Nextflow Modules
Showing module(s) with keyword "somatic variants"
| Module | Kind | Keywords | Description |
|---|---|---|---|
| nf-core/gridss/somaticfilter | Process | 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 | Process | 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 | Process | structural variants somatic variants copy number analysis long-read sequencing genomics | Tumour-only somatic SV calling with optional copy-number analysis in SAVANA |