name: fastp description: Perform adapter/quality trimming on sequencing reads keywords: - trimming - quality control - fastq tools: - fastp: description: | A tool designed to provide fast all-in-one preprocessing for FastQ files. This tool is developed in C++ with multithreading supported to afford high performance. documentation: https://github.com/OpenGene/fastp doi: https://doi.org/10.1093/bioinformatics/bty560 licence: ["MIT"] input: - meta: type: map description: | Groovy Map containing sample information. Use 'single_end: true' to specify single ended or interleaved FASTQs. Use 'single_end: false' for paired-end reads. 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. If you wish to run interleaved paired-end data, supply as single-end data but with `--interleaved_in` in your `modules.conf`'s `ext.args` for the module. - save_trimmed_fail: type: boolean description: Specify true to save files that failed to pass trimming thresholds ending in `*.fail.fastq.gz` - save_merged: type: boolean description: Specify true to save all merged reads to the a file ending in `*.merged.fastq.gz` output: - meta: type: map description: | Groovy Map containing sample information e.g. [ id:'test', single_end:false ] - reads: type: file description: The trimmed/modified/unmerged fastq reads pattern: "*fastp.fastq.gz" - json: type: file description: Results in JSON format pattern: "*.json" - html: type: file description: Results in HTML format pattern: "*.html" - log: type: file description: fastq log file pattern: "*.log" - versions: type: file description: File containing software versions pattern: "versions.yml" - reads_fail: type: file description: Reads the failed the preprocessing pattern: "*fail.fastq.gz" - reads_merged: type: file description: Reads that were successfully merged pattern: "*.{merged.fastq.gz}" authors: - "@drpatelh" - "@kevinmenden"