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.
29 March 2020
Leaders and contributors
|Brad Chapman||primary contact|
Resources and communication
|Debian (Ref) (R)||https://tracker.debian.org/pkg/bcbio|
|VCS Repository Webview||https://github.com/chapmanb/bcbio-nextgen|
|geomes and RNA-seq tools user group||Mailing List||https://groups.google.com/forum/#!forum/biovalidation|
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