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https://github.com/MillironX/nf-core_modules.git
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906577873b
* New functions.nf * Convert code to create versions.yml * Update meta.yml * update output channel * Fix more meta.yml * Manually update remaining modules * remove superflous echo * Fix misformatted meta.yml files * Fix yaml, was list instead of dict * fix version for bcftools Co-authored-by: Harshil Patel <drpatelh@users.noreply.github.com>
99 lines
3.8 KiB
Text
99 lines
3.8 KiB
Text
// Import generic module functions
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include { initOptions; saveFiles; getSoftwareName; getProcessName } from './functions'
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params.options = [:]
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options = initOptions(params.options)
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def VERSION = '2.2.0'
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process HISAT2_ALIGN {
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tag "$meta.id"
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label 'process_high'
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publishDir "${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::hisat2=2.2.0 bioconda::samtools=1.10" : null)
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if (workflow.containerEngine == 'singularity' && !params.singularity_pull_docker_container) {
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container "https://depot.galaxyproject.org/singularity/mulled-v2-a97e90b3b802d1da3d6958e0867610c718cb5eb1:2880dd9d8ad0a7b221d4eacda9a818e92983128d-0"
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} else {
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container "quay.io/biocontainers/mulled-v2-a97e90b3b802d1da3d6958e0867610c718cb5eb1:2880dd9d8ad0a7b221d4eacda9a818e92983128d-0"
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}
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input:
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tuple val(meta), path(reads)
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path index
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path splicesites
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output:
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tuple val(meta), path("*.bam"), emit: bam
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tuple val(meta), path("*.log"), emit: summary
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path "versions.yml" , emit: version
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tuple val(meta), path("*fastq.gz"), optional:true, emit: fastq
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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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def strandedness = ''
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if (meta.strandedness == 'forward') {
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strandedness = meta.single_end ? '--rna-strandness F' : '--rna-strandness FR'
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} else if (meta.strandedness == 'reverse') {
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strandedness = meta.single_end ? '--rna-strandness R' : '--rna-strandness RF'
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}
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def seq_center = params.seq_center ? "--rg-id ${prefix} --rg SM:$prefix --rg CN:${params.seq_center.replaceAll('\\s','_')}" : "--rg-id ${prefix} --rg SM:$prefix"
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if (meta.single_end) {
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def unaligned = params.save_unaligned ? "--un-gz ${prefix}.unmapped.fastq.gz" : ''
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"""
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INDEX=`find -L ./ -name "*.1.ht2" | sed 's/.1.ht2//'`
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hisat2 \\
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-x \$INDEX \\
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-U $reads \\
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$strandedness \\
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--known-splicesite-infile $splicesites \\
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--summary-file ${prefix}.hisat2.summary.log \\
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--threads $task.cpus \\
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$seq_center \\
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$unaligned \\
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$options.args \\
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| samtools view -bS -F 4 -F 256 - > ${prefix}.bam
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cat <<-END_VERSIONS > versions.yml
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${getProcessName(task.process)}:
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${getSoftwareName(task.process)}: \$(echo $VERSION)
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END_VERSIONS
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"""
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} else {
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def unaligned = params.save_unaligned ? "--un-conc-gz ${prefix}.unmapped.fastq.gz" : ''
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"""
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INDEX=`find -L ./ -name "*.1.ht2" | sed 's/.1.ht2//'`
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hisat2 \\
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-x \$INDEX \\
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-1 ${reads[0]} \\
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-2 ${reads[1]} \\
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$strandedness \\
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--known-splicesite-infile $splicesites \\
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--summary-file ${prefix}.hisat2.summary.log \\
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--threads $task.cpus \\
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$seq_center \\
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$unaligned \\
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--no-mixed \\
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--no-discordant \\
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$options.args \\
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| samtools view -bS -F 4 -F 8 -F 256 - > ${prefix}.bam
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if [ -f ${prefix}.unmapped.fastq.1.gz ]; then
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mv ${prefix}.unmapped.fastq.1.gz ${prefix}.unmapped_1.fastq.gz
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fi
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if [ -f ${prefix}.unmapped.fastq.2.gz ]; then
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mv ${prefix}.unmapped.fastq.2.gz ${prefix}.unmapped_2.fastq.gz
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fi
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cat <<-END_VERSIONS > versions.yml
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${getProcessName(task.process)}:
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${getSoftwareName(task.process)}: \$(echo $VERSION)
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END_VERSIONS
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"""
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}
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}
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