×

Nextflow Modules

Clear

Showing module(s) with keyword "variation"

Module Keywords Description
nf-core/htsnimtools/vcfcheck validation check variation This tools takes a background VCF, such as gnomad, that has full genome (though in some cases, users will instead want whole exome) coverage and uses that as an expectation of variants.
nf-core/severus structural variation somatic germline long-read Severus is a somatic structural variation (SV) caller for long reads (both PacBio and ONT)