{ "class": "Workflow", "cwlVersion": "v1.2", "id": "dna_resequencing_short_mem", "doc": "This workflow aligns short reads from fastq files using the\nbwa mem algorithm. It first starts by indexing the reference\ngenome if such index does not exist, performs quality control\nstep of the raw reads and performs adapter trimming. Trimmed\nreads are then aligned, sorted by reads name and pair end reads\nare corrected using samtools fixmate. All this steps, with the\nexception of the indexing, are scattered. After the alignment\nof each run, these files are merged and then a post-processing\nstep takes place which includes duplicate marking and base\nquality recalibration (for model organisms)\n", "requirements": [ { "class": "SubworkflowFeatureRequirement" }, { "class": "ScatterFeatureRequirement" }, { "class": "StepInputExpressionRequirement" }, { "class": "InlineJavascriptRequirement" } ], "inputs": [ { "type": { "type": "array", "items": { "type": "record", "fields": [ { "type": "string", "name": "run_id" }, { "type": { "type": "array", "items": "File" }, "name": "files" } ] } }, "id": "reads" }, { "type": "File", "secondaryFiles": [ "^.dict", ".fai", ".amb", ".ann", ".bwt", ".pac", ".sa" ], "id": "genome_index" }, { "type": "string", "id": "sample_name" }, { "type": "string", "id": "library" }, { "type": "string", "id": "platform" }, { "type": "File", "id": "target_regions" }, { "type": [ "null", "int" ], "id": "threads" }, { "type": { "type": "array", "items": "File" }, "secondaryFiles": [ ".tbi" ], "id": "known_sites" } ], "outputs": [ { "label": "FastQC html report file from original raw reads", "outputSource": "process_run/run_fastqc_folder", "type": { "type": "array", "items": "Directory" }, "id": "fastqc_folder" }, { "label": "BAM sorted by reads name from a sequencing run", "outputSource": "apply_quality_score/recalibrated_bam", "type": "File", "id": "bam_postprocessed" }, { "label": "statistics file of the alignment", "outputSource": "aln_quality_control/bam_samtools_stats", "type": "File", "id": "bam_samtools_stats" }, { "label": "statistics file of the alignment", "outputSource": "aln_quality_control/bam_bamdst_stats", "type": "Directory", "id": "bam_bamdst_stats" } ], "steps": [ { "run": { "class": "Workflow", "cwlVersion": "v1.2", "id": "scatters_alignment_runs_bwa_mem", "doc": "This workflow scatters the alignment step of multiple runs\nof the same sample using the bwa mem algorithm. DNA alignemnt\nbest pratices dictate that indivual runs should be first alignment\nindividually and then merged into a single file prior to the\npost-alignment step which includes duplicate marking and base\nquality recalibration (for model organisms with a dbsnp).\n", "label": "scatter short reads with bwa mem", "requirements": [ { "class": "InlineJavascriptRequirement" }, { "class": "StepInputExpressionRequirement" }, { "class": "MultipleInputFeatureRequirement" }, { "listing": [ { "entry": "$({class: 'Directory', listing: []})", "entryname": "FastQC_results", "writable": true } ], "class": "InitialWorkDirRequirement" }, { "class": "SubworkflowFeatureRequirement" } ], "inputs": [ { "type": { "type": "record", "fields": [ { "type": "string", "name": "run_id" }, { "type": { "type": "array", "items": "File" }, "name": "files" } ] }, "id": "input_reads" }, { "type": "File", "secondaryFiles": [ ".fai", ".amb", ".ann", ".bwt", ".pac", ".sa" ], "id": "genome_index" }, { "type": "string", "id": "run_sm" }, { "type": "string", "id": "run_lb" }, { "type": "string", "id": "run_pl" }, { "type": "int", "id": "threads" } ], "outputs": [ { "doc": "Folder containing the quality control\nresults before and after trim_galore\n", "outputSource": "qc_trimming/fastqc_folder", "type": "Directory", "id": "run_fastqc_folder" }, { "label": "BAM sorted by reads name from a sequencing run", "type": "File", "outputSource": [ "alignment_paired/bam", "alignment_single/bam" ], "pickValue": "first_non_null", "id": "bam_run" } ], "steps": [ { "run": { "cwlVersion": "v1.2", "class": "Workflow", "requirements": [ { "class": "InlineJavascriptRequirement" }, { "class": "StepInputExpressionRequirement" }, { "class": "MultipleInputFeatureRequirement" }, { "listing": [ { "entry": "$({class: 'Directory', listing: []})", "entryname": "FastQC_results", "writable": true } ], "class": "InitialWorkDirRequirement" } ], "inputs": [ { "type": { "type": "record", "fields": [ { "type": "string", "name": "run_id" }, { "type": { "type": "array", "items": "File" }, "name": "files" } ] }, "id": "input_reads" }, { "type": "int", "id": "qual_trim_cutoff" }, { "type": "int", "id": "min_adapter_overlap" }, { "type": "int", "id": "threads" } ], "outputs": [ { "doc": "Folder containing the quality control\nresults before and after trim_galore\n", "outputSource": "move_to_folder/outs", "type": "Directory", "id": "fastqc_folder" }, { "outputSource": "trim_adapters/fastq1_trimmed", "type": "File", "id": "fastq1_trimmed" }, { "outputSource": "trim_adapters/fastq2_trimmed", "type": [ "null", "File" ], "id": "fastq2_trimmed" } ], "steps": [ { "run": { "cwlVersion": "v1.0", "class": "CommandLineTool", "hints": { "DockerRequirement": { "dockerPull": "pegi3s/fastqc" }, "SoftwareRequirement": { "packages": { "fastqc": { "specs": [ "http://identifiers.org/biotools/fastqc" ], "version": [ "0.11.9--hdfd78af_1", "0.11.9" ] } } } }, "inputs": [ { "type": { "type": "array", "items": "File" }, "inputBinding": { "position": 50 }, "doc": "Input bam,sam,bam_mapped,sam_mapped or fastq file\n", "id": "reads_file" }, { "type": [ "null", { "type": "enum", "name": "format", "symbols": [ "bam", "sam", "bam_mapped", "sam_mapped", "fastq" ] } ], "inputBinding": { "position": 6, "prefix": "--format" }, "doc": "Bypasses the normal sequence file format detection and\nforces the program to use the specified format. Valid\nformats are bam,sam,bam_mapped,sam_mapped and fastq\n", "id": "format_enum" }, { "type": [ "null", "int" ], "inputBinding": { "position": 7, "prefix": "--threads" }, "doc": "Specifies the number of files which can be processed\nsimultaneously. Each thread will be allocated 250MB of\nmemory so you shouldn't run more threads than your\navailable memory will cope with, and not more than\n6 threads on a 32 bit machine\n", "id": "threads" }, { "type": [ "null", "File" ], "inputBinding": { "position": 8, "prefix": "--contaminants" }, "doc": "Specifies a non-default file which contains the list of\ncontaminants to screen overrepresented sequences against.\nThe file must contain sets of named contaminants in the\nform name[tab]sequence. Lines prefixed with a hash will\nbe ignored.\n", "id": "contaminants" }, { "type": [ "null", "File" ], "inputBinding": { "position": 9, "prefix": "--adapters" }, "doc": "Specifies a non-default file which contains the list of\nadapter sequences which will be explicity searched against\nthe library. The file must contain sets of named adapters\nin the form name[tab]sequence. Lines prefixed with a hash\nwill be ignored.\n", "id": "adapters" }, { "type": [ "null", "File" ], "inputBinding": { "position": 10, "prefix": "--limits" }, "doc": "Specifies a non-default file which contains a set of criteria\nwhich will be used to determine the warn/error limits for the\nvarious modules. This file can also be used to selectively\nremove some modules from the output all together. The format\nneeds to mirror the default limits.txt file found in the\nConfiguration folder.\n", "id": "limits" }, { "type": [ "null", "int" ], "inputBinding": { "position": 11, "prefix": "--kmers" }, "doc": "Specifies the length of Kmer to look for in the Kmer content\nmodule. Specified Kmer length must be between 2 and 10. Default\nlength is 7 if not specified.\n", "id": "kmers" }, { "type": [ "null", "boolean" ], "inputBinding": { "position": 13, "prefix": "--casava" }, "doc": "Files come from raw casava output. Files in the same sample\ngroup (differing only by the group number) will be analysed\nas a set rather than individually. Sequences with the filter\nflag set in the header will be excluded from the analysis.\nFiles must have the same names given to them by casava\n(including being gzipped and ending with .gz) otherwise they\nwon't be grouped together correctly.\n", "id": "casava" }, { "type": [ "null", "boolean" ], "inputBinding": { "position": 14, "prefix": "--nofilter" }, "doc": "If running with --casava then don't remove read flagged by\ncasava as poor quality when performing the QC analysis.\n", "id": "nofilter" }, { "type": [ "null", "boolean" ], "inputBinding": { "position": 15, "prefix": "--nogroup" }, "doc": "Disable grouping of bases for reads >50bp. All reports will\nshow data for every base in the read. WARNING: Using this\noption will cause fastqc to crash and burn if you use it on\nreally long reads, and your plots may end up a ridiculous size.\nYou have been warned!\n", "id": "hide_group" } ], "outputs": [ { "type": { "type": "array", "items": "File" }, "outputBinding": { "glob": "*.zip" }, "id": "zipped_file" }, { "type": { "type": "array", "items": "File" }, "outputBinding": { "glob": "*.html" }, "id": "html_file" }, { "type": { "type": "array", "items": "File" }, "outputBinding": { "glob": "*/summary.txt" }, "id": "summary_file" } ], "baseCommand": [ "--extract", "--outdir", "." ], "$namespaces": { "s": "http://schema.org/" }, "$schemas": [ "https://github.com/schemaorg/schemaorg/raw/main/data/releases/11.01/schemaorg-current-http.rdf" ], "doc": "Tool runs FastQC from Babraham Bioinformatics\n", "requirements": [] }, "label": "Run fastqc on raw reads", "in": [ { "source": "input_reads", "valueFrom": "$(self.files)", "id": "reads_file" }, { "source": "threads", "id": "threads" } ], "out": [ "zipped_file", "html_file" ], "id": "fastqc" }, { "run": { "cwlVersion": "v1.0", "class": "CommandLineTool", "doc": "Adaptor trimming of reads (single or paired end) in fastq format.\n", "requirements": [ { "class": "InlineJavascriptRequirement" } ], "hints": { "ResourceRequirement": { "coresMin": 1, "ramMin": 7000 }, "DockerRequirement": { "dockerPull": "i3sbioinformaticsservice/trim_galore:0.6.7" } }, "baseCommand": "trim_galore", "inputs": [ { "doc": "raw reads in fastq format; can be gzipped;\nif paired end, the file contains the first reads;\nif single end, the file contains all reads\n", "type": "File", "inputBinding": { "position": 10 }, "id": "fastq1" }, { "doc": "(optional) raw reads in fastq format; can be gzipped;\nif paired end, the file contains the second reads;\nif single end, the file does not exist\n", "type": [ "null", "File" ], "inputBinding": { "position": 11 }, "id": "fastq2" }, { "doc": "Adapter sequence for first reads.\nif not specified, trim_galore will try to autodetect whether ...\n- Illumina universal adapter (AGATCGGAAGAGC)\n- Nextera adapter (CTGTCTCTTATA)\n- Illumina Small RNA 3' Adapter (TGGAATTCTCGG)\n... was used.\nYou can directly choose one of the above configurations\nby setting the string to \"illumina\", \"nextera\", or \"small_rna\".\n", "type": [ "null", "string" ], "id": "adapter1" }, { "doc": "Adapter sequence for second reads - only for paired end data.\nif not specified, trim_galore will try to autodetect whether ...\n- Illumina universal adapter (AGATCGGAAGAGC)\n- Nextera adapter (CTGTCTCTTATA)\n- Illumina Small RNA 3' Adapter (TGGAATTCTCGG)\n... was used.\nYou can directly choose one of the above configurations\nby setting the adapter1 string to \"illumina\", \"nextera\", or \"small_rna\".\n", "type": [ "null", "string" ], "id": "adapter2" }, { "doc": "trim all base with a phred score lower than this valueFrom", "type": "int", "default": 20, "inputBinding": { "prefix": "--quality", "position": 1 }, "id": "qual_trim_cutoff" }, { "doc": "discard reads that get shorter than this value", "type": "int", "default": 20, "inputBinding": { "prefix": "--length", "position": 1 }, "id": "min_read_length" }, { "doc": "if only one read of a pair passes the qc and adapter trimming,\nit needs at least this length to be rescued\n", "type": "int", "default": 35, "id": "min_unpaired_read_rescue_length" }, { "doc": "minimum overlap with adapter seq in bp needed to trim", "type": "int", "default": 1, "inputBinding": { "prefix": "--stringency", "position": 1 }, "id": "min_adapter_overlap" }, { "doc": "basename for output files, instead of deriving the filenames from the input files", "type": [ "null", "string" ], "inputBinding": { "prefix": "--basename", "position": 1 }, "id": "out_basename" }, { "type": [ "null", "boolean" ], "default": true, "inputBinding": { "prefix": "--fastqc_args", "valueFrom": "\"--noextract\"", "position": 1 }, "id": "run_fastqc" }, { "doc": "Number of compression threads", "type": "int", "default": 1, "inputBinding": { "prefix": "--cores", "position": 1 }, "id": "n_threads" } ], "arguments": [ { "prefix": "--gzip", "position": 1 }, { "valueFrom": "${\n if ( inputs.adapter1 == \"illumina\" ){ return \"--illumina\" }\n else if ( inputs.adapter1 == \"nextera\" ){ return \"--nextera\" }\n else if ( inputs.adapter1 == \"small_rna\" ){ return \"--small_rna\" }\n else { return null }\n}\n", "position": 1 }, { "prefix": "--adapter", "valueFrom": "${\n if ( inputs.adapter1 != null && inputs.adapter1 != \"illumina\" && inputs.adapter1 != \"nextera\" && inputs.adapter1 != \"small_rna\" ){\n return inputs.adapter1\n } else {\n return null\n }\n}\n", "position": 1 }, { "prefix": "--adapter2", "valueFrom": "${\n if ( inputs.fastq2 != null && inputs.adapter2 != null && inputs.adapter1 != \"illumina\" && inputs.adapter1 != \"nextera\" && inputs.adapter1 != \"small_rna\" ){\n return inputs.adapter2\n } else {\n return null\n }\n}\n", "position": 1 }, { "valueFrom": "${\n if ( inputs.fastq2 == null ){ return null }\n else { return \"--paired\" }\n}\n", "position": 1 }, { "valueFrom": "${\n if ( inputs.fastq2 == null ){ return null }\n else { return \"--retain_unpaired\" }\n}\n", "position": 1 }, { "prefix": "--length_1", "valueFrom": "${\n if ( inputs.fastq2 == null ){ return null }\n else { return inputs.min_unpaired_read_rescue_length }\n}\n", "position": 1 }, { "prefix": "--length_2", "valueFrom": "${\n if ( inputs.fastq2 == null ){ return null }\n else { return inputs.min_unpaired_read_rescue_length }\n}\n", "position": 1 } ], "outputs": [ { "type": "File", "outputBinding": { "glob": "${\n if ( inputs.fastq2 == null ){\n \tif (inputs.out_basename == null ) { return \"*trimmed.fq*\" }\n else { return inputs.out_basename+\"*trimmed.fq*\"; }\n }\n else {\n \tif (inputs.out_basename == null ) { return \"*val_1.fq*\" }\n else { return inputs.out_basename+\"*val_1.fq*\"; }\n }\n }\n" }, "id": "fastq1_trimmed" }, { "type": [ "null", "File" ], "outputBinding": { "glob": "${\nif (inputs.out_basename == null ) { return \"*val_2.fq*\" }\nelse { return inputs.out_basename+\"*val_2.fq*\"; }\n}\n" }, "id": "fastq2_trimmed" }, { "type": [ "null", "File" ], "outputBinding": { "glob": "*unpaired_1.fq*" }, "id": "fastq1_trimmed_unpaired" }, { "type": [ "null", "File" ], "outputBinding": { "glob": "*unpaired_2.fq*" }, "id": "fastq2_trimmed_unpaired" }, { "type": { "type": "array", "items": "File" }, "outputBinding": { "glob": "*trimming_report.txt" }, "id": "trim_galore_log" }, { "doc": "html report of post-trimming fastqc", "type": { "type": "array", "items": "File" }, "outputBinding": { "glob": "*fastqc.html" }, "id": "trimmed_fastqc_html" }, { "doc": "all data of post-trimming fastqc e.g. figures", "type": { "type": "array", "items": "File" }, "outputBinding": { "glob": "*fastqc.zip" }, "id": "trimmed_fastqc_zip" } ] }, "label": "Run trim_galore for adapter removal", "doc": "Remove adapter sequences from reads. The quality\ntrimming cutoff is set to zero to ensure that no\nreads are removed due to low quality. For DNA\nsequencing it has been observed that by not removing\nlow quality reads we can increase specificity. This\ndoes not increase false positives because\nlow quality reads with several mismatches will be discarded\nduring the alignement step. Since base quality is taken into\naccount during variant calling, by mantaining all reads we\nare not increasing the amount of false positive variants.\nMin adapter overlap is increased from 1 to 3 mimicking\ncutadapt and trimmomatic default values.\n", "in": [ { "default": 0, "id": "qual_trim_cutoff" }, { "default": 3, "id": "min_adapter_overlap" }, { "source": "threads", "id": "n_threads" }, { "source": "input_reads", "valueFrom": "${ return self.files[0] }", "id": "fastq1" }, { "source": "input_reads", "valueFrom": "${\nif (self.files.length > 1) {\n\treturn self.files[1];\n}\nelse return null;\n}\n", "id": "fastq2" } ], "out": [ "fastq1_trimmed", "fastq2_trimmed", "trim_galore_log", "trimmed_fastqc_html", "trimmed_fastqc_zip" ], "id": "trim_adapters" }, { "label": "move all to Fastqc reports to a folder", "run": { "class": "CommandLineTool", "inputs": [ { "type": { "type": "array", "items": "File" }, "id": "item" } ], "outputs": [ { "type": "Directory", "outputBinding": { "glob": "FastQC_results/" }, "id": "outs" } ], "arguments": [ { "valueFrom": "cp", "position": 1 }, { "valueFrom": "$(inputs.item)", "position": 2 }, { "valueFrom": "FastQC_results/", "position": 101 } ], "requirements": [] }, "in": [ { "source": [ "fastqc/html_file", "fastqc/zipped_file", "trim_adapters/trim_galore_log", "trim_adapters/trimmed_fastqc_html", "trim_adapters/trimmed_fastqc_zip" ], "linkMerge": "merge_flattened", "id": "item" } ], "out": [ "outs" ], "id": "move_to_folder" } ] }, "label": "Run fastqc on raw reads and perform trimming", "in": [ { "source": "input_reads", "id": "input_reads" }, { "default": 0, "id": "qual_trim_cutoff" }, { "default": 3, "id": "min_adapter_overlap" }, { "source": "threads", "id": "threads" } ], "out": [ "fastq1_trimmed", "fastq2_trimmed", "fastqc_folder" ], "id": "qc_trimming" }, { "run": { "cwlVersion": "v1.2", "class": "CommandLineTool", "requirements": [ { "dockerPull": "i3sbioinformaticsservice/bwa-samtools", "class": "DockerRequirement" }, { "class": "ShellCommandRequirement" }, { "class": "InlineJavascriptRequirement" } ], "hints": { "ResourceRequirement": { "coresMin": "$(parseInt(inputs.n_threads))" } }, "baseCommand": [ "bwa", "mem" ], "inputs": [ { "type": { "type": "array", "items": "File" }, "label": "Fastq files for index.", "inputBinding": { "position": 99 }, "id": "input_file" }, { "type": "File", "label": "Reference genome", "inputBinding": { "position": 98 }, "secondaryFiles": [ ".fai", ".amb", ".ann", ".bwt", ".pac", ".sa" ], "id": "reference" }, { "type": [ "null", "string" ], "label": "Complete read group header lines.", "inputBinding": { "position": 3, "prefix": "-R" }, "id": "readgroup_line" }, { "type": [ "null", "boolean" ], "label": "Mark shorter split hits as secondary (for Picard compatibility).", "default": true, "inputBinding": { "position": 3, "prefix": "-M" }, "id": "mark_short_split" }, { "type": [ "null", "int" ], "label": "Number of threads [1].", "default": 1, "inputBinding": { "position": 3, "prefix": "-t" }, "id": "n_threads" }, { "doc": "If true, will sort by name, otherwise will sort by genomic position", "type": "boolean", "default": false, "inputBinding": { "position": 103, "prefix": "-n" }, "id": "by_name" }, { "doc": "Specify output format", "type": [ "null", { "type": "enum", "symbols": [ "SAM", "BAM", "CRAM" ] } ], "inputBinding": { "position": 103, "prefix": "-O" }, "id": "out_format" }, { "doc": "Add template cigar ct tag", "type": "boolean", "default": false, "inputBinding": { "position": 203, "prefix": "-c" }, "id": "cigar_tag" }, { "doc": "Add mate score tag", "type": "boolean", "default": false, "inputBinding": { "position": 203, "prefix": "-m" }, "id": "add_mate_score" }, { "type": [ "null", "string" ], "doc": "add a specific name to the stream.", "id": "out_filename" } ], "stdout": "$(inputs.out_filename)_fixmate_sort.bam", "outputs": [ { "type": "File", "format": "edam:format_2572", "label": "Alignments in BAM format", "outputBinding": { "glob": "*bam" }, "id": "bam" } ], "arguments": [ { "shellQuote": false, "position": 100, "valueFrom": "|" }, { "valueFrom": "samtools", "position": 101 }, { "valueFrom": "sort", "position": 102 }, { "valueFrom": "-@", "position": 196 }, { "valueFrom": "$(inputs.n_threads)", "position": 197 }, { "shellQuote": false, "position": 198, "valueFrom": "-" }, { "shellQuote": false, "position": 199, "valueFrom": "|" }, { "valueFrom": "samtools", "position": 201 }, { "valueFrom": "fixmate", "position": 202 }, { "valueFrom": "-@", "position": 296 }, { "valueFrom": "$(inputs.n_threads)", "position": 297 }, { "shellQuote": false, "position": 298, "valueFrom": "-" }, { "shellQuote": false, "position": 299, "valueFrom": "-" }, { "shellQuote": false, "position": 300, "valueFrom": "|" }, { "valueFrom": "samtools", "position": 301 }, { "valueFrom": "sort", "position": 302 }, { "valueFrom": "-@", "position": 396 }, { "valueFrom": "$(inputs.n_threads)", "position": 397 }, { "shellQuote": false, "position": 398, "valueFrom": "-" } ], "$namespaces": { "s": "https://schema.org/", "edam": "http://edamontology.org/" } }, "label": "bwa mem alignment", "in": [ { "source": "threads", "valueFrom": "$(Math.round(self/4))", "id": "n_threads" }, { "source": "input_reads", "valueFrom": "$(self.run_id)", "id": "out_filename" }, { "source": [ "qc_trimming/fastq1_trimmed", "qc_trimming/fastq2_trimmed" ], "valueFrom": "${\nif (self[1] == null) {\nreturn [ self[0] ];\n} else return self;\n}\n", "id": "input_file" }, { "source": "genome_index", "id": "reference" }, { "source": [ "input_reads", "run_sm", "run_lb", "run_pl" ], "valueFrom": "@RG\\tID:$(self[0].run_id)\\tSM:$(self[1])\\tLB:$(self[2])\\tPL:$(self[3])", "id": "readgroup_line" }, { "default": true, "id": "mark_short_split" }, { "default": true, "id": "by_name" }, { "default": "BAM", "id": "out_format" }, { "default": true, "id": "cigar_tag" }, { "default": true, "id": "add_mate_score" } ], "out": [ "bam" ], "when": "$(inputs.input_file.length > 1)", 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[input filename]", "inputBinding": { "prefix": "-P" }, "id": "split_prefix" }, { "type": [ "null", "int" ], "doc": "The BWA trimming parameter [0] ", "inputBinding": { "prefix": "-q" }, "id": "trim_quality" }, { "type": [ "null", "File" ], "doc": "Reference sequence (required for GC-depth and mismatches-per-cycle calculation). [] ", "inputBinding": { "prefix": "-r" }, "id": "ref_seq" }, { "type": [ "null", "string" ], "doc": "In addition to the complete statistics, also output categorised statistics based on the tagged field TAG (e.g., use --split RG to split into read groups). Categorised statistics are written to files named _.bamstat, where prefix is as given by --split-prefix (or the input filename by default) and value has been encountered as the specified tagged field's value in one or more alignment records. ", "inputBinding": { "prefix": "--split" }, "id": "split" }, { "type": [ "null", "File" ], "doc": "Do stats in these regions only. Tab-delimited file chr,from,to, 1-based, inclusive. []", "inputBinding": { "prefix": "--target-regions" }, "id": "target_regions" }, { "type": [ "null", "boolean" ], "doc": "Suppress outputting IS rows where there are no insertions.", "inputBinding": { "prefix": "--sparse" }, "id": "sparse" }, { "type": [ "null", "boolean" ], "doc": "Remove overlaps of paired-end reads from coverage and base count computations. ", "inputBinding": { "prefix": "--remove-overlaps" }, "id": "remove_overlaps" }, { "type": [ "null", "int" ], "doc": "Only bases with coverage above this value will be included in the target percentage computation [0] ", "inputBinding": { "prefix": "-g" }, "id": "cov_threshold" } ], "arguments": [ { "prefix": "--threads", "valueFrom": "$(runtime.cores)" } ], "outputs": [ { "type": "File", "outputBinding": { "glob": "$(inputs.input_file.nameroot).stats.txt" }, "id": "stats" } ], "stdout": "$(inputs.input_file.nameroot).stats.txt", "requirements": [] }, "label": "Samtools stats", "in": [ { "source": "input_file", "id": "input_file" } ], "out": [ "stats" ], "id": "samtools_stats" }, { "run": { "cwlVersion": "v1.0", "class": "CommandLineTool", "doc": "Bamdst is a lightweight tool to stat the depth coverage of target regions of bam file(s).\n", "requirements": [ { "class": "InlineJavascriptRequirement" }, { "dockerPull": "i3sbioinformaticsservice/bamdst:1.0.9", "class": "DockerRequirement" }, { "listing": [ { "entry": "$({class: 'Directory', listing: []})", "entryname": "$(inputs.output_folder)", "writable": true } ], "class": "InitialWorkDirRequirement" } ], "baseCommand": [ "bamdst" ], "inputs": [ { "doc": "Sorted bam file", "type": "File", "inputBinding": { "position": 100 }, "id": "input_file" }, { "doc": "Output folder name", "type": [ "null", "string" ], "default": "bamdst_stats", "inputBinding": { "position": 1, "prefix": "-o" }, "id": "output_folder" }, { "doc": "probe or target regions file, the region file will\nbe merged before calculate depths\n", "type": "File", "inputBinding": { "position": 1, "prefix": "-p" }, "id": "target_regions" }, { "doc": "flank n bp of each region", "type": [ "null", "int" ], "inputBinding": { "position": 1, "prefix": "-f" }, "id": "flank" }, { "doc": "map quality cutoff value, greater or equal to the value will be count", "type": [ "null", "int" ], "default": 20, "inputBinding": { "position": 1, "prefix": "-q" }, "id": "quality_cutoff" }, { "doc": "set the max depth to stat the cumu distribution.", "type": [ "null", "int" ], "default": 0, "inputBinding": { "position": 1, "prefix": "--maxdepth" }, "id": "max_depth" }, { "doc": "list the coverage of above depths", "type": [ "null", "int" ], "default": 0, "inputBinding": { "position": 1, "prefix": "--cutoffdepth" }, "id": "cutoff_depth" }, { "doc": "inferred insert size under this value", "type": [ "null", "int" ], "default": 2000, "inputBinding": { "position": 1, "prefix": "--isize" }, "id": "isize" }, { "doc": "region will included in uncover file if below it", "type": [ "null", "int" ], "default": 5, "inputBinding": { "position": 1, "prefix": "--uncover" }, "id": "uncover" }, { "doc": "begin position of bed file is 1-based", "type": [ "null", "boolean" ], "default": false, "inputBinding": { "position": 1, "prefix": "-1" }, "id": "one_based" } ], "outputs": [ { "type": "Directory", "outputBinding": { "glob": "$(inputs.output_folder)" }, "id": "statistics" } ] }, "label": "generates alignment statistics", "in": [ { "source": "input_file", "id": "input_file" }, { "source": "target_regions", "id": "target_regions" } ], "out": [ "statistics" ], "id": "bamdst_stats" } ] }, "label": "Quality control statistics of the alignment step", "in": [ { "source": "apply_quality_score/recalibrated_bam", "id": "input_file" }, { "source": "threads", "id": "threads" }, { "source": "target_regions", "id": "target_regions" } ], "out": [ "bam_samtools_stats", "bam_bamdst_stats" ], "id": "aln_quality_control" } ] }