Description

Merges several vcf files

Input

name:type
description
pattern

meta{:bash}

:map

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

vcf{:bash}

:list

Two or more VCF files

*.{vcf,vcf.gz}

meta2{:bash}

:map

Groovy Map containing reference information e.g. [ id:‘genome’]

dict{:bash}

:file

Optional Sequence Dictionary as input

*.dict

Output

name:type
description
pattern

vcf{:bash}

meta{:bash}

:file

merged vcf file

*.vcf.gz

*.vcf.gz{:bash}

:file

merged vcf file

*.vcf.gz

tbi{:bash}

meta{:bash}

:file

merged vcf file

*.vcf.gz

*.tbi{:bash}

:file

index files for the merged vcf files

*.tbi

versions{:bash}

versions.yml{:bash}

:file

File containing software versions

versions.yml

Tools

gatk4
Apache-2.0

Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size.

gatk.broadinstitute.org/hc/en-us gatk.broadinstitute.org/hc/en-us/categories/360002369672s 10.1158/1538-7445.AM2017-3590
included in
rarediseasernadnavarrnavarsarekvariantcatalogue
maintainer
Github user kevinmenden
get in touch
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