nf-core/subworkflows
Browse the 119 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 QUILT software. Variants location to impute are obtain through the tsv file given
Impute low-coverage BAM or CRAM inputs with QUILT2 and ligate chunked outputs per chromosome. 'regionout' key will be used to store temporarily the region and therefore shouldn't be used in the meta maps.
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