Filter variants based on Ensembl Variant Effect Predictor (VEP) annotations.
meta{:bash}
:map
Groovy Map containing sample information e.g. [ id:'test', single_end:false ]
[ id:'test', single_end:false ]
input{:bash}
:file
VCF/TAB file annotated with vep
*.{vcf,tab,tsv,txt}
feature_file{:bash}
File containing features on separate lines. To be used with —filter option.
output{:bash}
*.${extension}{:bash}
VCF/TAB file
*.{vcf,tab,txt,tsv}
versions_ensemblvep{:bash}
${task.process}{:bash}
:string
The process the versions were collected from
ensemblvep{:bash}
The tool name
vep --help | sed -n '/ensembl-vep/s/.*: //p'{:bash}
:eval
The command used to generate the version of the tool
versions_perlmathcdf{:bash}
perl-math-cdf{:bash}
perl -MMath::CDF -e 'print \$Math::CDF::VERSION'{:bash}
The expression to obtain the version of the tool
versions{:bash}
VEP determines the effect of your variants (SNPs, insertions, deletions, CNVs or structural variants) on genes, transcripts, and protein sequence, as well as regulatory regions.
