Merge branch 'master' into kat_hist

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Mahesh Binzer-Panchal 2022-05-23 08:52:13 +02:00 committed by GitHub
commit e06fb752c3
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@ -0,0 +1,68 @@
process ANTISMASH_ANTISMASHLITE {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::antismash-lite=6.0.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/antismash-lite:6.0.1--pyhdfd78af_1' :
'quay.io/biocontainers/antismash-lite:6.0.1--pyhdfd78af_1' }"
containerOptions {
workflow.containerEngine == 'singularity' ?
"-B $antismash_dir:/usr/local/lib/python3.8/site-packages/antismash" :
workflow.containerEngine == 'docker' ?
"-v \$PWD/$antismash_dir:/usr/local/lib/python3.8/site-packages/antismash" :
''
}
input:
tuple val(meta), path(sequence_input)
path(databases)
path(antismash_dir) // Optional input: AntiSMASH installation folder. It is not needed for using this module with conda, but required for docker/singularity (see meta.yml).
path(gff)
output:
tuple val(meta), path("${prefix}/clusterblast/*_c*.txt") , optional: true, emit: clusterblast_file
tuple val(meta), path("${prefix}/{css,images,js}") , emit: html_accessory_files
tuple val(meta), path("${prefix}/knownclusterblast/region*/ctg*.html") , optional: true, emit: knownclusterblast_html
tuple val(meta), path("${prefix}/knownclusterblast/*_c*.txt") , optional: true, emit: knownclusterblast_txt
tuple val(meta), path("${prefix}/svg/clusterblast*.svg") , optional: true, emit: svg_files_clusterblast
tuple val(meta), path("${prefix}/svg/knownclusterblast*.svg") , optional: true, emit: svg_files_knownclusterblast
tuple val(meta), path("${prefix}/*.gbk") , emit: gbk_input
tuple val(meta), path("${prefix}/*.json") , emit: json_results
tuple val(meta), path("${prefix}/*.log") , emit: log
tuple val(meta), path("${prefix}/*.zip") , emit: zip
tuple val(meta), path("${prefix}/*region*.gbk") , emit: gbk_results
tuple val(meta), path("${prefix}/clusterblastoutput.txt") , optional: true, emit: clusterblastoutput
tuple val(meta), path("${prefix}/index.html") , emit: html
tuple val(meta), path("${prefix}/knownclusterblastoutput.txt") , optional: true, emit: knownclusterblastoutput
tuple val(meta), path("${prefix}/regions.js") , emit: json_sideloading
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
prefix = task.ext.suffix ? "${meta.id}${task.ext.suffix}" : "${meta.id}"
gff_flag = "--genefinding-gff3 ${gff}"
"""
## We specifically do not include annotations (--genefinding-tool none) as
## this should be run as a separate module for versioning purposes
antismash \\
$args \\
$gff_flag \\
-c $task.cpus \\
--output-dir $prefix \\
--genefinding-tool none \\
--logfile $prefix/${prefix}.log \\
--databases $databases \\
$sequence_input
cat <<-END_VERSIONS > versions.yml
"${task.process}":
antismash-lite: \$(antismash --version | sed 's/antiSMASH //')
END_VERSIONS
"""
}

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@ -0,0 +1,128 @@
name: antismash_antismashlite
description: |
antiSMASH allows the rapid genome-wide identification, annotation
and analysis of secondary metabolite biosynthesis gene clusters.
keywords:
- secondary metabolites
- BGC
- biosynthetic gene cluster
- genome mining
- NRPS
- RiPP
- antibiotics
- prokaryotes
- bacteria
- eukaryotes
- fungi
- antismash
tools:
- antismashlite:
description: "antiSMASH - the antibiotics and Secondary Metabolite Analysis SHell"
homepage: "https://docs.antismash.secondarymetabolites.org"
documentation: "https://docs.antismash.secondarymetabolites.org"
tool_dev_url: "https://github.com/antismash/antismash"
doi: "10.1093/nar/gkab335"
licence: "['AGPL v3']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- sequence_input:
type: file
description: nucleotide sequence file (annotated)
pattern: "*.{gbk, gb, gbff, genbank, embl, fasta, fna}"
- databases:
type: directory
description: downloaded AntiSMASH databases e.g. data/databases
pattern: "*/"
- antismash_dir:
type: directory
description: |
A local copy of an AntiSMASH installation folder. This is required when running with
docker and singularity (not required for conda), due to attempted 'modifications' of
files during database checks in the installation directory, something that cannot
be done in immutable docker/singularity containers. Therefore, a local installation
directory needs to be mounted (including all modified files from the downloading step)
to the container as a workaround.
pattern: "*/"
- gff:
type: file
pattern: "*.gff"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- clusterblast_file:
type: file
description: Output of ClusterBlast algorithm
pattern: "clusterblast/*_c*.txt"
- html_accessory_files:
type: directory
description: Accessory files for the HTML output
pattern: "{css/,images/,js/}"
- knownclusterblast_html:
type: file
description: Tables with MIBiG hits in HTML format
pattern: "knownclusterblast/region*/ctg*.html"
- knownclusterblast_txt:
type: file
description: Tables with MIBiG hits
pattern: "knownclusterblast/*_c*.txt"
- svg_files_clusterblast:
type: file
description: SVG images showing the % identity of the aligned hits against their queries
pattern: "svg/clusterblast*.svg"
- svg_files_knownclusterblast:
type: file
description: SVG images showing the % identity of the aligned hits against their queries
pattern: "svg/knownclusterblast*.svg"
- gbk_input:
type: file
description: Nucleotide sequence and annotations in GenBank format; converted from input file
pattern: "*.gbk"
- json_results:
type: file
description: Nucleotide sequence and annotations in JSON format; converted from GenBank file (gbk_input)
pattern: "*.json"
- log:
type: file
description: Contains all the logging output that antiSMASH produced during its run
pattern: "*.log"
- zip:
type: file
description: Contains a compressed version of the output folder in zip format
pattern: "*.zip"
- gbk_results:
type: file
description: Nucleotide sequence and annotations in GenBank format; one file per antiSMASH hit
pattern: "*region*.gbk"
- clusterblastoutput:
type: file
description: Raw BLAST output of known clusters previously predicted by antiSMASH using the built-in ClusterBlast algorithm
pattern: "clusterblastoutput.txt"
- html:
type: file
description: Graphical web view of results in HTML format
patterN: "index.html"
- knownclusterblastoutput:
type: file
description: Raw BLAST output of known clusters of the MIBiG database
pattern: "knownclusterblastoutput.txt"
- json_sideloading:
type: file
description: Sideloaded annotations of protoclusters and/or subregions (see antiSMASH documentation "Annotation sideloading")
pattern: "regions.js"
authors:
- "@jasmezz"

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@ -0,0 +1,38 @@
process BEDTOOLS_SPLIT {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::bedtools=2.30.0" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/bedtools:2.30.0--h468198e_3':
'quay.io/biocontainers/bedtools:2.30.0--h7d7f7ad_2' }"
input:
tuple val(meta), path(bed)
val(number_of_files)
output:
tuple val(meta), path("*.bed"), emit: beds
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
"""
bedtools \\
split \\
$args \\
-i $bed \\
-p $prefix \\
-n $number_of_files
cat <<-END_VERSIONS > versions.yml
"${task.process}":
bedtools: \$(bedtools --version | sed -e "s/bedtools v//g")
END_VERSIONS
"""
}

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@ -0,0 +1,41 @@
name: "bedtools_split"
description: Split BED files into several smaller BED files
keywords:
- sort
tools:
- "bedtools":
description: "A powerful toolset for genome arithmetic"
documentation: "https://bedtools.readthedocs.io/en/latest/content/tools/sort.html"
licence: "['MIT', 'GPL v2']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- bed:
type: file
description: BED file
pattern: "*.bed"
- bed:
type: value
description: The number of files to split the BED into
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- beds:
type: file
description: list of split BED files
pattern: "*.bed"
authors:
- "@nvnieuwk"

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@ -0,0 +1,38 @@
process BIOBAMBAM_BAMMERGE {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::biobambam=2.0.183" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/biobambam:2.0.183--h9f5acd7_1':
'quay.io/biocontainers/biobambam:2.0.183--h9f5acd7_1' }"
input:
tuple val(meta), path(bam)
output:
tuple val(meta), path("${prefix}.bam") ,emit: bam
tuple val(meta), path("*.bai") ,optional:true, emit: bam_index
tuple val(meta), path("*.md5") ,optional:true, emit: checksum
path "versions.yml" ,emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
prefix = task.ext.prefix ?: "${meta.id}"
def input_string = bam.join(" I=")
"""
bammerge \\
I=${input_string} \\
$args \\
> ${prefix}.bam
cat <<-END_VERSIONS > versions.yml
"${task.process}":
bammerge: \$( bammerge --version |& sed '1!d; s/.*version //; s/.\$//' )
END_VERSIONS
"""
}

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@ -0,0 +1,46 @@
name: biobambam_bammerge
description: Merge a list of sorted bam files
keywords:
- merge
- bam
tools:
- biobambam:
description: |
biobambam is a set of tools for early stage alignment file processing.
homepage: https://gitlab.com/german.tischler/biobambam2
documentation: https://gitlab.com/german.tischler/biobambam2/-/blob/master/README.md
doi: 10.1186/1751-0473-9-13
licence: ["GPL v3"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- bam:
type: file
description: List containing 1 or more bam files
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- bam:
type: file
description: Merged BAM file
pattern: "*.bam"
- bam_index:
type: file
description: BAM index file
pattern: "*"
- checksum:
type: file
description: Checksum file
pattern: "*"
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
authors:
- "@matthdsm"

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@ -11,6 +11,7 @@ process BOWTIE2_ALIGN {
tuple val(meta), path(reads)
path index
val save_unaligned
val sort_bam
output:
tuple val(meta), path("*.bam") , emit: bam
@ -36,8 +37,7 @@ process BOWTIE2_ALIGN {
reads_args = "-1 ${reads[0]} -2 ${reads[1]}"
}
def samtools_command = "samtools view -@ $task.cpus --bam --with-header ${args2} > ${prefix}.bam"
def samtools_command = sort_bam ? 'sort' : 'view'
"""
INDEX=`find -L ./ -name "*.rev.1.bt2" | sed "s/.rev.1.bt2//"`
@ -51,7 +51,7 @@ process BOWTIE2_ALIGN {
$unaligned \\
$args \\
2> ${prefix}.bowtie2.log \\
| $samtools_command
| samtools $samtools_command $args2 --threads $task.cpus -o ${prefix}.bam -
if [ -f ${prefix}.unmapped.fastq.1.gz ]; then
mv ${prefix}.unmapped.fastq.1.gz ${prefix}.unmapped_1.fastq.gz
@ -69,4 +69,3 @@ process BOWTIE2_ALIGN {
END_VERSIONS
"""
}

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@ -29,6 +29,15 @@ input:
type: file
description: Bowtie2 genome index files
pattern: "*.ebwt"
- save_unaligned:
type: boolean
description: |
Save reads that do not map to the reference (true) or discard them (false)
(default: false)
- sort_bam:
type: boolean
description: use samtools sort (true) or samtools view (false)
pattern: "true or false"
output:
- bam:
type: file

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@ -2,10 +2,10 @@ process GATK4_APPLYBQSR {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(input), path(input_index), path(bqsr_table), path(intervals)

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@ -2,10 +2,10 @@ process GATK4_APPLYBQSR_SPARK {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.3.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.3.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.3.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(input), path(input_index), path(bqsr_table), path(intervals)

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@ -2,10 +2,10 @@ process GATK4_APPLYVQSR {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(vcf_tbi), path(recal), path(recal_index), path(tranches)

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@ -2,10 +2,10 @@ process GATK4_BASERECALIBRATOR {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(input), path(input_index), path(intervals)

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@ -2,10 +2,10 @@ process GATK4_BASERECALIBRATOR_SPARK {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.3.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.3.0--hdfd78af_0' :
'broadinstitute/gatk:4.2.3.0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(input), path(input_index), path(intervals)

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@ -2,10 +2,10 @@ process GATK4_BEDTOINTERVALLIST {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(bed)

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@ -2,10 +2,10 @@ process GATK4_CALCULATECONTAMINATION {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(pileup), path(matched)

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@ -0,0 +1,57 @@
process GATK4_CNNSCOREVARIANTS {
tag "$meta.id"
label 'process_low'
//Conda is not supported at the moment: https://github.com/broadinstitute/gatk/issues/7811
if (params.enable_conda) {
exit 1, "Conda environments cannot be used for GATK4/CNNScoreVariants at the moment. Please use docker or singularity containers."
}
container 'broadinstitute/gatk:4.2.6.1' //Biocontainers is missing a package
input:
tuple val(meta), path(vcf), path(aligned_input), path(intervals)
path fasta
path fai
path dict
path architecture
path weights
output:
tuple val(meta), path("*.vcf.gz"), emit: vcf
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def aligned_input = aligned_input ? "--input $aligned_input" : ""
def interval_command = intervals ? "--intervals $intervals" : ""
def architecture = architecture ? "--architecture $architecture" : ""
def weights = weights ? "--weights $weights" : ""
def avail_mem = 3
if (!task.memory) {
log.info '[GATK CnnScoreVariants] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
} else {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" CNNScoreVariants \\
--variant $vcf \\
--output ${prefix}.vcf.gz \\
--reference $fasta \\
$interval_command \\
$aligned_input \\
$architecture \\
$weights \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
gatk4: \$(echo \$(gatk --version 2>&1) | sed 's/^.*(GATK) v//; s/ .*\$//')
END_VERSIONS
"""
}

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@ -0,0 +1,72 @@
name: "gatk4_cnnscorevariants"
description: Apply a Convolutional Neural Net to filter annotated variants
keywords:
- gatk4_cnnscorevariants
- gatk4
- variants
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
licence: ["Apache-2.0"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- vcf:
type: file
description: VCF file
pattern: "*.vcf.gz"
- aligned_input:
type: file
description: BAM/CRAM file from alignment (optional)
pattern: "*.{bam,cram}"
- intervals:
type: file
description: Bed file with the genomic regions included in the library (optional)
- fasta:
type: file
description: The reference fasta file
pattern: "*.fasta"
- fai:
type: file
description: Index of reference fasta file
pattern: "*.fasta.fai"
- dict:
type: file
description: GATK sequence dictionary
pattern: "*.dict"
- architecture:
type: file
description: Neural Net architecture configuration json file (optional)
pattern: "*.json"
- weights:
type: file
description: Keras model HD5 file with neural net weights. (optional)
pattern: "*.hd5"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- vcf:
type: file
description: Annotated VCF file
pattern: "*.vcf"
authors:
- "@FriederikeHanssen"

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@ -2,10 +2,10 @@ process GATK4_COMBINEGVCFS {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(vcf_idx)

View file

@ -2,10 +2,10 @@ process GATK4_CREATESEQUENCEDICTIONARY {
tag "$fasta"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
path fasta

View file

@ -2,10 +2,10 @@ process GATK4_CREATESOMATICPANELOFNORMALS {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(genomicsdb)

View file

@ -2,10 +2,10 @@ process GATK4_ESTIMATELIBRARYCOMPLEXITY {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(input)

View file

@ -2,10 +2,10 @@ process GATK4_FASTQTOSAM {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(reads)

View file

@ -2,10 +2,10 @@ process GATK4_FILTERMUTECTCALLS {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(vcf_tbi), path(stats), path(orientationbias), path(segmentation), path(table), val(estimate)

View file

@ -2,10 +2,10 @@ process GATK4_GATHERBQSRREPORTS {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(table)

View file

@ -2,10 +2,10 @@ process GATK4_GATHERPILEUPSUMMARIES {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:

View file

@ -2,10 +2,10 @@ process GATK4_GENOMICSDBIMPORT {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(tbi), path(interval_file), val(interval_value), path(wspace)

View file

@ -2,10 +2,10 @@ process GATK4_GENOTYPEGVCFS {
tag "$meta.id"
label 'process_high'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(gvcf), path(gvcf_index), path(intervals), path(intervals_index)

View file

@ -2,10 +2,10 @@ process GATK4_GETPILEUPSUMMARIES {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(input), path(index), path(intervals)
@ -40,7 +40,7 @@ process GATK4_GETPILEUPSUMMARIES {
--variant $variants \\
--output ${prefix}.pileups.table \\
$reference_command \\
$sites_command \\
$interval_command \\
--tmp-dir . \\
$args

View file

@ -2,10 +2,10 @@ process GATK4_HAPLOTYPECALLER {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(input), path(input_index), path(intervals)

View file

@ -2,10 +2,10 @@ process GATK4_INDEXFEATUREFILE {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(feature_file)

View file

@ -2,10 +2,10 @@ process GATK4_INTERVALLISTTOBED {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(intervals)

View file

@ -2,10 +2,10 @@ process GATK4_INTERVALLISTTOOLS {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(intervals)

View file

@ -2,10 +2,10 @@ process GATK4_LEARNREADORIENTATIONMODEL {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(f1r2)

View file

@ -1,11 +1,11 @@
process GATK4_MARKDUPLICATES {
tag "$meta.id"
label 'process_low'
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(bam)

View file

@ -2,10 +2,10 @@ process GATK4_MERGEBAMALIGNMENT {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(aligned), path(unmapped)

View file

@ -2,10 +2,10 @@ process GATK4_MERGEMUTECTSTATS {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(stats)

View file

@ -2,10 +2,10 @@ process GATK4_MERGEVCFS {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(vcf)

View file

@ -2,10 +2,10 @@ process GATK4_MUTECT2 {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(input), path(input_index), path(intervals)

View file

@ -2,10 +2,10 @@ process GATK4_REVERTSAM {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(bam)

View file

@ -2,10 +2,10 @@ process GATK4_SAMTOFASTQ {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(bam)

View file

@ -2,10 +2,10 @@ process GATK4_SELECTVARIANTS {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(vcf_idx)

View file

@ -0,0 +1,48 @@
process GATK4_SPLITINTERVALS {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(intervals)
path(fasta)
path(fasta_fai)
path(dict)
output:
tuple val(meta), path("**.interval_list"), emit: split_intervals
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def reference = fasta ? "--reference $fasta" : ""
def avail_mem = 3
if (!task.memory) {
log.info '[GATK SplitIntervals] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
} else {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" SplitIntervals \\
--output ${prefix} \\
--intervals $intervals \\
$reference \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
gatk4: \$(echo \$(gatk --version 2>&1) | sed 's/^.*(GATK) v//; s/ .*\$//')
END_VERSIONS
"""
}

View file

@ -0,0 +1,53 @@
name: gatk4_splitintervals
keywords:
- interval
- bed
tools:
- gatk4:
description: Genome Analysis Toolkit (GATK4)
homepage: https://gatk.broadinstitute.org/hc/en-us
documentation: https://gatk.broadinstitute.org/hc/en-us/categories/360002369672s
tool_dev_url: https://github.com/broadinstitute/gatk
doi: "10.1158/1538-7445.AM2017-3590"
licence: ["BSD-3-clause"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test' ]
- interval:
type: file
description: Interval list or BED
pattern: "*.{interval,interval_list,bed}"
- fasta:
type: file
description: Reference FASTA
pattern: "*.{fa,fasta}"
- fasta_fai:
type: file
description: Reference FASTA index
pattern: "*.fai"
- dict:
type: file
description: Reference sequence dictionary
pattern: "*.dict"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test' ]
- bed:
type: file
description: A list of scattered interval lists
pattern: "*.interval_list"
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
authors:
- "@nvnieuwk"

View file

@ -2,10 +2,10 @@ process GATK4_SPLITNCIGARREADS {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(bam), path(bai), path(intervals)

View file

@ -2,10 +2,10 @@ process GATK4_VARIANTFILTRATION {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(tbi)

View file

@ -2,10 +2,10 @@ process GATK4_VARIANTRECALIBRATOR {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.5.0" : null)
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.5.0--hdfd78af_0' :
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(tbi)

View file

@ -0,0 +1,40 @@
process GENOMESCOPE2 {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::genomescope2=2.0" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/genomescope2:2.0--py310r41hdfd78af_5':
'quay.io/biocontainers/genomescope2:2.0--py310r41hdfd78af_5' }"
input:
tuple val(meta), path(histogram)
output:
tuple val(meta), path("*_linear_plot.png") , emit: linear_plot_png
tuple val(meta), path("*_transformed_linear_plot.png"), emit: transformed_linear_plot_png
tuple val(meta), path("*_log_plot.png") , emit: log_plot_png
tuple val(meta), path("*_transformed_log_plot.png") , emit: transformed_log_plot_png
tuple val(meta), path("*_model.txt") , emit: model
tuple val(meta), path("*_summary.txt") , emit: summary
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
prefix = task.ext.prefix ?: "${meta.id}"
"""
genomescope2 \\
--input $histogram \\
$args \\
--output . \\
--name_prefix $prefix
cat <<-END_VERSIONS > versions.yml
'${task.process}':
genomescope2: \$( genomescope2 -v | sed 's/GenomeScope //' )
END_VERSIONS
"""
}

View file

@ -0,0 +1,67 @@
name: "genomescope2"
description: Estimate genome heterozygosity, repeat content, and size from sequencing reads using a kmer-based statistical approach
keywords:
- "genome size"
- "genome heterozygosity"
- "repeat content"
tools:
- "genomescope2":
description: "Reference-free profiling of polyploid genomes"
homepage: "http://qb.cshl.edu/genomescope/genomescope2.0/"
documentation: "https://github.com/tbenavi1/genomescope2.0/blob/master/README.md"
tool_dev_url: "https://github.com/tbenavi1/genomescope2.0"
doi: "https://doi.org/10.1038/s41467-020-14998-3"
licence: "['Apache License, Version 2.0 (Apache-2.0)']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- histogram:
type: file
description: A K-mer histogram file
pattern: "*.hist"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- linear_plot_png:
type: file
description: A genomescope2 linear plot in PNG format
pattern: "*_linear_plot.png"
- linear_plot_png:
type: file
description: A genomescope2 linear plot in PNG format
pattern: "*_linear_plot.png"
- transformed_linear_plot_png:
type: file
description: A genomescope2 transformed linear plot in PNG format
pattern: "*_transformed_linear_plot.png"
- log_plot_png:
type: file
description: A genomescope2 log plot in PNG format
pattern: "*_log_plot.png"
- transformed_log_plot_png:
type: file
description: A genomescope2 transformed log plot in PNG format
pattern: "*_transformed_log_plot.png"
- model:
type: file
description: Genomescope2 model fit summary
pattern: "*_model.txt"
- summary:
type: file
description: Genomescope2 histogram summary
pattern: "*_summary.txt"
authors:
- "@mahesh-panchal"

45
modules/hmtnote/main.nf Normal file
View file

@ -0,0 +1,45 @@
process HMTNOTE {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::hmtnote=0.7.2" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/hmtnote:0.7.2--pyhdfd78af_0':
'quay.io/biocontainers/hmtnote:0.7.2--pyhdfd78af_0' }"
input:
tuple val(meta), path(vcf)
output:
tuple val(meta), path("*_annotated.vcf"), emit: vcf
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
"""
hmtnote \\
annotate \\
$vcf \\
${prefix}_annotated.vcf \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
hmtnote: \$(echo \$(hmtnote --version 2>&1) | sed 's/^.*hmtnote, version //; s/Using.*\$//' ))
END_VERSIONS
"""
stub:
def prefix = task.ext.prefix ?: "${meta.id}"
"""
touch ${prefix}_annotated.vcf
cat <<-END_VERSIONS > versions.yml
"${task.process}":
hmtnote: \$(echo \$(hmtnote --version 2>&1) | sed 's/^.*hmtnote, version //; s/Using.*\$//' ))
END_VERSIONS
"""
}

39
modules/hmtnote/meta.yml Normal file
View file

@ -0,0 +1,39 @@
name: hmtnote
description: Human mitochondrial variants annotation using HmtVar.
keywords:
- hmtnote mitochondria annotation
tools:
- hmtnote:
description: Human mitochondrial variants annotation using HmtVar.
homepage: https://github.com/robertopreste/HmtNote
documentation: https://hmtnote.readthedocs.io/en/latest/usage.html
tool_dev_url: None
doi: "https://doi.org/10.1101/600619"
licence: ["MIT"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
- vcf:
type: file
description: vcf file
pattern: "*.vcf"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- vcf:
type: file
description: annotated vcf
pattern: "*_annotated.vcf"
authors:
- "@sysbiocoder"

View file

@ -0,0 +1,38 @@
process MASH_SCREEN {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::mash=2.3" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mash:2.3--he348c14_1':
'quay.io/biocontainers/mash:2.3--he348c14_1' }"
input:
tuple val(meta), path(query_sketch)
path fastx_db
output:
tuple val(meta), path("*.screen"), emit: screen
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
"""
mash \\
screen \\
$args \\
-p $task.cpus \\
$query_sketch \\
$fastx_db \\
> ${prefix}.screen
cat <<-END_VERSIONS > versions.yml
"${task.process}":
mash: \$( mash --version )
END_VERSIONS
"""
}

View file

@ -0,0 +1,47 @@
name: "mash_screen"
description: Screens query sequences against large sequence databases
keywords:
- screen
- containment
- contamination
- taxonomic assignment
tools:
- "mash":
description: Fast sequence distance estimator that uses MinHash
homepage: https://github.com/marbl/Mash
documentation: https://mash.readthedocs.io/en/latest/sketches.html
tool_dev_url: https://github.com/marbl/Mash
doi: "10.1186/s13059-016-0997-x"
licence: ["https://github.com/marbl/Mash/blob/master/LICENSE.txt"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- query_sketch:
type: file
description: MinHash sketch of query sequences
pattern: "*.msh"
- fastx_db:
type: file
description: Sequence files to match against
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- screen:
type: file
description: List of sequences from fastx_db similar to query sequences
pattern: "*.screen"
authors:
- "@mahesh-panchal"

View file

@ -0,0 +1,37 @@
process MAXQUANT_LFQ {
tag "$meta.id"
label 'process_long'
conda (params.enable_conda ? "bioconda::maxquant=2.0.3.0=py310hdfd78af_1" : null)
if (workflow.containerEngine == 'singularity' && !params.singularity_pull_docker_container) {
container "https://depot.galaxyproject.org/singularity/maxquant:2.0.3.0--py310hdfd78af_1"
} else {
container "quay.io/biocontainers/maxquant:2.0.3.0--py310hdfd78af_1"
}
input:
tuple val(meta), path(fasta), path(paramfile)
path raw
output:
tuple val(meta), path("*.txt"), emit: maxquant_txt
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
"""
cat <<-END_VERSIONS > versions.yml
"${task.process}":
maxquant: \$(maxquant --version 2>&1 > /dev/null | cut -f2 -d\" \")
END_VERSIONS
sed \"s_<numThreads>.*_<numThreads>$task.cpus</numThreads>_\" ${paramfile} > mqpar_changed.xml
sed -i \"s|PLACEHOLDER|\$PWD/|g\" mqpar_changed.xml
mkdir temp
maxquant mqpar_changed.xml
mv combined/txt/*.txt .
"""
}

View file

@ -0,0 +1,52 @@
name: maxquant_lfq
description: Run standard proteomics data analysis with MaxQuant, mostly dedicated to label-free. Paths to fasta and raw files needs to be marked by "PLACEHOLDER"
keywords:
- sort
tools:
- maxquant:
description: MaxQuant is a quantitative proteomics software package designed for analyzing large mass-spectrometric data sets. License restricted.
homepage: None
documentation: None
tool_dev_url: None
doi: ""
licence: ["http://www.coxdocs.org/lib/exe/fetch.php?media=license_agreement.pdf"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- raw:
type: file
description: raw files with mass spectra
pattern: "*.{raw,RAW,Raw}"
- fasta:
type: file
description: fasta file with protein sequences
pattern: "*.{fasta}"
- parfile:
type: file
description: MaxQuant parameter file (XML)
pattern: "*.{xml}"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software version
pattern: "versions.yml"
- maxquant_txt:
type: file
description: tables with peptides and protein information
pattern: "*.{txt}"
authors:
- "@veitveit"

View file

@ -0,0 +1,54 @@
process MOTUS_PROFILE {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::motus=3.0.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/motus:3.0.1--pyhdfd78af_0':
'quay.io/biocontainers/motus:3.0.1--pyhdfd78af_0' }"
input:
tuple val(meta), path(reads)
path db
output:
tuple val(meta), path("*.out"), emit: out
tuple val(meta), path("*.bam"), optional: true, emit: bam
tuple val(meta), path("*.mgc"), optional: true, emit: mgc
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def inputs = reads[0].getExtension() == 'bam' ?
"-i ${reads}" :
reads[0].getExtension() == 'mgc' ? "-m $reads" :
meta.single_end ?
"-s $reads" : "-f ${reads[0]} -r ${reads[1]}"
def refdb = db ? "-db ${db}" : ""
"""
motus profile \\
$args \\
$inputs \\
$refdb \\
-t $task.cpus \\
-n $prefix \\
-o ${prefix}.out
## mOTUs version number is not available from command line.
## mOTUs save the version number in index database folder.
## mOTUs will check the database version is same version as exec version.
if [ "$db" == "" ]; then
VERSION=\$(echo \$(motus -h 2>&1) | sed 's/^.*Version: //; s/References.*\$//')
else
VERSION=\$(grep motus $db/db_mOTU_versions | sed 's/motus\\t//g')
fi
cat <<-END_VERSIONS > versions.yml
"${task.process}":
mOTUs: \$VERSION
END_VERSIONS
"""
}

View file

@ -0,0 +1,61 @@
name: "motus_profile"
description: Taxonomic meta-omics profiling using universal marker genes
keywords:
- classify
- metagenomics
- fastq
- taxonomic profiling
tools:
- "motus":
description: "Marker gene-based OTU (mOTU) profiling"
homepage: "https://motu-tool.org/"
documentation: "https://github.com/motu-tool/mOTUs/wiki"
tool_dev_url: "https://github.com/motu-tool/mOTUs"
doi: "10.1038/s41467-019-08844-4"
licence: "['GPL v3']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- reads:
type: file
description: |
List of input fastq/fasta files of size 1 and 2 for single-end and paired-end data,
respectively.
Or the intermediate bam file mapped by bwa to the mOTUs database or
the output bam file from motus profile.
Or the intermediate mgc read counts table.
pattern: "*.{fastq,fq,fasta,fa,fastq.gz,fq.gz,fasta.gz,fa.gz,.bam,.mgc}"
- db:
type: directory
description: |
mOTUs database downloaded by `motus downloadDB`
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- out:
type: file
description: Results with taxonomic classification of each read
pattern: "*.out"
- bam:
type: file
description: Optional intermediate sorted BAM file from BWA
pattern: "*.{bam}"
- mgc:
type: file
description: Optional intermediate mgc read count table file saved with `-M`.
pattern: "*.{mgc}"
authors:
- "@jianhong"

View file

@ -35,12 +35,13 @@ process RTGTOOLS_VCFEVAL {
def eval_regions = evaluation_regions ? "--evaluation-regions=$evaluation_regions" : ""
def truth_index = truth_vcf_tbi ? "" : "rtg index $truth_vcf"
def query_index = query_vcf_tbi ? "" : "rtg index $query_vcf"
def avail_mem = task.memory.toGiga() + "G"
"""
$truth_index
$query_index
rtg vcfeval \\
rtg RTG_MEM=$avail_mem vcfeval \\
$args \\
--baseline=$truth_vcf \\
$bed_regions \\

View file

@ -19,6 +19,7 @@ if ("$PROFILE" == "singularity") {
} else {
docker.enabled = true
docker.userEmulation = true
docker.runOptions = "--platform linux/x86_64"
}
// Increase time available to build Conda environment

View file

@ -42,6 +42,10 @@ amrfinderplus/update:
- modules/amrfinderplus/update/**
- tests/modules/amrfinderplus/update/**
antismash/antismashlite:
- modules/antismash/antismashlite/**
- tests/modules/antismash/antismashlite/**
antismash/antismashlitedownloaddatabases:
- modules/antismash/antismashlitedownloaddatabases/**
- tests/modules/antismash/antismashlitedownloaddatabases/**
@ -218,6 +222,10 @@ bedtools/sort:
- modules/bedtools/sort/**
- tests/modules/bedtools/sort/**
bedtools/split:
- modules/bedtools/split/**
- tests/modules/bedtools/split/**
bedtools/subtract:
- modules/bedtools/subtract/**
- tests/modules/bedtools/subtract/**
@ -226,6 +234,10 @@ biobambam/bammarkduplicates2:
- modules/biobambam/bammarkduplicates2/**
- tests/modules/biobambam/bammarkduplicates2/**
biobambam/bammerge:
- modules/biobambam/bammerge/**
- tests/modules/biobambam/bammerge/**
biobambam/bamsormadup:
- modules/biobambam/bamsormadup/**
- tests/modules/biobambam/bamsormadup/**
@ -719,6 +731,10 @@ gatk4/calculatecontamination:
- modules/gatk4/calculatecontamination/**
- tests/modules/gatk4/calculatecontamination/**
gatk4/cnnscorevariants:
- modules/gatk4/cnnscorevariants/**
- tests/modules/gatk4/cnnscorevariants/**
gatk4/combinegvcfs:
- modules/gatk4/combinegvcfs/**
- tests/modules/gatk4/combinegvcfs/**
@ -819,6 +835,10 @@ gatk4/selectvariants:
- modules/gatk4/selectvariants/**
- tests/modules/gatk4/selectvariants/**
gatk4/splitintervals:
- modules/gatk4/splitintervals/**
- tests/modules/gatk4/splitintervals/**
gatk4/splitncigarreads:
- modules/gatk4/splitncigarreads/**
- tests/modules/gatk4/splitncigarreads/**
@ -839,6 +859,10 @@ genmap/mappability:
- modules/genmap/mappability/**
- tests/modules/genmap/mappability/**
genomescope2:
- modules/genomescope2/**
- tests/modules/genomescope2/**
genrich:
- modules/genrich/**
- tests/modules/genrich/**
@ -954,6 +978,10 @@ hmmer/hmmsearch:
- modules/hmmer/hmmsearch/**
- tests/modules/hmmer/hmmsearch/**
hmtnote:
- modules/hmtnote/**
- tests/modules/hmtnote/**
homer/annotatepeaks:
- modules/homer/annotatepeaks/**
- tests/modules/homer/annotatepeaks/**
@ -1190,6 +1218,10 @@ mash/dist:
- modules/mash/dist/**
- tests/modules/mash/dist/**
mash/screen:
- modules/mash/screen/**
- tests/modules/mash/screen/**
mash/sketch:
- modules/mash/sketch/**
- tests/modules/mash/sketch/**
@ -1202,6 +1234,10 @@ maxbin2:
- modules/maxbin2/**
- tests/modules/maxbin2/**
maxquant/lfq:
- modules/maxquant/lfq/**
- tests/modules/maxquant/lfq/**
md5sum:
- modules/md5sum/**
- tests/modules/md5sum/**
@ -1286,6 +1322,10 @@ motus/downloaddb:
- modules/motus/downloaddb/**
- tests/modules/motus/downloaddb/**
motus/profile:
- modules/motus/profile/**
- tests/modules/motus/profile/**
msisensor/msi:
- modules/msisensor/msi/**
- tests/modules/msisensor/msi/**
@ -1651,14 +1691,14 @@ samtools/bam2fq:
- modules/samtools/bam2fq/**
- tests/modules/samtools/bam2fq/**
samtools/convert:
- modules/samtools/convert/**
- tests/modules/samtools/convert/**
samtools/collatefastq:
- modules/samtools/collatefastq/**
- tests/modules/samtools/collatefastq/**
samtools/convert:
- modules/samtools/convert/**
- tests/modules/samtools/convert/**
samtools/depth:
- modules/samtools/depth/**
- tests/modules/samtools/depth/**

View file

@ -430,5 +430,17 @@ params {
ncbi_user_settings = "${test_data_dir}/generic/config/ncbi_user_settings.mkfg"
}
}
'proteomics' {
'msspectra' {
ups_file1 = "${test_data_dir}/proteomics/msspectra/OVEMB150205_12.raw"
ups_file2 = "${test_data_dir}/proteomics/msspectra/OVEMB150205_14.raw"
}
'database' {
yeast_ups = "${test_data_dir}/proteomics/database/yeast_UPS.fasta"
}
'parameter' {
maxquant = "${test_data_dir}/proteomics/parameter/mqpar.xml"
}
}
}
}

View file

@ -0,0 +1,46 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { ANTISMASH_ANTISMASHLITE } from '../../../../modules/antismash/antismashlite/main.nf'
include { ANTISMASH_ANTISMASHLITEDOWNLOADDATABASES } from '../../../modules/antismash/antismashlitedownloaddatabases/main.nf'
include { GUNZIP as GUNZIP1 } from '../../../../modules/gunzip/main.nf'
include { GUNZIP as GUNZIP2 } from '../../../../modules/gunzip/main.nf'
include { UNTAR as UNTAR1 } from '../../../../modules/untar/main.nf'
include { UNTAR as UNTAR2 } from '../../../../modules/untar/main.nf'
include { UNTAR as UNTAR3 } from '../../../../modules/untar/main.nf'
workflow test_antismashlite {
genome_fna = [
[ id:'test' ],
file(params.test_data['bacteroides_fragilis']['genome']['genome_fna_gz'], checkIfExists: true)
]
genome_gff = [
[],
file(params.test_data['bacteroides_fragilis']['genome']['genome_gff_gz'], checkIfExists: true)
]
antismash_css = [
[],
file('https://github.com/nf-core/test-datasets/raw/modules/data/delete_me/antismash/css.tar.gz', checkIfExists: true)
]
antismash_detection = [
[],
file('https://github.com/nf-core/test-datasets/raw/modules/data/delete_me/antismash/detection.tar.gz', checkIfExists: true)
]
antismash_modules = [
[],
file('https://github.com/nf-core/test-datasets/raw/modules/data/delete_me/antismash/modules.tar.gz', checkIfExists: true)
]
GUNZIP1 ( genome_fna )
GUNZIP2 ( genome_gff )
UNTAR1 ( antismash_css )
UNTAR2 ( antismash_detection )
UNTAR3 ( antismash_modules )
ANTISMASH_ANTISMASHLITEDOWNLOADDATABASES ( UNTAR1.out.untar.map{ it[1] }, UNTAR2.out.untar.map{ it[1] }, UNTAR3.out.untar.map{ it[1] } )
ANTISMASH_ANTISMASHLITE ( GUNZIP1.out.gunzip, ANTISMASH_ANTISMASHLITEDOWNLOADDATABASES.out.database, ANTISMASH_ANTISMASHLITEDOWNLOADDATABASES.out.antismash_dir, GUNZIP2.out.gunzip.map{ it[1] } )
}

View file

@ -0,0 +1,5 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
}

View file

@ -0,0 +1,35 @@
- name: antismash antismashlite test_antismashlite
command: nextflow run tests/modules/antismash/antismashlite -entry test_antismashlite -c tests/config/nextflow.config
tags:
- antismash/antismashlite
- antismash
files:
- path: output/antismash/test/NZ_CP069563.1.region001.gbk
contains: ['/tool="antismash"']
- path: output/antismash/test/NZ_CP069563.1.region002.gbk
contains: ['/tool="antismash"']
- path: output/antismash/test/css/bacteria.css
md5sum: 8b3c2f8b143d5245a5f42f55803c532c
- path: output/antismash/test/genome.gbk
contains: ['/tool="antismash"']
- path: output/antismash/test/genome.json
contains: ['{"version": "6.0.1", "input_file": "genome.fna", "records": [{"id": "NZ_CP069563.1", "seq": {"data":']
- path: output/antismash/test/genome.zip
- path: output/antismash/test/index.html
md5sum: de787e865c3a1eec143a19d2facb4de4
- path: output/antismash/test/js/antismash.js
md5sum: 58e90c3d783ae014cc3d51849bcb50a2
- path: output/antismash/test/js/jquery.js
md5sum: 397754ba49e9e0cf4e7c190da78dda05
- path: output/antismash/test/js/jquery.tablesorter.min.js
md5sum: 5e9e08cef4d1be0eaa538e6eb28809a7
- path: output/antismash/test/regions.js
contains: ['"seq_id": "NZ_CP069563.1"']
- path: output/antismash/test/test.log
contains: ["antiSMASH version: 6.0.1"]
- path: output/antismash/versions.yml
md5sum: 759431a43da33e2ef8e2d0ebd79a439b
- path: output/gunzip1/genome.fna
md5sum: dafd38f5454b54fbea38245d773062a5
- path: output/gunzip2/genome.gff
md5sum: 9b9c848b1946d43fa68128f4d6316052

View file

@ -0,0 +1,17 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { BEDTOOLS_SPLIT } from '../../../../modules/bedtools/split/main.nf'
workflow test_bedtools_split {
input = [
[ id:'test' ], // meta map
file(params.test_data['homo_sapiens']['genome']['genome_multi_interval_bed'], checkIfExists: true)
]
number_of_files = 2
BEDTOOLS_SPLIT ( input, number_of_files )
}

View file

@ -0,0 +1,5 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
}

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@ -0,0 +1,10 @@
- name: bedtools split test_bedtools_split
command: nextflow run ./tests/modules/bedtools/split -entry test_bedtools_split -c ./tests/config/nextflow.config -c ./tests/modules/bedtools/split/nextflow.config
tags:
- bedtools
- bedtools/split
files:
- path: output/bedtools/test.00001.bed
md5sum: d58e5e46c2fcc3b8be5db0f023e93cb5
- path: output/bedtools/test.00002.bed
md5sum: 03caf952e9297a54620d2bbba8dc2823

View file

@ -0,0 +1,30 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { BIOBAMBAM_BAMMERGE } from '../../../../modules/biobambam/bammerge/main.nf'
workflow test_biobambam_bammerge_paired {
input = [
[ id:'test', single_end:false ], // meta map
[
file(params.test_data['homo_sapiens']['illumina']['test_paired_end_sorted_bam'], checkIfExists: true),
file(params.test_data['homo_sapiens']['illumina']['test2_paired_end_sorted_bam'], checkIfExists: true)
]
]
BIOBAMBAM_BAMMERGE ( input )
}
workflow test_biobambam_bammerge_single {
input = [
[ id:'test', single_end:false ], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_single_end_sorted_bam'], checkIfExists: true),
]
]
BIOBAMBAM_BAMMERGE ( input )
}

View file

@ -0,0 +1,13 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
withName: BIOBAMBAM_BAMMERGE {
ext.args = {[
"md5=1",
"md5filename=${meta.id}.md5",
"index=1",
"indexfilename=${meta.id}.bam.bai"
].join(" ").trim()}
}
}

View file

@ -0,0 +1,25 @@
- name: biobambam bammerge test_biobambam_bammerge_paired
command: nextflow run ./tests/modules/biobambam/bammerge -entry test_biobambam_bammerge_paired -c ./tests/config/nextflow.config -c ./tests/modules/biobambam/bammerge/nextflow.config
tags:
- biobambam/bammerge
- biobambam
files:
- path: output/biobambam/test.bam
md5sum: bc3d32ab6a54d1894ca7cc79387dec57
- path: output/biobambam/test.bam.bai
md5sum: b8ae542a37a73d79de1c15c765207c53
- path: output/biobambam/test.md5
md5sum: 31c59857990ceb392242136429e30243
- name: biobambam bammerge test_biobambam_bammerge_single
command: nextflow run ./tests/modules/biobambam/bammerge -entry test_biobambam_bammerge_single -c ./tests/config/nextflow.config -c ./tests/modules/biobambam/bammerge/nextflow.config
tags:
- biobambam/bammerge
- biobambam
files:
- path: output/biobambam/test.bam
md5sum: 86185d3d6895a7722d3b3a09c6f91bfc
- path: output/biobambam/test.bam.bai
md5sum: 973680feb6bc73cd1051ea83c7219418
- path: output/biobambam/test.md5
md5sum: 244a9d1cbc6d74724285c80220e5e427

View file

@ -14,9 +14,25 @@ workflow test_bowtie2_align_single_end {
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = false
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_single_end_sorted {
input = [
[ id:'test', single_end:true ], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true)
]
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = true
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_paired_end {
@ -29,7 +45,55 @@ workflow test_bowtie2_align_paired_end {
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = false
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned )
}
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_paired_end_sorted {
input = [
[ id:'test', single_end:false ], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true),
file(params.test_data['sarscov2']['illumina']['test_2_fastq_gz'], checkIfExists: true)
]
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = true
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_single_end_large_index {
input = [
[ id:'test', single_end:true ], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true)
]
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = false
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_paired_end_large_index {
input = [
[ id:'test', single_end:false ], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true),
file(params.test_data['sarscov2']['illumina']['test_2_fastq_gz'], checkIfExists: true)
]
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = false
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}

View file

@ -5,6 +5,7 @@ params {
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
}
if (params.force_large_index) {

View file

@ -1,21 +1,49 @@
- name: bowtie2 align test_bowtie2_align_single_end
command: nextflow run ./tests/modules/bowtie2/align -entry test_bowtie2_align_single_end -c ./tests/config/nextflow.config -c ./tests/modules/bowtie2/align/nextflow.config
tags:
- bowtie2/align
- bowtie2
- bowtie2/align
files:
- path: output/bowtie2/test.bam
- path: output/bowtie2/test.bowtie2.log
md5sum: 7b8a9e61b7646da1089b041333c41a87
- path: output/bowtie2/versions.yml
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml
- name: bowtie2 align test_bowtie2_align_single_end_sorted
command: nextflow run ./tests/modules/bowtie2/align -entry test_bowtie2_align_single_end_sorted -c ./tests/config/nextflow.config -c ./tests/modules/bowtie2/align/nextflow.config
tags:
- bowtie2
- bowtie2/align
files:
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml
- name: bowtie2 align test_bowtie2_align_paired_end
command: nextflow run ./tests/modules/bowtie2/align -entry test_bowtie2_align_paired_end -c ./tests/config/nextflow.config -c ./tests/modules/bowtie2/align/nextflow.config
command: nextflow run tests/modules/bowtie2/align -entry test_bowtie2_align_paired_end -c tests/config/nextflow.config -c tests/modules/bowtie2/align/nextflow.config
tags:
- bowtie2/align
- bowtie2
- bowtie2/align
files:
- path: output/bowtie2/test.bam
- path: output/bowtie2/test.bowtie2.log
md5sum: bd89ce1b28c93bf822bae391ffcedd19
- path: output/bowtie2/versions.yml
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml
- name: bowtie2 align test_bowtie2_align_single_end_large_index
command: nextflow run tests/modules/bowtie2/align -entry test_bowtie2_align_single_end_large_index -c tests/config/nextflow.config -c tests/modules/bowtie2/align/nextflow.config --force_large_index
tags:
- bowtie2
- bowtie2/align
files:
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml
- name: bowtie2 align test_bowtie2_align_paired_end_large_index
command: nextflow run tests/modules/bowtie2/align -entry test_bowtie2_align_paired_end_large_index -c tests/config/nextflow.config -c tests/modules/bowtie2/align/nextflow.config --force_large_index
tags:
- bowtie2
- bowtie2/align
files:
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml

View file

@ -5,7 +5,7 @@
- gatk4/applybqsr
files:
- path: output/gatk4/test.bam
md5sum: d088422be886dc8507ff97fcc7dd968a
md5sum: e11b7eaf2034740a953626518e3c3d6e
- path: output/gatk4/versions.yml
- name: gatk4 applybqsr test_gatk4_applybqsr_intervals
@ -15,7 +15,7 @@
- gatk4/applybqsr
files:
- path: output/gatk4/test.bam
md5sum: 4bfa18d651abd945e240b05e70107716
md5sum: e9e9aa753c106e43f936ad573e23d2e6
- path: output/gatk4/versions.yml
- name: gatk4 applybqsr test_gatk4_applybqsr_cram
@ -25,5 +25,5 @@
- gatk4/applybqsr
files:
- path: output/gatk4/test.cram
md5sum: 2e0bca197af4f043a4a85152e6edbe04
md5sum: bca9d234a5d484ce2a6f4826ca2ea308
- path: output/gatk4/versions.yml

View file

@ -5,7 +5,7 @@
- gatk4/applybqsrspark
files:
- path: output/gatk4/test.bam
md5sum: d088422be886dc8507ff97fcc7dd968a
md5sum: 1901c819fcba0fdd5e2482e6dc8285ef
- path: output/gatk4/versions.yml
- name: gatk4 applybqsr test_gatk4_applybqsr_spark_intervals
@ -15,7 +15,7 @@
- gatk4/applybqsrspark
files:
- path: output/gatk4/test.bam
md5sum: 4bfa18d651abd945e240b05e70107716
md5sum: 2ca2446f0125890280056fd7da822732
- path: output/gatk4/versions.yml
- name: gatk4 applybqsr test_gatk4_applybqsr_spark_cram
@ -25,5 +25,5 @@
- gatk4/applybqsrspark
files:
- path: output/gatk4/test.cram
md5sum: 2e0bca197af4f043a4a85152e6edbe04
md5sum: 60f7c822a9f2833e11eb7bfd16e4421f
- path: output/gatk4/versions.yml

View file

@ -0,0 +1,18 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { GATK4_CNNSCOREVARIANTS } from '../../../../modules/gatk4/cnnscorevariants/main.nf'
workflow test_gatk4_cnnscorevariants {
input = [ [ id:'test' ], // meta map
file(params.test_data['homo_sapiens']['illumina']['test_genome_vcf'], checkIfExists: true),
[],
[]
]
fasta = file(params.test_data['homo_sapiens']['genome']['genome_fasta'], checkIfExists: true)
fai = file(params.test_data['homo_sapiens']['genome']['genome_fasta_fai'], checkIfExists: true)
dict = file(params.test_data['homo_sapiens']['genome']['genome_dict'], checkIfExists: true)
GATK4_CNNSCOREVARIANTS ( input, fasta, fai, dict, [], [] )
}

View file

@ -0,0 +1,5 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
}

View file

@ -0,0 +1,9 @@
- name: gatk4 cnnscorevariants test_gatk4_cnnscorevariants
command: nextflow run ./tests/modules/gatk4/cnnscorevariants -entry test_gatk4_cnnscorevariants -c ./tests/config/nextflow.config -c ./tests/modules/gatk4/cnnscorevariants/nextflow.config
tags:
- gatk4
- gatk4/cnnscorevariants
files:
- path: output/gatk4/test.vcf.gz
contains:
- "##ALT=<ID=NON_REF,Description="

View file

@ -1,6 +1,5 @@
process {
ext.args = "--tmp-dir ."
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
}
}

View file

@ -65,7 +65,9 @@ workflow test_gatk4_genotypegvcfs_gz_input_intervals {
input = [ [ id:'test' ], // meta map
file(params.test_data['homo_sapiens']['illumina']['test_genome_vcf_gz'], checkIfExists: true),
file(params.test_data['homo_sapiens']['illumina']['test_genome_vcf_gz_tbi'], checkIfExists: true),
file(params.test_data['homo_sapiens']['genome']['genome_bed'], checkIfExists: true) ]
file(params.test_data['homo_sapiens']['genome']['genome_bed'], checkIfExists: true) ,
[]
]
fasta = file(params.test_data['homo_sapiens']['genome']['genome_fasta'], checkIfExists: true)
fai = file(params.test_data['homo_sapiens']['genome']['genome_fasta_fai'], checkIfExists: true)
@ -80,7 +82,8 @@ workflow test_gatk4_genotypegvcfs_gz_input_dbsnp_intervals {
input = [ [ id:'test' ], // meta map
file(params.test_data['homo_sapiens']['illumina']['test_genome_vcf_gz'], checkIfExists: true),
file(params.test_data['homo_sapiens']['illumina']['test_genome_vcf_gz_tbi'], checkIfExists: true),
file(params.test_data['homo_sapiens']['genome']['genome_bed'], checkIfExists: true)
file(params.test_data['homo_sapiens']['genome']['genome_bed'], checkIfExists: true),
[]
]
fasta = file(params.test_data['homo_sapiens']['genome']['genome_fasta'], checkIfExists: true)
@ -106,6 +109,7 @@ workflow test_gatk4_genotypegvcfs_gendb_input {
gendb = UNTAR.out.untar.map{ it[1] }.collect()
gendb.add([])
gendb.add([])
gendb.add([])
input = Channel.of([ id:'test' ]).combine(gendb)
@ -128,6 +132,7 @@ workflow test_gatk4_genotypegvcfs_gendb_input_dbsnp {
gendb = UNTAR.out.untar.map{ it[1] }.collect()
gendb.add([])
gendb.add([])
gendb.add([])
input = Channel.of([ id:'test' ]).combine(gendb)
GATK4_GENOTYPEGVCFS ( input, fasta, fai, dict, dbsnp, dbsnp_tbi)
@ -146,6 +151,8 @@ workflow test_gatk4_genotypegvcfs_gendb_input_intervals {
gendb = UNTAR.out.untar.map{ it[1] }.collect()
gendb.add([])
gendb.add([file(params.test_data['homo_sapiens']['genome']['genome_bed'], checkIfExists: true)])
gendb.add([])
input = Channel.of([ id:'test' ]).combine(gendb)
GATK4_GENOTYPEGVCFS ( input, fasta, fai, dict, [], [] )
@ -167,6 +174,8 @@ workflow test_gatk4_genotypegvcfs_gendb_input_dbsnp_intervals {
gendb = UNTAR.out.untar.map{ it[1] }.collect()
gendb.add([])
gendb.add([file(params.test_data['homo_sapiens']['genome']['genome_bed'], checkIfExists: true)])
gendb.add([])
input = Channel.of([ id:'test' ]).combine(gendb)
GATK4_GENOTYPEGVCFS ( input, fasta, fai, dict, dbsnp, dbsnp_tbi )

View file

@ -4,21 +4,6 @@ nextflow.enable.dsl = 2
include { GATK4_GETPILEUPSUMMARIES } from '../../../../modules/gatk4/getpileupsummaries/main.nf'
workflow test_gatk4_getpileupsummaries_just_variants {
input = [ [ id:'test' ], // meta map
file(params.test_data['homo_sapiens']['illumina']['test_paired_end_recalibrated_sorted_bam'], checkIfExists: true) ,
file(params.test_data['homo_sapiens']['illumina']['test_paired_end_recalibrated_sorted_bam_bai'], checkIfExists: true),
[]
]
variants = file(params.test_data['homo_sapiens']['genome']['gnomad_r2_1_1_21_vcf_gz'], checkIfExists: true)
variants_tbi = file(params.test_data['homo_sapiens']['genome']['gnomad_r2_1_1_21_vcf_gz_tbi'], checkIfExists: true)
fasta = []
fai = []
dict = []
GATK4_GETPILEUPSUMMARIES ( input , fasta, fai, dict, variants , variants_tbi )
}
workflow test_gatk4_getpileupsummaries_separate_sites {

View file

@ -1,13 +1,3 @@
- name: gatk4 getpileupsummaries test_gatk4_getpileupsummaries_just_variants
command: nextflow run tests/modules/gatk4/getpileupsummaries -entry test_gatk4_getpileupsummaries_just_variants -c tests/config/nextflow.config
tags:
- gatk4/getpileupsummaries
- gatk4
files:
- path: output/gatk4/test.pileups.table
md5sum: 8e0ca6f66e112bd2f7ec1d31a2d62469
- path: output/gatk4/versions.yml
- name: gatk4 getpileupsummaries test_gatk4_getpileupsummaries_separate_sites
command: nextflow run tests/modules/gatk4/getpileupsummaries -entry test_gatk4_getpileupsummaries_separate_sites -c tests/config/nextflow.config
tags:

View file

@ -7,11 +7,11 @@
- path: output/gatk4/test.interval_list
md5sum: e51101c9357fb2d59fd30e370eefa39c
- path: output/gatk4/test_split/temp_0001_of_6/1scattered.interval_list
md5sum: b8ba8a387200df76a0d1c577626dc265
md5sum: 39385d38ac6cb7c05190026fc3b81411
- path: output/gatk4/test_split/temp_0002_of_6/2scattered.interval_list
md5sum: 0728d164666d9264ef442a493e008dee
md5sum: 59f1978c5f4ef3fce3b110816283d9f5
- path: output/gatk4/test_split/temp_0003_of_6/3scattered.interval_list
md5sum: 55da0f3c69504148f4e7002a0e072cfe
md5sum: 709fe81bfcf700bd80d96c62a71629fd
- path: output/gatk4/test_split/temp_0004_of_6/4scattered.interval_list
md5sum: d29ca4447f32547f2936567fa902796a
md5sum: c24044490cfedbcba61dbc646d3aa570
- path: output/gatk4/versions.yml

View file

@ -5,9 +5,9 @@
- gatk4/markduplicates
files:
- path: output/gatk4/test.bai
md5sum: e9c125e82553209933883b4fe2b8d7c2
md5sum: c8f7a9e426c768577f88f59cb1336bf3
- path: output/gatk4/test.bam
md5sum: 2efd50b2e6b7fd9bdf242cd9e266cfa9
md5sum: 58533ddab47f7ac07f7b10e7f4aac234
- path: output/gatk4/test.metrics
- path: output/gatk4/versions.yml
@ -20,6 +20,6 @@
- path: output/gatk4/test.bai
md5sum: bad71df9c876e72a5bc0a3e0fd755f92
- path: output/gatk4/test.bam
md5sum: 8187febc6108ffef7f907e89b9c091a4
md5sum: 112580c24b43331950f24f9adea30788
- path: output/gatk4/test.metrics
- path: output/gatk4/versions.yml

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@ -0,0 +1,33 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { GATK4_SPLITINTERVALS } from '../../../../modules/gatk4/splitintervals/main.nf'
workflow test_gatk4_splitintervals_bed {
input = [
[ id:'test' ], // meta map
file(params.test_data['homo_sapiens']['genome']['genome_multi_interval_bed'], checkIfExists: true)
]
fasta = file(params.test_data['homo_sapiens']['genome']['genome_fasta'], checkIfExists: true)
fasta_fai = file(params.test_data['homo_sapiens']['genome']['genome_fasta_fai'], checkIfExists: true)
fasta_dict = file(params.test_data['homo_sapiens']['genome']['genome_dict'], checkIfExists: true)
GATK4_SPLITINTERVALS ( input, fasta, fasta_fai, fasta_dict)
}
workflow test_gatk4_splitintervals_intervals {
input = [
[ id:'test' ], // meta map
file(params.test_data['homo_sapiens']['genome']['genome_interval_list'], checkIfExists: true)
]
fasta = file(params.test_data['homo_sapiens']['genome']['genome_fasta'], checkIfExists: true)
fasta_fai = file(params.test_data['homo_sapiens']['genome']['genome_fasta_fai'], checkIfExists: true)
fasta_dict = file(params.test_data['homo_sapiens']['genome']['genome_dict'], checkIfExists: true)
GATK4_SPLITINTERVALS ( input, fasta, fasta_fai, fasta_dict)
}

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@ -0,0 +1,9 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
withName: GATK4_SPLITINTERVALS {
ext.args = "--scatter-count 2"
}
}

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@ -0,0 +1,23 @@
- name: gatk4 splitintervals test_gatk4_splitintervals_bed
command: nextflow run tests/modules/gatk4/splitintervals -entry test_gatk4_splitintervals_bed -c tests/config/nextflow.config
tags:
- gatk4/splitintervals
- gatk4
files:
- path: output/gatk4/test/0000-scattered.interval_list
md5sum: c8d6b19e7a92535b6ce9608eae558faa
- path: output/gatk4/test/0001-scattered.interval_list
md5sum: b1877ad96aec308906594c50ebbe3ded
- path: output/gatk4/versions.yml
- name: gatk4 splitintervals test_gatk4_splitintervals_intervals
command: nextflow run tests/modules/gatk4/splitintervals -entry test_gatk4_splitintervals_intervals -c tests/config/nextflow.config
tags:
- gatk4/splitintervals
- gatk4
files:
- path: output/gatk4/test/0000-scattered.interval_list
md5sum: ebd6b34a335efc6732ff541936c6d2d5
- path: output/gatk4/test/0001-scattered.interval_list
md5sum: 9459b0e124fa84ec1e64ac4615bc9af7
- path: output/gatk4/versions.yml

View file

@ -5,7 +5,7 @@
- gatk4/splitncigarreads
files:
- path: output/gatk4/test.bam
md5sum: 436d8e31285c6b588bdd1c7f1d07f6f2
md5sum: 37e5dbce8692b54c3292b539c91dfbd7
- path: output/gatk4/versions.yml
- name: gatk4 splitncigarreads test_gatk4_splitncigarreads_intervals
command: nextflow run tests/modules/gatk4/splitncigarreads -entry test_gatk4_splitncigarreads_intervals -c tests/config/nextflow.config
@ -14,5 +14,5 @@
- gatk4/splitncigarreads
files:
- path: output/gatk4/test.bam
md5sum: cd56e3225950f519fd47164cca60a0bb
md5sum: e5cd2fd1822298a9bf7bc8b8d42146af
- path: output/gatk4/versions.yml

View file

@ -9,7 +9,7 @@
- "#CHROM POS ID REF ALT QUAL FILTER INFO"
- path: output/gatk4/test.recal.idx
- path: output/gatk4/test.tranches
md5sum: d238e97bf996863969dac7751e345549
md5sum: c029e52fd63a893e1154cc9144a19eeb
- path: output/gatk4/versions.yml
- name: gatk4 variantrecalibrator test_gatk4_variantrecalibrator_allele_specific
@ -23,5 +23,5 @@
- "#CHROM POS ID REF ALT QUAL FILTER INFO"
- path: output/gatk4/test.recal.idx
- path: output/gatk4/test.tranches
md5sum: 444438d46716593634a6817958099292
md5sum: ad52fa69325c758f458a30ee5b43d6b5
- path: output/gatk4/versions.yml

View file

@ -0,0 +1,19 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { MERYL_COUNT } from '../../../modules/meryl/count/main.nf'
include { MERYL_HISTOGRAM } from '../../../modules/meryl/histogram/main.nf'
include { GENOMESCOPE2 } from '../../../modules/genomescope2/main.nf'
workflow test_genomescope2 {
input = [
[ id:'test', single_end:false ], // meta map
file(params.test_data['bacteroides_fragilis']['illumina']['test1_1_fastq_gz'], checkIfExists: true)
]
MERYL_COUNT ( input )
MERYL_HISTOGRAM ( MERYL_COUNT.out.meryl_db )
GENOMESCOPE2 ( MERYL_HISTOGRAM.out.hist )
}

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@ -0,0 +1,13 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
withName: 'MERYL.*' {
ext.args = 'k=21'
}
withName: 'GENOMESCOPE2' {
ext.args = '-k 21 -p 1'
}
}

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@ -0,0 +1,22 @@
- name: genomescope2 test_genomescope2
command: nextflow run tests/modules/genomescope2 -entry test_genomescope2 -c tests/config/nextflow.config
tags:
- genomescope2
files:
- path: output/genomescope2/test_linear_plot.png
md5sum: 94c165c5028156299a1d4d05766cac51
- path: output/genomescope2/test_log_plot.png
md5sum: 9d25ca463d92a0c73a893da7fd3979ba
- path: output/genomescope2/test_model.txt
md5sum: 3caf62f715f64a2f2b8fdff5d079cb84
- path: output/genomescope2/test_summary.txt
md5sum: 7452860e2cea99b85f3ff60daeac77f5
- path: output/genomescope2/test_transformed_linear_plot.png
md5sum: 99a64c1c18d8670f64cb863d4334abbb
- path: output/genomescope2/test_transformed_log_plot.png
md5sum: b4e029c9fb9987ca33b17392a691c1b4
- path: output/genomescope2/versions.yml
md5sum: 18afeb26f62a47f680b2bb3e27da9cbc
- path: output/meryl/test.hist
md5sum: f75362ab9cd70d96621b3690e952085f
- path: output/meryl/versions.yml

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@ -0,0 +1,14 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { HMTNOTE } from '../../../modules/hmtnote/main.nf'
workflow test_hmtnote {
input = [ [ id:'test' ], // meta map
file(params.test_data['sarscov2']['illumina']['test_vcf'], checkIfExists: true)
]
HMTNOTE ( input)
}

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@ -0,0 +1,7 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
withName: HMTNOTE {
ext.args = '--basic --variab'
}
}

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@ -0,0 +1,6 @@
- name: hmtnote test_hmtnote
command: nextflow run ./tests/modules/hmtnote -entry test_hmtnote -c ./tests/config/nextflow.config -c ./tests/modules/hmtnote/nextflow.config
tags:
- hmtnote
files:
- path: output/hmtnote/test_annotated.vcf

View file

@ -0,0 +1,21 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { MASH_SKETCH } from '../../../../modules/mash/sketch/main.nf'
include { MASH_SCREEN } from '../../../../modules/mash/screen/main.nf'
workflow test_mash_screen {
input = [
[ id:'test', single_end:false], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true),
file(params.test_data['sarscov2']['illumina']['test_2_fastq_gz'], checkIfExists: true)
]
]
fastx_db = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
MASH_SKETCH ( input )
MASH_SCREEN ( MASH_SKETCH.out.mash, fastx_db )
}

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@ -0,0 +1,5 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
}

View file

@ -0,0 +1,12 @@
- name: mash screen test_mash_screen
command: nextflow run ./tests/modules/mash/screen -entry test_mash_screen -c ./tests/config/nextflow.config -c ./tests/modules/mash/screen/nextflow.config
tags:
- mash
- mash/screen
files:
- path: output/mash/test.mash_stats
md5sum: 2a6f297d8e69a5e4160243bc6c89129c
- path: output/mash/test.msh
md5sum: d747145a43dad5f82342036f8f5d9133
- path: output/mash/test.screen
md5sum: d3c871dccd5cd57ab54781fa5c5d7278

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@ -0,0 +1,17 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { MAXQUANT_LFQ } from '../../../../modules/maxquant/lfq/main.nf' addParams( options: [:] )
workflow test_maxquant_lfq {
input = [ [ id:'test' ], // meta map
file(params.test_data['proteomics']['database']['yeast_ups'], checkIfExists: true), file(params.test_data['proteomics']['parameter']['maxquant'] , checkIfExists: true)
]
rawfiles = [file(params.test_data['proteomics']['msspectra']['ups_file1']) , file(params.test_data['proteomics']['msspectra']['ups_file2'])]
MAXQUANT_LFQ ( input, rawfiles.collect() )
}

View file

@ -0,0 +1,5 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
}

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@ -0,0 +1,8 @@
- name: maxquant lfq
command: nextflow run ./tests/modules/maxquant/lfq -entry test_maxquant_lfq -c tests/config/nextflow.config
tags:
- maxquant
- maxquant/lfq
files:
- path: output/maxquant/proteinGroups.txt
md5sum: 0d0f6aab54fe6dc717d1307bbc207324

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