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Showing module(s) with keyword "indels"

Module Keywords Description
nf-core/abra2 alignment realignment indels bam dna rna splice-junctions assembly Assembly Based ReAligner for next-generation sequencing data
nf-core/gatk4/mutect2 gatk4 haplotype indels mutect2 snvs somatic Call somatic SNVs and indels via local assembly of haplotypes.
nf-core/manta/convertinversion structural variants conversion indels Manta calls structural variants (SVs) and indels from mapped paired-end sequencing reads. This script reformats inversions into single inverted sequence junctions which was the format used in Manta versions <= 1.4.0.
nf-core/vt/decompose decompose multiallelic small variants snps indels decomposes multiallelic variants into biallelic in a VCF file.
nf-core/vt/decomposeblocksub decomposeblocksub multiallelic small variants snps indels block substitutions Decomposes biallelic block substitutions into its constituent SNPs.
nf-core/vt/normalize normalization vcf snps indels normalizes variants in a VCF file