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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
29 lines
832 B
Text
29 lines
832 B
Text
process SAMTOOLS_FAIDX {
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tag "$fasta"
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label 'process_low'
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conda (params.enable_conda ? "bioconda::samtools=1.14" : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/samtools:1.14--hb421002_0' :
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'quay.io/biocontainers/samtools:1.14--hb421002_0' }"
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input:
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tuple val(meta), path(fasta)
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output:
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tuple val(meta), path ("*.fai"), emit: fai
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path "versions.yml" , emit: versions
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script:
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def args = task.ext.args ?: ''
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"""
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samtools \\
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faidx \\
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$fasta
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cat <<-END_VERSIONS > versions.yml
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"${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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