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https://github.com/MillironX/nf-core_modules.git
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e751e5040a
* Bump software versions for viralrecon modules * Remove custom params.save_unaligned from bowtie2_align * Unify samtools modules and error if input and output names are the same * Fix ALL the tests
72 lines
2.8 KiB
Text
72 lines
2.8 KiB
Text
process FASTP {
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tag "$meta.id"
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label 'process_medium'
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conda (params.enable_conda ? 'bioconda::fastp=0.23.2' : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/fastp:0.23.2--h79da9fb_0' :
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'quay.io/biocontainers/fastp:0.23.2--h79da9fb_0' }"
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input:
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tuple val(meta), path(reads)
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val save_trimmed_fail
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val save_merged
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output:
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tuple val(meta), path('*.trim.fastq.gz') , emit: reads
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tuple val(meta), path('*.json') , emit: json
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tuple val(meta), path('*.html') , emit: html
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tuple val(meta), path('*.log') , emit: log
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path "versions.yml" , emit: versions
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tuple val(meta), path('*.fail.fastq.gz') , optional:true, emit: reads_fail
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tuple val(meta), path('*.merged.fastq.gz'), optional:true, emit: reads_merged
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script:
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def args = task.ext.args ?: ''
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// Added soft-links to original fastqs for consistent naming in MultiQC
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def prefix = task.ext.prefix ?: "${meta.id}"
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if (meta.single_end) {
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def fail_fastq = save_trimmed_fail ? "--failed_out ${prefix}.fail.fastq.gz" : ''
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"""
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[ ! -f ${prefix}.fastq.gz ] && ln -s $reads ${prefix}.fastq.gz
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fastp \\
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--in1 ${prefix}.fastq.gz \\
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--out1 ${prefix}.trim.fastq.gz \\
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--thread $task.cpus \\
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--json ${prefix}.fastp.json \\
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--html ${prefix}.fastp.html \\
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$fail_fastq \\
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$args \\
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2> ${prefix}.fastp.log
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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fastp: \$(fastp --version 2>&1 | sed -e "s/fastp //g")
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END_VERSIONS
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"""
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} else {
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def fail_fastq = save_trimmed_fail ? "--unpaired1 ${prefix}_1.fail.fastq.gz --unpaired2 ${prefix}_2.fail.fastq.gz" : ''
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def merge_fastq = save_merged ? "-m --merged_out ${prefix}.merged.fastq.gz" : ''
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"""
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[ ! -f ${prefix}_1.fastq.gz ] && ln -s ${reads[0]} ${prefix}_1.fastq.gz
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[ ! -f ${prefix}_2.fastq.gz ] && ln -s ${reads[1]} ${prefix}_2.fastq.gz
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fastp \\
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--in1 ${prefix}_1.fastq.gz \\
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--in2 ${prefix}_2.fastq.gz \\
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--out1 ${prefix}_1.trim.fastq.gz \\
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--out2 ${prefix}_2.trim.fastq.gz \\
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--json ${prefix}.fastp.json \\
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--html ${prefix}.fastp.html \\
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$fail_fastq \\
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$merge_fastq \\
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--thread $task.cpus \\
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--detect_adapter_for_pe \\
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$args \\
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2> ${prefix}.fastp.log
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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fastp: \$(fastp --version 2>&1 | sed -e "s/fastp //g")
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END_VERSIONS
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"""
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}
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}
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