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