nf-core_modules/software/bedtools/genomecov/meta.yml

name: bedtools_genomecov
description: Computes histograms (default), per-base reports (-d) and BEDGRAPH (-bg) summaries of feature coverage (e.g., aligned sequences) for a given genome.
keywords:
    - bed
    - bam
    - genomecov
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/genomecov.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 ]            
    - bam:
        type: file
        description: List of bam files
        pattern: "*.{bam}"
output:
    - meta:
        type: map
        description: |
            Groovy Map containing sample information
            e.g. [ id:'test', single_end:false ]            
    - bed:
        type: file
        description: Computed genomecov bed file
        pattern: "*.{bed}"

    - version:
        type: file
        description: File containing software version
        pattern: "*.{version.txt}"

authors:
    -"@Emiller88"
    -"@sruthipsuresh"