Description

Import variant genetic data using plink2

Input

name:type
description
pattern

meta:map

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

]

vcf:file

Variant calling file (vcf)

*.{vcf}, *.{vcf.gz}

Output

name:type
description
pattern

pgen

meta:map

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

]

*.pgen:file

PLINK 2 binary genotype table

*.{pgen}

psam

meta:map

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

]

*.psam:file

PLINK 2 sample information file

*.{psam}

pvar

meta:map

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

]

*.pvar:file

PLINK 2 variant information file

*.{pvar.zst}

pvar_zst

meta:map

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

]

*.pvar.zst:file

PLINK 2 variant information zst file

*.pvar.zst

versions

versions.yml:file

File containing software versions

versions.yml

Tools

plink2
GPL v3

Whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner