genome variant calling and RNA-seq analysis
A python toolkit providing best-practice pipelines for fully automated high throughput RNA sequencing analysis. It can work with BWA, .bam or .fastq files.
released on 20 June 2014
Extension or PluginThis package can be used as an extension, plugin, or add-on to:
|License||Verified by||Verified on||Notes|
Full license text: https://github.com/chapmanb/bcbio-nextgen/blob/master/LICENSE.txt
Leaders and contributors
|Brad Chapman||primary contact|
Resources and communication
|geomes and RNA-seq tools user group||Mailing List||https://groups.google.com/forum/#!forum/biovalidation|
Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.3 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts. A copy of the license is included in the page “GNU Free Documentation License”.
The copyright and license notices on this page only apply to the text on this page. Any software or copyright-licenses or other similar notices described in this text has its own copyright notice and license, which can usually be found in the distribution or license text itself.