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* added files * removed file * added file * changed files * changed files * edited file * edited file * edited files * edited files * edited files * edited tags * edited tags * edited tags * edited tags Co-authored-by: kaurravneet4123 <kaurravneet4123@yahoo.com@users.noreply.github.com>
62 lines
1.9 KiB
Text
62 lines
1.9 KiB
Text
// Import generic module functions
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include { initOptions; saveFiles; getSoftwareName } from './functions'
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params.options = [:]
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options = initOptions(params.options)
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process SEQTK_SAMPLE {
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tag "$meta.id"
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label 'process_low'
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publishDir "${params.outdir}",
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mode: params.publish_dir_mode,
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saveAs: { filename -> saveFiles(filename:filename, options:params.options, publish_dir:getSoftwareName(task.process), meta:meta, publish_by_meta:['id']) }
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conda (params.enable_conda ? "bioconda::seqtk=1.3" : null)
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if (workflow.containerEngine == 'singularity' && !params.singularity_pull_docker_container) {
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container "https://depot.galaxyproject.org/singularity/seqtk:1.3--h5bf99c6_3"
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} else {
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container "quay.io/biocontainers/seqtk:1.3--h5bf99c6_3"
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}
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input:
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tuple val(meta), path(reads)
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val sample_size
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output:
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tuple val(meta), path("*.fastq.gz"), emit: reads
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path "*.version.txt" , emit: version
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script:
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def software = getSoftwareName(task.process)
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def prefix = options.suffix ? "${meta.id}${options.suffix}" : "${meta.id}"
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if (meta.single_end) {
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"""
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seqtk \\
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sample \\
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$options.args \\
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$reads \\
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$sample_size \\
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| gzip > ${prefix}.fastq.gz \\
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echo \$(seqtk 2>&1) | sed 's/^.*Version: //; s/ .*\$//' > ${software}.version.txt
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"""
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} else {
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"""
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seqtk \\
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sample \\
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$options.args \\
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$reads[0] \\
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$sample_size \\
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| gzip > ${prefix}_1.fastq.gz \\
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seqtk \\
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sample \\
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$options.args \\
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$reads[1] \\
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$sample_size \\
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| gzip > ${prefix}_2.fastq.gz \\
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echo \$(seqtk 2>&1) | sed 's/^.*Version: //; s/ .*\$//' > ${software}.version.txt
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"""
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}
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}
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