You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Added run-cgprna command line tool, which can be used to complete a step in RNA-seq data workflow with just one command. Currently 4 subcommands are implemented:
map: uses star_mapping.pl to map and marks duplicates after mapping.
stats: generates mapping stats using bam_stats and RSeQC.
bigwig: generates bigwig file using bamToBw.pl
counts: counts reads using htseq-count.
Built a new set of reference files for run-cgprna to use. They're available on ftp://ftp.sanger.ac.uk/pub/cancer/support-files/cgpRna_container/.
CWL tools and workflows:
added a workflow to map sample by lanes, generate mapping stats for lanes, merge lane bams, generate bigwig file and count reads.
added CWL tools/workflows for the workflow above to use.