decomposes multiallelic variants into biallelic in a VCF file.
meta:map
Groovy Map containing sample information e.g. [ id:'test', single_end:false ]
[ id:'test', single_end:false ]
vcf:file
The VCF file to decompose
*.vcf(.gz)?
intervals:file
The intervals of the variants of decompose
*.bed
vcf
*.vcf.gz:file
The decomposed VCF file
*.vcf.gz
versions
versions.yml:file
File containing software versions
versions.yml
A tool set for short variant discovery in genetic sequence data
