Description

Ligatation of multiple phased BCF/VCF files into a single whole chromosome file. GLIMPSE2 is run in chunks that are ligated into chromosome-wide files maintaining the phasing.

Input

name:type
description
pattern

meta{:bash}

:map

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

input_list{:bash}

:file

VCF/BCF file containing genotype probabilities (GP field).

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

input_index{:bash}

:file

Index file of the input VCF/BCF file containing genotype likelihoods.

*.{csi,tbi}

Output

name:type
description
pattern

merged_variants{:bash}

meta{:bash}

:map

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

*.{vcf,bcf,vcf.gz,bcf.gz}{:bash}

:file

Output ligated (phased) file in VCF/BCF format.

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

versions_glimpse2{:bash}

${task.process}{:bash}

:string

The name of the process

glimpse2{:bash}

:string

The name of the tool

GLIMPSE2_ligate --help | grep -oE 'v[0-9.]+' | cut -c2-{:bash}

:eval

The expression to obtain the version of the tool

Topics

name:type
description
pattern

versions{:bash}

${task.process}{:bash}

:string

The name of the process

glimpse2{:bash}

:string

The name of the tool

GLIMPSE2_ligate --help | grep -oE 'v[0-9.]+' | cut -c2-{:bash}

:eval

The expression to obtain the version of the tool

Tools

glimpse2
MIT

GLIMPSE2 is a phasing and imputation method for large-scale low-coverage sequencing studies.