mirror of
https://github.com/MillironX/nf-core_modules.git
synced 2024-11-11 12:43:09 +00:00
c736817598
* changed genome size input position
* fixed...😊
42 lines
1.5 KiB
Text
42 lines
1.5 KiB
Text
// Import generic module functions
|
|
include { initOptions; saveFiles; getSoftwareName } from './functions'
|
|
|
|
params.options = [:]
|
|
options = initOptions(params.options)
|
|
|
|
process RASUSA {
|
|
tag "$meta.id"
|
|
label 'process_low'
|
|
publishDir "${params.outdir}",
|
|
mode: params.publish_dir_mode,
|
|
saveAs: { filename -> saveFiles(filename:filename, options:params.options, publish_dir:getSoftwareName(task.process), meta:meta, publish_by_meta:['id']) }
|
|
|
|
conda (params.enable_conda ? "bioconda::rasusa=0.3.0" : null)
|
|
if (workflow.containerEngine == 'singularity' && !params.singularity_pull_docker_container) {
|
|
container "https://depot.galaxyproject.org/singularity/rasusa:0.3.0--h779adbc_1"
|
|
} else {
|
|
container "quay.io/biocontainers/rasusa:0.3.0--h779adbc_1"
|
|
}
|
|
|
|
input:
|
|
tuple val(meta), path(reads), val(genome_size)
|
|
val depth_cutoff
|
|
|
|
output:
|
|
tuple val(meta), path('*.fastq.gz'), emit: reads
|
|
path '*.version.txt' , emit: version
|
|
|
|
script:
|
|
def software = getSoftwareName(task.process)
|
|
def prefix = options.suffix ? "${meta.id}${options.suffix}" : "${meta.id}"
|
|
def output = meta.single_end ? "--output ${prefix}.fastq.gz" : "--output ${prefix}_1.fastq.gz ${prefix}_2.fastq.gz"
|
|
"""
|
|
rasusa \\
|
|
$options.args \\
|
|
--coverage $depth_cutoff \\
|
|
--genome-size $genome_size \\
|
|
--input $reads \\
|
|
$output
|
|
echo \$(rasusa --version 2>&1) | sed -e "s/rasusa //g" > ${software}.version.txt
|
|
"""
|
|
}
|