name: bedtools_intersect
description: allows one to screen for overlaps between two sets of genomic features.
keywords:
    - bed
    - intersect
tools:
    - bedtools:
        description: |
            A set of tools for genomic analysis tasks, specifically enabling genome arithmetic (merge, count, complement) on various file types.
        documentation: https://bedtools.readthedocs.io/en/latest/content/tools/intersect.html
params:
    - outdir:
        type: string
        description: |
            The pipeline's output directory. By default, the module will
            output files into `$params.outdir/<SOFTWARE>`
    - publish_dir_mode:
        type: string
        description: |
            Value for the Nextflow `publishDir` mode parameter.
            Available: symlink, rellink, link, copy, copyNoFollow, move.
    - enable_conda:
        type: boolean
        description: |
            Run the module with Conda using the software specified
            via the `conda` directive

input:
    - meta:
        type: map
        description: |
            Groovy Map containing sample information
            e.g. [ id:'test', single_end:false ]
    - bed1:
        type: file
        description: Bed file, each feature in 1 is compared to 2 in search of overlaps
        pattern: "*.{bed}"
    - bed2:
        type: file
        description: Second bed file, used to compare to 1.
        pattern: "*.{bed}"

output:
    - meta:
        type: map
        description: |
            Groovy Map containing sample information
            e.g. [ id:'test', single_end:false ]
    - bed:
        type: file
        description: Overlapped bed file
        pattern: "*.{intersect.bed}"
    - version:
        type: file
        description: File containing software version
        pattern: "*.{version.txt}"
authors:
    -"@Emiller88"
    -"@sruthipsuresh"