From 0012b42458d97a3cbe336f3ebfc5cd5746b1637b Mon Sep 17 00:00:00 2001 From: Matthias Zepper Date: Fri, 3 Feb 2023 13:49:41 +0100 Subject: [PATCH] Linting with the new version of Black 23.1' --- bin/check_samplesheet.py | 2 - bin/filter_gtf_for_genes_in_genome.py | 1 - bin/mqc_features_stat.py | 1 - bin/prepare-for-rsem.py | 7 - modules.json | 114 +++++----- nextflow_schema.json | 306 +++++++++++--------------- 6 files changed, 190 insertions(+), 241 deletions(-) diff --git a/bin/check_samplesheet.py b/bin/check_samplesheet.py index 69d67446f6..05971a5d91 100755 --- a/bin/check_samplesheet.py +++ b/bin/check_samplesheet.py @@ -48,7 +48,6 @@ def check_samplesheet(file_in, file_out): sample_mapping_dict = {} with open(file_in, "r", encoding="utf-8-sig") as fin: - ## Check header MIN_COLS = 3 HEADER = ["sample", "fastq_1", "fastq_2", "strandedness"] @@ -142,7 +141,6 @@ def check_samplesheet(file_in, file_out): ",".join(["sample", "single_end", "fastq_1", "fastq_2", "strandedness"] + header[len(HEADER) :]) + "\n" ) for sample in sorted(sample_mapping_dict.keys()): - ## Check that multiple runs of the same sample are of the same datatype i.e. single-end / paired-end if not all(x[0] == sample_mapping_dict[sample][0][0] for x in sample_mapping_dict[sample]): print_error( diff --git a/bin/filter_gtf_for_genes_in_genome.py b/bin/filter_gtf_for_genes_in_genome.py index ef4c87cd41..9f876eaa03 100755 --- a/bin/filter_gtf_for_genes_in_genome.py +++ b/bin/filter_gtf_for_genes_in_genome.py @@ -46,7 +46,6 @@ def extract_genes_in_genome(fasta, gtf_in, gtf_out): n_lines_in_genome = 0 with open(gtf_out, "w") as f: with open(gtf_in) as g: - for line in g.readlines(): n_total_lines += 1 seq_name_gtf = line.split("\t")[0] diff --git a/bin/mqc_features_stat.py b/bin/mqc_features_stat.py index c0cb59dc97..689a3f2157 100755 --- a/bin/mqc_features_stat.py +++ b/bin/mqc_features_stat.py @@ -24,7 +24,6 @@ def mqc_feature_stat(bfile, features, outfile, sname=None): - # If sample name not given use file name if not sname: sname = os.path.splitext(os.path.basename(bfile))[0] diff --git a/bin/prepare-for-rsem.py b/bin/prepare-for-rsem.py index 95ef24686b..4a4009fa68 100755 --- a/bin/prepare-for-rsem.py +++ b/bin/prepare-for-rsem.py @@ -68,7 +68,6 @@ def chunk_bam(bamfile): output_buffer = list() for read in bamfile: - if last_query_name is not None and last_query_name != read.query_name: yield (output_buffer) output_buffer = list() @@ -84,7 +83,6 @@ def copy_tags(tags, read1, read2): to read2, if the tag is set""" for tag in tags: - try: read1_tag = read1.get_tag(tag, with_value_type=True) read2.set_tag(tag, value=read1_tag[0], value_type=read1_tag[1]) @@ -122,7 +120,6 @@ def pick_mate(read, template_dict, mate_key): def main(argv=None): - if argv is None: argv = sys.argv @@ -174,7 +171,6 @@ def main(argv=None): options.tags = options.tags.split(",") for template in chunk_bam(inbam): - assert len(set(r.query_name for r in template)) == 1 current_template = {True: defaultdict(list), False: defaultdict(list)} @@ -185,7 +181,6 @@ def main(argv=None): output = set() for read in template: - mate = None # if this read is a non_primary alignment, we first want to check if it has a mate @@ -231,7 +226,6 @@ def main(argv=None): # each pair twice - once when we scan read1 and once when we scan read2. Thus we need # to make sure we don't output something already output. if read.is_read1: - mate = copy_tags(options.tags, read, mate) output_key = str(read) + str(mate) @@ -242,7 +236,6 @@ def main(argv=None): skipped_stats["pairs_output"] += 1 elif read.is_read2: - read = copy_tags(options.tags, mate, read) output_key = str(mate) + str(read) diff --git a/modules.json b/modules.json index 0403e1f6a9..38d19ec1d0 100644 --- a/modules.json +++ b/modules.json @@ -8,143 +8,143 @@ "bbmap/bbsplit": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "cat/fastq": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "custom/dumpsoftwareversions": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "custom/getchromsizes": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", "installed_by": ["modules"], - "patch": "modules/nf-core/custom/getchromsizes/custom-getchromsizes.diff" + "patch": "modules/nf-core/custom/getchromsizes/custom-getchromsizes.diff", }, "fastqc": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["fastq_fastqc_umitools_trimgalore"] + "installed_by": ["fastq_fastqc_umitools_trimgalore"], }, "fq/subsample": { "branch": "master", "git_sha": "ad462aa294faf9a8c42688a08daf81a580594f70", - "installed_by": ["modules", "fastq_subsample_fq_salmon"] + "installed_by": ["modules", "fastq_subsample_fq_salmon"], }, "gffread": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "gunzip": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "hisat2/align": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["fastq_align_hisat2"] + "installed_by": ["fastq_align_hisat2"], }, "hisat2/build": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "hisat2/extractsplicesites": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "picard/markduplicates": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_markduplicates_picard"] + "installed_by": ["bam_markduplicates_picard"], }, "preseq/lcextrap": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "qualimap/rnaseq": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "rsem/calculateexpression": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "rsem/preparereference": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "rseqc/bamstat": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_rseqc"] + "installed_by": ["bam_rseqc"], }, "rseqc/inferexperiment": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_rseqc"] + "installed_by": ["bam_rseqc"], }, "rseqc/innerdistance": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_rseqc"] + "installed_by": ["bam_rseqc"], }, "rseqc/junctionannotation": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_rseqc"] + "installed_by": ["bam_rseqc"], }, "rseqc/junctionsaturation": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_rseqc"] + "installed_by": ["bam_rseqc"], }, "rseqc/readdistribution": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_rseqc"] + "installed_by": ["bam_rseqc"], }, "rseqc/readduplication": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_rseqc"] + "installed_by": ["bam_rseqc"], }, "rseqc/tin": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_rseqc"] + "installed_by": ["bam_rseqc"], }, "salmon/index": { "branch": "master", "git_sha": "94b06f1683ddf893cf06525f6e7f0573ad8fbf83", - "installed_by": ["fastq_subsample_fq_salmon"] + "installed_by": ["fastq_subsample_fq_salmon"], }, "salmon/quant": { "branch": "master", "git_sha": "94b06f1683ddf893cf06525f6e7f0573ad8fbf83", - "installed_by": ["modules", "fastq_subsample_fq_salmon"] + "installed_by": ["modules", "fastq_subsample_fq_salmon"], }, "samtools/flagstat": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_stats_samtools"] + "installed_by": ["bam_stats_samtools"], }, "samtools/idxstats": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_stats_samtools"] + "installed_by": ["bam_stats_samtools"], }, "samtools/index": { "branch": "master", @@ -152,74 +152,74 @@ "installed_by": [ "bam_markduplicates_picard", "bam_sort_stats_samtools", - "bam_dedup_stats_samtools_umitools" - ] + "bam_dedup_stats_samtools_umitools", + ], }, "samtools/sort": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_sort_stats_samtools"] + "installed_by": ["bam_sort_stats_samtools"], }, "samtools/stats": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_stats_samtools"] + "installed_by": ["bam_stats_samtools"], }, "sortmerna": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "star/align": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "star/genomegenerate": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "stringtie/stringtie": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "subread/featurecounts": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] + "installed_by": ["modules"], }, "trimgalore": { "branch": "master", "git_sha": "72ffbd7128015a1d4b65b95ff8d37be8fee2f981", - "installed_by": ["fastq_fastqc_umitools_trimgalore"] + "installed_by": ["fastq_fastqc_umitools_trimgalore"], }, "ucsc/bedclip": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bedgraph_bedclip_bedgraphtobigwig"] + "installed_by": ["bedgraph_bedclip_bedgraphtobigwig"], }, "ucsc/bedgraphtobigwig": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bedgraph_bedclip_bedgraphtobigwig"] + "installed_by": ["bedgraph_bedclip_bedgraphtobigwig"], }, "umitools/dedup": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["bam_dedup_stats_samtools_umitools"] + "installed_by": ["bam_dedup_stats_samtools_umitools"], }, "umitools/extract": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["fastq_fastqc_umitools_trimgalore"] + "installed_by": ["fastq_fastqc_umitools_trimgalore"], }, "untar": { "branch": "master", "git_sha": "c8e35eb2055c099720a75538d1b8adb3fb5a464c", - "installed_by": ["modules"] - } + "installed_by": ["modules"], + }, } }, "subworkflows": { @@ -227,22 +227,22 @@ "bam_dedup_stats_samtools_umitools": { "branch": "master", "git_sha": "41891ec2c3704911cd68b9317f26545b95a1c48d", - "installed_by": ["subworkflows"] + "installed_by": ["subworkflows"], }, "bam_markduplicates_picard": { "branch": "master", "git_sha": "6daac2bc63f4847e0c7cc661f4f5b043ac13faaf", - "installed_by": ["subworkflows"] + "installed_by": ["subworkflows"], }, "bam_rseqc": { "branch": "master", "git_sha": "36a77f7c6decf2d1fb9f639ae982bc148d6828aa", - "installed_by": ["subworkflows"] + "installed_by": ["subworkflows"], }, "bam_sort_stats_samtools": { "branch": "master", "git_sha": "3911652a6b24249358f79e8b8466338d63efb2a2", - "installed_by": ["fastq_align_hisat2"] + "installed_by": ["fastq_align_hisat2"], }, "bam_stats_samtools": { "branch": "master", @@ -250,31 +250,31 @@ "installed_by": [ "bam_sort_stats_samtools", "bam_dedup_stats_samtools_umitools", - "bam_markduplicates_picard" - ] + "bam_markduplicates_picard", + ], }, "bedgraph_bedclip_bedgraphtobigwig": { "branch": "master", "git_sha": "b81a313d8fac0a82a8a4ff0de80590b2f97f11ad", - "installed_by": ["subworkflows"] + "installed_by": ["subworkflows"], }, "fastq_align_hisat2": { "branch": "master", "git_sha": "9057e75e8ac959373a72a9402130fdea2e2d1398", - "installed_by": ["subworkflows"] + "installed_by": ["subworkflows"], }, "fastq_fastqc_umitools_trimgalore": { "branch": "master", "git_sha": "72ffbd7128015a1d4b65b95ff8d37be8fee2f981", - "installed_by": ["subworkflows"] + "installed_by": ["subworkflows"], }, "fastq_subsample_fq_salmon": { "branch": "master", "git_sha": "82d60046b4519e9dbef4a934371a53fa7666eabc", - "installed_by": ["subworkflows"] - } + "installed_by": ["subworkflows"], + }, } - } + }, } - } + }, } diff --git a/nextflow_schema.json b/nextflow_schema.json index 90a223cef4..da7d557755 100644 --- a/nextflow_schema.json +++ b/nextflow_schema.json @@ -20,32 +20,32 @@ "schema": "assets/schema_input.json", "description": "Path to comma-separated file containing information about the samples in the experiment.", "help_text": "You will need to create a design file with information about the samples in your experiment before running the pipeline. Use this parameter to specify its location. It has to be a comma-separated file with 4 columns, and a header row. See [usage docs](https://nf-co.re/rnaseq/usage#samplesheet-input).", - "fa_icon": "fas fa-file-csv" + "fa_icon": "fas fa-file-csv", }, "outdir": { "type": "string", "format": "directory-path", "description": "The output directory where the results will be saved. You have to use absolute paths to storage on Cloud infrastructure.", - "fa_icon": "fas fa-folder-open" + "fa_icon": "fas fa-folder-open", }, "email": { "type": "string", "description": "Email address for completion summary.", "fa_icon": "fas fa-envelope", "help_text": "Set this parameter to your e-mail address to get a summary e-mail with details of the run sent to you when the workflow exits. If set in your user config file (`~/.nextflow/config`) then you don't need to specify this on the command line for every run.", - "pattern": "^([a-zA-Z0-9_\\-\\.]+)@([a-zA-Z0-9_\\-\\.]+)\\.([a-zA-Z]{2,5})$" + "pattern": "^([a-zA-Z0-9_\\-\\.]+)@([a-zA-Z0-9_\\-\\.]+)\\.([a-zA-Z]{2,5})$", }, "multiqc_title": { "type": "string", "description": "MultiQC report title. Printed as page header, used for filename if not otherwise specified.", - "fa_icon": "fas fa-file-signature" + "fa_icon": "fas fa-file-signature", }, "save_merged_fastq": { "type": "boolean", "fa_icon": "fas fa-save", - "description": "Save FastQ files after merging re-sequenced libraries in the results directory." - } - } + "description": "Save FastQ files after merging re-sequenced libraries in the results directory.", + }, + }, }, "umi_options": { "title": "UMI options", @@ -56,61 +56,61 @@ "with_umi": { "type": "boolean", "fa_icon": "fas fa-barcode", - "description": "Enable UMI-based read deduplication." + "description": "Enable UMI-based read deduplication.", }, "umitools_extract_method": { "type": "string", "default": "string", "fa_icon": "fas fa-barcode", "description": "UMI pattern to use. Can be either 'string' (default) or 'regex'.", - "help_text": "More details can be found in the [UMI-tools documentation](https://umi-tools.readthedocs.io/en/latest/reference/extract.html#extract-method).\n" + "help_text": "More details can be found in the [UMI-tools documentation](https://umi-tools.readthedocs.io/en/latest/reference/extract.html#extract-method).\n", }, "skip_umi_extract": { "type": "boolean", "fa_icon": "fas fa-compress-alt", - "description": "Skip the UMI extraction from the read in case the UMIs have been moved to the headers in advance of the pipeline run." + "description": "Skip the UMI extraction from the read in case the UMIs have been moved to the headers in advance of the pipeline run.", }, "umitools_bc_pattern": { "type": "string", "fa_icon": "fas fa-barcode", "help_text": "More details can be found in the [UMI-tools documentation](https://umi-tools.readthedocs.io/en/latest/reference/extract.html#extract-method).", - "description": "The UMI barcode pattern to use e.g. 'NNNNNN' indicates that the first 6 nucleotides of the read are from the UMI." + "description": "The UMI barcode pattern to use e.g. 'NNNNNN' indicates that the first 6 nucleotides of the read are from the UMI.", }, "umitools_bc_pattern2": { "type": "string", "fa_icon": "fas fa-barcode", - "description": "The UMI barcode pattern to use if the UMI is located in read 2." + "description": "The UMI barcode pattern to use if the UMI is located in read 2.", }, "umi_discard_read": { "type": "integer", "fa_icon": "fas fa-barcode", - "description": "After UMI barcode extraction discard either R1 or R2 by setting this parameter to 1 or 2, respectively." + "description": "After UMI barcode extraction discard either R1 or R2 by setting this parameter to 1 or 2, respectively.", }, "umitools_umi_separator": { "type": "string", "fa_icon": "fas fa-star-half-alt", - "description": "The character that separates the UMI in the read name. Most likely a colon if you skipped the extraction with UMI-tools and used other software." + "description": "The character that separates the UMI in the read name. Most likely a colon if you skipped the extraction with UMI-tools and used other software.", }, "umitools_grouping_method": { "type": "string", "default": "directional", "fa_icon": "far fa-object-ungroup", "description": "Method to use to determine read groups by subsuming those with similar UMIs. All methods start by identifying the reads with the same mapping position, but treat similar yet nonidentical UMIs differently.", - "enum": ["unique", "percentile", "cluster", "adjacency", "directional"] + "enum": ["unique", "percentile", "cluster", "adjacency", "directional"], }, "umitools_dedup_stats": { "type": "boolean", "fa_icon": "fas fa-barcode", "help_text": "It can be quite time consuming generating these output stats - see [#827](https://github.com/nf-core/rnaseq/issues/827).", - "description": "Generate output stats when running \"umi_tools dedup\"." + "description": 'Generate output stats when running "umi_tools dedup".', }, "save_umi_intermeds": { "type": "boolean", "fa_icon": "fas fa-save", - "description": "If this option is specified, intermediate FastQ and BAM files produced by UMI-tools are also saved in the results directory." - } + "description": "If this option is specified, intermediate FastQ and BAM files produced by UMI-tools are also saved in the results directory.", + }, }, - "fa_icon": "fas fa-barcode" + "fa_icon": "fas fa-barcode", }, "read_filtering_options": { "title": "Read filtering options", @@ -122,45 +122,45 @@ "type": "string", "fa_icon": "fas fa-list-alt", "description": "Path to comma-separated file containing a list of reference genomes to filter reads against with BBSplit. You have to also explicitly set `--skip_bbsplit false` if you want to use BBSplit.", - "help_text": "The file should contain 2 columns: short name and full path to reference genome(s) e.g. \n```\nmm10,/path/to/mm10.fa\necoli,/path/to/ecoli.fa\n```" + "help_text": "The file should contain 2 columns: short name and full path to reference genome(s) e.g. \n```\nmm10,/path/to/mm10.fa\necoli,/path/to/ecoli.fa\n```", }, "bbsplit_index": { "type": "string", "fa_icon": "fas fa-bezier-curve", "description": "Path to directory or tar.gz archive for pre-built BBSplit index.", - "help_text": "The BBSplit index will have to be built at least once with this pipeline (see `--save_reference` to save index). It can then be provided via `--bbsplit_index` for future runs." + "help_text": "The BBSplit index will have to be built at least once with this pipeline (see `--save_reference` to save index). It can then be provided via `--bbsplit_index` for future runs.", }, "save_bbsplit_reads": { "type": "boolean", "fa_icon": "fas fa-save", - "description": "If this option is specified, FastQ files split by reference will be saved in the results directory." + "description": "If this option is specified, FastQ files split by reference will be saved in the results directory.", }, "skip_bbsplit": { "type": "boolean", "default": true, "fa_icon": "fas fa-fast-forward", - "description": "Skip BBSplit for removal of non-reference genome reads." + "description": "Skip BBSplit for removal of non-reference genome reads.", }, "remove_ribo_rna": { "type": "boolean", "fa_icon": "fas fa-trash-alt", "description": "Enable the removal of reads derived from ribosomal RNA using SortMeRNA.", - "help_text": "Any patterns found in the sequences defined by the '--ribo_database_manifest' parameter will be used." + "help_text": "Any patterns found in the sequences defined by the '--ribo_database_manifest' parameter will be used.", }, "ribo_database_manifest": { "type": "string", "default": "${projectDir}/assets/rrna-db-defaults.txt", "fa_icon": "fas fa-database", "description": "Text file containing paths to fasta files (one per line) that will be used to create the database for SortMeRNA.", - "help_text": "By default, [rRNA databases](https://github.com/biocore/sortmerna/tree/master/data/rRNA_databases) defined in the SortMeRNA GitHub repo are used. You can see an example in the pipeline Github repository in `assets/rrna-default-dbs.txt`.\nPlease note that commercial/non-academic entities require [`licensing for SILVA`](https://www.arb-silva.de/silva-license-information) for these default databases." + "help_text": "By default, [rRNA databases](https://github.com/biocore/sortmerna/tree/master/data/rRNA_databases) defined in the SortMeRNA GitHub repo are used. You can see an example in the pipeline Github repository in `assets/rrna-default-dbs.txt`.\nPlease note that commercial/non-academic entities require [`licensing for SILVA`](https://www.arb-silva.de/silva-license-information) for these default databases.", }, "save_non_ribo_reads": { "type": "boolean", "fa_icon": "fas fa-save", - "description": "If this option is specified, intermediate FastQ files containing non-rRNA reads will be saved in the results directory." - } + "description": "If this option is specified, intermediate FastQ files containing non-rRNA reads will be saved in the results directory.", + }, }, - "fa_icon": "fas fa-trash-alt" + "fa_icon": "fas fa-trash-alt", }, "reference_genome_options": { "title": "Reference genome options", @@ -172,7 +172,7 @@ "type": "string", "description": "Name of iGenomes reference.", "fa_icon": "fas fa-book", - "help_text": "If using a reference genome configured in the pipeline using iGenomes, use this parameter to give the ID for the reference. This is then used to build the full paths for all required reference genome files e.g. `--genome GRCh38`. \n\nSee the [nf-core website docs](https://nf-co.re/usage/reference_genomes) for more details." + "help_text": "If using a reference genome configured in the pipeline using iGenomes, use this parameter to give the ID for the reference. This is then used to build the full paths for all required reference genome files e.g. `--genome GRCh38`. \n\nSee the [nf-core website docs](https://nf-co.re/usage/reference_genomes) for more details.", }, "fasta": { "type": "string", @@ -181,7 +181,7 @@ "pattern": "^\\S+\\.fn?a(sta)?(\\.gz)?$", "description": "Path to FASTA genome file.", "help_text": "This parameter is *mandatory* if `--genome` is not specified. If you don't have the appropriate alignment index available this will be generated for you automatically. Combine with `--save_reference` to save alignment index for future runs.", - "fa_icon": "far fa-file-code" + "fa_icon": "far fa-file-code", }, "gtf": { "type": "string", @@ -190,7 +190,7 @@ "pattern": "^\\S+\\.gtf(\\.gz)?$", "description": "Path to GTF annotation file.", "fa_icon": "fas fa-code-branch", - "help_text": "This parameter is *mandatory* if `--genome` is not specified." + "help_text": "This parameter is *mandatory* if `--genome` is not specified.", }, "gff": { "type": "string", @@ -199,7 +199,7 @@ "pattern": "^\\S+\\.gff(\\.gz)?$", "fa_icon": "fas fa-code-branch", "description": "Path to GFF3 annotation file.", - "help_text": "This parameter must be specified if `--genome` or `--gtf` are not specified." + "help_text": "This parameter must be specified if `--genome` or `--gtf` are not specified.", }, "gene_bed": { "type": "string", @@ -207,7 +207,7 @@ "mimetype": "text/plain", "pattern": "^\\S+\\.bed(\\.gz)?$", "fa_icon": "fas fa-procedures", - "description": "Path to BED file containing gene intervals. This will be created from the GTF file if not specified." + "description": "Path to BED file containing gene intervals. This will be created from the GTF file if not specified.", }, "transcript_fasta": { "type": "string", @@ -215,7 +215,7 @@ "mimetype": "text/plain", "pattern": "^\\S+\\.fn?a(sta)?(\\.gz)?$", "fa_icon": "far fa-file-code", - "description": "Path to FASTA transcriptome file." + "description": "Path to FASTA transcriptome file.", }, "additional_fasta": { "type": "string", @@ -224,38 +224,38 @@ "pattern": "^\\S+\\.fn?a(sta)?(\\.gz)?$", "fa_icon": "far fa-file-code", "description": "FASTA file to concatenate to genome FASTA file e.g. containing spike-in sequences.", - "help_text": "If provided, the sequences in this file will get concatenated to the existing genome FASTA file, a GTF file will be automatically created using the entire sequence as the gene, transcript, and exon features, and any alignment index will get created from the combined FASTA and GTF. It is recommended to save the reference with `--save_reference` to re-use the index for future runs so you do not need to create it again." + "help_text": "If provided, the sequences in this file will get concatenated to the existing genome FASTA file, a GTF file will be automatically created using the entire sequence as the gene, transcript, and exon features, and any alignment index will get created from the combined FASTA and GTF. It is recommended to save the reference with `--save_reference` to re-use the index for future runs so you do not need to create it again.", }, "splicesites": { "type": "string", "format": "file-path", "mimetype": "text/plain", "fa_icon": "fas fa-hand-scissors", - "description": "Splice sites file required for HISAT2." + "description": "Splice sites file required for HISAT2.", }, "star_index": { "type": "string", "format": "path", "fa_icon": "fas fa-bezier-curve", - "description": "Path to directory or tar.gz archive for pre-built STAR index." + "description": "Path to directory or tar.gz archive for pre-built STAR index.", }, "hisat2_index": { "type": "string", "format": "path", "fa_icon": "fas fa-bezier-curve", - "description": "Path to directory or tar.gz archive for pre-built HISAT2 index." + "description": "Path to directory or tar.gz archive for pre-built HISAT2 index.", }, "rsem_index": { "type": "string", "format": "path", "fa_icon": "fas fa-bezier-curve", - "description": "Path to directory or tar.gz archive for pre-built RSEM index." + "description": "Path to directory or tar.gz archive for pre-built RSEM index.", }, "salmon_index": { "type": "string", "format": "path", "fa_icon": "fas fa-bezier-curve", - "description": "Path to directory or tar.gz archive for pre-built Salmon index." + "description": "Path to directory or tar.gz archive for pre-built Salmon index.", }, "hisat2_build_memory": { "type": "string", @@ -263,45 +263,45 @@ "fa_icon": "fas fa-memory", "pattern": "^\\d+(\\.\\d+)?\\.?\\s*(K|M|G|T)?B$", "description": "Minimum memory required to use splice sites and exons in the HiSAT2 index build process.", - "help_text": "HiSAT2 requires a huge amount of RAM to build a genome index for larger genomes, if including splice sites and exons e.g. the human genome might typically require 200GB. If you specify less than this threshold for the `HISAT2_BUILD` process then the splice sites and exons will be ignored, meaning that the process will require a lot less memory. If you are working with a small genome, set this parameter to a lower value to reduce the threshold for skipping this check. If using a larger genome, consider supplying more memory to the `HISAT2_BUILD` process." + "help_text": "HiSAT2 requires a huge amount of RAM to build a genome index for larger genomes, if including splice sites and exons e.g. the human genome might typically require 200GB. If you specify less than this threshold for the `HISAT2_BUILD` process then the splice sites and exons will be ignored, meaning that the process will require a lot less memory. If you are working with a small genome, set this parameter to a lower value to reduce the threshold for skipping this check. If using a larger genome, consider supplying more memory to the `HISAT2_BUILD` process.", }, "gencode": { "type": "boolean", "fa_icon": "fas fa-code-branch", "description": "Specify if your GTF annotation is in GENCODE format.", - "help_text": "If your GTF file is in GENCODE format and you would like to run Salmon i.e. `--pseudo_aligner salmon`, you will need to provide this parameter in order to build the Salmon index appropriately." + "help_text": "If your GTF file is in GENCODE format and you would like to run Salmon i.e. `--pseudo_aligner salmon`, you will need to provide this parameter in order to build the Salmon index appropriately.", }, "gtf_extra_attributes": { "type": "string", "default": "gene_name", "fa_icon": "fas fa-plus-square", "description": "By default, the pipeline uses the `gene_name` field to obtain additional gene identifiers from the input GTF file when running Salmon.", - "help_text": "This behaviour can be modified by specifying `--gtf_extra_attributes` when running the pipeline. Note that you can also specify more than one desired value, separated by a comma e.g. `--gtf_extra_attributes gene_id,...`.\n" + "help_text": "This behaviour can be modified by specifying `--gtf_extra_attributes` when running the pipeline. Note that you can also specify more than one desired value, separated by a comma e.g. `--gtf_extra_attributes gene_id,...`.\n", }, "gtf_group_features": { "type": "string", "default": "gene_id", "description": "Define the attribute type used to group features in the GTF file when running Salmon.", - "fa_icon": "fas fa-layer-group" + "fa_icon": "fas fa-layer-group", }, "featurecounts_group_type": { "type": "string", "default": "gene_biotype", "fa_icon": "fas fa-layer-group", - "description": "The attribute type used to group feature types in the GTF file when generating the biotype plot with featureCounts." + "description": "The attribute type used to group feature types in the GTF file when generating the biotype plot with featureCounts.", }, "featurecounts_feature_type": { "type": "string", "default": "exon", "description": "By default, the pipeline assigns reads based on the 'exon' attribute within the GTF file.", "fa_icon": "fas fa-indent", - "help_text": "The feature type used from the GTF file when generating the biotype plot with featureCounts." + "help_text": "The feature type used from the GTF file when generating the biotype plot with featureCounts.", }, "save_reference": { "type": "boolean", "description": "If generated by the pipeline save the STAR index in the results directory.", "help_text": "If an alignment index is generated by the pipeline use this parameter to save it to your results folder. These can then be used for future pipeline runs, reducing processing times.", - "fa_icon": "fas fa-save" + "fa_icon": "fas fa-save", }, "igenomes_base": { "type": "string", @@ -309,16 +309,16 @@ "description": "Directory / URL base for iGenomes references.", "default": "s3://ngi-igenomes/igenomes", "fa_icon": "fas fa-cloud-download-alt", - "hidden": true + "hidden": true, }, "igenomes_ignore": { "type": "boolean", "description": "Do not load the iGenomes reference config.", "fa_icon": "fas fa-ban", "hidden": true, - "help_text": "Do not load `igenomes.config` when running the pipeline. You may choose this option if you observe clashes between custom parameters and those supplied in `igenomes.config`." - } - } + "help_text": "Do not load `igenomes.config` when running the pipeline. You may choose this option if you observe clashes between custom parameters and those supplied in `igenomes.config`.", + }, + }, }, "read_trimming_options": { "title": "Read trimming options", @@ -329,48 +329,48 @@ "clip_r1": { "type": "integer", "description": "Instructs Trim Galore to remove bp from the 5' end of read 1 (or single-end reads).", - "fa_icon": "fas fa-cut" + "fa_icon": "fas fa-cut", }, "clip_r2": { "type": "integer", "description": "Instructs Trim Galore to remove bp from the 5' end of read 2 (paired-end reads only).", - "fa_icon": "fas fa-cut" + "fa_icon": "fas fa-cut", }, "three_prime_clip_r1": { "type": "integer", "description": "Instructs Trim Galore to remove bp from the 3' end of read 1 AFTER adapter/quality trimming has been performed.", - "fa_icon": "fas fa-cut" + "fa_icon": "fas fa-cut", }, "three_prime_clip_r2": { "type": "integer", "description": "Instructs Trim Galore to remove bp from the 3' end of read 2 AFTER adapter/quality trimming has been performed.", - "fa_icon": "fas fa-cut" + "fa_icon": "fas fa-cut", }, "trim_nextseq": { "type": "integer", "description": "Instructs Trim Galore to apply the --nextseq=X option, to trim based on quality after removing poly-G tails.", "help_text": "This enables the option Cutadapt `--nextseq-trim=3'CUTOFF` option via Trim Galore, which will set a quality cutoff (that is normally given with -q instead), but qualities of G bases are ignored. This trimming is in common for the NextSeq- and NovaSeq-platforms, where basecalls without any signal are called as high-quality G bases.", - "fa_icon": "fas fa-cut" + "fa_icon": "fas fa-cut", }, "min_trimmed_reads": { "type": "integer", "default": 10000, "fa_icon": "fas fa-hand-paper", - "description": "Minimum number of trimmed reads below which samples are removed from further processing. Some downstream steps in the pipeline will fail if this threshold is too low." + "description": "Minimum number of trimmed reads below which samples are removed from further processing. Some downstream steps in the pipeline will fail if this threshold is too low.", }, "skip_trimming": { "type": "boolean", "description": "Skip the adapter trimming step.", "help_text": "Use this if your input FastQ files have already been trimmed outside of the workflow or if you're very confident that there is no adapter contamination in your data.", - "fa_icon": "fas fa-fast-forward" + "fa_icon": "fas fa-fast-forward", }, "save_trimmed": { "type": "boolean", "description": "Save the trimmed FastQ files in the results directory.", "help_text": "By default, trimmed FastQ files will not be saved to the results directory. Specify this flag (or set to true in your config file) to copy these files to the results directory when complete.", - "fa_icon": "fas fa-save" - } - } + "fa_icon": "fas fa-save", + }, + }, }, "alignment_options": { "title": "Alignment options", @@ -383,80 +383,80 @@ "default": "star_salmon", "description": "Specifies the alignment algorithm to use - available options are 'star_salmon', 'star_rsem' and 'hisat2'.", "fa_icon": "fas fa-map-signs", - "enum": ["star_salmon", "star_rsem", "hisat2"] + "enum": ["star_salmon", "star_rsem", "hisat2"], }, "pseudo_aligner": { "type": "string", "description": "Specifies the pseudo aligner to use - available options are 'salmon'. Runs in addition to '--aligner'.", "fa_icon": "fas fa-hamburger", - "enum": ["salmon"] + "enum": ["salmon"], }, "bam_csi_index": { "type": "boolean", "description": "Create a CSI index for BAM files instead of the traditional BAI index. This will be required for genomes with larger chromosome sizes.", - "fa_icon": "fas fa-sort-alpha-down" + "fa_icon": "fas fa-sort-alpha-down", }, "star_ignore_sjdbgtf": { "type": "boolean", "fa_icon": "fas fa-ban", - "description": "When using pre-built STAR indices do not re-extract and use splice junctions from the GTF file." + "description": "When using pre-built STAR indices do not re-extract and use splice junctions from the GTF file.", }, "salmon_quant_libtype": { "type": "string", "fa_icon": "fas fa-fast-forward", "description": " Override Salmon library type inferred based on strandedness defined in meta object.", - "help_text": "See [Salmon docs](https://salmon.readthedocs.io/en/latest/library_type.html)." + "help_text": "See [Salmon docs](https://salmon.readthedocs.io/en/latest/library_type.html).", }, "min_mapped_reads": { "type": "number", "default": 5, "fa_icon": "fas fa-percentage", "description": "Minimum percentage of uniquely mapped reads below which samples are removed from further processing.", - "help_text": "Some downstream steps in the pipeline will fail if this threshold is too low." + "help_text": "Some downstream steps in the pipeline will fail if this threshold is too low.", }, "seq_center": { "type": "string", "description": "Sequencing center information to be added to read group of BAM files.", - "fa_icon": "fas fa-synagogue" + "fa_icon": "fas fa-synagogue", }, "stringtie_ignore_gtf": { "type": "boolean", "description": "Perform reference-guided de novo assembly of transcripts using StringTie i.e. dont restrict to those in GTF file.", - "fa_icon": "fas fa-ban" + "fa_icon": "fas fa-ban", }, "extra_star_align_args": { "type": "string", "description": "Extra arguments to pass to STAR alignment command in addition to defaults defined by the pipeline.", - "fa_icon": "fas fa-plus" + "fa_icon": "fas fa-plus", }, "extra_salmon_quant_args": { "type": "string", "description": "Extra arguments to pass to Salmon quant command in addition to defaults defined by the pipeline.", - "fa_icon": "fas fa-plus" + "fa_icon": "fas fa-plus", }, "save_unaligned": { "type": "boolean", "fa_icon": "fas fa-save", "description": "Where possible, save unaligned reads from either STAR, HISAT2 or Salmon to the results directory.", - "help_text": "This may either be in the form of FastQ or BAM files depending on the options available for that particular tool." + "help_text": "This may either be in the form of FastQ or BAM files depending on the options available for that particular tool.", }, "save_align_intermeds": { "type": "boolean", "description": "Save the intermediate BAM files from the alignment step.", "help_text": "By default, intermediate BAM files will not be saved. The final BAM files created after the appropriate filtering step are always saved to limit storage usage. Set this parameter to also save other intermediate BAM files.", - "fa_icon": "fas fa-save" + "fa_icon": "fas fa-save", }, "skip_markduplicates": { "type": "boolean", "fa_icon": "fas fa-fast-forward", - "description": "Skip picard MarkDuplicates step." + "description": "Skip picard MarkDuplicates step.", }, "skip_alignment": { "type": "boolean", "fa_icon": "fas fa-fast-forward", - "description": "Skip all of the alignment-based processes within the pipeline." - } - } + "description": "Skip all of the alignment-based processes within the pipeline.", + }, + }, }, "process_skipping_options": { "title": "Process skipping options", @@ -468,72 +468,52 @@ "type": "string", "default": "bam_stat,inner_distance,infer_experiment,junction_annotation,junction_saturation,read_distribution,read_duplication", "fa_icon": "fas fa-chart-pie", - "description": "Specify the RSeQC modules to run." + "description": "Specify the RSeQC modules to run.", }, "deseq2_vst": { "type": "boolean", "description": "Use vst transformation instead of rlog with DESeq2.", "help_text": "See [DESeq2 docs](http://bioconductor.org/packages/devel/bioc/vignettes/DESeq2/inst/doc/DESeq2.html#data-transformations-and-visualization).", "fa_icon": "fas fa-dolly", - "default": true + "default": true, }, "skip_bigwig": { "type": "boolean", "fa_icon": "fas fa-fast-forward", - "description": "Skip bigWig file creation." + "description": "Skip bigWig file creation.", }, "skip_stringtie": { "type": "boolean", "fa_icon": "fas fa-fast-forward", - "description": "Skip StringTie." - }, - "skip_fastqc": { - "type": "boolean", - "description": "Skip FastQC.", - "fa_icon": "fas fa-fast-forward" + "description": "Skip StringTie.", }, + "skip_fastqc": {"type": "boolean", "description": "Skip FastQC.", "fa_icon": "fas fa-fast-forward"}, "skip_preseq": { "type": "boolean", "description": "Skip Preseq.", "fa_icon": "fas fa-fast-forward", - "default": true - }, - "skip_dupradar": { - "type": "boolean", - "fa_icon": "fas fa-fast-forward", - "description": "Skip dupRadar." - }, - "skip_qualimap": { - "type": "boolean", - "fa_icon": "fas fa-fast-forward", - "description": "Skip Qualimap." - }, - "skip_rseqc": { - "type": "boolean", - "fa_icon": "fas fa-fast-forward", - "description": "Skip RSeQC." + "default": true, }, + "skip_dupradar": {"type": "boolean", "fa_icon": "fas fa-fast-forward", "description": "Skip dupRadar."}, + "skip_qualimap": {"type": "boolean", "fa_icon": "fas fa-fast-forward", "description": "Skip Qualimap."}, + "skip_rseqc": {"type": "boolean", "fa_icon": "fas fa-fast-forward", "description": "Skip RSeQC."}, "skip_biotype_qc": { "type": "boolean", "fa_icon": "fas fa-fast-forward", - "description": "Skip additional featureCounts process for biotype QC." + "description": "Skip additional featureCounts process for biotype QC.", }, "skip_deseq2_qc": { "type": "boolean", "fa_icon": "fas fa-fast-forward", - "description": "Skip DESeq2 PCA and heatmap plotting." - }, - "skip_multiqc": { - "type": "boolean", - "description": "Skip MultiQC.", - "fa_icon": "fas fa-fast-forward" + "description": "Skip DESeq2 PCA and heatmap plotting.", }, + "skip_multiqc": {"type": "boolean", "description": "Skip MultiQC.", "fa_icon": "fas fa-fast-forward"}, "skip_qc": { "type": "boolean", "fa_icon": "fas fa-fast-forward", - "description": "Skip all QC steps except for MultiQC." - } - } + "description": "Skip all QC steps except for MultiQC.", + }, + }, }, "institutional_config_options": { "title": "Institutional config options", @@ -547,7 +527,7 @@ "description": "Git commit id for Institutional configs.", "default": "master", "hidden": true, - "fa_icon": "fas fa-users-cog" + "fa_icon": "fas fa-users-cog", }, "custom_config_base": { "type": "string", @@ -555,33 +535,33 @@ "default": "https://raw.githubusercontent.com/nf-core/configs/master", "hidden": true, "help_text": "If you're running offline, Nextflow will not be able to fetch the institutional config files from the internet. If you don't need them, then this is not a problem. If you do need them, you should download the files from the repo and tell Nextflow where to find them with this parameter.", - "fa_icon": "fas fa-users-cog" + "fa_icon": "fas fa-users-cog", }, "config_profile_name": { "type": "string", "description": "Institutional config name.", "hidden": true, - "fa_icon": "fas fa-users-cog" + "fa_icon": "fas fa-users-cog", }, "config_profile_description": { "type": "string", "description": "Institutional config description.", "hidden": true, - "fa_icon": "fas fa-users-cog" + "fa_icon": "fas fa-users-cog", }, "config_profile_contact": { "type": "string", "description": "Institutional config contact information.", "hidden": true, - "fa_icon": "fas fa-users-cog" + "fa_icon": "fas fa-users-cog", }, "config_profile_url": { "type": "string", "description": "Institutional config URL link.", "hidden": true, - "fa_icon": "fas fa-users-cog" - } - } + "fa_icon": "fas fa-users-cog", + }, + }, }, "max_job_request_options": { "title": "Max job request options", @@ -596,7 +576,7 @@ "default": 16, "fa_icon": "fas fa-microchip", "hidden": true, - "help_text": "Use to set an upper-limit for the CPU requirement for each process. Should be an integer e.g. `--max_cpus 1`" + "help_text": "Use to set an upper-limit for the CPU requirement for each process. Should be an integer e.g. `--max_cpus 1`", }, "max_memory": { "type": "string", @@ -605,7 +585,7 @@ "fa_icon": "fas fa-memory", "pattern": "^\\d+(\\.\\d+)?\\.?\\s*(K|M|G|T)?B$", "hidden": true, - "help_text": "Use to set an upper-limit for the memory requirement for each process. Should be a string in the format integer-unit e.g. `--max_memory '8.GB'`" + "help_text": "Use to set an upper-limit for the memory requirement for each process. Should be a string in the format integer-unit e.g. `--max_memory '8.GB'`", }, "max_time": { "type": "string", @@ -614,9 +594,9 @@ "fa_icon": "far fa-clock", "pattern": "^(\\d+\\.?\\s*(s|m|h|day)\\s*)+$", "hidden": true, - "help_text": "Use to set an upper-limit for the time requirement for each process. Should be a string in the format integer-unit e.g. `--max_time '2.h'`" - } - } + "help_text": "Use to set an upper-limit for the time requirement for each process. Should be a string in the format integer-unit e.g. `--max_time '2.h'`", + }, + }, }, "generic_options": { "title": "Generic options", @@ -629,13 +609,13 @@ "type": "boolean", "description": "Display help text.", "fa_icon": "fas fa-question-circle", - "hidden": true + "hidden": true, }, "version": { "type": "boolean", "description": "Display version and exit.", "fa_icon": "fas fa-question-circle", - "hidden": true + "hidden": true, }, "publish_dir_mode": { "type": "string", @@ -644,7 +624,7 @@ "help_text": "The Nextflow `publishDir` option specifies which intermediate files should be saved to the output directory. This option tells the pipeline what method should be used to move these files. See [Nextflow docs](https://www.nextflow.io/docs/latest/process.html#publishdir) for details.", "fa_icon": "fas fa-copy", "enum": ["symlink", "rellink", "link", "copy", "copyNoFollow", "move"], - "hidden": true + "hidden": true, }, "email_on_fail": { "type": "string", @@ -652,105 +632,85 @@ "fa_icon": "fas fa-exclamation-triangle", "pattern": "^([a-zA-Z0-9_\\-\\.]+)@([a-zA-Z0-9_\\-\\.]+)\\.([a-zA-Z]{2,5})$", "help_text": "An email address to send a summary email to when the pipeline is completed - ONLY sent if the pipeline does not exit successfully.", - "hidden": true + "hidden": true, }, "plaintext_email": { "type": "boolean", "description": "Send plain-text email instead of HTML.", "fa_icon": "fas fa-remove-format", - "hidden": true + "hidden": true, }, "max_multiqc_email_size": { "type": "string", "description": "File size limit when attaching MultiQC reports to summary emails.", "default": "25.MB", "fa_icon": "fas fa-file-upload", - "hidden": true + "hidden": true, }, "monochrome_logs": { "type": "boolean", "description": "Do not use coloured log outputs.", "fa_icon": "fas fa-palette", - "hidden": true + "hidden": true, }, "hook_url": { "type": "string", "description": "Incoming hook URL for messaging service", "fa_icon": "fas fa-people-group", "help_text": "Incoming hook URL for messaging service. Currently, MS Teams and Slack are supported.", - "hidden": true + "hidden": true, }, "multiqc_config": { "type": "string", "description": "Custom config file to supply to MultiQC.", "fa_icon": "fas fa-cog", - "hidden": true + "hidden": true, }, "multiqc_logo": { "type": "string", "description": "Custom logo file to supply to MultiQC. File name must also be set in the MultiQC config file", "fa_icon": "fas fa-image", - "hidden": true + "hidden": true, }, "multiqc_methods_description": { "type": "string", "description": "Custom MultiQC yaml file containing HTML including a methods description.", - "fa_icon": "fas fa-cog" + "fa_icon": "fas fa-cog", }, "tracedir": { "type": "string", "description": "Directory to keep pipeline Nextflow logs and reports.", "default": "${params.outdir}/pipeline_info", "fa_icon": "fas fa-cogs", - "hidden": true + "hidden": true, }, "validate_params": { "type": "boolean", "description": "Boolean whether to validate parameters against the schema at runtime", "default": true, "fa_icon": "fas fa-check-square", - "hidden": true + "hidden": true, }, "show_hidden_params": { "type": "boolean", "fa_icon": "far fa-eye-slash", "description": "Show all params when using `--help`", "hidden": true, - "help_text": "By default, parameters set as _hidden_ in the schema are not shown on the command line when a user runs with `--help`. Specifying this option will tell the pipeline to show all parameters." - } - } - } + "help_text": "By default, parameters set as _hidden_ in the schema are not shown on the command line when a user runs with `--help`. Specifying this option will tell the pipeline to show all parameters.", + }, + }, + }, }, "allOf": [ - { - "$ref": "#/definitions/input_output_options" - }, - { - "$ref": "#/definitions/umi_options" - }, - { - "$ref": "#/definitions/read_filtering_options" - }, - { - "$ref": "#/definitions/reference_genome_options" - }, - { - "$ref": "#/definitions/read_trimming_options" - }, - { - "$ref": "#/definitions/alignment_options" - }, - { - "$ref": "#/definitions/process_skipping_options" - }, - { - "$ref": "#/definitions/institutional_config_options" - }, - { - "$ref": "#/definitions/max_job_request_options" - }, - { - "$ref": "#/definitions/generic_options" - } - ] + {"$ref": "#/definitions/input_output_options"}, + {"$ref": "#/definitions/umi_options"}, + {"$ref": "#/definitions/read_filtering_options"}, + {"$ref": "#/definitions/reference_genome_options"}, + {"$ref": "#/definitions/read_trimming_options"}, + {"$ref": "#/definitions/alignment_options"}, + {"$ref": "#/definitions/process_skipping_options"}, + {"$ref": "#/definitions/institutional_config_options"}, + {"$ref": "#/definitions/max_job_request_options"}, + {"$ref": "#/definitions/generic_options"}, + ], }