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 Plugin
|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|
This entry (in part or in whole) was last reviewed on 30 March 2018.
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