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FastQC module is working and now accepting arguments
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parent
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commit
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4 changed files with 49 additions and 31 deletions
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@ -1,20 +1,37 @@
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process fastqc {
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tag "FastQC - $sample_id"
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publishDir "${params.outdir}/fastqc", mode: 'copy',
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saveAs: {filename -> filename.indexOf(".zip") > 0 ? "zips/$filename" : "$filename"}
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nextflow.preview.dsl = 2
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container 'quay.io/biocontainers/fastqc:0.11.8--2'
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process FASTQC {
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// tag "FastQC - $sample_id"
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input:
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tuple sample_id, path(reads)
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input:
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tuple val(name), path(reads)
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val (outputdir)
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// fastqc_args are best passed into the workflow in the following manner:
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// --fastqc_args="--nogroup -a custom_adapter_file.txt"
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val (fastqc_args)
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val (verbose)
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output:
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path "*_fastqc.{zip,html}"
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output:
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tuple val(name), path ("*fastqc*"), emit: all
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path "*.zip", emit: report // e.g. for MultiQC later
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// container 'quay.io/biocontainers/fastqc:0.11.8--2'
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script:
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"""
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fastqc -q $reads
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publishDir "$outputdir",
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mode: "copy", overwrite: true
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script:
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if (verbose){
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println ("[MODULE] FASTQC ARGS: " + fastqc_args)
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}
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"""
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module load fastqc
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fastqc $fastqc_args -q -t 2 $reads
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fastqc --version &> fastqc.version.txt
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"""
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fastqc --version &> fastqc.version.txt
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"""
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}
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@ -16,7 +16,7 @@ tools:
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documentation: https://www.bioinformatics.babraham.ac.uk/projects/fastqc/Help/
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input:
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-
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- sample_id:
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- name:
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type: string
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description: Sample identifier
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- reads:
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@ -29,4 +29,6 @@ output:
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description: FastQC report
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pattern: *_fastqc.{zip,html}
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authors:
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- @ewels
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-
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- @ewels
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- @FelixKrueger
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25
tools/fastqc/test/main.nf
Normal file → Executable file
25
tools/fastqc/test/main.nf
Normal file → Executable file
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#!/usr/bin/env nextflow
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nextflow.preview.dsl = 2
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include '../../../nf-core/module_testing/check_process_outputs.nf' params(params)
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include '../main.nf' params(params)
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params.outdir = "." // gets set in nextflow.config file (as './results/fastqc')
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params.fastqc_args = ''
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params.verbose = false
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// TODO: check the output files in some way
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// include '../../../nf-core/module_testing/check_process_outputs.nf'
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include '../main.nf'
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// Define input channels
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readPaths = [
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['SRR4238351', ['../../../test-datasets/tools/fastqc/input/SRR4238351_subsamp.fastq.gz']],
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['SRR4238355', ['../../../test-datasets/tools/fastqc/input/SRR4238355_subsamp.fastq.gz']],
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['SRR4238359', ['../../../test-datasets/tools/fastqc/input/SRR4238359_subsamp.fastq.gz']],
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['SRR4238379', ['../../../test-datasets/tools/fastqc/input/SRR4238379_subsamp.fastq.gz']]
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]
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Channel
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.from(readPaths)
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.map { row -> [ row[0], [ file(row[1][0]) ] ] }
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.set { ch_read_files }
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ch_read_files = Channel
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.fromFilePairs('../../../test-datasets/test*{1,2}.fastq.gz',size:-1)
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// .view() // to check whether the input channel works
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// Run the workflow
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workflow {
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fastqc(ch_read_files)
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FASTQC (ch_read_files, params.outdir, params.fastqc_args, params.verbose)
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// .check_output()
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}
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@ -1,2 +1,2 @@
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docker.enabled = true
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params.outdir = './results'
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// docker.enabled = true
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params.outdir = './results/fastqc'
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