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:false ]

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:false ]

*.pgen

:file

PLINK 2 binary genotype table

*.{pgen}

psam

meta

:map

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

*.psam

:file

PLINK 2 sample information file

*.{psam}

pvar

meta

:map

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

*.pvar

:file

PLINK 2 variant information file

*.{pvar.zst}

pvar_zst

meta

:map

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

*.pvar.zst

:file

PLINK 2 variant information zst file

*.pvar.zst

versions_plink2

${task.process}

:string

The name of the process

plink2

:string

The name of the tool

The expression to obtain the version of the tool

Topics

name:type
description
pattern

versions

${task.process}

:string

The name of the process

plink2

:string

The name of the tool

The expression to obtain the version of the tool

Tools

plink2
GPL v3

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