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https://github.com/MillironX/nf-core_modules.git
synced 2024-11-13 05:13:09 +00:00
controlfreec significance (#1451)
* controlfreec significance * move freec files to own subfolder * Fix meta.yml naming * Fix meta.yml naming * Fix linting * Forgot to refactor * forgot more refactoring * Too much refactoring on output paths * Too little refactoring here * update checksum
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11 changed files with 187 additions and 23 deletions
30
modules/controlfreec/assesssignificance/main.nf
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30
modules/controlfreec/assesssignificance/main.nf
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@ -0,0 +1,30 @@
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process CONTROLFREEC_ASSESSSIGNIFICANCE {
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tag "$meta.id"
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label 'process_low'
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conda (params.enable_conda ? "bioconda::control-freec=11.6" : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/control-freec:11.6--h1b792b2_1':
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'quay.io/biocontainers/control-freec:11.6--h1b792b2_1' }"
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input:
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tuple val(meta), path(cnvs), path(ratio)
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output:
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tuple val(meta), path("*.p.value.txt"), emit: bam
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path "versions.yml" , emit: versions
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when:
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task.ext.when == null || task.ext.when
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script:
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def args = task.ext.args ?: ''
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"""
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cat /usr/local/bin/assess_significance.R | R --slave --args ${cnvs} ${ratio}
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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controlfreec: \$(echo \$(freec -version 2>&1) | sed 's/^.*Control-FREEC //; s/:.*\$//' | sed -e "s/Control-FREEC v//g" )
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END_VERSIONS
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"""
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}
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50
modules/controlfreec/assesssignificance/meta.yml
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50
modules/controlfreec/assesssignificance/meta.yml
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@ -0,0 +1,50 @@
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name: controlfreec_assesssignificance
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description: Add both Wilcoxon test and Kolmogorov-Smirnov test p-values to each CNV output of FREEC
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keywords:
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- cna
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- cnv
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- somatic
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- single
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- tumor-only
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tools:
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- controlfreec/assesssignificance:
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description: Copy number and genotype annotation from whole genome and whole exome sequencing data.
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homepage: http://boevalab.inf.ethz.ch/FREEC
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documentation: http://boevalab.inf.ethz.ch/FREEC/tutorial.html
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tool_dev_url: https://github.com/BoevaLab/FREEC/
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doi: "10.1093/bioinformatics/btq635"
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licence: ["GPL >=2"]
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input:
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# Only when we have meta
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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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- cnvs:
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type: file
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description: _CNVs file generated by FREEC
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pattern: "*._CNVs"
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- ratio:
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type: file
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description: ratio file generated by FREEC
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pattern: "*.ratio.txt"
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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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- versions:
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type: file
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description: File containing software versions
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pattern: "versions.yml"
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- p_value_txt:
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type: file
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description: CNV file containing p_values for each call
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pattern: "*.p.value.txt"
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authors:
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- "@FriederikeHanssen"
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@ -1,4 +1,4 @@
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process CONTROLFREEC {
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process CONTROLFREEC_FREEC {
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tag "$meta.id"
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label 'process_low'
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@ -1,4 +1,4 @@
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name: controlfreec
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name: controlfreec_freec
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description: Copy number and genotype annotation from whole genome and whole exome sequencing data
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keywords:
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- cna
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@ -7,7 +7,7 @@ keywords:
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- single
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- tumor-only
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tools:
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- controlfreec:
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- controlfreec/freec:
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description: Copy number and genotype annotation from whole genome and whole exome sequencing data.
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homepage: http://boevalab.inf.ethz.ch/FREEC
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documentation: http://boevalab.inf.ethz.ch/FREEC/tutorial.html
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@ -419,9 +419,13 @@ cnvkit/batch:
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- modules/cnvkit/batch/**
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- tests/modules/cnvkit/batch/**
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controlfreec:
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- modules/controlfreec/**
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- tests/modules/controlfreec/**
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controlfreec/assesssignificance:
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- modules/controlfreec/assesssignificance/**
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- tests/modules/controlfreec/assesssignificance/**
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controlfreec/freec:
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- modules/controlfreec/freec/**
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- tests/modules/controlfreec/freec/**
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cooler/cload:
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- modules/cooler/cload/**
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42
tests/modules/controlfreec/assesssignificance/main.nf
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42
tests/modules/controlfreec/assesssignificance/main.nf
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#!/usr/bin/env nextflow
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nextflow.enable.dsl = 2
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include { CONTROLFREEC_ASSESSSIGNIFICANCE } from '../../../../modules/controlfreec/assesssignificance/main.nf'
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include { CONTROLFREEC_FREEC } from '../../../../modules/controlfreec/freec/main.nf'
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include { UNTAR } from '../../../../modules/untar/main.nf'
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workflow test_controlfreec_assesssignificance {
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input = [
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[ id:'test', single_end:false, sex:'XX' ], // meta map
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file(params.test_data['homo_sapiens']['illumina']['test_mpileup'], checkIfExists: true),
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file(params.test_data['homo_sapiens']['illumina']['test2_mpileup'], checkIfExists: true),
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[],[],[],[]
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]
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fasta = file(params.test_data['homo_sapiens']['genome']['genome_21_fasta'], checkIfExists: true)
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fai = file(params.test_data['homo_sapiens']['genome']['genome_21_fasta_fai'], checkIfExists: true)
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dbsnp = file(params.test_data['homo_sapiens']['genome']['dbsnp_138_hg38_21_vcf_gz'], checkIfExists: true)
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dbsnp_tbi = file(params.test_data['homo_sapiens']['genome']['dbsnp_138_hg38_21_vcf_gz_tbi'], checkIfExists: true)
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chrfiles = [ [], file(params.test_data['homo_sapiens']['genome']['genome_21_chromosomes_dir'], checkIfExists: true) ]
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target_bed = file(params.test_data['homo_sapiens']['genome']['genome_21_multi_interval_bed'], checkIfExists: true)
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UNTAR(chrfiles)
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CONTROLFREEC_FREEC (input,
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fasta,
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fai,
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[],
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dbsnp,
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dbsnp_tbi,
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UNTAR.out.untar.map{ it[1] },
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[],
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target_bed,
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[]
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)
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sig_in = CONTROLFREEC_FREEC.out.CNV.join(CONTROLFREEC_FREEC.out.ratio)
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CONTROLFREEC_ASSESSSIGNIFICANCE ( sig_in )
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}
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@ -2,7 +2,7 @@ process {
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publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
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withName:CONTROLFREEC{
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withName:CONTROLFREEC_FREEC{
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ext.args = { [
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"sample":[
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inputformat: 'pileup',
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10
tests/modules/controlfreec/assesssignificance/test.yml
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10
tests/modules/controlfreec/assesssignificance/test.yml
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- name: controlfreec assesssignificance test_controlfreec_assesssignificance
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command: nextflow run tests/modules/controlfreec/assesssignificance -entry test_controlfreec_assesssignificance -c tests/config/nextflow.config
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tags:
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- controlfreec/assesssignificance
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- controlfreec
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files:
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- path: output/controlfreec/test2.mpileup.gz_CNVs.p.value.txt
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md5sum: 44e23b916535fbc1a3f47b57fad292df
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- path: output/controlfreec/versions.yml
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md5sum: 0aa42fed10d61e4570fe1e0e83ffe932
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@ -2,9 +2,10 @@
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nextflow.enable.dsl = 2
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include { CONTROLFREEC } from '../../../modules/controlfreec/main.nf'
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include { UNTAR } from '../../../modules/untar/main.nf'
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workflow test_controlfreec {
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include { CONTROLFREEC_FREEC } from '../../../../modules/controlfreec/freec/main.nf'
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include { UNTAR } from '../../../../modules/untar/main.nf'
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workflow test_controlfreec_freec {
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input = [
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[ id:'test', single_end:false, sex:'XX' ], // meta map
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target_bed = file(params.test_data['homo_sapiens']['genome']['genome_21_multi_interval_bed'], checkIfExists: true)
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UNTAR(chrfiles)
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CONTROLFREEC ( input,
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fasta,
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fai,
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[],
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dbsnp,
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dbsnp_tbi,
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UNTAR.out.untar.map{ it[1] },
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[],
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target_bed,
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[]
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CONTROLFREEC_FREEC (input,
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fasta,
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fai,
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[],
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dbsnp,
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dbsnp_tbi,
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UNTAR.out.untar.map{ it[1] },
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[],
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target_bed,
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[]
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)
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}
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26
tests/modules/controlfreec/freec/nextflow.config
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26
tests/modules/controlfreec/freec/nextflow.config
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process {
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publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
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withName:CONTROLFREEC_FREEC{
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ext.args = { [
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"sample":[
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inputformat: 'pileup',
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mateorientation: 'FR'
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],
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"general" :[
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bedgraphoutput: "TRUE",
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noisydata: "TRUE",
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minexpectedgc: "0",
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readcountthreshold: "1",
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sex: meta.sex,
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window: "10",
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],
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"control":[
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inputformat: "pileup",
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mateorientation: "FR"
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]
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]
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}
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}
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}
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@ -1,7 +1,8 @@
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- name: controlfreec test_controlfreec
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command: nextflow run tests/modules/controlfreec -entry test_controlfreec -c tests/config/nextflow.config
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- name: controlfreec test_controlfreec_freec
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command: nextflow run tests/modules/controlfreec/freec -entry test_controlfreec_freec -c tests/config/nextflow.config
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tags:
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- controlfreec
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- controlfreec/freec
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files:
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- path: output/controlfreec/config.txt
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- path: output/controlfreec/test.mpileup.gz_control.cpn
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- path: output/controlfreec/test2.mpileup.gz_sample.cpn
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md5sum: c80dad58a77b1d7ba6d273999f4b4b4b
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- path: output/controlfreec/versions.yml
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md5sum: ff93f6466d4686aab708425782c6c848
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md5sum: 3ab250a2ab3be22628124c7c65324651
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