name: star_align description: Align reads to a reference genome using STAR keywords: - align - fasta - genome - reference tools: - star: description: | STAR is a software package for mapping DNA sequences against a large reference genome, such as the human genome. homepage: https://github.com/alexdobin/STAR manual: https://github.com/alexdobin/STAR/blob/master/doc/STARmanual.pdf doi: 10.1093/bioinformatics/bts635 params: - outdir: type: string description: | The pipeline's output directory. By default, the module will output files into `$params.outdir/` - publish_dir_mode: type: string description: | Value for the Nextflow `publishDir` mode parameter. Available: symlink, rellink, link, copy, copyNoFollow, move. - enable_conda: type: boolean description: | Run the module with Conda using the software specified via the `conda` directive - singularity_pull_docker_container: type: boolean description: | Instead of directly downloading Singularity images for use with Singularity, force the workflow to pull and convert Docker containers instead. input: - meta: type: map description: | Groovy Map containing sample information e.g. [ id:'test', single_end:false ] - reads: type: file description: | List of input FastQ files of size 1 and 2 for single-end and paired-end data, respectively. - index: type: directory description: STAR genome index pattern: "star" output: - bam: type: file description: Output BAM file containing read alignments pattern: "*.{bam}" - log_final: type: file description: STAR final log file pattern: "*Log.final.out" - log_out: type: file description: STAR lot out file pattern: "*Log.out" - log_progress: type: file description: STAR log progress file pattern: "*Log.progress.out" - version: type: file description: File containing software version pattern: "*.{version.txt}" authors: - "@kevinmenden" - "@drpatelh"