// Import generic module functions include { initOptions; saveFiles; getSoftwareName } from './functions' params.options = [:] options = initOptions(params.options) process STAR_GENOMEGENERATE { tag "$fasta" label 'process_high' publishDir "${params.outdir}", mode: params.publish_dir_mode, saveAs: { filename -> saveFiles(filename:filename, options:params.options, publish_dir:'index', meta:[:], publish_by_meta:[]) } // Note: 2.7X indices incompatible with AWS iGenomes. conda (params.enable_conda ? "bioconda::star=2.7.9a bioconda::samtools=1.13 conda-forge::gawk=5.1.0" : null) if (workflow.containerEngine == 'singularity' && !params.singularity_pull_docker_container) { container "https://depot.galaxyproject.org/singularity/mulled-v2-1fa26d1ce03c295fe2fdcf85831a92fbcbd7e8c2:a7908dfb0485a80ca94e4d17b0ac991532e4e989-0" } else { container "quay.io/biocontainers/mulled-v2-1fa26d1ce03c295fe2fdcf85831a92fbcbd7e8c2:a7908dfb0485a80ca94e4d17b0ac991532e4e989-0" } input: path fasta path gtf output: path "star" , emit: index path "*.version.txt", emit: version script: def software = getSoftwareName(task.process) def memory = task.memory ? "--limitGenomeGenerateRAM ${task.memory.toBytes() - 100000000}" : '' def args = options.args.tokenize() if (args.contains('--genomeSAindexNbases')) { """ mkdir star STAR \\ --runMode genomeGenerate \\ --genomeDir star/ \\ --genomeFastaFiles $fasta \\ --sjdbGTFfile $gtf \\ --runThreadN $task.cpus \\ $memory \\ $options.args STAR --version | sed -e "s/STAR_//g" > ${software}.version.txt """ } else { """ samtools faidx $fasta NUM_BASES=`gawk '{sum = sum + \$2}END{if ((log(sum)/log(2))/2 - 1 > 14) {printf "%.0f", 14} else {printf "%.0f", (log(sum)/log(2))/2 - 1}}' ${fasta}.fai` mkdir star STAR \\ --runMode genomeGenerate \\ --genomeDir star/ \\ --genomeFastaFiles $fasta \\ --sjdbGTFfile $gtf \\ --runThreadN $task.cpus \\ --genomeSAindexNbases \$NUM_BASES \\ $memory \\ $options.args STAR --version | sed -e "s/STAR_//g" > ${software}.version.txt """ } }