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Merge pull request #218 from phue/samtools_faidx
add samtools/faidx + tests
This commit is contained in:
commit
78cf182ed4
6 changed files with 167 additions and 0 deletions
4
.github/filters.yml
vendored
4
.github/filters.yml
vendored
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@ -193,6 +193,10 @@ salmon_quant:
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- software/salmon/quant/**
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- software/salmon/quant/**
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- tests/software/salmon/quant/**
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- tests/software/salmon/quant/**
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samtools_faidx:
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- software/samtools/faidx/**
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- tests/software/samtools/faidx/**
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samtools_flagstat:
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samtools_flagstat:
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- software/samtools/flagstat/**
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- software/samtools/flagstat/**
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- tests/software/samtools/flagstat/**
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- tests/software/samtools/flagstat/**
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59
software/samtools/faidx/functions.nf
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59
software/samtools/faidx/functions.nf
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@ -0,0 +1,59 @@
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/*
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* -----------------------------------------------------
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* Utility functions used in nf-core DSL2 module files
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* -----------------------------------------------------
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*/
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/*
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* Extract name of software tool from process name using $task.process
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*/
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def getSoftwareName(task_process) {
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return task_process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()
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}
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/*
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* Function to initialise default values and to generate a Groovy Map of available options for nf-core modules
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*/
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def initOptions(Map args) {
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def Map options = [:]
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options.args = args.args ?: ''
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options.args2 = args.args2 ?: ''
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options.publish_by_id = args.publish_by_id ?: false
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options.publish_dir = args.publish_dir ?: ''
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options.publish_files = args.publish_files
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options.suffix = args.suffix ?: ''
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return options
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}
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/*
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* Tidy up and join elements of a list to return a path string
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*/
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def getPathFromList(path_list) {
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def paths = path_list.findAll { item -> !item?.trim().isEmpty() } // Remove empty entries
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paths = paths.collect { it.trim().replaceAll("^[/]+|[/]+\$", "") } // Trim whitespace and trailing slashes
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return paths.join('/')
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}
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/*
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* Function to save/publish module results
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*/
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def saveFiles(Map args) {
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if (!args.filename.endsWith('.version.txt')) {
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def ioptions = initOptions(args.options)
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def path_list = [ ioptions.publish_dir ?: args.publish_dir ]
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if (ioptions.publish_by_id) {
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path_list.add(args.publish_id)
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}
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if (ioptions.publish_files instanceof Map) {
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for (ext in ioptions.publish_files) {
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if (args.filename.endsWith(ext.key)) {
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def ext_list = path_list.collect()
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ext_list.add(ext.value)
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return "${getPathFromList(ext_list)}/$args.filename"
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}
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}
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} else if (ioptions.publish_files == null) {
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return "${getPathFromList(path_list)}/$args.filename"
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}
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}
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}
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33
software/samtools/faidx/main.nf
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33
software/samtools/faidx/main.nf
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// Import generic module functions
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include { saveFiles; getSoftwareName } from './functions'
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params.options = [:]
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process SAMTOOLS_FAIDX {
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tag "$fasta"
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label 'process_low'
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publishDir "${params.outdir}",
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mode: params.publish_dir_mode,
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saveAs: { filename -> saveFiles(filename:filename, options:params.options, publish_dir:getSoftwareName(task.process), publish_id:'') }
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conda (params.enable_conda ? "bioconda::samtools=1.10" : null)
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if (workflow.containerEngine == 'singularity' && !params.singularity_pull_docker_container) {
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container "https://depot.galaxyproject.org/singularity/samtools:1.10--h9402c20_2"
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} else {
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container "quay.io/biocontainers/samtools:1.10--h9402c20_2"
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}
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input:
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path fasta
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output:
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path "*.fai" , emit: fai
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path "*.version.txt", emit: version
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script:
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def software = getSoftwareName(task.process)
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"""
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samtools faidx $fasta
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echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//' > ${software}.version.txt
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"""
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}
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53
software/samtools/faidx/meta.yml
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53
software/samtools/faidx/meta.yml
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name: samtools_faidx
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description: Index FASTA file
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keywords:
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- index
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- fasta
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tools:
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- samtools:
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description: |
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SAMtools is a set of utilities for interacting with and post-processing
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short DNA sequence read alignments in the SAM, BAM and CRAM formats, written by Heng Li.
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These files are generated as output by short read aligners like BWA.
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homepage: http://www.htslib.org/
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documentation: http://www.htslib.org/doc/samtools.html
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doi: 10.1093/bioinformatics/btp352
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params:
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- outdir:
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type: string
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description: |
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The pipeline's output directory. By default, the module will
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output files into `$params.outdir/<SOFTWARE>`
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- publish_dir_mode:
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type: string
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description: |
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Value for the Nextflow `publishDir` mode parameter.
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Available: symlink, rellink, link, copy, copyNoFollow, move.
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- enable_conda:
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type: boolean
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description: |
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Run the module with Conda using the software specified
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via the `conda` directive
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- singularity_pull_docker_container:
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type: boolean
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description: |
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Instead of directly downloading Singularity images for use with Singularity,
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force the workflow to pull and convert Docker containers instead.
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input:
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- fasta:
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type: file
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description: FASTA file
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pattern: "*.{fa,fasta}"
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output:
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- fai:
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type: file
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description: FASTA index file
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pattern: "*.{fai}"
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- version:
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type: file
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description: File containing software version
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pattern: "*.{version.txt}"
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authors:
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- "@drpatelh"
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- "@ewels"
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- "@phue"
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10
tests/software/samtools/faidx/main.nf
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10
tests/software/samtools/faidx/main.nf
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#!/usr/bin/env nextflow
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nextflow.enable.dsl = 2
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include { SAMTOOLS_FAIDX } from '../../../../software/samtools/faidx/main.nf' addParams( options: [:] )
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workflow test_samtools_faidx {
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SAMTOOLS_FAIDX ( file("${launchDir}/tests/data/fasta/E_coli/NC_010473.fa", checkIfExists: true) )
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}
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8
tests/software/samtools/faidx/test.yml
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8
tests/software/samtools/faidx/test.yml
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- name: Run samtools faidx test workflow
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command: nextflow run ./tests/software/samtools/faidx -entry test_samtools_faidx -c tests/config/nextflow.config
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tags:
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- samtools
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- samtools_faidx
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files:
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- path: output/samtools/NC_010473.fa.fai
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md5sum: 082de78397fbe9bd3500c7d5c9edc03e
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