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 25 March 2020
Extension or Plugin
29 March 2020
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|
|Debian (Ref) (R)||https://tracker.debian.org/pkg/bcbio|
|VCS Repository Webview||https://github.com/chapmanb/bcbio-nextgen|
This entry (in part or in whole) was last reviewed on 29 March 2020.
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