nf-core_modules/modules/samtools/fastq/main.nf

process SAMTOOLS_FASTQ {
    tag "$meta.id"
    label 'process_low'

    conda (params.enable_conda ? "bioconda::samtools=1.14" : null)
    container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
        'https://depot.galaxyproject.org/singularity/samtools:1.14--hb421002_0' :
        'quay.io/biocontainers/samtools:1.14--hb421002_0' }"

    input:
    tuple val(meta), path(bam)

    output:
    tuple val(meta), path("*.fastq.gz"), emit: fastq
    path  "versions.yml"               , emit: versions

    script:
    def args = task.ext.args ?: ''
    def prefix = task.ext.suffix ? "${meta.id}${task.ext.suffix}" : "${meta.id}"
    def endedness = meta.single_end ? "-0 ${prefix}.fastq.gz" : "-1 ${prefix}_1.fastq.gz -2 ${prefix}_2.fastq.gz"

    """
    samtools fastq \\
        $args \\
        --threads ${task.cpus-1} \\
        $endedness \\
        $bam
    cat <<-END_VERSIONS > versions.yml
    "${task.process}":
        samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
    END_VERSIONS
    """
}