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Showing module(s) with keyword "somatic variants"

Module Keywords Description
nf-core/gridss/somaticfilter gridss structural variants somatic variants vcf GRIDSS is a module software suite containing tools useful for the detection of genomic rearrangements.
nf-core/happy/sompy happy sompy benchmark haplotype validation somatic variants Hap.py is a tool to compare diploid genotypes at haplotype level. som.py is a part of hap.py compares somatic variations.
nf-core/savana/to structural variants somatic variants copy number analysis long-read sequencing genomics Tumour-only somatic SV calling with optional copy-number analysis in SAVANA