nf-core/subworkflows
Browse the 96 subworkflows that are currently available as part of nf-core.
A subworkflow for filtering differential abundance results
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.
umicollapse, index BAM file and run samtools stats, flagstat and idxstats
UMI-tools dedup, index BAM file and run samtools stats, flagstat and idxstats
BAM deduplication with UMI processing for both genome and transcriptome alignments
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
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.