mirror of
https://github.com/MillironX/nf-core_modules.git
synced 2024-12-22 11:08:17 +00:00
Merge branch 'master' into maxulysse-patch-1
This commit is contained in:
commit
e2acf28c8f
15 changed files with 125 additions and 184 deletions
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@ -1,4 +1,4 @@
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process SNAPALIGNER_PAIRED {
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process SNAPALIGNER_ALIGN {
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tag '$meta.id'
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label 'process_high'
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@ -21,15 +21,16 @@ process SNAPALIGNER_PAIRED {
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script:
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def args = task.ext.args ?: ''
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def prefix = task.ext.prefix ?: "${meta.id}"
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def subcmd = meta.single_end ? "single" : "paired"
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"""
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mkdir -p index
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mv $index index/
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snap-aligner paired \\
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snap-aligner ${subcmd} \\
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index \\
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${reads.join(" ")} \\
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-o -bam ${prefix}.bam \\
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-o ${prefix}.bam \\
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-t ${task.cpus} \\
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$args
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@ -1,5 +1,5 @@
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name: "snapaligner_paired"
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description: Performs paired end fastq alignment to a fasta reference using SNAP
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name: "snapaligner_align"
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description: Performs fastq alignment to a fasta reference using SNAP
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keywords:
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- alignment
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- map
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@ -22,7 +22,7 @@ input:
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e.g. [ id:'test', single_end:false ]
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- reads:
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type: file
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description: List of input fastq files of size 2 for fastq or 1 for bam
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description: List of input fastq files of size 2 for paired fastq or 1 for bam or single fastq
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pattern: "*.{fastq.gz,fq.gz,fastq,fq,bam}"
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- index:
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type: file
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@ -1,41 +0,0 @@
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process SNAPALIGNER_SINGLE {
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tag '$meta.id'
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label 'process_high'
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conda (params.enable_conda ? "bioconda::snap-aligner=2.0.1" : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/snap-aligner:2.0.1--hd03093a_1':
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'quay.io/biocontainers/snap-aligner:2.0.1--hd03093a_1' }"
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input:
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tuple val(meta), path(reads)
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path index
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output:
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tuple val(meta), path("*.bam"), 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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def prefix = task.ext.prefix ?: "${meta.id}"
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"""
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mkdir -p index
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mv $index index/
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snap-aligner single \\
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index \\
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${reads.join(" ")} \\
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-o -bam ${prefix}.bam \\
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-t ${task.cpus} \\
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$args
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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snapaligner: \$(snap-aligner 2>&1| head -n 1 | sed 's/^.*version //;s/.\$//')
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END_VERSIONS
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"""
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}
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@ -1,48 +0,0 @@
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name: "snapaligner_single"
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description: Performs single end fastq alignment to a fasta reference using SNAP
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keywords:
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- alignment
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- map
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- fastq
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- bam
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- sam
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tools:
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- "snapaligner":
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description: "Scalable Nucleotide Alignment Program -- a fast and accurate read aligner for high-throughput sequencing data"
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homepage: "http://snap.cs.berkeley.edu"
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documentation: "https://1drv.ms/b/s!AhuEg_0yZD86hcpblUt-muHKYsG8fA?e=R8ogug"
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tool_dev_url: "https://github.com/amplab/snap"
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doi: "10.1101/2021.11.23.469039"
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licence: "['Apache v2']"
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input:
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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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- reads:
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type: file
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description: List of single end input files
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pattern: "*.{fastq.gz,fq.gz,fastq,fq,bam}"
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- index:
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type: file
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description: List of SNAP genome index files
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pattern: "{Genome,GenomeIndex,GenomeIndexHash,OverflowTable}"
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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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- bam:
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type: file
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description: Aligned BAM file
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pattern: "*.{bam}"
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authors:
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- "@matthdsm"
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@ -1,43 +1,26 @@
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process SRATOOLS_PREFETCH {
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tag "$id"
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label 'process_low'
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label 'error_retry'
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conda (params.enable_conda ? 'bioconda::sra-tools=2.11.0' : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/sra-tools:2.11.0--pl5262h314213e_0' :
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'quay.io/biocontainers/sra-tools:2.11.0--pl5262h314213e_0' }"
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'https://depot.galaxyproject.org/singularity/sra-tools:2.11.0--pl5321ha49a11a_3' :
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'quay.io/biocontainers/sra-tools:2.11.0--pl5321ha49a11a_3' }"
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input:
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tuple val(meta), val(id)
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output:
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tuple val(meta), path("$id"), emit: sra
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tuple val(meta), path(id), emit: sra
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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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def config = "/LIBS/GUID = \"${UUID.randomUUID().toString()}\"\\n/libs/cloud/report_instance_identity = \"true\"\\n"
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"""
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eval "\$(vdb-config -o n NCBI_SETTINGS | sed 's/[" ]//g')"
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if [[ ! -f "\${NCBI_SETTINGS}" ]]; then
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mkdir -p "\$(dirname "\${NCBI_SETTINGS}")"
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printf '${config}' > "\${NCBI_SETTINGS}"
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fi
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shell:
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args = task.ext.args ?: ''
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args2 = task.ext.args2 ?: '5 1 100' // <num retries> <base delay in seconds> <max delay in seconds>
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config = "/LIBS/GUID = \"${UUID.randomUUID().toString()}\"\\n/libs/cloud/report_instance_identity = \"true\"\\n"
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prefetch \\
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$args \\
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--progress \\
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$id
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vdb-validate $id
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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sratools: \$(prefetch --version 2>&1 | grep -Eo '[0-9.]+')
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END_VERSIONS
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"""
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template 'retry_with_backoff.sh'
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}
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59
modules/sratools/prefetch/templates/retry_with_backoff.sh
Executable file
59
modules/sratools/prefetch/templates/retry_with_backoff.sh
Executable file
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@ -0,0 +1,59 @@
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#!/usr/bin/env bash
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set -u
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retry_with_backoff() {
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local max_attempts=${1}
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local delay=${2}
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local max_time=${3}
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local attempt=1
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local output=
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local status=
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# Remove the first three arguments to this function in order to access
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# the 'real' command with `${@}`.
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shift 3
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while [ ${attempt} -le ${max_attempts} ]; do
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output=$("${@}")
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status=${?}
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if [ ${status} -eq 0 ]; then
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break
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fi
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if [ ${attempt} -lt ${max_attempts} ]; then
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echo "Failed attempt ${attempt} of ${max_attempts}. Retrying in ${delay} s." >&2
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sleep ${delay}
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elif [ ${attempt} -eq ${max_attempts} ]; then
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echo "Failed after ${attempt} attempts." >&2
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return ${status}
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fi
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attempt=$(( ${attempt} + 1 ))
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delay=$(( ${delay} * 2 ))
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if [ ${delay} -ge ${max_time} ]; then
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delay=${max_time}
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fi
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done
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echo "${output}"
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}
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eval "$(vdb-config -o n NCBI_SETTINGS | sed 's/[" ]//g')"
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if [[ ! -f "${NCBI_SETTINGS}" ]]; then
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mkdir -p "$(dirname "${NCBI_SETTINGS}")"
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printf '!{config}' > "${NCBI_SETTINGS}"
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fi
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retry_with_backoff !{args2} \
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prefetch \
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!{args} \
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!{id}
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vdb-validate !{id}
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cat <<-END_VERSIONS > versions.yml
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"!{task.process}":
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sratools: $(prefetch --version 2>&1 | grep -Eo '[0-9.]+')
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END_VERSIONS
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@ -1767,13 +1767,9 @@ snapaligner/index:
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- modules/snapaligner/index/**
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- tests/modules/snapaligner/index/**
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snapaligner/paired:
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- modules/snapaligner/paired/**
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- tests/modules/snapaligner/paired/**
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snapaligner/single:
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- modules/snapaligner/single/**
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- tests/modules/snapaligner/single/**
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snapaligner/align:
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- modules/snapaligner/align/**
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- tests/modules/snapaligner/align/**
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snpdists:
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- modules/snpdists/**
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29
tests/modules/snapaligner/align/main.nf
Normal file
29
tests/modules/snapaligner/align/main.nf
Normal file
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#!/usr/bin/env nextflow
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nextflow.enable.dsl = 2
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include { SNAPALIGNER_INDEX } from '../../../../modules/snapaligner/index/main.nf'
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include { SNAPALIGNER_ALIGN as SNAPALIGNER_SINGLE } from '../../../../modules/snapaligner/align/main.nf'
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include { SNAPALIGNER_ALIGN as SNAPALIGNER_PAIRED } from '../../../../modules/snapaligner/align/main.nf'
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workflow test_snapaligner_single {
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input = [
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[ id:'test', single_end:true ], // meta map
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[file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true)]
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]
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SNAPALIGNER_INDEX ( file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true),[],[],[])
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SNAPALIGNER_SINGLE ( input, SNAPALIGNER_INDEX.out.index )
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}
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workflow test_snapaligner_paired {
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input = [
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[ id:'test', single_end:false ], // meta map
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[file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true), file(params.test_data['sarscov2']['illumina']['test_2_fastq_gz'], checkIfExists: true)]
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]
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SNAPALIGNER_INDEX ( file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true),[],[],[])
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SNAPALIGNER_PAIRED ( input, SNAPALIGNER_INDEX.out.index )
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}
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19
tests/modules/snapaligner/align/test.yml
Normal file
19
tests/modules/snapaligner/align/test.yml
Normal file
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@ -0,0 +1,19 @@
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- name: snapaligner align test_snapaligner_single
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command: nextflow run tests/modules/snapaligner/align -entry test_snapaligner_single -c tests/config/nextflow.config
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tags:
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- snapaligner/align
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- snapaligner
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files:
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- path: output/snapaligner/test.bam
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md5sum: 5d95594e4ef1ee23ce56e6a7cb64f0f2
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- path: output/snapaligner/versions.yml
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- name: snapaligner align test_snapaligner_paired
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command: nextflow run tests/modules/snapaligner/align -entry test_snapaligner_paired -c tests/config/nextflow.config
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tags:
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- snapaligner/align
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- snapaligner
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files:
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- path: output/snapaligner/test.bam
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md5sum: a1405da5876f15dbe8a81516b94c2a15
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- path: output/snapaligner/versions.yml
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@ -1,17 +0,0 @@
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#!/usr/bin/env nextflow
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nextflow.enable.dsl = 2
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include { SNAPALIGNER_INDEX } from '../../../../modules/snapaligner/index/main.nf'
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include { SNAPALIGNER_PAIRED } from '../../../../modules/snapaligner/paired/main.nf'
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workflow test_snapaligner_paired {
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input = [
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[ id:'test', single_end:false ], // meta map
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[file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true), file(params.test_data['sarscov2']['illumina']['test_2_fastq_gz'], checkIfExists: true)]
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]
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SNAPALIGNER_INDEX ( file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true),[],[],[])
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SNAPALIGNER_PAIRED ( input, SNAPALIGNER_INDEX.out.index )
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}
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@ -1,9 +0,0 @@
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- name: snapaligner paired test_snapaligner_paired
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command: nextflow run tests/modules/snapaligner/paired -entry test_snapaligner_paired -c tests/config/nextflow.config
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tags:
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- snapaligner
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- snapaligner/paired
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files:
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- path: output/snapaligner/test.bam
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md5sum: 2ac92e9539fa246dd6db52b5de56fca5
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- path: output/snapaligner/versions.yml
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@ -1,17 +0,0 @@
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#!/usr/bin/env nextflow
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nextflow.enable.dsl = 2
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include { SNAPALIGNER_INDEX } from '../../../../modules/snapaligner/index/main.nf'
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include { SNAPALIGNER_SINGLE } from '../../../../modules/snapaligner/single/main.nf'
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workflow test_snapaligner_single {
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input = [
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[ id:'test', single_end:false ], // meta map
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[file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true)]
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]
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SNAPALIGNER_INDEX ( file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true),[],[],[])
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SNAPALIGNER_SINGLE ( input, SNAPALIGNER_INDEX.out.index )
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}
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@ -1,5 +0,0 @@
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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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@ -1,9 +0,0 @@
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- name: snapaligner single test_snapaligner_single
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command: nextflow run tests/modules/snapaligner/single -entry test_snapaligner_single -c tests/config/nextflow.config
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tags:
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- snapaligner/single
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- snapaligner
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files:
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- path: output/snapaligner/test.bam
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||||
md5sum: 696f7ea8e1aa5f9d7dafb9d0134fe25d
|
||||
- path: output/snapaligner/versions.yml
|
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