Description

Subset plink pfiles with a text file of variant identifiers

Input

name:type
description
pattern

meta{:bash}

:map

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

pgen{:bash}

:file

PLINK 2 binary genotype table

*.{pgen}

psam{:bash}

:file

PLINK 2 sample information file

*.{psam}

pvar{:bash}

:file

PLINK 2 variant information file

*.{pvar}

variants{:bash}

:file

A text file containing variant identifiers to keep (one per line)

*.{keep}

Output

name:type
description
pattern

extract_pgen{:bash}

meta{:bash}

:map

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

*.pgen{:bash}

:file

PLINK 2 binary genotype table, containing extracted variants

*.{pgen}

extract_psam{:bash}

meta{:bash}

:map

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

*.psam{:bash}

:file

PLINK 2 sample information file associated with the extracted data

*.{psam}

extract_pvar{:bash}

meta{:bash}

:map

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

*.pvar.zst{:bash}

:file

PLINK 2 variant information file, containing extracted variants

*.{pvar.zst}

versions{:bash}

versions.yml{:bash}

: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