nf-core/plink/epistasis @ 0.0.0-6c4ed3a
Summary
Epistasis in PLINK, analyzing how the effects of one gene depend on the presence of others.
Get started
Add the following snippet to your workflow script to include this module.
include { PLINK_EPISTASIS } from 'nf-core/plink/epistasis'
License
MIT License
Name
|
PLINK_EPISTASIS |
|---|
meta
map
|
Groovy Map containing sample information e.g. [ id:'test', single_end:false ] meta is associated to the PLINK native file input |
|---|---|
bed
file
|
PLINK binary biallelic genotype table file *.{bed}
|
bim
file
|
PLINK extended MAP file *.{bim}
|
fam
file
|
PLINK sample information file *.{fam}
|
meta2
map
|
Groovy Map containing sample information, e.g. [ id:'test', single_end:false ] meta2 is associated to VCF file input |
|---|---|
vcf
file
|
Variant calling file (vcf) *.{vcf}
|
meta3
map
|
Groovy Map containing sample information, e.g. [ id:'test', single_end:false ] meta3 is associated to BCF file input |
|---|---|
bcf
file
|
PLINK variant information + sample ID + genotype call binary file *.{bcf}
|
meta4
map
|
Groovy Map containing sample information, e.g. [ id:'test', single_end:false ] meta4 is associated to phenotype file input |
|---|---|
phe
file
|
PLINK file containing phenotype information. This phenotype information can be read from the third column with the --pheno option or from a specific column with the --pheno-name option. *.{phe}
|
epi
tuple
meta
map
|
Groovy Map containing sample information e.g. |
|---|---|
*.epi.cc
file
|
PLINK epistasis file *.{epi.cc}
|
log
tuple
meta
map
|
Groovy Map containing sample information e.g. |
|---|---|
*.log
file
|
PLINK epistasis log file *.{log}
|
nosex
tuple
meta
map
|
Groovy Map containing sample information e.g. |
|---|---|
*.nosex
file
|
Ambiguous sex ID file *.{nosex}
|
episummary
tuple
meta
map
|
Groovy Map containing sample information e.g. |
|---|---|
*.epi.cc.summary
file
|
PLINK epistasis summary file *.{epi.cc.summary}
|
versions_plink
tuple
${task.process}
string
|
The name of the process |
|---|---|
plink
string
|
The name of the tool |
plink --version 2>&1 | sed 's/^PLINK v//;s/ .*//'
eval
|
The expression to obtain the version of the tool |
| Tool | Description | Homepage |
|---|---|---|
| plink | Whole genome association analysis toolset, designed to perform a range of basic, large-scale analyses in a computationally efficient manner. | https://www.cog-genomics.org/plink |
| Version | 0.0.0-6c4ed3a |
|---|---|
| Commit ID | 6c4ed3a220310b905a1fc9d04f05be2e0837142b |
| Release Date | 23 Apr 2026 15:37:40 (UTC) |
| Download URL | https://registry.nextflow.io/api/v1/modules/nf-core%2Fplink%2Fepistasis/0.0.0-6c4ed3a/download |