process FASTQC {
    tag "$meta.id"
    label 'process_micro'

    module (params.enable_module ? "${params.swmodulepath}${params.fs}fastqc${params.fs}0.11.9" : null)
    conda (params.enable_conda ? "conda-forge::perl bioconda::fastqc=0.11.9" : null)
    container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
        'https://depot.galaxyproject.org/singularity/fastqc:0.11.9--0' :
        'quay.io/biocontainers/fastqc:0.11.9--0' }"

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

    output:
    tuple val(meta), path("*.html"), emit: html
    tuple val(meta), path("*.zip") , emit: zip
    path  "versions.yml"           , emit: versions

    when:
    task.ext.when == null || task.ext.when

    script:
    def args = task.ext.args ?: ''
    // Add soft-links to original FastQs for consistent naming in pipeline
    def prefix = task.ext.prefix ?: "${meta.id}"
    if (meta.single_end) {
        """
        [ ! -f  ${prefix}.fastq.gz ] && ln -s $reads ${prefix}.fastq.gz
        fastqc $args --threads $task.cpus ${prefix}.fastq.gz

        cat <<-END_VERSIONS > versions.yml
        "${task.process}":
            fastqc: \$( fastqc --version | sed -e "s/FastQC v//g" )
        END_VERSIONS
        """
    } else {
        """
        [ ! -f  ${prefix}_1.fastq.gz ] && ln -s ${reads[0]} ${prefix}_1.fastq.gz
        [ ! -f  ${prefix}_2.fastq.gz ] && ln -s ${reads[1]} ${prefix}_2.fastq.gz
        fastqc $args --threads $task.cpus ${prefix}_1.fastq.gz ${prefix}_2.fastq.gz

        cat <<-END_VERSIONS > versions.yml
        "${task.process}":
            fastqc: \$( fastqc --version | sed -e "s/FastQC v//g" )
        END_VERSIONS
        """
    }
}