mirror of
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45 lines
1.6 KiB
Text
45 lines
1.6 KiB
Text
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process SAMTOOLS_FASTQ {
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tag "$meta.id"
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label 'process_low'
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conda "bioconda::samtools=1.16.1"
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/samtools:1.16.1--h6899075_1' :
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'quay.io/biocontainers/samtools:1.16.1--h6899075_1' }"
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input:
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tuple val(meta), path(input)
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val(interleave)
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output:
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tuple val(meta), path("*_{1,2}.fastq.gz") , optional:true, emit: fastq
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tuple val(meta), path("*_interleaved.fastq.gz"), optional:true, emit: interleaved
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tuple val(meta), path("*_singleton.fastq.gz") , optional:true, emit: singleton
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tuple val(meta), path("*_other.fastq.gz") , optional:true, emit: other
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path "versions.yml" , emit: versions
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when:
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task.ext.when == null || task.ext.when
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script:
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def args = task.ext.args ?: ''
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def prefix = task.ext.prefix ?: "${meta.id}"
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def output = ( interleave && ! meta.single_end ) ? "> ${prefix}_interleaved.fastq.gz" :
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meta.single_end ? "-1 ${prefix}_1.fastq.gz -s ${prefix}_singleton.fastq.gz" :
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"-1 ${prefix}_1.fastq.gz -2 ${prefix}_2.fastq.gz -s ${prefix}_singleton.fastq.gz"
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"""
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samtools \\
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fastq \\
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$args \\
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--threads ${task.cpus-1} \\
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-0 ${prefix}_other.fastq.gz \\
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$input \\
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$output
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
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END_VERSIONS
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"""
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}
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