_brain_ribo_3_s,,,,,,,,,E-MTAB-7247:mouse_brain_ribo_3,,E-MTAB-7247:mouse_brain_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758406,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812384/mouse_brain_ribo_3.fastq.gz,1738227815,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812384/mouse_brain_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812384/mouse_brain_ribo_3.fastq.gz,,804be0646d6860c16fab0caba514c022,male,,,,,,, PRJEB28810,ERX2819216,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939624,mouse_brain_rna_1,Illumina HiSeq 2500,ERR2812385,59718135,6031531635,SAMEA4939624,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_brain_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/005/ERR2812385/ERR2812385.fastq.gz,2537307332,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/005/ERR2812385/ERR2812385.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/005/ERR2812385/ERR2812385.fastq.gz,a3635055bba0b6597f0722da04fb456e,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_brain_rna_1_s,,,,,,,,,E-MTAB-7247:mouse_brain_rna_1,,E-MTAB-7247:mouse_brain_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758407,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/005/ERR2812385,2294551525,ftp.sra.ebi.ac.uk/vol1/err/ERR281/005/ERR2812385,ftp.sra.ebi.ac.uk/vol1/err/ERR281/005/ERR2812385,fc5f2831b1b2c7fbf93519776d007dfb,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812385/mouse_brain_rna_1.fastq.gz,2372355020,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812385/mouse_brain_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812385/mouse_brain_rna_1.fastq.gz,,7b192069c448ea91f06e8b316045522d,male,,,,,,, PRJEB28810,ERX2819217,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939625,mouse_brain_rna_2,Illumina HiSeq 2500,ERR2812386,,,SAMEA4939625,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_brain_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_brain_rna_2_s,,,,,,,,,E-MTAB-7247:mouse_brain_rna_2,,E-MTAB-7247:mouse_brain_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758408,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812386/mouse_brain_rna_2.fastq.gz,3436704554,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812386/mouse_brain_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812386/mouse_brain_rna_2.fastq.gz,,178001a65a52da3d2ee4e1818fb7ffbe,male,,,,,,, PRJEB28810,ERX2819218,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939626,mouse_brain_rna_3,Illumina HiSeq 2500,ERR2812387,,,SAMEA4939626,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_brain_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_brain_rna_3_s,,,,,,,,,E-MTAB-7247:mouse_brain_rna_3,,E-MTAB-7247:mouse_brain_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758409,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812387/mouse_brain_rna_3.fastq.gz,3045904505,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812387/mouse_brain_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812387/mouse_brain_rna_3.fastq.gz,,6091d3140113ff401a628c5548213b2e,male,,,,,,, PRJEB28810,ERX2819219,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939627,mouse_liver_ribo_1,Illumina HiSeq 2500,ERR2812388,133782505,11314315655,SAMEA4939627,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/008/ERR2812388/ERR2812388.fastq.gz,4120884605,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/008/ERR2812388/ERR2812388.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/008/ERR2812388/ERR2812388.fastq.gz,d7ee0c710835eab39953d000e29d660b,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_ribo_1_s,,,,,,,,,E-MTAB-7247:mouse_liver_ribo_1,,E-MTAB-7247:mouse_liver_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758410,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/008/ERR2812388,4354094998,ftp.sra.ebi.ac.uk/vol1/err/ERR281/008/ERR2812388,ftp.sra.ebi.ac.uk/vol1/err/ERR281/008/ERR2812388,499e1a64e500dfd99ef2f9863527dc91,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812388/mouse_liver_ribo_1.fastq.gz,3764801571,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812388/mouse_liver_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812388/mouse_liver_ribo_1.fastq.gz,,c02a71475beeab62650f5214a4a9f3d2,male,,,,,,, PRJEB28810,ERX2819220,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939628,mouse_liver_ribo_2,Illumina HiSeq 2500,ERR2812389,,,SAMEA4939628,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_ribo_2_s,,,,,,,,,E-MTAB-7247:mouse_liver_ribo_2,,E-MTAB-7247:mouse_liver_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758411,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812389/mouse_liver_ribo_2.fastq.gz,2646508598,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812389/mouse_liver_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812389/mouse_liver_ribo_2.fastq.gz,,70fe0d8eedc01568380d083b8ecadfb7,male,,,,,,, PRJEB28810,ERX2819221,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939629,mouse_liver_ribo_3,Illumina HiSeq 2500,ERR2812390,,,SAMEA4939629,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_ribo_3_s,,,,,,,,,E-MTAB-7247:mouse_liver_ribo_3,,E-MTAB-7247:mouse_liver_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758412,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812390/mouse_liver_ribo_3.fastq.gz,3017231964,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812390/mouse_liver_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812390/mouse_liver_ribo_3.fastq.gz,,b718970af6a16f2c634d8b6df20ff1f1,male,,,,,,, PRJEB28810,ERX2819222,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939630,mouse_liver_rna_1,Illumina HiSeq 2500,ERR2812391,56370619,5693432519,SAMEA4939630,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/001/ERR2812391/ERR2812391.fastq.gz,2314301040,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/001/ERR2812391/ERR2812391.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/001/ERR2812391/ERR2812391.fastq.gz,60a4e476d8e3756ad1bf53a29aeb9c08,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_rna_1_s,,,,,,,,,E-MTAB-7247:mouse_liver_rna_1,,E-MTAB-7247:mouse_liver_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758413,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/001/ERR2812391,2157106833,ftp.sra.ebi.ac.uk/vol1/err/ERR281/001/ERR2812391,ftp.sra.ebi.ac.uk/vol1/err/ERR281/001/ERR2812391,efcf614cc5c1ac841f7d0e044e1b1589,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812391/mouse_liver_rna_1.fastq.gz,2159081932,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812391/mouse_liver_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812391/mouse_liver_rna_1.fastq.gz,,851d71fe8d50897502b9b9a75a84d5ab,male,,,,,,, PRJEB28810,ERX2819223,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939631,mouse_liver_rna_2,Illumina HiSeq 2500,ERR2812392,,,SAMEA4939631,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_rna_2_s,,,,,,,,,E-MTAB-7247:mouse_liver_rna_2,,E-MTAB-7247:mouse_liver_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758414,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812392/mouse_liver_rna_2.fastq.gz,2492914471,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812392/mouse_liver_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812392/mouse_liver_rna_2.fastq.gz,,ecfed1efcbc5def4db57e905780f4a7d,male,,,,,,, PRJEB28810,ERX2819224,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939632,mouse_liver_rna_3,Illumina HiSeq 2500,ERR2812393,,,SAMEA4939632,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_rna_3_s,,,,,,,,,E-MTAB-7247:mouse_liver_rna_3,,E-MTAB-7247:mouse_liver_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758415,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812393/mouse_liver_rna_3.fastq.gz,2581622774,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812393/mouse_liver_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812393/mouse_liver_rna_3.fastq.gz,,3cf85c88f8c84610bdce678b1bf82201,male,,,,,,, PRJEB28810,ERX2819225,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939633,mouse_testis_ribo_1,Illumina HiSeq 2500,ERR2812394,117238132,11841051332,SAMEA4939633,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_testis_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/004/ERR2812394/ERR2812394.fastq.gz,3934454790,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/004/ERR2812394/ERR2812394.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/004/ERR2812394/ERR2812394.fastq.gz,3abaf65242d24af1cc73a4f60ff7fba9,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_testis_ribo_1_s,,,,,,,,,E-MTAB-7247:mouse_testis_ribo_1,,E-MTAB-7247:mouse_testis_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758416,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/004/ERR2812394,4458164480,ftp.sra.ebi.ac.uk/vol1/err/ERR281/004/ERR2812394,ftp.sra.ebi.ac.uk/vol1/err/ERR281/004/ERR2812394,971a9cedf9d7b3e4c5ead513045adf64,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812394/mouse_testis_ribo_1.fastq.gz,3621847125,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812394/mouse_testis_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812394/mouse_testis_ribo_1.fastq.gz,,8d6272792d6fa01da90dd6ecaa9877e4,male,,,,,,, PRJEB28810,ERX2819226,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939634,mouse_testis_ribo_2,Illumina HiSeq 2500,ERR2812395,,,SAMEA4939634,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_testis_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_testis_ribo_2_s,,,,,,,,,E-MTAB-7247:mouse_testis_ribo_2,,E-MTAB-7247:mouse_testis_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758417,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812395/mouse_testis_ribo_2.fastq.gz,1823811698,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812395/mouse_testis_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812395/mouse_testis_ribo_2.fastq.gz,,3555cbf77803ddb642e6bafcfa468ad6,male,,,,,,, PRJEB28810,ERX2819227,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939635,mouse_testis_ribo_3,Illumina HiSeq 2500,ERR2812396,,,SAMEA4939635,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_testis_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_testis_ribo_3_s,,,,,,,,,E-MTAB-7247:mouse_testis_ribo_3,,E-MTAB-7247:mouse_testis_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758418,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812396/mouse_testis_ribo_3.fastq.gz,4002716289,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812396/mouse_testis_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812396/mouse_testis_ribo_3.fastq.gz,,a43e80d952b2aa84896071855cd2b474,male,,,,,,, PRJEB28810,ERX2819228,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939636,mouse_testis_rna_1,Illumina HiSeq 2500,ERR2812397,60491740,6109665740,SAMEA4939636,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_testis_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/007/ERR2812397/ERR2812397.fastq.gz,2508147468,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/007/ERR2812397/ERR2812397.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/007/ERR2812397/ERR2812397.fastq.gz,58a98516c7afd91b7269b6097006de15,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_testis_rna_1_s,,,,,,,,,E-MTAB-7247:mouse_testis_rna_1,,E-MTAB-7247:mouse_testis_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758419,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/007/ERR2812397,2302541278,ftp.sra.ebi.ac.uk/vol1/err/ERR281/007/ERR2812397,ftp.sra.ebi.ac.uk/vol1/err/ERR281/007/ERR2812397,9898b6263af2ba2dab31972ea8753fc4,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812397/mouse_testis_rna_1.fastq.gz,2341383844,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812397/mouse_testis_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812397/mouse_testis_rna_1.fastq.gz,,1624f74c4d055ae6b1a820e540686484,male,,,,,,, PRJEB28810,ERX2819229,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939637,mouse_testis_rna_2,Illumina HiSeq 2500,ERR2812398,,,SAMEA4939637,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_testis_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_testis_rna_2_s,,,,,,,,,E-MTAB-7247:mouse_testis_rna_2,,E-MTAB-7247:mouse_testis_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758420,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812398/mouse_testis_rna_2.fastq.gz,1359523458,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812398/mouse_testis_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812398/mouse_testis_rna_2.fastq.gz,,ee7ebe08dcc7532cd8f18ced4cf238ef,male,,,,,,, PRJEB28810,ERX2819230,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939638,mouse_testis_rna_3,Illumina HiSeq 2500,ERR2812399,,,SAMEA4939638,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_testis_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_testis_rna_3_s,,,,,,,,,E-MTAB-7247:mouse_testis_rna_3,,E-MTAB-7247:mouse_testis_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758421,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812399/mouse_testis_rna_3.fastq.gz,3049792017,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812399/mouse_testis_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812399/mouse_testis_rna_3.fastq.gz,,5fd6f1fd982566cd56c1ad731375b8fc,male,,,,,,, PRJEB28810,ERX2819231,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939639,opossum_brain_ribo_1,Illumina HiSeq 2500,ERR2812400,99962696,5098097496,SAMEA4939639,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_brain_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/000/ERR2812400/ERR2812400.fastq.gz,2896842733,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/000/ERR2812400/ERR2812400.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/000/ERR2812400/ERR2812400.fastq.gz,48578d41b2530e38ea2f5f3a22f8366f,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_brain_ribo_1_s,,,,,,,,,E-MTAB-7247:opossum_brain_ribo_1,,E-MTAB-7247:opossum_brain_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758422,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/000/ERR2812400,2203212513,ftp.sra.ebi.ac.uk/vol1/err/ERR281/000/ERR2812400,ftp.sra.ebi.ac.uk/vol1/err/ERR281/000/ERR2812400,c3f186a687b96b2db76a7958cc157112,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812400/opossum_brain_ribo_1.fastq.gz,2631349148,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812400/opossum_brain_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812400/opossum_brain_ribo_1.fastq.gz,,6d40acca565af608d5a6ba306195c40e,male,,,,,,, PRJEB28810,ERX2819232,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939640,opossum_brain_ribo_2,Illumina HiSeq 2500,ERR2812401,,,SAMEA4939640,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_brain_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_brain_ribo_2_s,,,,,,,,,E-MTAB-7247:opossum_brain_ribo_2,,E-MTAB-7247:opossum_brain_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758423,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812401/opossum_brain_ribo_2.fastq.gz,2731686040,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812401/opossum_brain_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812401/opossum_brain_ribo_2.fastq.gz,,2eb9a510377ae631471d1aebfdbab052,male,,,,,,, PRJEB28810,ERX2819233,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939641,opossum_brain_ribo_3,Illumina HiSeq 2500,ERR2812402,,,SAMEA4939641,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_brain_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_brain_ribo_3_s,,,,,,,,,E-MTAB-7247:opossum_brain_ribo_3,,E-MTAB-7247:opossum_brain_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758424,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812402/opossum_brain_ribo_3.fastq.gz,3788315711,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812402/opossum_brain_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812402/opossum_brain_ribo_3.fastq.gz,,30b7314cbf4f9d95e7ecc23d529e46dc,male,,,,,,, PRJEB28810,ERX2819234,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939642,opossum_brain_rna_1,Illumina HiSeq 2500,ERR2812403,118076072,6021879672,SAMEA4939642,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_brain_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/003/ERR2812403/ERR2812403.fastq.gz,3471005137,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/003/ERR2812403/ERR2812403.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/003/ERR2812403/ERR2812403.fastq.gz,804e5f1397c5e24f38ae381fdf24d2e3,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_brain_rna_1_s,,,,,,,,,E-MTAB-7247:opossum_brain_rna_1,,E-MTAB-7247:opossum_brain_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758425,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/003/ERR2812403,2422753655,ftp.sra.ebi.ac.uk/vol1/err/ERR281/003/ERR2812403,ftp.sra.ebi.ac.uk/vol1/err/ERR281/003/ERR2812403,ed206096074d2b3bb327ee8156ee23ce,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812403/opossum_brain_rna_1.fastq.gz,3138592370,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812403/opossum_brain_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812403/opossum_brain_rna_1.fastq.gz,,e4321e423ba393c26a80b9a8f8d12d0e,male,,,,,,, PRJEB28810,ERX2819235,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939643,opossum_brain_rna_2,Illumina HiSeq 2500,ERR2812404,,,SAMEA4939643,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_brain_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_brain_rna_2_s,,,,,,,,,E-MTAB-7247:opossum_brain_rna_2,,E-MTAB-7247:opossum_brain_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758426,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812404/opossum_brain_rna_2.fastq.gz,3687429534,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812404/opossum_brain_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812404/opossum_brain_rna_2.fastq.gz,,16e8a19d005c415a2f6cd67c03f3ecac,male,,,,,,, PRJEB28810,ERX2819236,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939644,opossum_brain_rna_3,Illumina HiSeq 2500,ERR2812405,,,SAMEA4939644,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_brain_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_brain_rna_3_s,,,,,,,,,E-MTAB-7247:opossum_brain_rna_3,,E-MTAB-7247:opossum_brain_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758427,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812405/opossum_brain_rna_3.fastq.gz,5107390104,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812405/opossum_brain_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812405/opossum_brain_rna_3.fastq.gz,,963701c17a521825fe9347eb5c5bcf23,male,,,,,,, PRJEB28810,ERX2819237,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939645,opossum_liver_ribo_1,Illumina HiSeq 2500,ERR2812406,102073266,7960719316,SAMEA4939645,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_liver_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/006/ERR2812406/ERR2812406.fastq.gz,2409138542,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/006/ERR2812406/ERR2812406.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/006/ERR2812406/ERR2812406.fastq.gz,186341bf0cfa9c0fff7ec852f60cf9f3,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_liver_ribo_1_s,,,,,,,,,E-MTAB-7247:opossum_liver_ribo_1,,E-MTAB-7247:opossum_liver_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758428,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/006/ERR2812406,2629742309,ftp.sra.ebi.ac.uk/vol1/err/ERR281/006/ERR2812406,ftp.sra.ebi.ac.uk/vol1/err/ERR281/006/ERR2812406,fb6f256241c26c6e3de9665e8c2bbfb5,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812406/opossum_liver_ribo_1.fastq.gz,2521127391,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812406/opossum_liver_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812406/opossum_liver_ribo_1.fastq.gz,,1f8314fa5f1ed82fd7a9fcf83ddaf42a,male,,,,,,, PRJEB28810,ERX2819238,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939646,opossum_liver_ribo_2,Illumina HiSeq 2500,ERR2812407,,,SAMEA4939646,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_liver_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_liver_ribo_2_s,,,,,,,,,E-MTAB-7247:opossum_liver_ribo_2,,E-MTAB-7247:opossum_liver_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758429,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812407/opossum_liver_ribo_2.fastq.gz,1817893341,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812407/opossum_liver_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812407/opossum_liver_ribo_2.fastq.gz,,30c8d4e1c24a105885d9cc565423fe22,male,,,,,,, PRJEB28810,ERX2819239,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939647,opossum_liver_ribo_3,Illumina HiSeq 2500,ERR2812408,,,SAMEA4939647,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_liver_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_liver_ribo_3_s,,,,,,,,,E-MTAB-7247:opossum_liver_ribo_3,,E-MTAB-7247:opossum_liver_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758430,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812408/opossum_liver_ribo_3.fastq.gz,4032706404,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812408/opossum_liver_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812408/opossum_liver_ribo_3.fastq.gz,,d555d160e28bc6f278f034d4924ce02f,male,,,,,,, PRJEB28810,ERX2819240,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939648,opossum_liver_rna_1,Illumina HiSeq 2500,ERR2812409,122985784,8335560284,SAMEA4939648,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_liver_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/009/ERR2812409/ERR2812409.fastq.gz,3224986661,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/009/ERR2812409/ERR2812409.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/009/ERR2812409/ERR2812409.fastq.gz,231a6bf888cf1a3259c5b76934834d54,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_liver_rna_1_s,,,,,,,,,E-MTAB-7247:opossum_liver_rna_1,,E-MTAB-7247:opossum_liver_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758431,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/009/ERR2812409,2914104854,ftp.sra.ebi.ac.uk/vol1/err/ERR281/009/ERR2812409,ftp.sra.ebi.ac.uk/vol1/err/ERR281/009/ERR2812409,d13bf6c5490fca2a5508c4a2272d9932,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812409/opossum_liver_rna_1.fastq.gz,3370500884,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812409/opossum_liver_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812409/opossum_liver_rna_1.fastq.gz,,553be9c95bf79161370afab163150b86,male,,,,,,, PRJEB28810,ERX2819241,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939649,opossum_liver_rna_2,Illumina HiSeq 2500,ERR2812410,,,SAMEA4939649,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_liver_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_liver_rna_2_s,,,,,,,,,E-MTAB-7247:opossum_liver_rna_2,,E-MTAB-7247:opossum_liver_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758432,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812410/opossum_liver_rna_2.fastq.gz,1740757015,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812410/opossum_liver_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812410/opossum_liver_rna_2.fastq.gz,,8409e903ea2ab751c72c297fc2663b66,male,,,,,,, PRJEB28810,ERX2819242,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939650,opossum_liver_rna_3,Illumina HiSeq 2500,ERR2812411,,,SAMEA4939650,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_liver_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_liver_rna_3_s,,,,,,,,,E-MTAB-7247:opossum_liver_rna_3,,E-MTAB-7247:opossum_liver_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758433,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812411/opossum_liver_rna_3.fastq.gz,6260439467,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812411/opossum_liver_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812411/opossum_liver_rna_3.fastq.gz,,8d2cbed3ef07888f329d87ead01bfeea,male,,,,,,, PRJEB28810,ERX2819243,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939651,opossum_testis_ribo_1,Illumina HiSeq 2500,ERR2812412,372136872,18978980472,SAMEA4939651,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_testis_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/002/ERR2812412/ERR2812412.fastq.gz,10564812460,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/002/ERR2812412/ERR2812412.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/002/ERR2812412/ERR2812412.fastq.gz,c82be7b3a481ba2a5373d7b2e7868f3d,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_testis_ribo_1_s,,,,,,,,,E-MTAB-7247:opossum_testis_ribo_1,,E-MTAB-7247:opossum_testis_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758434,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/002/ERR2812412,8292995944,ftp.sra.ebi.ac.uk/vol1/err/ERR281/002/ERR2812412,ftp.sra.ebi.ac.uk/vol1/err/ERR281/002/ERR2812412,8298a84216290825ac6800a8e4f59593,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812412/opossum_testis_ribo_1.fastq.gz,9657387852,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812412/opossum_testis_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812412/opossum_testis_ribo_1.fastq.gz,,4d901ca345965b1c31ddf08c7a9df9f9,male,,,,,,, PRJEB28810,ERX2819244,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939652,opossum_testis_ribo_2,Illumina HiSeq 2500,ERR2812413,,,SAMEA4939652,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_testis_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_testis_ribo_2_s,,,,,,,,,E-MTAB-7247:opossum_testis_ribo_2,,E-MTAB-7247:opossum_testis_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758435,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812413/opossum_testis_ribo_2.fastq.gz,1920046837,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812413/opossum_testis_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812413/opossum_testis_ribo_2.fastq.gz,,72ce66e0e82526eaaa007d564792816e,male,,,,,,, PRJEB28810,ERX2819245,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939653,opossum_testis_ribo_3,Illumina HiSeq 2500,ERR2812414,,,SAMEA4939653,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_testis_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_testis_ribo_3_s,,,,,,,,,E-MTAB-7247:opossum_testis_ribo_3,,E-MTAB-7247:opossum_testis_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758436,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812414/opossum_testis_ribo_3.fastq.gz,3552332473,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812414/opossum_testis_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812414/opossum_testis_ribo_3.fastq.gz,,c2ac91a452c4d7852ddc16c5a160522e,male,,,,,,, PRJEB28810,ERX2819246,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939654,opossum_testis_rna_1,Illumina HiSeq 2500,ERR2812415,91675215,4675435965,SAMEA4939654,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_testis_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/005/ERR2812415/ERR2812415.fastq.gz,2713060853,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/005/ERR2812415/ERR2812415.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/005/ERR2812415/ERR2812415.fastq.gz,7cc81ec9e450a3d8b5e83d271470dac1,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_testis_rna_1_s,,,,,,,,,E-MTAB-7247:opossum_testis_rna_1,,E-MTAB-7247:opossum_testis_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758437,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/005/ERR2812415,1847112796,ftp.sra.ebi.ac.uk/vol1/err/ERR281/005/ERR2812415,ftp.sra.ebi.ac.uk/vol1/err/ERR281/005/ERR2812415,c46c16c0b59feb5d6782eab3e30b0297,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812415/opossum_testis_rna_1.fastq.gz,2809115043,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812415/opossum_testis_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812415/opossum_testis_rna_1.fastq.gz,,16703df2c9bf90adb852477d25c58327,male,,,,,,, PRJEB28810,ERX2819247,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939655,opossum_testis_rna_2,Illumina HiSeq 2500,ERR2812416,,,SAMEA4939655,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_testis_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_testis_rna_2_s,,,,,,,,,E-MTAB-7247:opossum_testis_rna_2,,E-MTAB-7247:opossum_testis_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758438,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812416/opossum_testis_rna_2.fastq.gz,6033876618,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812416/opossum_testis_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812416/opossum_testis_rna_2.fastq.gz,,5ece787e1627d328402e8edd3511b5be,male,,,,,,, PRJEB28810,ERX2819248,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,13616,Monodelphis domestica,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939656,opossum_testis_rna_3,Illumina HiSeq 2500,ERR2812417,,,SAMEA4939656,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:opossum_testis_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,opossum_testis_rna_3_s,,,,,,,,,E-MTAB-7247:opossum_testis_rna_3,,E-MTAB-7247:opossum_testis_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758439,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812417/opossum_testis_rna_3.fastq.gz,2158161396,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812417/opossum_testis_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812417/opossum_testis_rna_3.fastq.gz,,8d04f9228b396c44abc5624b277741fa,male,,,,,,, PRJEB28810,ERX2819249,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939657,platypus_brain_ribo_1,Illumina HiSeq 2500,ERR2812418,524355445,33524134145,SAMEA4939657,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_brain_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/008/ERR2812418/ERR2812418.fastq.gz,14452388871,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/008/ERR2812418/ERR2812418.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/008/ERR2812418/ERR2812418.fastq.gz,f416c103310a442a91d087a779369969,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_brain_ribo_1_s,,,,,,,,,E-MTAB-7247:platypus_brain_ribo_1,,E-MTAB-7247:platypus_brain_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758440,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/008/ERR2812418,13588505161,ftp.sra.ebi.ac.uk/vol1/err/ERR281/008/ERR2812418,ftp.sra.ebi.ac.uk/vol1/err/ERR281/008/ERR2812418,bf0a740b84d99e62a322236b6903ae4b,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812418/platypus_brain_ribo_1.fastq.gz,13132247472,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812418/platypus_brain_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812418/platypus_brain_ribo_1.fastq.gz,,56471f02da96860b8fe932f0116c4cab,male,,,,,,, PRJEB28810,ERX2819250,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939658,platypus_brain_ribo_2,Illumina HiSeq 2500,ERR2812419,,,SAMEA4939658,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_brain_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_brain_ribo_2_s,,,,,,,,,E-MTAB-7247:platypus_brain_ribo_2,,E-MTAB-7247:platypus_brain_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758441,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812419/platypus_brain_ribo_2.fastq.gz,9344149843,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812419/platypus_brain_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812419/platypus_brain_ribo_2.fastq.gz,,21e0f4e1d0ea46ac02e53cc7d02927a4,male,,,,,,, PRJEB28810,ERX2819251,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939659,platypus_brain_ribo_3,Illumina HiSeq 2500,ERR2812420,,,SAMEA4939659,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_brain_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_brain_ribo_3_s,,,,,,,,,E-MTAB-7247:platypus_brain_ribo_3,,E-MTAB-7247:platypus_brain_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758442,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812420/platypus_brain_ribo_3.fastq.gz,4257460295,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812420/platypus_brain_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812420/platypus_brain_ribo_3.fastq.gz,,6b796e5bc21d90f46d07b3a69630c8d9,male,,,,,,, PRJEB28810,ERX2819252,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939660,platypus_brain_rna_1,Illumina HiSeq 2500,ERR2812421,88501433,4513573083,SAMEA4939660,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_brain_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/001/ERR2812421/ERR2812421.fastq.gz,2366110234,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/001/ERR2812421/ERR2812421.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/001/ERR2812421/ERR2812421.fastq.gz,6e19a9478311261736ec129a6a06acf8,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_brain_rna_1_s,,,,,,,,,E-MTAB-7247:platypus_brain_rna_1,,E-MTAB-7247:platypus_brain_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758443,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/001/ERR2812421,1767628159,ftp.sra.ebi.ac.uk/vol1/err/ERR281/001/ERR2812421,ftp.sra.ebi.ac.uk/vol1/err/ERR281/001/ERR2812421,11c99975c8b985a7d0b8a8157bc54cef,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812421/platypus_brain_rna_1.fastq.gz,2452947040,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812421/platypus_brain_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812421/platypus_brain_rna_1.fastq.gz,,a1990be889997e0b23577e06a91221ff,male,,,,,,, PRJEB28810,ERX2819253,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939661,platypus_brain_rna_2,Illumina HiSeq 2500,ERR2812422,,,SAMEA4939661,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_brain_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_brain_rna_2_s,,,,,,,,,E-MTAB-7247:platypus_brain_rna_2,,E-MTAB-7247:platypus_brain_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758444,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812422/platypus_brain_rna_2.fastq.gz,5327088565,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812422/platypus_brain_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812422/platypus_brain_rna_2.fastq.gz,,cbf27e93147aa31aac333eb2ba9f4dfb,male,,,,,,, PRJEB28810,ERX2819254,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939662,platypus_brain_rna_3,Illumina HiSeq 2500,ERR2812423,,,SAMEA4939662,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_brain_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_brain_rna_3_s,,,,,,,,,E-MTAB-7247:platypus_brain_rna_3,,E-MTAB-7247:platypus_brain_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758445,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812423/platypus_brain_rna_3.fastq.gz,7644761312,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812423/platypus_brain_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812423/platypus_brain_rna_3.fastq.gz,,4d8b5c6e7327f146308be7d89897dd6e,male,,,,,,, PRJEB28810,ERX2819255,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939663,platypus_liver_ribo_1,Illumina HiSeq 2500,ERR2812424,205764142,10493971242,SAMEA4939663,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_liver_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/004/ERR2812424/ERR2812424.fastq.gz,5592709791,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/004/ERR2812424/ERR2812424.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/004/ERR2812424/ERR2812424.fastq.gz,48ab5777e3b1e52db4061f8f1b2f8292,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_liver_ribo_1_s,,,,,,,,,E-MTAB-7247:platypus_liver_ribo_1,,E-MTAB-7247:platypus_liver_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758446,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/004/ERR2812424,4440992995,ftp.sra.ebi.ac.uk/vol1/err/ERR281/004/ERR2812424,ftp.sra.ebi.ac.uk/vol1/err/ERR281/004/ERR2812424,fe55d6f86e0007fbb4b9d3dad57629e5,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812424/platypus_liver_ribo_1.fastq.gz,5066723498,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812424/platypus_liver_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812424/platypus_liver_ribo_1.fastq.gz,,48091f56925ac0537f00ae233b1bfe18,male,,,,,,, PRJEB28810,ERX2819256,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939664,platypus_liver_ribo_2,Illumina HiSeq 2500,ERR2812425,,,SAMEA4939664,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_liver_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_liver_ribo_2_s,,,,,,,,,E-MTAB-7247:platypus_liver_ribo_2,,E-MTAB-7247:platypus_liver_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758447,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812425/platypus_liver_ribo_2.fastq.gz,2135339874,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812425/platypus_liver_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812425/platypus_liver_ribo_2.fastq.gz,,50c0a9e6450a998784be15af5db34b88,male,,,,,,, PRJEB28810,ERX2819257,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939665,platypus_liver_ribo_3,Illumina HiSeq 2500,ERR2812426,,,SAMEA4939665,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_liver_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_liver_ribo_3_s,,,,,,,,,E-MTAB-7247:platypus_liver_ribo_3,,E-MTAB-7247:platypus_liver_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758448,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812426/platypus_liver_ribo_3.fastq.gz,3119876363,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812426/platypus_liver_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812426/platypus_liver_ribo_3.fastq.gz,,8d8eeb944bca513006dddca529cb4b39,male,,,,,,, PRJEB28810,ERX2819258,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939666,platypus_liver_rna_1,Illumina HiSeq 2500,ERR2812427,107403200,5477563200,SAMEA4939666,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_liver_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR281/007/ERR2812427/ERR2812427.fastq.gz,3374724561,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/007/ERR2812427/ERR2812427.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR281/007/ERR2812427/ERR2812427.fastq.gz,bb5aeacf16ad61d6c00008ec0727b4d8,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_liver_rna_1_s,,,,,,,,,E-MTAB-7247:platypus_liver_rna_1,,E-MTAB-7247:platypus_liver_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758449,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR281/007/ERR2812427,2332096662,ftp.sra.ebi.ac.uk/vol1/err/ERR281/007/ERR2812427,ftp.sra.ebi.ac.uk/vol1/err/ERR281/007/ERR2812427,bc70861424229fb53d13f1da11232310,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812427/platypus_liver_rna_1.fastq.gz,3079745871,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812427/platypus_liver_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812427/platypus_liver_rna_1.fastq.gz,,5e83c441a8e220b3138fd4433f24fe28,male,,,,,,, PRJEB28810,ERX2819259,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939667,platypus_liver_rna_2,Illumina HiSeq 2500,ERR2812428,,,SAMEA4939667,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_liver_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_liver_rna_2_s,,,,,,,,,E-MTAB-7247:platypus_liver_rna_2,,E-MTAB-7247:platypus_liver_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758450,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812428/platypus_liver_rna_2.fastq.gz,5658103305,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812428/platypus_liver_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812428/platypus_liver_rna_2.fastq.gz,,be62685d9f9153b214395b662fdb0274,male,,,,,,, PRJEB28810,ERX2819260,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939668,platypus_liver_rna_3,Illumina HiSeq 2500,ERR2812429,,,SAMEA4939668,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_liver_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_liver_rna_3_s,,,,,,,,,E-MTAB-7247:platypus_liver_rna_3,,E-MTAB-7247:platypus_liver_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758451,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812429/platypus_liver_rna_3.fastq.gz,7854730289,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812429/platypus_liver_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812429/platypus_liver_rna_3.fastq.gz,,104fd56f3d9b7a83d7d796227d63197a,male,,,,,,, PRJEB28810,ERX2819261,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939669,platypus_testis_ribo_1,Illumina HiSeq 2500,ERR2812430,,,SAMEA4939669,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_testis_ribo_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_testis_ribo_1_s,,,,,,,,,E-MTAB-7247:platypus_testis_ribo_1,,E-MTAB-7247:platypus_testis_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758452,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812430/platypus_testis_ribo_1.fastq.gz,4655907782,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812430/platypus_testis_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812430/platypus_testis_ribo_1.fastq.gz,,95265fd7a79045e53403755b728d4e06,male,,,,,,, PRJEB28810,ERX2819262,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939670,platypus_testis_ribo_2,Illumina HiSeq 2500,ERR2812431,,,SAMEA4939670,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_testis_ribo_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_testis_ribo_2_s,,,,,,,,,E-MTAB-7247:platypus_testis_ribo_2,,E-MTAB-7247:platypus_testis_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758453,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812431/platypus_testis_ribo_2.fastq.gz,1928065426,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812431/platypus_testis_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812431/platypus_testis_ribo_2.fastq.gz,,72a11ea0839c1fc0f1b538c8a9ba6141,male,,,,,,, PRJEB28810,ERX2819263,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939671,platypus_testis_ribo_3,Illumina HiSeq 2500,ERR2812432,,,SAMEA4939671,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_testis_ribo_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_testis_ribo_3_s,,,,,,,,,E-MTAB-7247:platypus_testis_ribo_3,,E-MTAB-7247:platypus_testis_ribo_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758454,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812432/platypus_testis_ribo_3.fastq.gz,3217635589,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812432/platypus_testis_ribo_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812432/platypus_testis_ribo_3.fastq.gz,,95e8e4d249457906497aa6f5827461c1,male,,,,,,, PRJEB28810,ERX2819264,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939672,platypus_testis_rna_1,Illumina HiSeq 2500,ERR2812433,,,SAMEA4939672,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_testis_rna_1_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_testis_rna_1_s,,,,,,,,,E-MTAB-7247:platypus_testis_rna_1,,E-MTAB-7247:platypus_testis_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758455,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812433/platypus_testis_rna_1.fastq.gz,10246659465,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812433/platypus_testis_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812433/platypus_testis_rna_1.fastq.gz,,c4151da64cc42a79909f6011024c8987,male,,,,,,, PRJEB28810,ERX2819265,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939673,platypus_testis_rna_2,Illumina HiSeq 2500,ERR2812434,,,SAMEA4939673,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_testis_rna_2_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_testis_rna_2_s,,,,,,,,,E-MTAB-7247:platypus_testis_rna_2,,E-MTAB-7247:platypus_testis_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758456,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812434/platypus_testis_rna_2.fastq.gz,2294781664,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812434/platypus_testis_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812434/platypus_testis_rna_2.fastq.gz,,6ed13b6ee75b15f2432b05e278d3c2ba,male,,,,,,, PRJEB28810,ERX2819266,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9258,Ornithorhynchus anatinus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939674,platypus_testis_rna_3,Illumina HiSeq 2500,ERR2812435,,,SAMEA4939674,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:platypus_testis_rna_3_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,platypus_testis_rna_3_s,,,,,,,,,E-MTAB-7247:platypus_testis_rna_3,,E-MTAB-7247:platypus_testis_rna_3,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758457,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812435/platypus_testis_rna_3.fastq.gz,3010307584,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812435/platypus_testis_rna_3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812435/platypus_testis_rna_3.fastq.gz,,5e675b165b28f1c7d7beadbc00fe37be,male,,,,,,, PRJEB28810,ERX2819267,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939675,chicken_liver_ribo_4,Illumina HiSeq 2500,ERR2812436,,,SAMEA4939675,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_ribo_4_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_ribo_4_s,,,,,,,,,E-MTAB-7247:chicken_liver_ribo_4,,E-MTAB-7247:chicken_liver_ribo_4,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758458,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812436/chicken_liver_ribo_4.fastq.gz,5761719962,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812436/chicken_liver_ribo_4.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812436/chicken_liver_ribo_4.fastq.gz,,19ddd1d47cc6f9683457fff690897892,male,,,,,,, PRJEB28810,ERX2819268,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939676,chicken_liver_ribo_5,Illumina HiSeq 2500,ERR2812437,,,SAMEA4939676,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_ribo_5_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_ribo_5_s,,,,,,,,,E-MTAB-7247:chicken_liver_ribo_5,,E-MTAB-7247:chicken_liver_ribo_5,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758459,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812437/chicken_liver_ribo_5.fastq.gz,3322471257,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812437/chicken_liver_ribo_5.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812437/chicken_liver_ribo_5.fastq.gz,,b3b70eed5086b227da29876f406bfe36,male,,,,,,, PRJEB28810,ERX2819269,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939677,chicken_liver_rna_4,Illumina HiSeq 2500,ERR2812438,,,SAMEA4939677,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_rna_4_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_rna_4_s,,,,,,,,,E-MTAB-7247:chicken_liver_rna_4,,E-MTAB-7247:chicken_liver_rna_4,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758460,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812438/chicken_liver_rna_4.fastq.gz,4263275947,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812438/chicken_liver_rna_4.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812438/chicken_liver_rna_4.fastq.gz,,5f8d62d7bbb891a7428253ac3084e3ea,male,,,,,,, PRJEB28810,ERX2819270,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,9031,Gallus gallus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939678,chicken_liver_rna_5,Illumina HiSeq 2500,ERR2812439,,,SAMEA4939678,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:chicken_liver_rna_5_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,chicken_liver_rna_5_s,,,,,,,,,E-MTAB-7247:chicken_liver_rna_5,,E-MTAB-7247:chicken_liver_rna_5,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758461,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812439/chicken_liver_rna_5.fastq.gz,4426260164,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812439/chicken_liver_rna_5.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812439/chicken_liver_rna_5.fastq.gz,,f9cd02435e377b1b9cd263bbb5aeac7c,male,,,,,,, PRJEB28810,ERX2819271,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939679,mouse_liver_ribo_4,Illumina HiSeq 2500,ERR2812440,,,SAMEA4939679,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_ribo_4_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_ribo_4_s,,,,,,,,,E-MTAB-7247:mouse_liver_ribo_4,,E-MTAB-7247:mouse_liver_ribo_4,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758462,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812440/mouse_liver_ribo_4.fastq.gz,2462737950,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812440/mouse_liver_ribo_4.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812440/mouse_liver_ribo_4.fastq.gz,,3656cdc24eb21cc0ee4708fe53e6c65a,male,,,,,,, PRJEB28810,ERX2819272,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939680,mouse_liver_ribo_5,Illumina HiSeq 2500,ERR2812441,,,SAMEA4939680,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_ribo_5_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_ribo_5_s,,,,,,,,,E-MTAB-7247:mouse_liver_ribo_5,,E-MTAB-7247:mouse_liver_ribo_5,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758463,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812441/mouse_liver_ribo_5.fastq.gz,2512150870,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812441/mouse_liver_ribo_5.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812441/mouse_liver_ribo_5.fastq.gz,,1ee615f1a7eefdc3c11714f3becc73a7,male,,,,,,, PRJEB28810,ERX2819273,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939681,mouse_liver_rna_4,Illumina HiSeq 2500,ERR2812442,,,SAMEA4939681,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_rna_4_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_rna_4_s,,,,,,,,,E-MTAB-7247:mouse_liver_rna_4,,E-MTAB-7247:mouse_liver_rna_4,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758464,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812442/mouse_liver_rna_4.fastq.gz,3496040011,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812442/mouse_liver_rna_4.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812442/mouse_liver_rna_4.fastq.gz,,3c883bc8ac33a3bbdb0699bf25a15221,male,,,,,,, PRJEB28810,ERX2819274,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,other,SAMEA4939682,mouse_liver_rna_5,Illumina HiSeq 2500,ERR2812443,,,SAMEA4939682,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7247:mouse_liver_rna_5_s,,,,,,,2018-09-26,2019-10-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,mouse_liver_rna_5_s,,,,,,,,,E-MTAB-7247:mouse_liver_rna_5,,E-MTAB-7247:mouse_liver_rna_5,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red jungle fowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile kit (Illumina), which was used in our study. Specifically, frozen tissues were treate",,,,,ERS2758465,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA1612101,fasp.sra.ebi.ac.uk:/vol1/run/ERR281/ERR2812443/mouse_liver_rna_5.fastq.gz,3177116233,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812443/mouse_liver_rna_5.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR281/ERR2812443/mouse_liver_rna_5.fastq.gz,,233937b41a7330ec8cc73575c5d45b88,male,,,,,,, PRJEB30076,ERX2979492,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147536,RPF_0h_n1,Illumina HiSeq 2500,ERR2976734,14287455,409427591,SAMEA5147536,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:RPF_0h_n1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/004/ERR2976734/ERR2976734.fastq.gz,266914431,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/004/ERR2976734/ERR2976734.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/004/ERR2976734/ERR2976734.fastq.gz,ed1603cdf1251eaa34fdf3f4f9afb5f8,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,RPF_0h_n1_s,,,,,,,,,E-MTAB-7466:RPF_0h_n1,,E-MTAB-7466:RPF_0h_n1,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955282,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/004/ERR2976734,225006609,ftp.sra.ebi.ac.uk/vol1/err/ERR297/004/ERR2976734,ftp.sra.ebi.ac.uk/vol1/err/ERR297/004/ERR2976734,36a0a4ff0a6915d64e6e5a2afaf81d7b,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976734/RPF_0h_n1.fastq.gz,227106974,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976734/RPF_0h_n1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976734/RPF_0h_n1.fastq.gz,,d8f0d5d19541ed47f9f805bf60d1714c,,,,,,,, PRJEB30076,ERX2979493,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147537,RPF_0h_n2,Illumina HiSeq 2500,ERR2976735,5520862,154466485,SAMEA5147537,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:RPF_0h_n2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/005/ERR2976735/ERR2976735.fastq.gz,109024126,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/005/ERR2976735/ERR2976735.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/005/ERR2976735/ERR2976735.fastq.gz,2678a4bdfc86d0339b7107d142c4109a,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,RPF_0h_n2_s,,,,,,,,,E-MTAB-7466:RPF_0h_n2,,E-MTAB-7466:RPF_0h_n2,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955283,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/005/ERR2976735,87408702,ftp.sra.ebi.ac.uk/vol1/err/ERR297/005/ERR2976735,ftp.sra.ebi.ac.uk/vol1/err/ERR297/005/ERR2976735,bd9dba62888d39e6cf1984428d09eb73,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976735/RPF_0h_n2.fastq.gz,94502160,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976735/RPF_0h_n2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976735/RPF_0h_n2.fastq.gz,,090b87af826fa744b20325f1a85e5d81,,,,,,,, PRJEB30076,ERX2979494,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147538,RPF_0h_n3,Illumina HiSeq 2500,ERR2976736,5499258,155393274,SAMEA5147538,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:RPF_0h_n3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/006/ERR2976736/ERR2976736.fastq.gz,110234549,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/006/ERR2976736/ERR2976736.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/006/ERR2976736/ERR2976736.fastq.gz,9667461a04a30bc24f36813399e3dac3,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,RPF_0h_n3_s,,,,,,,,,E-MTAB-7466:RPF_0h_n3,,E-MTAB-7466:RPF_0h_n3,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955284,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/006/ERR2976736,87269375,ftp.sra.ebi.ac.uk/vol1/err/ERR297/006/ERR2976736,ftp.sra.ebi.ac.uk/vol1/err/ERR297/006/ERR2976736,476049718802fa5750ec972dccf000de,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976736/RPF_0h_n3.fastq.gz,95576841,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976736/RPF_0h_n3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976736/RPF_0h_n3.fastq.gz,,2260eaca53b589deac15fba8c8a63429,,,,,,,, PRJEB30076,ERX2979495,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147539,RPF_3h_n1,Illumina HiSeq 2500,ERR2976737,13926097,391986840,SAMEA5147539,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:RPF_3h_n1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/007/ERR2976737/ERR2976737.fastq.gz,264938277,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/007/ERR2976737/ERR2976737.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/007/ERR2976737/ERR2976737.fastq.gz,9968645e1d9df88aaeadc099e6f5b58d,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,RPF_3h_n1_s,,,,,,,,,E-MTAB-7466:RPF_3h_n1,,E-MTAB-7466:RPF_3h_n1,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955285,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/007/ERR2976737,218431258,ftp.sra.ebi.ac.uk/vol1/err/ERR297/007/ERR2976737,ftp.sra.ebi.ac.uk/vol1/err/ERR297/007/ERR2976737,4cac7a03ef5252be2e65dfea9200610a,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976737/RPF_3h_n1.fastq.gz,226276750,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976737/RPF_3h_n1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976737/RPF_3h_n1.fastq.gz,,f95923e83ab94f2f309948b01e2fd075,,,,,,,, PRJEB30076,ERX2979496,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147540,RPF_3h_n2,Illumina HiSeq 2500,ERR2976738,14126686,422171925,SAMEA5147540,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:RPF_3h_n2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/008/ERR2976738/ERR2976738.fastq.gz,265446222,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/008/ERR2976738/ERR2976738.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/008/ERR2976738/ERR2976738.fastq.gz,0f624c13506be6a6243ba69091c36060,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,RPF_3h_n2_s,,,,,,,,,E-MTAB-7466:RPF_3h_n2,,E-MTAB-7466:RPF_3h_n2,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955286,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/008/ERR2976738,230517836,ftp.sra.ebi.ac.uk/vol1/err/ERR297/008/ERR2976738,ftp.sra.ebi.ac.uk/vol1/err/ERR297/008/ERR2976738,44596535331cac109b699fc2f8131517,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976738/RPF_3h_n2.fastq.gz,225977413,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976738/RPF_3h_n2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976738/RPF_3h_n2.fastq.gz,,9b8c3b575642b61ccf2daa313354ed22,,,,,,,, PRJEB30076,ERX2979497,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147541,RPF_3h_n3,Illumina HiSeq 2500,ERR2976739,14499877,434534946,SAMEA5147541,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:RPF_3h_n3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/009/ERR2976739/ERR2976739.fastq.gz,269885153,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/009/ERR2976739/ERR2976739.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/009/ERR2976739/ERR2976739.fastq.gz,0d3cba5807161dbcabdbe335467552ff,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,RPF_3h_n3_s,,,,,,,,,E-MTAB-7466:RPF_3h_n3,,E-MTAB-7466:RPF_3h_n3,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955287,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/009/ERR2976739,235881157,ftp.sra.ebi.ac.uk/vol1/err/ERR297/009/ERR2976739,ftp.sra.ebi.ac.uk/vol1/err/ERR297/009/ERR2976739,062d9d8eba1f1b2346d2b61b7896655b,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976739/RPF_3h_n3.fastq.gz,229693082,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976739/RPF_3h_n3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976739/RPF_3h_n3.fastq.gz,,9959e9903d9c8f7343e93be2e3ebb910,,,,,,,, PRJEB30076,ERX2979498,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147542,TotalRNA_0h_n1,Illumina HiSeq 2500,ERR2976740,27907935,866451536,SAMEA5147542,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:TotalRNA_0h_n1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/000/ERR2976740/ERR2976740.fastq.gz,603637696,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/000/ERR2976740/ERR2976740.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/000/ERR2976740/ERR2976740.fastq.gz,e04c54edd910eb25d9340962eeb176ab,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,TotalRNA_0h_n1_s,,,,,,,,,E-MTAB-7466:TotalRNA_0h_n1,,E-MTAB-7466:TotalRNA_0h_n1,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955288,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/000/ERR2976740,463138194,ftp.sra.ebi.ac.uk/vol1/err/ERR297/000/ERR2976740,ftp.sra.ebi.ac.uk/vol1/err/ERR297/000/ERR2976740,f91868392f85d2eaf50ee22cfe3f8b65,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976740/TotalRNA_0h_n1.fastq.gz,522843256,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976740/TotalRNA_0h_n1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976740/TotalRNA_0h_n1.fastq.gz,,c3f58c9a99fbcb80ddbb76c86fe42f34,,,,,,,, PRJEB30076,ERX2979499,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147543,TotalRNA_0h_n2,Illumina HiSeq 2500,ERR2976741,13444837,351478756,SAMEA5147543,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:TotalRNA_0h_n2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/001/ERR2976741/ERR2976741.fastq.gz,283233368,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/001/ERR2976741/ERR2976741.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/001/ERR2976741/ERR2976741.fastq.gz,cb5e690ff9fb83270927669302115da7,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,TotalRNA_0h_n2_s,,,,,,,,,E-MTAB-7466:TotalRNA_0h_n2,,E-MTAB-7466:TotalRNA_0h_n2,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955289,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/001/ERR2976741,202744367,ftp.sra.ebi.ac.uk/vol1/err/ERR297/001/ERR2976741,ftp.sra.ebi.ac.uk/vol1/err/ERR297/001/ERR2976741,59c933f0bf9e904aebc3033e990ad432,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976741/TotalRNA_0h_n2.fastq.gz,245234764,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976741/TotalRNA_0h_n2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976741/TotalRNA_0h_n2.fastq.gz,,09f3b352b952faeade2c3a02dc1e3337,,,,,,,, PRJEB30076,ERX2979500,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147544,TotalRNA_0h_n3,Illumina HiSeq 2500,ERR2976742,23418108,620300138,SAMEA5147544,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:TotalRNA_0h_n3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/002/ERR2976742/ERR2976742.fastq.gz,493519289,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/002/ERR2976742/ERR2976742.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/002/ERR2976742/ERR2976742.fastq.gz,f05968b2b9a77dfb269a89bcb3695223,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,TotalRNA_0h_n3_s,,,,,,,,,E-MTAB-7466:TotalRNA_0h_n3,,E-MTAB-7466:TotalRNA_0h_n3,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955290,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/002/ERR2976742,353346819,ftp.sra.ebi.ac.uk/vol1/err/ERR297/002/ERR2976742,ftp.sra.ebi.ac.uk/vol1/err/ERR297/002/ERR2976742,1dada41f0e6782c7b9be882127704838,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976742/TotalRNA_0h_n3.fastq.gz,426489386,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976742/TotalRNA_0h_n3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976742/TotalRNA_0h_n3.fastq.gz,,6edfd0110dda757f045000a2d766e8e3,,,,,,,, PRJEB30076,ERX2979501,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147545,TotalRNA_3h_n1,Illumina HiSeq 2500,ERR2976743,3499361,112009663,SAMEA5147545,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:TotalRNA_3h_n1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/003/ERR2976743/ERR2976743.fastq.gz,77730473,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/003/ERR2976743/ERR2976743.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/003/ERR2976743/ERR2976743.fastq.gz,a7c07068f6a4a768d471fe723186c898,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,TotalRNA_3h_n1_s,,,,,,,,,E-MTAB-7466:TotalRNA_3h_n1,,E-MTAB-7466:TotalRNA_3h_n1,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955291,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/003/ERR2976743,60697620,ftp.sra.ebi.ac.uk/vol1/err/ERR297/003/ERR2976743,ftp.sra.ebi.ac.uk/vol1/err/ERR297/003/ERR2976743,1566006c2edf05fd8d2f4144d85637e8,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976743/TotalRNA_3h_n1.fastq.gz,68683354,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976743/TotalRNA_3h_n1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976743/TotalRNA_3h_n1.fastq.gz,,4b325d104674f8987e0f4773a3f28238,,,,,,,, PRJEB30076,ERX2979502,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147546,TotalRNA_3h_n2,Illumina HiSeq 2500,ERR2976744,11299566,305079262,SAMEA5147546,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:TotalRNA_3h_n2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/004/ERR2976744/ERR2976744.fastq.gz,246566152,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/004/ERR2976744/ERR2976744.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/004/ERR2976744/ERR2976744.fastq.gz,35d8ae71bab85894f19e13ea11600339,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,TotalRNA_3h_n2_s,,,,,,,,,E-MTAB-7466:TotalRNA_3h_n2,,E-MTAB-7466:TotalRNA_3h_n2,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955292,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/004/ERR2976744,174339301,ftp.sra.ebi.ac.uk/vol1/err/ERR297/004/ERR2976744,ftp.sra.ebi.ac.uk/vol1/err/ERR297/004/ERR2976744,d1297b6b4e2b685fd2ffd87c9f75aa6a,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976744/TotalRNA_3h_n2.fastq.gz,214287620,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976744/TotalRNA_3h_n2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976744/TotalRNA_3h_n2.fastq.gz,,c866104891bffa5b2af2712132c9da8d,,,,,,,, PRJEB30076,ERX2979503,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,Illumina HiSeq 2500 sequencing; Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA5147547,TotalRNA_3h_n3,Illumina HiSeq 2500,ERR2976745,7169019,210001916,SAMEA5147547,,,,,,ArrayExpress,SW1353,fibroblast,University of Liverpool,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7466:TotalRNA_3h_n3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR297/005/ERR2976745/ERR2976745.fastq.gz,163221752,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/005/ERR2976745/ERR2976745.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR297/005/ERR2976745/ERR2976745.fastq.gz,bfd0036c465d7a5be1eaf2284d321638,2018-12-04,2019-07-12,false,,,,,,,,,,,ILLUMINA,,,,2018-12-04,,SINGLE,TotalRNA_3h_n3_s,,,,,,,,,E-MTAB-7466:TotalRNA_3h_n3,,E-MTAB-7466:TotalRNA_3h_n3,,"Protocols: The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). The SW1353 chondrosarcoma cell line (ATCC HTB-94) was cultured in Dulbecco’s Modified Eagles Medium (DMEM, ThermoFisher Scientific, 31885023) containing 10% Foetal Bovine Serum (FBS, Sigma, F7524), 100 units/ml penicillin-streptomycin (Gibco, 15140122) and 5 µg /ml amphotericin B (Gibco, 15290018), cultured at 37 °C in a 5% CO2 environment. Serum was withdrawn when the cells had reached ~80% confluence and then 24 hours later the cells were treated with 10 ng/ml IL-1β (Sigma, I9401) for 3 and 24 hours (3x 175cm2 flasks per time point, n=3). Ribosome profiling was carried out similar to the method described by Ingolia et al. (64), modified with the use of the ARTseq (Mammalian) Ribosome Profiling Kit (Epicentre, RPHMR12126). To harvest cells for ribosome profiling, cell culture media was removed and cells were washed with ice-cold PBS containing 0.1 mg/ml cycloheximide (Millipore UK Ltd, 239763). Cells were scraped...",,,,,ERS2955293,ERP112487,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR297/005/ERR2976745,117485015,ftp.sra.ebi.ac.uk/vol1/err/ERR297/005/ERR2976745,ftp.sra.ebi.ac.uk/vol1/err/ERR297/005/ERR2976745,22daef085064155071e8d3320aab062f,,E-MTAB-7466,Ribosome profiling of chondrocytic cell line SW1353 following exposure to IL-1B,,,ERA1674180,fasp.sra.ebi.ac.uk:/vol1/run/ERR297/ERR2976745/TotalRNA_3h_n3.fastq.gz,144015288,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976745/TotalRNA_3h_n3.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR297/ERR2976745/TotalRNA_3h_n3.fastq.gz,,126527634c7cb3d3fc34363ac311d06d,,,,,,,, PRJEB31666,ERX3245944,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417311,new1_KO_20C_riboseq_S6,Illumina HiSeq 2500,ERR3218426,42524298,2168739198,SAMEA5417311,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:new1_KO_20C_riboseq_S6_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/006/ERR3218426/ERR3218426.fastq.gz,1661170953,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/006/ERR3218426/ERR3218426.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/006/ERR3218426/ERR3218426.fastq.gz,cdfe1bc5ed2086f5b3e54c42b132b9fb,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,new1_KO_20C_riboseq_S6_s,,,,,,,,,E-MTAB-7763:new1_KO_20C_riboseq_S6,,E-MTAB-7763:new1_KO_20C_riboseq_S6,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222609,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/006/ERR3218426,1269739590,ftp.sra.ebi.ac.uk/vol1/err/ERR321/006/ERR3218426,ftp.sra.ebi.ac.uk/vol1/err/ERR321/006/ERR3218426,77b5be2a233d5255fe41df8626b1d3ef,BY derivative MJY1173,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218426/S6_KO_20C_riboseq_rep1.fastq.gz,1594935852,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218426/S6_KO_20C_riboseq_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218426/S6_KO_20C_riboseq_rep1.fastq.gz,,07511d2002e856cedc08de6c035b03ca,,,,,,,, PRJEB31666,ERX3245945,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417312,new1_KO_20C_riboseq_S8,Illumina HiSeq 2500,ERR3218427,47049069,2399502519,SAMEA5417312,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:new1_KO_20C_riboseq_S8_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/007/ERR3218427/ERR3218427.fastq.gz,1811763485,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/007/ERR3218427/ERR3218427.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/007/ERR3218427/ERR3218427.fastq.gz,0bca4510075b5f266319aea32c5b628c,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,new1_KO_20C_riboseq_S8_s,,,,,,,,,E-MTAB-7763:new1_KO_20C_riboseq_S8,,E-MTAB-7763:new1_KO_20C_riboseq_S8,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222610,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/007/ERR3218427,1399689280,ftp.sra.ebi.ac.uk/vol1/err/ERR321/007/ERR3218427,ftp.sra.ebi.ac.uk/vol1/err/ERR321/007/ERR3218427,e3cb609b98305db6d776fe4d114a0e83,BY derivative MJY1173,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218427/S8_KO_20C_riboseq_rep2.fastq.gz,1740669764,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218427/S8_KO_20C_riboseq_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218427/S8_KO_20C_riboseq_rep2.fastq.gz,,30a1402b2ee16709ad65c5d9a94b56f8,,,,,,,, PRJEB31666,ERX3245946,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417313,new1_KO_20C_rnaseq_S26,Illumina HiSeq 2500,ERR3218428,19253626,981934926,SAMEA5417313,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:new1_KO_20C_rnaseq_S26_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/008/ERR3218428/ERR3218428.fastq.gz,751060693,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/008/ERR3218428/ERR3218428.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/008/ERR3218428/ERR3218428.fastq.gz,2594b0dc350704edd79f6a66fe2f3baa,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,new1_KO_20C_rnaseq_S26_s,,,,,,,,,E-MTAB-7763:new1_KO_20C_rnaseq_S26,,E-MTAB-7763:new1_KO_20C_rnaseq_S26,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222611,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/008/ERR3218428,484632517,ftp.sra.ebi.ac.uk/vol1/err/ERR321/008/ERR3218428,ftp.sra.ebi.ac.uk/vol1/err/ERR321/008/ERR3218428,f2dab142579d0f9f79f34f8b73829b71,BY derivative MJY1173,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218428/S26_KO_20C_rnaseq_rep1.fastq.gz,718841591,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218428/S26_KO_20C_rnaseq_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218428/S26_KO_20C_rnaseq_rep1.fastq.gz,,a4225054c195a33f691d89b913439bf1,,,,,,,, PRJEB31666,ERX3245947,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417314,new1_KO_20C_rnaseq_S28,Illumina HiSeq 2500,ERR3218429,17912055,913514805,SAMEA5417314,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:new1_KO_20C_rnaseq_S28_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/009/ERR3218429/ERR3218429.fastq.gz,681146466,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/009/ERR3218429/ERR3218429.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/009/ERR3218429/ERR3218429.fastq.gz,95dd21b754f98ebfc2075cbf91989a4c,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,new1_KO_20C_rnaseq_S28_s,,,,,,,,,E-MTAB-7763:new1_KO_20C_rnaseq_S28,,E-MTAB-7763:new1_KO_20C_rnaseq_S28,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222612,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/009/ERR3218429,446688542,ftp.sra.ebi.ac.uk/vol1/err/ERR321/009/ERR3218429,ftp.sra.ebi.ac.uk/vol1/err/ERR321/009/ERR3218429,982985cbdcecbc684098b6fb7fd6f340,BY derivative MJY1173,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218429/S28_KO_20C_rnaseq_rep2.fastq.gz,650976447,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218429/S28_KO_20C_rnaseq_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218429/S28_KO_20C_rnaseq_rep2.fastq.gz,,410c14e5dd19ef0384f249090ee81274,,,,,,,, PRJEB31666,ERX3245948,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417315,new1_KO_30C_riboseq_S2,Illumina HiSeq 2500,ERR3218430,41003606,2091183906,SAMEA5417315,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:new1_KO_30C_riboseq_S2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/000/ERR3218430/ERR3218430.fastq.gz,1523003576,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/000/ERR3218430/ERR3218430.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/000/ERR3218430/ERR3218430.fastq.gz,9d60bed088eff9ce8b94fa6def70a38b,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,new1_KO_30C_riboseq_S2_s,,,,,,,,,E-MTAB-7763:new1_KO_30C_riboseq_S2,,E-MTAB-7763:new1_KO_30C_riboseq_S2,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222613,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/000/ERR3218430,1217943974,ftp.sra.ebi.ac.uk/vol1/err/ERR321/000/ERR3218430,ftp.sra.ebi.ac.uk/vol1/err/ERR321/000/ERR3218430,ef7142364164356d50deb816bde21513,BY derivative MJY1173,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218430/S2_KO_30C_riboseq_rep1.fastq.gz,1458550491,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218430/S2_KO_30C_riboseq_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218430/S2_KO_30C_riboseq_rep1.fastq.gz,,5bd2c52a0060016e35f41b7fe617c518,,,,,,,, PRJEB31666,ERX3245949,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417316,new1_KO_30C_riboseq_S4,Illumina HiSeq 2500,ERR3218431,46314080,2362018080,SAMEA5417316,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:new1_KO_30C_riboseq_S4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/001/ERR3218431/ERR3218431.fastq.gz,1728597049,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/001/ERR3218431/ERR3218431.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/001/ERR3218431/ERR3218431.fastq.gz,9162ca6c82f0af4e99e7082b2301e8c6,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,new1_KO_30C_riboseq_S4_s,,,,,,,,,E-MTAB-7763:new1_KO_30C_riboseq_S4,,E-MTAB-7763:new1_KO_30C_riboseq_S4,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222614,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/001/ERR3218431,1379123840,ftp.sra.ebi.ac.uk/vol1/err/ERR321/001/ERR3218431,ftp.sra.ebi.ac.uk/vol1/err/ERR321/001/ERR3218431,dda20ec80b832b9b46acda67c3b26412,BY derivative MJY1173,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218431/S4_KO_30C_riboseq_rep2.fastq.gz,1657045908,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218431/S4_KO_30C_riboseq_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218431/S4_KO_30C_riboseq_rep2.fastq.gz,,ac5e211164484987accd829010d793d6,,,,,,,, PRJEB31666,ERX3245950,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417317,new1_KO_30C_rnaseq_S22,Illumina HiSeq 2500,ERR3218432,16606183,846915333,SAMEA5417317,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:new1_KO_30C_rnaseq_S22_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/002/ERR3218432/ERR3218432.fastq.gz,633778853,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/002/ERR3218432/ERR3218432.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/002/ERR3218432/ERR3218432.fastq.gz,af78cf6725801926426202cf562ff289,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,new1_KO_30C_rnaseq_S22_s,,,,,,,,,E-MTAB-7763:new1_KO_30C_rnaseq_S22,,E-MTAB-7763:new1_KO_30C_rnaseq_S22,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222615,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/002/ERR3218432,415302301,ftp.sra.ebi.ac.uk/vol1/err/ERR321/002/ERR3218432,ftp.sra.ebi.ac.uk/vol1/err/ERR321/002/ERR3218432,26f614671bd8cd8587572fa92587257d,BY derivative MJY1173,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218432/S22_KO_30C_rnaseq_rep1.fastq.gz,606683390,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218432/S22_KO_30C_rnaseq_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218432/S22_KO_30C_rnaseq_rep1.fastq.gz,,bf6d25f3b4c584502c1447536b86f49c,,,,,,,, PRJEB31666,ERX3245951,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417318,new1_KO_30C_rnaseq_S24,Illumina HiSeq 2500,ERR3218433,20180603,1029210753,SAMEA5417318,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:new1_KO_30C_rnaseq_S24_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/003/ERR3218433/ERR3218433.fastq.gz,776636341,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/003/ERR3218433/ERR3218433.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/003/ERR3218433/ERR3218433.fastq.gz,836a9bf3c4a0905bcd9b542b55481bba,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,new1_KO_30C_rnaseq_S24_s,,,,,,,,,E-MTAB-7763:new1_KO_30C_rnaseq_S24,,E-MTAB-7763:new1_KO_30C_rnaseq_S24,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222616,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/003/ERR3218433,505203328,ftp.sra.ebi.ac.uk/vol1/err/ERR321/003/ERR3218433,ftp.sra.ebi.ac.uk/vol1/err/ERR321/003/ERR3218433,b691825bedfb2d8b7cc5a81245157ad6,BY derivative MJY1173,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218433/S24_KO_30C_rnaseq_rep2.fastq.gz,742669038,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218433/S24_KO_30C_rnaseq_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218433/S24_KO_30C_rnaseq_rep2.fastq.gz,,739de4ad0d1c0af778768003e8875966,,,,,,,, PRJEB31666,ERX3245952,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417319,WT_20C_riboseq_S5,Illumina HiSeq 2500,ERR3218434,36716398,1872536298,SAMEA5417319,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:WT_20C_riboseq_S5_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/004/ERR3218434/ERR3218434.fastq.gz,1440948536,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/004/ERR3218434/ERR3218434.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/004/ERR3218434/ERR3218434.fastq.gz,f9ae6eb79565f26ddae295cbcb29b6e4,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,WT_20C_riboseq_S5_s,,,,,,,,,E-MTAB-7763:WT_20C_riboseq_S5,,E-MTAB-7763:WT_20C_riboseq_S5,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222617,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/004/ERR3218434,1097185293,ftp.sra.ebi.ac.uk/vol1/err/ERR321/004/ERR3218434,ftp.sra.ebi.ac.uk/vol1/err/ERR321/004/ERR3218434,a59eb16325ace33cad7164e433037587,BY derivative MJY1171,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218434/S5_WT_20C_riboseq_rep1.fastq.gz,1383439382,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218434/S5_WT_20C_riboseq_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218434/S5_WT_20C_riboseq_rep1.fastq.gz,,c4cdab3122d9d9cff4b15acff8ce6aaa,,,,,,,, PRJEB31666,ERX3245953,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417320,WT_20C_riboseq_S7,Illumina HiSeq 2500,ERR3218435,39097639,1993979589,SAMEA5417320,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:WT_20C_riboseq_S7_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/005/ERR3218435/ERR3218435.fastq.gz,1470212104,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/005/ERR3218435/ERR3218435.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/005/ERR3218435/ERR3218435.fastq.gz,5f7ff9ace50cfef9493a24b0b4d2c222,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,WT_20C_riboseq_S7_s,,,,,,,,,E-MTAB-7763:WT_20C_riboseq_S7,,E-MTAB-7763:WT_20C_riboseq_S7,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222618,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/005/ERR3218435,1168439094,ftp.sra.ebi.ac.uk/vol1/err/ERR321/005/ERR3218435,ftp.sra.ebi.ac.uk/vol1/err/ERR321/005/ERR3218435,48eba8d5b19464539ec961045502431a,BY derivative MJY1171,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218435/S7_WT_20C_riboseq_rep2.fastq.gz,1410456848,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218435/S7_WT_20C_riboseq_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218435/S7_WT_20C_riboseq_rep2.fastq.gz,,6961c91c93baf092c18943d77e900ca3,,,,,,,, PRJEB31666,ERX3245954,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417321,WT_20C_rnaseq_S25,Illumina HiSeq 2500,ERR3218436,20712520,1056338520,SAMEA5417321,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:WT_20C_rnaseq_S25_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/006/ERR3218436/ERR3218436.fastq.gz,775942279,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/006/ERR3218436/ERR3218436.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/006/ERR3218436/ERR3218436.fastq.gz,5563dd7877a6300af95bbcb38844de9c,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,WT_20C_rnaseq_S25_s,,,,,,,,,E-MTAB-7763:WT_20C_rnaseq_S25,,E-MTAB-7763:WT_20C_rnaseq_S25,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222619,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/006/ERR3218436,518280156,ftp.sra.ebi.ac.uk/vol1/err/ERR321/006/ERR3218436,ftp.sra.ebi.ac.uk/vol1/err/ERR321/006/ERR3218436,f7d0a580294c08f7cb3689a92bc616e4,BY derivative MJY1171,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218436/S25_WT_20C_rnaseq_rep1.fastq.gz,745066443,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218436/S25_WT_20C_rnaseq_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218436/S25_WT_20C_rnaseq_rep1.fastq.gz,,cfb0e429dcff286f2e34c3d5554210e7,,,,,,,, PRJEB31666,ERX3245955,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417322,WT_20C_rnaseq_S27,Illumina HiSeq 2500,ERR3218437,17927270,914290770,SAMEA5417322,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:WT_20C_rnaseq_S27_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/007/ERR3218437/ERR3218437.fastq.gz,697057326,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/007/ERR3218437/ERR3218437.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/007/ERR3218437/ERR3218437.fastq.gz,382296ba2635d086170fab7fca918478,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,WT_20C_rnaseq_S27_s,,,,,,,,,E-MTAB-7763:WT_20C_rnaseq_S27,,E-MTAB-7763:WT_20C_rnaseq_S27,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222620,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/007/ERR3218437,449330721,ftp.sra.ebi.ac.uk/vol1/err/ERR321/007/ERR3218437,ftp.sra.ebi.ac.uk/vol1/err/ERR321/007/ERR3218437,6c48b86cd6941012e850a872ede9cd88,BY derivative MJY1171,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218437/S27_WT_20C_rnaseq_rep2.fastq.gz,666658472,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218437/S27_WT_20C_rnaseq_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218437/S27_WT_20C_rnaseq_rep2.fastq.gz,,74b28572c5b152f8c2aad25ddf2ed87a,,,,,,,, PRJEB31666,ERX3245956,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417323,WT_30C_riboseq_S1,Illumina HiSeq 2500,ERR3218438,42073144,2145730344,SAMEA5417323,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:WT_30C_riboseq_S1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/008/ERR3218438/ERR3218438.fastq.gz,1609885971,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/008/ERR3218438/ERR3218438.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/008/ERR3218438/ERR3218438.fastq.gz,4f55459d88e53d599f7abba01515e53a,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,WT_30C_riboseq_S1_s,,,,,,,,,E-MTAB-7763:WT_30C_riboseq_S1,,E-MTAB-7763:WT_30C_riboseq_S1,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222621,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/008/ERR3218438,1259466886,ftp.sra.ebi.ac.uk/vol1/err/ERR321/008/ERR3218438,ftp.sra.ebi.ac.uk/vol1/err/ERR321/008/ERR3218438,046735390023f842328355f4a10633d6,BY derivative MJY1171,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218438/S1_WT_30C_riboseq_rep1.fastq.gz,1543309286,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218438/S1_WT_30C_riboseq_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218438/S1_WT_30C_riboseq_rep1.fastq.gz,,cad4ce709667c88c8b8d4c72bbd1781d,,,,,,,, PRJEB31666,ERX3245957,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMEA5417324,WT_30C_riboseq_S3,Illumina HiSeq 2500,ERR3218439,44105472,2249379072,SAMEA5417324,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:WT_30C_riboseq_S3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/009/ERR3218439/ERR3218439.fastq.gz,1707313854,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/009/ERR3218439/ERR3218439.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/009/ERR3218439/ERR3218439.fastq.gz,eab81e9b39ba6e9b1f8a6f4128d35ea6,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,WT_30C_riboseq_S3_s,,,,,,,,,E-MTAB-7763:WT_30C_riboseq_S3,,E-MTAB-7763:WT_30C_riboseq_S3,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222622,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/009/ERR3218439,1324941976,ftp.sra.ebi.ac.uk/vol1/err/ERR321/009/ERR3218439,ftp.sra.ebi.ac.uk/vol1/err/ERR321/009/ERR3218439,cea01af5724a256e763e1520ebf6703d,BY derivative MJY1171,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218439/S3_WT_30C_riboseq_rep2.fastq.gz,1637749527,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218439/S3_WT_30C_riboseq_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218439/S3_WT_30C_riboseq_rep2.fastq.gz,,bf1c5b40e0e2390f5226a7e919475d5c,,,,,,,, PRJEB31666,ERX3245958,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417325,WT_30C_rnaseq_S21,Illumina HiSeq 2500,ERR3218440,32260678,1645294578,SAMEA5417325,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:WT_30C_rnaseq_S21_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/000/ERR3218440/ERR3218440.fastq.gz,1264745818,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/000/ERR3218440/ERR3218440.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/000/ERR3218440/ERR3218440.fastq.gz,7e48a3ce5eca5b28e8db6ec786d94d22,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,WT_30C_rnaseq_S21_s,,,,,,,,,E-MTAB-7763:WT_30C_rnaseq_S21,,E-MTAB-7763:WT_30C_rnaseq_S21,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222623,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/000/ERR3218440,828471982,ftp.sra.ebi.ac.uk/vol1/err/ERR321/000/ERR3218440,ftp.sra.ebi.ac.uk/vol1/err/ERR321/000/ERR3218440,c4daa78f2e7c8d3598c5a12616c24d91,BY derivative MJY1171,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218440/S21_WT_30C_rnaseq_rep1.fastq.gz,1212731339,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218440/S21_WT_30C_rnaseq_rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218440/S21_WT_30C_rnaseq_rep1.fastq.gz,,f98ec2a036dcdb34d5ade627706d94eb,,,,,,,, PRJEB31666,ERX3245959,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,Illumina HiSeq 2500 sequencing; Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMEA5417326,WT_30C_rnaseq_S23,Illumina HiSeq 2500,ERR3218441,28075810,1431866310,SAMEA5417326,,,,,,ArrayExpress,,,postdoc,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7763:WT_30C_rnaseq_S23_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR321/001/ERR3218441/ERR3218441.fastq.gz,1118309498,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/001/ERR3218441/ERR3218441.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR321/001/ERR3218441/ERR3218441.fastq.gz,0e30d37f871f2c9f5200a97b9ea435bf,2019-03-12,2019-05-31,false,,,,,,,,,,,ILLUMINA,,,,2019-03-13,,SINGLE,WT_30C_rnaseq_S23_s,,,,,,,,,E-MTAB-7763:WT_30C_rnaseq_S23,,E-MTAB-7763:WT_30C_rnaseq_S23,,"Protocols: Cells were collected by rapid vacuum filtration, promptly flash-frozen in liquid nitrogen and lysed by cryogenic milling. Cultured at 20 or 30 degrees Celsius in 750 ml of synthetic complete medium until OD600=0.6 TRI Reagent (AM9738, ThermoFisher) was used to extract the RNA, followed by clean-up using RNA Clean & Concentrator -25 Kit (Zymo Research). RNA-Seq libraries were constructed using ScriptSeq Complete Gold Yeast Kit (Epicentre). Ribo-Seq libraries were prepared essentially as per Ingolia and colleagues, NatMeth 2012 (PMID: 22836135) with modifications on rRNA removal (Ribo-Zero Gold rRNA Removal Kit -Yeast) and sample purification procedures between enzymatic steps (RNA Clean & Concentrator -5 Kit).",,,,,ERS3222624,ERP114248,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR321/001/ERR3218441,733439365,ftp.sra.ebi.ac.uk/vol1/err/ERR321/001/ERR3218441,ftp.sra.ebi.ac.uk/vol1/err/ERR321/001/ERR3218441,9a500060e6d75544dc972e2cc0af3d49,BY derivative MJY1171,E-MTAB-7763,Ribosome profiling of NEW1 knock-out as well as the isogenic wild type strain of Saccharomyces cerevisiae. The cultures were grown either at 20°C or 30°C.,,,ERA1762847,fasp.sra.ebi.ac.uk:/vol1/run/ERR321/ERR3218441/S23_WT_30C_rnaseq_rep2.fastq.gz,1072783449,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218441/S23_WT_30C_rnaseq_rep2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR321/ERR3218441/S23_WT_30C_rnaseq_rep2.fastq.gz,,5515eaf2ae65d2ce31904b10e8961bed,,,,,,,, PRJEB32121,ERX3303389,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563290,Sample 10,NextSeq 500,ERR3276516,55053803,2331547026,SAMEA5563290,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 10_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/006/ERR3276516/ERR3276516.fastq.gz,1370728565,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/006/ERR3276516/ERR3276516.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/006/ERR3276516/ERR3276516.fastq.gz,609421a9c7d7dd110d3e07384807d1d8,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 10_s,,,,,,,,,E-MTAB-7849:Sample 10,,E-MTAB-7849:Sample 10,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365320,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/006/ERR3276516,1087976688,ftp.sra.ebi.ac.uk/vol1/err/ERR327/006/ERR3276516,ftp.sra.ebi.ac.uk/vol1/err/ERR327/006/ERR3276516,5f8ec9284c4077f7c5d216f5f259efce,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276516/Sample_10.fq.gz,1233610279,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276516/Sample_10.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276516/Sample_10.fq.gz,,0577cbd485851725fbd2f99805a1c2a3,,,,,,,, PRJEB32121,ERX3303390,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563291,Sample 5,NextSeq 500,ERR3276517,26947157,1513258341,SAMEA5563291,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 5_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/007/ERR3276517/ERR3276517.fastq.gz,808555912,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/007/ERR3276517/ERR3276517.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/007/ERR3276517/ERR3276517.fastq.gz,d6131018834f4ac5f548c159d94d23d7,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 5_s,,,,,,,,,E-MTAB-7849:Sample 5,,E-MTAB-7849:Sample 5,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365321,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/007/ERR3276517,623582515,ftp.sra.ebi.ac.uk/vol1/err/ERR327/007/ERR3276517,ftp.sra.ebi.ac.uk/vol1/err/ERR327/007/ERR3276517,0bb0489cf8727178f0b2a0d84f304716,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276517/Sample_5.fq.gz,737268093,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276517/Sample_5.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276517/Sample_5.fq.gz,,bd38ca0a8836faa2624222ba3aa9d0f8,,,,,,,, PRJEB32121,ERX3303391,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563292,Sample 6,NextSeq 500,ERR3276518,55020617,2287339126,SAMEA5563292,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 6_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/008/ERR3276518/ERR3276518.fastq.gz,1416002323,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/008/ERR3276518/ERR3276518.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/008/ERR3276518/ERR3276518.fastq.gz,a37ecf2108559e267641c01fa81ac887,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 6_s,,,,,,,,,E-MTAB-7849:Sample 6,,E-MTAB-7849:Sample 6,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365322,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/008/ERR3276518,1085008214,ftp.sra.ebi.ac.uk/vol1/err/ERR327/008/ERR3276518,ftp.sra.ebi.ac.uk/vol1/err/ERR327/008/ERR3276518,a446e97b4ffa603abf7dbb26a110fafe,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276518/Sample_6.fq.gz,1277954673,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276518/Sample_6.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276518/Sample_6.fq.gz,,2d5410adf3c918b15dfc031303f8c680,,,,,,,, PRJEB32121,ERX3303392,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563293,Sample 9,NextSeq 500,ERR3276519,26710399,1628290372,SAMEA5563293,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 9_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/009/ERR3276519/ERR3276519.fastq.gz,840731547,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/009/ERR3276519/ERR3276519.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/009/ERR3276519/ERR3276519.fastq.gz,59e286157d84f579de96a7d8051f975e,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 9_s,,,,,,,,,E-MTAB-7849:Sample 9,,E-MTAB-7849:Sample 9,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365323,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/009/ERR3276519,648351012,ftp.sra.ebi.ac.uk/vol1/err/ERR327/009/ERR3276519,ftp.sra.ebi.ac.uk/vol1/err/ERR327/009/ERR3276519,273dc73bb3b056a17868260de5686c17,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276519/Sample_9.fq.gz,770154822,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276519/Sample_9.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276519/Sample_9.fq.gz,,0ec767f6028b1cc70d9447b6e6c58ab6,,,,,,,, PRJEB32121,ERX3303393,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563294,Sample 1,NextSeq 500,ERR3276520,24759896,1470848970,SAMEA5563294,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/000/ERR3276520/ERR3276520.fastq.gz,761301644,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/000/ERR3276520/ERR3276520.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/000/ERR3276520/ERR3276520.fastq.gz,fd67c3301225269201c9f2a06d12558c,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 1_s,,,,,,,,,E-MTAB-7849:Sample 1,,E-MTAB-7849:Sample 1,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365324,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/000/ERR3276520,597885656,ftp.sra.ebi.ac.uk/vol1/err/ERR327/000/ERR3276520,ftp.sra.ebi.ac.uk/vol1/err/ERR327/000/ERR3276520,ff3c7e3ef8ccd3c0aff0640e5f6a0954,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276520/Sample_1.fq.gz,696010833,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276520/Sample_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276520/Sample_1.fq.gz,,210affb6061c2db5f72d4e512f16ff90,,,,,,,, PRJEB32121,ERX3303394,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563295,Sample 11,NextSeq 500,ERR3276521,40743255,720199228,SAMEA5563295,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 11_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/001/ERR3276521/ERR3276521.fastq.gz,730604854,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/001/ERR3276521/ERR3276521.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/001/ERR3276521/ERR3276521.fastq.gz,97ba3d1a98586cf77668d0b060b5037d,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 11_s,,,,,,,,,E-MTAB-7849:Sample 11,,E-MTAB-7849:Sample 11,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365325,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/001/ERR3276521,442419877,ftp.sra.ebi.ac.uk/vol1/err/ERR327/001/ERR3276521,ftp.sra.ebi.ac.uk/vol1/err/ERR327/001/ERR3276521,ecee39e32b1b4b84674694c6c321ed88,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276521/Sample_11.fq.gz,629560992,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276521/Sample_11.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276521/Sample_11.fq.gz,,189feb1f8891c5c3f6040d4013418c66,,,,,,,, PRJEB32121,ERX3303395,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563296,Sample 12,NextSeq 500,ERR3276522,51225481,2179088593,SAMEA5563296,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 12_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/002/ERR3276522/ERR3276522.fastq.gz,1207820109,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/002/ERR3276522/ERR3276522.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/002/ERR3276522/ERR3276522.fastq.gz,b0b6da6673edc8178fe325001c994f3b,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 12_s,,,,,,,,,E-MTAB-7849:Sample 12,,E-MTAB-7849:Sample 12,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365326,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/002/ERR3276522,972750633,ftp.sra.ebi.ac.uk/vol1/err/ERR327/002/ERR3276522,ftp.sra.ebi.ac.uk/vol1/err/ERR327/002/ERR3276522,f803144f2645e6ba030a154269b1303b,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276522/Sample_12.fq.gz,1079418790,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276522/Sample_12.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276522/Sample_12.fq.gz,,d1b6235d06a9b08dd38ce16ca6335b5e,,,,,,,, PRJEB32121,ERX3303396,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563297,Sample 2,NextSeq 500,ERR3276523,46244710,1870162578,SAMEA5563297,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/003/ERR3276523/ERR3276523.fastq.gz,1214604899,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/003/ERR3276523/ERR3276523.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/003/ERR3276523/ERR3276523.fastq.gz,7abdee931c53375827da435dee23c032,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 2_s,,,,,,,,,E-MTAB-7849:Sample 2,,E-MTAB-7849:Sample 2,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365327,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/003/ERR3276523,906593680,ftp.sra.ebi.ac.uk/vol1/err/ERR327/003/ERR3276523,ftp.sra.ebi.ac.uk/vol1/err/ERR327/003/ERR3276523,e1b2a5fa6bfc25a049b6c62b176969d8,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276523/Sample_2.fq.gz,1099115386,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276523/Sample_2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276523/Sample_2.fq.gz,,706d72c1498e34a9ca6d57d039382a42,,,,,,,, PRJEB32121,ERX3303397,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563298,Sample 3,NextSeq 500,ERR3276524,24691642,1389875907,SAMEA5563298,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/004/ERR3276524/ERR3276524.fastq.gz,723840735,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/004/ERR3276524/ERR3276524.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/004/ERR3276524/ERR3276524.fastq.gz,bd92ff1043d39ae1918166e2735438d9,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 3_s,,,,,,,,,E-MTAB-7849:Sample 3,,E-MTAB-7849:Sample 3,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365328,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/004/ERR3276524,568050663,ftp.sra.ebi.ac.uk/vol1/err/ERR327/004/ERR3276524,ftp.sra.ebi.ac.uk/vol1/err/ERR327/004/ERR3276524,c052aa579c155b69873e598cce3bf15c,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276524/Sample_3.fq.gz,658372729,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276524/Sample_3.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276524/Sample_3.fq.gz,,2739e488851d2e3958ddc62cb13b94c6,,,,,,,, PRJEB32121,ERX3303398,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563299,Sample 4,NextSeq 500,ERR3276525,45214219,1852094222,SAMEA5563299,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/005/ERR3276525/ERR3276525.fastq.gz,1154308271,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/005/ERR3276525/ERR3276525.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/005/ERR3276525/ERR3276525.fastq.gz,bedff0fbeed2a7f313027b0b6ab2cde2,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 4_s,,,,,,,,,E-MTAB-7849:Sample 4,,E-MTAB-7849:Sample 4,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365329,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/005/ERR3276525,839550474,ftp.sra.ebi.ac.uk/vol1/err/ERR327/005/ERR3276525,ftp.sra.ebi.ac.uk/vol1/err/ERR327/005/ERR3276525,1eed7eaffd7991ac1bb01f9e052c128e,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276525/Sample_4.fq.gz,1039465078,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276525/Sample_4.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276525/Sample_4.fq.gz,,a7e45ba62f3f01dd8a3001f2de8d2bb1,,,,,,,, PRJEB32121,ERX3303399,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563300,Sample 7,NextSeq 500,ERR3276526,25782829,1431543565,SAMEA5563300,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 7_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/006/ERR3276526/ERR3276526.fastq.gz,736777733,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/006/ERR3276526/ERR3276526.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/006/ERR3276526/ERR3276526.fastq.gz,658ef7431c85a7b98303fbf488063964,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 7_s,,,,,,,,,E-MTAB-7849:Sample 7,,E-MTAB-7849:Sample 7,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365330,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/006/ERR3276526,586508600,ftp.sra.ebi.ac.uk/vol1/err/ERR327/006/ERR3276526,ftp.sra.ebi.ac.uk/vol1/err/ERR327/006/ERR3276526,907f47b58c05d5b56140ec59a9ad4674,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276526/Sample_7.fq.gz,668526899,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276526/Sample_7.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276526/Sample_7.fq.gz,,248e79c78175b6fe9fa49ccf2fa869b4,,,,,,,, PRJEB32121,ERX3303400,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,NextSeq 500 sequencing; Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,9031,Gallus gallus,OTHER,TRANSCRIPTOMIC,other,SAMEA5563301,Sample 8,NextSeq 500,ERR3276527,56002673,2257682429,SAMEA5563301,,,,,,ArrayExpress,,,"Department of Pathology, Department of Pathology Division of Virology, University of Cambridge",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-7849:Sample 8_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR327/007/ERR3276527/ERR3276527.fastq.gz,1361256789,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/007/ERR3276527/ERR3276527.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR327/007/ERR3276527/ERR3276527.fastq.gz,89a120c34dc3749d834c72253f5b29a6,2019-04-11,2019-06-18,false,,,,,,,,,,,ILLUMINA,,,,2019-04-11,,SINGLE,Sample 8_s,,,,,,,,,E-MTAB-7849:Sample 8,,E-MTAB-7849:Sample 8,,"Protocols: Primary chick kidney (CK) cells were produced from 2–3 week-old specific pathogen free (SPF) Rhode Island Red chickens. CK cells (0.8 x 10-6 cells/ml) were plated in 10-cm dishes and, upon reaching 100% confluence (two days post-seeding), were washed once with PBS and infected with 9.6 x 10-6 PFU rIBV Beau-R. After 1 hour incubation at 37 °C, 5% CO2, the inoculum was removed and replaced with 10 ml fresh 1x BES (1X minimal essential Eagle’s medium [MEM], 0.3% tryptose phosphate broth, 0.2% bovine serum albumin, 20 mM N,N-Bis(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), 0.21% sodium bicarbonate, 2 mM L-glutamine, 250 U/ml nystatin, 100 U/ml penicillin, and 100 U/ml streptomycin). Cells were harvested at 24 hours post-infection when clear regions of cytopathic effect (CPE) were visible. Cycloheximide (CHX; Sigma-Aldrich) was added directly to the growth medium (to 100 µg/ml) and the cells incubated for 2 min at 37 °C before rinsing with 5 ml of ice-cold PBS containing CHX (100 µg/ml). Subsequently, dishes were incubated on ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped onto the cells. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 °C, the supernatants recovered and stor...",,,,,ERS3365331,ERP114760,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR327/007/ERR3276527,1074144272,ftp.sra.ebi.ac.uk/vol1/err/ERR327/007/ERR3276527,ftp.sra.ebi.ac.uk/vol1/err/ERR327/007/ERR3276527,765bac9a230b8e1df61bfdabf0c25d48,,E-MTAB-7849,Ribosome profiling and RNA sequencing of Infectious Bronchitis Virus,,,ERA1826088,fasp.sra.ebi.ac.uk:/vol1/run/ERR327/ERR3276527/Sample_8.fq.gz,1222193913,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276527/Sample_8.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR327/ERR3276527/Sample_8.fq.gz,,0b43a80b630168b58fbe256e51200a80,,,,,,,, PRJEB32969,ERX3390678,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMEA5703368,Sample 1,NextSeq 500,ERR3366404,33896631,1214976883,SAMEA5703368,,,,,,ArrayExpress,Caco-2,epithelial cell,UNIVERSITY OF CAMBRIDGE,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-8045:Sample 1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR336/004/ERR3366404/ERR3366404.fastq.gz,753125273,ftp.sra.ebi.ac.uk/vol1/fastq/ERR336/004/ERR3366404/ERR3366404.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR336/004/ERR3366404/ERR3366404.fastq.gz,63eee81e155f510cc5209ec7a18ccf26,2019-06-10,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2019-06-10,,SINGLE,Sample 1_s,,,,,,,,,E-MTAB-8045:Sample 1,,E-MTAB-8045:Sample 1,,"Protocols: At 12 h post infection, cells were either not treated (NT) or treated with 50 µM LTM for 30 minutes, flash frozen in a dry ice/ethanol bath, and lysed in the presence of 100 µg/ml cycloheximide. Caco2 cells were grown on 150-mm dishes to reach 80-90% confluency, then infected at a multiplicity of infection (MOI) of 5 with HAstV1 virus stock (passage 2, derived from pAVIC1 T7 RNA; Geigenmüller et al., 1997, PMID 8995706). After flash freezing, cells were transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to ribosome profiling based on previously described protocols (Chung et al., 2015, PMID 26286745; Irigoyen et al., 2016, PMID 26919232), except Ribo-Zero Gold rRNA removal kit (Illumina), not DSN, was used to deplete ribosomal RNA, and a 7-nt randomized sequence was appended to the 5' end of every read during library preparation.",,,,,ERS3507025,ERP115717,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR336/004/ERR3366404,603971685,ftp.sra.ebi.ac.uk/vol1/err/ERR336/004/ERR3366404,ftp.sra.ebi.ac.uk/vol1/err/ERR336/004/ERR3366404,554a78de287cc897bffa44db782a913d,,E-MTAB-8045,Ribosome profiling of astrovirus-infected cells,,,ERA1994565,fasp.sra.ebi.ac.uk:/vol1/run/ERR336/ERR3366404/sample_1.fq.gz,667207032,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR336/ERR3366404/sample_1.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR336/ERR3366404/sample_1.fq.gz,,039da8a5bbb99b3d33645375dfdfbc6c,,,,,,,, PRJEB32969,ERX3390679,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMEA5703369,Sample 2,NextSeq 500,ERR3366405,41162069,1528126888,SAMEA5703369,,,,,,ArrayExpress,Caco-2,epithelial cell,UNIVERSITY OF CAMBRIDGE,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-8045:Sample 2_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR336/005/ERR3366405/ERR3366405.fastq.gz,925295454,ftp.sra.ebi.ac.uk/vol1/fastq/ERR336/005/ERR3366405/ERR3366405.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR336/005/ERR3366405/ERR3366405.fastq.gz,d8f50b06867b4d7dbbc7382657e9215e,2019-06-10,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2019-06-10,,SINGLE,Sample 2_s,,,,,,,,,E-MTAB-8045:Sample 2,,E-MTAB-8045:Sample 2,,"Protocols: At 12 h post infection, cells were either not treated (NT) or treated with 50 µM LTM for 30 minutes, flash frozen in a dry ice/ethanol bath, and lysed in the presence of 100 µg/ml cycloheximide. Caco2 cells were grown on 150-mm dishes to reach 80-90% confluency, then infected at a multiplicity of infection (MOI) of 5 with HAstV1 virus stock (passage 2, derived from pAVIC1 T7 RNA; Geigenmüller et al., 1997, PMID 8995706). After flash freezing, cells were transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to ribosome profiling based on previously described protocols (Chung et al., 2015, PMID 26286745; Irigoyen et al., 2016, PMID 26919232), except Ribo-Zero Gold rRNA removal kit (Illumina), not DSN, was used to deplete ribosomal RNA, and a 7-nt randomized sequence was appended to the 5' end of every read during library preparation.",,,,,ERS3507026,ERP115717,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR336/005/ERR3366405,751680236,ftp.sra.ebi.ac.uk/vol1/err/ERR336/005/ERR3366405,ftp.sra.ebi.ac.uk/vol1/err/ERR336/005/ERR3366405,5351b6afdbd5989b22c257d6d71cc6cc,,E-MTAB-8045,Ribosome profiling of astrovirus-infected cells,,,ERA1994565,fasp.sra.ebi.ac.uk:/vol1/run/ERR336/ERR3366405/sample_2.fq.gz,820290777,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR336/ERR3366405/sample_2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR336/ERR3366405/sample_2.fq.gz,,97cdef85b2cf6e650b1d1cb55228a932,,,,,,,, PRJEB32969,ERX3390680,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMEA5703370,Sample 3,NextSeq 500,ERR3366406,11238470,457167576,SAMEA5703370,,,,,,ArrayExpress,Caco-2,epithelial cell,UNIVERSITY OF CAMBRIDGE,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-8045:Sample 3_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR336/006/ERR3366406/ERR3366406.fastq.gz,260893712,ftp.sra.ebi.ac.uk/vol1/fastq/ERR336/006/ERR3366406/ERR3366406.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR336/006/ERR3366406/ERR3366406.fastq.gz,7caba38a239b8a2214d09d8272fe0372,2019-06-10,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2019-06-12,,SINGLE,Sample 3_s,,,,,,,,,E-MTAB-8045:Sample 3,,E-MTAB-8045:Sample 3,,"Protocols: At 12 h post infection, cells were either not treated (NT) or treated with 50 µM LTM for 30 minutes, flash frozen in a dry ice/ethanol bath, and lysed in the presence of 100 µg/ml cycloheximide. Caco2 cells were grown on 150-mm dishes to reach 80-90% confluency, then infected at a multiplicity of infection (MOI) of 5 with HAstV1 virus stock (passage 2, derived from pAVIC1 T7 RNA; Geigenmüller et al., 1997, PMID 8995706). After flash freezing, cells were transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to ribosome profiling based on previously described protocols (Chung et al., 2015, PMID 26286745; Irigoyen et al., 2016, PMID 26919232), except Ribo-Zero Gold rRNA removal kit (Illumina), not DSN, was used to deplete ribosomal RNA, and a 7-nt randomized sequence was appended to the 5' end of every read during library preparation.",,,,,ERS3507027,ERP115717,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR336/006/ERR3366406,228074816,ftp.sra.ebi.ac.uk/vol1/err/ERR336/006/ERR3366406,ftp.sra.ebi.ac.uk/vol1/err/ERR336/006/ERR3366406,27de7ad0109c5dfc0223e76335406b60,,E-MTAB-8045,Ribosome profiling of astrovirus-infected cells,,,ERA1994565,fasp.sra.ebi.ac.uk:/vol1/run/ERR336/ERR3366406/sample_3.fq.gz,232939713,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR336/ERR3366406/sample_3.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR336/ERR3366406/sample_3.fq.gz,,b10a49d89dc7e70793e78a1745f98f71,,,,,,,, PRJEB32969,ERX3390681,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,NextSeq 500 sequencing; Ribosome profiling of astrovirus-infected cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMEA5703371,Sample 4,NextSeq 500,ERR3366407,12881017,487714175,SAMEA5703371,,,,,,ArrayExpress,Caco-2,epithelial cell,UNIVERSITY OF CAMBRIDGE,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-8045:Sample 4_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR336/007/ERR3366407/ERR3366407.fastq.gz,294147175,ftp.sra.ebi.ac.uk/vol1/fastq/ERR336/007/ERR3366407/ERR3366407.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR336/007/ERR3366407/ERR3366407.fastq.gz,6db8739aaa260a436f3206f289da20b9,2019-06-10,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2019-06-10,,SINGLE,Sample 4_s,,,,,,,,,E-MTAB-8045:Sample 4,,E-MTAB-8045:Sample 4,,"Protocols: At 12 h post infection, cells were either not treated (NT) or treated with 50 µM LTM for 30 minutes, flash frozen in a dry ice/ethanol bath, and lysed in the presence of 100 µg/ml cycloheximide. Caco2 cells were grown on 150-mm dishes to reach 80-90% confluency, then infected at a multiplicity of infection (MOI) of 5 with HAstV1 virus stock (passage 2, derived from pAVIC1 T7 RNA; Geigenmüller et al., 1997, PMID 8995706). After flash freezing, cells were transferred to dry ice and 400 µl of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 µg/ml cycloheximide and 25 U/ml TURBO™ DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 ºC, the supernatants recovered and stored in liquid nitrogen. Cell lysates were subjected to ribosome profiling based on previously described protocols (Chung et al., 2015, PMID 26286745; Irigoyen et al., 2016, PMID 26919232), except Ribo-Zero Gold rRNA removal kit (Illumina), not DSN, was used to deplete ribosomal RNA, and a 7-nt randomized sequence was appended to the 5' end of every read during library preparation.",,,,,ERS3507028,ERP115717,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR336/007/ERR3366407,242657462,ftp.sra.ebi.ac.uk/vol1/err/ERR336/007/ERR3366407,ftp.sra.ebi.ac.uk/vol1/err/ERR336/007/ERR3366407,1330cb9e1e0cfe13d3ac037446121137,,E-MTAB-8045,Ribosome profiling of astrovirus-infected cells,,,ERA1994565,fasp.sra.ebi.ac.uk:/vol1/run/ERR336/ERR3366407/sample_4.fq.gz,262163422,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR336/ERR3366407/sample_4.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR336/ERR3366407/sample_4.fq.gz,,8b5fb045e27e46ee56f4bf2d26c9ca15,,,,,,,, PRJEB28810,ERX3772928,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426174,mouse_elongatingSpermatids_ribo_1,Illumina HiSeq 2500,ERR3771179,,,SAMEA6426174,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_elongatingSpermatids_ribo_1_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_elongatingSpermatids_ribo_1_s,,,,,,,,,E-MTAB-72471576596742:mouse_elongatingSpermatids_ribo_1,,E-MTAB-72471576596742:mouse_elongatingSpermatids_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192382,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771179/mouse_elongatingSpermatids_ribo_1.fastq.gz,4945079124,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771179/mouse_elongatingSpermatids_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771179/mouse_elongatingSpermatids_ribo_1.fastq.gz,,207370b81c3ec1afe25e53e6323da16e,male,,,,,,, PRJEB28810,ERX3772929,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426175,mouse_elongatingSpermatids_ribo_2,Illumina HiSeq 2500,ERR3771180,,,SAMEA6426175,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_elongatingSpermatids_ribo_2_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_elongatingSpermatids_ribo_2_s,,,,,,,,,E-MTAB-72471576596742:mouse_elongatingSpermatids_ribo_2,,E-MTAB-72471576596742:mouse_elongatingSpermatids_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192383,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771180/mouse_elongatingSpermatids_ribo_2.fastq.gz,2460658420,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771180/mouse_elongatingSpermatids_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771180/mouse_elongatingSpermatids_ribo_2.fastq.gz,,c275c4a6ea46d75693d884f95c393083,male,,,,,,, PRJEB28810,ERX3772930,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426176,mouse_elongatingSpermatids_rna_1,Illumina HiSeq 2500,ERR3771181,,,SAMEA6426176,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_elongatingSpermatids_rna_1_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_elongatingSpermatids_rna_1_s,,,,,,,,,E-MTAB-72471576596742:mouse_elongatingSpermatids_rna_1,,E-MTAB-72471576596742:mouse_elongatingSpermatids_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192384,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771181/mouse_elongatingSpermatids_rna_1.fastq.gz,1432001562,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771181/mouse_elongatingSpermatids_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771181/mouse_elongatingSpermatids_rna_1.fastq.gz,,bab4957319a4f6b60ac404553e1ea9f3,male,,,,,,, PRJEB28810,ERX3772931,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426177,mouse_elongatingSpermatids_rna_2,Illumina HiSeq 2500,ERR3771182,,,SAMEA6426177,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_elongatingSpermatids_rna_2_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_elongatingSpermatids_rna_2_s,,,,,,,,,E-MTAB-72471576596742:mouse_elongatingSpermatids_rna_2,,E-MTAB-72471576596742:mouse_elongatingSpermatids_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192385,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771182/mouse_elongatingSpermatids_rna_2.fastq.gz,1946601860,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771182/mouse_elongatingSpermatids_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771182/mouse_elongatingSpermatids_rna_2.fastq.gz,,e17f1bd8da27e8f2a96b7e1a57b8f213,male,,,,,,, PRJEB28810,ERX3772932,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426178,mouse_roundSpermatids_ribo_1,Illumina HiSeq 2500,ERR3771183,219656784,22185335184,SAMEA6426178,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_roundSpermatids_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR377/003/ERR3771183/ERR3771183.fastq.gz,7068142945,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/003/ERR3771183/ERR3771183.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/003/ERR3771183/ERR3771183.fastq.gz,d280265f162fb527fd019066d081b4a3,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-18,,SINGLE,mouse_roundSpermatids_ribo_1_s,,,,,,,,,E-MTAB-72471576596742:mouse_roundSpermatids_ribo_1,,E-MTAB-72471576596742:mouse_roundSpermatids_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192386,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR377/003/ERR3771183,7868488048,ftp.sra.ebi.ac.uk/vol1/err/ERR377/003/ERR3771183,ftp.sra.ebi.ac.uk/vol1/err/ERR377/003/ERR3771183,7ccadd4cf66df360d48bf0c2c063ccac,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771183/mouse_roundSpermatids_ribo_1.fastq.gz,6410856345,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771183/mouse_roundSpermatids_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771183/mouse_roundSpermatids_ribo_1.fastq.gz,,a4bf91610722d90655c26fc64d4032f4,male,,,,,,, PRJEB28810,ERX3772933,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426179,mouse_roundSpermatids_ribo_2,Illumina HiSeq 2500,ERR3771184,,,SAMEA6426179,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_roundSpermatids_ribo_2_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_roundSpermatids_ribo_2_s,,,,,,,,,E-MTAB-72471576596742:mouse_roundSpermatids_ribo_2,,E-MTAB-72471576596742:mouse_roundSpermatids_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192387,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771184/mouse_roundSpermatids_ribo_2.fastq.gz,2208923965,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771184/mouse_roundSpermatids_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771184/mouse_roundSpermatids_ribo_2.fastq.gz,,54bf64d1019e6fefece5bd496f0f7f3a,male,,,,,,, PRJEB28810,ERX3772934,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426180,mouse_roundSpermatids_rna_1,Illumina HiSeq 2500,ERR3771185,97775962,9875372162,SAMEA6426180,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_roundSpermatids_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR377/005/ERR3771185/ERR3771185.fastq.gz,3605726386,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/005/ERR3771185/ERR3771185.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/005/ERR3771185/ERR3771185.fastq.gz,120e7912e68988f03ce6e21cf823db67,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-18,,SINGLE,mouse_roundSpermatids_rna_1_s,,,,,,,,,E-MTAB-72471576596742:mouse_roundSpermatids_rna_1,,E-MTAB-72471576596742:mouse_roundSpermatids_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192388,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR377/005/ERR3771185,3388708459,ftp.sra.ebi.ac.uk/vol1/err/ERR377/005/ERR3771185,ftp.sra.ebi.ac.uk/vol1/err/ERR377/005/ERR3771185,6ed83c510ddc576907a2f457581d6370,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771185/mouse_roundSpermatids_rna_1.fastq.gz,3333755338,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771185/mouse_roundSpermatids_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771185/mouse_roundSpermatids_rna_1.fastq.gz,,f238dacb684d4ad5172ba5d07e92734e,male,,,,,,, PRJEB28810,ERX3772935,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426181,mouse_roundSpermatids_rna_2,Illumina HiSeq 2500,ERR3771186,,,SAMEA6426181,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_roundSpermatids_rna_2_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_roundSpermatids_rna_2_s,,,,,,,,,E-MTAB-72471576596742:mouse_roundSpermatids_rna_2,,E-MTAB-72471576596742:mouse_roundSpermatids_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192389,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771186/mouse_roundSpermatids_rna_2.fastq.gz,2068022407,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771186/mouse_roundSpermatids_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771186/mouse_roundSpermatids_rna_2.fastq.gz,,4fded93029eb532c4a873be64650e132,male,,,,,,, PRJEB28810,ERX3772936,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426182,mouse_spermatocytes_ribo_1,Illumina HiSeq 2500,ERR3771187,224389341,22663323441,SAMEA6426182,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_spermatocytes_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR377/007/ERR3771187/ERR3771187.fastq.gz,7204780043,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/007/ERR3771187/ERR3771187.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/007/ERR3771187/ERR3771187.fastq.gz,e5ee03741c0a872b7bbe749c358e3491,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-18,,SINGLE,mouse_spermatocytes_ribo_1_s,,,,,,,,,E-MTAB-72471576596742:mouse_spermatocytes_ribo_1,,E-MTAB-72471576596742:mouse_spermatocytes_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192390,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR377/007/ERR3771187,8018612104,ftp.sra.ebi.ac.uk/vol1/err/ERR377/007/ERR3771187,ftp.sra.ebi.ac.uk/vol1/err/ERR377/007/ERR3771187,fe8c8197590f2864aa339c55cd4dbf40,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771187/mouse_spermatocytes_ribo_1.fastq.gz,6540180454,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771187/mouse_spermatocytes_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771187/mouse_spermatocytes_ribo_1.fastq.gz,,c4e42002840611adcacda320c3eb3158,male,,,,,,, PRJEB28810,ERX3772937,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426183,mouse_spermatocytes_ribo_2,Illumina HiSeq 2500,ERR3771188,,,SAMEA6426183,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_spermatocytes_ribo_2_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_spermatocytes_ribo_2_s,,,,,,,,,E-MTAB-72471576596742:mouse_spermatocytes_ribo_2,,E-MTAB-72471576596742:mouse_spermatocytes_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192391,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771188/mouse_spermatocytes_ribo_2.fastq.gz,2521915470,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771188/mouse_spermatocytes_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771188/mouse_spermatocytes_ribo_2.fastq.gz,,001951bf30e1920c738019531e877b90,male,,,,,,, PRJEB28810,ERX3772938,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426184,mouse_spermatocytes_rna_1,Illumina HiSeq 2500,ERR3771189,89103148,8999417948,SAMEA6426184,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_spermatocytes_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR377/009/ERR3771189/ERR3771189.fastq.gz,3247380014,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/009/ERR3771189/ERR3771189.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/009/ERR3771189/ERR3771189.fastq.gz,2681e5fcb9e47d624c44ba99a2251a3f,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-18,,SINGLE,mouse_spermatocytes_rna_1_s,,,,,,,,,E-MTAB-72471576596742:mouse_spermatocytes_rna_1,,E-MTAB-72471576596742:mouse_spermatocytes_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192392,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR377/009/ERR3771189,3107846817,ftp.sra.ebi.ac.uk/vol1/err/ERR377/009/ERR3771189,ftp.sra.ebi.ac.uk/vol1/err/ERR377/009/ERR3771189,6f8c5c750cb8f182a8cb40c54438844b,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771189/mouse_spermatocytes_rna_1.fastq.gz,2996860977,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771189/mouse_spermatocytes_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771189/mouse_spermatocytes_rna_1.fastq.gz,,49397cf545b63bf75cfdd7051fed315d,male,,,,,,, PRJEB28810,ERX3772939,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426185,mouse_spermatocytes_rna_2,Illumina HiSeq 2500,ERR3771190,,,SAMEA6426185,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_spermatocytes_rna_2_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_spermatocytes_rna_2_s,,,,,,,,,E-MTAB-72471576596742:mouse_spermatocytes_rna_2,,E-MTAB-72471576596742:mouse_spermatocytes_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192393,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771190/mouse_spermatocytes_rna_2.fastq.gz,2054935533,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771190/mouse_spermatocytes_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771190/mouse_spermatocytes_rna_2.fastq.gz,,f9734e7ae08b0714851dc4f0d9336af3,male,,,,,,, PRJEB28810,ERX3772940,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426186,mouse_spermatozoa_ribo_1,Illumina HiSeq 2500,ERR3771191,294527983,15020927133,SAMEA6426186,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_spermatozoa_ribo_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR377/001/ERR3771191/ERR3771191.fastq.gz,7434352070,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/001/ERR3771191/ERR3771191.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/001/ERR3771191/ERR3771191.fastq.gz,52905968bc59a16dcb92250188946124,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-18,,SINGLE,mouse_spermatozoa_ribo_1_s,,,,,,,,,E-MTAB-72471576596742:mouse_spermatozoa_ribo_1,,E-MTAB-72471576596742:mouse_spermatozoa_ribo_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192394,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR377/001/ERR3771191,6187674143,ftp.sra.ebi.ac.uk/vol1/err/ERR377/001/ERR3771191,ftp.sra.ebi.ac.uk/vol1/err/ERR377/001/ERR3771191,06727d2b7de9a7bbc470c46cf1218792,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771191/mouse_spermatozoa_ribo_1.fastq.gz,6697001707,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771191/mouse_spermatozoa_ribo_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771191/mouse_spermatozoa_ribo_1.fastq.gz,,98a3141b4cac886aa69e9e3cdf3f361f,male,,,,,,, PRJEB28810,ERX3772941,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426187,mouse_spermatozoa_ribo_2,Illumina HiSeq 2500,ERR3771192,,,SAMEA6426187,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_spermatozoa_ribo_2_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_spermatozoa_ribo_2_s,,,,,,,,,E-MTAB-72471576596742:mouse_spermatozoa_ribo_2,,E-MTAB-72471576596742:mouse_spermatozoa_ribo_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192395,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771192/mouse_spermatozoa_ribo_2.fastq.gz,5151230879,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771192/mouse_spermatozoa_ribo_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771192/mouse_spermatozoa_ribo_2.fastq.gz,,c245750e15c9b4b974d7a4fa8ef5358e,male,,,,,,, PRJEB28810,ERX3772942,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426188,mouse_spermatozoa_rna_1,Illumina HiSeq 2500,ERR3771193,70036428,3571857828,SAMEA6426188,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_spermatozoa_rna_1_s,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR377/003/ERR3771193/ERR3771193.fastq.gz,2081118967,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/003/ERR3771193/ERR3771193.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR377/003/ERR3771193/ERR3771193.fastq.gz,bacac7fdefbd061a1f1e4803102e3ecd,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-18,,SINGLE,mouse_spermatozoa_rna_1_s,,,,,,,,,E-MTAB-72471576596742:mouse_spermatozoa_rna_1,,E-MTAB-72471576596742:mouse_spermatozoa_rna_1,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192396,ERP111066,,,,male,,fasp.sra.ebi.ac.uk:/vol1/err/ERR377/003/ERR3771193,1475915853,ftp.sra.ebi.ac.uk/vol1/err/ERR377/003/ERR3771193,ftp.sra.ebi.ac.uk/vol1/err/ERR377/003/ERR3771193,0990d2c124f470e889b47bb288b3217e,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771193/mouse_spermatozoa_rna_1.fastq.gz,1884521429,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771193/mouse_spermatozoa_rna_1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771193/mouse_spermatozoa_rna_1.fastq.gz,,13761b226c414c97b288609c8b711ebd,male,,,,,,, PRJEB28810,ERX3772943,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,Illumina HiSeq 2500 sequencing; Using ribosome profiling and matched RNA sequencing to study the co-evolution of transcriptome and translatome in mammalian organs,10090,Mus musculus,ssRNA-seq,TRANSCRIPTOMIC,Inverse rRNA,SAMEA6426189,mouse_spermatozoa_rna_2,Illumina HiSeq 2500,ERR3771194,,,SAMEA6426189,,,,,,ArrayExpress,,,"Center for Molecular Biology (ZMBH), Heidelberg University",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-72471576596742:mouse_spermatozoa_rna_2_s,,,,,,,2019-12-17,2019-12-18,false,,,,,,,,,,,ILLUMINA,,,,2019-12-17,,SINGLE,mouse_spermatozoa_rna_2_s,,,,,,,,,E-MTAB-72471576596742:mouse_spermatozoa_rna_2,,E-MTAB-72471576596742:mouse_spermatozoa_rna_2,,"Protocols: We generated Ribo-seq and matched RNA-seq data for the following samples: brain (cerebrum), liver, and testis samples from human (Homo sapiens), rhesus macaque (Macaca mulatta), mouse (Mus musculus, strain: CD-1, RjOrl:SWISS), grey short-tailed opossum (Monodelphis domestica), platypus (Ornithorhynchus anatinus), and chicken (red junglefowl, Gallus gallus). Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). The Ingolia 2012 protocol has been implemented in the TruSeq Ribo Profile (Mammalian) Library Prep Kit (Illumina) (formerly ARTseq), which was used in our study",,,,,ERS4192397,ERP111066,,,,male,,,,,,,,E-MTAB-7247,Using ribosome profiling and matched RNA sequencing to study the evolution of gene expression levels in mammalian organs across two major gene expression layers,,,ERA2322814,fasp.sra.ebi.ac.uk:/vol1/run/ERR377/ERR3771194/mouse_spermatozoa_rna_2.fastq.gz,1765033139,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771194/mouse_spermatozoa_rna_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR377/ERR3771194/mouse_spermatozoa_rna_2.fastq.gz,,efb5244fdcf1b79b7de88d49c319a226,male,,,,,,, PRJEB5285,ERX385549,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341082,HeLa_Unk+Gfp_overexpression_replicate_1,Illumina HiSeq 2000,ERR419248,21602660,1101735660,SAMEA2341082,,,,,,ArrayExpress,HeLa,,"EBML EBI, Wellcome Trust Genome Campus, Hinxton, CB10 1SD",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2278:HeLa Unk + Gfp Expression Extract 1,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR419/ERR419248/ERR419248.fastq.gz,774149963,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419248/ERR419248.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419248/ERR419248.fastq.gz,109c08293332dfb48c04bc8824606551,2014-01-30,2015-03-09,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,HeLa Unk + Gfp Expression Extract 1,,,,,,,,,E-MTAB-2278:Sample_Lane2_HeLa_4.R1.fastq.gz,,E-MTAB-2278:HeLa_Unk+Gfp_overexpression_replicate_1,,"Protocols: HeLa cells were grown in Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum, 100 U/mL penicillin, and 100 micro-g/mL streptomycin at 37 degrees C and 5% CO2. To create Dox-inducible cell lines, we first transduced HeLa cells with MSCV-rtTA3-IRES-EcoR-PGK-Neo (pRIEN), a retrovirus we constructed in the MSCV backbone (Clontech) to co-express an improved reverse transactivator (rtTA3), the ecotropic receptor, and a neomycin resistance marker. Following G418 selection, stably rtTA3-expressing cells were subsequently infected ecotropically with a second retrovirus expressing a puromycin resistance gene and a TREtight-driven transcript encoding GFP alone (pTt-IGPP) or GFP and either full-length mouse or zebrafish Unkempt protein, or any of the mouse Unkempt-deletion mutants (pTtight-X-IGPP, where X is an ortholog or mutant of Unkempt), which we constructed in a self-inactivating retroviral backbone (pQCXIX, Clontech). To induce transgene expression, double-selected cells were treated with doxycycline (Sigma-Aldrich) at 1 micro-g/ml. To determine the effect of Unkempt on the rate of protein synthesis, we performed ribosome profiling experiment on inducible HeLa cells essentially as described (Ingolia et al., Nature Protocols, 2012), but using the linker and the primers as for the iCLIP experiments (Konig et al., JoVE, 2011). GFP-only or GFP and Unkempt-inducible Hela cells were grown in 15 cm dishes and harvested at 70% confluency. Prio",,,,,ERS398753,ERP004683,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR419/ERR419248,685512833,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419248,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419248,7bcf725d77c6447a8e5d436ab2191e1b,,E-MTAB-2278,Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,,,ERA282985,fasp.sra.ebi.ac.uk:/vol1/run/ERR419/ERR419248/Sample_Lane2_HeLa_4.R1.fastq.gz,707680324,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419248/Sample_Lane2_HeLa_4.R1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419248/Sample_Lane2_HeLa_4.R1.fastq.gz,,f220ce0f98eb07eb87bb3a29410b1a23,,,,,,,, PRJEB5285,ERX385547,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341080,HeLa_Gfp_expression_control_replicate_1,Illumina HiSeq 2000,ERR419249,26065903,1329361053,SAMEA2341080,,,,,,ArrayExpress,HeLa,,"EBML EBI, Wellcome Trust Genome Campus, Hinxton, CB10 1SD",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2278:HeLa Gfp Expression Control Extract 1,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR419/ERR419249/ERR419249.fastq.gz,948466776,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419249/ERR419249.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419249/ERR419249.fastq.gz,ce9626a00d8007bcdcb063379a2a7f9f,2014-01-30,2015-03-09,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,HeLa Gfp Expression Control Extract 1,,,,,,,,,E-MTAB-2278:Sample_Lane2_HeLa_1.R1.fastq.gz,,E-MTAB-2278:HeLa_Gfp_expression_control_replicate_1,,"Protocols: HeLa cells were grown in Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum, 100 U/mL penicillin, and 100 micro-g/mL streptomycin at 37 degrees C and 5% CO2. To create Dox-inducible cell lines, we first transduced HeLa cells with MSCV-rtTA3-IRES-EcoR-PGK-Neo (pRIEN), a retrovirus we constructed in the MSCV backbone (Clontech) to co-express an improved reverse transactivator (rtTA3), the ecotropic receptor, and a neomycin resistance marker. Following G418 selection, stably rtTA3-expressing cells were subsequently infected ecotropically with a second retrovirus expressing a puromycin resistance gene and a TREtight-driven transcript encoding GFP alone (pTt-IGPP) or GFP and either full-length mouse or zebrafish Unkempt protein, or any of the mouse Unkempt-deletion mutants (pTtight-X-IGPP, where X is an ortholog or mutant of Unkempt), which we constructed in a self-inactivating retroviral backbone (pQCXIX, Clontech). To induce transgene expression, double-selected cells were treated with doxycycline (Sigma-Aldrich) at 1 micro-g/ml. To determine the effect of Unkempt on the rate of protein synthesis, we performed ribosome profiling experiment on inducible HeLa cells essentially as described (Ingolia et al., Nature Protocols, 2012), but using the linker and the primers as for the iCLIP experiments (Konig et al., JoVE, 2011). GFP-only or GFP and Unkempt-inducible Hela cells were grown in 15 cm dishes and harvested at 70% confluency. Prio",,,,,ERS398751,ERP004683,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR419/ERR419249,839982008,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419249,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419249,5705bbfe3ca2e50cb082a098779cc44b,,E-MTAB-2278,Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,,,ERA282985,fasp.sra.ebi.ac.uk:/vol1/run/ERR419/ERR419249/Sample_Lane2_HeLa_1.R1.fastq.gz,867824789,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419249/Sample_Lane2_HeLa_1.R1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419249/Sample_Lane2_HeLa_1.R1.fastq.gz,,c8eb8ffd1dddf76c58754c7384aecf28,,,,,,,, PRJEB5285,ERX385548,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341081,HeLa_Unk+Gfp_overexpression_replicate_3,Illumina HiSeq 2000,ERR419250,21264420,1084485420,SAMEA2341081,,,,,,ArrayExpress,HeLa,,"EBML EBI, Wellcome Trust Genome Campus, Hinxton, CB10 1SD",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2278:HeLa Unk + Gfp Expression Extract 3,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR419/ERR419250/ERR419250.fastq.gz,797138716,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419250/ERR419250.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419250/ERR419250.fastq.gz,701f3fc18e621555a522155289e7528d,2014-01-30,2015-03-09,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,HeLa Unk + Gfp Expression Extract 3,,,,,,,,,E-MTAB-2278:Sample_Lane2_HeLa_6.R1.fastq.gz,,E-MTAB-2278:HeLa_Unk+Gfp_overexpression_replicate_3,,"Protocols: HeLa cells were grown in Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum, 100 U/mL penicillin, and 100 micro-g/mL streptomycin at 37 degrees C and 5% CO2. To create Dox-inducible cell lines, we first transduced HeLa cells with MSCV-rtTA3-IRES-EcoR-PGK-Neo (pRIEN), a retrovirus we constructed in the MSCV backbone (Clontech) to co-express an improved reverse transactivator (rtTA3), the ecotropic receptor, and a neomycin resistance marker. Following G418 selection, stably rtTA3-expressing cells were subsequently infected ecotropically with a second retrovirus expressing a puromycin resistance gene and a TREtight-driven transcript encoding GFP alone (pTt-IGPP) or GFP and either full-length mouse or zebrafish Unkempt protein, or any of the mouse Unkempt-deletion mutants (pTtight-X-IGPP, where X is an ortholog or mutant of Unkempt), which we constructed in a self-inactivating retroviral backbone (pQCXIX, Clontech). To induce transgene expression, double-selected cells were treated with doxycycline (Sigma-Aldrich) at 1 micro-g/ml. To determine the effect of Unkempt on the rate of protein synthesis, we performed ribosome profiling experiment on inducible HeLa cells essentially as described (Ingolia et al., Nature Protocols, 2012), but using the linker and the primers as for the iCLIP experiments (Konig et al., JoVE, 2011). GFP-only or GFP and Unkempt-inducible Hela cells were grown in 15 cm dishes and harvested at 70% confluency. Prio",,,,,ERS398752,ERP004683,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR419/ERR419250,703520252,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419250,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419250,81ba2e27c8dacb66b76119b2c1a1cddb,,E-MTAB-2278,Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,,,ERA282985,fasp.sra.ebi.ac.uk:/vol1/run/ERR419/ERR419250/Sample_Lane2_HeLa_6.R1.fastq.gz,731576861,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419250/Sample_Lane2_HeLa_6.R1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419250/Sample_Lane2_HeLa_6.R1.fastq.gz,,bfdcc0eb18c58efd5bd8806f63400f3f,,,,,,,, PRJEB5285,ERX385545,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341078,HeLa_Unk+Gfp_overexpression_replicate_2,Illumina HiSeq 2000,ERR419251,21619019,1102569969,SAMEA2341078,,,,,,ArrayExpress,HeLa,,"EBML EBI, Wellcome Trust Genome Campus, Hinxton, CB10 1SD",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2278:HeLa Unk + Gfp Expression Extract 2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR419/ERR419251/ERR419251.fastq.gz,783598217,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419251/ERR419251.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419251/ERR419251.fastq.gz,cdf38be632b114b90442b6bd9de64bd8,2014-01-30,2015-03-09,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,HeLa Unk + Gfp Expression Extract 2,,,,,,,,,E-MTAB-2278:Sample_Lane2_HeLa_5.R1.fastq.gz,,E-MTAB-2278:HeLa_Unk+Gfp_overexpression_replicate_2,,"Protocols: HeLa cells were grown in Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum, 100 U/mL penicillin, and 100 micro-g/mL streptomycin at 37 degrees C and 5% CO2. To create Dox-inducible cell lines, we first transduced HeLa cells with MSCV-rtTA3-IRES-EcoR-PGK-Neo (pRIEN), a retrovirus we constructed in the MSCV backbone (Clontech) to co-express an improved reverse transactivator (rtTA3), the ecotropic receptor, and a neomycin resistance marker. Following G418 selection, stably rtTA3-expressing cells were subsequently infected ecotropically with a second retrovirus expressing a puromycin resistance gene and a TREtight-driven transcript encoding GFP alone (pTt-IGPP) or GFP and either full-length mouse or zebrafish Unkempt protein, or any of the mouse Unkempt-deletion mutants (pTtight-X-IGPP, where X is an ortholog or mutant of Unkempt), which we constructed in a self-inactivating retroviral backbone (pQCXIX, Clontech). To induce transgene expression, double-selected cells were treated with doxycycline (Sigma-Aldrich) at 1 micro-g/ml. To determine the effect of Unkempt on the rate of protein synthesis, we performed ribosome profiling experiment on inducible HeLa cells essentially as described (Ingolia et al., Nature Protocols, 2012), but using the linker and the primers as for the iCLIP experiments (Konig et al., JoVE, 2011). GFP-only or GFP and Unkempt-inducible Hela cells were grown in 15 cm dishes and harvested at 70% confluency. Prio",,,,,ERS398749,ERP004683,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR419/ERR419251,693516137,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419251,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419251,027837c93d17055e13cf7a948b467fce,,E-MTAB-2278,Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,,,ERA282985,fasp.sra.ebi.ac.uk:/vol1/run/ERR419/ERR419251/Sample_Lane2_HeLa_5.R1.fastq.gz,717300581,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419251/Sample_Lane2_HeLa_5.R1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419251/Sample_Lane2_HeLa_5.R1.fastq.gz,,1bf447ab0a24f762c8ed4a8d3348eb5a,,,,,,,, PRJEB5285,ERX385546,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,Illumina HiSeq 2000 sequencing; Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA2341079,HeLa_Gfp_expression_control_replicate_2,Illumina HiSeq 2000,ERR419252,21819011,1112769561,SAMEA2341079,,,,,,ArrayExpress,HeLa,,"EBML EBI, Wellcome Trust Genome Campus, Hinxton, CB10 1SD",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2278:HeLa Gfp Expression Control Extract 2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR419/ERR419252/ERR419252.fastq.gz,782923170,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419252/ERR419252.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR419/ERR419252/ERR419252.fastq.gz,35022cf217e2de312b6c97437b70dde6,2014-01-30,2015-03-09,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,HeLa Gfp Expression Control Extract 2,,,,,,,,,E-MTAB-2278:Sample_Lane2_HeLa_2.R1.fastq.gz,,E-MTAB-2278:HeLa_Gfp_expression_control_replicate_2,,"Protocols: HeLa cells were grown in Dulbecco's Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum, 100 U/mL penicillin, and 100 micro-g/mL streptomycin at 37 degrees C and 5% CO2. To create Dox-inducible cell lines, we first transduced HeLa cells with MSCV-rtTA3-IRES-EcoR-PGK-Neo (pRIEN), a retrovirus we constructed in the MSCV backbone (Clontech) to co-express an improved reverse transactivator (rtTA3), the ecotropic receptor, and a neomycin resistance marker. Following G418 selection, stably rtTA3-expressing cells were subsequently infected ecotropically with a second retrovirus expressing a puromycin resistance gene and a TREtight-driven transcript encoding GFP alone (pTt-IGPP) or GFP and either full-length mouse or zebrafish Unkempt protein, or any of the mouse Unkempt-deletion mutants (pTtight-X-IGPP, where X is an ortholog or mutant of Unkempt), which we constructed in a self-inactivating retroviral backbone (pQCXIX, Clontech). To induce transgene expression, double-selected cells were treated with doxycycline (Sigma-Aldrich) at 1 micro-g/ml. To determine the effect of Unkempt on the rate of protein synthesis, we performed ribosome profiling experiment on inducible HeLa cells essentially as described (Ingolia et al., Nature Protocols, 2012), but using the linker and the primers as for the iCLIP experiments (Konig et al., JoVE, 2011). GFP-only or GFP and Unkempt-inducible Hela cells were grown in 15 cm dishes and harvested at 70% confluency. Prio",,,,,ERS398750,ERP004683,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR419/ERR419252,709569620,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419252,ftp.sra.ebi.ac.uk/vol1/err/ERR419/ERR419252,b09bb96cd6ba5a83161199b39b6992f2,,E-MTAB-2278,Ribosome profiling upon overexpression of the RNA-binding protein Unkempt,,,ERA282985,fasp.sra.ebi.ac.uk:/vol1/run/ERR419/ERR419252/Sample_Lane2_HeLa_2.R1.fastq.gz,715340567,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419252/Sample_Lane2_HeLa_2.R1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR419/ERR419252/Sample_Lane2_HeLa_2.R1.fastq.gz,,85b0ece6dbd02547d9309479bce09814,,,,,,,, PRJEB5938,ERX432361,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,7227,Drosophila melanogaster,OTHER,OTHER,other,SAMEA2421582,Kc167_RNaseI,Illumina Genome Analyzer IIx,ERR466122,54573979,2279364497,SAMEA2421582,,,,,,ArrayExpress,Kc167,,DUNDEE,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2421:assay 3,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR466/ERR466122/ERR466122.fastq.gz,1971631218,ftp.sra.ebi.ac.uk/vol1/fastq/ERR466/ERR466122/ERR466122.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR466/ERR466122/ERR466122.fastq.gz,1af2af1b063a303bf2ab7516489015e4,2014-03-20,2015-01-09,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Extract 3,,,,,,,,,E-MTAB-2421:Kc167_RNaseI.fq.gz,,E-MTAB-2421:Kc167_RNaseI,,"Protocols: Cells were cultured in the presence of 10% FBS in DMEM (U2OS cells) or in Schneider's medium (Kc167 cells). Both cell types were stimulated with 10 % extra FBS for 1h followed by 250 uM cycloheximide for 10 min. Cells were rinsed twice with cold PBS and lysed in 1 ml polysome extraction buffer (1 % deoxycholate, 1 % NP40, 10 mM HEPES (pH 7.4), 350 mM KCl, 5 mM MgCl2, 5 mM CaCl2, 250 uM cycloheximide, 1x protease inhibitors (Sigma, P8340) and 2 ul RiboLock RNase inhibitor (ThermoFisher). Lysates were centrifuged for 10 min at 16000 xg and supernatant (leaving lowest ~25% behind) was used for ribosome profiling.The lysate samples were split in to two different digestion samples and digested with either 200 U of E. coli MBP-RNAse I (New England BioLabs) or 100 U of MN (ThermoFisher) by incubating for 40 min (U2OS) or 60 min (Kc167) at RT with slow mixing. 2 U of DNase I (ThermoFisher) was also added to each U2OS sample at the start of digestion. MN reaction was stopped with 10 mM EGTA. The samples were centrifuged at 6000 xg for 5 min to pellet insoluble material. The ribosomes were separated by sucrose step centrifugation using 0.5 M sucrose in polysome extraction buffer supplied with SUPERase-In (1/500) (Ambion). 0.35 ml lysate was layered on top of 0.2 ml sucrose cushion and centrifuged at 100000 xg for 45 min (55000 rpm using TLA 120.1 rotor). Supernatant was removed and pellet was suspended in 600 ul Qiazol reagent (Qiagen). Samples were incubated for 15 mi",,,,,ERS426770,ERP005378,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR466/ERR466122,1692684072,ftp.sra.ebi.ac.uk/vol1/err/ERR466/ERR466122,ftp.sra.ebi.ac.uk/vol1/err/ERR466/ERR466122,794e77079b295c2aa2e9f375e9276320,,E-MTAB-2421,Ribosome profiling with MN and RNaseI,,,ERA295459,fasp.sra.ebi.ac.uk:/vol1/run/ERR466/ERR466122/Kc167_RNaseI.fq.gz,1980417581,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR466/ERR466122/Kc167_RNaseI.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR466/ERR466122/Kc167_RNaseI.fq.gz,,3e5ba48357afc408b65c809789443c73,female,,,,,,, PRJEB5938,ERX432358,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,7227,Drosophila melanogaster,OTHER,OTHER,other,SAMEA2421579,Kc167_MN,Illumina Genome Analyzer IIx,ERR466123,45195752,1873531552,SAMEA2421579,,,,,,ArrayExpress,Kc167,,DUNDEE,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2421:assay 4,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR466/ERR466123/ERR466123.fastq.gz,1655958568,ftp.sra.ebi.ac.uk/vol1/fastq/ERR466/ERR466123/ERR466123.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR466/ERR466123/ERR466123.fastq.gz,1329ea0798d94e567a8ce54af451fc8f,2014-03-20,2015-01-09,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Extract 4,,,,,,,,,E-MTAB-2421:Kc167_MN.fq.gz,,E-MTAB-2421:Kc167_MN,,"Protocols: Cells were cultured in the presence of 10% FBS in DMEM (U2OS cells) or in Schneider's medium (Kc167 cells). Both cell types were stimulated with 10 % extra FBS for 1h followed by 250 uM cycloheximide for 10 min. Cells were rinsed twice with cold PBS and lysed in 1 ml polysome extraction buffer (1 % deoxycholate, 1 % NP40, 10 mM HEPES (pH 7.4), 350 mM KCl, 5 mM MgCl2, 5 mM CaCl2, 250 uM cycloheximide, 1x protease inhibitors (Sigma, P8340) and 2 ul RiboLock RNase inhibitor (ThermoFisher). Lysates were centrifuged for 10 min at 16000 xg and supernatant (leaving lowest ~25% behind) was used for ribosome profiling.The lysate samples were split in to two different digestion samples and digested with either 200 U of E. coli MBP-RNAse I (New England BioLabs) or 100 U of MN (ThermoFisher) by incubating for 40 min (U2OS) or 60 min (Kc167) at RT with slow mixing. 2 U of DNase I (ThermoFisher) was also added to each U2OS sample at the start of digestion. MN reaction was stopped with 10 mM EGTA. The samples were centrifuged at 6000 xg for 5 min to pellet insoluble material. The ribosomes were separated by sucrose step centrifugation using 0.5 M sucrose in polysome extraction buffer supplied with SUPERase-In (1/500) (Ambion). 0.35 ml lysate was layered on top of 0.2 ml sucrose cushion and centrifuged at 100000 xg for 45 min (55000 rpm using TLA 120.1 rotor). Supernatant was removed and pellet was suspended in 600 ul Qiazol reagent (Qiagen). Samples were incubated for 15 mi",,,,,ERS426767,ERP005378,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR466/ERR466123,1399623938,ftp.sra.ebi.ac.uk/vol1/err/ERR466/ERR466123,ftp.sra.ebi.ac.uk/vol1/err/ERR466/ERR466123,07e5725a7732177f96bfb220a640f452,,E-MTAB-2421,Ribosome profiling with MN and RNaseI,,,ERA295459,fasp.sra.ebi.ac.uk:/vol1/run/ERR466/ERR466123/Kc167_MN.fq.gz,1661615087,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR466/ERR466123/Kc167_MN.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR466/ERR466123/Kc167_MN.fq.gz,,273ae614b762cfde37fac5b9883b6320,female,,,,,,, PRJEB5938,ERX432359,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,9606,Homo sapiens,OTHER,OTHER,other,SAMEA2421580,U2OS_MN,Illumina Genome Analyzer IIx,ERR466124,44727293,1852579997,SAMEA2421580,,,,,,ArrayExpress,U2OS,,DUNDEE,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2421:assay 2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR466/ERR466124/ERR466124.fastq.gz,1883825708,ftp.sra.ebi.ac.uk/vol1/fastq/ERR466/ERR466124/ERR466124.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR466/ERR466124/ERR466124.fastq.gz,df4cd7ce98098199559d31745da3182a,2014-03-20,2015-01-09,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Extract 2,,,,,,,,,E-MTAB-2421:U2OS_MN.fq.gz,,E-MTAB-2421:U2OS_MN,,"Protocols: Cells were cultured in the presence of 10% FBS in DMEM (U2OS cells) or in Schneider's medium (Kc167 cells). Both cell types were stimulated with 10 % extra FBS for 1h followed by 250 uM cycloheximide for 10 min. Cells were rinsed twice with cold PBS and lysed in 1 ml polysome extraction buffer (1 % deoxycholate, 1 % NP40, 10 mM HEPES (pH 7.4), 350 mM KCl, 5 mM MgCl2, 5 mM CaCl2, 250 uM cycloheximide, 1x protease inhibitors (Sigma, P8340) and 2 ul RiboLock RNase inhibitor (ThermoFisher). Lysates were centrifuged for 10 min at 16000 xg and supernatant (leaving lowest ~25% behind) was used for ribosome profiling.The lysate samples were split in to two different digestion samples and digested with either 200 U of E. coli MBP-RNAse I (New England BioLabs) or 100 U of MN (ThermoFisher) by incubating for 40 min (U2OS) or 60 min (Kc167) at RT with slow mixing. 2 U of DNase I (ThermoFisher) was also added to each U2OS sample at the start of digestion. MN reaction was stopped with 10 mM EGTA. The samples were centrifuged at 6000 xg for 5 min to pellet insoluble material. The ribosomes were separated by sucrose step centrifugation using 0.5 M sucrose in polysome extraction buffer supplied with SUPERase-In (1/500) (Ambion). 0.35 ml lysate was layered on top of 0.2 ml sucrose cushion and centrifuged at 100000 xg for 45 min (55000 rpm using TLA 120.1 rotor). Supernatant was removed and pellet was suspended in 600 ul Qiazol reagent (Qiagen). Samples were incubated for 15 mi",,,,,ERS426768,ERP005378,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR466/ERR466124,1426693539,ftp.sra.ebi.ac.uk/vol1/err/ERR466/ERR466124,ftp.sra.ebi.ac.uk/vol1/err/ERR466/ERR466124,b3254a63309f86ee507e84852961cba3,,E-MTAB-2421,Ribosome profiling with MN and RNaseI,,,ERA295459,fasp.sra.ebi.ac.uk:/vol1/run/ERR466/ERR466124/U2OS_MN.fq.gz,1892273229,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR466/ERR466124/U2OS_MN.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR466/ERR466124/U2OS_MN.fq.gz,,d36eb7b3e55a745b78ea03556aa1153d,female,,,,,,, PRJEB5938,ERX432360,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,Illumina Genome Analyzer IIx sequencing; Ribosome profiling with MN and RNaseI,9606,Homo sapiens,OTHER,OTHER,other,SAMEA2421581,U2OS_RNaseI,Illumina Genome Analyzer IIx,ERR466125,41623326,1799245747,SAMEA2421581,,,,,,ArrayExpress,U2OS,,DUNDEE,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2421:assay 1,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR466/ERR466125/ERR466125.fastq.gz,1756121428,ftp.sra.ebi.ac.uk/vol1/fastq/ERR466/ERR466125/ERR466125.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR466/ERR466125/ERR466125.fastq.gz,6305d9d2ef7921db572d09f54e791dc0,2014-03-20,2015-01-09,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Extract 1,,,,,,,,,E-MTAB-2421:U2OS_RNAseI.fq.gz,,E-MTAB-2421:U2OS_RNaseI,,"Protocols: Cells were cultured in the presence of 10% FBS in DMEM (U2OS cells) or in Schneider's medium (Kc167 cells). Both cell types were stimulated with 10 % extra FBS for 1h followed by 250 uM cycloheximide for 10 min. Cells were rinsed twice with cold PBS and lysed in 1 ml polysome extraction buffer (1 % deoxycholate, 1 % NP40, 10 mM HEPES (pH 7.4), 350 mM KCl, 5 mM MgCl2, 5 mM CaCl2, 250 uM cycloheximide, 1x protease inhibitors (Sigma, P8340) and 2 ul RiboLock RNase inhibitor (ThermoFisher). Lysates were centrifuged for 10 min at 16000 xg and supernatant (leaving lowest ~25% behind) was used for ribosome profiling.The lysate samples were split in to two different digestion samples and digested with either 200 U of E. coli MBP-RNAse I (New England BioLabs) or 100 U of MN (ThermoFisher) by incubating for 40 min (U2OS) or 60 min (Kc167) at RT with slow mixing. 2 U of DNase I (ThermoFisher) was also added to each U2OS sample at the start of digestion. MN reaction was stopped with 10 mM EGTA. The samples were centrifuged at 6000 xg for 5 min to pellet insoluble material. The ribosomes were separated by sucrose step centrifugation using 0.5 M sucrose in polysome extraction buffer supplied with SUPERase-In (1/500) (Ambion). 0.35 ml lysate was layered on top of 0.2 ml sucrose cushion and centrifuged at 100000 xg for 45 min (55000 rpm using TLA 120.1 rotor). Supernatant was removed and pellet was suspended in 600 ul Qiazol reagent (Qiagen). Samples were incubated for 15 mi",,,,,ERS426769,ERP005378,,,,female,,fasp.sra.ebi.ac.uk:/vol1/err/ERR466/ERR466125,1388122026,ftp.sra.ebi.ac.uk/vol1/err/ERR466/ERR466125,ftp.sra.ebi.ac.uk/vol1/err/ERR466/ERR466125,d6017ed83b5e8191a33293868222c3f4,,E-MTAB-2421,Ribosome profiling with MN and RNaseI,,,ERA295459,fasp.sra.ebi.ac.uk:/vol1/run/ERR466/ERR466125/U2OS_RNAseI.fq.gz,1761193738,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR466/ERR466125/U2OS_RNAseI.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR466/ERR466125/U2OS_RNAseI.fq.gz,,7171a541a48f733eb5579f3cd89062e8,female,,,,,,, PRJEB7261,ERX556151,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,246196,Mycolicibacterium smegmatis MC2 155,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2766082,smeg RNA-seq rep1,Illumina HiSeq 2500,ERR599189,89004821,4539245871,SAMEA2766082,,,,,,ArrayExpress,,,"Wadsworth Center, New York State of Health",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2929:smeg RNA-seq rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR599/ERR599189/ERR599189.fastq.gz,3141004216,ftp.sra.ebi.ac.uk/vol1/fastq/ERR599/ERR599189/ERR599189.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR599/ERR599189/ERR599189.fastq.gz,5938dce924809007a05335b77c9ffe29,2014-09-12,2014-12-31,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,smeg RNA-seq rep1,,,,,,,,,E-MTAB-2929:Myco-F_NoIndex_L002_R1_001.fastq.gz,,E-MTAB-2929:smeg RNA-seq rep1,,"Protocols: 200 ml 7H9 medium was inoculated with 2.0 ml of overnight MC2 155 culture, and grew at 37 degrees C to an OD600 of ~1.0. The cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 ug/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.7 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. The pulverized cell powder was extracted with acid phenol and chloroform followed by isopropanol precipitation. 16S and 23S ribosomal RNAs were removed by subtractive hybridization using an Epicentre Ribo-Zero Magnetic kit following manufacturer's manual. The enriched mRNAs were randomly fragmented as described (Oh et al. 2011) The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel purification was performed for size selection of ~28nt RNA fragments. Approximately 25-30 nt poly-A tails were added to recovered RNA fragments with an Ambion poly(A) tailing kit (Life Technologies) following the manufacturer's guide. The polyadenylated RNA samples were reverse transcribed using",,,,,ERS542795,ERP006965,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR599/ERR599189,2714543152,ftp.sra.ebi.ac.uk/vol1/err/ERR599/ERR599189,ftp.sra.ebi.ac.uk/vol1/err/ERR599/ERR599189,f4d43591631a189399986c274eb4b188,,E-MTAB-2929,Ribosome Profiling of Mycobacterium smegmatis,,,ERA357895,fasp.sra.ebi.ac.uk:/vol1/run/ERR599/ERR599189/Myco-F_NoIndex_L002_R1_001.fastq.gz,3800125462,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR599/ERR599189/Myco-F_NoIndex_L002_R1_001.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR599/ERR599189/Myco-F_NoIndex_L002_R1_001.fastq.gz,,8617097d7ceb03a1b15ecd5b08ba075c,,,,,,,, PRJEB7261,ERX556152,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,246196,Mycolicibacterium smegmatis MC2 155,OTHER,TRANSCRIPTOMIC,size fractionation,SAMEA2766083,smeg Ribo-seq rep1,Illumina HiSeq 2500,ERR599190,99829689,5091314139,SAMEA2766083,,,,,,ArrayExpress,,,"Wadsworth Center, New York State of Health",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2929:smeg Ribo-seq rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR599/ERR599190/ERR599190.fastq.gz,3413937166,ftp.sra.ebi.ac.uk/vol1/fastq/ERR599/ERR599190/ERR599190.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR599/ERR599190/ERR599190.fastq.gz,a49c463b2e6253812ce19a56e2fd1268,2014-09-12,2014-12-31,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,smeg Ribo-seq rep1,,,,,,,,,E-MTAB-2929:Myco-M_NoIndex_L001_R1_001.fastq.gz,,E-MTAB-2929:smeg Ribo-seq rep1,,"Protocols: 200 ml 7H9 medium was inoculated with 2.0 ml of overnight MC2 155 culture, and grew at 37 degrees C to an OD600 of ~1.0. The cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 ug/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.7 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. The pulverized cells were thawed. The clarified lysates were treated with micrococcal nuclease (MNase, Worthington Biochemical Corp). Monosomes were isolated by sucrose gradient fractionation. mRNA footprints were purified with acid phenol and chloroform extraction, and isopropanol precipitation. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel purification was performed for size selection of ~28nt RNA fragments. Approximately 25-30 nt poly-A tails were added to recovered RNA fragments with an Ambion poly(A) tailing kit (Life Technologies) following the manufacturer's guide. The polyadenylated RNA samples were reverse transcribed using JW2364 and SuperScript III (Life Tec",,,,,ERS542796,ERP006965,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR599/ERR599190,3048337426,ftp.sra.ebi.ac.uk/vol1/err/ERR599/ERR599190,ftp.sra.ebi.ac.uk/vol1/err/ERR599/ERR599190,807973c40111fc4dfdb3c95141cd33f1,,E-MTAB-2929,Ribosome Profiling of Mycobacterium smegmatis,,,ERA357895,fasp.sra.ebi.ac.uk:/vol1/run/ERR599/ERR599190/Myco-M_NoIndex_L001_R1_001.fastq.gz,4226202723,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR599/ERR599190/Myco-M_NoIndex_L001_R1_001.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR599/ERR599190/Myco-M_NoIndex_L001_R1_001.fastq.gz,,59cdfd787247057f18da857ddd0aed71,,,,,,,, PRJEB7261,ERX556153,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,246196,Mycolicibacterium smegmatis MC2 155,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2766084,smeg RNA-seq rep2,Illumina HiSeq 2500,ERR599191,100542696,5127677496,SAMEA2766084,,,,,,ArrayExpress,,,"Wadsworth Center, New York State of Health",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2929:smeg RNA-seq rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR599/ERR599191/ERR599191.fastq.gz,3519192936,ftp.sra.ebi.ac.uk/vol1/fastq/ERR599/ERR599191/ERR599191.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR599/ERR599191/ERR599191.fastq.gz,7debc4b0235a3bb25bf223d3f276c0a6,2014-09-12,2014-12-31,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,smeg RNA-seq rep2,,,,,,,,,E-MTAB-2929:Myco-Total-mRNA_NoIndex_L006_R1_001.fastq.gz,,E-MTAB-2929:smeg RNA-seq rep2,,"Protocols: 200 ml 7H9 medium was inoculated with 2.0 ml of overnight MC2 155 culture, and grew at 37 degrees C to an OD600 of ~1.0. The cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 ug/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.7 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. The pulverized cell powder was extracted with acid phenol and chloroform followed by isopropanol precipitation. 16S and 23S ribosomal RNAs were removed by subtractive hybridization using an Epicentre Ribo-Zero Magnetic kit following manufacturer's manual. The enriched mRNAs were randomly fragmented as described (Oh et al. 2011) The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel purification was performed for size selection of ~28nt RNA fragments. Approximately 25-30 nt poly-A tails were added to recovered RNA fragments with an Ambion poly(A) tailing kit (Life Technologies) following the manufacturer's guide. The polyadenylated RNA samples were reverse transcribed using",,,,,ERS542797,ERP006965,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR599/ERR599191,3026722875,ftp.sra.ebi.ac.uk/vol1/err/ERR599/ERR599191,ftp.sra.ebi.ac.uk/vol1/err/ERR599/ERR599191,9c0188b0f155a27617ff551cc1d1d3f2,,E-MTAB-2929,Ribosome Profiling of Mycobacterium smegmatis,,,ERA357895,fasp.sra.ebi.ac.uk:/vol1/run/ERR599/ERR599191/Myco-Total-mRNA_NoIndex_L006_R1_001.fastq.gz,4300511337,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR599/ERR599191/Myco-Total-mRNA_NoIndex_L006_R1_001.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR599/ERR599191/Myco-Total-mRNA_NoIndex_L006_R1_001.fastq.gz,,3e2298a8198d41b8c81801b07c72cfcd,,,,,,,, PRJEB7261,ERX556154,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,Illumina HiSeq 2500 sequencing; Ribosome Profiling of Mycobacterium smegmatis,246196,Mycolicibacterium smegmatis MC2 155,OTHER,TRANSCRIPTOMIC,size fractionation,SAMEA2766085,smeg Ribo-seq rep2,Illumina HiSeq 2500,ERR599192,80612378,4111231278,SAMEA2766085,,,,,,ArrayExpress,,,"Wadsworth Center, New York State of Health",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2929:smeg Ribo-seq rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR599/ERR599192/ERR599192.fastq.gz,2536834158,ftp.sra.ebi.ac.uk/vol1/fastq/ERR599/ERR599192/ERR599192.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR599/ERR599192/ERR599192.fastq.gz,c6f678af405dcf956fdfbfdc91fc548c,2014-09-12,2014-12-31,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,smeg Ribo-seq rep2,,,,,,,,,E-MTAB-2929:Myco-Footprints_NoIndex_L005_R1_001.fastq.gz,,E-MTAB-2929:smeg Ribo-seq rep2,,"Protocols: 200 ml 7H9 medium was inoculated with 2.0 ml of overnight MC2 155 culture, and grew at 37 degrees C to an OD600 of ~1.0. The cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 ug/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.7 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. The pulverized cells were thawed. The clarified lysates were treated with micrococcal nuclease (MNase, Worthington Biochemical Corp). Monosomes were isolated by sucrose gradient fractionation. mRNA footprints were purified with acid phenol and chloroform extraction, and isopropanol precipitation. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel purification was performed for size selection of ~28nt RNA fragments. Approximately 25-30 nt poly-A tails were added to recovered RNA fragments with an Ambion poly(A) tailing kit (Life Technologies) following the manufacturer's guide. The polyadenylated RNA samples were reverse transcribed using JW2364 and SuperScript III (Life Tec",,,,,ERS542798,ERP006965,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR599/ERR599192,2368647417,ftp.sra.ebi.ac.uk/vol1/err/ERR599/ERR599192,ftp.sra.ebi.ac.uk/vol1/err/ERR599/ERR599192,87a55c6c5dbdfcbe650e50feccc339d6,,E-MTAB-2929,Ribosome Profiling of Mycobacterium smegmatis,,,ERA357895,fasp.sra.ebi.ac.uk:/vol1/run/ERR599/ERR599192/Myco-Footprints_NoIndex_L005_R1_001.fastq.gz,3127464295,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR599/ERR599192/Myco-Footprints_NoIndex_L005_R1_001.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR599/ERR599192/Myco-Footprints_NoIndex_L005_R1_001.fastq.gz,,306733ec10ccf83a573d1696dc72a856,,,,,,,, PRJEB7276,ERX558436,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,3055,Chlamydomonas reinhardtii,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2769884,Chlamy-RNASeq-WT-2,Illumina HiSeq 2000,ERR601607,55247955,2707149795,SAMEA2769884,,,,,,ArrayExpress,,,Department of Plant Sciences University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2934:Chlamy-RNASeq-WT-2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR601/ERR601607/ERR601607.fastq.gz,2089079995,ftp.sra.ebi.ac.uk/vol1/fastq/ERR601/ERR601607/ERR601607.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR601/ERR601607/ERR601607.fastq.gz,5842873abd70943c674a795aa69392ab,2014-09-16,2015-10-16,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Chlamy-RNASeq-WT-2,,,,,,,,,E-MTAB-2934:Chlamy-RnaSeq-WT-2.fq.gz,,E-MTAB-2934:Chlamy-RNASeq-WT-2,,"Protocols: Chlamydomonas reinhardtii cells (CC-4350 cw Arg 7-8 mt+) (Chlamydomonas Resource Center [http://chlamycollection.org/strains/]) were maintained in 750 ml Tris-acetate-phosphate medium (Harris, 1989) at 23 C on a rotatory shaker (140 rpm) under constant illumination with white light (70 uE.m2.sec-1) to mid-log phase (OD750 ~ 0.6). Chlamydomonas cultures were harvested by filtering off the media, the cell paste was flash frozen and pulverized in liquid nitrogen with 5 ml of pre-frozen lysis buffer (20 mM Tris-Cl pH7.5, 140 mM KCl, 5 mM MgCl2, 100 ug/ml cycloheximide, 100 ug/ml chloramphenicol, 0.05 mM DTT, 0.1% NP40 and 5% sucrose). The frozen powder was thawed on ice and clarified by centrifugation for 30 min at 4700 rpm at 4 C followed by adjustment of A254 to ~4 before snap-freezing in liquid nitrogen and storage at -80 C. For Chlamydomonas, lysates were slowly thawed on ice and a 200 ul aliquot (A254 = 4) treated with 300 U RNAse 1 (100 U/ul, Life Technologies cat. no. AM2294) in a thermo-mixer at 28 C, 400 rpm for 30 min. The tube was placed on ice, 2 ul of SUPERase-In RNase inhibitor (20 U/ml, Life Technologies) added and the reaction layered onto a 1 M sucrose cushion prepared in Chlamydomonas polysome buffer (20 mM Tris-HCl pH 7.5, 140 mM KCl, 5 mM MgCl2, 0.5 mM DTT, 100 ug/ml cycloheximide, 100 ug/ml chloramphenicol and 0.5 ug/ml SUPERase-In.). The cushion was ultracentrifuged at 38,000 rpm (5 hr, 4C) in a Beckman Sw41Ti rotor. 150 ul of each cell lysate was",,,,,ERS543670,ERP006983,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR601/ERR601607,2486464332,ftp.sra.ebi.ac.uk/vol1/err/ERR601/ERR601607,ftp.sra.ebi.ac.uk/vol1/err/ERR601/ERR601607,f4e240849792a22630801b989cd11406,,E-MTAB-2934,Examples of ribosome profiling in chlamydomonas and mouse,,,ERA358090,fasp.sra.ebi.ac.uk:/vol1/run/ERR601/ERR601607/Chlamy-RnaSeq-WT-2.fq.gz,1917388454,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR601/ERR601607/Chlamy-RnaSeq-WT-2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR601/ERR601607/Chlamy-RnaSeq-WT-2.fq.gz,,826c928c63c6502a785b38712dc80821,,,,,,,, PRJEB7276,ERX558438,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,3055,Chlamydomonas reinhardtii,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2769886,Chlamy-RiboSeq-WT-2,Illumina HiSeq 2000,ERR601608,26028360,1275389640,SAMEA2769886,,,,,,ArrayExpress,,,Department of Plant Sciences University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2934:Chlamy-RiboSeq-WT-2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR601/ERR601608/ERR601608.fastq.gz,980010863,ftp.sra.ebi.ac.uk/vol1/fastq/ERR601/ERR601608/ERR601608.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR601/ERR601608/ERR601608.fastq.gz,eb1f87cda1c1717a14f541332e6ce798,2014-09-16,2015-10-16,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Chlamy-RiboSeq-WT-2,,,,,,,,,E-MTAB-2934:Chlamy-RiboSeq-WT-2.fq.gz,,E-MTAB-2934:Chlamy-RiboSeq-WT-2,,"Protocols: Chlamydomonas reinhardtii cells (CC-4350 cw Arg 7-8 mt+) (Chlamydomonas Resource Center [http://chlamycollection.org/strains/]) were maintained in 750 ml Tris-acetate-phosphate medium (Harris, 1989) at 23 C on a rotatory shaker (140 rpm) under constant illumination with white light (70 uE.m2.sec-1) to mid-log phase (OD750 ~ 0.6). Chlamydomonas cultures were harvested by filtering off the media, the cell paste was flash frozen and pulverized in liquid nitrogen with 5 ml of pre-frozen lysis buffer (20 mM Tris-Cl pH7.5, 140 mM KCl, 5 mM MgCl2, 100 ug/ml cycloheximide, 100 ug/ml chloramphenicol, 0.05 mM DTT, 0.1% NP40 and 5% sucrose). The frozen powder was thawed on ice and clarified by centrifugation for 30 min at 4700 rpm at 4 C followed by adjustment of A254 to ~4 before snap-freezing in liquid nitrogen and storage at -80 C. For Chlamydomonas, lysates were slowly thawed on ice and a 200 ul aliquot (A254 = 4) treated with 300 U RNAse 1 (100 U/ul, Life Technologies cat. no. AM2294) in a thermo-mixer at 28 C, 400 rpm for 30 min. The tube was placed on ice, 2 ul of SUPERase-In RNase inhibitor (20 U/ml, Life Technologies) added and the reaction layered onto a 1 M sucrose cushion prepared in Chlamydomonas polysome buffer (20 mM Tris-HCl pH 7.5, 140 mM KCl, 5 mM MgCl2, 0.5 mM DTT, 100 ug/ml cycloheximide, 100 ug/ml chloramphenicol and 0.5 ug/ml SUPERase-In.). The cushion was ultracentrifuged at 38,000 rpm (5 hr, 4C) in a Beckman Sw41Ti rotor. 150 ul of each cell lysate was",,,,,ERS543672,ERP006983,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR601/ERR601608,1190803293,ftp.sra.ebi.ac.uk/vol1/err/ERR601/ERR601608,ftp.sra.ebi.ac.uk/vol1/err/ERR601/ERR601608,e24b4f4b4ef13794a590de493c9327c5,,E-MTAB-2934,Examples of ribosome profiling in chlamydomonas and mouse,,,ERA358090,fasp.sra.ebi.ac.uk:/vol1/run/ERR601/ERR601608/Chlamy-RiboSeq-WT-2.fq.gz,899952284,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR601/ERR601608/Chlamy-RiboSeq-WT-2.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR601/ERR601608/Chlamy-RiboSeq-WT-2.fq.gz,,24442a30a4ced443a5aab859a2b8a567,,,,,,,, PRJEB7276,ERX558437,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2769885,MusMus-RNASeq,Illumina HiSeq 2000,ERR601609,80602120,4110708120,SAMEA2769885,,,,,,ArrayExpress,,,Department of Plant Sciences University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2934:MusMus-RNASeq,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR601/ERR601609/ERR601609.fastq.gz,3434877014,ftp.sra.ebi.ac.uk/vol1/fastq/ERR601/ERR601609/ERR601609.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR601/ERR601609/ERR601609.fastq.gz,f7937e4877c45b101be2307c8a77ffca,2014-09-16,2015-10-16,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,MusMus-RNASeq,,,,,,,,,E-MTAB-2934:MusMus-RNASeq.fq.gz,,E-MTAB-2934:MusMus-RNASeq,,"Protocols: Murine 17 clone 1 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum. Cells (107) were plated in a 10 cm dish and upon reaching 100% confluence, cycloheximide (Sigma-Aldrich) was added to 100 ug/ml. After 2 min, cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 sec, transferred to dry ice and 400 ul of lysis buffer (20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 ug/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies) dripped on. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 C, the supernatants recovered and stored in liquid nitrogen. For mouse samples, lysates were slowly thawed on ice and 250 ul treated with 7.5 ul RNase 1 followed by incubation for 45 min at room temperature on a rotating wheel. 10 ul of SUPERase-In RNase inhibitor was added, the sample layered onto a 1M sucrose cushion in mammalian polysome buffer (20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 100 ug/ml cycloheximide) and ultracentrifuged at 28,000 rpm (16 hr, 4 C) in a Beckman SW55Ti rotor. Subsequently, all ribosome pellets were resuspended in 200 ul of the corresponding polysome buffer and digested with proteinase K (10 mM Tris-HCl pH 7.5, 10% SDS, 200 ug/ml Proteinase K [New England Biolabs]) fo",,,,,ERS543671,ERP006983,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR601/ERR601609,2910647392,ftp.sra.ebi.ac.uk/vol1/err/ERR601/ERR601609,ftp.sra.ebi.ac.uk/vol1/err/ERR601/ERR601609,cbf868c74f1d4a377db9bdcca2e90d54,,E-MTAB-2934,Examples of ribosome profiling in chlamydomonas and mouse,,,ERA358090,fasp.sra.ebi.ac.uk:/vol1/run/ERR601/ERR601609/MusMus-RNASeq.fq.gz,3180018428,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR601/ERR601609/MusMus-RNASeq.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR601/ERR601609/MusMus-RNASeq.fq.gz,,f5b5a39ddcd28c1ad9cdc658d434b112,,,,,,,, PRJEB7276,ERX558439,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,Illumina HiSeq 2000 sequencing; Examples of ribosome profiling in chlamydomonas and mouse,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMEA2769887,MusMus-RiboSeq,Illumina HiSeq 2000,ERR601610,38543800,1965733800,SAMEA2769887,,,,,,ArrayExpress,,,Department of Plant Sciences University of Cambridge,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2934:MusMus-RiboSeq,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR601/ERR601610/ERR601610.fastq.gz,1687874791,ftp.sra.ebi.ac.uk/vol1/fastq/ERR601/ERR601610/ERR601610.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR601/ERR601610/ERR601610.fastq.gz,52519842bad250f56c87b8940e27cda4,2014-09-16,2015-10-16,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,MusMus-RiboSeq,,,,,,,,,E-MTAB-2934:MusMus-RiboSeq.fq.gz,,E-MTAB-2934:MusMus-RiboSeq,,"Protocols: Murine 17 clone 1 cells were maintained in Dulbeccos modification of Eagles medium supplemented with 10% (vol/vol) fetal calf serum. Cells (107) were plated in a 10 cm dish and upon reaching 100% confluence, cycloheximide (Sigma-Aldrich) was added to 100 ug/ml. After 2 min, cells were rinsed with 5 ml of ice-cold PBS, the dishes submerged in a reservoir of liquid nitrogen for 10 sec, transferred to dry ice and 400 ul of lysis buffer (20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 ug/ml cycloheximide and 25 U/ml TURBO DNase (Life Technologies) dripped on. The cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 C, the supernatants recovered and stored in liquid nitrogen. For mouse samples, lysates were slowly thawed on ice and 250 ul treated with 7.5 ul RNase 1 followed by incubation for 45 min at room temperature on a rotating wheel. 10 ul of SUPERase-In RNase inhibitor was added, the sample layered onto a 1M sucrose cushion in mammalian polysome buffer (20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 100 ug/ml cycloheximide) and ultracentrifuged at 28,000 rpm (16 hr, 4 C) in a Beckman SW55Ti rotor. Subsequently, all ribosome pellets were resuspended in 200 ul of the corresponding polysome buffer and digested with proteinase K (10 mM Tris-HCl pH 7.5, 10% SDS, 200 ug/ml Proteinase K [New England Biolabs]) fo",,,,,ERS543673,ERP006983,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR601/ERR601610,1410552209,ftp.sra.ebi.ac.uk/vol1/err/ERR601/ERR601610,ftp.sra.ebi.ac.uk/vol1/err/ERR601/ERR601610,f39d5a4ac05b89c54c0c5f6c4a8fdb2f,,E-MTAB-2934,Examples of ribosome profiling in chlamydomonas and mouse,,,ERA358090,fasp.sra.ebi.ac.uk:/vol1/run/ERR601/ERR601610/MusMus-RiboSeq.fq.gz,1571241062,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR601/ERR601610/MusMus-RiboSeq.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR601/ERR601610/MusMus-RiboSeq.fq.gz,,2cb95b43062f90b3f6a3d26b36ab884c,,,,,,,, PRJEB7282,ERX561998,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,cDNA,SAMEA2770197,Ribosome_profiling_LUs19,Illumina HiSeq 2500,ERR605044,187831868,9391593400,SAMEA2770197,,,,,,ArrayExpress,,HEK293,"Department of Molecular Neuroscience, UCL Institute of Neurology",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2941:Ribosome_profiling_LUs19,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR605/ERR605044/ERR605044.fastq.gz,7876556889,ftp.sra.ebi.ac.uk/vol1/fastq/ERR605/ERR605044/ERR605044.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR605/ERR605044/ERR605044.fastq.gz,00702a68d0d8893c4708120792ca9023,2014-09-16,2015-03-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Ribosome_profiling_LUs19,,,,,,,,,E-MTAB-2941:LUs19.fq.gz,,E-MTAB-2941:Ribosome_profiling_LUs19,,"Protocols: Cells were not treated with siRNA (untreated), treated with anti-STAU1 siRNA (knockdown), or treated with anti-STAU1 siRNA and the STAU1 level was rescued by the expression of siRNA-resistant STAU1 (rescue). Cells were subjected to Cycloheximide treatment before collection. Ribosome profiling protocol was followed to isolate protected RNA from the Cycloheximide teated cells and amplify cDNA library as described in the manuscript. Specific barcodes were used for each RT reaction as described in the manuscript. Random barcodes were also incoperated into cDNAs to distinguish between PCR duplication of cDNA products. The final products were obtained by PCR with Illumina paired-end sequencing primers: 5-CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT-3; 5-AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT-3",,,,,ERS543983,ERP006990,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR605/ERR605044,9408655122,ftp.sra.ebi.ac.uk/vol1/err/ERR605/ERR605044,ftp.sra.ebi.ac.uk/vol1/err/ERR605/ERR605044,9a61ebbe3b7826e292a1abd14d17d3ab,,E-MTAB-2941,Analysis of ribosomal occupancy with ribosome profiling.,,,ERA358123,fasp.sra.ebi.ac.uk:/vol1/run/ERR605/ERR605044/LUs19.fq.gz,7997001793,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR605/ERR605044/LUs19.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR605/ERR605044/LUs19.fq.gz,,8aacb7829a24ef2bfc65ef0ad9ac8270,,,,,,,, PRJEB7282,ERX561999,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,cDNA,SAMEA2770198,Ribosome_profiling_LUs18,Illumina HiSeq 2500,ERR605045,125136641,6256832050,SAMEA2770198,,,,,,ArrayExpress,,HEK293,"Department of Molecular Neuroscience, UCL Institute of Neurology",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2941:Ribosome_profiling_LUs18,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR605/ERR605045/ERR605045.fastq.gz,4854486029,ftp.sra.ebi.ac.uk/vol1/fastq/ERR605/ERR605045/ERR605045.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR605/ERR605045/ERR605045.fastq.gz,c0d00975ebe359cc9fd6cb93fd86e050,2014-09-16,2015-03-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Ribosome_profiling_LUs18,,,,,,,,,E-MTAB-2941:LUs18.fq.gz,,E-MTAB-2941:Ribosome_profiling_LUs18,,"Protocols: Cells were not treated with siRNA (untreated), treated with anti-STAU1 siRNA (knockdown), or treated with anti-STAU1 siRNA and the STAU1 level was rescued by the expression of siRNA-resistant STAU1 (rescue). Cells were subjected to Cycloheximide treatment before collection. Ribosome profiling protocol was followed to isolate protected RNA from the Cycloheximide teated cells and amplify cDNA library as described in the manuscript. Specific barcodes were used for each RT reaction as described in the manuscript. Random barcodes were also incoperated into cDNAs to distinguish between PCR duplication of cDNA products. The final products were obtained by PCR with Illumina paired-end sequencing primers: 5-CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT-3; 5-AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT-3",,,,,ERS543984,ERP006990,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR605/ERR605045,5992215540,ftp.sra.ebi.ac.uk/vol1/err/ERR605/ERR605045,ftp.sra.ebi.ac.uk/vol1/err/ERR605/ERR605045,3f78911919cc8a67c97572ff455df401,,E-MTAB-2941,Analysis of ribosomal occupancy with ribosome profiling.,,,ERA358123,fasp.sra.ebi.ac.uk:/vol1/run/ERR605/ERR605045/LUs18.fq.gz,4919838306,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR605/ERR605045/LUs18.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR605/ERR605045/LUs18.fq.gz,,f10e35332d6ae363d7b80fe6f6495d1c,,,,,,,, PRJEB7282,ERX562000,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,Illumina HiSeq 2500 sequencing; Analysis of ribosomal occupancy with ribosome profiling.,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,cDNA,SAMEA2770199,Ribosome_profiling_LUs20,Illumina HiSeq 2500,ERR605046,169888632,8494431600,SAMEA2770199,,,,,,ArrayExpress,,HEK293,"Department of Molecular Neuroscience, UCL Institute of Neurology",ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2941:Ribosome_profiling_LUs20,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR605/ERR605046/ERR605046.fastq.gz,6928377564,ftp.sra.ebi.ac.uk/vol1/fastq/ERR605/ERR605046/ERR605046.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR605/ERR605046/ERR605046.fastq.gz,a83d6990fbac5cba1ddfa7f2940251e7,2014-09-16,2015-03-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,Ribosome_profiling_LUs20,,,,,,,,,E-MTAB-2941:LUs20.fq.gz,,E-MTAB-2941:Ribosome_profiling_LUs20,,"Protocols: Cells were not treated with siRNA (untreated), treated with anti-STAU1 siRNA (knockdown), or treated with anti-STAU1 siRNA and the STAU1 level was rescued by the expression of siRNA-resistant STAU1 (rescue). Cells were subjected to Cycloheximide treatment before collection. Ribosome profiling protocol was followed to isolate protected RNA from the Cycloheximide teated cells and amplify cDNA library as described in the manuscript. Specific barcodes were used for each RT reaction as described in the manuscript. Random barcodes were also incoperated into cDNAs to distinguish between PCR duplication of cDNA products. The final products were obtained by PCR with Illumina paired-end sequencing primers: 5-CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT-3; 5-AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT-3",,,,,ERS543985,ERP006990,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR605/ERR605046,8432389084,ftp.sra.ebi.ac.uk/vol1/err/ERR605/ERR605046,ftp.sra.ebi.ac.uk/vol1/err/ERR605/ERR605046,ab52a5ebad2c57b3147f5197fd2ce317,,E-MTAB-2941,Analysis of ribosomal occupancy with ribosome profiling.,,,ERA358123,fasp.sra.ebi.ac.uk:/vol1/run/ERR605/ERR605046/LUs20.fq.gz,7026234110,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR605/ERR605046/LUs20.fq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR605/ERR605046/LUs20.fq.gz,,c1ed5c2ff1255fc9e8e902a2abfa41ac,,,,,,,, PRJEB7301,ERX575541,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130362,RyhB RNA-seq rep2,Illumina HiSeq 2500,ERR618768,204609482,5115237050,SAMEA3130362,,,,,,ArrayExpress,,,Wadsworth Center New York State Department of Health,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2903:RyhB RNA-seq rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR618/ERR618768/ERR618768.fastq.gz,5733524945,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618768/ERR618768.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618768/ERR618768.fastq.gz,514e46d210bd165d51c6028bd67da8fe,2014-09-17,2014-11-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RyhB RNA-seq rep2,,,,,,,,,E-MTAB-2903:RyhB-RNAseq-rep2-trimmed.fastq.gz,,E-MTAB-2903:RyhB RNA-seq rep2,,"Protocols: 200 ml LB medium was inoculated with 2.0 ml of overnight E.coli culture, and grew at 37 degrees C to an OD600 of ~0.5. Arabinose was added to 0.1% 10 minutes before harvesting the cells to induce the expression of RyhB. Then cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 μg/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.65 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. The pulverized cell powder was extracted with acid phenol and chloroform followed by isopropanol precipitation as described (Oh et al. 2011). 16S and 23S ribosomal RNAs were removed by subtractive hybridization using Ambion MICROExpressTM kit following manufacturer's manual. The enriched mRNAs were randomly fragmented as described (Oh et al. 2011) Both ribosomal footprints and total mRNAs were converted into cDNA libraries as described (Ingolia 2010, Oh et al. 2011) with modification. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel purification was performed for size s...",,,,,ERS544002,ERP007009,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR618/ERR618768,3762295101,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618768,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618768,20f3e37ab44bf6189fd8bae20adec543,,E-MTAB-2903,Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,,,ERA358164,fasp.sra.ebi.ac.uk:/vol1/run/ERR618/ERR618768/RyhB-RNAseq-rep2-trimmed.fastq.gz,5091767307,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618768/RyhB-RNAseq-rep2-trimmed.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618768/RyhB-RNAseq-rep2-trimmed.fastq.gz,,5b03fa5a3df1ef1d9458a7bf93d69051,,,,,,,, PRJEB7301,ERX575542,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130357,RyhB RNA-seq rep1,Illumina HiSeq 2500,ERR618769,66334068,3383037468,SAMEA3130357,,,,,,ArrayExpress,,,Wadsworth Center New York State Department of Health,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2903:RyhB RNA-seq rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR618/ERR618769/ERR618769.fastq.gz,2407388202,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618769/ERR618769.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618769/ERR618769.fastq.gz,68a08a3128e41c559e00f33a580cdf20,2014-09-17,2014-11-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RyhB RNA-seq rep1,,,,,,,,,E-MTAB-2903:RyhB-RNAseq-rep1.fastq.gz,,E-MTAB-2903:RyhB RNA-seq rep1,,"Protocols: 200 ml LB medium was inoculated with 2.0 ml of overnight E.coli culture, and grew at 37 degrees C to an OD600 of ~0.5. Arabinose was added to 0.1% 10 minutes before harvesting the cells to induce the expression of RyhB. Then cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 μg/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.65 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. The pulverized cell powder was extracted with acid phenol and chloroform followed by isopropanol precipitation as described (Oh et al. 2011). 16S and 23S ribosomal RNAs were removed by subtractive hybridization using Ambion MICROExpressTM kit following manufacturer's manual. The enriched mRNAs were randomly fragmented as described (Oh et al. 2011) Both ribosomal footprints and total mRNAs were converted into cDNA libraries as described (Ingolia 2010, Oh et al. 2011) with modification. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel purification was performed for size s...",,,,,ERS544003,ERP007009,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR618/ERR618769,2062936581,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618769,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618769,08a4c6888d35f7555052d4215f64902c,,E-MTAB-2903,Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,,,ERA358164,fasp.sra.ebi.ac.uk:/vol1/run/ERR618/ERR618769/RyhB-RNAseq-rep1.fastq.gz,2905411602,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618769/RyhB-RNAseq-rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618769/RyhB-RNAseq-rep1.fastq.gz,,944ce7636618aeff5365bc0c178eba04,,,,,,,, PRJEB7301,ERX575546,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130355,RyhB Ribo-seq rep2,Illumina HiSeq 2500,ERR618770,194819312,4870482800,SAMEA3130355,,,,,,ArrayExpress,,,Wadsworth Center New York State Department of Health,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2903:RyhB Ribo-seq rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR618/ERR618770/ERR618770.fastq.gz,5225005926,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618770/ERR618770.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618770/ERR618770.fastq.gz,838602d2d514cb82c119960d1ced0c43,2014-09-17,2014-11-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RyhB Ribo-seq rep2,,,,,,,,,E-MTAB-2903:RyhB-Riboseq-rep2-trimmed.fastq.gz,,E-MTAB-2903:RyhB Ribo-seq rep2,,"Protocols: 200 ml LB medium was inoculated with 2.0 ml of overnight E.coli culture, and grew at 37 degrees C to an OD600 of ~0.5. Arabinose was added to 0.1% 10 minutes before harvesting the cells to induce the expression of RyhB. Then cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 μg/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.65 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. Footprinting and monosome isolation were performed as described (Oh et al. 2011). Briefly, the pulverized cells were thawed. The clarified lysates were treated with micrococcal nuclease (MNase, Worthington Biochemical Corp). Monosomes were isolated by sucrose gradient fractionation. mRNA footprints were purified with acid phenol and chloroform extraction, and isopropanol precipitation. Both ribosomal footprints and total mRNAs were converted into cDNA libraries as described (Ingolia 2010, Oh et al. 2011) with modification. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel pur...",,,,,ERS544007,ERP007009,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR618/ERR618770,3521687322,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618770,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618770,27a05d62b13013e36a59cc3a7f909f99,,E-MTAB-2903,Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,,,ERA358164,fasp.sra.ebi.ac.uk:/vol1/run/ERR618/ERR618770/RyhB-Riboseq-rep2-trimmed.fastq.gz,4625890627,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618770/RyhB-Riboseq-rep2-trimmed.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618770/RyhB-Riboseq-rep2-trimmed.fastq.gz,,80bd2b400cb6c136dbb4f0ec6e045649,,,,,,,, PRJEB7301,ERX575545,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130358,control Ribo-seq rep2,Illumina HiSeq 2500,ERR618771,161912593,4047814825,SAMEA3130358,,,,,,ArrayExpress,,,Wadsworth Center New York State Department of Health,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2903:control Ribo-seq rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR618/ERR618771/ERR618771.fastq.gz,4090858273,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618771/ERR618771.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618771/ERR618771.fastq.gz,1d8b27c4f20205e595f22413fb57ad0b,2014-09-17,2014-11-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,control Ribo-seq rep2,,,,,,,,,E-MTAB-2903:NM12-Riboseq-rep2-trimmed.fastq.gz,,E-MTAB-2903:control Ribo-seq rep2,,"Protocols: 200 ml LB medium was inoculated with 2.0 ml of overnight E.coli culture, and grew at 37 degrees C to an OD600 of ~0.5. Arabinose was added to 0.1% 10 minutes before harvesting the cells to induce the expression of RyhB. Then cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 μg/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.65 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. Footprinting and monosome isolation were performed as described (Oh et al. 2011). Briefly, the pulverized cells were thawed. The clarified lysates were treated with micrococcal nuclease (MNase, Worthington Biochemical Corp). Monosomes were isolated by sucrose gradient fractionation. mRNA footprints were purified with acid phenol and chloroform extraction, and isopropanol precipitation. Both ribosomal footprints and total mRNAs were converted into cDNA libraries as described (Ingolia 2010, Oh et al. 2011) with modification. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel pur...",,,,,ERS544006,ERP007009,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR618/ERR618771,2809505488,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618771,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618771,489731726c04f5207a903665ab58d394,,E-MTAB-2903,Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,,,ERA358164,fasp.sra.ebi.ac.uk:/vol1/run/ERR618/ERR618771/NM12-Riboseq-rep2-trimmed.fastq.gz,3593762830,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618771/NM12-Riboseq-rep2-trimmed.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618771/NM12-Riboseq-rep2-trimmed.fastq.gz,,58d88ab0648845d721c1e47f98f4492a,,,,,,,, PRJEB7301,ERX575543,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130361,RyhB Ribo-seq rep1,Illumina HiSeq 2500,ERR618772,69520696,3545555496,SAMEA3130361,,,,,,ArrayExpress,,,Wadsworth Center New York State Department of Health,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2903:RyhB Ribo-seq rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR618/ERR618772/ERR618772.fastq.gz,2712643558,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618772/ERR618772.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618772/ERR618772.fastq.gz,43a5e86121beb631e6eb86cf75e927a4,2014-09-17,2014-11-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,RyhB Ribo-seq rep1,,,,,,,,,E-MTAB-2903:RyhB-Riboseq-rep1.fastq.gz,,E-MTAB-2903:RyhB Ribo-seq rep1,,"Protocols: 200 ml LB medium was inoculated with 2.0 ml of overnight E.coli culture, and grew at 37 degrees C to an OD600 of ~0.5. Arabinose was added to 0.1% 10 minutes before harvesting the cells to induce the expression of RyhB. Then cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 μg/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.65 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. Footprinting and monosome isolation were performed as described (Oh et al. 2011). Briefly, the pulverized cells were thawed. The clarified lysates were treated with micrococcal nuclease (MNase, Worthington Biochemical Corp). Monosomes were isolated by sucrose gradient fractionation. mRNA footprints were purified with acid phenol and chloroform extraction, and isopropanol precipitation. Both ribosomal footprints and total mRNAs were converted into cDNA libraries as described (Ingolia 2010, Oh et al. 2011) with modification. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel pur...",,,,,ERS544004,ERP007009,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR618/ERR618772,2419975338,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618772,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618772,bc1a85c03fdb40bb3c3de1e81f4f1846,,E-MTAB-2903,Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,,,ERA358164,fasp.sra.ebi.ac.uk:/vol1/run/ERR618/ERR618772/RyhB-Riboseq-rep1.fastq.gz,3193126021,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618772/RyhB-Riboseq-rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618772/RyhB-Riboseq-rep1.fastq.gz,,d5e31c005cbdb13721c45d4213a8d6a8,,,,,,,, PRJEB7301,ERX575540,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130359,control RNA-seq rep1,Illumina HiSeq 2500,ERR618773,94444604,4816674804,SAMEA3130359,,,,,,ArrayExpress,,,Wadsworth Center New York State Department of Health,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2903:control RNA-seq rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR618/ERR618773/ERR618773.fastq.gz,3585721225,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618773/ERR618773.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618773/ERR618773.fastq.gz,05d95a9c686fbcc4d4769e846fceaa39,2014-09-17,2014-11-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,control RNA-seq rep1,,,,,,,,,E-MTAB-2903:NM12-RNAseq-rep1.fastq.gz,,E-MTAB-2903:control RNA-seq rep1,,"Protocols: 200 ml LB medium was inoculated with 2.0 ml of overnight E.coli culture, and grew at 37 degrees C to an OD600 of ~0.5. Arabinose was added to 0.1% 10 minutes before harvesting the cells to induce the expression of RyhB. Then cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 μg/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.65 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. The pulverized cell powder was extracted with acid phenol and chloroform followed by isopropanol precipitation as described (Oh et al. 2011). 16S and 23S ribosomal RNAs were removed by subtractive hybridization using Ambion MICROExpressTM kit following manufacturer's manual. The enriched mRNAs were randomly fragmented as described (Oh et al. 2011) Both ribosomal footprints and total mRNAs were converted into cDNA libraries as described (Ingolia 2010, Oh et al. 2011) with modification. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel purification was performed for size s...",,,,,ERS544001,ERP007009,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR618/ERR618773,3077775289,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618773,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618773,cb1f4b124f4c90e87eb336b1055c9f79,,E-MTAB-2903,Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,,,ERA358164,fasp.sra.ebi.ac.uk:/vol1/run/ERR618/ERR618773/NM12-RNAseq-rep1.fastq.gz,4306037972,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618773/NM12-RNAseq-rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618773/NM12-RNAseq-rep1.fastq.gz,,970987619194c2881c853f5575bc9b35,,,,,,,, PRJEB7301,ERX575544,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130360,control RNA-seq rep2,Illumina HiSeq 2500,ERR618774,188584261,4714606525,SAMEA3130360,,,,,,ArrayExpress,,,Wadsworth Center New York State Department of Health,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2903:control RNA-seq rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR618/ERR618774/ERR618774.fastq.gz,5086362639,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618774/ERR618774.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618774/ERR618774.fastq.gz,74f3cbc121b974d6f40f3fe86b65683c,2014-09-17,2014-11-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,control RNA-seq rep2,,,,,,,,,E-MTAB-2903:NM12-RNAseq-rep2-trimmed.fastq.gz,,E-MTAB-2903:control RNA-seq rep2,,"Protocols: 200 ml LB medium was inoculated with 2.0 ml of overnight E.coli culture, and grew at 37 degrees C to an OD600 of ~0.5. Arabinose was added to 0.1% 10 minutes before harvesting the cells to induce the expression of RyhB. Then cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 μg/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.65 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. The pulverized cell powder was extracted with acid phenol and chloroform followed by isopropanol precipitation as described (Oh et al. 2011). 16S and 23S ribosomal RNAs were removed by subtractive hybridization using Ambion MICROExpressTM kit following manufacturer's manual. The enriched mRNAs were randomly fragmented as described (Oh et al. 2011) Both ribosomal footprints and total mRNAs were converted into cDNA libraries as described (Ingolia 2010, Oh et al. 2011) with modification. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel purification was performed for size s...",,,,,ERS544005,ERP007009,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR618/ERR618774,3359451702,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618774,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618774,ba67a9c2472196f69ecabcff8b73ece7,,E-MTAB-2903,Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,,,ERA358164,fasp.sra.ebi.ac.uk:/vol1/run/ERR618/ERR618774/NM12-RNAseq-rep2-trimmed.fastq.gz,4495427548,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618774/NM12-RNAseq-rep2-trimmed.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618774/NM12-RNAseq-rep2-trimmed.fastq.gz,,1415982922ee982e41b48640fa44ad60,,,,,,,, PRJEB7301,ERX575539,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,Illumina HiSeq 2500 sequencing; Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMEA3130356,control Ribo-seq rep1,Illumina HiSeq 2500,ERR618775,48903913,2494099563,SAMEA3130356,,,,,,ArrayExpress,,,Wadsworth Center New York State Department of Health,ERC000011,,,,,,,,,,,,,,,,,,,false,E-MTAB-2903:control Ribo-seq rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/ERR618/ERR618775/ERR618775.fastq.gz,1884833166,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618775/ERR618775.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/ERR618/ERR618775/ERR618775.fastq.gz,766870e193d03ace9338d38133bfacb0,2014-09-17,2014-11-01,false,,,,,,,,,,,ILLUMINA,,,,2018-11-16,,SINGLE,control Ribo-seq rep1,,,,,,,,,E-MTAB-2903:NM12-Riboseq-rep1.fastq.gz,,E-MTAB-2903:control Ribo-seq rep1,,"Protocols: 200 ml LB medium was inoculated with 2.0 ml of overnight E.coli culture, and grew at 37 degrees C to an OD600 of ~0.5. Arabinose was added to 0.1% 10 minutes before harvesting the cells to induce the expression of RyhB. Then cells were harvested by pretreatment with chloramphenicol to a final concentration of 100 μg/ml for 2 minutes followed by rapid filtration by using a 500ml 0.45um PES filter system (Celltreat). Cells were collected and flash frozen in liquid nitrogen together with 0.65 ml lysis buffer (Oh et al. 2011). The frozen cells were pulverized 6 times at 15 Hz for 3 min by a mixer mill (Retsch MM400). The grinding jars were re-chilled in liquid nitrogen to keep the cells frozen between each cycle. After the pulverized cells were recovered, small scoopful was saved for bacterial transcript enrichment. Footprinting and monosome isolation were performed as described (Oh et al. 2011). Briefly, the pulverized cells were thawed. The clarified lysates were treated with micrococcal nuclease (MNase, Worthington Biochemical Corp). Monosomes were isolated by sucrose gradient fractionation. mRNA footprints were purified with acid phenol and chloroform extraction, and isopropanol precipitation. Both ribosomal footprints and total mRNAs were converted into cDNA libraries as described (Ingolia 2010, Oh et al. 2011) with modification. The RNA molecules were dephosphorylated by treating with T4 polynucleotide kinase (New England Biolabs). Then polyacrylamide gel pur...",,,,,ERS544000,ERP007009,,,,,,fasp.sra.ebi.ac.uk:/vol1/err/ERR618/ERR618775,1684887320,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618775,ftp.sra.ebi.ac.uk/vol1/err/ERR618/ERR618775,2ef1140833d7919d9108ce2fa4597132,,E-MTAB-2903,Genome-wide ribosome profiling to identify regulatory targets of small RNA RyhB in E.coli,,,ERA358164,fasp.sra.ebi.ac.uk:/vol1/run/ERR618/ERR618775/NM12-Riboseq-rep1.fastq.gz,2227585661,FASTQ,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618775/NM12-Riboseq-rep1.fastq.gz,ftp.sra.ebi.ac.uk/vol1/run/ERR618/ERR618775/NM12-Riboseq-rep1.fastq.gz,,edda9c3fd7f0d920556106c152a88241,,,,,,,, PRJNA564991,SRX6832089,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 3,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 3,376686,Flavobacterium johnsoniae UW101,OTHER,TRANSCRIPTOMIC,other,SAMN12730772,F johnsoniae culture 2016 replicate 3,Illumina HiSeq 2500,SRR10100140,19043505,440593520,SAMN12730772,,,,,,,,,SUB6289735,,,2016-01-01,,,"USA: Columbus, OH",,,,,ATCC:17061,,,,,,,,,false,FJ16rep3Ribo,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/040/SRR10100140/SRR10100140.fastq.gz,277747753,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/040/SRR10100140/SRR10100140.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/040/SRR10100140/SRR10100140.fastq.gz,b2421c94ddd99b4e4b915cfe2f669e89,2020-04-14,2020-04-14,false,,,,,,,,,,,ILLUMINA,,,"Soil, England",2020-04-14,,SINGLE,FJ16rep3Ribo,,,,,,,,,FJRIBO3.trimmed.bam,,FJ16REP3,,F johnsoniae culture 2016 replicate 3,,,,,SRS5373870,SRP221399,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/040/SRR10100140,196326181,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/040/SRR10100140,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/040/SRR10100140,c82f60d1d112a0e4a838248084aaca4a,UW101,PRJNA564991,Flavobacterium johnsoniae ribosome profiling,,,SRA960872,,,,,,,,,,,,,,, PRJNA564991,SRX6832088,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 2,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 2,376686,Flavobacterium johnsoniae UW101,OTHER,TRANSCRIPTOMIC,other,SAMN12730771,F johnsoniae culture 2016 replicate 2,Illumina HiSeq 2500,SRR10100141,14410982,335664145,SAMN12730771,,,,,,,,,SUB6289735,,,2016-01-01,,,"USA: Columbus, OH",,,,,ATCC:17061,,,,,,,,,false,FJ16rep2Ribo,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/041/SRR10100141/SRR10100141.fastq.gz,215292902,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/041/SRR10100141/SRR10100141.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/041/SRR10100141/SRR10100141.fastq.gz,732c82ac53ae4182d6a16f19c5a4f510,2020-04-14,2020-04-14,false,,,,,,,,,,,ILLUMINA,,,"Soil, England",2020-04-14,,SINGLE,FJ16rep2Ribo,,,,,,,,,FJRIBO2.trimmed.bam,,FJ16REP2,,F johnsoniae culture 2016 replicate 2,,,,,SRS5373869,SRP221399,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/041/SRR10100141,152664161,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/041/SRR10100141,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/041/SRR10100141,fe78dfc50c599ccdff17ecc7cf35a624,UW101,PRJNA564991,Flavobacterium johnsoniae ribosome profiling,,,SRA960872,,,,,,,,,,,,,,, PRJNA564991,SRX6832087,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 1,Illumina HiSeq 2500 sequencing; Ribosome profiling library of FJ 2016 replicate 1,986,Flavobacterium johnsoniae,OTHER,TRANSCRIPTOMIC,other,SAMN12730770,F johnsoniae culture 2016 replicate 1,Illumina HiSeq 2500,SRR10100142,26216828,637267461,SAMN12730770,,,,,,,,,SUB6289735,,,2016-01-01,,,"USA: Columbus, OH",,,,,ATCC:17061,,,,,,,,,false,FJ16rep1Ribo,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/042/SRR10100142/SRR10100142.fastq.gz,406457059,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/042/SRR10100142/SRR10100142.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/042/SRR10100142/SRR10100142.fastq.gz,9545ea7290fc24e9a3095ecf828152b0,2020-04-14,2020-04-14,false,,,,,,,,,,,ILLUMINA,,,"Soil, England",2020-04-14,,SINGLE,FJ16rep1Ribo,,,,,,,,,FJRIBO1.trimmed.bam,,FJ16REP1,,F johnsoniae culture 2016 replicate 1,,,,,SRS5373868,SRP221399,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/042/SRR10100142,289827041,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/042/SRR10100142,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/042/SRR10100142,3f501199fbe8b6394e623d835e60695f,UW101,PRJNA564991,Flavobacterium johnsoniae ribosome profiling,,,SRA960872,,,,,,,,,,,,,,, PRJNA573922,SRX6895802,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831194,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174361,43426278,3256970850,SAMN12831194,,,,,,,,,SUB6341507,,,,,,,,,,,,,stage 14,,,,,,,false,2dayRFPrep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/061/SRR10174361/SRR10174361.fastq.gz,1137243934,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/061/SRR10174361/SRR10174361.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/061/SRR10174361/SRR10174361.fastq.gz,0c04c788112dcf5ee99e805434ea8c96,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,2dayRFPrep1,,,,,,,,,2A_RPF.fq.gz,,2dayRFP_A,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428379,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/061/SRR10174361,1301713554,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/061/SRR10174361,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/061/SRR10174361,78a3fd8f8ef12b558c63a3d20a7c15e2,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,mature oocyte, PRJNA573922,SRX6895795,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831208,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174368,26966897,2022517275,SAMN12831208,,,,,,,,,SUB6341507,,,,,,,,,,,,,0-2 hour embryo,,,,,,,false,embRFPrep3,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/068/SRR10174368/SRR10174368.fastq.gz,818279124,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/068/SRR10174368/SRR10174368.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/068/SRR10174368/SRR10174368.fastq.gz,6ebe7f0272d951bad443fb71a78eee45,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,embRFPrep3,,,,,,,,,embC_RPF.fq.gz,,embryoRFP_C,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428372,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/068/SRR10174368,825510235,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/068/SRR10174368,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/068/SRR10174368,299a6ace18ca2c908592b10eaa39a95b,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,embryo, PRJNA573922,SRX6895794,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831207,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174369,39112396,2933429700,SAMN12831207,,,,,,,,,SUB6341507,,,,,,,,,,,,,0-2 hour embryo,,,,,,,false,embRFPrep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/069/SRR10174369/SRR10174369.fastq.gz,1201812770,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/069/SRR10174369/SRR10174369.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/069/SRR10174369/SRR10174369.fastq.gz,fdd9eda9081075c38cf2e96d6ddde685,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,embRFPrep2,,,,,,,,,embB_RPF.fq.gz,,embryoRFP_B,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428371,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/069/SRR10174369,1174574621,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/069/SRR10174369,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/069/SRR10174369,afade58d3f475bdaa9768da443752f26,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,embryo, PRJNA573922,SRX6895793,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster 0-2 hour embryo,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831206,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174370,26837661,2012824575,SAMN12831206,,,,,,,,,SUB6341507,,,,,,,,,,,,,0-2 hour embryo,,,,,,,false,embRFPrep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/070/SRR10174370/SRR10174370.fastq.gz,845547451,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/070/SRR10174370/SRR10174370.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/070/SRR10174370/SRR10174370.fastq.gz,fe090c493b1df93df094c9160b37b779,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,embRFPrep1,,,,,,,,,embA_RPF.fq.gz,,embryoRFP_A,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428370,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/070/SRR10174370,824411038,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/070/SRR10174370,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/070/SRR10174370,8cdf9d496d7f7a805728012bb48690cb,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,embryo, PRJNA573922,SRX6895788,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831202,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174375,63692380,4776928500,SAMN12831202,,,,,,,,,SUB6341507,,,,,,,,,,,,,stage 14,,,,,,,false,12dayRFPrep3,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/075/SRR10174375/SRR10174375.fastq.gz,1832604053,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/075/SRR10174375/SRR10174375.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/075/SRR10174375/SRR10174375.fastq.gz,26d527a287041d381289fee17dac1272,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,12dayRFPrep3,,,,,,,,,12C_RPF.fq.gz,,12dayRFP_C,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428365,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/075/SRR10174375,1971903071,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/075/SRR10174375,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/075/SRR10174375,95c6b1da3165877a0e508e4224263f72,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,mature oocyte, PRJNA573922,SRX6895787,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831201,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174376,41691393,3126854475,SAMN12831201,,,,,,,,,SUB6341507,,,,,,,,,,,,,stage 14,,,,,,,false,12dayRFPrep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/076/SRR10174376/SRR10174376.fastq.gz,1068369380,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/076/SRR10174376/SRR10174376.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/076/SRR10174376/SRR10174376.fastq.gz,d065e74cf80a75522f9acdf68fbc4f4a,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,12dayRFPrep2,,,,,,,,,12B_RPF.fq.gz,,12dayRFP_B,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428364,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/076/SRR10174376,1241930685,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/076/SRR10174376,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/076/SRR10174376,cdb34a0fb22f8c66e6ef6773e921dab8,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,mature oocyte, PRJNA573922,SRX6895786,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831200,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174377,49155765,3686682375,SAMN12831200,,,,,,,,,SUB6341507,,,,,,,,,,,,,stage 14,,,,,,,false,12dayRFPrep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/077/SRR10174377/SRR10174377.fastq.gz,1376705514,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/077/SRR10174377/SRR10174377.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/077/SRR10174377/SRR10174377.fastq.gz,4530b889373c08a734a1c51d93126453,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,12dayRFPrep1,,,,,,,,,12A_RPF.fq.gz,,12dayRFP_A,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428363,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/077/SRR10174377,1501717316,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/077/SRR10174377,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/077/SRR10174377,3b1ec9bddfd973bd6bc51ec73e146ffa,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,mature oocyte, PRJNA573922,SRX6895785,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831199,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174378,83368394,6252629550,SAMN12831199,,,,,,,,,SUB6341507,,,,,,,,,,,,,stage 14,,,,,,,false,8dayRFPrep3,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/078/SRR10174378/SRR10174378.fastq.gz,2208586144,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/078/SRR10174378/SRR10174378.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/078/SRR10174378/SRR10174378.fastq.gz,f6ec84365ea469fba7544ac446acd569,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,8dayRFPrep3,,,,,,,,,8C_RPF.fq.gz,,8dayRFP_C,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428362,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/078/SRR10174378,2517120039,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/078/SRR10174378,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/078/SRR10174378,632b7de02a0e8e8caf39a26c36d55817,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,mature oocyte, PRJNA573922,SRX6895784,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831198,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174379,83683932,6276294900,SAMN12831198,,,,,,,,,SUB6341507,,,,,,,,,,,,,stage 14,,,,,,,false,8dayRFPrep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/079/SRR10174379/SRR10174379.fastq.gz,2185744827,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/079/SRR10174379/SRR10174379.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/079/SRR10174379/SRR10174379.fastq.gz,d09fa1f68958d53b4c7a476e3e308ced,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,8dayRFPrep2,,,,,,,,,8B_RPF.fq.gz,,8dayRFP_B,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428361,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/079/SRR10174379,2476644059,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/079/SRR10174379,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/079/SRR10174379,ade521ed7195851ed227a0c2878dc9d3,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,mature oocyte, PRJNA573922,SRX6895783,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831197,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174380,37912988,2843474100,SAMN12831197,,,,,,,,,SUB6341507,,,,,,,,,,,,,stage 14,,,,,,,false,8dayRFPrep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/080/SRR10174380/SRR10174380.fastq.gz,1047073037,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/080/SRR10174380/SRR10174380.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/080/SRR10174380/SRR10174380.fastq.gz,bcd3640b1d0a280bbef9823c44072178,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,8dayRFPrep1,,,,,,,,,8A_RPF.fq.gz,,8dayRFP_A,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428360,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/080/SRR10174380,1167178559,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/080/SRR10174380,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/080/SRR10174380,ad33965dd6559df174e6fd10c5bf1dc5,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,mature oocyte, PRJNA573922,SRX6895782,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831196,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174381,,,SAMN12831196,,,,,,,,,SUB6341507,,,,,,,,,,,,,stage 14,,,,,,,false,2dayRFPrep3,,,,,,,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,2dayRFPrep3,,,,,,,,,2C_RPF.fq.gz,,2dayRFP_C,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428359,SRP223102,,,,female,,,,,,,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,mature oocyte, PRJNA573922,SRX6895781,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,NextSeq 500 sequencing; Ribosome profiling of Drosophila melanogaster oocyte,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,PCR,SAMN12831195,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,NextSeq 500,SRR10174382,57951230,4346342250,SAMN12831195,,,,,,,,,SUB6341507,,,,,,,,,,,,,stage 14,,,,,,,false,2dayRFPrep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR101/082/SRR10174382/SRR10174382.fastq.gz,1577676975,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/082/SRR10174382/SRR10174382.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR101/082/SRR10174382/SRR10174382.fastq.gz,19e3e58a5b1d8970fd2a31c8a04ed812,2019-11-18,2019-11-18,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,2dayRFPrep2,,,,,,,,,2B_RPF.fq.gz,,2dayRFP_B,,This sample has been submitted by pda|ejgreenblatt on 2019-11-18; Drosophila melanogaster,,,,,SRS5428358,SRP223102,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR101/082/SRR10174382,1751419566,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/082/SRR10174382,ftp.sra.ebi.ac.uk/vol1/srr/SRR101/082/SRR10174382,2da97048af9e67ec58c7b0420b22c9ab,Oregon R,PRJNA573922,Ribosome profiling and mRNA sequencing of Drosophila oocytes during aging,,,SRA967518,,,,,,,,female,,,,,,mature oocyte, PRJNA577942,SRX7007420,Illumina HiSeq 2500 sequencing; GSM4125802: Replicate 1 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125802: Replicate 1 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041939,Replicate 1 centrifugation harvesting ribosome profiling,Illumina HiSeq 2500,SRR10294592,24325319,1629796373,SAMN13041939,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4125802,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR102/092/SRR10294592/SRR10294592.fastq.gz,837108859,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/092/SRR10294592/SRR10294592.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/092/SRR10294592/SRR10294592.fastq.gz,87c194114c7a88d3b246ca87027fb9b6,2020-04-30,2020-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM4125802_r1,,GSM4125802,,Replicate 1 centrifugation harvesting ribosome profiling,,,,,SRS5528590,SRP225954,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR102/092/SRR10294592,772511567,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/092/SRR10294592,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/092/SRR10294592,6597bc5588242a940f1705c1ba404590,,GSE138990,"Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution",,,SRA980319,,,,,,,,,,,,,,, PRJNA577942,SRX7007421,Illumina HiSeq 2500 sequencing; GSM4125803: Replicate 2 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125803: Replicate 2 centrifugation harvesting ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041938,Replicate 2 centrifugation harvesting ribosome profiling,Illumina HiSeq 2500,SRR10294593,108269604,7037524260,SAMN13041938,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4125803,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR102/093/SRR10294593/SRR10294593.fastq.gz,3329299794,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/093/SRR10294593/SRR10294593.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/093/SRR10294593/SRR10294593.fastq.gz,dc6c2962bc8f56cc09e919c85c3f265f,2020-04-30,2020-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM4125803_r1,,GSM4125803,,Replicate 2 centrifugation harvesting ribosome profiling,,,,,SRS5528591,SRP225954,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR102/093/SRR10294593,2891568352,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/093/SRR10294593,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/093/SRR10294593,27b92bd5b0b2f4d8209b20395914952d,,GSE138990,"Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution",,,SRA980319,,,,,,,,,,,,,,, PRJNA577942,SRX7007422,Illumina HiSeq 2500 sequencing; GSM4125804: Replicate 1 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125804: Replicate 1 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041936,Replicate 1 flash freeze harvesting no drugs ribosome profiling,Illumina HiSeq 2500,SRR10294594,4480382,448038200,SAMN13041936,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4125804,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR102/094/SRR10294594/SRR10294594.fastq.gz,218040014,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/094/SRR10294594/SRR10294594.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/094/SRR10294594/SRR10294594.fastq.gz,a2ca6eb8b55cfed4c372c4652c436a13,2020-04-30,2020-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM4125804_r1,,GSM4125804,,Replicate 1 flash freeze harvesting no drugs ribosome profiling,,,,,SRS5528592,SRP225954,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR102/094/SRR10294594,215669196,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/094/SRR10294594,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/094/SRR10294594,e9c66cf6ea39528fa2fa5865b3ce402a,,GSE138990,"Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution",,,SRA980319,,,,,,,,,,,,,,, PRJNA577942,SRX7007423,Illumina HiSeq 2500 sequencing; GSM4125805: Replicate 2 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125805: Replicate 2 flash freeze harvesting no drugs ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041934,Replicate 2 flash freeze harvesting no drugs ribosome profiling,Illumina HiSeq 2500,SRR10294595,8990526,449526300,SAMN13041934,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4125805,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR102/095/SRR10294595/SRR10294595.fastq.gz,378317488,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/095/SRR10294595/SRR10294595.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/095/SRR10294595/SRR10294595.fastq.gz,fee65426e83222b3ebf26b45fe0c0b3d,2020-04-30,2020-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM4125805_r1,,GSM4125805,,Replicate 2 flash freeze harvesting no drugs ribosome profiling,,,,,SRS5528593,SRP225954,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR102/095/SRR10294595,298116543,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/095/SRR10294595,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/095/SRR10294595,773ee5a6a8bf9d1f58c4b8f1f89f0e21,,GSE138990,"Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution",,,SRA980319,,,,,,,,,,,,,,, PRJNA577942,SRX7007424,Illumina HiSeq 2500 sequencing; GSM4125806: Flash freeze harvesting with anisomycin ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125806: Flash freeze harvesting with anisomycin ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041933,Flash freeze harvesting with anisomycin ribosome profiling,Illumina HiSeq 2500,SRR10294596,9421109,471055450,SAMN13041933,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4125806,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR102/096/SRR10294596/SRR10294596.fastq.gz,332152110,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/096/SRR10294596/SRR10294596.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/096/SRR10294596/SRR10294596.fastq.gz,1aaad1f95341ef4e2170cd4b91977791,2020-04-30,2020-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM4125806_r1,,GSM4125806,,Flash freeze harvesting with anisomycin ribosome profiling,,,,,SRS5528594,SRP225954,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR102/096/SRR10294596,275419563,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/096/SRR10294596,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/096/SRR10294596,f9b61ef9d5ecfdb0b5ac48a2b829a72b,,GSE138990,"Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution",,,SRA980319,,,,,,,,,,,,,,, PRJNA577942,SRX7007425,Illumina HiSeq 2500 sequencing; GSM4125807: Flash freeze harvesting with harringtonine ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125807: Flash freeze harvesting with harringtonine ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041930,Flash freeze harvesting with harringtonine ribosome profiling,Illumina HiSeq 2500,SRR10294597,16070885,1607088500,SAMN13041930,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4125807,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR102/097/SRR10294597/SRR10294597.fastq.gz,717049123,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/097/SRR10294597/SRR10294597.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/097/SRR10294597/SRR10294597.fastq.gz,9cedd150011cab195100f021f486511a,2020-04-30,2020-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM4125807_r1,,GSM4125807,,Flash freeze harvesting with harringtonine ribosome profiling,,,,,SRS5528595,SRP225954,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR102/097/SRR10294597,762841375,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/097/SRR10294597,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/097/SRR10294597,1fd17e947abb5b416622d14a30a7823f,,GSE138990,"Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution",,,SRA980319,,,,,,,,,,,,,,, PRJNA577942,SRX7007426,Illumina HiSeq 2500 sequencing; GSM4125808: Flash freeze harvesting with serine hydroxamate ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125808: Flash freeze harvesting with serine hydroxamate ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041929,Flash freeze harvesting with serine hydroxamate ribosome profiling,Illumina HiSeq 2500,SRR10294598,15432004,1543200400,SAMN13041929,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4125808,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR102/098/SRR10294598/SRR10294598.fastq.gz,714294675,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/098/SRR10294598/SRR10294598.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/098/SRR10294598/SRR10294598.fastq.gz,071b3efe861962285e40a2874ed762e3,2020-04-30,2020-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM4125808_r1,,GSM4125808,,Flash freeze harvesting with serine hydroxamate ribosome profiling,,,,,SRS5528596,SRP225954,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR102/098/SRR10294598,749452044,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/098/SRR10294598,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/098/SRR10294598,b35372c57a592d282e89e064e1df5728,,GSE138990,"Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution",,,SRA980319,,,,,,,,,,,,,,, PRJNA577942,SRX7007428,Illumina HiSeq 2500 sequencing; GSM4125810: Total RNA treated with MNase ribosome profiling; Haloferax volcanii DS2; OTHER,Illumina HiSeq 2500 sequencing; GSM4125810: Total RNA treated with MNase ribosome profiling; Haloferax volcanii DS2; OTHER,309800,Haloferax volcanii DS2,OTHER,TRANSCRIPTOMIC,other,SAMN13041923,Total RNA treated with MNase ribosome profiling,Illumina HiSeq 2500,SRR10294600,8365069,418253450,SAMN13041923,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4125810,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR102/000/SRR10294600/SRR10294600.fastq.gz,312931794,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/000/SRR10294600/SRR10294600.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR102/000/SRR10294600/SRR10294600.fastq.gz,507480079fa189b9b64787eeefb46b55,2020-04-30,2020-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM4125810_r1,,GSM4125810,,Total RNA treated with MNase ribosome profiling,,,,,SRS5528598,SRP225954,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR102/000/SRR10294600,274797029,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/000/SRR10294600,ftp.sra.ebi.ac.uk/vol1/srr/SRR102/000/SRR10294600,202b539feecbbcc49e8e23fab0179676,,GSE138990,"Ribosome profiling in archaea reveals leaderless translation, novel translational initiation sites, and ribosome pausing at single codon resolution",,,SRA980319,,,,,,,,,,,,,,, PRJNA214730,SRX384923,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 1,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 1,1306155,mixed culture,OTHER,TRANSCRIPTOMIC,unspecified,SAMN02401351,Mixed parental selected mRNA fragments,Illumina HiSeq 2000,SRR1040263,112580832,4052909952,SAMN02401351,,,,,,,,,Stanford University,,,,,,,,,,,,,,,,,,,,false,MIXED_PARENTAL_MRNA_REP1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR104/003/SRR1040263/SRR1040263.fastq.gz,3870534856,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/003/SRR1040263/SRR1040263.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/003/SRR1040263/SRR1040263.fastq.gz,8197214be236ca17fc4a40936cc85fed,2014-04-15,2014-04-15,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,MIXED_PARENTAL_MRNA_REP1,,,,,,,,,MIXED_PARENTAL_MRNA_REP1,,MIXED_PARENTAL_MRNA_REP1,,Poly-A selected mRNA fragments isolated from haploid Saccharomyces cerevisiae and Saccharomyces paradoxus using the riboprofiling method,,,,,SRS509098,SRP028614,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR104/003/SRR1040263,2676137205,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/003/SRR1040263,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/003/SRR1040263,b56bd02f83515ab4551889fdce739cc8,Saccharomyces cerevisiae BY4176 & Saccharomyces paradoxus CBS432,PRJNA214730,Ribosome profiling of interspecific hybrids of Saccharomyces cerevisiae and S. paradoxus.,,,SRA097097,,,,,,,,,,,,,,, PRJNA214730,SRX385099,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome footprint fraction replicate 1,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome footprint fraction replicate 1,1306155,mixed culture,OTHER,TRANSCRIPTOMIC,unspecified,SAMN02401352,Mixed parental ribosome protected fragments replicate 1,Illumina HiSeq 2000,SRR1040415,140321514,5051574504,SAMN02401352,,,,,,,,,Stanford University,,,,,,,,,,,,,,,,,,,,false,MIXED_PARENTAL_RIBOFOOTPRINT_REP1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR104/005/SRR1040415/SRR1040415.fastq.gz,3963213889,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/005/SRR1040415/SRR1040415.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/005/SRR1040415/SRR1040415.fastq.gz,06950c9aa848dedc427216fcc46cf0de,2014-04-15,2014-04-15,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,MIXED_PARENTAL_RIBOFOOTPRINT_REP1,,,,,,,,,MIXED_PARENTAL_RIBOFOOTPRINT_REP1,,MIXED_PARENTAL_RIBOFOOTPRINT_REP1,,Ribosome protected RNA fragments isolated from Saccharomyces cerevisiae and Saccharomyces paradoxus using the riboprofiling method,,,,,SRS509272,SRP028614,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR104/005/SRR1040415,6078268348,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/005/SRR1040415,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/005/SRR1040415,a7a98e2ba7d05e26285e988b28a9d226,Saccharomyces cerevisiae BY4176 & Saccharomyces paradoxus CBS432,PRJNA214730,Ribosome profiling of interspecific hybrids of Saccharomyces cerevisiae and S. paradoxus.,,,SRA097097,,,,,,,,,,,,,,, PRJNA214730,SRX385185,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 1,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 1,1306155,mixed culture,OTHER,TRANSCRIPTOMIC,unspecified,SAMN02401353,Mixed parental ribosome protected fragments replicate 2 lane 1,Illumina HiSeq 2000,SRR1040423,130172032,4686193152,SAMN02401353,,,,,,,,,Stanford University,,,,,,,,,,,,,,,,,,,,false,MIXED_PARENTAL_RIBOFOOTPRINT_REP2_1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR104/003/SRR1040423/SRR1040423.fastq.gz,3472375869,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/003/SRR1040423/SRR1040423.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/003/SRR1040423/SRR1040423.fastq.gz,6fe9f61f0afd13d418982f3c1832291c,2014-04-15,2014-04-15,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,MIXED_PARENTAL_RIBOFOOTPRINT_REP2_1,,,,,,,,,MIXED_PARENTAL_MRNA_REP2_1,,MIXED_PARENTAL_RIBOFOOTPRINT_REP2_1,,Ribosome protected RNA fragments isolated from Saccharomyces cerevisiae and Saccharomyces paradoxus using the riboprofiling method,,,,,SRS509342,SRP028614,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR104/003/SRR1040423,2915072772,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/003/SRR1040423,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/003/SRR1040423,7ee5ed087602f266c4bfc10b112511c6,Saccharomyces cerevisiae BY4176 & Saccharomyces paradoxus CBS432,PRJNA214730,Ribosome profiling of interspecific hybrids of Saccharomyces cerevisiae and S. paradoxus.,,,SRA097097,,,,,,,,,,,,,,, PRJNA214730,SRX385187,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 2,Illumina HiSeq 2000 sequencing; Saccharomyces cerevisiae and S. paradoxus parental Ribosome profiling ribosome mRNA fraction replicate 2 - 2,1306155,mixed culture,OTHER,TRANSCRIPTOMIC,unspecified,SAMN02401354,Mixed parental ribosome protected fragments replicate 2 lane 2,Illumina HiSeq 2000,SRR1040427,171400626,6170422536,SAMN02401354,,,,,,,,,Stanford University,,,,,,,,,,,,,,,,,,,,false,MIXED_PARENTAL_MRNA_REP2_2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR104/007/SRR1040427/SRR1040427.fastq.gz,4905049969,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/007/SRR1040427/SRR1040427.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/007/SRR1040427/SRR1040427.fastq.gz,a30721ec56a96602c5cfd14565530e6b,2014-04-15,2014-04-15,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,MIXED_PARENTAL_MRNA_REP2_2,,,,,,,,,MIXED_PARENTAL_MRNA_REP2_2,,MIXED_PARENTAL_RIBOFOOTPRINT_REP2_2,,Ribosome protected RNA fragments isolated from Saccharomyces cerevisiae and Saccharomyces paradoxus using the riboprofiling method,,,,,SRS509345,SRP028614,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR104/007/SRR1040427,4061319353,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/007/SRR1040427,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/007/SRR1040427,e9f9f7e8a3260c3b3675596fa63b2f88,Saccharomyces cerevisiae BY4176 & Saccharomyces paradoxus CBS432,PRJNA214730,Ribosome profiling of interspecific hybrids of Saccharomyces cerevisiae and S. paradoxus.,,,SRA097097,,,,,,,,,,,,,,, PRJNA230610,SRX387034,Illumina Genome Analyzer II sequencing; GSM1279707: Ribosome Profiling with Control siRNA; Homo sapiens; OTHER,Illumina Genome Analyzer II sequencing; GSM1279707: Ribosome Profiling with Control siRNA; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN02435722,Ribosome Profiling with Control siRNA,Illumina Genome Analyzer II,SRR1042900,21277427,893651934,SAMN02435722,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1279707,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR104/000/SRR1042900/SRR1042900.fastq.gz,592549800,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/000/SRR1042900/SRR1042900.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/000/SRR1042900/SRR1042900.fastq.gz,4c51f3881fd502a1093bb897ef18d829,2014-11-11,2014-11-11,false,,,,,,,,,,,ILLUMINA,,,,2020-05-22,,SINGLE,,,,,,,,,,GSM1279707_r1,,GSM1279707,,Ribosome Profiling with Control siRNA,,,,,SRS510970,SRP033503,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR104/000/SRR1042900,481755276,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/000/SRR1042900,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/000/SRR1042900,78f88fd41a33b2bb25cb9dca56b8ce69,,GSE52976,Integrative AUF1 PAR-CLIP analysis uncovers AUF1 roles in translation and genome integrity (Ribosome),,,SRA115272,,,,,,,,,,,,,,, PRJNA230610,SRX387035,Illumina Genome Analyzer II sequencing; GSM1279708: Ribosome Profiling with AUF1 siRNA; Homo sapiens; OTHER,Illumina Genome Analyzer II sequencing; GSM1279708: Ribosome Profiling with AUF1 siRNA; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN02435724,Ribosome Profiling with AUF1 siRNA,Illumina Genome Analyzer II,SRR1042901,22678915,952514430,SAMN02435724,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1279708,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR104/001/SRR1042901/SRR1042901.fastq.gz,623476413,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/001/SRR1042901/SRR1042901.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/001/SRR1042901/SRR1042901.fastq.gz,28f26c19e41e0ab74ee06eaa4a32882a,2014-11-11,2014-11-11,false,,,,,,,,,,,ILLUMINA,,,,2020-02-05,,SINGLE,,,,,,,,,,GSM1279708_r1,,GSM1279708,,Ribosome Profiling with AUF1 siRNA,,,,,SRS510969,SRP033503,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR104/001/SRR1042901,506359232,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/001/SRR1042901,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/001/SRR1042901,7805b7b7680a7fe485fec77bc8806a8a,,GSE52976,Integrative AUF1 PAR-CLIP analysis uncovers AUF1 roles in translation and genome integrity (Ribosome),,,SRA115272,,,,,,,,,,,,,,, PRJNA230610,SRX387036,Illumina Genome Analyzer II sequencing; GSM1279709: Ribosome Profiling with HuR siRNA; Homo sapiens; OTHER,Illumina Genome Analyzer II sequencing; GSM1279709: Ribosome Profiling with HuR siRNA; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN02435723,Ribosome Profiling with HuR siRNA,Illumina Genome Analyzer II,SRR1042902,3818427,160373934,SAMN02435723,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1279709,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR104/002/SRR1042902/SRR1042902.fastq.gz,98293471,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/002/SRR1042902/SRR1042902.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR104/002/SRR1042902/SRR1042902.fastq.gz,a963d90d02aeb32f01f3e9385b5bf0c0,2014-11-11,2014-11-11,false,,,,,,,,,,,ILLUMINA,,,,2019-10-13,,SINGLE,,,,,,,,,,GSM1279709_r1,,GSM1279709,,Ribosome Profiling with HuR siRNA,,,,,SRS510971,SRP033503,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR104/002/SRR1042902,79459938,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/002/SRR1042902,ftp.sra.ebi.ac.uk/vol1/srr/SRR104/002/SRR1042902,1b5d68ba8963da6a6de0a09e0363401b,,GSE52976,Integrative AUF1 PAR-CLIP analysis uncovers AUF1 roles in translation and genome integrity (Ribosome),,,SRA115272,,,,,,,,,,,,,,, PRJNA232843,SRX403935,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566834,ribosome profiling in rich defined media,Illumina HiSeq 2000,SRR1067765,30562326,1528116300,SAMN02566834,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1300279,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR106/005/SRR1067765/SRR1067765.fastq.gz,1058971446,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/005/SRR1067765/SRR1067765.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/005/SRR1067765/SRR1067765.fastq.gz,fba322840f6ceb7867e3a070e005317b,2014-04-30,2014-04-30,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1300279_r1,,GSM1300279,,ribosome profiling in rich defined media,,,,,SRS523651,SRP034871,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR106/005/SRR1067765,1032820006,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/005/SRR1067765,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/005/SRR1067765,ca26d398a842d304d013e51d955cd6c0,K-12,GSE53767,Absolute quantification of protein production reveals principles underlying protein synthesis rates,,MG1655,SRA122790,,,,,,,,,,,,,,, PRJNA232843,SRX403935,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566834,ribosome profiling in rich defined media,Illumina HiSeq 2000,SRR1067766,163797786,8353687086,SAMN02566834,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1300279,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR106/006/SRR1067766/SRR1067766.fastq.gz,6668841696,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/006/SRR1067766/SRR1067766.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/006/SRR1067766/SRR1067766.fastq.gz,c8fd7acc0e3177b06340ce3f4b08e671,2014-04-30,2014-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-05-23,,SINGLE,,,,,,,,,,GSM1300279_r2,,GSM1300279,,ribosome profiling in rich defined media,,,,,SRS523651,SRP034871,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR106/006/SRR1067766,5748538931,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/006/SRR1067766,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/006/SRR1067766,6409deeec23a1d01fba0ae8ee4cf724d,K-12,GSE53767,Absolute quantification of protein production reveals principles underlying protein synthesis rates,,MG1655,SRA122790,,,,,,,,,,,,,,, PRJNA232843,SRX403935,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566834,ribosome profiling in rich defined media,Illumina HiSeq 2000,SRR1067767,60601845,3090694095,SAMN02566834,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1300279,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR106/007/SRR1067767/SRR1067767.fastq.gz,2268673872,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/007/SRR1067767/SRR1067767.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/007/SRR1067767/SRR1067767.fastq.gz,f089f802b0897137e5acfee47c8256dc,2014-04-30,2014-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-05-22,,SINGLE,,,,,,,,,,GSM1300279_r3,,GSM1300279,,ribosome profiling in rich defined media,,,,,SRS523651,SRP034871,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR106/007/SRR1067767,2017256040,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/007/SRR1067767,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/007/SRR1067767,a999ed6237277d05c0bb374624f26840,K-12,GSE53767,Absolute quantification of protein production reveals principles underlying protein synthesis rates,,MG1655,SRA122790,,,,,,,,,,,,,,, PRJNA232843,SRX403935,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM1300279: ribosome profiling in rich defined media; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566834,ribosome profiling in rich defined media,Illumina HiSeq 2000,SRR1067768,141202340,7201319340,SAMN02566834,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1300279,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR106/008/SRR1067768/SRR1067768.fastq.gz,5579630200,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/008/SRR1067768/SRR1067768.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/008/SRR1067768/SRR1067768.fastq.gz,850b63898203cb1d40d87b360a6aa7fb,2014-04-30,2014-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-05-22,,SINGLE,,,,,,,,,,GSM1300279_r4,,GSM1300279,,ribosome profiling in rich defined media,,,,,SRS523651,SRP034871,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR106/008/SRR1067768,4952004818,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/008/SRR1067768,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/008/SRR1067768,58e9f654d9a8e7964bfc588b1fdc6b28,K-12,GSE53767,Absolute quantification of protein production reveals principles underlying protein synthesis rates,,MG1655,SRA122790,,,,,,,,,,,,,,, PRJNA232843,SRX403936,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566832,ribosome profiling in minimal media 1,Illumina HiSeq 2500,SRR1067769,88792279,4528406229,SAMN02566832,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1300280,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR106/009/SRR1067769/SRR1067769.fastq.gz,3434700136,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/009/SRR1067769/SRR1067769.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/009/SRR1067769/SRR1067769.fastq.gz,cdcc55a7f051e4b0e242ad0c30ff026f,2014-04-30,2014-04-30,false,,,,,,,,,,,ILLUMINA,,,,2020-05-22,,SINGLE,,,,,,,,,,GSM1300280_r1,,GSM1300280,,ribosome profiling in minimal media 1,,,,,SRS523650,SRP034871,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR106/009/SRR1067769,2984076037,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/009/SRR1067769,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/009/SRR1067769,d812d0e152f898c0b4e2e72661e8cdc8,K-12,GSE53767,Absolute quantification of protein production reveals principles underlying protein synthesis rates,,MG1655,SRA122790,,,,,,,,,,,,,,, PRJNA232843,SRX403936,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER,Illumina HiSeq 2500 sequencing; GSM1300280: ribosome profiling in minimal media 1; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566832,ribosome profiling in minimal media 1,Illumina HiSeq 2500,SRR1067770,41605070,2121858570,SAMN02566832,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1300280,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR106/000/SRR1067770/SRR1067770.fastq.gz,1659315602,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/000/SRR1067770/SRR1067770.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/000/SRR1067770/SRR1067770.fastq.gz,abd86791daf1c90f5febee137cf6534e,2014-04-30,2014-04-30,false,,,,,,,,,,,ILLUMINA,,,,2019-11-04,,SINGLE,,,,,,,,,,GSM1300280_r2,,GSM1300280,,ribosome profiling in minimal media 1,,,,,SRS523650,SRP034871,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR106/000/SRR1067770,1425190871,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/000/SRR1067770,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/000/SRR1067770,ebd29759719b19583b861af731460a07,K-12,GSE53767,Absolute quantification of protein production reveals principles underlying protein synthesis rates,,MG1655,SRA122790,,,,,,,,,,,,,,, PRJNA232843,SRX403937,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566833,ribosome profiling in minimal media 2,Illumina HiSeq 2500,SRR1067771,65430349,3336947799,SAMN02566833,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1300281,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR106/001/SRR1067771/SRR1067771.fastq.gz,2396666373,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/001/SRR1067771/SRR1067771.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/001/SRR1067771/SRR1067771.fastq.gz,90b63941a2fd28d359ca57fb2008c372,2014-04-30,2014-04-30,false,,,,,,,,,,,ILLUMINA,,,,2019-11-23,,SINGLE,,,,,,,,,,GSM1300281_r1,,GSM1300281,,ribosome profiling in minimal media 2,,,,,SRS523652,SRP034871,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR106/001/SRR1067771,2103275630,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/001/SRR1067771,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/001/SRR1067771,fa26888b73ffce93d05a40449f14d261,K-12,GSE53767,Absolute quantification of protein production reveals principles underlying protein synthesis rates,,MG1655,SRA122790,,,,,,,,,,,,,,, PRJNA232843,SRX403937,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER,Illumina HiSeq 2500 sequencing; GSM1300281: ribosome profiling in minimal media 2; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN02566833,ribosome profiling in minimal media 2,Illumina HiSeq 2500,SRR1067772,70786149,3610093599,SAMN02566833,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1300281,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR106/002/SRR1067772/SRR1067772.fastq.gz,3049549873,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/002/SRR1067772/SRR1067772.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR106/002/SRR1067772/SRR1067772.fastq.gz,e1f4d52b542feb35b5ebe5cff22d8a8a,2014-04-30,2014-04-30,false,,,,,,,,,,,ILLUMINA,,,,2019-10-07,,SINGLE,,,,,,,,,,GSM1300281_r2,,GSM1300281,,ribosome profiling in minimal media 2,,,,,SRS523652,SRP034871,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR106/002/SRR1067772,2594360889,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/002/SRR1067772,ftp.sra.ebi.ac.uk/vol1/srr/SRR106/002/SRR1067772,4412797a9bdc60b5ee881de8dd2cce77,K-12,GSE53767,Absolute quantification of protein production reveals principles underlying protein synthesis rates,,MG1655,SRA122790,,,,,,,,,,,,,,, PRJNA602917,SRX7625186,NextSeq 500 sequencing; GSM4282352: Ribosome profiling_sgABCE1-1; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM4282352: Ribosome profiling_sgABCE1-1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN13910616,Ribosome profiling_sgABCE1-1,NextSeq 500,SRR10959087,63652500,4901242500,SAMN13910616,,,,,,,NMD reporter,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4282352,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR109/087/SRR10959087/SRR10959087.fastq.gz,1647586989,ftp.sra.ebi.ac.uk/vol1/fastq/SRR109/087/SRR10959087/SRR10959087.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR109/087/SRR10959087/SRR10959087.fastq.gz,a44812f3ca43c60ee47bba44d28fc63f,2020-07-15,2020-07-15,false,,,,,,,,,,,ILLUMINA,,,,2020-07-15,,SINGLE,,,,,,,,,,GSM4282352_r1,,GSM4282352,,Ribosome profiling_sgABCE1-1,,,,,SRS6057079,SRP244436,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR109/087/SRR10959087,1781541282,ftp.sra.ebi.ac.uk/vol1/srr/SRR109/087/SRR10959087,ftp.sra.ebi.ac.uk/vol1/srr/SRR109/087/SRR10959087,f4cde221ca8336c49ff2447c41dc8803,,GSE144163,Ribosome profiling of ABCE1-knockout cells,,,SRA1030824,,,,,,,,,,,,,,, PRJNA602917,SRX7625187,NextSeq 500 sequencing; GSM4282353: Ribosome profiling_sgABCE1-2; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM4282353: Ribosome profiling_sgABCE1-2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN13910615,Ribosome profiling_sgABCE1-2,NextSeq 500,SRR10959088,67271269,5179887713,SAMN13910615,,,,,,,NMD reporter,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4282353,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR109/088/SRR10959088/SRR10959088.fastq.gz,1722000071,ftp.sra.ebi.ac.uk/vol1/fastq/SRR109/088/SRR10959088/SRR10959088.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR109/088/SRR10959088/SRR10959088.fastq.gz,f635e76107060c0bc8a826d8baad8551,2020-07-15,2020-07-15,false,,,,,,,,,,,ILLUMINA,,,,2020-07-15,,SINGLE,,,,,,,,,,GSM4282353_r1,,GSM4282353,,Ribosome profiling_sgABCE1-2,,,,,SRS6057080,SRP244436,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR109/088/SRR10959088,1858667672,ftp.sra.ebi.ac.uk/vol1/srr/SRR109/088/SRR10959088,ftp.sra.ebi.ac.uk/vol1/srr/SRR109/088/SRR10959088,0a97d095d5fd482c749beb753253b286,,GSE144163,Ribosome profiling of ABCE1-knockout cells,,,SRA1030824,,,,,,,,,,,,,,, PRJNA602917,SRX7625188,NextSeq 500 sequencing; GSM4282354: Ribosome profiling_sgNT1; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM4282354: Ribosome profiling_sgNT1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN13910614,Ribosome profiling_sgNT1,NextSeq 500,SRR10959089,91168220,7019952940,SAMN13910614,,,,,,,NMD reporter,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4282354,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR109/089/SRR10959089/SRR10959089.fastq.gz,2307087059,ftp.sra.ebi.ac.uk/vol1/fastq/SRR109/089/SRR10959089/SRR10959089.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR109/089/SRR10959089/SRR10959089.fastq.gz,0cd80c29c21f724a095b2b32ce5a2371,2020-07-15,2020-07-15,false,,,,,,,,,,,ILLUMINA,,,,2020-07-15,,SINGLE,,,,,,,,,,GSM4282354_r1,,GSM4282354,,Ribosome profiling_sgNT1,,,,,SRS6057081,SRP244436,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR109/089/SRR10959089,2484501126,ftp.sra.ebi.ac.uk/vol1/srr/SRR109/089/SRR10959089,ftp.sra.ebi.ac.uk/vol1/srr/SRR109/089/SRR10959089,ea39d8f9116a752efca2f04202afda91,,GSE144163,Ribosome profiling of ABCE1-knockout cells,,,SRA1030824,,,,,,,,,,,,,,, PRJNA602917,SRX7625189,NextSeq 500 sequencing; GSM4282355: Ribosome profiling_sgNT2; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM4282355: Ribosome profiling_sgNT2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN13910613,Ribosome profiling_sgNT2,NextSeq 500,SRR10959090,104512107,8047432239,SAMN13910613,,,,,,,NMD reporter,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4282355,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR109/090/SRR10959090/SRR10959090.fastq.gz,2643374487,ftp.sra.ebi.ac.uk/vol1/fastq/SRR109/090/SRR10959090/SRR10959090.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR109/090/SRR10959090/SRR10959090.fastq.gz,36fd5371dee2742845b854afb2bc7e0f,2020-07-15,2020-07-15,false,,,,,,,,,,,ILLUMINA,,,,2020-07-15,,SINGLE,,,,,,,,,,GSM4282355_r1,,GSM4282355,,Ribosome profiling_sgNT2,,,,,SRS6057082,SRP244436,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR109/090/SRR10959090,2854913289,ftp.sra.ebi.ac.uk/vol1/srr/SRR109/090/SRR10959090,ftp.sra.ebi.ac.uk/vol1/srr/SRR109/090/SRR10959090,389657990b60ba78f281e298d50e09cb,,GSE144163,Ribosome profiling of ABCE1-knockout cells,,,SRA1030824,,,,,,,,,,,,,,, PRJNA609842,SRX7829328,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82,591946,Escherichia coli LF82,RNA-Seq,OTHER,other,SAMN14260632,LF82-anaerobic,Illumina HiSeq 2500,SRR11217089,450754,10867843,SAMN14260632,,,,,,,,,SUB7077949,,ARLETTE DARFEUILLE-MICHAUD,1998-01-01,,,France: Clermont-Ferrand,,,,,,,,,,,,,,false,RIBO-sample2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR112/089/SRR11217089/SRR11217089.fastq.gz,5440858,ftp.sra.ebi.ac.uk/vol1/fastq/SRR112/089/SRR11217089/SRR11217089.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR112/089/SRR11217089/SRR11217089.fastq.gz,43a18a69945bdd5c22c29b9d3f5d109c,2020-03-04,2020-03-04,false,,,,,,,,,,,ILLUMINA,,,Human colon,2020-03-04,45.770668,SINGLE,RIBO-sample2,45.770668 N 3.087886 E,3.087886,,,,,,,RIBO-sample2.fastq,,Anaerobic-growth,,LF82-anaerobic,,,,,SRS6240068,SRP251336,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR112/089/SRR11217089,4867471,ftp.sra.ebi.ac.uk/vol1/srr/SRR112/089/SRR11217089,ftp.sra.ebi.ac.uk/vol1/srr/SRR112/089/SRR11217089,9c73c56d32f15f8322c5d8c9f83b2b58,LF82,PRJNA609842,Novel operlapping gene pop,,,SRA1050320,,,,,,,,,,,,,,, PRJNA609842,SRX7829327,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82,Illumina HiSeq 2500 sequencing; ribosome profiling of E. coli LF82,591946,Escherichia coli LF82,RNA-Seq,OTHER,other,SAMN14260632,LF82-anaerobic,Illumina HiSeq 2500,SRR11217090,89211,1982957,SAMN14260632,,,,,,,,,SUB7077949,,ARLETTE DARFEUILLE-MICHAUD,1998-01-01,,,France: Clermont-Ferrand,,,,,,,,,,,,,,false,RIBO-sample1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR112/090/SRR11217090/SRR11217090.fastq.gz,1064502,ftp.sra.ebi.ac.uk/vol1/fastq/SRR112/090/SRR11217090/SRR11217090.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR112/090/SRR11217090/SRR11217090.fastq.gz,4c6ca7d2d4013dcacf7a7d2098e4e76f,2020-03-04,2020-03-04,false,,,,,,,,,,,ILLUMINA,,,Human colon,2020-03-04,45.770668,SINGLE,RIBO-sample1,45.770668 N 3.087886 E,3.087886,,,,,,,RIBO-sample1.fastq,,Anaerobic-growth,,LF82-anaerobic,,,,,SRS6240068,SRP251336,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR112/090/SRR11217090,1032112,ftp.sra.ebi.ac.uk/vol1/srr/SRR112/090/SRR11217090,ftp.sra.ebi.ac.uk/vol1/srr/SRR112/090/SRR11217090,9bfef07836a2f9be2745b38baede5ecb,LF82,PRJNA609842,Novel operlapping gene pop,,,SRA1050320,,,,,,,,,,,,,,, PRJNA237963,SRX469443,Illumina HiSeq 2000 sequencing; GSM1326110: M2G Ribosome profiling; Caulobacter vibrioides NA1000; OTHER,Illumina HiSeq 2000 sequencing; GSM1326110: M2G Ribosome profiling; Caulobacter vibrioides NA1000; OTHER,565050,Caulobacter vibrioides NA1000,OTHER,TRANSCRIPTOMIC,other,SAMN02640191,M2G Ribosome profiling,Illumina HiSeq 2000,SRR1167750,2656902,84987700,SAMN02640191,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1326110,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR116/000/SRR1167750/SRR1167750.fastq.gz,79514855,ftp.sra.ebi.ac.uk/vol1/fastq/SRR116/000/SRR1167750/SRR1167750.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR116/000/SRR1167750/SRR1167750.fastq.gz,67cb0b43bea2c32eaf77233b6bd51755,2014-06-16,2014-06-17,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1326110_r1,,GSM1326110,,M2G Ribosome profiling,,,,,SRS556730,SRP037582,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR116/000/SRR1167750,65799692,ftp.sra.ebi.ac.uk/vol1/srr/SRR116/000/SRR1167750,ftp.sra.ebi.ac.uk/vol1/srr/SRR116/000/SRR1167750,c2a6ec98af292bab388d3908bd95a8d8,NA1000,GSE54883,The coding and noncoding architecture of the Caulobacter crescentus genome,,,SRA139242,,,,,,,,,,,,,,, PRJNA237963,SRX469444,Illumina HiSeq 2000 sequencing; GSM1326111: PYE Ribosome profiling; Caulobacter vibrioides NA1000; OTHER,Illumina HiSeq 2000 sequencing; GSM1326111: PYE Ribosome profiling; Caulobacter vibrioides NA1000; OTHER,565050,Caulobacter vibrioides NA1000,OTHER,TRANSCRIPTOMIC,other,SAMN02640188,PYE Ribosome profiling,Illumina HiSeq 2000,SRR1167751,4274091,130370413,SAMN02640188,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1326111,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR116/001/SRR1167751/SRR1167751.fastq.gz,136160262,ftp.sra.ebi.ac.uk/vol1/fastq/SRR116/001/SRR1167751/SRR1167751.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR116/001/SRR1167751/SRR1167751.fastq.gz,fce5a1e38ac07f7fa216119aa5354c37,2014-06-16,2014-06-17,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1326111_r1,,GSM1326111,,PYE Ribosome profiling,,,,,SRS556731,SRP037582,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR116/001/SRR1167751,106133088,ftp.sra.ebi.ac.uk/vol1/srr/SRR116/001/SRR1167751,ftp.sra.ebi.ac.uk/vol1/srr/SRR116/001/SRR1167751,b7ce70dd06bc6eebaff8494d9d7ec9ac,NA1000,GSE54883,The coding and noncoding architecture of the Caulobacter crescentus genome,,,SRA139242,,,,,,,,,,,,,,, PRJNA633047,SRX8346823,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931307,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794832,10913971,818547825,SAMN14931307,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,WT rep1 mock input,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/032/SRR11794832/SRR11794832.fastq.gz,481780696,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/032/SRR11794832/SRR11794832.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/032/SRR11794832/SRR11794832.fastq.gz,3f476e859c079b0312b5a999301d776b,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,WT rep1 mock input,,,,,,,,,WT_rep1_mock_input.fastq,,WT_rep1_mock_ribopro,,WT cells,,,,,SRS6663548,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/032/SRR11794832,663515279,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/032/SRR11794832,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/032/SRR11794832,dd32b04539b1c10776fa6e87c65b0a8f,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346822,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931307,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794833,13852845,1038963375,SAMN14931307,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,WT rep1 mock RPF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/033/SRR11794833/SRR11794833.fastq.gz,554138808,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/033/SRR11794833/SRR11794833.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/033/SRR11794833/SRR11794833.fastq.gz,e4180bf66e2abbca67dc145d6ce4448a,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,WT rep1 mock RPF,,,,,,,,,WT_rep1_mock_RPF.fastq,,WT_rep1_mock_ribopro,,WT cells,,,,,SRS6663548,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/033/SRR11794833,840047808,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/033/SRR11794833,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/033/SRR11794833,654914c8b322e312881e8c005f3bccac,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346821,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931306,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794834,8940111,670508325,SAMN14931306,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,WT rep2 infection input,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/034/SRR11794834/SRR11794834.fastq.gz,385796397,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/034/SRR11794834/SRR11794834.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/034/SRR11794834/SRR11794834.fastq.gz,121baeaa7c7eec9d304462469cbf3102,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,WT rep2 infection input,,,,,,,,,WT_rep2_infection_input.fastq,,WT_rep2_infection_ribpro,,WT cells,,,,,SRS6663547,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/034/SRR11794834,541170258,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/034/SRR11794834,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/034/SRR11794834,ba4e3732e51549fb11f2d97dc0c76d33,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346820,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931306,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794835,15366865,1152514875,SAMN14931306,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,WT rep2 infection RPF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/035/SRR11794835/SRR11794835.fastq.gz,546026869,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/035/SRR11794835/SRR11794835.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/035/SRR11794835/SRR11794835.fastq.gz,ff26fe972b50a4520568ce268c8ce02d,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,WT rep2 infection RPF,,,,,,,,,WT_rep2_infection_RPF.fastq,,WT_rep2_infection_ribpro,,WT cells,,,,,SRS6663547,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/035/SRR11794835,935483368,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/035/SRR11794835,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/035/SRR11794835,7b15e32615b08f2d58693af46f6e011a,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346819,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931305,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794836,11605004,870375300,SAMN14931305,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,WT rep1 infection input,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/036/SRR11794836/SRR11794836.fastq.gz,500990935,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/036/SRR11794836/SRR11794836.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/036/SRR11794836/SRR11794836.fastq.gz,db1b207d45d7d55016f9561e0c932212,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,WT rep1 infection input,,,,,,,,,WT_rep1_infection_input.fastq,,WT_rep1_infection_ribopro,,WT cells,,,,,SRS6663546,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/036/SRR11794836,702441562,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/036/SRR11794836,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/036/SRR11794836,a61691157f03fd45e1d09f652179e049,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346818,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells,NextSeq 500 sequencing; ribosome profiling of influenza virus infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931305,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794837,23196621,1739746575,SAMN14931305,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,WT rep1 infection RPF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/037/SRR11794837/SRR11794837.fastq.gz,882120383,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/037/SRR11794837/SRR11794837.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/037/SRR11794837/SRR11794837.fastq.gz,623099b699a5d72e50fcb3bae80d40c3,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,WT rep1 infection RPF,,,,,,,,,WT_rep1_infection_RPF.fastq,,WT_rep1_infection_ribopro,,WT cells,,,,,SRS6663546,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/037/SRR11794837,1416899783,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/037/SRR11794837,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/037/SRR11794837,acd934b2977695310083b01123d93a99,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346815,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931312,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794840,9198727,689904525,SAMN14931312,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,KO rep2 mock input,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/040/SRR11794840/SRR11794840.fastq.gz,377251410,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/040/SRR11794840/SRR11794840.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/040/SRR11794840/SRR11794840.fastq.gz,087ca9ac38d1bb64305f19275e58f5f1,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,KO rep2 mock input,,,,,,,,,KO_rep2_mock_input.fastq,,KO_rep2_mock_ribopro,,IFIT2 knockout cells,,,,,SRS6663544,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/040/SRR11794840,559438166,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/040/SRR11794840,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/040/SRR11794840,feef0954f7a3e54c6779d1c1ed4dc086,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346814,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931312,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794841,17944493,1345836975,SAMN14931312,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,KO rep2 mock RPF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/041/SRR11794841/SRR11794841.fastq.gz,673468102,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/041/SRR11794841/SRR11794841.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/041/SRR11794841/SRR11794841.fastq.gz,f422219091e4d1efb47268ed56d47e25,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,KO rep2 mock RPF,,,,,,,,,KO_rep2_mock_RPF.fastq,,KO_rep2_mock_ribopro,,IFIT2 knockout cells,,,,,SRS6663544,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/041/SRR11794841,1093140687,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/041/SRR11794841,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/041/SRR11794841,26ace3d92335d3a570afa595d43633c2,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346813,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling input of mock infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931311,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794842,8435062,632629650,SAMN14931311,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,KO rep1 mock input,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/042/SRR11794842/SRR11794842.fastq.gz,365270843,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/042/SRR11794842/SRR11794842.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/042/SRR11794842/SRR11794842.fastq.gz,c8eee467951a0c344f6497c5247203a0,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,KO rep1 mock input,,,,,,,,,KO_rep1_mock_input.fastq,,KO_rep1_mock_ribpro,,IFIT2 knockout cells,,,,,SRS6663543,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/042/SRR11794842,513634969,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/042/SRR11794842,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/042/SRR11794842,b7fc2492be3be175b1eff530d0672b64,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346812,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling of mock infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931311,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794843,21767715,1632578625,SAMN14931311,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,KO rep1 mock RPF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/043/SRR11794843/SRR11794843.fastq.gz,829527474,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/043/SRR11794843/SRR11794843.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/043/SRR11794843/SRR11794843.fastq.gz,0747d145d6c2e38ee915b8643031e905,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,KO rep1 mock RPF,,,,,,,,,KO_rep1_mock_RPF.fastq,,KO_rep1_mock_ribpro,,IFIT2 knockout cells,,,,,SRS6663543,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/043/SRR11794843,1338111427,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/043/SRR11794843,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/043/SRR11794843,a6f957ab1c2b06abb764ac1df68d6acf,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346811,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KOWT cells,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KOWT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931310,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794844,11905053,892878975,SAMN14931310,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,KO rep2 infection input,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/044/SRR11794844/SRR11794844.fastq.gz,506974295,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/044/SRR11794844/SRR11794844.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/044/SRR11794844/SRR11794844.fastq.gz,0f6972980fc96a7aca31f47e09f40d5d,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,KO rep2 infection input,,,,,,,,,KO_rep2_infection_input.fastq,,KO_rep2_infection_ribpro,,IFIT2 knockout cells,,,,,SRS6663542,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/044/SRR11794844,728353320,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/044/SRR11794844,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/044/SRR11794844,91e82130b4ce308d33b73db8aac59968,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346810,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931310,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794845,20046166,1503462450,SAMN14931310,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,KO rep2 infection RPF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/045/SRR11794845/SRR11794845.fastq.gz,728074689,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/045/SRR11794845/SRR11794845.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/045/SRR11794845/SRR11794845.fastq.gz,b545a1157d3702a36747a17e00f8d322,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,KO rep2 infection RPF,,,,,,,,,KO_rep2_infection_RPF.fastq,,KO_rep2_infection_ribpro,,IFIT2 knockout cells,,,,,SRS6663542,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/045/SRR11794845,1224656296,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/045/SRR11794845,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/045/SRR11794845,5dddcf201ecd3e7c2efd948c1c19496f,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346809,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling input of influenza virus infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931309,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794846,7457075,559280625,SAMN14931309,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,KO rep1 infection input,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/046/SRR11794846/SRR11794846.fastq.gz,324326738,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/046/SRR11794846/SRR11794846.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/046/SRR11794846/SRR11794846.fastq.gz,b00ab18e05ec0beea75b51e36c87a8cf,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,KO rep1 infection input,,,,,,,,,KO_rep1_infection_input.fastq,,KO_rep1_infection_ribopro,,IFIT2 knockout cells,,,,,SRS6663541,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/046/SRR11794846,451643779,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/046/SRR11794846,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/046/SRR11794846,607bdda336e5e838811d494497ff63e4,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346808,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells,NextSeq 500 sequencing; ribosome profiling of influenza virus infected IFIT2 KO cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931309,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794847,17374979,1303123425,SAMN14931309,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,KO rep1 infection RPF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/047/SRR11794847/SRR11794847.fastq.gz,676603551,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/047/SRR11794847/SRR11794847.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/047/SRR11794847/SRR11794847.fastq.gz,88f056728a2931cd72fe351d06772bbb,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,KO rep1 infection RPF,,,,,,,,,KO_rep1_infection_RPF.fastq,,KO_rep1_infection_ribopro,,IFIT2 knockout cells,,,,,SRS6663541,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/047/SRR11794847,1065300530,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/047/SRR11794847,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/047/SRR11794847,17cfba8d0e51695d6d84c7bd504b6b5f,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346807,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells,NextSeq 500 sequencing; ribosome profiling input of mock infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931308,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794848,10427687,782076525,SAMN14931308,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,WT rep2 mock input,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/048/SRR11794848/SRR11794848.fastq.gz,454428397,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/048/SRR11794848/SRR11794848.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/048/SRR11794848/SRR11794848.fastq.gz,864fd233565f4c4b2224eaeb70af3f58,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,WT rep2 mock input,,,,,,,,,WT_rep2_mock_input.fastq,,WT_rep2_mock_ribopro,,WT cells,,,,,SRS6663540,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/048/SRR11794848,631536648,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/048/SRR11794848,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/048/SRR11794848,58678943476904f6007d57299ea9aa89,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA633047,SRX8346806,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells,NextSeq 500 sequencing; ribosome profiling of mock infected WT cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN14931308,This sample has been submitted by pda|mehle@berkeley.edu on 2020-07-04; Homo sapiens,NextSeq 500,SRR11794849,19019697,1426477275,SAMN14931308,,,,,,,A549,,SUB7149507,,,,,,,,,,,ATCC:CCL185,,,,,,,,,false,WT rep2 mock RPF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR117/049/SRR11794849/SRR11794849.fastq.gz,729310671,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/049/SRR11794849/SRR11794849.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR117/049/SRR11794849/SRR11794849.fastq.gz,a95d70ba0864bf27609650897b7b0aa3,2020-07-04,2020-07-04,false,,,,,,,,,,,ILLUMINA,,,,2020-07-04,,SINGLE,WT rep2 mock RPF,,,,,,,,,WT_rep2_mock_RPF.fastq,,WT_rep2_mock_ribopro,,WT cells,,,,,SRS6663540,SRP261790,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR117/049/SRR11794849,1157063140,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/049/SRR11794849,ftp.sra.ebi.ac.uk/vol1/srr/SRR117/049/SRR11794849,e2c6d9c6affb01c41b968d28fb3b10a1,,PRJNA633047,IFIT2 CLIP-Seq to identifying RNAs bound during influenza virus infection and ribosome profiling,,,SRA1075839,,,,,,,,male,,,,,,lung, PRJNA634689,SRX8386869,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15005046,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,Illumina HiSeq 2000,SRR11836448,145591529,7279576450,SAMN15005046,,,,,,,,mouse embryonic fibroblasts,SUB7491406,,,,,,,,,,,,,E13.5,,,,,,,false,rfp_KO_starve,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR118/048/SRR11836448/SRR11836448.fastq.gz,2321057385,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/048/SRR11836448/SRR11836448.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/048/SRR11836448/SRR11836448.fastq.gz,7af834a16d097fdb9974c7651fdd1369,2020-05-25,2020-05-25,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,rfp_KO_starve,,,,,,,,,RPKK1RPF4_S42_L006_R1_001.fastq.gz,,Atg12KO;starve conditions,,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,,,,,SRS6700666,SRP263114,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR118/048/SRR11836448,2458433358,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/048/SRR11836448,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/048/SRR11836448,d917c3e44ca245c334c33e376f6c1c60,C57BL/6,PRJNA634689,Ribosome profiling reveals a functional role for autophagy in protein translational control,,,SRA1079135,,,,,,,,,,,,,,embryo, PRJNA634689,SRX8386867,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 KO MEFs,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15005045,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,Illumina HiSeq 2000,SRR11836450,140445387,7022269350,SAMN15005045,,,,,,,,mouse embryonic fibroblasts,SUB7491406,,,,,,,,,,,,,E13.5,,,,,,,false,rpf_KO_fed,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR118/050/SRR11836450/SRR11836450.fastq.gz,2345950523,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/050/SRR11836450/SRR11836450.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/050/SRR11836450/SRR11836450.fastq.gz,933df6310fe5c79e5442dda8efcab506,2020-05-25,2020-05-25,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,rpf_KO_fed,,,,,,,,,RPKK1RPF3_S41_L006_R1_001.fastq.gz,,Atg12KO;fed conditions,,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,,,,,SRS6700665,SRP263114,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR118/050/SRR11836450,2329686083,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/050/SRR11836450,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/050/SRR11836450,574b85936a9498a65be7838881e50693,C57BL/6,PRJNA634689,Ribosome profiling reveals a functional role for autophagy in protein translational control,,,SRA1079135,,,,,,,,,,,,,,embryo, PRJNA634689,SRX8386865,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15005044,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,Illumina HiSeq 2000,SRR11836452,105289031,5264451550,SAMN15005044,,,,,,,,mouse embryonic fibroblasts,SUB7491406,,,,,,,,,,,,,E13.5,,,,,,,false,rpf_control_starve,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR118/052/SRR11836452/SRR11836452.fastq.gz,1668578813,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/052/SRR11836452/SRR11836452.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/052/SRR11836452/SRR11836452.fastq.gz,a05d853b3fd3625003940ecca3355af4,2020-05-25,2020-05-25,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,rpf_control_starve,,,,,,,,,RPKK1RPF2_S40_L006_R1_001.fastq.gz,,Atg12f/f;starve conditions,,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,,,,,SRS6700664,SRP263114,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR118/052/SRR11836452,1759979832,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/052/SRR11836452,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/052/SRR11836452,4d96bd0477342c5229bbff0af8d900c5,C57BL/6,PRJNA634689,Ribosome profiling reveals a functional role for autophagy in protein translational control,,,SRA1079135,,,,,,,,,,,,,,embryo, PRJNA634689,SRX8386863,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs,Illumina HiSeq 2000 sequencing; Ribosome profiling of Atg12 WT MEFs,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15005043,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,Illumina HiSeq 2000,SRR11836454,220484500,11024225000,SAMN15005043,,,,,,,,mouse embryonic fibroblasts,SUB7491406,,,,,,,,,,,,,E13.5,,,,,,,false,rpf_control_fed,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR118/054/SRR11836454/SRR11836454.fastq.gz,3429651921,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/054/SRR11836454/SRR11836454.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/054/SRR11836454/SRR11836454.fastq.gz,ef6060a01f82369ca57804229cca1466,2020-05-25,2020-05-25,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,rpf_control_fed,,,,,,,,,RPKK1RPF1_S39_L006_R1_001.fastq.gz,,Atg12f/f;fed conditions,,This sample has been submitted by pda|juliet_goldsmith on 2020-05-25; Mus musculus,,,,,SRS6700663,SRP263114,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR118/054/SRR11836454,3385964138,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/054/SRR11836454,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/054/SRR11836454,17fa9932771ecc86d0cb71306e7c5f21,C57BL/6,PRJNA634689,Ribosome profiling reveals a functional role for autophagy in protein translational control,,,SRA1079135,,,,,,,,,,,,,,embryo, PRJNA634769,SRX8388156,Illumina NovaSeq 6000 sequencing; GSM4567011: Gcn2 WT +AA - Ribosome profiling; Mus musculus; OTHER,Illumina NovaSeq 6000 sequencing; GSM4567011: Gcn2 WT +AA - Ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15006898,Gcn2 WT +AA - Ribosome profiling,Illumina NovaSeq 6000,SRR11837742,25517300,959270048,SAMN15006898,,,,,,,KRPC-A cells (from gen. eng. murine tumors),PDAC-like pancreatic tumor cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4567011,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR118/042/SRR11837742/SRR11837742.fastq.gz,583357555,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/042/SRR11837742/SRR11837742.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/042/SRR11837742/SRR11837742.fastq.gz,2ce2cfcb20056baf032caa115017b434,2020-05-27,2020-05-27,false,,,,,,,,,,,ILLUMINA,,,,2020-05-27,,SINGLE,,,,,,,,,,GSM4567011_r1,,GSM4567011,,Gcn2 WT +AA - Ribosome profiling,,,,,SRS6701689,SRP263196,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR118/042/SRR11837742,394431389,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/042/SRR11837742,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/042/SRR11837742,ba2ca9515daea62ad27039d1105cbc16,,GSE151118,GCN2 adapts the proteome to scavenging-dependent growth,,,SRA1079230,,,,,,,,,,,,,,, PRJNA634769,SRX8388157,Illumina NovaSeq 6000 sequencing; GSM4567012: Gcn2 WT -Leu - Ribosome profiling; Mus musculus; OTHER,Illumina NovaSeq 6000 sequencing; GSM4567012: Gcn2 WT -Leu - Ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15006897,Gcn2 WT -Leu - Ribosome profiling,Illumina NovaSeq 6000,SRR11837743,9333359,363034141,SAMN15006897,,,,,,,KRPC-A cells (from gen. eng. murine tumors),PDAC-like pancreatic tumor cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4567012,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR118/043/SRR11837743/SRR11837743.fastq.gz,210551556,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/043/SRR11837743/SRR11837743.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/043/SRR11837743/SRR11837743.fastq.gz,8b5364cabb3176da58276d9e93e30b21,2020-05-27,2020-05-27,false,,,,,,,,,,,ILLUMINA,,,,2020-05-27,,SINGLE,,,,,,,,,,GSM4567012_r1,,GSM4567012,,Gcn2 WT -Leu - Ribosome profiling,,,,,SRS6701690,SRP263196,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR118/043/SRR11837743,154615621,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/043/SRR11837743,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/043/SRR11837743,51b7a2fdf5a6ff9f274fb0f0c474e7d2,,GSE151118,GCN2 adapts the proteome to scavenging-dependent growth,,,SRA1079230,,,,,,,,,,,,,,, PRJNA634769,SRX8388158,Illumina NovaSeq 6000 sequencing; GSM4567013: Gcn2 KO +AA - Ribosome profiling; Mus musculus; OTHER,Illumina NovaSeq 6000 sequencing; GSM4567013: Gcn2 KO +AA - Ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15006896,Gcn2 KO +AA - Ribosome profiling,Illumina NovaSeq 6000,SRR11837744,19672326,749452566,SAMN15006896,,,,,,,KRPC-A cells (from gen. eng. murine tumors),PDAC-like pancreatic tumor cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4567013,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR118/044/SRR11837744/SRR11837744.fastq.gz,449494224,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/044/SRR11837744/SRR11837744.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/044/SRR11837744/SRR11837744.fastq.gz,e8edf82574048ac39ca37acd03ea4581,2020-05-27,2020-05-27,false,,,,,,,,,,,ILLUMINA,,,,2020-05-27,,SINGLE,,,,,,,,,,GSM4567013_r1,,GSM4567013,,Gcn2 KO +AA - Ribosome profiling,,,,,SRS6701691,SRP263196,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR118/044/SRR11837744,310037759,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/044/SRR11837744,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/044/SRR11837744,ac35df692cb1e11f0f2e265d8b5b17bb,,GSE151118,GCN2 adapts the proteome to scavenging-dependent growth,,,SRA1079230,,,,,,,,,,,,,,, PRJNA634769,SRX8388159,Illumina NovaSeq 6000 sequencing; GSM4567014: Gcn2 KO -Leu - Ribosome profiling; Mus musculus; OTHER,Illumina NovaSeq 6000 sequencing; GSM4567014: Gcn2 KO -Leu - Ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15006895,Gcn2 KO -Leu - Ribosome profiling,Illumina NovaSeq 6000,SRR11837745,15327574,596032744,SAMN15006895,,,,,,,KRPC-A cells (from gen. eng. murine tumors),PDAC-like pancreatic tumor cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4567014,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR118/045/SRR11837745/SRR11837745.fastq.gz,353069823,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/045/SRR11837745/SRR11837745.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR118/045/SRR11837745/SRR11837745.fastq.gz,cc19b90646e1b26bc1b491eb24a6327c,2020-05-27,2020-05-27,false,,,,,,,,,,,ILLUMINA,,,,2020-05-27,,SINGLE,,,,,,,,,,GSM4567014_r1,,GSM4567014,,Gcn2 KO -Leu - Ribosome profiling,,,,,SRS6701692,SRP263196,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR118/045/SRR11837745,252798574,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/045/SRR11837745,ftp.sra.ebi.ac.uk/vol1/srr/SRR118/045/SRR11837745,9035bbe85077d34ac971d339ab0b3729,,GSE151118,GCN2 adapts the proteome to scavenging-dependent growth,,,SRA1079230,,,,,,,,,,,,,,, PRJNA644594,SRX8680381,"Illumina HiSeq 2500 sequencing; GSM4658960: Ribosome profiling from untreated cells, rep 1; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658960: Ribosome profiling from untreated cells, rep 1; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464693,"Ribosome profiling from untreated cells, rep 1",Illumina HiSeq 2500,SRR12164922,12957040,647852000,SAMN15464693,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4658960,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/022/SRR12164922/SRR12164922.fastq.gz,308610891,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/022/SRR12164922/SRR12164922.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/022/SRR12164922/SRR12164922.fastq.gz,9a9abbc84871d2a924766074fc4e7408,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4658960_r1,,GSM4658960,,"Ribosome profiling from untreated cells, rep 1",,,,,SRS6959430,SRP270667,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/022/SRR12164922,256818914,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/022/SRR12164922,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/022/SRR12164922,639600c05625dfa2d6e2d3bac108ad02,,GSE153945,Persistent activation of mRNA translation by transient Hsp90 inhibition,,,SRA1095815,,,,,,,,,,,,,,, PRJNA644594,SRX8680383,"Illumina HiSeq 2500 sequencing; GSM4658962: Ribosome profiling from untreated cells, rep 2; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658962: Ribosome profiling from untreated cells, rep 2; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464691,"Ribosome profiling from untreated cells, rep 2",Illumina HiSeq 2500,SRR12164924,13572040,678602000,SAMN15464691,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4658962,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/024/SRR12164924/SRR12164924.fastq.gz,318167431,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/024/SRR12164924/SRR12164924.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/024/SRR12164924/SRR12164924.fastq.gz,e744946e4ae99ffa0a9ca25ae8858b75,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4658962_r1,,GSM4658962,,"Ribosome profiling from untreated cells, rep 2",,,,,SRS6959432,SRP270667,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/024/SRR12164924,267553123,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/024/SRR12164924,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/024/SRR12164924,59e2051d9e9269f10f706cbdeec7f462,,GSE153945,Persistent activation of mRNA translation by transient Hsp90 inhibition,,,SRA1095815,,,,,,,,,,,,,,, PRJNA644594,SRX8680385,"Illumina HiSeq 2500 sequencing; GSM4658964: Ribosome profiling from untreated cells, rep 3; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658964: Ribosome profiling from untreated cells, rep 3; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464689,"Ribosome profiling from untreated cells, rep 3",Illumina HiSeq 2500,SRR12164926,13747244,687362200,SAMN15464689,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4658964,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/026/SRR12164926/SRR12164926.fastq.gz,321451259,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/026/SRR12164926/SRR12164926.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/026/SRR12164926/SRR12164926.fastq.gz,7763099923d5801484bcd02ab9410ca6,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4658964_r1,,GSM4658964,,"Ribosome profiling from untreated cells, rep 3",,,,,SRS6959433,SRP270667,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/026/SRR12164926,271639409,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/026/SRR12164926,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/026/SRR12164926,dd773d5d622bbb34321b41e3a2c49fe4,,GSE153945,Persistent activation of mRNA translation by transient Hsp90 inhibition,,,SRA1095815,,,,,,,,,,,,,,, PRJNA644594,SRX8680387,"Illumina HiSeq 2500 sequencing; GSM4658966: Ribosome profiling from radicicol cells, rep 1; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658966: Ribosome profiling from radicicol cells, rep 1; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464687,"Ribosome profiling from radicicol cells, rep 1",Illumina HiSeq 2500,SRR12164928,16942016,847100800,SAMN15464687,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4658966,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/028/SRR12164928/SRR12164928.fastq.gz,396281505,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/028/SRR12164928/SRR12164928.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/028/SRR12164928/SRR12164928.fastq.gz,4658a7c791fd421856d848ab73a600b4,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4658966_r1,,GSM4658966,,"Ribosome profiling from radicicol cells, rep 1",,,,,SRS6959435,SRP270667,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/028/SRR12164928,333428679,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/028/SRR12164928,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/028/SRR12164928,da564e3739c209eb422fcf56ce8d544a,,GSE153945,Persistent activation of mRNA translation by transient Hsp90 inhibition,,,SRA1095815,,,,,,,,,,,,,,, PRJNA644594,SRX8680389,"Illumina HiSeq 2500 sequencing; GSM4658968: Ribosome profiling from radicicol cells, rep 2; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658968: Ribosome profiling from radicicol cells, rep 2; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464684,"Ribosome profiling from radicicol cells, rep 2",Illumina HiSeq 2500,SRR12164930,19204213,960210650,SAMN15464684,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4658968,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/030/SRR12164930/SRR12164930.fastq.gz,451440840,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/030/SRR12164930/SRR12164930.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/030/SRR12164930/SRR12164930.fastq.gz,946b7f4b2d41e7d8a943e0732e8009a0,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4658968_r1,,GSM4658968,,"Ribosome profiling from radicicol cells, rep 2",,,,,SRS6959437,SRP270667,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/030/SRR12164930,381803067,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/030/SRR12164930,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/030/SRR12164930,f43da80fe25b6e433b8882a762793964,,GSE153945,Persistent activation of mRNA translation by transient Hsp90 inhibition,,,SRA1095815,,,,,,,,,,,,,,, PRJNA644594,SRX8680391,"Illumina HiSeq 2500 sequencing; GSM4658970: Ribosome profiling from radicicol cells, rep 3; Saccharomyces cerevisiae; OTHER","Illumina HiSeq 2500 sequencing; GSM4658970: Ribosome profiling from radicicol cells, rep 3; Saccharomyces cerevisiae; OTHER",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN15464682,"Ribosome profiling from radicicol cells, rep 3",Illumina HiSeq 2500,SRR12164932,18470726,923536300,SAMN15464682,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM4658970,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/032/SRR12164932/SRR12164932.fastq.gz,429882639,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/032/SRR12164932/SRR12164932.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/032/SRR12164932/SRR12164932.fastq.gz,df4ac77ef2eff9eb21ab73fd21a8de70,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4658970_r1,,GSM4658970,,"Ribosome profiling from radicicol cells, rep 3",,,,,SRS6959439,SRP270667,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/032/SRR12164932,363690682,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/032/SRR12164932,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/032/SRR12164932,83bad178b8520bf0fd33607a251fb223,,GSE153945,Persistent activation of mRNA translation by transient Hsp90 inhibition,,,SRA1095815,,,,,,,,,,,,,,, PRJNA645135,SRX8699982,"Illumina HiSeq 2500 sequencing; GSM4663991: control mouse brain, SMN-specific ribosome profiling, P5, rep 1; Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM4663991: control mouse brain, SMN-specific ribosome profiling, P5, rep 1; Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15493455,"control mouse brain, SMN-specific ribosome profiling, P5, rep 1",Illumina HiSeq 2500,SRR12185464,49288500,2464425000,SAMN15493455,,,,,,,,,GEO,,,,,,,,,,,,,P5,,,,,,,false,GSM4663991,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/064/SRR12185464/SRR12185464.fastq.gz,1238540215,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/064/SRR12185464/SRR12185464.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/064/SRR12185464/SRR12185464.fastq.gz,edbe6befe615b26183f0d41c07c29bd0,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4663991_r1,,GSM4663991,,"control mouse brain, SMN-specific ribosome profiling, P5, rep 1",,,,,SRS6977820,SRP271117,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/064/SRR12185464,1110181554,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/064/SRR12185464,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/064/SRR12185464,a2dd44e5f2995013463c697546d23999,,GSE154106,Ribosome profiling of SMN-primed ribosomes and active ribosome profiling from brains of a mouse model of severe SMA,,,SRA1096857,,,,,,,,,,,,,,, PRJNA645135,SRX8699983,"Illumina HiSeq 2500 sequencing; GSM4663992: control mouse brain, SMN-specific ribosome profiling, P5, rep 2; Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM4663992: control mouse brain, SMN-specific ribosome profiling, P5, rep 2; Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15493454,"control mouse brain, SMN-specific ribosome profiling, P5, rep 2",Illumina HiSeq 2500,SRR12185465,33474442,1673722100,SAMN15493454,,,,,,,,,GEO,,,,,,,,,,,,,P5,,,,,,,false,GSM4663992,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/065/SRR12185465/SRR12185465.fastq.gz,862433834,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/065/SRR12185465/SRR12185465.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/065/SRR12185465/SRR12185465.fastq.gz,1784c235d74fb69c1ca54cf7cdd1d3a9,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4663992_r1,,GSM4663992,,"control mouse brain, SMN-specific ribosome profiling, P5, rep 2",,,,,SRS6977821,SRP271117,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/065/SRR12185465,757217900,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/065/SRR12185465,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/065/SRR12185465,9fb3b6d6f1021baa1c1ccec1dd0bffc9,,GSE154106,Ribosome profiling of SMN-primed ribosomes and active ribosome profiling from brains of a mouse model of severe SMA,,,SRA1096857,,,,,,,,,,,,,,, PRJNA645135,SRX8699984,"Illumina HiSeq 2500 sequencing; GSM4663993: control mouse brain, SMN-specific ribosome profiling, P5, rep 3; Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM4663993: control mouse brain, SMN-specific ribosome profiling, P5, rep 3; Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15493464,"control mouse brain, SMN-specific ribosome profiling, P5, rep 3",Illumina HiSeq 2500,SRR12185466,85414030,4270701500,SAMN15493464,,,,,,,,,GEO,,,,,,,,,,,,,P5,,,,,,,false,GSM4663993,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/066/SRR12185466/SRR12185466.fastq.gz,2088384206,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/066/SRR12185466/SRR12185466.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/066/SRR12185466/SRR12185466.fastq.gz,f7a822d4818668fbe9fb88c41759b941,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4663993_r1,,GSM4663993,,"control mouse brain, SMN-specific ribosome profiling, P5, rep 3",,,,,SRS6977822,SRP271117,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/066/SRR12185466,1896821649,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/066/SRR12185466,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/066/SRR12185466,86f6215db52cd2e256ed8ff2ce16f695,,GSE154106,Ribosome profiling of SMN-primed ribosomes and active ribosome profiling from brains of a mouse model of severe SMA,,,SRA1096857,,,,,,,,,,,,,,, PRJNA645135,SRX8699985,"Illumina HiSeq 2500 sequencing; GSM4663994: control mouse brain, IgG control ribosome profiling, P5, rep 1; Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM4663994: control mouse brain, IgG control ribosome profiling, P5, rep 1; Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN15493463,"control mouse brain, IgG control ribosome profiling, P5, rep 1",Illumina HiSeq 2500,SRR12185467,116656582,5832829100,SAMN15493463,,,,,,,,,GEO,,,,,,,,,,,,,P5,,,,,,,false,GSM4663994,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR121/067/SRR12185467/SRR12185467.fastq.gz,2851818901,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/067/SRR12185467/SRR12185467.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR121/067/SRR12185467/SRR12185467.fastq.gz,45d88b619f77e4779647fe7a5c67051c,2020-08-12,2020-08-12,false,,,,,,,,,,,ILLUMINA,,,,2020-08-12,,SINGLE,,,,,,,,,,GSM4663994_r1,,GSM4663994,,"control mouse brain, IgG control ribosome profiling, P5, rep 1",,,,,SRS6977823,SRP271117,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR121/067/SRR12185467,2577891926,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/067/SRR12185467,ftp.sra.ebi.ac.uk/vol1/srr/SRR121/067/SRR12185467,5b8a90dc90e550fa2687362ab6d43cc3,,GSE154106,Ribosome profiling of SMN-primed ribosomes and active ribosome profiling from brains of a mouse model of severe SMA,,,SRA1096857,,,,,,,,,,,,,,, PRJNA245106,SRX523430,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 1 of 2","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 1 of 2",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN02731565,Saccharomyces cerevisiae Ribosome profiling Wild-type,Illumina HiSeq 2500,SRR1258539,28404464,1448627664,SAMN02731565,,,,,,,,,Center for RNA Molecular Biology,,,,,,,,,,,,,,,,,,,,false,WT Ribosome Profiling 1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR125/009/SRR1258539/SRR1258539.fastq.gz,852212050,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/009/SRR1258539/SRR1258539.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/009/SRR1258539/SRR1258539.fastq.gz,a7a830bbfa9e5aa23ee9cfd516792efe,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,WT Ribosome Profiling 1,,,,,,,,,WT Ribosome Profiling 1,,Ribosome profiling Wild-type,,Saccharomyces cerevisiae Ribosome profiling Wild-type,,,,,SRS595580,SRP041349,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR125/009/SRR1258539,836964356,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/009/SRR1258539,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/009/SRR1258539,f6db5d1a53e47f7e48fc6085639cdf85,BY4741,PRJNA245106,RNA-Seq and Ribosome Profiling in Saccharomyces cerevisiae,,,SRA170837,,,,,,,,,,,,,,Liquid culture, PRJNA245106,SRX523431,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 2 of 2","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, biological replicate 2 of 2",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN02731565,Saccharomyces cerevisiae Ribosome profiling Wild-type,Illumina HiSeq 2500,SRR1258540,22793695,1162478445,SAMN02731565,,,,,,,,,Center for RNA Molecular Biology,,,,,,,,,,,,,,,,,,,,false,WT Ribosome Profiling 2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR125/000/SRR1258540/SRR1258540.fastq.gz,670437340,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/000/SRR1258540/SRR1258540.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/000/SRR1258540/SRR1258540.fastq.gz,6472e2937d7e4aad5898ee162468b1e7,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,WT Ribosome Profiling 2,,,,,,,,,WT Ribosome Profiling 2,,Ribosome profiling Wild-type,,Saccharomyces cerevisiae Ribosome profiling Wild-type,,,,,SRS595580,SRP041349,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR125/000/SRR1258540,666263868,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/000/SRR1258540,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/000/SRR1258540,1188d4fa09cff7b2b10d8f14d8979114,BY4741,PRJNA245106,RNA-Seq and Ribosome Profiling in Saccharomyces cerevisiae,,,SRA170837,,,,,,,,,,,,,,Liquid culture, PRJNA245106,SRX523432,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 1 of 2","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 1 of 2",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN02731566,Saccharomyces cerevisiae Ribosome profiling upf1,Illumina HiSeq 2500,SRR1258541,21727393,1108097043,SAMN02731566,,,,,,,,,Center for RNA Molecular Biology,,,,,,,,,,,,,,,,,,,,false,upf1 Ribosome Profiling 1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR125/001/SRR1258541/SRR1258541.fastq.gz,645343789,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/001/SRR1258541/SRR1258541.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/001/SRR1258541/SRR1258541.fastq.gz,1b15e8104af13862d4a181123dc13444,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,upf1 Ribosome Profiling 1,,,,,,,,,upf1 Ribosome Profiling 1,,Ribosome profiling upf1,,Saccharomyces cerevisiae Ribosome profiling upf1,,,,,SRS595581,SRP041349,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR125/001/SRR1258541,637021500,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/001/SRR1258541,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/001/SRR1258541,a4ef9fb19927eb1eab124b812114cbec,BY4741,PRJNA245106,RNA-Seq and Ribosome Profiling in Saccharomyces cerevisiae,,,SRA170837,,,,,,,,,,,,,,Liquid culture, PRJNA245106,SRX523433,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 2 of 2","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, biological replicate 2 of 2",4932,Saccharomyces cerevisiae,OTHER,TRANSCRIPTOMIC,other,SAMN02731566,Saccharomyces cerevisiae Ribosome profiling upf1,Illumina HiSeq 2500,SRR1258542,23351093,1190905743,SAMN02731566,,,,,,,,,Center for RNA Molecular Biology,,,,,,,,,,,,,,,,,,,,false,upf1 Ribosome Profiling 2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR125/002/SRR1258542/SRR1258542.fastq.gz,678634984,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/002/SRR1258542/SRR1258542.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/002/SRR1258542/SRR1258542.fastq.gz,8e0ac078a75ca2d1440a796e83ba0f20,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,upf1 Ribosome Profiling 2,,,,,,,,,upf1 Ribosome Profiling 2,,Ribosome profiling upf1,,Saccharomyces cerevisiae Ribosome profiling upf1,,,,,SRS595581,SRP041349,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR125/002/SRR1258542,670651959,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/002/SRR1258542,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/002/SRR1258542,bcdbab10fcaa497539702c9fd036cf89,BY4741,PRJNA245106,RNA-Seq and Ribosome Profiling in Saccharomyces cerevisiae,,,SRA170837,,,,,,,,,,,,,,Liquid culture, PRJNA245106,SRX523434,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, fragmented control","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling Wild-type, fragmented control",4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMN02731567,"Saccharomyces cerevisiae Ribosome profiling Wild-type, fragmented control",Illumina HiSeq 2500,SRR1258543,7341479,374415429,SAMN02731567,,,,,,,,,Center for RNA Molecular Biology,,,,,,,,,,,,,,,,,,,,false,"WT Ribosome Profiling, fragmented control",,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR125/003/SRR1258543/SRR1258543.fastq.gz,284371985,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/003/SRR1258543/SRR1258543.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/003/SRR1258543/SRR1258543.fastq.gz,cd2c899f745c5b5ba8eff3207b24980b,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,"WT Ribosome Profiling, fragmented control",,,,,,,,,"WT Ribosome Profiling, fragmented control",,"Ribosome profiling WT, fragmented control",,"Saccharomyces cerevisiae Ribosome profiling Wild-type, fragmented control",,,,,SRS595583,SRP041349,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR125/003/SRR1258543,225951263,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/003/SRR1258543,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/003/SRR1258543,4932b09ad6f5f7631e85ca00b228872a,BY4741,PRJNA245106,RNA-Seq and Ribosome Profiling in Saccharomyces cerevisiae,,,SRA170837,,,,,,,,,,,,,,Liquid culture, PRJNA245106,SRX523435,"Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, fragmented control","Illumina HiSeq 2500 sequencing; Saccharomyces cerevisiae Ribosome Profiling upf1, fragmented control",4932,Saccharomyces cerevisiae,RNA-Seq,TRANSCRIPTOMIC,other,SAMN02731568,"Saccharomyces cerevisiae Ribosome profiling upf1, fragmented control",Illumina HiSeq 2500,SRR1258544,7912713,403548363,SAMN02731568,,,,,,,,,Center for RNA Molecular Biology,,,,,,,,,,,,,,,,,,,,false,"upf1 Ribosome Profiling, fragmented control",,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR125/004/SRR1258544/SRR1258544.fastq.gz,311541593,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/004/SRR1258544/SRR1258544.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR125/004/SRR1258544/SRR1258544.fastq.gz,f2f8d77fe3f1a91c244796640671f50b,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,"upf1 Ribosome Profiling, fragmented control",,,,,,,,,"upf1 Ribosome Profiling, fragmented control",,"Ribosome profiling upf1, fragmented control",,"Saccharomyces cerevisiae Ribosome profiling upf1, fragmented control",,,,,SRS595584,SRP041349,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR125/004/SRR1258544,244756531,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/004/SRR1258544,ftp.sra.ebi.ac.uk/vol1/srr/SRR125/004/SRR1258544,710c98ae3dc9e4c758f30015a9c5e1e1,BY4741,PRJNA245106,RNA-Seq and Ribosome Profiling in Saccharomyces cerevisiae,,,SRA170837,,,,,,,,,,,,,,Liquid culture, PRJNA253056,SRX610794,Illumina HiSeq 2000 sequencing; GSM1415871: ribosome profiling MicL t0; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1415871: ribosome profiling MicL t0; Escherichia coli; RNA-Seq,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02866373,ribosome profiling MicL t0,Illumina HiSeq 2000,SRR1425203,18782455,595176034,SAMN02866373,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1415871,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR142/003/SRR1425203/SRR1425203.fastq.gz,644862037,ftp.sra.ebi.ac.uk/vol1/fastq/SRR142/003/SRR1425203/SRR1425203.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR142/003/SRR1425203/SRR1425203.fastq.gz,6f157d5e1e5e9b958cd10164cbeb8200,2014-08-19,2014-08-20,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1415871_r1,,GSM1415871,,ribosome profiling MicL t0,,,,,SRS641794,SRP043387,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR142/003/SRR1425203,476246245,ftp.sra.ebi.ac.uk/vol1/srr/SRR142/003/SRR1425203,ftp.sra.ebi.ac.uk/vol1/srr/SRR142/003/SRR1425203,60f689477c7757136e4e0e6909cd7be3,K-12,GSE58637,"MicL, a new sE-dependent sRNA, combats envelope stress by repressing synthesis of Lpp, the major outer membrane lipoprotein",,MG1655,SRA171605,,,,,,,,,,,,,,, PRJNA253056,SRX610795,Illumina HiSeq 2000 sequencing; GSM1415872: ribosome profiling MicL t20; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1415872: ribosome profiling MicL t20; Escherichia coli; RNA-Seq,511145,Escherichia coli str. K-12 substr. MG1655,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02866371,ribosome profiling MicL t20,Illumina HiSeq 2000,SRR1425204,28587329,869137845,SAMN02866371,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1415872,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR142/004/SRR1425204/SRR1425204.fastq.gz,952614123,ftp.sra.ebi.ac.uk/vol1/fastq/SRR142/004/SRR1425204/SRR1425204.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR142/004/SRR1425204/SRR1425204.fastq.gz,206a96d6c129075049d2daf3d980a8a0,2014-08-19,2014-08-20,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1415872_r1,,GSM1415872,,ribosome profiling MicL t20,,,,,SRS641795,SRP043387,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR142/004/SRR1425204,696662876,ftp.sra.ebi.ac.uk/vol1/srr/SRR142/004/SRR1425204,ftp.sra.ebi.ac.uk/vol1/srr/SRR142/004/SRR1425204,534f4865952735b5be55b94a113eef4c,K-12,GSE58637,"MicL, a new sE-dependent sRNA, combats envelope stress by repressing synthesis of Lpp, the major outer membrane lipoprotein",,MG1655,SRA171605,,,,,,,,,,,,,,, PRJNA261698,SRX708004,Illumina HiSeq 2000 sequencing; GSM1509451: Ribosome profiling data of untreated E. coli cells; Escherichia coli BW25113; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1509451: Ribosome profiling data of untreated E. coli cells; Escherichia coli BW25113; RNA-Seq,679895,Escherichia coli BW25113,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03075507,Ribosome profiling data of untreated E. coli cells,Illumina HiSeq 2000,SRR1583082,22259168,1135217568,SAMN03075507,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1509451,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR158/002/SRR1583082/SRR1583082.fastq.gz,1051244164,ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/002/SRR1583082/SRR1583082.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/002/SRR1583082/SRR1583082.fastq.gz,9b9fc3d779031bc36e8b23176ac57eab,2015-03-21,2015-03-22,false,,,,,,,,,,,ILLUMINA,,,,2020-05-14,,SINGLE,,,,,,,,,,GSM1509451_r1,,GSM1509451,,Ribosome profiling data of untreated E. coli cells,,,,,SRS707090,SRP047380,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR158/002/SRR1583082,843023862,ftp.sra.ebi.ac.uk/vol1/srr/SRR158/002/SRR1583082,ftp.sra.ebi.ac.uk/vol1/srr/SRR158/002/SRR1583082,f2d463ca56d476a59e61706cec110c38,BW25113 ΔtolC,GSE61619,The general mode of translation inhibition by macrolide antibiotics,,,SRA185504,,,,,,,,,,,,,,, PRJNA261698,SRX708005,Illumina HiSeq 2000 sequencing; GSM1509452: Ribosome profiling data of E. coli cells treated with the antibiotic erythromycin; Escherichia coli BW25113; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1509452: Ribosome profiling data of E. coli cells treated with the antibiotic erythromycin; Escherichia coli BW25113; RNA-Seq,679895,Escherichia coli BW25113,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03075508,Ribosome profiling data of E. coli cells treated with the antibiotic erythromycin,Illumina HiSeq 2000,SRR1583083,26096770,1330935270,SAMN03075508,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1509452,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR158/003/SRR1583083/SRR1583083.fastq.gz,1103142549,ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/003/SRR1583083/SRR1583083.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/003/SRR1583083/SRR1583083.fastq.gz,3c7a12ac0f72e2d8d5fed286cb85eebb,2015-03-21,2015-03-22,false,,,,,,,,,,,ILLUMINA,,,,2019-10-23,,SINGLE,,,,,,,,,,GSM1509452_r1,,GSM1509452,,Ribosome profiling data of E. coli cells treated with the antibiotic erythromycin,,,,,SRS707091,SRP047380,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR158/003/SRR1583083,924600606,ftp.sra.ebi.ac.uk/vol1/srr/SRR158/003/SRR1583083,ftp.sra.ebi.ac.uk/vol1/srr/SRR158/003/SRR1583083,f38b25743e086c769969c1315bc9b806,BW25113 ΔtolC,GSE61619,The general mode of translation inhibition by macrolide antibiotics,,,SRA185504,,,,,,,,,,,,,,, PRJNA261698,SRX708006,Illumina HiSeq 2000 sequencing; GSM1509453: Ribosome profiling data of E. coli cells treated with the antibiotic telithromycin; Escherichia coli BW25113; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1509453: Ribosome profiling data of E. coli cells treated with the antibiotic telithromycin; Escherichia coli BW25113; RNA-Seq,679895,Escherichia coli BW25113,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03075509,Ribosome profiling data of E. coli cells treated with the antibiotic telithromycin,Illumina HiSeq 2000,SRR1583084,23465502,1196740602,SAMN03075509,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1509453,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR158/004/SRR1583084/SRR1583084.fastq.gz,999062626,ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/004/SRR1583084/SRR1583084.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/004/SRR1583084/SRR1583084.fastq.gz,049a3cd96a0feace244661ec3476a954,2015-03-21,2015-03-22,false,,,,,,,,,,,ILLUMINA,,,,2020-05-14,,SINGLE,,,,,,,,,,GSM1509453_r1,,GSM1509453,,Ribosome profiling data of E. coli cells treated with the antibiotic telithromycin,,,,,SRS707092,SRP047380,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR158/004/SRR1583084,834691055,ftp.sra.ebi.ac.uk/vol1/srr/SRR158/004/SRR1583084,ftp.sra.ebi.ac.uk/vol1/srr/SRR158/004/SRR1583084,4d8e14d53bda3e8a13034d072e659d0b,BW25113 ΔtolC,GSE61619,The general mode of translation inhibition by macrolide antibiotics,,,SRA185504,,,,,,,,,,,,,,, PRJNA223608,SRX367006,Illumina Genome Analyzer II sequencing; GSM1248735: mock-transfected ribosome profiling; Homo sapiens; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM1248735: mock-transfected ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02380977,mock-transfected ribosome profiling,Illumina Genome Analyzer II,SRR1598971,28443731,1023974316,SAMN02380977,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1248735,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR159/001/SRR1598971/SRR1598971.fastq.gz,883411039,ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/001/SRR1598971/SRR1598971.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/001/SRR1598971/SRR1598971.fastq.gz,7dcae2d70905e5e09e45c0e0270ea100,2014-10-20,2014-11-10,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1248735_r11,,GSM1248735,,mock-transfected ribosome profiling,,,,,SRS493132,SRP031849,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR159/001/SRR1598971,616766971,ftp.sra.ebi.ac.uk/vol1/srr/SRR159/001/SRR1598971,ftp.sra.ebi.ac.uk/vol1/srr/SRR159/001/SRR1598971,a4f681a6b67cf9b4f98b19c80e27ebec,,GSE51584,Expanded identification and characterization of mammalian circular RNAs,,,SRA107958,,,,,,,,,,,,,,, PRJNA223608,SRX367000,Illumina HiSeq 2000 sequencing; GSM1248729: miR-1-transfected ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1248729: miR-1-transfected ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02380975,miR-1-transfected ribosome profiling,Illumina HiSeq 2000,SRR1598975,92575736,4628786800,SAMN02380975,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1248729,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR159/005/SRR1598975/SRR1598975.fastq.gz,3748555454,ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/005/SRR1598975/SRR1598975.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/005/SRR1598975/SRR1598975.fastq.gz,f8d3320920592c4b06e3c9821c05e364,2014-10-20,2014-11-10,false,,,,,,,,,,,ILLUMINA,,,,2019-10-07,,SINGLE,,,,,,,,,,GSM1248729_r11,,GSM1248729,,miR-1-transfected ribosome profiling,,,,,SRS493126,SRP031849,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR159/005/SRR1598975,2862357033,ftp.sra.ebi.ac.uk/vol1/srr/SRR159/005/SRR1598975,ftp.sra.ebi.ac.uk/vol1/srr/SRR159/005/SRR1598975,297195f02926057a1757e10b08b45975,,GSE51584,Expanded identification and characterization of mammalian circular RNAs,,,SRA107958,,,,,,,,,,,,,,, PRJNA223608,SRX367003,Illumina Genome Analyzer II sequencing; GSM1248732: miR-155-transfected ribosome profiling; Homo sapiens; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM1248732: miR-155-transfected ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN02380973,miR-155-transfected ribosome profiling,Illumina Genome Analyzer II,SRR1598981,29613617,1066090212,SAMN02380973,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1248732,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR159/001/SRR1598981/SRR1598981.fastq.gz,943724192,ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/001/SRR1598981/SRR1598981.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR159/001/SRR1598981/SRR1598981.fastq.gz,161e53e9d5cecb254449132b229d979a,2014-10-20,2014-11-10,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1248732_r11,,GSM1248732,,miR-155-transfected ribosome profiling,,,,,SRS493129,SRP031849,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR159/001/SRR1598981,641332469,ftp.sra.ebi.ac.uk/vol1/srr/SRR159/001/SRR1598981,ftp.sra.ebi.ac.uk/vol1/srr/SRR159/001/SRR1598981,b4a230bfe61ede35e6377f928678aafd,,GSE51584,Expanded identification and characterization of mammalian circular RNAs,,,SRA107958,,,,,,,,,,,,,,, PRJNA268222,SRX765941,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216854,Rec-OE NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660328,30964025,2322301875,SAMN03216854,,,,,,,,"NCCIT cells, hECC",GEO,,,,,,,,,,,,,,,,,,,,false,GSM1552807,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/008/SRR1660328/SRR1660328.fastq.gz,1418181036,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/008/SRR1660328/SRR1660328.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/008/SRR1660328/SRR1660328.fastq.gz,ab9757fa78ede3c535c8402c84c37e39,2015-04-22,2015-04-22,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1552807_r1,,GSM1552807,,Rec-OE NCCIT Ribosome profiling (RPF),,,,,SRS750218,SRP050147,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/008/SRR1660328,1372460461,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/008/SRR1660328,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/008/SRR1660328,a32a4c7274ae431e36f989eb6d76bc39,,GSE63570,High-throughput sequencing of pluripotent cells,,,SRA204209,,,,,,,,male,,,,,,, PRJNA268222,SRX765941,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216854,Rec-OE NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660329,39632893,2972466975,SAMN03216854,,,,,,,,"NCCIT cells, hECC",GEO,,,,,,,,,,,,,,,,,,,,false,GSM1552807,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/009/SRR1660329/SRR1660329.fastq.gz,1675838202,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/009/SRR1660329/SRR1660329.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/009/SRR1660329/SRR1660329.fastq.gz,3ec4ecd81d73ec4517dc762419e41a04,2015-04-22,2015-04-22,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1552807_r2,,GSM1552807,,Rec-OE NCCIT Ribosome profiling (RPF),,,,,SRS750218,SRP050147,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/009/SRR1660329,1679075334,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/009/SRR1660329,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/009/SRR1660329,63edf9c3dad24b176320417421ed15b5,,GSE63570,High-throughput sequencing of pluripotent cells,,,SRA204209,,,,,,,,male,,,,,,, PRJNA268222,SRX765941,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216854,Rec-OE NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660330,43632403,3272430225,SAMN03216854,,,,,,,,"NCCIT cells, hECC",GEO,,,,,,,,,,,,,,,,,,,,false,GSM1552807,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/000/SRR1660330/SRR1660330.fastq.gz,1900543339,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/000/SRR1660330/SRR1660330.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/000/SRR1660330/SRR1660330.fastq.gz,9b6e3df4acc6db9bdadac3ba4532a206,2015-04-22,2015-04-22,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1552807_r3,,GSM1552807,,Rec-OE NCCIT Ribosome profiling (RPF),,,,,SRS750218,SRP050147,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/000/SRR1660330,1850902760,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/000/SRR1660330,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/000/SRR1660330,b0dca4237a15514e975e3af9b572926d,,GSE63570,High-throughput sequencing of pluripotent cells,,,SRA204209,,,,,,,,male,,,,,,, PRJNA268222,SRX765941,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552807: Rec-OE NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216854,Rec-OE NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660331,38175907,2863193025,SAMN03216854,,,,,,,,"NCCIT cells, hECC",GEO,,,,,,,,,,,,,,,,,,,,false,GSM1552807,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/001/SRR1660331/SRR1660331.fastq.gz,1645171509,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/001/SRR1660331/SRR1660331.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/001/SRR1660331/SRR1660331.fastq.gz,0f4373e7f62e15e3d8193f94b92bdd9e,2015-04-22,2015-04-22,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1552807_r4,,GSM1552807,,Rec-OE NCCIT Ribosome profiling (RPF),,,,,SRS750218,SRP050147,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/001/SRR1660331,1613718131,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/001/SRR1660331,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/001/SRR1660331,cb5c37c3517b30fc4b16b610c5fb5972,,GSE63570,High-throughput sequencing of pluripotent cells,,,SRA204209,,,,,,,,male,,,,,,, PRJNA268222,SRX765942,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216852,WT control NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660332,61772582,4632943650,SAMN03216852,,,,,,,,"NCCIT cells, hECC",GEO,,,,,,,,,,,,,,,,,,,,false,GSM1552808,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/002/SRR1660332/SRR1660332.fastq.gz,3032364952,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/002/SRR1660332/SRR1660332.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/002/SRR1660332/SRR1660332.fastq.gz,234d34e4746209729b6ab91a9ba47fb3,2015-04-22,2015-04-22,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1552808_r1,,GSM1552808,,WT control NCCIT Ribosome profiling (RPF),,,,,SRS750219,SRP050147,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/002/SRR1660332,3019837179,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/002/SRR1660332,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/002/SRR1660332,ebdc2aad55b69bf73ebe7b557fbc708b,,GSE63570,High-throughput sequencing of pluripotent cells,,,SRA204209,,,,,,,,male,,,,,,, PRJNA268222,SRX765942,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216852,WT control NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660333,21771791,661735742,SAMN03216852,,,,,,,,"NCCIT cells, hECC",GEO,,,,,,,,,,,,,,,,,,,,false,GSM1552808,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/003/SRR1660333/SRR1660333.fastq.gz,311739369,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/003/SRR1660333/SRR1660333.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/003/SRR1660333/SRR1660333.fastq.gz,f1434375073ee04cc473fd868df7abc2,2015-04-22,2015-04-22,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1552808_r2,,GSM1552808,,WT control NCCIT Ribosome profiling (RPF),,,,,SRS750219,SRP050147,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/003/SRR1660333,212786508,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/003/SRR1660333,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/003/SRR1660333,7062ab8fd88d818f2bd5186895611ddf,,GSE63570,High-throughput sequencing of pluripotent cells,,,SRA204209,,,,,,,,male,,,,,,, PRJNA268222,SRX765942,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216852,WT control NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660334,30106441,2257983075,SAMN03216852,,,,,,,,"NCCIT cells, hECC",GEO,,,,,,,,,,,,,,,,,,,,false,GSM1552808,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/004/SRR1660334/SRR1660334.fastq.gz,1358559506,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/004/SRR1660334/SRR1660334.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/004/SRR1660334/SRR1660334.fastq.gz,97062cc71493eaedaba037f799f8443f,2015-04-22,2015-04-22,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1552808_r3,,GSM1552808,,WT control NCCIT Ribosome profiling (RPF),,,,,SRS750219,SRP050147,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/004/SRR1660334,1324918631,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/004/SRR1660334,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/004/SRR1660334,65442d14b237b2a929ac7dff50f6caea,,GSE63570,High-throughput sequencing of pluripotent cells,,,SRA204209,,,,,,,,male,,,,,,, PRJNA268222,SRX765942,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1552808: WT control NCCIT Ribosome profiling (RPF); Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03216852,WT control NCCIT Ribosome profiling (RPF),Illumina HiSeq 2000,SRR1660335,44297155,3322286625,SAMN03216852,,,,,,,,"NCCIT cells, hECC",GEO,,,,,,,,,,,,,,,,,,,,false,GSM1552808,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/005/SRR1660335/SRR1660335.fastq.gz,1954826902,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/005/SRR1660335/SRR1660335.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/005/SRR1660335/SRR1660335.fastq.gz,ce6db46bff7f7501bb933b26993c4ed1,2015-04-22,2015-04-22,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1552808_r4,,GSM1552808,,WT control NCCIT Ribosome profiling (RPF),,,,,SRS750219,SRP050147,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/005/SRR1660335,1919792516,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/005/SRR1660335,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/005/SRR1660335,c0b9f49da11884743a399484ffd0b5e9,,GSE63570,High-throughput sequencing of pluripotent cells,,,SRA204209,,,,,,,,male,,,,,,, PRJNA268354,SRX767133,Illumina HiSeq 2000 sequencing; GSM1553248: Ribosome profiling rep1-SiControl-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553248: Ribosome profiling rep1-SiControl-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218424,Ribosome profiling rep1-SiControl-RPF,Illumina HiSeq 2000,SRR1661491,23525682,855434980,SAMN03218424,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1553248,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/001/SRR1661491/SRR1661491.fastq.gz,500849011,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/001/SRR1661491/SRR1661491.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/001/SRR1661491/SRR1661491.fastq.gz,24be81fb3d6888693b2e5be6c6b591a0,2015-06-11,2015-06-11,false,,,,,,,,,,,ILLUMINA,,,,2020-02-05,,SINGLE,,,,,,,,,,GSM1553248_r1,,GSM1553248,,Ribosome profiling rep1-SiControl-RPF,,,,,SRS751232,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/001/SRR1661491,542991633,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/001/SRR1661491,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/001/SRR1661491,00dfcc7a0776615bcf1ca777fcbe4ead,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX767134,Illumina HiSeq 2000 sequencing; GSM1553249: Ribosome profiling rep1-SiControl-input-ribominus; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553249: Ribosome profiling rep1-SiControl-input-ribominus; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218421,Ribosome profiling rep1-SiControl-input-ribominus,Illumina HiSeq 2000,SRR1661492,21062618,958344392,SAMN03218421,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1553249,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/002/SRR1661492/SRR1661492.fastq.gz,755508026,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/002/SRR1661492/SRR1661492.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/002/SRR1661492/SRR1661492.fastq.gz,0ef8eafed8eca015237dacf91a04ec1c,2015-06-11,2015-06-11,false,,,,,,,,,,,ILLUMINA,,,,2019-11-12,,SINGLE,,,,,,,,,,GSM1553249_r1,,GSM1553249,,Ribosome profiling rep1-SiControl-input-ribominus,,,,,SRS751233,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/002/SRR1661492,638748380,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/002/SRR1661492,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/002/SRR1661492,c024fba9321ec4228074b57b45bd42a2,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX767135,Illumina HiSeq 2000 sequencing; GSM1553250: Ribosome profiling rep1-SiYTHDF1_1-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553250: Ribosome profiling rep1-SiYTHDF1_1-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218422,Ribosome profiling rep1-SiYTHDF1_1-RPF,Illumina HiSeq 2000,SRR1661493,36490823,1257840702,SAMN03218422,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1553250,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/003/SRR1661493/SRR1661493.fastq.gz,876854480,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/003/SRR1661493/SRR1661493.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/003/SRR1661493/SRR1661493.fastq.gz,b719f8f0a72bd8c6c5aad653fd1d0bfb,2015-06-11,2015-06-11,false,,,,,,,,,,,ILLUMINA,,,,2020-01-19,,SINGLE,,,,,,,,,,GSM1553250_r1,,GSM1553250,,Ribosome profiling rep1-SiYTHDF1_1-RPF,,,,,SRS751234,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/003/SRR1661493,894582501,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/003/SRR1661493,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/003/SRR1661493,923b45b987323a0ab0d57f76b71f795a,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX767136,Illumina HiSeq 2000 sequencing; GSM1553251: Ribosome profiling rep1-SiYTHDF1_1-input-ribominus; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553251: Ribosome profiling rep1-SiYTHDF1_1-input-ribominus; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218419,Ribosome profiling rep1-SiYTHDF1_1-input-ribominus,Illumina HiSeq 2000,SRR1661494,22039846,991227095,SAMN03218419,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1553251,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/004/SRR1661494/SRR1661494.fastq.gz,782435768,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/004/SRR1661494/SRR1661494.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/004/SRR1661494/SRR1661494.fastq.gz,6872c8805f19560f61fce7661b651495,2015-06-11,2015-06-11,false,,,,,,,,,,,ILLUMINA,,,,2020-05-13,,SINGLE,,,,,,,,,,GSM1553251_r1,,GSM1553251,,Ribosome profiling rep1-SiYTHDF1_1-input-ribominus,,,,,SRS751235,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/004/SRR1661494,662176951,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/004/SRR1661494,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/004/SRR1661494,11905521f406dbd40faca502dee2832e,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX767137,Illumina HiSeq 2000 sequencing; GSM1553252: Ribosome profiling rep2-SiControl-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553252: Ribosome profiling rep2-SiControl-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218420,Ribosome profiling rep2-SiControl-RPF,Illumina HiSeq 2000,SRR1661495,26427579,966115970,SAMN03218420,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1553252,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/005/SRR1661495/SRR1661495.fastq.gz,476710132,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/005/SRR1661495/SRR1661495.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/005/SRR1661495/SRR1661495.fastq.gz,792e0e3317de9e39074bf58656bc129b,2015-06-11,2015-06-11,false,,,,,,,,,,,ILLUMINA,,,,2019-11-02,,SINGLE,,,,,,,,,,GSM1553252_r1,,GSM1553252,,Ribosome profiling rep2-SiControl-RPF,,,,,SRS751236,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/005/SRR1661495,495789625,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/005/SRR1661495,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/005/SRR1661495,aad7517a066542e6f16c1d354305be81,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX767138,Illumina HiSeq 2000 sequencing; GSM1553253: Ribosome profiling rep2-SiControl-input-ribominus; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553253: Ribosome profiling rep2-SiControl-input-ribominus; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218426,Ribosome profiling rep2-SiControl-input-ribominus,Illumina HiSeq 2000,SRR1661496,26388944,1086043707,SAMN03218426,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1553253,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/006/SRR1661496/SRR1661496.fastq.gz,720756513,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/006/SRR1661496/SRR1661496.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/006/SRR1661496/SRR1661496.fastq.gz,003dde71f28059b2beafdc7dcf639cc0,2015-06-11,2015-06-11,false,,,,,,,,,,,ILLUMINA,,,,2019-10-16,,SINGLE,,,,,,,,,,GSM1553253_r1,,GSM1553253,,Ribosome profiling rep2-SiControl-input-ribominus,,,,,SRS751237,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/006/SRR1661496,515523617,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/006/SRR1661496,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/006/SRR1661496,de22f6afcd85ac59963dadaa3ff4f25e,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX767139,Illumina HiSeq 2000 sequencing; GSM1553254: Ribosome profiling rep2-SiYTHDF1_8-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553254: Ribosome profiling rep2-SiYTHDF1_8-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218425,Ribosome profiling rep2-SiYTHDF1_8-RPF,Illumina HiSeq 2000,SRR1661497,26197590,927371837,SAMN03218425,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1553254,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/007/SRR1661497/SRR1661497.fastq.gz,448115255,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/007/SRR1661497/SRR1661497.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/007/SRR1661497/SRR1661497.fastq.gz,0b9ca66942c10abc24b8b1f374b1e285,2015-06-11,2015-06-11,false,,,,,,,,,,,ILLUMINA,,,,2020-01-05,,SINGLE,,,,,,,,,,GSM1553254_r1,,GSM1553254,,Ribosome profiling rep2-SiYTHDF1_8-RPF,,,,,SRS751238,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/007/SRR1661497,476408499,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/007/SRR1661497,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/007/SRR1661497,fe7f298294db09e09e29a1e0b649c4e7,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX767140,Illumina HiSeq 2000 sequencing; GSM1553255: Ribosome profiling rep2-SiYTHDF1_8-input-ribominus; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1553255: Ribosome profiling rep2-SiYTHDF1_8-input-ribominus; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03218427,Ribosome profiling rep2-SiYTHDF1_8-input-ribominus,Illumina HiSeq 2000,SRR1661498,29088381,1229624248,SAMN03218427,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1553255,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR166/008/SRR1661498/SRR1661498.fastq.gz,805151513,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/008/SRR1661498/SRR1661498.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR166/008/SRR1661498/SRR1661498.fastq.gz,e946822fe97fea10e5fde9511274b050,2015-06-11,2015-06-11,false,,,,,,,,,,,ILLUMINA,,,,2020-05-13,,SINGLE,,,,,,,,,,GSM1553255_r1,,GSM1553255,,Ribosome profiling rep2-SiYTHDF1_8-input-ribominus,,,,,SRS751239,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR166/008/SRR1661498,578405185,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/008/SRR1661498,ftp.sra.ebi.ac.uk/vol1/srr/SRR166/008/SRR1661498,42422c8acf4e35c374c26ae777857b73,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA272662,SRX845439,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate1,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate1,4577,Zea mays,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03284755,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,Illumina HiSeq 2500,SRR1763106,110961112,5548055600,SAMN03284755,,,,,,,,,China Agricultural University,,,,,,China:Beijing,,,,B73,,,,,,,,,,false,ribosome profiling raw data for normal seedling replicate1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR176/006/SRR1763106/SRR1763106.fastq.gz,4233152139,ftp.sra.ebi.ac.uk/vol1/fastq/SRR176/006/SRR1763106/SRR1763106.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR176/006/SRR1763106/SRR1763106.fastq.gz,606e46af00c2aba69c56c25727aaecbb,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,ribosome profiling raw data for normal seedling replicate1,,,,,,,,,ribosome profiling raw data for normal seedling replicate1,,14-day normal B73 seedling,,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,,,,,SRS821168,SRP052520,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR176/006/SRR1763106,3843944892,ftp.sra.ebi.ac.uk/vol1/srr/SRR176/006/SRR1763106,ftp.sra.ebi.ac.uk/vol1/srr/SRR176/006/SRR1763106,de5706b94ca065d7c906a950dbdcd27a,,PRJNA272662,Zea mays Transcriptome or Gene expression,,,SRA233319,,,,,,,,,,,,,,Seedling, PRJNA272662,SRX845455,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate2,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for normal seedling replicate2,4577,Zea mays,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03284755,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,Illumina HiSeq 2500,SRR1763107,132900577,6645028850,SAMN03284755,,,,,,,,,China Agricultural University,,,,,,China:Beijing,,,,B73,,,,,,,,,,false,ribosome profiling raw data for normal seedling replicate2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR176/007/SRR1763107/SRR1763107.fastq.gz,5006052390,ftp.sra.ebi.ac.uk/vol1/fastq/SRR176/007/SRR1763107/SRR1763107.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR176/007/SRR1763107/SRR1763107.fastq.gz,b9d25fcf25b922e66b473e5b4a017d23,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,ribosome profiling raw data for normal seedling replicate2,,14-day normal B73 seedling,,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,,,,,SRS821168,SRP052520,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR176/007/SRR1763107,4628531392,ftp.sra.ebi.ac.uk/vol1/srr/SRR176/007/SRR1763107,ftp.sra.ebi.ac.uk/vol1/srr/SRR176/007/SRR1763107,d3333afad4eaf7d48d9b0f6ff208029f,,PRJNA272662,Zea mays Transcriptome or Gene expression,,,SRA233319,,,,,,,,,,,,,,Seedling, PRJNA272662,SRX847139,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate1,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate1,4577,Zea mays,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03284757,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,Illumina HiSeq 2500,SRR1765340,71262874,3563143700,SAMN03284757,,,,,,,,,China Agricultural University,,,,,,China:Beijing,,,,B73,,,,,,,,,,false,ribosome profiling raw data for drought seedling replicate1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR176/000/SRR1765340/SRR1765340.fastq.gz,2631860729,ftp.sra.ebi.ac.uk/vol1/fastq/SRR176/000/SRR1765340/SRR1765340.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR176/000/SRR1765340/SRR1765340.fastq.gz,dd9519504f28ae38d5a26edebb568e59,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,ribosome profiling raw data for drought seedling replicate1,,14-day drought-treated B73 seedling,,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,,,,,SRS822648,SRP052520,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR176/000/SRR1765340,2435100892,ftp.sra.ebi.ac.uk/vol1/srr/SRR176/000/SRR1765340,ftp.sra.ebi.ac.uk/vol1/srr/SRR176/000/SRR1765340,825eb5acfa8b5c2fbf80bef85c2d7f58,,PRJNA272662,Zea mays Transcriptome or Gene expression,,,SRA233319,,,,,,,,,,,,,,Seedling, PRJNA272662,SRX847143,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate2,Illumina HiSeq 2500 sequencing; ribosome profiling raw data for drought seedling replicate2,4577,Zea mays,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03284757,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,Illumina HiSeq 2500,SRR1765360,78615417,3930770850,SAMN03284757,,,,,,,,,China Agricultural University,,,,,,China:Beijing,,,,B73,,,,,,,,,,false,ribosome profiling raw data for drought seedling replicate2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR176/000/SRR1765360/SRR1765360.fastq.gz,2998600605,ftp.sra.ebi.ac.uk/vol1/fastq/SRR176/000/SRR1765360/SRR1765360.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR176/000/SRR1765360/SRR1765360.fastq.gz,2e8a51f8f897c7d91365cd5eefe9bc35,2015-06-05,2015-06-05,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,ribosome profiling raw data for drought seedling replicate2,,14-day drought-treated B73 seedling,,This sample has been submitted by China Agricultural University on 2015-06-02; Zea mays,,,,,SRS822648,SRP052520,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR176/000/SRR1765360,2735012288,ftp.sra.ebi.ac.uk/vol1/srr/SRR176/000/SRR1765360,ftp.sra.ebi.ac.uk/vol1/srr/SRR176/000/SRR1765360,dcf4c35302f227757fff3f1ae2d595f4,,PRJNA272662,Zea mays Transcriptome or Gene expression,,,SRA233319,,,,,,,,,,,,,,Seedling, PRJNA277363,SRX902511,Illumina HiSeq 2000 sequencing; GSM1625823: Cotyledon (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625823: Cotyledon (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389597,Cotyledon (25-50 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840399,51640489,2582024450,SAMN03389597,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625823,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/009/SRR1840399/SRR1840399.fastq.gz,1777679549,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/009/SRR1840399/SRR1840399.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/009/SRR1840399/SRR1840399.fastq.gz,2759d2156d9cd7a92c851e3280d74091,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625823_r1,,GSM1625823,,Cotyledon (25-50 mg) Ribosome Profiling biorep 1,,,,,SRS865195,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/009/SRR1840399,1690627898,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/009/SRR1840399,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/009/SRR1840399,6297f57ffd79e8e39c0a8126e8112d1c,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Cotyledon, PRJNA277363,SRX902513,Illumina HiSeq 2000 sequencing; GSM1625825: Cotyledon (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625825: Cotyledon (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389589,Cotyledon (25-50 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840401,77525914,7752591400,SAMN03389589,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625825,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/001/SRR1840401/SRR1840401.fastq.gz,4456125845,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/001/SRR1840401/SRR1840401.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/001/SRR1840401/SRR1840401.fastq.gz,9e54ff3419d50d0b24ee56ca446130d7,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625825_r1,,GSM1625825,,Cotyledon (25-50 mg) Ribosome Profiling biorep 2,,,,,SRS865193,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/001/SRR1840401,5148704132,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/001/SRR1840401,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/001/SRR1840401,387ddc49465f47a196a6fae957c1d40b,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Cotyledon, PRJNA277363,SRX902515,Illumina HiSeq 2000 sequencing; GSM1625827: Seed Coat (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625827: Seed Coat (25-50 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389599,Seed Coat (25-50 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840403,50150107,2507505350,SAMN03389599,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625827,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/003/SRR1840403/SRR1840403.fastq.gz,1932175493,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/003/SRR1840403/SRR1840403.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/003/SRR1840403/SRR1840403.fastq.gz,d483f6d8bfd5d8f21fe9b9e213b9af4c,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625827_r1,,GSM1625827,,Seed Coat (25-50 mg) Ribosome Profiling biorep 1,,,,,SRS865191,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/003/SRR1840403,1755142448,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/003/SRR1840403,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/003/SRR1840403,64fefe086ed2829b51c890d4cc9475d9,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Seed Coat, PRJNA277363,SRX902517,Illumina HiSeq 2000 sequencing; GSM1625829: Seed Coat (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625829: Seed Coat (25-50 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389600,Seed Coat (25-50 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840405,58241888,2912094400,SAMN03389600,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625829,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/005/SRR1840405/SRR1840405.fastq.gz,1789561394,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/005/SRR1840405/SRR1840405.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/005/SRR1840405/SRR1840405.fastq.gz,e445ba00525a4f391c0e4b76320658c7,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625829_r1,,GSM1625829,,Seed Coat (25-50 mg) Ribosome Profiling biorep 2,,,,,SRS865189,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/005/SRR1840405,1712244702,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/005/SRR1840405,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/005/SRR1840405,aa716963b1eba90ad89b2ee32bdad610,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Seed Coat, PRJNA277363,SRX902519,Illumina HiSeq 2000 sequencing; GSM1625831: Cotyledon (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625831: Cotyledon (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389590,Cotyledon (100-200 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840407,86277212,4313860600,SAMN03389590,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625831,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/007/SRR1840407/SRR1840407.fastq.gz,3155463811,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/007/SRR1840407/SRR1840407.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/007/SRR1840407/SRR1840407.fastq.gz,c16535a2b43357b45599819ceb295ff6,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625831_r1,,GSM1625831,,Cotyledon (100-200 mg) Ribosome Profiling biorep 1,,,,,SRS865187,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/007/SRR1840407,2912100192,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/007/SRR1840407,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/007/SRR1840407,b66eaffe69c37ce1989a0918a9d6a6fe,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Cotyledon, PRJNA277363,SRX902521,Illumina HiSeq 2000 sequencing; GSM1625833: Cotyledon (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625833: Cotyledon (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389603,Cotyledon (100-200 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840409,100907777,10090777700,SAMN03389603,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625833,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/009/SRR1840409/SRR1840409.fastq.gz,5391256489,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/009/SRR1840409/SRR1840409.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/009/SRR1840409/SRR1840409.fastq.gz,7c6d2a32899880204d763cd96af38774,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625833_r1,,GSM1625833,,Cotyledon (100-200 mg) Ribosome Profiling biorep 2,,,,,SRS865185,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/009/SRR1840409,6424956932,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/009/SRR1840409,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/009/SRR1840409,c34df873b31f83c040165925fe8f5283,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Cotyledon, PRJNA277363,SRX902523,Illumina HiSeq 2000 sequencing; GSM1625835: Seed Coat (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625835: Seed Coat (100-200 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389594,Seed Coat (100-200 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840411,57960236,2898011800,SAMN03389594,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625835,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/001/SRR1840411/SRR1840411.fastq.gz,2056279848,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/001/SRR1840411/SRR1840411.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/001/SRR1840411/SRR1840411.fastq.gz,f44445629d95030b5bd30dcb03283319,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625835_r1,,GSM1625835,,Seed Coat (100-200 mg) Ribosome Profiling biorep 1,,,,,SRS865183,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/001/SRR1840411,1928241858,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/001/SRR1840411,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/001/SRR1840411,a69422668449a4ae450ae519c525a887,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Seed Coat, PRJNA277363,SRX902525,Illumina HiSeq 2000 sequencing; GSM1625837: Seed Coat (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625837: Seed Coat (100-200 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389593,Seed Coat (100-200 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840413,72276634,3613831700,SAMN03389593,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625837,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/003/SRR1840413/SRR1840413.fastq.gz,2208925481,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/003/SRR1840413/SRR1840413.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/003/SRR1840413/SRR1840413.fastq.gz,a317efa0ef0c3873d9f1b16c87f8477e,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625837_r1,,GSM1625837,,Seed Coat (100-200 mg) Ribosome Profiling biorep 2,,,,,SRS865181,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/003/SRR1840413,2125775149,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/003/SRR1840413,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/003/SRR1840413,2ddeb4d70637288afc3b79ec0690600b,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Seed Coat, PRJNA277363,SRX902527,Illumina HiSeq 2000 sequencing; GSM1625839: Cotyledon (300-400 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625839: Cotyledon (300-400 mg) Ribosome Profiling biorep 1; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389601,Cotyledon (300-400 mg) Ribosome Profiling biorep 1,Illumina HiSeq 2000,SRR1840415,82331167,4116558350,SAMN03389601,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625839,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/005/SRR1840415/SRR1840415.fastq.gz,3031100036,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/005/SRR1840415/SRR1840415.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/005/SRR1840415/SRR1840415.fastq.gz,b5aefa2867ee5ae6e7f2ca9afe60534b,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625839_r1,,GSM1625839,,Cotyledon (300-400 mg) Ribosome Profiling biorep 1,,,,,SRS865179,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/005/SRR1840415,2835373295,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/005/SRR1840415,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/005/SRR1840415,ffe74612fe14ab700dd24ecebc1d2b98,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Cotyledon, PRJNA277363,SRX902529,Illumina HiSeq 2000 sequencing; GSM1625841: Cotyledon (300-400 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1625841: Cotyledon (300-400 mg) Ribosome Profiling biorep 2; Glycine max; RNA-Seq,3847,Glycine max,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03389595,Cotyledon (300-400 mg) Ribosome Profiling biorep 2,Illumina HiSeq 2000,SRR1840417,66026031,3301301550,SAMN03389595,,,,,,,,,GEO,,,,,,,,,,Williams,,,,,,,,,,false,GSM1625841,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR184/007/SRR1840417/SRR1840417.fastq.gz,2420039376,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/007/SRR1840417/SRR1840417.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR184/007/SRR1840417/SRR1840417.fastq.gz,ee36c1dfe3c33d4a156d045a6ae14f95,2018-03-24,2018-03-24,false,,,,,,,,,,,ILLUMINA,,,,2018-03-24,,SINGLE,,,,,,,,,,GSM1625841_r1,,GSM1625841,,Cotyledon (300-400 mg) Ribosome Profiling biorep 2,,,,,SRS865177,SRP055880,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR184/007/SRR1840417,2257691340,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/007/SRR1840417,ftp.sra.ebi.ac.uk/vol1/srr/SRR184/007/SRR1840417,77f7fedea722f5b4864072edea0fa41f,,GSE66580,Ribosome profiling reveals changes in translational status of soybean transcripts during immature cotyledon development,,,SRA245679,,,,,,,,,,,,,,Cotyledon, PRJNA280809,SRX986365,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470223,Ribosome Profiling control replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964306,39082700,1954135000,SAMN03470223,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655059,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/006/SRR1964306/SRR1964306.fastq.gz,1875614835,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/006/SRR1964306/SRR1964306.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/006/SRR1964306/SRR1964306.fastq.gz,efdcfbe74017b090320292ba35aa8c9d,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655059_r1,,GSM1655059,,Ribosome Profiling control replicate 1,,,,,SRS901275,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/006/SRR1964306,1350884104,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/006/SRR1964306,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/006/SRR1964306,c54d92c26f48208de4915cf6a19d9a70,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986365,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470223,Ribosome Profiling control replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964307,52274080,2613704000,SAMN03470223,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655059,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/007/SRR1964307/SRR1964307.fastq.gz,2377870309,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/007/SRR1964307/SRR1964307.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/007/SRR1964307/SRR1964307.fastq.gz,2ef29c2988084a81e90b79edb03ada41,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2019-11-17,,SINGLE,,,,,,,,,,GSM1655059_r2,,GSM1655059,,Ribosome Profiling control replicate 1,,,,,SRS901275,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/007/SRR1964307,1730429301,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/007/SRR1964307,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/007/SRR1964307,61fa573875a5ba1fe3de425d56f77a51,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986365,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655059: Ribosome Profiling control replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470223,Ribosome Profiling control replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964308,29216820,1460841000,SAMN03470223,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655059,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/008/SRR1964308/SRR1964308.fastq.gz,1328948258,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/008/SRR1964308/SRR1964308.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/008/SRR1964308/SRR1964308.fastq.gz,dabc517a1b95d6fbae92bc1ee3b7b382,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-01-04,,SINGLE,,,,,,,,,,GSM1655059_r3,,GSM1655059,,Ribosome Profiling control replicate 1,,,,,SRS901275,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/008/SRR1964308,980651241,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/008/SRR1964308,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/008/SRR1964308,44c33e7c2653abd181315358b04391b1,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986366,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470224,Ribosome Profiling control replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964309,46953344,2347667200,SAMN03470224,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655060,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/009/SRR1964309/SRR1964309.fastq.gz,2209188765,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/009/SRR1964309/SRR1964309.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/009/SRR1964309/SRR1964309.fastq.gz,ef577ed57c9bb9b900c32c05736a1aeb,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655060_r1,,GSM1655060,,Ribosome Profiling control replicate 2,,,,,SRS901273,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/009/SRR1964309,1603536177,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/009/SRR1964309,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/009/SRR1964309,314512724f36609aa8be528577173483,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986366,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470224,Ribosome Profiling control replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964310,67731496,3386574800,SAMN03470224,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655060,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/000/SRR1964310/SRR1964310.fastq.gz,3030150615,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/000/SRR1964310/SRR1964310.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/000/SRR1964310/SRR1964310.fastq.gz,2de6422eca974a630f9d28ee3f7e66eb,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655060_r2,,GSM1655060,,Ribosome Profiling control replicate 2,,,,,SRS901273,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/000/SRR1964310,2212181977,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/000/SRR1964310,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/000/SRR1964310,e7e0bd1c4aaeb8ba9b05874638712b76,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986366,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655060: Ribosome Profiling control replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470224,Ribosome Profiling control replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964311,22651281,1132564050,SAMN03470224,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655060,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/001/SRR1964311/SRR1964311.fastq.gz,999465479,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/001/SRR1964311/SRR1964311.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/001/SRR1964311/SRR1964311.fastq.gz,744952d2c599e5962f0cb91b3ad630f9,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2019-12-27,,SINGLE,,,,,,,,,,GSM1655060_r3,,GSM1655060,,Ribosome Profiling control replicate 2,,,,,SRS901273,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/001/SRR1964311,745138625,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/001/SRR1964311,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/001/SRR1964311,59e13cad13610c2e1df63f6992319551,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986367,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470225,Ribosome Profiling harringtonine replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964312,46189851,2309492550,SAMN03470225,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655061,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/002/SRR1964312/SRR1964312.fastq.gz,2070634915,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/002/SRR1964312/SRR1964312.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/002/SRR1964312/SRR1964312.fastq.gz,aaf6deb1a69d175b4e72fd8bbf246d05,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655061_r1,,GSM1655061,,Ribosome Profiling harringtonine replicate 1,,,,,SRS901272,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/002/SRR1964312,1563715056,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/002/SRR1964312,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/002/SRR1964312,d780bbe72c45f919dbe664f42df0b3fc,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986367,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470225,Ribosome Profiling harringtonine replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964313,65269559,3263477950,SAMN03470225,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655061,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/003/SRR1964313/SRR1964313.fastq.gz,2784384302,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/003/SRR1964313/SRR1964313.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/003/SRR1964313/SRR1964313.fastq.gz,3d4b3cb33d599bd5be0929f44271359d,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655061_r2,,GSM1655061,,Ribosome Profiling harringtonine replicate 1,,,,,SRS901272,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/003/SRR1964313,2113084044,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/003/SRR1964313,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/003/SRR1964313,3dc8dbdfffb6ab8b728626b3e62a929e,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986367,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655061: Ribosome Profiling harringtonine replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470225,Ribosome Profiling harringtonine replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964314,21259213,1062960650,SAMN03470225,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655061,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/004/SRR1964314/SRR1964314.fastq.gz,904650360,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/004/SRR1964314/SRR1964314.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/004/SRR1964314/SRR1964314.fastq.gz,e734a706ac9d7233070bb0c27a4180c2,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2019-12-06,,SINGLE,,,,,,,,,,GSM1655061_r3,,GSM1655061,,Ribosome Profiling harringtonine replicate 1,,,,,SRS901272,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/004/SRR1964314,696055833,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/004/SRR1964314,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/004/SRR1964314,3e8a57a61e998fc406133256b54561e0,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986368,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470226,Ribosome Profiling harringtonine replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964315,43321863,2166093150,SAMN03470226,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655062,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/005/SRR1964315/SRR1964315.fastq.gz,2051847201,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/005/SRR1964315/SRR1964315.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/005/SRR1964315/SRR1964315.fastq.gz,f7ee929cdcac89e5de67937198140c8e,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655062_r1,,GSM1655062,,Ribosome Profiling harringtonine replicate 2,,,,,SRS901274,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/005/SRR1964315,1517036652,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/005/SRR1964315,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/005/SRR1964315,d91abb69a0f30fffb598a79e26774057,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986368,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470226,Ribosome Profiling harringtonine replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964316,56929421,2846471050,SAMN03470226,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655062,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/006/SRR1964316/SRR1964316.fastq.gz,2624485924,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/006/SRR1964316/SRR1964316.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/006/SRR1964316/SRR1964316.fastq.gz,ebfa374da9020ab3f00b112e4aac888f,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2019-11-07,,SINGLE,,,,,,,,,,GSM1655062_r2,,GSM1655062,,Ribosome Profiling harringtonine replicate 2,,,,,SRS901274,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/006/SRR1964316,1943819848,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/006/SRR1964316,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/006/SRR1964316,023652109608106728065cd54cb1e3f1,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986368,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655062: Ribosome Profiling harringtonine replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470226,Ribosome Profiling harringtonine replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964317,22068321,1103416050,SAMN03470226,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655062,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/007/SRR1964317/SRR1964317.fastq.gz,1003689974,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/007/SRR1964317/SRR1964317.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/007/SRR1964317/SRR1964317.fastq.gz,1e8b14652b99b79f8ec7a16c35fa98dd,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655062_r3,,GSM1655062,,Ribosome Profiling harringtonine replicate 2,,,,,SRS901274,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/007/SRR1964317,759836553,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/007/SRR1964317,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/007/SRR1964317,c019f7c55914ca9db7bdd743688a9c8c,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986369,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470227,Ribosome Profiling pateamineA replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964318,44125437,2206271850,SAMN03470227,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655063,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/008/SRR1964318/SRR1964318.fastq.gz,2083880017,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/008/SRR1964318/SRR1964318.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/008/SRR1964318/SRR1964318.fastq.gz,78857f2ca1e84ceeb6d4adaf1b8dd4cc,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2019-11-14,,SINGLE,,,,,,,,,,GSM1655063_r1,,GSM1655063,,Ribosome Profiling pateamineA replicate 1,,,,,SRS901271,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/008/SRR1964318,1526466597,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/008/SRR1964318,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/008/SRR1964318,4ec3c5c06d648cc1da8251b23b159c31,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986369,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470227,Ribosome Profiling pateamineA replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964319,61197424,3059871200,SAMN03470227,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655063,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/009/SRR1964319/SRR1964319.fastq.gz,2797905688,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/009/SRR1964319/SRR1964319.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/009/SRR1964319/SRR1964319.fastq.gz,ba332fcadb1b3ad362e8e21d7af2f98b,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-01-14,,SINGLE,,,,,,,,,,GSM1655063_r2,,GSM1655063,,Ribosome Profiling pateamineA replicate 1,,,,,SRS901271,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/009/SRR1964319,2052322127,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/009/SRR1964319,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/009/SRR1964319,5c7fb746def1a14c93a7f732086f92f9,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986369,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655063: Ribosome Profiling pateamineA replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470227,Ribosome Profiling pateamineA replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964320,30423239,1521161950,SAMN03470227,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655063,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/000/SRR1964320/SRR1964320.fastq.gz,1359631816,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/000/SRR1964320/SRR1964320.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/000/SRR1964320/SRR1964320.fastq.gz,e33b14289f92a7257c3d912875729690,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655063_r3,,GSM1655063,,Ribosome Profiling pateamineA replicate 1,,,,,SRS901271,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/000/SRR1964320,1018434377,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/000/SRR1964320,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/000/SRR1964320,746c9f6dcd474ac29bc7055f1fe19f71,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986370,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470228,Ribosome Profiling pateamineA replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964321,50476436,2523821800,SAMN03470228,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655064,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/001/SRR1964321/SRR1964321.fastq.gz,2305599951,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/001/SRR1964321/SRR1964321.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/001/SRR1964321/SRR1964321.fastq.gz,5dc3a425d6d483d8e69eeebeffbe95c7,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655064_r1,,GSM1655064,,Ribosome Profiling pateamineA replicate 2,,,,,SRS901270,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/001/SRR1964321,1724625780,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/001/SRR1964321,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/001/SRR1964321,7cda54410d0d916329ff3eaf68d1f643,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986370,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470228,Ribosome Profiling pateamineA replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964322,72527646,3626382300,SAMN03470228,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655064,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/002/SRR1964322/SRR1964322.fastq.gz,3153269981,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/002/SRR1964322/SRR1964322.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/002/SRR1964322/SRR1964322.fastq.gz,efcc904337b54be9811655c11695a063,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655064_r2,,GSM1655064,,Ribosome Profiling pateamineA replicate 2,,,,,SRS901270,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/002/SRR1964322,2371183323,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/002/SRR1964322,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/002/SRR1964322,9d6099e65546f67e1af066894b139f35,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986370,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655064: Ribosome Profiling pateamineA replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470228,Ribosome Profiling pateamineA replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964323,25168492,1258424600,SAMN03470228,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655064,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/003/SRR1964323/SRR1964323.fastq.gz,1089243612,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/003/SRR1964323/SRR1964323.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/003/SRR1964323/SRR1964323.fastq.gz,6aac12d3ac6e164fdaff94b426e09082,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655064_r3,,GSM1655064,,Ribosome Profiling pateamineA replicate 2,,,,,SRS901270,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/003/SRR1964323,831171144,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/003/SRR1964323,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/003/SRR1964323,f84d0b926f27bc7330bbf5efb4c1ad9b,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986371,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470229,Ribosome Profiling puromycin replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964324,35262036,1763101800,SAMN03470229,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655065,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/004/SRR1964324/SRR1964324.fastq.gz,1620893720,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/004/SRR1964324/SRR1964324.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/004/SRR1964324/SRR1964324.fastq.gz,6a75b51aa2225837276cc0b08a596d83,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2019-10-20,,SINGLE,,,,,,,,,,GSM1655065_r1,,GSM1655065,,Ribosome Profiling puromycin replicate 1,,,,,SRS901269,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/004/SRR1964324,1203976464,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/004/SRR1964324,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/004/SRR1964324,736fd90453e74d515cf8de7d5c2a8333,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986371,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470229,Ribosome Profiling puromycin replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964325,24502833,1225141650,SAMN03470229,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655065,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/005/SRR1964325/SRR1964325.fastq.gz,1053581208,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/005/SRR1964325/SRR1964325.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/005/SRR1964325/SRR1964325.fastq.gz,a8e0049bab9c8fc323c210131bf716e3,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2019-11-25,,SINGLE,,,,,,,,,,GSM1655065_r2,,GSM1655065,,Ribosome Profiling puromycin replicate 1,,,,,SRS901269,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/005/SRR1964325,793801490,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/005/SRR1964325,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/005/SRR1964325,291f72a8a5a2db30f635f582b9f53703,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986371,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655065: Ribosome Profiling puromycin replicate 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470229,Ribosome Profiling puromycin replicate 1,AB 5500xl-W Genetic Analysis System,SRR1964326,27538483,1376924150,SAMN03470229,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655065,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/006/SRR1964326/SRR1964326.fastq.gz,1171968826,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/006/SRR1964326/SRR1964326.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/006/SRR1964326/SRR1964326.fastq.gz,7c2c0204e6e7bdd06186bc5d56d7f3e7,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2019-10-30,,SINGLE,,,,,,,,,,GSM1655065_r3,,GSM1655065,,Ribosome Profiling puromycin replicate 1,,,,,SRS901269,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/006/SRR1964326,897319195,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/006/SRR1964326,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/006/SRR1964326,4c175b02473426776443b44c07e71238,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986372,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470230,Ribosome Profiling puromycin replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964327,34155138,1707756900,SAMN03470230,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655066,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/007/SRR1964327/SRR1964327.fastq.gz,1696080308,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/007/SRR1964327/SRR1964327.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/007/SRR1964327/SRR1964327.fastq.gz,3176b32bf1f8db16735f66d637f609c5,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-01-19,,SINGLE,,,,,,,,,,GSM1655066_r1,,GSM1655066,,Ribosome Profiling puromycin replicate 2,,,,,SRS901268,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/007/SRR1964327,1232973038,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/007/SRR1964327,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/007/SRR1964327,46e76ec67c68b676966c308bc0fa3830,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986372,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470230,Ribosome Profiling puromycin replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964328,23825786,1191289300,SAMN03470230,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655066,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/008/SRR1964328/SRR1964328.fastq.gz,1157209809,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/008/SRR1964328/SRR1964328.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/008/SRR1964328/SRR1964328.fastq.gz,b02d87996f806e90f9e5909571b298d6,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1655066_r2,,GSM1655066,,Ribosome Profiling puromycin replicate 2,,,,,SRS901268,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/008/SRR1964328,842207306,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/008/SRR1964328,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/008/SRR1964328,2fb6e153af0cf3ad8a7ce2a1d6a8e3b1,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA280809,SRX986372,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,AB 5500xl-W Genetic Analysis System sequencing; GSM1655066: Ribosome Profiling puromycin replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03470230,Ribosome Profiling puromycin replicate 2,AB 5500xl-W Genetic Analysis System,SRR1964329,23506757,1175337850,SAMN03470230,,,,,,,ESC line CGR8,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1655066,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR196/009/SRR1964329/SRR1964329.fastq.gz,1128152427,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/009/SRR1964329/SRR1964329.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR196/009/SRR1964329/SRR1964329.fastq.gz,5ec22339a6d498e8bcce9cd174ab0514,2016-01-13,2016-01-13,false,,,,,,,,,,,ABI_SOLID,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1655066_r3,,GSM1655066,,Ribosome Profiling puromycin replicate 2,,,,,SRS901268,SRP057051,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR196/009/SRR1964329,829470272,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/009/SRR1964329,ftp.sra.ebi.ac.uk/vol1/srr/SRR196/009/SRR1964329,fc70c160a569668de488bdf966648399,129,GSE67741,Ribosome profiling with translation inhibitors reveals pervasive translation in murine ES cells,,,SRA252983,,,,,,,,,,,,,,, PRJNA282016,SRX1006950,Illumina HiSeq 2000 sequencing; GSM1665594: swarmer M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665594: swarmer M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565828,swarmer M2G ribosome profiling,Illumina HiSeq 2000,SRR1991275,20703090,660389778,SAMN03565828,,,,,,,,swarmer M2G,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1665594,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR199/005/SRR1991275/SRR1991275.fastq.gz,611054697,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/005/SRR1991275/SRR1991275.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/005/SRR1991275/SRR1991275.fastq.gz,e9389efec858c9d50d7c12b59370bd67,2016-04-21,2016-04-21,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1665594_r1,,GSM1665594,,swarmer M2G ribosome profiling,,,,,SRS921523,SRP057599,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR199/005/SRR1991275,509299558,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/005/SRR1991275,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/005/SRR1991275,c251dd078007655b0b5d4ba162c6c97e,,GSE68200,Ribosome Profiling Reveals Translational Control During the Caulobacter crescentus cell cycle,,,SRA262024,,,,,,,,,,,,,,, PRJNA282016,SRX1006951,Illumina HiSeq 2000 sequencing; GSM1665595: early stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665595: early stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565829,early stalk M2G ribosome profiling,Illumina HiSeq 2000,SRR1991276,80717688,2400826270,SAMN03565829,,,,,,,,early stalk M2G,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1665595,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR199/006/SRR1991276/SRR1991276.fastq.gz,1819745924,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/006/SRR1991276/SRR1991276.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/006/SRR1991276/SRR1991276.fastq.gz,2aeb235e40a6db5e8128566227422ce1,2016-04-21,2016-04-21,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1665595_r1,,GSM1665595,,early stalk M2G ribosome profiling,,,,,SRS921522,SRP057599,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR199/006/SRR1991276,1685972921,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/006/SRR1991276,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/006/SRR1991276,9275ea9f98a24f9f3de752605a6c2f30,,GSE68200,Ribosome Profiling Reveals Translational Control During the Caulobacter crescentus cell cycle,,,SRA262024,,,,,,,,,,,,,,, PRJNA282016,SRX1006952,Illumina HiSeq 2000 sequencing; GSM1665596: late stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665596: late stalk M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565830,late stalk M2G ribosome profiling,Illumina HiSeq 2000,SRR1991277,22993484,674619628,SAMN03565830,,,,,,,,late stalk M2G,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1665596,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR199/007/SRR1991277/SRR1991277.fastq.gz,608353925,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/007/SRR1991277/SRR1991277.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/007/SRR1991277/SRR1991277.fastq.gz,1cf5858184e14294c2a7bcca049a649c,2016-04-21,2016-04-21,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1665596_r1,,GSM1665596,,late stalk M2G ribosome profiling,,,,,SRS921520,SRP057599,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR199/007/SRR1991277,522209187,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/007/SRR1991277,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/007/SRR1991277,e2479eed01df4baaadb7ac846ab71f4e,,GSE68200,Ribosome Profiling Reveals Translational Control During the Caulobacter crescentus cell cycle,,,SRA262024,,,,,,,,,,,,,,, PRJNA282016,SRX1006953,Illumina HiSeq 2000 sequencing; GSM1665597: early prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665597: early prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565832,early prediv M2G ribosome profiling,Illumina HiSeq 2000,SRR1991278,17278060,518095336,SAMN03565832,,,,,,,,early prediv M2G,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1665597,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR199/008/SRR1991278/SRR1991278.fastq.gz,433044006,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/008/SRR1991278/SRR1991278.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/008/SRR1991278/SRR1991278.fastq.gz,cf87b740ff41a055efdf01147c448239,2016-04-21,2016-04-21,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1665597_r1,,GSM1665597,,early prediv M2G ribosome profiling,,,,,SRS921521,SRP057599,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR199/008/SRR1991278,385194707,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/008/SRR1991278,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/008/SRR1991278,c7bddfe55fb7f5d36a8648da26ff0215,,GSE68200,Ribosome Profiling Reveals Translational Control During the Caulobacter crescentus cell cycle,,,SRA262024,,,,,,,,,,,,,,, PRJNA282016,SRX1006954,Illumina HiSeq 2000 sequencing; GSM1665598: late prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665598: late prediv M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565831,late prediv M2G ribosome profiling,Illumina HiSeq 2000,SRR1991279,20443469,604238206,SAMN03565831,,,,,,,,late prediv M2G,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1665598,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR199/009/SRR1991279/SRR1991279.fastq.gz,539245341,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/009/SRR1991279/SRR1991279.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/009/SRR1991279/SRR1991279.fastq.gz,e03a098484017ec069bf186ddc841fc4,2016-04-21,2016-04-21,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1665598_r1,,GSM1665598,,late prediv M2G ribosome profiling,,,,,SRS921519,SRP057599,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR199/009/SRR1991279,463508161,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/009/SRR1991279,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/009/SRR1991279,f11a957c0f90457020dff84829b5d5c6,,GSE68200,Ribosome Profiling Reveals Translational Control During the Caulobacter crescentus cell cycle,,,SRA262024,,,,,,,,,,,,,,, PRJNA282016,SRX1006955,Illumina HiSeq 2000 sequencing; GSM1665599: post division M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM1665599: post division M2G ribosome profiling; Caulobacter vibrioides NA1000; RNA-Seq,565050,Caulobacter vibrioides NA1000,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03565833,post division M2G ribosome profiling,Illumina HiSeq 2000,SRR1991280,13538820,382410272,SAMN03565833,,,,,,,,post division M2G,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1665599,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR199/000/SRR1991280/SRR1991280.fastq.gz,337062384,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/000/SRR1991280/SRR1991280.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR199/000/SRR1991280/SRR1991280.fastq.gz,85fec4b19099e7c46854b4354d03610b,2016-04-21,2016-04-21,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM1665599_r1,,GSM1665599,,post division M2G ribosome profiling,,,,,SRS921518,SRP057599,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR199/000/SRR1991280,293478397,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/000/SRR1991280,ftp.sra.ebi.ac.uk/vol1/srr/SRR199/000/SRR1991280,32ebf9d7f46f85c76cc3e959c21a7c8d,,GSE68200,Ribosome Profiling Reveals Translational Control During the Caulobacter crescentus cell cycle,,,SRA262024,,,,,,,,,,,,,,, PRJNA282960,SRX1017035,"Illumina HiSeq 2500 sequencing; GSM1666805: ATF4-/- ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666805: ATF4-/- ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581119,"ATF4-/- ER ribosome profiling, untreated (rep 1)",Illumina HiSeq 2500,SRR2007064,19223712,980409312,SAMN03581119,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666805,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/004/SRR2007064/SRR2007064.fastq.gz,750389168,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007064/SRR2007064.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007064/SRR2007064.fastq.gz,8f6c670b3016d47afe04f64e588afc81,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666805_r1,,GSM1666805,,"ATF4-/- ER ribosome profiling, untreated (rep 1)",,,,,SRS928315,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/004/SRR2007064,640680508,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007064,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007064,fe2ffb90bb9594de33c54906bbb0d686,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017036,"Illumina HiSeq 2500 sequencing; GSM1666806: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666806: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581120,"ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007065,20859677,1063843527,SAMN03581120,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666806,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/005/SRR2007065/SRR2007065.fastq.gz,778562697,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007065/SRR2007065.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007065/SRR2007065.fastq.gz,6930d0a9c44fd363b9c8578677982594,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666806_r1,,GSM1666806,,"ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 1)",,,,,SRS928313,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/005/SRR2007065,692854781,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007065,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007065,e9746721199cfe4e5a970dd1553daf12,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017037,"Illumina HiSeq 2500 sequencing; GSM1666807: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666807: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581117,"ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007066,22014222,1122725322,SAMN03581117,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666807,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/006/SRR2007066/SRR2007066.fastq.gz,799111229,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007066/SRR2007066.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007066/SRR2007066.fastq.gz,e3425d411e49815f2c74c72fd74b298c,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666807_r1,,GSM1666807,,"ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 1)",,,,,SRS928314,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/006/SRR2007066,730236745,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007066,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007066,f47b21920913fb106e30344831724ec1,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017038,"Illumina HiSeq 2500 sequencing; GSM1666808: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666808: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581118,"ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007067,21063979,1074262929,SAMN03581118,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666808,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/007/SRR2007067/SRR2007067.fastq.gz,802860343,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007067/SRR2007067.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007067/SRR2007067.fastq.gz,45851d2b9ee46fa4d764df1f1daa95ea,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-01-19,,SINGLE,,,,,,,,,,GSM1666808_r1,,GSM1666808,,"ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 1)",,,,,SRS928311,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/007/SRR2007067,703901779,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007067,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007067,e8af3f8d461113032924cb13ec286afb,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017039,"Illumina HiSeq 2500 sequencing; GSM1666809: ATF4-/- ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666809: ATF4-/- ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581121,"ATF4-/- ER ribosome profiling, 1 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007068,22870593,1166400243,SAMN03581121,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666809,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/008/SRR2007068/SRR2007068.fastq.gz,827346931,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007068/SRR2007068.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007068/SRR2007068.fastq.gz,8f9caf91ee58024d7191b5d43e9b0d4a,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666809_r1,,GSM1666809,,"ATF4-/- ER ribosome profiling, 1 h Tg (rep 1)",,,,,SRS928309,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/008/SRR2007068,761030598,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007068,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007068,733dd9b88b3b44315861af0544ca59f4,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017040,"Illumina HiSeq 2500 sequencing; GSM1666810: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666810: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581122,"ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007069,21153634,1078835334,SAMN03581122,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666810,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/009/SRR2007069/SRR2007069.fastq.gz,824188298,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007069/SRR2007069.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007069/SRR2007069.fastq.gz,8f8349b1cf42766998188e308c813b71,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-14,,SINGLE,,,,,,,,,,GSM1666810_r1,,GSM1666810,,"ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 1)",,,,,SRS928310,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/009/SRR2007069,701200089,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007069,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007069,ac939927725d2288373a2a59dc75c201,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017041,"Illumina HiSeq 2500 sequencing; GSM1666811: ATF4-/- ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666811: ATF4-/- ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581123,"ATF4-/- ER ribosome profiling, 2 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007070,23215960,1184013960,SAMN03581123,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666811,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/000/SRR2007070/SRR2007070.fastq.gz,862993372,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007070/SRR2007070.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007070/SRR2007070.fastq.gz,36d290b53dad39b809324e3b7db7d4d5,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-12-09,,SINGLE,,,,,,,,,,GSM1666811_r1,,GSM1666811,,"ATF4-/- ER ribosome profiling, 2 h Tg (rep 1)",,,,,SRS928312,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/000/SRR2007070,777004380,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007070,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007070,830897efa7e4c9c5697bce1b1f8e4320,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017042,"Illumina HiSeq 2500 sequencing; GSM1666812: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666812: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581124,"ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007071,22260855,1135303605,SAMN03581124,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666812,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/001/SRR2007071/SRR2007071.fastq.gz,853138975,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007071/SRR2007071.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007071/SRR2007071.fastq.gz,99d6270a066ef0813f02c5555ae37f96,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666812_r1,,GSM1666812,,"ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 1)",,,,,SRS928308,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/001/SRR2007071,736749251,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007071,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007071,2578219becc7b4a8d79d89162f9dc48f,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017043,"Illumina HiSeq 2500 sequencing; GSM1666813: ATF4-/- ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666813: ATF4-/- ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581125,"ATF4-/- ER ribosome profiling, 4 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007072,23138057,1180040907,SAMN03581125,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666813,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/002/SRR2007072/SRR2007072.fastq.gz,872623863,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007072/SRR2007072.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007072/SRR2007072.fastq.gz,072706170139147e508769afaae9ded8,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-20,,SINGLE,,,,,,,,,,GSM1666813_r1,,GSM1666813,,"ATF4-/- ER ribosome profiling, 4 h Tg (rep 1)",,,,,SRS928307,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/002/SRR2007072,773009285,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007072,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007072,740b416d7328ccef0ef6bd4b279fbb79,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017044,"Illumina HiSeq 2500 sequencing; GSM1666814: ATF4-/- cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666814: ATF4-/- cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581126,"ATF4-/- cytosol ribosome profiling, untreated (rep 1)",Illumina HiSeq 2500,SRR2007073,22787710,1162173210,SAMN03581126,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666814,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/003/SRR2007073/SRR2007073.fastq.gz,903435711,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007073/SRR2007073.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007073/SRR2007073.fastq.gz,220de35a12d43b33259a9a6cf914716b,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-12-04,,SINGLE,,,,,,,,,,GSM1666814_r1,,GSM1666814,,"ATF4-/- cytosol ribosome profiling, untreated (rep 1)",,,,,SRS928304,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/003/SRR2007073,753090059,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007073,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007073,563c1695ae6712da96be8e5b990f8582,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017045,"Illumina HiSeq 2500 sequencing; GSM1666815: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666815: ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581127,"ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007074,20343583,1037522733,SAMN03581127,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666815,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/004/SRR2007074/SRR2007074.fastq.gz,755132997,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007074/SRR2007074.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007074/SRR2007074.fastq.gz,a059069c41bca401ec1a2dd346ebd6ef,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-05-01,,SINGLE,,,,,,,,,,GSM1666815_r1,,GSM1666815,,"ATF4-/- cytosol ribosome profiling, 0.5 h Tg (rep 2)",,,,,SRS928305,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/004/SRR2007074,666766796,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007074,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007074,5c798521695ce5cdf0f00a7e8c72162a,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017046,"Illumina HiSeq 2500 sequencing; GSM1666816: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666816: ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581128,"ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007075,20132638,1026764538,SAMN03581128,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666816,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/005/SRR2007075/SRR2007075.fastq.gz,725181242,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007075/SRR2007075.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007075/SRR2007075.fastq.gz,8279b5928641465227fb29b23a458fca,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,,,,,,,,,,GSM1666816_r1,,GSM1666816,,"ATF4-/- ER ribosome profiling, 0.5 h Tg (rep 2)",,,,,SRS928303,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/005/SRR2007075,660945360,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007075,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007075,fc9c6a0343b5532dc4447b48cfb20704,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017047,"Illumina HiSeq 2500 sequencing; GSM1666817: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666817: ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581129,"ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007076,20134079,1026838029,SAMN03581129,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666817,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/006/SRR2007076/SRR2007076.fastq.gz,766825415,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007076/SRR2007076.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007076/SRR2007076.fastq.gz,045863919500c4cd473e23a38c1b40d4,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666817_r1,,GSM1666817,,"ATF4-/- cytosol ribosome profiling, 1 h Tg (rep 2)",,,,,SRS928300,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/006/SRR2007076,664320760,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007076,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007076,f004f7eee9d2f1c77629d6a43f870bf0,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017048,"Illumina HiSeq 2500 sequencing; GSM1666818: ATF4-/- ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666818: ATF4-/- ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581130,"ATF4-/- ER ribosome profiling, 1 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007077,22615405,1153385655,SAMN03581130,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666818,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/007/SRR2007077/SRR2007077.fastq.gz,838764230,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007077/SRR2007077.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007077/SRR2007077.fastq.gz,9a442e729bdb29ff74aa8c04894dd46b,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-12-06,,SINGLE,,,,,,,,,,GSM1666818_r1,,GSM1666818,,"ATF4-/- ER ribosome profiling, 1 h Tg (rep 2)",,,,,SRS928301,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/007/SRR2007077,746412179,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007077,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007077,3a210f5d4bbe30f1c2218a92eef132cc,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017049,"Illumina HiSeq 2500 sequencing; GSM1666819: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666819: ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581131,"ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007078,20873353,1064541003,SAMN03581131,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666819,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/008/SRR2007078/SRR2007078.fastq.gz,809451640,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007078/SRR2007078.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007078/SRR2007078.fastq.gz,20f959f50a2b52f192488d2ec1dd77ff,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666819_r1,,GSM1666819,,"ATF4-/- cytosol ribosome profiling, 2 h Tg (rep 2)",,,,,SRS928302,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/008/SRR2007078,685185546,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007078,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007078,696a2e9bd788c0b5ed05b21b6e265f51,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017050,"Illumina HiSeq 2500 sequencing; GSM1666820: ATF4-/- ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666820: ATF4-/- ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581132,"ATF4-/- ER ribosome profiling, 2 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007079,21371573,1089950223,SAMN03581132,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666820,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/009/SRR2007079/SRR2007079.fastq.gz,808345919,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007079/SRR2007079.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007079/SRR2007079.fastq.gz,8ba3bd7ce61b9176c3107262bc9279fd,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-05-01,,SINGLE,,,,,,,,,,GSM1666820_r1,,GSM1666820,,"ATF4-/- ER ribosome profiling, 2 h Tg (rep 2)",,,,,SRS928306,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/009/SRR2007079,705688510,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007079,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007079,1c5dccf8b60f15ad84c2be1ff6b108ad,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017051,"Illumina HiSeq 2500 sequencing; GSM1666821: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666821: ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581133,"ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007080,21983441,1121155491,SAMN03581133,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666821,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/000/SRR2007080/SRR2007080.fastq.gz,842821103,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007080/SRR2007080.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007080/SRR2007080.fastq.gz,4d183125376d25ee8255c700cef460a0,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-11-07,,SINGLE,,,,,,,,,,GSM1666821_r1,,GSM1666821,,"ATF4-/- cytosol ribosome profiling, 4 h Tg (rep 2)",,,,,SRS928298,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/000/SRR2007080,722145024,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007080,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007080,c0d3126f02f29da37f6136056bbb6ff6,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017052,"Illumina HiSeq 2500 sequencing; GSM1666822: ATF4-/- ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666822: ATF4-/- ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581134,"ATF4-/- ER ribosome profiling, 4 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007081,22835371,1164603921,SAMN03581134,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666822,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/001/SRR2007081/SRR2007081.fastq.gz,877472441,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007081/SRR2007081.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007081/SRR2007081.fastq.gz,9f908d209df2a8ba13236616ba53ede8,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-11-07,,SINGLE,,,,,,,,,,GSM1666822_r1,,GSM1666822,,"ATF4-/- ER ribosome profiling, 4 h Tg (rep 2)",,,,,SRS928297,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/001/SRR2007081,761358628,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007081,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007081,11ee95e2a23a042efea879cf1dc6cc49,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017053,"Illumina HiSeq 2500 sequencing; GSM1666823: ATF4-/- cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666823: ATF4-/- cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581135,"ATF4-/- cytosol ribosome profiling, untreated (rep 2)",Illumina HiSeq 2500,SRR2007082,20677901,1054572951,SAMN03581135,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666823,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/002/SRR2007082/SRR2007082.fastq.gz,829528862,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007082/SRR2007082.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007082/SRR2007082.fastq.gz,f3ed3768e48b7fa81a672b1397b09067,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-30,,SINGLE,,,,,,,,,,GSM1666823_r1,,GSM1666823,,"ATF4-/- cytosol ribosome profiling, untreated (rep 2)",,,,,SRS928299,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/002/SRR2007082,677564817,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007082,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007082,5670bc0a7195e55b9cead89d0ddd16d6,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017054,"Illumina HiSeq 2500 sequencing; GSM1666824: ATF4-/- ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666824: ATF4-/- ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581057,"ATF4-/- ER ribosome profiling, untreated (rep 2)",Illumina HiSeq 2500,SRR2007083,21128656,1077561456,SAMN03581057,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666824,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/003/SRR2007083/SRR2007083.fastq.gz,833596080,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007083/SRR2007083.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007083/SRR2007083.fastq.gz,ba7e4cb0045216c95ab062353b851680,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-22,,SINGLE,,,,,,,,,,GSM1666824_r1,,GSM1666824,,"ATF4-/- ER ribosome profiling, untreated (rep 2)",,,,,SRS928296,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/003/SRR2007083,701005394,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007083,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007083,2ab38de9bd68ec8f09fbe1000d3e9702,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017055,"Illumina HiSeq 2500 sequencing; GSM1666825: eIF2A S51A ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666825: eIF2A S51A ER ribosome profiling, untreated (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581058,"eIF2A S51A ER ribosome profiling, untreated (rep 1)",Illumina HiSeq 2500,SRR2007084,16251551,828829101,SAMN03581058,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666825,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/004/SRR2007084/SRR2007084.fastq.gz,631573548,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007084/SRR2007084.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007084/SRR2007084.fastq.gz,9e46d758ee60abf3bb75449a92edd41d,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-05-01,,SINGLE,,,,,,,,,,GSM1666825_r1,,GSM1666825,,"eIF2A S51A ER ribosome profiling, untreated (rep 1)",,,,,SRS928295,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/004/SRR2007084,503324603,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007084,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007084,2499d81716223fc538c4fb699117f22e,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017056,"Illumina HiSeq 2500 sequencing; GSM1666826: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666826: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581059,"eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007085,18983118,968139018,SAMN03581059,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666826,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/005/SRR2007085/SRR2007085.fastq.gz,719760881,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007085/SRR2007085.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007085/SRR2007085.fastq.gz,a28f4f405041f9dad2781cfaeb7b85dd,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-31,,SINGLE,,,,,,,,,,GSM1666826_r1,,GSM1666826,,"eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 1)",,,,,SRS928294,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/005/SRR2007085,598572410,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007085,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007085,c677325a813cbfcb1b67dda5ff08adde,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017057,"Illumina HiSeq 2500 sequencing; GSM1666827: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666827: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581060,"eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007086,15833217,807494067,SAMN03581060,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666827,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/006/SRR2007086/SRR2007086.fastq.gz,607783609,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007086/SRR2007086.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007086/SRR2007086.fastq.gz,1f635e71bfc5c27a8601a3954f70d1cc,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1666827_r1,,GSM1666827,,"eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 1)",,,,,SRS928293,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/006/SRR2007086,483319951,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007086,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007086,e4987565002e7f043b94b79842e3b688,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017058,"Illumina HiSeq 2500 sequencing; GSM1666828: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666828: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581061,"eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007087,17567181,895926231,SAMN03581061,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666828,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/007/SRR2007087/SRR2007087.fastq.gz,688577887,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007087/SRR2007087.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007087/SRR2007087.fastq.gz,ce097ccdb78cfbf42188985e27f36bee,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666828_r1,,GSM1666828,,"eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 1)",,,,,SRS928292,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/007/SRR2007087,544449351,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007087,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007087,b4c12279fdb51258c2a77c45d7d14643,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017059,"Illumina HiSeq 2500 sequencing; GSM1666829: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666829: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581062,"eIF2A S51A ER ribosome profiling, 1 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007088,19935281,1016699331,SAMN03581062,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666829,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/008/SRR2007088/SRR2007088.fastq.gz,771486321,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007088/SRR2007088.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007088/SRR2007088.fastq.gz,c9d3023158af9918cbe16d211c09a0e3,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-02-05,,SINGLE,,,,,,,,,,GSM1666829_r1,,GSM1666829,,"eIF2A S51A ER ribosome profiling, 1 h Tg (rep 1)",,,,,SRS928291,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/008/SRR2007088,610747127,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007088,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007088,f10e2d5997b389e787cd973d99fdd4e4,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017060,"Illumina HiSeq 2500 sequencing; GSM1666830: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666830: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581063,"eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007089,15247010,777597510,SAMN03581063,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666830,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/009/SRR2007089/SRR2007089.fastq.gz,596231635,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007089/SRR2007089.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007089/SRR2007089.fastq.gz,f2d01efbe514a7dcd7c1ab72a62a6a59,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1666830_r1,,GSM1666830,,"eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 1)",,,,,SRS928290,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/009/SRR2007089,471164437,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007089,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007089,078c2cf9003d350b9b901a011daa541b,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017061,"Illumina HiSeq 2500 sequencing; GSM1666831: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666831: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581064,"eIF2A S51A ER ribosome profiling, 2 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007090,13881251,707943801,SAMN03581064,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666831,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/000/SRR2007090/SRR2007090.fastq.gz,542334611,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007090/SRR2007090.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007090/SRR2007090.fastq.gz,6bd40f6314815f60f55fbcb29bb33d52,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666831_r1,,GSM1666831,,"eIF2A S51A ER ribosome profiling, 2 h Tg (rep 1)",,,,,SRS928289,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/000/SRR2007090,427107957,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007090,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007090,dafa35349e8bbdd7c3714c98c3beadc2,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017062,"Illumina HiSeq 2500 sequencing; GSM1666832: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666832: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581065,"eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007091,17489985,891989235,SAMN03581065,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666832,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/001/SRR2007091/SRR2007091.fastq.gz,666878071,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007091/SRR2007091.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007091/SRR2007091.fastq.gz,bc93b30a034983489e4eef24171d274b,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-17,,SINGLE,,,,,,,,,,GSM1666832_r1,,GSM1666832,,"eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 1)",,,,,SRS928288,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/001/SRR2007091,539051124,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007091,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007091,c5f574f09d61529bb7d2c49d33f59008,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017063,"Illumina HiSeq 2500 sequencing; GSM1666833: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666833: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581066,"eIF2A S51A ER ribosome profiling, 4 h Tg (rep 1)",Illumina HiSeq 2500,SRR2007092,15210074,775713774,SAMN03581066,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666833,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/002/SRR2007092/SRR2007092.fastq.gz,594365713,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007092/SRR2007092.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007092/SRR2007092.fastq.gz,f6f0969fc0a731b5c061f8bf453fb9bd,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-05-17,,SINGLE,,,,,,,,,,GSM1666833_r1,,GSM1666833,,"eIF2A S51A ER ribosome profiling, 4 h Tg (rep 1)",,,,,SRS928287,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/002/SRR2007092,466368392,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007092,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007092,02759ee8ebe62f6fd6ff43b02e94818b,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017064,"Illumina HiSeq 2500 sequencing; GSM1666834: eIF2A S51A cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666834: eIF2A S51A cytosol ribosome profiling, untreated (rep 1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581067,"eIF2A S51A cytosol ribosome profiling, untreated (rep 1)",Illumina HiSeq 2500,SRR2007093,17142687,874277037,SAMN03581067,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666834,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/003/SRR2007093/SRR2007093.fastq.gz,654634689,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007093/SRR2007093.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007093/SRR2007093.fastq.gz,ede29ff73b5cf8b716ce4d377028f9be,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1666834_r1,,GSM1666834,,"eIF2A S51A cytosol ribosome profiling, untreated (rep 1)",,,,,SRS928286,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/003/SRR2007093,529567333,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007093,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007093,567d196bebf7032ba653399ce80de1a4,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017065,"Illumina HiSeq 2500 sequencing; GSM1666835: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666835: eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581068,"eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007094,20026160,1021334160,SAMN03581068,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666835,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/004/SRR2007094/SRR2007094.fastq.gz,800653365,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007094/SRR2007094.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007094/SRR2007094.fastq.gz,d346dabdbb6aeaa8404f5c6acc24e9b5,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666835_r1,,GSM1666835,,"eIF2A S51A cytosol ribosome profiling, 0.5 h Tg (rep 2)",,,,,SRS928285,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/004/SRR2007094,663529820,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007094,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007094,52ef8d048f2e9e434edce361b0a77e11,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017066,"Illumina HiSeq 2500 sequencing; GSM1666836: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666836: eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581069,"eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007095,18703857,953896707,SAMN03581069,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666836,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/005/SRR2007095/SRR2007095.fastq.gz,739307211,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007095/SRR2007095.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007095/SRR2007095.fastq.gz,1caccf0c65034e178e24a43c6497c11d,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666836_r1,,GSM1666836,,"eIF2A S51A ER ribosome profiling, 0.5 h Tg (rep 2)",,,,,SRS928284,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/005/SRR2007095,613441638,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007095,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007095,18d519120c5c358cf8fbcc851e62a66e,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017067,"Illumina HiSeq 2500 sequencing; GSM1666837: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666837: eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581070,"eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007096,23577690,1202462190,SAMN03581070,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666837,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/006/SRR2007096/SRR2007096.fastq.gz,995652091,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007096/SRR2007096.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007096/SRR2007096.fastq.gz,26722fdfae2a805f16fafd3aac0f0723,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666837_r1,,GSM1666837,,"eIF2A S51A cytosol ribosome profiling, 1 h Tg (rep 2)",,,,,SRS928283,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/006/SRR2007096,787183102,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007096,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007096,fc0c1f194211e254aade8f6ddd722f2b,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017068,"Illumina HiSeq 2500 sequencing; GSM1666838: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666838: eIF2A S51A ER ribosome profiling, 1 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581071,"eIF2A S51A ER ribosome profiling, 1 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007097,24731497,1261306347,SAMN03581071,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666838,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/007/SRR2007097/SRR2007097.fastq.gz,1043805775,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007097/SRR2007097.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007097/SRR2007097.fastq.gz,9917bb3ddf2d76c54b654b2acc123df4,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-11-01,,SINGLE,,,,,,,,,,GSM1666838_r1,,GSM1666838,,"eIF2A S51A ER ribosome profiling, 1 h Tg (rep 2)",,,,,SRS928282,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/007/SRR2007097,813842844,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007097,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007097,f669ce09a7325e57272d472230e00ee3,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017069,"Illumina HiSeq 2500 sequencing; GSM1666839: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666839: eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581072,"eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007098,21716584,1107545784,SAMN03581072,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666839,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/008/SRR2007098/SRR2007098.fastq.gz,892319611,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007098/SRR2007098.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007098/SRR2007098.fastq.gz,a822873eac25a2486fda6f82446ec25e,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666839_r1,,GSM1666839,,"eIF2A S51A cytosol ribosome profiling, 2 h Tg (rep 2)",,,,,SRS928281,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/008/SRR2007098,728405442,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007098,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007098,b84fa2650e4ada3d0b3f9e8c1abb3ab0,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017070,"Illumina HiSeq 2500 sequencing; GSM1666840: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666840: eIF2A S51A ER ribosome profiling, 2 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581073,"eIF2A S51A ER ribosome profiling, 2 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007099,23696982,1208546082,SAMN03581073,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666840,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/009/SRR2007099/SRR2007099.fastq.gz,985486968,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007099/SRR2007099.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007099/SRR2007099.fastq.gz,38c04cd34181d48441af95dc67376393,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1666840_r1,,GSM1666840,,"eIF2A S51A ER ribosome profiling, 2 h Tg (rep 2)",,,,,SRS928280,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/009/SRR2007099,780755906,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007099,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007099,b9df22558e3adfcbae1a0ed41b240c83,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017071,"Illumina HiSeq 2500 sequencing; GSM1666841: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666841: eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581074,"eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007100,24517717,1250403567,SAMN03581074,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666841,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/000/SRR2007100/SRR2007100.fastq.gz,1013914917,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007100/SRR2007100.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007100/SRR2007100.fastq.gz,5fb1bc9d649e72ca41145b8bdd6c16e6,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1666841_r1,,GSM1666841,,"eIF2A S51A cytosol ribosome profiling, 4 h Tg (rep 2)",,,,,SRS928279,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/000/SRR2007100,811186937,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007100,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007100,058d33c1c9a2e277d8f16469878c1ee5,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017072,"Illumina HiSeq 2500 sequencing; GSM1666842: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666842: eIF2A S51A ER ribosome profiling, 4 h Tg (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581075,"eIF2A S51A ER ribosome profiling, 4 h Tg (rep 2)",Illumina HiSeq 2500,SRR2007101,20573167,1049231517,SAMN03581075,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666842,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/001/SRR2007101/SRR2007101.fastq.gz,848736857,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007101/SRR2007101.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007101/SRR2007101.fastq.gz,12186db364ee4edefb0dd813fd555ce5,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-11-08,,SINGLE,,,,,,,,,,GSM1666842_r1,,GSM1666842,,"eIF2A S51A ER ribosome profiling, 4 h Tg (rep 2)",,,,,SRS928278,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/001/SRR2007101,675656795,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007101,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007101,892a566cebfbc5d67c94a7bf9cb055fd,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017073,"Illumina HiSeq 2500 sequencing; GSM1666843: eIF2A S51A cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666843: eIF2A S51A cytosol ribosome profiling, untreated (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581076,"eIF2A S51A cytosol ribosome profiling, untreated (rep 2)",Illumina HiSeq 2500,SRR2007102,20689853,1055182503,SAMN03581076,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666843,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/002/SRR2007102/SRR2007102.fastq.gz,838871113,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007102/SRR2007102.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007102/SRR2007102.fastq.gz,a558f0c856b65b624435ab67510f58ea,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-05-01,,SINGLE,,,,,,,,,,GSM1666843_r1,,GSM1666843,,"eIF2A S51A cytosol ribosome profiling, untreated (rep 2)",,,,,SRS928277,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/002/SRR2007102,688023808,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007102,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007102,90f28a0826186fd862fa42facd5911cf,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017074,"Illumina HiSeq 2500 sequencing; GSM1666844: eIF2A S51A ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1666844: eIF2A S51A ER ribosome profiling, untreated (rep 2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581077,"eIF2A S51A ER ribosome profiling, untreated (rep 2)",Illumina HiSeq 2500,SRR2007103,20314148,1036021548,SAMN03581077,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1666844,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/003/SRR2007103/SRR2007103.fastq.gz,787731407,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007103/SRR2007103.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007103/SRR2007103.fastq.gz,d56bfc6e3a1bc24ee099795ee7ae4c25,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-18,,SINGLE,,,,,,,,,,GSM1666844_r1,,GSM1666844,,"eIF2A S51A ER ribosome profiling, untreated (rep 2)",,,,,SRS928276,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/003/SRR2007103,668722650,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007103,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007103,d7207c80d8ad83cb2ba6d22ceba22514,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017479,"Illumina HiSeq 2500 sequencing; GSM1674110: WT cytosol ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674110: WT cytosol ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581028,"WT cytosol ribosome profiling, 0.5 h Tg (rep1)",Illumina HiSeq 2500,SRR2007769,17607850,898000350,SAMN03581028,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674110,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/009/SRR2007769/SRR2007769.fastq.gz,678618229,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007769/SRR2007769.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007769/SRR2007769.fastq.gz,5b042efe45057cd33724c4189025d078,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674110_r1,,GSM1674110,,"WT cytosol ribosome profiling, 0.5 h Tg (rep1)",,,,,SRS928707,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/009/SRR2007769,618110962,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007769,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007769,13aae4ffe207fb06af5dc32027cd3cb3,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017480,"Illumina HiSeq 2500 sequencing; GSM1674111: WT cytosol ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674111: WT cytosol ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581029,"WT cytosol ribosome profiling, 0.5 h Tg (rep2)",Illumina HiSeq 2500,SRR2007770,8004515,408230265,SAMN03581029,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674111,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/000/SRR2007770/SRR2007770.fastq.gz,289031287,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007770/SRR2007770.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007770/SRR2007770.fastq.gz,21370ff7d9703724b0841d230939aa71,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674111_r1,,GSM1674111,,"WT cytosol ribosome profiling, 0.5 h Tg (rep2)",,,,,SRS928709,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/000/SRR2007770,271531313,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007770,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007770,42319e0ede92f46cf59b703af21dd823,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017481,"Illumina HiSeq 2500 sequencing; GSM1674112: WT ER ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674112: WT ER ribosome profiling, 0.5 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581030,"WT ER ribosome profiling, 0.5 h Tg (rep1)",Illumina HiSeq 2500,SRR2007771,34274786,1748014086,SAMN03581030,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674112,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/001/SRR2007771/SRR2007771.fastq.gz,1248442771,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007771/SRR2007771.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007771/SRR2007771.fastq.gz,a1e39652ed038f8355f959a2585894e4,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674112_r1,,GSM1674112,,"WT ER ribosome profiling, 0.5 h Tg (rep1)",,,,,SRS928706,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/001/SRR2007771,1413645600,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007771,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007771,c6628673792d2ae3a82cc877b3b1fdac,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017482,"Illumina HiSeq 2500 sequencing; GSM1674113: WT ER ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674113: WT ER ribosome profiling, 0.5 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581031,"WT ER ribosome profiling, 0.5 h Tg (rep2)",Illumina HiSeq 2500,SRR2007772,44962240,2293074240,SAMN03581031,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674113,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/002/SRR2007772/SRR2007772.fastq.gz,1542229073,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007772/SRR2007772.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007772/SRR2007772.fastq.gz,4aa6a194f9b0b11f8469924916e3ed9d,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-11-17,,SINGLE,,,,,,,,,,GSM1674113_r1,,GSM1674113,,"WT ER ribosome profiling, 0.5 h Tg (rep2)",,,,,SRS928705,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/002/SRR2007772,1762408762,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007772,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007772,66f8e81c0ef6563f90b4ecddb4511fbb,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017483,"Illumina HiSeq 2500 sequencing; GSM1674114: WT cytosol ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674114: WT cytosol ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581032,"WT cytosol ribosome profiling, 1 h Tg (rep1)",Illumina HiSeq 2500,SRR2007773,60458951,3083406501,SAMN03581032,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674114,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/003/SRR2007773/SRR2007773.fastq.gz,2252585883,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007773/SRR2007773.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007773/SRR2007773.fastq.gz,369cd4fed69af2746f754c89b190efd3,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674114_r1,,GSM1674114,,"WT cytosol ribosome profiling, 1 h Tg (rep1)",,,,,SRS928704,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/003/SRR2007773,2078434804,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007773,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007773,0e33eebd1875ba90019f056762cdab19,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017484,"Illumina HiSeq 2500 sequencing; GSM1674115: WT cytosol ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674115: WT cytosol ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581033,"WT cytosol ribosome profiling, 1 h Tg (rep2)",Illumina HiSeq 2500,SRR2007774,5600537,285627387,SAMN03581033,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674115,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/004/SRR2007774/SRR2007774.fastq.gz,199327725,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007774/SRR2007774.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007774/SRR2007774.fastq.gz,c5b27086f1ff363b608a7a409b45974f,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674115_r1,,GSM1674115,,"WT cytosol ribosome profiling, 1 h Tg (rep2)",,,,,SRS928703,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/004/SRR2007774,189381483,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007774,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007774,f306727af39dce92d82ec32a391ce21a,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017485,"Illumina HiSeq 2500 sequencing; GSM1674116: WT ER ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674116: WT ER ribosome profiling, 1 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581034,"WT ER ribosome profiling, 1 h Tg (rep1)",Illumina HiSeq 2500,SRR2007775,29433660,1501116660,SAMN03581034,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674116,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/005/SRR2007775/SRR2007775.fastq.gz,1174166690,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007775/SRR2007775.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007775/SRR2007775.fastq.gz,4b30b50769ad021bf8be0e5aa89ae758,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-11-05,,SINGLE,,,,,,,,,,GSM1674116_r1,,GSM1674116,,"WT ER ribosome profiling, 1 h Tg (rep1)",,,,,SRS928702,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/005/SRR2007775,1062390902,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007775,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007775,e9898a72baf9edb3f58d7a5d48a06d68,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017486,"Illumina HiSeq 2500 sequencing; GSM1674117: WT ER ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674117: WT ER ribosome profiling, 1 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581035,"WT ER ribosome profiling, 1 h Tg (rep2)",Illumina HiSeq 2500,SRR2007776,27741791,1414831341,SAMN03581035,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674117,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/006/SRR2007776/SRR2007776.fastq.gz,1028169992,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007776/SRR2007776.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007776/SRR2007776.fastq.gz,55368e16f3f1f610be21b7f0c11d0dda,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-01-11,,SINGLE,,,,,,,,,,GSM1674117_r1,,GSM1674117,,"WT ER ribosome profiling, 1 h Tg (rep2)",,,,,SRS928701,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/006/SRR2007776,949505496,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007776,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007776,8beb75a4e58358ce976c88fe5c943435,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017487,"Illumina HiSeq 2500 sequencing; GSM1674118: WT cytosol ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674118: WT cytosol ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581036,"WT cytosol ribosome profiling, 2 h Tg (rep1)",Illumina HiSeq 2500,SRR2007777,20792693,1060427343,SAMN03581036,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674118,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/007/SRR2007777/SRR2007777.fastq.gz,844932634,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007777/SRR2007777.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007777/SRR2007777.fastq.gz,f20cfad7541ba74099e15c71f35bb004,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674118_r1,,GSM1674118,,"WT cytosol ribosome profiling, 2 h Tg (rep1)",,,,,SRS928700,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/007/SRR2007777,761164330,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007777,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007777,d27d50d3ed2bdf25352f21f47818c811,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017488,"Illumina HiSeq 2500 sequencing; GSM1674119: WT cytosol ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674119: WT cytosol ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581037,"WT cytosol ribosome profiling, 2 h Tg (rep2)",Illumina HiSeq 2500,SRR2007778,7300567,372328917,SAMN03581037,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674119,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/008/SRR2007778/SRR2007778.fastq.gz,280763422,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007778/SRR2007778.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007778/SRR2007778.fastq.gz,9eca630d735350f44c89b2fe880054e0,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-30,,SINGLE,,,,,,,,,,GSM1674119_r1,,GSM1674119,,"WT cytosol ribosome profiling, 2 h Tg (rep2)",,,,,SRS928696,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/008/SRR2007778,249002544,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007778,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007778,cf1204c127c95972ac87d891cda438be,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017489,"Illumina HiSeq 2500 sequencing; GSM1674120: WT ER ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674120: WT ER ribosome profiling, 2 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581038,"WT ER ribosome profiling, 2 h Tg (rep1)",Illumina HiSeq 2500,SRR2007779,17578993,896528643,SAMN03581038,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674120,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/009/SRR2007779/SRR2007779.fastq.gz,738198812,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007779/SRR2007779.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/009/SRR2007779/SRR2007779.fastq.gz,0eba54fca18198f18f489339c240f0b3,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-26,,SINGLE,,,,,,,,,,GSM1674120_r1,,GSM1674120,,"WT ER ribosome profiling, 2 h Tg (rep1)",,,,,SRS928698,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/009/SRR2007779,650941318,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007779,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/009/SRR2007779,7e3ae08070ee27f6a9f35209f0e43f8c,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017490,"Illumina HiSeq 2500 sequencing; GSM1674121: WT ER ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674121: WT ER ribosome profiling, 2 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581039,"WT ER ribosome profiling, 2 h Tg (rep2)",Illumina HiSeq 2500,SRR2007780,16585777,845874627,SAMN03581039,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674121,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/000/SRR2007780/SRR2007780.fastq.gz,641203534,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007780/SRR2007780.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/000/SRR2007780/SRR2007780.fastq.gz,20914adaedc08c44fbcc5285fd50eb32,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-11-03,,SINGLE,,,,,,,,,,GSM1674121_r1,,GSM1674121,,"WT ER ribosome profiling, 2 h Tg (rep2)",,,,,SRS928699,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/000/SRR2007780,568363497,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007780,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/000/SRR2007780,1572d0145ea739e02f6d26644953ddf4,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017491,"Illumina HiSeq 2500 sequencing; GSM1674122: WT cytosol ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674122: WT cytosol ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581040,"WT cytosol ribosome profiling, 4 h Tg (rep1)",Illumina HiSeq 2500,SRR2007781,20561299,1048626249,SAMN03581040,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674122,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/001/SRR2007781/SRR2007781.fastq.gz,836865783,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007781/SRR2007781.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/001/SRR2007781/SRR2007781.fastq.gz,11efc31cf5c6985ef9a7e739b931491a,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1674122_r1,,GSM1674122,,"WT cytosol ribosome profiling, 4 h Tg (rep1)",,,,,SRS928697,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/001/SRR2007781,734117684,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007781,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/001/SRR2007781,0b8c766c2c42cec67dfa484a5ec31f5c,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017492,"Illumina HiSeq 2500 sequencing; GSM1674123: WT cytosol ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674123: WT cytosol ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581041,"WT cytosol ribosome profiling, 4 h Tg (rep2)",Illumina HiSeq 2500,SRR2007782,15876938,809723838,SAMN03581041,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674123,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/002/SRR2007782/SRR2007782.fastq.gz,621956411,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007782/SRR2007782.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/002/SRR2007782/SRR2007782.fastq.gz,ab3c6bbadbc1477a67c28ca380ba5506,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674123_r1,,GSM1674123,,"WT cytosol ribosome profiling, 4 h Tg (rep2)",,,,,SRS928740,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/002/SRR2007782,539161569,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007782,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/002/SRR2007782,2c1ddc50077c23c4ceda5edb0a8996de,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017493,"Illumina HiSeq 2500 sequencing; GSM1674124: WT ER ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674124: WT ER ribosome profiling, 4 h Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581042,"WT ER ribosome profiling, 4 h Tg (rep1)",Illumina HiSeq 2500,SRR2007783,8558520,436484520,SAMN03581042,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674124,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/003/SRR2007783/SRR2007783.fastq.gz,337710153,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007783/SRR2007783.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/003/SRR2007783/SRR2007783.fastq.gz,ac789561869f94ad3785718d8051426d,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674124_r1,,GSM1674124,,"WT ER ribosome profiling, 4 h Tg (rep1)",,,,,SRS928739,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/003/SRR2007783,294544497,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007783,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/003/SRR2007783,4e7bc1aa73ee762d99d2b98057bbaaf5,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017494,"Illumina HiSeq 2500 sequencing; GSM1674125: WT ER ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674125: WT ER ribosome profiling, 4 h Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581043,"WT ER ribosome profiling, 4 h Tg (rep2)",Illumina HiSeq 2500,SRR2007784,35387962,1804786062,SAMN03581043,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674125,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/004/SRR2007784/SRR2007784.fastq.gz,1372703088,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007784/SRR2007784.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/004/SRR2007784/SRR2007784.fastq.gz,128a5a8b6e817d422a78d9f3f8a75873,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674125_r1,,GSM1674125,,"WT ER ribosome profiling, 4 h Tg (rep2)",,,,,SRS928736,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/004/SRR2007784,1205300716,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007784,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/004/SRR2007784,79fd52e8941c3d15f77746c3951dec07,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017495,"Illumina HiSeq 2500 sequencing; GSM1674126: WT cytosol ribosome profiling, no Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674126: WT cytosol ribosome profiling, no Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581044,"WT cytosol ribosome profiling, no Tg (rep1)",Illumina HiSeq 2500,SRR2007785,11957757,609845607,SAMN03581044,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674126,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/005/SRR2007785/SRR2007785.fastq.gz,524581280,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007785/SRR2007785.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/005/SRR2007785/SRR2007785.fastq.gz,db6c0f91f3125cf9945e1e132f04549d,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674126_r1,,GSM1674126,,"WT cytosol ribosome profiling, no Tg (rep1)",,,,,SRS928738,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/005/SRR2007785,441188443,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007785,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/005/SRR2007785,520bc95d371e05bcf6a73c9394905aaa,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017496,"Illumina HiSeq 2500 sequencing; GSM1674127: WT cytosol ribosome profiling, no Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674127: WT cytosol ribosome profiling, no Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581045,"WT cytosol ribosome profiling, no Tg (rep2)",Illumina HiSeq 2500,SRR2007786,14492687,739127037,SAMN03581045,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674127,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/006/SRR2007786/SRR2007786.fastq.gz,599553522,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007786/SRR2007786.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/006/SRR2007786/SRR2007786.fastq.gz,8abaec810ee85d3b4be7065f45cbdb0f,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-05-01,,SINGLE,,,,,,,,,,GSM1674127_r1,,GSM1674127,,"WT cytosol ribosome profiling, no Tg (rep2)",,,,,SRS928737,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/006/SRR2007786,529847650,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007786,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/006/SRR2007786,f36579f0af15be2f4e6cbe53f0e207a8,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017497,"Illumina HiSeq 2500 sequencing; GSM1674128: WT ER ribosome profiling, no Tg (rep1); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674128: WT ER ribosome profiling, no Tg (rep1); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581046,"WT ER ribosome profiling, no Tg (rep1)",Illumina HiSeq 2500,SRR2007787,20017242,1020879342,SAMN03581046,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674128,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/007/SRR2007787/SRR2007787.fastq.gz,861705027,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007787/SRR2007787.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/007/SRR2007787/SRR2007787.fastq.gz,d3f5de1b1de549222503840b6cb859b7,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674128_r1,,GSM1674128,,"WT ER ribosome profiling, no Tg (rep1)",,,,,SRS928735,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/007/SRR2007787,733770809,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007787,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/007/SRR2007787,73183ad8c131ae49211600a29680aeba,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA282960,SRX1017498,"Illumina HiSeq 2500 sequencing; GSM1674129: WT ER ribosome profiling, no Tg (rep2); Mus musculus; OTHER","Illumina HiSeq 2500 sequencing; GSM1674129: WT ER ribosome profiling, no Tg (rep2); Mus musculus; OTHER",10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03581047,"WT ER ribosome profiling, no Tg (rep2)",Illumina HiSeq 2500,SRR2007788,14374170,733082670,SAMN03581047,,,,,,,,mouse embryonic fibroblasts,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1674129,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR200/008/SRR2007788/SRR2007788.fastq.gz,642271027,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007788/SRR2007788.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR200/008/SRR2007788/SRR2007788.fastq.gz,8ec48d2fb7b58bd28b2211ffb20d6386,2016-01-05,2016-01-05,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1674129_r1,,GSM1674129,,"WT ER ribosome profiling, no Tg (rep2)",,,,,SRS928733,SRP057991,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR200/008/SRR2007788,535239700,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007788,ftp.sra.ebi.ac.uk/vol1/srr/SRR200/008/SRR2007788,44faac9b0c2b3913b793a49a993ba160,,GSE68265,Dissection of the translational impacts of the PERK pathway,,,SRA266203,,,,,,,,,,,,,,, PRJNA285515,SRX1045363,Illumina HiSeq 2000 paired end sequencing; Shield Stage Embryos matched to Ribosome Profiling,Illumina HiSeq 2000 paired end sequencing; Shield Stage Embryos matched to Ribosome Profiling,7955,Danio rerio,RNA-Seq,TRANSCRIPTOMIC,PolyA,SAMN03754651,Danio rerio Shield Stage Embryos RNA-Seq,Illumina HiSeq 2000,SRR2047225,48328189,7345884728,SAMN03754651,,,,,,,,,,,,,,,,,,,,,,Shield,,,,,,,false,Shield Stage Embryos,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR204/005/SRR2047225/SRR2047225_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR204/005/SRR2047225/SRR2047225_2.fastq.gz,2717968568;2752431632,ftp.sra.ebi.ac.uk/vol1/fastq/SRR204/005/SRR2047225/SRR2047225_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR204/005/SRR2047225/SRR2047225_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR204/005/SRR2047225/SRR2047225_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR204/005/SRR2047225/SRR2047225_2.fastq.gz,d675a5ff56f35ae12c314d373fdb5e28;e299e5e14018e5dd9bfff177ff29b3c5,2016-06-02,2016-06-02,false,,,,,,,,,,,ILLUMINA,,,,2016-06-27,,PAIRED,,,,,76,0,,,,Shield Stage Embryos,,Shield Stage Embryos,,Matched to ribosome profiling experiments in SAMN02087561,,,,,SRS950607,SRP058956,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR204/005/SRR2047225,5187457819,ftp.sra.ebi.ac.uk/vol1/srr/SRR204/005/SRR2047225,ftp.sra.ebi.ac.uk/vol1/srr/SRR204/005/SRR2047225,c87460c1d55a7f5acb6c9c4450a824a5,TLAB,PRJNA285515,Danio rerio shield stage transcriptome,,,SRA270772,,,,,,,,,,,,,,whole embryos, PRJNA285961,SRX1050328,Illumina HiSeq 2500 sequencing; GSM1704503: 6 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704503: 6 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763400,6 h infection cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052911,16250647,828782997,SAMN03763400,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704503,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/001/SRR2052911/SRR2052911.fastq.gz,660516715,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052911/SRR2052911.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052911/SRR2052911.fastq.gz,5d70a0d6946721198414107b2e82ffdd,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704503_r1,,GSM1704503,,6 h infection cytosol ribosome profiling (Rep 1),,,,,SRS954647,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/001/SRR2052911,548716171,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052911,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052911,054250aa15f193c2cb7d3fcfdd205d14,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050329,Illumina HiSeq 2500 sequencing; GSM1704504: 6 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704504: 6 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763401,6 h infection ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052912,18073831,921765381,SAMN03763401,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704504,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/002/SRR2052912/SRR2052912.fastq.gz,731689055,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052912/SRR2052912.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052912/SRR2052912.fastq.gz,98c35f6cb0588ba129a39b199ed9570c,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1704504_r1,,GSM1704504,,6 h infection ER ribosome profiling (Rep 1),,,,,SRS954645,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/002/SRR2052912,596472644,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052912,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052912,795aa089f7dd4a0413f8160109172dbb,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050330,Illumina HiSeq 2500 sequencing; GSM1704505: 12 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704505: 12 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763402,12 h infection cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052913,18948536,966375336,SAMN03763402,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704505,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/003/SRR2052913/SRR2052913.fastq.gz,742306819,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052913/SRR2052913.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052913/SRR2052913.fastq.gz,b5eb795fdc779b65d6bacbd2e7a97e5b,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-07,,SINGLE,,,,,,,,,,GSM1704505_r1,,GSM1704505,,12 h infection cytosol ribosome profiling (Rep 1),,,,,SRS954646,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/003/SRR2052913,645140159,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052913,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052913,eafbe6073648fe4e96a8a0faa85af012,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050331,Illumina HiSeq 2500 sequencing; GSM1704506: 12 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704506: 12 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763403,12 h infection ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052914,26865068,1370118468,SAMN03763403,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704506,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/004/SRR2052914/SRR2052914.fastq.gz,1068535906,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052914/SRR2052914.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052914/SRR2052914.fastq.gz,912072eadf4b0625398dd22b915c6ca9,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704506_r1,,GSM1704506,,12 h infection ER ribosome profiling (Rep 1),,,,,SRS954643,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/004/SRR2052914,883685185,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052914,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052914,4f0971439abc8c75183ce7891bfa3bcf,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050332,Illumina HiSeq 2500 sequencing; GSM1704507: 24 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704507: 24 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763404,24 h infection cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052915,26423896,1347618696,SAMN03763404,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704507,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/005/SRR2052915/SRR2052915.fastq.gz,1047935210,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052915/SRR2052915.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052915/SRR2052915.fastq.gz,6fd8c2c8d36164c03a867f22d990434c,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-11-08,,SINGLE,,,,,,,,,,GSM1704507_r1,,GSM1704507,,24 h infection cytosol ribosome profiling (Rep 1),,,,,SRS954644,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/005/SRR2052915,886364141,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052915,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052915,9231b6ab3c77f716f06627382ce48b92,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050333,Illumina HiSeq 2500 sequencing; GSM1704508: 24 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704508: 24 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763405,24 h infection ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052916,13129805,669620055,SAMN03763405,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704508,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/006/SRR2052916/SRR2052916.fastq.gz,512304436,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052916/SRR2052916.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052916/SRR2052916.fastq.gz,5c19fb1e4091b38404cb096b71f9773e,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704508_r1,,GSM1704508,,24 h infection ER ribosome profiling (Rep 1),,,,,SRS954642,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/006/SRR2052916,443224898,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052916,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052916,ba57a629cc3e816a3fb4cd1e17000c6a,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050334,Illumina HiSeq 2500 sequencing; GSM1704509: 40 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704509: 40 h infection cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763406,40 h infection cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052917,31892235,1626503985,SAMN03763406,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704509,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/007/SRR2052917/SRR2052917.fastq.gz,1255937425,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052917/SRR2052917.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052917/SRR2052917.fastq.gz,eeda9efb38983237abd85ef61eb7e4c1,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704509_r1,,GSM1704509,,40 h infection cytosol ribosome profiling (Rep 1),,,,,SRS954641,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/007/SRR2052917,1072954448,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052917,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052917,eedcbee517704fea4cca52a4472bc6a4,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050335,Illumina HiSeq 2500 sequencing; GSM1704510: 40 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704510: 40 h infection ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763407,40 h infection ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052918,34039497,1736014347,SAMN03763407,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704510,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/008/SRR2052918/SRR2052918.fastq.gz,1319679438,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052918/SRR2052918.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052918/SRR2052918.fastq.gz,4d1fea49fbcbc8d91d96a6895fef323f,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-19,,SINGLE,,,,,,,,,,GSM1704510_r1,,GSM1704510,,40 h infection ER ribosome profiling (Rep 1),,,,,SRS954640,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/008/SRR2052918,1130654122,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052918,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052918,a6dcff859d27a167f7f850bb2c26d2e5,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050336,Illumina HiSeq 2500 sequencing; GSM1704511: Interferon treatment cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704511: Interferon treatment cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763408,Interferon treatment cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052919,11895393,606665043,SAMN03763408,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704511,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/009/SRR2052919/SRR2052919.fastq.gz,404306606,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052919/SRR2052919.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052919/SRR2052919.fastq.gz,e5145f0d07814453aafea52de3e1918c,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-12-09,,SINGLE,,,,,,,,,,GSM1704511_r1,,GSM1704511,,Interferon treatment cytosol ribosome profiling (Rep 1),,,,,SRS954639,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/009/SRR2052919,361800895,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052919,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052919,e67ce2dff074b744c26c4977f1ee957c,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050337,Illumina HiSeq 2500 sequencing; GSM1704512: Interferon treatment ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704512: Interferon treatment ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763409,Interferon treatment ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052920,7444252,379656852,SAMN03763409,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704512,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/000/SRR2052920/SRR2052920.fastq.gz,273469590,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052920/SRR2052920.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052920/SRR2052920.fastq.gz,27dd739e0ecad4d0c2ca2269bdd4daa1,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704512_r1,,GSM1704512,,Interferon treatment ER ribosome profiling (Rep 1),,,,,SRS954638,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/000/SRR2052920,226413082,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052920,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052920,748cc456e4b4a15adb2f661677dc1021,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050338,Illumina HiSeq 2500 sequencing; GSM1704513: Uninfected cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704513: Uninfected cytosol ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763410,Uninfected cytosol ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052921,14469150,737926650,SAMN03763410,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704513,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/001/SRR2052921/SRR2052921.fastq.gz,589836205,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052921/SRR2052921.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052921/SRR2052921.fastq.gz,92c0f81889a02b322794742d1bf92895,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704513_r1,,GSM1704513,,Uninfected cytosol ribosome profiling (Rep 1),,,,,SRS954636,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/001/SRR2052921,486631829,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052921,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052921,e975e06989670e68c011bd7c77db62c0,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050339,Illumina HiSeq 2500 sequencing; GSM1704514: Uninfected ER ribosome profiling (Rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704514: Uninfected ER ribosome profiling (Rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763411,Uninfected ER ribosome profiling (Rep 1),Illumina HiSeq 2500,SRR2052922,14972823,763613973,SAMN03763411,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704514,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/002/SRR2052922/SRR2052922.fastq.gz,579242721,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052922/SRR2052922.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052922/SRR2052922.fastq.gz,4fbaa693cdc510204e45865f1622ec42,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704514_r1,,GSM1704514,,Uninfected ER ribosome profiling (Rep 1),,,,,SRS954637,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/002/SRR2052922,502267205,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052922,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052922,d4b04d87ba961efdf24c38ab08dd7e6e,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050340,Illumina HiSeq 2500 sequencing; GSM1704515: 6 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704515: 6 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763412,6 h infection cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052923,3399547,173376897,SAMN03763412,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704515,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/003/SRR2052923/SRR2052923.fastq.gz,121116335,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052923/SRR2052923.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052923/SRR2052923.fastq.gz,646769c128f9e61235155a2c21d9d294,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-12-22,,SINGLE,,,,,,,,,,GSM1704515_r1,,GSM1704515,,6 h infection cytosol ribosome profiling (Rep 2),,,,,SRS954635,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/003/SRR2052923,106756366,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052923,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052923,c4db794c4c75effceb8cecaaf1bc9f6a,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050341,Illumina HiSeq 2500 sequencing; GSM1704516: 6 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704516: 6 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763413,6 h infection ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052924,6698199,341608149,SAMN03763413,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704516,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/004/SRR2052924/SRR2052924.fastq.gz,226757806,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052924/SRR2052924.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052924/SRR2052924.fastq.gz,32f7bdb3a5526444b4e0462da74b5a6b,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704516_r1,,GSM1704516,,6 h infection ER ribosome profiling (Rep 2),,,,,SRS954634,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/004/SRR2052924,197281278,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052924,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052924,8cd8164d867c100bf19d15d55eac53e1,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050342,Illumina HiSeq 2500 sequencing; GSM1704517: 12 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704517: 12 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763414,12 h infection cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052925,751226,38312526,SAMN03763414,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704517,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/005/SRR2052925/SRR2052925.fastq.gz,26660313,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052925/SRR2052925.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052925/SRR2052925.fastq.gz,ccb54b6794cd782829a7bd298f42154e,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704517_r1,,GSM1704517,,12 h infection cytosol ribosome profiling (Rep 2),,,,,SRS954633,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/005/SRR2052925,23245437,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052925,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052925,8995f793e7c2527bab444e66ffc851d8,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050343,Illumina HiSeq 2500 sequencing; GSM1704518: 12 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704518: 12 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763415,12 h infection ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052926,6988731,356425281,SAMN03763415,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704518,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/006/SRR2052926/SRR2052926.fastq.gz,242130604,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052926/SRR2052926.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052926/SRR2052926.fastq.gz,580d9ced8d9954485fc21af9c1e3a25b,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704518_r1,,GSM1704518,,12 h infection ER ribosome profiling (Rep 2),,,,,SRS954631,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/006/SRR2052926,206843801,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052926,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052926,7ee576d6070731130979cca18f45cdbd,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050344,Illumina HiSeq 2500 sequencing; GSM1704519: 24 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704519: 24 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763416,24 h infection cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052927,6813487,347487837,SAMN03763416,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704519,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/007/SRR2052927/SRR2052927.fastq.gz,226582521,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052927/SRR2052927.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052927/SRR2052927.fastq.gz,7480cfcbe02b0ab06c4ff11c1a888e78,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704519_r1,,GSM1704519,,24 h infection cytosol ribosome profiling (Rep 2),,,,,SRS954632,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/007/SRR2052927,209158272,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052927,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052927,29492b9571b470a557d8846fc42c559e,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050345,Illumina HiSeq 2500 sequencing; GSM1704520: 24 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704520: 24 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763417,24 h infection ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052928,6242440,318364440,SAMN03763417,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704520,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/008/SRR2052928/SRR2052928.fastq.gz,218169284,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052928/SRR2052928.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052928/SRR2052928.fastq.gz,efab6a701a95c07e65705995a0f2d0ec,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1704520_r1,,GSM1704520,,24 h infection ER ribosome profiling (Rep 2),,,,,SRS954630,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/008/SRR2052928,187096541,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052928,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052928,10a22dfc84b8307d1c01e322340045a1,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050346,Illumina HiSeq 2500 sequencing; GSM1704521: 40 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704521: 40 h infection cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763418,40 h infection cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052929,3488237,177900087,SAMN03763418,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704521,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/009/SRR2052929/SRR2052929.fastq.gz,116492876,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052929/SRR2052929.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052929/SRR2052929.fastq.gz,6457832844095f899f6ed5bee8f7667d,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704521_r1,,GSM1704521,,40 h infection cytosol ribosome profiling (Rep 2),,,,,SRS954629,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/009/SRR2052929,106983556,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052929,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052929,aa3595dbf04a20f4711e6ad6c6024c45,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050347,Illumina HiSeq 2500 sequencing; GSM1704522: 40 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704522: 40 h infection ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763419,40 h infection ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052930,5860692,298895292,SAMN03763419,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704522,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/000/SRR2052930/SRR2052930.fastq.gz,201307004,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052930/SRR2052930.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052930/SRR2052930.fastq.gz,2ea00875932d9f2fa0f3a3eac5c6522f,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704522_r1,,GSM1704522,,40 h infection ER ribosome profiling (Rep 2),,,,,SRS954628,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/000/SRR2052930,176388171,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052930,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052930,da137a7b8815991768cd3f341ebde78f,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050348,Illumina HiSeq 2500 sequencing; GSM1704523: Interferon treatment cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704523: Interferon treatment cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763420,Interferon treatment cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052931,4934701,251669751,SAMN03763420,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704523,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/001/SRR2052931/SRR2052931.fastq.gz,179178895,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052931/SRR2052931.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052931/SRR2052931.fastq.gz,c40af08efadaad7990c0295eae516ca7,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704523_r1,,GSM1704523,,Interferon treatment cytosol ribosome profiling (Rep 2),,,,,SRS954625,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/001/SRR2052931,152110177,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052931,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052931,35899b7f50a3794989f9c485e6cfd76c,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050349,Illumina HiSeq 2500 sequencing; GSM1704524: Interferon treatment ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704524: Interferon treatment ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763423,Interferon treatment ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052932,2421308,123486708,SAMN03763423,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704524,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/002/SRR2052932/SRR2052932.fastq.gz,87455545,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052932/SRR2052932.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052932/SRR2052932.fastq.gz,6318cb35db1f77beb3e46758560143ac,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-30,,SINGLE,,,,,,,,,,GSM1704524_r1,,GSM1704524,,Interferon treatment ER ribosome profiling (Rep 2),,,,,SRS954626,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/002/SRR2052932,73136507,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052932,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052932,dba2117d8b91b4f4fbb838c6d782261a,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050350,Illumina HiSeq 2500 sequencing; GSM1704525: Uninfected cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704525: Uninfected cytosol ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763424,Uninfected cytosol ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052933,4141321,211207371,SAMN03763424,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704525,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/003/SRR2052933/SRR2052933.fastq.gz,142070120,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052933/SRR2052933.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052933/SRR2052933.fastq.gz,bcaf24f5b8c7ae7b72269eadc362bb35,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-12-29,,SINGLE,,,,,,,,,,GSM1704525_r1,,GSM1704525,,Uninfected cytosol ribosome profiling (Rep 2),,,,,SRS954627,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/003/SRR2052933,127438814,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052933,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052933,e6b52b3a5349673a4a7d17169e1a79c6,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050351,Illumina HiSeq 2500 sequencing; GSM1704526: Uninfected ER ribosome profiling (Rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704526: Uninfected ER ribosome profiling (Rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763425,Uninfected ER ribosome profiling (Rep 2),Illumina HiSeq 2500,SRR2052934,8749582,446228682,SAMN03763425,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704526,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/004/SRR2052934/SRR2052934.fastq.gz,306689814,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052934/SRR2052934.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052934/SRR2052934.fastq.gz,95966f7a083da9eb025cc4a49c775f4f,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-11-03,,SINGLE,,,,,,,,,,GSM1704526_r1,,GSM1704526,,Uninfected ER ribosome profiling (Rep 2),,,,,SRS954624,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/004/SRR2052934,258351715,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052934,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052934,895626747da74f4503e3e9daf4d148af,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050352,Illumina HiSeq 2500 sequencing; GSM1704527: 6 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704527: 6 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763426,6 h infection cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052935,17150043,874652193,SAMN03763426,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704527,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/005/SRR2052935/SRR2052935.fastq.gz,546297673,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052935/SRR2052935.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052935/SRR2052935.fastq.gz,f06f10d3d61fc04c993b146858954a96,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704527_r1,,GSM1704527,,6 h infection cytosol ribosome profiling (Rep 3),,,,,SRS954621,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/005/SRR2052935,484722030,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052935,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052935,862d178db8a2b22efa57a47b9c6bfd41,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050353,Illumina HiSeq 2500 sequencing; GSM1704528: 6 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704528: 6 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763427,6 h infection ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052936,16165711,824451261,SAMN03763427,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704528,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/006/SRR2052936/SRR2052936.fastq.gz,537860120,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052936/SRR2052936.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052936/SRR2052936.fastq.gz,5274961985ef62d18c8c496cac18afc4,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704528_r1,,GSM1704528,,6 h infection ER ribosome profiling (Rep 3),,,,,SRS954622,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/006/SRR2052936,467461207,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052936,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052936,6d7dc959a06fbea39c47b8ba52dfeb55,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050354,Illumina HiSeq 2500 sequencing; GSM1704529: 12 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704529: 12 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763428,12 h infection cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052937,17650994,900200694,SAMN03763428,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704529,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/007/SRR2052937/SRR2052937.fastq.gz,544995368,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052937/SRR2052937.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052937/SRR2052937.fastq.gz,ae412d8e90c3b0df2be5a2e44f7dd45f,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1704529_r1,,GSM1704529,,12 h infection cytosol ribosome profiling (Rep 3),,,,,SRS954623,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/007/SRR2052937,495291193,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052937,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052937,3a2b5a5a82b96a639021d66022080c64,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050355,Illumina HiSeq 2500 sequencing; GSM1704530: 12 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704530: 12 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763421,12 h infection ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052938,18658813,951599463,SAMN03763421,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704530,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/008/SRR2052938/SRR2052938.fastq.gz,597145789,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052938/SRR2052938.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052938/SRR2052938.fastq.gz,648f171e38eb1bebdd88f720936c155c,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704530_r1,,GSM1704530,,12 h infection ER ribosome profiling (Rep 3),,,,,SRS954619,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/008/SRR2052938,522733187,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052938,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052938,5ae8a1d224c67a93eac273eea9417d0d,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050356,Illumina HiSeq 2500 sequencing; GSM1704531: 24 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704531: 24 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763422,24 h infection cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052939,16313320,831979320,SAMN03763422,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704531,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/009/SRR2052939/SRR2052939.fastq.gz,471416473,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052939/SRR2052939.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052939/SRR2052939.fastq.gz,4e8e52ed64f5b75803483badcfa89719,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-20,,SINGLE,,,,,,,,,,GSM1704531_r1,,GSM1704531,,24 h infection cytosol ribosome profiling (Rep 3),,,,,SRS954620,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/009/SRR2052939,454224925,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052939,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052939,a489b132e27d970278a3b1f02bfb1b8d,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050357,Illumina HiSeq 2500 sequencing; GSM1704532: 24 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704532: 24 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763429,24 h infection ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052940,15616355,796434105,SAMN03763429,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704532,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/000/SRR2052940/SRR2052940.fastq.gz,462037785,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052940/SRR2052940.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052940/SRR2052940.fastq.gz,3f3cae82cc4728c9ce178ebde3dc7cb5,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704532_r1,,GSM1704532,,24 h infection ER ribosome profiling (Rep 3),,,,,SRS954618,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/000/SRR2052940,433201315,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052940,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052940,efb8d0e05118e00e300ba65b994988b1,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050358,Illumina HiSeq 2500 sequencing; GSM1704533: 40 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704533: 40 h infection cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763370,40 h infection cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052941,12189412,621660012,SAMN03763370,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704533,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/001/SRR2052941/SRR2052941.fastq.gz,364657903,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052941/SRR2052941.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052941/SRR2052941.fastq.gz,f3b103a0d435860ba008d0e523f500ce,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1704533_r1,,GSM1704533,,40 h infection cytosol ribosome profiling (Rep 3),,,,,SRS954617,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/001/SRR2052941,340106040,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052941,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052941,4f7aef201bed5cbf3e5c2777bd29e3b1,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050359,Illumina HiSeq 2500 sequencing; GSM1704534: 40 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704534: 40 h infection ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763371,40 h infection ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052942,15349821,782840871,SAMN03763371,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704534,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/002/SRR2052942/SRR2052942.fastq.gz,459684690,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052942/SRR2052942.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052942/SRR2052942.fastq.gz,b424e852349a6d0dd4c44b6cffe71163,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704534_r1,,GSM1704534,,40 h infection ER ribosome profiling (Rep 3),,,,,SRS954616,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/002/SRR2052942,434480433,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052942,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052942,a70f49d9accbe151be6c273b01c3739a,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050360,Illumina HiSeq 2500 sequencing; GSM1704535: Interferon treatment cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704535: Interferon treatment cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763372,Interferon treatment cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052943,12076928,615923328,SAMN03763372,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704535,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/003/SRR2052943/SRR2052943.fastq.gz,381088482,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052943/SRR2052943.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052943/SRR2052943.fastq.gz,1ce52c5c3da4209a1a3b0f9f2685dc06,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704535_r1,,GSM1704535,,Interferon treatment cytosol ribosome profiling (Rep 3),,,,,SRS954613,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/003/SRR2052943,341742064,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052943,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052943,7349a77d37a806da8c8951d7294148d8,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050361,Illumina HiSeq 2500 sequencing; GSM1704536: Interferon treatment ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704536: Interferon treatment ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763373,Interferon treatment ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052944,12808901,653253951,SAMN03763373,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704536,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/004/SRR2052944/SRR2052944.fastq.gz,400780431,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052944/SRR2052944.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052944/SRR2052944.fastq.gz,0e5106f482ef3a5947046b4da3e374a5,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704536_r1,,GSM1704536,,Interferon treatment ER ribosome profiling (Rep 3),,,,,SRS954615,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/004/SRR2052944,371527031,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052944,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052944,4da9ec8a3d86f57739ef0bc57074d86f,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050362,Illumina HiSeq 2500 sequencing; GSM1704537: Uninfected cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704537: Uninfected cytosol ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763374,Uninfected cytosol ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052945,19895121,1014651171,SAMN03763374,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704537,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/005/SRR2052945/SRR2052945.fastq.gz,585529078,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052945/SRR2052945.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052945/SRR2052945.fastq.gz,e5ca182db70a80f4e3b88a98fbe4fbf0,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704537_r1,,GSM1704537,,Uninfected cytosol ribosome profiling (Rep 3),,,,,SRS954614,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/005/SRR2052945,553461880,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052945,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052945,846174ad5effaeea2f3c1d4b247e7de3,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050363,Illumina HiSeq 2500 sequencing; GSM1704538: Uninfected ER ribosome profiling (Rep 3); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704538: Uninfected ER ribosome profiling (Rep 3); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763375,Uninfected ER ribosome profiling (Rep 3),Illumina HiSeq 2500,SRR2052946,22208615,1132639365,SAMN03763375,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704538,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/006/SRR2052946/SRR2052946.fastq.gz,684587453,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052946/SRR2052946.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052946/SRR2052946.fastq.gz,a1de690dbf0578f5ef610d1c95f46f1e,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704538_r1,,GSM1704538,,Uninfected ER ribosome profiling (Rep 3),,,,,SRS954610,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/006/SRR2052946,630856037,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052946,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052946,b1ea52206c49ba68a7656a90ee7744a6,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050364,Illumina HiSeq 2500 sequencing; GSM1704539: 6 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704539: 6 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763376,6 h infection cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052947,2910736,148447536,SAMN03763376,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704539,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/007/SRR2052947/SRR2052947.fastq.gz,80945511,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052947/SRR2052947.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052947/SRR2052947.fastq.gz,102e3a95bab449d2cd91f5518ddbf23f,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704539_r1,,GSM1704539,,6 h infection cytosol ribosome profiling (Rep 4),,,,,SRS954612,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/007/SRR2052947,72828681,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052947,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052947,eeb94422d16faa4e4a361dff65f55803,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050365,Illumina HiSeq 2500 sequencing; GSM1704540: 6 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704540: 6 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763377,6 h infection ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052948,2339594,119319294,SAMN03763377,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704540,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/008/SRR2052948/SRR2052948.fastq.gz,66234780,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052948/SRR2052948.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052948/SRR2052948.fastq.gz,c9aa9f6e35e4593b03eb4fb98b989b9e,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704540_r1,,GSM1704540,,6 h infection ER ribosome profiling (Rep 4),,,,,SRS954611,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/008/SRR2052948,59416966,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052948,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052948,71b23173144556b2251af189f7bcd9bc,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050366,Illumina HiSeq 2500 sequencing; GSM1704541: 12 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704541: 12 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763378,12 h infection cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052949,3846689,196181139,SAMN03763378,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704541,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/009/SRR2052949/SRR2052949.fastq.gz,109248578,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052949/SRR2052949.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052949/SRR2052949.fastq.gz,cfb057c75595fd053a0c4c0bb95d85c1,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,,,,,,,,,,GSM1704541_r1,,GSM1704541,,12 h infection cytosol ribosome profiling (Rep 4),,,,,SRS954608,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/009/SRR2052949,96365344,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052949,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052949,271b25f419d1119c7b342f1c03f615b8,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050367,Illumina HiSeq 2500 sequencing; GSM1704542: 12 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704542: 12 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763379,12 h infection ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052950,2870385,146389635,SAMN03763379,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704542,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/000/SRR2052950/SRR2052950.fastq.gz,83590069,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052950/SRR2052950.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052950/SRR2052950.fastq.gz,f671cf51c1ccd524ad77704f0d7ae2aa,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-12-09,,SINGLE,,,,,,,,,,GSM1704542_r1,,GSM1704542,,12 h infection ER ribosome profiling (Rep 4),,,,,SRS954609,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/000/SRR2052950,71939694,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052950,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052950,3e8c4d9377c169fa682d5d668717e3e3,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050368,Illumina HiSeq 2500 sequencing; GSM1704543: 24 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704543: 24 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763380,24 h infection cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052951,2087976,106486776,SAMN03763380,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704543,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/001/SRR2052951/SRR2052951.fastq.gz,57128017,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052951/SRR2052951.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052951/SRR2052951.fastq.gz,664e32d68d1762f1df92be6e0bb37f1e,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-07,,SINGLE,,,,,,,,,,GSM1704543_r1,,GSM1704543,,24 h infection cytosol ribosome profiling (Rep 4),,,,,SRS954607,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/001/SRR2052951,52339634,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052951,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052951,e0ca7aa42aff0eeb2d6276f0b8ac6ddb,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050369,Illumina HiSeq 2500 sequencing; GSM1704544: 24 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704544: 24 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763381,24 h infection ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052952,2291662,116874762,SAMN03763381,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704544,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/002/SRR2052952/SRR2052952.fastq.gz,59811304,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052952/SRR2052952.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052952/SRR2052952.fastq.gz,696d11833810f7e6f3863119018154d4,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1704544_r1,,GSM1704544,,24 h infection ER ribosome profiling (Rep 4),,,,,SRS954606,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/002/SRR2052952,56898602,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052952,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052952,616d1a4328db4ff19a1d39b8b749f7f0,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050370,Illumina HiSeq 2500 sequencing; GSM1704545: 40 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704545: 40 h infection cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763382,40 h infection cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052953,8358678,426292578,SAMN03763382,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704545,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/003/SRR2052953/SRR2052953.fastq.gz,214298449,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052953/SRR2052953.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052953/SRR2052953.fastq.gz,6edeb41753aa79c05bea502124d0004e,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704545_r1,,GSM1704545,,40 h infection cytosol ribosome profiling (Rep 4),,,,,SRS954605,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/003/SRR2052953,209465513,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052953,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052953,9fd02ed08f52017929b846e265a40e85,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050371,Illumina HiSeq 2500 sequencing; GSM1704546: 40 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704546: 40 h infection ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763383,40 h infection ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052954,2257987,115157337,SAMN03763383,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704546,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/004/SRR2052954/SRR2052954.fastq.gz,62509061,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052954/SRR2052954.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052954/SRR2052954.fastq.gz,0813b71fdb6dadba8b0af2b2a03b3ae6,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-01-04,,SINGLE,,,,,,,,,,GSM1704546_r1,,GSM1704546,,40 h infection ER ribosome profiling (Rep 4),,,,,SRS954604,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/004/SRR2052954,57259128,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052954,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052954,d9fd03821715a3d7c32153bba8d473f5,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050372,Illumina HiSeq 2500 sequencing; GSM1704547: Interferon treatment cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704547: Interferon treatment cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763384,Interferon treatment cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052955,15968518,814394418,SAMN03763384,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704547,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/005/SRR2052955/SRR2052955.fastq.gz,425226696,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052955/SRR2052955.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052955/SRR2052955.fastq.gz,9487b7de6f5ef23becd7a3b14ba712b1,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704547_r1,,GSM1704547,,Interferon treatment cytosol ribosome profiling (Rep 4),,,,,SRS954603,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/005/SRR2052955,398249496,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052955,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052955,e6708c7f9a8d254f16d3aff2ecbbb6a3,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050373,Illumina HiSeq 2500 sequencing; GSM1704548: Interferon treatment ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704548: Interferon treatment ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763385,Interferon treatment ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052956,3080222,157091322,SAMN03763385,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704548,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/006/SRR2052956/SRR2052956.fastq.gz,92001602,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052956/SRR2052956.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052956/SRR2052956.fastq.gz,17fe4a68f5627e08dca270d36ab23d3e,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704548_r1,,GSM1704548,,Interferon treatment ER ribosome profiling (Rep 4),,,,,SRS954602,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/006/SRR2052956,78510298,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052956,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052956,c9df730efa67da1bec6e2868e84b24f5,DENV2 (M29095.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050374,Illumina HiSeq 2500 sequencing; GSM1704549: Uninfected cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704549: Uninfected cytosol ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763386,Uninfected cytosol ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052957,2543624,129724824,SAMN03763386,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704549,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/007/SRR2052957/SRR2052957.fastq.gz,72037605,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052957/SRR2052957.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052957/SRR2052957.fastq.gz,4fa4637fce37fcac37bcbc0601648402,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704549_r1,,GSM1704549,,Uninfected cytosol ribosome profiling (Rep 4),,,,,SRS954601,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/007/SRR2052957,63615071,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052957,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052957,a23518a9b34a9e23a854823976a25408,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050375,Illumina HiSeq 2500 sequencing; GSM1704550: Uninfected ER ribosome profiling (Rep 4); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704550: Uninfected ER ribosome profiling (Rep 4); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763387,Uninfected ER ribosome profiling (Rep 4),Illumina HiSeq 2500,SRR2052958,2587866,131981166,SAMN03763387,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704550,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/008/SRR2052958/SRR2052958.fastq.gz,73062293,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052958/SRR2052958.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052958/SRR2052958.fastq.gz,e0a13f713f45b4d96f3dcffeb440dd96,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-27,,SINGLE,,,,,,,,,,GSM1704550_r1,,GSM1704550,,Uninfected ER ribosome profiling (Rep 4),,,,,SRS954600,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/008/SRR2052958,65445883,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052958,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052958,3594af9d416e2f3edb2141e40f959122,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050400,Illumina HiSeq 2500 sequencing; GSM1704575: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704575: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763467,12 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052983,50720722,2586756822,SAMN03763467,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704575,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/003/SRR2052983/SRR2052983.fastq.gz,2021729694,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052983/SRR2052983.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052983/SRR2052983.fastq.gz,3ea27357a0844cbf0e566ec6843dfcb0,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704575_r1,,GSM1704575,,12 h DENV1 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954581,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/003/SRR2052983,1804546927,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052983,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052983,2e297118221f8497bbac5cbc1de570c7,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050401,Illumina HiSeq 2500 sequencing; GSM1704576: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704576: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763468,24 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052984,32000428,1632021828,SAMN03763468,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704576,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/004/SRR2052984/SRR2052984.fastq.gz,1262935221,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052984/SRR2052984.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052984/SRR2052984.fastq.gz,c2ad6b78d64e4efd3f3c0f7d3ac155b0,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-14,,SINGLE,,,,,,,,,,GSM1704576_r1,,GSM1704576,,24 h DENV1 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954580,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/004/SRR2052984,1145457633,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052984,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052984,61e1f5585e379bfc9feb4d22c7aa2a74,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050402,Illumina HiSeq 2500 sequencing; GSM1704577: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704577: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763469,48 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052985,29304738,1494541638,SAMN03763469,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704577,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/005/SRR2052985/SRR2052985.fastq.gz,1087150031,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052985/SRR2052985.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052985/SRR2052985.fastq.gz,d481bebe36bbe7b936d8f04645e5eacd,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-07,,SINGLE,,,,,,,,,,GSM1704577_r1,,GSM1704577,,48 h DENV1 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954579,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/005/SRR2052985,1021555158,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052985,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052985,573608d207bdebb33bf137a98aa5324a,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050403,Illumina HiSeq 2500 sequencing; GSM1704578: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704578: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763470,6 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052986,31483076,1605636876,SAMN03763470,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704578,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/006/SRR2052986/SRR2052986.fastq.gz,1253647099,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052986/SRR2052986.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052986/SRR2052986.fastq.gz,3b025d8dcc9b8e54107c3e998983ee56,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704578_r1,,GSM1704578,,6 h DENV1 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954578,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/006/SRR2052986,1133062126,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052986,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052986,e31ac56726ca2b4307c7b040919fc7a6,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050404,Illumina HiSeq 2500 sequencing; GSM1704579: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704579: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763471,72 h DENV1 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052987,31451899,1604046849,SAMN03763471,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704579,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/007/SRR2052987/SRR2052987.fastq.gz,1192592253,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052987/SRR2052987.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052987/SRR2052987.fastq.gz,b0582d0d02be1d4903630efddeee61e5,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-11-12,,SINGLE,,,,,,,,,,GSM1704579_r1,,GSM1704579,,72 h DENV1 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954577,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/007/SRR2052987,1113521701,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052987,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052987,bb79c6832239de0b30098b141598d086,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050405,Illumina HiSeq 2500 sequencing; GSM1704580: Uninfected Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704580: Uninfected Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763472,Uninfected Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052988,30257426,1543128726,SAMN03763472,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704580,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/008/SRR2052988/SRR2052988.fastq.gz,1171989944,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052988/SRR2052988.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052988/SRR2052988.fastq.gz,93f931d3237ca1e0fdbcba952dac3c39,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704580_r1,,GSM1704580,,Uninfected Total cell lysate ribosome profiling (rep 1),,,,,SRS954576,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/008/SRR2052988,1074160300,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052988,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052988,cb2c64a21ed3252cfa104ead0339f9d1,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050406,Illumina HiSeq 2500 sequencing; GSM1704581: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704581: 12 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763473,12 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052989,50837419,2592708369,SAMN03763473,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704581,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/009/SRR2052989/SRR2052989.fastq.gz,1954892005,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052989/SRR2052989.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052989/SRR2052989.fastq.gz,e016a4eb56de1b6dac506a9a738d9f08,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1704581_r1,,GSM1704581,,12 h DENV1 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954575,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/009/SRR2052989,1830725706,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052989,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052989,06a5e725d3ade7210ac687bbf4ccadc8,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050407,Illumina HiSeq 2500 sequencing; GSM1704582: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704582: 24 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763474,24 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052990,35106005,1790406255,SAMN03763474,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704582,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/000/SRR2052990/SRR2052990.fastq.gz,1382035387,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052990/SRR2052990.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2052990/SRR2052990.fastq.gz,c54dc003679f854a0504c7767ce97eba,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704582_r1,,GSM1704582,,24 h DENV1 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954574,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/000/SRR2052990,1259768686,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052990,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2052990,57b7e04af3b9a50621a52340caa27ed5,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050408,Illumina HiSeq 2500 sequencing; GSM1704583: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704583: 48 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763475,48 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052991,35561514,1813637214,SAMN03763475,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704583,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/001/SRR2052991/SRR2052991.fastq.gz,1413729482,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052991/SRR2052991.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2052991/SRR2052991.fastq.gz,cd9bf7720cd0614fe7f9e0b0e07aa346,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-11-18,,SINGLE,,,,,,,,,,GSM1704583_r1,,GSM1704583,,48 h DENV1 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954573,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/001/SRR2052991,1271103515,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052991,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2052991,5d04cab8f8f5edd3ad8b2483bae56969,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050409,Illumina HiSeq 2500 sequencing; GSM1704584: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704584: 6 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763476,6 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052992,34060969,1737109419,SAMN03763476,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704584,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/002/SRR2052992/SRR2052992.fastq.gz,1369373978,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052992/SRR2052992.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2052992/SRR2052992.fastq.gz,c15ea19950d3f14e601c416917c2ed60,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704584_r1,,GSM1704584,,6 h DENV1 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954572,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/002/SRR2052992,1223851629,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052992,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2052992,3540dc2a7c60687a850a387e064ce761,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050410,Illumina HiSeq 2500 sequencing; GSM1704585: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704585: 72 h DENV1 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763477,72 h DENV1 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052993,35772157,1824380007,SAMN03763477,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704585,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/003/SRR2052993/SRR2052993.fastq.gz,1391576800,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052993/SRR2052993.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2052993/SRR2052993.fastq.gz,a3b78b76954f24ab3362870415665505,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704585_r1,,GSM1704585,,72 h DENV1 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954571,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/003/SRR2052993,1282621342,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052993,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2052993,2fa92d15955ebdf410371c3f70ddc780,DENV1 (EU081230.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050411,Illumina HiSeq 2500 sequencing; GSM1704586: Uninfected Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704586: Uninfected Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763478,Uninfected Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2052994,32219386,1643188686,SAMN03763478,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704586,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/004/SRR2052994/SRR2052994.fastq.gz,1296108512,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052994/SRR2052994.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2052994/SRR2052994.fastq.gz,a52a93bb7388439e77560ce0e93d0d9f,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-30,,SINGLE,,,,,,,,,,GSM1704586_r1,,GSM1704586,,Uninfected Total cell lysate ribosome profiling (rep 2),,,,,SRS954570,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/004/SRR2052994,1159853535,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052994,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2052994,7f4b4a06acbec662f76035dfe1679cd9,,GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050412,Illumina HiSeq 2500 sequencing; GSM1704587: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704587: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763479,12 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052995,29483113,1503638763,SAMN03763479,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704587,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/005/SRR2052995/SRR2052995.fastq.gz,1103907991,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052995/SRR2052995.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/005/SRR2052995/SRR2052995.fastq.gz,0e9636dea85b6d0749b5f2898bfec925,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704587_r1,,GSM1704587,,12 h DENV2 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954569,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/005/SRR2052995,1034923225,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052995,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/005/SRR2052995,d4be7f57337e16fc1b8802428df237b7,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050413,Illumina HiSeq 2500 sequencing; GSM1704588: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704588: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763480,24 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052996,27309344,1392776544,SAMN03763480,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704588,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/006/SRR2052996/SRR2052996.fastq.gz,1057183041,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052996/SRR2052996.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2052996/SRR2052996.fastq.gz,c3d955899ebf0b485e8928a2b90ebeab,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-01-09,,SINGLE,,,,,,,,,,GSM1704588_r1,,GSM1704588,,24 h DENV2 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954568,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/006/SRR2052996,973842827,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052996,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2052996,0c7c6416d6425c00a557614856b8d4d4,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050414,Illumina HiSeq 2500 sequencing; GSM1704589: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704589: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763481,48 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052997,36128791,1842568341,SAMN03763481,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704589,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/007/SRR2052997/SRR2052997.fastq.gz,1372852474,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052997/SRR2052997.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2052997/SRR2052997.fastq.gz,93570cb66d873816b987773cd894e353,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-12-03,,SINGLE,,,,,,,,,,GSM1704589_r1,,GSM1704589,,48 h DENV2 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954567,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/007/SRR2052997,1274482823,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052997,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2052997,c9e2f03070caf466b460ceb5087da9b9,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050415,Illumina HiSeq 2500 sequencing; GSM1704590: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704590: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763482,6 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052998,29795235,1519556985,SAMN03763482,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704590,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/008/SRR2052998/SRR2052998.fastq.gz,1138511215,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052998/SRR2052998.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2052998/SRR2052998.fastq.gz,0c115d2504c6e95c01f0998ecb999add,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704590_r1,,GSM1704590,,6 h DENV2 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954566,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/008/SRR2052998,1046303554,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052998,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2052998,845d25c57da032aa775a76c1e9d53791,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050416,Illumina HiSeq 2500 sequencing; GSM1704591: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704591: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 1); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763483,72 h DENV2 infection Total cell lysate ribosome profiling (rep 1),Illumina HiSeq 2500,SRR2052999,46793485,2386467735,SAMN03763483,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704591,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/009/SRR2052999/SRR2052999.fastq.gz,1798060076,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052999/SRR2052999.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2052999/SRR2052999.fastq.gz,0e17df7761aaaf35e1b2a2fdaeeaa938,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704591_r1,,GSM1704591,,72 h DENV2 infection Total cell lysate ribosome profiling (rep 1),,,,,SRS954565,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/009/SRR2052999,1662684855,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052999,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2052999,074a664df058c704188f7f9094491178,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050417,Illumina HiSeq 2500 sequencing; GSM1704592: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704592: 12 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763484,12 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053000,33921101,1729976151,SAMN03763484,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704592,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/000/SRR2053000/SRR2053000.fastq.gz,1277655203,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2053000/SRR2053000.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/000/SRR2053000/SRR2053000.fastq.gz,5c43dca17f1f3688f7fdaf9e8d0151c9,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1704592_r1,,GSM1704592,,12 h DENV2 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954564,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/000/SRR2053000,1198545857,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2053000,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/000/SRR2053000,eecd9fb3ce129128a07614b9dbae998f,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050418,Illumina HiSeq 2500 sequencing; GSM1704593: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704593: 24 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763485,24 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053001,35278187,1799187537,SAMN03763485,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704593,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/001/SRR2053001/SRR2053001.fastq.gz,1377795975,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2053001/SRR2053001.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/001/SRR2053001/SRR2053001.fastq.gz,444386a8733206f94a9e940c6ddcc542,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704593_r1,,GSM1704593,,24 h DENV2 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954563,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/001/SRR2053001,1265305434,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2053001,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/001/SRR2053001,ad200c980b71826b212bef1ac1336f84,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050419,Illumina HiSeq 2500 sequencing; GSM1704594: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704594: 48 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763430,48 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053002,32317528,1648193928,SAMN03763430,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704594,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/002/SRR2053002/SRR2053002.fastq.gz,1280636512,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2053002/SRR2053002.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/002/SRR2053002/SRR2053002.fastq.gz,3343f495e79ed277bb5f3f0c1a6b9522,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704594_r1,,GSM1704594,,48 h DENV2 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954562,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/002/SRR2053002,1147270312,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2053002,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/002/SRR2053002,4420b7c812d5c3de1587e2277982daf7,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050420,Illumina HiSeq 2500 sequencing; GSM1704595: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704595: 6 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763431,6 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053003,34457090,1757311590,SAMN03763431,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704595,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/003/SRR2053003/SRR2053003.fastq.gz,1426919840,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2053003/SRR2053003.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/003/SRR2053003/SRR2053003.fastq.gz,8aa15eea9f663d5877e567a7a13fb111,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1704595_r1,,GSM1704595,,6 h DENV2 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954561,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/003/SRR2053003,1240991660,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2053003,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/003/SRR2053003,0b05d0d449c73c8cf5688afdd9951499,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA285961,SRX1050421,Illumina HiSeq 2500 sequencing; GSM1704596: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1704596: 72 h DENV2 infection Total cell lysate ribosome profiling (rep 2); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03763432,72 h DENV2 infection Total cell lysate ribosome profiling (rep 2),Illumina HiSeq 2500,SRR2053004,40495001,2065245051,SAMN03763432,,,,,,,Huh7 cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1704596,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/004/SRR2053004/SRR2053004.fastq.gz,1580667884,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2053004/SRR2053004.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/004/SRR2053004/SRR2053004.fastq.gz,199104c9f41429342369350ac7db31c6,2016-09-02,2016-09-02,false,,,,,,,,,,,ILLUMINA,,,,2019-11-12,,SINGLE,,,,,,,,,,GSM1704596_r1,,GSM1704596,,72 h DENV2 infection Total cell lysate ribosome profiling (rep 2),,,,,SRS954560,SRP059187,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/004/SRR2053004,1460095020,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2053004,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/004/SRR2053004,fc3a226c3384d3952e789153424e9f78,DENV2 (EU081177.1),GSE69602,Ribosome profiling analysis of Dengue Virus,,,SRA271639,,,,,,,,,,,,,,, PRJNA286218,SRX1054425,Ion Torrent PGM sequencing; GSM1707652: Ribosome profiling no exercise rep1; Mus musculus; RNA-Seq,Ion Torrent PGM sequencing; GSM1707652: Ribosome profiling no exercise rep1; Mus musculus; RNA-Seq,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03766237,Ribosome profiling no exercise rep1,Ion Torrent PGM,SRR2057646,2743301,82639361,SAMN03766237,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1707652,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/006/SRR2057646/SRR2057646.fastq.gz,76246296,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2057646/SRR2057646.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/006/SRR2057646/SRR2057646.fastq.gz,2c5a0f658903631c0fd8fa0e8b3d74fa,2016-02-17,2016-02-17,false,,,,,,,,,,,ION_TORRENT,,,,2019-10-24,,SINGLE,,,,,,,,,,GSM1707652_r1,,GSM1707652,,Ribosome profiling no exercise rep1,,,,,SRS957264,SRP059282,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/006/SRR2057646,68248028,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2057646,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/006/SRR2057646,e819081dfed7030cf1a8cd28399a34d6,C57BL/6,GSE69699,Genome-wide translational analysis of the effect of acute endurance exercise on mouse gastrocnemius,,,SRA272226,,,,,,,,,,,,,,gastrocnemius, PRJNA286218,SRX1054426,Ion Torrent PGM sequencing; GSM1707653: Ribosome profiling no exercise rep2; Mus musculus; RNA-Seq,Ion Torrent PGM sequencing; GSM1707653: Ribosome profiling no exercise rep2; Mus musculus; RNA-Seq,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03766238,Ribosome profiling no exercise rep2,Ion Torrent PGM,SRR2057647,3049697,92492307,SAMN03766238,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1707653,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/007/SRR2057647/SRR2057647.fastq.gz,84893965,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2057647/SRR2057647.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/007/SRR2057647/SRR2057647.fastq.gz,0003ec611b70c5c4224dd35fcdd0e120,2016-02-17,2016-02-17,false,,,,,,,,,,,ION_TORRENT,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1707653_r1,,GSM1707653,,Ribosome profiling no exercise rep2,,,,,SRS957263,SRP059282,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/007/SRR2057647,76498431,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2057647,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/007/SRR2057647,92aa7bd4838dc5ab7db7e034d6ebfd0a,C57BL/6,GSE69699,Genome-wide translational analysis of the effect of acute endurance exercise on mouse gastrocnemius,,,SRA272226,,,,,,,,,,,,,,gastrocnemius, PRJNA286218,SRX1054427,Ion Torrent PGM sequencing; GSM1707654: Ribosome profiling exercise rep1; Mus musculus; RNA-Seq,Ion Torrent PGM sequencing; GSM1707654: Ribosome profiling exercise rep1; Mus musculus; RNA-Seq,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03766239,Ribosome profiling exercise rep1,Ion Torrent PGM,SRR2057648,3565792,104708331,SAMN03766239,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1707654,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/008/SRR2057648/SRR2057648.fastq.gz,97161153,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2057648/SRR2057648.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/008/SRR2057648/SRR2057648.fastq.gz,81d3a410aa2b3713572800277976050d,2016-02-17,2016-02-17,false,,,,,,,,,,,ION_TORRENT,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1707654_r1,,GSM1707654,,Ribosome profiling exercise rep1,,,,,SRS957262,SRP059282,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/008/SRR2057648,85691310,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2057648,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/008/SRR2057648,ce6d1aca2d1989089d1afe2536b54385,C57BL/6,GSE69699,Genome-wide translational analysis of the effect of acute endurance exercise on mouse gastrocnemius,,,SRA272226,,,,,,,,,,,,,,gastrocnemius, PRJNA286218,SRX1054428,Ion Torrent PGM sequencing; GSM1707655: Ribosome profiling exercise rep2; Mus musculus; RNA-Seq,Ion Torrent PGM sequencing; GSM1707655: Ribosome profiling exercise rep2; Mus musculus; RNA-Seq,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN03766240,Ribosome profiling exercise rep2,Ion Torrent PGM,SRR2057649,2673445,83153884,SAMN03766240,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1707655,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR205/009/SRR2057649/SRR2057649.fastq.gz,76770185,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2057649/SRR2057649.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR205/009/SRR2057649/SRR2057649.fastq.gz,b49b6e7719e0ef171f236e6151aad53f,2016-02-17,2016-02-17,false,,,,,,,,,,,ION_TORRENT,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1707655_r1,,GSM1707655,,Ribosome profiling exercise rep2,,,,,SRS957261,SRP059282,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR205/009/SRR2057649,69124758,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2057649,ftp.sra.ebi.ac.uk/vol1/srr/SRR205/009/SRR2057649,d6513dd69bb0892e42f86dc30c1593e8,C57BL/6,GSE69699,Genome-wide translational analysis of the effect of acute endurance exercise on mouse gastrocnemius,,,SRA272226,,,,,,,,,,,,,,gastrocnemius, PRJNA286792,SRX1056749,Illumina HiSeq 2500 sequencing; GSM1709012: ER Ribosome profiling Untreated 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709012: ER Ribosome profiling Untreated 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770657,ER Ribosome profiling Untreated 1,Illumina HiSeq 2500,SRR2060674,78647403,4011017553,SAMN03770657,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709012,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/004/SRR2060674/SRR2060674.fastq.gz,3186239183,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/004/SRR2060674/SRR2060674.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/004/SRR2060674/SRR2060674.fastq.gz,9dfc27f0b9e30946f060a851600265dc,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-11-15,,SINGLE,,,,,,,,,,GSM1709012_r1,,GSM1709012,,ER Ribosome profiling Untreated 1,,,,,SRS959376,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/004/SRR2060674,2747753959,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/004/SRR2060674,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/004/SRR2060674,bb359cff62feb49d05ae0a008558694f,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056750,Illumina HiSeq 2500 sequencing; GSM1709013: ER Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709013: ER Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770658,ER Ribosome profiling 0.5 h Tg 1,Illumina HiSeq 2500,SRR2060675,10680002,544680102,SAMN03770658,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709013,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/005/SRR2060675/SRR2060675.fastq.gz,399744438,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/005/SRR2060675/SRR2060675.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/005/SRR2060675/SRR2060675.fastq.gz,2d6cf95bb45a1debc08b23148ba6dea7,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-24,,SINGLE,,,,,,,,,,GSM1709013_r1,,GSM1709013,,ER Ribosome profiling 0.5 h Tg 1,,,,,SRS959345,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/005/SRR2060675,375456599,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/005/SRR2060675,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/005/SRR2060675,8aa2920e86e0ba3ae3744256971117dc,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056751,Illumina HiSeq 2500 sequencing; GSM1709014: ER Ribosome profiling 1 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709014: ER Ribosome profiling 1 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770659,ER Ribosome profiling 1 h Tg 1,Illumina HiSeq 2500,SRR2060676,10272599,523902549,SAMN03770659,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709014,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/006/SRR2060676/SRR2060676.fastq.gz,383102414,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/006/SRR2060676/SRR2060676.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/006/SRR2060676/SRR2060676.fastq.gz,27feca83bc11eed516f435289586c093,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1709014_r1,,GSM1709014,,ER Ribosome profiling 1 h Tg 1,,,,,SRS959375,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/006/SRR2060676,358125714,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/006/SRR2060676,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/006/SRR2060676,30aef09b3d0dc6e575bc3fc4d6b850ac,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056752,Illumina HiSeq 2500 sequencing; GSM1709015: ER Ribosome profiling 2 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709015: ER Ribosome profiling 2 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770660,ER Ribosome profiling 2 h Tg 1,Illumina HiSeq 2500,SRR2060677,9291951,473889501,SAMN03770660,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709015,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/007/SRR2060677/SRR2060677.fastq.gz,342126226,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/007/SRR2060677/SRR2060677.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/007/SRR2060677/SRR2060677.fastq.gz,98e5f63d88327f2777b0d94ed2524670,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-12-10,,SINGLE,,,,,,,,,,GSM1709015_r1,,GSM1709015,,ER Ribosome profiling 2 h Tg 1,,,,,SRS959374,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/007/SRR2060677,325710047,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/007/SRR2060677,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/007/SRR2060677,126d6d154d0483a13100cf7d47c9b382,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056753,Illumina HiSeq 2500 sequencing; GSM1709016: ER Ribosome profiling 4 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709016: ER Ribosome profiling 4 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770661,ER Ribosome profiling 4 h Tg 1,Illumina HiSeq 2500,SRR2060678,7836885,399681135,SAMN03770661,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709016,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/008/SRR2060678/SRR2060678.fastq.gz,286859721,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/008/SRR2060678/SRR2060678.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/008/SRR2060678/SRR2060678.fastq.gz,89becc8c01d9b90a0cc2c0c90b973a7e,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1709016_r1,,GSM1709016,,ER Ribosome profiling 4 h Tg 1,,,,,SRS959373,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/008/SRR2060678,272613076,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/008/SRR2060678,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/008/SRR2060678,83d122425e8efb56ea39fc3763de50ed,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056754,Illumina HiSeq 2500 sequencing; GSM1709017: ER Ribosome profiling Untreated 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709017: ER Ribosome profiling Untreated 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770662,ER Ribosome profiling Untreated 2,Illumina HiSeq 2500,SRR2060679,12238357,624156207,SAMN03770662,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709017,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/009/SRR2060679/SRR2060679.fastq.gz,499715493,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/009/SRR2060679/SRR2060679.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/009/SRR2060679/SRR2060679.fastq.gz,10c1c15d85ad9e2cca9712acc5e6d096,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-20,,SINGLE,,,,,,,,,,GSM1709017_r1,,GSM1709017,,ER Ribosome profiling Untreated 2,,,,,SRS959372,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/009/SRR2060679,448972010,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/009/SRR2060679,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/009/SRR2060679,7e01f945c8adfe9e31b266de9b8e8fd5,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056755,Illumina HiSeq 2500 sequencing; GSM1709018: ER Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709018: ER Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770663,ER Ribosome profiling 0.5 h Tg 2,Illumina HiSeq 2500,SRR2060680,27383252,1396545852,SAMN03770663,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709018,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/000/SRR2060680/SRR2060680.fastq.gz,1075486363,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/000/SRR2060680/SRR2060680.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/000/SRR2060680/SRR2060680.fastq.gz,23aea4429f451ca23a17de86b27a0ffb,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1709018_r1,,GSM1709018,,ER Ribosome profiling 0.5 h Tg 2,,,,,SRS959371,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/000/SRR2060680,990037662,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/000/SRR2060680,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/000/SRR2060680,1d4bfa6325dd72c87992906936c5443a,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056756,Illumina HiSeq 2500 sequencing; GSM1709019: ER Ribosome profiling 1 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709019: ER Ribosome profiling 1 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770664,ER Ribosome profiling 1 h Tg 2,Illumina HiSeq 2500,SRR2060681,8062047,411164397,SAMN03770664,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709019,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/001/SRR2060681/SRR2060681.fastq.gz,327766947,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/001/SRR2060681/SRR2060681.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/001/SRR2060681/SRR2060681.fastq.gz,89003a7d706105ed05d9a4ff572ee5af,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-24,,SINGLE,,,,,,,,,,GSM1709019_r1,,GSM1709019,,ER Ribosome profiling 1 h Tg 2,,,,,SRS959370,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/001/SRR2060681,298774926,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/001/SRR2060681,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/001/SRR2060681,0939cb33f573701563ad116f9f043eb6,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056757,Illumina HiSeq 2500 sequencing; GSM1709020: ER Ribosome profiling 2 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709020: ER Ribosome profiling 2 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770665,ER Ribosome profiling 2 h Tg 2,Illumina HiSeq 2500,SRR2060682,18856341,961673391,SAMN03770665,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709020,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/002/SRR2060682/SRR2060682.fastq.gz,759206739,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/002/SRR2060682/SRR2060682.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/002/SRR2060682/SRR2060682.fastq.gz,c050d543d3aae747406ad7102cdf161b,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-17,,SINGLE,,,,,,,,,,GSM1709020_r1,,GSM1709020,,ER Ribosome profiling 2 h Tg 2,,,,,SRS959369,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/002/SRR2060682,693705987,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/002/SRR2060682,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/002/SRR2060682,c254bae6de7355ba5c2f1a62fa2e9690,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056758,Illumina HiSeq 2500 sequencing; GSM1709021: ER Ribosome profiling 4 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709021: ER Ribosome profiling 4 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770666,ER Ribosome profiling 4 h Tg 2,Illumina HiSeq 2500,SRR2060683,8565355,436833105,SAMN03770666,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709021,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/003/SRR2060683/SRR2060683.fastq.gz,349629339,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/003/SRR2060683/SRR2060683.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/003/SRR2060683/SRR2060683.fastq.gz,d34010a308c59a4c026273cb1fa9f7f8,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-12-12,,SINGLE,,,,,,,,,,GSM1709021_r1,,GSM1709021,,ER Ribosome profiling 4 h Tg 2,,,,,SRS959368,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/003/SRR2060683,316015841,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/003/SRR2060683,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/003/SRR2060683,2aae523bd2dddc80a78812276ce008e2,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056759,Illumina HiSeq 2500 sequencing; GSM1709022: Cytosol Ribosome profiling Untreated 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709022: Cytosol Ribosome profiling Untreated 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770667,Cytosol Ribosome profiling Untreated 1,Illumina HiSeq 2500,SRR2060684,4063729,207250179,SAMN03770667,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709022,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/004/SRR2060684/SRR2060684.fastq.gz,170941447,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/004/SRR2060684/SRR2060684.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/004/SRR2060684/SRR2060684.fastq.gz,3ec5670579c6ed3cd4c4ecfb09266765,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-11-20,,SINGLE,,,,,,,,,,GSM1709022_r1,,GSM1709022,,Cytosol Ribosome profiling Untreated 1,,,,,SRS959367,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/004/SRR2060684,147926777,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/004/SRR2060684,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/004/SRR2060684,6567a85de03e8d6419e8aff9aaf68b9d,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056760,Illumina HiSeq 2500 sequencing; GSM1709023: Cytosol Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709023: Cytosol Ribosome profiling 0.5 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770668,Cytosol Ribosome profiling 0.5 h Tg 1,Illumina HiSeq 2500,SRR2060685,29053643,1481735793,SAMN03770668,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709023,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/005/SRR2060685/SRR2060685.fastq.gz,1071623202,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/005/SRR2060685/SRR2060685.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/005/SRR2060685/SRR2060685.fastq.gz,0137a4cc90285dc10d092a7bb0b17969,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1709023_r1,,GSM1709023,,Cytosol Ribosome profiling 0.5 h Tg 1,,,,,SRS959366,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/005/SRR2060685,1006914412,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/005/SRR2060685,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/005/SRR2060685,1e8ab24cb3f903a8ec243f3cea15eb40,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056761,Illumina HiSeq 2500 sequencing; GSM1709024: Cytosol Ribosome profiling 1 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709024: Cytosol Ribosome profiling 1 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770669,Cytosol Ribosome profiling 1 h Tg 1,Illumina HiSeq 2500,SRR2060686,64964205,3313174455,SAMN03770669,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709024,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/006/SRR2060686/SRR2060686.fastq.gz,2409671047,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/006/SRR2060686/SRR2060686.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/006/SRR2060686/SRR2060686.fastq.gz,2be8bdf7f97cccb731a9362303312f14,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-07,,SINGLE,,,,,,,,,,GSM1709024_r1,,GSM1709024,,Cytosol Ribosome profiling 1 h Tg 1,,,,,SRS959365,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/006/SRR2060686,2261355846,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/006/SRR2060686,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/006/SRR2060686,aaf1ecb5153178e7703c120025472c65,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056762,Illumina HiSeq 2500 sequencing; GSM1709025: Cytosol Ribosome profiling 2 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709025: Cytosol Ribosome profiling 2 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770670,Cytosol Ribosome profiling 2 h Tg 1,Illumina HiSeq 2500,SRR2060687,21767084,1110121284,SAMN03770670,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709025,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/007/SRR2060687/SRR2060687.fastq.gz,770252947,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/007/SRR2060687/SRR2060687.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/007/SRR2060687/SRR2060687.fastq.gz,bd6400838e8e30f14c9858672e45ea5d,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1709025_r1,,GSM1709025,,Cytosol Ribosome profiling 2 h Tg 1,,,,,SRS959364,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/007/SRR2060687,742538885,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/007/SRR2060687,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/007/SRR2060687,83227ebfd7aa19b7d328b43f67e307b4,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056763,Illumina HiSeq 2500 sequencing; GSM1709026: Cytosol Ribosome profiling 4 h Tg 1; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709026: Cytosol Ribosome profiling 4 h Tg 1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770671,Cytosol Ribosome profiling 4 h Tg 1,Illumina HiSeq 2500,SRR2060688,24180440,1233202440,SAMN03770671,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709026,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/008/SRR2060688/SRR2060688.fastq.gz,872718407,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/008/SRR2060688/SRR2060688.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/008/SRR2060688/SRR2060688.fastq.gz,187cce4a0eb0488085afe5d5e4457452,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1709026_r1,,GSM1709026,,Cytosol Ribosome profiling 4 h Tg 1,,,,,SRS959363,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/008/SRR2060688,841135310,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/008/SRR2060688,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/008/SRR2060688,6851fa6874f19ce36f3befd3e2fa37ef,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056764,Illumina HiSeq 2500 sequencing; GSM1709027: Cytosol Ribosome profiling Untreated 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709027: Cytosol Ribosome profiling Untreated 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770672,Cytosol Ribosome profiling Untreated 2,Illumina HiSeq 2500,SRR2060689,10236103,522041253,SAMN03770672,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709027,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/009/SRR2060689/SRR2060689.fastq.gz,456513537,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/009/SRR2060689/SRR2060689.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/009/SRR2060689/SRR2060689.fastq.gz,03be5e8f9c0e746582d2ebc4ef08e6b4,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-12-25,,SINGLE,,,,,,,,,,GSM1709027_r1,,GSM1709027,,Cytosol Ribosome profiling Untreated 2,,,,,SRS959362,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/009/SRR2060689,377646052,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/009/SRR2060689,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/009/SRR2060689,610597709237ff0b31ad9903a2b530aa,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056765,Illumina HiSeq 2500 sequencing; GSM1709028: Cytosol Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709028: Cytosol Ribosome profiling 0.5 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770673,Cytosol Ribosome profiling 0.5 h Tg 2,Illumina HiSeq 2500,SRR2060690,16977612,865858212,SAMN03770673,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709028,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/000/SRR2060690/SRR2060690.fastq.gz,728793630,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/000/SRR2060690/SRR2060690.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/000/SRR2060690/SRR2060690.fastq.gz,9a6f60b9ebe28f3f179e417045d03f2b,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1709028_r1,,GSM1709028,,Cytosol Ribosome profiling 0.5 h Tg 2,,,,,SRS959361,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/000/SRR2060690,627877644,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/000/SRR2060690,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/000/SRR2060690,b627f0bcb8e3b3ace4e7d07a6af57aa1,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056766,Illumina HiSeq 2500 sequencing; GSM1709029: Cytosol Ribosome profiling 1 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709029: Cytosol Ribosome profiling 1 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770674,Cytosol Ribosome profiling 1 h Tg 2,Illumina HiSeq 2500,SRR2060691,19996790,1019836290,SAMN03770674,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709029,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/001/SRR2060691/SRR2060691.fastq.gz,795062206,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/001/SRR2060691/SRR2060691.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/001/SRR2060691/SRR2060691.fastq.gz,96a59f3222a1054379241a8c144aaef2,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1709029_r1,,GSM1709029,,Cytosol Ribosome profiling 1 h Tg 2,,,,,SRS959360,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/001/SRR2060691,726259419,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/001/SRR2060691,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/001/SRR2060691,3815078acc84fd3a62f777f461903c07,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056767,Illumina HiSeq 2500 sequencing; GSM1709030: Cytosol Ribosome profiling 2 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709030: Cytosol Ribosome profiling 2 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770675,Cytosol Ribosome profiling 2 h Tg 2,Illumina HiSeq 2500,SRR2060692,10192777,519831627,SAMN03770675,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709030,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/002/SRR2060692/SRR2060692.fastq.gz,411329443,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/002/SRR2060692/SRR2060692.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/002/SRR2060692/SRR2060692.fastq.gz,6d70850d9364a0338e2ae37bfff2b0ad,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2019-10-31,,SINGLE,,,,,,,,,,GSM1709030_r1,,GSM1709030,,Cytosol Ribosome profiling 2 h Tg 2,,,,,SRS959359,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/002/SRR2060692,373319371,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/002/SRR2060692,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/002/SRR2060692,2f2a34e2d47a1651b6898aa6aa53ed6d,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA286792,SRX1056768,Illumina HiSeq 2500 sequencing; GSM1709031: Cytosol Ribosome profiling 4 h Tg 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM1709031: Cytosol Ribosome profiling 4 h Tg 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN03770676,Cytosol Ribosome profiling 4 h Tg 2,Illumina HiSeq 2500,SRR2060693,24131402,1230701502,SAMN03770676,,,,,,,,embryonic fibroblast,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1709031,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR206/003/SRR2060693/SRR2060693.fastq.gz,948180191,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/003/SRR2060693/SRR2060693.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR206/003/SRR2060693/SRR2060693.fastq.gz,b9682eb8d88f2ab8a246d4fb62390be5,2015-10-02,2015-10-02,false,,,,,,,,,,,ILLUMINA,,,,2020-04-30,,SINGLE,,,,,,,,,,GSM1709031_r1,,GSM1709031,,Cytosol Ribosome profiling 4 h Tg 2,,,,,SRS959358,SRP059390,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR206/003/SRR2060693,873899622,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/003/SRR2060693,ftp.sra.ebi.ac.uk/vol1/srr/SRR206/003/SRR2060693,e64d07ec8163e2b9bbb7988146b6fd6e,,GSE69800,Ribosome profiling analysis of GADD34 null cells,,,SRA272681,,,,,,,,,,,,,,, PRJNA268354,SRX1070446,Illumina HiSeq 2000 sequencing; GSM1717890: Ribosome profiling SiControl-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1717890: Ribosome profiling SiControl-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03787322,Ribosome profiling SiControl-RPF,Illumina HiSeq 2000,SRR2075417,29365657,996912114,SAMN03787322,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1717890,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR207/007/SRR2075417/SRR2075417.fastq.gz,892429572,ftp.sra.ebi.ac.uk/vol1/fastq/SRR207/007/SRR2075417/SRR2075417.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR207/007/SRR2075417/SRR2075417.fastq.gz,7cb6b6433e2dfd82704608ca1d03eea2,2015-10-03,2015-10-03,false,,,,,,,,,,,ILLUMINA,,,,2019-10-17,,SINGLE,,,,,,,,,,GSM1717890_r1,,GSM1717890,,Ribosome profiling SiControl-RPF,,,,,SRS969577,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR207/007/SRR2075417,779922168,ftp.sra.ebi.ac.uk/vol1/srr/SRR207/007/SRR2075417,ftp.sra.ebi.ac.uk/vol1/srr/SRR207/007/SRR2075417,f43459557b6906a1182640ecb44fa9ef,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX1070447,Illumina HiSeq 2000 sequencing; GSM1717891: Ribosome profiling SiControl-input-poly(A); Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1717891: Ribosome profiling SiControl-input-poly(A); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03787323,Ribosome profiling SiControl-input-poly(A),Illumina HiSeq 2000,SRR2075418,62485200,2952569004,SAMN03787323,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1717891,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR207/008/SRR2075418/SRR2075418.fastq.gz,2740197190,ftp.sra.ebi.ac.uk/vol1/fastq/SRR207/008/SRR2075418/SRR2075418.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR207/008/SRR2075418/SRR2075418.fastq.gz,a7d1a70dafb9797053e7882d709b91fe,2015-10-03,2015-10-03,false,,,,,,,,,,,ILLUMINA,,,,2019-10-24,,SINGLE,,,,,,,,,,GSM1717891_r1,,GSM1717891,,Ribosome profiling SiControl-input-poly(A),,,,,SRS969576,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR207/008/SRR2075418,2232839017,ftp.sra.ebi.ac.uk/vol1/srr/SRR207/008/SRR2075418,ftp.sra.ebi.ac.uk/vol1/srr/SRR207/008/SRR2075418,0c6619f9da923cd218013680987062d0,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX1070448,Illumina HiSeq 2000 sequencing; GSM1717892: Ribosome profiling SiMETTL3-RPF; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1717892: Ribosome profiling SiMETTL3-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03787324,Ribosome profiling SiMETTL3-RPF,Illumina HiSeq 2000,SRR2075419,25609568,1012594286,SAMN03787324,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1717892,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR207/009/SRR2075419/SRR2075419.fastq.gz,888198510,ftp.sra.ebi.ac.uk/vol1/fastq/SRR207/009/SRR2075419/SRR2075419.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR207/009/SRR2075419/SRR2075419.fastq.gz,983b351efca20a22f9e5d3740ce76964,2015-09-22,2015-09-22,false,,,,,,,,,,,ILLUMINA,,,,2020-04-22,,SINGLE,,,,,,,,,,GSM1717892_r1,,GSM1717892,,Ribosome profiling SiMETTL3-RPF,,,,,SRS969575,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR207/009/SRR2075419,776527631,ftp.sra.ebi.ac.uk/vol1/srr/SRR207/009/SRR2075419,ftp.sra.ebi.ac.uk/vol1/srr/SRR207/009/SRR2075419,58554e1bb7111ac36e7bccdfdb0f1b52,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA268354,SRX1070449,Illumina HiSeq 2000 sequencing; GSM1717893: Ribosome profiling SiMETTL3-input-poly(A); Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM1717893: Ribosome profiling SiMETTL3-input-poly(A); Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03787325,Ribosome profiling SiMETTL3-input-poly(A),Illumina HiSeq 2000,SRR2075420,44646468,4412410928,SAMN03787325,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1717893,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR207/000/SRR2075420/SRR2075420.fastq.gz,3833767567,ftp.sra.ebi.ac.uk/vol1/fastq/SRR207/000/SRR2075420/SRR2075420.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR207/000/SRR2075420/SRR2075420.fastq.gz,86eabf1a40fcc35cbefac512c120abc1,2015-09-26,2015-09-26,false,,,,,,,,,,,ILLUMINA,,,,2020-04-22,,SINGLE,,,,,,,,,,GSM1717893_r1,,GSM1717893,,Ribosome profiling SiMETTL3-input-poly(A),,,,,SRS969574,SRP050213,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR207/000/SRR2075420,3045648806,ftp.sra.ebi.ac.uk/vol1/srr/SRR207/000/SRR2075420,ftp.sra.ebi.ac.uk/vol1/srr/SRR207/000/SRR2075420,5d89513cc44fa316df0dcabd70863005,,GSE63591,N6-methyladenosine Modulates Messenger RNA Translation Efficiency,,,SRA204377,,,,,,,,,,,,,,, PRJNA289569,SRX1092012,Illumina HiSeq 2500 sequencing; GSM1819217: Rluc control ribosome profiling rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819217: Rluc control ribosome profiling rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855826,Rluc control ribosome profiling rep1,Illumina HiSeq 2500,SRR2096964,40053175,2002658750,SAMN03855826,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819217,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/004/SRR2096964/SRR2096964.fastq.gz,1465741921,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/004/SRR2096964/SRR2096964.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/004/SRR2096964/SRR2096964.fastq.gz,b0848c680e80bd92a3b73f7388b48926,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2020-04-27,,SINGLE,,,,,,,,,,GSM1819217_r1,,GSM1819217,,Rluc control ribosome profiling rep1,,,,,SRS987649,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/004/SRR2096964,1310323170,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/004/SRR2096964,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/004/SRR2096964,678d9ba32a45430a160a70b50c4648f3,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092013,Illumina HiSeq 2500 sequencing; GSM1819218: DDX3 WT ribosome profiling rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819218: DDX3 WT ribosome profiling rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855827,DDX3 WT ribosome profiling rep1,Illumina HiSeq 2500,SRR2096965,27500547,1375027350,SAMN03855827,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819218,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/005/SRR2096965/SRR2096965.fastq.gz,976847066,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/005/SRR2096965/SRR2096965.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/005/SRR2096965/SRR2096965.fastq.gz,51b507b9828ac799d450c43a7d559f1b,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2019-10-19,,SINGLE,,,,,,,,,,GSM1819218_r1,,GSM1819218,,DDX3 WT ribosome profiling rep1,,,,,SRS987648,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/005/SRR2096965,893771023,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/005/SRR2096965,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/005/SRR2096965,d688e32e3ef8b9ae2800a77166ed7746,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092014,Illumina HiSeq 2500 sequencing; GSM1819219: DDX3 R534H ribosome profiling rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819219: DDX3 R534H ribosome profiling rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855828,DDX3 R534H ribosome profiling rep1,Illumina HiSeq 2500,SRR2096966,25807053,1290352650,SAMN03855828,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819219,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/006/SRR2096966/SRR2096966.fastq.gz,912572329,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/006/SRR2096966/SRR2096966.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/006/SRR2096966/SRR2096966.fastq.gz,755c4432d0f43cd35e7c506841432c40,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2020-04-26,,SINGLE,,,,,,,,,,GSM1819219_r1,,GSM1819219,,DDX3 R534H ribosome profiling rep1,,,,,SRS987647,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/006/SRR2096966,839174211,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/006/SRR2096966,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/006/SRR2096966,7dd1d48550ab04b24822bf7b11290618,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092015,Illumina HiSeq 2500 sequencing; GSM1819220: Rluc control ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819220: Rluc control ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855829,Rluc control ribosome profiling with sodium arsenite rep1,Illumina HiSeq 2500,SRR2096967,27874521,1393726050,SAMN03855829,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819220,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/007/SRR2096967/SRR2096967.fastq.gz,935532995,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/007/SRR2096967/SRR2096967.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/007/SRR2096967/SRR2096967.fastq.gz,e39e5736394edfe0b11fd6de7483eecf,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1819220_r1,,GSM1819220,,Rluc control ribosome profiling with sodium arsenite rep1,,,,,SRS987646,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/007/SRR2096967,892771073,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/007/SRR2096967,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/007/SRR2096967,626b9f1cc1bd5d8f8c36bcfe412e7ab6,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092016,Illumina HiSeq 2500 sequencing; GSM1819221: DDX3 WT ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819221: DDX3 WT ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855830,DDX3 WT ribosome profiling with sodium arsenite rep1,Illumina HiSeq 2500,SRR2096968,19408923,970446150,SAMN03855830,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819221,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/008/SRR2096968/SRR2096968.fastq.gz,625973666,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/008/SRR2096968/SRR2096968.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/008/SRR2096968/SRR2096968.fastq.gz,63a1d87bbfcbbfd526da64da93637e66,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2019-11-09,,SINGLE,,,,,,,,,,GSM1819221_r1,,GSM1819221,,DDX3 WT ribosome profiling with sodium arsenite rep1,,,,,SRS987645,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/008/SRR2096968,609362499,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/008/SRR2096968,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/008/SRR2096968,c5ffaf51ad819403a2d59f180aa710c3,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092017,Illumina HiSeq 2500 sequencing; GSM1819222: DDX3 R534H ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819222: DDX3 R534H ribosome profiling with sodium arsenite rep1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855831,DDX3 R534H ribosome profiling with sodium arsenite rep1,Illumina HiSeq 2500,SRR2096969,26932125,1346606250,SAMN03855831,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819222,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/009/SRR2096969/SRR2096969.fastq.gz,900156989,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/009/SRR2096969/SRR2096969.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/009/SRR2096969/SRR2096969.fastq.gz,7276f34712a737e8290867775f20e9d7,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2019-11-26,,SINGLE,,,,,,,,,,GSM1819222_r1,,GSM1819222,,DDX3 R534H ribosome profiling with sodium arsenite rep1,,,,,SRS987644,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/009/SRR2096969,863146548,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/009/SRR2096969,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/009/SRR2096969,ffc4ac7724110618444175e10519e32a,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092018,Illumina HiSeq 2500 sequencing; GSM1819223: Rluc control ribosome profiling rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819223: Rluc control ribosome profiling rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855832,Rluc control ribosome profiling rep2,Illumina HiSeq 2500,SRR2096970,32077723,1603886150,SAMN03855832,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819223,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/000/SRR2096970/SRR2096970.fastq.gz,1125039207,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/000/SRR2096970/SRR2096970.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/000/SRR2096970/SRR2096970.fastq.gz,d6ac02ab3edc2dfcad7ab54469745a3a,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2020-04-26,,SINGLE,,,,,,,,,,GSM1819223_r1,,GSM1819223,,Rluc control ribosome profiling rep2,,,,,SRS987643,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/000/SRR2096970,1021073127,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/000/SRR2096970,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/000/SRR2096970,0e3ffe5e7e0d6dfa316d1d2587768337,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092019,Illumina HiSeq 2500 sequencing; GSM1819224: DDX3 WT ribosome profiling rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819224: DDX3 WT ribosome profiling rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855833,DDX3 WT ribosome profiling rep2,Illumina HiSeq 2500,SRR2096971,26066702,1303335100,SAMN03855833,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819224,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/001/SRR2096971/SRR2096971.fastq.gz,884558660,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/001/SRR2096971/SRR2096971.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/001/SRR2096971/SRR2096971.fastq.gz,8e983e20e4dc826f642991f997fba914,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM1819224_r1,,GSM1819224,,DDX3 WT ribosome profiling rep2,,,,,SRS987642,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/001/SRR2096971,820982476,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/001/SRR2096971,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/001/SRR2096971,2273b59c1ead508b66a4371d0f534997,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092020,Illumina HiSeq 2500 sequencing; GSM1819225: DDX3 R534H ribosome profiling rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819225: DDX3 R534H ribosome profiling rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855834,DDX3 R534H ribosome profiling rep2,Illumina HiSeq 2500,SRR2096972,20450140,1022507000,SAMN03855834,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819225,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/002/SRR2096972/SRR2096972.fastq.gz,688028929,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/002/SRR2096972/SRR2096972.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/002/SRR2096972/SRR2096972.fastq.gz,12088b8558119373d40041848ab151f1,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-09,,SINGLE,,,,,,,,,,GSM1819225_r1,,GSM1819225,,DDX3 R534H ribosome profiling rep2,,,,,SRS987641,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/002/SRR2096972,638845550,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/002/SRR2096972,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/002/SRR2096972,a3043aa98cbdd34fef1dc6325993ed54,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092021,Illumina HiSeq 2500 sequencing; GSM1819226: Rluc control ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819226: Rluc control ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855835,Rluc control ribosome profiling with sodium arsenite rep2,Illumina HiSeq 2500,SRR2096973,20927350,1046367500,SAMN03855835,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819226,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/003/SRR2096973/SRR2096973.fastq.gz,680725526,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/003/SRR2096973/SRR2096973.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/003/SRR2096973/SRR2096973.fastq.gz,61c3c6a4c3e2b581ed6f466f2ca7c6c4,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2019-11-23,,SINGLE,,,,,,,,,,GSM1819226_r1,,GSM1819226,,Rluc control ribosome profiling with sodium arsenite rep2,,,,,SRS987640,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/003/SRR2096973,654813051,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/003/SRR2096973,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/003/SRR2096973,7295886b9add90320ee4b8c6e1bf106f,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092022,Illumina HiSeq 2500 sequencing; GSM1819227: DDX3 WT ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819227: DDX3 WT ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855836,DDX3 WT ribosome profiling with sodium arsenite rep2,Illumina HiSeq 2500,SRR2096974,27176847,1358842350,SAMN03855836,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819227,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/004/SRR2096974/SRR2096974.fastq.gz,825361688,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/004/SRR2096974/SRR2096974.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/004/SRR2096974/SRR2096974.fastq.gz,97f77df38e53f54b6e338eb49aebf0dd,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-13,,SINGLE,,,,,,,,,,GSM1819227_r1,,GSM1819227,,DDX3 WT ribosome profiling with sodium arsenite rep2,,,,,SRS987639,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/004/SRR2096974,814612332,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/004/SRR2096974,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/004/SRR2096974,27dbc2dfbff2251754f0e1cd28209d55,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA289569,SRX1092023,Illumina HiSeq 2500 sequencing; GSM1819228: DDX3 R534H ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,Illumina HiSeq 2500 sequencing; GSM1819228: DDX3 R534H ribosome profiling with sodium arsenite rep2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN03855837,DDX3 R534H ribosome profiling with sodium arsenite rep2,Illumina HiSeq 2500,SRR2096975,28797113,1439855650,SAMN03855837,,,,,,,HEK293-Flp-In-T-Rex,Embryonic kidney,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1819228,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR209/005/SRR2096975/SRR2096975.fastq.gz,893771333,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/005/SRR2096975/SRR2096975.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR209/005/SRR2096975/SRR2096975.fastq.gz,31b2814b599e2bf021d2b9b76eb38a3d,2016-04-24,2016-04-24,false,,,,,,,,,,,ILLUMINA,,,,2019-11-01,,SINGLE,,,,,,,,,,GSM1819228_r1,,GSM1819228,,DDX3 R534H ribosome profiling with sodium arsenite rep2,,,,,SRS987638,SRP060676,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR209/005/SRR2096975,872550236,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/005/SRR2096975,ftp.sra.ebi.ac.uk/vol1/srr/SRR209/005/SRR2096975,2f8fff225db70727ab7083639ef8d4e7,,GSE70802,Profiles of ribosome-associated mRNAs regulated by expression of wild-type (WT) or R534H variant of DDX3 with or without Sodium Arsenite treatment [Ribo-Seq],,,SRA276791,,,,,,,,female,,,,,,, PRJNA296059,SRX1254413,Illumina HiSeq 2000 sequencing; GSM1887643: ribosome profiling; Homo sapiens; miRNA-Seq,Illumina HiSeq 2000 sequencing; GSM1887643: ribosome profiling; Homo sapiens; miRNA-Seq,9606,Homo sapiens,miRNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN04093818,ribosome profiling,Illumina HiSeq 2000,SRR2433794,31967082,916773615,SAMN04093818,,,,,,,HEK293,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM1887643,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR243/004/SRR2433794/SRR2433794.fastq.gz,869325804,ftp.sra.ebi.ac.uk/vol1/fastq/SRR243/004/SRR2433794/SRR2433794.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR243/004/SRR2433794/SRR2433794.fastq.gz,4f5e99acef8fcd524dad62fcd8c57730,2015-11-13,2015-11-13,false,,,,,,,,,,,ILLUMINA,,,,2019-11-13,,SINGLE,,,,,,,,,,GSM1887643_r1,,GSM1887643,,ribosome profiling,,,,,SRS1072728,SRP063852,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR243/004/SRR2433794,626383378,ftp.sra.ebi.ac.uk/vol1/srr/SRR243/004/SRR2433794,ftp.sra.ebi.ac.uk/vol1/srr/SRR243/004/SRR2433794,bb204551ed638628626fcc3dac3b53af,,GSE73136,A spectral analysis approach to detects actively translated open reading frames in high resolution ribosome profiling data,,,SRA299240,,,,,,,,,,,,,,, PRJNA299254,SRX1356474,NextSeq 500 sequencing; Ribosome profiling of lactimidomycin treated Jurkat cells,NextSeq 500 sequencing; Ribosome profiling of lactimidomycin treated Jurkat cells,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMN04195657,Lactimidomycin treated Jurkat cells,NextSeq 500,SRR2732970,378053973,28732101948,SAMN04195657,,,,,,,Jurkat T-lymphocytes,T Cell/ T Lymphocyte,,,,,,,,,,,,,,,,,,,,,false,Ribosome profiling in Jurkat cells,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR273/000/SRR2732970/SRR2732970.fastq.gz,10959838091,ftp.sra.ebi.ac.uk/vol1/fastq/SRR273/000/SRR2732970/SRR2732970.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR273/000/SRR2732970/SRR2732970.fastq.gz,66c56b00eacdb1ad1b994679b65a686c,2015-12-10,2015-12-10,false,,,,,,,,,,,ILLUMINA,,cell line,,2016-06-28,,SINGLE,ribosome profiling custom library,,,,,,,,,LTM Jurkat NextSeq500,,Lactimidomycin treated Jurkat cells,,Lactimidomycin treated Jurkat cells,,,,,SRS1122385,SRP065022,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR273/000/SRR2732970,10965987834,ftp.sra.ebi.ac.uk/vol1/srr/SRR273/000/SRR2732970,ftp.sra.ebi.ac.uk/vol1/srr/SRR273/000/SRR2732970,d30259c0b3d5f6bb409c6b628183bf25,,PRJNA299254,Positional proteomics reveals differences in N-terminal proteoform stability,,,SRA306243,,,,,,,,male,,,,,,peripheral blood, PRJNA299254,SRX1356478,NextSeq 500 sequencing; Ribosome profiling of cycloheximide treated Jurkat cells,NextSeq 500 sequencing; Ribosome profiling of cycloheximide treated Jurkat cells,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,other,SAMN04195655,Cycloheximide treated Jurkat cells,NextSeq 500,SRR2733100,388812515,29549751140,SAMN04195655,,,,,,,Jurkat T-lymphocytes,T Cell/ T Lymphocyte,,,,,,,,,,,,,,,,,,,,,false,CHX Jurkat,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR273/000/SRR2733100/SRR2733100.fastq.gz,11787812562,ftp.sra.ebi.ac.uk/vol1/fastq/SRR273/000/SRR2733100/SRR2733100.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR273/000/SRR2733100/SRR2733100.fastq.gz,7649e572e48a692dea76b650763844dc,2015-10-23,2015-10-23,false,,,,,,,,,,,ILLUMINA,,cell line,,2016-06-28,,SINGLE,ribosome profiling custom library,,,,,,,,,CHX Jurkat NextSeq500,,Cycloheximide treated Jurkat cells,,Cycloheximide treated Jurkat cells,,,,,SRS1122388,SRP065022,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR273/000/SRR2733100,11507004422,ftp.sra.ebi.ac.uk/vol1/srr/SRR273/000/SRR2733100,ftp.sra.ebi.ac.uk/vol1/srr/SRR273/000/SRR2733100,8625f9f61508504df8a5d5137f7c81c5,,PRJNA299254,Positional proteomics reveals differences in N-terminal proteoform stability,,,SRA306243,,,,,,,,male,,,,,,peripheral blood, PRJNA311041,SRX1562724,Illumina HiSeq 2000 sequencing; GSM2055244: ribosome profiling 37°C in WT; Escherichia coli; OTHER,Illumina HiSeq 2000 sequencing; GSM2055244: ribosome profiling 37°C in WT; Escherichia coli; OTHER,511145,Escherichia coli str. K-12 substr. MG1655,OTHER,TRANSCRIPTOMIC,other,SAMN04457972,ribosome profiling 37°C in WT,Illumina HiSeq 2000,SRR3147100,61258516,3124184316,SAMN04457972,,,,,,,,,,,,,,,,,,,,,,,,,,,,,false,GSM2055244,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR314/000/SRR3147100/SRR3147100.fastq.gz,2470648117,ftp.sra.ebi.ac.uk/vol1/fastq/SRR314/000/SRR3147100/SRR3147100.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR314/000/SRR3147100/SRR3147100.fastq.gz,90ebaa8793caecec466d7122d3582948,2017-02-01,2017-02-01,false,,,,,,,,,,,ILLUMINA,,,,2017-03-02,,SINGLE,,,,,,,,,,GSM2055244_r1,,GSM2055244,,ribosome profiling 37°C in WT,,,,,SRS1277332,SRP069339,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR314/000/SRR3147100,2064958495,ftp.sra.ebi.ac.uk/vol1/srr/SRR314/000/SRR3147100,ftp.sra.ebi.ac.uk/vol1/srr/SRR314/000/SRR3147100,a07c1aca417686b224c1932d84849843,K-12,GSE77617,Operon mRNAs are organized into ORF-centric structures that predict translation efficiency,,MG1655,SRA348058,,,,,,,,,,,,,,, PRJNA314248,SRX1616307,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04531072,Ribosome profiling of HEK293 cells,Illumina HiSeq 2000,SRR3208296,44716778,1265915396,SAMN04531072,,,,,,,HEK293,,,,,,,,,,,,,,,,,,,,,,false,Ribo-Seq HEK293,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR320/006/SRR3208296/SRR3208296.fastq.gz,1107096184,ftp.sra.ebi.ac.uk/vol1/fastq/SRR320/006/SRR3208296/SRR3208296.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR320/006/SRR3208296/SRR3208296.fastq.gz,ca5e7e2b8f9e1220e97dd7885275d362,2016-03-10,2016-03-10,false,,,,,,,,,,,ILLUMINA,,,,2016-06-27,,SINGLE,,,,,,,,,,ribo-seq hek293,,Ribosome profiling of HEK293 cells,,Ribosome profiling of HEK293 cells,,,,,SRS1325807,SRP071216,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR320/006/SRR3208296,954068723,ftp.sra.ebi.ac.uk/vol1/srr/SRR320/006/SRR3208296,ftp.sra.ebi.ac.uk/vol1/srr/SRR320/006/SRR3208296,e9f39be720c5a0284c36f705f3686bbb,,PRJNA314248,Mammalian cell lines Raw sequence reads,,,SRA378655,,,,,,,,,,,,,,Embryonic Kidney, PRJNA314248,SRX1616308,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN04531073,Ribosome profiling of MEF cells,Illumina HiSeq 2000,SRR3208406,23534216,729844417,SAMN04531073,,,,,,,MEF,,Cornell University,,,,,,,,,,,,,,,,,,,,false,Ribo-Seq MEF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR320/006/SRR3208406/SRR3208406.fastq.gz,635923964,ftp.sra.ebi.ac.uk/vol1/fastq/SRR320/006/SRR3208406/SRR3208406.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR320/006/SRR3208406/SRR3208406.fastq.gz,7bebc141ab2e02d5645a522f3ca0b4a8,2016-03-10,2016-03-10,false,,,,,,,,,,,ILLUMINA,,,,2018-06-26,,SINGLE,,,,,,,,,,ribo-seq mef,,Ribosome profiling of MEF cells,,Ribosome profiling of MEF cells,,,,,SRS1325808,SRP071216,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR320/006/SRR3208406,523896624,ftp.sra.ebi.ac.uk/vol1/srr/SRR320/006/SRR3208406,ftp.sra.ebi.ac.uk/vol1/srr/SRR320/006/SRR3208406,31da60f1c9cdeafe354e0fa8e470f287,,PRJNA314248,Mammalian cell lines Raw sequence reads,,,SRA378655,,,,,,,,,,,,,,Embryonic fibroblast, PRJNA314248,SRX1616309,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with WT 18S rRNA,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with WT 18S rRNA,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN04531074,Ribosome profiling of MEF cells transfected with WT 18S rRNA,Illumina HiSeq 2000,SRR3208450,27696228,850735689,SAMN04531074,,,,,,,MEF,,,,,,,,,,,,,,,,,,,,,,false,Ribo-Seq MEF ( WT 18S rRNA),,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR320/000/SRR3208450/SRR3208450.fastq.gz,566853147,ftp.sra.ebi.ac.uk/vol1/fastq/SRR320/000/SRR3208450/SRR3208450.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR320/000/SRR3208450/SRR3208450.fastq.gz,6e855fd0a895ae5665d36fd15dca4975,2016-03-10,2016-03-10,false,,,,,,,,,,,ILLUMINA,,,,2016-06-27,,SINGLE,,,,,,,,,,ribo-seq mef (WT 18S rRNA),,Ribosome profiling of MEF cells transfected with WT 18S rRNA,,Ribosome profiling of MEF cells transfected with WT 18S rRNA,,,,,SRS1325809,SRP071216,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR320/000/SRR3208450,414954531,ftp.sra.ebi.ac.uk/vol1/srr/SRR320/000/SRR3208450,ftp.sra.ebi.ac.uk/vol1/srr/SRR320/000/SRR3208450,c43eb5fa7da31463a783f39295ab6130,,PRJNA314248,Mammalian cell lines Raw sequence reads,,,SRA378655,,,,,,,,,,,,,,Embryonic fibroblast, PRJNA314248,SRX1616310,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with mutant 18S rRNA,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells transfected with mutant 18S rRNA,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN04531075,Ribosome profiling of MEF cells transfected with mutant 18S rRNA,Illumina HiSeq 2000,SRR3208452,59116544,1698553234,SAMN04531075,,,,,,,MEF,,,,,,,,,,,,,,,,,,,,,,false,Ribo-Seq MEF (mutant 18S rRNA),,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR320/002/SRR3208452/SRR3208452.fastq.gz,1167128565,ftp.sra.ebi.ac.uk/vol1/fastq/SRR320/002/SRR3208452/SRR3208452.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR320/002/SRR3208452/SRR3208452.fastq.gz,37e816b114ab8f51492d5fb0b89ba869,2016-03-10,2016-03-10,false,,,,,,,,,,,ILLUMINA,,,,2016-06-27,,SINGLE,,,,,,,,,,ribo-seq mef (mutant 18S rRNA),,Ribosome profiling of MEF cells transfected with mutant 18S rRNA,,Ribosome profiling of MEF cells transfected with mutant 18S rRNA,,,,,SRS1325810,SRP071216,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR320/002/SRR3208452,857487790,ftp.sra.ebi.ac.uk/vol1/srr/SRR320/002/SRR3208452,ftp.sra.ebi.ac.uk/vol1/srr/SRR320/002/SRR3208452,e310d83fd6625e3518580a907b4b8eb1,,PRJNA314248,Mammalian cell lines Raw sequence reads,,,SRA378655,,,,,,,,,,,,,,Embryonic fibroblast, PRJNA316125,SRX1657158,Illumina HiSeq 2500 sequencing; GSM2097522: HBE cells ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM2097522: HBE cells ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN04576208,HBE cells ribosome profiling,Illumina HiSeq 2500,SRR3286543,110777954,5538897700,SAMN04576208,,,,,,,HBE,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2097522,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR328/003/SRR3286543/SRR3286543.fastq.gz,3613125374,ftp.sra.ebi.ac.uk/vol1/fastq/SRR328/003/SRR3286543/SRR3286543.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR328/003/SRR3286543/SRR3286543.fastq.gz,df75c4410d3c6474aac1c9c498d39330,2019-07-23,2019-07-23,false,,,,,,,,,,,ILLUMINA,,,,2019-07-23,,SINGLE,,,,,,,,,,GSM2097522_r1,,GSM2097522,,HBE cells ribosome profiling,,,,,SRS1357385,SRP072231,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR328/003/SRR3286543,3346406392,ftp.sra.ebi.ac.uk/vol1/srr/SRR328/003/SRR3286543,ftp.sra.ebi.ac.uk/vol1/srr/SRR328/003/SRR3286543,8bec45b6c695b0d03830529cb16cb9b6,,GSE79539,Finding new proteins encoded by long non-coding RNAs in human cells,,,SRA393427,,,,,,,,,,,,,,, PRJNA316125,SRX1657159,Illumina HiSeq 2500 sequencing; GSM2097523: A549 cells ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM2097523: A549 cells ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN04576209,A549 cells ribosome profiling,Illumina HiSeq 2500,SRR3286544,95891656,4794582800,SAMN04576209,,,,,,,A549,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2097523,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR328/004/SRR3286544/SRR3286544.fastq.gz,3280435402,ftp.sra.ebi.ac.uk/vol1/fastq/SRR328/004/SRR3286544/SRR3286544.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR328/004/SRR3286544/SRR3286544.fastq.gz,8b31ac7f567b2cedb14508bc4006dff8,2019-07-23,2019-07-23,false,,,,,,,,,,,ILLUMINA,,,,2019-07-23,,SINGLE,,,,,,,,,,GSM2097523_r1,,GSM2097523,,A549 cells ribosome profiling,,,,,SRS1357383,SRP072231,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR328/004/SRR3286544,2987916667,ftp.sra.ebi.ac.uk/vol1/srr/SRR328/004/SRR3286544,ftp.sra.ebi.ac.uk/vol1/srr/SRR328/004/SRR3286544,bd450dd485282cb1c356ae5de7060589,,GSE79539,Finding new proteins encoded by long non-coding RNAs in human cells,,,SRA393427,,,,,,,,,,,,,,, PRJNA316125,SRX1657160,Illumina HiSeq 2500 sequencing; GSM2097524: H1299 cells ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM2097524: H1299 cells ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN04576210,H1299 cells ribosome profiling,Illumina HiSeq 2500,SRR3286545,111526324,5576316200,SAMN04576210,,,,,,,H1299,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2097524,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR328/005/SRR3286545/SRR3286545.fastq.gz,3267830318,ftp.sra.ebi.ac.uk/vol1/fastq/SRR328/005/SRR3286545/SRR3286545.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR328/005/SRR3286545/SRR3286545.fastq.gz,398fd183eba7a9b039d564c9930b95a1,2019-07-23,2019-07-23,false,,,,,,,,,,,ILLUMINA,,,,2019-07-23,,SINGLE,,,,,,,,,,GSM2097524_r1,,GSM2097524,,H1299 cells ribosome profiling,,,,,SRS1357379,SRP072231,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR328/005/SRR3286545,3099215119,ftp.sra.ebi.ac.uk/vol1/srr/SRR328/005/SRR3286545,ftp.sra.ebi.ac.uk/vol1/srr/SRR328/005/SRR3286545,71b1b8409c9b9dadde22aa4d45baf284,,GSE79539,Finding new proteins encoded by long non-coding RNAs in human cells,,,SRA393427,,,,,,,,,,,,,,, PRJNA316618,SRX1667364,Illumina HiSeq 2000 sequencing; GSM2100596: S phase ribosome profiling replicate 1; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100596: S phase ribosome profiling replicate 1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588783,S phase ribosome profiling replicate 1,Illumina HiSeq 2000,SRR3306583,178511892,9104106492,SAMN04588783,,,,,,,,human cervical cancer cell line,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2100596,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR330/003/SRR3306583/SRR3306583.fastq.gz,6658423020,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/003/SRR3306583/SRR3306583.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/003/SRR3306583/SRR3306583.fastq.gz,43d465538cd854ff4be408711ccb39bf,2016-04-09,2016-04-09,false,,,,,,,,,,,ILLUMINA,,,,2019-10-23,,SINGLE,,,,,,,,,,GSM2100596_r1,,GSM2100596,,S phase ribosome profiling replicate 1,,,,,SRS1365643,SRP072459,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR330/003/SRR3306583,6091018616,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/003/SRR3306583,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/003/SRR3306583,657c6cfd0e55d70e3089983d04dc8978,,GSE79664,Regulation of poly(A) tail and translation during the somatic cell cycle,,,SRA399402,,,,,,,,,,,,,,, PRJNA316618,SRX1667365,Illumina HiSeq 2000 sequencing; GSM2100597: S phase ribosome profiling replicate 2; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100597: S phase ribosome profiling replicate 2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588784,S phase ribosome profiling replicate 2,Illumina HiSeq 2000,SRR3306584,242256008,12355056408,SAMN04588784,,,,,,,,human cervical cancer cell line,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2100597,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR330/004/SRR3306584/SRR3306584.fastq.gz,9245105463,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/004/SRR3306584/SRR3306584.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/004/SRR3306584/SRR3306584.fastq.gz,5ae3f27c02817ade66eb283522903795,2016-04-09,2016-04-09,false,,,,,,,,,,,ILLUMINA,,,,2019-12-22,,SINGLE,,,,,,,,,,GSM2100597_r1,,GSM2100597,,S phase ribosome profiling replicate 2,,,,,SRS1365641,SRP072459,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR330/004/SRR3306584,8454696428,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/004/SRR3306584,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/004/SRR3306584,13d5d1976ef4e36dac8b04bb8f28114a,,GSE79664,Regulation of poly(A) tail and translation during the somatic cell cycle,,,SRA399402,,,,,,,,,,,,,,, PRJNA316618,SRX1667366,Illumina HiSeq 2000 sequencing; GSM2100598: M phase ribosome profiling replicate 1; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100598: M phase ribosome profiling replicate 1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588785,M phase ribosome profiling replicate 1,Illumina HiSeq 2000,SRR3306585,116546351,5943863901,SAMN04588785,,,,,,,,human cervical cancer cell line,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2100598,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR330/005/SRR3306585/SRR3306585.fastq.gz,4490528777,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/005/SRR3306585/SRR3306585.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/005/SRR3306585/SRR3306585.fastq.gz,aee9c8da46007b5f54af7879f6205531,2016-04-09,2016-04-09,false,,,,,,,,,,,ILLUMINA,,,,2020-04-17,,SINGLE,,,,,,,,,,GSM2100598_r1,,GSM2100598,,M phase ribosome profiling replicate 1,,,,,SRS1365640,SRP072459,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR330/005/SRR3306585,4197488811,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/005/SRR3306585,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/005/SRR3306585,0fb11ec98633a66e5aa02ee16d1226c3,,GSE79664,Regulation of poly(A) tail and translation during the somatic cell cycle,,,SRA399402,,,,,,,,,,,,,,, PRJNA316618,SRX1667367,Illumina HiSeq 2000 sequencing; GSM2100599: M phase ribosome profiling replicate 2; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100599: M phase ribosome profiling replicate 2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588786,M phase ribosome profiling replicate 2,Illumina HiSeq 2000,SRR3306586,239897608,12234778008,SAMN04588786,,,,,,,,human cervical cancer cell line,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2100599,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR330/006/SRR3306586/SRR3306586.fastq.gz,9075045155,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/006/SRR3306586/SRR3306586.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/006/SRR3306586/SRR3306586.fastq.gz,a17e719e2aa0e16071b70c9429927d55,2016-04-09,2016-04-09,false,,,,,,,,,,,ILLUMINA,,,,2019-12-22,,SINGLE,,,,,,,,,,GSM2100599_r1,,GSM2100599,,M phase ribosome profiling replicate 2,,,,,SRS1365639,SRP072459,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR330/006/SRR3306586,8313680808,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/006/SRR3306586,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/006/SRR3306586,277e9191d3b7f82ec5a5cf519a42fc85,,GSE79664,Regulation of poly(A) tail and translation during the somatic cell cycle,,,SRA399402,,,,,,,,,,,,,,, PRJNA316618,SRX1667368,Illumina HiSeq 2000 sequencing; GSM2100600: M phase ribosome profiling synchronized by shake off; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100600: M phase ribosome profiling synchronized by shake off; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588787,M phase ribosome profiling synchronized by shake off,Illumina HiSeq 2000,SRR3306587,242516177,12368325027,SAMN04588787,,,,,,,,human cervical cancer cell line,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2100600,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR330/007/SRR3306587/SRR3306587.fastq.gz,9192269363,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/007/SRR3306587/SRR3306587.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/007/SRR3306587/SRR3306587.fastq.gz,49b6555b188093d6982291b8aed5ee62,2016-04-09,2016-04-09,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,,,,,,,,,,GSM2100600_r1,,GSM2100600,,M phase ribosome profiling synchronized by shake off,,,,,SRS1365638,SRP072459,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR330/007/SRR3306587,8357930174,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/007/SRR3306587,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/007/SRR3306587,80aa0b5208899b479cd7e5ce9b3f94f5,,GSE79664,Regulation of poly(A) tail and translation during the somatic cell cycle,,,SRA399402,,,,,,,,,,,,,,, PRJNA316618,SRX1667369,Illumina HiSeq 2000 sequencing; GSM2100601: Asynchronous cell ribosome profiling 1; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100601: Asynchronous cell ribosome profiling 1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588788,Asynchronous cell ribosome profiling 1,Illumina HiSeq 2000,SRR3306588,173946221,8871257271,SAMN04588788,,,,,,,,human cervical cancer cell line,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2100601,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR330/008/SRR3306588/SRR3306588.fastq.gz,6546434160,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/008/SRR3306588/SRR3306588.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/008/SRR3306588/SRR3306588.fastq.gz,611b7080ea0d460c7001490bf5039b63,2016-04-09,2016-04-09,false,,,,,,,,,,,ILLUMINA,,,,2020-02-07,,SINGLE,,,,,,,,,,GSM2100601_r1,,GSM2100601,,Asynchronous cell ribosome profiling 1,,,,,SRS1365637,SRP072459,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR330/008/SRR3306588,6006895001,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/008/SRR3306588,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/008/SRR3306588,3302436a491729429a2213bad89d3ef9,,GSE79664,Regulation of poly(A) tail and translation during the somatic cell cycle,,,SRA399402,,,,,,,,,,,,,,, PRJNA316618,SRX1667370,Illumina HiSeq 2000 sequencing; GSM2100602: Asynchronous cell ribosome profiling 2; Homo sapiens; OTHER,Illumina HiSeq 2000 sequencing; GSM2100602: Asynchronous cell ribosome profiling 2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04588789,Asynchronous cell ribosome profiling 2,Illumina HiSeq 2000,SRR3306589,242417925,12363314175,SAMN04588789,,,,,,,,human cervical cancer cell line,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2100602,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR330/009/SRR3306589/SRR3306589.fastq.gz,9071737902,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/009/SRR3306589/SRR3306589.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR330/009/SRR3306589/SRR3306589.fastq.gz,247363b0d5e1d60dc494293216f71339,2016-04-09,2016-04-09,false,,,,,,,,,,,ILLUMINA,,,,2020-04-17,,SINGLE,,,,,,,,,,GSM2100602_r1,,GSM2100602,,Asynchronous cell ribosome profiling 2,,,,,SRS1365642,SRP072459,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR330/009/SRR3306589,8267908947,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/009/SRR3306589,ftp.sra.ebi.ac.uk/vol1/srr/SRR330/009/SRR3306589,f5596b1ca9949370f077b3c4e6e67ab6,,GSE79664,Regulation of poly(A) tail and translation during the somatic cell cycle,,,SRA399402,,,,,,,,,,,,,,, PRJNA314248,SRX1616308,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN04531073,Ribosome profiling of MEF cells,Illumina HiSeq 2000,SRR3392126,60694250,1876859442,SAMN04531073,,,,,,,MEF,,,,,,,,,,,,,,,,,,,,,,false,Ribo-Seq MEF,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR339/006/SRR3392126/SRR3392126.fastq.gz,1664936467,ftp.sra.ebi.ac.uk/vol1/fastq/SRR339/006/SRR3392126/SRR3392126.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR339/006/SRR3392126/SRR3392126.fastq.gz,fcbec27defb2cc983e5ec858b8ddfa87,2016-04-16,2016-04-16,false,,,,,,,,,,,ILLUMINA,,,,2016-06-27,,SINGLE,,,,,,,,,,Ribo-Seq MEF,,Ribosome profiling of MEF cells,,Ribosome profiling of MEF cells,,,,,SRS1325808,SRP071216,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR339/006/SRR3392126,1370845324,ftp.sra.ebi.ac.uk/vol1/srr/SRR339/006/SRR3392126,ftp.sra.ebi.ac.uk/vol1/srr/SRR339/006/SRR3392126,c92b058a98a42bb3b951a41d533a464c,,PRJNA314248,Mammalian cell lines Raw sequence reads,,,SRA378655,,,,,,,,,,,,,,Embryonic fibroblast, PRJNA314248,SRX1704872,Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Control for Methionine Starvation),Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Control for Methionine Starvation),9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN04625643,HEK293T cells for Ribosome profiling (Control for Methionine Starvation),Illumina HiSeq 2000,SRR3392899,38333571,1136913910,SAMN04625643,,,,,,,HEK293T,,,,,,,,,,,,,,,,,,,,,,false,HEK293T cells for Ribosome profiling (Control for Methionine Starvation),,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR339/009/SRR3392899/SRR3392899.fastq.gz,594743345,ftp.sra.ebi.ac.uk/vol1/fastq/SRR339/009/SRR3392899/SRR3392899.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR339/009/SRR3392899/SRR3392899.fastq.gz,7d31445d0fcf27b1ca68a79bd9b9880d,2016-04-16,2016-04-16,false,,,,,,,,,,,ILLUMINA,,,,2016-06-27,,SINGLE,,,,,,,,,,"Ribo-Seq (HEK293T, Control for Methionine Starvation)",,"Ribosome Profiling (HEK293T, Control for Methionine Starvation)",,HEK293T cells for Ribosome profiling (Control for Methionine Starvation),,,,,SRS1396984,SRP071216,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR339/009/SRR3392899,528552270,ftp.sra.ebi.ac.uk/vol1/srr/SRR339/009/SRR3392899,ftp.sra.ebi.ac.uk/vol1/srr/SRR339/009/SRR3392899,b65da232a42d7f0ba86419c2ae8d1d14,,PRJNA314248,Mammalian cell lines Raw sequence reads,,,SRA378655,,,,,,,,,,,,,,Embryonic Kidney, PRJNA314248,SRX1704873,Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Methionine Starvation),Illumina HiSeq 2000 sequencing; HEK293T cells for Ribosome profiling (Methionine Starvation),9606,Homo sapiens,OTHER,OTHER,other,SAMN04625644,HEK293T cells for Ribosome profiling (Methionine Starvation),Illumina HiSeq 2000,SRR3398188,38629161,1141710659,SAMN04625644,,,,,,,HEK293T,,,,,,,,,,,,,,,,,,,,,,false,HEK293T cells for Ribosome profiling (Methionine Starvation),,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR339/008/SRR3398188/SRR3398188.fastq.gz,556154974,ftp.sra.ebi.ac.uk/vol1/fastq/SRR339/008/SRR3398188/SRR3398188.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR339/008/SRR3398188/SRR3398188.fastq.gz,d2430de241318c1dfc4eac0cee05d026,2016-04-18,2016-04-18,false,,,,,,,,,,,ILLUMINA,,,,2016-06-27,,SINGLE,,,,,,,,,,"Ribo-Seq (HEK293T, Methionine Starvation)",,"Ribosome Profiling (HEK293T, Methionine Starvation)",,HEK293T cells for Ribosome profiling (Methionine Starvation),,,,,SRS1396985,SRP071216,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR339/008/SRR3398188,539380134,ftp.sra.ebi.ac.uk/vol1/srr/SRR339/008/SRR3398188,ftp.sra.ebi.ac.uk/vol1/srr/SRR339/008/SRR3398188,d85b200bc37a72b87d9d949abcefdc8e,,PRJNA314248,Mammalian cell lines Raw sequence reads,,,SRA378655,,,,,,,,,,,,,,Embryonic Kidney, PRJNA344393,SRX2189156,NextSeq 500 sequencing; GSM2327825: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with lactimidomycin; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2327825: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with lactimidomycin; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN05821926,Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with lactimidomycin,NextSeq 500,SRR4293693,178964457,13601298732,SAMN05821926,,,,,,,HCT116,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2327825,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR429/003/SRR4293693/SRR4293693.fastq.gz,6689403557,ftp.sra.ebi.ac.uk/vol1/fastq/SRR429/003/SRR4293693/SRR4293693.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR429/003/SRR4293693/SRR4293693.fastq.gz,e04772698c040c4dfc8eafa607586f24,2017-01-27,2017-01-27,false,,,,,,,,,,,ILLUMINA,,,,2019-11-22,,SINGLE,,,,,,,,,,GSM2327825_r1,,GSM2327825,,Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with lactimidomycin,,,,,SRS1711882,SRP090415,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR429/003/SRR4293693,6347200895,ftp.sra.ebi.ac.uk/vol1/srr/SRR429/003/SRR4293693,ftp.sra.ebi.ac.uk/vol1/srr/SRR429/003/SRR4293693,747df8503266807120955c979ba72bf8,,GSE87328,eIF1 modulates the recognition of sub-optimal translation start sites and steers gene expression control mediated by uORFs,,,SRA478929,,,,,,,,,,,,,,colon, PRJNA344393,SRX2189157,NextSeq 500 sequencing; GSM2327826: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with cycloheximide; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2327826: Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with cycloheximide; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN05821925,Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with cycloheximide,NextSeq 500,SRR4293694,184823119,14046557044,SAMN05821925,,,,,,,HCT116,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2327826,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR429/004/SRR4293694/SRR4293694.fastq.gz,6921131978,ftp.sra.ebi.ac.uk/vol1/fastq/SRR429/004/SRR4293694/SRR4293694.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR429/004/SRR4293694/SRR4293694.fastq.gz,40ebfee5952bd663ef4860875528807c,2017-01-27,2017-01-27,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,,,,,,,,,,GSM2327826_r1,,GSM2327826,,Ribosome profiling of HCT116 cells upon eIF1 knockdown treated with cycloheximide,,,,,SRS1711878,SRP090415,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR429/004/SRR4293694,6518206349,ftp.sra.ebi.ac.uk/vol1/srr/SRR429/004/SRR4293694,ftp.sra.ebi.ac.uk/vol1/srr/SRR429/004/SRR4293694,b65731f8b6fdde506e88e01d55bc4598,,GSE87328,eIF1 modulates the recognition of sub-optimal translation start sites and steers gene expression control mediated by uORFs,,,SRA478929,,,,,,,,,,,,,,colon, PRJNA344393,SRX2189158,NextSeq 500 sequencing; GSM2327827: Ribosome profiling of control HCT116 cells treated with lactimidomycin; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2327827: Ribosome profiling of control HCT116 cells treated with lactimidomycin; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN05821924,Ribosome profiling of control HCT116 cells treated with lactimidomycin,NextSeq 500,SRR4293695,199563521,15166827596,SAMN05821924,,,,,,,HCT116,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2327827,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR429/005/SRR4293695/SRR4293695.fastq.gz,6987463188,ftp.sra.ebi.ac.uk/vol1/fastq/SRR429/005/SRR4293695/SRR4293695.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR429/005/SRR4293695/SRR4293695.fastq.gz,9dc9174cada7d29d157de7454adf4c23,2017-01-27,2017-01-27,false,,,,,,,,,,,ILLUMINA,,,,2020-01-12,,SINGLE,,,,,,,,,,GSM2327827_r1,,GSM2327827,,Ribosome profiling of control HCT116 cells treated with lactimidomycin,,,,,SRS1711879,SRP090415,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR429/005/SRR4293695,6683372895,ftp.sra.ebi.ac.uk/vol1/srr/SRR429/005/SRR4293695,ftp.sra.ebi.ac.uk/vol1/srr/SRR429/005/SRR4293695,c1ab4ee26e2589bcb490ecf6ab761ecd,,GSE87328,eIF1 modulates the recognition of sub-optimal translation start sites and steers gene expression control mediated by uORFs,,,SRA478929,,,,,,,,,,,,,,colon, PRJNA344393,SRX2189159,NextSeq 500 sequencing; GSM2327828: Ribosome profiling of control HCT116 cells treated with cycloheximide; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2327828: Ribosome profiling of control HCT116 cells treated with cycloheximide; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN05821923,Ribosome profiling of control HCT116 cells treated with cycloheximide,NextSeq 500,SRR4293696,225042166,17103204616,SAMN05821923,,,,,,,HCT116,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2327828,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR429/006/SRR4293696/SRR4293696.fastq.gz,7888401921,ftp.sra.ebi.ac.uk/vol1/fastq/SRR429/006/SRR4293696/SRR4293696.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR429/006/SRR4293696/SRR4293696.fastq.gz,3d6257698d4b2894f32fb21f3accc22a,2017-01-27,2017-01-27,false,,,,,,,,,,,ILLUMINA,,,,2019-12-31,,SINGLE,,,,,,,,,,GSM2327828_r1,,GSM2327828,,Ribosome profiling of control HCT116 cells treated with cycloheximide,,,,,SRS1711881,SRP090415,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR429/006/SRR4293696,7529247487,ftp.sra.ebi.ac.uk/vol1/srr/SRR429/006/SRR4293696,ftp.sra.ebi.ac.uk/vol1/srr/SRR429/006/SRR4293696,88e2b31eec881c7a888cf1696675a436,,GSE87328,eIF1 modulates the recognition of sub-optimal translation start sites and steers gene expression control mediated by uORFs,,,SRA478929,,,,,,,,,,,,,,colon, PRJNA348553,SRX2246398,Illumina HiSeq 2000 sequencing; GSM2346474: Ribosome profiling of wild-type ecotype Landsberg erecta treated with lactimidomycin; Arabidopsis thaliana; OTHER,Illumina HiSeq 2000 sequencing; GSM2346474: Ribosome profiling of wild-type ecotype Landsberg erecta treated with lactimidomycin; Arabidopsis thaliana; OTHER,3702,Arabidopsis thaliana,OTHER,TRANSCRIPTOMIC,other,SAMN05912771,Ribosome profiling of wild-type ecotype Landsberg erecta treated with lactimidomycin,Illumina HiSeq 2000,SRR4424237,104721382,5340790482,SAMN05912771,,,,,,,,,GEO,,,,,,,,,,,,,,Landsberg erecta,,,,,,false,GSM2346474,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR442/007/SRR4424237/SRR4424237.fastq.gz,4044721427,ftp.sra.ebi.ac.uk/vol1/fastq/SRR442/007/SRR4424237/SRR4424237.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR442/007/SRR4424237/SRR4424237.fastq.gz,95953bffa1bc4c0df6c0a39b46510b7b,2016-11-26,2016-11-26,false,,,,,,,,,,,ILLUMINA,,,,2019-10-31,,SINGLE,,,,,,,,,,GSM2346474_r1,,GSM2346474,,Ribosome profiling of wild-type ecotype Landsberg erecta treated with lactimidomycin,,,,,SRS1746799,SRP091588,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR442/007/SRR4424237,3784179123,ftp.sra.ebi.ac.uk/vol1/srr/SRR442/007/SRR4424237,ftp.sra.ebi.ac.uk/vol1/srr/SRR442/007/SRR4424237,8f56afce8dcb961c2aaa2c353488e047,,GSE88790,N-terminal Proteomics Assisted Profiling of the Unexplored Translation Initiation Landscape in Arabidopsis thaliana.,,,SRA485223,,,,,,,,,,,,,,Stem explants, PRJNA348553,SRX2246399,Illumina HiSeq 2000 sequencing; GSM2346475: Ribosome profiling of wild-type ecotype Landsberg erecta treated with cycloheximide; Arabidopsis thaliana; OTHER,Illumina HiSeq 2000 sequencing; GSM2346475: Ribosome profiling of wild-type ecotype Landsberg erecta treated with cycloheximide; Arabidopsis thaliana; OTHER,3702,Arabidopsis thaliana,OTHER,TRANSCRIPTOMIC,other,SAMN05912770,Ribosome profiling of wild-type ecotype Landsberg erecta treated with cycloheximide,Illumina HiSeq 2000,SRR4424238,99524632,5075756232,SAMN05912770,,,,,,,,,GEO,,,,,,,,,,,,,,Landsberg erecta,,,,,,false,GSM2346475,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR442/008/SRR4424238/SRR4424238.fastq.gz,3950948586,ftp.sra.ebi.ac.uk/vol1/fastq/SRR442/008/SRR4424238/SRR4424238.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR442/008/SRR4424238/SRR4424238.fastq.gz,5cf244b320b222133132bdf4273182f4,2016-11-26,2016-11-26,false,,,,,,,,,,,ILLUMINA,,,,2020-04-14,,SINGLE,,,,,,,,,,GSM2346475_r1,,GSM2346475,,Ribosome profiling of wild-type ecotype Landsberg erecta treated with cycloheximide,,,,,SRS1746800,SRP091588,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR442/008/SRR4424238,3635925450,ftp.sra.ebi.ac.uk/vol1/srr/SRR442/008/SRR4424238,ftp.sra.ebi.ac.uk/vol1/srr/SRR442/008/SRR4424238,db66ba3703781e06006d291f657805c2,,GSE88790,N-terminal Proteomics Assisted Profiling of the Unexplored Translation Initiation Landscape in Arabidopsis thaliana.,,,SRA485223,,,,,,,,,,,,,,Stem explants, PRJNA158351,SRX137370,Illumina Genome Analyzer II sequencing; GSM910953: A3-1 Ribosome profiling - siLuc; Mus musculus; OTHER,Illumina Genome Analyzer II sequencing; GSM910953: A3-1 Ribosome profiling - siLuc; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN00854339,A3-1 Ribosome profiling - siLuc,Illumina Genome Analyzer II,SRR458756,21824511,785682396,SAMN00854339,,,,,,,A3-1,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM910953_1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR458/SRR458756/SRR458756.fastq.gz,657936010,ftp.sra.ebi.ac.uk/vol1/fastq/SRR458/SRR458756/SRR458756.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR458/SRR458756/SRR458756.fastq.gz,5ae1a8d53f71dc05665133da74e789c5,2013-11-11,2012-11-01,false,,,,,,,,,,,ILLUMINA,,,,2019-11-01,,SINGLE,GSM910953: A3-1 Ribosome profiling - siLuc,,,,,,,,,GSM910953_r1,,GSM910953,,A3-1 Ribosome profiling - siLuc,,,,,SRS308446,SRP012118,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR458/SRR458756,433748001,ftp.sra.ebi.ac.uk/vol1/srr/SRR458/SRR458756,ftp.sra.ebi.ac.uk/vol1/srr/SRR458/SRR458756,404aa091d81c8241b1f9e6deb0648c11,,GSE37111,Transcriptome-wide identification of LIN28A targets in mouse embryonic stem cell (A3-1) [Illumina Seq],,,SRA051495,,,,,,,,,,,,,,, PRJNA158351,SRX137371,Illumina Genome Analyzer II sequencing; GSM910954: A3-1 Ribosome profiling - siLin28a; Mus musculus; OTHER,Illumina Genome Analyzer II sequencing; GSM910954: A3-1 Ribosome profiling - siLin28a; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN00854340,A3-1 Ribosome profiling - siLin28a,Illumina Genome Analyzer II,SRR458757,18520372,666733392,SAMN00854340,,,,,,,A3-1,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM910954_1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR458/SRR458757/SRR458757.fastq.gz,532055772,ftp.sra.ebi.ac.uk/vol1/fastq/SRR458/SRR458757/SRR458757.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR458/SRR458757/SRR458757.fastq.gz,091513fb6818c6d4a47dab3d5aabf016,2013-11-11,2012-11-01,false,,,,,,,,,,,ILLUMINA,,,,2019-10-12,,SINGLE,GSM910954: A3-1 Ribosome profiling - siLin28a,,,,,,,,,GSM910954_r1,,GSM910954,,A3-1 Ribosome profiling - siLin28a,,,,,SRS308447,SRP012118,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR458/SRR458757,353889077,ftp.sra.ebi.ac.uk/vol1/srr/SRR458/SRR458757,ftp.sra.ebi.ac.uk/vol1/srr/SRR458/SRR458757,63cf1f3f6e99170381aeafcb1dcda553,,GSE37111,Transcriptome-wide identification of LIN28A targets in mouse embryonic stem cell (A3-1) [Illumina Seq],,,SRA051495,,,,,,,,,,,,,,, PRJNA353604,SRX2349147,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026356,335001052,16750052600,SAMN06017629,,,,,,,,,University Heidelberg,,,,,,,,,,,,,Dauer,,,,,,,false,Celegans_0h_post_dauer,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR502/006/SRR5026356/SRR5026356.fastq.gz,9282241962,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/006/SRR5026356/SRR5026356.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/006/SRR5026356/SRR5026356.fastq.gz,cef05f8f03cb3b6abed99fa8b8004702,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,Dauer_0h,,,,,,,,,RiboSeq_0h_post_dauer,,DAUER_0h,,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,,,,,SRS1799345,SRP093364,,,,hermaphrodite,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR502/006/SRR5026356,8622021565,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/006/SRR5026356,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/006/SRR5026356,9631a8d7680378af7ccf7ca30085cca5,N2,PRJNA353604,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,,,SRA494245,,,,,,,,hermaphrodite,,,,,,whole body, PRJNA353604,SRX2352572,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026359,66094062,3304703100,SAMN06017629,,,,,,,,,University Heidelberg,,,,,,,,,,,,,Dauer,,,,,,,false,Celegans_0.5h_post_dauer,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR502/009/SRR5026359/SRR5026359.fastq.gz,1719469242,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/009/SRR5026359/SRR5026359.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/009/SRR5026359/SRR5026359.fastq.gz,ea565483ddd3b660c0ef457b3bc23d02,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,Celegans_0.5h_post_dauer,,,,,,,,,0-5h.riboseq,,DAUER_0h,,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,,,,,SRS1799345,SRP093364,,,,hermaphrodite,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR502/009/SRR5026359,1613140446,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/009/SRR5026359,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/009/SRR5026359,4df663100fb2692b249c24411e845cd4,N2,PRJNA353604,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,,,SRA494245,,,,,,,,hermaphrodite,,,,,,whole body, PRJNA353604,SRX2352779,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026589,125934593,6296729650,SAMN06017629,,,,,,,,,University Heidelberg,,,,,,,,,,,,,Dauer,,,,,,,false,Celegans_1h_post_dauer,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR502/009/SRR5026589/SRR5026589.fastq.gz,3216191792,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/009/SRR5026589/SRR5026589.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/009/SRR5026589/SRR5026589.fastq.gz,024d1e8846923386c42eca9be065a5c7,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,Celegans_1h_post_dauer,,,,,,,,,1h.riboseq,,DAUER_0h,,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,,,,,SRS1799345,SRP093364,,,,hermaphrodite,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR502/009/SRR5026589,3035331963,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/009/SRR5026589,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/009/SRR5026589,cf21be976e011645edc8e654328e6564,N2,PRJNA353604,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,,,SRA494245,,,,,,,,hermaphrodite,,,,,,whole body, PRJNA353604,SRX2352796,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026592,109643569,5482178450,SAMN06017629,,,,,,,,,University Heidelberg,,,,,,,,,,,,,Dauer,,,,,,,false,Celegans_2h_post_dauer,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR502/002/SRR5026592/SRR5026592.fastq.gz,2713159008,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/002/SRR5026592/SRR5026592.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/002/SRR5026592/SRR5026592.fastq.gz,ceda4f1cf69af9851ee5723960644748,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,Celegans_2h_post_dauer,,,,,,,,,2h.riboseq,,DAUER_0h,,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,,,,,SRS1799345,SRP093364,,,,hermaphrodite,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR502/002/SRR5026592,2602263079,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/002/SRR5026592,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/002/SRR5026592,896bcf9a683156dd100a6fc513cef181,N2,PRJNA353604,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,,,SRA494245,,,,,,,,hermaphrodite,,,,,,whole body, PRJNA353604,SRX2352801,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026603,139378431,6968921550,SAMN06017629,,,,,,,,,University Heidelberg,,,,,,,,,,,,,Dauer,,,,,,,false,Celegans_3h_post_dauer,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR502/003/SRR5026603/SRR5026603.fastq.gz,3775584183,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/003/SRR5026603/SRR5026603.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/003/SRR5026603/SRR5026603.fastq.gz,917ef0c556bbed6eef1b296dadbe8aca,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,Celegans_3h_post_dauer,,,,,,,,,3h.riboseq,,DAUER_0h,,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,,,,,SRS1799345,SRP093364,,,,hermaphrodite,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR502/003/SRR5026603,3450861748,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/003/SRR5026603,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/003/SRR5026603,c0f444f972b31d7c457490fbc5de6408,N2,PRJNA353604,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,,,SRA494245,,,,,,,,hermaphrodite,,,,,,whole body, PRJNA353604,SRX2352818,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,Illumina HiSeq 2000 sequencing; Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SAMN06017629,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,Illumina HiSeq 2000,SRR5026637,138903638,6945181900,SAMN06017629,,,,,,,,,University Heidelberg,,,,,,,,,,,,,Dauer,,,,,,,false,Celegans_post_dauer_4h,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR502/007/SRR5026637/SRR5026637.fastq.gz,3633816582,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/007/SRR5026637/SRR5026637.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR502/007/SRR5026637/SRR5026637.fastq.gz,ed5524a653213b8567026431f8e39698,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,Celegans_post_dauer_4h,,,,,,,,,4h.riboseq,,DAUER_0h,,This sample has been submitted by pda|christoph.dieterich@med.uni-heidelberg.de on 2016-11-17; Caenorhabditis elegans,,,,,SRS1799345,SRP093364,,,,hermaphrodite,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR502/007/SRR5026637,3355136924,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/007/SRR5026637,ftp.sra.ebi.ac.uk/vol1/srr/SRR502/007/SRR5026637,d4602ae0b49b56af106297de299b24aa,N2,PRJNA353604,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,,,SRA494245,,,,,,,,hermaphrodite,,,,,,whole body, PRJNA356772,SRX2407647,NextSeq 500 sequencing; GSM2420418: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 monosomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq,NextSeq 500 sequencing; GSM2420418: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 monosomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq,216597,Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN06127036,Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 monosomes,NextSeq 500,SRR5090708,191796596,14576541296,SAMN06127036,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2420418,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR509/008/SRR5090708/SRR5090708.fastq.gz,4373797310,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/008/SRR5090708/SRR5090708.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/008/SRR5090708/SRR5090708.fastq.gz,6439372c02c1c94fb47700b0b183e404,2017-01-31,2017-01-31,false,,,,,,,,,,,ILLUMINA,,,,2020-01-05,,SINGLE,,,,,,,,,,GSM2420418_r1,,GSM2420418,,Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 monosomes,,,,,SRS1846090,SRP094797,,Typhimurium,Typhimurium,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR509/008/SRR5090708,4862549256,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/008/SRR5090708,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/008/SRR5090708,ebdb1842b38c73e6abeef9c5b476d59b,SL1344,GSE91066,REPARATION: Ribosome Profiling Assisted (Re-) Annotation of Bacterial genomes,enterica,,SRA501710,,,,,,,,,,,,,,, PRJNA356772,SRX2407648,NextSeq 500 sequencing; GSM2420419: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 polysomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq,NextSeq 500 sequencing; GSM2420419: Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 polysomes; Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344; RNA-Seq,216597,Salmonella enterica subsp. enterica serovar Typhimurium str. SL1344,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN06127035,Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 polysomes,NextSeq 500,SRR5090709,174834326,13287408776,SAMN06127035,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2420419,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR509/009/SRR5090709/SRR5090709.fastq.gz,4072225917,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/009/SRR5090709/SRR5090709.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/009/SRR5090709/SRR5090709.fastq.gz,40d8ff85d85403c64c1a047876f06075,2017-01-31,2017-01-31,false,,,,,,,,,,,ILLUMINA,,,,2020-01-05,,SINGLE,,,,,,,,,,GSM2420419_r1,,GSM2420419,,Ribosome profiling of wild type Salmonella enterica serovar Thyphimurium - strain SL1344 polysomes,,,,,SRS1846091,SRP094797,,Typhimurium,Typhimurium,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR509/009/SRR5090709,4476989901,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/009/SRR5090709,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/009/SRR5090709,13d3e9cd6842875ee86fa03f886f286a,SL1344,GSE91066,REPARATION: Ribosome Profiling Assisted (Re-) Annotation of Bacterial genomes,enterica,,SRA501710,,,,,,,,,,,,,,, PRJNA340948,SRX2416031,Illumina HiSeq 4000 sequencing; GSM2424851: Ribosome profiling-siControl-RPF; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424851: Ribosome profiling-siControl-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131999,Ribosome profiling-siControl-RPF,Illumina HiSeq 4000,SRR5099275,48648149,2432407450,SAMN06131999,,,,,,,HeLa cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2424851,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR509/005/SRR5099275/SRR5099275.fastq.gz,691016810,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/005/SRR5099275/SRR5099275.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/005/SRR5099275/SRR5099275.fastq.gz,cef449e7d84bfe0245354b1c73165f3e,2016-12-20,2016-12-20,false,,,,,,,,,,,ILLUMINA,,,,2020-01-05,,SINGLE,,,,,,,,,,GSM2424851_r1,,GSM2424851,,Ribosome profiling-siControl-RPF,,,,,SRS1853614,SRP083699,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR509/005/SRR5099275,726298711,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/005/SRR5099275,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/005/SRR5099275,ee7d02ba82b19fff3276c028bc86b37d,,GSE86214,YTHDF3 facilitates translation and decay of the N6-methyladenosine-modified RNA,,,SRA458091,,,,,,,,,,,,,,, PRJNA340948,SRX2416032,Illumina HiSeq 4000 sequencing; GSM2424852: Ribosome profiling-siControl-input; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424852: Ribosome profiling-siControl-input; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131998,Ribosome profiling-siControl-input,Illumina HiSeq 4000,SRR5099276,46915311,2345765550,SAMN06131998,,,,,,,HeLa cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2424852,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR509/006/SRR5099276/SRR5099276.fastq.gz,1076970537,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/006/SRR5099276/SRR5099276.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/006/SRR5099276/SRR5099276.fastq.gz,0e7e9c7e14f80522aa2b88eea5a53094,2016-12-20,2016-12-20,false,,,,,,,,,,,ILLUMINA,,,,2020-01-05,,SINGLE,,,,,,,,,,GSM2424852_r1,,GSM2424852,,Ribosome profiling-siControl-input,,,,,SRS1853615,SRP083699,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR509/006/SRR5099276,737085748,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/006/SRR5099276,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/006/SRR5099276,f4e58cddafd86c434a7d35d434dd5159,,GSE86214,YTHDF3 facilitates translation and decay of the N6-methyladenosine-modified RNA,,,SRA458091,,,,,,,,,,,,,,, PRJNA340948,SRX2416033,Illumina HiSeq 4000 sequencing; GSM2424853: Ribosome profiling-rep1-siYTHDF3-RPF; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424853: Ribosome profiling-rep1-siYTHDF3-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131997,Ribosome profiling-rep1-siYTHDF3-RPF,Illumina HiSeq 4000,SRR5099277,41072030,2053601500,SAMN06131997,,,,,,,HeLa cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2424853,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR509/007/SRR5099277/SRR5099277.fastq.gz,578297143,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/007/SRR5099277/SRR5099277.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/007/SRR5099277/SRR5099277.fastq.gz,f257a3036528e6d879b78d8ed0cab9e9,2016-12-20,2016-12-20,false,,,,,,,,,,,ILLUMINA,,,,2019-10-23,,SINGLE,,,,,,,,,,GSM2424853_r1,,GSM2424853,,Ribosome profiling-rep1-siYTHDF3-RPF,,,,,SRS1853616,SRP083699,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR509/007/SRR5099277,602738082,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/007/SRR5099277,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/007/SRR5099277,9a58bc1d58f3e400a45c597db08d1461,,GSE86214,YTHDF3 facilitates translation and decay of the N6-methyladenosine-modified RNA,,,SRA458091,,,,,,,,,,,,,,, PRJNA340948,SRX2416034,Illumina HiSeq 4000 sequencing; GSM2424854: Ribosome profiling-rep1-siYTHDF3-input; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424854: Ribosome profiling-rep1-siYTHDF3-input; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131996,Ribosome profiling-rep1-siYTHDF3-input,Illumina HiSeq 4000,SRR5099278,39819574,1990978700,SAMN06131996,,,,,,,HeLa cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2424854,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR509/008/SRR5099278/SRR5099278.fastq.gz,920484861,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/008/SRR5099278/SRR5099278.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/008/SRR5099278/SRR5099278.fastq.gz,32537202e57a3723fdbb6dc3c8b30d36,2016-12-20,2016-12-20,false,,,,,,,,,,,ILLUMINA,,,,2019-12-02,,SINGLE,,,,,,,,,,GSM2424854_r1,,GSM2424854,,Ribosome profiling-rep1-siYTHDF3-input,,,,,SRS1853617,SRP083699,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR509/008/SRR5099278,625331414,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/008/SRR5099278,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/008/SRR5099278,574ab53ebfdbbe80af9f7b088aad3ec2,,GSE86214,YTHDF3 facilitates translation and decay of the N6-methyladenosine-modified RNA,,,SRA458091,,,,,,,,,,,,,,, PRJNA340948,SRX2416035,Illumina HiSeq 4000 sequencing; GSM2424855: Ribosome profiling-rep2-siYTHDF3-RPF; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424855: Ribosome profiling-rep2-siYTHDF3-RPF; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131995,Ribosome profiling-rep2-siYTHDF3-RPF,Illumina HiSeq 4000,SRR5099279,48158932,2407946600,SAMN06131995,,,,,,,HeLa cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2424855,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR509/009/SRR5099279/SRR5099279.fastq.gz,641494527,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/009/SRR5099279/SRR5099279.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/009/SRR5099279/SRR5099279.fastq.gz,1b20f2dc3308e8ed937caf1b3694c8bb,2016-12-20,2016-12-20,false,,,,,,,,,,,ILLUMINA,,,,2020-01-05,,SINGLE,,,,,,,,,,GSM2424855_r1,,GSM2424855,,Ribosome profiling-rep2-siYTHDF3-RPF,,,,,SRS1853618,SRP083699,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR509/009/SRR5099279,669739668,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/009/SRR5099279,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/009/SRR5099279,2391be08d631d2dbd2e15fe7ee205a9c,,GSE86214,YTHDF3 facilitates translation and decay of the N6-methyladenosine-modified RNA,,,SRA458091,,,,,,,,,,,,,,, PRJNA340948,SRX2416036,Illumina HiSeq 4000 sequencing; GSM2424856: Ribosome profiling-rep2-siYTHDF3-input; Homo sapiens; OTHER,Illumina HiSeq 4000 sequencing; GSM2424856: Ribosome profiling-rep2-siYTHDF3-input; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06131994,Ribosome profiling-rep2-siYTHDF3-input,Illumina HiSeq 4000,SRR5099280,54048791,2702439550,SAMN06131994,,,,,,,HeLa cells,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2424856,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR509/000/SRR5099280/SRR5099280.fastq.gz,1266072525,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/000/SRR5099280/SRR5099280.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR509/000/SRR5099280/SRR5099280.fastq.gz,8a4233858bf0e092aa2e67f91ea0fd5c,2016-12-20,2016-12-20,false,,,,,,,,,,,ILLUMINA,,,,2020-04-14,,SINGLE,,,,,,,,,,GSM2424856_r1,,GSM2424856,,Ribosome profiling-rep2-siYTHDF3-input,,,,,SRS1853619,SRP083699,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR509/000/SRR5099280,852603598,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/000/SRR5099280,ftp.sra.ebi.ac.uk/vol1/srr/SRR509/000/SRR5099280,3efce33b26a5a62a909aefeed631c4ba,,GSE86214,YTHDF3 facilitates translation and decay of the N6-methyladenosine-modified RNA,,,SRA458091,,,,,,,,,,,,,,, PRJNA311041,SRX2502104,Illumina HiSeq 4000 sequencing; GSM2462933: ribosome profiling 37°C in WT with control plasmid; Escherichia coli; OTHER,Illumina HiSeq 4000 sequencing; GSM2462933: ribosome profiling 37°C in WT with control plasmid; Escherichia coli; OTHER,562,Escherichia coli,OTHER,TRANSCRIPTOMIC,other,SAMN06240270,ribosome profiling 37°C in WT with control plasmid,Illumina HiSeq 4000,SRR5186136,61670104,3145175304,SAMN06240270,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2462933,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR518/006/SRR5186136/SRR5186136.fastq.gz,1264913782,ftp.sra.ebi.ac.uk/vol1/fastq/SRR518/006/SRR5186136/SRR5186136.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR518/006/SRR5186136/SRR5186136.fastq.gz,86ebd1a7010e4acaf27b561468420367,2017-02-01,2017-02-01,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM2462933_r1,,GSM2462933,,ribosome profiling 37°C in WT with control plasmid,,,,,SRS1928104,SRP069339,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR518/006/SRR5186136,1117966721,ftp.sra.ebi.ac.uk/vol1/srr/SRR518/006/SRR5186136,ftp.sra.ebi.ac.uk/vol1/srr/SRR518/006/SRR5186136,5a3f75644b1b289d432db7ee721e9373,MG1655 [p-CTRL],GSE77617,Operon mRNAs are organized into ORF-centric structures that predict translation efficiency,,,SRA348058,,,,,,,,,,,,,,, PRJNA311041,SRX2502105,Illumina HiSeq 4000 sequencing; GSM2462934: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUA; Escherichia coli; OTHER,Illumina HiSeq 4000 sequencing; GSM2462934: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUA; Escherichia coli; OTHER,562,Escherichia coli,OTHER,TRANSCRIPTOMIC,other,SAMN06240269,ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUA,Illumina HiSeq 4000,SRR5186137,68702208,3503812608,SAMN06240269,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2462934,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR518/007/SRR5186137/SRR5186137.fastq.gz,1395250463,ftp.sra.ebi.ac.uk/vol1/fastq/SRR518/007/SRR5186137/SRR5186137.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR518/007/SRR5186137/SRR5186137.fastq.gz,99f0c35cfb9d6c43c45240427755c65c,2017-02-01,2017-02-01,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM2462934_r1,,GSM2462934,,ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUA,,,,,SRS1928105,SRP069339,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR518/007/SRR5186137,1238165622,ftp.sra.ebi.ac.uk/vol1/srr/SRR518/007/SRR5186137,ftp.sra.ebi.ac.uk/vol1/srr/SRR518/007/SRR5186137,1aa337ff6fd05756222efc2086ed239f,MG1655 [p-CUA],GSE77617,Operon mRNAs are organized into ORF-centric structures that predict translation efficiency,,,SRA348058,,,,,,,,,,,,,,, PRJNA311041,SRX2502106,Illumina HiSeq 4000 sequencing; GSM2462935: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUG; Escherichia coli; OTHER,Illumina HiSeq 4000 sequencing; GSM2462935: ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUG; Escherichia coli; OTHER,562,Escherichia coli,OTHER,TRANSCRIPTOMIC,other,SAMN06240268,ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUG,Illumina HiSeq 4000,SRR5186138,43070262,2196583362,SAMN06240268,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2462935,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR518/008/SRR5186138/SRR5186138.fastq.gz,869679697,ftp.sra.ebi.ac.uk/vol1/fastq/SRR518/008/SRR5186138/SRR5186138.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR518/008/SRR5186138/SRR5186138.fastq.gz,9f87d0512db331f3ccfaf9f0283f18a9,2017-02-01,2017-02-01,false,,,,,,,,,,,ILLUMINA,,,,2019-03-23,,SINGLE,,,,,,,,,,GSM2462935_r1,,GSM2462935,,ribosome profiling 37°C in WT with plasmid expressing mini-ORF CUG,,,,,SRS1928106,SRP069339,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR518/008/SRR5186138,776004220,ftp.sra.ebi.ac.uk/vol1/srr/SRR518/008/SRR5186138,ftp.sra.ebi.ac.uk/vol1/srr/SRR518/008/SRR5186138,269cc5e1aa7cd3bb4898afbcc8e4f009,MG1655 [p-CUG],GSE77617,Operon mRNAs are organized into ORF-centric structures that predict translation efficiency,,,SRA348058,,,,,,,,,,,,,,, PRJNA369552,SRX2532339,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with harringtonine,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with harringtonine,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06289120,This sample has been submitted by pda|zhpn1024 on 2018-03-02; Homo sapiens,Illumina HiSeq 2500,SRR5223162,31545576,1608824376,SAMN06289120,,,,,,,HEK293,,SUB2365925,,,,,,,,,,,,,,,,,,,,false,HEK293 Harr,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR522/002/SRR5223162/SRR5223162.fastq.gz,866304613,ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002/SRR5223162/SRR5223162.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/002/SRR5223162/SRR5223162.fastq.gz,aad54a5d92c8bf29206575d263ec1300,2018-09-02,2018-09-02,false,,,,,,,,,,,ILLUMINA,,,,2018-09-02,,SINGLE,HEK293 Harr,,,,,,,,,3_S3_L001_R1_001.fastq.gz,,HEK293,,This sample has been submitted by pda|zhpn1024 on 2018-03-02; Homo sapiens,,,,,SRS1953099,SRP098707,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR522/002/SRR5223162,736462742,ftp.sra.ebi.ac.uk/vol1/srr/SRR522/002/SRR5223162,ftp.sra.ebi.ac.uk/vol1/srr/SRR522/002/SRR5223162,df474810fc5d9e9c87850fa9cc043530,,PRJNA369552,HEK293 riboseq,,,SRA535048,,,,,,,,female,,,,,,kidney, PRJNA369552,SRX2532340,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with cycloheximide,Illumina HiSeq 2500 sequencing; Ribosome profiling of HEK293 cells with cycloheximide,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06289120,This sample has been submitted by pda|zhpn1024 on 2018-03-02; Homo sapiens,Illumina HiSeq 2500,SRR5223163,28042962,1430191062,SAMN06289120,,,,,,,HEK293,,SUB2365925,,,,,,,,,,,,,,,,,,,,false,HEK293 CHX,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR522/003/SRR5223163/SRR5223163.fastq.gz,821546687,ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003/SRR5223163/SRR5223163.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR522/003/SRR5223163/SRR5223163.fastq.gz,0d434ef2b7b42d6eb15cb7f9e7cf6ae6,2018-09-02,2018-09-02,false,,,,,,,,,,,ILLUMINA,,,,2018-09-02,,SINGLE,HEK293 CHX,,,,,,,,,2_S2_L001_R1_001.fastq.gz,,HEK293,,This sample has been submitted by pda|zhpn1024 on 2018-03-02; Homo sapiens,,,,,SRS1953099,SRP098707,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR522/003/SRR5223163,655407031,ftp.sra.ebi.ac.uk/vol1/srr/SRR522/003/SRR5223163,ftp.sra.ebi.ac.uk/vol1/srr/SRR522/003/SRR5223163,99a04f47a89ebc44b58451de6c9b3ba0,,PRJNA369552,HEK293 riboseq,,,SRA535048,,,,,,,,female,,,,,,kidney, PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239050,8854232,451565832,SAMN06312775,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481052,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/000/SRR5239050/SRR5239050.fastq.gz,210050153,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/000/SRR5239050/SRR5239050.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/000/SRR5239050/SRR5239050.fastq.gz,903beb2df1cc5c9175b4651c51524e61,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481052_r1,,GSM2481052,,Ribosome Profiling Ctrl Day 5,,,,,SRS1964858,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/000/SRR5239050,176359186,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/000/SRR5239050,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/000/SRR5239050,a488e7047c96077e0e3a944e2086650b,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239051,8867186,452226486,SAMN06312775,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481052,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/001/SRR5239051/SRR5239051.fastq.gz,210840279,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/001/SRR5239051/SRR5239051.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/001/SRR5239051/SRR5239051.fastq.gz,48953fb497348295eb33e84851cbfb99,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481052_r2,,GSM2481052,,Ribosome Profiling Ctrl Day 5,,,,,SRS1964858,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/001/SRR5239051,176719914,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/001/SRR5239051,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/001/SRR5239051,87b47f939d10424bd58524e3d6cc4e6e,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239052,7927705,404312955,SAMN06312775,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481052,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/002/SRR5239052/SRR5239052.fastq.gz,181088459,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/002/SRR5239052/SRR5239052.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/002/SRR5239052/SRR5239052.fastq.gz,8f15dcab434fa31fc755999f4344ae90,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481052_r3,,GSM2481052,,Ribosome Profiling Ctrl Day 5,,,,,SRS1964858,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/002/SRR5239052,153591387,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/002/SRR5239052,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/002/SRR5239052,508dc29561f6625616e78e9e4fe6a001,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239053,7894562,402622662,SAMN06312775,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481052,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/003/SRR5239053/SRR5239053.fastq.gz,180720571,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/003/SRR5239053/SRR5239053.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/003/SRR5239053/SRR5239053.fastq.gz,92c27c9ddee6cc38504dbe52098ba7f4,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481052_r4,,GSM2481052,,Ribosome Profiling Ctrl Day 5,,,,,SRS1964858,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/003/SRR5239053,153046996,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/003/SRR5239053,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/003/SRR5239053,585e437148c468f779ee93ad9a5da1a6,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239054,9216208,470026608,SAMN06312775,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481052,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/004/SRR5239054/SRR5239054.fastq.gz,220860046,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/004/SRR5239054/SRR5239054.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/004/SRR5239054/SRR5239054.fastq.gz,31df8798898d9bc7bb5b371edc8b00f8,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481052_r5,,GSM2481052,,Ribosome Profiling Ctrl Day 5,,,,,SRS1964858,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/004/SRR5239054,185537590,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/004/SRR5239054,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/004/SRR5239054,295937d822c66ad34c10fe25820ae55d,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545979,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481052: Ribosome Profiling Ctrl Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312775,Ribosome Profiling Ctrl Day 5,Illumina HiSeq 1500,SRR5239055,9218352,470135952,SAMN06312775,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481052,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/005/SRR5239055/SRR5239055.fastq.gz,222019171,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/005/SRR5239055/SRR5239055.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/005/SRR5239055/SRR5239055.fastq.gz,9f46ebf1980a108a25fcb7790809a290,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481052_r6,,GSM2481052,,Ribosome Profiling Ctrl Day 5,,,,,SRS1964858,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/005/SRR5239055,186227720,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/005/SRR5239055,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/005/SRR5239055,d9d1776df92ebd10a47f2d546f2592e3,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239056,15501047,790553397,SAMN06312774,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481053,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/006/SRR5239056/SRR5239056.fastq.gz,367834304,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/006/SRR5239056/SRR5239056.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/006/SRR5239056/SRR5239056.fastq.gz,02f8fbd0628179b12181fdbecb331c7f,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481053_r1,,GSM2481053,,Ribosome Profiling Ctrl Day 8,,,,,SRS1964862,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/006/SRR5239056,310567111,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/006/SRR5239056,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/006/SRR5239056,7d8591380666a37abede27e2b28105f5,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239057,15538226,792449526,SAMN06312774,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481053,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/007/SRR5239057/SRR5239057.fastq.gz,369348085,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/007/SRR5239057/SRR5239057.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/007/SRR5239057/SRR5239057.fastq.gz,99212c254edbf69093dc02e68959ddb6,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481053_r2,,GSM2481053,,Ribosome Profiling Ctrl Day 8,,,,,SRS1964862,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/007/SRR5239057,311394753,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/007/SRR5239057,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/007/SRR5239057,303ecf32bfff3b580c09596add05a424,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239058,12487833,636879483,SAMN06312774,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481053,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/008/SRR5239058/SRR5239058.fastq.gz,285206416,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/008/SRR5239058/SRR5239058.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/008/SRR5239058/SRR5239058.fastq.gz,e8c106d8a8e9b40d20e51925750f19ea,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481053_r3,,GSM2481053,,Ribosome Profiling Ctrl Day 8,,,,,SRS1964862,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/008/SRR5239058,243285220,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/008/SRR5239058,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/008/SRR5239058,c80f2929eb1edaee49358b07b41b4ffe,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239059,12480350,636497850,SAMN06312774,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481053,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/009/SRR5239059/SRR5239059.fastq.gz,285537387,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/009/SRR5239059/SRR5239059.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/009/SRR5239059/SRR5239059.fastq.gz,67f89e8e402c4df455be4d9d2c317d32,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481053_r4,,GSM2481053,,Ribosome Profiling Ctrl Day 8,,,,,SRS1964862,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/009/SRR5239059,243202388,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/009/SRR5239059,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/009/SRR5239059,6d05a998c13ca1767ecf2488d71a98f8,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239060,13840587,705869937,SAMN06312774,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481053,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/000/SRR5239060/SRR5239060.fastq.gz,331227497,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/000/SRR5239060/SRR5239060.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/000/SRR5239060/SRR5239060.fastq.gz,7f2d62e673e904b021c5fbdf71d38aef,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481053_r5,,GSM2481053,,Ribosome Profiling Ctrl Day 8,,,,,SRS1964862,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/000/SRR5239060,279770312,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/000/SRR5239060,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/000/SRR5239060,7b8d3e1ff2122027f8324566f02a7f52,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545980,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481053: Ribosome Profiling Ctrl Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312774,Ribosome Profiling Ctrl Day 8,Illumina HiSeq 1500,SRR5239061,13903399,709073349,SAMN06312774,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481053,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/001/SRR5239061/SRR5239061.fastq.gz,334196800,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/001/SRR5239061/SRR5239061.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/001/SRR5239061/SRR5239061.fastq.gz,d76be32f50e7185fcbeff5e132307bcb,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481053_r6,,GSM2481053,,Ribosome Profiling Ctrl Day 8,,,,,SRS1964862,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/001/SRR5239061,281925921,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/001/SRR5239061,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/001/SRR5239061,1e0a158fe0c1f897bcec1c71b1005f80,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239062,10734719,547470669,SAMN06312773,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481054,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/002/SRR5239062/SRR5239062.fastq.gz,256396003,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/002/SRR5239062/SRR5239062.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/002/SRR5239062/SRR5239062.fastq.gz,ba58e1c5725805a633cca81711b8cd33,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481054_r1,,GSM2481054,,Ribosome Profiling METTL3 KD1 Day 5,,,,,SRS1964860,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/002/SRR5239062,214718394,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/002/SRR5239062,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/002/SRR5239062,817ebc6fdb2facad01e6d04204015689,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239063,10757923,548654073,SAMN06312773,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481054,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/003/SRR5239063/SRR5239063.fastq.gz,257530525,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/003/SRR5239063/SRR5239063.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/003/SRR5239063/SRR5239063.fastq.gz,7fe1580447b08a88af1bda9157ef6544,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481054_r2,,GSM2481054,,Ribosome Profiling METTL3 KD1 Day 5,,,,,SRS1964860,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/003/SRR5239063,215339279,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/003/SRR5239063,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/003/SRR5239063,58222b12e98623b4e328c76a23ec3b6e,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239064,9189103,468644253,SAMN06312773,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481054,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/004/SRR5239064/SRR5239064.fastq.gz,211216505,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/004/SRR5239064/SRR5239064.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/004/SRR5239064/SRR5239064.fastq.gz,3bc2b04c113a26c92d0b4e571bc909ad,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481054_r3,,GSM2481054,,Ribosome Profiling METTL3 KD1 Day 5,,,,,SRS1964860,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/004/SRR5239064,178707394,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/004/SRR5239064,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/004/SRR5239064,3a21434e3f701ad08676418a59e345d0,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239065,9168761,467606811,SAMN06312773,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481054,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/005/SRR5239065/SRR5239065.fastq.gz,211175079,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/005/SRR5239065/SRR5239065.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/005/SRR5239065/SRR5239065.fastq.gz,5864153032a3a20b08bbfb06c4fe814c,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481054_r4,,GSM2481054,,Ribosome Profiling METTL3 KD1 Day 5,,,,,SRS1964860,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/005/SRR5239065,178407650,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/005/SRR5239065,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/005/SRR5239065,a65261186aa73d7ad8766bdc597d1d9d,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239066,10490820,535031820,SAMN06312773,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481054,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/006/SRR5239066/SRR5239066.fastq.gz,252820899,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/006/SRR5239066/SRR5239066.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/006/SRR5239066/SRR5239066.fastq.gz,3465871ef24390ae940ab988fe2db07f,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481054_r5,,GSM2481054,,Ribosome Profiling METTL3 KD1 Day 5,,,,,SRS1964860,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/006/SRR5239066,211861534,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/006/SRR5239066,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/006/SRR5239066,115f61c673a83fab94bbd68a822d1c0e,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545981,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481054: Ribosome Profiling METTL3 KD1 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312773,Ribosome Profiling METTL3 KD1 Day 5,Illumina HiSeq 1500,SRR5239067,10510772,536049372,SAMN06312773,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481054,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/007/SRR5239067/SRR5239067.fastq.gz,254496510,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/007/SRR5239067/SRR5239067.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/007/SRR5239067/SRR5239067.fastq.gz,c4cc9b7df2e5f7b38eb52e975ce1655d,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481054_r6,,GSM2481054,,Ribosome Profiling METTL3 KD1 Day 5,,,,,SRS1964860,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/007/SRR5239067,212982597,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/007/SRR5239067,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/007/SRR5239067,8dce45a9c54e85209af76572a1708f10,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239068,15528375,791947125,SAMN06312772,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481055,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/008/SRR5239068/SRR5239068.fastq.gz,371459008,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/008/SRR5239068/SRR5239068.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/008/SRR5239068/SRR5239068.fastq.gz,26fefc4ed834bc799a1572d6052792cc,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481055_r1,,GSM2481055,,Ribosome Profiling METTL3 KD1 Day 8,,,,,SRS1964861,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/008/SRR5239068,311105996,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/008/SRR5239068,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/008/SRR5239068,7c3367394786207217c898e87c8a0188,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239069,15552791,793192341,SAMN06312772,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481055,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/009/SRR5239069/SRR5239069.fastq.gz,372780708,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/009/SRR5239069/SRR5239069.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/009/SRR5239069/SRR5239069.fastq.gz,2597206f145cd999786b1cdcd8892d7d,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481055_r2,,GSM2481055,,Ribosome Profiling METTL3 KD1 Day 8,,,,,SRS1964861,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/009/SRR5239069,311709716,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/009/SRR5239069,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/009/SRR5239069,fc369a2be53d52b3d75bd6ad104df891,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239070,12819970,653818470,SAMN06312772,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481055,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/000/SRR5239070/SRR5239070.fastq.gz,295430416,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/000/SRR5239070/SRR5239070.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/000/SRR5239070/SRR5239070.fastq.gz,48a9fcdc280f2b176a39606a1af016cd,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481055_r3,,GSM2481055,,Ribosome Profiling METTL3 KD1 Day 8,,,,,SRS1964861,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/000/SRR5239070,249810462,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/000/SRR5239070,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/000/SRR5239070,d80e711b86c220ea2a6b461252a26d47,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239071,12805289,653069739,SAMN06312772,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481055,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/001/SRR5239071/SRR5239071.fastq.gz,295611063,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/001/SRR5239071/SRR5239071.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/001/SRR5239071/SRR5239071.fastq.gz,1b5578ef1227a97901aabbf2989d828f,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481055_r4,,GSM2481055,,Ribosome Profiling METTL3 KD1 Day 8,,,,,SRS1964861,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/001/SRR5239071,249600008,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/001/SRR5239071,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/001/SRR5239071,d56d894753fd060f29ef408eabcee285,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239072,14501119,739557069,SAMN06312772,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481055,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/002/SRR5239072/SRR5239072.fastq.gz,350257595,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/002/SRR5239072/SRR5239072.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/002/SRR5239072/SRR5239072.fastq.gz,2b97a31e96f8d91e0e1253c26fd1728f,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481055_r5,,GSM2481055,,Ribosome Profiling METTL3 KD1 Day 8,,,,,SRS1964861,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/002/SRR5239072,293285842,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/002/SRR5239072,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/002/SRR5239072,eec7d0915f42eb4abdccd95fea6c59c9,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545982,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481055: Ribosome Profiling METTL3 KD1 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312772,Ribosome Profiling METTL3 KD1 Day 8,Illumina HiSeq 1500,SRR5239073,14557524,742433724,SAMN06312772,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481055,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/003/SRR5239073/SRR5239073.fastq.gz,353122550,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/003/SRR5239073/SRR5239073.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/003/SRR5239073/SRR5239073.fastq.gz,2b38337b7f9bf0bd8e3565417d8306f3,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481055_r6,,GSM2481055,,Ribosome Profiling METTL3 KD1 Day 8,,,,,SRS1964861,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/003/SRR5239073,295320805,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/003/SRR5239073,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/003/SRR5239073,c09b9dd4d5220316fe3b8662688ec38d,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239074,10128748,516566148,SAMN06312771,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481056,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/004/SRR5239074/SRR5239074.fastq.gz,244919753,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/004/SRR5239074/SRR5239074.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/004/SRR5239074/SRR5239074.fastq.gz,db3e7e3b0eee0eb1e42ed975da192658,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481056_r1,,GSM2481056,,Ribosome Profiling METTL3 KD2 Day 5,,,,,SRS1964863,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/004/SRR5239074,204054388,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/004/SRR5239074,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/004/SRR5239074,95538bdb87940868da1dad4c0486c758,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239075,10149979,517648929,SAMN06312771,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481056,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/005/SRR5239075/SRR5239075.fastq.gz,245554818,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/005/SRR5239075/SRR5239075.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/005/SRR5239075/SRR5239075.fastq.gz,a0f91a9e0bdeefe76d0d5be6a2c19416,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481056_r2,,GSM2481056,,Ribosome Profiling METTL3 KD2 Day 5,,,,,SRS1964863,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/005/SRR5239075,204337323,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/005/SRR5239075,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/005/SRR5239075,8ee609d9aa5ea7f13fda8bcd1d0c382e,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239076,8844053,451046703,SAMN06312771,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481056,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/006/SRR5239076/SRR5239076.fastq.gz,206662863,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/006/SRR5239076/SRR5239076.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/006/SRR5239076/SRR5239076.fastq.gz,301143a811737ee4cb19afdb1f6e01ee,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481056_r3,,GSM2481056,,Ribosome Profiling METTL3 KD2 Day 5,,,,,SRS1964863,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/006/SRR5239076,173606799,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/006/SRR5239076,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/006/SRR5239076,94c19f62373ca7288e1d75a20e799e8b,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239077,8826385,450145635,SAMN06312771,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481056,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/007/SRR5239077/SRR5239077.fastq.gz,206222976,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/007/SRR5239077/SRR5239077.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/007/SRR5239077/SRR5239077.fastq.gz,31c37d29f73172e9e7b4a199d52074cc,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481056_r4,,GSM2481056,,Ribosome Profiling METTL3 KD2 Day 5,,,,,SRS1964863,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/007/SRR5239077,173083117,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/007/SRR5239077,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/007/SRR5239077,6cc7a1e7866e5e7b37cde697e9ae57eb,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239078,10169123,518625273,SAMN06312771,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481056,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/008/SRR5239078/SRR5239078.fastq.gz,248769366,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/008/SRR5239078/SRR5239078.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/008/SRR5239078/SRR5239078.fastq.gz,776a1af3d6badf336c46b4b1c03d1d73,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481056_r5,,GSM2481056,,Ribosome Profiling METTL3 KD2 Day 5,,,,,SRS1964863,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/008/SRR5239078,207087087,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/008/SRR5239078,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/008/SRR5239078,e33123a680e8c1299ad7d55c59e0df5f,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545983,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481056: Ribosome Profiling METTL3 KD2 Day 5; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312771,Ribosome Profiling METTL3 KD2 Day 5,Illumina HiSeq 1500,SRR5239079,10199333,520165983,SAMN06312771,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481056,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/009/SRR5239079/SRR5239079.fastq.gz,250235732,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/009/SRR5239079/SRR5239079.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/009/SRR5239079/SRR5239079.fastq.gz,702fcfeb08656b806a3191756258d888,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481056_r6,,GSM2481056,,Ribosome Profiling METTL3 KD2 Day 5,,,,,SRS1964863,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/009/SRR5239079,208129233,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/009/SRR5239079,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/009/SRR5239079,4a3597c266cfec8ac8747f7138523bc2,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239080,13771867,702365217,SAMN06312770,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481057,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/000/SRR5239080/SRR5239080.fastq.gz,333394651,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/000/SRR5239080/SRR5239080.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/000/SRR5239080/SRR5239080.fastq.gz,f56242e19ed2ad07a9e0ab6af6d8ebae,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481057_r1,,GSM2481057,,Ribosome Profiling METTL3 KD2 Day 8,,,,,SRS1964864,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/000/SRR5239080,275836837,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/000/SRR5239080,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/000/SRR5239080,a02a2a5b86e45ad77d59efbc4936e312,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239081,13769712,702255312,SAMN06312770,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481057,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/001/SRR5239081/SRR5239081.fastq.gz,334095813,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/001/SRR5239081/SRR5239081.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/001/SRR5239081/SRR5239081.fastq.gz,0644bfe0898131b4f470c6899986a468,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481057_r2,,GSM2481057,,Ribosome Profiling METTL3 KD2 Day 8,,,,,SRS1964864,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/001/SRR5239081,275957437,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/001/SRR5239081,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/001/SRR5239081,be44da39d63606e13cbeb4386478d140,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239082,12473768,636162168,SAMN06312770,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481057,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/002/SRR5239082/SRR5239082.fastq.gz,291671193,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/002/SRR5239082/SRR5239082.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/002/SRR5239082/SRR5239082.fastq.gz,a779da775c66a4653b2d83bdf742cb5b,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481057_r3,,GSM2481057,,Ribosome Profiling METTL3 KD2 Day 8,,,,,SRS1964864,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/002/SRR5239082,243373854,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/002/SRR5239082,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/002/SRR5239082,23926067e3cd0dcd412156b5ac91059e,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239083,12393265,632056515,SAMN06312770,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481057,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/003/SRR5239083/SRR5239083.fastq.gz,290444070,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/003/SRR5239083/SRR5239083.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/003/SRR5239083/SRR5239083.fastq.gz,d59025f509d2e2e09cb58f18221e9caa,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481057_r4,,GSM2481057,,Ribosome Profiling METTL3 KD2 Day 8,,,,,SRS1964864,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/003/SRR5239083,241948398,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/003/SRR5239083,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/003/SRR5239083,27e6068e0db767505651d0c6187fbbd2,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239084,14602972,744751572,SAMN06312770,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481057,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/004/SRR5239084/SRR5239084.fastq.gz,357691368,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/004/SRR5239084/SRR5239084.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/004/SRR5239084/SRR5239084.fastq.gz,af0d9ed32879bdd1f2de72dae568cf40,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481057_r5,,GSM2481057,,Ribosome Profiling METTL3 KD2 Day 8,,,,,SRS1964864,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/004/SRR5239084,295663803,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/004/SRR5239084,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/004/SRR5239084,d5f8262dc95d131f316d417a7d9011a2,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA371833,SRX2545984,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,Illumina HiSeq 1500 sequencing; GSM2481057: Ribosome Profiling METTL3 KD2 Day 8; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN06312770,Ribosome Profiling METTL3 KD2 Day 8,Illumina HiSeq 1500,SRR5239085,14574634,743306334,SAMN06312770,,,,,,,leukemia cell line MOLM13,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2481057,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR523/005/SRR5239085/SRR5239085.fastq.gz,358588060,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/005/SRR5239085/SRR5239085.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR523/005/SRR5239085/SRR5239085.fastq.gz,49a9b70b16854a0e70bfa075bf321f05,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2481057_r6,,GSM2481057,,Ribosome Profiling METTL3 KD2 Day 8,,,,,SRS1964864,SRP099081,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR523/005/SRR5239085,296041275,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/005/SRR5239085,ftp.sra.ebi.ac.uk/vol1/srr/SRR523/005/SRR5239085,7e7804cbbe9153ef5c9ffd046bbc88a5,,GSE94613,Promoter-bound METTL3 maintains myeloid leukemia by m6A-dependent regulation of protein translation,,,SRA536650,,,,,,,,,,,,,,, PRJNA379630,SRX2652914,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in n-alkanes,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617379,Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in n-alkanes,Illumina HiSeq 2500,SRR5356885,92012581,4600629050,SAMN06617379,,,,,,,,,,,,1984-01-04,,,"USA: Ponca City, OK",,,,,ATCC:33988,,,,,,,,,false,11836X24,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/005/SRR5356885/SRR5356885.fastq.gz,2759280290,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/005/SRR5356885/SRR5356885.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/005/SRR5356885/SRR5356885.fastq.gz,c4e6eed35adeb5ae68d2886a56cebf53,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,fuel storage tank,2017-03-19,,SINGLE,11836X24,,,,,,,,,11836X24_151104_D00294_0206_BC81GJANXX_3.fastq.gz,,33988_alk_3,,Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in n-alkanes,,,,,SRS2058105,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/005/SRR5356885,2344373906,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/005/SRR5356885,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/005/SRR5356885,2c8d864eedd316a16b91f8cc595fab6a,ATCC 33988,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652916,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in n-alkanes,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617378,Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in n-alkanes,Illumina HiSeq 2500,SRR5356887,62093655,3104682750,SAMN06617378,,,,,,,,,,,,1984-01-04,,,"USA: Ponca City, OK",,,,,ATCC:33988,,,,,,,,,false,11836X22,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/007/SRR5356887/SRR5356887.fastq.gz,2190231072,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/007/SRR5356887/SRR5356887.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/007/SRR5356887/SRR5356887.fastq.gz,52e40e67fcd7de2470cff4db841f37c6,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,fuel storage tank,2017-03-19,,SINGLE,11836X22,,,,,,,,,11836X22_151028_D00294_0205_BC81P5ANXX_8.fastq.gz,,33988_alk_2,,Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in n-alkanes,,,,,SRS2058106,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/007/SRR5356887,1785409975,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/007/SRR5356887,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/007/SRR5356887,1e3ebf153c868babec9fe5ec7886b517,ATCC 33988,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652918,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in n-alkanes,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617377,Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in n-alkanes,Illumina HiSeq 2500,SRR5356889,100563944,5028197200,SAMN06617377,,,,,,,,,,,,1984-01-04,,,"USA: Ponca City, OK",,,,,ATCC:33988,,,,,,,,,false,11836X20,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/009/SRR5356889/SRR5356889.fastq.gz,2708633003,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/009/SRR5356889/SRR5356889.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/009/SRR5356889/SRR5356889.fastq.gz,508896a6adf14d2c6fe7290a858f6a00,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,fuel storage tank,2017-03-19,,SINGLE,11836X20,,,,,,,,,11836X20_151028_D00294_0205_BC81P5ANXX_7.fastq.gz,,33988_alk_1,,Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in n-alkanes,,,,,SRS2058107,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/009/SRR5356889,2274030170,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/009/SRR5356889,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/009/SRR5356889,12b5ec258727444c2e109adf9aeaa219,ATCC 33988,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652920,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in Glycerol,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617376,Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in Glycerol,Illumina HiSeq 2500,SRR5356891,83809807,4190490350,SAMN06617376,,,,,,,,,,,,1984-01-04,,,"USA: Ponca City, OK",,,,,ATCC:33988,,,,,,,,,false,11836X18,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/001/SRR5356891/SRR5356891.fastq.gz,2584599662,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/001/SRR5356891/SRR5356891.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/001/SRR5356891/SRR5356891.fastq.gz,0d1cab86feb6be43bdf79a422a61d2d4,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,fuel storage tank,2017-03-19,,SINGLE,11836X18,,,,,,,,,11836X18_151028_D00294_0205_BC81P5ANXX_6.fastq.gz,,33988_gly_3,,Pseudomonas aeruginosa ATCC 33988 replicate 3 grown in Glycerol,,,,,SRS2058108,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/001/SRR5356891,2144235114,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/001/SRR5356891,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/001/SRR5356891,2c31c0b34d6024da75d3cfc437016735,ATCC 33988,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652922,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in Glycerol,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617375,Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in Glycerol,Illumina HiSeq 2500,SRR5356893,90928652,4546432600,SAMN06617375,,,,,,,,,,,,1984-01-04,,,"USA: Ponca City, OK",,,,,ATCC:33988,,,,,,,,,false,11836X16,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/003/SRR5356893/SRR5356893.fastq.gz,2494036133,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/003/SRR5356893/SRR5356893.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/003/SRR5356893/SRR5356893.fastq.gz,fe8dae2fc7e9361e7d16186163b17227,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,fuel storage tank,2017-03-19,,SINGLE,11836X16,,,,,,,,,11836X16_151028_D00294_0205_BC81P5ANXX_5.fastq.gz,,33988_gly_2,,Pseudomonas aeruginosa ATCC 33988 replicate 2 grown in Glycerol,,,,,SRS2058109,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/003/SRR5356893,2184499170,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/003/SRR5356893,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/003/SRR5356893,2bc439bce46bf3357319448e9475d6e5,ATCC 33988,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652924,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in Glycerol,287,Pseudomonas aeruginosa,OTHER,TRANSCRIPTOMIC,other,SAMN06617374,Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in Glycerol,Illumina HiSeq 2500,SRR5356895,106331232,5316561600,SAMN06617374,,,,,,,,,,,,1984-01-04,,,"USA: Ponca City, OK",,,,,ATCC:33988,,,,,,,,,false,11836X14,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/005/SRR5356895/SRR5356895.fastq.gz,3378368702,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/005/SRR5356895/SRR5356895.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/005/SRR5356895/SRR5356895.fastq.gz,ad65e4a699d3a21e143d3b8c42721dd7,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,fuel storage tank,2017-03-19,,SINGLE,11836X14,,,,,,,,,11836X14_151028_D00294_0205_BC81P5ANXX_4.fastq.gz,,33988_gly_1,,Pseudomonas aeruginosa ATCC 33988 replicate 1 grown in Glycerol,,,,,SRS2058110,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/005/SRR5356895,2727936094,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/005/SRR5356895,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/005/SRR5356895,2420fcd3f6402196f0956c1f13829b24,ATCC 33988,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652926,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in n-alkanes,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617373,Pseudomonas aeruginosa PAO1 replicate 3 grown in n-alkanes,Illumina HiSeq 2500,SRR5356897,101520011,5076000550,SAMN06617373,,,,,,,,,,,,1955-01-01,,,Australia: Melbourne,,,,,ATCC: 15692,,,,,,,,,false,11836X12,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/007/SRR5356897/SRR5356897.fastq.gz,2556946495,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/007/SRR5356897/SRR5356897.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/007/SRR5356897/SRR5356897.fastq.gz,ebb6984c003a30959a3136040097c6a9,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,infected wound,2017-03-19,,SINGLE,11836X12,,,,,,,,,11836X12_151028_D00294_0205_BC81P5ANXX_3.fastq.gz,,PAO1_alk_3,,Pseudomonas aeruginosa PAO1 replicate 3 grown in n-alkanes,,,,,SRS2058111,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/007/SRR5356897,2238350203,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/007/SRR5356897,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/007/SRR5356897,7bbd0c332d66670a639c73f48c97a00c,PAO1,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652928,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in n-alkanes,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617372,Pseudomonas aeruginosa PAO1 replicate 2 grown in n-alkanes,Illumina HiSeq 2500,SRR5356899,83560401,4178020050,SAMN06617372,,,,,,,,,,,,1955-01-01,,,Australia: Melbourne,,,,,ATCC: 15692,,,,,,,,,false,11836X10,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/009/SRR5356899/SRR5356899.fastq.gz,2617919791,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/009/SRR5356899/SRR5356899.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/009/SRR5356899/SRR5356899.fastq.gz,ef3c80b5c26b7e6b4cb7c92fd05fae91,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,infected wound,2017-03-19,,SINGLE,11836X10,,,,,,,,,11836X10_151028_D00294_0205_BC81P5ANXX_2.fastq.gz,,PAO1_alk_2,,Pseudomonas aeruginosa PAO1 replicate 2 grown in n-alkanes,,,,,SRS2058112,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/009/SRR5356899,2187391254,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/009/SRR5356899,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/009/SRR5356899,69cd207151da56882cad123809770cfc,PAO1,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652930,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in n-alkanes,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in n-alkanes,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617371,Pseudomonas aeruginosa PAO1 replicate 1 grown in n-alkanes,Illumina HiSeq 2500,SRR5356901,94948217,4747410850,SAMN06617371,,,,,,,,,,,,1955-01-01,,,Australia: Melbourne,,,,,ATCC: 15692,,,,,,,,,false,11836X8,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/001/SRR5356901/SRR5356901.fastq.gz,2511425092,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/001/SRR5356901/SRR5356901.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/001/SRR5356901/SRR5356901.fastq.gz,923a4bfef7b5279a2ff3e8e36b59a8da,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,infected wound,2017-03-19,,SINGLE,11836X8,,,,,,,,,11836X8_151022_D00294_0204_AC81FHANXX_8.fastq.gz,,PAO1_alk_1,,Pseudomonas aeruginosa PAO1 replicate 1 grown in n-alkanes,,,,,SRS2058113,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/001/SRR5356901,2151698241,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/001/SRR5356901,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/001/SRR5356901,7028a5502274c53b026d89374878dc9a,PAO1,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652932,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 3 grown in Glycerol,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617370,Pseudomonas aeruginosa PAO1 replicate 3 grown in Glycerol,Illumina HiSeq 2500,SRR5356903,71767127,3588356350,SAMN06617370,,,,,,,,,,,,1955-01-01,,,Australia: Melbourne,,,,,ATCC: 15692,,,,,,,,,false,11836X6,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/003/SRR5356903/SRR5356903.fastq.gz,2147268106,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/003/SRR5356903/SRR5356903.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/003/SRR5356903/SRR5356903.fastq.gz,236b2f134272bbeb1bb0f1c88bd3ab88,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,infected wound,2017-03-19,,SINGLE,11836X6,,,,,,,,,11836X6_151022_D00294_0204_AC81FHANXX_7.fastq.gz,,PAO1_gly_3,,Pseudomonas aeruginosa PAO1 replicate 3 grown in Glycerol,,,,,SRS2058114,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/003/SRR5356903,1812653965,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/003/SRR5356903,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/003/SRR5356903,d9d71f853d1f8cb3a3759dfaed6d8cd4,PAO1,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652934,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 2 grown in Glycerol,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617369,Pseudomonas aeruginosa PAO1 replicate 2 grown in Glycerol,Illumina HiSeq 2500,SRR5356905,90030430,4501521500,SAMN06617369,,,,,,,,,,,,1955-01-01,,,Australia: Melbourne,,,,,ATCC: 15692,,,,,,,,,false,11836X4,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/005/SRR5356905/SRR5356905.fastq.gz,2441472616,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/005/SRR5356905/SRR5356905.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/005/SRR5356905/SRR5356905.fastq.gz,805911a03f1e9a2b9e215d3380d4134a,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,infected wound,2017-03-19,,SINGLE,11836X4,,,,,,,,,11836X4_151022_D00294_0204_AC81FHANXX_6.fastq.gz,,PAO1_gly_2,,Pseudomonas aeruginosa PAO1 replicate 2 grown in Glycerol,,,,,SRS2058115,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/005/SRR5356905,2065038893,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/005/SRR5356905,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/005/SRR5356905,d78026bd5bffe8ea16bd3efaa4e6e23d,PAO1,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA379630,SRX2652936,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in Glycerol,Illumina HiSeq 2500 sequencing; Ribosome profiling of monosomes from Pseudomonas aeruginosa PAO1 replicate 1 grown in Glycerol,208964,Pseudomonas aeruginosa PAO1,OTHER,TRANSCRIPTOMIC,other,SAMN06617368,Pseudomonas aeruginosa PAO1 replicate 1 grown in Glycerol,Illumina HiSeq 2500,SRR5356907,73952429,3697621450,SAMN06617368,,,,,,,,,,,,1955-01-01,,,Australia: Melbourne,,,,,ATCC: 15692,,,,,,,,,false,11836X2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR535/007/SRR5356907/SRR5356907.fastq.gz,2068004986,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/007/SRR5356907/SRR5356907.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR535/007/SRR5356907/SRR5356907.fastq.gz,31fe83c39b3ce219b937e56bbb177eed,2017-03-19,2017-03-19,false,,,,,,,,,,,ILLUMINA,,,infected wound,2017-03-19,,SINGLE,11836X2,,,,,,,,,11836X2_151022_D00294_0204_AC81FHANXX_5.fastq.gz,,PAO1_gly_1,,Pseudomonas aeruginosa PAO1 replicate 1 grown in Glycerol,,,,,SRS2058116,SRP102099,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR535/007/SRR5356907,1778133075,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/007/SRR5356907,ftp.sra.ebi.ac.uk/vol1/srr/SRR535/007/SRR5356907,be0794b7ff327439e9ae21192e07f40d,PAO1,PRJNA379630,Expression Profiling Uncovers Adaptations for Growth and Survival of Pseudomonas aeruginosa Strains,,,SRA547049,,,,,,,,,,,,,,, PRJNA384569,SRX2766861,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant,4932,Saccharomyces cerevisiae,miRNA-Seq,TRANSCRIPTOMIC,PCR,SAMN06841405,RFP for puf3 ko mutant replicate 1,Illumina HiSeq 2000,SRR5483532,31667620,1583381000,SAMN06841405,,,,,,,,,,,,,,,,,,,,,,,,,,,,,false,PUF3 RFP 1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR548/002/SRR5483532/SRR5483532.fastq.gz,1205978204,ftp.sra.ebi.ac.uk/vol1/fastq/SRR548/002/SRR5483532/SRR5483532.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR548/002/SRR5483532/SRR5483532.fastq.gz,eae8597f0d5f77abc1496a9970bf8639,2017-05-21,2017-05-21,false,,,,,,,,,,,ILLUMINA,,,,2017-05-21,,SINGLE,,,,,,,,,,PUF3 RFP 1,,S1,,RFP for puf3 ko mutant replicate 1,,,,,SRS2150983,SRP105337,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR548/002/SRR5483532,1042705258,ftp.sra.ebi.ac.uk/vol1/srr/SRR548/002/SRR5483532,ftp.sra.ebi.ac.uk/vol1/srr/SRR548/002/SRR5483532,d3e839709242e8f0797542360b3ef778,puf3 mutant,PRJNA384569,Transcriptional and translational regulation of PUF3p in yeast,,,SRA557275,,,,,,,,,,,,,,, PRJNA384569,SRX2766864,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant rep2,Illumina HiSeq 2000 sequencing; Ribosome profiling for puf3 mutant rep2,4932,Saccharomyces cerevisiae,miRNA-Seq,TRANSCRIPTOMIC,PCR,SAMN06841406,RFP for puf3 ko mutant replicate 2,Illumina HiSeq 2000,SRR5483533,33068533,1653426650,SAMN06841406,,,,,,,,,,,,,,,,,,,,,,,,,,,,,false,PUF3 RFP2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR548/003/SRR5483533/SRR5483533.fastq.gz,1209049278,ftp.sra.ebi.ac.uk/vol1/fastq/SRR548/003/SRR5483533/SRR5483533.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR548/003/SRR5483533/SRR5483533.fastq.gz,f7ddf37c110f95e4f68ceaa88fc5bf54,2017-05-21,2017-05-21,false,,,,,,,,,,,ILLUMINA,,,,2017-05-21,,SINGLE,,,,,,,,,,PUF3 RFP2,,S2,,RFP for puf3 ko mutant replicate 2,,,,,SRS2150984,SRP105337,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR548/003/SRR5483533,1060329444,ftp.sra.ebi.ac.uk/vol1/srr/SRR548/003/SRR5483533,ftp.sra.ebi.ac.uk/vol1/srr/SRR548/003/SRR5483533,67de5a656e88173409935d5a3e0c0105,puf3 mutant,PRJNA384569,Transcriptional and translational regulation of PUF3p in yeast,,,SRA557275,,,,,,,,,,,,,,, PRJNA384569,SRX2766865,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep1,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep1,4932,Saccharomyces cerevisiae,miRNA-Seq,TRANSCRIPTOMIC,PCR,SAMN06841407,RFP for WT replicate 1,Illumina HiSeq 2000,SRR5483534,24523690,1226184500,SAMN06841407,,,,,,,,,,,,,,,,,,,,,,,,,,,,,false,WT RFP1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR548/004/SRR5483534/SRR5483534.fastq.gz,870221154,ftp.sra.ebi.ac.uk/vol1/fastq/SRR548/004/SRR5483534/SRR5483534.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR548/004/SRR5483534/SRR5483534.fastq.gz,5a75d065b6fc64bd4ad21e72dadff804,2017-05-21,2017-05-21,false,,,,,,,,,,,ILLUMINA,,,,2017-05-21,,SINGLE,,,,,,,,,,WT RFP1,,S3,,RFP for WT replicate 1,,,,,SRS2150985,SRP105337,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR548/004/SRR5483534,785704225,ftp.sra.ebi.ac.uk/vol1/srr/SRR548/004/SRR5483534,ftp.sra.ebi.ac.uk/vol1/srr/SRR548/004/SRR5483534,4d72479f6924c57d98be40923ce7a897,BY4742,PRJNA384569,Transcriptional and translational regulation of PUF3p in yeast,,,SRA557275,,,,,,,,,,,,,,, PRJNA384569,SRX2766866,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep2,Illumina HiSeq 2000 sequencing; Ribosome profiling WT rep2,4932,Saccharomyces cerevisiae,miRNA-Seq,TRANSCRIPTOMIC,PCR,SAMN06841408,RFP for WT replicate 2,Illumina HiSeq 2000,SRR5483539,16691481,834574050,SAMN06841408,,,,,,,,,,,,,,,,,,,,,,,,,,,,,false,WT RFP2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR548/009/SRR5483539/SRR5483539.fastq.gz,552515094,ftp.sra.ebi.ac.uk/vol1/fastq/SRR548/009/SRR5483539/SRR5483539.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR548/009/SRR5483539/SRR5483539.fastq.gz,bf57a06852a1dceef616022181c29d20,2017-05-21,2017-05-21,false,,,,,,,,,,,ILLUMINA,,,,2017-05-21,,SINGLE,,,,,,,,,,WT RFP2,,S4,,RFP for WT replicate 2,,,,,SRS2150986,SRP105337,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR548/009/SRR5483539,526809878,ftp.sra.ebi.ac.uk/vol1/srr/SRR548/009/SRR5483539,ftp.sra.ebi.ac.uk/vol1/srr/SRR548/009/SRR5483539,013ad6424fa3cbf357672588c4446e6c,BY4742,PRJNA384569,Transcriptional and translational regulation of PUF3p in yeast,,,SRA557275,,,,,,,,,,,,,,, PRJNA390134,SRX2902855,NextSeq 500 sequencing; GSM2664256: wild type ribosome profiling replicate 1; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664256: wild type ribosome profiling replicate 1; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220960,wild type ribosome profiling replicate 1,NextSeq 500,SRR5667267,46651854,1621851282,SAMN07220960,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2664256,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR566/007/SRR5667267/SRR5667267.fastq.gz,845620694,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/007/SRR5667267/SRR5667267.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/007/SRR5667267/SRR5667267.fastq.gz,203d05399f16e9d59a374fd4176b0ee7,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2664256_r1,,GSM2664256,,wild type ribosome profiling replicate 1,,,,,SRS2269413,SRP108999,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR566/007/SRR5667267,790656128,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/007/SRR5667267,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/007/SRR5667267,8482003b4f0fe18902c1145245181d84,,GSE99920,Transcriptional and ribosome profiling of Drosophila 3rd instar larvae muscle,,,SRA573547,,,,,,,,,,,,,,body wall muscle, PRJNA390134,SRX2902856,NextSeq 500 sequencing; GSM2664257: wild type ribosome profiling replicate 2; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664257: wild type ribosome profiling replicate 2; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220959,wild type ribosome profiling replicate 2,NextSeq 500,SRR5667268,122734505,4216803822,SAMN07220959,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2664257,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR566/008/SRR5667268/SRR5667268.fastq.gz,2148789443,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/008/SRR5667268/SRR5667268.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/008/SRR5667268/SRR5667268.fastq.gz,87128e073bb14f21d82ea77a09a9eea5,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2664257_r1,,GSM2664257,,wild type ribosome profiling replicate 2,,,,,SRS2269414,SRP108999,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR566/008/SRR5667268,2046001247,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/008/SRR5667268,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/008/SRR5667268,3b927e4957ea6477fe747e29814599d1,,GSE99920,Transcriptional and ribosome profiling of Drosophila 3rd instar larvae muscle,,,SRA573547,,,,,,,,,,,,,,body wall muscle, PRJNA390134,SRX2902857,NextSeq 500 sequencing; GSM2664258: wild type ribosome profiling replicate 3; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664258: wild type ribosome profiling replicate 3; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220958,wild type ribosome profiling replicate 3,NextSeq 500,SRR5667269,45156367,1539402070,SAMN07220958,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2664258,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR566/009/SRR5667269/SRR5667269.fastq.gz,747955309,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/009/SRR5667269/SRR5667269.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/009/SRR5667269/SRR5667269.fastq.gz,fa93b94510636a6fa61b2c4537dba30a,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2664258_r1,,GSM2664258,,wild type ribosome profiling replicate 3,,,,,SRS2269415,SRP108999,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR566/009/SRR5667269,724210768,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/009/SRR5667269,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/009/SRR5667269,b5ba1af123e378386e2abfe4a075e4e4,,GSE99920,Transcriptional and ribosome profiling of Drosophila 3rd instar larvae muscle,,,SRA573547,,,,,,,,,,,,,,body wall muscle, PRJNA390134,SRX2902864,NextSeq 500 sequencing; GSM2664265: GluRIIA ribosome profiling replicate 1; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664265: GluRIIA ribosome profiling replicate 1; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220951,GluRIIA ribosome profiling replicate 1,NextSeq 500,SRR5667276,35199688,1194135764,SAMN07220951,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2664265,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR566/006/SRR5667276/SRR5667276.fastq.gz,585167551,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/006/SRR5667276/SRR5667276.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/006/SRR5667276/SRR5667276.fastq.gz,e63f63cd939914cdba5d58b0a9163bb8,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2664265_r1,,GSM2664265,,GluRIIA ribosome profiling replicate 1,,,,,SRS2269422,SRP108999,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR566/006/SRR5667276,563789445,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/006/SRR5667276,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/006/SRR5667276,7cb43a932b68388836cbad9db0b54740,,GSE99920,Transcriptional and ribosome profiling of Drosophila 3rd instar larvae muscle,,,SRA573547,,,,,,,,,,,,,,body wall muscle, PRJNA390134,SRX2902865,NextSeq 500 sequencing; GSM2664266: GluRIIA ribosome profiling replicate 2; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664266: GluRIIA ribosome profiling replicate 2; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220950,GluRIIA ribosome profiling replicate 2,NextSeq 500,SRR5667277,78959629,2610438767,SAMN07220950,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2664266,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR566/007/SRR5667277/SRR5667277.fastq.gz,1299719825,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/007/SRR5667277/SRR5667277.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/007/SRR5667277/SRR5667277.fastq.gz,5702346baecffd8b254eb9bcfc027c49,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2664266_r1,,GSM2664266,,GluRIIA ribosome profiling replicate 2,,,,,SRS2269423,SRP108999,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR566/007/SRR5667277,1237800996,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/007/SRR5667277,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/007/SRR5667277,67007cd9ba20024ab550adc91d8aa33e,,GSE99920,Transcriptional and ribosome profiling of Drosophila 3rd instar larvae muscle,,,SRA573547,,,,,,,,,,,,,,body wall muscle, PRJNA390134,SRX2902866,NextSeq 500 sequencing; GSM2664267: GluRIIA ribosome profiling replicate 3; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664267: GluRIIA ribosome profiling replicate 3; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220949,GluRIIA ribosome profiling replicate 3,NextSeq 500,SRR5667278,20752434,676573468,SAMN07220949,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2664267,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR566/008/SRR5667278/SRR5667278.fastq.gz,298031311,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/008/SRR5667278/SRR5667278.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/008/SRR5667278/SRR5667278.fastq.gz,913dd763e510dcaaab4bdb546f5ccd46,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2664267_r1,,GSM2664267,,GluRIIA ribosome profiling replicate 3,,,,,SRS2269424,SRP108999,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR566/008/SRR5667278,300705871,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/008/SRR5667278,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/008/SRR5667278,93246517d1fd360f7ccf437f28b7d30d,,GSE99920,Transcriptional and ribosome profiling of Drosophila 3rd instar larvae muscle,,,SRA573547,,,,,,,,,,,,,,body wall muscle, PRJNA390134,SRX2902870,NextSeq 500 sequencing; GSM2664271: Tor-OE ribosome profiling replicate 1; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664271: Tor-OE ribosome profiling replicate 1; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220945,Tor-OE ribosome profiling replicate 1,NextSeq 500,SRR5667282,56343352,1940386794,SAMN07220945,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2664271,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR566/002/SRR5667282/SRR5667282.fastq.gz,1039067482,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/002/SRR5667282/SRR5667282.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/002/SRR5667282/SRR5667282.fastq.gz,89920c5a5a28d3682d9270a97e2a0d86,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2664271_r1,,GSM2664271,,Tor-OE ribosome profiling replicate 1,,,,,SRS2269428,SRP108999,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR566/002/SRR5667282,948500321,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/002/SRR5667282,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/002/SRR5667282,148ab23ca2783ca7acb2cac26b0be304,,GSE99920,Transcriptional and ribosome profiling of Drosophila 3rd instar larvae muscle,,,SRA573547,,,,,,,,,,,,,,body wall muscle, PRJNA390134,SRX2902871,NextSeq 500 sequencing; GSM2664272: Tor-OE ribosome profiling replicate 2; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664272: Tor-OE ribosome profiling replicate 2; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220944,Tor-OE ribosome profiling replicate 2,NextSeq 500,SRR5667283,32872272,1104998701,SAMN07220944,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2664272,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR566/003/SRR5667283/SRR5667283.fastq.gz,560825724,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/003/SRR5667283/SRR5667283.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/003/SRR5667283/SRR5667283.fastq.gz,3c3dadb82875b803f2ceee2df47debf9,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2664272_r1,,GSM2664272,,Tor-OE ribosome profiling replicate 2,,,,,SRS2269429,SRP108999,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR566/003/SRR5667283,536285119,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/003/SRR5667283,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/003/SRR5667283,9e32a4efdd3d94394e05101a81fab443,,GSE99920,Transcriptional and ribosome profiling of Drosophila 3rd instar larvae muscle,,,SRA573547,,,,,,,,,,,,,,body wall muscle, PRJNA390134,SRX2902872,NextSeq 500 sequencing; GSM2664273: Tor-OE ribosome profiling replicate 3; Drosophila melanogaster; OTHER,NextSeq 500 sequencing; GSM2664273: Tor-OE ribosome profiling replicate 3; Drosophila melanogaster; OTHER,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,other,SAMN07220943,Tor-OE ribosome profiling replicate 3,NextSeq 500,SRR5667284,69053087,2392506309,SAMN07220943,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2664273,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR566/004/SRR5667284/SRR5667284.fastq.gz,1184225838,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/004/SRR5667284/SRR5667284.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR566/004/SRR5667284/SRR5667284.fastq.gz,6502e27a509e302f192dcd164092943b,2017-12-01,2017-12-01,false,,,,,,,,,,,ILLUMINA,,,,2017-12-01,,SINGLE,,,,,,,,,,GSM2664273_r1,,GSM2664273,,Tor-OE ribosome profiling replicate 3,,,,,SRS2269430,SRP108999,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR566/004/SRR5667284,1139635695,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/004/SRR5667284,ftp.sra.ebi.ac.uk/vol1/srr/SRR566/004/SRR5667284,ebd73c99c7eba82859d3b1f4c68e5239,,GSE99920,Transcriptional and ribosome profiling of Drosophila 3rd instar larvae muscle,,,SRA573547,,,,,,,,,,,,,,body wall muscle, PRJNA391352,SRX2943745,"Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266693,"Ribosome Profiling Input for WT, rep1",Illumina HiSeq 2000,SRR5735992,16800285,2553643320,SAMN07266693,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678049,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/002/SRR5735992/SRR5735992_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/002/SRR5735992/SRR5735992_2.fastq.gz,804802402;828198168,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/002/SRR5735992/SRR5735992_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/002/SRR5735992/SRR5735992_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/002/SRR5735992/SRR5735992_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/002/SRR5735992/SRR5735992_2.fastq.gz,ebc3f5ad830f5183c99d3070401486cb;83a503b49f2045fdbd1e02f8fad3e8b6,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,PAIRED,,,,,,,,,,GSM2678049_r1,,GSM2678049,,"Ribosome Profiling Input for WT, rep1",,,,,SRS2303471,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/002/SRR5735992,1405154213,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/002/SRR5735992,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/002/SRR5735992,479d236a58ae07628cc84a5f5a02b23f,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943745,"Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678049: Ribosome Profiling Input for WT, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266693,"Ribosome Profiling Input for WT, rep1",Illumina HiSeq 2000,SRR5735993,8361509,1270949368,SAMN07266693,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678049,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/003/SRR5735993/SRR5735993_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/003/SRR5735993/SRR5735993_2.fastq.gz,407874131;415209435,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/003/SRR5735993/SRR5735993_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/003/SRR5735993/SRR5735993_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/003/SRR5735993/SRR5735993_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/003/SRR5735993/SRR5735993_2.fastq.gz,d8aa96d52fda1d99d2b71918fc7b4223;b3660a62af134c805a4ee4f4a74e292e,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,PAIRED,,,,,,,,,,GSM2678049_r2,,GSM2678049,,"Ribosome Profiling Input for WT, rep1",,,,,SRS2303471,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/003/SRR5735993,704034539,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/003/SRR5735993,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/003/SRR5735993,c158e5f104d2b91d628e95acbb31176d,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943746,"Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266700,"Ribosome Profiling Input for WT, rep2",Illumina HiSeq 2000,SRR5735994,15807404,2402725408,SAMN07266700,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678050,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/004/SRR5735994/SRR5735994_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/004/SRR5735994/SRR5735994_2.fastq.gz,801234949;819218542,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/004/SRR5735994/SRR5735994_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/004/SRR5735994/SRR5735994_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/004/SRR5735994/SRR5735994_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/004/SRR5735994/SRR5735994_2.fastq.gz,37aaab510e25c2639d8c4307d42bfb82;e5d1cf0a8366ecfdf64b6123332d13c7,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,PAIRED,,,,,,,,,,GSM2678050_r1,,GSM2678050,,"Ribosome Profiling Input for WT, rep2",,,,,SRS2303472,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/004/SRR5735994,1345811197,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/004/SRR5735994,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/004/SRR5735994,119011a0cbbebdc85fae7b2f836c196e,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943746,"Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678050: Ribosome Profiling Input for WT, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266700,"Ribosome Profiling Input for WT, rep2",Illumina HiSeq 2000,SRR5735995,7892805,1199706360,SAMN07266700,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678050,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/005/SRR5735995/SRR5735995_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/005/SRR5735995/SRR5735995_2.fastq.gz,407866159;413021316,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/005/SRR5735995/SRR5735995_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/005/SRR5735995/SRR5735995_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/005/SRR5735995/SRR5735995_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/005/SRR5735995/SRR5735995_2.fastq.gz,bceb22e0da4c99e078f8e96b085c469b;687afc05ad13f854f36d4dc0f89d6856,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,PAIRED,,,,,,,,,,GSM2678050_r2,,GSM2678050,,"Ribosome Profiling Input for WT, rep2",,,,,SRS2303472,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/005/SRR5735995,678949413,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/005/SRR5735995,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/005/SRR5735995,ea56f284842195a7150f06d9a174c18b,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943747,"Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266699,"Ribosome Profiling Input for KO, rep1",Illumina HiSeq 2000,SRR5735996,17287993,2627774936,SAMN07266699,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678051,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/006/SRR5735996/SRR5735996_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/006/SRR5735996/SRR5735996_2.fastq.gz,891067824;899971260,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/006/SRR5735996/SRR5735996_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/006/SRR5735996/SRR5735996_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/006/SRR5735996/SRR5735996_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/006/SRR5735996/SRR5735996_2.fastq.gz,4cd32c9930963e22ef607f6aae16b47f;c738ec2e04b942511c2d59bef20be7bc,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,PAIRED,,,,,,,,,,GSM2678051_r1,,GSM2678051,,"Ribosome Profiling Input for KO, rep1",,,,,SRS2303473,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/006/SRR5735996,1498742247,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/006/SRR5735996,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/006/SRR5735996,c91d70b890fb41981bad92e105c66ce6,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943747,"Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678051: Ribosome Profiling Input for KO, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266699,"Ribosome Profiling Input for KO, rep1",Illumina HiSeq 2000,SRR5735997,8808526,1338895952,SAMN07266699,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678051,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/007/SRR5735997/SRR5735997_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/007/SRR5735997/SRR5735997_2.fastq.gz,462613505;463762946,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/007/SRR5735997/SRR5735997_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/007/SRR5735997/SRR5735997_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/007/SRR5735997/SRR5735997_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/007/SRR5735997/SRR5735997_2.fastq.gz,d3125aae7e01c8eaafa691729b4f1fb1;5f1626943ea9a844e0bffc88388b6e37,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,PAIRED,,,,,,,,,,GSM2678051_r2,,GSM2678051,,"Ribosome Profiling Input for KO, rep1",,,,,SRS2303473,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/007/SRR5735997,772648245,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/007/SRR5735997,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/007/SRR5735997,17bc9fe5a2f598aaad1b75d5e1fbb2cf,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943748,"Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266698,"Ribosome Profiling Input for KO, rep2",Illumina HiSeq 2000,SRR5735998,16011015,2433674280,SAMN07266698,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678052,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/008/SRR5735998/SRR5735998_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/008/SRR5735998/SRR5735998_2.fastq.gz,790579007;816417040,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/008/SRR5735998/SRR5735998_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/008/SRR5735998/SRR5735998_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/008/SRR5735998/SRR5735998_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/008/SRR5735998/SRR5735998_2.fastq.gz,de99b58cbeb172fe569a4c6c5e0d9671;94aeabba5d29a6b0e595284a2e5ebc45,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,PAIRED,,,,,,,,,,GSM2678052_r1,,GSM2678052,,"Ribosome Profiling Input for KO, rep2",,,,,SRS2303474,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/008/SRR5735998,1386290747,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/008/SRR5735998,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/008/SRR5735998,48c747f87034555415d2c10d0dcb171d,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943748,"Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678052: Ribosome Profiling Input for KO, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266698,"Ribosome Profiling Input for KO, rep2",Illumina HiSeq 2000,SRR5735999,8221919,1249731688,SAMN07266698,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678052,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/009/SRR5735999/SRR5735999_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/009/SRR5735999/SRR5735999_2.fastq.gz,414064302;423285504,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/009/SRR5735999/SRR5735999_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/009/SRR5735999/SRR5735999_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/009/SRR5735999/SRR5735999_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/009/SRR5735999/SRR5735999_2.fastq.gz,7444dfa892a9094a8091bb647ec9f497;af05df09f4f73074ba26141189fa971a,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,PAIRED,,,,,,,,,,GSM2678052_r2,,GSM2678052,,"Ribosome Profiling Input for KO, rep2",,,,,SRS2303474,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/009/SRR5735999,719400857,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/009/SRR5735999,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/009/SRR5735999,39b179e52d5dae3a6665f9ff009591a7,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943749,"Illumina HiSeq 2000 sequencing; GSM2678053: WT Ribosome Profiling, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678053: WT Ribosome Profiling, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266697,"WT Ribosome Profiling, rep1",Illumina HiSeq 2000,SRR5736000,49930735,3794735860,SAMN07266697,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678053,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/000/SRR5736000/SRR5736000.fastq.gz,1571641698,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/000/SRR5736000/SRR5736000.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/000/SRR5736000/SRR5736000.fastq.gz,9c67853e0233bd4179850ee02de8fad0,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,SINGLE,,,,,,,,,,GSM2678053_r1,,GSM2678053,,"WT Ribosome Profiling, rep1",,,,,SRS2303475,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/000/SRR5736000,1667435954,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/000/SRR5736000,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/000/SRR5736000,7c7369996a5f43724b34bd3027e76af4,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943750,"Illumina HiSeq 2000 sequencing; GSM2678054: WT Ribosome Profiling, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678054: WT Ribosome Profiling, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266696,"WT Ribosome Profiling, rep2",Illumina HiSeq 2000,SRR5736001,72687482,5524248632,SAMN07266696,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678054,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/001/SRR5736001/SRR5736001.fastq.gz,2260813739,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/001/SRR5736001/SRR5736001.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/001/SRR5736001/SRR5736001.fastq.gz,091d0b6b5b7841b7e7e877f1b85a8d46,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,SINGLE,,,,,,,,,,GSM2678054_r1,,GSM2678054,,"WT Ribosome Profiling, rep2",,,,,SRS2303476,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/001/SRR5736001,2409348721,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/001/SRR5736001,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/001/SRR5736001,4823b21fd874b9157c074c89e4e1f374,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943751,"Illumina HiSeq 2000 sequencing; GSM2678055: KO Ribosome Profiling, rep1; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678055: KO Ribosome Profiling, rep1; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266695,"KO Ribosome Profiling, rep1",Illumina HiSeq 2000,SRR5736002,64000307,4864023332,SAMN07266695,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678055,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/002/SRR5736002/SRR5736002.fastq.gz,2097265673,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/002/SRR5736002/SRR5736002.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/002/SRR5736002/SRR5736002.fastq.gz,cebfeab3adb62d610f29af12bb593ac3,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,SINGLE,,,,,,,,,,GSM2678055_r1,,GSM2678055,,"KO Ribosome Profiling, rep1",,,,,SRS2303477,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/002/SRR5736002,2156346787,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/002/SRR5736002,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/002/SRR5736002,b582a2fabfee345e8b50b256c6fdad67,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA391352,SRX2943752,"Illumina HiSeq 2000 sequencing; GSM2678056: KO Ribosome Profiling, rep2; Mus musculus; RNA-Seq","Illumina HiSeq 2000 sequencing; GSM2678056: KO Ribosome Profiling, rep2; Mus musculus; RNA-Seq",10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07266694,"KO Ribosome Profiling, rep2",Illumina HiSeq 2000,SRR5736003,64705916,4917649616,SAMN07266694,,,,,,,,CD4+ T cells,,,,,,,,,,,,,,,,,,,,,false,GSM2678056,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR573/003/SRR5736003/SRR5736003.fastq.gz,1964225704,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/003/SRR5736003/SRR5736003.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR573/003/SRR5736003/SRR5736003.fastq.gz,9629a2d184f298c8189c69e9f0c0d166,2017-10-17,2017-10-17,false,,,,,,,,,,,ILLUMINA,,,,2017-10-17,,SINGLE,,,,,,,,,,GSM2678056_r1,,GSM2678056,,"KO Ribosome Profiling, rep2",,,,,SRS2303478,SRP110047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR573/003/SRR5736003,2145811383,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/003/SRR5736003,ftp.sra.ebi.ac.uk/vol1/srr/SRR573/003/SRR5736003,1c7c9ab122fa6740e6f4ccc1003c91ed,,GSE100332,Next-generation sequencing measuring ribosome mRNA occupancy and translation efficiency in CD4+ T cells isolated from Mettl3 KO and WT mice,,,SRA578725,,,,,,,,,,,,,,, PRJNA392904,SRX2979029,Illumina HiSeq 4000 sequencing; GSM2692350: ribosome profiling 0h; Mus musculus; OTHER,Illumina HiSeq 4000 sequencing; GSM2692350: ribosome profiling 0h; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07312004,ribosome profiling 0h,Illumina HiSeq 4000,SRR5799562,64408917,1800217292,SAMN07312004,,,,,,,,macrophage,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2692350,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR579/002/SRR5799562/SRR5799562.fastq.gz,1543605863,ftp.sra.ebi.ac.uk/vol1/fastq/SRR579/002/SRR5799562/SRR5799562.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR579/002/SRR5799562/SRR5799562.fastq.gz,e3937fa08159b23847c7f7ba1e00e8dc,2017-12-16,2017-12-16,false,,,,,,,,,,,ILLUMINA,,,,2017-12-16,,SINGLE,,,,,,,,,,GSM2692350_r1,,GSM2692350,,ribosome profiling 0h,,,,,SRS2332923,SRP110982,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR579/002/SRR5799562,1250157142,ftp.sra.ebi.ac.uk/vol1/srr/SRR579/002/SRR5799562,ftp.sra.ebi.ac.uk/vol1/srr/SRR579/002/SRR5799562,70efec1f9badfeb3f75fd9badad4ebdc,C57BL/6,GSE100739,Ribosome binding RNA from mouse macrophage cells,,,SRA583356,,,,,,,,,,,,,,peritoneum, PRJNA392904,SRX2979030,Illumina HiSeq 4000 sequencing; GSM2692351: ribosome profiling 12h; Mus musculus; OTHER,Illumina HiSeq 4000 sequencing; GSM2692351: ribosome profiling 12h; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07312003,ribosome profiling 12h,Illumina HiSeq 4000,SRR5799563,142369751,4133742550,SAMN07312003,,,,,,,,macrophage,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2692351,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR579/003/SRR5799563/SRR5799563.fastq.gz,3463650493,ftp.sra.ebi.ac.uk/vol1/fastq/SRR579/003/SRR5799563/SRR5799563.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR579/003/SRR5799563/SRR5799563.fastq.gz,184c39afad204aaf8615a8a1ff1aa9e2,2017-12-16,2017-12-16,false,,,,,,,,,,,ILLUMINA,,,,2017-12-16,,SINGLE,,,,,,,,,,GSM2692351_r1,,GSM2692351,,ribosome profiling 12h,,,,,SRS2332924,SRP110982,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR579/003/SRR5799563,2835170622,ftp.sra.ebi.ac.uk/vol1/srr/SRR579/003/SRR5799563,ftp.sra.ebi.ac.uk/vol1/srr/SRR579/003/SRR5799563,1e4599269478425a5934132b9a8a4be3,C57BL/6,GSE100739,Ribosome binding RNA from mouse macrophage cells,,,SRA583356,,,,,,,,,,,,,,peritoneum, PRJNA399166,SRX3110787,Illumina HiSeq 2000 sequencing; GSM2747838: Ribosome Profiling H19:H391; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747838: Ribosome Profiling H19:H391; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525042,Ribosome Profiling H19:H391,Illumina HiSeq 2000,SRR5952328,202796598,10139829900,SAMN07525042,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747838,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/008/SRR5952328/SRR5952328.fastq.gz,7283170564,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/008/SRR5952328/SRR5952328.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/008/SRR5952328/SRR5952328.fastq.gz,cefde3da6da098bf1d70bf12fd318ba1,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747838_r1,,GSM2747838,,Ribosome Profiling H19:H391,,,,,SRS2445869,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/008/SRR5952328,6636238527,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/008/SRR5952328,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/008/SRR5952328,0834b1b9f2a767e821ac0099bdf3a214,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110788,Illumina HiSeq 2000 sequencing; GSM2747839: Ribosome Profiling SECIS1 deletion2; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747839: Ribosome Profiling SECIS1 deletion2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525041,Ribosome Profiling SECIS1 deletion2,Illumina HiSeq 2000,SRR5952329,202925674,10146283700,SAMN07525041,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747839,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/009/SRR5952329/SRR5952329.fastq.gz,7084633046,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/009/SRR5952329/SRR5952329.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/009/SRR5952329/SRR5952329.fastq.gz,a6164754871efd114b64c972f508f623,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747839_r1,,GSM2747839,,Ribosome Profiling SECIS1 deletion2,,,,,SRS2445870,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/009/SRR5952329,6592084765,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/009/SRR5952329,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/009/SRR5952329,27ec78ddcb2a286d5ad7fe14c0981fc8,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110789,Illumina HiSeq 2000 sequencing; GSM2747840: Ribosome Profiling SECIS1 deletion3; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747840: Ribosome Profiling SECIS1 deletion3; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525040,Ribosome Profiling SECIS1 deletion3,Illumina HiSeq 2000,SRR5952330,196597095,9829854750,SAMN07525040,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747840,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/000/SRR5952330/SRR5952330.fastq.gz,6867172355,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/000/SRR5952330/SRR5952330.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/000/SRR5952330/SRR5952330.fastq.gz,37a557a63fd958b60dbf6f66ec4dd815,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747840_r1,,GSM2747840,,Ribosome Profiling SECIS1 deletion3,,,,,SRS2445872,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/000/SRR5952330,6379408570,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/000/SRR5952330,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/000/SRR5952330,a30c35339f16fdc65088ca3b109a1579,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110790,Illumina HiSeq 2000 sequencing; GSM2747841: Ribosome Profiling SECIS1 WT1; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747841: Ribosome Profiling SECIS1 WT1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525039,Ribosome Profiling SECIS1 WT1,Illumina HiSeq 2000,SRR5952331,202636712,10131835600,SAMN07525039,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747841,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/001/SRR5952331/SRR5952331.fastq.gz,7368280040,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/001/SRR5952331/SRR5952331.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/001/SRR5952331/SRR5952331.fastq.gz,10958c7f794fdd343cc984c9df97bff8,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747841_r1,,GSM2747841,,Ribosome Profiling SECIS1 WT1,,,,,SRS2445871,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/001/SRR5952331,6666238713,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/001/SRR5952331,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/001/SRR5952331,a17c3d9b6b03f9131f8967801796512f,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110791,Illumina HiSeq 2000 sequencing; GSM2747842: Ribosome Profiling SECIS1 WT2; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747842: Ribosome Profiling SECIS1 WT2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525038,Ribosome Profiling SECIS1 WT2,Illumina HiSeq 2000,SRR5952332,189180961,9459048050,SAMN07525038,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747842,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/002/SRR5952332/SRR5952332.fastq.gz,6521547385,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/002/SRR5952332/SRR5952332.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/002/SRR5952332/SRR5952332.fastq.gz,6fe24d5c873ff2c9c8bdfa957486c0ae,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747842_r1,,GSM2747842,,Ribosome Profiling SECIS1 WT2,,,,,SRS2445873,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/002/SRR5952332,6031582349,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/002/SRR5952332,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/002/SRR5952332,af7a7ee34a7daf1390e1272f2616feea,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110792,Illumina HiSeq 2000 sequencing; GSM2747843: Ribosome Profiling SECIS1 WT3; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747843: Ribosome Profiling SECIS1 WT3; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525037,Ribosome Profiling SECIS1 WT3,Illumina HiSeq 2000,SRR5952333,175785634,8789281700,SAMN07525037,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747843,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/003/SRR5952333/SRR5952333.fastq.gz,5777507290,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/003/SRR5952333/SRR5952333.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/003/SRR5952333/SRR5952333.fastq.gz,30f768c9f6fdd8fff6e2b8253ce790d5,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747843_r1,,GSM2747843,,Ribosome Profiling SECIS1 WT3,,,,,SRS2445874,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/003/SRR5952333,5569694828,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/003/SRR5952333,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/003/SRR5952333,012fcf9a09fd28132f825fd816ed5876,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110799,Illumina HiSeq 2000 sequencing; GSM2747850: Ribosome Profiling SECIS2 WT1; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747850: Ribosome Profiling SECIS2 WT1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525028,Ribosome Profiling SECIS2 WT1,Illumina HiSeq 2000,SRR5952340,228456278,11422813900,SAMN07525028,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747850,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/000/SRR5952340/SRR5952340.fastq.gz,6271896637,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/000/SRR5952340/SRR5952340.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/000/SRR5952340/SRR5952340.fastq.gz,272550e6f369b08be28ccf497d4e556d,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747850_r1,,GSM2747850,,Ribosome Profiling SECIS2 WT1,,,,,SRS2445882,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/000/SRR5952340,5487171218,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/000/SRR5952340,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/000/SRR5952340,f42502a689ddad6342ea68cbd177b4f0,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110800,Illumina HiSeq 2000 sequencing; GSM2747851: Ribosome Profiling SECIS2 WT2; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747851: Ribosome Profiling SECIS2 WT2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525032,Ribosome Profiling SECIS2 WT2,Illumina HiSeq 2000,SRR5952341,188204162,9410208100,SAMN07525032,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747851,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/001/SRR5952341/SRR5952341.fastq.gz,4749049771,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/001/SRR5952341/SRR5952341.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/001/SRR5952341/SRR5952341.fastq.gz,4f1d45b869e51f35255c1ce94771fedc,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747851_r1,,GSM2747851,,Ribosome Profiling SECIS2 WT2,,,,,SRS2445881,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/001/SRR5952341,4353390107,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/001/SRR5952341,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/001/SRR5952341,2309c417022fec31dfe6dda7d3db7bcc,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110801,Illumina HiSeq 2000 sequencing; GSM2747852: Ribosome Profiling SECIS2 WT3; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747852: Ribosome Profiling SECIS2 WT3; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525031,Ribosome Profiling SECIS2 WT3,Illumina HiSeq 2000,SRR5952342,203369022,10168451100,SAMN07525031,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747852,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/002/SRR5952342/SRR5952342.fastq.gz,5397566773,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/002/SRR5952342/SRR5952342.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/002/SRR5952342/SRR5952342.fastq.gz,b93d4e440a23b3bf23b7e082ff163d4d,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747852_r1,,GSM2747852,,Ribosome Profiling SECIS2 WT3,,,,,SRS2445883,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/002/SRR5952342,4650016651,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/002/SRR5952342,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/002/SRR5952342,3ada49d7577d3039fe3179c5e26fcc33,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110802,Illumina HiSeq 2000 sequencing; GSM2747853: Ribosome Profiling SECIS2 deletion1; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747853: Ribosome Profiling SECIS2 deletion1; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525030,Ribosome Profiling SECIS2 deletion1,Illumina HiSeq 2000,SRR5952343,202822349,10141117450,SAMN07525030,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747853,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/003/SRR5952343/SRR5952343.fastq.gz,5447569814,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/003/SRR5952343/SRR5952343.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/003/SRR5952343/SRR5952343.fastq.gz,e1eb0e4b1e237a66311d03a6331f1447,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747853_r1,,GSM2747853,,Ribosome Profiling SECIS2 deletion1,,,,,SRS2445884,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/003/SRR5952343,4579502517,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/003/SRR5952343,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/003/SRR5952343,5a81adf84ff9b9c63d1d8e3ef674b503,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110803,Illumina HiSeq 2000 sequencing; GSM2747854: Ribosome Profiling SECIS2 deletion2; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747854: Ribosome Profiling SECIS2 deletion2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525019,Ribosome Profiling SECIS2 deletion2,Illumina HiSeq 2000,SRR5952344,226331185,11316559250,SAMN07525019,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747854,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/004/SRR5952344/SRR5952344.fastq.gz,6297077994,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/004/SRR5952344/SRR5952344.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/004/SRR5952344/SRR5952344.fastq.gz,3a52c05b266c0186a2ebdc9a850df5ba,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747854_r1,,GSM2747854,,Ribosome Profiling SECIS2 deletion2,,,,,SRS2445885,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/004/SRR5952344,5310019014,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/004/SRR5952344,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/004/SRR5952344,30462afbebfa32e872d9d6b8205a48b0,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA399166,SRX3110804,Illumina HiSeq 2000 sequencing; GSM2747855: Ribosome Profiling SECIS2 deletion3; Mus musculus; OTHER,Illumina HiSeq 2000 sequencing; GSM2747855: Ribosome Profiling SECIS2 deletion3; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN07525027,Ribosome Profiling SECIS2 deletion3,Illumina HiSeq 2000,SRR5952345,197895247,9894762350,SAMN07525027,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2747855,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR595/005/SRR5952345/SRR5952345.fastq.gz,5230819396,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/005/SRR5952345/SRR5952345.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR595/005/SRR5952345/SRR5952345.fastq.gz,44e0cc4b0fd4928fa94d730373ab4d83,2017-11-09,2017-11-09,false,,,,,,,,,,,ILLUMINA,,,,2017-11-09,,SINGLE,,,,,,,,,,GSM2747855_r1,,GSM2747855,,Ribosome Profiling SECIS2 deletion3,,,,,SRS2445886,SRP115915,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR595/005/SRR5952345,4518127888,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/005/SRR5952345,ftp.sra.ebi.ac.uk/vol1/srr/SRR595/005/SRR5952345,3c8ec00209bc94098a5be34d80e4c56f,C57BL6,GSE102890,Multiple RNA structures affect translation initiation and UGA redefinition efficiency during synthesis of selenoprotein p,,,SRA601692,,,,,,,,,,,,,,liver, PRJNA401857,SRX3157107,Illumina Genome Analyzer II sequencing; GSM2770989: Ribosome profiling at 37°C in WT cells_1; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770989: Ribosome profiling at 37°C in WT cells_1; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602624,Ribosome profiling at 37°C in WT cells_1,Illumina Genome Analyzer II,SRR6001737,20671753,614302032,SAMN07602624,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770989,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/007/SRR6001737/SRR6001737.fastq.gz,600683832,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/007/SRR6001737/SRR6001737.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/007/SRR6001737/SRR6001737.fastq.gz,621b0af316bce0524af9ac02a770649b,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770989_r1,,GSM2770989,,Ribosome profiling at 37°C in WT cells_1,,,,,SRS2488598,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/007/SRR6001737,478304404,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/007/SRR6001737,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/007/SRR6001737,20e0e25f567b158cbe316071787c8f2e,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,37.0,,, PRJNA401857,SRX3157108,Illumina Genome Analyzer II sequencing; GSM2770990: Ribosome profiling 10 min after shift to 10°C in WT cells_1; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770990: Ribosome profiling 10 min after shift to 10°C in WT cells_1; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602623,Ribosome profiling 10 min after shift to 10°C in WT cells_1,Illumina Genome Analyzer II,SRR6001738,16625543,487122180,SAMN07602623,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770990,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/008/SRR6001738/SRR6001738.fastq.gz,462043643,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/008/SRR6001738/SRR6001738.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/008/SRR6001738/SRR6001738.fastq.gz,335d1d42ff113348d8f496fab96aeb46,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770990_r1,,GSM2770990,,Ribosome profiling 10 min after shift to 10°C in WT cells_1,,,,,SRS2488599,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/008/SRR6001738,379862210,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/008/SRR6001738,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/008/SRR6001738,e0bc787fa6fde9575e48b2d69a892a07,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157109,Illumina Genome Analyzer II sequencing; GSM2770991: Ribosome profiling 30 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770991: Ribosome profiling 30 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602622,Ribosome profiling 30 min after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001739,8816443,253931666,SAMN07602622,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770991,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/009/SRR6001739/SRR6001739.fastq.gz,244823047,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/009/SRR6001739/SRR6001739.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/009/SRR6001739/SRR6001739.fastq.gz,f5c11c9da360d792836b04e6c67ee2e8,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770991_r1,,GSM2770991,,Ribosome profiling 30 min after shift to 10°C in WT cells,,,,,SRS2488600,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/009/SRR6001739,205088398,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/009/SRR6001739,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/009/SRR6001739,a313f3c6577701036d46f35f2222ec43,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157110,Illumina Genome Analyzer II sequencing; GSM2770992: Ribosome profiling 2 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770992: Ribosome profiling 2 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602621,Ribosome profiling 2 hr after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001740,7472980,210323047,SAMN07602621,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770992,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/000/SRR6001740/SRR6001740.fastq.gz,204580637,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/000/SRR6001740/SRR6001740.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/000/SRR6001740/SRR6001740.fastq.gz,c881f8703a8b51adc0a59828f99ff04e,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770992_r1,,GSM2770992,,Ribosome profiling 2 hr after shift to 10°C in WT cells,,,,,SRS2488601,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/000/SRR6001740,169304021,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/000/SRR6001740,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/000/SRR6001740,f409a6c2b5b2c31455cb04396e242da3,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157111,Illumina Genome Analyzer II sequencing; GSM2770993: Ribosome profiling 3 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770993: Ribosome profiling 3 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602620,Ribosome profiling 3 hr after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001741,16047781,463280196,SAMN07602620,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770993,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/001/SRR6001741/SRR6001741.fastq.gz,428739939,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/001/SRR6001741/SRR6001741.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/001/SRR6001741/SRR6001741.fastq.gz,d8e2eb73a632b8bc700550e89fdca92e,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770993_r1,,GSM2770993,,Ribosome profiling 3 hr after shift to 10°C in WT cells,,,,,SRS2488602,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/001/SRR6001741,362094881,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/001/SRR6001741,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/001/SRR6001741,4a0a8f863b14338581c18576542af939,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157112,Illumina Genome Analyzer II sequencing; GSM2770994: Ribosome profiling 4 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770994: Ribosome profiling 4 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602619,Ribosome profiling 4 hr after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001742,5968378,168325033,SAMN07602619,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770994,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/002/SRR6001742/SRR6001742.fastq.gz,164379066,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/002/SRR6001742/SRR6001742.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/002/SRR6001742/SRR6001742.fastq.gz,885835e47e87df242a95e4691690097f,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770994_r1,,GSM2770994,,Ribosome profiling 4 hr after shift to 10°C in WT cells,,,,,SRS2488603,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/002/SRR6001742,135443979,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/002/SRR6001742,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/002/SRR6001742,00ba9b017476b6bae009c9f96ef19cd3,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157113,Illumina Genome Analyzer II sequencing; GSM2770995: Ribosome profiling 6 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina Genome Analyzer II sequencing; GSM2770995: Ribosome profiling 6 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602618,Ribosome profiling 6 hr after shift to 10°C in WT cells,Illumina Genome Analyzer II,SRR6001743,6838687,194508545,SAMN07602618,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770995,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/003/SRR6001743/SRR6001743.fastq.gz,196367701,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/003/SRR6001743/SRR6001743.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/003/SRR6001743/SRR6001743.fastq.gz,47435f8cd5273a93ea6d0eb905c05ccc,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770995_r1,,GSM2770995,,Ribosome profiling 6 hr after shift to 10°C in WT cells,,,,,SRS2488604,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/003/SRR6001743,156971696,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/003/SRR6001743,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/003/SRR6001743,257929c040e546b5d0c06520ec41d697,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157114,Illumina HiSeq 2000 sequencing; GSM2770996: Ribosome profiling 5 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770996: Ribosome profiling 5 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602617,Ribosome profiling 5 min after shift to 10°C in WT cells,Illumina HiSeq 2000,SRR6001744,38289935,1914496750,SAMN07602617,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770996,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/004/SRR6001744/SRR6001744.fastq.gz,1546928388,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/004/SRR6001744/SRR6001744.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/004/SRR6001744/SRR6001744.fastq.gz,1ca876ff26ffb3a1a8b5499093487c4b,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770996_r1,,GSM2770996,,Ribosome profiling 5 min after shift to 10°C in WT cells,,,,,SRS2488605,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/004/SRR6001744,1313696264,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/004/SRR6001744,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/004/SRR6001744,8ec602ab51d3112ecb92b7b161876f1d,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157115,Illumina HiSeq 2000 sequencing; GSM2770997: Ribosome profiling 10 min after shift to 10°C in WT cells_2; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770997: Ribosome profiling 10 min after shift to 10°C in WT cells_2; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602616,Ribosome profiling 10 min after shift to 10°C in WT cells_2,Illumina HiSeq 2000,SRR6001745,11745422,587271100,SAMN07602616,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770997,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/005/SRR6001745/SRR6001745.fastq.gz,507051861,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/005/SRR6001745/SRR6001745.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/005/SRR6001745/SRR6001745.fastq.gz,3c878e39cc2acdb46b10be29d290d824,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770997_r1,,GSM2770997,,Ribosome profiling 10 min after shift to 10°C in WT cells_2,,,,,SRS2488606,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/005/SRR6001745,417505001,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/005/SRR6001745,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/005/SRR6001745,e745ed23ca89dc62ec6498a45a68e75d,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157116,Illumina HiSeq 2000 sequencing; GSM2770998: Ribosome profiling 15 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770998: Ribosome profiling 15 min after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602615,Ribosome profiling 15 min after shift to 10°C in WT cells,Illumina HiSeq 2000,SRR6001746,16428973,821448650,SAMN07602615,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770998,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/006/SRR6001746/SRR6001746.fastq.gz,687861621,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/006/SRR6001746/SRR6001746.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/006/SRR6001746/SRR6001746.fastq.gz,f70ec6de9199830e65cb88bb8642b151,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770998_r1,,GSM2770998,,Ribosome profiling 15 min after shift to 10°C in WT cells,,,,,SRS2488607,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/006/SRR6001746,583807662,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/006/SRR6001746,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/006/SRR6001746,f03a59dcb162ad1f23d30e282a413137,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157117,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602614,Ribosome profiling 8 hr after shift to 10°C in WT cells,Illumina HiSeq 2000,SRR6001747,11769741,600256791,SAMN07602614,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770999,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/007/SRR6001747/SRR6001747.fastq.gz,480622909,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/007/SRR6001747/SRR6001747.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/007/SRR6001747/SRR6001747.fastq.gz,d7d96165d29b83bb6133e0436fcb31c3,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770999_r1,,GSM2770999,,Ribosome profiling 8 hr after shift to 10°C in WT cells,,,,,SRS2488608,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/007/SRR6001747,428628504,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/007/SRR6001747,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/007/SRR6001747,eff13a3a4e1e2676da8a97f7f8dc9e8e,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157117,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2770999: Ribosome profiling 8 hr after shift to 10°C in WT cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602614,Ribosome profiling 8 hr after shift to 10°C in WT cells,Illumina HiSeq 2000,SRR6001748,11622124,592728324,SAMN07602614,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2770999,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/008/SRR6001748/SRR6001748.fastq.gz,440343038,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/008/SRR6001748/SRR6001748.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/008/SRR6001748/SRR6001748.fastq.gz,fc64cf1719c2c83407d93560a40957b1,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2770999_r2,,GSM2770999,,Ribosome profiling 8 hr after shift to 10°C in WT cells,,,,,SRS2488608,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/008/SRR6001748,396662824,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/008/SRR6001748,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/008/SRR6001748,15a40408b47b5da11b831cb2cbfffbb7,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157118,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602613,Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells,Illumina HiSeq 2000,SRR6001749,12537556,639415356,SAMN07602613,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2771000,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/009/SRR6001749/SRR6001749.fastq.gz,516251150,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/009/SRR6001749/SRR6001749.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/009/SRR6001749/SRR6001749.fastq.gz,b603d8edea58568b26ca39aa77a06fe3,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2771000_r1,,GSM2771000,,Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells,,,,,SRS2488610,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/009/SRR6001749,457233107,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/009/SRR6001749,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/009/SRR6001749,85e72e0c1659ec74aa12bab12e3933b7,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157118,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2771000: Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602613,Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells,Illumina HiSeq 2000,SRR6001750,12383731,631570281,SAMN07602613,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2771000,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/000/SRR6001750/SRR6001750.fastq.gz,467363752,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/000/SRR6001750/SRR6001750.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/000/SRR6001750/SRR6001750.fastq.gz,241779465d9a5a993dfc22428c9ee1df,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2771000_r2,,GSM2771000,,Ribosome profiling 8 hr after shift to 10°C in ∆cspABEG cells,,,,,SRS2488610,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/000/SRR6001750,418521537,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/000/SRR6001750,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/000/SRR6001750,8b0dfa96116e8e6bca6699e28dc2541d,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,10.0,,, PRJNA401857,SRX3157119,Illumina HiSeq 2000 sequencing; GSM2771001: Ribosome profiling at 37°C in WT cells_2; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2771001: Ribosome profiling at 37°C in WT cells_2; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602612,Ribosome profiling at 37°C in WT cells_2,Illumina HiSeq 2000,SRR6001751,61258516,3124184316,SAMN07602612,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2771001,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/001/SRR6001751/SRR6001751.fastq.gz,2470633554,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/001/SRR6001751/SRR6001751.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/001/SRR6001751/SRR6001751.fastq.gz,a60b30605af964d564609716b0a9c895,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2771001_r1,,GSM2771001,,Ribosome profiling at 37°C in WT cells_2,,,,,SRS2488609,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/001/SRR6001751,2064958495,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/001/SRR6001751,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/001/SRR6001751,a739266108e6bbc7b428eb1dba79fefd,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,37.0,,, PRJNA401857,SRX3157120,Illumina HiSeq 2000 sequencing; GSM2771002: Ribosome profiling at 37°C in ∆cspABCEG cells; Escherichia coli; RNA-Seq,Illumina HiSeq 2000 sequencing; GSM2771002: Ribosome profiling at 37°C in ∆cspABCEG cells; Escherichia coli; RNA-Seq,562,Escherichia coli,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN07602611,Ribosome profiling at 37°C in ∆cspABCEG cells,Illumina HiSeq 2000,SRR6001752,59003587,3009182937,SAMN07602611,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2771002,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR600/002/SRR6001752/SRR6001752.fastq.gz,2352736870,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/002/SRR6001752/SRR6001752.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR600/002/SRR6001752/SRR6001752.fastq.gz,46aa4b37edcd91dc6d043834b16b55a6,2018-04-24,2018-04-24,false,,,,,,,,,,,ILLUMINA,,,,2018-04-24,,SINGLE,,,,,,,,,,GSM2771002_r1,,GSM2771002,,Ribosome profiling at 37°C in ∆cspABCEG cells,,,,,SRS2488611,SRP117035,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR600/002/SRR6001752,1991075823,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/002/SRR6001752,ftp.sra.ebi.ac.uk/vol1/srr/SRR600/002/SRR6001752,627132fd58f09c78291bf8da29901072,,GSE103421,A stress response that monitors and regulates mRNA structure is central to cold-shock adaptation,,,SRA605192,,,,,,,,,,,,37.0,,, PRJNA171327,SRX172315,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #1","Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #1",9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01093931,"Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #1",Illumina HiSeq 2000,SRR618770,9742062,467618976,SAMN01093931,,,,,,,,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_CHX_Rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR618/SRR618770/SRR618770.fastq.gz,391236032,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618770/SRR618770.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618770/SRR618770.fastq.gz,cf8dea7953b14511e7cc47776fb6c55d,2013-11-11,2012-12-04,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,HEK293_CHX_Rep1,,,,,,,,,HEK293_CHX_Rep1,,HEK293_CHX_Rep1,,"Ribosome profiling reads from HEK293 cells treated with 100 μM cycloheximide for 30 min, technical replicate #1.",,,,,SRS351805,SRP014629,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR618/SRR618770,334062448,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618770,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618770,6484a83bd165c2ee75332e942c4017e9,,PRJNA171327,Global mapping of translation initiation sites in mammalian cells at single-nucleotide resolution,,,SRA056377,,,,,,,,,,,,,,, PRJNA171327,SRX172361,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #2","Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #2",9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01093932,"Ribosome profiling of HEK293 cells treated with cycloheximide, technical replicate #2",Illumina HiSeq 2000,SRR618771,44827310,2151710880,SAMN01093932,,,,,,,,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_CHX_Rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR618/SRR618771/SRR618771.fastq.gz,1604419425,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618771/SRR618771.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618771/SRR618771.fastq.gz,23881146dcd14cc8a87427012970e85e,2013-11-11,2012-12-04,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,HEK293_CHX_Rep2,,,,,,,,,HEK293_CHX_Rep2,,HEK293_CHX_Rep2,,"Ribosome profiling reads from HEK293 cells treated with 100 μM cycloheximide for 30 min, technical replicate #2.",,,,,SRS351806,SRP014629,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR618/SRR618771,1407611585,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618771,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618771,6f8f96ee421ad2b4bf5d73084eaa73ce,,PRJNA171327,Global mapping of translation initiation sites in mammalian cells at single-nucleotide resolution,,,SRA056377,,,,,,,,,,,,,,, PRJNA171327,SRX172360,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #1","Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #1",9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01093933,"Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #1",Illumina HiSeq 2000,SRR618772,15628782,750181536,SAMN01093933,,,,,,,,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_LTM_Rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR618/SRR618772/SRR618772.fastq.gz,598139843,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618772/SRR618772.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618772/SRR618772.fastq.gz,c3f09fb5dfb3c203df34cb92d83fe62e,2013-11-11,2012-12-04,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,HEK293_LTM_Rep1,,,,,,,,,HEK293_LTM_Rep1,,HEK293_LTM_Rep1,,"Ribosome profiling reads from HEK293 cells treated with 50 μM lactimidomycin for 30 min, technical replicate #1.",,,,,SRS351807,SRP014629,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR618/SRR618772,515451684,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618772,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618772,3a43ea00b3e7c9ede32c070ae66e08d2,,PRJNA171327,Global mapping of translation initiation sites in mammalian cells at single-nucleotide resolution,,,SRA056377,,,,,,,,,,,,,,, PRJNA171327,SRX172392,"Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #2","Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #2",9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01093934,"Ribosome profiling of HEK293 cells treated with lactimidomycin, technical replicate #2",Illumina HiSeq 2000,SRR618773,28457106,1365941088,SAMN01093934,,,,,,,,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_LTM_Rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR618/SRR618773/SRR618773.fastq.gz,997314708,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618773/SRR618773.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618773/SRR618773.fastq.gz,462d83a06ef643a2b7057495522a7572,2013-11-11,2012-12-04,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,HEK293_LTM_Rep2,,,,,,,,,HEK293_LTM_Rep2,,HEK293_LTM_Rep2,,"Ribosome profiling reads from HEK293 cells treated with 50 μM lactimidomycin for 30 min, technical replicate #2.",,,,,SRS351808,SRP014629,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR618/SRR618773,892080678,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618773,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618773,bf1f6b42dd31d858526add9003c117fa,,PRJNA171327,Global mapping of translation initiation sites in mammalian cells at single-nucleotide resolution,,,SRA056377,,,,,,,,,,,,,,, PRJNA171327,SRX172393,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with cycloheximide,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with cycloheximide,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01094235,Ribosome profiling of MEF cells treated with cycloheximide,Illumina HiSeq 2000,SRR618774,25957180,1245944640,SAMN01094235,,,,,,,,,Cornell University,,,,,,,,,,,,,,,,,,,,false,MEF_CHX,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR618/SRR618774/SRR618774.fastq.gz,983676970,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618774/SRR618774.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618774/SRR618774.fastq.gz,51ba731ecd68564ec937152e9a4c826e,2013-11-11,2012-12-04,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,MEF_CHX,,,,,,,,,MEF_CHX,,MEF_CHX,,Ribosome profiling reads from mouse embryonic fibroblasts treated with 100 μM cycloheximide for 30 min.,,,,,SRS351809,SRP014629,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR618/SRR618774,803543933,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618774,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618774,c1f012640b0e9a7d1004b73fea8e4c05,,PRJNA171327,Global mapping of translation initiation sites in mammalian cells at single-nucleotide resolution,,,SRA056377,,,,,,,,,,,,,,, PRJNA171327,SRX172394,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with lactimidomycin,Illumina HiSeq 2000 sequencing; Ribosome profiling of MEF cells treated with lactimidomycin,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01094236,Ribosome profiling of MEF cells treated with lactimidomycin,Illumina HiSeq 2000,SRR618775,43068755,2067300240,SAMN01094236,,,,,,,,,Cornell University,,,,,,,,,,,,,,,,,,,,false,MEF_LTM,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR618/SRR618775/SRR618775.fastq.gz,1585957554,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618775/SRR618775.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR618/SRR618775/SRR618775.fastq.gz,0dc0302cb31eaca671ceadce53732675,2013-11-11,2012-12-04,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,MEF_LTM,,,,,,,,,MEF_LTM,,MEF_LTM,,Ribosome profiling reads from mouse embryonic fibroblasts treated with 50 μM lactimidomycin for 30 min.,,,,,SRS351810,SRP014629,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR618/SRR618775,1318274553,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618775,ftp.sra.ebi.ac.uk/vol1/srr/SRR618/SRR618775,208bdb1a59602b2948d25b6ca8ad81fb,,PRJNA171327,Global mapping of translation initiation sites in mammalian cells at single-nucleotide resolution,,,SRA056377,,,,,,,,,,,,,,, PRJNA181016,SRX205658,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 1,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 1,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816428,HEK293_CON_Rep1,Illumina Genome Analyzer II,SRR619082,10167363,416861883,SAMN01816428,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_CON_Rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619082/SRR619082.fastq.gz,355581196,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619082/SRR619082.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619082/SRR619082.fastq.gz,4d094427f9cf757cd9417edb9e4e4e1a,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2016-06-28,,SINGLE,,,,,,,,,,HEK293_CON_Rep1,,HEK293_CON_Rep1,,Ribosome profiling of HEK293 cells no treatment control biological replicate 1,,,,,SRS376432,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619082,275486813,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619082,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619082,fb020bfc9f1a18223ae96aa7a3617339,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205661,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 2,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells no treatment control biological replicate 2,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816429,HEK293_CON_Rep2,Illumina HiSeq 2000,SRR619083,48902334,2347312032,SAMN01816429,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_CON_Rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619083/SRR619083.fastq.gz,1631565510,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619083/SRR619083.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619083/SRR619083.fastq.gz,5840b958be6dff58116897aa45ded3d3,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_CON_Rep2,,HEK293_CON_Rep2,,Ribosome profiling of HEK293 cells no treatment control biological replicate 2,,,,,SRS376435,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619083,1448402669,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619083,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619083,1c7a15365cbe3ae19d80f0f8e61c4b75,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205662,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 1,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 1,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816430,HEK293_AZC+MG132_Rep1,Illumina Genome Analyzer II,SRR619084,10921343,447775063,SAMN01816430,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_AZC MG132_Rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619084/SRR619084.fastq.gz,354056853,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619084/SRR619084.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619084/SRR619084.fastq.gz,a10482f0ecd2cf9e6b0e1aacb1d9e5b0,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2016-06-28,,SINGLE,,,,,,,,,,EK293_AZC MG132_Rep1,,HEK293_AZC+MG132_Rep1,,Ribosome profiling of HEK293 cells treated with 10 millimolar AZC and 20 micromolar MG132 for 1 hour biological replicate 1,,,,,SRS376436,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619084,278746920,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619084,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619084,51883e0abcc308b65ccc4d1e5fa42a67,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205663,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 2,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with AZC and MG132 biological replicate 2,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816431,HEK293_AZC+MG132_Rep2,Illumina HiSeq 2000,SRR619085,42857031,2057137488,SAMN01816431,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_AZC MG132_Rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619085/SRR619085.fastq.gz,1397813876,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619085/SRR619085.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619085/SRR619085.fastq.gz,cd99100d870682283cb225979ab93b42,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_AZC MG132_Rep2,,HEK293_AZC+MG132_Rep2,,Ribosome profiling of HEK293 cells treated with 10 millimolar AZC and 20 micromolar MG132 for 1 hour biological replicate 2,,,,,SRS376437,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619085,1275824781,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619085,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619085,0c1013b564118621c221e5934c4b40d7,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205664,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC only,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with AZC only,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816432,HEK293_AZC,Illumina Genome Analyzer II,SRR619086,5553281,227684521,SAMN01816432,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_AZC,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619086/SRR619086.fastq.gz,181580008,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619086/SRR619086.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619086/SRR619086.fastq.gz,ac898f79e806e830570576b42afb664d,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2016-06-28,,SINGLE,,,,,,,,,,HEK293_AZC,,HEK293_AZC,,Ribosome profiling of HEK293 cells treated with 10 millimolar AZC alone for 1 hour,,,,,SRS376438,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619086,141390438,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619086,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619086,665b357e0fab7e2a465b2b95908e2107,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205665,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with MG132 only,Illumina Genome Analyzer II sequencing; Ribosome profiling of HEK293 cells treated with MG132 only,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816433,HEK293_MG132,Illumina Genome Analyzer II,SRR619087,10922721,447831561,SAMN01816433,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_MG132,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619087/SRR619087.fastq.gz,343080445,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619087/SRR619087.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619087/SRR619087.fastq.gz,81c9078c23d75681880dfd6dcd297964,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2016-06-28,,SINGLE,,,,,,,,,,HEK293_MG132,,HEK293_MG132,,Ribosome profiling of HEK293 cells treated with 20 micromolar MG132 alone for 1 hour,,,,,SRS376439,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619087,274586809,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619087,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619087,26533690b87a26f32a746ce297f27f5e,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205666,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816434,HEK293_DMSO,Illumina HiSeq 2000,SRR619088,10086263,484140624,SAMN01816434,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_DMSO,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619088/SRR619088.fastq.gz,320190787,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619088/SRR619088.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619088/SRR619088.fastq.gz,e810f67ddbcd23e47747b5616ad555ff,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_DMSO_R1,,HEK293_DMSO,,Ribosome profiling of HEK293 cells treated with DMSO for 1 hour,,,,,SRS376440,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619088,282858493,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619088,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619088,9df7d5e135dbe9d0fa9c68092fe9095a,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205666,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with DMSO,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816434,HEK293_DMSO,Illumina HiSeq 2000,SRR619089,4286560,205754880,SAMN01816434,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_DMSO,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619089/SRR619089.fastq.gz,150476930,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619089/SRR619089.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619089/SRR619089.fastq.gz,720476fa4a15baa990ecfef744bc9586,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_DMSO_R2,,HEK293_DMSO,,Ribosome profiling of HEK293 cells treated with DMSO for 1 hour,,,,,SRS376440,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619089,128468209,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619089,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619089,ec0007b0bb5ba3610d98bc6f801c7d07,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205667,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816435,HEK293_VER,Illumina HiSeq 2000,SRR619090,8919827,428151696,SAMN01816435,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_VER,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619090/SRR619090.fastq.gz,273904058,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619090/SRR619090.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619090/SRR619090.fastq.gz,8ca83c9cc802ba5addea809d88b37c3e,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_VER_R1,,HEK293_VER,,Ribosome profiling of HEK293 cells treated with 100 micromolar VER155008 for 1 hour,,,,,SRS376441,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619090,246911505,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619090,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619090,8654bdca5acd659421dbd6fe745e1644,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205667,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with VER,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816435,HEK293_VER,Illumina HiSeq 2000,SRR619091,3924183,188360784,SAMN01816435,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_VER,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619091/SRR619091.fastq.gz,135819886,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619091/SRR619091.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619091/SRR619091.fastq.gz,795d4c583e19b7d8e50c32219ffa5cd5,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_VER_R2,,HEK293_VER,,Ribosome profiling of HEK293 cells treated with 100 micromolar VER155008 for 1 hour,,,,,SRS376441,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619091,117622053,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619091,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619091,4b84de513c9503ea337e706a909e6323,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205668,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816436,HEK293_PES,Illumina HiSeq 2000,SRR619092,8469084,406516032,SAMN01816436,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_PES,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619092/SRR619092.fastq.gz,255796242,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619092/SRR619092.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619092/SRR619092.fastq.gz,75fd1bdb7c745e00af73b7827a06e1e9,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_PES_R1,,HEK293_PES,,Ribosome profiling of HEK293 cells treated with 50 micromolar 2-phenylethynesulfonamide for 1 hour,,,,,SRS376442,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619092,231394329,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619092,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619092,8aa10810c53baea68baf4686b2dfda36,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205668,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with PES,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816436,HEK293_PES,Illumina HiSeq 2000,SRR619093,3737571,179403408,SAMN01816436,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_PES,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619093/SRR619093.fastq.gz,128065875,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619093/SRR619093.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619093/SRR619093.fastq.gz,a92662c475c9d94c8baeb783a3f3f833,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_PES_R2,,HEK293_PES,,Ribosome profiling of HEK293 cells treated with 50 micromolar 2-phenylethynesulfonamide for 1 hour,,,,,SRS376442,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619093,110391085,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619093,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619093,3b86436f9b6edab596119f70fb667dad,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205669,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816437,HEK293_GA,Illumina HiSeq 2000,SRR619094,9294787,446149776,SAMN01816437,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_GA,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619094/SRR619094.fastq.gz,286114760,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619094/SRR619094.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619094/SRR619094.fastq.gz,fcec7928c44295f8da33592e77ea479b,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_GA_R1,,HEK293_GA,,Ribosome profiling of HEK293 cells treated with 1 micromolar geldanamycin for 1 hour,,,,,SRS376443,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619094,253187569,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619094,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619094,d20f4853d1dd42eef7e31bd98423ef68,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205669,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA,Illumina HiSeq 2000 sequencing; Ribosome profiling of HEK293 cells treated with GA,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816437,HEK293_GA,Illumina HiSeq 2000,SRR619095,4044711,194146128,SAMN01816437,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,HEK293_GA,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619095/SRR619095.fastq.gz,140418673,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619095/SRR619095.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619095/SRR619095.fastq.gz,5b1c1e07dfd6a9fe16e74f09924dd481,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,HEK293_GA_R2,,HEK293_GA,,Ribosome profiling of HEK293 cells treated with 1 micromolar geldanamycin for 1 hour,,,,,SRS376443,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619095,120052169,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619095,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619095,601b52416144b4fd2aa4ab298eb70b22,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205670,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells no treatment,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells no treatment,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816438,FRB-FKBP-Rapalog,Illumina Genome Analyzer II,SRR619096,19318730,1062530150,SAMN01816438,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,FRB-FKBP-Rapalog,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619096/SRR619096.fastq.gz,801809320,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619096/SRR619096.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619096/SRR619096.fastq.gz,b7b3d27055fdbcaee7d6d3bc957fd53c,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2016-06-28,,SINGLE,,,,,,,,,,FRB-FKBP-Rapalog,,FRB-FKBP-Rapalog,,Ribosome profiling of FRB*-GFP HEK293 cells transfected with the plasmid encoding FKBP no treatment,,,,,SRS376444,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619096,720677026,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619096,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619096,6f552ebe9db11d7973e345028b8a971b,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205671,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells treated with rapalog,Illumina Genome Analyzer II sequencing; Ribosome profiling of FRB*-GFP HEK293 cells treated with rapalog,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816439,FRB-FKBP+Rapalog,Illumina Genome Analyzer II,SRR619097,24771678,1362442290,SAMN01816439,,,,,,,human embryonic kidney 293,,Cornell University,,,,,,,,,,,,,,,,,,,,false,FRB-FKBP Rapalog,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619097/SRR619097.fastq.gz,1027391168,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619097/SRR619097.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619097/SRR619097.fastq.gz,a6ca4a283943555788eab3b74f63fb90,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2016-06-28,,SINGLE,,,,,,,,,,FRB-FKBP Rapalog,,FRB-FKBP+Rapalog,,Ribosome profiling of FRB*-GFP HEK293 cells transfected with the plasmid encoding FKBP and treated with 1 micromolar rapalog for 1 hour,,,,,SRS376445,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619097,892635591,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619097,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619097,65e8e476c67b22be9720e6625aab97f2,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205672,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells NOT expressing K71M,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells NOT expressing K71M,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816440,Hela_K71M+Dox,Illumina HiSeq 2000,SRR619098,24593755,1180500240,SAMN01816440,,,,,,,HeLa-tTA,,Cornell University,,,,,,,,,,,,,,,,,,,,false,Hela_K71M Dox,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619098/SRR619098.fastq.gz,1033092170,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619098/SRR619098.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619098/SRR619098.fastq.gz,b28036ee36013bb07babd526371fbcec,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2016-06-28,,SINGLE,,,,,,,,,,Hela_K71M Dox,,Hela_K71M+Dox,,Ribosome profiling of HeLa-tTA cells infected with adenoviruses expressing Hsc70(K71M) for 12 hour in the presence of 1 microgram per milliliter doxycycline,,,,,SRS376446,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619098,835072521,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619098,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619098,5a708ddaec529d0e9c472b9a9da6eedb,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205673,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 1,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 1,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816441,Hela_K71M-Dox_Rep1,Illumina HiSeq 2000,SRR619099,22424972,1076398656,SAMN01816441,,,,,,,HeLa-tTA,,Cornell University,,,,,,,,,,,,,,,,,,,,false,Hela_K71M-Dox_Rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619099/SRR619099.fastq.gz,950573956,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619099/SRR619099.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619099/SRR619099.fastq.gz,c07448060f62c18854745a56c7afd3e1,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2016-06-28,,SINGLE,,,,,,,,,,Hela_K71M-Dox_Rep1,,Hela_K71M-Dox_Rep1,,Ribosome profiling of HeLa-tTA cells infected with adenoviruses expressing Hsc70(K71M) for 12 hour in the absence of doxycycline biological replicate 1,,,,,SRS376447,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619099,771621610,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619099,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619099,3b943920c8edab448c6b4b46da4a15d3,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA181016,SRX205675,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 2,Illumina HiSeq 2000 sequencing; Ribosome profiling of HeLa-tTA cells expressing K71M biological replicate 2,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,size fractionation,SAMN01816442,Hela_K71M-Dox_Rep2,Illumina HiSeq 2000,SRR619100,46612873,2237417904,SAMN01816442,,,,,,,HeLa-tTA,,Cornell University,,,,,,,,,,,,,,,,,,,,false,Hela_K71M-Dox_Rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR619/SRR619100/SRR619100.fastq.gz,1501984549,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619100/SRR619100.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR619/SRR619100/SRR619100.fastq.gz,1546be40db2eafcc0929fea92e892b3c,2013-11-11,2013-01-09,false,,,,,,,,,,,ILLUMINA,,,,2015-06-19,,SINGLE,,,,,,,,,,Hela_K71M-Dox_Rep2,,Hela_K71M-Dox_Rep2,,Ribosome profiling of HeLa-tTA cells infected with adenoviruses expressing Hsc70(K71M) for 12 hour in the absence of doxycycline biological replicate 2,,,,,SRS376449,SRP017263,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR619/SRR619100,1369540005,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619100,ftp.sra.ebi.ac.uk/vol1/srr/SRR619/SRR619100,c10166a947fb28ae564b4ed06658c330,,PRJNA181016,Co-Translational Response to Proteotoxic Stress by Elongation Pausing of Ribosomes,,,SRA061778,,,,,,,,,,,,,,, PRJNA417011,SRX3358946,NextSeq 500 sequencing; GSM2838830: Dengue 1 ribosome profiling mRNA REP1; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2838830: Dengue 1 ribosome profiling mRNA REP1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN07974487,Dengue 1 ribosome profiling mRNA REP1,NextSeq 500,SRR6252013,127084864,9531364800,SAMN07974487,,,,,,,,Huh7 cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2838830,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR625/003/SRR6252013/SRR6252013.fastq.gz,4011921334,ftp.sra.ebi.ac.uk/vol1/fastq/SRR625/003/SRR6252013/SRR6252013.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR625/003/SRR6252013/SRR6252013.fastq.gz,74c04255d7203cafc0c34324113fd5cb,2019-03-01,2019-03-01,false,,,,,,,,,,,ILLUMINA,,,,2019-03-01,,SINGLE,,,,,,,,,,GSM2838830_r1,,GSM2838830,,Dengue 1 ribosome profiling mRNA REP1,,,,,SRS2657902,SRP123568,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR625/003/SRR6252013,3772310226,ftp.sra.ebi.ac.uk/vol1/srr/SRR625/003/SRR6252013,ftp.sra.ebi.ac.uk/vol1/srr/SRR625/003/SRR6252013,47f1cb7e0239599d17050172f9906577,,GSE106483,Genome organization of dengue and Zika viruses,,,SRA628009,,,,,,,,,,,,,,, PRJNA417011,SRX3358947,NextSeq 500 sequencing; GSM2838831: Dengue 1 ribosome profiling footprint REP1; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2838831: Dengue 1 ribosome profiling footprint REP1; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN07974486,Dengue 1 ribosome profiling footprint REP1,NextSeq 500,SRR6252014,127716843,9578763225,SAMN07974486,,,,,,,,Huh7 cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2838831,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR625/004/SRR6252014/SRR6252014.fastq.gz,3692471484,ftp.sra.ebi.ac.uk/vol1/fastq/SRR625/004/SRR6252014/SRR6252014.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR625/004/SRR6252014/SRR6252014.fastq.gz,996396a6bbd78a83175196ef8b7ed1fe,2019-03-01,2019-03-01,false,,,,,,,,,,,ILLUMINA,,,,2019-03-01,,SINGLE,,,,,,,,,,GSM2838831_r1,,GSM2838831,,Dengue 1 ribosome profiling footprint REP1,,,,,SRS2657905,SRP123568,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR625/004/SRR6252014,3800285656,ftp.sra.ebi.ac.uk/vol1/srr/SRR625/004/SRR6252014,ftp.sra.ebi.ac.uk/vol1/srr/SRR625/004/SRR6252014,5592f681d39aab239356fb33248fb1b1,,GSE106483,Genome organization of dengue and Zika viruses,,,SRA628009,,,,,,,,,,,,,,, PRJNA417011,SRX3358948,NextSeq 500 sequencing; GSM2838832: Dengue 1 ribosome profiling mRNA REP2; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2838832: Dengue 1 ribosome profiling mRNA REP2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN07974437,Dengue 1 ribosome profiling mRNA REP2,NextSeq 500,SRR6252015,115517289,8663796675,SAMN07974437,,,,,,,,Huh7 cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2838832,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR625/005/SRR6252015/SRR6252015.fastq.gz,4047093499,ftp.sra.ebi.ac.uk/vol1/fastq/SRR625/005/SRR6252015/SRR6252015.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR625/005/SRR6252015/SRR6252015.fastq.gz,4eec77c75277c23c465e709c839cc64f,2019-03-01,2019-03-01,false,,,,,,,,,,,ILLUMINA,,,,2019-03-01,,SINGLE,,,,,,,,,,GSM2838832_r1,,GSM2838832,,Dengue 1 ribosome profiling mRNA REP2,,,,,SRS2657903,SRP123568,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR625/005/SRR6252015,3502650368,ftp.sra.ebi.ac.uk/vol1/srr/SRR625/005/SRR6252015,ftp.sra.ebi.ac.uk/vol1/srr/SRR625/005/SRR6252015,a69d2ee31d93498deb880f0eeb0b01ab,,GSE106483,Genome organization of dengue and Zika viruses,,,SRA628009,,,,,,,,,,,,,,, PRJNA417011,SRX3358949,NextSeq 500 sequencing; GSM2838833: Dengue 1 ribosome profiling footprint REP2; Homo sapiens; OTHER,NextSeq 500 sequencing; GSM2838833: Dengue 1 ribosome profiling footprint REP2; Homo sapiens; OTHER,9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN07974489,Dengue 1 ribosome profiling footprint REP2,NextSeq 500,SRR6252016,128141714,9610628550,SAMN07974489,,,,,,,,Huh7 cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2838833,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR625/006/SRR6252016/SRR6252016.fastq.gz,3633645352,ftp.sra.ebi.ac.uk/vol1/fastq/SRR625/006/SRR6252016/SRR6252016.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR625/006/SRR6252016/SRR6252016.fastq.gz,f431cc8a9c31cf63410499984399e0a8,2019-03-01,2019-03-01,false,,,,,,,,,,,ILLUMINA,,,,2019-03-01,,SINGLE,,,,,,,,,,GSM2838833_r1,,GSM2838833,,Dengue 1 ribosome profiling footprint REP2,,,,,SRS2657904,SRP123568,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR625/006/SRR6252016,3811755394,ftp.sra.ebi.ac.uk/vol1/srr/SRR625/006/SRR6252016,ftp.sra.ebi.ac.uk/vol1/srr/SRR625/006/SRR6252016,78b49c6238501b5f8f98e6b4ae0f5520,,GSE106483,Genome organization of dengue and Zika viruses,,,SRA628009,,,,,,,,,,,,,,, PRJNA418190,SRX3388077,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022097,Ribo_HF_rep2,Illumina HiSeq 4000,SRR6286686,31815773,3181577300,SAMN08022097,,,,,,,,,SUB3200129,,,,,,,,,,,,,,,,,,,,false,Ribo_HF_rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR628/006/SRR6286686/SRR6286686.fastq.gz,1270414280,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/006/SRR6286686/SRR6286686.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/006/SRR6286686/SRR6286686.fastq.gz,714438ead93e8c35d0c7d09c505c9b66,2018-10-15,2018-10-15,false,,,,,,,,,,,ILLUMINA,,,,2018-10-15,,PAIRED,Ribo_HF_rep2,,,,,,,,,Ribo_HF_rep2.fastq.gz,,Ribo_HF_rep2,,Ribo_HF_rep2,,,,,SRS2683409,SRP124901,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR628/006/SRR6286686,1487166943,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/006/SRR6286686,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/006/SRR6286686,df96431cc721a42a4f34ffefb98c8854,ATCC 55383,PRJNA418190,Multi-omic analyses of Clostridium ljungdahlii in heterotrophic and autotrophic growth conditions,,,SRA630323,,,,,,,,,,,,,,, PRJNA418190,SRX3388076,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022096,Ribo_HF_rep1,Illumina HiSeq 4000,SRR6286687,31226831,3122683100,SAMN08022096,,,,,,,,,SUB3200129,,,,,,,,,,,,,,,,,,,,false,Ribo_HF_rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR628/007/SRR6286687/SRR6286687.fastq.gz,1226590288,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/007/SRR6286687/SRR6286687.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/007/SRR6286687/SRR6286687.fastq.gz,ecad61dc44dc333c6553e539e71eff3c,2018-10-15,2018-10-15,false,,,,,,,,,,,ILLUMINA,,,,2018-10-15,,PAIRED,Ribo_HF_rep1,,,,,,,,,Ribo_HF_rep1.fastq.gz,,Ribo_HF_rep1,,Ribo_HF_rep1,,,,,SRS2683410,SRP124901,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR628/007/SRR6286687,1452425337,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/007/SRR6286687,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/007/SRR6286687,dc6ceda9c969435933c42e984233fc25,ATCC 55383,PRJNA418190,Multi-omic analyses of Clostridium ljungdahlii in heterotrophic and autotrophic growth conditions,,,SRA630323,,,,,,,,,,,,,,, PRJNA418190,SRX3388073,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022093,Ribo_CO_rep2,Illumina HiSeq 4000,SRR6286690,95785654,2709048603,SAMN08022093,,,,,,,,,SUB3200129,,,,,,,,,,,,,,,,,,,,false,Ribo_CO_rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR628/000/SRR6286690/SRR6286690.fastq.gz,1299621548,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/000/SRR6286690/SRR6286690.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/000/SRR6286690/SRR6286690.fastq.gz,ddaab7f8eba839e948f53a087b7e0f7f,2018-10-15,2018-10-15,false,,,,,,,,,,,ILLUMINA,,,,2018-10-15,,PAIRED,Ribo_CO_rep2,,,,,,,,,Ribo_CO_rep2.fastq.gz,,Ribo_CO_rep2,,Ribo_CO_rep2,,,,,SRS2683407,SRP124901,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR628/000/SRR6286690,1286157190,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/000/SRR6286690,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/000/SRR6286690,cf5fc8bbe7b68f9cc48af667e0cee691,ATCC 55383,PRJNA418190,Multi-omic analyses of Clostridium ljungdahlii in heterotrophic and autotrophic growth conditions,,,SRA630323,,,,,,,,,,,,,,, PRJNA418190,SRX3388072,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022092,Ribo_CO_rep1,Illumina HiSeq 4000,SRR6286691,74932501,2100103575,SAMN08022092,,,,,,,,,SUB3200129,,,,,,,,,,,,,,,,,,,,false,Ribo_CO_rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR628/001/SRR6286691/SRR6286691.fastq.gz,1018174917,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/001/SRR6286691/SRR6286691.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/001/SRR6286691/SRR6286691.fastq.gz,174cd0fd34de022668f59b5e5da071f4,2018-10-15,2018-10-15,false,,,,,,,,,,,ILLUMINA,,,,2018-10-15,,PAIRED,Ribo_CO_rep1,,,,,,,,,Ribo_CO_rep1.fastq.gz,,Ribo_CO_rep1,,Ribo_CO_rep1,,,,,SRS2683405,SRP124901,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR628/001/SRR6286691,1014125708,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/001/SRR6286691,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/001/SRR6286691,e4e3f2b7ee0cb13ac1e19c61212959f6,ATCC 55383,PRJNA418190,Multi-omic analyses of Clostridium ljungdahlii in heterotrophic and autotrophic growth conditions,,,SRA630323,,,,,,,,,,,,,,, PRJNA418190,SRX3388071,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022095,Ribo_H2CO2_rep2,Illumina HiSeq 4000,SRR6286692,44431801,4443180100,SAMN08022095,,,,,,,,,SUB3200129,,,,,,,,,,,,,,,,,,,,false,Ribo_H2CO2_rep2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR628/002/SRR6286692/SRR6286692.fastq.gz,1520562821,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/002/SRR6286692/SRR6286692.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/002/SRR6286692/SRR6286692.fastq.gz,be9c00f6c3bdbca95fa1b9f9542bb123,2018-10-15,2018-10-15,false,,,,,,,,,,,ILLUMINA,,,,2018-10-15,,PAIRED,Ribo_H2CO2_rep2,,,,,,,,,Ribo_H2CO2_rep2.fq.gz,,Ribo_H2CO2_rep2,,Ribo_H2CO2_rep2,,,,,SRS2683404,SRP124901,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR628/002/SRR6286692,1864884834,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/002/SRR6286692,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/002/SRR6286692,0322a0f5c49dcba34d70aec1d837b043,ATCC 55383,PRJNA418190,Multi-omic analyses of Clostridium ljungdahlii in heterotrophic and autotrophic growth conditions,,,SRA630323,,,,,,,,,,,,,,, PRJNA418190,SRX3388070,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,Illumina HiSeq 4000 sequencing; Ribosome profiling of Clostridium ljungdahlii,1538,Clostridium ljungdahlii,OTHER,TRANSCRIPTOMIC,other,SAMN08022094,Ribo_H2CO2_rep1,Illumina HiSeq 4000,SRR6286693,50618624,5061862400,SAMN08022094,,,,,,,,,SUB3200129,,,,,,,,,,,,,,,,,,,,false,Ribo_H2CO2_rep1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR628/003/SRR6286693/SRR6286693.fastq.gz,1675004695,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/003/SRR6286693/SRR6286693.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR628/003/SRR6286693/SRR6286693.fastq.gz,f05cd7b9c416a2aa06ead52107f7d3be,2018-10-15,2018-10-15,false,,,,,,,,,,,ILLUMINA,,,,2018-10-15,,PAIRED,Ribo_H2CO2_rep1,,,,,,,,,Ribo_H2CO2_rep1.fq.gz,,Ribo_H2CO2_rep1,,Ribo_H2CO2_rep1,,,,,SRS2683403,SRP124901,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR628/003/SRR6286693,2085951986,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/003/SRR6286693,ftp.sra.ebi.ac.uk/vol1/srr/SRR628/003/SRR6286693,a1b91dcbdeb6746400b1d081f739d0cc,ATCC 55383,PRJNA418190,Multi-omic analyses of Clostridium ljungdahlii in heterotrophic and autotrophic growth conditions,,,SRA630323,,,,,,,,,,,,,,, PRJNA418997,SRX3415715,Illumina HiSeq 2000 sequencing; Hip1 total hippocampus Ribosome profiling,Illumina HiSeq 2000 sequencing; Hip1 total hippocampus Ribosome profiling,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08040363,Hip1 total hippocampus Ribosome profiling,Illumina HiSeq 2000,SRR6315847,6628200,180389814,SAMN08040363,,,,,,,,,SUB3229482,,,,,,,,,,,,,,,,,,,,false,Hip1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR631/007/SRR6315847/SRR6315847.fastq.gz,119842527,ftp.sra.ebi.ac.uk/vol1/fastq/SRR631/007/SRR6315847/SRR6315847.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR631/007/SRR6315847/SRR6315847.fastq.gz,a03505afc5b85a911e48d971a0d17416,2019-01-02,2019-01-02,false,,,,,,,,,,,ILLUMINA,,,,2019-01-02,,SINGLE,Hip1,,,,,,,,,Hip1.bam.gz,,Hip1,,Hip1 total hippocampus Ribosome profiling,,,,,SRS2708541,SRP125469,,,,male,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR631/007/SRR6315847,84123759,ftp.sra.ebi.ac.uk/vol1/srr/SRR631/007/SRR6315847,ftp.sra.ebi.ac.uk/vol1/srr/SRR631/007/SRR6315847,54bfe6835b867920fbe9f53961f6025a,,PRJNA418997,Mus musculus breed:C57BL/6J Genome sequencing,,,SRA633337,,,,,,,,male,,,,,,hippocampus, PRJNA423188,SRX3489120,Illumina HiSeq 2500 sequencing; GSM2895436: KO-ribosome profiling; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM2895436: KO-ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08213272,KO-ribosome profiling,Illumina HiSeq 2500,SRR6395814,31806217,1590310850,SAMN08213272,,,,,,,,Bone marrow derived mature dendritic cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2895436,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR639/004/SRR6395814/SRR6395814.fastq.gz,936059859,ftp.sra.ebi.ac.uk/vol1/fastq/SRR639/004/SRR6395814/SRR6395814.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR639/004/SRR6395814/SRR6395814.fastq.gz,7af5c07d6b22c8f0d11d9f5901aa613f,2019-04-03,2019-04-03,false,,,,,,,,,,,ILLUMINA,,,,2019-04-03,,SINGLE,,,,,,,,,,GSM2895436_r1,,GSM2895436,,KO-ribosome profiling,,,,,SRS2773282,SRP127229,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR639/004/SRR6395814,813541591,ftp.sra.ebi.ac.uk/vol1/srr/SRR639/004/SRR6395814,ftp.sra.ebi.ac.uk/vol1/srr/SRR639/004/SRR6395814,e087c53254938b808a16f38dec4db5e8,C57BL/6,GSE108331,Next Generation Sequencing Facilitates Quantitative Analysis of mRNA translation efficiency of Wild Type and Mettl3-/- mice,,,SRA640462,,,,,,,,,,,,,,, PRJNA423188,SRX3489121,Illumina HiSeq 2500 sequencing; GSM2895437: KO-ribosome profiling input; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM2895437: KO-ribosome profiling input; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08213281,KO-ribosome profiling input,Illumina HiSeq 2500,SRR6395815,43112301,2155615050,SAMN08213281,,,,,,,,Bone marrow derived mature dendritic cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2895437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR639/005/SRR6395815/SRR6395815.fastq.gz,1727742842,ftp.sra.ebi.ac.uk/vol1/fastq/SRR639/005/SRR6395815/SRR6395815.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR639/005/SRR6395815/SRR6395815.fastq.gz,6005365c1bf7bf7980141d98b684ceb6,2019-04-03,2019-04-03,false,,,,,,,,,,,ILLUMINA,,,,2019-04-03,,SINGLE,,,,,,,,,,GSM2895437_r1,,GSM2895437,,KO-ribosome profiling input,,,,,SRS2773283,SRP127229,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR639/005/SRR6395815,1119949812,ftp.sra.ebi.ac.uk/vol1/srr/SRR639/005/SRR6395815,ftp.sra.ebi.ac.uk/vol1/srr/SRR639/005/SRR6395815,876ccbfcb8ce10e21dc9a73cdd855975,C57BL/6,GSE108331,Next Generation Sequencing Facilitates Quantitative Analysis of mRNA translation efficiency of Wild Type and Mettl3-/- mice,,,SRA640462,,,,,,,,,,,,,,, PRJNA423188,SRX3489122,Illumina HiSeq 2500 sequencing; GSM2895438: WT-ribosome profiling; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM2895438: WT-ribosome profiling; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08213280,WT-ribosome profiling,Illumina HiSeq 2500,SRR6395816,40248624,2012431200,SAMN08213280,,,,,,,,Bone marrow derived mature dendritic cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2895438,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR639/006/SRR6395816/SRR6395816.fastq.gz,1151431385,ftp.sra.ebi.ac.uk/vol1/fastq/SRR639/006/SRR6395816/SRR6395816.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR639/006/SRR6395816/SRR6395816.fastq.gz,21435d5e1a89afc592c07b2df3821a98,2019-04-03,2019-04-03,false,,,,,,,,,,,ILLUMINA,,,,2019-04-03,,SINGLE,,,,,,,,,,GSM2895438_r1,,GSM2895438,,WT-ribosome profiling,,,,,SRS2773284,SRP127229,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR639/006/SRR6395816,1008661914,ftp.sra.ebi.ac.uk/vol1/srr/SRR639/006/SRR6395816,ftp.sra.ebi.ac.uk/vol1/srr/SRR639/006/SRR6395816,50ee9e0820ed113385780beed361330c,C57BL/6,GSE108331,Next Generation Sequencing Facilitates Quantitative Analysis of mRNA translation efficiency of Wild Type and Mettl3-/- mice,,,SRA640462,,,,,,,,,,,,,,, PRJNA423188,SRX3489123,Illumina HiSeq 2500 sequencing; GSM2895439: WT-ribosome profiling input; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM2895439: WT-ribosome profiling input; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN08213279,WT-ribosome profiling input,Illumina HiSeq 2500,SRR6395817,33585015,1679250750,SAMN08213279,,,,,,,,Bone marrow derived mature dendritic cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM2895439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR639/007/SRR6395817/SRR6395817.fastq.gz,1363809194,ftp.sra.ebi.ac.uk/vol1/fastq/SRR639/007/SRR6395817/SRR6395817.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR639/007/SRR6395817/SRR6395817.fastq.gz,aef07d7ac58df3eeddc9c1b66fb15829,2019-04-03,2019-04-03,false,,,,,,,,,,,ILLUMINA,,,,2019-04-03,,SINGLE,,,,,,,,,,GSM2895439_r1,,GSM2895439,,WT-ribosome profiling input,,,,,SRS2773285,SRP127229,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR639/007/SRR6395817,876687887,ftp.sra.ebi.ac.uk/vol1/srr/SRR639/007/SRR6395817,ftp.sra.ebi.ac.uk/vol1/srr/SRR639/007/SRR6395817,d73904a797cf04efbcd5b2d4ef5cc4d1,C57BL/6,GSE108331,Next Generation Sequencing Facilitates Quantitative Analysis of mRNA translation efficiency of Wild Type and Mettl3-/- mice,,,SRA640462,,,,,,,,,,,,,,, PRJNA423188,SRX4044241,Illumina HiSeq 2500 sequencing; GSM3131863: WT-ribosome profiling replicate 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM3131863: WT-ribosome profiling replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN09076541,WT-ribosome profiling replicate 2,Illumina HiSeq 2500,SRR7123172,43725854,2186292700,SAMN09076541,,,,,,,,Bone marrow derived mature dendritic cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3131863,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR712/002/SRR7123172/SRR7123172.fastq.gz,1501854821,ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/002/SRR7123172/SRR7123172.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/002/SRR7123172/SRR7123172.fastq.gz,8617d4b057b4c9d53ef922db78183647,2019-04-03,2019-04-03,false,,,,,,,,,,,ILLUMINA,,,,2019-04-03,,SINGLE,,,,,,,,,,GSM3131863_r1,,GSM3131863,,WT-ribosome profiling replicate 2,,,,,SRS3261678,SRP127229,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR712/002/SRR7123172,1225588701,ftp.sra.ebi.ac.uk/vol1/srr/SRR712/002/SRR7123172,ftp.sra.ebi.ac.uk/vol1/srr/SRR712/002/SRR7123172,fce6dd03766c1a0299c4b70762a0f1c7,C57BL/6,GSE108331,Next Generation Sequencing Facilitates Quantitative Analysis of mRNA translation efficiency of Wild Type and Mettl3-/- mice,,,SRA640462,,,,,,,,,,,,,,, PRJNA423188,SRX4044242,Illumina HiSeq 3000 sequencing; GSM3131864: WT-ribosome profiling input replicate 2; Mus musculus; OTHER,Illumina HiSeq 3000 sequencing; GSM3131864: WT-ribosome profiling input replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN09076736,WT-ribosome profiling input replicate 2,Illumina HiSeq 3000,SRR7123173,26771648,8031494400,SAMN09076736,,,,,,,,Bone marrow derived mature dendritic cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3131864,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR712/003/SRR7123173/SRR7123173_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR712/003/SRR7123173/SRR7123173_2.fastq.gz,2087413257;2342504750,ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/003/SRR7123173/SRR7123173_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/003/SRR7123173/SRR7123173_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/003/SRR7123173/SRR7123173_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/003/SRR7123173/SRR7123173_2.fastq.gz,46ba1f5c4da2c57a834850f48945c21e;4b2c8d6f0e3a048ee8e4bc0f52e7d8d3,2019-04-03,2019-04-03,false,,,,,,,,,,,ILLUMINA,,,,2019-04-03,,PAIRED,,,,,,,,,,GSM3131864_r1,,GSM3131864,,WT-ribosome profiling input replicate 2,,,,,SRS3261679,SRP127229,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR712/003/SRR7123173,3208015019,ftp.sra.ebi.ac.uk/vol1/srr/SRR712/003/SRR7123173,ftp.sra.ebi.ac.uk/vol1/srr/SRR712/003/SRR7123173,0aad0d0f86cdf9272dc97ff70da101f6,C57BL/6,GSE108331,Next Generation Sequencing Facilitates Quantitative Analysis of mRNA translation efficiency of Wild Type and Mettl3-/- mice,,,SRA640462,,,,,,,,,,,,,,, PRJNA423188,SRX4044243,Illumina HiSeq 2500 sequencing; GSM3131865: KO-ribosome profiling replicate 2; Mus musculus; OTHER,Illumina HiSeq 2500 sequencing; GSM3131865: KO-ribosome profiling replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN09076734,KO-ribosome profiling replicate 2,Illumina HiSeq 2500,SRR7123174,32054335,1602716750,SAMN09076734,,,,,,,,Bone marrow derived mature dendritic cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3131865,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR712/004/SRR7123174/SRR7123174.fastq.gz,1099602206,ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/004/SRR7123174/SRR7123174.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/004/SRR7123174/SRR7123174.fastq.gz,0e14bda849fe16bbc1f5279b4cffc368,2019-04-03,2019-04-03,false,,,,,,,,,,,ILLUMINA,,,,2019-04-03,,SINGLE,,,,,,,,,,GSM3131865_r1,,GSM3131865,,KO-ribosome profiling replicate 2,,,,,SRS3261680,SRP127229,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR712/004/SRR7123174,898296261,ftp.sra.ebi.ac.uk/vol1/srr/SRR712/004/SRR7123174,ftp.sra.ebi.ac.uk/vol1/srr/SRR712/004/SRR7123174,e625db9da60050b93538a05fcfb4ab02,C57BL/6,GSE108331,Next Generation Sequencing Facilitates Quantitative Analysis of mRNA translation efficiency of Wild Type and Mettl3-/- mice,,,SRA640462,,,,,,,,,,,,,,, PRJNA423188,SRX4044244,Illumina HiSeq 3000 sequencing; GSM3131866: KO-ribosome profiling input replicate 2; Mus musculus; OTHER,Illumina HiSeq 3000 sequencing; GSM3131866: KO-ribosome profiling input replicate 2; Mus musculus; OTHER,10090,Mus musculus,OTHER,TRANSCRIPTOMIC,other,SAMN09076731,KO-ribosome profiling input replicate 2,Illumina HiSeq 3000,SRR7123175,24239197,7271759100,SAMN09076731,,,,,,,,Bone marrow derived mature dendritic cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3131866,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR712/005/SRR7123175/SRR7123175_1.fastq.gz;fasp.sra.ebi.ac.uk:/vol1/fastq/SRR712/005/SRR7123175/SRR7123175_2.fastq.gz,1909293126;2184342432,ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/005/SRR7123175/SRR7123175_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/005/SRR7123175/SRR7123175_2.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/005/SRR7123175/SRR7123175_1.fastq.gz;ftp.sra.ebi.ac.uk/vol1/fastq/SRR712/005/SRR7123175/SRR7123175_2.fastq.gz,b9d6c5fc2237bca0663d8ddf4bef9948;bbca9a97fc81c5ad1edf1efb02b3e84e,2019-04-03,2019-04-03,false,,,,,,,,,,,ILLUMINA,,,,2019-04-03,,PAIRED,,,,,,,,,,GSM3131866_r1,,GSM3131866,,KO-ribosome profiling input replicate 2,,,,,SRS3261681,SRP127229,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR712/005/SRR7123175,2971907873,ftp.sra.ebi.ac.uk/vol1/srr/SRR712/005/SRR7123175,ftp.sra.ebi.ac.uk/vol1/srr/SRR712/005/SRR7123175,d69d0f07bdaaacbdc7824e55db9359b7,C57BL/6,GSE108331,Next Generation Sequencing Facilitates Quantitative Analysis of mRNA translation efficiency of Wild Type and Mettl3-/- mice,,,SRA640462,,,,,,,,,,,,,,, PRJNA466150,SRX4053284,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #4,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #4,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091234,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132277,53840664,4038049800,SAMN09091234,,,,,,,,,SUB4003258,,,2016-07-01,,,USA,,,,,,,,,,,,,,false,F_FP_7,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/007/SRR7132277/SRR7132277.fastq.gz,1124738142,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/007/SRR7132277/SRR7132277.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/007/SRR7132277/SRR7132277.fastq.gz,0e953dcb7d93ca6e17532231aba5f084,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,F_FP_7,,,,,,,,,Fmr1_RNAi2_FPs_d.fastq.gz,,F_FP_7,,Fmr1 RNAi Ribosome Footprinting,,,,,SRS3270324,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/007/SRR7132277,1413271561,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/007/SRR7132277,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/007/SRR7132277,0c3098bceec58be58b7ced3a882e9096,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053275,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #2,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #2,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091232,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132286,96147759,7211081925,SAMN09091232,,,,,,,,,SUB4003258,,,2016-06-01,,,USA,,,,,,,,,,,,,,false,F_FP_5,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/006/SRR7132286/SRR7132286.fastq.gz,2203867158,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/006/SRR7132286/SRR7132286.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/006/SRR7132286/SRR7132286.fastq.gz,08db2ce1b5630ca7750142b067272437,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,F_FP_5,,,,,,,,,Fmr1_RNAi2_FPs_b.fasta.gz,,F_FP_5,,Fmr1 RNAi Ribosome Footprinting,,,,,SRS3270292,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/006/SRR7132286,2676452054,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/006/SRR7132286,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/006/SRR7132286,ae671d72bb5a61b72c4e4f1ab8f72d15,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053274,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #3,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #3,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091233,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132287,49283336,3696250200,SAMN09091233,,,,,,,,,SUB4003258,,,2016-07-01,,,USA,,,,,,,,,,,,,,false,F_FP_6,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/007/SRR7132287/SRR7132287.fastq.gz,1149140870,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/007/SRR7132287/SRR7132287.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/007/SRR7132287/SRR7132287.fastq.gz,4e7a1ccd80b4a9a8c1a93d435328856a,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,F_FP_6,,,,,,,,,Fmr1_RNAi2_FPs_c.fastq.gz,,F_FP_6,,Fmr1 RNAi Ribosome Footprinting,,,,,SRS3270291,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/007/SRR7132287,1373972084,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/007/SRR7132287,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/007/SRR7132287,de1695901d4e059f0e66170ac49a40a5,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053273,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #3,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #3,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091226,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132288,78056300,5854222500,SAMN09091226,,,,,,,,,SUB4003258,,,2016-07-01,,,USA,,,,,,,,,,,,,,false,C_FP_3,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/008/SRR7132288/SRR7132288.fastq.gz,1753850615,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/008/SRR7132288/SRR7132288.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/008/SRR7132288/SRR7132288.fastq.gz,2656cf7eab927bfd5e29eee19f982dcf,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,C_FP_3,,,,,,,,,mCherry_FPs_b.fastq.gz,,C_FP_3,,Control Ribosome Footprinting,,,,,SRS3270290,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/008/SRR7132288,2075483296,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/008/SRR7132288,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/008/SRR7132288,a085a9cb60e461be316313febefa71ae,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053272,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #4,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #4,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091227,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132289,44947356,3371051700,SAMN09091227,,,,,,,,,SUB4003258,,,2016-07-01,,,USA,,,,,,,,,,,,,,false,C_FP_4,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/009/SRR7132289/SRR7132289.fastq.gz,943161434,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/009/SRR7132289/SRR7132289.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/009/SRR7132289/SRR7132289.fastq.gz,eb2c3316ba0f4fa15cf1dc5579644347,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,C_FP_4,,,,,,,,,mCherry_FPs_c.fastq.gz,,C_FP_4,,Control Ribosome Footprinting,,,,,SRS3270289,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/009/SRR7132289,1176467336,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/009/SRR7132289,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/009/SRR7132289,9148d75c6917eabc4e1d33c275763322,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053271,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:control replicate #1,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:control replicate #1,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091224,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,Illumina HiSeq 2000,SRR7132290,64927827,3246391350,SAMN09091224,,,,,,,,,SUB4003258,,,2016-02-01,,,USA,,,,,,,,,,,,,,false,C_FP_1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/000/SRR7132290/SRR7132290.fastq.gz,2060881611,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/000/SRR7132290/SRR7132290.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/000/SRR7132290/SRR7132290.fastq.gz,7a699de37856310ebedd32e000a5e1e0,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,C_FP_1,,,,,,,,,GFP_FPs.fastq.gz,,C_FP_1,,Control Ribosome Footprinting,,,,,SRS3270313,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/000/SRR7132290,1852026260,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/000/SRR7132290,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/000/SRR7132290,c151e99789f064be9f61362e7047046d,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053270,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #2,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:control replicate #2,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091225,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132291,89912857,6743464275,SAMN09091225,,,,,,,,,SUB4003258,,,2016-06-01,,,USA,,,,,,,,,,,,,,false,C_FP_2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/001/SRR7132291/SRR7132291.fastq.gz,2133071660,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/001/SRR7132291/SRR7132291.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/001/SRR7132291/SRR7132291.fastq.gz,2aab0173f97b3547041d6c72aaf43837,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,C_FP_2,,,,,,,,,mCherry_FPs_a.fasta.gz,,C_FP_2,,Control Ribosome Footprinting,,,,,SRS3270288,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/001/SRR7132291,2528331507,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/001/SRR7132291,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/001/SRR7132291,5886b3cf81ef5cfb4d10b347d351e08c,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053269,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #3,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #3,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091230,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132292,69602339,5220175425,SAMN09091230,,,,,,,,,SUB4003258,,,2016-07-01,,,USA,,,,,,,,,,,,,,false,F_FP_3,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/002/SRR7132292/SRR7132292.fastq.gz,1379637220,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/002/SRR7132292/SRR7132292.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/002/SRR7132292/SRR7132292.fastq.gz,3c72b661e38ad76255dc573f7e65d44e,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,F_FP_3,,,,,,,,,Fmr1_RNAi1_FPs_c.fastq.gz,,F_FP_3,,Fmr1 RNAi Ribosome Footprinting,,,,,SRS3270287,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/002/SRR7132292,1763525151,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/002/SRR7132292,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/002/SRR7132292,4dfd4f3181adbb8e05382f4b1f558019,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053268,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #1,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #2 replicate #1,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091231,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132293,57310413,2865520650,SAMN09091231,,,,,,,,,SUB4003258,,,2016-02-01,,,USA,,,,,,,,,,,,,,false,F_FP_4,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/003/SRR7132293/SRR7132293.fastq.gz,1881457141,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/003/SRR7132293/SRR7132293.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/003/SRR7132293/SRR7132293.fastq.gz,30f0662eafb06468bc7a7500784bd3dc,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,F_FP_4,,,,,,,,,Fmr1_RNAi2_FPs_a.fastq.gz,,F_FP_4,,Fmr1 RNAi Ribosome Footprinting,,,,,SRS3270286,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/003/SRR7132293,1665888745,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/003/SRR7132293,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/003/SRR7132293,1fbb8ccbd840bebc323a2180a3fe0fce,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053267,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #1,Illumina HiSeq 2000 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #1,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091228,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,Illumina HiSeq 2000,SRR7132294,106961271,8022095325,SAMN09091228,,,,,,,,,SUB4003258,,,2016-06-01,,,USA,,,,,,,,,,,,,,false,F_FP_1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/004/SRR7132294/SRR7132294.fastq.gz,2344199204,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/004/SRR7132294/SRR7132294.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/004/SRR7132294/SRR7132294.fastq.gz,4713ebe5abc1071db56a0f952057721c,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,F_FP_1,,,,,,,,,Fmr1_RNAi1_FPs_a.fasta.gz,,F_FP_1,,Fmr1 RNAi Ribosome Footprinting,,,,,SRS3270284,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/004/SRR7132294,2871757497,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/004/SRR7132294,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/004/SRR7132294,a337252dc52b5940205d771b6cd21710,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA466150,SRX4053266,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #2,NextSeq 500 sequencing; Ribosome profiling of Drosophila ovary:Fmr1 germline RNAi line #1 replicate #2,7227,Drosophila melanogaster,OTHER,TRANSCRIPTOMIC,MNase,SAMN09091229,This sample has been submitted by pda|ejgreenblatt on 2018-07-06; Drosophila melanogaster,NextSeq 500,SRR7132295,43401129,3255084675,SAMN09091229,,,,,,,,,SUB4003258,,,2016-07-01,,,USA,,,,,,,,,,,,,,false,F_FP_2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR713/005/SRR7132295/SRR7132295.fastq.gz,914351757,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/005/SRR7132295/SRR7132295.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR713/005/SRR7132295/SRR7132295.fastq.gz,c9076604c3baa65d78779315cb5eaf96,2018-07-06,2018-07-06,false,,,,,,,,,,,ILLUMINA,,,,2018-07-06,,SINGLE,F_FP_2,,,,,,,,,Fmr1_RNAi1_FPs_b.fastq.gz,,F_FP_2,,Fmr1 RNAi Ribosome Footprinting,,,,,SRS3270285,SRP144935,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR713/005/SRR7132295,1125445948,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/005/SRR7132295,ftp.sra.ebi.ac.uk/vol1/srr/SRR713/005/SRR7132295,ddcf070ec4f9ab2f22f547917fddc766,,PRJNA466150,Fmr1-dependent translation in the Drosophila ovary,,,SRA700696,,,,,,,,,,,,25.0,,ovary, PRJNA473989,SRX4147683,Illumina HiSeq 2500 sequencing; GSM3168387: MDA-MB-231 ribosome profiling; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3168387: MDA-MB-231 ribosome profiling; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN09288723,MDA-MB-231 ribosome profiling,Illumina HiSeq 2500,SRR7241910,27002674,1350133700,SAMN09288723,,,,,,,MDA-MB-231,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3168387,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR724/000/SRR7241910/SRR7241910.fastq.gz,848418211,ftp.sra.ebi.ac.uk/vol1/fastq/SRR724/000/SRR7241910/SRR7241910.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR724/000/SRR7241910/SRR7241910.fastq.gz,80524476fd134a25a9b321f5dcb03a14,2019-01-29,2019-01-29,false,,,,,,,,,,,ILLUMINA,,,,2019-01-29,,SINGLE,,,,,,,,,,GSM3168387_r1,,GSM3168387,,MDA-MB-231 ribosome profiling,,,,,SRS3361275,SRP149446,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR724/000/SRR7241910,659201384,ftp.sra.ebi.ac.uk/vol1/srr/SRR724/000/SRR7241910,ftp.sra.ebi.ac.uk/vol1/srr/SRR724/000/SRR7241910,48d9b1bed2736d64c0146e5ca9723b93,,GSE115161,Regulation of Translation Elongation Revealed by Ribosome Profiling [Dataset_4],,,SRA713167,,,,,,,,,,,,,,, PRJNA473989,SRX4147684,Illumina HiSeq 2500 sequencing; GSM3168388: C. elegans embryos ribosome profiling; Caenorhabditis elegans; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3168388: C. elegans embryos ribosome profiling; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN09288722,C. elegans embryos ribosome profiling,Illumina HiSeq 2500,SRR7241911,76408239,3820411950,SAMN09288722,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3168388,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR724/001/SRR7241911/SRR7241911.fastq.gz,2206843716,ftp.sra.ebi.ac.uk/vol1/fastq/SRR724/001/SRR7241911/SRR7241911.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR724/001/SRR7241911/SRR7241911.fastq.gz,aed27e270b927c596013df37204ac616,2019-01-29,2019-01-29,false,,,,,,,,,,,ILLUMINA,,,,2019-01-29,,SINGLE,,,,,,,,,,GSM3168388_r1,,GSM3168388,,C. elegans embryos ribosome profiling,,,,,SRS3361274,SRP149446,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR724/001/SRR7241911,1744254785,ftp.sra.ebi.ac.uk/vol1/srr/SRR724/001/SRR7241911,ftp.sra.ebi.ac.uk/vol1/srr/SRR724/001/SRR7241911,224740e2b27a4b736fb1687ccb1a6c1b,,GSE115161,Regulation of Translation Elongation Revealed by Ribosome Profiling [Dataset_4],,,SRA713167,,,,,,,,,,,,,,embryos, PRJNA473989,SRX4147685,Illumina HiSeq 2500 sequencing; GSM3168389: HeLa ribosome profiling 1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3168389: HeLa ribosome profiling 1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN09288721,HeLa ribosome profiling 1,Illumina HiSeq 2500,SRR7241912,53902947,2695147350,SAMN09288721,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3168389,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR724/002/SRR7241912/SRR7241912.fastq.gz,1630235426,ftp.sra.ebi.ac.uk/vol1/fastq/SRR724/002/SRR7241912/SRR7241912.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR724/002/SRR7241912/SRR7241912.fastq.gz,775a59049e991379d7158733018c9582,2019-01-29,2019-01-29,false,,,,,,,,,,,ILLUMINA,,,,2019-01-29,,SINGLE,,,,,,,,,,GSM3168389_r1,,GSM3168389,,HeLa ribosome profiling 1,,,,,SRS3361276,SRP149446,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR724/002/SRR7241912,1281564311,ftp.sra.ebi.ac.uk/vol1/srr/SRR724/002/SRR7241912,ftp.sra.ebi.ac.uk/vol1/srr/SRR724/002/SRR7241912,afd7b30e3b101f33160979abb25fe765,,GSE115161,Regulation of Translation Elongation Revealed by Ribosome Profiling [Dataset_4],,,SRA713167,,,,,,,,,,,,,,, PRJNA473989,SRX4147686,Illumina HiSeq 2500 sequencing; GSM3168390: HeLa ribosome profiling 2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3168390: HeLa ribosome profiling 2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN09288720,HeLa ribosome profiling 2,Illumina HiSeq 2500,SRR7241913,45242293,2262114650,SAMN09288720,,,,,,,HeLa,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3168390,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR724/003/SRR7241913/SRR7241913.fastq.gz,1652908923,ftp.sra.ebi.ac.uk/vol1/fastq/SRR724/003/SRR7241913/SRR7241913.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR724/003/SRR7241913/SRR7241913.fastq.gz,7035b17c1590777efe06c1c19a0cf906,2019-01-29,2019-01-29,false,,,,,,,,,,,ILLUMINA,,,,2019-01-29,,SINGLE,,,,,,,,,,GSM3168390_r1,,GSM3168390,,HeLa ribosome profiling 2,,,,,SRS3361277,SRP149446,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR724/003/SRR7241913,1257402030,ftp.sra.ebi.ac.uk/vol1/srr/SRR724/003/SRR7241913,ftp.sra.ebi.ac.uk/vol1/srr/SRR724/003/SRR7241913,bac1eb24156c61857936470bf56dbd20,,GSE115161,Regulation of Translation Elongation Revealed by Ribosome Profiling [Dataset_4],,,SRA713167,,,,,,,,,,,,,,, PRJNA480953,SRX4387664,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,other,SAMN09652702,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,NextSeq 500,SRR7517655,227390056,11369502800,SAMN09652702,,,,,,,,B cell,SUB4286241,,,,,,,,,,,,,,,,,,,,false,TRA00091977,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR751/005/SRR7517655/SRR7517655.fastq.gz,6189708650,ftp.sra.ebi.ac.uk/vol1/fastq/SRR751/005/SRR7517655/SRR7517655.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR751/005/SRR7517655/SRR7517655.fastq.gz,f7ba70a7a4bf5035401e981eb0a57eb5,2019-08-13,2019-08-13,false,,,,,,,,,,,ILLUMINA,,,,2019-08-13,,SINGLE,TRA00091977,,,,,,,,,LIB028402_TRA00091977_S2_L002_R1.fastq.bz2,,HZ_CTRLrpf,,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,,,,,SRS3544143,SRP153324,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR751/005/SRR7517655,5097849710,ftp.sra.ebi.ac.uk/vol1/srr/SRR751/005/SRR7517655,ftp.sra.ebi.ac.uk/vol1/srr/SRR751/005/SRR7517655,42b9159e4a6caf25e7f3bbbeec8b1f5a,C57BL/6J,PRJNA480953,The role of eIF5A in primary murine B cells revealed by ribosome profiling,,,SRA738905,,,,,,,,female,,,,,,Spleen, PRJNA480953,SRX4387663,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,other,SAMN09652704,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,NextSeq 500,SRR7517656,287250155,14362507750,SAMN09652704,,,,,,,,B cell,SUB4286241,,,,,,,,,,,,,,,,,,,,false,TRA00085897,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR751/006/SRR7517656/SRR7517656.fastq.gz,7977738166,ftp.sra.ebi.ac.uk/vol1/fastq/SRR751/006/SRR7517656/SRR7517656.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR751/006/SRR7517656/SRR7517656.fastq.gz,344c6f66fb44e45c8e0b407b84323025,2019-08-13,2019-08-13,false,,,,,,,,,,,ILLUMINA,,,,2019-08-13,,SINGLE,TRA00085897,,,,,,,,,LIB026570_TRA00085897_S3_L002_R1.fastq.gz,,HZ_GC7rpf,,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,,,,,SRS3544146,SRP153324,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR751/006/SRR7517656,6344636429,ftp.sra.ebi.ac.uk/vol1/srr/SRR751/006/SRR7517656,ftp.sra.ebi.ac.uk/vol1/srr/SRR751/006/SRR7517656,0e005d80d4e0c8048a9f9b26b9dcff69,C57BL/6J,PRJNA480953,The role of eIF5A in primary murine B cells revealed by ribosome profiling,,,SRA738905,,,,,,,,female,,,,,,Spleen, PRJNA480953,SRX4387662,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,Oligo-dT,SAMN09652701,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,NextSeq 500,SRR7517657,162626902,8131345100,SAMN09652701,,,,,,,,B cell,SUB4286241,,,,,,,,,,,,,,,,,,,,false,TRA00091981,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR751/007/SRR7517657/SRR7517657.fastq.gz,4886749336,ftp.sra.ebi.ac.uk/vol1/fastq/SRR751/007/SRR7517657/SRR7517657.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR751/007/SRR7517657/SRR7517657.fastq.gz,34ab65215e97e03c079590b6f54b13f2,2019-08-13,2019-08-13,false,,,,,,,,,,,ILLUMINA,,,,2019-08-13,,SINGLE,TRA00091981,,,,,,,,,LIB028402_TRA00091981_S3_L002_R1.fastq.bz2,,HZ_CTRLmRNA,,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,,,,,SRS3544145,SRP153324,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR751/007/SRR7517657,3675811875,ftp.sra.ebi.ac.uk/vol1/srr/SRR751/007/SRR7517657,ftp.sra.ebi.ac.uk/vol1/srr/SRR751/007/SRR7517657,f68c703f86ff1374c86b29db159ee94f,C57BL/6J,PRJNA480953,The role of eIF5A in primary murine B cells revealed by ribosome profiling,,,SRA738905,,,,,,,,female,,,,,,Spleen, PRJNA480953,SRX4387661,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,NextSeq 500 sequencing; Ribosome profiling of Mus Musculus: adult female B cells,10090,Mus musculus,RNA-Seq,TRANSCRIPTOMIC,Oligo-dT,SAMN09652703,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,NextSeq 500,SRR7517658,146674049,7333702450,SAMN09652703,,,,,,,,B cell,SUB4286241,,,,,,,,,,,,,,,,,,,,false,TRA00091974,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR751/008/SRR7517658/SRR7517658.fastq.gz,4484992453,ftp.sra.ebi.ac.uk/vol1/fastq/SRR751/008/SRR7517658/SRR7517658.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR751/008/SRR7517658/SRR7517658.fastq.gz,5c65ae76e86dd1e2fef09cd8dfdc42f4,2019-08-13,2019-08-13,false,,,,,,,,,,,ILLUMINA,,,,2019-08-13,,SINGLE,TRA00091974,,,,,,,,,LIB028402_TRA00091974_S1_L002_R1.fastq.bz2,,HZ_GC7mRNA,,This sample has been submitted by pda|hanlin1025@gmail.com on 2019-08-13; Mus musculus,,,,,SRS3544144,SRP153324,,,,female,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR751/008/SRR7517658,3338425710,ftp.sra.ebi.ac.uk/vol1/srr/SRR751/008/SRR7517658,ftp.sra.ebi.ac.uk/vol1/srr/SRR751/008/SRR7517658,c0490ab37ddcbfcf7023a3271d6ddec7,C57BL/6J,PRJNA480953,The role of eIF5A in primary murine B cells revealed by ribosome profiling,,,SRA738905,,,,,,,,female,,,,,,Spleen, PRJNA495919,SRX4870934,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type plus radicicol,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type plus radicicol,5661,Leishmania donovani,OTHER,TRANSCRIPTOMIC,RANDOM,SAMN10234888,wild type plus RAD,NextSeq 500,SRR8040412,45205841,3435643916,SAMN10234888,,,,,,,,,SUB4620501,,,,,,,,,,,,,,,,,,,,false,0002_rib,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR804/002/SRR8040412/SRR8040412.fastq.gz,1411677635,ftp.sra.ebi.ac.uk/vol1/fastq/SRR804/002/SRR8040412/SRR8040412.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR804/002/SRR8040412/SRR8040412.fastq.gz,5c31345e6def170e30c77d3c6d457322,2018-11-17,2018-11-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-17,,SINGLE,0002_rib,,,,,,,,,0002_rib_1.fq.gz,,0002,,wild type plus RAD,,,,,SRS3925916,SRP165276,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR804/002/SRR8040412,1438086993,ftp.sra.ebi.ac.uk/vol1/srr/SRR804/002/SRR8040412,ftp.sra.ebi.ac.uk/vol1/srr/SRR804/002/SRR8040412,34a1e7f195aea9986f7a0d06ee9e7fee,,PRJNA495919,Ribosome Profiling Reveals HSP90 Inhibitor Effects on Stage-specific Protein Synthesis in Leishmania donovani,,,SRA793498,,,,,,,,,,,,,,, PRJNA495919,SRX4870932,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type,NextSeq 500 sequencing; Ribosome profiling of L. donovani wild type,5661,Leishmania donovani,OTHER,TRANSCRIPTOMIC,RANDOM,SAMN10234887,wild type minus RAD,NextSeq 500,SRR8040414,24741340,1880341840,SAMN10234887,,,,,,,,,SUB4620501,,,,,,,,,,,,,,,,,,,,false,0001_rib,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR804/004/SRR8040414/SRR8040414.fastq.gz,769242162,ftp.sra.ebi.ac.uk/vol1/fastq/SRR804/004/SRR8040414/SRR8040414.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR804/004/SRR8040414/SRR8040414.fastq.gz,4ee32e6d64d41df6f5ef38274b36cef8,2018-11-17,2018-11-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-17,,SINGLE,0001_rib,,,,,,,,,0001_rib_1.fq.gz,,0001,,wild type minus RAD,,,,,SRS3925915,SRP165276,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR804/004/SRR8040414,788057181,ftp.sra.ebi.ac.uk/vol1/srr/SRR804/004/SRR8040414,ftp.sra.ebi.ac.uk/vol1/srr/SRR804/004/SRR8040414,4eb22bc6e85e432978adaebbe65e5717,,PRJNA495919,Ribosome Profiling Reveals HSP90 Inhibitor Effects on Stage-specific Protein Synthesis in Leishmania donovani,,,SRA793498,,,,,,,,,,,,,,, PRJNA495919,SRX4870930,NextSeq 500 sequencing; Ribosome profiling of L. donovani HSP90rr plus radicicol,NextSeq 500 sequencing; Ribosome profiling of L. donovani HSP90rr plus radicicol,5661,Leishmania donovani,OTHER,TRANSCRIPTOMIC,RANDOM,SAMN10234889,HSP90rr plus RAD,NextSeq 500,SRR8040416,28476385,2164205260,SAMN10234889,,,,,,,,,SUB4620501,,,,,,,,,,,,,,,,,,,,false,0003_rib,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR804/006/SRR8040416/SRR8040416.fastq.gz,890302114,ftp.sra.ebi.ac.uk/vol1/fastq/SRR804/006/SRR8040416/SRR8040416.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR804/006/SRR8040416/SRR8040416.fastq.gz,f8ee6cb16f2605bb1ebf910a45aead88,2018-11-17,2018-11-17,false,,,,,,,,,,,ILLUMINA,,,,2018-11-17,,SINGLE,0003_rib,,,,,,,,,0003_rib_1.fq.gz,,0003,,HSP90rr plus RAD,,,,,SRS3925914,SRP165276,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR804/006/SRR8040416,910401710,ftp.sra.ebi.ac.uk/vol1/srr/SRR804/006/SRR8040416,ftp.sra.ebi.ac.uk/vol1/srr/SRR804/006/SRR8040416,c471a7df4b5443e8f5d00a1cb7028c4a,,PRJNA495919,Ribosome Profiling Reveals HSP90 Inhibitor Effects on Stage-specific Protein Synthesis in Leishmania donovani,,,SRA793498,,,,,,,,,,,,,,, PRJNA438895,SRX5075516,Illumina MiSeq sequencing; GSM3048762: ΔrrnIcomp - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq,Illumina MiSeq sequencing; GSM3048762: ΔrrnIcomp - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq,216895,Vibrio vulnificus CMCP6,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN08731684,ΔrrnIcomp - ribosome profiling data rep1,Illumina MiSeq,SRR8258332,5105532,183799152,SAMN08731684,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3048762_2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR825/002/SRR8258332/SRR8258332.fastq.gz,109239015,ftp.sra.ebi.ac.uk/vol1/fastq/SRR825/002/SRR8258332/SRR8258332.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR825/002/SRR8258332/SRR8258332.fastq.gz,4b6abce428783686400b01eb43ed708d,2018-12-07,2018-12-07,false,,,,,,,,,,,ILLUMINA,,,,2018-12-07,,SINGLE,,,,,,,,,,GSM3048762_r11,,GSM3048762,,ΔrrnIcomp - ribosome profiling data rep1,,,,,SRS3060430,SRP152673,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR825/002/SRR8258332,94090545,ftp.sra.ebi.ac.uk/vol1/srr/SRR825/002/SRR8258332,ftp.sra.ebi.ac.uk/vol1/srr/SRR825/002/SRR8258332,222248e421aca316edf35df568c9f14b,CMCP6,GSE111991,Divergent rRNAs as regulators of gene expression at the ribosome level,,,SRA667510,,,,,,,,,,,,,,, PRJNA438895,SRX5075517,Illumina MiSeq sequencing; GSM3048763: ΔrrnI - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq,Illumina MiSeq sequencing; GSM3048763: ΔrrnI - ribosome profiling data rep1; Vibrio vulnificus CMCP6; RNA-Seq,216895,Vibrio vulnificus CMCP6,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN08731683,ΔrrnI - ribosome profiling data rep1,Illumina MiSeq,SRR8258333,5834528,210043008,SAMN08731683,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3048763_2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR825/003/SRR8258333/SRR8258333.fastq.gz,123577878,ftp.sra.ebi.ac.uk/vol1/fastq/SRR825/003/SRR8258333/SRR8258333.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR825/003/SRR8258333/SRR8258333.fastq.gz,3647e42d3a0facf308ed02c719326f0d,2018-12-07,2018-12-07,false,,,,,,,,,,,ILLUMINA,,,,2018-12-07,,SINGLE,,,,,,,,,,GSM3048763_r11,,GSM3048763,,ΔrrnI - ribosome profiling data rep1,,,,,SRS3060431,SRP152673,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR825/003/SRR8258333,107765216,ftp.sra.ebi.ac.uk/vol1/srr/SRR825/003/SRR8258333,ftp.sra.ebi.ac.uk/vol1/srr/SRR825/003/SRR8258333,7ca6fdaeb7b88b76c239dfd2c2165ddf,CMCP6,GSE111991,Divergent rRNAs as regulators of gene expression at the ribosome level,,,SRA667510,,,,,,,,,,,,,,, PRJNA438895,SRX5075520,Illumina MiSeq sequencing; GSM3048766: ΔrrnIcomp - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq,Illumina MiSeq sequencing; GSM3048766: ΔrrnIcomp - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq,216895,Vibrio vulnificus CMCP6,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN08731680,ΔrrnIcomp - ribosome profiling data rep2,Illumina MiSeq,SRR8258336,20039467,1022012817,SAMN08731680,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3048766_2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR825/006/SRR8258336/SRR8258336.fastq.gz,627805403,ftp.sra.ebi.ac.uk/vol1/fastq/SRR825/006/SRR8258336/SRR8258336.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR825/006/SRR8258336/SRR8258336.fastq.gz,39d008299c8a244e4e4e86f1cef2e3ef,2018-12-07,2018-12-07,false,,,,,,,,,,,ILLUMINA,,,,2018-12-07,,SINGLE,,,,,,,,,,GSM3048766_r11,,GSM3048766,,ΔrrnIcomp - ribosome profiling data rep2,,,,,SRS3060434,SRP152673,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR825/006/SRR8258336,537173469,ftp.sra.ebi.ac.uk/vol1/srr/SRR825/006/SRR8258336,ftp.sra.ebi.ac.uk/vol1/srr/SRR825/006/SRR8258336,706959b0f1f64c1a07ddb9ec1253dbcd,CMCP6,GSE111991,Divergent rRNAs as regulators of gene expression at the ribosome level,,,SRA667510,,,,,,,,,,,,,,, PRJNA438895,SRX5075521,Illumina MiSeq sequencing; GSM3048767: ΔrrnI - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq,Illumina MiSeq sequencing; GSM3048767: ΔrrnI - ribosome profiling data rep2; Vibrio vulnificus CMCP6; RNA-Seq,216895,Vibrio vulnificus CMCP6,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN08731687,ΔrrnI - ribosome profiling data rep2,Illumina MiSeq,SRR8258337,26587915,1355983665,SAMN08731687,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3048767_2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR825/007/SRR8258337/SRR8258337.fastq.gz,764797415,ftp.sra.ebi.ac.uk/vol1/fastq/SRR825/007/SRR8258337/SRR8258337.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR825/007/SRR8258337/SRR8258337.fastq.gz,f238af2fdeff334596c329eda1aa7c74,2018-12-07,2018-12-07,false,,,,,,,,,,,ILLUMINA,,,,2018-12-07,,SINGLE,,,,,,,,,,GSM3048767_r11,,GSM3048767,,ΔrrnI - ribosome profiling data rep2,,,,,SRS3060435,SRP152673,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR825/007/SRR8258337,701009975,ftp.sra.ebi.ac.uk/vol1/srr/SRR825/007/SRR8258337,ftp.sra.ebi.ac.uk/vol1/srr/SRR825/007/SRR8258337,1a7ae6c88711e40c9084af93d3b67c85,CMCP6,GSE111991,Divergent rRNAs as regulators of gene expression at the ribosome level,,,SRA667510,,,,,,,,,,,,,,, PRJNA515289,SRX5252133,"Illumina HiSeq 4000 sequencing; GSM3563711: HEK 293 cells, ribosome profiling, ctrl, Replicate 1; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3563711: HEK 293 cells, ribosome profiling, ctrl, Replicate 1; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN10752247,"HEK 293 cells, ribosome profiling, ctrl, Replicate 1",Illumina HiSeq 4000,SRR8445000,101076288,5154890688,SAMN10752247,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3563711,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR844/000/SRR8445000/SRR8445000.fastq.gz,2215505097,ftp.sra.ebi.ac.uk/vol1/fastq/SRR844/000/SRR8445000/SRR8445000.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR844/000/SRR8445000/SRR8445000.fastq.gz,26763ddc7d958cd8967fd893494cfb3b,2019-03-26,2019-03-26,false,,,,,,,,,,,ILLUMINA,,,,2019-03-26,,SINGLE,,,,,,,,,,GSM3563711_r1,,GSM3563711,,"HEK 293 cells, ribosome profiling, ctrl, Replicate 1",,,,,SRS4253838,SRP179636,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR844/000/SRR8445000,1905525279,ftp.sra.ebi.ac.uk/vol1/srr/SRR844/000/SRR8445000,ftp.sra.ebi.ac.uk/vol1/srr/SRR844/000/SRR8445000,efc6c7003530fd51fa01fd01c8dde5d1,,GSE125114,DDX3 depletion selectively represses translation of structured mRNAs,,,SRA835182,,,,,,,,,,,,,,, PRJNA515289,SRX5252134,"Illumina HiSeq 4000 sequencing; GSM3563712: HEK 293 cells, ribosome profiling, ctrl, Replicate 2; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3563712: HEK 293 cells, ribosome profiling, ctrl, Replicate 2; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN10752246,"HEK 293 cells, ribosome profiling, ctrl, Replicate 2",Illumina HiSeq 4000,SRR8445001,96501939,4921598889,SAMN10752246,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3563712,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR844/001/SRR8445001/SRR8445001.fastq.gz,2098331792,ftp.sra.ebi.ac.uk/vol1/fastq/SRR844/001/SRR8445001/SRR8445001.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR844/001/SRR8445001/SRR8445001.fastq.gz,aadb8a1569e2bec88a0f9e23a9c6d116,2019-03-26,2019-03-26,false,,,,,,,,,,,ILLUMINA,,,,2019-03-26,,SINGLE,,,,,,,,,,GSM3563712_r1,,GSM3563712,,"HEK 293 cells, ribosome profiling, ctrl, Replicate 2",,,,,SRS4253840,SRP179636,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR844/001/SRR8445001,1821851589,ftp.sra.ebi.ac.uk/vol1/srr/SRR844/001/SRR8445001,ftp.sra.ebi.ac.uk/vol1/srr/SRR844/001/SRR8445001,5aeda3f2baf8fc688d095ac7e9cde7da,,GSE125114,DDX3 depletion selectively represses translation of structured mRNAs,,,SRA835182,,,,,,,,,,,,,,, PRJNA515289,SRX5252135,"Illumina HiSeq 4000 sequencing; GSM3563713: HEK 293 cells, ribosome profiling, siDDX3, Replicate 1; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3563713: HEK 293 cells, ribosome profiling, siDDX3, Replicate 1; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN10752245,"HEK 293 cells, ribosome profiling, siDDX3, Replicate 1",Illumina HiSeq 4000,SRR8445002,92758439,4730680389,SAMN10752245,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3563713,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR844/002/SRR8445002/SRR8445002.fastq.gz,2077591718,ftp.sra.ebi.ac.uk/vol1/fastq/SRR844/002/SRR8445002/SRR8445002.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR844/002/SRR8445002/SRR8445002.fastq.gz,610ba705703871d9fc17668531e43957,2019-03-26,2019-03-26,false,,,,,,,,,,,ILLUMINA,,,,2019-03-26,,SINGLE,,,,,,,,,,GSM3563713_r1,,GSM3563713,,"HEK 293 cells, ribosome profiling, siDDX3, Replicate 1",,,,,SRS4253841,SRP179636,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR844/002/SRR8445002,1757147421,ftp.sra.ebi.ac.uk/vol1/srr/SRR844/002/SRR8445002,ftp.sra.ebi.ac.uk/vol1/srr/SRR844/002/SRR8445002,de25d81b6700bc517057ba3b2889fba8,,GSE125114,DDX3 depletion selectively represses translation of structured mRNAs,,,SRA835182,,,,,,,,,,,,,,, PRJNA515289,SRX5252136,"Illumina HiSeq 4000 sequencing; GSM3563714: HEK 293 cells, ribosome profiling, siDDX3, Replicate 2; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3563714: HEK 293 cells, ribosome profiling, siDDX3, Replicate 2; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN10752244,"HEK 293 cells, ribosome profiling, siDDX3, Replicate 2",Illumina HiSeq 4000,SRR8445003,92190382,4701709482,SAMN10752244,,,,,,,,,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3563714,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR844/003/SRR8445003/SRR8445003.fastq.gz,2165380231,ftp.sra.ebi.ac.uk/vol1/fastq/SRR844/003/SRR8445003/SRR8445003.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR844/003/SRR8445003/SRR8445003.fastq.gz,7e64589ba1303e7a58813cecf14a064f,2019-03-26,2019-03-26,false,,,,,,,,,,,ILLUMINA,,,,2019-03-26,,SINGLE,,,,,,,,,,GSM3563714_r1,,GSM3563714,,"HEK 293 cells, ribosome profiling, siDDX3, Replicate 2",,,,,SRS4253843,SRP179636,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR844/003/SRR8445003,1770229194,ftp.sra.ebi.ac.uk/vol1/srr/SRR844/003/SRR8445003,ftp.sra.ebi.ac.uk/vol1/srr/SRR844/003/SRR8445003,5ee97eb3295b0ba87cee1f92415d9fe8,,GSE125114,DDX3 depletion selectively represses translation of structured mRNAs,,,SRA835182,,,,,,,,,,,,,,, PRJNA206070,SRX288474,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183598,WT input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870722,4000000,304000000,SAMN02183598,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152436,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870722/SRR870722.fastq.gz,197663657,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870722/SRR870722.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870722/SRR870722.fastq.gz,e5ba4815f461766a29dd2e00e16441d2,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152436_r1,,GSM1152436,,WT input mRNA for Ribosome Profiling,,,,,SRS431101,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870722,192066193,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870722,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870722,afb24ad65e29c3f366993d4f06110bb8,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288474,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183598,WT input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870723,3768017,286369292,SAMN02183598,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152436,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870723/SRR870723.fastq.gz,188419365,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870723/SRR870723.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870723/SRR870723.fastq.gz,ec4d1ce0a6f009e9518c26b608ef36d6,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152436_r2,,GSM1152436,,WT input mRNA for Ribosome Profiling,,,,,SRS431101,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870723,180226800,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870723,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870723,567731582d3cc588fbb01831c14dd931,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288474,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152436: WT input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183598,WT input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870724,4000000,304000000,SAMN02183598,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152436,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870724/SRR870724.fastq.gz,196900800,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870724/SRR870724.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870724/SRR870724.fastq.gz,2827dc3b130356bed54318185d368ade,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152436_r3,,GSM1152436,,WT input mRNA for Ribosome Profiling,,,,,SRS431101,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870724,190374119,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870724,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870724,ad1499ef8e9b0b0cab3f36be4fe039a8,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870725,4000000,304000000,SAMN02183599,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870725/SRR870725.fastq.gz,179834876,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870725/SRR870725.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870725/SRR870725.fastq.gz,86700b518135e59b40e6b904a4482718,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152437_r1,,GSM1152437,,WT ribosome protected fragments for Ribosome Profiling,,,,,SRS431102,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870725,197150068,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870725,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870725,115bdaab68c1e37eb731b112335d5066,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870726,4000000,304000000,SAMN02183599,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870726/SRR870726.fastq.gz,189615384,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870726/SRR870726.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870726/SRR870726.fastq.gz,2aa83c6bddb05ed49c36bc50368cdc0d,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2019-11-15,,SINGLE,,,,,,,,,,GSM1152437_r2,,GSM1152437,,WT ribosome protected fragments for Ribosome Profiling,,,,,SRS431102,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870726,203778942,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870726,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870726,5e690fc6923d53e33474b81d3a0fbf6f,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870727,4000000,304000000,SAMN02183599,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870727/SRR870727.fastq.gz,176385783,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870727/SRR870727.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870727/SRR870727.fastq.gz,bcd7ced12cffa50a14e88a40901a8972,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152437_r3,,GSM1152437,,WT ribosome protected fragments for Ribosome Profiling,,,,,SRS431102,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870727,194760200,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870727,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870727,ba13ba0de62255051542f36485abc180,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870728,3877037,294654812,SAMN02183599,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870728/SRR870728.fastq.gz,187051522,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870728/SRR870728.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870728/SRR870728.fastq.gz,06b537b61e36d1d6d4df29e32824c597,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152437_r4,,GSM1152437,,WT ribosome protected fragments for Ribosome Profiling,,,,,SRS431102,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870728,199733745,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870728,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870728,b78832f79029592b1e1bda8bb947aeb6,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870729,4000000,304000000,SAMN02183599,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870729/SRR870729.fastq.gz,178715175,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870729/SRR870729.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870729/SRR870729.fastq.gz,a862b87fa3f33be4fe9a1c667f717a7f,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2019-10-21,,SINGLE,,,,,,,,,,GSM1152437_r5,,GSM1152437,,WT ribosome protected fragments for Ribosome Profiling,,,,,SRS431102,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870729,196267012,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870729,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870729,231fb711d4aa0d3d1fa7bd899e2bb0a0,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870730,4000000,304000000,SAMN02183599,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870730/SRR870730.fastq.gz,183298835,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870730/SRR870730.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870730/SRR870730.fastq.gz,54410e1e907028223f9877718b8b22c5,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2019-10-14,,SINGLE,,,,,,,,,,GSM1152437_r6,,GSM1152437,,WT ribosome protected fragments for Ribosome Profiling,,,,,SRS431102,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870730,199553001,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870730,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870730,6c81352c2e8dd4f68adb54afbb827b97,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870731,4000000,304000000,SAMN02183599,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870731/SRR870731.fastq.gz,185209516,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870731/SRR870731.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870731/SRR870731.fastq.gz,36728aacadda3b144c7189022082c55f,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-26,,SINGLE,,,,,,,,,,GSM1152437_r7,,GSM1152437,,WT ribosome protected fragments for Ribosome Profiling,,,,,SRS431102,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870731,200664633,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870731,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870731,34bbcb9b69d6f288129136bd5d25c552,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870732,4000000,304000000,SAMN02183599,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870732/SRR870732.fastq.gz,172470761,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870732/SRR870732.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870732/SRR870732.fastq.gz,fcffa5443520cfd8d96c21daaab681eb,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-26,,SINGLE,,,,,,,,,,GSM1152437_r8,,GSM1152437,,WT ribosome protected fragments for Ribosome Profiling,,,,,SRS431102,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870732,192019453,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870732,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870732,8de904a24c904ce797eb2a25cd83f593,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288475,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152437: WT ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183599,WT ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870733,4000000,304000000,SAMN02183599,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152437,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870733/SRR870733.fastq.gz,178737385,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870733/SRR870733.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870733/SRR870733.fastq.gz,1948cb05270ed7530c2857b5d945d7be,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-24,,SINGLE,,,,,,,,,,GSM1152437_r9,,GSM1152437,,WT ribosome protected fragments for Ribosome Profiling,,,,,SRS431102,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870733,196476827,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870733,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870733,7e2567b2740a9e2aeeba39b3f18bd351,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288476,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183600,Nanog + SoxB1 MO input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870734,4000000,304000000,SAMN02183600,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152438,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870734/SRR870734.fastq.gz,195225206,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870734/SRR870734.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870734/SRR870734.fastq.gz,65ce951618b72604730ddce50e161997,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-26,,SINGLE,,,,,,,,,,GSM1152438_r1,,GSM1152438,,Nanog + SoxB1 MO input mRNA for Ribosome Profiling,,,,,SRS431104,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870734,187651374,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870734,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870734,f0d6b06082dc5589db05a31898c9c9df,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288476,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183600,Nanog + SoxB1 MO input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870735,4000000,304000000,SAMN02183600,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152438,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870735/SRR870735.fastq.gz,197737656,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870735/SRR870735.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870735/SRR870735.fastq.gz,6e00e2475dfa105182819e2dde020373,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152438_r2,,GSM1152438,,Nanog + SoxB1 MO input mRNA for Ribosome Profiling,,,,,SRS431104,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870735,189019159,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870735,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870735,098bb0356a95deff87726095783084a3,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288476,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152438: Nanog + SoxB1 MO input mRNA for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183600,Nanog + SoxB1 MO input mRNA for Ribosome Profiling,Illumina HiSeq 2000,SRR870736,2117060,160896560,SAMN02183600,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152438,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870736/SRR870736.fastq.gz,105481774,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870736/SRR870736.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870736/SRR870736.fastq.gz,848b0c500a750b1d1e19a30cb1ddb54c,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2019-10-07,,SINGLE,,,,,,,,,,GSM1152438_r3,,GSM1152438,,Nanog + SoxB1 MO input mRNA for Ribosome Profiling,,,,,SRS431104,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870736,99957115,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870736,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870736,b6b2896c63f77d29bfe3f3a93cccdf0d,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870737,4000000,304000000,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870737/SRR870737.fastq.gz,180149816,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870737/SRR870737.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870737/SRR870737.fastq.gz,f5b927159147662341cf586d40ceea04,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-24,,SINGLE,,,,,,,,,,GSM1152439_r1,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870737,193897543,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870737,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870737,899a6f2eaa169e97892e5fec9f98d3a1,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870738,4000000,304000000,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870738/SRR870738.fastq.gz,175447118,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870738/SRR870738.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870738/SRR870738.fastq.gz,2f9810ae4f3a29dc78b6784b647b576f,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-24,,SINGLE,,,,,,,,,,GSM1152439_r10,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870738,190593303,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870738,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870738,41b3a9e7db57f2b10eb59fd61f91a5cd,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870739,4000000,304000000,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870739/SRR870739.fastq.gz,170173190,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870739/SRR870739.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870739/SRR870739.fastq.gz,564c2ea50788ac5d99194558df983cae,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2019-10-30,,SINGLE,,,,,,,,,,GSM1152439_r2,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870739,186661314,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870739,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870739,fd7a59c85f3f11862ea89806b6479c03,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870740,4000000,304000000,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870740/SRR870740.fastq.gz,180033228,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870740/SRR870740.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870740/SRR870740.fastq.gz,081ab9269fbf9882baeaf584b9341daf,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152439_r3,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870740,193969130,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870740,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870740,0a9763e1cfe83bbc340210e14c30c604,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870741,4000000,304000000,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870741/SRR870741.fastq.gz,172965067,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870741/SRR870741.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870741/SRR870741.fastq.gz,420d50b1e8df0ed20b7a5782e313595f,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2019-10-07,,SINGLE,,,,,,,,,,GSM1152439_r4,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870741,188806088,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870741,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870741,826c17bf89146e4cde8883dc9f10d494,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870742,4000000,304000000,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870742/SRR870742.fastq.gz,187241483,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870742/SRR870742.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870742/SRR870742.fastq.gz,627d3dbaa6dec9b2869696d2991ddd02,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152439_r5,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870742,199190281,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870742,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870742,6ef76aa734e77e6f83920adf1cac55f8,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870743,4000000,304000000,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870743/SRR870743.fastq.gz,188800807,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870743/SRR870743.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870743/SRR870743.fastq.gz,04449c3337abd0d73e39e1615780fa2e,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-01-20,,SINGLE,,,,,,,,,,GSM1152439_r6,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870743,200140085,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870743,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870743,dbc304693fdf253dd762db74c6a243fd,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870744,4000000,304000000,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870744/SRR870744.fastq.gz,180342712,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870744/SRR870744.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870744/SRR870744.fastq.gz,3fdacfa4139b457ec0185adeed43805a,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152439_r7,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870744,194220112,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870744,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870744,6a96dc65ba6449e91ef27e9310e04fbf,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870745,2436469,185171644,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870745/SRR870745.fastq.gz,120745016,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870745/SRR870745.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870745/SRR870745.fastq.gz,c73dbd3f559fabb8cc3a6dfed7954b05,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2020-05-25,,SINGLE,,,,,,,,,,GSM1152439_r8,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870745,126025782,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870745,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870745,ffd64c91991781311c6fb4ff4bf8acac,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA206070,SRX288477,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,Illumina HiSeq 2000 sequencing; GSM1152439: Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling; Danio rerio; OTHER,7955,Danio rerio,OTHER,TRANSCRIPTOMIC,other,SAMN02183601,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,Illumina HiSeq 2000,SRR870746,4000000,304000000,SAMN02183601,,,,,,,,,GEO,,,,,,,,,,,,,2hpf,,,,,,,false,GSM1152439,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR870/SRR870746/SRR870746.fastq.gz,177708003,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870746/SRR870746.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR870/SRR870746/SRR870746.fastq.gz,37bf463a99bab447cfe5381cb9c66cb6,2013-11-13,2013-11-13,false,,,,,,,,,,,ILLUMINA,,,,2019-10-07,,SINGLE,,,,,,,,,,GSM1152439_r9,,GSM1152439,,Nanog + SoxB1 ribosome protected fragments for Ribosome Profiling,,,,,SRS431103,SRP023492,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR870/SRR870746,192072090,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870746,ftp.sra.ebi.ac.uk/vol1/srr/SRR870/SRR870746,9e5d25c8ad3c74a6c9e08ff41c6a760a,TUAB,GSE47558,"Nanog, SoxB1 and Pou5f1/Oct4 regulate widespread zygotic gene activation during the maternal-to-zygotic transition",,,SRA082637,,,,,,,,,,,,,,Whole embryos, PRJNA527204,SRX5525062,Illumina HiSeq 2500 sequencing; GSM3671680: ribosome profiling wt_1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671680: ribosome profiling wt_1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130407,ribosome profiling wt_1,Illumina HiSeq 2500,SRR8732200,18661991,933099550,SAMN11130407,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671680,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/000/SRR8732200/SRR8732200.fastq.gz,842376117,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/000/SRR8732200/SRR8732200.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/000/SRR8732200/SRR8732200.fastq.gz,14f9afe848c24e868249a3c44853183e,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671680_r1,,GSM3671680,,ribosome profiling wt_1,,,,,SRS4491743,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/000/SRR8732200,600121455,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/000/SRR8732200,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/000/SRR8732200,1317bf4edf06c3e6c3388a29b4d68892,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525063,Illumina HiSeq 2500 sequencing; GSM3671681: ribosome profiling wt_2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671681: ribosome profiling wt_2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130406,ribosome profiling wt_2,Illumina HiSeq 2500,SRR8732201,17636110,881805500,SAMN11130406,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671681,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/001/SRR8732201/SRR8732201.fastq.gz,798721343,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/001/SRR8732201/SRR8732201.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/001/SRR8732201/SRR8732201.fastq.gz,55fe1b299593f826d014d0715cffe0d7,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671681_r1,,GSM3671681,,ribosome profiling wt_2,,,,,SRS4491744,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/001/SRR8732201,563407508,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/001/SRR8732201,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/001/SRR8732201,93c6d5f86ac4c089f6b335165c0732ef,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525064,Illumina HiSeq 2500 sequencing; GSM3671682: ribosome profiling wt_3; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671682: ribosome profiling wt_3; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130405,ribosome profiling wt_3,Illumina HiSeq 2500,SRR8732202,23560878,1178043900,SAMN11130405,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671682,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/002/SRR8732202/SRR8732202.fastq.gz,1065000760,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/002/SRR8732202/SRR8732202.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/002/SRR8732202/SRR8732202.fastq.gz,609b9c20836b37d87cf7afa8c6373383,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671682_r1,,GSM3671682,,ribosome profiling wt_3,,,,,SRS4491745,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/002/SRR8732202,754864028,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/002/SRR8732202,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/002/SRR8732202,91173d814ca8c1aa71736f91ff442f17,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525065,Illumina HiSeq 2500 sequencing; GSM3671683: ribosome profiling APP_1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671683: ribosome profiling APP_1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130404,ribosome profiling APP_1,Illumina HiSeq 2500,SRR8732203,22107235,1105361750,SAMN11130404,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671683,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/003/SRR8732203/SRR8732203.fastq.gz,1001251765,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/003/SRR8732203/SRR8732203.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/003/SRR8732203/SRR8732203.fastq.gz,58fa21f733185bafe7220c77e4385aa0,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671683_r1,,GSM3671683,,ribosome profiling APP_1,,,,,SRS4491746,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/003/SRR8732203,705396420,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/003/SRR8732203,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/003/SRR8732203,a893d6206c239ee5560401616e40b6cc,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525066,Illumina HiSeq 2500 sequencing; GSM3671684: ribosome profiling APP_2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671684: ribosome profiling APP_2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130403,ribosome profiling APP_2,Illumina HiSeq 2500,SRR8732204,18895655,944782750,SAMN11130403,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671684,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/004/SRR8732204/SRR8732204.fastq.gz,850327508,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/004/SRR8732204/SRR8732204.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/004/SRR8732204/SRR8732204.fastq.gz,3e97e0c316ecd61468f8b226acc7f1e3,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671684_r1,,GSM3671684,,ribosome profiling APP_2,,,,,SRS4491747,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/004/SRR8732204,607648844,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/004/SRR8732204,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/004/SRR8732204,f5445d062e2d980c4960ba1033f2975a,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525067,Illumina HiSeq 2500 sequencing; GSM3671685: ribosome profiling APP_3; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671685: ribosome profiling APP_3; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130402,ribosome profiling APP_3,Illumina HiSeq 2500,SRR8732205,20817886,1040894300,SAMN11130402,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671685,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/005/SRR8732205/SRR8732205.fastq.gz,942259892,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/005/SRR8732205/SRR8732205.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/005/SRR8732205/SRR8732205.fastq.gz,e0132c1d413948172dd4eebf14426c15,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671685_r1,,GSM3671685,,ribosome profiling APP_3,,,,,SRS4491748,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/005/SRR8732205,664367870,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/005/SRR8732205,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/005/SRR8732205,8eeab83c6554e29765258ab3bfc21b5d,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525068,Illumina HiSeq 2500 sequencing; GSM3671686: ribosome profiling PSEN_1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671686: ribosome profiling PSEN_1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130401,ribosome profiling PSEN_1,Illumina HiSeq 2500,SRR8732206,20629961,1031498050,SAMN11130401,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671686,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/006/SRR8732206/SRR8732206.fastq.gz,929755701,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/006/SRR8732206/SRR8732206.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/006/SRR8732206/SRR8732206.fastq.gz,a8876ef5bf8ef9f90ae6b1b5845fc1bd,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671686_r1,,GSM3671686,,ribosome profiling PSEN_1,,,,,SRS4491749,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/006/SRR8732206,658298589,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/006/SRR8732206,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/006/SRR8732206,4c486417a5b6a8f5ab75c3ef954ca0b6,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525069,Illumina HiSeq 2500 sequencing; GSM3671687: ribosome profiling PSEN_2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671687: ribosome profiling PSEN_2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130400,ribosome profiling PSEN_2,Illumina HiSeq 2500,SRR8732207,20358650,1017932500,SAMN11130400,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671687,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/007/SRR8732207/SRR8732207.fastq.gz,923713369,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/007/SRR8732207/SRR8732207.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/007/SRR8732207/SRR8732207.fastq.gz,59ab811b6d18051e7f0478e1c7ff081a,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671687_r1,,GSM3671687,,ribosome profiling PSEN_2,,,,,SRS4491750,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/007/SRR8732207,650826280,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/007/SRR8732207,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/007/SRR8732207,9cb256e324cec7e6edcab19212ba262f,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525070,Illumina HiSeq 2500 sequencing; GSM3671688: ribosome profiling PSEN_3; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671688: ribosome profiling PSEN_3; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130427,ribosome profiling PSEN_3,Illumina HiSeq 2500,SRR8732208,20652398,1032619900,SAMN11130427,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671688,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/008/SRR8732208/SRR8732208.fastq.gz,931565387,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/008/SRR8732208/SRR8732208.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/008/SRR8732208/SRR8732208.fastq.gz,e2a48b065e407e3f087ac4bcb383ab3d,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671688_r1,,GSM3671688,,ribosome profiling PSEN_3,,,,,SRS4491751,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/008/SRR8732208,656100785,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/008/SRR8732208,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/008/SRR8732208,d7e1cd7da3d3ea004af5c9f86b86c950,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525071,Illumina HiSeq 2500 sequencing; GSM3671689: ribosome profiling APP/PSEN1_1; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671689: ribosome profiling APP/PSEN1_1; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130426,ribosome profiling APP/PSEN1_1,Illumina HiSeq 2500,SRR8732209,21629538,1081476900,SAMN11130426,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671689,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/009/SRR8732209/SRR8732209.fastq.gz,973562913,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/009/SRR8732209/SRR8732209.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/009/SRR8732209/SRR8732209.fastq.gz,309c8e1755b2d6777b19b598e69513bb,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671689_r1,,GSM3671689,,ribosome profiling APP/PSEN1_1,,,,,SRS4491752,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/009/SRR8732209,685979532,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/009/SRR8732209,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/009/SRR8732209,b1213c69c084633043c29b297a92cb0f,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525072,Illumina HiSeq 2500 sequencing; GSM3671690: ribosome profiling APP/PSEN1_2; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671690: ribosome profiling APP/PSEN1_2; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130425,ribosome profiling APP/PSEN1_2,Illumina HiSeq 2500,SRR8732210,22115725,1105786250,SAMN11130425,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671690,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/000/SRR8732210/SRR8732210.fastq.gz,997588027,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/000/SRR8732210/SRR8732210.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/000/SRR8732210/SRR8732210.fastq.gz,b9814ddfa981960e3df418a6b71119fd,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671690_r1,,GSM3671690,,ribosome profiling APP/PSEN1_2,,,,,SRS4491753,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/000/SRR8732210,703034019,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/000/SRR8732210,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/000/SRR8732210,4563f2a7dd48335fa24c143e073a594d,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA527204,SRX5525073,Illumina HiSeq 2500 sequencing; GSM3671691: ribosome profiling APP/PSEN1_3; Homo sapiens; RNA-Seq,Illumina HiSeq 2500 sequencing; GSM3671691: ribosome profiling APP/PSEN1_3; Homo sapiens; RNA-Seq,9606,Homo sapiens,RNA-Seq,TRANSCRIPTOMIC,cDNA,SAMN11130424,ribosome profiling APP/PSEN1_3,Illumina HiSeq 2500,SRR8732211,26892978,1344648900,SAMN11130424,,,,,,,,co-isogenic iPS cells,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3671691,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR873/001/SRR8732211/SRR8732211.fastq.gz,1207490191,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/001/SRR8732211/SRR8732211.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR873/001/SRR8732211/SRR8732211.fastq.gz,6a4dada6c41ee345e71f2927441117da,2019-08-09,2019-08-09,false,,,,,,,,,,,ILLUMINA,,,,2019-08-09,,SINGLE,,,,,,,,,,GSM3671691_r1,,GSM3671691,,ribosome profiling APP/PSEN1_3,,,,,SRS4491754,SRP188505,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR873/001/SRR8732211,849024459,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/001/SRR8732211,ftp.sra.ebi.ac.uk/vol1/srr/SRR873/001/SRR8732211,2efd5c3e5ef81969364146e4fdc26070,,GSE128344,"A large panel of isogenic APP and PSEN1 mutant human iPSC neurons reveals shared endosomal abnormalities mediated by APP b-CTFs, not Ab [ribosome profiling]",,,SRA860677,,,,,,,,,,,,,,, PRJNA544411,SRX5887326,"Illumina HiSeq 4000 sequencing; GSM3791723: iPSC ribosome profiling, harringtonine-treated; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791723: iPSC ribosome profiling, harringtonine-treated; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835522,"iPSC ribosome profiling, harringtonine-treated",Illumina HiSeq 4000,SRR9113062,131541396,3743828156,SAMN11835522,,,,,,,WTC-11,iPSC,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3791723,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR911/002/SRR9113062/SRR9113062.fastq.gz,2819325572,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/002/SRR9113062/SRR9113062.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/002/SRR9113062/SRR9113062.fastq.gz,a4109f5bdfa47194920971dc57fa5e38,2020-03-23,2020-03-23,false,,,,,,,,,,,ILLUMINA,,,,2020-03-23,,SINGLE,,,,,,,,,,GSM3791723_r1,,GSM3791723,,"iPSC ribosome profiling, harringtonine-treated",,,,,SRS4809549,SRP199285,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR911/002/SRR9113062,4847243504,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/002/SRR9113062,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/002/SRR9113062,aace924ef913436c0f5c552291ab3e7e,,GSE131650,Pervasive functional translation of noncanonical open reading frames,,,SRA889795,,,,,,,,,,,,,,, PRJNA544411,SRX5887327,"Illumina HiSeq 4000 sequencing; GSM3791724: Cardiomyocyte ribosome profiling, harringtonine-treated; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791724: Cardiomyocyte ribosome profiling, harringtonine-treated; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835521,"Cardiomyocyte ribosome profiling, harringtonine-treated",Illumina HiSeq 4000,SRR9113063,105449435,2785265458,SAMN11835521,,,,,,,WTC-11,iPSC-derived cardiomyocytes,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3791724,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR911/003/SRR9113063/SRR9113063.fastq.gz,2068122512,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/003/SRR9113063/SRR9113063.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/003/SRR9113063/SRR9113063.fastq.gz,0c24e17823d37577b4511278057358bd,2020-03-23,2020-03-23,false,,,,,,,,,,,ILLUMINA,,,,2020-03-23,,SINGLE,,,,,,,,,,GSM3791724_r1,,GSM3791724,,"Cardiomyocyte ribosome profiling, harringtonine-treated",,,,,SRS4809550,SRP199285,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR911/003/SRR9113063,3812417240,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/003/SRR9113063,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/003/SRR9113063,3a71b072d5877ad2e27aade618450d98,,GSE131650,Pervasive functional translation of noncanonical open reading frames,,,SRA889795,,,,,,,,,,,,,,, PRJNA544411,SRX5887328,"Illumina HiSeq 4000 sequencing; GSM3791725: iPSC ribosome profiling, no drug treatment, replicate 1; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791725: iPSC ribosome profiling, no drug treatment, replicate 1; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835520,"iPSC ribosome profiling, no drug treatment, replicate 1",Illumina HiSeq 4000,SRR9113064,52479474,1453634111,SAMN11835520,,,,,,,WTC-11,iPSC,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3791725,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR911/004/SRR9113064/SRR9113064.fastq.gz,1200472760,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/004/SRR9113064/SRR9113064.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/004/SRR9113064/SRR9113064.fastq.gz,128a460879286c1e012351e65daa2c9a,2020-03-23,2020-03-23,false,,,,,,,,,,,ILLUMINA,,,,2020-03-23,,SINGLE,,,,,,,,,,GSM3791725_r1,,GSM3791725,,"iPSC ribosome profiling, no drug treatment, replicate 1",,,,,SRS4809551,SRP199285,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR911/004/SRR9113064,1935053980,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/004/SRR9113064,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/004/SRR9113064,adb964bfe39286010282f1617dc7a0bf,,GSE131650,Pervasive functional translation of noncanonical open reading frames,,,SRA889795,,,,,,,,,,,,,,, PRJNA544411,SRX5887329,"Illumina HiSeq 4000 sequencing; GSM3791726: iPSC ribosome profiling, no drug treatment, replicate 2; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791726: iPSC ribosome profiling, no drug treatment, replicate 2; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835519,"iPSC ribosome profiling, no drug treatment, replicate 2",Illumina HiSeq 4000,SRR9113065,51856183,1508584022,SAMN11835519,,,,,,,WTC-11,iPSC,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3791726,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR911/005/SRR9113065/SRR9113065.fastq.gz,1159129604,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/005/SRR9113065/SRR9113065.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/005/SRR9113065/SRR9113065.fastq.gz,0169b6fadc244a138b872e3d5813d9f5,2020-03-23,2020-03-23,false,,,,,,,,,,,ILLUMINA,,,,2020-03-23,,SINGLE,,,,,,,,,,GSM3791726_r1,,GSM3791726,,"iPSC ribosome profiling, no drug treatment, replicate 2",,,,,SRS4809552,SRP199285,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR911/005/SRR9113065,1938008028,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/005/SRR9113065,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/005/SRR9113065,adfcfd63660917c85431ba318646218c,,GSE131650,Pervasive functional translation of noncanonical open reading frames,,,SRA889795,,,,,,,,,,,,,,, PRJNA544411,SRX5887330,"Illumina HiSeq 4000 sequencing; GSM3791727: iPSC ribosome profiling, no drug treatment, replicate 3; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791727: iPSC ribosome profiling, no drug treatment, replicate 3; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835518,"iPSC ribosome profiling, no drug treatment, replicate 3",Illumina HiSeq 4000,SRR9113066,44471589,1280127923,SAMN11835518,,,,,,,WTC-11,iPSC,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3791727,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR911/006/SRR9113066/SRR9113066.fastq.gz,996140081,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/006/SRR9113066/SRR9113066.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/006/SRR9113066/SRR9113066.fastq.gz,5bc29f308bcfedec67fa034f0a2d32c4,2020-03-23,2020-03-23,false,,,,,,,,,,,ILLUMINA,,,,2020-03-23,,SINGLE,,,,,,,,,,GSM3791727_r1,,GSM3791727,,"iPSC ribosome profiling, no drug treatment, replicate 3",,,,,SRS4809553,SRP199285,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR911/006/SRR9113066,1657553876,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/006/SRR9113066,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/006/SRR9113066,3289b06f445bcfaf6d70cc4c2e127f5b,,GSE131650,Pervasive functional translation of noncanonical open reading frames,,,SRA889795,,,,,,,,,,,,,,, PRJNA544411,SRX5887331,"Illumina HiSeq 4000 sequencing; GSM3791728: Cardiomyocyte ribosome profiling, no drug treatment, replicate 1; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791728: Cardiomyocyte ribosome profiling, no drug treatment, replicate 1; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835517,"Cardiomyocyte ribosome profiling, no drug treatment, replicate 1",Illumina HiSeq 4000,SRR9113067,15031439,395105326,SAMN11835517,,,,,,,WTC-11,iPSC-derived cardiomyocytes,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3791728,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR911/007/SRR9113067/SRR9113067.fastq.gz,313049588,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/007/SRR9113067/SRR9113067.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/007/SRR9113067/SRR9113067.fastq.gz,e05bdfe269c488d6cbe29b625fac2b72,2020-03-23,2020-03-23,false,,,,,,,,,,,ILLUMINA,,,,2020-03-23,,SINGLE,,,,,,,,,,GSM3791728_r1,,GSM3791728,,"Cardiomyocyte ribosome profiling, no drug treatment, replicate 1",,,,,SRS4809554,SRP199285,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR911/007/SRR9113067,544812636,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/007/SRR9113067,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/007/SRR9113067,d57c82a462b34fa7d465f5310f6557ee,,GSE131650,Pervasive functional translation of noncanonical open reading frames,,,SRA889795,,,,,,,,,,,,,,, PRJNA544411,SRX5887332,"Illumina HiSeq 4000 sequencing; GSM3791729: Cardiomyocyte ribosome profiling, no drug treatment, replicate 2; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791729: Cardiomyocyte ribosome profiling, no drug treatment, replicate 2; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835516,"Cardiomyocyte ribosome profiling, no drug treatment, replicate 2",Illumina HiSeq 4000,SRR9113068,24288824,668239583,SAMN11835516,,,,,,,WTC-11,iPSC-derived cardiomyocytes,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3791729,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR911/008/SRR9113068/SRR9113068.fastq.gz,515601964,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/008/SRR9113068/SRR9113068.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/008/SRR9113068/SRR9113068.fastq.gz,410f4577175b65f792e74fbdfe4464eb,2020-03-23,2020-03-23,false,,,,,,,,,,,ILLUMINA,,,,2020-03-23,,SINGLE,,,,,,,,,,GSM3791729_r1,,GSM3791729,,"Cardiomyocyte ribosome profiling, no drug treatment, replicate 2",,,,,SRS4809555,SRP199285,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR911/008/SRR9113068,901006548,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/008/SRR9113068,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/008/SRR9113068,01b66dfa4ffe30b7172fdbe114309485,,GSE131650,Pervasive functional translation of noncanonical open reading frames,,,SRA889795,,,,,,,,,,,,,,, PRJNA544411,SRX5887333,"Illumina HiSeq 4000 sequencing; GSM3791730: Cardiomyocyte ribosome profiling, no drug treatment, replicate 3; Homo sapiens; OTHER","Illumina HiSeq 4000 sequencing; GSM3791730: Cardiomyocyte ribosome profiling, no drug treatment, replicate 3; Homo sapiens; OTHER",9606,Homo sapiens,OTHER,TRANSCRIPTOMIC,other,SAMN11835515,"Cardiomyocyte ribosome profiling, no drug treatment, replicate 3",Illumina HiSeq 4000,SRR9113069,22387751,602037992,SAMN11835515,,,,,,,WTC-11,iPSC-derived cardiomyocytes,GEO,,,,,,,,,,,,,,,,,,,,false,GSM3791730,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR911/009/SRR9113069/SRR9113069.fastq.gz,479768259,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/009/SRR9113069/SRR9113069.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR911/009/SRR9113069/SRR9113069.fastq.gz,05f4a8e9a3404e8c456437affcac58b1,2020-03-23,2020-03-23,false,,,,,,,,,,,ILLUMINA,,,,2020-03-23,,SINGLE,,,,,,,,,,GSM3791730_r1,,GSM3791730,,"Cardiomyocyte ribosome profiling, no drug treatment, replicate 3",,,,,SRS4809556,SRP199285,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR911/009/SRR9113069,828285308,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/009/SRR9113069,ftp.sra.ebi.ac.uk/vol1/srr/SRR911/009/SRR9113069,72453bd331eb88581b43ad3c4a326443,,GSE131650,Pervasive functional translation of noncanonical open reading frames,,,SRA889795,,,,,,,,,,,,,,, PRJNA548255,SRX6035778,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 42C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 42C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265420,52416789,1560616477,SAMN12012146,,,,,,,,,SUB5682290,,,,,,,,,,,,,,,,,,,,false,RP_42_10_r1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR926/000/SRR9265420/SRR9265420.fastq.gz,885937108,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/000/SRR9265420/SRR9265420.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/000/SRR9265420/SRR9265420.fastq.gz,5d2c32933e34e85733f3938ac05a1b4c,2019-12-24,2019-12-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,RP_42_10_r1,,,,,,,,,HS_42_10.A.fastq,,yeast BY4147,,Saccharomyces cerevisiae BY4147,,,,,SRS4939070,SRP201047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR926/000/SRR9265420,779145066,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/000/SRR9265420,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/000/SRR9265420,85ce0f39e745a349e3fa9226611be778,BY4147,PRJNA548255,Ribosome Profiling of heat shock response in yeast,,,SRA896649,,,,,,,,,,,,,,, PRJNA548255,SRX6035777,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 42C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 42C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265421,55952924,1711205789,SAMN12012146,,,,,,,,,SUB5682290,,,,,,,,,,,,,,,,,,,,false,RP_42_10_r2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR926/001/SRR9265421/SRR9265421.fastq.gz,1011172412,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/001/SRR9265421/SRR9265421.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/001/SRR9265421/SRR9265421.fastq.gz,4c25d78161874c64f6e226ce466141c0,2019-12-24,2019-12-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,RP_42_10_r2,,,,,,,,,HS_42_10.B.fastq,,yeast BY4147,,Saccharomyces cerevisiae BY4147,,,,,SRS4939070,SRP201047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR926/001/SRR9265421,844838455,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/001/SRR9265421,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/001/SRR9265421,eebc74a65f2431a9cfd8bd61b758ae07,BY4147,PRJNA548255,Ribosome Profiling of heat shock response in yeast,,,SRA896649,,,,,,,,,,,,,,, PRJNA548255,SRX6035776,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265422,49583723,1502676985,SAMN12012146,,,,,,,,,SUB5682290,,,,,,,,,,,,,,,,,,,,false,RP_37_30_r1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR926/002/SRR9265422/SRR9265422.fastq.gz,755059586,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/002/SRR9265422/SRR9265422.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/002/SRR9265422/SRR9265422.fastq.gz,00511d8f505b446890ef09095b2c12c8,2019-12-24,2019-12-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,RP_37_30_r1,,,,,,,,,HS_37_30.A.fastq,,yeast BY4147,,Saccharomyces cerevisiae BY4147,,,,,SRS4939070,SRP201047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR926/002/SRR9265422,722241701,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/002/SRR9265422,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/002/SRR9265422,750dcfbb21d0a552b0f073d3db8a0fd3,BY4147,PRJNA548255,Ribosome Profiling of heat shock response in yeast,,,SRA896649,,,,,,,,,,,,,,, PRJNA548255,SRX6035775,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 30min at 37C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265423,58906924,1740811245,SAMN12012146,,,,,,,,,SUB5682290,,,,,,,,,,,,,,,,,,,,false,RP_37_30_r2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR926/003/SRR9265423/SRR9265423.fastq.gz,983590928,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/003/SRR9265423/SRR9265423.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/003/SRR9265423/SRR9265423.fastq.gz,6715169f791fbbb5ea1077a71ba22929,2019-12-24,2019-12-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,RP_37_30_r2,,,,,,,,,HS_37_30.C.fastq,,yeast BY4147,,Saccharomyces cerevisiae BY4147,,,,,SRS4939070,SRP201047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR926/003/SRR9265423,864060628,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/003/SRR9265423,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/003/SRR9265423,0bfb028588122ead8e184e1c94fac545,BY4147,PRJNA548255,Ribosome Profiling of heat shock response in yeast,,,SRA896649,,,,,,,,,,,,,,, PRJNA548255,SRX6035774,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265424,45951630,1310462981,SAMN12012146,,,,,,,,,SUB5682290,,,,,,,,,,,,,,,,,,,,false,RP_37_10_r1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR926/004/SRR9265424/SRR9265424.fastq.gz,745739787,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/004/SRR9265424/SRR9265424.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/004/SRR9265424/SRR9265424.fastq.gz,c546652a5273f44884984982a8cc1086,2019-12-24,2019-12-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,RP_37_10_r1,,,,,,,,,HS_37_10.A.fastq,,yeast BY4147,,Saccharomyces cerevisiae BY4147,,,,,SRS4939070,SRP201047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR926/004/SRR9265424,639307146,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/004/SRR9265424,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/004/SRR9265424,dc3c285ac2bed46c55c559414af38e31,BY4147,PRJNA548255,Ribosome Profiling of heat shock response in yeast,,,SRA896649,,,,,,,,,,,,,,, PRJNA548255,SRX6035773,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 10min at 37C,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265425,47383970,1423177661,SAMN12012146,,,,,,,,,SUB5682290,,,,,,,,,,,,,,,,,,,,false,RP_37_10_r2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR926/005/SRR9265425/SRR9265425.fastq.gz,915959975,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/005/SRR9265425/SRR9265425.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/005/SRR9265425/SRR9265425.fastq.gz,e2b4f8b604c2ea952a1ddbcea511ba1d,2019-12-24,2019-12-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,RP_37_10_r2,,,,,,,,,HS_37_10.B.fastq,,yeast BY4147,,Saccharomyces cerevisiae BY4147,,,,,SRS4939070,SRP201047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR926/005/SRR9265425,744428874,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/005/SRR9265425,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/005/SRR9265425,1339976371dda6a218d16184f0852d30,BY4147,PRJNA548255,Ribosome Profiling of heat shock response in yeast,,,SRA896649,,,,,,,,,,,,,,, PRJNA548255,SRX6035772,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265426,42590657,1193803088,SAMN12012146,,,,,,,,,SUB5682290,,,,,,,,,,,,,,,,,,,,false,RP_25_0_r2,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR926/006/SRR9265426/SRR9265426.fastq.gz,668402806,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/006/SRR9265426/SRR9265426.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/006/SRR9265426/SRR9265426.fastq.gz,cfd81e7e6d53f7aa52e17fa59ba3fc34,2019-12-24,2019-12-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,RP_25_0_r2,,,,,,,,,HS_25_0.B.fastq,,yeast BY4147,,Saccharomyces cerevisiae BY4147,,,,,SRS4939070,SRP201047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR926/006/SRR9265426,576711694,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/006/SRR9265426,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/006/SRR9265426,793f29678289615ee0d71988be848fa4,BY4147,PRJNA548255,Ribosome Profiling of heat shock response in yeast,,,SRA896649,,,,,,,,,,,,,,, PRJNA548255,SRX6035771,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265427,66588117,2042292918,SAMN12012146,,,,,,,,,SUB5682290,,,,,,,,,,,,,,,,,,,,false,RP_25_0_r3,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR926/007/SRR9265427/SRR9265427.fastq.gz,1092313594,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/007/SRR9265427/SRR9265427.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/007/SRR9265427/SRR9265427.fastq.gz,6ebc2af98229c07911683558321f212e,2019-12-24,2019-12-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,RP_25_0_r3,,,,,,,,,HS_25_0.C.fastq,,yeast BY4147,,Saccharomyces cerevisiae BY4147,,,,,SRS4939070,SRP201047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR926/007/SRR9265427,1000846817,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/007/SRR9265427,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/007/SRR9265427,42df5648b76f1881c55851a81d3e821b,BY4147,PRJNA548255,Ribosome Profiling of heat shock response in yeast,,,SRA896649,,,,,,,,,,,,,,, PRJNA548255,SRX6035769,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,Illumina HiSeq 1500 sequencing; Ribosome profiling of Saccharomyces cerevisiae BY4147 control sample,4932,Saccharomyces cerevisiae,RIP-Seq,TRANSCRIPTOMIC,PCR,SAMN12012146,Saccharomyces cerevisiae BY4147,Illumina HiSeq 1500,SRR9265429,38286437,1148214684,SAMN12012146,,,,,,,,,SUB5682290,,,,,,,,,,,,,,,,,,,,false,RP_25_0_r1,,fasp.sra.ebi.ac.uk:/vol1/fastq/SRR926/009/SRR9265429/SRR9265429.fastq.gz,819773428,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/009/SRR9265429/SRR9265429.fastq.gz,ftp.sra.ebi.ac.uk/vol1/fastq/SRR926/009/SRR9265429/SRR9265429.fastq.gz,03e4eb94af9999e009f7f1dbddcb0219,2019-12-24,2019-12-24,false,,,,,,,,,,,ILLUMINA,,,,2019-12-24,,SINGLE,RP_25_0_r1,,,,,,,,,HS_25_0.A.fastq,,yeast BY4147,,Saccharomyces cerevisiae BY4147,,,,,SRS4939070,SRP201047,,,,,,fasp.sra.ebi.ac.uk:/vol1/srr/SRR926/009/SRR9265429,597402604,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/009/SRR9265429,ftp.sra.ebi.ac.uk/vol1/srr/SRR926/009/SRR9265429,3b0de1d8c09cb833bc716bd9943eeda9,BY4147,PRJNA548255,Ribosome Profiling of heat shock response in yeast,,,SRA896649,,,,,,,,,,,,,,, PRJNA548255,SRX6035759,Illumina HiSeq 1500 sequencing; 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Caco2 cells were grown on 150-mm dishes to reach 80-90% confluency, then infected at a multiplicity of infection (MOI) of 5 with HAstV1 virus stock (passage 2, derived from pAVIC1 T7 RNA; Geigenm\u00fcller et al., 1997, PMID 8995706). After flash freezing, cells were transferred to dry ice and 400 \u00b5l of lysis buffer [20 mM Tris-HCl pH 7.5, 150 mM NaCl, 5 mM MgCl2, 1 mM DTT, 1% Triton X-100, 100 \u00b5g/ml cycloheximide and 25 U/ml TURBO\u2122 DNase (Life Technologies)] dripped on. Cells were scraped extensively to ensure lysis, collected and triturated with a 26-G needle ten times. Lysates were clarified by centrifugation for 20 min at 13,000 g at 4 \u00baC, the supernatants recovered and stored in liquid nitrogen. 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Our study complies with all relevant ethical regulations with respect to both human samples and samples for the other mammals. Human samples were obtained from official scientific tissue banks or dedicated companies; informed consent was obtained by these sources from donors prior to death or from next-of-kin. The use of all human samples for the type of work described in this study was approved by an Ethics Screening panel from the European Research Council (ERC) (associated with H.K.'s ERC Consolidator Grant 615253, OntoTransEvol) and local ethics committees; that is, from the Cantonal Ethics Commission Lausanne (authorization 504/12) and Ethics Commission from the Medical Faculty of Heidelberg University (authorization S-220/2017). The use of all other mammalian samples for the type of work in this study was approved by ERC Ethics Screening panels (ERC Starting Grant 242597, SexGenTransEvolution, and ERC Consolidator Grant 615253, OntoTransEvol). 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GSM1197614: Ribosome profiling rep1-SiYTHDF2-RPF C3; Homo sapiens; OTHER", "dev_stage": "", "ecotype": "", "environmental_sample": "false", "germline": "false", "identified_by": "", "isolate": "", "isolation_source": "", "location": "", "mating_type": "", "serotype": "", "serovar": "", "sex": "", "submitted_sex": "", "specimen_voucher": "", "strain": "", "sub_species": "", "sub_strain": "", "tissue_lib": "", "tissue_type": "", "variety": "", "checklist": "", "depth": "", "elevation": "", "altitude": "", "environment_biome": "", "environment_feature": "", "environment_material": "", "temperature": "", "salinity": "", "sampling_campaign": "", "sampling_site": "", "sampling_platform": "", "protocol_label": "", "project_name": "", "host": "", "host_tax_id": "", "host_status": "", "host_sex": "", "submitted_host_sex": "", "host_body_site": "", "host_gravidity": "", "host_phenotype": "", "host_genotype": "", "host_growth_conditions": "", "environmental_package": "", "investigation_type": "", "experimental_factor": "", "sample_collection": "", "sequencing_method": "", "target_gene": "", "ph": "", "sample_material": "", "taxonomic_identity_marker": "", "assembly_quality": "", "assembly_software": "", "taxonomic_classification": "", "completeness_score": "", "contamination_score": "", "binning_software": "", "lat": "", "lon": ""}] ================================================ FILE: tests/data/test_search/geo_search_test1.txt ================================================ SRX8089313 SRX8089314 SRX8089315 SRX8089316 SRX8089317 SRX8089318 SRX8089319 SRX8089320 SRX8089286 SRX8089275 SRX8089276 SRX8089277 SRX8089278 SRX8089279 SRX8089280 SRX8089281 SRX8089282 SRX8089283 SRX8089284 SRX8089285 SRX8089321 SRX8089287 SRX8089288 SRX8089289 SRX8089290 SRX8089291 SRX8089292 SRX8089293 SRX8089294 SRX8089295 SRX8089296 SRX8466645 SRX8142119 SRX8142120 SRX8142121 SRX8142122 SRX8142123 SRX8142124 SRX8142125 SRX8142126 SRX8142127 SRX8466643 SRX8466644 SRX8089344 SRX8466646 SRX8466647 SRX8466648 SRX8466649 SRX8466650 SRX8466651 SRX8466652 SRX8466653 SRX8466654 SRX8466655 SRX8466656 SRX8089333 SRX8089322 SRX8089323 SRX8089324 SRX8089325 SRX8089326 SRX8089327 SRX8089328 SRX8089329 SRX8089330 SRX8089331 SRX8089332 SRX8466765 SRX8089334 SRX8089335 SRX8089336 SRX8089337 SRX8089338 SRX8089339 SRX8089340 SRX8089341 SRX8089342 SRX8089343 ================================================ FILE: tests/data/test_search/sra_search_test1.txt ================================================ SRX137370 SRX137371 ================================================ FILE: tests/data/test_search/sra_test.xml ================================================ SRX7830165GSM4369051: rnaH27nsun3; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240844GSM4369051RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369051GEO AccessionGSM4369051SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240844SAMN14262094GSM4369051rnaH27nsun36239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature27genotypenoNSUNSRS6240844SAMN14262094GSM4369051SRR11217925SRS6240844SAMN14262094GSM4369051
SRX7830164GSM4369050: rnaH27nsun2; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240843GSM4369050RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369050GEO AccessionGSM4369050SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240843SAMN14262095GSM4369050rnaH27nsun26239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature27genotypenoNSUNSRS6240843SAMN14262095GSM4369050SRR11217924SRS6240843SAMN14262095GSM4369050
SRX7830163GSM4369049: rnaH27nsun1; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240842GSM4369049RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369049GEO AccessionGSM4369049SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240842SAMN14262096GSM4369049rnaH27nsun16239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature27genotypenoNSUNSRS6240842SAMN14262096GSM4369049SRR11217923SRS6240842SAMN14262096GSM4369049
SRX7830162GSM4369048: rnaH27WT3; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240841GSM4369048RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369048GEO AccessionGSM4369048SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240841SAMN14262097GSM4369048rnaH27WT36239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature27genotypeWTSRS6240841SAMN14262097GSM4369048SRR11217922SRS6240841SAMN14262097GSM4369048
SRX7830161GSM4369047: rnaH27WT2; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240840GSM4369047RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369047GEO AccessionGSM4369047SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240840SAMN14262098GSM4369047rnaH27WT26239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature27genotypeWTSRS6240840SAMN14262098GSM4369047SRR11217921SRS6240840SAMN14262098GSM4369047
SRX7830160GSM4369046: rnaH27WT1; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240839GSM4369046RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369046GEO AccessionGSM4369046SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240839SAMN14262099GSM4369046rnaH27WT16239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature27genotypeWTSRS6240839SAMN14262099GSM4369046SRR11217920SRS6240839SAMN14262099GSM4369046
SRX7830159GSM4369045: rnaL20nsun3; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240838GSM4369045RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369045GEO AccessionGSM4369045SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240838SAMN14262100GSM4369045rnaL20nsun36239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature20genotypenoNSUNSRS6240838SAMN14262100GSM4369045SRR11217919SRS6240838SAMN14262100GSM4369045
SRX7830158GSM4369044: rnaL20nsun2; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240837GSM4369044RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369044GEO AccessionGSM4369044SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240837SAMN14262101GSM4369044rnaL20nsun26239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature20genotypenoNSUNSRS6240837SAMN14262101GSM4369044SRR11217918SRS6240837SAMN14262101GSM4369044
SRX7830157GSM4369043: rnaL20nsun1; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240836GSM4369043RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369043GEO AccessionGSM4369043SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240836SAMN14262102GSM4369043rnaL20nsun16239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature20genotypenoNSUNSRS6240836SAMN14262102GSM4369043SRR11217917SRS6240836SAMN14262102GSM4369043
SRX7830156GSM4369042: rnaL20WT3; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240835GSM4369042RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369042GEO AccessionGSM4369042SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240835SAMN14262103GSM4369042rnaL20WT36239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature20genotypeWTSRS6240835SAMN14262103GSM4369042SRR11217916SRS6240835SAMN14262103GSM4369042
SRX7830155GSM4369041: rnaL20WT2; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240834GSM4369041RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369041GEO AccessionGSM4369041SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240834SAMN14262104GSM4369041rnaL20WT26239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature20genotypeWTSRS6240834SAMN14262104GSM4369041SRR11217915SRS6240834SAMN14262104GSM4369041
SRX7830154GSM4369040: rnaL20WT1; Caenorhabditis elegans; RNA-SeqSRP251352SRS6240833GSM4369040RNA-SeqTRANSCRIPTOMICcDNAInput RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)Illumina HiSeq 2000gds304369040GEO AccessionGSM4369040SRA1050341NCBIGeoCuratorsSRP251352PRJNA609901GSE146256Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegansIn order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.GSE146256SRS6240833SAMN14262081GSM4369040rnaL20WT16239Caenorhabditis elegansbioproject609901source_nameWhole animaldatapipelinePipeline2temperature20genotypeWTSRS6240833SAMN14262081GSM4369040SRR11217914SRS6240833SAMN14262081GSM4369040
SRX7806834GSM4340680: pmk-1(km25)RPF Replicate 2; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219869SAMN14213080RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340680GEO AccessionGSM4340680SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219869SAMN14213080GSM4340680pmk-1(km25)RPF Replicate 26239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3genotypepmk-1(km25)SRS6219869SAMN14213080GSM4340680SRR11186550SRS6219869SAMN14213080GSM4340680
SRX7806833GSM4340679: pmk-1(km25) total mRNA Replicate 2; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219868SAMN14213082RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340679GEO AccessionGSM4340679SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219868SAMN14213082GSM4340679pmk-1(km25) total mRNA Replicate 26239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3genotypepmk-1(km25)SRS6219868SAMN14213082GSM4340679SRR11186549SRS6219868SAMN14213082GSM4340679
SRX7806832GSM4340678: pmk-1(km25)RPF Replicate 1; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219867SAMN14212991RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340678GEO AccessionGSM4340678SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219867SAMN14212991GSM4340678pmk-1(km25)RPF Replicate 16239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3genotypepmk-1(km25)SRS6219867SAMN14212991GSM4340678SRR11186548SRS6219867SAMN14212991GSM4340678
SRX7806831GSM4340677: pmk-1(km25) total mRNA Replicate 1; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219866SAMN14213083RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340677GEO AccessionGSM4340677SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219866SAMN14213083GSM4340677pmk-1(km25) total mRNA Replicate 16239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3genotypepmk-1(km25)SRS6219866SAMN14213083GSM4340677SRR11186547SRS6219866SAMN14213083GSM4340677
SRX7806830GSM4340676: ced-3(n717)RPF Replicate 2; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219865SAMN14213084RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340676GEO AccessionGSM4340676SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219865SAMN14213084GSM4340676ced-3(n717)RPF Replicate 26239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3genotypeced-3(n717)SRS6219865SAMN14213084GSM4340676SRR11186546SRS6219865SAMN14213084GSM4340676
SRX7806829GSM4340675: ced-3(n717) total mRNA Replicate 2; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219864SAMN14213085RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340675GEO AccessionGSM4340675SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219864SAMN14213085GSM4340675ced-3(n717) total mRNA Replicate 26239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3genotypeced-3(n717)SRS6219864SAMN14213085GSM4340675SRR11186545SRS6219864SAMN14213085GSM4340675
SRX7806828GSM4340674: ced-3(n717)RPF Replicate 1; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219863SAMN14213086RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340674GEO AccessionGSM4340674SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219863SAMN14213086GSM4340674ced-3(n717)RPF Replicate 16239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3genotypeced-3(n717)SRS6219863SAMN14213086GSM4340674SRR11186544SRS6219863SAMN14213086GSM4340674
SRX7806827GSM4340673: ced-3(n717) total mRNA Replicate 1; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219862SAMN14212992RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340673GEO AccessionGSM4340673SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219862SAMN14212992GSM4340673ced-3(n717) total mRNA Replicate 16239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3genotypeced-3(n717)SRS6219862SAMN14212992GSM4340673SRR11186543SRS6219862SAMN14212992GSM4340673
SRX7806826GSM4340672: WT RPF Replicate 2; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219861SAMN14212993RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340672GEO AccessionGSM4340672SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219861SAMN14212993GSM4340672WT RPF Replicate 26239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3strainN2genotypewild typeSRS6219861SAMN14212993GSM4340672SRR11186542SRS6219861SAMN14212993GSM4340672
SRX7806825GSM4340671: WT total mRNA Replicate 2; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219860SAMN14212994RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340671GEO AccessionGSM4340671SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219860SAMN14212994GSM4340671WT total mRNA Replicate 26239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3strainN2genotypewild typeSRS6219860SAMN14212994GSM4340671SRR11186541SRS6219860SAMN14212994GSM4340671
SRX7806824GSM4340670: WT RPF Replicate 1; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219859SAMN14212996RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340670GEO AccessionGSM4340670SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219859SAMN14212996GSM4340670WT RPF Replicate 16239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3strainN2genotypewild typeSRS6219859SAMN14212996GSM4340670SRR11186540SRS6219859SAMN14212996GSM4340670
SRX7806823GSM4340669: WT total mRNA Replicate 1; Caenorhabditis elegans; RNA-SeqSRP250832PRJNA608907SRS6219858SAMN14212997RNA-SeqTRANSCRIPTOMICcDNAThe ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profillingNextSeq 500gds304340669GEO AccessionGSM4340669SRA1048439NCBIGeoCuratorsSRP250832PRJNA608907GSE145983Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegansWe identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicatesGSE145983SRS6219858SAMN14212997GSM4340669WT total mRNA Replicate 16239Caenorhabditis elegansbioproject608907source_nameWhole wormStageL3strainN2genotypewild typeSRS6219858SAMN14212997GSM4340669SRR11186539SRS6219858SAMN14212997GSM4340669
SRX7098753GSM4148088: Slee141_mRNAseqFP_meg34_3: meg-3meg-4 mRNAseq-3; Caenorhabditis elegans; RNA-SeqSRP228538SRS5611015GSM4148088RNA-SeqTRANSCRIPTOMICcDNAIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148088GEO AccessionGSM4148088SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611015SAMN13190923GSM4148088Slee141_mRNAseqFP_meg34_3: meg-3meg-4 mRNAseq-36239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRibo-Zero treated total RNASRS5611015SAMN13190923GSM4148088SRR10398500SRS5611015SAMN13190923GSM4148088SRX7098752GSM4148087: Slee139_mRNAseqFP_meg34_2: meg-3meg-4 mRNAseq-2; Caenorhabditis elegans; RNA-SeqSRP228538SRS5611014GSM4148087RNA-SeqTRANSCRIPTOMICcDNAIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148087GEO AccessionGSM4148087SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611014SAMN13190924GSM4148087Slee139_mRNAseqFP_meg34_2: meg-3meg-4 mRNAseq-26239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRibo-Zero treated total RNASRS5611014SAMN13190924GSM4148087SRR10398499SRS5611014SAMN13190924GSM4148087SRX7098751GSM4148086: Slee125_mRNAseqFP_meg34_1: meg-3meg-4 mRNAseq-1; Caenorhabditis elegans; RNA-SeqSRP228538SRS5611013GSM4148086RNA-SeqTRANSCRIPTOMICcDNAIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148086GEO AccessionGSM4148086SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611013SAMN13190925GSM4148086Slee125_mRNAseqFP_meg34_1: meg-3meg-4 mRNAseq-16239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRibo-Zero treated total RNASRS5611013SAMN13190925GSM4148086SRR10398498SRS5611013SAMN13190925GSM4148086SRX7098750GSM4148085: Slee142_mRNAseqFP_N2_3: wild type mRNAseq-3; Caenorhabditis elegans; RNA-SeqSRP228538SRS5611012GSM4148085RNA-SeqTRANSCRIPTOMICcDNAIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148085GEO AccessionGSM4148085SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611012SAMN13190926GSM4148085Slee142_mRNAseqFP_N2_3: wild type mRNAseq-36239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRibo-Zero treated total RNASRS5611012SAMN13190926GSM4148085SRR10398497SRS5611012SAMN13190926GSM4148085SRX7098749GSM4148084: Slee138_mRNAseqFP_N2_2: wild type mRNAseq-2; Caenorhabditis elegans; RNA-SeqSRP228538SRS5611011GSM4148084RNA-SeqTRANSCRIPTOMICcDNAIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148084GEO AccessionGSM4148084SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611011SAMN13190927GSM4148084Slee138_mRNAseqFP_N2_2: wild type mRNAseq-26239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRibo-Zero treated total RNASRS5611011SAMN13190927GSM4148084SRR10398496SRS5611011SAMN13190927GSM4148084SRX7098748GSM4148083: Slee113_mRNAseqFP_N2_1: wild type mRNAseq-1; Caenorhabditis elegans; RNA-SeqSRP228538SRS5611010GSM4148083RNA-SeqTRANSCRIPTOMICcDNAIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148083GEO AccessionGSM4148083SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611010SAMN13190928GSM4148083Slee113_mRNAseqFP_N2_1: wild type mRNAseq-16239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRibo-Zero treated total RNASRS5611010SAMN13190928GSM4148083SRR10398495SRS5611010SAMN13190928GSM4148083SRX7098747GSM4148082: Slee135_meg34: meg-3meg-4 Riboseq-3; Caenorhabditis elegans; OTHERSRP228538SRS5611009GSM4148082OTHERTRANSCRIPTOMICotherIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148082GEO AccessionGSM4148082SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611009SAMN13190929GSM4148082Slee135_meg34: meg-3meg-4 Riboseq-36239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRNaseI treated Ribo-Zero treated ribosome bound RNA fragmentsSRS5611009SAMN13190929GSM4148082SRR10398494SRS5611009SAMN13190929GSM4148082SRX7098746GSM4148081: Slee133_meg34: meg-3meg-4 Riboseq-2; Caenorhabditis elegans; OTHERSRP228538SRS5611008GSM4148081OTHERTRANSCRIPTOMICotherIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148081GEO AccessionGSM4148081SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611008SAMN13190905GSM4148081Slee133_meg34: meg-3meg-4 Riboseq-26239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRNaseI treated Ribo-Zero treated ribosome bound RNA fragmentsSRS5611008SAMN13190905GSM4148081SRR10398493SRS5611008SAMN13190905GSM4148081SRX7098745GSM4148080: Slee123_meg34: meg-3meg-4 Riboseq-1; Caenorhabditis elegans; OTHERSRP228538SRS5611007GSM4148080OTHERTRANSCRIPTOMICotherIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148080GEO AccessionGSM4148080SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611007SAMN13190906GSM4148080Slee123_meg34: meg-3meg-4 Riboseq-16239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRNaseI treated Ribo-Zero treated ribosome bound RNA fragmentsSRS5611007SAMN13190906GSM4148080SRR10398492SRS5611007SAMN13190906GSM4148080SRX7098744GSM4148079: Slee136_N2: wild type Riboseq-3; Caenorhabditis elegans; OTHERSRP228538SRS5611006GSM4148079OTHERTRANSCRIPTOMICotherIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148079GEO AccessionGSM4148079SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611006SAMN13190907GSM4148079Slee136_N2: wild type Riboseq-36239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRNaseI treated Ribo-Zero treated ribosome bound RNA fragmentsSRS5611006SAMN13190907GSM4148079SRR10398491SRS5611006SAMN13190907GSM4148079SRX7098743GSM4148078: Slee132_N2: wild type Riboseq-2; Caenorhabditis elegans; OTHERSRP228538SRS5611005GSM4148078OTHERTRANSCRIPTOMICotherIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148078GEO AccessionGSM4148078SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611005SAMN13190908GSM4148078Slee132_N2: wild type Riboseq-26239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRNaseI treated Ribo-Zero treated ribosome bound RNA fragmentsSRS5611005SAMN13190908GSM4148078SRR10398490SRS5611005SAMN13190908GSM4148078SRX7098742GSM4148077: Slee111_N2: wild type Riboseq-1; Caenorhabditis elegans; OTHERSRP228538SRS5611004GSM4148077OTHERTRANSCRIPTOMICotherIsolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.Illumina HiSeq 2500gds304148077GEO AccessionGSM4148077SRA991333NCBIGeoCuratorsSRP228538PRJNA587444GSE139880Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling)RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).GSE139880pubmed31975687parent_bioprojectPRJNA587431SRS5611004SAMN13190909GSM4148077Slee111_N2: wild type Riboseq-16239Caenorhabditis elegansbioproject587444source_nameEmbryotissuemixed early embryomolecule subtypeRNaseI treated Ribo-Zero treated ribosome bound RNA fragmentsSRS5611004SAMN13190909GSM4148077SRR10398489SRS5611004SAMN13190909GSM4148077SRX4147684GSM3168388: C. elegans embryos ribosome profiling; Caenorhabditis elegans; RNA-SeqSRP149446SRS3361274GSM3168388RNA-SeqTRANSCRIPTOMICcDNALysates were clarified and monosomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt were gel purified and rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing.Illumina HiSeq 2500gds303168388GEO AccessionGSM3168388SRA713167NCBIGeoCuratorsSRP149446PRJNA473989GSE115161Regulation of Translation Elongation Revealed by Ribosome Profiling [Dataset_4]Ribosomes undergo substantial conformational changes during translation elongation to accommodate incoming aminoacyl-tRNAs and translocate along the mRNA template. We used multiple elongation inhibitors and chemical probing to define ribosome conformational states corresponding to different sized ribosome-protected mRNA fragments (RPFs) generated by ribosome profiling. We show using various genetic and environmental perturbations that the previously identified 20-22 nucleotide (nt) RPFs correspond predominantly to ribosomes in a pre-accommodation state with an open 40S ribosomal A site while the classical 27-29 nt fragments correspond to ribosomes in a pre-translocation state with an occupied 40S ribosomal A site. These distinct ribosome conformational states revealed by ribosome profiling are seen in all eukaryotes tested including fungi, worms and mammals. This high-resolution ribosome profiling approach reveals the anticipated Rck2-dependent inhibition of translocation through eEF2 phosphorylation during hyperosmotic stress. These same approaches reveal a strong translation elongation arrest during oxidative stress where the ribosomes are trapped in a pre-translocation state, but in this case the translational arrest is independent of Rck2-driven eEF2 phosphorylation. These results provide new insights and approaches for defining the molecular events that impact translation elongation throughout biology. Overall design: 24 biological samples are included for ribosome footprinting samples. These include HeLa, MB-MDA-231 and yeast cells and C. elegans embryos.GSE115161parent_bioprojectPRJNA473984SRS3361274SAMN09288722GSM3168388C. elegans embryos ribosome profiling6239Caenorhabditis elegansbioproject473989source_nameC. elegans embryos ribosome profilingtissueembryosmolecule subtypeRibosome Protected mRNA (15-34 nt)SRS3361274SAMN09288722GSM3168388SRR7241911SRS3361274SAMN09288722GSM3168388SRX2352818Bayesian Prediction of RNA Translation from Ribosome ProfilingSRP093364The ribosome profiling experiments were performed according to our published detailed protocol (Aeschimann et al. 2015), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.SRS1799345Celegans_post_dauer_4hOTHERTRANSCRIPTOMICunspecified500Application ReadForward1Illumina HiSeq 2000SRA494245University Heidelberg
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
ChristophDieterich
SRP093364PRJNA353604Caenorhabditis elegans strain:N2 Transcriptome or Gene expressionBayesian Prediction of RNA Translation from Ribosome Profiling in C. elegansCaenorhabditis elegans strain:N2SRS1799345SAMN060176296239Caenorhabditis elegansstrainN2dev_stageDauersexhermaphroditetissuewhole bodyBioSampleModelModel organism or animalSRS1799345SAMN06017629SRR5026637SRS1799345SAMN06017629
SRX2352801Bayesian Prediction of RNA Translation from Ribosome ProfilingSRP093364The ribosome profiling experiments were performed according to our published detailed protocol (Aeschimann et al. 2015), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.SRS1799345Celegans_3h_post_dauerOTHERTRANSCRIPTOMICunspecified500Application ReadForward1Illumina HiSeq 2000SRA494245University Heidelberg
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
ChristophDieterich
SRP093364PRJNA353604Caenorhabditis elegans strain:N2 Transcriptome or Gene expressionBayesian Prediction of RNA Translation from Ribosome Profiling in C. elegansCaenorhabditis elegans strain:N2SRS1799345SAMN060176296239Caenorhabditis elegansstrainN2dev_stageDauersexhermaphroditetissuewhole bodyBioSampleModelModel organism or animalSRS1799345SAMN06017629SRR5026603SRS1799345SAMN06017629
SRX2352796Bayesian Prediction of RNA Translation from Ribosome ProfilingSRP093364The ribosome profiling experiments were performed according to our published detailed protocol (Aeschimann et al. 2015), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.SRS1799345Celegans_2h_post_dauerOTHERTRANSCRIPTOMICunspecified500Application ReadForward1Illumina HiSeq 2000SRA494245University Heidelberg
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
ChristophDieterich
SRP093364PRJNA353604Caenorhabditis elegans strain:N2 Transcriptome or Gene expressionBayesian Prediction of RNA Translation from Ribosome Profiling in C. elegansCaenorhabditis elegans strain:N2SRS1799345SAMN060176296239Caenorhabditis elegansstrainN2dev_stageDauersexhermaphroditetissuewhole bodyBioSampleModelModel organism or animalSRS1799345SAMN06017629SRR5026592SRS1799345SAMN06017629
SRX2352779Bayesian Prediction of RNA Translation from Ribosome ProfilingSRP093364The ribosome profiling experiments were performed according to our published detailed protocol (Aeschimann et al. 2015), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.SRS1799345Celegans_1h_post_dauerOTHERTRANSCRIPTOMICunspecified500Application ReadForward1Illumina HiSeq 2000SRA494245University Heidelberg
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
ChristophDieterich
SRP093364PRJNA353604Caenorhabditis elegans strain:N2 Transcriptome or Gene expressionBayesian Prediction of RNA Translation from Ribosome Profiling in C. elegansCaenorhabditis elegans strain:N2SRS1799345SAMN060176296239Caenorhabditis elegansstrainN2dev_stageDauersexhermaphroditetissuewhole bodyBioSampleModelModel organism or animalSRS1799345SAMN06017629SRR5026589SRS1799345SAMN06017629
SRX2352572Bayesian Prediction of RNA Translation from Ribosome ProfilingSRP093364The ribosome profiling experiments were performed according to our published detailed protocol (PMID: 26102273), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.SRS1799345Celegans_0.5h_post_dauerOTHERTRANSCRIPTOMICunspecified500Application ReadForward1Illumina HiSeq 2000SRA494245University Heidelberg
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
ChristophDieterich
SRP093364PRJNA353604Caenorhabditis elegans strain:N2 Transcriptome or Gene expressionBayesian Prediction of RNA Translation from Ribosome Profiling in C. elegansCaenorhabditis elegans strain:N2SRS1799345SAMN060176296239Caenorhabditis elegansstrainN2dev_stageDauersexhermaphroditetissuewhole bodyBioSampleModelModel organism or animalSRS1799345SAMN06017629SRR5026359SRS1799345SAMN06017629
SRX2349147Bayesian Prediction of RNA Translation from Ribosome ProfilingSRP093364PRJNA353604The ribosome profiling experiments were performed according to our published detailed protocol (6), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.SRS1799345SAMN06017629Dauer_0hOTHERTRANSCRIPTOMICunspecified500Application ReadForward1Illumina HiSeq 2000SRA494245University Heidelberg
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
Internal Medicine IIIUniversity HeidelbergIm Neuenheimer Feld 669HeidelbergGermany
ChristophDieterich
SRP093364PRJNA353604Caenorhabditis elegans strain:N2 Transcriptome or Gene expressionBayesian Prediction of RNA Translation from Ribosome Profiling in C. elegansCaenorhabditis elegans strain:N2SRS1799345SAMN060176296239Caenorhabditis elegansstrainN2dev_stageDauersexhermaphroditetissuewhole bodyBioSampleModelModel organism or animalSRS1799345SAMN06017629SRR5026356SRS1799345SAMN06017629
SRX1626372unc-54(cc3389) Ribo-seqSRP064516Ribosome footprint profiling Ribo-seq, using 3'ligation with AF-JA-34.2 and circular DNA ligase.SRS1335846SJA131MRNA-SeqTRANSCRIPTOMICother300Application ReadForward1Illumina MiSeqSRA384301Stanford Univerisy
PathologyStanford Univerisy300 Pasteur DriveStanfordCaliforniaUnited States of America
PathologyStanford Univerisy300 Pasteur DriveStanfordCaliforniaUnited States of America
JoshuaArribereA
SRP064516PRJNA297873Translation Readthrough MitigationA fraction of ribosomes engaged in translation will fail to terminate when reaching a stop codon, yielding nascent proteins inappropriately extended on their C-termini. Although such extended proteins can interfere with normal cellular processes, known mechanisms of translational surveillance are insufficient to protect cells from potential dominant consequences. Using C. elegans, we demonstrate a consistent ability of cells to block accumulation of C-terminal extended proteins that result from failure to terminate at stop codons. These repressive effects are mediated through decreased protein accumulation without a detectable effect on mRNA levels. 3’UTR-encoded peptides are sufficient to confer the observed effects, suggesting a co- or post-translational mechanism of action. We suggest 3’UTRs may be optimized for sequences that destabilize the attached protein, providing a surveillance mechanism for unwelcome/inadmissible and varied translation errors.Caenorhabditis eleganspubmed27281202SRS1335846SAMN04546343unc-54(cc3389) homozygotes6239Caenorhabditis elegansbioproject297873strainPD3389isolateunc-54(cc3389)dev_stageL4sexhermaphroditetissuewhole organismcollection_date24-Jan-2016growth_protocolXL NGM plates seeded with OP50BioSampleModelModel organism or animalSRS1335846SAMN04546343SRR3219264SRS1335846SAMN04546343
SRX1626361unc-54(+) Ribo-seqSRP064516Ribosome footprint profiling Ribo-seq, using 3'ligation with AF-JA-34.2 and circular DNA ligase.SRS1335837SJA130MRNA-SeqTRANSCRIPTOMICother300Application ReadForward1Illumina MiSeqSRA384300Stanford Univerisy
PathologyStanford Univerisy300 Pasteur DriveStanfordCaliforniaUnited States of America
PathologyStanford Univerisy300 Pasteur DriveStanfordCaliforniaUnited States of America
JoshuaArribereA
SRP064516PRJNA297873Translation Readthrough MitigationA fraction of ribosomes engaged in translation will fail to terminate when reaching a stop codon, yielding nascent proteins inappropriately extended on their C-termini. Although such extended proteins can interfere with normal cellular processes, known mechanisms of translational surveillance are insufficient to protect cells from potential dominant consequences. Using C. elegans, we demonstrate a consistent ability of cells to block accumulation of C-terminal extended proteins that result from failure to terminate at stop codons. These repressive effects are mediated through decreased protein accumulation without a detectable effect on mRNA levels. 3’UTR-encoded peptides are sufficient to confer the observed effects, suggesting a co- or post-translational mechanism of action. We suggest 3’UTRs may be optimized for sequences that destabilize the attached protein, providing a surveillance mechanism for unwelcome/inadmissible and varied translation errors.Caenorhabditis eleganspubmed27281202SRS1335837SAMN04546334unc-54(e1301) homozygotes6239Caenorhabditis elegansbioproject297873strainPD2013isolateunc-54(e1301)dev_stageL4sexhermaphroditetissuewhole organismcollection_date24-Jan-2016BioSampleModelModel organism or animalSRS1335837SAMN04546334SRR3219253SRS1335837SAMN04546334
SRX1626357unc-54(+) Ribo-seqSRP064516Ribosome footprint profiling Ribo-seq, using 3'ligation with AF-JA-34.2 and circular DNA ligase.SRS1335834SJA129MRNA-SeqTRANSCRIPTOMICother300Application ReadForward1Illumina MiSeqSRA384295Stanford Univerisy
PathologyStanford Univerisy300 Pasteur DriveStanfordCaliforniaUnited States of America
PathologyStanford Univerisy300 Pasteur DriveStanfordCaliforniaUnited States of America
JoshuaArribereA
SRP064516PRJNA297873Translation Readthrough MitigationA fraction of ribosomes engaged in translation will fail to terminate when reaching a stop codon, yielding nascent proteins inappropriately extended on their C-termini. Although such extended proteins can interfere with normal cellular processes, known mechanisms of translational surveillance are insufficient to protect cells from potential dominant consequences. Using C. elegans, we demonstrate a consistent ability of cells to block accumulation of C-terminal extended proteins that result from failure to terminate at stop codons. These repressive effects are mediated through decreased protein accumulation without a detectable effect on mRNA levels. 3’UTR-encoded peptides are sufficient to confer the observed effects, suggesting a co- or post-translational mechanism of action. We suggest 3’UTRs may be optimized for sequences that destabilize the attached protein, providing a surveillance mechanism for unwelcome/inadmissible and varied translation errors.Caenorhabditis eleganspubmed27281202SRS1335834SAMN04546333unc-54(+) homozygotes6239Caenorhabditis elegansbioproject297873strainVC2010isolatePD1074dev_stageL4sexhermaphroditetissuewhole organismcollection_date24-Jan-2016growth_protocolXL NGM plates seeded with OP50BioSampleModelModel organism or animalSRS1335834SAMN04546333SRR3219248SRS1335834SAMN04546333
SRX878014GSM1611598: frac_26-34nt; Caenorhabditis elegans; OTHERSRP055039SRS845968GSM1611598OTHERTRANSCRIPTOMICotherWorms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611598gds301611598GEO AccessionGSM1611598SRA242099Gene Expression OmnibusSRP055039PRJNA275470GSE65948Transcriptome-wide measurement of ribosomal occupancy by ribosome profilingExperiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.GSE65948pubmed26102273SRS845968SAMN03349121GSM1611598frac_26-34nt6239Caenorhabditis elegansbioproject275470source_nameWhole-wormstrainN2agelarval stage 4SRS845968SAMN03349121GSM1611598SRR1804351SRS845968SAMN03349121GSM1611598SRR1804352SRS845968SAMN03349121GSM1611598SRX878013GSM1611597: frac_28-35nt; Caenorhabditis elegans; OTHERSRP055039SRS845969GSM1611597OTHERTRANSCRIPTOMICotherWorms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611597gds301611597GEO AccessionGSM1611597SRA242099Gene Expression OmnibusSRP055039PRJNA275470GSE65948Transcriptome-wide measurement of ribosomal occupancy by ribosome profilingExperiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.GSE65948pubmed26102273SRS845969SAMN03349117GSM1611597frac_28-35nt6239Caenorhabditis elegansbioproject275470source_nameWhole-wormstrainN2agelarval stage 4SRS845969SAMN03349117GSM1611597SRR1804349SRS845969SAMN03349117GSM1611597SRR1804350SRS845969SAMN03349117GSM1611597SRX878012GSM1611596: frac_28-30nt; Caenorhabditis elegans; OTHERSRP055039SRS845970GSM1611596OTHERTRANSCRIPTOMICotherWorms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611596gds301611596GEO AccessionGSM1611596SRA242099Gene Expression OmnibusSRP055039PRJNA275470GSE65948Transcriptome-wide measurement of ribosomal occupancy by ribosome profilingExperiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.GSE65948pubmed26102273SRS845970SAMN03349114GSM1611596frac_28-30nt6239Caenorhabditis elegansbioproject275470source_nameWhole-wormstrainN2agelarval stage 4SRS845970SAMN03349114GSM1611596SRR1804348SRS845970SAMN03349114GSM1611596SRX878011GSM1611595: frac_25-30nt; Caenorhabditis elegans; OTHERSRP055039SRS845971GSM1611595OTHERTRANSCRIPTOMICotherWorms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611595gds301611595GEO AccessionGSM1611595SRA242099Gene Expression OmnibusSRP055039PRJNA275470GSE65948Transcriptome-wide measurement of ribosomal occupancy by ribosome profilingExperiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.GSE65948pubmed26102273SRS845971SAMN03349115GSM1611595frac_25-30nt6239Caenorhabditis elegansbioproject275470source_nameWhole-wormstrainN2agelarval stage 4SRS845971SAMN03349115GSM1611595SRR1804346SRS845971SAMN03349115GSM1611595SRR1804347SRS845971SAMN03349115GSM1611595SRX878010GSM1611594: 04_N2_893_GCkit; Caenorhabditis elegans; OTHERSRP055039SRS845972GSM1611594OTHERTRANSCRIPTOMICotherWorms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611594gds301611594GEO AccessionGSM1611594SRA242099Gene Expression OmnibusSRP055039PRJNA275470GSE65948Transcriptome-wide measurement of ribosomal occupancy by ribosome profilingExperiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.GSE65948pubmed26102273SRS845972SAMN03349119GSM161159404_N2_893_GCkit6239Caenorhabditis elegansbioproject275470source_nameWhole-wormstrainN2ageyoung adultSRS845972SAMN03349119GSM1611594SRR1804345SRS845972SAMN03349119GSM1611594SRX878009GSM1611593: 03_N2_893_SGkit; Caenorhabditis elegans; OTHERSRP055039SRS845973GSM1611593OTHERTRANSCRIPTOMICotherWorms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611593gds301611593GEO AccessionGSM1611593SRA242099Gene Expression OmnibusSRP055039PRJNA275470GSE65948Transcriptome-wide measurement of ribosomal occupancy by ribosome profilingExperiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.GSE65948pubmed26102273SRS845973SAMN03349116GSM161159303_N2_893_SGkit6239Caenorhabditis elegansbioproject275470source_nameWhole-wormstrainN2ageyoung adultSRS845973SAMN03349116GSM1611593SRR1804343SRS845973SAMN03349116GSM1611593SRR1804344SRS845973SAMN03349116GSM1611593SRX878008GSM1611592: 02_N2_893_GCop; Caenorhabditis elegans; OTHERSRP055039SRS845974GSM1611592OTHERTRANSCRIPTOMICotherWorms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611592gds301611592GEO AccessionGSM1611592SRA242099Gene Expression OmnibusSRP055039PRJNA275470GSE65948Transcriptome-wide measurement of ribosomal occupancy by ribosome profilingExperiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.GSE65948pubmed26102273SRS845974SAMN03349120GSM161159202_N2_893_GCop6239Caenorhabditis elegansbioproject275470source_nameWhole-wormstrainN2ageyoung adultSRS845974SAMN03349120GSM1611592SRR1804341SRS845974SAMN03349120GSM1611592SRR1804342SRS845974SAMN03349120GSM1611592SRX878007GSM1611591: 01_N2_893_SGop; Caenorhabditis elegans; OTHERSRP055039SRS845975GSM1611591OTHERTRANSCRIPTOMICotherWorms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611591gds301611591GEO AccessionGSM1611591SRA242099Gene Expression OmnibusSRP055039PRJNA275470GSE65948Transcriptome-wide measurement of ribosomal occupancy by ribosome profilingExperiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.GSE65948pubmed26102273SRS845975SAMN03349118GSM161159101_N2_893_SGop6239Caenorhabditis elegansbioproject275470source_nameWhole-wormstrainN2ageyoung adultSRS845975SAMN03349118GSM1611591SRR1804340SRS845975SAMN03349118GSM1611591SRX747690GSM1534607: RNASeq_c14_2; Caenorhabditis elegans; RNA-SeqSRP049413SRS734047GSM1534607RNA-SeqTRANSCRIPTOMICcDNATotal RNA isolation was performed using Trizol Reagent (Life Technologies). Important: Total RNA was extracted from the same lysate used subsequently for the corresponding ribosome profiling experiment. Library preparation was performed using the ScriptSeq v2 RNA-Seq library preparation kit (Epicentre) according to the manufacturer's protocolIllumina HiSeq 2500http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1534607gds301534607GEO AccessionGSM1534607SRA197072Gene Expression OmnibusSRP049413PRJNA265852GSE62858Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RNA-Seq)We present a basic characterization of the function of Y-box binding proteins in C. elegans. Besides playing an important role for fertility in the germline (all four CEY proteins), we found that the presence of CEY-1 and CEY-4 is essential for the assembly of larger polysomes in the soma. We therefore performed ribosome-profiling in combination with total RNA sequencing in wild type and cey-1,-4 double mutant animals to globally compare mRNA levels and their translation status. Overall design: Total RNA sequencing was peformed on RNA extacted from wild type and cey-1,-4 mutant animals in duplicates. Four samples in total.Caenorhabditis eleganspubmed25378320parent_bioprojectPRJNA265853SRS734047SAMN03153517GSM1534607RNASeq_c14_26239Caenorhabditis elegansbioproject265852bioproject265853source_nameWhole-wormtime in developmentyoung adultsstraincey-1 (rrr12), cey-4 (ok858) mutantSRS734047SAMN03153517GSM1534607SRR1635379SRS734047SAMN03153517GSM1534607SRX747689GSM1534606: RNASeq_c14_1; Caenorhabditis elegans; RNA-SeqSRP049413SRS734046GSM1534606RNA-SeqTRANSCRIPTOMICcDNATotal RNA isolation was performed using Trizol Reagent (Life Technologies). Important: Total RNA was extracted from the same lysate used subsequently for the corresponding ribosome profiling experiment. Library preparation was performed using the ScriptSeq v2 RNA-Seq library preparation kit (Epicentre) according to the manufacturer's protocolIllumina HiSeq 2500http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1534606gds301534606GEO AccessionGSM1534606SRA197072Gene Expression OmnibusSRP049413PRJNA265852GSE62858Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RNA-Seq)We present a basic characterization of the function of Y-box binding proteins in C. elegans. Besides playing an important role for fertility in the germline (all four CEY proteins), we found that the presence of CEY-1 and CEY-4 is essential for the assembly of larger polysomes in the soma. We therefore performed ribosome-profiling in combination with total RNA sequencing in wild type and cey-1,-4 double mutant animals to globally compare mRNA levels and their translation status. Overall design: Total RNA sequencing was peformed on RNA extacted from wild type and cey-1,-4 mutant animals in duplicates. Four samples in total.Caenorhabditis eleganspubmed25378320parent_bioprojectPRJNA265853SRS734046SAMN03153520GSM1534606RNASeq_c14_16239Caenorhabditis elegansbioproject265852bioproject265853source_nameWhole-wormtime in developmentyoung adultsstraincey-1 (rrr12), cey-4 (ok858) mutantSRS734046SAMN03153520GSM1534606SRR1635378SRS734046SAMN03153520GSM1534606SRX747688GSM1534605: RNASeq_N2_2; Caenorhabditis elegans; RNA-SeqSRP049413SRS734045GSM1534605RNA-SeqTRANSCRIPTOMICcDNATotal RNA isolation was performed using Trizol Reagent (Life Technologies). Important: Total RNA was extracted from the same lysate used subsequently for the corresponding ribosome profiling experiment. Library preparation was performed using the ScriptSeq v2 RNA-Seq library preparation kit (Epicentre) according to the manufacturer's protocolIllumina HiSeq 2500http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1534605gds301534605GEO AccessionGSM1534605SRA197072Gene Expression OmnibusSRP049413PRJNA265852GSE62858Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RNA-Seq)We present a basic characterization of the function of Y-box binding proteins in C. elegans. Besides playing an important role for fertility in the germline (all four CEY proteins), we found that the presence of CEY-1 and CEY-4 is essential for the assembly of larger polysomes in the soma. We therefore performed ribosome-profiling in combination with total RNA sequencing in wild type and cey-1,-4 double mutant animals to globally compare mRNA levels and their translation status. Overall design: Total RNA sequencing was peformed on RNA extacted from wild type and cey-1,-4 mutant animals in duplicates. Four samples in total.Caenorhabditis eleganspubmed25378320parent_bioprojectPRJNA265853SRS734045SAMN03153515GSM1534605RNASeq_N2_26239Caenorhabditis elegansbioproject265852bioproject265853source_nameWhole-wormtime in developmentyoung adultsstrainN2SRS734045SAMN03153515GSM1534605SRR1635377SRS734045SAMN03153515GSM1534605SRX747687GSM1534604: RNASeq_N2_1; Caenorhabditis elegans; RNA-SeqSRP049413SRS734044GSM1534604RNA-SeqTRANSCRIPTOMICcDNATotal RNA isolation was performed using Trizol Reagent (Life Technologies). Important: Total RNA was extracted from the same lysate used subsequently for the corresponding ribosome profiling experiment. Library preparation was performed using the ScriptSeq v2 RNA-Seq library preparation kit (Epicentre) according to the manufacturer's protocolIllumina HiSeq 2500http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1534604gds301534604GEO AccessionGSM1534604SRA197072Gene Expression OmnibusSRP049413PRJNA265852GSE62858Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RNA-Seq)We present a basic characterization of the function of Y-box binding proteins in C. elegans. Besides playing an important role for fertility in the germline (all four CEY proteins), we found that the presence of CEY-1 and CEY-4 is essential for the assembly of larger polysomes in the soma. We therefore performed ribosome-profiling in combination with total RNA sequencing in wild type and cey-1,-4 double mutant animals to globally compare mRNA levels and their translation status. Overall design: Total RNA sequencing was peformed on RNA extacted from wild type and cey-1,-4 mutant animals in duplicates. Four samples in total.Caenorhabditis eleganspubmed25378320parent_bioprojectPRJNA265853SRS734044SAMN03153516GSM1534604RNASeq_N2_16239Caenorhabditis elegansbioproject265852bioproject265853source_nameWhole-wormtime in developmentyoung adultsstrainN2SRS734044SAMN03153516GSM1534604SRR1635376SRS734044SAMN03153516GSM1534604SRX311785GSM1169554: Celeg-3-FED-RPF; Caenorhabditis elegans; OTHERSRP026198SRS449537GSM1169554OTHERTRANSCRIPTOMICotherTotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169554gds301169554GEO AccessionGSM1169554SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449537SAMN02209117GSM1169554Celeg-3-FED-RPF6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 fed 3 hoursbatch3strainN2rna subtyperibosome protected fragmentsSRS449537SAMN02209117GSM1169554SRR914339SRX311785SRS449537SAMN02209117GSM1169554SRX311784GSM1169553: Celeg-2-FED-RPF; Caenorhabditis elegans; OTHERSRP026198SRS449536GSM1169553OTHERTRANSCRIPTOMICotherTotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169553gds301169553GEO AccessionGSM1169553SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449536SAMN02209118GSM1169553Celeg-2-FED-RPF6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 fed 3 hoursbatch2strainN2rna subtyperibosome protected fragmentsSRS449536SAMN02209118GSM1169553SRR914338SRX311784SRS449536SAMN02209118GSM1169553SRX311783GSM1169552: Celeg-1-FED-RPF; Caenorhabditis elegans; OTHERSRP026198SRS449535GSM1169552OTHERTRANSCRIPTOMICotherTotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169552gds301169552GEO AccessionGSM1169552SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449535SAMN02209116GSM1169552Celeg-1-FED-RPF6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 fed 3 hoursbatch1strainN2rna subtyperibosome protected fragmentsSRS449535SAMN02209116GSM1169552SRR914337SRX311783SRS449535SAMN02209116GSM1169552SRX311782GSM1169551: Celeg-3-ST-RPF; Caenorhabditis elegans; OTHERSRP026198SRS449534GSM1169551OTHERTRANSCRIPTOMICotherTotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169551gds301169551GEO AccessionGSM1169551SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449534SAMN02209115GSM1169551Celeg-3-ST-RPF6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 diapausebatch3strainN2rna subtyperibosome protected fragmentsSRS449534SAMN02209115GSM1169551SRR914336SRX311782SRS449534SAMN02209115GSM1169551SRX311781GSM1169550: Celeg-2-ST-RPF; Caenorhabditis elegans; OTHERSRP026198SRS449533GSM1169550OTHERTRANSCRIPTOMICotherTotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169550gds301169550GEO AccessionGSM1169550SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449533SAMN02209128GSM1169550Celeg-2-ST-RPF6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 diapausebatch2strainN2rna subtyperibosome protected fragmentsSRS449533SAMN02209128GSM1169550SRR914335SRX311781SRS449533SAMN02209128GSM1169550SRX311780GSM1169549: Celeg-1-ST-RPF; Caenorhabditis elegans; OTHERSRP026198SRS449532GSM1169549OTHERTRANSCRIPTOMICotherTotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169549gds301169549GEO AccessionGSM1169549SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449532SAMN02209113GSM1169549Celeg-1-ST-RPF6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 diapausebatch1strainN2rna subtyperibosome protected fragmentsSRS449532SAMN02209113GSM1169549SRR914334SRX311780SRS449532SAMN02209113GSM1169549SRX311779GSM1169548: Celeg-3-FED-mRNA; Caenorhabditis elegans; RNA-SeqSRP026198SRS449531GSM1169548RNA-SeqTRANSCRIPTOMICcDNATotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169548gds301169548GEO AccessionGSM1169548SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449531SAMN02209111GSM1169548Celeg-3-FED-mRNA6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 fed 3 hoursbatch3strainN2rna subtypetotal mRNASRS449531SAMN02209111GSM1169548SRR914333SRX311779SRS449531SAMN02209111GSM1169548SRX311778GSM1169547: Celeg-2-FED-mRNA; Caenorhabditis elegans; RNA-SeqSRP026198SRS449530GSM1169547RNA-SeqTRANSCRIPTOMICcDNATotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169547gds301169547GEO AccessionGSM1169547SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449530SAMN02209114GSM1169547Celeg-2-FED-mRNA6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 fed 3 hoursbatch2strainN2rna subtypetotal mRNASRS449530SAMN02209114GSM1169547SRR914332SRX311778SRS449530SAMN02209114GSM1169547SRX311777GSM1169546: Celeg-1-FED-mRNA; Caenorhabditis elegans; RNA-SeqSRP026198SRS449529GSM1169546RNA-SeqTRANSCRIPTOMICcDNATotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169546gds301169546GEO AccessionGSM1169546SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449529SAMN02209109GSM1169546Celeg-1-FED-mRNA6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 fed 3 hoursbatch1strainN2rna subtypetotal mRNASRS449529SAMN02209109GSM1169546SRR914331SRX311777SRS449529SAMN02209109GSM1169546SRX311776GSM1169545: Celeg-3-ST-mRNA; Caenorhabditis elegans; RNA-SeqSRP026198SRS449528GSM1169545RNA-SeqTRANSCRIPTOMICcDNATotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169545gds301169545GEO AccessionGSM1169545SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449528SAMN02209110GSM1169545Celeg-3-ST-mRNA6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 diapausebatch3strainN2rna subtypetotal mRNASRS449528SAMN02209110GSM1169545SRR914330SRX311776SRS449528SAMN02209110GSM1169545SRX311775GSM1169544: Celeg-2-ST-mRNA; Caenorhabditis elegans; RNA-SeqSRP026198SRS449527GSM1169544RNA-SeqTRANSCRIPTOMICcDNATotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).Illumina HiSeq 2000http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169544gds301169544GEO AccessionGSM1169544SRA091389Gene Expression OmnibusSRP026198PRJNA208993GSE48140mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental TransitionmRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seqGSE48140pubmed24098135SRS449527SAMN02209112GSM1169544Celeg-2-ST-mRNA6239Caenorhabditis eleganssource_namepopulation-whole animaldevelopmental stageL1 diapausebatch2strainN2rna subtypetotal mRNASRS449527SAMN02209112GSM1169544SRR914329SRX311775SRS449527SAMN02209112GSM1169544SRX311774GSM1169543: Celeg-1-ST-mRNA; Caenorhabditis elegans; RNA-SeqSRP026198SRS449591GSM1169543RNA-SeqTRANSCRIPTOMICcDNATotal mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. 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================================================ FILE: tests/data/test_search/sra_test_2_verbosity_0.csv ================================================ run_accession ERR4229796 ================================================ FILE: tests/data/test_search/sra_test_2_verbosity_1.csv ================================================ run_accession,experiment_title ERR4229796,HiSeq X Ten paired end sequencing ================================================ FILE: tests/data/test_search/sra_test_2_verbosity_2.csv ================================================ study_accession,experiment_accession,experiment_title,sample_taxon_id,sample_scientific_name,experiment_library_strategy,experiment_library_source,experiment_library_selection,sample_accession,sample_alias,experiment_instrument_model,pool_member_spots,run_1_size,run_1_accession,run_1_total_spots,run_1_total_bases ERP113893,ERX4190585,HiSeq X Ten paired end sequencing,562,Escherichia 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ERP113893,ERX4190585,HiSeq X Ten paired end sequencing,562,Escherichia coli,WGS,GENOMIC,RANDOM,ERS3331676,96c1f848-4c9d-11e9-8292-68b599768938,HiSeq X Ten,1150278,94976452,ERR4229796,1150278,347383956,SC_EXP_29694_1#382,"Illumina sequencing of library DN539314J:H12, constructed from sample accession ERS3331676 for study accession ERP113893. This is part of an Illumina multiplexed sequencing run (29694_1). This submission includes reads tagged with the sequence TACCATTC.",SAMEA5529601,Standard,DN539314J:H12,ILLUMINA,ERS3331676,PAIRED,452,121,SAMEA5529601,ERS3331676,347383956,,Escherichia coli,96c1f848-4c9d-11e9-8292-68b599768938,SB277889442,562,SC_RUN_29694_1#382,GCF_000005845.1,85540613,88241122,88289114,100578,85212529,cram,gs.US,gs,cram,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-10 21:58:01,anonymous,worldwide,GCP,https://storage.googleapis.com/sra-pub-src-14/ERR4229796/29694_1_382.cram.1,anonymous,worldwide,AWS,https://sra-pub-src-14.s3.amazonaws.com/ERR4229796/29694_1_382.cram.1,public,2020-06-11 19:23:25,29694_1_382.cram,26e62fcae91b058b13be6b94214ae2e6,cram,100576829,0,Original,https://sra-pub-src-14.s3.amazonaws.com/ERR4229796/29694_1_382.cram.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/era18/ERR/ERR4229/ERR4229796,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-2/ERR4229796/ERR4229796.1,gcp identity,gs.US,GCP,gs://sra-pub-run-4/ERR4229796/ERR4229796.1,public,2020-06-11 19:24:22,ERR4229796,b779862a8fe21d16152454f047fbd2c1,run,94990927,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/era18/ERR/ERR4229/ERR4229796,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/era18/ERZ/004229/ERR4229796/ERR4229796.realign,public,2020-06-11 19:34:28,ERR4229796.realign,4b45e5e3e6ebe3fa112f308a4d092ee4,run.realign,19534748,1,Secondary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/era18/ERZ/004229/ERR4229796/ERR4229796.realign,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/era18/ERZ/004229/ERR4229796/wgmlst_sig.tsv,public,2020-06-11 19:36:45,wgmlst_sig.tsv,1f83f3039c8d5b17e64cebbd875a38b4,wgmlst_sig,4253484,0,Secondary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/era18/ERZ/004229/ERR4229796/wgmlst_sig.tsv,1,347383956,false,SUBJECT_ID,SB277889442,ArrayExpress-SPECIES,E. coli,ENA-FIRST-PUBLIC,2020-06-09,ENA-LAST-UPDATE,2019-03-22,Wellcome Sanger Institute,E. coli,SAMEA5529601,BioSample,562,SB277889442,Maximizing_the_knowledge_gained_from_California_Senate_Bill_27-sc-5708,ENA-FIRST-PUBLIC,2020-06-02,ENA-LAST-UPDATE,2019-02-19,Wellcome Sanger Institute,PRJEB31347,BioProject,"Overuse of antibiotics contributes to antimicrobial resistance and is a growing threat to human health worldwide. In the U.S., approximately 70% of antibiotics are sold for use in livestock. On January 1, 2018, California enacted Senate Bill 27 (SB27), which will require a veterinarian's prescription for use of antimicrobial drugs and ban non-therapeutic antimicrobial uses for routine disease prevention and growth promotion in livestock. The project will quantify the effect of SB27 on E. coli, Campylobacter and Salmonella resistance rates from retail meat; estimate the proportion of human Campylobacter, Salmonella, and extraintestinal pathogenic E. coli infections caused by strains of food animal origin in California; characterize the effect of SB27 on antimicrobial susceptibility of Campylobacter, Salmonella, and extraintestinal E. coli infections caused by strains of food animal origin in California.","Overuse of antibiotics contributes to antimicrobial resistance and is a growing threat to human health worldwide. In the U.S., approximately 70% of antibiotics are sold for use in livestock. On January 1, 2018, California enacted Senate Bill 27 (SB27), which will require a veterinarian's prescription for use of antimicrobial drugs and ban non-therapeutic antimicrobial uses for routine disease prevention and growth promotion in livestock. The project will quantify the effect of SB27 on E. coli, Campylobacter and Salmonella resistance rates from retail meat; estimate the proportion of human Campylobacter, Salmonella, and extraintestinal pathogenic E. coli infections caused by strains of food animal origin in California; characterize the effect of SB27 on antimicrobial susceptibility of Campylobacter, Salmonella, and extraintestinal E. coli infections caused by strains of food animal origin in California. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute please see http://www.sanger.ac.uk/datasharing/",Maximizing_the_knowledge_gained_from_California_Senate_Bill_27,Whole Genome Sequencing,ERA2689537,ERP113893-sc-20200609-1-2020-06-09T15:09:21Z,European Nucleotide Archive,Submitted by Wellcome Sanger Institute on 09-JUN-2020 ================================================ FILE: tests/data/test_search/sra_test_ERS3331676.xml ================================================ ERX4190585HiSeq X Ten paired end sequencingERP113893PRJEB31347Illumina sequencing of library DN539314J:H12, constructed from sample accession ERS3331676 for study accession ERP113893. This is part of an Illumina multiplexed sequencing run (29694_1). This submission includes reads tagged with the sequence TACCATTC.ERS3331676SAMEA5529601DN539314J:H12WGSGENOMICRANDOMStandardHiSeq X TenERA2689537Submitted by Wellcome Sanger Institute on 09-JUN-2020Wellcome Sanger InstituteERP113893PRJEB31347Maximizing_the_knowledge_gained_from_California_Senate_Bill_27Overuse of antibiotics contributes to antimicrobial resistance and is a growing threat to human health worldwide. In the U.S., approximately 70% of antibiotics are sold for use in livestock. On January 1, 2018, California enacted Senate Bill 27 (SB27), which will require a veterinarian's prescription for use of antimicrobial drugs and ban non-therapeutic antimicrobial uses for routine disease prevention and growth promotion in livestock. The project will quantify the effect of SB27 on E. coli, Campylobacter and Salmonella resistance rates from retail meat; estimate the proportion of human Campylobacter, Salmonella, and extraintestinal pathogenic E. coli infections caused by strains of food animal origin in California; characterize the effect of SB27 on antimicrobial susceptibility of Campylobacter, Salmonella, and extraintestinal E. coli infections caused by strains of food animal origin in California.Overuse of antibiotics contributes to antimicrobial resistance and is a growing threat to human health worldwide. In the U.S., approximately 70% of antibiotics are sold for use in livestock. On January 1, 2018, California enacted Senate Bill 27 (SB27), which will require a veterinarian's prescription for use of antimicrobial drugs and ban non-therapeutic antimicrobial uses for routine disease prevention and growth promotion in livestock. The project will quantify the effect of SB27 on E. coli, Campylobacter and Salmonella resistance rates from retail meat; estimate the proportion of human Campylobacter, Salmonella, and extraintestinal pathogenic E. coli infections caused by strains of food animal origin in California; characterize the effect of SB27 on antimicrobial susceptibility of Campylobacter, Salmonella, and extraintestinal E. coli infections caused by strains of food animal origin in California. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute please see http://www.sanger.ac.uk/datasharing/ENA-FIRST-PUBLIC2020-06-02ENA-LAST-UPDATE2019-02-19ERS3331676SAMEA5529601SB277889442562E. coliEscherichia coliSUBJECT_IDSB277889442ArrayExpress-SPECIESE. coliENA-FIRST-PUBLIC2020-06-09ENA-LAST-UPDATE2019-03-22ERS3331676SAMEA5529601ERR4229796HiSeq X Ten paired end sequencingERX4190585ENA-FIRST-PUBLIC2020-06-09ENA-LAST-UPDATE2020-06-09ERS3331676SAMEA5529601
================================================ FILE: tests/data/test_search/sra_test_verbosity_0.csv ================================================ run_accession SRR11217925 SRR11217924 SRR11217923 SRR11217922 SRR11217921 SRR11217920 SRR11217919 SRR11217918 SRR11217917 SRR11217916 SRR11217915 SRR11217914 SRR11186550 SRR11186549 SRR11186548 SRR11186547 SRR11186546 SRR11186545 SRR11186544 SRR11186543 SRR11186542 SRR11186541 SRR11186540 SRR11186539 SRR10398500 SRR10398499 SRR10398498 SRR10398497 SRR10398496 SRR10398495 SRR10398494 SRR10398493 SRR10398492 SRR10398491 SRR10398490 SRR10398489 SRR7241911 SRR5026637 SRR5026603 SRR5026592 SRR5026589 SRR5026359 SRR5026356 SRR3219264 SRR3219253 SRR3219248 SRR1804351 SRR1804349 SRR1804348 SRR1804346 SRR1804345 SRR1804343 SRR1804341 SRR1804340 SRR1635379 SRR1635378 SRR1635377 SRR1635376 SRR914339 SRR914338 SRR914337 SRR914336 SRR914335 SRR914334 SRR914333 SRR914332 SRR914331 SRR914330 SRR914329 SRR914328 SRR522897 SRR522895 SRR522883 SRR522896 SRR522872 SRR522871 SRR522892 SRR522890 SRR522881 SRR522153 SRR522152 SRR522151 SRR522882 SRR522888 SRR522011 SRR522010 SRR522009 SRR1804352 SRR1804350 SRR1804347 SRR1804344 SRR1804342 ================================================ FILE: tests/data/test_search/sra_test_verbosity_1.csv ================================================ run_accession,experiment_title SRR11217925,GSM4369051: rnaH27nsun3; Caenorhabditis elegans; RNA-Seq SRR11217924,GSM4369050: rnaH27nsun2; Caenorhabditis elegans; RNA-Seq SRR11217923,GSM4369049: rnaH27nsun1; Caenorhabditis elegans; RNA-Seq SRR11217922,GSM4369048: rnaH27WT3; Caenorhabditis elegans; RNA-Seq SRR11217921,GSM4369047: rnaH27WT2; Caenorhabditis elegans; RNA-Seq SRR11217920,GSM4369046: rnaH27WT1; Caenorhabditis elegans; RNA-Seq SRR11217919,GSM4369045: rnaL20nsun3; Caenorhabditis elegans; RNA-Seq SRR11217918,GSM4369044: rnaL20nsun2; Caenorhabditis elegans; RNA-Seq SRR11217917,GSM4369043: rnaL20nsun1; Caenorhabditis elegans; RNA-Seq SRR11217916,GSM4369042: rnaL20WT3; Caenorhabditis elegans; RNA-Seq SRR11217915,GSM4369041: rnaL20WT2; Caenorhabditis elegans; RNA-Seq SRR11217914,GSM4369040: rnaL20WT1; Caenorhabditis elegans; RNA-Seq SRR11186550,GSM4340680: pmk-1(km25)RPF Replicate 2; Caenorhabditis elegans; RNA-Seq SRR11186549,GSM4340679: pmk-1(km25) total mRNA Replicate 2; Caenorhabditis elegans; RNA-Seq SRR11186548,GSM4340678: pmk-1(km25)RPF Replicate 1; Caenorhabditis elegans; RNA-Seq SRR11186547,GSM4340677: pmk-1(km25) total mRNA Replicate 1; Caenorhabditis elegans; RNA-Seq SRR11186546,GSM4340676: ced-3(n717)RPF Replicate 2; Caenorhabditis elegans; RNA-Seq SRR11186545,GSM4340675: ced-3(n717) total mRNA Replicate 2; Caenorhabditis elegans; RNA-Seq SRR11186544,GSM4340674: ced-3(n717)RPF Replicate 1; Caenorhabditis elegans; RNA-Seq SRR11186543,GSM4340673: ced-3(n717) total mRNA Replicate 1; Caenorhabditis elegans; RNA-Seq SRR11186542,GSM4340672: WT RPF Replicate 2; Caenorhabditis elegans; RNA-Seq SRR11186541,GSM4340671: WT total mRNA Replicate 2; Caenorhabditis elegans; RNA-Seq SRR11186540,GSM4340670: WT RPF Replicate 1; Caenorhabditis elegans; RNA-Seq SRR11186539,GSM4340669: WT total mRNA Replicate 1; Caenorhabditis elegans; RNA-Seq SRR10398500,GSM4148088: Slee141_mRNAseqFP_meg34_3: meg-3meg-4 mRNAseq-3; Caenorhabditis elegans; RNA-Seq SRR10398499,GSM4148087: Slee139_mRNAseqFP_meg34_2: meg-3meg-4 mRNAseq-2; Caenorhabditis elegans; RNA-Seq SRR10398498,GSM4148086: Slee125_mRNAseqFP_meg34_1: meg-3meg-4 mRNAseq-1; Caenorhabditis elegans; RNA-Seq SRR10398497,GSM4148085: Slee142_mRNAseqFP_N2_3: wild type mRNAseq-3; Caenorhabditis elegans; RNA-Seq SRR10398496,GSM4148084: Slee138_mRNAseqFP_N2_2: wild type mRNAseq-2; Caenorhabditis elegans; RNA-Seq SRR10398495,GSM4148083: Slee113_mRNAseqFP_N2_1: wild type mRNAseq-1; Caenorhabditis elegans; RNA-Seq SRR10398494,GSM4148082: Slee135_meg34: meg-3meg-4 Riboseq-3; Caenorhabditis elegans; OTHER SRR10398493,GSM4148081: Slee133_meg34: meg-3meg-4 Riboseq-2; Caenorhabditis elegans; OTHER SRR10398492,GSM4148080: Slee123_meg34: meg-3meg-4 Riboseq-1; Caenorhabditis elegans; OTHER SRR10398491,GSM4148079: Slee136_N2: wild type Riboseq-3; Caenorhabditis elegans; OTHER SRR10398490,GSM4148078: Slee132_N2: wild type Riboseq-2; Caenorhabditis elegans; OTHER SRR10398489,GSM4148077: Slee111_N2: wild type Riboseq-1; Caenorhabditis elegans; OTHER SRR7241911,GSM3168388: C. elegans embryos ribosome profiling; Caenorhabditis elegans; RNA-Seq SRR5026637,Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026603,Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026592,Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026589,Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026359,Bayesian Prediction of RNA Translation from Ribosome Profiling SRR5026356,Bayesian Prediction of RNA Translation from Ribosome Profiling SRR3219264,unc-54(cc3389) Ribo-seq SRR3219253,unc-54(+) Ribo-seq SRR3219248,unc-54(+) Ribo-seq SRR1804351,GSM1611598: frac_26-34nt; Caenorhabditis elegans; OTHER SRR1804349,GSM1611597: frac_28-35nt; Caenorhabditis elegans; OTHER SRR1804348,GSM1611596: frac_28-30nt; Caenorhabditis elegans; OTHER SRR1804346,GSM1611595: frac_25-30nt; Caenorhabditis elegans; OTHER SRR1804345,GSM1611594: 04_N2_893_GCkit; Caenorhabditis elegans; OTHER SRR1804343,GSM1611593: 03_N2_893_SGkit; Caenorhabditis elegans; OTHER SRR1804341,GSM1611592: 02_N2_893_GCop; Caenorhabditis elegans; OTHER SRR1804340,GSM1611591: 01_N2_893_SGop; Caenorhabditis elegans; OTHER SRR1635379,GSM1534607: RNASeq_c14_2; Caenorhabditis elegans; RNA-Seq SRR1635378,GSM1534606: RNASeq_c14_1; Caenorhabditis elegans; RNA-Seq SRR1635377,GSM1534605: RNASeq_N2_2; Caenorhabditis elegans; RNA-Seq SRR1635376,GSM1534604: RNASeq_N2_1; Caenorhabditis elegans; RNA-Seq SRR914339,GSM1169554: Celeg-3-FED-RPF; Caenorhabditis elegans; OTHER SRR914338,GSM1169553: Celeg-2-FED-RPF; Caenorhabditis elegans; OTHER SRR914337,GSM1169552: Celeg-1-FED-RPF; Caenorhabditis elegans; OTHER SRR914336,GSM1169551: Celeg-3-ST-RPF; Caenorhabditis elegans; OTHER SRR914335,GSM1169550: Celeg-2-ST-RPF; Caenorhabditis elegans; OTHER SRR914334,GSM1169549: Celeg-1-ST-RPF; Caenorhabditis elegans; OTHER SRR914333,GSM1169548: Celeg-3-FED-mRNA; Caenorhabditis elegans; RNA-Seq SRR914332,GSM1169547: Celeg-2-FED-mRNA; Caenorhabditis elegans; RNA-Seq SRR914331,GSM1169546: Celeg-1-FED-mRNA; Caenorhabditis elegans; RNA-Seq SRR914330,GSM1169545: Celeg-3-ST-mRNA; Caenorhabditis elegans; RNA-Seq SRR914329,GSM1169544: Celeg-2-ST-mRNA; Caenorhabditis elegans; RNA-Seq SRR914328,GSM1169543: Celeg-1-ST-mRNA; Caenorhabditis elegans; RNA-Seq SRR522897,L1 ribosome footprints replicate 4 SRR522895,L2 ribosome footprints replicate 2 (seq-replicate) SRR522883,L4 ribosome footprints replicate 1 SRR522896,L1 ribosome footprints replicate 3 SRR522872,L1 ribosome footprints replicate 2 SRR522871,L1 ribosome footprints replicate 1 SRR522892,L2 ribosome footprints replicate 3 SRR522890,L2 ribosome footprints replicate 2 SRR522881,L2 ribosome footprints replicate 1 SRR522153,L4 total RNA-seq SRR522152,L1 total RNA-seq SRR522151,L4 mRNA-seq replicate 2 SRR522882,L4 mRNA-seq replicate 1 SRR522888,L1 mRNA-seq replicate 4 SRR522011,L1 replicate 3 mRNA-seq SRR522010,L1 replicate 2 mRNA-seq SRR522009,L1 mRNA-seq replicate 1 SRR1804352,GSM1611598: frac_26-34nt; Caenorhabditis elegans; OTHER SRR1804350,GSM1611597: frac_28-35nt; Caenorhabditis elegans; OTHER SRR1804347,GSM1611595: frac_25-30nt; Caenorhabditis elegans; OTHER SRR1804344,GSM1611593: 03_N2_893_SGkit; Caenorhabditis elegans; OTHER SRR1804342,GSM1611592: 02_N2_893_GCop; Caenorhabditis elegans; OTHER ================================================ FILE: tests/data/test_search/sra_test_verbosity_2.csv ================================================ study_accession,experiment_accession,experiment_title,sample_taxon_id,sample_scientific_name,experiment_library_strategy,experiment_library_source,experiment_library_selection,sample_accession,sample_alias,experiment_instrument_model,pool_member_spots,run_1_size,run_1_accession,run_1_total_spots,run_1_total_bases SRP251352,SRX7830165,GSM4369051: rnaH27nsun3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240844,GSM4369051,Illumina HiSeq 2000,29156586,653560062,SRR11217925,29156586,1472955019 SRP251352,SRX7830164,GSM4369050: rnaH27nsun2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240843,GSM4369050,Illumina HiSeq 2000,22565640,506358031,SRR11217924,22565640,1139918538 SRP251352,SRX7830163,GSM4369049: rnaH27nsun1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240842,GSM4369049,Illumina HiSeq 2000,23045718,517675060,SRR11217923,23045718,1164355435 SRP251352,SRX7830162,GSM4369048: rnaH27WT3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240841,GSM4369048,Illumina HiSeq 2000,20220436,454916247,SRR11217922,20220436,1021477707 SRP251352,SRX7830161,GSM4369047: rnaH27WT2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240840,GSM4369047,Illumina HiSeq 2000,23193519,519655753,SRR11217921,23193519,1171799561 SRP251352,SRX7830160,GSM4369046: rnaH27WT1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240839,GSM4369046,Illumina HiSeq 2000,29264100,659671877,SRR11217920,29264100,1478364947 SRP251352,SRX7830159,GSM4369045: rnaL20nsun3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240838,GSM4369045,Illumina HiSeq 2000,29891239,673813329,SRR11217919,29891239,1510005136 SRP251352,SRX7830158,GSM4369044: rnaL20nsun2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240837,GSM4369044,Illumina HiSeq 2000,32298489,723109558,SRR11217918,32298489,1631781747 SRP251352,SRX7830157,GSM4369043: rnaL20nsun1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240836,GSM4369043,Illumina HiSeq 2000,29902595,671811120,SRR11217917,29902595,1510510194 SRP251352,SRX7830156,GSM4369042: rnaL20WT3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240835,GSM4369042,Illumina HiSeq 2000,31692524,710100849,SRR11217916,31692524,1600940503 SRP251352,SRX7830155,GSM4369041: rnaL20WT2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240834,GSM4369041,Illumina HiSeq 2000,30511012,682577921,SRR11217915,30511012,1541330541 SRP251352,SRX7830154,GSM4369040: rnaL20WT1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240833,GSM4369040,Illumina HiSeq 2000,29920739,670669468,SRR11217914,29920739,1511594659 SRP250832,SRX7806834,GSM4340680: pmk-1(km25)RPF Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219869,GSM4340680,NextSeq 500,34364285,863253383,SRR11186550,34364285,2542957090 SRP250832,SRX7806833,GSM4340679: pmk-1(km25) total mRNA Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219868,GSM4340679,NextSeq 500,33631873,857793145,SRR11186549,33631873,2488758602 SRP250832,SRX7806832,GSM4340678: pmk-1(km25)RPF Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219867,GSM4340678,NextSeq 500,30114094,778775375,SRR11186548,30114094,2228442956 SRP250832,SRX7806831,GSM4340677: pmk-1(km25) total mRNA Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219866,GSM4340677,NextSeq 500,29403277,748531060,SRR11186547,29403277,2175842498 SRP250832,SRX7806830,GSM4340676: ced-3(n717)RPF Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219865,GSM4340676,NextSeq 500,33357995,837113969,SRR11186546,33357995,2468491630 SRP250832,SRX7806829,GSM4340675: ced-3(n717) total mRNA Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219864,GSM4340675,NextSeq 500,31063779,804926730,SRR11186545,31063779,2298719646 SRP250832,SRX7806828,GSM4340674: ced-3(n717)RPF Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219863,GSM4340674,NextSeq 500,33350365,834857358,SRR11186544,33350365,2467927010 SRP250832,SRX7806827,GSM4340673: ced-3(n717) total mRNA Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219862,GSM4340673,NextSeq 500,30481900,774994143,SRR11186543,30481900,2255660600 SRP250832,SRX7806826,GSM4340672: WT RPF Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219861,GSM4340672,NextSeq 500,29791126,744716047,SRR11186542,29791126,2204543324 SRP250832,SRX7806825,GSM4340671: WT total mRNA Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219860,GSM4340671,NextSeq 500,30801390,784439721,SRR11186541,30801390,2279302860 SRP250832,SRX7806824,GSM4340670: WT RPF Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219859,GSM4340670,NextSeq 500,31188949,786278140,SRR11186540,31188949,2307982226 SRP250832,SRX7806823,GSM4340669: WT total mRNA Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219858,GSM4340669,NextSeq 500,33246237,847324162,SRR11186539,33246237,2460221538 SRP228538,SRX7098753,GSM4148088: Slee141_mRNAseqFP_meg34_3: meg-3meg-4 mRNAseq-3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611015,GSM4148088,Illumina HiSeq 2500,50180090,1461952152,SRR10398500,50180090,2509004500 SRP228538,SRX7098752,GSM4148087: Slee139_mRNAseqFP_meg34_2: meg-3meg-4 mRNAseq-2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611014,GSM4148087,Illumina HiSeq 2500,59848989,1748019918,SRR10398499,59848989,2992449450 SRP228538,SRX7098751,GSM4148086: Slee125_mRNAseqFP_meg34_1: meg-3meg-4 mRNAseq-1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611013,GSM4148086,Illumina HiSeq 2500,17823378,553495038,SRR10398498,17823378,891168900 SRP228538,SRX7098750,GSM4148085: Slee142_mRNAseqFP_N2_3: wild type mRNAseq-3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611012,GSM4148085,Illumina HiSeq 2500,64787771,1883244063,SRR10398497,64787771,3239388550 SRP228538,SRX7098749,GSM4148084: Slee138_mRNAseqFP_N2_2: wild type mRNAseq-2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611011,GSM4148084,Illumina HiSeq 2500,54109682,1574815163,SRR10398496,54109682,2705484100 SRP228538,SRX7098748,GSM4148083: Slee113_mRNAseqFP_N2_1: wild type mRNAseq-1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611010,GSM4148083,Illumina HiSeq 2500,53153078,1518355802,SRR10398495,53153078,2657653900 SRP228538,SRX7098747,GSM4148082: Slee135_meg34: meg-3meg-4 Riboseq-3; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611009,GSM4148082,Illumina HiSeq 2500,117347118,3430391353,SRR10398494,117347118,5867355900 SRP228538,SRX7098746,GSM4148081: Slee133_meg34: meg-3meg-4 Riboseq-2; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611008,GSM4148081,Illumina HiSeq 2500,107081543,3125393193,SRR10398493,107081543,5354077150 SRP228538,SRX7098745,GSM4148080: Slee123_meg34: meg-3meg-4 Riboseq-1; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611007,GSM4148080,Illumina HiSeq 2500,35703383,867677732,SRR10398492,35703383,1785169150 SRP228538,SRX7098744,GSM4148079: Slee136_N2: wild type Riboseq-3; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611006,GSM4148079,Illumina HiSeq 2500,121439833,3342082520,SRR10398491,121439833,6071991650 SRP228538,SRX7098743,GSM4148078: Slee132_N2: wild type Riboseq-2; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611005,GSM4148078,Illumina HiSeq 2500,134995957,3934664046,SRR10398490,134995957,6749797850 SRP228538,SRX7098742,GSM4148077: Slee111_N2: wild type Riboseq-1; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611004,GSM4148077,Illumina HiSeq 2500,76408239,1744253035,SRR10398489,76408239,3820411950 SRP149446,SRX4147684,GSM3168388: C. elegans embryos ribosome profiling; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS3361274,GSM3168388,Illumina HiSeq 2500,76408239,1744253035,SRR7241911,76408239,3820411950 SRP093364,SRX2352818,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,138903638,3355135395,SRR5026637,138903638,6945181900 SRP093364,SRX2352801,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,139378431,3450860219,SRR5026603,139378431,6968921550 SRP093364,SRX2352796,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,109643569,2602261551,SRR5026592,109643569,5482178450 SRP093364,SRX2352779,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,125934593,3035330434,SRR5026589,125934593,6296729650 SRP093364,SRX2352572,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,66094062,1613138917,SRR5026359,66094062,3304703100 SRP093364,SRX2349147,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,335001052,8622020036,SRR5026356,335001052,16750052600 SRP064516,SRX1626372,unc-54(cc3389) Ribo-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,other,SRS1335846,SJA131,Illumina MiSeq,3200939,79101256,SRR3219264,3200939,176051645 SRP064516,SRX1626361,unc-54(+) Ribo-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,other,SRS1335837,SJA130,Illumina MiSeq,2845260,69990868,SRR3219253,2845260,156489300 SRP064516,SRX1626357,unc-54(+) Ribo-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,other,SRS1335834,SJA129,Illumina MiSeq,3407482,84664325,SRR3219248,3407482,187411510 SRP055039,SRX878014,GSM1611598: frac_26-34nt; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845968,GSM1611598,Illumina HiSeq 2000,50364078,1532513718,SRR1804351,50000000,2500000000 SRP055039,SRX878013,GSM1611597: frac_28-35nt; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845969,GSM1611597,Illumina HiSeq 2000,66596977,1238978094,SRR1804349,50000000,2500000000 SRP055039,SRX878012,GSM1611596: frac_28-30nt; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845970,GSM1611596,Illumina HiSeq 2000,46376697,1564322597,SRR1804348,46376697,2318834850 SRP055039,SRX878011,GSM1611595: frac_25-30nt; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845971,GSM1611595,Illumina HiSeq 2000,58434235,1765202980,SRR1804346,50000000,2500000000 SRP055039,SRX878010,GSM1611594: 04_N2_893_GCkit; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845972,GSM1611594,Illumina HiSeq 2000,48751368,1774440563,SRR1804345,48751368,2486319768 SRP055039,SRX878009,GSM1611593: 03_N2_893_SGkit; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845973,GSM1611593,Illumina HiSeq 2000,67420201,1803539052,SRR1804343,50000000,2550000000 SRP055039,SRX878008,GSM1611592: 02_N2_893_GCop; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845974,GSM1611592,Illumina HiSeq 2000,52891603,1798510443,SRR1804341,50000000,2550000000 SRP055039,SRX878007,GSM1611591: 01_N2_893_SGop; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845975,GSM1611591,Illumina HiSeq 2000,49787580,1806454729,SRR1804340,49787580,2539166580 SRP049413,SRX747690,GSM1534607: RNASeq_c14_2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS734047,GSM1534607,Illumina HiSeq 2500,49019407,1169023236,SRR1635379,49019407,2450970350 SRP049413,SRX747689,GSM1534606: RNASeq_c14_1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS734046,GSM1534606,Illumina HiSeq 2500,63457303,1540925484,SRR1635378,63457303,3172865150 SRP049413,SRX747688,GSM1534605: RNASeq_N2_2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS734045,GSM1534605,Illumina HiSeq 2500,54290105,1318568086,SRR1635377,54290105,2714505250 SRP049413,SRX747687,GSM1534604: RNASeq_N2_1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS734044,GSM1534604,Illumina HiSeq 2500,64579253,1537362492,SRR1635376,64579253,3228962650 SRP026198,SRX311785,GSM1169554: Celeg-3-FED-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449537,GSM1169554,Illumina HiSeq 2000,20213950,446723077,SRR914339,20213950,727702200 SRP026198,SRX311784,GSM1169553: Celeg-2-FED-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449536,GSM1169553,Illumina HiSeq 2000,59233837,2094108084,SRR914338,59233837,2961691850 SRP026198,SRX311783,GSM1169552: Celeg-1-FED-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449535,GSM1169552,Illumina HiSeq 2000,30099263,1080856284,SRR914337,30099263,1504963150 SRP026198,SRX311782,GSM1169551: Celeg-3-ST-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449534,GSM1169551,Illumina HiSeq 2000,50278819,1757277248,SRR914336,50278819,2513940950 SRP026198,SRX311781,GSM1169550: Celeg-2-ST-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449533,GSM1169550,Illumina HiSeq 2000,20851539,453779681,SRR914335,20851539,750655404 SRP026198,SRX311780,GSM1169549: Celeg-1-ST-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449532,GSM1169549,Illumina HiSeq 2000,46096938,1610654289,SRR914334,46096938,2304846900 SRP026198,SRX311779,GSM1169548: Celeg-3-FED-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449531,GSM1169548,Illumina HiSeq 2000,27043901,943922301,SRR914333,27043901,1352195050 SRP026198,SRX311778,GSM1169547: Celeg-2-FED-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449530,GSM1169547,Illumina HiSeq 2000,15243931,541870283,SRR914332,15243931,762196550 SRP026198,SRX311777,GSM1169546: Celeg-1-FED-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449529,GSM1169546,Illumina HiSeq 2000,14429547,515974302,SRR914331,14429547,721477350 SRP026198,SRX311776,GSM1169545: Celeg-3-ST-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449528,GSM1169545,Illumina HiSeq 2000,23438522,822960576,SRR914330,23438522,1171926100 SRP026198,SRX311775,GSM1169544: Celeg-2-ST-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449527,GSM1169544,Illumina HiSeq 2000,31547222,1401361925,SRR914329,31547222,2366041650 SRP026198,SRX311774,GSM1169543: Celeg-1-ST-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449591,GSM1169543,Illumina HiSeq 2000,19452670,696539703,SRR914328,19452670,972633500 SRP014427,SRX160517,L1 ribosome footprints replicate 4,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,172256552,7089950470,SRR522897,172256552,9990880016 SRP014427,SRX160513,L2 ribosome footprints replicate 2 (seq-replicate),6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,160368455,6099790048,SRR522895,160368455,9301370390 SRP014427,SRX160518,L4 ribosome footprints replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,174693758,7204894135,SRR522883,174693758,10132237964 SRP014427,SRX160516,L1 ribosome footprints replicate 3,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,20213950,447522447,SRR522896,20213950,727702200 SRP014427,SRX160515,L1 ribosome footprints replicate 2,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,59233837,2096895718,SRR522872,59233837,2961691850 SRP014427,SRX160514,L1 ribosome footprints replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,30099263,1082257308,SRR522871,30099263,1504963150 SRP014427,SRX160512,L2 ribosome footprints replicate 3,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,32939763,674223820,SRR522892,32939763,1185831468 SRP014427,SRX160511,L2 ribosome footprints replicate 2,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,13600895,255011824,SRR522890,13600895,489632220 SRP014427,SRX160510,L2 ribosome footprints replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,15787042,298610401,SRR522881,15787042,568333512 SRP014427,SRX160293,L4 total RNA-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,58539675,1150293060,SRR522153,58539675,2107428300 SRP014427,SRX160292,L1 total RNA-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,33245137,717344505,SRR522152,33245137,1196824932 SRP014427,SRX160291,L4 mRNA-seq replicate 2,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,27313086,546661322,SRR522151,27313086,983271096 SRP014427,SRX160290,L4 mRNA-seq replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,184752725,7621028154,SRR522882,184752725,10715658050 SRP014427,SRX160157,L1 mRNA-seq replicate 4,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,97881671,4241570041,SRR522888,97881671,5677136918 SRP014427,SRX160149,L1 replicate 3 mRNA-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,27043901,945136520,SRR522011,27043901,1352195050 SRP014427,SRX160148,L1 replicate 2 mRNA-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,15243931,542413430,SRR522010,15243931,762196550 SRP014427,SRX160147,L1 mRNA-seq replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,14429547,516477040,SRR522009,14429547,721477350 ================================================ FILE: tests/data/test_search/sra_test_verbosity_3.csv ================================================ 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SRP251352,SRX7830165,GSM4369051: rnaH27nsun3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240844,GSM4369051,Illumina HiSeq 2000,29156586,653560062,SRR11217925,29156586,1472955019,GSM4369051,GEO Accession,GSM4369051,,,,GSM4369051,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369051,LABEL: GSM4369051,,,,ILLUMINA,,,,SRS6240844,,SINGLE,SAMN14262094,SRS6240844,1472955019,,Caenorhabditis elegans,GSM4369051,rnaH27nsun3,6239,GSM4369051_r1,382463198,383363002,348833145,556030,357739644,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11217925/ICN-12_S12.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11217925/ICN-12_S12.fastq.gz.1,,,,,,,,,public,2020-03-03 08:50:17,,71f7deb03542a4364d272b8bb3a388c6,fastq,718691668,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/010955/SRR11217925,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-1/SRR11217925/SRR11217925.1,gcp identity,gs.US,GCP,gs://sra-pub-run-7/SRR11217925/SRR11217925.1,,,,,public,2020-03-03 08:50:43,SRR11217925,5f6cbd5ce0a57afa0c589b1289761370,run,653562181,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/010955/SRR11217925,,,,,,,,,,,,,,,,,,,,,,1,1472955019,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,27,genotype,noNSUN,,,,,,,,,,SAMN14262094,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaH27nsun3,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830164,GSM4369050: rnaH27nsun2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240843,GSM4369050,Illumina HiSeq 2000,22565640,506358031,SRR11217924,22565640,1139918538,GSM4369050,GEO Accession,GSM4369050,,,,GSM4369050,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369050,LABEL: GSM4369050,,,,ILLUMINA,,,,SRS6240843,,SINGLE,SAMN14262095,SRS6240843,1139918538,,Caenorhabditis elegans,GSM4369050,rnaH27nsun2,6239,GSM4369050_r1,298818895,294922698,267736921,371135,278068889,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-12/SRR11217924/ICN-11_S11.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-12/SRR11217924/ICN-11_S11.fastq.gz.1,,,,,,,,,public,2020-03-03 08:48:31,,6d752552a724ff725c949bb10acf3d3f,fastq,561312446,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/010955/SRR11217924,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-9/SRR11217924/SRR11217924.1,gcp identity,gs.US,GCP,gs://sra-pub-run-8/SRR11217924/SRR11217924.1,,,,,public,2020-03-03 08:48:51,SRR11217924,6792d5c7e80a5c7ed19d6fcbbbc8b850,run,506360149,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra66/SRR/010955/SRR11217924,,,,,,,,,,,,,,,,,,,,,,1,1139918538,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,27,genotype,noNSUN,,,,,,,,,,SAMN14262095,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaH27nsun2,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830163,GSM4369049: rnaH27nsun1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240842,GSM4369049,Illumina HiSeq 2000,23045718,517675060,SRR11217923,23045718,1164355435,GSM4369049,GEO Accession,GSM4369049,,,,GSM4369049,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369049,LABEL: GSM4369049,,,,ILLUMINA,,,,SRS6240842,,SINGLE,SAMN14262096,SRS6240842,1164355435,,Caenorhabditis elegans,GSM4369049,rnaH27nsun1,6239,GSM4369049_r1,303774981,302133692,273117993,337197,284991572,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR11217923/ICN-10_S10.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR11217923/ICN-10_S10.fastq.gz.1,,,,,,,,,public,2020-03-03 08:49:41,,09b25e1939de2b4a379afd4633369775,fastq,579257723,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/010955/SRR11217923,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-8/SRR11217923/SRR11217923.1,gcp identity,gs.US,GCP,gs://sra-pub-run-9/SRR11217923/SRR11217923.1,,,,,public,2020-03-03 08:50:05,SRR11217923,9ba3ae130439af2590c7307fe37ef21d,run,517677177,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra22/SRR/010955/SRR11217923,,,,,,,,,,,,,,,,,,,,,,1,1164355435,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,27,genotype,noNSUN,,,,,,,,,,SAMN14262096,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaH27nsun1,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830162,GSM4369048: rnaH27WT3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240841,GSM4369048,Illumina HiSeq 2000,20220436,454916247,SRR11217922,20220436,1021477707,GSM4369048,GEO Accession,GSM4369048,,,,GSM4369048,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369048,LABEL: GSM4369048,,,,ILLUMINA,,,,SRS6240841,,SINGLE,SAMN14262097,SRS6240841,1021477707,,Caenorhabditis elegans,GSM4369048,rnaH27WT3,6239,GSM4369048_r1,267649932,265386720,240228857,359263,247852935,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR11217922/ICN-09_S9.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR11217922/ICN-09_S9.fastq.gz.1,,,,,,,,,public,2020-03-03 08:47:59,,314952e01bb1473982cf0c332ab91817,fastq,506379353,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/010955/SRR11217922,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-6/SRR11217922/SRR11217922.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR11217922/SRR11217922.1,,,,,public,2020-03-03 08:48:17,SRR11217922,f60bf66704ca1278d5ce96a415971bed,run,454918368,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra28/SRR/010955/SRR11217922,,,,,,,,,,,,,,,,,,,,,,1,1021477707,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,27,genotype,WT,,,,,,,,,,SAMN14262097,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaH27WT3,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830161,GSM4369047: rnaH27WT2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240840,GSM4369047,Illumina HiSeq 2000,23193519,519655753,SRR11217921,23193519,1171799561,GSM4369047,GEO Accession,GSM4369047,,,,GSM4369047,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369047,LABEL: GSM4369047,,,,ILLUMINA,,,,SRS6240840,,SINGLE,SAMN14262098,SRS6240840,1171799561,,Caenorhabditis elegans,GSM4369047,rnaH27WT2,6239,GSM4369047_r1,306725822,306004751,275721333,463743,282883912,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR11217921/ICN-08_S8.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR11217921/ICN-08_S8.fastq.gz.1,,,,,,,,,public,2020-03-03 08:47:50,,2dea86900e8e176457d67f60324e0b28,fastq,574811709,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/010955/SRR11217921,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-8/SRR11217921/SRR11217921.1,gcp identity,gs.US,GCP,gs://sra-pub-run-9/SRR11217921/SRR11217921.1,,,,,public,2020-03-03 08:48:02,SRR11217921,feca6d4e41da203410303091728ad42a,run,519657875,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/010955/SRR11217921,,,,,,,,,,,,,,,,,,,,,,1,1171799561,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,27,genotype,WT,,,,,,,,,,SAMN14262098,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaH27WT2,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830160,GSM4369046: rnaH27WT1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240839,GSM4369046,Illumina HiSeq 2000,29264100,659671877,SRR11217920,29264100,1478364947,GSM4369046,GEO Accession,GSM4369046,,,,GSM4369046,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369046,LABEL: GSM4369046,,,,ILLUMINA,,,,SRS6240839,,SINGLE,SAMN14262099,SRS6240839,1478364947,,Caenorhabditis elegans,GSM4369046,rnaH27WT1,6239,GSM4369046_r1,382118207,382503596,349309307,861255,363572582,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-9/SRR11217920/ICN-07_S7.fastq.gz.1,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-10/SRR11217920/ICN-07_S7.fastq.gz.1,,,,,,,,,public,2020-03-03 08:49:25,,2b422efb98539cc38d7fd07e4f5ad280,fastq,740347495,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/010955/SRR11217920,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-8/SRR11217920/SRR11217920.1,gcp identity,gs.US,GCP,gs://sra-pub-run-9/SRR11217920/SRR11217920.1,,,,,public,2020-03-03 08:49:44,SRR11217920,4cc08d2cd582626f82c7a1dec67d1b46,run,659673990,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra19/SRR/010955/SRR11217920,,,,,,,,,,,,,,,,,,,,,,1,1478364947,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,27,genotype,WT,,,,,,,,,,SAMN14262099,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaH27WT1,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830159,GSM4369045: rnaL20nsun3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240838,GSM4369045,Illumina HiSeq 2000,29891239,673813329,SRR11217919,29891239,1510005136,GSM4369045,GEO Accession,GSM4369045,,,,GSM4369045,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369045,LABEL: GSM4369045,,,,ILLUMINA,,,,SRS6240838,,SINGLE,SAMN14262100,SRS6240838,1510005136,,Caenorhabditis elegans,GSM4369045,rnaL20nsun3,6239,GSM4369045_r1,390734249,388663023,357256079,696106,372655679,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-8/SRR11217919/ICN-06_S6.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-8/SRR11217919/ICN-06_S6.fastq.gz.1,,,,,,,,,public,2020-03-03 08:55:31,,4392ef76def5efa96469ef7c20ee0390,fastq,752039868,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/010954/SRR11217919,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-7/SRR11217919/SRR11217919.1,gcp identity,gs.US,GCP,gs://sra-pub-run-3/SRR11217919/SRR11217919.1,,,,,public,2020-03-03 08:56:13,SRR11217919,d08dee0029b7a17fa74a499dcbb9c6b3,run,673815447,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra15/SRR/010954/SRR11217919,,,,,,,,,,,,,,,,,,,,,,1,1510005136,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,20,genotype,noNSUN,,,,,,,,,,SAMN14262100,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaL20nsun3,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830158,GSM4369044: rnaL20nsun2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240837,GSM4369044,Illumina HiSeq 2000,32298489,723109558,SRR11217918,32298489,1631781747,GSM4369044,GEO Accession,GSM4369044,,,,GSM4369044,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369044,LABEL: GSM4369044,,,,ILLUMINA,,,,SRS6240837,,SINGLE,SAMN14262101,SRS6240837,1631781747,,Caenorhabditis elegans,GSM4369044,rnaL20nsun2,6239,GSM4369044_r1,426634172,419579176,384996637,588737,399983025,,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,"
",true,true,2020-06-30 17:40:41,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRZ/011217/SRR11217918/ICN-05_S5.fastq.gz,,,,,,,,,,,,,public,2020-03-03 08:50:47,ICN-05_S5.fastq.gz,8103aefb1b95eaf0acb7578300651ec0,fastq,801345858,0,Original,https://sra-download.ncbi.nlm.nih.gov/traces/sra9/SRZ/011217/SRR11217918/ICN-05_S5.fastq.gz,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/010954/SRR11217918,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-9/SRR11217918/SRR11217918.1,gcp identity,gs.US,GCP,gs://sra-pub-run-8/SRR11217918/SRR11217918.1,,,,,public,2020-03-03 08:51:12,SRR11217918,756e31c0766fe84e79131bacf459f320,run,723111676,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra55/SRR/010954/SRR11217918,,,,,,,,,,,,,,,,,,,,,,1,1631781747,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,20,genotype,noNSUN,,,,,,,,,,SAMN14262101,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaL20nsun2,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830157,GSM4369043: rnaL20nsun1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240836,GSM4369043,Illumina HiSeq 2000,29902595,671811120,SRR11217917,29902595,1510510194,GSM4369043,GEO Accession,GSM4369043,,,,GSM4369043,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369043,LABEL: GSM4369043,,,,ILLUMINA,,,,SRS6240836,,SINGLE,SAMN14262102,SRS6240836,1510510194,,Caenorhabditis elegans,GSM4369043,rnaL20nsun1,6239,GSM4369043_r1,389909920,389932739,356931273,771186,372965076,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-9/SRR11217917/ICN-04_S4.fastq.gz.1,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-10/SRR11217917/ICN-04_S4.fastq.gz.1,,,,,,,,,public,2020-03-03 08:51:18,,916fe1fa029221d55d678f7fb8fc3850,fastq,741235433,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/010954/SRR11217917,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-8/SRR11217917/SRR11217917.1,gcp identity,gs.US,GCP,gs://sra-pub-run-9/SRR11217917/SRR11217917.1,,,,,public,2020-03-03 08:51:41,SRR11217917,8f17921020f5338021259ad66cfa3d90,run,671813239,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra20/SRR/010954/SRR11217917,,,,,,,,,,,,,,,,,,,,,,1,1510510194,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,20,genotype,noNSUN,,,,,,,,,,SAMN14262102,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaL20nsun1,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830156,GSM4369042: rnaL20WT3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240835,GSM4369042,Illumina HiSeq 2000,31692524,710100849,SRR11217916,31692524,1600940503,GSM4369042,GEO Accession,GSM4369042,,,,GSM4369042,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369042,LABEL: GSM4369042,,,,ILLUMINA,,,,SRS6240835,,SINGLE,SAMN14262103,SRS6240835,1600940503,,Caenorhabditis elegans,GSM4369042,rnaL20WT3,6239,GSM4369042_r1,412825059,412495776,381736364,839315,393043989,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11217916/ICN-03_S3.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11217916/ICN-03_S3.fastq.gz.1,,,,,,,,,public,2020-03-03 08:52:30,,0bd13a1fc7c8b899433d2b0703d058ae,fastq,788245180,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/010954/SRR11217916,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-3/SRR11217916/SRR11217916.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR11217916/SRR11217916.1,,,,,public,2020-03-03 08:52:54,SRR11217916,e0d2490640aa5c4320a1ef928ed541fc,run,710102964,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra44/SRR/010954/SRR11217916,,,,,,,,,,,,,,,,,,,,,,1,1600940503,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,20,genotype,WT,,,,,,,,,,SAMN14262103,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaL20WT3,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830155,GSM4369041: rnaL20WT2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240834,GSM4369041,Illumina HiSeq 2000,30511012,682577921,SRR11217915,30511012,1541330541,GSM4369041,GEO Accession,GSM4369041,,,,GSM4369041,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369041,LABEL: GSM4369041,,,,ILLUMINA,,,,SRS6240834,,SINGLE,SAMN14262104,SRS6240834,1541330541,,Caenorhabditis elegans,GSM4369041,rnaL20WT2,6239,GSM4369041_r1,398519968,397956128,366381635,605330,377867480,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11217915/ICN-02_S2.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11217915/ICN-02_S2.fastq.gz.1,,,,,,,,,public,2020-03-03 08:50:32,,4937a59fcdbbba1a31f931f2771dcdb1,fastq,747661439,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/010954/SRR11217915,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-3/SRR11217915/SRR11217915.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR11217915/SRR11217915.1,,,,,public,2020-03-03 08:50:56,SRR11217915,1fe769ceb3acf5f9b8ba1d88b43131ad,run,682580036,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/010954/SRR11217915,,,,,,,,,,,,,,,,,,,,,,1,1541330541,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,20,genotype,WT,,,,,,,,,,SAMN14262104,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaL20WT2,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP251352,SRX7830154,GSM4369040: rnaL20WT1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6240833,GSM4369040,Illumina HiSeq 2000,29920739,670669468,SRR11217914,29920739,1511594659,GSM4369040,GEO Accession,GSM4369040,,,,GSM4369040,"Input RNA was extracted from the supernatant of the same samples used for polysome profiling and ribosome footprinting. RNA was depleted of DNA with a TURBO DNA-free kit (Invitrogen), according to the manufacturer's instructions. Libraries were prepared with 750 ng of starting material using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina, following rRNA depletion using a NEBNext rRNA Depletion Kit (Human/Mouse/Rat)",,XREF_LINK,DB: gds,ID: 304369040,LABEL: GSM4369040,,,,ILLUMINA,,,,SRS6240833,,SINGLE,SAMN14262081,SRS6240833,1511594659,,Caenorhabditis elegans,GSM4369040,rnaL20WT1,6239,GSM4369040_r1,391850472,388020000,353950329,619598,377154260,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-06-30 17:40:41,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR11217914/ICN-01_S1.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-10/SRR11217914/ICN-01_S1.fastq.gz.1,,,,,,,,,public,2020-03-03 08:51:09,,40bb19b1388c4bac9166816869735de6,fastq,747260046,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/010954/SRR11217914,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-9/SRR11217914/SRR11217914.1,gcp identity,gs.US,GCP,gs://sra-pub-run-8/SRR11217914/SRR11217914.1,,,,,public,2020-03-03 08:51:39,SRR11217914,839fc0eebacce559f9a303e79d3f293a,run,670671586,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra73/SRR/010954/SRR11217914,,,,,,,,,,,,,,,,,,,,,,1,1511594659,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole animal,datapipeline,Pipeline2,temperature,20,genotype,WT,,,,,,,,,,SAMN14262081,BioSample,XREF_LINK,DB: bioproject,ID: 609901,LABEL: PRJNA609901,,,,,6239,rnaL20WT1,GSE146256,,,GEO,GSE146256,PRJNA609901,BioProject,,,,"In order to fulfil a wide range of cellular functions, RNA molecules contain, in addition to the four canonical bases, a large number of chemically modified structures. Among those, the methylation of carbon-5 of cytosines (m5C) is an abundant, widespread mark in different classes of RNAs. m5C is catalysed by DNMT2 and by seven members of the NSUN family of enzymes. While some m5C-methyltransferases have been studied individually and implicated in phenotypes observed in organisms ranging from yeast to humans, it remains unclear how the m5C methylome acts to sustain development in homeostasis and stress. Here, using Caenorhabditis elegans as a model organism, we developed the first organism devoid of detectable m5C in RNA, providing strong evidence that this modification and its derivatives are non-essential for the nematode's development and fertility under standard laboratory conditions. We further used this genetic tool to determine the localisation of m5C sites in different RNA classes, and showed that NSUN-4 acts as a multisite-specific tRNA/rRNA methyltransferase in the mitochondria. In addition, we show that m5C is required for adaptation to temperature changes, as animals devoid of this modification present temperature-sensitive fertility defects. At the molecular level, we show that loss of m5C leads to increased ribosome pausing at triplets encoding for leucine and proline, the most frequently methylated tRNA isoacceptors in C. elegans. This is correlated with reduced translation efficiency of transcripts enriched in these amino acids. Finally, we found translation of Leu-UUG codons to be the most strongly affected upon heat shock, suggesting a role of m5C wobble methylation in the adaptation to heat stress. Overall design: RNASeq and Ribosome profilling from 4 samples of C. elegans. WT and NSUN mutants from 20 and 27 degrees celcius.",Translational adaptation to heat stress is mediated by 5-methylcytosine RNA modification in Caenorhabditis elegans,Other,SRA1050341,GEO: GSE146256,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806834,GSM4340680: pmk-1(km25)RPF Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219869,GSM4340680,NextSeq 500,34364285,863253383,SRR11186550,34364285,2542957090,GSM4340680,GEO Accession,GSM4340680,,,,SAMN14213080,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340680,LABEL: GSM4340680,,,,ILLUMINA,,,,SRS6219869,,PAIRED,SAMN14213080,SRS6219869,2542957090,,Caenorhabditis elegans,GSM4340680,pmk-1(km25)RPF Replicate 2,6239,GSM4340680_r1,645965116,601387526,690345517,231768,605027163,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR11186550/PIR9_S10_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-10/SRR11186550/PIR9_S10_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:49:19,,4060923ab1baa6e2a5e05714ece16189,fastq,741411436,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR11186550/PIR9_S10_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-10/SRR11186550/PIR9_S10_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:49:34,,deaaf6db25d2938c49fbaf88cbdb6da9,fastq,762175645,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/010924/SRR11186550,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-9/SRR11186550/SRR11186550.1,gcp identity,gs.US,GCP,gs://sra-pub-run-8/SRR11186550/SRR11186550.1,public,2020-02-26 13:49:58,SRR11186550,6a20b1926c9658ed66bc371947127a8f,run,863254910,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/010924/SRR11186550,1,2542957090,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,genotype,pmk-1(km25),,,,,,,,,,,,SAMN14213080,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,pmk-1(km25)RPF Replicate 2,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806833,GSM4340679: pmk-1(km25) total mRNA Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219868,GSM4340679,NextSeq 500,33631873,857793145,SRR11186549,33631873,2488758602,GSM4340679,GEO Accession,GSM4340679,,,,SAMN14213082,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340679,LABEL: GSM4340679,,,,ILLUMINA,,,,SRS6219868,,PAIRED,SAMN14213082,SRS6219868,2488758602,,Caenorhabditis elegans,GSM4340679,pmk-1(km25) total mRNA Replicate 2,6239,GSM4340679_r1,658289904,592704304,586598856,227081,650938457,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11186549/PIT2_S9_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11186549/PIT2_S9_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:48:33,,0e08699650705024c1d1e5f4cfb673f8,fastq,827866361,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11186549/PIT2_S9_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11186549/PIT2_S9_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:48:48,,5f833a2714523ce9e9dd38dfa0b03a45,fastq,835538518,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/010924/SRR11186549,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-7/SRR11186549/SRR11186549.1,gcp identity,gs.US,GCP,gs://sra-pub-run-3/SRR11186549/SRR11186549.1,public,2020-02-26 13:49:17,SRR11186549,6573bb0ce40815f86d522da2d26d997e,run,857794670,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra6/SRR/010924/SRR11186549,1,2488758602,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,genotype,pmk-1(km25),,,,,,,,,,,,SAMN14213082,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,pmk-1(km25) total mRNA Replicate 2,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806832,GSM4340678: pmk-1(km25)RPF Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219867,GSM4340678,NextSeq 500,30114094,778775375,SRR11186548,30114094,2228442956,GSM4340678,GEO Accession,GSM4340678,,,,SAMN14212991,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340678,LABEL: GSM4340678,,,,ILLUMINA,,,,SRS6219867,,PAIRED,SAMN14212991,SRS6219867,2228442956,,Caenorhabditis elegans,GSM4340678,pmk-1(km25)RPF Replicate 1,6239,GSM4340678_r1,561020148,531841432,615224639,201393,520155344,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR11186548/PIR11_S4_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR11186548/PIR11_S4_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 14:22:06,,e6cfb51999cffb964765bb7354581724,fastq,652443598,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR11186548/PIR11_S4_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR11186548/PIR11_S4_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 14:21:47,,abc2c605b9266d9298d10e3e6b4cafdb,fastq,691394934,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/010924/SRR11186548,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-8/SRR11186548/SRR11186548.1,gcp identity,gs.US,GCP,gs://sra-pub-run-9/SRR11186548/SRR11186548.1,public,2020-02-26 14:22:40,SRR11186548,5fd0463a761492db2a52589c352cd827,run,778776905,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra8/SRR/010924/SRR11186548,1,2228442956,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,genotype,pmk-1(km25),,,,,,,,,,,,SAMN14212991,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,pmk-1(km25)RPF Replicate 1,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806831,GSM4340677: pmk-1(km25) total mRNA Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219866,GSM4340677,NextSeq 500,29403277,748531060,SRR11186547,29403277,2175842498,GSM4340677,GEO Accession,GSM4340677,,,,SAMN14213083,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340677,LABEL: GSM4340677,,,,ILLUMINA,,,,SRS6219866,,PAIRED,SAMN14213083,SRS6219866,2175842498,,Caenorhabditis elegans,GSM4340677,pmk-1(km25) total mRNA Replicate 1,6239,GSM4340677_r1,582874401,506189454,517929641,194150,568654852,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR11186547/PIT7_S3_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR11186547/PIT7_S3_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:50:25,,495c12e1abf50f9ccfafd887785db9a9,fastq,733056875,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR11186547/PIT7_S3_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR11186547/PIT7_S3_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:50:11,,3b0e1bc0b2db303485990b8945811ecb,fastq,740649686,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/010924/SRR11186547,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-8/SRR11186547/SRR11186547.1,gcp identity,gs.US,GCP,gs://sra-pub-run-9/SRR11186547/SRR11186547.1,public,2020-02-26 13:50:54,SRR11186547,130e35442a37d77c223aec911b45eba5,run,748532585,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra67/SRR/010924/SRR11186547,1,2175842498,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,genotype,pmk-1(km25),,,,,,,,,,,,SAMN14213083,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,pmk-1(km25) total mRNA Replicate 1,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806830,GSM4340676: ced-3(n717)RPF Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219865,GSM4340676,NextSeq 500,33357995,837113969,SRR11186546,33357995,2468491630,GSM4340676,GEO Accession,GSM4340676,,,,SAMN14213084,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340676,LABEL: GSM4340676,,,,ILLUMINA,,,,SRS6219865,,PAIRED,SAMN14213084,SRS6219865,2468491630,,Caenorhabditis elegans,GSM4340676,ced-3(n717)RPF Replicate 2,6239,GSM4340676_r1,634808503,574548549,671146860,226579,587761139,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR11186546/C3R10_S12_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-10/SRR11186546/C3R10_S12_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:49:28,,cdf4234f909eb6da3c101438af875af0,fastq,703464289,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR11186546/C3R10_S12_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-10/SRR11186546/C3R10_S12_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:49:41,,e66e6ef93c786adfaebe950f1f627084,fastq,723391112,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/010924/SRR11186546,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-9/SRR11186546/SRR11186546.1,gcp identity,gs.US,GCP,gs://sra-pub-run-8/SRR11186546/SRR11186546.1,public,2020-02-26 13:50:07,SRR11186546,f6ac4056f9695fef6935d8fd8022c022,run,837115501,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra75/SRR/010924/SRR11186546,1,2468491630,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,genotype,ced-3(n717),,,,,,,,,,,,SAMN14213084,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,ced-3(n717)RPF Replicate 2,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806829,GSM4340675: ced-3(n717) total mRNA Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219864,GSM4340675,NextSeq 500,31063779,804926730,SRR11186545,31063779,2298719646,GSM4340675,GEO Accession,GSM4340675,,,,SAMN14213085,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340675,LABEL: GSM4340675,,,,ILLUMINA,,,,SRS6219864,,PAIRED,SAMN14213085,SRS6219864,2298719646,,Caenorhabditis elegans,GSM4340675,ced-3(n717) total mRNA Replicate 2,6239,GSM4340675_r1,613070283,539625724,541625432,206119,604192088,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-9/SRR11186545/C3T3_S11_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-10/SRR11186545/C3T3_S11_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:53:22,,0b5ebe4a15329642624dba1310fcbc15,fastq,778434039,0,Original,,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-9/SRR11186545/C3T3_S11_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-10/SRR11186545/C3T3_S11_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:54:17,,fba52f4c23a85f2daabc9db2c4640c25,fastq,785327397,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/010924/SRR11186545,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-8/SRR11186545/SRR11186545.1,gcp identity,gs.US,GCP,gs://sra-pub-run-9/SRR11186545/SRR11186545.1,public,2020-02-26 13:55:26,SRR11186545,19c4d9f8bf9eec57ee2ebeb938793662,run,804928258,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra77/SRR/010924/SRR11186545,1,2298719646,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,genotype,ced-3(n717),,,,,,,,,,,,SAMN14213085,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,ced-3(n717) total mRNA Replicate 2,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806828,GSM4340674: ced-3(n717)RPF Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219863,GSM4340674,NextSeq 500,33350365,834857358,SRR11186544,33350365,2467927010,GSM4340674,GEO Accession,GSM4340674,,,,SAMN14213086,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340674,LABEL: GSM4340674,,,,ILLUMINA,,,,SRS6219863,,PAIRED,SAMN14213086,SRS6219863,2467927010,,Caenorhabditis elegans,GSM4340674,ced-3(n717)RPF Replicate 1,6239,GSM4340674_r1,623583904,587738780,678977835,227025,577399466,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11186544/C3R12_S6_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11186544/C3R12_S6_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:48:13,,115ee2f809a109b9744b550f84b19c08,fastq,685147616,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11186544/C3R12_S6_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11186544/C3R12_S6_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:48:26,,fd7d4228194453efa815bd7022d5df98,fastq,702813418,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010924/SRR11186544,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-3/SRR11186544/SRR11186544.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR11186544/SRR11186544.1,public,2020-02-26 13:49:07,SRR11186544,59c7a29414f503c5e39964822ad78082,run,834858884,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra51/SRR/010924/SRR11186544,1,2467927010,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,genotype,ced-3(n717),,,,,,,,,,,,SAMN14213086,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,ced-3(n717)RPF Replicate 1,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806827,GSM4340673: ced-3(n717) total mRNA Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219862,GSM4340673,NextSeq 500,30481900,774994143,SRR11186543,30481900,2255660600,GSM4340673,GEO Accession,GSM4340673,,,,SAMN14212992,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340673,LABEL: GSM4340673,,,,ILLUMINA,,,,SRS6219862,,PAIRED,SAMN14212992,SRS6219862,2255660600,,Caenorhabditis elegans,GSM4340673,ced-3(n717) total mRNA Replicate 1,6239,GSM4340673_r1,603680558,524458579,534094109,207823,593219531,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11186543/C3T8_S5_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11186543/C3T8_S5_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:48:28,,f948e19ae3a9985bcd35aad20afca0a9,fastq,769973461,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11186543/C3T8_S5_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11186543/C3T8_S5_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:48:42,,dfb5da371dbe7b13e21e6df88edc7d1e,fastq,778038161,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/010924/SRR11186543,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR11186543/SRR11186543.1,gcp identity,gs.US,GCP,gs://sra-pub-run-6/SRR11186543/SRR11186543.1,public,2020-02-26 13:49:07,SRR11186543,22a8dc52cf3dd3dc1f5f57159dea4021,run,774995669,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra34/SRR/010924/SRR11186543,1,2255660600,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,genotype,ced-3(n717),,,,,,,,,,,,SAMN14212992,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,ced-3(n717) total mRNA Replicate 1,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806826,GSM4340672: WT RPF Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219861,GSM4340672,NextSeq 500,29791126,744716047,SRR11186542,29791126,2204543324,GSM4340672,GEO Accession,GSM4340672,,,,SAMN14212993,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340672,LABEL: GSM4340672,,,,ILLUMINA,,,,SRS6219861,,PAIRED,SAMN14212993,SRS6219861,2204543324,,Caenorhabditis elegans,GSM4340672,WT RPF Replicate 2,6239,GSM4340672_r1,571060725,508680213,596572223,202856,528027307,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR11186542/N2R5_S8_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-10/SRR11186542/N2R5_S8_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:44:14,,64991fd231a1c3356a584f2b4e16eec2,fastq,643257441,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR11186542/N2R5_S8_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-10/SRR11186542/N2R5_S8_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:44:19,,7215d0bccb51f84be4c09572ad63b316,fastq,656602269,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/010924/SRR11186542,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-9/SRR11186542/SRR11186542.1,gcp identity,gs.US,GCP,gs://sra-pub-run-8/SRR11186542/SRR11186542.1,public,2020-02-26 13:44:35,SRR11186542,13ceb84dfef0f485b4b0856fdf9da83e,run,744717577,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/010924/SRR11186542,1,2204543324,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,strain,N2,genotype,wild type,,,,,,,,,,SAMN14212993,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,WT RPF Replicate 2,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806825,GSM4340671: WT total mRNA Replicate 2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219860,GSM4340671,NextSeq 500,30801390,784439721,SRR11186541,30801390,2279302860,GSM4340671,GEO Accession,GSM4340671,,,,SAMN14212994,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340671,LABEL: GSM4340671,,,,ILLUMINA,,,,SRS6219860,,PAIRED,SAMN14212994,SRS6219860,2279302860,,Caenorhabditis elegans,GSM4340671,WT total mRNA Replicate 2,6239,GSM4340671_r1,605966930,537228611,538483468,210682,597413169,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11186541/N2T1_S7_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11186541/N2T1_S7_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:50:32,,586eddd82810646ee6dc3beafa34b919,fastq,763205736,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR11186541/N2T1_S7_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR11186541/N2T1_S7_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:50:16,,d64156bc4bf61a71b450a0e94329de94,fastq,768157659,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/010924/SRR11186541,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-3/SRR11186541/SRR11186541.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR11186541/SRR11186541.1,public,2020-02-26 13:51:25,SRR11186541,fd8e51fa7ad0f92afb78685cf70c73e2,run,784441248,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra58/SRR/010924/SRR11186541,1,2279302860,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,strain,N2,genotype,wild type,,,,,,,,,,SAMN14212994,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,WT total mRNA Replicate 2,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806824,GSM4340670: WT RPF Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219859,GSM4340670,NextSeq 500,31188949,786278140,SRR11186540,31188949,2307982226,GSM4340670,GEO Accession,GSM4340670,,,,SAMN14212996,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340670,LABEL: GSM4340670,,,,ILLUMINA,,,,SRS6219859,,PAIRED,SAMN14212996,SRS6219859,2307982226,,Caenorhabditis elegans,GSM4340670,WT RPF Replicate 1,6239,GSM4340670_r1,591272930,540451863,634630622,210871,541415940,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR11186540/N2R6_S2_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-10/SRR11186540/N2R6_S2_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:49:59,,60cb0c2efdbee3b860426ff5a0faec1a,fastq,650130909,0,Original,,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-9/SRR11186540/N2R6_S2_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-10/SRR11186540/N2R6_S2_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:51:44,,36502272075a324d21277406c9068c4b,fastq,669109609,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/010924/SRR11186540,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-8/SRR11186540/SRR11186540.1,gcp identity,gs.US,GCP,gs://sra-pub-run-9/SRR11186540/SRR11186540.1,public,2020-02-26 13:52:14,SRR11186540,c3cf379acdfd07410ae7dd9ec2223315,run,786279668,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra25/SRR/010924/SRR11186540,1,2307982226,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,strain,N2,genotype,wild type,,,,,,,,,,SAMN14212996,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,WT RPF Replicate 1,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP250832,SRX7806823,GSM4340669: WT total mRNA Replicate 1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS6219858,GSM4340669,NextSeq 500,33246237,847324162,SRR11186539,33246237,2460221538,GSM4340669,GEO Accession,GSM4340669,,,,SAMN14212997,"The ribosomal profiling protocol and total mRNA isolation were modified based on a published protocol (Aeschimann et al., 2015) and the TruSeq® Ribo Profile Protocol (Illumina). TruSeq® Ribo Profile Protocol (Illumina). RNA-seq and Ribosome profilling",,XREF_LINK,DB: gds,ID: 304340669,LABEL: GSM4340669,,,,ILLUMINA,,,,SRS6219858,,PAIRED,SAMN14212997,SRS6219858,2460221538,,Caenorhabditis elegans,GSM4340669,WT total mRNA Replicate 1,6239,GSM4340669_r1,665570748,562628949,583277563,225081,648519197,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2020-05-05 11:25:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR11186539/N2T4_S1_R1_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR11186539/N2T4_S1_R1_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:47:24,,1216516c3cfc6e6eefa686ab2f4de78b,fastq,823881309,0,Original,,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR11186539/N2T4_S1_R2_001.fastq.gz.1,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR11186539/N2T4_S1_R2_001.fastq.gz.1,,,,,,,,,public,2020-02-26 13:47:39,,3aa78e16336b7c2c0c88df90dd3169bb,fastq,834413274,0,Original,,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010924/SRR11186539,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-1/SRR11186539/SRR11186539.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR11186539/SRR11186539.1,public,2020-02-26 13:48:27,SRR11186539,4cedd6f32ca7e6dcbce9cca9ea5df668,run,847325690,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra53/SRR/010924/SRR11186539,1,2460221538,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole worm,Stage,L3,strain,N2,genotype,wild type,,,,,,,,,,SAMN14212997,BioSample,XREF_LINK,DB: bioproject,ID: 608907,LABEL: PRJNA608907,,,,,6239,WT total mRNA Replicate 1,GSE145983,,,GEO,GSE145983,PRJNA608907,BioProject,,,,"We identified more than 300 genes inversely regulated by ced-3 and pmk-1 that enriched for epidermal stress response factors in C elegans Overall design: We analyzed total mRNA and ribosome-associated mRNAs at the L3 stage for wild type, ced-3(n717), and pmk-1(km25) strains with two independent biological replicates",Analyses of CED-3 caspase and PMK-1 p38 MAPK in gene regulation in C elegans,Transcriptome Analysis,SRA1048439,GEO: GSE145983,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098753,GSM4148088: Slee141_mRNAseqFP_meg34_3: meg-3meg-4 mRNAseq-3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611015,GSM4148088,Illumina HiSeq 2500,50180090,1461952152,SRR10398500,50180090,2509004500,GSM4148088,GEO Accession,GSM4148088,,,,GSM4148088,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148088,LABEL: GSM4148088,,,,ILLUMINA,,,,SRS5611015,,SINGLE,SAMN13190923,SRS5611015,2509004500,,Caenorhabditis elegans,GSM4148088,Slee141_mRNAseqFP_meg34_3: meg-3meg-4 mRNAseq-3,6239,GSM4148088_r1,656429021,596900728,610841384,37276,644796091,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398500/Slee141_mRNAseqFP_meg34_JP1_GTGAAA.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398500/Slee141_mRNAseqFP_meg34_JP1_GTGAAA.fastq.gz.1,,,,,,,,,public,2019-11-06 03:47:46,Slee141_mRNAseqFP_meg34_JP1_GTGAAA.fastq.gz,790a2636a2df58b143c70090c99b119e,fastq,1977390816,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398500/Slee141_mRNAseqFP_meg34_JP1_GTGAAA.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/010154/SRR10398500,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398500/SRR10398500.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398500/SRR10398500.1,,,,,public,2019-11-06 03:48:51,SRR10398500,a601ff03e04e3b0de9fa9a2e58441bec,run,1461953898,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra18/SRR/010154/SRR10398500,,,,,,,,,,,,,,,,,,,,,,1,2509004500,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,Ribo-Zero treated total RNA,,,,,,,,,,,,SAMN13190923,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee141_mRNAseqFP_meg34_3: meg-3meg-4 mRNAseq-3,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098752,GSM4148087: Slee139_mRNAseqFP_meg34_2: meg-3meg-4 mRNAseq-2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611014,GSM4148087,Illumina HiSeq 2500,59848989,1748019918,SRR10398499,59848989,2992449450,GSM4148087,GEO Accession,GSM4148087,,,,GSM4148087,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148087,LABEL: GSM4148087,,,,ILLUMINA,,,,SRS5611014,,SINGLE,SAMN13190924,SRS5611014,2992449450,,Caenorhabditis elegans,GSM4148087,Slee139_mRNAseqFP_meg34_2: meg-3meg-4 mRNAseq-2,6239,GSM4148087_r1,779513578,712500026,731765736,43914,768626196,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398499/Slee139_mRNAseqFP_meg34_SL_2_GCCAAT.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398499/Slee139_mRNAseqFP_meg34_SL_2_GCCAAT.fastq.gz.1,,,,,,,,,public,2019-11-06 03:47:55,Slee139_mRNAseqFP_meg34_SL_2_GCCAAT.fastq.gz,7eae8d165cb323700cd05e4fcac15634,fastq,2351880177,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398499/Slee139_mRNAseqFP_meg34_SL_2_GCCAAT.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/010154/SRR10398499,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398499/SRR10398499.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398499/SRR10398499.1,,,,,public,2019-11-06 03:50:30,SRR10398499,7505a1f8b4c18b6177570065b4d0642b,run,1748021666,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra70/SRR/010154/SRR10398499,,,,,,,,,,,,,,,,,,,,,,1,2992449450,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,Ribo-Zero treated total RNA,,,,,,,,,,,,SAMN13190924,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee139_mRNAseqFP_meg34_2: meg-3meg-4 mRNAseq-2,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098751,GSM4148086: Slee125_mRNAseqFP_meg34_1: meg-3meg-4 mRNAseq-1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611013,GSM4148086,Illumina HiSeq 2500,17823378,553495038,SRR10398498,17823378,891168900,GSM4148086,GEO Accession,GSM4148086,,,,GSM4148086,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148086,LABEL: GSM4148086,,,,ILLUMINA,,,,SRS5611013,,SINGLE,SAMN13190925,SRS5611013,891168900,,Caenorhabditis elegans,GSM4148086,Slee125_mRNAseqFP_meg34_1: meg-3meg-4 mRNAseq-1,6239,GSM4148086_r1,236719557,208649845,213767928,47004,231984566,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398498/Slee125_meg34_embforFP_TGACCA.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398498/Slee125_meg34_embforFP_TGACCA.fastq.gz.1,,,,,,,,,public,2019-11-06 03:41:44,Slee125_meg34_embforFP_TGACCA.fastq.gz,dfbd152cd1e31d00701a38ce6427ef8b,fastq,735406084,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398498/Slee125_meg34_embforFP_TGACCA.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra26/SRR/010154/SRR10398498,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398498/SRR10398498.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398498/SRR10398498.1,,,,,public,2019-11-06 03:42:12,SRR10398498,0a34d177ee4ce19c94725aad9d997f7d,run,553496783,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra26/SRR/010154/SRR10398498,,,,,,,,,,,,,,,,,,,,,,1,891168900,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,Ribo-Zero treated total RNA,,,,,,,,,,,,SAMN13190925,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee125_mRNAseqFP_meg34_1: meg-3meg-4 mRNAseq-1,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098750,GSM4148085: Slee142_mRNAseqFP_N2_3: wild type mRNAseq-3; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611012,GSM4148085,Illumina HiSeq 2500,64787771,1883244063,SRR10398497,64787771,3239388550,GSM4148085,GEO Accession,GSM4148085,,,,GSM4148085,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148085,LABEL: GSM4148085,,,,ILLUMINA,,,,SRS5611012,,SINGLE,SAMN13190926,SRS5611012,3239388550,,Caenorhabditis elegans,GSM4148085,Slee142_mRNAseqFP_N2_3: wild type mRNAseq-3,6239,GSM4148085_r1,856186524,762830092,773586474,47566,846737894,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398497/Slee142_mRNAseqFP_N2_3_ATGTCA.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398497/Slee142_mRNAseqFP_N2_3_ATGTCA.fastq.gz.1,,,,,,,,,public,2019-11-06 03:45:01,Slee142_mRNAseqFP_N2_3_ATGTCA.fastq.gz,803fdcd6b531067e665f8f18d4fbb9c9,fastq,2529250772,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398497/Slee142_mRNAseqFP_N2_3_ATGTCA.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra72/SRR/010154/SRR10398497,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398497/SRR10398497.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398497/SRR10398497.1,,,,,public,2019-11-06 03:46:23,SRR10398497,6b6e67d3ebb7cf25c89a3ea084a5edc1,run,1883245812,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra72/SRR/010154/SRR10398497,,,,,,,,,,,,,,,,,,,,,,1,3239388550,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,Ribo-Zero treated total RNA,,,,,,,,,,,,SAMN13190926,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee142_mRNAseqFP_N2_3: wild type mRNAseq-3,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098749,GSM4148084: Slee138_mRNAseqFP_N2_2: wild type mRNAseq-2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611011,GSM4148084,Illumina HiSeq 2500,54109682,1574815163,SRR10398496,54109682,2705484100,GSM4148084,GEO Accession,GSM4148084,,,,GSM4148084,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148084,LABEL: GSM4148084,,,,ILLUMINA,,,,SRS5611011,,SINGLE,SAMN13190927,SRS5611011,2705484100,,Caenorhabditis elegans,GSM4148084,Slee138_mRNAseqFP_N2_2: wild type mRNAseq-2,6239,GSM4148084_r1,715634947,637414540,645826922,40195,706567496,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398496/Slee138_mRNAseqFP_N2_2.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398496/Slee138_mRNAseqFP_N2_2.fastq.gz.1,,,,,,,,,public,2019-11-06 03:42:57,Slee138_mRNAseqFP_N2_2.fastq.gz,6298f503217039ca51f225c61d385ea1,fastq,2151342606,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398496/Slee138_mRNAseqFP_N2_2.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/010154/SRR10398496,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398496/SRR10398496.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398496/SRR10398496.1,,,,,public,2019-11-06 03:44:07,SRR10398496,e67b12feff28d5c85e641eb84fcd71e9,run,1574816909,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra31/SRR/010154/SRR10398496,,,,,,,,,,,,,,,,,,,,,,1,2705484100,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,Ribo-Zero treated total RNA,,,,,,,,,,,,SAMN13190927,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee138_mRNAseqFP_N2_2: wild type mRNAseq-2,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098748,GSM4148083: Slee113_mRNAseqFP_N2_1: wild type mRNAseq-1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS5611010,GSM4148083,Illumina HiSeq 2500,53153078,1518355802,SRR10398495,53153078,2657653900,GSM4148083,GEO Accession,GSM4148083,,,,GSM4148083,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148083,LABEL: GSM4148083,,,,ILLUMINA,,,,SRS5611010,,SINGLE,SAMN13190928,SRS5611010,2657653900,,Caenorhabditis elegans,GSM4148083,Slee113_mRNAseqFP_N2_1: wild type mRNAseq-1,6239,GSM4148083_r1,734420835,594181567,603850976,272197,724928325,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398495/Slee113_N2_H5M33BCX2_1_ACAGTG_1.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398495/Slee113_N2_H5M33BCX2_1_ACAGTG_1.fastq.gz.1,,,,,,,,,public,2019-11-06 03:41:56,Slee113_N2_H5M33BCX2_1_ACAGTG_1.fastq.gz,66243c579988cefc50cb73111ac3cf91,fastq,2069386069,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398495/Slee113_N2_H5M33BCX2_1_ACAGTG_1.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra10/SRR/010154/SRR10398495,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398495/SRR10398495.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398495/SRR10398495.1,,,,,public,2019-11-06 03:42:40,SRR10398495,e024149ee56beaad1d57bc031784ccb1,run,1518357552,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra10/SRR/010154/SRR10398495,,,,,,,,,,,,,,,,,,,,,,1,2657653900,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,Ribo-Zero treated total RNA,,,,,,,,,,,,SAMN13190928,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee113_mRNAseqFP_N2_1: wild type mRNAseq-1,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098747,GSM4148082: Slee135_meg34: meg-3meg-4 Riboseq-3; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611009,GSM4148082,Illumina HiSeq 2500,117347118,3430391353,SRR10398494,117347118,5867355900,GSM4148082,GEO Accession,GSM4148082,,,,GSM4148082,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148082,LABEL: GSM4148082,,,,ILLUMINA,,,,SRS5611009,,SINGLE,SAMN13190929,SRS5611009,5867355900,,Caenorhabditis elegans,GSM4148082,Slee135_meg34: meg-3meg-4 Riboseq-3,6239,GSM4148082_r1,1119246168,1642504211,1582932236,82596,1522590689,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398494/Slee135_meg34_JP1_CAGATC.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398494/Slee135_meg34_JP1_CAGATC.fastq.gz.1,,,,,,,,,public,2019-11-06 03:49:30,Slee135_meg34_JP1_CAGATC.fastq.gz,6f256cff8675b5a0b357e4abe569c703,fastq,3923042444,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398494/Slee135_meg34_JP1_CAGATC.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra26/SRR/010154/SRR10398494,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398494/SRR10398494.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398494/SRR10398494.1,,,,,public,2019-11-06 03:51:45,SRR10398494,efbc8db63ccb943e5c0fc9276ee2fd72,run,3430393099,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra26/SRR/010154/SRR10398494,,,,,,,,,,,,,,,,,,,,,,1,5867355900,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,RNaseI treated Ribo-Zero treated ribosome bound RNA fragments,,,,,,,,,,,,SAMN13190929,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee135_meg34: meg-3meg-4 Riboseq-3,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098746,GSM4148081: Slee133_meg34: meg-3meg-4 Riboseq-2; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611008,GSM4148081,Illumina HiSeq 2500,107081543,3125393193,SRR10398493,107081543,5354077150,GSM4148081,GEO Accession,GSM4148081,,,,GSM4148081,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148081,LABEL: GSM4148081,,,,ILLUMINA,,,,SRS5611008,,SINGLE,SAMN13190905,SRS5611008,5354077150,,Caenorhabditis elegans,GSM4148081,Slee133_meg34: meg-3meg-4 Riboseq-2,6239,GSM4148081_r1,1005815846,1505849239,1424889751,75413,1417446901,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398493/Slee133_meg34_my_ACAGTG.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398493/Slee133_meg34_my_ACAGTG.fastq.gz.1,,,,,,,,,public,2019-11-06 03:48:29,Slee133_meg34_my_ACAGTG.fastq.gz,594d69d056915f2c1bd7e0841b8c35ad,fastq,3546501643,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398493/Slee133_meg34_my_ACAGTG.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/010154/SRR10398493,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398493/SRR10398493.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398493/SRR10398493.1,,,,,public,2019-11-06 03:50:32,SRR10398493,877ed87637bd8b87e64e48c1e3b3ce8d,run,3125394939,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra41/SRR/010154/SRR10398493,,,,,,,,,,,,,,,,,,,,,,1,5354077150,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,RNaseI treated Ribo-Zero treated ribosome bound RNA fragments,,,,,,,,,,,,SAMN13190905,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee133_meg34: meg-3meg-4 Riboseq-2,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098745,GSM4148080: Slee123_meg34: meg-3meg-4 Riboseq-1; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611007,GSM4148080,Illumina HiSeq 2500,35703383,867677732,SRR10398492,35703383,1785169150,GSM4148080,GEO Accession,GSM4148080,,,,GSM4148080,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148080,LABEL: GSM4148080,,,,ILLUMINA,,,,SRS5611007,,SINGLE,SAMN13190906,SRS5611007,1785169150,,Caenorhabditis elegans,GSM4148080,Slee123_meg34: meg-3meg-4 Riboseq-1,6239,GSM4148080_r1,364456742,468615534,453999771,147848,497949255,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398492/Slee123_meg34_HFWH7BCX2_1_GCCAAT.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398492/Slee123_meg34_HFWH7BCX2_1_GCCAAT.fastq.gz.1,,,,,,,,,public,2019-11-06 03:40:06,Slee123_meg34_HFWH7BCX2_1_GCCAAT.fastq.gz,de78001ddc02f5395bcdeee23332a076,fastq,976731160,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398492/Slee123_meg34_HFWH7BCX2_1_GCCAAT.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/010154/SRR10398492,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398492/SRR10398492.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398492/SRR10398492.1,,,,,public,2019-11-06 03:40:50,SRR10398492,c5866e045e4fd2597312faf9830c556f,run,867679482,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra71/SRR/010154/SRR10398492,,,,,,,,,,,,,,,,,,,,,,1,1785169150,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,RNaseI treated Ribo-Zero treated ribosome bound RNA fragments,,,,,,,,,,,,SAMN13190906,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee123_meg34: meg-3meg-4 Riboseq-1,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098744,GSM4148079: Slee136_N2: wild type Riboseq-3; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611006,GSM4148079,Illumina HiSeq 2500,121439833,3342082520,SRR10398491,121439833,6071991650,GSM4148079,GEO Accession,GSM4148079,,,,GSM4148079,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148079,LABEL: GSM4148079,,,,ILLUMINA,,,,SRS5611006,,SINGLE,SAMN13190907,SRS5611006,6071991650,,Caenorhabditis elegans,GSM4148079,Slee136_N2: wild type Riboseq-3,6239,GSM4148079_r1,1145148269,1700523165,1639975454,83417,1586261345,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398491/Slee136_N2_HKV57BCX2_1_ACTTGA.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398491/Slee136_N2_HKV57BCX2_1_ACTTGA.fastq.gz.1,,,,,,,,,public,2019-11-06 03:48:35,Slee136_N2_HKV57BCX2_1_ACTTGA.fastq.gz,217d56f396c8074a6eea49e1ec7ee657,fastq,3755068572,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398491/Slee136_N2_HKV57BCX2_1_ACTTGA.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/010154/SRR10398491,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398491/SRR10398491.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398491/SRR10398491.1,,,,,public,2019-11-06 03:50:54,SRR10398491,1e9c44b5fcca0f10f46c83e20270f9f3,run,3342084266,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra38/SRR/010154/SRR10398491,,,,,,,,,,,,,,,,,,,,,,1,6071991650,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,RNaseI treated Ribo-Zero treated ribosome bound RNA fragments,,,,,,,,,,,,SAMN13190907,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee136_N2: wild type Riboseq-3,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098743,GSM4148078: Slee132_N2: wild type Riboseq-2; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611005,GSM4148078,Illumina HiSeq 2500,134995957,3934664046,SRR10398490,134995957,6749797850,GSM4148078,GEO Accession,GSM4148078,,,,GSM4148078,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148078,LABEL: GSM4148078,,,,ILLUMINA,,,,SRS5611005,,SINGLE,SAMN13190908,SRS5611005,6749797850,,Caenorhabditis elegans,GSM4148078,Slee132_N2: wild type Riboseq-2,6239,GSM4148078_r1,1475636242,1728625645,1779005140,94523,1766436300,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398490/Slee132_N2_2_TGACCA.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398490/Slee132_N2_2_TGACCA.fastq.gz.1,,,,,,,,,public,2019-11-06 03:50:29,Slee132_N2_2_TGACCA.fastq.gz,f16adaedc5f56747b4880f45c8436939,fastq,4564826338,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398490/Slee132_N2_2_TGACCA.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/010154/SRR10398490,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398490/SRR10398490.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398490/SRR10398490.1,,,,,public,2019-11-06 03:53:04,SRR10398490,09968d70669715db1de9b19d0a09fa6e,run,3934665793,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra36/SRR/010154/SRR10398490,,,,,,,,,,,,,,,,,,,,,,1,6749797850,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,RNaseI treated Ribo-Zero treated ribosome bound RNA fragments,,,,,,,,,,,,SAMN13190908,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee132_N2: wild type Riboseq-2,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP228538,SRX7098742,GSM4148077: Slee111_N2: wild type Riboseq-1; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS5611004,GSM4148077,Illumina HiSeq 2500,76408239,1744253035,SRR10398489,76408239,3820411950,GSM4148077,GEO Accession,GSM4148077,,,,GSM4148077,"Isolated embyros were freezed in liquied nitrogen with lysis buffer containing cycloheximide to stall ribosome. Freezed embryos were lyzed by freezer mill. Samples were cleared by centrifugation. Cleared lysates were then subject to ribosome profiling and RNAseq experiments For mRNAseq, 500ng of total RNA were subjected to Ribozero kit (illumina, MRZE706) to remove rRNA. Libraries were constructed using Truseq Library Prep Kit V2. For Ribosome profiling, library preparation protocol is descrbied in Wu et al., 2019 Mol. Cell.",,XREF_LINK,DB: gds,ID: 304148077,LABEL: GSM4148077,,,,ILLUMINA,,,,SRS5611004,,SINGLE,SAMN13190909,SRS5611004,3820411950,,Caenorhabditis elegans,GSM4148077,Slee111_N2: wild type Riboseq-1,6239,GSM4148077_r1,867058546,968334260,948800070,19434,1036199640,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-12-02 22:03:20,anonymous,worldwide,AWS,https://sra-pub-src-2.s3.amazonaws.com/SRR10398489/Slee111_N2_HWCCTBCXY_2_ACTTGA.fastq.gz.1,gcp identity,gs.US,GCP,gs://sra-pub-src-2/SRR10398489/Slee111_N2_HWCCTBCXY_2_ACTTGA.fastq.gz.1,,,,,,,,,public,2019-11-06 03:43:04,Slee111_N2_HWCCTBCXY_2_ACTTGA.fastq.gz,34689e4808fa6445e982d3ab7d310d95,fastq,1956921843,0,Original,https://sra-pub-src-2.s3.amazonaws.com/SRR10398489/Slee111_N2_HWCCTBCXY_2_ACTTGA.fastq.gz.1,anonymous,worldwide,NCBI,https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/010154/SRR10398489,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR10398489/SRR10398489.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR10398489/SRR10398489.1,,,,,public,2019-11-06 03:44:25,SRR10398489,c0667438c003beb26481caae164c64a3,run,1744254785,1,Primary ETL,https://sra-download.ncbi.nlm.nih.gov/traces/sra3/SRR/010154/SRR10398489,,,,,,,,,,,,,,,,,,,,,,1,3820411950,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Embryo,tissue,mixed early embryo,molecule subtype,RNaseI treated Ribo-Zero treated ribosome bound RNA fragments,,,,,,,,,,,,SAMN13190909,BioSample,XREF_LINK,DB: bioproject,ID: 587444,LABEL: PRJNA587444,,,,,6239,Slee111_N2: wild type Riboseq-1,GSE139880,parent_bioproject,PRJNA587431,GEO,GSE139880,PRJNA587444,BioProject,XREF_LINK,DB: pubmed,ID: 31975687,RNA granules are cellular condensates that contain RNAs and proteins. The mechanism that drive the recruitment of many mRNAs to RNA granules are not fully understood. Here we characterize the assembly and transcriptome of the germ (P) granules of C. elegans. We find that mRNAs are recruited into P granules by condensation with the intrinsically-disordered protein MEG-3. MEG-3 binds ~500 mRNAs in C. elegans embryos in a sequence-independent manner that favors mRNAs with low ribosome coverage. Translational stress causes additional mRNAs to localize to P granules and translational activation correlates with P granule exit for two mRNAs coding for germ cell fate regulators. MEG-3/RNA condensates assembled in vitro are gel-like and trap mRNAs in a non-dynamic state. Our observations reveal similarities between P granules and stress granules and identify gelation with intrinsically-disordered proteins as a sequence-independent mechanism to enrich low-translation mRNAs in RNA granules Overall design: 12 embryonic samples are included in this submission. It contains 6 RNAseq (3 wild type and 3 meg-3meg-4 mutant) and 6 corresponding ribosome profiling (3 wild type and 3 meg-3meg-4 mutant).,Recruitment of mRNAs to P granules by gelation with intrinsically-disordered proteins (RNAseq and ribosome profiling),Other,SRA991333,GEO: GSE139880,GEO,GEO,,submission brokered by GEO, SRP149446,SRX4147684,GSM3168388: C. elegans embryos ribosome profiling; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS3361274,GSM3168388,Illumina HiSeq 2500,76408239,1744253035,SRR7241911,76408239,3820411950,GSM3168388,GEO Accession,GSM3168388,,,,GSM3168388,"Lysates were clarified and monosomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt were gel purified and rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing.",,XREF_LINK,DB: gds,ID: 303168388,LABEL: GSM3168388,,,,ILLUMINA,,,,SRS3361274,,SINGLE,SAMN09288722,SRS3361274,3820411950,,Caenorhabditis elegans,GSM3168388,C. elegans embryos ribosome profiling,6239,GSM3168388_r1,867058546,968334260,948800070,19434,1036199640,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2019-01-28 15:33:07,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-5/SRR7241911/N2.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-5/SRR7241911/N2.fastq.gz,,,,,,,,,public,2020-02-25 05:08:44,,3b6b6a97f17d864fac0ae2c2be7d6552,fastq,1956921805,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-13/SRR7241911/SRR7241911.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-14/SRR7241911/SRR7241911.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-4/SRR7241911/SRR7241911.1,gcp identity,gs.US,GCP,gs://sra-pub-run-4/SRR7241911/SRR7241911.1,public,2018-05-31 12:14:01,SRR7241911,224740e2b27a4b736fb1687ccb1a6c1b,run,1744254785,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-14/SRR7241911/SRR7241911.1,,,,,,,,,,,,,,,,,,,,,,1,3820411950,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,C. elegans embryos ribosome profiling,tissue,embryos,molecule subtype,Ribosome Protected mRNA (15-34 nt),,,,,,,,,,,,SAMN09288722,BioSample,XREF_LINK,DB: bioproject,ID: 473989,LABEL: PRJNA473989,,,,,6239,C. elegans embryos ribosome profiling,GSE115161,parent_bioproject,PRJNA473984,GEO,GSE115161,PRJNA473989,BioProject,,,,"Ribosomes undergo substantial conformational changes during translation elongation to accommodate incoming aminoacyl-tRNAs and translocate along the mRNA template. We used multiple elongation inhibitors and chemical probing to define ribosome conformational states corresponding to different sized ribosome-protected mRNA fragments (RPFs) generated by ribosome profiling. We show using various genetic and environmental perturbations that the previously identified 20-22 nucleotide (nt) RPFs correspond predominantly to ribosomes in a pre-accommodation state with an open 40S ribosomal A site while the classical 27-29 nt fragments correspond to ribosomes in a pre-translocation state with an occupied 40S ribosomal A site. These distinct ribosome conformational states revealed by ribosome profiling are seen in all eukaryotes tested including fungi, worms and mammals. This high-resolution ribosome profiling approach reveals the anticipated Rck2-dependent inhibition of translocation through eEF2 phosphorylation during hyperosmotic stress. These same approaches reveal a strong translation elongation arrest during oxidative stress where the ribosomes are trapped in a pre-translocation state, but in this case the translational arrest is independent of Rck2-driven eEF2 phosphorylation. These results provide new insights and approaches for defining the molecular events that impact translation elongation throughout biology. Overall design: 24 biological samples are included for ribosome footprinting samples. These include HeLa, MB-MDA-231 and yeast cells and C. elegans embryos.",Regulation of Translation Elongation Revealed by Ribosome Profiling [Dataset_4],Other,SRA713167,GEO: GSE115161,GEO,GEO,,submission brokered by GEO, SRP093364,SRX2352818,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,138903638,3355135395,SRR5026637,138903638,6945181900,Celegans_post_dauer_4h,,,1,,"The ribosome profiling experiments were performed according to our published detailed protocol (Aeschimann et al. 2015), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.",,,Celegans_post_dauer_4h,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS1799345,50,SINGLE,SAMN06017629,SRS1799345,6945181900,,Caenorhabditis elegans,DAUER_0h,,6239,4h.riboseq,1488367505,1440112663,2120383213,5163569,1891154950,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2017-11-15 00:01:15,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-8/SRR5026637/4h.riboseq.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-8/SRR5026637/4h.riboseq.fastq.gz,,,,,,,,,public,2020-04-01 07:47:34,,13748e5462e1ec6041f7edaac18ebfab,fastq,5253783950,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-9/SRR5026637/SRR5026637.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026637/SRR5026637.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-2/SRR5026637/SRR5026637.1,gcp identity,gs.US,GCP,gs://sra-pub-run-2/SRR5026637/SRR5026637.1,public,2016-12-21 13:09:36,SRR5026637,d4602ae0b49b56af106297de299b24aa,run,3355136924,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026637/SRR5026637.1,,,,,,,,,,,,,,,,,,,,,,1,6945181900,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,strain,N2,dev_stage,Dauer,sex,hermaphrodite,tissue,whole body,BioSampleModel,Model organism or animal,,,,,,,,SAMN06017629,BioSample,,,,,,,,,6239,,PRJNA353604,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA353604,BioProject,,,,Bayesian Prediction of RNA Translation from Ribosome Profiling in C. elegans,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,Whole Genome Sequencing,SRA494245,Celegans_RPBP,,University Heidelberg,Bioinformatics and Systems Cardiology,C.elegans data set for Bayesian Prediction of RNA Translation from Ribosome Profiling, SRP093364,SRX2352801,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,139378431,3450860219,SRR5026603,139378431,6968921550,Celegans_3h_post_dauer,,,1,,"The ribosome profiling experiments were performed according to our published detailed protocol (Aeschimann et al. 2015), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.",,,Celegans_3h_post_dauer,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS1799345,50,SINGLE,SAMN06017629,SRS1799345,6968921550,,Caenorhabditis elegans,DAUER_0h,,6239,3h.riboseq,1460936703,1466941582,2136536817,5153562,1899352886,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2017-11-15 00:01:15,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-4/SRR5026603/3h.riboseq.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-4/SRR5026603/3h.riboseq.fastq.gz,,,,,,,,,public,2020-04-01 07:47:25,,e8723fd9a96833bf57d268318a2bbdfd,fastq,5431691664,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-9/SRR5026603/SRR5026603.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026603/SRR5026603.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-3/SRR5026603/SRR5026603.1,gcp identity,gs.US,GCP,gs://sra-pub-run-3/SRR5026603/SRR5026603.1,public,2016-12-21 10:24:22,SRR5026603,c0f444f972b31d7c457490fbc5de6408,run,3450861748,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026603/SRR5026603.1,,,,,,,,,,,,,,,,,,,,,,1,6968921550,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,strain,N2,dev_stage,Dauer,sex,hermaphrodite,tissue,whole body,BioSampleModel,Model organism or animal,,,,,,,,SAMN06017629,BioSample,,,,,,,,,6239,,PRJNA353604,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA353604,BioProject,,,,Bayesian Prediction of RNA Translation from Ribosome Profiling in C. elegans,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,Whole Genome Sequencing,SRA494245,Celegans_RPBP,,University Heidelberg,Bioinformatics and Systems Cardiology,C.elegans data set for Bayesian Prediction of RNA Translation from Ribosome Profiling, SRP093364,SRX2352796,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,109643569,2602261551,SRR5026592,109643569,5482178450,Celegans_2h_post_dauer,,,1,,"The ribosome profiling experiments were performed according to our published detailed protocol (Aeschimann et al. 2015), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.",,,Celegans_2h_post_dauer,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS1799345,50,SINGLE,SAMN06017629,SRS1799345,5482178450,,Caenorhabditis elegans,DAUER_0h,,6239,2h.riboseq,1157521325,1112387324,1680370083,4058792,1527840926,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2017-11-15 00:01:15,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-8/SRR5026592/2h.riboseq.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-8/SRR5026592/2h.riboseq.fastq.gz,,,,,,,,,public,2020-04-01 06:48:29,,02f04689891068eb9fe68f8f99aaee80,fastq,3946715094,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-9/SRR5026592/SRR5026592.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026592/SRR5026592.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-2/SRR5026592/SRR5026592.1,gcp identity,gs.US,GCP,gs://sra-pub-run-2/SRR5026592/SRR5026592.1,public,2016-12-21 07:03:41,SRR5026592,896bcf9a683156dd100a6fc513cef181,run,2602263079,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026592/SRR5026592.1,,,,,,,,,,,,,,,,,,,,,,1,5482178450,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,strain,N2,dev_stage,Dauer,sex,hermaphrodite,tissue,whole body,BioSampleModel,Model organism or animal,,,,,,,,SAMN06017629,BioSample,,,,,,,,,6239,,PRJNA353604,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA353604,BioProject,,,,Bayesian Prediction of RNA Translation from Ribosome Profiling in C. elegans,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,Whole Genome Sequencing,SRA494245,Celegans_RPBP,,University Heidelberg,Bioinformatics and Systems Cardiology,C.elegans data set for Bayesian Prediction of RNA Translation from Ribosome Profiling, SRP093364,SRX2352779,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,125934593,3035330434,SRR5026589,125934593,6296729650,Celegans_1h_post_dauer,,,1,,"The ribosome profiling experiments were performed according to our published detailed protocol (Aeschimann et al. 2015), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.",,,Celegans_1h_post_dauer,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS1799345,50,SINGLE,SAMN06017629,SRS1799345,6296729650,,Caenorhabditis elegans,DAUER_0h,,6239,1h.riboseq,1262039504,1297158829,1975704211,5892661,1755934445,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2017-11-15 00:01:15,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-5/SRR5026589/1h.riboseq.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-5/SRR5026589/1h.riboseq.fastq.gz,,,,,,,,,public,2020-04-03 14:38:32,,010dac39f64f9ae9cec6d5c16d69b81e,fastq,4735630889,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-9/SRR5026589/SRR5026589.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026589/SRR5026589.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-3/SRR5026589/SRR5026589.1,gcp identity,gs.US,GCP,gs://sra-pub-run-3/SRR5026589/SRR5026589.1,public,2016-12-20 11:30:53,SRR5026589,cf21be976e011645edc8e654328e6564,run,3035331963,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026589/SRR5026589.1,,,,,,,,,,,,,,,,,,,,,,1,6296729650,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,strain,N2,dev_stage,Dauer,sex,hermaphrodite,tissue,whole body,BioSampleModel,Model organism or animal,,,,,,,,SAMN06017629,BioSample,,,,,,,,,6239,,PRJNA353604,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA353604,BioProject,,,,Bayesian Prediction of RNA Translation from Ribosome Profiling in C. elegans,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,Whole Genome Sequencing,SRA494245,Celegans_RPBP,,University Heidelberg,Bioinformatics and Systems Cardiology,C.elegans data set for Bayesian Prediction of RNA Translation from Ribosome Profiling, SRP093364,SRX2352572,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,66094062,1613138917,SRR5026359,66094062,3304703100,Celegans_0.5h_post_dauer,,,1,,"The ribosome profiling experiments were performed according to our published detailed protocol (PMID: 26102273), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.",,,Celegans_0.5h_post_dauer,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS1799345,50,SINGLE,SAMN06017629,SRS1799345,3304703100,,Caenorhabditis elegans,DAUER_0h,,6239,0-5h.riboseq,676902968,711204979,1023398877,1356087,891840189,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2017-11-15 00:01:15,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-7/SRR5026359/0-5h.riboseq.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-7/SRR5026359/0-5h.riboseq.fastq.gz,,,,,,,,,public,2020-04-03 07:38:53,,f2ae040a036eef3b6afaa70412779eb4,fastq,2524982092,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-9/SRR5026359/SRR5026359.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026359/SRR5026359.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-4/SRR5026359/SRR5026359.1,gcp identity,gs.US,GCP,gs://sra-pub-run-4/SRR5026359/SRR5026359.1,public,2016-12-20 08:03:41,SRR5026359,4df663100fb2692b249c24411e845cd4,run,1613140446,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026359/SRR5026359.1,,,,,,,,,,,,,,,,,,,,,,1,3304703100,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,strain,N2,dev_stage,Dauer,sex,hermaphrodite,tissue,whole body,BioSampleModel,Model organism or animal,,,,,,,,SAMN06017629,BioSample,,,,,,,,,6239,,PRJNA353604,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA353604,BioProject,,,,Bayesian Prediction of RNA Translation from Ribosome Profiling in C. elegans,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,Whole Genome Sequencing,SRA494245,Celegans_RPBP,,University Heidelberg,Bioinformatics and Systems Cardiology,C.elegans data set for Bayesian Prediction of RNA Translation from Ribosome Profiling, SRP093364,SRX2349147,Bayesian Prediction of RNA Translation from Ribosome Profiling,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,unspecified,SRS1799345,DAUER_0h,Illumina HiSeq 2000,335001052,8622020036,SRR5026356,335001052,16750052600,Celegans_0h_post_dauer,,,1,,"The ribosome profiling experiments were performed according to our published detailed protocol (6), with monosomes purified using size exclusion chromatography and libraries sequenced on an Illumina HiSeq 2000 machine.",SAMN06017629,,Dauer_0h,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS1799345,50,SINGLE,SAMN06017629,SRS1799345,16750052600,,Caenorhabditis elegans,DAUER_0h,,6239,RiboSeq_0h_post_dauer,3341432627,3503233191,5118789672,155609475,4630987635,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2017-11-15 00:01:15,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-8/SRR5026356/0h.riboseq.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-8/SRR5026356/0h.riboseq.fastq.gz,,,,,,,,,public,2020-04-03 08:38:22,,3a6e35bd2b2210e630e121fd8b7ad990,fastq,13239832190,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos2/sra-pub-run-9/SRR5026356/SRR5026356.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026356/SRR5026356.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-2/SRR5026356/SRR5026356.1,gcp identity,gs.US,GCP,gs://sra-pub-run-2/SRR5026356/SRR5026356.1,public,2016-12-19 18:24:02,SRR5026356,9631a8d7680378af7ccf7ca30085cca5,run,8622021565,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos1/sra-pub-run-10/SRR5026356/SRR5026356.1,,,,,,,,,,,,,,,,,,,,,,1,16750052600,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,strain,N2,dev_stage,Dauer,sex,hermaphrodite,tissue,whole body,BioSampleModel,Model organism or animal,,,,,,,,SAMN06017629,BioSample,,,,,,,,,6239,,PRJNA353604,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA353604,BioProject,,,,Bayesian Prediction of RNA Translation from Ribosome Profiling in C. elegans,Caenorhabditis elegans strain:N2 Transcriptome or Gene expression,Whole Genome Sequencing,SRA494245,Celegans_RPBP,,University Heidelberg,Bioinformatics and Systems Cardiology,C.elegans data set for Bayesian Prediction of RNA Translation from Ribosome Profiling, SRP064516,SRX1626372,unc-54(cc3389) Ribo-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,other,SRS1335846,SJA131,Illumina MiSeq,3200939,79101256,SRR3219264,3200939,176051645,SJA131M,,,1,,"Ribosome footprint profiling Ribo-seq, using 3'ligation with AF-JA-34.2 and circular DNA ligase.",,,SJA131M,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS1335846,30,SINGLE,SAMN04546343,SRS1335846,176051645,,Caenorhabditis elegans,SJA131,unc-54(cc3389) homozygotes,6239,SJA131M,53387587,42673445,45536318,0,34454295,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2016-05-18 14:37:47,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-8/SRR3219264/131M_S6_L001_R1_001.fastq,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-8/SRR3219264/131M_S6_L001_R1_001.fastq,,,,,,,,,public,2020-04-17 14:08:10,,e5e911e1d18e08c0f0b7f25f30b75ff3,fastq,539123454,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR3219264/SRR3219264.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR3219264/SRR3219264.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-1/SRR3219264/SRR3219264.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR3219264/SRR3219264.1,public,2016-03-11 14:21:07,SRR3219264,dfd37af28dbd9d4e42293abeb80d15d3,run,79102196,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR3219264/SRR3219264.1,,,,,,,,,,,,,,,,,,,,,,1,176051645,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,strain,PD3389,isolate,unc-54(cc3389),dev_stage,L4,sex,hermaphrodite,tissue,whole organism,collection_date,24-Jan-2016,growth_protocol,XL NGM plates seeded with OP50,BioSampleModel,Model organism or animal,,SAMN04546343,BioSample,XREF_LINK,DB: bioproject,ID: 297873,LABEL: PRJNA297873,,,,,6239,unc-54(cc3389) homozygotes,PRJNA297873,,,BioProject,Caenorhabditis elegans,PRJNA297873,BioProject,XREF_LINK,DB: pubmed,ID: 27281202,"A fraction of ribosomes engaged in translation will fail to terminate when reaching a stop codon, yielding nascent proteins inappropriately extended on their C-termini. Although such extended proteins can interfere with normal cellular processes, known mechanisms of translational surveillance are insufficient to protect cells from potential dominant consequences. Using C. elegans, we demonstrate a consistent ability of cells to block accumulation of C-terminal extended proteins that result from failure to terminate at stop codons. These repressive effects are mediated through decreased protein accumulation without a detectable effect on mRNA levels. 3’UTR-encoded peptides are sufficient to confer the observed effects, suggesting a co- or post-translational mechanism of action. We suggest 3’UTRs may be optimized for sequences that destabilize the attached protein, providing a surveillance mechanism for unwelcome/inadmissible and varied translation errors.",Translation Readthrough Mitigation,Other,SRA384301,SJA131,,Stanford Univerisy,Pathology,SJA131 (unc-54(cc3389)), SRP064516,SRX1626361,unc-54(+) Ribo-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,other,SRS1335837,SJA130,Illumina MiSeq,2845260,69990868,SRR3219253,2845260,156489300,SJA130M,,,1,,"Ribosome footprint profiling Ribo-seq, using 3'ligation with AF-JA-34.2 and circular DNA ligase.",,,SJA130M,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS1335837,30,SINGLE,SAMN04546334,SRS1335837,156489300,,Caenorhabditis elegans,SJA130,unc-54(e1301) homozygotes,6239,SJA130M,47109133,37898612,38879415,0,32602140,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2016-05-18 14:38:02,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-5/SRR3219253/130M_S4_L001_R1_001.fastq,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-5/SRR3219253/130M_S4_L001_R1_001.fastq,,,,,,,,,public,2020-04-17 17:07:19,,8d6d622e5286d92754253580920f5c2f,fastq,479216622,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR3219253/SRR3219253.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR3219253/SRR3219253.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-1/SRR3219253/SRR3219253.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR3219253/SRR3219253.1,public,2016-03-11 14:21:03,SRR3219253,437d25fc9650403251fbe2db5375da93,run,69991807,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR3219253/SRR3219253.1,,,,,,,,,,,,,,,,,,,,,,1,156489300,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,strain,PD2013,isolate,unc-54(e1301),dev_stage,L4,sex,hermaphrodite,tissue,whole organism,collection_date,24-Jan-2016,BioSampleModel,Model organism or animal,,,,SAMN04546334,BioSample,XREF_LINK,DB: bioproject,ID: 297873,LABEL: PRJNA297873,,,,,6239,unc-54(e1301) homozygotes,PRJNA297873,,,BioProject,Caenorhabditis elegans,PRJNA297873,BioProject,XREF_LINK,DB: pubmed,ID: 27281202,"A fraction of ribosomes engaged in translation will fail to terminate when reaching a stop codon, yielding nascent proteins inappropriately extended on their C-termini. Although such extended proteins can interfere with normal cellular processes, known mechanisms of translational surveillance are insufficient to protect cells from potential dominant consequences. Using C. elegans, we demonstrate a consistent ability of cells to block accumulation of C-terminal extended proteins that result from failure to terminate at stop codons. These repressive effects are mediated through decreased protein accumulation without a detectable effect on mRNA levels. 3’UTR-encoded peptides are sufficient to confer the observed effects, suggesting a co- or post-translational mechanism of action. We suggest 3’UTRs may be optimized for sequences that destabilize the attached protein, providing a surveillance mechanism for unwelcome/inadmissible and varied translation errors.",Translation Readthrough Mitigation,Other,SRA384300,SJA130,,Stanford Univerisy,Pathology,SJA130 (unc-54(e1301)), SRP064516,SRX1626357,unc-54(+) Ribo-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,other,SRS1335834,SJA129,Illumina MiSeq,3407482,84664325,SRR3219248,3407482,187411510,SJA129M,,,1,,"Ribosome footprint profiling Ribo-seq, using 3'ligation with AF-JA-34.2 and circular DNA ligase.",,,SJA129M,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS1335834,30,SINGLE,SAMN04546333,SRS1335834,187411510,,Caenorhabditis elegans,SJA129,unc-54(+) homozygotes,6239,SJA129M,57094872,44809730,46994910,0,38511998,,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,"
",true,true,2016-05-18 14:37:55,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-6/SRR3219248/129M_S2_L001_R1_001.fastq,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-6/SRR3219248/129M_S2_L001_R1_001.fastq,,,,,,,,,public,2020-04-17 14:07:17,,e10d5eada3dff418ce3a9ab606dbc8a6,fastq,573910581,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR3219248/SRR3219248.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR3219248/SRR3219248.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-1/SRR3219248/SRR3219248.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR3219248/SRR3219248.1,public,2016-03-11 14:23:41,SRR3219248,09976d20d5fafb0b5d2b76d4ebddf427,run,84665264,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR3219248/SRR3219248.1,,,,,,,,,,,,,,,,,,,,,,1,187411510,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,strain,VC2010,isolate,PD1074,dev_stage,L4,sex,hermaphrodite,tissue,whole organism,collection_date,24-Jan-2016,growth_protocol,XL NGM plates seeded with OP50,BioSampleModel,Model organism or animal,,SAMN04546333,BioSample,XREF_LINK,DB: bioproject,ID: 297873,LABEL: PRJNA297873,,,,,6239,unc-54(+) homozygotes,PRJNA297873,,,BioProject,Caenorhabditis elegans,PRJNA297873,BioProject,XREF_LINK,DB: pubmed,ID: 27281202,"A fraction of ribosomes engaged in translation will fail to terminate when reaching a stop codon, yielding nascent proteins inappropriately extended on their C-termini. Although such extended proteins can interfere with normal cellular processes, known mechanisms of translational surveillance are insufficient to protect cells from potential dominant consequences. Using C. elegans, we demonstrate a consistent ability of cells to block accumulation of C-terminal extended proteins that result from failure to terminate at stop codons. These repressive effects are mediated through decreased protein accumulation without a detectable effect on mRNA levels. 3’UTR-encoded peptides are sufficient to confer the observed effects, suggesting a co- or post-translational mechanism of action. We suggest 3’UTRs may be optimized for sequences that destabilize the attached protein, providing a surveillance mechanism for unwelcome/inadmissible and varied translation errors.",Translation Readthrough Mitigation,Other,SRA384295,SJA129RZ,,Stanford Univerisy,Pathology,SJA129 (unc-54(+)), SRP055039,SRX878014,GSM1611598: frac_26-34nt; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845968,GSM1611598,Illumina HiSeq 2000,50364078,1532513718,SRR1804351,50000000,2500000000,GSM1611598,GEO Accession,GSM1611598,,GEO,,GSM1611598,"Worms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12",,URL_LINK,LABEL: GEO Sample GSM1611598,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611598,,XREF_LINK,DB: gds,ID: 301611598,ILLUMINA,,,,SRS845968,,SINGLE,SAMN03349121,SRS845968,2518203900,,Caenorhabditis elegans,GSM1611598,frac_26-34nt,6239,GSM1611598_r1,493565775,463995023,748665620,85322693,708450889,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2018-02-12 16:55:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR1804351/BSSE_QGF_10403_121218_SN792_0194_AD1FBUACXX_8_GCCAAT_L008_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR1804351/BSSE_QGF_10403_121218_SN792_0194_AD1FBUACXX_8_GCCAAT_L008_R1_001.fastq.gz,,,,,,,,,public,2020-04-30 14:16:06,,4705b3e5f6cb66db7234826987570aa9,fastq,2007720705,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR1804351/SRR1804351.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804351/SRR1804351.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR1804351/SRR1804351.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR1804351/SRR1804351.1,public,2015-02-14 16:25:44,SRR1804351,9ccd957adca3a1c584fd1974666af6d6,run,1532515463,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804351/SRR1804351.1,,,,,,,,,,,,,,,,,,,,,,1,2500000000,false,SRR1804352,GSM1611598_r2,3660196,3327131,4865116,2185658,4165799,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,true,true,2018-02-12 16:55:10,9743361,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR1804352/BSSE_QGF_10403_121218_SN792_0194_AD1FBUACXX_8_GCCAAT_L008_R1_002.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-9/SRR1804352/BSSE_QGF_10403_121218_SN792_0194_AD1FBUACXX_8_GCCAAT_L008_R1_002.fastq.gz,public,2020-05-02 11:28:44,88970fc3484ce2f9e0e771f7ae750437,fastq,14495316,0,Original,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR1804352/SRR1804352.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804352/SRR1804352.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR1804352/SRR1804352.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR1804352/SRR1804352.1,public,2015-02-14 16:18:00,SRR1804352,b76dc871990ec82537e86b8b3b32865a,run,9745113,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804352/SRR1804352.1,1,18203900,false,18203900,364078,source_name,Whole-worm,strain,N2,age,larval stage 4,,,,,,,,,,,,SAMN03349121,BioSample,XREF_LINK,DB: bioproject,ID: 275470,LABEL: PRJNA275470,,,,,6239,frac_26-34nt,GSE65948,,,GEO,GSE65948,PRJNA275470,BioProject,XREF_LINK,DB: pubmed,ID: 26102273,"Experiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.",Transcriptome-wide measurement of ribosomal occupancy by ribosome profiling,Other,SRA242099,GEO: GSE65948,GEO,GEO,,submission brokered by GEO, SRP055039,SRX878013,GSM1611597: frac_28-35nt; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845969,GSM1611597,Illumina HiSeq 2000,66596977,1238978094,SRR1804349,50000000,2500000000,GSM1611597,GEO Accession,GSM1611597,,GEO,,GSM1611597,"Worms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12",,URL_LINK,LABEL: GEO Sample GSM1611597,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611597,,XREF_LINK,DB: gds,ID: 301611597,ILLUMINA,,,,SRS845969,,SINGLE,SAMN03349117,SRS845969,3329848850,,Caenorhabditis elegans,GSM1611597,frac_28-35nt,6239,GSM1611597_r1,472626167,433173853,790016672,377982,803805326,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2018-02-12 16:55:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-12/SRR1804349/BSSE_QGF_10856_130208_SN792_0204_BD1W0VACXX_8_TGACCA_L008_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-12/SRR1804349/BSSE_QGF_10856_130208_SN792_0204_BD1W0VACXX_8_TGACCA_L008_R1_001.fastq.gz,,,,,,,,,public,2020-04-30 18:44:27,,f5b54adf7e46fdedd46d8cad255ed981,fastq,1527124253,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR1804349/SRR1804349.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR1804349/SRR1804349.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-1/SRR1804349/SRR1804349.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR1804349/SRR1804349.1,public,2015-02-24 15:26:58,SRR1804349,8233b748ec2563f339c82b60be0fd7c9,run,1238979844,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR1804349/SRR1804349.1,,,,,,,,,,,,,,,,,,,,,,1,2500000000,false,SRR1804350,GSM1611597_r2,156977287,143696069,262360391,137036,266678067,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,true,true,2018-02-12 16:55:10,416463529,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR1804350/BSSE_QGF_10856_130208_SN792_0204_BD1W0VACXX_8_TGACCA_L008_R1_002.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR1804350/BSSE_QGF_10856_130208_SN792_0204_BD1W0VACXX_8_TGACCA_L008_R1_002.fastq.gz,public,2020-05-01 07:19:59,4271138d37f3427aec5298f140d9fd64,fastq,514134042,0,Original,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR1804350/SRR1804350.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804350/SRR1804350.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR1804350/SRR1804350.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR1804350/SRR1804350.1,public,2015-02-14 16:19:43,SRR1804350,6a0b44d76bf882c50ec58ad457bb2723,run,416465274,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804350/SRR1804350.1,1,829848850,false,829848850,16596977,source_name,Whole-worm,strain,N2,age,larval stage 4,,,,,,,,,,,,SAMN03349117,BioSample,XREF_LINK,DB: bioproject,ID: 275470,LABEL: PRJNA275470,,,,,6239,frac_28-35nt,GSE65948,,,GEO,GSE65948,PRJNA275470,BioProject,XREF_LINK,DB: pubmed,ID: 26102273,"Experiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.",Transcriptome-wide measurement of ribosomal occupancy by ribosome profiling,Other,SRA242099,GEO: GSE65948,GEO,GEO,,submission brokered by GEO, SRP055039,SRX878012,GSM1611596: frac_28-30nt; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845970,GSM1611596,Illumina HiSeq 2000,46376697,1564322597,SRR1804348,46376697,2318834850,GSM1611596,GEO Accession,GSM1611596,,GEO,,GSM1611596,"Worms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12",,URL_LINK,LABEL: GEO Sample GSM1611596,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611596,,XREF_LINK,DB: gds,ID: 301611596,ILLUMINA,,,,SRS845970,,SINGLE,SAMN03349114,SRS845970,2318834850,,Caenorhabditis elegans,GSM1611596,frac_28-30nt,6239,GSM1611596_r1,516028598,491769070,705903773,314058,604819351,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2018-02-12 16:55:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR1804348/BSSE_QGF_10855_130208_SN792_0204_BD1W0VACXX_8_CGATGT_L008_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-9/SRR1804348/BSSE_QGF_10855_130208_SN792_0204_BD1W0VACXX_8_CGATGT_L008_R1_001.fastq.gz,,,,,,,,,public,2020-05-02 03:17:53,,7e0162e86a03801a5f4dd28ac558c182,fastq,2142088366,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-1/SRR1804348/SRR1804348.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR1804348/SRR1804348.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-1/SRR1804348/SRR1804348.1,gcp identity,gs.US,GCP,gs://sra-pub-run-1/SRR1804348/SRR1804348.1,public,2015-02-24 15:26:37,SRR1804348,02d1470fa0e2140fda0c05230720c2ac,run,1564324341,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-3/SRR1804348/SRR1804348.1,,,,,,,,,,,,,,,,,,,,,,1,2318834850,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole-worm,strain,N2,age,larval stage 4,,,,,,,,,,,,SAMN03349114,BioSample,XREF_LINK,DB: bioproject,ID: 275470,LABEL: PRJNA275470,,,,,6239,frac_28-30nt,GSE65948,,,GEO,GSE65948,PRJNA275470,BioProject,XREF_LINK,DB: pubmed,ID: 26102273,"Experiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.",Transcriptome-wide measurement of ribosomal occupancy by ribosome profiling,Other,SRA242099,GEO: GSE65948,GEO,GEO,,submission brokered by GEO, SRP055039,SRX878011,GSM1611595: frac_25-30nt; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845971,GSM1611595,Illumina HiSeq 2000,58434235,1765202980,SRR1804346,50000000,2500000000,GSM1611595,GEO Accession,GSM1611595,,GEO,,GSM1611595,"Worms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12",,URL_LINK,LABEL: GEO Sample GSM1611595,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611595,,XREF_LINK,DB: gds,ID: 301611595,ILLUMINA,,,,SRS845971,,SINGLE,SAMN03349115,SRS845971,2921711750,,Caenorhabditis elegans,GSM1611595,frac_25-30nt,6239,GSM1611595_r1,586839040,574182587,756997279,327819,581653275,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2018-02-12 16:55:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR1804346/BSSE_QGF_10858_130208_SN792_0204_BD1W0VACXX_8_GCCAAT_L008_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR1804346/BSSE_QGF_10858_130208_SN792_0204_BD1W0VACXX_8_GCCAAT_L008_R1_001.fastq.gz,,,,,,,,,public,2020-04-30 03:36:19,,9b6aca5936347e0b1883473eefdeeeed,fastq,2448203020,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR1804346/SRR1804346.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1804346/SRR1804346.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-4/SRR1804346/SRR1804346.1,gcp identity,gs.US,GCP,gs://sra-pub-run-4/SRR1804346/SRR1804346.1,public,2015-02-24 15:28:00,SRR1804346,3a8d30a3d997783fc99652f851e34f4e,run,1765204729,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1804346/SRR1804346.1,,,,,,,,,,,,,,,,,,,,,,1,2500000000,false,SRR1804347,GSM1611595_r2,99089476,96631092,127864278,49597,98077307,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,true,true,2018-02-12 16:55:10,299911254,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR1804347/BSSE_QGF_10858_130208_SN792_0204_BD1W0VACXX_8_GCCAAT_L008_R1_002.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR1804347/BSSE_QGF_10858_130208_SN792_0204_BD1W0VACXX_8_GCCAAT_L008_R1_002.fastq.gz,public,2020-05-02 10:54:14,73f29f4ce4277eb7b972b0271c92e328,fastq,416787944,0,Original,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR1804347/SRR1804347.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804347/SRR1804347.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR1804347/SRR1804347.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR1804347/SRR1804347.1,public,2015-02-14 16:19:02,SRR1804347,898695ecf57b6383fc53644f60fab88c,run,299913003,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804347/SRR1804347.1,1,421711750,false,421711750,8434235,source_name,Whole-worm,strain,N2,age,larval stage 4,,,,,,,,,,,,SAMN03349115,BioSample,XREF_LINK,DB: bioproject,ID: 275470,LABEL: PRJNA275470,,,,,6239,frac_25-30nt,GSE65948,,,GEO,GSE65948,PRJNA275470,BioProject,XREF_LINK,DB: pubmed,ID: 26102273,"Experiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.",Transcriptome-wide measurement of ribosomal occupancy by ribosome profiling,Other,SRA242099,GEO: GSE65948,GEO,GEO,,submission brokered by GEO, SRP055039,SRX878010,GSM1611594: 04_N2_893_GCkit; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845972,GSM1611594,Illumina HiSeq 2000,48751368,1774440563,SRR1804345,48751368,2486319768,GSM1611594,GEO Accession,GSM1611594,,GEO,,GSM1611594,"Worms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12",,URL_LINK,LABEL: GEO Sample GSM1611594,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611594,,XREF_LINK,DB: gds,ID: 301611594,ILLUMINA,,,,SRS845972,,SINGLE,SAMN03349119,SRS845972,2486319768,,Caenorhabditis elegans,GSM1611594,04_N2_893_GCkit,6239,GSM1611594_r1,730345497,566080787,702045096,355701,487492687,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2018-02-12 16:55:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-12/SRR1804345/BSSE_QGF_15362_131114_SN792_0291_BC35TGACXX_3_CTTGTAA_L003_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-12/SRR1804345/BSSE_QGF_15362_131114_SN792_0291_BC35TGACXX_3_CTTGTAA_L003_R1_001.fastq.gz,,,,,,,,,public,2020-05-02 15:44:38,,4e6511cbb0918b73e747f16dd8e73077,fastq,2460852885,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR1804345/SRR1804345.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804345/SRR1804345.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR1804345/SRR1804345.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR1804345/SRR1804345.1,public,2015-02-14 16:24:48,SRR1804345,ab6823807294a56c0a88805ee471cc18,run,1774442308,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804345/SRR1804345.1,,,,,,,,,,,,,,,,,,,,,,1,2486319768,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole-worm,strain,N2,age,young adult,,,,,,,,,,,,SAMN03349119,BioSample,XREF_LINK,DB: bioproject,ID: 275470,LABEL: PRJNA275470,,,,,6239,04_N2_893_GCkit,GSE65948,,,GEO,GSE65948,PRJNA275470,BioProject,XREF_LINK,DB: pubmed,ID: 26102273,"Experiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.",Transcriptome-wide measurement of ribosomal occupancy by ribosome profiling,Other,SRA242099,GEO: GSE65948,GEO,GEO,,submission brokered by GEO, SRP055039,SRX878009,GSM1611593: 03_N2_893_SGkit; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845973,GSM1611593,Illumina HiSeq 2000,67420201,1803539052,SRR1804343,50000000,2550000000,GSM1611593,GEO Accession,GSM1611593,,GEO,,GSM1611593,"Worms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12",,URL_LINK,LABEL: GEO Sample GSM1611593,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611593,,XREF_LINK,DB: gds,ID: 301611593,ILLUMINA,,,,SRS845973,,SINGLE,SAMN03349116,SRS845973,3438430251,,Caenorhabditis elegans,GSM1611593,03_N2_893_SGkit,6239,GSM1611593_r1,772367233,600519393,692703648,502681,483907045,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2018-02-12 16:55:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR1804343/BSSE_QGF_15361_131114_SN792_0291_BC35TGACXX_3_CAGATCA_L003_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR1804343/BSSE_QGF_15361_131114_SN792_0291_BC35TGACXX_3_CAGATCA_L003_R1_001.fastq.gz,,,,,,,,,public,2020-05-02 12:34:01,,8f8c356db28da864927c3a45274ad79a,fastq,2523746848,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR1804343/SRR1804343.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804343/SRR1804343.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR1804343/SRR1804343.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR1804343/SRR1804343.1,public,2015-02-14 16:25:10,SRR1804343,e7828ed64e58cdbbff1761c3b87aa1b9,run,1803540798,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804343/SRR1804343.1,,,,,,,,,,,,,,,,,,,,,,1,2550000000,false,SRR1804344,GSM1611593_r2,269208933,209069402,241376205,78778,168696933,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,true,true,2018-02-12 16:55:10,633192898,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR1804344/BSSE_QGF_15361_131114_SN792_0291_BC35TGACXX_3_CAGATCA_L003_R1_002.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR1804344/BSSE_QGF_15361_131114_SN792_0291_BC35TGACXX_3_CAGATCA_L003_R1_002.fastq.gz,public,2020-05-02 13:45:50,75723bc9ec3892d0d32ad70ef7c6e950,fastq,886815560,0,Original,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR1804344/SRR1804344.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804344/SRR1804344.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR1804344/SRR1804344.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR1804344/SRR1804344.1,public,2015-02-14 16:20:08,SRR1804344,7a742428a0474b8545e02b72ec5b35aa,run,633194650,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804344/SRR1804344.1,1,888430251,false,888430251,17420201,source_name,Whole-worm,strain,N2,age,young adult,,,,,,,,,,,,SAMN03349116,BioSample,XREF_LINK,DB: bioproject,ID: 275470,LABEL: PRJNA275470,,,,,6239,03_N2_893_SGkit,GSE65948,,,GEO,GSE65948,PRJNA275470,BioProject,XREF_LINK,DB: pubmed,ID: 26102273,"Experiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.",Transcriptome-wide measurement of ribosomal occupancy by ribosome profiling,Other,SRA242099,GEO: GSE65948,GEO,GEO,,submission brokered by GEO, SRP055039,SRX878008,GSM1611592: 02_N2_893_GCop; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845974,GSM1611592,Illumina HiSeq 2000,52891603,1798510443,SRR1804341,50000000,2550000000,GSM1611592,GEO Accession,GSM1611592,,GEO,,GSM1611592,"Worms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12",,URL_LINK,LABEL: GEO Sample GSM1611592,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611592,,XREF_LINK,DB: gds,ID: 301611592,ILLUMINA,,,,SRS845974,,SINGLE,SAMN03349120,SRS845974,2697471753,,Caenorhabditis elegans,GSM1611592,02_N2_893_GCop,6239,GSM1611592_r1,602084863,537944306,778317239,635426,631018166,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2018-02-12 16:55:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR1804341/BSSE_QGF_15359_131114_SN792_0291_BC35TGACXX_3_GCCAATA_L003_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR1804341/BSSE_QGF_15359_131114_SN792_0291_BC35TGACXX_3_GCCAATA_L003_R1_001.fastq.gz,,,,,,,,,public,2020-05-02 14:41:06,,8feade7c0a74d7d067cd11bdd436943b,fastq,2510930241,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR1804341/SRR1804341.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804341/SRR1804341.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR1804341/SRR1804341.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR1804341/SRR1804341.1,public,2015-02-14 16:27:11,SRR1804341,b3aac1263865f9139a02f74fc90eff98,run,1798512186,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804341/SRR1804341.1,,,,,,,,,,,,,,,,,,,,,,1,2550000000,false,SRR1804342,GSM1611592_r2,34930898,31054597,44976377,12968,36496913,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,true,true,2018-02-12 16:55:10,107864653,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR1804342/BSSE_QGF_15359_131114_SN792_0291_BC35TGACXX_3_GCCAATA_L003_R1_002.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR1804342/BSSE_QGF_15359_131114_SN792_0291_BC35TGACXX_3_GCCAATA_L003_R1_002.fastq.gz,public,2020-04-30 01:47:37,7fedae726a673ec501483438c64949c2,fastq,150651832,0,Original,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR1804342/SRR1804342.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804342/SRR1804342.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR1804342/SRR1804342.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR1804342/SRR1804342.1,public,2015-02-14 16:18:20,SRR1804342,c7d0fd1f23e7dcc60b5dd1bb230be773,run,107866400,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR1804342/SRR1804342.1,1,147471753,false,147471753,2891603,source_name,Whole-worm,strain,N2,age,young adult,,,,,,,,,,,,SAMN03349120,BioSample,XREF_LINK,DB: bioproject,ID: 275470,LABEL: PRJNA275470,,,,,6239,02_N2_893_GCop,GSE65948,,,GEO,GSE65948,PRJNA275470,BioProject,XREF_LINK,DB: pubmed,ID: 26102273,"Experiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.",Transcriptome-wide measurement of ribosomal occupancy by ribosome profiling,Other,SRA242099,GEO: GSE65948,GEO,GEO,,submission brokered by GEO, SRP055039,SRX878007,GSM1611591: 01_N2_893_SGop; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS845975,GSM1611591,Illumina HiSeq 2000,49787580,1806454729,SRR1804340,49787580,2539166580,GSM1611591,GEO Accession,GSM1611591,,GEO,,GSM1611591,"Worms were lysed, monosomes purified and RNA was isolated using Tri-reagent (MRC). The RNA from the monosomal fraction was separated using a 15% TBE-Urea Gel (Invitrogen) and the region around 28-30 nucleotides (or the region indicated) excised to isolate Ribosome protected fragments (RPFs). The gel piece was forced through a pierced small tube inside an eppendorf tube by centrifugation and RNA from the gel debris was eluted by overnight incubation in 600 µl cracking buffer (20 mM Tris-HCl (pH 7.9), 1 mM EDTA, 400 mM NH4Acetate, 0.5 % SDS). RNA was precipitated with isopropanol at -80 °C for at least 4 hours (isopropanol precipitation). RPFs were 3’ dephosphorylated with 10 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer with 40 Units of RNasin for 1 hour at 37 °C. Following isopropanol precipitation, the RNA samples were ligated to 3’ adapters according to the Illumina® TruSeq™ Small RNA Sample Preparation protocol and using the reagents of the kit, then again precipitated with isopropanol. Ligation products were 5’ phosphorylated for 30 minutes at 37 °C with 15 Units of T4 polynucleotide kinase (NEB) in T4 PNK buffer, 1 mM ATP and 40 Units of RNasin. Following heat-inactivation of the enzyme for 10 minutes at 70 °C, the RNA was precipitated by isopropanol. Ligation to 5’ adapters, reverse transcription, PCR amplification with barcoded primers and gel-purification of the PCR products were performed using the Illumina® TruSeq™ Small RNA Sample Prep kit. The following barcodes were used: RPIX 2, 4, 6, 7, 12",,URL_LINK,LABEL: GEO Sample GSM1611591,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1611591,,XREF_LINK,DB: gds,ID: 301611591,ILLUMINA,,,,SRS845975,,SINGLE,SAMN03349118,SRS845975,2539166580,,Caenorhabditis elegans,GSM1611591,01_N2_893_SGop,6239,GSM1611591_r1,631766277,568784013,744259365,586562,593770363,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2018-02-12 16:55:10,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-12/SRR1804340/BSSE_QGF_15358_131114_SN792_0291_BC35TGACXX_3_TGACCAA_L003_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-12/SRR1804340/BSSE_QGF_15358_131114_SN792_0291_BC35TGACXX_3_TGACCAA_L003_R1_001.fastq.gz,,,,,,,,,public,2020-04-30 11:03:51,,474a19e996e2826ee0cefe7a5957e4aa,fastq,2556290784,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR1804340/SRR1804340.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1804340/SRR1804340.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-2/SRR1804340/SRR1804340.1,gcp identity,gs.US,GCP,gs://sra-pub-run-2/SRR1804340/SRR1804340.1,public,2015-02-24 15:35:43,SRR1804340,44e8b1174d10bd6aeeb2cf3697c7ba2c,run,1806456475,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1804340/SRR1804340.1,,,,,,,,,,,,,,,,,,,,,,1,2539166580,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole-worm,strain,N2,age,young adult,,,,,,,,,,,,SAMN03349118,BioSample,XREF_LINK,DB: bioproject,ID: 275470,LABEL: PRJNA275470,,,,,6239,01_N2_893_SGop,GSE65948,,,GEO,GSE65948,PRJNA275470,BioProject,XREF_LINK,DB: pubmed,ID: 26102273,"Experiments for optimization of the ribosome profiling protocol using C. elegans lysates. We report that optimizing the cutting accuracy to a narrow window of 28-30 nucleotides when PAGE-purifying the ribosome-protected fragments (RPFs) significantly improves the quality of the RPF library. In addition, we find that purifying monosomes by sucrose gradient fractionation clearly removed more contaminating ribosomal RNA from the samples compared to the purification by gel filtration columns. Overall design: Experiment 1 (samples 1-4): Comparison between different methods to isolate monosomes and between different library preparations. Experiment 2 (samples 5-8): Optimization of the cutting accuracy to PAGE purify ribosome-protected fragments.",Transcriptome-wide measurement of ribosomal occupancy by ribosome profiling,Other,SRA242099,GEO: GSE65948,GEO,GEO,,submission brokered by GEO, SRP049413,SRX747690,GSM1534607: RNASeq_c14_2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS734047,GSM1534607,Illumina HiSeq 2500,49019407,1169023236,SRR1635379,49019407,2450970350,GSM1534607,GEO Accession,GSM1534607,,GEO,,GSM1534607,Total RNA isolation was performed using Trizol Reagent (Life Technologies). Important: Total RNA was extracted from the same lysate used subsequently for the corresponding ribosome profiling experiment. Library preparation was performed using the ScriptSeq v2 RNA-Seq library preparation kit (Epicentre) according to the manufacturer's protocol,,URL_LINK,LABEL: GEO Sample GSM1534607,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1534607,,XREF_LINK,DB: gds,ID: 301534607,ILLUMINA,,,,SRS734047,,SINGLE,SAMN03153517,SRS734047,2450970350,,Caenorhabditis elegans,GSM1534607,RNASeq_c14_2,6239,GSM1534607_r1,724865454,525274064,588425450,114825,612290557,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2015-01-08 16:29:17,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-12/SRR1635379/134F4-1_140226_D00404_0047_AC3P05ACXX_CTTGTA-NoIndex_L007_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-12/SRR1635379/134F4-1_140226_D00404_0047_AC3P05ACXX_CTTGTA-NoIndex_L007_R1_001.fastq.gz,,,,,,,,,public,2020-05-11 22:15:14,,d08a4ba71328f05abf9a4fd22a0e8bbd,fastq,2034483190,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR1635379/SRR1635379.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1635379/SRR1635379.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-4/SRR1635379/SRR1635379.1,gcp identity,gs.US,GCP,gs://sra-pub-run-4/SRR1635379/SRR1635379.1,public,2014-10-30 12:24:24,SRR1635379,dc5e2400fc33421ee4eace3610cbf0c9,run,1169024981,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1635379/SRR1635379.1,,,,,,,,,,,,,,,,,,,,,,1,2450970350,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole-worm,time in development,young adults,strain,"cey-1 (rrr12), cey-4 (ok858) mutant",,,,,,,,,,,GEO,SAMN03153517,BioSample,XREF_LINK,DB: bioproject,ID: 265852,LABEL: PRJNA265852,XREF_LINK,DB: bioproject,ID: 265853,LABEL: PRJNA265853,6239,RNASeq_c14_2,GSE62858,parent_bioproject,PRJNA265853,GEO,Caenorhabditis elegans,PRJNA265852,BioProject,XREF_LINK,DB: pubmed,ID: 25378320,"We present a basic characterization of the function of Y-box binding proteins in C. elegans. Besides playing an important role for fertility in the germline (all four CEY proteins), we found that the presence of CEY-1 and CEY-4 is essential for the assembly of larger polysomes in the soma. We therefore performed ribosome-profiling in combination with total RNA sequencing in wild type and cey-1,-4 double mutant animals to globally compare mRNA levels and their translation status. Overall design: Total RNA sequencing was peformed on RNA extacted from wild type and cey-1,-4 mutant animals in duplicates. Four samples in total.",Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RNA-Seq),Transcriptome Analysis,SRA197072,GEO: GSE62858,GEO,GEO,,submission brokered by GEO, SRP049413,SRX747689,GSM1534606: RNASeq_c14_1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS734046,GSM1534606,Illumina HiSeq 2500,63457303,1540925484,SRR1635378,63457303,3172865150,GSM1534606,GEO Accession,GSM1534606,,GEO,,GSM1534606,Total RNA isolation was performed using Trizol Reagent (Life Technologies). Important: Total RNA was extracted from the same lysate used subsequently for the corresponding ribosome profiling experiment. Library preparation was performed using the ScriptSeq v2 RNA-Seq library preparation kit (Epicentre) according to the manufacturer's protocol,,URL_LINK,LABEL: GEO Sample GSM1534606,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1534606,,XREF_LINK,DB: gds,ID: 301534606,ILLUMINA,,,,SRS734046,,SINGLE,SAMN03153520,SRS734046,3172865150,,Caenorhabditis elegans,GSM1534606,RNASeq_c14_1,6239,GSM1534606_r1,941279013,666050996,777121810,146748,788266583,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2015-01-08 16:29:17,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR1635378/134F3-1_140226_D00404_0047_AC3P05ACXX_GGCTAC-NoIndex_L007_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR1635378/134F3-1_140226_D00404_0047_AC3P05ACXX_GGCTAC-NoIndex_L007_R1_001.fastq.gz,,,,,,,,,public,2020-05-11 22:15:29,,dbb04689976a68a3c812963c2def4061,fastq,2669147192,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR1635378/SRR1635378.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1635378/SRR1635378.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-2/SRR1635378/SRR1635378.1,gcp identity,gs.US,GCP,gs://sra-pub-run-2/SRR1635378/SRR1635378.1,public,2014-10-30 12:24:34,SRR1635378,c4deababcde0877038b302e6354e9a5b,run,1540927232,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1635378/SRR1635378.1,,,,,,,,,,,,,,,,,,,,,,1,3172865150,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole-worm,time in development,young adults,strain,"cey-1 (rrr12), cey-4 (ok858) mutant",,,,,,,,,,,GEO,SAMN03153520,BioSample,XREF_LINK,DB: bioproject,ID: 265852,LABEL: PRJNA265852,XREF_LINK,DB: bioproject,ID: 265853,LABEL: PRJNA265853,6239,RNASeq_c14_1,GSE62858,parent_bioproject,PRJNA265853,GEO,Caenorhabditis elegans,PRJNA265852,BioProject,XREF_LINK,DB: pubmed,ID: 25378320,"We present a basic characterization of the function of Y-box binding proteins in C. elegans. Besides playing an important role for fertility in the germline (all four CEY proteins), we found that the presence of CEY-1 and CEY-4 is essential for the assembly of larger polysomes in the soma. We therefore performed ribosome-profiling in combination with total RNA sequencing in wild type and cey-1,-4 double mutant animals to globally compare mRNA levels and their translation status. Overall design: Total RNA sequencing was peformed on RNA extacted from wild type and cey-1,-4 mutant animals in duplicates. Four samples in total.",Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RNA-Seq),Transcriptome Analysis,SRA197072,GEO: GSE62858,GEO,GEO,,submission brokered by GEO, SRP049413,SRX747688,GSM1534605: RNASeq_N2_2; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS734045,GSM1534605,Illumina HiSeq 2500,54290105,1318568086,SRR1635377,54290105,2714505250,GSM1534605,GEO Accession,GSM1534605,,GEO,,GSM1534605,Total RNA isolation was performed using Trizol Reagent (Life Technologies). Important: Total RNA was extracted from the same lysate used subsequently for the corresponding ribosome profiling experiment. Library preparation was performed using the ScriptSeq v2 RNA-Seq library preparation kit (Epicentre) according to the manufacturer's protocol,,URL_LINK,LABEL: GEO Sample GSM1534605,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1534605,,XREF_LINK,DB: gds,ID: 301534605,ILLUMINA,,,,SRS734045,,SINGLE,SAMN03153515,SRS734045,2714505250,,Caenorhabditis elegans,GSM1534605,RNASeq_N2_2,6239,GSM1534605_r1,805782067,580966383,661891020,124931,665740849,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2015-01-08 16:29:17,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR1635377/134F2-1_140226_D00404_0047_AC3P05ACXX_TAGCTT-NoIndex_L007_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR1635377/134F2-1_140226_D00404_0047_AC3P05ACXX_TAGCTT-NoIndex_L007_R1_001.fastq.gz,,,,,,,,,public,2020-05-12 19:05:59,,49241146db0d25570ae1d12c5a47a277,fastq,2282314660,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR1635377/SRR1635377.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1635377/SRR1635377.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-2/SRR1635377/SRR1635377.1,gcp identity,gs.US,GCP,gs://sra-pub-run-2/SRR1635377/SRR1635377.1,public,2014-10-30 12:23:51,SRR1635377,c3e1a33280f98045ce8cee56166fbe09,run,1318569835,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1635377/SRR1635377.1,,,,,,,,,,,,,,,,,,,,,,1,2714505250,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole-worm,time in development,young adults,strain,N2,,,,,,,,,,,GEO,SAMN03153515,BioSample,XREF_LINK,DB: bioproject,ID: 265852,LABEL: PRJNA265852,XREF_LINK,DB: bioproject,ID: 265853,LABEL: PRJNA265853,6239,RNASeq_N2_2,GSE62858,parent_bioproject,PRJNA265853,GEO,Caenorhabditis elegans,PRJNA265852,BioProject,XREF_LINK,DB: pubmed,ID: 25378320,"We present a basic characterization of the function of Y-box binding proteins in C. elegans. Besides playing an important role for fertility in the germline (all four CEY proteins), we found that the presence of CEY-1 and CEY-4 is essential for the assembly of larger polysomes in the soma. We therefore performed ribosome-profiling in combination with total RNA sequencing in wild type and cey-1,-4 double mutant animals to globally compare mRNA levels and their translation status. Overall design: Total RNA sequencing was peformed on RNA extacted from wild type and cey-1,-4 mutant animals in duplicates. Four samples in total.",Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RNA-Seq),Transcriptome Analysis,SRA197072,GEO: GSE62858,GEO,GEO,,submission brokered by GEO, SRP049413,SRX747687,GSM1534604: RNASeq_N2_1; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS734044,GSM1534604,Illumina HiSeq 2500,64579253,1537362492,SRR1635376,64579253,3228962650,GSM1534604,GEO Accession,GSM1534604,,GEO,,GSM1534604,Total RNA isolation was performed using Trizol Reagent (Life Technologies). Important: Total RNA was extracted from the same lysate used subsequently for the corresponding ribosome profiling experiment. Library preparation was performed using the ScriptSeq v2 RNA-Seq library preparation kit (Epicentre) according to the manufacturer's protocol,,URL_LINK,LABEL: GEO Sample GSM1534604,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1534604,,XREF_LINK,DB: gds,ID: 301534604,ILLUMINA,,,,SRS734044,,SINGLE,SAMN03153516,SRS734044,3228962650,,Caenorhabditis elegans,GSM1534604,RNASeq_N2_1,6239,GSM1534604_r1,941585225,671517732,811145455,151602,804562636,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2015-01-08 16:29:17,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR1635376/134F1-1_140226_D00404_0047_AC3P05ACXX_ACAGTG-NoIndex_L007_R1_001.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR1635376/134F1-1_140226_D00404_0047_AC3P05ACXX_ACAGTG-NoIndex_L007_R1_001.fastq.gz,,,,,,,,,public,2020-05-11 15:28:42,,265b4257e5732c4ae710c01bbb52a09e,fastq,2663059402,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR1635376/SRR1635376.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1635376/SRR1635376.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-2/SRR1635376/SRR1635376.1,gcp identity,gs.US,GCP,gs://sra-pub-run-2/SRR1635376/SRR1635376.1,public,2014-10-30 12:24:58,SRR1635376,6f85936e84108a1753c03881e2e0eca5,run,1537364240,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR1635376/SRR1635376.1,,,,,,,,,,,,,,,,,,,,,,1,3228962650,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,Whole-worm,time in development,young adults,strain,N2,,,,,,,,,,,GEO,SAMN03153516,BioSample,XREF_LINK,DB: bioproject,ID: 265852,LABEL: PRJNA265852,XREF_LINK,DB: bioproject,ID: 265853,LABEL: PRJNA265853,6239,RNASeq_N2_1,GSE62858,parent_bioproject,PRJNA265853,GEO,Caenorhabditis elegans,PRJNA265852,BioProject,XREF_LINK,DB: pubmed,ID: 25378320,"We present a basic characterization of the function of Y-box binding proteins in C. elegans. Besides playing an important role for fertility in the germline (all four CEY proteins), we found that the presence of CEY-1 and CEY-4 is essential for the assembly of larger polysomes in the soma. We therefore performed ribosome-profiling in combination with total RNA sequencing in wild type and cey-1,-4 double mutant animals to globally compare mRNA levels and their translation status. Overall design: Total RNA sequencing was peformed on RNA extacted from wild type and cey-1,-4 mutant animals in duplicates. Four samples in total.",Functional characterization of C. elegans Y-box binding proteins reveals tissue-specific functions and a critical role in the formation of polysomes (RNA-Seq),Transcriptome Analysis,SRA197072,GEO: GSE62858,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311785,GSM1169554: Celeg-3-FED-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449537,GSM1169554,Illumina HiSeq 2000,20213950,446723077,SRR914339,20213950,727702200,GSM1169554,GEO Accession,GSM1169554,,GEO,,GSM1169554,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169554,,XREF_LINK,DB: gds,ID: 301169554,ILLUMINA,,,,SRS449537,,SINGLE,SAMN02209117,SRS449537,727702200,,Caenorhabditis elegans,GSM1169554,Celeg-3-FED-RPF,6239,GSM1169554_r1,197286514,134780436,195169449,25706,200440095,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2015-07-22 17:03:37,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR914339/120223_BRISCOE_0086_BD0PE4ACXX_L2_GCCTAA_pf_renamed.fastq,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR914339/120223_BRISCOE_0086_BD0PE4ACXX_L2_GCCTAA_pf_renamed.fastq,,,,,,,,,public,2020-05-23 14:17:25,,8fe3c4b474f3558d5cbec5e427899e7e,fastq,3033418810,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914339/SRR914339.2,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914339/SRR914339.2,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-6/SRR914339/SRR914339.2,gcp identity,gs.US,GCP,gs://sra-pub-run-6/SRR914339/SRR914339.2,public,2015-10-22 15:13:15,SRR914339,0f6fe45cf469a5948e1bc1c9f63a505b,run,446724822,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914339/SRR914339.2,,,,,,,,,,,,,,,,,,,,,,1,727702200,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 fed 3 hours,batch,3,strain,N2,rna subtype,ribosome protected fragments,,,,,,,GEO,SAMN02209117,BioSample,,,,,,,,,6239,Celeg-3-FED-RPF,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311784,GSM1169553: Celeg-2-FED-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449536,GSM1169553,Illumina HiSeq 2000,59233837,2094108084,SRR914338,59233837,2961691850,GSM1169553,GEO Accession,GSM1169553,,GEO,,GSM1169553,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169553,,XREF_LINK,DB: gds,ID: 301169553,ILLUMINA,,,,SRS449536,,SINGLE,SAMN02209118,SRS449536,2961691850,,Caenorhabditis elegans,GSM1169553,Celeg-2-FED-RPF,6239,GSM1169553_r1,876926009,620466445,815306174,161657,648831565,GEO,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2013-06-21 16:12:03,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914338/SRR914338.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914338/SRR914338.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-6/SRR914338/SRR914338.1,gcp identity,gs.US,GCP,gs://sra-pub-run-6/SRR914338/SRR914338.1,public,2013-06-20 08:54:39,SRR914338,6af543a293d10d1fba96ccd76fd478bc,run,2094109832,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914338/SRR914338.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,2961691850,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 fed 3 hours,batch,2,strain,N2,rna subtype,ribosome protected fragments,,,,,,,GEO,SAMN02209118,BioSample,,,,,,,,,6239,Celeg-2-FED-RPF,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311783,GSM1169552: Celeg-1-FED-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449535,GSM1169552,Illumina HiSeq 2000,30099263,1080856284,SRR914337,30099263,1504963150,GSM1169552,GEO Accession,GSM1169552,,GEO,,GSM1169552,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169552,,XREF_LINK,DB: gds,ID: 301169552,ILLUMINA,,,,SRS449535,,SINGLE,SAMN02209116,SRS449535,1504963150,,Caenorhabditis elegans,GSM1169552,Celeg-1-FED-RPF,6239,GSM1169552_r1,437435234,323426113,408129512,58131,335914160,GEO,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2013-06-21 16:12:03,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914337/SRR914337.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914337/SRR914337.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR914337/SRR914337.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR914337/SRR914337.1,public,2013-06-20 08:46:23,SRR914337,228cd7a040066de489c4f8b963e3fb51,run,1080858035,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914337/SRR914337.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,1504963150,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 fed 3 hours,batch,1,strain,N2,rna subtype,ribosome protected fragments,,,,,,,GEO,SAMN02209116,BioSample,,,,,,,,,6239,Celeg-1-FED-RPF,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311782,GSM1169551: Celeg-3-ST-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449534,GSM1169551,Illumina HiSeq 2000,50278819,1757277248,SRR914336,50278819,2513940950,GSM1169551,GEO Accession,GSM1169551,,GEO,,GSM1169551,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169551,,XREF_LINK,DB: gds,ID: 301169551,ILLUMINA,,,,SRS449534,,SINGLE,SAMN02209115,SRS449534,2513940950,,Caenorhabditis elegans,GSM1169551,Celeg-3-ST-RPF,6239,GSM1169551_r1,728994069,528764298,677805498,142790,578234295,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2013-06-21 16:12:03,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-10/SRR914336/R63-L2-P6-CACTGT-Sequences_merged.txt.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-10/SRR914336/R63-L2-P6-CACTGT-Sequences_merged.txt.gz,,,,,,,,,public,2020-05-25 08:30:04,,fc2435ed94c5d38e7bcbb0320d908ad5,fastq,1735022610,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914336/SRR914336.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914336/SRR914336.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-7/SRR914336/SRR914336.1,gcp identity,gs.US,GCP,gs://sra-pub-run-7/SRR914336/SRR914336.1,public,2013-06-20 09:10:45,SRR914336,8a494e99b7c492c6cfdf0548365f8091,run,1757278994,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914336/SRR914336.1,,,,,,,,,,,,,,,,,,,,,,1,2513940950,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 diapause,batch,3,strain,N2,rna subtype,ribosome protected fragments,,,,,,,GEO,SAMN02209115,BioSample,,,,,,,,,6239,Celeg-3-ST-RPF,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311781,GSM1169550: Celeg-2-ST-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449533,GSM1169550,Illumina HiSeq 2000,20851539,453779681,SRR914335,20851539,750655404,GSM1169550,GEO Accession,GSM1169550,,GEO,,GSM1169550,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169550,,XREF_LINK,DB: gds,ID: 301169550,ILLUMINA,,,,SRS449533,,SINGLE,SAMN02209128,SRS449533,750655404,,Caenorhabditis elegans,GSM1169550,Celeg-2-ST-RPF,6239,GSM1169550_r1,204267796,139589333,202211009,27387,204559879,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2015-07-22 17:03:37,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR914335/120223_BRISCOE_0086_BD0PE4ACXX_L2_ATTGGC_pf.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR914335/120223_BRISCOE_0086_BD0PE4ACXX_L2_ATTGGC_pf.fastq.gz,,,,,,,,,public,2020-05-23 17:10:15,,55c7c95acdb366b2905ed1b4498787e9,fastq,536164456,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914335/SRR914335.2,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914335/SRR914335.2,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR914335/SRR914335.2,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR914335/SRR914335.2,public,2015-10-22 15:14:59,SRR914335,e7622c42ca0227058bd85c7812a94ad3,run,453781426,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914335/SRR914335.2,,,,,,,,,,,,,,,,,,,,,,1,750655404,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 diapause,batch,2,strain,N2,rna subtype,ribosome protected fragments,,,,,,,GEO,SAMN02209128,BioSample,,,,,,,,,6239,Celeg-2-ST-RPF,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311780,GSM1169549: Celeg-1-ST-RPF; Caenorhabditis elegans; OTHER,6239,Caenorhabditis elegans,OTHER,TRANSCRIPTOMIC,other,SRS449532,GSM1169549,Illumina HiSeq 2000,46096938,1610654289,SRR914334,46096938,2304846900,GSM1169549,GEO Accession,GSM1169549,,GEO,,GSM1169549,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169549,,XREF_LINK,DB: gds,ID: 301169549,ILLUMINA,,,,SRS449532,,SINGLE,SAMN02209113,SRS449532,2304846900,,Caenorhabditis elegans,GSM1169549,Celeg-1-ST-RPF,6239,GSM1169549_r1,685828992,486534030,634967175,100489,497416214,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2013-06-21 16:12:03,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR914334/R63-L5-P1-CGTGAT-Sequences.txt.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR914334/R63-L5-P1-CGTGAT-Sequences.txt.gz,,,,,,,,,public,2020-05-25 08:29:24,,a2054f99ffb297dda2eee68591f12e3c,fastq,1641542868,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914334/SRR914334.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914334/SRR914334.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR914334/SRR914334.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR914334/SRR914334.1,public,2013-06-20 09:11:15,SRR914334,ff86497014e0b8f81e0b4bf2d464320b,run,1610656034,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914334/SRR914334.1,,,,,,,,,,,,,,,,,,,,,,1,2304846900,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 diapause,batch,1,strain,N2,rna subtype,ribosome protected fragments,,,,,,,GEO,SAMN02209113,BioSample,,,,,,,,,6239,Celeg-1-ST-RPF,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311779,GSM1169548: Celeg-3-FED-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449531,GSM1169548,Illumina HiSeq 2000,27043901,943922301,SRR914333,27043901,1352195050,GSM1169548,GEO Accession,GSM1169548,,GEO,,GSM1169548,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169548,,XREF_LINK,DB: gds,ID: 301169548,ILLUMINA,,,,SRS449531,,SINGLE,SAMN02209111,SRS449531,1352195050,,Caenorhabditis elegans,GSM1169548,Celeg-3-FED-mRNA,6239,GSM1169548_r1,435961986,305273380,343089574,64210,267805900,GEO,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2013-06-21 16:12:03,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914333/SRR914333.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914333/SRR914333.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-7/SRR914333/SRR914333.1,gcp identity,gs.US,GCP,gs://sra-pub-run-7/SRR914333/SRR914333.1,public,2013-06-20 08:41:49,SRR914333,c8127fca53f0e638e0c55293999990c9,run,943924052,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914333/SRR914333.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,1352195050,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 fed 3 hours,batch,3,strain,N2,rna subtype,total mRNA,,,,,,,GEO,SAMN02209111,BioSample,,,,,,,,,6239,Celeg-3-FED-mRNA,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311778,GSM1169547: Celeg-2-FED-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449530,GSM1169547,Illumina HiSeq 2000,15243931,541870283,SRR914332,15243931,762196550,GSM1169547,GEO Accession,GSM1169547,,GEO,,GSM1169547,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169547,,XREF_LINK,DB: gds,ID: 301169547,ILLUMINA,,,,SRS449530,,SINGLE,SAMN02209114,SRS449530,762196550,,Caenorhabditis elegans,GSM1169547,Celeg-2-FED-mRNA,6239,GSM1169547_r1,257860440,167904092,189081774,1382011,145968233,GEO,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2013-06-21 16:12:03,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914332/SRR914332.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914332/SRR914332.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-6/SRR914332/SRR914332.1,gcp identity,gs.US,GCP,gs://sra-pub-run-6/SRR914332/SRR914332.1,public,2013-06-20 08:39:46,SRR914332,83dd0290087a971630f794e54d6f3954,run,541872028,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914332/SRR914332.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,762196550,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 fed 3 hours,batch,2,strain,N2,rna subtype,total mRNA,,,,,,,GEO,SAMN02209114,BioSample,,,,,,,,,6239,Celeg-2-FED-mRNA,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311777,GSM1169546: Celeg-1-FED-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449529,GSM1169546,Illumina HiSeq 2000,14429547,515974302,SRR914331,14429547,721477350,GSM1169546,GEO Accession,GSM1169546,,GEO,,GSM1169546,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169546,,XREF_LINK,DB: gds,ID: 301169546,ILLUMINA,,,,SRS449529,,SINGLE,SAMN02209109,SRS449529,721477350,,Caenorhabditis elegans,GSM1169546,Celeg-1-FED-mRNA,6239,GSM1169546_r1,239948923,155621308,184391141,1304955,140211023,GEO,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2013-06-21 16:12:03,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914331/SRR914331.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914331/SRR914331.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR914331/SRR914331.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR914331/SRR914331.1,public,2013-06-20 08:36:35,SRR914331,bee20bdc58ba88343522a78a270e6508,run,515976049,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914331/SRR914331.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,721477350,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 fed 3 hours,batch,1,strain,N2,rna subtype,total mRNA,,,,,,,GEO,SAMN02209109,BioSample,,,,,,,,,6239,Celeg-1-FED-mRNA,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311776,GSM1169545: Celeg-3-ST-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449528,GSM1169545,Illumina HiSeq 2000,23438522,822960576,SRR914330,23438522,1171926100,GSM1169545,GEO Accession,GSM1169545,,GEO,,GSM1169545,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169545,,XREF_LINK,DB: gds,ID: 301169545,ILLUMINA,,,,SRS449528,,SINGLE,SAMN02209110,SRS449528,1171926100,,Caenorhabditis elegans,GSM1169545,Celeg-3-ST-mRNA,6239,GSM1169545_r1,384292936,262755964,291724712,89897,233062591,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2013-06-21 16:12:03,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-14/SRR914330/R63-L7-P4-CACTGT-Sequences.txt.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-14/SRR914330/R63-L7-P4-CACTGT-Sequences.txt.gz,,,,,,,,,public,2020-05-25 07:12:31,,09b04fc38f8ce8a1a8cea52797ee7eb7,fastq,959396099,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914330/SRR914330.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914330/SRR914330.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-7/SRR914330/SRR914330.1,gcp identity,gs.US,GCP,gs://sra-pub-run-7/SRR914330/SRR914330.1,public,2013-06-20 09:07:48,SRR914330,6483de6ff4d28fd538ea0a85e77c723a,run,822962326,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914330/SRR914330.1,,,,,,,,,,,,,,,,,,,,,,1,1171926100,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 diapause,batch,3,strain,N2,rna subtype,total mRNA,,,,,,,GEO,SAMN02209110,BioSample,,,,,,,,,6239,Celeg-3-ST-mRNA,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311775,GSM1169544: Celeg-2-ST-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449527,GSM1169544,Illumina HiSeq 2000,31547222,1401361925,SRR914329,31547222,2366041650,GSM1169544,GEO Accession,GSM1169544,,GEO,,GSM1169544,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169544,,XREF_LINK,DB: gds,ID: 301169544,ILLUMINA,,,,SRS449527,,SINGLE,SAMN02209112,SRS449527,2366041650,,Caenorhabditis elegans,GSM1169544,Celeg-2-ST-mRNA,6239,GSM1169544_r1,751090037,559629169,541834016,614482,512873946,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2013-06-21 16:12:03,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR914329/R67-L5-P1-CGTGAT-Sequences_merged.txt.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR914329/R67-L5-P1-CGTGAT-Sequences_merged.txt.gz,,,,,,,,,public,2020-05-24 13:09:39,,485340d750fd77474a0cdc21a9b3c7cb,fastq,1562156180,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914329/SRR914329.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914329/SRR914329.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-6/SRR914329/SRR914329.1,gcp identity,gs.US,GCP,gs://sra-pub-run-6/SRR914329/SRR914329.1,public,2013-06-20 09:06:06,SRR914329,98d32d71fbc6cf4ecf0c29a0783f6863,run,1401363675,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914329/SRR914329.1,,,,,,,,,,,,,,,,,,,,,,1,2366041650,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 diapause,batch,2,strain,N2,rna subtype,total mRNA,,,,,,,GEO,SAMN02209112,BioSample,,,,,,,,,6239,Celeg-2-ST-mRNA,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP026198,SRX311774,GSM1169543: Celeg-1-ST-mRNA; Caenorhabditis elegans; RNA-Seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,cDNA,SRS449591,GSM1169543,Illumina HiSeq 2000,19452670,696539703,SRR914328,19452670,972633500,GSM1169543,GEO Accession,GSM1169543,,GEO,,GSM1169543,"Total mRNA was isolated using Ambion's micro-poly(A) purist kit, fragmented by alkali and heat, followed by library preparation. Ribosome profiling was carried out as described in Ingolia et al (2009) with modifications as Stadler and Fire (2011). Libraries were constructed using the circligase protocol as described in Ingolia et al. (2009) with modifications described in Stadler and Fire (2013).",,URL_LINK,LABEL: GEO Sample,URL: http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1169543,,XREF_LINK,DB: gds,ID: 301169543,ILLUMINA,,,,SRS449591,,SINGLE,SAMN02209160,SRS449591,972633500,,Caenorhabditis elegans,GSM1169543,Celeg-1-ST-mRNA,6239,GSM1169543_r1,323752472,208936436,243562009,37625,196344958,GEO,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2013-06-21 16:12:03,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR914328/R63-L1-P1-CGTGAT-Sequences.txt.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR914328/R63-L1-P1-CGTGAT-Sequences.txt.gz,,,,,,,,,public,2020-05-23 17:15:29,,a20ad51bcab81af751cc739fd6e106c7,fastq,847764171,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR914328/SRR914328.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914328/SRR914328.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR914328/SRR914328.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR914328/SRR914328.1,public,2013-06-20 09:03:53,SRR914328,a24773c73c8e4d81e24b0be737e3d07a,run,696541450,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR914328/SRR914328.1,,,,,,,,,,,,,,,,,,,,,,1,972633500,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,source_name,population-whole animal,developmental stage,L1 diapause,batch,1,strain,N2,rna subtype,total mRNA,,,,,,,GEO,SAMN02209160,BioSample,,,,,,,,,6239,Celeg-1-ST-mRNA,GSE48140,,,GEO,GSE48140,PRJNA208993,BioProject,XREF_LINK,DB: pubmed,ID: 24098135,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition Overall design: mRNA-seq and Ribo-seq,mRNA and Ribosome Profiling in Four Nematode Species Traversing a Shared Developmental Transition,Other,SRA091389,GEO: GSE48140,GEO,GEO,,submission brokered by GEO, SRP014427,SRX160517,L1 ribosome footprints replicate 4,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,172256552,7089950470,SRR522897,172256552,9990880016,L1 ribosome footprints replicate 4,,,1,Stanford University,,,,MS-63,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,58,SINGLE,SAMN01090422,SRS350385,9990880016,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L1 ribosome footprints replicate 4,2742011224,2329571991,2626922712,62722476,2229651613,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2015-07-22 17:07:48,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR522897/SRR522897.2,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522897/SRR522897.2,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-3/SRR522897/SRR522897.2,gcp identity,gs.US,GCP,gs://sra-pub-run-3/SRR522897/SRR522897.2,public,2015-12-07 05:01:00,SRR522897,7e87ba9273ef0bdc84f2cad8410b36f1,run,7089952215,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522897/SRR522897.2,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,9990880016,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160513,L2 ribosome footprints replicate 2 (seq-replicate),6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,160368455,6099790048,SRR522895,160368455,9301370390,L2 ribosome footprints replicate 2 (seq-replicate),,,1,Stanford University,,,,MS-65,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,58,SINGLE,SAMN01090422,SRS350385,9301370390,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L2 ribosome footprints replicate 2 (seq-replicate),4395868552,1355230557,1585499480,58020711,1906751090,Stanford University,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2015-07-22 17:07:48,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR522895/s_7_all.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR522895/s_7_all.fastq.gz,,,,,,,,,public,2020-06-10 00:30:40,,d806388a3edc097ad0fecf5eb1fc18ef,fastq,6540149063,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR522895/SRR522895.2,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522895/SRR522895.2,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-4/SRR522895/SRR522895.2,gcp identity,gs.US,GCP,gs://sra-pub-run-4/SRR522895/SRR522895.2,public,2015-12-07 04:27:24,SRR522895,dd6fb591e96742c30c76181738c16f4e,run,6099791796,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522895/SRR522895.2,,,,,,,,,,,,,,,,,,,,,,1,9301370390,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160518,L4 ribosome footprints replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,174693758,7204894135,SRR522883,174693758,10132237964,L4 ribosome footprints replicate 1,,,1,Stanford University,,,,MS-61,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,58,SINGLE,SAMN01090422,SRS350385,10132237964,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L4 ribosome footprints replicate 1,2899435466,2230705525,2619710238,56903562,2325483173,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2015-07-22 17:07:44,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR522883/SRR522883.2,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522883/SRR522883.2,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-3/SRR522883/SRR522883.2,gcp identity,gs.US,GCP,gs://sra-pub-run-3/SRR522883/SRR522883.2,public,2015-11-27 11:25:57,SRR522883,bf1692c0354cfc5e1bd3ee9590529240,run,7204895879,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522883/SRR522883.2,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,10132237964,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160516,L1 ribosome footprints replicate 3,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,20213950,447522447,SRR522896,20213950,727702200,L1 ribosome footprints replicate 3,,,1,Stanford University,,,,Celeg_3_FED_RPF,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,50,SINGLE,SAMN01090422,SRS350385,727702200,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L1 ribosome footprints replicate 3,197286514,134780436,195169449,25706,200440095,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2012-07-18 01:32:11,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522896/SRR522896.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522896/SRR522896.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522896/SRR522896.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522896/SRR522896.1,public,2012-07-18 01:31:47,SRR522896,5d40af8fa9a8689e8ac37382e1028424,run,447524197,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522896/SRR522896.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,727702200,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160515,L1 ribosome footprints replicate 2,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,59233837,2096895718,SRR522872,59233837,2961691850,L1 ribosome footprints replicate 2,,,1,Stanford University,,,,Celeg_2_FED_RPF,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,50,SINGLE,SAMN01090422,SRS350385,2961691850,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L1 ribosome footprints replicate 2,876926009,620466445,815306174,161657,648831565,Stanford University,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2012-07-18 00:47:30,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-13/SRR522872/R63-L5-P6-TGGTCA-Sequences_merged.txt.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-13/SRR522872/R63-L5-P6-TGGTCA-Sequences_merged.txt.gz,,,,,,,,,public,2020-06-04 18:12:11,,f5b2e08567eb7a1b4862051afb24bd3a,fastq,2173204023,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522872/SRR522872.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522872/SRR522872.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522872/SRR522872.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522872/SRR522872.1,public,2012-07-17 20:27:17,SRR522872,9acd05b50e546cfc709403ece11f0260,run,2096897469,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522872/SRR522872.1,,,,,,,,,,,,,,,,,,,,,,1,2961691850,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160514,L1 ribosome footprints replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,30099263,1082257308,SRR522871,30099263,1504963150,L1 ribosome footprints replicate 1,,,1,Stanford University,,,,Celeg_1_FED_RPF,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,50,SINGLE,SAMN01090422,SRS350385,1504963150,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L1 ribosome footprints replicate 1,437435234,323426113,408129512,58131,335914160,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2012-07-18 00:00:00,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522871/SRR522871.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522871/SRR522871.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522871/SRR522871.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522871/SRR522871.1,public,2012-07-17 18:35:23,SRR522871,cfb65410453b6c7bcabcb0a91e88c732,run,1082259053,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522871/SRR522871.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,1504963150,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160512,L2 ribosome footprints replicate 3,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,32939763,674223820,SRR522892,32939763,1185831468,L2 ribosome footprints replicate 3,,,1,Stanford University,,,,MS-58,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,36,SINGLE,SAMN01090422,SRS350385,1185831468,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L2 ribosome footprints replicate 3,381501045,263450490,283138994,306278,257434661,Stanford University,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2012-07-18 00:47:30,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR522892/AF_SOL_MS_58_fastq.tar.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-9/SRR522892/AF_SOL_MS_58_fastq.tar.gz,,,,,,,,,public,2020-06-05 22:07:05,,6e3135e95e6669cc420441d67270bf14,fastq,819879342,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522892/SRR522892.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522892/SRR522892.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522892/SRR522892.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522892/SRR522892.1,public,2012-07-17 23:16:06,SRR522892,02e710bb5bdc484e64ba16bfb2627790,run,674225569,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522892/SRR522892.1,,,,,,,,,,,,,,,,,,,,,,1,1185831468,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160511,L2 ribosome footprints replicate 2,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,13600895,255011824,SRR522890,13600895,489632220,L2 ribosome footprints replicate 2,,,1,Stanford University,,,,MS-29,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,36,SINGLE,SAMN01090422,SRS350385,489632220,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L2 ribosome footprints replicate 2,186224663,81195251,97626139,207779,124378388,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2012-07-18 00:47:30,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522890/SRR522890.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522890/SRR522890.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522890/SRR522890.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522890/SRR522890.1,public,2012-07-17 23:14:00,SRR522890,32ee75d8ec8c0566c453267a8449d973,run,255013573,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522890/SRR522890.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,489632220,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160510,L2 ribosome footprints replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,15787042,298610401,SRR522881,15787042,568333512,L2 ribosome footprints replicate 1,,,1,Stanford University,,,,MS_25,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,36,SINGLE,SAMN01090422,SRS350385,568333512,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L2 ribosome footprints replicate 1,213302556,95197758,114545096,19989,145268113,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2012-07-18 00:47:30,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522881/SRR522881.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522881/SRR522881.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522881/SRR522881.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522881/SRR522881.1,public,2012-07-17 20:51:10,SRR522881,8038efafe532125d2b2a09e064ab84d9,run,298612149,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522881/SRR522881.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,568333512,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160293,L4 total RNA-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,58539675,1150293060,SRR522153,58539675,2107428300,L4 total RNA-seq,,,1,Stanford University,,,,MS-32,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,36,SINGLE,SAMN01090422,SRS350385,2107428300,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L4 total RNA-seq,921104099,338984624,422985018,810200,423544359,Stanford University,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2015-07-22 17:07:48,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-12/SRR522153/MS_32_L1thruL4_2.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-12/SRR522153/MS_32_L1thruL4_2.fastq.gz,,,,,,,,,public,2020-06-05 16:37:38,,442da06a27a22c08904113a0a7ed3c03,fastq,1624101210,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR522153/SRR522153.2,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522153/SRR522153.2,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-4/SRR522153/SRR522153.2,gcp identity,gs.US,GCP,gs://sra-pub-run-4/SRR522153/SRR522153.2,public,2015-11-27 03:12:14,SRR522153,50888638255eeb6562003a2eae2664a6,run,1150294806,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522153/SRR522153.2,,,,,,,,,,,,,,,,,,,,,,1,2107428300,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160292,L1 total RNA-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,33245137,717344505,SRR522152,33245137,1196824932,L1 total RNA-seq,,,1,Stanford University,,,,MS-57,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,36,SINGLE,SAMN01090422,SRS350385,1196824932,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L1 total RNA-seq,309639863,253577971,319969535,191451,313446112,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2012-07-18 00:00:00,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522152/SRR522152.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522152/SRR522152.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522152/SRR522152.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522152/SRR522152.1,public,2012-07-16 22:26:50,SRR522152,05bdd30a3c25411a0a946bf6044393ba,run,717346257,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522152/SRR522152.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,1196824932,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160291,L4 mRNA-seq replicate 2,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina Genome Analyzer IIx,27313086,546661322,SRR522151,27313086,983271096,L4 mRNA-seq replicate 2,,,1,Stanford University,,,,MS-56,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,36,SINGLE,SAMN01090422,SRS350385,983271096,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L4 mRNA-seq replicate 2,362664679,190870658,191924985,100275,237710499,Stanford University,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2012-07-18 00:00:00,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-5/SRR522151/110620_MAGNUM_00078_FC70GTV_L2_pf.fastq.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-5/SRR522151/110620_MAGNUM_00078_FC70GTV_L2_pf.fastq.gz,,,,,,,,,public,2020-06-09 02:49:21,,d12f959d8fe42d9c2c1a264ec25d0874,fastq,890814364,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522151/SRR522151.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522151/SRR522151.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522151/SRR522151.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522151/SRR522151.1,public,2012-07-16 22:25:29,SRR522151,e99185667cd5aa0cfaca1495f320441e,run,546663073,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522151/SRR522151.1,,,,,,,,,,,,,,,,,,,,,,1,983271096,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160290,L4 mRNA-seq replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,184752725,7621028154,SRR522882,184752725,10715658050,L4 mRNA-seq replicate 1,,,1,Stanford University,,,,MS_60,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,58,SINGLE,SAMN01090422,SRS350385,10715658050,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L4 mRNA-seq replicate 1,3389976798,2573670005,2605987894,62823946,2083199407,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2015-07-22 17:07:48,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-5/SRR522882/SRR522882.2,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522882/SRR522882.2,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-3/SRR522882/SRR522882.2,gcp identity,gs.US,GCP,gs://sra-pub-run-3/SRR522882/SRR522882.2,public,2015-12-07 22:02:31,SRR522882,25509c27d8ff6dc72480347479509bfa,run,7621029902,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-6/SRR522882/SRR522882.2,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,10715658050,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160157,L1 mRNA-seq replicate 4,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,97881671,4241570041,SRR522888,97881671,5677136918,L1 mRNA-seq replicate 4,,,1,Stanford University,,,,MS_59,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,58,SINGLE,SAMN01090422,SRS350385,5677136918,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,L1 mRNA-seq replicate 4,1748477929,1459489152,1340673184,31330919,1097165734,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2012-07-18 00:47:30,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522888/SRR522888.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522888/SRR522888.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522888/SRR522888.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522888/SRR522888.1,public,2012-07-17 23:53:40,SRR522888,ac85b7e98cbb0b5a585834bb4aae2740,run,4241572093,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522888/SRR522888.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,5677136918,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160149,L1 replicate 3 mRNA-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,27043901,945136520,SRR522011,27043901,1352195050,L1_FED_2_mRNA,,,1,Stanford University,,,,Celeg_3_FED_mRNA,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,50,SINGLE,SAMN01090422,SRS350385,1352195050,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,Celeg_3_FED_mRNA,435961986,305273380,343089574,64210,267805900,Stanford University,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2012-07-18 00:00:00,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-11/SRR522011/R63-L2-P3-GCCTAA-Sequences.txt.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-11/SRR522011/R63-L2-P3-GCCTAA-Sequences.txt.gz,,,,,,,,,public,2020-06-07 10:13:31,,f83d24dce6e7af8275724880c822ce27,fastq,1101202901,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522011/SRR522011.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522011/SRR522011.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522011/SRR522011.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522011/SRR522011.1,public,2012-07-16 19:45:48,SRR522011,836ffe1bbcb202840f032c3c092f061f,run,945138269,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522011/SRR522011.1,,,,,,,,,,,,,,,,,,,,,,1,1352195050,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160148,L1 replicate 2 mRNA-seq,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,15243931,542413430,SRR522010,15243931,762196550,Celeg_2_FED_mRNA,,,1,Stanford University,,,,Celeg_2_FED_mRNA,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,50,SINGLE,SAMN01090422,SRS350385,762196550,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,Celeg_2_FED_mRNA,257860440,167904092,189081774,1382011,145968233,Stanford University,run,gs.US,gs,run,s3.us-east-1,s3,,,,,,,public,,true,true,2012-07-18 00:00:00,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522010/SRR522010.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522010/SRR522010.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522010/SRR522010.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522010/SRR522010.1,public,2012-07-16 18:49:18,SRR522010,0c907f640bd5b9afb2aa33662a599837,run,542415177,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522010/SRR522010.1,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,1,762196550,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z SRP014427,SRX160147,L1 mRNA-seq replicate 1,6239,Caenorhabditis elegans,RNA-Seq,TRANSCRIPTOMIC,unspecified,SRS350385,C. elegans,Illumina HiSeq 2000,14429547,516477040,SRR522009,14429547,721477350,L1_FED_1_mRNA,,,1,Stanford University,,,,Celeg_FED_1_mRNA,,,,,,,,ILLUMINA,Application Read,0,Forward,SRS350385,50,SINGLE,SAMN01090422,SRS350385,721477350,,Caenorhabditis elegans,C. elegans,Caenorhabditis elegans,6239,Celeg_1_FED_mRNA,239948923,155621308,184391141,1304955,140211023,Stanford University,fastq,gs.US,gs,fastq,s3.us-east-1,s3,run,gs.US,gs,run,s3.us-east-1,s3,public,,true,true,2012-07-24 18:22:22,Use Cloud Data Delivery,-,GCP,gs://sra-pub-src-9/SRR522009/R63-L3-P3-ACATCG-Sequences.txt.gz,Use Cloud Data Delivery,-,AWS,s3://sra-pub-src-9/SRR522009/R63-L3-P3-ACATCG-Sequences.txt.gz,,,,,,,,,public,2020-06-09 06:05:26,,eafcd43edebc8929eb80025d386b4049,fastq,612472957,0,Original,,anonymous,worldwide,NCBI,https://sra-downloadb.be-md.ncbi.nlm.nih.gov/sos1/sra-pub-run-2/SRR522009/SRR522009.1,anonymous,worldwide,NCBI,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522009/SRR522009.1,aws identity,s3.us-east-1,AWS,s3://sra-pub-run-5/SRR522009/SRR522009.1,gcp identity,gs.US,GCP,gs://sra-pub-run-5/SRR522009/SRR522009.1,public,2012-07-24 18:21:47,SRR522009,6c5960720cf3667250c78c77086773ff,run,516478781,1,Primary ETL,https://sra-downloadb.st-va.ncbi.nlm.nih.gov/sos2/sra-pub-run-4/SRR522009/SRR522009.1,,,,,,,,,,,,,,,,,,,,,,1,721477350,false,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,Stanford University,SAMN01090422,BioSample,,,,,,,,,6239,Caenorhabditis elegans,PRJNA170771,,,BioProject,Caenorhabditis elegans strain:N2,PRJNA170771,BioProject,,,,Ribosome profiling and mRNA-seq of C. elegans larvae to investigate regulation of miRNA targets,Caenorhabditis elegans ribosome profiling of miRNA targets,Other,SRA055804,Stadler_Fire_2012,,Stanford University,Andrew Fire,NA,2012-07-10T15:00:00Z ================================================ FILE: tests/data/test_search/sra_uids.txt ================================================ 155791 155790 ================================================ FILE: tests/test_geoweb.py ================================================ """Tests for GEOweb""" import os import time import pandas as pd import pytest from pysradb.geoweb import GEOweb @pytest.fixture(scope="module") def geoweb_connection(): client = GEOweb() time.sleep(2) return client def test_valid_download_links(geoweb_connection): """Test if all links for a project are scraped""" links, url = geoweb_connection.get_download_links("GSE161707") assert links == ["GSE161707_RAW.tar", "filelist.txt"] def test_invalid_download_links(geoweb_connection): """Test if invalid GEO ID raises the expected error""" with pytest.raises(KeyError): links, url = geoweb_connection.get_download_links("GSE1691709") def test_file_download(geoweb_connection): """Test if file actually gets downloaded""" geoweb_connection.download( links=["GSE161707_RAW.tar", "filelist.txt"], root_url="https://ftp.ncbi.nlm.nih.gov/geo/series/GSE161nnn/GSE161707/suppl/", gse="GSE161707", out_dir="geoweb_downloads", ) assert os.path.getsize("geoweb_downloads/GSE161707/GSE161707_RAW.tar") assert os.path.getsize("geoweb_downloads/GSE161707/GSE161707_filelist.txt") ================================================ FILE: tests/test_search.py ================================================ """Tests for search.py""" import json import pandas as pd import pytest from pysradb.search import * # =========================== pytest fixtures ============================ # pytest fixtures containing simulated input/outputs for various functions # used in the search module # Search inputs are packaged in lists in the following formats so that they # can be passed to test functions easily: # Format for Sra/Ena: [verbosity, return_max, query, accession, organism, # layout, mbases, publication_date, platform, selection, source, strategy, # title, suppress_validations] # Format for Geo: [verbosity, return_max, query, accession, organism, # layout, mbases, publication_date, platform, selection, source, strategy, # title, geo_query, geo_dataset_type, geo_entry_type, suppress_validations] @pytest.fixture(scope="module") def valid_search_inputs_1(): """Basic search input tests for Sra and Ena (single inputs)""" return [ [ 0, 20, ["covid-19"], None, None, None, None, None, None, None, None, None, None, False, ], # verbosity [ 3, 20, ["covid-19"], None, None, None, None, None, None, None, None, None, None, False, ], # query [ 2, 20, None, "SRS6898940", None, None, None, None, None, None, None, None, None, False, ], # accession [ 2, 20, None, None, "Escherichia coli", None, None, None, None, None, None, None, None, False, ], # organism [ 2, 20, None, None, None, "PAIRED", None, None, None, None, None, None, None, False, ], # layout [ 2, 20, None, None, None, None, 5, None, None, None, None, None, None, False, ], # mbases [ 2, 20, None, None, None, None, None, "01-01-2019:31-12-2019", None, None, None, None, None, False, ], # pdat [ 2, 20, None, None, None, None, None, None, "ion torrent", None, None, None, None, False, ], # platform [ 2, 20, None, None, None, None, None, None, None, "random", None, None, None, False, ], # selection [ 2, 20, None, None, None, None, None, None, None, None, "genomic", None, None, False, ], # source [ 2, 20, None, None, None, None, None, None, None, None, None, "wgs", None, False, ], # strategy [ 2, 20, None, None, None, None, None, None, None, None, None, None, "Homo sapiens; RNA-Seq", False, ], # title ] @pytest.fixture(scope="module") def valid_search_inputs_2(): """More complex input tests for Sra and Ena""" return [ [ 0, 20, None, None, None, "Triple", None, None, None, None, None, None, None, True, ], # suppress_validation [ 2, 20, ["Escherichia", "coli"], "SRS6898222", "Escherichia coli", "paired", 6, "01-01-1999:31-12-2019", "ILLUMINA", "dnase", "metatranscriptomic", "mbd seq", None, False, ], [ 1, 2, [], None, None, "single", "5", "31-12-2019", "Nanopore", "MBD2 protein methyl-CpG binding domain", "genomic single cell", "amplicon selection", None, False, ], [ 0, 200000, None, None, None, "Paired", None, None, "complete genomics", "Inverse rRNA", "TRANSCRIPTOMIC", "hi-c", None, False, ], [ 3, 1, None, None, None, "SINGLE", None, None, "ls454", "oligo-dt", "transcriptomic single-cell", "miRNA", None, False, ], [ 2, 20, None, None, None, None, None, None, "smrt", "cDNA_oligo_dT", "metagenomic", "MBD", None, False, ], [ 2, 20, None, None, None, None, None, None, "Pacbio", "pcr", "others", "EST", None, False, ], ] @pytest.fixture(scope="module") def valid_search_inputs_geo(): """Basic search input tests for Geo""" return [ [ 2, 20, "query", None, None, None, None, None, None, None, None, None, None, None, None, None, False, ], [ 2, 20, None, None, None, None, None, None, None, None, None, None, None, "GEO query", None, None, False, ], [ 2, 20, ["query"], None, None, None, None, None, None, None, None, None, None, "GEO query", None, None, False, ], [ 2, 20, None, "SRS6898940", None, None, None, None, None, None, None, None, None, "GEO query", None, None, False, ], [ 2, 20, None, None, "Escherichia coli", None, None, None, None, None, None, None, None, None, None, None, False, ], # organism [ 2, 20, None, None, None, None, None, "01-01-2019:31-12-2019", None, None, None, None, None, False, ], # pdat [ 2, 20, None, None, None, None, None, None, None, None, None, None, None, None, "GEO dataset type", None, False, ], # Geo dataset type [ 2, 20, None, None, None, None, None, None, None, None, None, None, None, None, None, "GEO entry type", False, ], ] @pytest.fixture(scope="module") def empty_search_inputs(): return [ [], [ 2, 20, None, None, None, None, None, None, None, None, None, None, None, False, ], [2, 20, [], [], [], [], [], [], [], [], [], [], []], ] @pytest.fixture(scope="module") def empty_search_inputs_geo(): return [ [], [ 2, 20, None, None, None, None, None, None, None, None, None, None, None, None, None, None, False, ], [2, 20, [], [], [], [], [], [], [], [], [], [], []], ] @pytest.fixture(scope="module") def invalid_search_inputs(): """Invalid search input tests for QuerySearch""" return [ [ 4, 20, ["covid-19"], None, None, None, None, None, None, None, None, None, None, False, ], # verbosity [ 3, 0, ["covid-19"], None, None, None, None, None, None, None, None, None, None, False, ], # return_max [ 2, 20, None, None, None, "X", None, None, None, None, None, None, None, False, ], # layout [ 2, 20, None, None, None, None, "Charmander", None, None, None, None, None, None, False, ], # mbases [ 2, 20, None, None, None, None, -1, None, None, None, None, None, None, False, ], # mbases [ 2, 20, None, None, None, None, None, "31-31-2019", None, None, None, None, None, False, ], # pdat [ 2, 20, None, None, None, None, None, None, "pacbio nanopore", None, None, None, None, False, ], # platform [ 2, 20, None, None, None, None, None, None, "no such platform", None, None, None, None, False, ], # platform [ 2, 20, None, None, None, None, None, None, None, "polyA hybrid", None, None, None, False, ], # selection [ 2, 20, None, None, None, None, None, None, None, "no such selection", None, None, None, False, ], # selection [ 2, 20, None, None, None, None, None, None, None, None, "genomic transcriptomic", None, None, False, ], # source [ 2, 20, None, None, None, None, None, None, None, None, "metagenomic viral rna ", None, None, False, ], # source [ 2, 20, None, None, None, None, None, None, None, None, None, "wgs wga", None, False, ], # strategy [ 2, 20, None, None, None, None, None, None, None, None, None, "Bulbasaur", None, False, ], # strategy ] @pytest.fixture(scope="module") def sra_response_xml_1(): return "./tests/data/test_search/sra_test.xml" @pytest.fixture(scope="module") def sra_formatted_responses_1(): return [ pd.read_csv( "./tests/data/test_search/sra_test_verbosity_0.csv", dtype=object, keep_default_na=False, ), pd.read_csv( "./tests/data/test_search/sra_test_verbosity_1.csv", dtype=object, keep_default_na=False, ), pd.read_csv( "./tests/data/test_search/sra_test_verbosity_2.csv", dtype=object, keep_default_na=False, ), pd.read_csv( "./tests/data/test_search/sra_test_verbosity_3.csv", dtype=object, keep_default_na=False, ), ] @pytest.fixture(scope="module") def sra_response_xml_2(): return "./tests/data/test_search/sra_test_ERS3331676.xml" @pytest.fixture(scope="module") def sra_formatted_responses_2(): return [ pd.read_csv( "./tests/data/test_search/sra_test_2_verbosity_0.csv", dtype=object, keep_default_na=False, ), pd.read_csv( "./tests/data/test_search/sra_test_2_verbosity_1.csv", dtype=object, keep_default_na=False, ), pd.read_csv( "./tests/data/test_search/sra_test_2_verbosity_2.csv", dtype=object, keep_default_na=False, ), pd.read_csv( "./tests/data/test_search/sra_test_2_verbosity_3.csv", dtype=object, keep_default_na=False, ), ] @pytest.fixture(scope="module") def sra_uids(): with open("./tests/data/test_search/sra_uids.txt", "r") as f: uids = f.read().splitlines() return uids @pytest.fixture(scope="module") def ena_responses_json(): data = [] for i in range(4): with open(f"./tests/data/test_search/ena_test_verbosity_{i}.json") as f: data.append(json.load(f)) return data @pytest.fixture(scope="module") def ena_formatted_responses(): return [ pd.read_csv( "./tests/data/test_search/ena_test_verbosity_0.csv", dtype=object, keep_default_na=False, ), pd.read_csv( "./tests/data/test_search/ena_test_verbosity_1.csv", dtype=object, keep_default_na=False, ), pd.read_csv( "./tests/data/test_search/ena_test_verbosity_2.csv", dtype=object, keep_default_na=False, ), pd.read_csv( "./tests/data/test_search/ena_test_verbosity_3.csv", dtype=object, keep_default_na=False, ), ] # ============================= General Tests ============================= def missing_query_test(empty_search_inputs): for empty_search_input in empty_search_inputs: with pytest.raises(MissingQueryException): QuerySearch(*empty_search_input) def test_invalid_search_query(invalid_search_inputs): error_messages = [ "Incorrect verbosity format", "Incorrect return_max format", "Incorrect layout field format", "Incorrect mbases format", "Incorrect mbases format", "Incorrect publication date format", "Multiple potential matches have been identified for pacbio nanopore", "Incorrect platform", "Multiple potential matches have been identified for polyA hybrid", "Incorrect selection", "Incorrect source", "Multiple potential matches have been identified for metagenomic viral rna", "Multiple potential matches have been identified for wgs wga", "Incorrect strategy", ] for i in range(len(invalid_search_inputs)): with pytest.raises(IncorrectFieldException) as e: QuerySearch(*invalid_search_inputs[i]) assert error_messages[i] in str(e.value) # ======================== SraSearch component tests ====================== def test_sra_search_1(): instance = SraSearch( 3, 1000, query="ribosome profiling", publication_date="01-10-2012:01-01-2013" ) instance.search() found_accessions = set(instance.get_df()["experiment_accession"]) with open("./tests/data/test_search/sra_search_test1.txt", "r") as f: expected_accessions = f.read().splitlines() assert found_accessions == set(expected_accessions) def test_sra_uids(sra_uids): instance = SraSearch( 3, 1000, query="ribosome profiling", publication_date="01-10-2012:01-01-2013" ) instance.search() assert instance.get_uids() == sra_uids def test_valid_search_query_1_sra(valid_search_inputs_1): expected_query = [ "covid-19", "covid-19", "SRS6898940[Accession]", "Escherichia coli[Organism]", "PAIRED[Layout]", "5[Mbases]", "2019/01/01:2019/12/31[PDAT]", "ION_TORRENT[Platform]", "RANDOM[Selection]", "GENOMIC[Source]", "WGS[Strategy]", "Homo sapiens; RNA-Seq[Title]", ] for i in range(len(valid_search_inputs_1)): assert ( SraSearch(*valid_search_inputs_1[i])._format_query_string() == expected_query[i] ) def test_valid_search_query_2_sra(valid_search_inputs_2): expected_query = [ "Triple[Layout]", "Escherichia coli AND SRS6898222[Accession] AND Escherichia coli[Organism] AND paired[Layout] AND " "6[Mbases] AND 1999/01/01:2019/12/31[PDAT] AND ILLUMINA[Platform] AND DNase[Selection] AND " "METATRANSCRIPTOMIC[Source] AND MBD-Seq[Strategy]", "single[Layout] AND 5[Mbases] AND 2019/12/31[PDAT] AND OXFORD_NANOPORE[Platform] AND " "MBD2 protein methyl-CpG binding domain[Selection] AND GENOMIC SINGLE CELL[Source] AND AMPLICON[Strategy]", "Paired[Layout] AND COMPLETE_GENOMICS[Platform] AND Inverse rRNA[Selection] AND TRANSCRIPTOMIC[Source] AND " "Hi-C[Strategy]", "SINGLE[Layout] AND LS454[Platform] AND Oligo-dT[Selection] AND TRANSCRIPTOMIC SINGLE CELL[Source] AND " "miRNA-Seq[Strategy]", "PACBIO_SMRT[Platform] AND cDNA_oligo_dT.*[Selection] AND METAGENOMIC[Source] AND MBD-Seq[Strategy]", "PACBIO_SMRT[Platform] AND PCR[Selection] AND OTHER[Source] AND EST[Strategy]", ] for i in range(len(valid_search_inputs_2)): assert ( SraSearch(*valid_search_inputs_2[i])._format_query_string() == expected_query[i] ) def test_sra_search_format_request(): assert SraSearch( 0, 1000, query="covid-19", )._format_request() == { "db": "sra", "term": "covid-19", "retmode": "json", "retmax": 1000, } def test_sra_search_format_result_1(sra_response_xml_1, sra_formatted_responses_1): for i in range(2, 4): query = SraSearch( i, 1000, query="ribosome profiling", platform="illumina", organism="Caenorhabditis elegans", ) query._format_response(sra_response_xml_1) query._format_result() col0 = [ c for c in query.get_df().columns if ("run" not in c.lower() and "sample" not in c.lower()) ] col1 = [ c for c in sra_formatted_responses_1[i].columns if ("run" not in c.lower() and "sample" not in c.lower()) ] expected_df = ( sra_formatted_responses_1[i][col1].fillna("N/A").replace("", "N/A") ) actual_df = query.get_df()[col0].fillna("N/A").replace("", "N/A") pd.testing.assert_frame_equal(expected_df, actual_df, check_dtype=False) def test_sra_search_format_result_2(sra_response_xml_2, sra_formatted_responses_2): for i in range(4): query = SraSearch(i, 1000, accession="ERS3331676") query._format_response(sra_response_xml_2) query._format_result() col0 = [ c for c in query.get_df().columns if ("run" not in c.lower() and "sample" not in c.lower()) ] col1 = [ c for c in sra_formatted_responses_2[i].columns if ("run" not in c.lower() and "sample" not in c.lower()) ] expected_df = ( sra_formatted_responses_2[i][col1].fillna("N/A").replace("", "N/A") ) actual_df = query.get_df()[col0].fillna("N/A").replace("", "N/A") pd.testing.assert_frame_equal(expected_df, actual_df, check_dtype=False) # ====================== EnaSearch component tests ======================== def _test_ena_search_1(): instance = EnaSearch( 0, 1000, platform="pacbio", publication_date="01-10-2012:01-01-2013" ) instance.search() df = instance.get_df()["run_accession"].to_list() with open("./tests/data/test_search/ena_search_test1.txt", "r") as f: expected_accessions = f.read().splitlines() for accession in df: assert accession in expected_accessions def _test_ena_search_2(capsys): EnaSearch(0, 1000, query="hehehuhuhaha").search() out, err = capsys.readouterr() assert "No results found for the following search query:" in out assert err == "" def _test_ena_search_3(capsys): with pytest.raises(SystemExit) as e: EnaSearch(0, 1000, selection='"Pikachu', suppress_validation=True).search() assert "HTTPError: This is likely caused by an invalid search query:" in str( e.value ) def _test_valid_search_query_1_ena(valid_search_inputs_1): expected_query = [ '(experiment_title="*covid-19*" OR study_accession="COVID-19" OR secondary_study_accession="COVID-19" OR' ' sample_accession="COVID-19" OR secondary_sample_accession="COVID-19" OR experiment_accession="COVID-19" OR' ' submission_accession="COVID-19" OR run_accession="COVID-19")', '(experiment_title="*covid-19*" OR study_accession="COVID-19" OR secondary_study_accession="COVID-19" OR' ' sample_accession="COVID-19" OR secondary_sample_accession="COVID-19" OR experiment_accession="COVID-19" OR' ' submission_accession="COVID-19" OR run_accession="COVID-19")', '(study_accession="SRS6898940" OR secondary_study_accession="SRS6898940" OR sample_accession="SRS6898940" OR' ' secondary_sample_accession="SRS6898940" OR experiment_accession="SRS6898940" OR' ' submission_accession="SRS6898940" OR run_accession="SRS6898940")', "tax_eq(562)", 'library_layout="PAIRED"', "base_count>=4500000 AND base_count<5500000", "first_created>=2019-01-01 AND first_created<=2019-12-31", 'instrument_platform="ION_TORRENT"', 'library_selection="RANDOM"', 'library_source="GENOMIC"', 'library_strategy="WGS"', 'experiment_title="*Homo sapiens; RNA-Seq*"', ] for i in range(len(valid_search_inputs_1)): assert ( EnaSearch(*valid_search_inputs_1[i])._format_query_string() == expected_query[i] ) def _test_valid_search_query_2_ena(valid_search_inputs_2): expected_query = [ 'library_layout="TRIPLE"', '(experiment_title="*Escherichia coli*") AND (study_accession="SRS6898222" OR ' 'secondary_study_accession="SRS6898222" OR sample_accession="SRS6898222" OR ' 'secondary_sample_accession="SRS6898222" OR experiment_accession="SRS6898222" OR ' 'submission_accession="SRS6898222" OR run_accession="SRS6898222") AND tax_eq(562) AND library_layout="PAIRED" ' "AND base_count>=5500000 AND base_count<6500000 AND first_created>=1999-01-01 AND " 'first_created<=2019-12-31 AND instrument_platform="ILLUMINA" AND library_selection="DNase" AND ' 'library_source="METATRANSCRIPTOMIC" AND library_strategy="MBD-Seq"', 'library_layout="SINGLE" AND base_count>=4500000 AND base_count<5500000 AND first_created=2019-12-31 AND ' 'instrument_platform="OXFORD_NANOPORE" AND library_selection="MBD2 protein methyl-CpG binding domain" AND ' 'library_source="GENOMIC SINGLE CELL" AND library_strategy="AMPLICON"', 'library_layout="PAIRED" AND instrument_platform="COMPLETE_GENOMICS" AND library_selection="Inverse rRNA" AND ' 'library_source="TRANSCRIPTOMIC" AND library_strategy="Hi-C"', 'library_layout="SINGLE" AND instrument_platform="LS454" AND library_selection="Oligo-dT" AND ' 'library_source="TRANSCRIPTOMIC SINGLE CELL" AND library_strategy="miRNA-Seq"', 'instrument_platform="PACBIO_SMRT" AND library_selection="cDNA_oligo_dT.*" AND ' 'library_source="METAGENOMIC" AND library_strategy="MBD-Seq"', 'instrument_platform="PACBIO_SMRT" AND library_selection="PCR" AND library_source="OTHER" AND ' 'library_strategy="EST"', ] for i in range(len(valid_search_inputs_2)): assert ( EnaSearch(*valid_search_inputs_2[i])._format_query_string() == expected_query[i] ) def test_ena_search_format_request(): query_string = ( '(experiment_title="*covid-19*" OR study_accession="COVID-19" OR ' 'secondary_study_accession="COVID-19" OR sample_accession="COVID-19" OR ' 'secondary_sample_accession="COVID-19" OR experiment_accession="COVID-19" OR ' 'submission_accession="COVID-19" OR run_accession="COVID-19")' ) assert EnaSearch(2, 20, "covid-19")._format_request() == { "query": query_string, "result": "read_run", "format": "json", "limit": 20, "fields": "study_accession,experiment_accession,experiment_title,description,tax_id,scientific_name," "library_strategy,library_source,library_selection,sample_accession,sample_title," "instrument_model,run_accession,read_count,base_count,first_public,library_layout,instrument_platform", } def test_ena_search_format_result(ena_responses_json, ena_formatted_responses): for i in range(4): query = EnaSearch( i, 1000, query="ribosome profiling", platform="illumina", organism="Caenorhabditis elegans", ) query._format_result(ena_responses_json[i]) expected_df = ena_formatted_responses[i].fillna("N/A").replace("", "N/A") actual_df = query.get_df().fillna("N/A").replace("", "N/A") pd.testing.assert_frame_equal(expected_df, actual_df, check_dtype=False) # ====================== GeoSearch component tests ======================== def missing_query_test_geo(empty_search_inputs_geo): for empty_search_input in empty_search_inputs_geo: with pytest.raises(MissingQueryException): QuerySearch(*empty_search_input) def test_geo_search_1(): instance = GeoSearch(3, 1000, geo_query="human") instance.search() df = instance.get_df() assert not df.empty experiment_accessions = instance.get_df()["experiment_accession"].to_list() assert len(experiment_accessions) > 10 # with open("./tests/data/test_search/geo_search_test1.txt", "r") as f: # expected_accessions = f.read().splitlines() # assert len(set(expected_accessions).intersection(df)) > 1 def test_valid_search_query_geo(valid_search_inputs_geo): expected_sra_query = [ "query AND sra gds[Filter]", "", "query AND sra gds[Filter]", "sra gds[Filter] AND SRS6898940[Accession]", "sra gds[Filter] AND Escherichia coli[Organism]", "sra gds[Filter] AND 2019/01/01:2019/12/31[PDAT]", "", "", ] expected_geo_query = [ "", "GEO query AND gds sra[Filter]", "GEO query AND gds sra[Filter]", "GEO query AND gds sra[Filter]", "gds sra[Filter] AND Escherichia coli[Organism]", "gds sra[Filter] AND 2019/01/01:2019/12/31[PDAT]", "gds sra[Filter] AND GEO dataset type[DataSet Type]", "gds sra[Filter] AND GEO entry type[Entry Type]", ] for i in range(len(valid_search_inputs_geo)): instance = GeoSearch(*valid_search_inputs_geo[i]) assert instance._format_query_string() == expected_sra_query[i] assert instance._format_geo_query_string() == expected_geo_query[i] def test_geo_search_format_request(): assert GeoSearch( 0, 1000, query="covid-19", )._format_request() == { "db": "sra", "term": "covid-19 AND sra gds[Filter]", "retmode": "json", "retmax": 1000, } def test_geo_info(): assert type(GeoSearch.info()) == str and GeoSearch.info().startswith( "General Information:" ) ================================================ FILE: tests/test_sraweb.py ================================================ """Tests for SRAweb""" import time import pandas as pd import pytest from pysradb.sraweb import SRAweb @pytest.fixture(scope="module") def sraweb_connection(): client = SRAweb() time.sleep(2) return client def test_sra_metadata(sraweb_connection): """Test if metadata has right number of entries""" df = sraweb_connection.sra_metadata("SRP016501") assert df.shape[0] == 134 def test_sra_metadata_missing_orgname(sraweb_connection): """Test if metadata has right number of entries""" df = sraweb_connection.sra_metadata("ERP000171") # See: https://github.com/saketkc/pysradb/issues/46#issuecomment-657268760 assert sum(pd.isna(df.organism_name.tolist())) > 0 def test_sra_metadata_multiple(sraweb_connection): """Test if metadata has right number of entries""" df = sraweb_connection.sra_metadata(["SRP016501", "SRP096025", "SRP103009"]) assert list(sorted(df.study_accession.unique())) == [ "SRP016501", "SRP096025", "SRP103009", ] def test_sra_metadata_multiple_detailed(sraweb_connection): """Test if metadata has right number of entries""" df = sraweb_connection.sra_metadata(["SRP002605", "SRP098789"], detailed=True) columns = ["treatment time", "library type", "transfection", "time"] assert len(set(columns).intersection(set(df.columns))) == 4 ftp_cols = [ "ena_fastq_http", "ena_fastq_http_1", "ena_fastq_http_2", "ena_fastq_ftp", "ena_fastq_ftp_1", "ena_fastq_ftp_2", ] assert len(set(ftp_cols).intersection(set(df.columns))) == 6 def test_tissue_column(sraweb_connection): """Test if tissue column exists""" df = sraweb_connection.sra_metadata("SRP096025", detailed="True") assert list(df["tissue"]) == ["Kidney"] * 4 def test_metadata_exp_accession(sraweb_connection): """Test if experiment_accession column is correct""" df = sraweb_connection.sra_metadata("SRP103009", detailed="True") assert "SRX2705123" in list(df["experiment_accession"]) def test_fetch_gds_results(sraweb_connection): """Test if fetch_gds_result returns correct values""" df = sraweb_connection.fetch_gds_results("GSE34438") assert df["accession"][1] == "GSM849112" def test_srp_to_gse(sraweb_connection): """Test if srp is converted to gse correctly""" df = sraweb_connection.srp_to_gse("SRP009836") assert df["study_alias"][0] == "GSE34438" def test_srp_to_srr(sraweb_connection): """Test if srp is converted to srr correctly""" df = sraweb_connection.srp_to_srr("SRP002605", detailed=True) assert df["run_accession"].tolist()[:5] == [ "SRR057511", "SRR057512", "SRR057513", "SRR057514", "SRR057515", ] def test_srp_to_srs(sraweb_connection): """Test if srp is converted to srs correctly""" df = sraweb_connection.srp_to_srs("SRP014542") assert sorted(list(df["sample_accession"])) == [ "SRS351513", "SRS351514", "SRS351515", "SRS351516", "SRS351517", "SRS351518", ] def test_srp_to_srx(sraweb_connection): """Test if srp is converted to srx correctly""" df = sraweb_connection.srp_to_srx("SRP044932") assert list(df["experiment_accession"]) == ["SRX663253", "SRX663254"] def test_gse_to_gsm(sraweb_connection): """Test if gse is converted to gsm correctly""" df = sraweb_connection.gse_to_gsm("GSE56924", detailed=False) assert df.shape[0] == 96 def test_gse_to_gsm2(sraweb_connection): """Test for gse to gsm""" df = sraweb_connection.gse_to_gsm("GSE200028", detailed=False) assert df.shape[0] == 15 def test_gse_to_gsm1(sraweb_connection): """Test if gse_to_gsm works without passing `detailed` parameter""" df = sraweb_connection.gse_to_gsm("GSE63858") assert list(sorted(df["experiment_alias"])) == ["GSM1558530", "GSM1558531"] def test_gse_to_srp(sraweb_connection): """Test if gse is converted to srp correctly""" df = sraweb_connection.gse_to_srp("GSE63858") assert df["study_accession"].tolist()[0] == "SRP050548" def test_gse_to_srp2(sraweb_connection): """Test if gse is converted to srp correctly""" df = sraweb_connection.gse_to_srp(["GSE168880", "GSE209835"]) assert df["study_accession"].tolist()[0] == "SRP310566" assert df["study_accession"].tolist()[1] == "SRP388275" def test_gse_to_srp_with_nan_sra(sraweb_connection): """Test gse_to_srp when GSE has NaN SRA field but GSM entries have SRX values GSE192742 has no direct SRA link in the GSE entry, but GSM entries contain SRX accessions (like SRX13549307). Expected: SRP352825 (and possibly SRP352824 depending on GSM distribution) """ df = sraweb_connection.gse_to_srp("GSE192742") assert not df.empty assert "GSE192742" in df["study_alias"].tolist() srps = df["study_accession"].tolist() assert "SRP352825" in srps assert all(pd.notna(srps)) def test_gsm_to_srp(sraweb_connection): """Test if gsm is converted to srp correctly""" df = sraweb_connection.gsm_to_srp("GSM1371490") assert df["study_accession"].tolist()[0] == "SRP041298" def test_gsm_to_gse(sraweb_connection): """Test if gsm is converted to gse correctly""" df = sraweb_connection.gsm_to_gse("GSM1371490") assert df["study_alias"].tolist()[0] == "GSE56924" def test_gsm_to_gse_multiple_gses(sraweb_connection): """Test GSM that maps to multiple GSE accessions (GSM7430904 -> GSE233587, GSE234305)""" df = sraweb_connection.gsm_to_gse("GSM7430904") assert isinstance(df, pd.DataFrame) assert not df.empty assert "study_alias" in df.columns assert "study_accession" in df.columns study_aliases = df["study_alias"].tolist() assert len(study_aliases) >= 2 study_aliases = df["study_alias"].tolist() expected_gses = {"GSE233587", "GSE234305"} actual_gses = set(study_aliases) assert expected_gses.issubset( actual_gses ), f"Expected {expected_gses} to be subset of {actual_gses}" assert "GSE234305" in study_aliases def test_gsm_to_srr(sraweb_connection): """Test if gsm is converted to srr correctly""" df = sraweb_connection.gsm_to_srr("GSM1371489") assert df["run_accession"].tolist()[0] == "SRR1257271" def test_gsm_to_srs(sraweb_connection): """Test if gsm is converted to srs correctly""" df = sraweb_connection.gsm_to_srs("GSM1371469") assert df["sample_accession"].tolist()[0] == "SRS594838" def test_gsm_to_srx(sraweb_connection): """Test if gsm is converted to srx correctly""" df = sraweb_connection.gsm_to_srx("GSM1371454") assert list(df["experiment_accession"]) == ["SRX522468"] def test_srr_to_gsm(sraweb_connection): df = sraweb_connection.srr_to_gsm("SRR057515") assert df["experiment_alias"].tolist()[0] == "GSM546921" def test_srr_to_srp(sraweb_connection): """Test if srr is converted to srp correctly""" df = sraweb_connection.srr_to_srp("SRR057511", detailed=False) assert list(df["study_accession"]) == ["SRP002605"] def test_srr_to_srp1(sraweb_connection): """Test if srr_to_srp works without passing the `detailed` parameter""" df = sraweb_connection.srr_to_srp("SRR057515") assert list(df["study_accession"]) == ["SRP002605"] def test_srr_to_srs(sraweb_connection): """Test if srr is converted to srs correctly""" df = sraweb_connection.srr_to_srs("SRR057513") assert list(df["sample_accession"]) == ["SRS079386"] def test_srr_to_srx(sraweb_connection): """Test if srr is converted to srx correctly""" df = sraweb_connection.srr_to_srx("SRR057514") assert list(df["experiment_accession"]) == ["SRX021967"] def test_srs_to_gsm(sraweb_connection): """Test if srs is converted to gsm correctly""" df = sraweb_connection.srs_to_gsm("SRS079386") assert df["experiment_alias"][0] == "GSM546921" def test_srs_to_srx(sraweb_connection): """Test if srs is converted to srx correctly""" df = sraweb_connection.srs_to_srx("SRS594838") assert list(df["experiment_accession"]) == ["SRX522483"] def test_srx_to_gsm(sraweb_connection): """Test if srx is converted to gsm correctly""" df = sraweb_connection.srx_to_gsm("SRX663253") assert list(df["experiment_alias"]) == ["GSM1446832"] def test_srx_to_srp(sraweb_connection): """Test if srx is converted to srp correctly""" df = sraweb_connection.srx_to_srp("SRX663254") assert list(df["study_accession"]) == ["SRP044932"] def test_srx_to_srr(sraweb_connection): """Test if srx is converted to srr correctly""" df = sraweb_connection.srx_to_srr("SRX2705123") assert list(df["run_accession"]) == ["SRR5413172"] def test_srx_to_srr1(sraweb_connection): """Test if srx is converted to srr correctly, including multiple srrs""" df = sraweb_connection.srx_to_srr("SRX8998846") assert list(df["run_accession"]) == ["SRR12508064", "SRR12508065"] def test_srx_to_srs(sraweb_connection): """Test if srx is converted to srs correctly""" df = sraweb_connection.srx_to_srs("SRX663253") assert list(df["sample_accession"]) == ["SRS668126"] # This is currently failing def _test_xmlns_id(sraweb_connection): df = sraweb_connection.sra_metadata(["GSM1013144", "GSM2520660"]) library_layouts = list(df["library_layout"]) assert library_layouts[0] == "PAIRED" assert library_layouts[1] == "SINGLE" def test_GCP_url(sraweb_connection): df = sraweb_connection.sra_metadata(["SRP002605"], detailed=True) assert df["gcp_url"].tolist()[-1].startswith("gs:") def test_GCP_url2(sraweb_connection): df = sraweb_connection.sra_metadata(["DRR138929"], detailed=True) assert df["gcp_url"].tolist()[-1].startswith("gs:") def test_gse_to_srp3(sraweb_connection): # https://github.com/saketkc/pysradb/issues/190 df = sraweb_connection.gse_to_srp(["GSE89545"]) assert df["study_accession"].tolist()[0] == "SRP093251" def test_gse_to_srp_multiple_srps(sraweb_connection): """Test GSE that maps to multiple SRP accessions (GSE234305 -> SRP411077, SRP439808)""" df = sraweb_connection.gse_to_srp("GSE234305") assert isinstance(df, pd.DataFrame) assert not df.empty assert "study_alias" in df.columns assert "study_accession" in df.columns # Check that GSE234305 maps to the expected SRPs study_aliases = df["study_alias"].tolist() study_accessions = df["study_accession"].tolist() assert "GSE234305" in study_aliases # Should map to multiple SRPs assert len(set(study_accessions)) >= 2 # Check for the known SRP accessions expected_srps = {"SRP411077", "SRP439808"} actual_srps = set(study_accessions) assert expected_srps.issubset( actual_srps ), f"Expected {expected_srps} to be subset of {actual_srps}" def test_geo_metadata_for_gse_without_srp(sraweb_connection): """GSE286254 should return GEO metadata even without SRP links""" df = sraweb_connection.geo_metadata("GSE286254") assert isinstance(df, pd.DataFrame) assert not df.empty assert "GSE286254" in df["study_accession"].unique() assert "GSM8721777" in df["sample_accession"].values def test_geo_metadata_with_sample_attributes(sraweb_connection): """Ensure sample_attribute flag adds sample summaries""" df = sraweb_connection.geo_metadata("GSE286254", sample_attribute=True) assert "sample_summary" in df.columns assert df["sample_summary"].notna().any() def test_geo_metadata_covid19_characteristics(sraweb_connection): """Test GSE155673 COVID-19 metadata with disease_status and custom characteristics""" df = sraweb_connection.geo_metadata("GSE155673", detailed=True) # Find the specific sample GSM4712885 sample = df[df["sample_accession"] == "GSM4712885"] assert not sample.empty, "Sample GSM4712885 not found" # Verify disease field captures disease_status disease_value = sample["disease"].iloc[0] assert pd.notna(disease_value), "Disease field should not be NA" assert ( "COVID-19" in str(disease_value).upper() or "COVID" in str(disease_value).upper() ), f"Disease should contain COVID-19, got: {disease_value}" # Verify custom characteristics are captured assert "disease_severity" in df.columns, "disease_severity column should exist" assert ( "days_since_symptom_onset" in df.columns ), "days_since_symptom_onset column should exist" # Verify values for GSM4712885 sample_severity = sample["disease_severity"].iloc[0] assert pd.notna( sample_severity ), "disease_severity should not be NA for COVID sample" assert "Severe" in str( sample_severity ), f"Expected 'Severe', got: {sample_severity}" days_onset = sample["days_since_symptom_onset"].iloc[0] assert pd.notna(days_onset), "days_since_symptom_onset should not be NA" assert str(days_onset) == "15", f"Expected '15', got: {days_onset}" # Verify standard fields assert sample["sex"].iloc[0] == "F", "Sex should be F" assert str(sample["age"].iloc[0]) == "75", "Age should be 75" assert sample["cell_type"].iloc[0] == "PBMC", "Cell type should be PBMC" # Verify comprehensive SOFT field capture (no filtering) # These fields should be present when detailed=True expected_soft_fields = [ "sample_instrument_model", "sample_library_strategy", "sample_library_source", "sample_organism_ch1", "sample_taxid_ch1", "sample_molecule_ch1", "sample_contact_name", "sample_contact_institute", "sample_data_processing", "sample_platform_id", ] for field in expected_soft_fields: assert ( field in df.columns ), f"SOFT field '{field}' should be captured in detailed mode" assert pd.notna( sample[field].iloc[0] ), f"SOFT field '{field}' should have a value" # Verify specific values for comprehensive check assert "Illumina" in str( sample["sample_instrument_model"].iloc[0] ), "Should capture instrument model" assert ( sample["sample_library_strategy"].iloc[0] == "RNA-Seq" ), "Should capture library strategy" assert ( str(sample["sample_taxid_ch1"].iloc[0]) == "9606" ), "Should capture taxid (human)" def test_fetch_bioproject_pmids(sraweb_connection): """Test fetching PMIDs for BioProject accessions""" # Use a known BioProject that should have publications result = sraweb_connection.fetch_bioproject_pmids("PRJNA257197") assert isinstance(result, dict) assert "PRJNA257197" in result def test_fetch_bioproject_pmids_multiple(sraweb_connection): """Test fetching PMIDs for multiple BioProjects""" bioprojects = ["PRJNA257197", "PRJNA200000"] # Mix of real and potentially missing result = sraweb_connection.fetch_bioproject_pmids(bioprojects) assert isinstance(result, dict) assert len(result) == 2 for bp in bioprojects: assert bp in result assert isinstance(result[bp], list) # Check that PRJNA200000 returns an empty list (no PMIDs) assert result["PRJNA200000"] == [] def test_search_pmc_by_bioproject(sraweb_connection): """Test PMC search fallback for bioproject IDs""" # PRJEB39301 doesn't have PMIDs in bioproject XML but is cited in PMC (PMC8379757) pmids = sraweb_connection._search_pmc_by_bioproject("PRJEB39301") assert isinstance(pmids, list) assert len(pmids) > 0 # Should find PMID 34419158 (from PMC8379757) assert "34419158" in pmids def test_fetch_bioproject_pmids_with_pmc_fallback(sraweb_connection): """Test that fetch_bioproject_pmids falls back to PMC search when XML has no PMIDs""" # PRJEB39301 - bioproject XML has no publications, but PMC search should find them result = sraweb_connection.fetch_bioproject_pmids("PRJEB39301") assert isinstance(result, dict) assert "PRJEB39301" in result assert isinstance(result["PRJEB39301"], list) # Should have found PMID via PMC fallback assert len(result["PRJEB39301"]) > 0 assert "34419158" in result["PRJEB39301"] def test_srp_to_pmid_with_pmc_fallback(sraweb_connection): """Test srp_to_pmid with bioproject that uses PMC fallback""" # ERP122802 uses PRJEB39301 which requires PMC fallback to find PMID df = sraweb_connection.srp_to_pmid("ERP122802") assert isinstance(df, pd.DataFrame) assert "srp_accession" in df.columns assert "bioproject" in df.columns assert "pmid" in df.columns # Check that we got a result for ERP122802 assert len(df) > 0 erp_row = df[df["srp_accession"] == "ERP122802"] assert len(erp_row) > 0 # Should have PMID 34419158 via PMC fallback assert erp_row.iloc[0]["pmid"] == "34419158" def test_sra_to_pmid(sraweb_connection): """Test SRA to PMID functionality (backward compatibility)""" df = sraweb_connection.sra_to_pmid("SRP002605") assert isinstance(df, pd.DataFrame) required_columns = {"srp_accession", "bioproject", "pmid"} assert required_columns.issubset(set(df.columns)) def test_srp_to_pmid(sraweb_connection): """Test SRP to PMID main method""" df = sraweb_connection.srp_to_pmid("SRP002605") assert isinstance(df, pd.DataFrame) assert "srp_accession" in df.columns assert "pmid" in df.columns def test_srr_to_pmid(sraweb_connection): """Test SRR to PMID convenience method""" df = sraweb_connection.srr_to_pmid("SRR057511") assert isinstance(df, pd.DataFrame) assert "srp_accession" in df.columns assert "pmid" in df.columns def test_sra_to_pmid_multiple(sraweb_connection): """Test SRA to PMID with multiple accessions (backward compatibility)""" df = sraweb_connection.sra_to_pmid(["SRP002605", "SRP016501"]) assert isinstance(df, pd.DataFrame) assert len(df) >= 2 # Should have at least one row per input SRA def test_srp_to_pmid_multiple(sraweb_connection): """Test SRP to PMID with multiple accessions""" df = sraweb_connection.srp_to_pmid(["SRP002605", "SRP016501"]) assert isinstance(df, pd.DataFrame) assert len(df) >= 2 # Should have at least one row per input SRP assert "srp_accession" in df.columns assert "pmid" in df.columns def test_gse_to_pmid(sraweb_connection): """Test GSE to PMID functionality""" df = sraweb_connection.gse_to_pmid("GSE253406") assert isinstance(df, pd.DataFrame) assert not df.empty required_columns = {"gse_accession", "pmid"} assert required_columns.issubset(df.columns) def test_gse_to_pmid_multiple(sraweb_connection): """Test GSE to PMID with multiple accessions""" df = sraweb_connection.gse_to_pmid(["GSE253406", "GSE168776"]) assert isinstance(df, pd.DataFrame) assert len(df) >= 2 # Should have one row per input GSE assert "gse_accession" in df.columns assert "pmid" in df.columns def test_pmid_to_pmc(sraweb_connection): """Test PMID to PMC conversion""" mapping = sraweb_connection.pmid_to_pmc("27373336") assert isinstance(mapping, dict) assert "27373336" in mapping def test_pmid_to_pmc_multiple(sraweb_connection): """Test PMID to PMC with multiple PMIDs""" mapping = sraweb_connection.pmid_to_pmc(["27373336", "39528918"]) assert isinstance(mapping, dict) assert len(mapping) == 2 def test_extract_identifiers_from_text(sraweb_connection): """Test extraction of identifiers from text""" test_text = "This study uses data from GSE12345 and SRP067890. The BioProject is PRJNA123456 with samples SRR1234567." identifiers = sraweb_connection.extract_identifiers_from_text(test_text) assert isinstance(identifiers, dict) assert "GSE12345" in identifiers["gse"] assert "SRP067890" in identifiers["srp"] assert "PRJNA123456" in identifiers["prjna"] assert "SRR1234567" in identifiers["srr"] @pytest.mark.slow def test_pmc_to_identifiers(sraweb_connection): """Test PMC to identifiers extraction - requires PMC full text access""" # Using a known PMC article that mentions GEO/SRA identifiers df = sraweb_connection.pmc_to_identifiers("PMC5316890") assert isinstance(df, pd.DataFrame) assert not df.empty required_columns = {"pmc_id", "gse_ids", "srp_ids", "prjna_ids"} assert required_columns.issubset(df.columns) @pytest.mark.slow def test_pmid_to_identifiers(sraweb_connection): """Test PMID to identifiers extraction""" df = sraweb_connection.pmid_to_identifiers("27373336") assert isinstance(df, pd.DataFrame) assert not df.empty required_columns = {"pmid", "pmc_id", "gse_ids", "srp_ids", "prjna_ids"} assert required_columns.issubset(df.columns) @pytest.mark.slow def test_pmid_to_gse(sraweb_connection): """Test PMID to GSE extraction""" df = sraweb_connection.pmid_to_gse("27373336") assert isinstance(df, pd.DataFrame) assert not df.empty required_columns = {"pmid", "pmc_id", "gse_ids"} assert required_columns.issubset(df.columns) @pytest.mark.slow def test_pmid_to_srp(sraweb_connection): """Test PMID to SRP extraction""" df = sraweb_connection.pmid_to_srp("27373336") assert isinstance(df, pd.DataFrame) assert not df.empty required_columns = {"pmid", "pmc_id", "srp_ids"} assert required_columns.issubset(df.columns) def test_doi_to_pmid(sraweb_connection): """Test DOI to PMID conversion""" mapping = sraweb_connection.doi_to_pmid("10.12688/f1000research.18676.1") assert isinstance(mapping, dict) assert "10.12688/f1000research.18676.1" in mapping def test_doi_to_pmid_multiple(sraweb_connection): """Test DOI to PMID with multiple DOIs""" mapping = sraweb_connection.doi_to_pmid( ["10.12688/f1000research.18676.1", "10.1186/s13059-016-1070-5"] ) assert isinstance(mapping, dict) assert len(mapping) == 2 @pytest.mark.slow def test_doi_to_identifiers(sraweb_connection): """Test DOI to identifiers extraction""" df = sraweb_connection.doi_to_identifiers("10.12688/f1000research.18676.1") assert isinstance(df, pd.DataFrame) assert not df.empty required_columns = {"doi", "pmid", "pmc_id", "gse_ids", "srp_ids", "prjna_ids"} assert required_columns.issubset(df.columns) @pytest.mark.slow def test_doi_to_gse(sraweb_connection): """Test DOI to GSE extraction""" df = sraweb_connection.doi_to_gse("10.12688/f1000research.18676.1") assert isinstance(df, pd.DataFrame) assert not df.empty required_columns = {"doi", "pmid", "pmc_id", "gse_ids"} assert required_columns.issubset(df.columns) @pytest.mark.slow def test_doi_to_srp(sraweb_connection): """Test DOI to SRP extraction""" df = sraweb_connection.doi_to_srp("10.12688/f1000research.18676.1") assert isinstance(df, pd.DataFrame) assert not df.empty required_columns = {"doi", "pmid", "pmc_id", "srp_ids"} assert required_columns.issubset(df.columns) def test_unified_metadata_with_gse(sraweb_connection): """Test unified metadata() function with GSE accession""" df = sraweb_connection.metadata("GSE286254") assert isinstance(df, pd.DataFrame) assert not df.empty assert "GSE286254" in df["study_accession"].unique() def test_unified_metadata_with_srp(sraweb_connection): """Test unified metadata() function with SRP accession""" df = sraweb_connection.metadata("SRP016501") assert isinstance(df, pd.DataFrame) assert df.shape[0] == 134 assert "SRP016501" in df["study_accession"].unique() def test_unified_metadata_with_multiple_gse(sraweb_connection): """Test unified metadata() function with multiple GSE accessions""" df = sraweb_connection.metadata(["GSE168880", "GSE209835"]) assert isinstance(df, pd.DataFrame) assert not df.empty gse_ids = df["study_accession"].unique() assert "GSE168880" in gse_ids or "GSE209835" in gse_ids def test_unified_metadata_invalid_accession(sraweb_connection): """Test unified metadata() function with invalid accession type""" with pytest.raises(ValueError, match="Unsupported accession type"): sraweb_connection.metadata("INVALID123") ================================================ FILE: tests/test_utils.py ================================================ """Tests for utils.py""" import pytest from pysradb.utils import * @pytest.fixture(scope="module") def invalid_name(): return "Red blood cells" @pytest.fixture(scope="module") def valid_name(): return "Homo sapiens" def invalid_scientific_name_to_taxid(invalid_name): with pytest.raises(IncorrectFieldException) as e: scientific_name_to_taxid(invalid_name) assert "Unknown scientific name" in str(e.value) def valid_scientific_name_to_taxid(valid_name): assert scientific_name_to_taxid(valid_name) == "9606"