How to Cite Galaxy. Galaxy Tool Shed / (sandbox for testing). 3382 valid tools on Aug 13, 2015. Search for valid tools. Login to create a repository.
http://testtoolshed.g2.bx.psu.edu/
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Galaxy Tool Shed / (sandbox for testing) | testtoolshed.g2.bx.psu.edu Reviews
https://testtoolshed.g2.bx.psu.edu
How to Cite Galaxy. Galaxy Tool Shed / (sandbox for testing). 3382 valid tools on Aug 13, 2015. Search for valid tools. Login to create a repository.
testtoolshed.g2.bx.psu.edu
Custom datatypes in this tool shed
https://testtoolshed.g2.bx.psu.edu/repository/browse_datatypes
Galaxy Tool Shed / (sandbox for testing)
https://testtoolshed.g2.bx.psu.edu/repository
How to Cite Galaxy. Galaxy Tool Shed / (sandbox for testing). 5484 valid tools on Oct 16, 2016. Search for valid tools. Login to create a repository.
Galaxy Tool Shed / (sandbox for testing)
https://testtoolshed.g2.bx.psu.edu/groups
How to Cite Galaxy. Galaxy Tool Shed / (sandbox for testing).
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etalog: Preview and preprint: CNVkit, copy number detection for targeted sequencing
http://etalog.blogspot.com/2014/11/preview-and-preprint-cnvkit-copy-number.html
More of a comment than a question. Tuesday, November 4, 2014. Preview and preprint: CNVkit, copy number detection for targeted sequencing. I've posted a preprint of the CNVkit manuscript. On bioRxiv. If you think this software or method might suit your needs, please take a look and let me know what you think of it! CNVkit is a software toolkit for detecting and visualizing germline copy number variants and somatic copy number alterations in targeted or whole-exome DNA sequencing data. ( Source code.
The Galaxy Tool Shed: Primary Repository Features - Greg Von Kuster
http://gregvonkuster.org/galaxy-tool-shed-primary-repository-features
History of the Galaxy Tool Shed. The Galaxy Tool Shed: the First Biomedical App Store. The Galaxy Tool Shed: Primary Repository Features. The Galaxy Tool Shed. Release. Watch for future articles here as well as future Galaxy News Briefs. Which are published for each new release, for details about upcoming features. A Repository’s Main Page. Clicking the name link of a repository in the Tool Shed displays the repository’s main page. The Tool Shed provides an Install and Test Framework. We introduced the T...
etalog: November 2014
http://etalog.blogspot.com/2014_11_01_archive.html
More of a comment than a question. Tuesday, November 4, 2014. Preview and preprint: CNVkit, copy number detection for targeted sequencing. I've posted a preprint of the CNVkit manuscript. On bioRxiv. If you think this software or method might suit your needs, please take a look and let me know what you think of it! CNVkit is a software toolkit for detecting and visualizing germline copy number variants and somatic copy number alterations in targeted or whole-exome DNA sequencing data. ( Source code.
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Galaxy Tool Shed / (sandbox for testing)
How to Cite Galaxy. Galaxy Tool Shed / (sandbox for testing). 3382 valid tools on Aug 13, 2015. Search for valid tools. Login to create a repository.
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