A subworkflow for filtering differential abundance results

Extract archive(s) from any format Currently supported format are .gz, .tar.gz, .zip

Includes: gunzipuntarunzip

A subworkflow for calling CNVs using WisecondorX

Perform variant calling on a set of normal samples using mutect2 panel of normals mode. Group them into a genomicsdbworkspace using genomicsdbimport, then use this to create a panel of normals using createsomaticpanelofnormals.

Included in: createpanelrefs

umicollapse, index BAM file and run samtools stats, flagstat and idxstats

Included in: lncpiperiboseqrnaseq
Includes: umicollapsesamtools/indexsamtools/stats and 3 more modules

UMI-tools dedup, index BAM file and run samtools stats, flagstat and idxstats

Included in: lncpipenascentriboseq and 1 more pipeline
Includes: umitools/dedupsamtools/indexsamtools/stats and 3 more modules

BAM deduplication with UMI processing for both genome and transcriptome alignments

Included in: lncpiperiboseqrnaseq

Calculate contamination of the X-chromosome with ANGSD

Subworkflow to impute BAM files using STITCH software. Variants location to impute are obtain through the legend file given

Picard MarkDuplicates, index BAM file and run samtools stats, flagstat and idxstats

Included in: atacseqchipseqcircdna and 4 more pipelines

Samtools markduplicate SAM/BAM/CRAM file

Performs methylation quantification based on negative readout of C to T conversion of 3-letter genome alignments using Methyldackel.