nf-core/subworkflows
Browse the 78 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
Picard MarkDuplicates, index BAM file and run samtools stats, flagstat and idxstats
Samtools markduplicate SAM/BAM/CRAM file
Take a set of bam files and run NGSCheckMate to determine whether samples match with each other, using a set of SNPs.
Produces comprehensive statistics from BAM file