// // Notes to End Users. // // The workflow should run without editing this configuration file, // however there may be instances in which you wish to edit this // file for compute performance or other reasons. Please see: // // https://nextflow.io/docs/latest/config.html#configuration // // for further help editing this file. params { help = false fastq = null ref_genome = null ref_annotation = null // Process cDNA reads using pychopper, turn off for direct RNA: use_pychopper = true threads = 4 out_dir = null sample = null sample_sheet = null sanitize_fastq = false wfversion = "v0.0.1" aws_image_prefix = null aws_queue = null report_name = "report" monochrome_logs = false validate_params = true show_hidden_params = false schema_ignore_params = 'show_hidden_params,validate_params,monochrome_logs,aws_queue,aws_image_prefix,wfversion' // Options passed to pychopper: pychopper_opts = "" // Extra option passed to minimap2 when generating index minimap_index_opts = "-k14" // Extra options passed to minimap2 minimap2_opts = "-uf" // Add this for SIRV data: // "--splice-flank=no" // Minmum mapping quality minimum_mapping_quality = 40 // Internal priming filter context size: poly_context = 24 // Maximum allowed poly(A) length in the genome near the 3' end of mapping: max_poly_run = 8 // Minimium number of reads in BAM bundles: bundle_min_reads = 50000 // Options passed to stringtie: stringtie_opts = " --conservative " // Options passed to gffcompare: gffcompare_opts = " -R " // Plot gffcompare results: plot_gffcmp_stats = true disable_ping = false } manifest { name = 'epi2me-labs/wf-isoforms' author = 'Oxford Nanopore Technologies' homePage = 'https://github.com/epi2me-labs/wf-isoforms' description = 'RNA/cDNA isoform analysis workflow' mainScript = 'main.nf' nextflowVersion = '>=20.10.0' //version = 'v0.0.7' // TODO: do switch to this? } executor { $local { cpus = 4 memory = "8 GB" } } // used by default for "standard" (docker) and singularity profiles, // other profiles may override. process { withLabel:isoforms { container = "ontresearch/wf-isoforms:${params.wfversion}" } shell = ['/bin/bash', '-euo', 'pipefail'] } profiles { // the "standard" profile is used implicitely by nextflow // if no other profile is given on the CLI standard { docker { enabled = true // this ensures container is run as host user and group, but // also adds host user to the within-container group runOptions = "--user \$(id -u):\$(id -g) --group-add 100" } } // using singularity instead of docker singularity { singularity { enabled = true autoMounts = true } } // profile using conda environments conda { docker.enabled = false process { withLabel:isoforms { conda = "${projectDir}/environment.yaml" } shell = ['/bin/bash', '-euo', 'pipefail'] } conda { cacheDir = "" useMamba = true } } // Using AWS batch. // May need to set aws.region and aws.batch.cliPath awsbatch { process { executor = 'awsbatch' queue = "${params.aws_queue}" memory = '8G' withLabel:isoforms { container = "${params.aws_image_prefix}-wf-isoforms:${params.wfversion}" } shell = ['/bin/bash', '-euo', 'pipefail'] } } // local profile for simplified development testing local { process.executor = 'local' } } timeline { enabled = true file = "${params.out_dir}/execution/timeline.html" } report { enabled = true file = "${params.out_dir}/execution/report.html" } trace { enabled = true file = "${params.out_dir}/execution/trace.txt" } dag { enabled = true file = "${params.out_dir}/execution/pipeline.svg" }