nf-core_modules/modules/scramble/clusteridentifier/main.nf

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process SCRAMBLE_CLUSTERIDENTIFIER {
tag "$meta.id"
label 'process_single'
conda (params.enable_conda ? "bioconda::scramble=1.0.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/scramble:1.0.1--h779adbc_1':
'quay.io/biocontainers/scramble:1.0.1--h779adbc_1' }"
input:
tuple val(meta), path(input), path(input_index)
path fasta
output:
tuple val(meta), path("*.clusters.txt") , emit: clusters
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def VERSION = '1.0.1' // WARN: Version information not provided by tool on CLI. Please update this string when bumping container versions.
// The tool does not contain a way to specify the reference file when using CRAM files.
// It just looks in the header of the CRAM file where the reference file is located,
// but that reference can't always be fetched since most test data is created on
// another machine. I had to find another way to specify the reference and I
// found that I could create an md5 cache of a specified fasta and supply it to
// the REF_PATH environment variable. This way the tool uses the correct reference.
// An issue has been made about this: https://github.com/GeneDx/scramble/issues/27
// The reference code is a placeholder until this issue has been fixed.
def reference = fasta ? "wget https://raw.githubusercontent.com/samtools/samtools/master/misc/seq_cache_populate.pl && perl seq_cache_populate.pl -root ./md5_ref ${fasta} && export REF_PATH=`pwd`/md5_ref/%2s/%2s/%s" : ""
"""
${reference}
cluster_identifier \\
${args} \\
${input} \\
> ${prefix}.clusters.txt
cat <<-END_VERSIONS > versions.yml
"${task.process}":
scramble: ${VERSION}
END_VERSIONS
"""
}