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Rewritten module fgbio/fastqtobam (#916)
* added template for fastqtobam * porting old code into new template * update with missing getprocessname function * test completed - updating all * fixed linting issues * improved reading Co-authored-by: FriederikeHanssen <Friederike.hanssen@qbic.uni-tuebingen.de> Co-authored-by: FriederikeHanssen <Friederike.hanssen@qbic.uni-tuebingen.de>
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78
modules/fgbio/fastqtobam/functions.nf
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78
modules/fgbio/fastqtobam/functions.nf
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//
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// Utility functions used in nf-core DSL2 module files
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//
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//
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// Extract name of software tool from process name using $task.process
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//
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def getSoftwareName(task_process) {
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return task_process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()
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}
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//
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// Extract name of module from process name using $task.process
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//
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def getProcessName(task_process) {
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return task_process.tokenize(':')[-1]
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}
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//
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// Function to initialise default values and to generate a Groovy Map of available options for nf-core modules
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//
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def initOptions(Map args) {
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def Map options = [:]
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options.args = args.args ?: ''
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options.args2 = args.args2 ?: ''
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options.args3 = args.args3 ?: ''
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options.publish_by_meta = args.publish_by_meta ?: []
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options.publish_dir = args.publish_dir ?: ''
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options.publish_files = args.publish_files
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options.suffix = args.suffix ?: ''
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return options
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}
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//
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// Tidy up and join elements of a list to return a path string
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//
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def getPathFromList(path_list) {
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def paths = path_list.findAll { item -> !item?.trim().isEmpty() } // Remove empty entries
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paths = paths.collect { it.trim().replaceAll("^[/]+|[/]+\$", "") } // Trim whitespace and trailing slashes
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return paths.join('/')
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}
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//
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// Function to save/publish module results
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//
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def saveFiles(Map args) {
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def ioptions = initOptions(args.options)
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def path_list = [ ioptions.publish_dir ?: args.publish_dir ]
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// Do not publish versions.yml unless running from pytest workflow
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if (args.filename.equals('versions.yml') && !System.getenv("NF_CORE_MODULES_TEST")) {
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return null
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}
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if (ioptions.publish_by_meta) {
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def key_list = ioptions.publish_by_meta instanceof List ? ioptions.publish_by_meta : args.publish_by_meta
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for (key in key_list) {
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if (args.meta && key instanceof String) {
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def path = key
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if (args.meta.containsKey(key)) {
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path = args.meta[key] instanceof Boolean ? "${key}_${args.meta[key]}".toString() : args.meta[key]
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}
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path = path instanceof String ? path : ''
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path_list.add(path)
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}
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}
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}
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if (ioptions.publish_files instanceof Map) {
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for (ext in ioptions.publish_files) {
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if (args.filename.endsWith(ext.key)) {
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def ext_list = path_list.collect()
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ext_list.add(ext.value)
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return "${getPathFromList(ext_list)}/$args.filename"
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}
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}
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} else if (ioptions.publish_files == null) {
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return "${getPathFromList(path_list)}/$args.filename"
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}
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}
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51
modules/fgbio/fastqtobam/main.nf
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modules/fgbio/fastqtobam/main.nf
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// Import generic module functions
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include { initOptions; saveFiles; getSoftwareName; getProcessName } from './functions'
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params.options = [:]
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options = initOptions(params.options)
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process FGBIO_FASTQTOBAM {
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tag "$meta.id"
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label 'process_low'
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publishDir "${params.outdir}",
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mode: params.publish_dir_mode,
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saveAs: { filename -> saveFiles(filename:filename, options:params.options, publish_dir:getSoftwareName(task.process), meta:meta, publish_by_meta:['id']) }
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conda (params.enable_conda ? "bioconda::fgbio=1.4.0" : null)
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if (workflow.containerEngine == 'singularity' && !params.singularity_pull_docker_container) {
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container "https://depot.galaxyproject.org/singularity/fgbio:1.4.0--hdfd78af_0"
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} else {
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container "quay.io/biocontainers/fgbio:1.4.0--hdfd78af_0"
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}
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input:
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tuple val(meta), path(reads)
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val(read_structure)
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output:
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tuple val(meta), path("*_umi_converted.bam"), emit: umibam
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path "versions.yml" , emit: version
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script:
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def software = getSoftwareName(task.process)
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def prefix = options.suffix ? "${meta.id}${options.suffix}" : "${meta.id}"
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"""
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mkdir tmpFolder
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fgbio \\
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--tmp-dir=${PWD}/tmpFolder \\
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FastqToBam \\
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-i $reads \\
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-o "${prefix}_umi_converted.bam" \\
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--read-structures $read_structure \\
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--sample $meta.id \\
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--library $meta.id \\
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$options.args
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cat <<-END_VERSIONS > versions.yml
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${getProcessName(task.process)}:
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${getSoftwareName(task.process)}: \$( echo \$(fgbio --version 2>&1 | tr -d '[:cntrl:]' ) | sed -e 's/^.*Version: //;s/\\[.*\$//')
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END_VERSIONS
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"""
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}
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47
modules/fgbio/fastqtobam/meta.yml
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47
modules/fgbio/fastqtobam/meta.yml
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name: fgbio_fastqtobam
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description: |
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Using the FGBIO tools, converts FASTQ files sequenced with UMIs into BAM files, moving the UMI barcode into the RX field of the BAM file
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keywords:
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- fastqtobam
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- fgbio
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tools:
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- fgbio:
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description: A set of tools for working with genomic and high throughput sequencing data, including UMIs
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homepage: http://fulcrumgenomics.github.io/fgbio/
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documentation: http://fulcrumgenomics.github.io/fgbio/tools/latest/
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tool_dev_url: https://github.com/fulcrumgenomics/fgbio
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doi: ""
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licence: ['MIT']
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input:
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- reads:
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type: file
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description: pair of reads to be converted into BAM file
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pattern: "*.{fastq.gz}"
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- read_structure:
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type: string
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description: |
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A read structure should always be provided for each of the fastq files.
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If single end, the string will contain only one structure (i.e. "2M11S+T"), if paired-end the string
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will contain two structures separated by a blank space (i.e. "2M11S+T 2M11S+T").
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If the read does not contain any UMI, the structure will be +T (i.e. only template of any length).
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https://github.com/fulcrumgenomics/fgbio/wiki/Read-Structures
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output:
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- meta:
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type: map
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description: |
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Groovy Map containing sample information
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e.g. [ id:'test', single_end:false ]
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- version:
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type: file
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description: File containing software version
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pattern: "*.{version.yml}"
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- umibam:
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type: file
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description: Converted, unsorted BAM file with RX tag reporting UMI sequence (if any)
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pattern: "*.{bam}"
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authors:
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- "@lescai"
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@ -378,6 +378,10 @@ fgbio/callmolecularconsensusreads:
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- modules/fgbio/callmolecularconsensusreads/**
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- modules/fgbio/callmolecularconsensusreads/**
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- tests/modules/fgbio/callmolecularconsensusreads/**
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- tests/modules/fgbio/callmolecularconsensusreads/**
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fgbio/fastqtobam:
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- modules/fgbio/fastqtobam/**
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- tests/modules/fgbio/fastqtobam/**
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fgbio/sortbam:
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fgbio/sortbam:
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- modules/fgbio/sortbam/**
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- modules/fgbio/sortbam/**
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- tests/modules/fgbio/sortbam/**
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- tests/modules/fgbio/sortbam/**
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16
tests/modules/fgbio/fastqtobam/main.nf
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16
tests/modules/fgbio/fastqtobam/main.nf
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#!/usr/bin/env nextflow
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nextflow.enable.dsl = 2
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params.read_structure = "+T 12M11S+T"
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include { FGBIO_FASTQTOBAM } from '../../../../modules/fgbio/fastqtobam/main.nf' addParams( options: [:] )
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workflow test_fgbio_fastqtobam {
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input = [ [ id:'test', single_end:false ], // meta map
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[ file(params.test_data['homo_sapiens']['illumina']['test_umi_1_fastq_gz'], checkIfExists: true),
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file(params.test_data['homo_sapiens']['illumina']['test_umi_2_fastq_gz'], checkIfExists: true) ]
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]
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FGBIO_FASTQTOBAM ( input, "${params.read_structure}" )
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}
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10
tests/modules/fgbio/fastqtobam/test.yml
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tests/modules/fgbio/fastqtobam/test.yml
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- name: fgbio fastqtobam test_fgbio_fastqtobam
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command: nextflow run tests/modules/fgbio/fastqtobam -entry test_fgbio_fastqtobam -c tests/config/nextflow.config
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tags:
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- fgbio/fastqtobam
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- fgbio
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files:
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- path: output/fgbio/test_umi_converted.bam
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md5sum: 9510735554e5eff29244077a72075fb6
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- path: output/fgbio/versions.yml
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md5sum: 524815093b96759060d0d800fc6a3f25
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