Description

Perform joint genotyping on one or more samples pre-called with HaplotypeCaller.

Input

name:type
description
pattern

meta:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end

]

input:file

gVCF(.gz) file or a GenomicsDB

*.{vcf,vcf.gz}

gvcf_index:file

index of gvcf file, or empty when providing GenomicsDB

*.{idx,tbi}

intervals:file

Interval file with the genomic regions included in the library (optional)

intervals_index:file

Interval index file (optional)

meta2:map

Groovy Map containing fasta information e.g. [ id:‘test’ ]

fasta:file

Reference fasta file

*.fasta

meta3:map

Groovy Map containing fai information e.g. [ id:‘test’ ]

fai:file

Reference fasta index file

*.fai

meta4:map

Groovy Map containing dict information e.g. [ id:‘test’ ]

dict:file

Reference fasta sequence dict file

*.dict

meta5:map

Groovy Map containing dbsnp information e.g. [ id:‘test’ ]

dbsnp:file

dbSNP VCF file

*.vcf.gz

meta6:map

Groovy Map containing dbsnp tbi information e.g. [ id:‘test’ ]

dbsnp_tbi:file

dbSNP VCF index file

*.tbi

Output

name:type
description
pattern

vcf

meta:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end

]

*.vcf.gz:file

Genotyped VCF file

*.vcf.gz

tbi

meta:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end

]

*.tbi:file

Tbi index for VCF file

*.vcf.gz

versions

versions.yml:file

File containing software versions

versions.yml