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Showing module(s) with keyword "small indels"

Module Keywords Description
nf-core/manta/germline somatic wgs wxs panel vcf structural variants small indels Manta calls structural variants (SVs) and indels from mapped paired-end sequencing reads. It is optimized for analysis of germline variation in small sets of individuals and somatic variation in tumor/normal sample pairs.
nf-core/manta/somatic somatic wgs wxs panel vcf structural variants small indels Manta calls structural variants (SVs) and indels from mapped paired-end sequencing reads. It is optimized for analysis of germline variation in small sets of individuals and somatic variation in tumor/normal sample pairs.
nf-core/manta/tumoronly somatic wgs wxs panel vcf structural variants small indels Manta calls structural variants (SVs) and indels from mapped paired-end sequencing reads. It is optimized for analysis of germline variation in small sets of individuals and somatic variation in tumor/normal sample pairs.