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add new module cnvkit/reference
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39
modules/cnvkit/reference/main.nf
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39
modules/cnvkit/reference/main.nf
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@ -0,0 +1,39 @@
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process CNVKIT_REFERENCE {
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tag "$reference"
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label 'process_low'
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conda (params.enable_conda ? "bioconda::cnvkit=0.9.9" : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/cnvkit:0.9.9--pyhdfd78af_0':
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'quay.io/biocontainers/cnvkit:0.9.9--pyhdfd78af_0' }"
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input:
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path fasta
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path targets
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path antitargets
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output:
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path("*.cnn") , emit: cnn
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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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cnvkit.py \\
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reference \\
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--fasta $fasta \\
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--targets $targets \\
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--antitargets $antitargets \\
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--output reference.cnn \\
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$args
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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cnvkit: \$(cnvkit.py version | sed -e "s/cnvkit v//g")
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END_VERSIONS
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"""
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}
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47
modules/cnvkit/reference/meta.yml
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47
modules/cnvkit/reference/meta.yml
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name: cnvkit_reference
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description:
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keywords:
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- cnvkit
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- reference
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tools:
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- cnvkit:
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description: |
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CNVkit is a Python library and command-line software toolkit to infer and visualize copy number from high-throughput DNA sequencing data.
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It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina and Ion Torrent.
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homepage: https://cnvkit.readthedocs.io/en/stable/index.html
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documentation: https://cnvkit.readthedocs.io/en/stable/index.html
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tool_dev_url: https://github.com/etal/cnvkit
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doi: 10.1371/journal.pcbi.1004873
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licence: ["Apache-2.0"]
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input:
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- fasta:
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type: file
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description: File containing reference genome
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pattern: "*.{fasta}"
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- targets:
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type: file
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description: File containing genomic regions
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pattern: "*.{bed}"
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- antitargets:
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type: file
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description: File containing off-target genomic regions
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pattern: "*.{bed}"
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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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- reference:
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type: file
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description: File containing a copy-number reference (required for CNV calling in tumor_only mode)
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pattern: "*.{cnn}"
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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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authors:
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- "@SusiJo"
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@ -451,6 +451,10 @@ cnvkit/batch:
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- modules/cnvkit/batch/**
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- modules/cnvkit/batch/**
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- tests/modules/cnvkit/batch/**
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- tests/modules/cnvkit/batch/**
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cnvkit/reference:
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- modules/cnvkit/reference/**
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- tests/modules/cnvkit/reference/**
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controlfreec/assesssignificance:
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controlfreec/assesssignificance:
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- modules/controlfreec/assesssignificance/**
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- modules/controlfreec/assesssignificance/**
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- tests/modules/controlfreec/assesssignificance/**
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- tests/modules/controlfreec/assesssignificance/**
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14
tests/modules/cnvkit/reference/main.nf
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14
tests/modules/cnvkit/reference/main.nf
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#!/usr/bin/env nextflow
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nextflow.enable.dsl = 2
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include { CNVKIT_REFERENCE } from '../../../../modules/cnvkit/reference/main.nf'
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workflow test_cnvkit_reference {
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fasta = file(params.test_data['homo_sapiens']['genome']['genome_21_fasta'], checkIfExists: true)
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targets = file(params.test_data['homo_sapiens']['genome']['genome_21_multi_interval_bed'], checkIfExists: true)
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antitargets = file("/Users/susanne/Documents/repos/forks/modules/test_antitarget/output/cnvkit/test.antitarget.bed", checkIfExists: true)
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CNVKIT_REFERENCE ( fasta, targets, antitargets )
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}
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5
tests/modules/cnvkit/reference/nextflow.config
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5
tests/modules/cnvkit/reference/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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}
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8
tests/modules/cnvkit/reference/test.yml
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8
tests/modules/cnvkit/reference/test.yml
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- name: cnvkit reference test_cnvkit_reference
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command: nextflow run ./tests/modules/cnvkit/reference -entry test_cnvkit_reference -c ./tests/config/nextflow.config -c ./tests/modules/cnvkit/reference/nextflow.config
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tags:
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- cnvkit/reference
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- cnvkit
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files:
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- path: output/cnvkit/reference.cnn
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md5sum: 7c4a7902f5ab101b1f9d6038d331b3d9
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