Merge pull request #218 from phue/samtools_faidx

add samtools/faidx + tests
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Patrick Hüther 2021-02-17 17:37:16 +01:00 committed by GitHub
commit 78cf182ed4
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6 changed files with 167 additions and 0 deletions

4
.github/filters.yml vendored
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@ -193,6 +193,10 @@ salmon_quant:
- software/salmon/quant/** - software/salmon/quant/**
- tests/software/salmon/quant/** - tests/software/salmon/quant/**
samtools_faidx:
- software/samtools/faidx/**
- tests/software/samtools/faidx/**
samtools_flagstat: samtools_flagstat:
- software/samtools/flagstat/** - software/samtools/flagstat/**
- tests/software/samtools/flagstat/** - tests/software/samtools/flagstat/**

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@ -0,0 +1,59 @@
/*
* -----------------------------------------------------
* Utility functions used in nf-core DSL2 module files
* -----------------------------------------------------
*/
/*
* Extract name of software tool from process name using $task.process
*/
def getSoftwareName(task_process) {
return task_process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()
}
/*
* Function to initialise default values and to generate a Groovy Map of available options for nf-core modules
*/
def initOptions(Map args) {
def Map options = [:]
options.args = args.args ?: ''
options.args2 = args.args2 ?: ''
options.publish_by_id = args.publish_by_id ?: false
options.publish_dir = args.publish_dir ?: ''
options.publish_files = args.publish_files
options.suffix = args.suffix ?: ''
return options
}
/*
* Tidy up and join elements of a list to return a path string
*/
def getPathFromList(path_list) {
def paths = path_list.findAll { item -> !item?.trim().isEmpty() } // Remove empty entries
paths = paths.collect { it.trim().replaceAll("^[/]+|[/]+\$", "") } // Trim whitespace and trailing slashes
return paths.join('/')
}
/*
* Function to save/publish module results
*/
def saveFiles(Map args) {
if (!args.filename.endsWith('.version.txt')) {
def ioptions = initOptions(args.options)
def path_list = [ ioptions.publish_dir ?: args.publish_dir ]
if (ioptions.publish_by_id) {
path_list.add(args.publish_id)
}
if (ioptions.publish_files instanceof Map) {
for (ext in ioptions.publish_files) {
if (args.filename.endsWith(ext.key)) {
def ext_list = path_list.collect()
ext_list.add(ext.value)
return "${getPathFromList(ext_list)}/$args.filename"
}
}
} else if (ioptions.publish_files == null) {
return "${getPathFromList(path_list)}/$args.filename"
}
}
}

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@ -0,0 +1,33 @@
// Import generic module functions
include { saveFiles; getSoftwareName } from './functions'
params.options = [:]
process SAMTOOLS_FAIDX {
tag "$fasta"
label 'process_low'
publishDir "${params.outdir}",
mode: params.publish_dir_mode,
saveAs: { filename -> saveFiles(filename:filename, options:params.options, publish_dir:getSoftwareName(task.process), publish_id:'') }
conda (params.enable_conda ? "bioconda::samtools=1.10" : null)
if (workflow.containerEngine == 'singularity' && !params.singularity_pull_docker_container) {
container "https://depot.galaxyproject.org/singularity/samtools:1.10--h9402c20_2"
} else {
container "quay.io/biocontainers/samtools:1.10--h9402c20_2"
}
input:
path fasta
output:
path "*.fai" , emit: fai
path "*.version.txt", emit: version
script:
def software = getSoftwareName(task.process)
"""
samtools faidx $fasta
echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//' > ${software}.version.txt
"""
}

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@ -0,0 +1,53 @@
name: samtools_faidx
description: Index FASTA file
keywords:
- index
- fasta
tools:
- samtools:
description: |
SAMtools is a set of utilities for interacting with and post-processing
short DNA sequence read alignments in the SAM, BAM and CRAM formats, written by Heng Li.
These files are generated as output by short read aligners like BWA.
homepage: http://www.htslib.org/
documentation: http://www.htslib.org/doc/samtools.html
doi: 10.1093/bioinformatics/btp352
params:
- outdir:
type: string
description: |
The pipeline's output directory. By default, the module will
output files into `$params.outdir/<SOFTWARE>`
- publish_dir_mode:
type: string
description: |
Value for the Nextflow `publishDir` mode parameter.
Available: symlink, rellink, link, copy, copyNoFollow, move.
- enable_conda:
type: boolean
description: |
Run the module with Conda using the software specified
via the `conda` directive
- singularity_pull_docker_container:
type: boolean
description: |
Instead of directly downloading Singularity images for use with Singularity,
force the workflow to pull and convert Docker containers instead.
input:
- fasta:
type: file
description: FASTA file
pattern: "*.{fa,fasta}"
output:
- fai:
type: file
description: FASTA index file
pattern: "*.{fai}"
- version:
type: file
description: File containing software version
pattern: "*.{version.txt}"
authors:
- "@drpatelh"
- "@ewels"
- "@phue"

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@ -0,0 +1,10 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { SAMTOOLS_FAIDX } from '../../../../software/samtools/faidx/main.nf' addParams( options: [:] )
workflow test_samtools_faidx {
SAMTOOLS_FAIDX ( file("${launchDir}/tests/data/fasta/E_coli/NC_010473.fa", checkIfExists: true) )
}

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@ -0,0 +1,8 @@
- name: Run samtools faidx test workflow
command: nextflow run ./tests/software/samtools/faidx -entry test_samtools_faidx -c tests/config/nextflow.config
tags:
- samtools
- samtools_faidx
files:
- path: output/samtools/NC_010473.fa.fai
md5sum: 082de78397fbe9bd3500c7d5c9edc03e