Add gatk4/applybqsr (#331)

* Add applybqsr module

* Solve problem in functions.nf

* Add to pytest
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yocra3 2021-03-23 14:15:26 +01:00 committed by GitHub
parent 9115c12f88
commit 614d61dc13
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6 changed files with 221 additions and 1 deletions

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/*
* -----------------------------------------------------
* Utility functions used in nf-core DSL2 module files
* -----------------------------------------------------
*/
/*
* Extract name of software tool from process name using $task.process
*/
def getSoftwareName(task_process) {
return task_process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()
}
/*
* Function to initialise default values and to generate a Groovy Map of available options for nf-core modules
*/
def initOptions(Map args) {
def Map options = [:]
options.args = args.args ?: ''
options.args2 = args.args2 ?: ''
options.args3 = args.args3 ?: ''
options.publish_by_id = args.publish_by_id ?: false
options.publish_dir = args.publish_dir ?: ''
options.publish_files = args.publish_files
options.suffix = args.suffix ?: ''
return options
}
/*
* Tidy up and join elements of a list to return a path string
*/
def getPathFromList(path_list) {
def paths = path_list.findAll { item -> !item?.trim().isEmpty() } // Remove empty entries
paths = paths.collect { it.trim().replaceAll("^[/]+|[/]+\$", "") } // Trim whitespace and trailing slashes
return paths.join('/')
}
/*
* Function to save/publish module results
*/
def saveFiles(Map args) {
if (!args.filename.endsWith('.version.txt')) {
def ioptions = initOptions(args.options)
def path_list = [ ioptions.publish_dir ?: args.publish_dir ]
if (ioptions.publish_by_id) {
path_list.add(args.publish_id)
}
if (ioptions.publish_files instanceof Map) {
for (ext in ioptions.publish_files) {
if (args.filename.endsWith(ext.key)) {
def ext_list = path_list.collect()
ext_list.add(ext.value)
return "${getPathFromList(ext_list)}/$args.filename"
}
}
} else if (ioptions.publish_files == null) {
return "${getPathFromList(path_list)}/$args.filename"
}
}
}

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// Import generic module functions
include { initOptions; saveFiles; getSoftwareName } from './functions'
params.options = [:]
options = initOptions(params.options)
process GATK4_APPLYBQSR {
tag "$meta.id"
label 'process_low'
publishDir "${params.outdir}",
mode: params.publish_dir_mode,
saveAs: { filename -> saveFiles(filename:filename, options:params.options, publish_dir:getSoftwareName(task.process), publish_id:meta.id) }
conda (params.enable_conda ? "bioconda::gatk4=4.2.0.0" : null)
if (workflow.containerEngine == 'singularity' && !params.singularity_pull_docker_container) {
container "https://depot.galaxyproject.org/singularity/gatk4:4.2.0.0--0"
} else {
container "quay.io/biocontainers/gatk4:4.2.0.0--0"
}
input:
tuple val(meta), path(bam), path(bqsr_table)
path fasta
path fastaidx
path dict
path intervalsBed
output:
tuple val(meta), path("*.bam"), emit: bam
path "*.version.txt" , emit: version
script:
def software = getSoftwareName(task.process)
def prefix = options.suffix ? "${meta.id}${options.suffix}" : "${meta.id}"
def intervalsCommand = intervalsBed ? "-L ${intervalsBed}" : ""
"""
gatk ApplyBQSR \\
-R $fasta \\
-I $bam \\
--bqsr-recal-file $bqsr_table \\
$intervalsCommand \\
-O ${prefix}.bam \\
$options.args
gatk --version | grep Picard | sed "s/Picard Version: //g" > ${software}.version.txt
"""
}

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name: gatk4_applybqsr
description: Apply base quality score recalibration (BQSR) to a bam file
keywords:
- bqsr
- bam
tools:
- gatk4:
description: |
Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools
with a primary focus on variant discovery and genotyping. Its powerful processing engine
and high-performance computing features make it capable of taking on projects of any size.
homepage: https://gatk.broadinstitute.org/hc/en-us
documentation: https://gatk.broadinstitute.org/hc/en-us/categories/360002369672s
doi: 10.1158/1538-7445.AM2017-3590
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- bam:
type: file
description: BAM file from alignment
pattern: "*.{bam}"
- bqsr_table:
type: file
description: Recalibration table from gatk4_baserecalibrator
- fasta:
type: file
description: The reference fasta file
- fastaidx:
type: file
description: Index of reference fasta file
- dict:
type: file
description: GATK sequence dictionary
- intervalsBed:
type: file
description: Bed file with the genomic regions included in the library (optional)
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- version:
type: file
description: File containing software version
pattern: "*.{version.txt}"
- bam:
type: file
description: Recalibrated BAM file
pattern: "*.{bam}"
authors:
- "@yocra3"

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@ -99,7 +99,7 @@ bismark_summary:
blast_blastn:
- software/blast/blastn/**
- tests/software/blast/blastn/**
blast_makeblastdb:
- software/blast/makeblastdb/**
- tests/software/blast/makeblastdb/**
@ -174,6 +174,10 @@ fastqc:
- software/fastqc/**
- tests/software/fastqc/**
gatk4_applybqsr:
- software/gatk4/applybqsr/**
- tests/software/gatk4/applybqsr/**
gatk4_bedtointervallist:
- software/gatk4/bedtointervallist/**
- tests/software/gatk4/bedtointervallist/**

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#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { GATK4_APPLYBQSR } from '../../../../software/gatk4/applybqsr/main.nf' addParams( options: [:] )
workflow test_gatk4_applybqsr {
def input = []
input = [ [ id:'test' ], // meta map
file("${launchDir}/tests/data/genomics/sarscov2/bam/test_paired_end.sorted.bam", checkIfExists: true),
file("${launchDir}/tests/data/genomics/sarscov2/table/test.table", checkIfExists: true) ]
fasta = file("${launchDir}/tests/data/genomics/sarscov2/fasta/test_genome.fasta", checkIfExists: true)
fastaidx = file("${launchDir}/tests/data/genomics/sarscov2/fasta/test_genome.fasta.fai", checkIfExists: true)
dict = file("${launchDir}/tests/data/genomics/sarscov2/fasta/test_genome.dict", checkIfExists: true)
GATK4_APPLYBQSR ( input, fasta, fastaidx, dict, [] )
}
workflow test_gatk4_applybqsr_intervals {
def input = []
input = [ [ id:'test' ], // meta map
file("${launchDir}/tests/data/genomics/sarscov2/bam/test_paired_end.sorted.bam", checkIfExists: true),
file("${launchDir}/tests/data/genomics/sarscov2/table/test.table", checkIfExists: true) ]
fasta = file("${launchDir}/tests/data/genomics/sarscov2/fasta/test_genome.fasta", checkIfExists: true)
fastaidx = file("${launchDir}/tests/data/genomics/sarscov2/fasta/test_genome.fasta.fai", checkIfExists: true)
dict = file("${launchDir}/tests/data/genomics/sarscov2/fasta/test_genome.dict", checkIfExists: true)
intervals = file("${launchDir}/tests/data/genomics/sarscov2/bed/test.bed", checkIfExists: true)
GATK4_APPLYBQSR ( input, fasta, fastaidx, dict, intervals)
}

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- name: gatk4 applybqsr test_gatk4_applybqsr
command: nextflow run tests/software/gatk4/applybqsr -entry test_gatk4_applybqsr -c tests/config/nextflow.config
tags:
- gatk4
- gatk4_applybqsr
files:
- path: output/gatk4/test.bam
md5sum: 943a43de5f575a0435fe13072cbc15c8
- name: "\e[3~"
command: nextflow run tests/software/gatk4/applybqsr -entry test_gatk4_applybqsr_intervals -c tests/config/nextflow.config
tags:
- gatk4
- gatk4_applybqsr_intervals
- gatk4_applybqsr
files:
- path: output/gatk4/test.bam
md5sum: a92238a9a78da48bf437fd5b7d9790a3