nf-core/subworkflows
Browse the 78 subworkflows that are currently available as part of nf-core.
A subworkflow for filtering differential abundance results
differentialabundanceexpressioncount matrixfold-change
Extract archive(s) from any format Currently supported format are .gz, .tar.gz, .zip
archivegziptarzip
A subworkflow for calling CNVs using WisecondorX
cnvbambedcramplotsgenomics
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.
gatk4mutect2genomicsdbimportcreatesomaticpanelofnormalsvariant_callinggenomicsdb_workspacepanel_of_normals
BAM deduplication with UMI processing for both genome and transcriptome alignments
deduplicationUMIBAMgenometranscriptomeumicollapseumitools
Calculate contamination of the X-chromosome with ANGSD
angsdbamcontaminationdocounts
Samtools markduplicate SAM/BAM/CRAM file
markdupbamsamcram
Take a set of bam files and run NGSCheckMate to determine whether samples match with each other, using a set of SNPs.
ngscheckmateqcbamsnp
Produces comprehensive statistics from BAM file
statisticscountshs_metricswgs_metricsbamsamcram