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4
modules/allelecounter/meta.yml
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@ -32,8 +32,8 @@ input:
description: loci file <CHR><tab><POS1>
pattern: "*.{tsv}"
- fasta:
type: file
description: Input genome fasta file. Required when passing CRAM files.
type: file
description: Input genome fasta file. Required when passing CRAM files.
output:
- meta:

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modules/amplify/predict/main.nf Normal file
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def VERSION = '1.0.3' // Version information not provided by tool
process AMPLIFY_PREDICT {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::amplify=1.0.3" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/amplify:1.0.3--py36hdfd78af_0':
'quay.io/biocontainers/amplify:1.0.3--py36hdfd78af_0' }"
input:
tuple val(meta), path(faa)
path(model_dir)
output:
tuple val(meta), path('*.tsv'), emit: tsv
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 custom_model_dir = model_dir ? "-md ${model_dir}" : ""
"""
AMPlify \\
$args \\
${custom_model_dir} \\
-s '${faa}'
#rename output, because tool includes date and time in name
mv *.tsv ${prefix}.tsv
cat <<-END_VERSIONS > versions.yml
"${task.process}":
AMPlify: $VERSION
END_VERSIONS
"""
}

47
modules/amplify/predict/meta.yml Normal file
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@ -0,0 +1,47 @@
name: "amplify_predict"
description: AMPlify is an attentive deep learning model for antimicrobial peptide prediction.
keywords:
- antimicrobial peptides
- AMPs
- prediction
- model
tools:
- "amplify":
description: "Attentive deep learning model for antimicrobial peptide prediction"
homepage: "https://github.com/bcgsc/AMPlify"
documentation: "https://github.com/bcgsc/AMPlify"
tool_dev_url: "https://github.com/bcgsc/AMPlify"
doi: "https://doi.org/10.1186/s12864-022-08310-4"
licence: "['GPL v3']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- faa:
type: file
description: amino acid sequences fasta
pattern: "*.{fa,fa.gz,faa,faa.gz,fasta,fasta.gz}"
- model_dir:
type: directory
description: Directory of where models are stored (optional)
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"
- tsv:
type: file
description: amino acid sequences with prediction (AMP, non-AMP) and probability scores
pattern: "*.{tsv}"
authors:
- "@louperelo"

46
modules/antismash/antismashlitedownloaddatabases/main.nf Normal file
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@ -0,0 +1,46 @@
process ANTISMASH_ANTISMASHLITEDOWNLOADDATABASES {
label 'process_low'
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' }"
/*
These files are normally downloaded by download-antismash-databases itself, and must be retrieved for input by manually running the command with conda or a standalone installation of antiSMASH. Therefore we do not recommend using this module for production pipelines, but rather require users to specify their own local copy of the antiSMASH database in pipelines. This is solely for use for CI tests of the nf-core/module version of antiSMASH.
Reason: Upon execution, the tool checks if certain database files are present within the container and if not, it tries to create them in /usr/local/bin, for which only root user has write permissions. Mounting those database files with this module prevents the tool from trying to create them.
*/
containerOptions {
workflow.containerEngine == 'singularity' ?
"-B $database_css:/usr/local/lib/python3.8/site-packages/antismash/outputs/html/css,$database_detection:/usr/local/lib/python3.8/site-packages/antismash/detection,$database_modules:/usr/local/lib/python3.8/site-packages/antismash/modules" :
workflow.containerEngine == 'docker' ?
"-v \$PWD/$database_css:/usr/local/lib/python3.8/site-packages/antismash/outputs/html/css -v \$PWD/$database_detection:/usr/local/lib/python3.8/site-packages/antismash/detection -v \$PWD/$database_modules:/usr/local/lib/python3.8/site-packages/antismash/modules" :
''
}
input:
path database_css
path database_detection
path database_modules
output:
path("antismash_db") , emit: database
path "versions.yml", emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
"""
download-antismash-databases \\
--database-dir antismash_db \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
antismash: \$(antismash --version | sed 's/antiSMASH //')
END_VERSIONS
"""
}

55
modules/antismash/antismashlitedownloaddatabases/meta.yml Normal file
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@ -0,0 +1,55 @@
name: antismash_antismashlitedownloaddatabases
description: antiSMASH allows the rapid genome-wide identification, annotation and analysis of secondary metabolite biosynthesis gene clusters. This module downloads the antiSMASH databases.
keywords:
- secondary metabolites
- BGC
- biosynthetic gene cluster
- genome mining
- NRPS
- RiPP
- antibiotics
- prokaryotes
- bacteria
- eukaryotes
- fungi
- antismash
- database
tools:
- antismash:
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:
- database_css:
type: directory
description: |
antismash/outputs/html/css folder which is being created during the antiSMASH database downloading step. These files are normally downloaded by download-antismash-databases itself, and must be retrieved by the use by manually running the command with conda or a standalone installation of antiSMASH. Therefore we do not recommend using this module for production pipelines, but rather require users to specify their own local copy of the antiSMASH database in pipelines.
pattern: "css"
- database_detection:
type: directory
description: |
antismash/detection folder which is being created during the antiSMASH database downloading step. These files are normally downloaded by download-antismash-databases itself, and must be retrieved by the use by manually running the command with conda or a standalone installation of antiSMASH. Therefore we do not recommend using this module for production pipelines, but rather require users to specify their own local copy of the antiSMASH database in pipelines.
pattern: "detection"
- database_modules:
type: directory
description: |
antismash/modules folder which is being created during the antiSMASH database downloading step. These files are normally downloaded by download-antismash-databases itself, and must be retrieved by the use by manually running the command with conda or a standalone installation of antiSMASH. Therefore we do not recommend using this module for production pipelines, but rather require users to specify their own local copy of the antiSMASH database in pipelines.
pattern: "modules"
output:
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- database:
type: directory
description: Download directory for antiSMASH databases
pattern: "antismash_db"
authors:
- "@jasmezz"

6
modules/bbmap/align/main.nf
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@ -2,10 +2,10 @@ process BBMAP_ALIGN {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::bbmap=38.92 bioconda::samtools=1.13 pigz=2.6" : null)
conda (params.enable_conda ? "bioconda::bbmap=38.92 bioconda::samtools=1.15.1 pigz=2.6" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-008daec56b7aaf3f162d7866758142b9f889d690:f5f55fc5623bb7b3f725e8d2f86bedacfd879510-0' :
'quay.io/biocontainers/mulled-v2-008daec56b7aaf3f162d7866758142b9f889d690:f5f55fc5623bb7b3f725e8d2f86bedacfd879510-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-008daec56b7aaf3f162d7866758142b9f889d690:2fee0e0facec1dfe32a1ee4aa516aef7d0296ebf-0' :
'quay.io/biocontainers/mulled-v2-008daec56b7aaf3f162d7866758142b9f889d690:2fee0e0facec1dfe32a1ee4aa516aef7d0296ebf-0' }"
input:
tuple val(meta), path(fastq)

6
modules/bbmap/pileup/main.nf
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@ -2,10 +2,10 @@ process BBMAP_PILEUP {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::bbmap=38.92 bioconda::samtools=1.13 pigz=2.6" : null)
conda (params.enable_conda ? "bioconda::bbmap=38.92 bioconda::samtools=1.15.1 pigz=2.6" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-008daec56b7aaf3f162d7866758142b9f889d690:f5f55fc5623bb7b3f725e8d2f86bedacfd879510-0' :
'quay.io/biocontainers/mulled-v2-008daec56b7aaf3f162d7866758142b9f889d690:f5f55fc5623bb7b3f725e8d2f86bedacfd879510-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-008daec56b7aaf3f162d7866758142b9f889d690:2fee0e0facec1dfe32a1ee4aa516aef7d0296ebf-0' :
'quay.io/biocontainers/mulled-v2-008daec56b7aaf3f162d7866758142b9f889d690:2fee0e0facec1dfe32a1ee4aa516aef7d0296ebf-0' }"
input:
tuple val(meta), path(bam)

2
modules/bclconvert/.gitignore vendored Normal file
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@ -0,0 +1,2 @@
bcl-convert
*.rpm

15
modules/bclconvert/Dockerfile Normal file
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@ -0,0 +1,15 @@
# Dockerfile to create container with bcl-convert
# Push to nfcore/bclconvert:<VER>
FROM debian:bullseye-slim
LABEL authors="Matthias De Smet <matthias.desmet@ugent.be>" \
description="Docker image containing bcl-convert"
# Disclaimer: this container is not provided nor supported by Illumina
# 'ps' command is need by some nextflow executions to collect system stats
# Install procps and clean apt cache
RUN apt-get update \
&& apt-get install -y \
procps \
&& apt-get clean -y && rm -rf /var/lib/apt/lists/*
COPY bcl-convert /usr/local/bin/bcl-convert
RUN chmod +x /usr/local/bin/bcl-convert

30
modules/bclconvert/LICENSE Normal file
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@ -0,0 +1,30 @@
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# Updating the docker container and making a new module release
bcl-convert is a commercial tool from Illumina. The container provided for the bcl-convert nf-core module is not provided nor supported by Illumina. Updating the bcl-convert versions in the container and pushing the update to Dockerhub needs to be done manually.
1. Navigate to the appropriate download page. - [BCL Convert](https://support.illumina.com/sequencing/sequencing_software/bcl-convert/downloads.html): download the rpm of the desired bcl-convert version with `curl` or `wget`.
2. Unpack the RPM package using `rpm2cpio bcl-convert-*.rpm | cpio -i --make-directories`. Place the executable located in `<unpack_dir>/usr/bin/bcl-convert` in the same folder where the Dockerfile lies.
3. Create and test the container:
```bash
docker build . -t nfcore/bclconvert:<VERSION>
```
4. Access rights are needed to push the container to the Dockerhub nfcore organization, please ask a core team member to do so.
```bash
docker push nfcore/bclconvert:<VERSION>
```

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process BCLCONVERT {
tag '$samplesheet'
label 'process_high'
if (params.enable_conda) {
exit 1, "Conda environments cannot be used when using bcl-convert. Please use docker or singularity containers."
}
container "nfcore/bclconvert:3.9.3"
input:
path samplesheet
path run_dir
output:
path "*.fastq.gz" ,emit: fastq
path "Reports/*.{csv,xml,bin}" ,emit: reports
path "Logs/*.{log,txt}" ,emit: logs
path "InterOp/*.bin" ,emit: interop
path "versions.yml" ,emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
"""
bcl-convert \
$args \\
--output-directory . \\
--bcl-input-directory ${run_dir} \\
--sample-sheet ${samplesheet} \\
--bcl-num-parallel-tiles ${task.cpus}
mkdir InterOp
cp ${run_dir}/InterOp/*.bin InterOp/
mv Reports/*.bin InterOp/
cat <<-END_VERSIONS > versions.yml
"${task.process}":
bclconvert: \$(bcl-convert -V 2>&1 | head -n 1 | sed 's/^.*Version //')
END_VERSIONS
"""
stub:
"""
echo "sample1_S1_L001_R1_001" > sample1_S1_L001_R1_001.fastq.gz
echo "sample1_S1_L001_R2_001" > sample1_S1_L001_R2_001.fastq.gz
echo "sample1_S1_L002_R1_001" > sample1_S1_L002_R1_001.fastq.gz
echo "sample1_S1_L002_R2_001" > sample1_S1_L002_R2_001.fastq.gz
echo "sample2_S2_L001_R1_001" > sample2_S2_L001_R1_001.fastq.gz
echo "sample2_S2_L001_R2_001" > sample2_S2_L001_R2_001.fastq.gz
echo "sample2_S2_L002_R1_001" > sample2_S2_L002_R1_001.fastq.gz
echo "sample2_S2_L002_R2_001" > sample2_S2_L002_R2_001.fastq.gz
mkdir Reports
echo "Adapter_Metrics" > Reports/Adapter_Metrics.csv
echo "Demultiplex_Stats" > Reports/Demultiplex_Stats.csv
echo "fastq_list" > Reports/fastq_list.csv
echo "Index_Hopping_Counts" > Reports/Index_Hopping_Counts.csv
echo "IndexMetricsOut" > Reports/IndexMetricsOut.bin
echo "Quality_Metrics" > Reports/Quality_Metrics.csv
echo "RunInfo" > Reports/RunInfo.xml
echo "SampleSheet" > Reports/SampleSheet.csv
echo "Top_Unknown_Barcodes" > Reports/Top_Unknown_Barcodes.csv
mkdir Logs
echo "Errors" > Logs/Errors.log
echo "FastqComplete" > Logs/FastqComplete.txt
echo "Info" > Logs/Info.log
echo "Warnings" > Logs/Warnings.log
mkdir InterOp/
echo "InterOp" > InterOp/InterOp.bin
cat <<-END_VERSIONS > versions.yml
"${task.process}":
bclconvert: \$(bcl-convert -V 2>&1 | head -n 1 | sed 's/^.*Version //')
END_VERSIONS
"""
}

45
modules/bclconvert/meta.yml Normal file
View file

@ -0,0 +1,45 @@
name: "bclconvert"
description: Demultiplex Illumina BCL files
keywords:
- demultiplex
- illumina
- fastq
tools:
- "bclconvert":
description: "Demultiplex Illumina BCL files"
homepage: "https://support.illumina.com/sequencing/sequencing_software/bcl-convert.html"
documentation: "https://support-docs.illumina.com/SW/BCL_Convert/Content/SW/FrontPages/BCL_Convert.htm"
licence: "ILLUMINA"
input:
- samplesheet:
type: file
description: "Input samplesheet"
pattern: "*.{csv}"
- run_dir:
type: directory
description: "Input run directory containing RunInfo.xml and BCL data"
output:
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- fastq:
type: file
description: Demultiplexed FASTQ files
pattern: "*.{fastq.gz}"
- reports:
type: file
description: Demultiplexing Reports
pattern: "Reports/*.{csv,xml}"
- logs:
type: file
description: Log files
pattern: "Logs/*.{log,txt}"
- interop:
type: file
description: Interop files
pattern: "Interop/*.{bin}"
authors:
- "@matthdsm"

6
modules/bowtie/align/main.nf
View file

@ -2,10 +2,10 @@ process BOWTIE_ALIGN {
tag "$meta.id"
label 'process_high'
conda (params.enable_conda ? 'bioconda::bowtie=1.3.0 bioconda::samtools=1.11' : null)
conda (params.enable_conda ? 'bioconda::bowtie=1.3.0 bioconda::samtools=1.15.1' : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-ffbf83a6b0ab6ec567a336cf349b80637135bca3:9e14e16c284d6860574cf5b624bbc44c793cb024-0' :
'quay.io/biocontainers/mulled-v2-ffbf83a6b0ab6ec567a336cf349b80637135bca3:9e14e16c284d6860574cf5b624bbc44c793cb024-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-ffbf83a6b0ab6ec567a336cf349b80637135bca3:676c5bcfe34af6097728fea60fb7ea83f94a4a5f-0' :
'quay.io/biocontainers/mulled-v2-ffbf83a6b0ab6ec567a336cf349b80637135bca3:676c5bcfe34af6097728fea60fb7ea83f94a4a5f-0' }"
input:
tuple val(meta), path(reads)

6
modules/bowtie2/align/main.nf
View file

@ -2,10 +2,10 @@ process BOWTIE2_ALIGN {
tag "$meta.id"
label 'process_high'
conda (params.enable_conda ? 'bioconda::bowtie2=2.4.4 bioconda::samtools=1.14 conda-forge::pigz=2.6' : null)
conda (params.enable_conda ? 'bioconda::bowtie2=2.4.4 bioconda::samtools=1.15.1 conda-forge::pigz=2.6' : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-ac74a7f02cebcfcc07d8e8d1d750af9c83b4d45a:4d235f41348a00533f18e47c9669f1ecb327f629-0' :
'quay.io/biocontainers/mulled-v2-ac74a7f02cebcfcc07d8e8d1d750af9c83b4d45a:4d235f41348a00533f18e47c9669f1ecb327f629-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-ac74a7f02cebcfcc07d8e8d1d750af9c83b4d45a:1744f68fe955578c63054b55309e05b41c37a80d-0' :
'quay.io/biocontainers/mulled-v2-ac74a7f02cebcfcc07d8e8d1d750af9c83b4d45a:1744f68fe955578c63054b55309e05b41c37a80d-0' }"
input:
tuple val(meta), path(reads)

8
modules/bwa/mem/main.nf
View file

@ -2,10 +2,10 @@ process BWA_MEM {
tag "$meta.id"
label 'process_high'
conda (params.enable_conda ? "bioconda::bwa=0.7.17 bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::bwa=0.7.17 bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:c56a3aabc8d64e52d5b9da1e8ecec2031668596d-0' :
'quay.io/biocontainers/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:c56a3aabc8d64e52d5b9da1e8ecec2031668596d-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:8110a70be2bfe7f75a2ea7f2a89cda4cc7732095-0' :
'quay.io/biocontainers/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:8110a70be2bfe7f75a2ea7f2a89cda4cc7732095-0' }"
input:
tuple val(meta), path(reads)
@ -23,14 +23,12 @@ process BWA_MEM {
def args = task.ext.args ?: ''
def args2 = task.ext.args2 ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def read_group = meta.read_group ? "-R ${meta.read_group}" : ""
def samtools_command = sort_bam ? 'sort' : 'view'
"""
INDEX=`find -L ./ -name "*.amb" | sed 's/.amb//'`
bwa mem \\
$args \\
$read_group \\
-t $task.cpus \\
\$INDEX \\
$reads \\

6
modules/bwa/sampe/main.nf
View file

@ -2,10 +2,10 @@ process BWA_SAMPE {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::bwa=0.7.17 bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::bwa=0.7.17 bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:c56a3aabc8d64e52d5b9da1e8ecec2031668596d-0' :
'quay.io/biocontainers/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:c56a3aabc8d64e52d5b9da1e8ecec2031668596d-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:8110a70be2bfe7f75a2ea7f2a89cda4cc7732095-0' :
'quay.io/biocontainers/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:8110a70be2bfe7f75a2ea7f2a89cda4cc7732095-0' }"
input:
tuple val(meta), path(reads), path(sai)

6
modules/bwa/samse/main.nf
View file

@ -2,10 +2,10 @@ process BWA_SAMSE {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::bwa=0.7.17 bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::bwa=0.7.17 bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:c56a3aabc8d64e52d5b9da1e8ecec2031668596d-0' :
'quay.io/biocontainers/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:c56a3aabc8d64e52d5b9da1e8ecec2031668596d-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:8110a70be2bfe7f75a2ea7f2a89cda4cc7732095-0' :
'quay.io/biocontainers/mulled-v2-fe8faa35dbf6dc65a0f7f5d4ea12e31a79f73e40:8110a70be2bfe7f75a2ea7f2a89cda4cc7732095-0' }"
input:
tuple val(meta), path(reads), path(sai)

8
modules/bwamem2/mem/main.nf
View file

@ -2,10 +2,10 @@ process BWAMEM2_MEM {
tag "$meta.id"
label 'process_high'
conda (params.enable_conda ? "bioconda::bwa-mem2=2.2.1 bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::bwa-mem2=2.2.1 bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-e5d375990341c5aef3c9aff74f96f66f65375ef6:8ee25ae85d7a2bacac3e3139db209aff3d605a18-0' :
'quay.io/biocontainers/mulled-v2-e5d375990341c5aef3c9aff74f96f66f65375ef6:8ee25ae85d7a2bacac3e3139db209aff3d605a18-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-e5d375990341c5aef3c9aff74f96f66f65375ef6:38aed4501da19db366dc7c8d52d31d94e760cfaf-0' :
'quay.io/biocontainers/mulled-v2-e5d375990341c5aef3c9aff74f96f66f65375ef6:38aed4501da19db366dc7c8d52d31d94e760cfaf-0' }"
input:
tuple val(meta), path(reads)
@ -23,7 +23,6 @@ process BWAMEM2_MEM {
def args = task.ext.args ?: ''
def args2 = task.ext.args2 ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def read_group = meta.read_group ? "-R ${meta.read_group}" : ""
def samtools_command = sort_bam ? 'sort' : 'view'
"""
INDEX=`find -L ./ -name "*.amb" | sed 's/.amb//'`
@ -31,7 +30,6 @@ process BWAMEM2_MEM {
bwa-mem2 \\
mem \\
$args \\
$read_group \\
-t $task.cpus \\
\$INDEX \\
$reads \\

33
modules/centrifuge/kreport/main.nf Normal file
View file

@ -0,0 +1,33 @@
process CENTRIFUGE_KREPORT {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::centrifuge=1.0.4_beta" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/centrifuge:1.0.4_beta--h9a82719_6':
'quay.io/biocontainers/centrifuge:1.0.4_beta--h9a82719_6' }"
input:
tuple val(meta), path(results)
path db
output:
tuple val(meta), path('*.txt') , emit: kreport
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}"
"""
db_name=`find -L ${db} -name "*.1.cf" -not -name "._*" | sed 's/.1.cf//'`
centrifuge-kreport -x \$db_name ${results} > ${prefix}.txt
cat <<-END_VERSIONS > versions.yml
"${task.process}":
centrifuge: \$( centrifuge --version | sed -n 1p | sed 's/^.*centrifuge-class version //')
END_VERSIONS
"""
}

41
modules/centrifuge/kreport/meta.yml Normal file
View file

@ -0,0 +1,41 @@
name: "centrifuge_kreport"
description: Creates Kraken-style reports from centrifuge out files
keywords:
- metagenomics
tools:
- centrifuge:
description: Centrifuge is a classifier for metagenomic sequences.
homepage: https://ccb.jhu.edu/software/centrifuge/
documentation: https://ccb.jhu.edu/software/centrifuge/manual.shtml
doi: 10.1101/gr.210641.116
licence: ["GPL v3"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- results:
type: file
description: File containing the centrifuge classification results
pattern: "*.{txt}"
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"
- kreport:
type: file
description: |
File containing kraken-style report from centrifuge
out files.
pattern: "*.{txt}"
authors:
- "@sofstam"
- "@jfy133"

6
modules/chromap/chromap/main.nf
View file

@ -2,10 +2,10 @@ process CHROMAP_CHROMAP {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::chromap=0.2.1 bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::chromap=0.2.1 bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-1f09f39f20b1c4ee36581dc81cc323c70e661633:bd74d08a359024829a7aec1638a28607bbcd8a58-0' :
'quay.io/biocontainers/mulled-v2-1f09f39f20b1c4ee36581dc81cc323c70e661633:bd74d08a359024829a7aec1638a28607bbcd8a58-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-1f09f39f20b1c4ee36581dc81cc323c70e661633:963e4fe6a85c548a4018585660aed79780a175d3-0' :
'quay.io/biocontainers/mulled-v2-1f09f39f20b1c4ee36581dc81cc323c70e661633:963e4fe6a85c548a4018585660aed79780a175d3-0' }"
input:
tuple val(meta), path(reads)

59
modules/dragmap/align/main.nf
View file

@ -2,10 +2,10 @@ process DRAGMAP_ALIGN {
tag "$meta.id"
label 'process_high'
conda (params.enable_conda ? "bioconda::dragmap=1.2.1 bioconda::samtools=1.14 conda-forge::pigz=2.3.4" : null)
conda (params.enable_conda ? "bioconda::dragmap=1.2.1 bioconda::samtools=1.15.1 conda-forge::pigz=2.3.4" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-580d344d9d4a496cd403932da8765f9e0187774d:f7aad9060cde739c95685fc5ff6d6f7e3ec629c8-0':
'quay.io/biocontainers/mulled-v2-580d344d9d4a496cd403932da8765f9e0187774d:f7aad9060cde739c95685fc5ff6d6f7e3ec629c8-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-580d344d9d4a496cd403932da8765f9e0187774d:5ebebbc128cd624282eaa37d2c7fe01505a91a69-0':
'quay.io/biocontainers/mulled-v2-580d344d9d4a496cd403932da8765f9e0187774d:5ebebbc128cd624282eaa37d2c7fe01505a91a69-0' }"
input:
tuple val(meta), path(reads)
@ -24,44 +24,23 @@ process DRAGMAP_ALIGN {
def args = task.ext.args ?: ''
def args2 = task.ext.args2 ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def read_group = meta.read_group ? "--RGSM ${meta.read_group}" : ""
def reads_command = meta.single_end ? "-1 $reads" : "-1 ${reads[0]} -2 ${reads[1]}"
def samtools_command = sort_bam ? 'sort' : 'view'
if (meta.single_end) {
"""
dragen-os \\
-r $hashmap \\
$args \\
$read_group \\
--num-threads $task.cpus \\
-1 $reads \\
2> ${prefix}.dragmap.log \\
| samtools $samtools_command $args2 --threads $task.cpus -o ${prefix}.bam -
cat <<-END_VERSIONS > versions.yml
"${task.process}":
dragmap: \$(echo \$(dragen-os --version 2>&1))
samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
pigz: \$( pigz --version 2>&1 | sed 's/pigz //g' )
END_VERSIONS
"""
} else {
"""
dragen-os \\
-r $hashmap \\
$args \\
$read_group \\
--num-threads $task.cpus \\
-1 ${reads[0]} \\
-2 ${reads[1]} \\
2> ${prefix}.dragmap.log \\
| samtools $samtools_command $args2 --threads $task.cpus -o ${prefix}.bam -
"""
dragen-os \\
-r $hashmap \\
$args \\
--num-threads $task.cpus \\
$reads_command \\
2> ${prefix}.dragmap.log \\
| samtools $samtools_command $args2 --threads $task.cpus -o ${prefix}.bam -
cat <<-END_VERSIONS > versions.yml
"${task.process}":
dragmap: \$(echo \$(dragen-os --version 2>&1))
samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
pigz: \$( pigz --version 2>&1 | sed 's/pigz //g' )
END_VERSIONS
"""
}
cat <<-END_VERSIONS > versions.yml
"${task.process}":
dragmap: \$(echo \$(dragen-os --version 2>&1))
samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
pigz: \$( pigz --version 2>&1 | sed 's/pigz //g' )
END_VERSIONS
"""
}

89
modules/elprep/filter/main.nf Normal file
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@ -0,0 +1,89 @@
process ELPREP_FILTER {
tag "$meta.id"
label 'process_high'
conda (params.enable_conda ? "bioconda::elprep=5.1.2" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/elprep:5.1.2--he881be0_0':
'quay.io/biocontainers/elprep:5.1.2--he881be0_0' }"
input:
tuple val(meta), path(bam)
val(run_haplotypecaller)
val(run_bqsr)
path(reference_sequences)
path(filter_regions_bed)
path(reference_elfasta)
path(known_sites_elsites)
path(target_regions_bed)
path(intermediate_bqsr_tables)
val(bqsr_tables_only)
val(get_activity_profile)
val(get_assembly_regions)
output:
tuple val(meta), path("output/**.{bam,sam}") ,emit: bam
tuple val(meta), path("*.metrics.txt") ,optional: true, emit: metrics
tuple val(meta), path("*.recall") ,optional: true, emit: recall
tuple val(meta), path("*.vcf.gz") ,optional: true, emit: gvcf
tuple val(meta), path("*.table") ,optional: true, emit: table
tuple val(meta), path("*.activity_profile.igv") ,optional: true, emit: activity_profile
tuple val(meta), path("*.assembly_regions.igv") ,optional: true, emit: assembly_regions
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 suffix = args.contains("--output-type sam") ? "sam" : "bam"
// filter args
def reference_sequences_cmd = reference_sequences ? " --replace-reference-sequences ${reference_sequences}" : ""
def filter_regions_cmd = filter_regions_bed ? " --filter-non-overlapping-reads ${filter_regions_bed}" : ""
// markdup args
def markdup_cmd = args.contains("--mark-duplicates") ? " --mark-optical-duplicates ${prefix}.metrics.txt": ""
// variant calling args
def haplotyper_cmd = run_haplotypecaller ? " --haplotypecaller ${prefix}.g.vcf.gz": ""
def fasta_cmd = reference_elfasta ? " --reference ${reference_elfasta}": ""
def known_sites_cmd = known_sites_elsites ? " --known-sites ${known_sites_elsites}": ""
def target_regions_cmd = target_regions_bed ? " --target-regions ${target_regions_bed}": ""
// bqsr args
def bqsr_cmd = run_bqsr ? " --bqsr ${prefix}.recall": ""
def bqsr_tables_only_cmd = bqsr_tables_only ? " --bqsr-tables-only ${prefix}.table": ""
def intermediate_bqsr_cmd = intermediate_bqsr_tables ? " --bqsr-apply .": ""
// misc
def activity_profile_cmd = get_activity_profile ? " --activity-profile ${prefix}.activity_profile.igv": ""
def assembly_regions_cmd = get_assembly_regions ? " --assembly-regions ${prefix}.assembly_regions.igv": ""
"""
elprep filter ${bam} output/${prefix}.${suffix} \\
${reference_sequences_cmd} \\
${filter_regions_cmd} \\
${markdup_cmd} \\
${haplotyper_cmd} \\
${fasta_cmd} \\
${known_sites_cmd} \\
${target_regions_cmd} \\
${bqsr_cmd} \\
${bqsr_tables_only_cmd} \\
${intermediate_bqsr_cmd} \\
${activity_profile_cmd} \\
${assembly_regions_cmd} \\
--nr-of-threads ${task.cpus} \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
elprep: \$(elprep 2>&1 | head -n2 | tail -n1 |sed 's/^.*version //;s/ compiled.*\$//')
END_VERSIONS
"""
}

106
modules/elprep/filter/meta.yml Normal file
View file

@ -0,0 +1,106 @@
name: "elprep_filter"
description: "Filter, sort and markdup sam/bam files, with optional BQSR and variant calling."
keywords:
- sort
- bam
- sam
- filter
- variant calling
tools:
- "elprep":
description: "elPrep is a high-performance tool for preparing .sam/.bam files for variant calling in sequencing pipelines. It can be used as a drop-in replacement for SAMtools/Picard/GATK4."
homepage: "https://github.com/ExaScience/elprep"
documentation: "https://github.com/ExaScience/elprep"
tool_dev_url: "https://github.com/ExaScience/elprep"
doi: "10.1371/journal.pone.0244471"
licence: "['AGPL v3']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- bam:
type: file
description: Input SAM/BAM file
pattern: "*.{bam,sam}"
- run_haplotypecaller:
type: boolean
description: Run variant calling on the input files. Needed to generate gvcf output.
- run_bqsr:
type: boolean
description: Run BQSR on the input files. Needed to generate recall metrics.
- reference_sequences:
type: file
description: Optional SAM header to replace existing header.
pattern: "*.sam"
- filter_regions_bed:
type: file
description: Optional BED file containing regions to filter.
pattern: "*.bed"
- reference_elfasta:
type: file
description: Elfasta file, required for BQSR and variant calling.
pattern: "*.elfasta"
- known_sites:
type: file
description: Optional elsites file containing known SNPs for BQSR.
pattern: "*.elsites"
- target_regions_bed:
type: file
description: Optional BED file containing target regions for BQSR and variant calling.
pattern: "*.bed"
- intermediate_bqsr_tables:
type: file
description: Optional list of BQSR tables, used when parsing files created by `elprep split`
pattern: "*.table"
- bqsr_tables_only:
type: boolean
description: Write intermediate BQSR tables, used when parsing files created by `elprep split`.
- get_activity_profile:
type: boolean
description: Get the activity profile calculated by the haplotypecaller to the given file in IGV format.
- get_assembly_regions:
type: boolean
description: Get the assembly regions calculated by haplotypecaller to the speficied file in IGV format.
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"
- bam:
type: file
description: Sorted, markdup, optionally BQSR BAM/SAM file
pattern: "*.{bam,sam}"
- metrics:
type: file
description: Optional duplicate metrics file generated by elprep
pattern: "*.{metrics.txt}"
- recall:
type: file
description: Optional recall metrics file generated by elprep
pattern: "*.{recall}"
- gvcf:
type: file
description: Optional GVCF output file
pattern: "*.{vcf.gz}"
- table:
type: file
description: Optional intermediate BQSR table output file
pattern: "*.{table}"
- activity_profile:
type: file
description: Optional activity profile output file
pattern: "*.{activity_profile.igv}"
- assembly_regions:
type: file
description: Optional activity regions output file
pattern: "*.{assembly_regions.igv}"
authors:
- "@matthdsm"

45
modules/elprep/split/main.nf Normal file
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@ -0,0 +1,45 @@
process ELPREP_SPLIT {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::elprep=5.1.2" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/elprep:5.1.2--he881be0_0':
'quay.io/biocontainers/elprep:5.1.2--he881be0_0' }"
input:
tuple val(meta), path(bam)
output:
tuple val(meta), path("output/**.{bam,sam}"), emit: bam
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 single_end = meta.single_end ? " --single-end": ""
"""
# create directory and move all input so elprep can find and merge them before splitting
mkdir input
mv ${bam} input/
mkdir ${prefix}
elprep split \\
input \\
output/ \\
$args \\
$single_end \\
--nr-of-threads $task.cpus \\
--output-prefix $prefix
cat <<-END_VERSIONS > versions.yml
"${task.process}":
elprep: \$(elprep 2>&1 | head -n2 | tail -n1 |sed 's/^.*version //;s/ compiled.*\$//')
END_VERSIONS
"""
}

43
modules/elprep/split/meta.yml Normal file
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@ -0,0 +1,43 @@
name: "elprep_split"
description: Split bam file into manageable chunks
keywords:
- bam
- split by chromosome
tools:
- "elprep":
description: "elPrep is a high-performance tool for preparing .sam/.bam files for variant calling in sequencing pipelines. It can be used as a drop-in replacement for SAMtools/Picard/GATK4."
homepage: "https://github.com/ExaScience/elprep"
documentation: "https://github.com/ExaScience/elprep"
tool_dev_url: "https://github.com/ExaScience/elprep"
doi: "10.1371"
licence: "['AGPL v3']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- bam:
type: file
description: List of BAM/SAM files
pattern: "*.{bam,sam}"
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"
- bam:
type: file
description: List of split BAM/SAM files
pattern: "*.{bam,sam}"
authors:
- "@matthdsm"

15
modules/gatk4/applybqsr/main.nf
View file

@ -14,9 +14,9 @@ process GATK4_APPLYBQSR {
path dict
output:
tuple val(meta), path("*.bam"), emit: bam, optional: true
tuple val(meta), path("*.bam") , emit: bam, optional: true
tuple val(meta), path("*.cram"), emit: cram, optional: true
path "versions.yml" , emit: versions
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -24,8 +24,7 @@ process GATK4_APPLYBQSR {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def interval = intervals ? "-L ${intervals}" : ""
def file_type = input.getExtension()
def interval_command = intervals ? "--intervals $intervals" : ""
def avail_mem = 3
if (!task.memory) {
@ -35,12 +34,12 @@ process GATK4_APPLYBQSR {
}
"""
gatk --java-options "-Xmx${avail_mem}g" ApplyBQSR \\
-R $fasta \\
-I $input \\
--input $input \\
--output ${prefix}.${input.getExtension()} \\
--reference $fasta \\
--bqsr-recal-file $bqsr_table \\
$interval \\
$interval_command \\
--tmp-dir . \\
-O ${prefix}.${file_type} \\
$args
cat <<-END_VERSIONS > versions.yml

4
modules/gatk4/applybqsr/meta.yml
View file

@ -61,6 +61,10 @@ output:
type: file
description: Recalibrated BAM file
pattern: "*.{bam}"
- cram:
type: file
description: Recalibrated CRAM file
pattern: "*.{cram}"
authors:
- "@yocra3"

51
modules/gatk4/applybqsrspark/main.nf Normal file
View file

@ -0,0 +1,51 @@
process GATK4_APPLYBQSR_SPARK {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.3.0" : null)
container "${ 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' }"
input:
tuple val(meta), path(input), path(input_index), path(bqsr_table), path(intervals)
path fasta
path fai
path dict
output:
tuple val(meta), path("*.bam") , emit: bam, optional: true
tuple val(meta), path("*.cram"), emit: cram, optional: true
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 interval_command = intervals ? "--intervals $intervals" : ""
def avail_mem = 3
if (!task.memory) {
log.info '[GATK ApplyBQSRSpark] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
} else {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" ApplyBQSRSpark \\
--input $input \\
--output ${prefix}.${input.getExtension()} \\
--reference $fasta \\
--bqsr-recal-file $bqsr_table \\
$interval_command \\
--spark-master local[${task.cpus}] \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
gatk4: \$(echo \$(gatk --version 2>&1) | sed 's/^.*(GATK) v//; s/ .*\$//')
END_VERSIONS
"""
}

72
modules/gatk4/applybqsrspark/meta.yml Normal file
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@ -0,0 +1,72 @@
name: gatk4_applybqsr_spark
description: Apply base quality score recalibration (BQSR) to a bam file
keywords:
- bqsr
- bam
tools:
- gatk4:
description: |
Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools
with a primary focus on variant discovery and genotyping. Its powerful processing engine
and high-performance computing features make it capable of taking on projects of any size.
homepage: https://gatk.broadinstitute.org/hc/en-us
documentation: https://gatk.broadinstitute.org/hc/en-us/categories/360002369672s
doi: 10.1158/1538-7445.AM2017-3590
licence: ["Apache-2.0"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- input:
type: file
description: BAM/CRAM file from alignment
pattern: "*.{bam,cram}"
- input_index:
type: file
description: BAI/CRAI file from alignment
pattern: "*.{bai,crai}"
- bqsr_table:
type: file
description: Recalibration table from gatk4_baserecalibrator
- 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"
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"
- bam:
type: file
description: Recalibrated BAM file
pattern: "*.{bam}"
- cram:
type: file
description: Recalibrated CRAM file
pattern: "*.{cram}"
authors:
- "@yocra3"
- "@FriederikeHanssen"
- "@maxulysse"

23
modules/gatk4/applyvqsr/main.nf
View file

@ -8,15 +8,15 @@ process GATK4_APPLYVQSR {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(tbi), path(recal), path(recalidx), path(tranches)
path fasta
path fai
path dict
tuple val(meta), path(vcf), path(vcf_tbi), path(recal), path(recal_index), path(tranches)
path fasta
path fai
path dict
output:
tuple val(meta), path("*.vcf.gz") , emit: vcf
tuple val(meta), path("*.tbi") , emit: tbi
path "versions.yml" , emit: versions
tuple val(meta), path("*.vcf.gz"), emit: vcf
tuple val(meta), path("*.tbi") , emit: tbi
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -24,7 +24,7 @@ process GATK4_APPLYVQSR {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
refCommand = fasta ? "-R ${fasta} " : ''
def reference_command = fasta ? "--reference $fasta" : ''
def avail_mem = 3
if (!task.memory) {
@ -34,11 +34,12 @@ process GATK4_APPLYVQSR {
}
"""
gatk --java-options "-Xmx${avail_mem}g" ApplyVQSR \\
${refCommand} \\
-V ${vcf} \\
-O ${prefix}.vcf.gz \\
--variant ${vcf} \\
--output ${prefix}.vcf.gz \\
$reference_command \\
--tranches-file $tranches \\
--recal-file $recal \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

8
modules/gatk4/applyvqsr/meta.yml
View file

@ -29,20 +29,20 @@ input:
type: file
description: VCF file to be recalibrated, this should be the same file as used for the first stage VariantRecalibrator.
pattern: "*.vcf"
- tbi:
- vcf_tbi:
type: file
description: Tbi index for the input vcf file.
description: tabix index for the input vcf file.
pattern: "*.vcf.tbi"
- recal:
type: file
description: Recalibration file produced when the input vcf was run through VariantRecalibrator in stage 1.
pattern: "*.recal"
- recalidx:
- recal_index:
type: file
description: Index file for the recalibration file.
pattern: ".recal.idx"
- tranches:
type: boolean
type: file
description: Tranches file produced when the input vcf was run through VariantRecalibrator in stage 1.
pattern: ".tranches"
- fasta:

33
modules/gatk4/baserecalibrator/main.nf
View file

@ -9,15 +9,15 @@ process GATK4_BASERECALIBRATOR {
input:
tuple val(meta), path(input), path(input_index), path(intervals)
path fasta
path fai
path dict
path knownSites
path knownSites_tbi
path fasta
path fai
path dict
path known_sites
path known_sites_tbi
output:
tuple val(meta), path("*.table"), emit: table
path "versions.yml" , emit: versions
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -25,8 +25,8 @@ process GATK4_BASERECALIBRATOR {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def intervalsCommand = intervals ? "-L ${intervals}" : ""
def sitesCommand = knownSites.collect{"--known-sites ${it}"}.join(' ')
def interval_command = intervals ? "--intervals $intervals" : ""
def sites_command = known_sites.collect{"--known-sites $it"}.join(' ')
def avail_mem = 3
if (!task.memory) {
@ -34,16 +34,15 @@ process GATK4_BASERECALIBRATOR {
} else {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" BaseRecalibrator \
-R $fasta \
-I $input \
$sitesCommand \
$intervalsCommand \
--tmp-dir . \
$args \
-O ${prefix}.table
gatk --java-options "-Xmx${avail_mem}g" BaseRecalibrator \\
--input $input \\
--output ${prefix}.table \\
--reference $fasta \\
$interval_command \\
$sites_command \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":

10
modules/gatk4/baserecalibrator/meta.yml
View file

@ -42,9 +42,14 @@ input:
type: file
description: GATK sequence dictionary
pattern: "*.dict"
- knownSites:
- known_sites:
type: file
description: Bed file with the genomic regions included in the library (optional)
description: VCF files with known sites for indels / snps (optional)
pattern: "*.vcf.gz"
- known_sites_tbi:
type: file
description: Tabix index of the known_sites (optional)
pattern: "*.vcf.gz.tbi"
output:
- meta:
@ -64,3 +69,4 @@ output:
authors:
- "@yocra3"
- "@FriederikeHanssen"
- "@maxulysse"

53
modules/gatk4/baserecalibratorspark/main.nf Normal file
View file

@ -0,0 +1,53 @@
process GATK4_BASERECALIBRATOR_SPARK {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.3.0" : null)
container "${ 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' }"
input:
tuple val(meta), path(input), path(input_index), path(intervals)
path fasta
path fai
path dict
path known_sites
path known_sites_tbi
output:
tuple val(meta), path("*.table"), emit: table
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 interval_command = intervals ? "--intervals $intervals" : ""
def sites_command = known_sites.collect{"--known-sites $it"}.join(' ')
def avail_mem = 3
if (!task.memory) {
log.info '[GATK BaseRecalibratorSpark] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
} else {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" BaseRecalibratorSpark \\
--input $input \\
--output ${prefix}.table \\
--reference $fasta \\
$interval_command \\
$sites_command \\
--spark-master local[${task.cpus}] \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
gatk4: \$(echo \$(gatk --version 2>&1) | sed 's/^.*(GATK) v//; s/ .*\$//')
END_VERSIONS
"""
}

72
modules/gatk4/baserecalibratorspark/meta.yml Normal file
View file

@ -0,0 +1,72 @@
name: gatk4_baserecalibrator_spark
description: Generate recalibration table for Base Quality Score Recalibration (BQSR)
keywords:
- sort
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 ]
- input:
type: file
description: BAM/CRAM file from alignment
pattern: "*.{bam,cram}"
- input_index:
type: file
description: BAI/CRAI file from alignment
pattern: "*.{bai,crai}"
- 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"
- known_sites:
type: file
description: VCF files with known sites for indels / snps (optional)
pattern: "*.vcf.gz"
- known_sites_tbi:
type: file
description: Tabix index of the known_sites (optional)
pattern: "*.vcf.gz.tbi"
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"
- table:
type: file
description: Recalibration table from BaseRecalibrator
pattern: "*.{table}"
authors:
- "@yocra3"
- "@FriederikeHanssen"
- "@maxulysse"

10
modules/gatk4/bedtointervallist/main.nf
View file

@ -9,7 +9,7 @@ process GATK4_BEDTOINTERVALLIST {
input:
tuple val(meta), path(bed)
path sequence_dict
path dict
output:
tuple val(meta), path('*.interval_list'), emit: interval_list
@ -21,6 +21,7 @@ process GATK4_BEDTOINTERVALLIST {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK BedToIntervalList] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -29,9 +30,10 @@ process GATK4_BEDTOINTERVALLIST {
}
"""
gatk --java-options "-Xmx${avail_mem}g" BedToIntervalList \\
-I $bed \\
-SD $sequence_dict \\
-O ${prefix}.interval_list \\
--INPUT $bed \\
--OUTPUT ${prefix}.interval_list \\
--SEQUENCE_DICTIONARY $dict \\
--TMP_DIR . \\
$args
cat <<-END_VERSIONS > versions.yml

11
modules/gatk4/calculatecontamination/main.nf
View file

@ -9,7 +9,6 @@ process GATK4_CALCULATECONTAMINATION {
input:
tuple val(meta), path(pileup), path(matched)
val segmentout
output:
tuple val(meta), path('*.contamination.table'), emit: contamination
@ -22,8 +21,8 @@ process GATK4_CALCULATECONTAMINATION {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def matched_command = matched ? " -matched ${matched} " : ''
def segment_command = segmentout ? " -segments ${prefix}.segmentation.table" : ''
def matched_command = matched ? "--matched-normal $matched" : ''
def avail_mem = 3
if (!task.memory) {
log.info '[GATK CalculateContamination] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -32,10 +31,10 @@ process GATK4_CALCULATECONTAMINATION {
}
"""
gatk --java-options "-Xmx${avail_mem}g" CalculateContamination \\
-I $pileup \\
--input $pileup \\
--output ${prefix}.contamination.table \\
$matched_command \\
-O ${prefix}.contamination.table \\
$segment_command \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

6
modules/gatk4/calculatecontamination/meta.yml
View file

@ -32,9 +32,6 @@ input:
type: file
description: File containing the pileups summary table of a normal sample that matches with the tumor sample specified in pileup argument. This is an optional input.
pattern: "*.pileups.table"
- segmentout:
type: boolean
description: specifies whether to output the segmentation table.
output:
- contamination:
@ -43,7 +40,7 @@ output:
pattern: "*.contamination.table"
- segmentation:
type: file
description: optional output table containing segmentation of tumor minor allele fractions.
description: output table containing segmentation of tumor minor allele fractions (optional)
pattern: "*.segmentation.table"
- versions:
type: file
@ -52,3 +49,4 @@ output:
authors:
- "@GCJMackenzie"
- "@maxulysse"

24
modules/gatk4/combinegvcfs/main.nf
View file

@ -9,9 +9,9 @@ process GATK4_COMBINEGVCFS {
input:
tuple val(meta), path(vcf), path(vcf_idx)
path (fasta)
path (fasta_fai)
path (fasta_dict)
path fasta
path fai
path dict
output:
tuple val(meta), path("*.combined.g.vcf.gz"), emit: combined_gvcf
@ -23,21 +23,21 @@ process GATK4_COMBINEGVCFS {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def avail_mem = 3
def input_list = vcf.collect{"--variant $it"}.join(' ')
def avail_mem = 3
if (!task.memory) {
log.info '[GATK COMBINEGVCFS] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
} else {
avail_mem = task.memory.giga
}
def input_files = vcf.collect{"-V ${it}"}.join(' ') // add '-V' to each vcf file
"""
gatk \\
--java-options "-Xmx${avail_mem}g" \\
CombineGVCFs \\
-R ${fasta} \\
-O ${prefix}.combined.g.vcf.gz \\
${args} \\
${input_files}
gatk --java-options "-Xmx${avail_mem}g" CombineGVCFs \\
$input_list \\
--output ${prefix}.combined.g.vcf.gz \\
--reference ${fasta} \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":

32
modules/gatk4/combinegvcfs/meta.yml
View file

@ -19,18 +19,11 @@ tools:
licence: ["Apache-2.0"]
input:
- fasta:
type: file
description: The reference fasta file
pattern: "*.fasta"
- fai:
type: file
description: FASTA index file
pattern: "*.{fai}"
- dict:
type: file
description: FASTA dictionary file
pattern: "*.{dict}"
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test' ]
- vcf:
type: file
description: Compressed VCF files
@ -38,7 +31,19 @@ input:
- vcf_idx:
type: file
description: VCF Index file
pattern: "*.{fai}"
pattern: "*.vcf.gz.idx"
- fasta:
type: file
description: The reference fasta file
pattern: "*.fasta"
- fai:
type: file
description: FASTA index file
pattern: "*.fasta.fai"
- dict:
type: file
description: FASTA dictionary file
pattern: "*.dict"
output:
- gvcf:
type: file
@ -53,3 +58,4 @@ authors:
- "@sateeshperi"
- "@mjcipriano"
- "@hseabolt"
- "@maxulysse"

9
modules/gatk4/createsequencedictionary/main.nf
View file

@ -11,14 +11,15 @@ process GATK4_CREATESEQUENCEDICTIONARY {
path fasta
output:
path "*.dict" , emit: dict
path "versions.yml" , emit: versions
path "*.dict" , emit: dict
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def avail_mem = 6
if (!task.memory) {
log.info '[GATK CreateSequenceDictionary] Available memory not known - defaulting to 6GB. Specify process memory requirements to change this.'
@ -26,10 +27,10 @@ process GATK4_CREATESEQUENCEDICTIONARY {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" \\
CreateSequenceDictionary \\
gatk --java-options "-Xmx${avail_mem}g" CreateSequenceDictionary \\
--REFERENCE $fasta \\
--URI $fasta \\
--TMP_DIR . \\
$args
cat <<-END_VERSIONS > versions.yml

17
modules/gatk4/createsomaticpanelofnormals/main.nf
View file

@ -9,9 +9,9 @@ process GATK4_CREATESOMATICPANELOFNORMALS {
input:
tuple val(meta), path(genomicsdb)
path fasta
path fai
path dict
path fasta
path fai
path dict
output:
tuple val(meta), path("*.vcf.gz"), emit: vcf
@ -24,6 +24,7 @@ process GATK4_CREATESOMATICPANELOFNORMALS {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK CreateSomaticPanelOfNormals] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -31,11 +32,11 @@ process GATK4_CREATESOMATICPANELOFNORMALS {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" \\
CreateSomaticPanelOfNormals \\
-R $fasta \\
-V gendb://$genomicsdb \\
-O ${prefix}.vcf.gz \\
gatk --java-options "-Xmx${avail_mem}g" CreateSomaticPanelOfNormals \\
--variant gendb://$genomicsdb \\
--output ${prefix}.vcf.gz \\
--reference $fasta \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

2
modules/gatk4/createsomaticpanelofnormals/meta.yml
View file

@ -44,7 +44,7 @@ output:
pattern: "*.vcf.gz"
- tbi:
type: file
description: Index of vcf file
description: Tabix index of vcf file
pattern: "*vcf.gz.tbi"
- versions:
type: file

24
modules/gatk4/estimatelibrarycomplexity/main.nf
View file

@ -8,14 +8,14 @@ process GATK4_ESTIMATELIBRARYCOMPLEXITY {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(cram)
path(fasta)
path(fai)
path(dict)
tuple val(meta), path(input)
path fasta
path fai
path dict
output:
tuple val(meta), path('*.metrics'), emit: metrics
path "versions.yml" , emit: versions
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -23,7 +23,7 @@ process GATK4_ESTIMATELIBRARYCOMPLEXITY {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def crams = cram.collect(){ x -> "-I ".concat(x.toString()) }.join(" ")
def input_list = input.collect(){"--INPUT $it"}.join(" ")
def avail_mem = 3
if (!task.memory) {
@ -32,12 +32,12 @@ process GATK4_ESTIMATELIBRARYCOMPLEXITY {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" EstimateLibraryComplexity \
${crams} \
-O ${prefix}.metrics \
--REFERENCE_SEQUENCE ${fasta} \
--VALIDATION_STRINGENCY SILENT \
--TMP_DIR . $args
gatk --java-options "-Xmx${avail_mem}g" EstimateLibraryComplexity \\
$input_list \\
--OUTPUT ${prefix}.metrics \\
--REFERENCE_SEQUENCE ${fasta} \\
--TMP_DIR . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":

3
modules/gatk4/estimatelibrarycomplexity/meta.yml
View file

@ -20,7 +20,7 @@ input:
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- cram:
- input:
type: file
description: BAM/CRAM/SAM file
pattern: "*.{bam,cram,sam}"
@ -54,3 +54,4 @@ output:
authors:
- "@FriederikeHanssen"
- "@maxulysse"

10
modules/gatk4/fastqtosam/main.nf
View file

@ -20,7 +20,8 @@ process GATK4_FASTQTOSAM {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def read_files = meta.single_end ? "-F1 $reads" : "-F1 ${reads[0]} -F2 ${reads[1]}"
def reads_command = meta.single_end ? "--FASTQ $reads" : "--FASTQ ${reads[0]} --FASTQ2 ${reads[1]}"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK FastqToSam] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -29,9 +30,10 @@ process GATK4_FASTQTOSAM {
}
"""
gatk --java-options "-Xmx${avail_mem}g" FastqToSam \\
$read_files \\
-O ${prefix}.bam \\
-SM $prefix \\
$reads_command \\
--OUTPUT ${prefix}.bam \\
--SAMPLE_NAME $prefix \\
--TMP_DIR . \\
$args
cat <<-END_VERSIONS > versions.yml

8
modules/gatk4/fastqtosam/meta.yml
View file

@ -34,14 +34,14 @@ output:
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- bam:
type: file
description: Converted BAM file
pattern: "*.bam"
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
authors:
- "@ntoda03"

39
modules/gatk4/filtermutectcalls/main.nf
View file

@ -8,10 +8,10 @@ process GATK4_FILTERMUTECTCALLS {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(tbi), path(stats), path(orientationbias), path(segmentation), path(contaminationfile), val(contaminationest)
path fasta
path fai
path dict
tuple val(meta), path(vcf), path(vcf_tbi), path(stats), path(orientationbias), path(segmentation), path(table), val(estimate)
path fasta
path fai
path dict
output:
tuple val(meta), path("*.vcf.gz") , emit: vcf
@ -26,20 +26,11 @@ process GATK4_FILTERMUTECTCALLS {
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def orientationbias_options = ''
if (orientationbias) {
orientationbias_options = '--orientation-bias-artifact-priors ' + orientationbias.join(' --orientation-bias-artifact-priors ')
}
def orientationbias_command = orientationbias ? orientationbias.collect{"--orientation-bias-artifact-priors $it"}.join(' ') : ''
def segmentation_command = segmentation ? segmentation.collect{"--tumor-segmentation $it"}.join(' ') : ''
def estimate_command = estimate ? " --contamination-estimate ${estimate} " : ''
def table_command = table ? " --contamination-table ${table} " : ''
def segmentation_options = ''
if (segmentation) {
segmentation_options = '--tumor-segmentation ' + segmentation.join(' --tumor-segmentation ')
}
def contamination_options = contaminationest ? " --contamination-estimate ${contaminationest} " : ''
if (contaminationfile) {
contamination_options = '--contamination-table ' + contaminationfile.join(' --contamination-table ')
}
def avail_mem = 3
if (!task.memory) {
log.info '[GATK FilterMutectCalls] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -48,12 +39,14 @@ process GATK4_FILTERMUTECTCALLS {
}
"""
gatk --java-options "-Xmx${avail_mem}g" FilterMutectCalls \\
-R $fasta \\
-V $vcf \\
$orientationbias_options \\
$segmentation_options \\
$contamination_options \\
-O ${prefix}.vcf.gz \\
--variant $vcf \\
--output ${prefix}.vcf.gz \\
--reference $fasta \\
$orientationbias_command \\
$segmentation_command \\
$estimate_command \\
$table_command \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

13
modules/gatk4/filtermutectcalls/meta.yml
View file

@ -26,9 +26,9 @@ input:
type: file
description: compressed vcf file of mutect2calls
pattern: "*.vcf.gz"
- tbi:
- vcf_tbi:
type: file
description: Index of vcf file
description: Tabix index of vcf file
pattern: "*vcf.gz.tbi"
- stats:
type: file
@ -42,13 +42,13 @@ input:
type: list
description: tables containing segmentation information for input vcf. Optional input.
pattern: "*.segmentation.table"
- contaminationfile:
- table:
type: list
description: table(s) containing contamination contamination data for input vcf. Optional input, takes priority over contaminationest.
description: table(s) containing contamination data for input vcf. Optional input, takes priority over estimate.
pattern: "*.contamination.table"
- contaminationest:
- estimate:
type: val
description: estimation of contamination value as a double. Optional input, will only be used if contaminationfile is not specified.
description: estimation of contamination value as a double. Optional input, will only be used if table is not specified.
- fasta:
type: file
description: The reference fasta file
@ -82,3 +82,4 @@ output:
authors:
- "@GCJMackenzie"
- "@maxulysse"

15
modules/gatk4/gatherbqsrreports/main.nf
View file

@ -8,7 +8,7 @@ process GATK4_GATHERBQSRREPORTS {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(recal_table)
tuple val(meta), path(table)
output:
tuple val(meta), path("*.table"), emit: table
@ -20,7 +20,7 @@ process GATK4_GATHERBQSRREPORTS {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def input = recal_table.collect{"-I ${it}"}.join(' ')
def input_list = table.collect{"--input $it"}.join(' ')
def avail_mem = 3
if (!task.memory) {
@ -29,12 +29,11 @@ process GATK4_GATHERBQSRREPORTS {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" \\
GatherBQSRReports \
${input} \
--tmp-dir . \
$args \
--output ${prefix}.table
gatk --java-options "-Xmx${avail_mem}g" GatherBQSRReports \\
$input_list \\
--output ${prefix}.table \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":

10
modules/gatk4/gatherbqsrreports/meta.yml
View file

@ -19,7 +19,7 @@ input:
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- recal_table:
- table:
type: file
description: File(s) containing BQSR table(s)
pattern: "*.table"
@ -30,14 +30,14 @@ output:
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- table:
type: file
description: File containing joined BQSR table
pattern: "*.table"
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- recal_table:
type: file
description: File containing joined BQSR table
pattern: "*.table"
authors:
- "@FriederikeHanssen"

17
modules/gatk4/gatherpileupsummaries/main.nf
View file

@ -10,11 +10,11 @@ process GATK4_GATHERPILEUPSUMMARIES {
input:
tuple val(meta), path(pileup)
path dict
path dict
output:
tuple val(meta), path("*.pileupsummaries.table"), emit: table
path "versions.yml" , emit: versions
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -22,7 +22,7 @@ process GATK4_GATHERPILEUPSUMMARIES {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def input = pileup.collect{ "-I ${it} " }.join(' ')
def input_list = pileup.collect{ "--I $it" }.join(' ')
def avail_mem = 3
if (!task.memory) {
@ -31,11 +31,12 @@ process GATK4_GATHERPILEUPSUMMARIES {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" \
GatherPileupSummaries \
--sequence-dictionary ${dict} \
${input} \
-O ${prefix}.pileupsummaries.table
gatk --java-options "-Xmx${avail_mem}g" GatherPileupSummaries \\
$input_list \\
--O ${prefix}.pileupsummaries.table \\
--sequence-dictionary $dict \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":

9
modules/gatk4/gatherpileupsummaries/meta.yml
View file

@ -28,14 +28,15 @@ output:
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- table:
type: file
description: pileup summaries table file
pattern: "*.pileupsummaries.table"
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
- table:
type: file
description: Pileup file
pattern: "*.pileups.table"
authors:
- "@FriederikeHanssen"
- "@maxulysse"

37
modules/gatk4/genomicsdbimport/main.nf
View file

@ -8,13 +8,13 @@ process GATK4_GENOMICSDBIMPORT {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(tbi), path(intervalfile), val(intervalval), path(wspace)
val run_intlist
val run_updatewspace
val input_map
tuple val(meta), path(vcf), path(tbi), path(interval_file), val(interval_value), path(wspace)
val run_intlist
val run_updatewspace
val input_map
output:
tuple val(meta), path("${prefix}") , optional:true, emit: genomicsdb
tuple val(meta), path("$prefix") , optional:true, emit: genomicsdb
tuple val(meta), path("$updated_db") , optional:true, emit: updatedb
tuple val(meta), path("*.interval_list"), optional:true, emit: intervallist
path "versions.yml" , emit: versions
@ -27,22 +27,22 @@ process GATK4_GENOMICSDBIMPORT {
prefix = task.ext.prefix ?: "${meta.id}"
// settings for running default create gendb mode
inputs_command = input_map ? "--sample-name-map ${vcf[0]}" : "${'-V ' + vcf.join(' -V ')}"
dir_command = "--genomicsdb-workspace-path ${prefix}"
intervals_command = intervalfile ? " -L ${intervalfile} " : " -L ${intervalval} "
input_command = input_map ? "--sample-name-map ${vcf[0]}" : vcf.collect(){"--variant $it"}.join(' ')
genomicsdb_command = "--genomicsdb-workspace-path ${prefix}"
interval_command = interval_file ? "--intervals ${interval_file}" : "--intervals ${interval_value}"
// settings changed for running get intervals list mode if run_intlist is true
if (run_intlist) {
inputs_command = ''
dir_command = "--genomicsdb-update-workspace-path ${wspace}"
intervals_command = "--output-interval-list-to-file ${prefix}.interval_list"
genomicsdb_command = "--genomicsdb-update-workspace-path ${wspace}"
interval_command = "--output-interval-list-to-file ${prefix}.interval_list"
}
// settings changed for running update gendb mode. inputs_command same as default, update_db forces module to emit the updated gendb
// settings changed for running update gendb mode. input_command same as default, update_db forces module to emit the updated gendb
if (run_updatewspace) {
dir_command = "--genomicsdb-update-workspace-path ${wspace}"
intervals_command = ''
updated_db = wspace.toString()
genomicsdb_command = "--genomicsdb-update-workspace-path ${wspace}"
interval_command = ''
updated_db = "${wspace}"
}
def avail_mem = 3
@ -53,9 +53,10 @@ process GATK4_GENOMICSDBIMPORT {
}
"""
gatk --java-options "-Xmx${avail_mem}g" GenomicsDBImport \\
$inputs_command \\
$dir_command \\
$intervals_command \\
$input_command \\
$genomicsdb_command \\
$interval_command \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

29
modules/gatk4/genotypegvcfs/main.nf
View file

@ -10,10 +10,10 @@ process GATK4_GENOTYPEGVCFS {
input:
tuple val(meta), path(gvcf), path(gvcf_index), path(intervals), path(intervals_index)
path fasta
path fasta_index
path fasta_dict
path fai
path dict
path dbsnp
path dbsnp_index
path dbsnp_tbi
output:
tuple val(meta), path("*.vcf.gz"), emit: vcf
@ -26,9 +26,10 @@ process GATK4_GENOTYPEGVCFS {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def dbsnp_options = dbsnp ? "-D ${dbsnp}" : ""
def interval_options = intervals ? "-L ${intervals}" : ""
def gvcf_options = gvcf.name.endsWith(".vcf") || gvcf.name.endsWith(".vcf.gz") ? "$gvcf" : "gendb://$gvcf"
def gvcf_command = gvcf.name.endsWith(".vcf") || gvcf.name.endsWith(".vcf.gz") ? "$gvcf" : "gendb://$gvcf"
def dbsnp_command = dbsnp ? "--dbsnp $dbsnp" : ""
def interval_command = intervals ? "--intervals $intervals" : ""
def avail_mem = 3
if (!task.memory) {
log.info '[GATK GenotypeGVCFs] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -36,14 +37,14 @@ process GATK4_GENOTYPEGVCFS {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" \\
GenotypeGVCFs \\
$args \\
$interval_options \\
$dbsnp_options \\
-R $fasta \\
-V $gvcf_options \\
-O ${prefix}.vcf.gz
gatk --java-options "-Xmx${avail_mem}g" GenotypeGVCFs \\
--variant $gvcf_command \\
--output ${prefix}.vcf.gz \\
--reference $fasta \\
$interval_command \\
$dbsnp_command \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":

20
modules/gatk4/genotypegvcfs/meta.yml
View file

@ -21,10 +21,15 @@ input:
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- gvcf:
type: tuple of files
type: file
description: |
Tuple of gVCF(.gz) file (first) and its index (second) or the path to a GenomicsDB (and empty)
pattern: ["*.{vcf,vcf.gz}", "*.{idx,tbi}"]
gVCF(.gz) file or to a GenomicsDB
pattern: "*.{vcf,vcf.gz}"
- gvcf_index:
type: file
description: |
index of gvcf file, or empty when providing GenomicsDB
pattern: "*.{idx,tbi}"
- intervals:
type: file
description: Interval file with the genomic regions included in the library (optional)
@ -35,11 +40,11 @@ input:
type: file
description: Reference fasta file
pattern: "*.fasta"
- fasta_index:
- fai:
type: file
description: Reference fasta index file
pattern: "*.fai"
- fasta_dict:
- dict:
type: file
description: Reference fasta sequence dict file
pattern: "*.dict"
@ -47,8 +52,8 @@ input:
type: file
description: dbSNP VCF file
pattern: "*.vcf.gz"
- dbsnp_index:
type: tuple of files
- dbsnp_tbi:
type: file
description: dbSNP VCF index file
pattern: "*.tbi"
@ -73,3 +78,4 @@ output:
authors:
- "@santiagorevale"
- "@maxulysse"

27
modules/gatk4/getpileupsummaries/main.nf
View file

@ -9,15 +9,15 @@ process GATK4_GETPILEUPSUMMARIES {
input:
tuple val(meta), path(input), path(index), path(intervals)
path fasta
path fai
path dict
path variants
path variants_tbi
path fasta
path fai
path dict
path variants
path variants_tbi
output:
tuple val(meta), path('*.pileups.table'), emit: table
path "versions.yml" , emit: versions
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -25,8 +25,8 @@ process GATK4_GETPILEUPSUMMARIES {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def sitesCommand = intervals ? " -L ${intervals} " : " -L ${variants} "
def reference = fasta ? " -R ${fasta}" :""
def interval_command = intervals ? "--intervals $intervals" : ""
def reference_command = fasta ? "--reference $fasta" : ''
def avail_mem = 3
if (!task.memory) {
@ -36,11 +36,12 @@ process GATK4_GETPILEUPSUMMARIES {
}
"""
gatk --java-options "-Xmx${avail_mem}g" GetPileupSummaries \\
-I $input \\
-V $variants \\
$sitesCommand \\
${reference} \\
-O ${prefix}.pileups.table \\
--input $input \\
--variant $variants \\
--output ${prefix}.pileups.table \\
$reference_command \\
$sites_command \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

35
modules/gatk4/haplotypecaller/main.nf
View file

@ -9,11 +9,11 @@ process GATK4_HAPLOTYPECALLER {
input:
tuple val(meta), path(input), path(input_index), path(intervals)
path fasta
path fai
path dict
path dbsnp
path dbsnp_tbi
path fasta
path fai
path dict
path dbsnp
path dbsnp_tbi
output:
tuple val(meta), path("*.vcf.gz"), emit: vcf
@ -26,25 +26,24 @@ process GATK4_HAPLOTYPECALLER {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def interval_option = intervals ? "-L ${intervals}" : ""
def dbsnp_option = dbsnp ? "-D ${dbsnp}" : ""
def avail_mem = 3
def dbsnp_command = dbsnp ? "--dbsnp $dbsnp" : ""
def interval_command = intervals ? "--intervals $intervals" : ""
def avail_mem = 3
if (!task.memory) {
log.info '[GATK HaplotypeCaller] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
} else {
avail_mem = task.memory.giga
}
"""
gatk \\
--java-options "-Xmx${avail_mem}g" \\
HaplotypeCaller \\
-R $fasta \\
-I $input \\
${dbsnp_option} \\
${interval_option} \\
-O ${prefix}.vcf.gz \\
$args \\
--tmp-dir .
gatk --java-options "-Xmx${avail_mem}g" HaplotypeCaller \\
--input $input \\
--output ${prefix}.vcf.gz \\
--reference $fasta \\
$dbsnp_command \\
$interval_command \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":

9
modules/gatk4/indexfeaturefile/main.nf
View file

@ -19,6 +19,7 @@ process GATK4_INDEXFEATUREFILE {
script:
def args = task.ext.args ?: ''
def avail_mem = 3
if (!task.memory) {
log.info '[GATK IndexFeatureFile] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -26,10 +27,10 @@ process GATK4_INDEXFEATUREFILE {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" \\
IndexFeatureFile \\
$args \\
-I $feature_file
gatk --java-options "-Xmx${avail_mem}g" IndexFeatureFile \\
--input $feature_file \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":

5
modules/gatk4/intervallisttobed/main.nf
View file

@ -8,7 +8,7 @@ process GATK4_INTERVALLISTTOBED {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(interval)
tuple val(meta), path(intervals)
output:
tuple val(meta), path("*.bed"), emit: bed
@ -29,8 +29,9 @@ process GATK4_INTERVALLISTTOBED {
}
"""
gatk --java-options "-Xmx${avail_mem}g" IntervalListToBed \\
--INPUT ${interval} \\
--INPUT $intervals \\
--OUTPUT ${prefix}.bed \\
--TMP_DIR . \\
$args
cat <<-END_VERSIONS > versions.yml

13
modules/gatk4/intervallisttools/main.nf
View file

@ -8,11 +8,11 @@ process GATK4_INTERVALLISTTOOLS {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(interval_list)
tuple val(meta), path(intervals)
output:
tuple val(meta), path("*_split/*/*.interval_list"), emit: interval_list
path "versions.yml" , emit: versions
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -20,6 +20,7 @@ process GATK4_INTERVALLISTTOOLS {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK IntervalListTools] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -30,10 +31,10 @@ process GATK4_INTERVALLISTTOOLS {
mkdir ${prefix}_split
gatk --java-options "-Xmx${avail_mem}g" \\
IntervalListTools \\
-I ${interval_list} \\
-O ${prefix}_split \\
gatk --java-options "-Xmx${avail_mem}g" IntervalListTools \\
--INPUT $intervals \\
--OUTPUT ${prefix}_split \\
--TMP_DIR . \\
$args
python3 <<CODE

12
modules/gatk4/learnreadorientationmodel/main.nf
View file

@ -20,8 +20,8 @@ process GATK4_LEARNREADORIENTATIONMODEL {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def inputs_list = []
f1r2.each() { a -> inputs_list.add(" -I " + a) }
def input_list = f1r2.collect{"--input $it"}.join(' ')
def avail_mem = 3
if (!task.memory) {
log.info '[GATK LearnReadOrientationModel] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -29,10 +29,10 @@ process GATK4_LEARNREADORIENTATIONMODEL {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" \\
LearnReadOrientationModel \\
${inputs_list.join(' ')} \\
-O ${prefix}.tar.gz \\
gatk --java-options "-Xmx${avail_mem}g" LearnReadOrientationModel \\
$input_list \\
--output ${prefix}.tar.gz \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

10
modules/gatk4/markduplicates/main.nf
View file

@ -8,7 +8,7 @@ process GATK4_MARKDUPLICATES {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(bams)
tuple val(meta), path(bam)
output:
tuple val(meta), path("*.bam") , emit: bam
@ -22,7 +22,8 @@ process GATK4_MARKDUPLICATES {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def bam_list = bams.collect(){ bam -> "--INPUT ".concat(bam.toString()) }.join(" ")
def input_list = bam.collect{"--INPUT $it"}.join(' ')
def avail_mem = 3
if (!task.memory) {
log.info '[GATK MarkDuplicates] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -31,11 +32,10 @@ process GATK4_MARKDUPLICATES {
}
"""
gatk --java-options "-Xmx${avail_mem}g" MarkDuplicates \\
$bam_list \\
$input_list \\
--OUTPUT ${prefix}.bam \\
--METRICS_FILE ${prefix}.metrics \\
--TMP_DIR . \\
--CREATE_INDEX true \\
--OUTPUT ${prefix}.bam \\
$args
cat <<-END_VERSIONS > versions.yml

1
modules/gatk4/markduplicates/meta.yml
View file

@ -49,3 +49,4 @@ output:
authors:
- "@ajodeh-juma"
- "@FriederikeHanssen"
- "@maxulysse"

50
modules/gatk4/markduplicatesspark/main.nf Normal file
View file

@ -0,0 +1,50 @@
process GATK4_MARKDUPLICATES_SPARK {
tag "$meta.id"
label 'process_high'
conda (params.enable_conda ? "bioconda::gatk4=4.2.3.0" : null)
container "${ 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' }"
input:
tuple val(meta), path(bam)
path fasta
path fasta_fai
path dict
output:
tuple val(meta), path("${prefix}"), emit: output
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
prefix = task.ext.prefix ?: "${meta.id}"
def input_list = bam.collect{"--input $it"}.join(' ')
def avail_mem = 3
if (!task.memory) {
log.info '[GATK MarkDuplicatesSpark] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
} else {
avail_mem = task.memory.giga
}
"""
export SPARK_USER=spark3
gatk --java-options "-Xmx${avail_mem}g" MarkDuplicatesSpark \\
$input_list \\
--output $prefix \\
--reference $fasta \\
--spark-master local[${task.cpus}] \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
gatk4: \$(echo \$(gatk --version 2>&1) | sed 's/^.*(GATK) v//; s/ .*\$//')
END_VERSIONS
"""
}

60
modules/gatk4/markduplicatesspark/meta.yml Normal file
View file

@ -0,0 +1,60 @@
name: gatk4_markduplicates_spark
description: This tool locates and tags duplicate reads in a BAM or SAM file, where duplicate reads are defined as originating from a single fragment of DNA.
keywords:
- markduplicates
- bam
- sort
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/articles/360037052812-MarkDuplicates-Picard-
tool_dev_url: https://github.com/broadinstitute/gatk
doi: 10.1158/1538-7445.AM2017-3590
licence: ["MIT"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- bam:
type: file
description: Sorted BAM file
pattern: "*.{bam}"
- 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"
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"
- bam:
type: file
description: Marked duplicates BAM file
pattern: "*.{bam}"
authors:
- "@ajodeh-juma"
- "@FriederikeHanssen"
- "@maxulysse"

10
modules/gatk4/mergebamalignment/main.nf
View file

@ -22,6 +22,7 @@ process GATK4_MERGEBAMALIGNMENT {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK MergeBamAlignment] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -30,10 +31,11 @@ process GATK4_MERGEBAMALIGNMENT {
}
"""
gatk --java-options "-Xmx${avail_mem}g" MergeBamAlignment \\
-ALIGNED $aligned \\
-UNMAPPED $unmapped \\
-R $fasta \\
-O ${prefix}.bam \\
--UNMAPPED_BAM $unmapped \\
--ALIGNED_BAM $aligned \\
--OUTPUT ${prefix}.bam \\
--REFERENCE_SEQUENCE $fasta \\
--TMP_DIR . \\
$args
cat <<-END_VERSIONS > versions.yml

8
modules/gatk4/mergemutectstats/main.nf
View file

@ -9,6 +9,7 @@ process GATK4_MERGEMUTECTSTATS {
input:
tuple val(meta), path(stats)
output:
tuple val(meta), path("*.vcf.gz.stats"), emit: stats
path "versions.yml" , emit: versions
@ -19,7 +20,7 @@ process GATK4_MERGEMUTECTSTATS {
script:
def args = task.ext.args ?: ''
prefix = task.ext.prefix ?: "${meta.id}"
def input = stats.collect{ " -stats ${it} "}.join()
def input_list = stats.collect{ "--stats ${it}"}.join(' ')
def avail_mem = 3
if (!task.memory) {
@ -29,8 +30,9 @@ process GATK4_MERGEMUTECTSTATS {
}
"""
gatk --java-options "-Xmx${avail_mem}g" MergeMutectStats \\
${input} \\
-output ${meta.id}.vcf.gz.stats \\
$input_list \\
--output ${prefix}.vcf.gz.stats \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

20
modules/gatk4/mergevcfs/main.nf
View file

@ -8,9 +8,8 @@ process GATK4_MERGEVCFS {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(vcfs)
path ref_dict
val use_ref_dict
tuple val(meta), path(vcf)
path dict
output:
tuple val(meta), path('*.vcf.gz'), emit: vcf
@ -22,13 +21,9 @@ process GATK4_MERGEVCFS {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def input_list = vcf.collect{ "--INPUT $it"}.join(' ')
def reference_command = dict ? "--SEQUENCE_DICTIONARY $dict" : ""
// Make list of VCFs to merge
def input = ""
for (vcf in vcfs) {
input += " I=${vcf}"
}
def ref = use_ref_dict ? "D=${ref_dict}" : ""
def avail_mem = 3
if (!task.memory) {
log.info '[GATK MergeVcfs] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -37,9 +32,10 @@ process GATK4_MERGEVCFS {
}
"""
gatk --java-options "-Xmx${avail_mem}g" MergeVcfs \\
$input \\
O=${prefix}.vcf.gz \\
$ref \\
$input_list \\
--OUTPUT ${prefix}.vcf.gz \\
$reference_command \\
--TMP_DIR . \\
$args
cat <<-END_VERSIONS > versions.yml

44
modules/gatk4/mutect2/main.nf
View file

@ -8,10 +8,7 @@ process GATK4_MUTECT2 {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta) , path(input) , path(input_index) , path(intervals), val(which_norm)
val run_single
val run_pon
val run_mito
tuple val(meta), path(input), path(input_index), path(intervals)
path fasta
path fai
path dict
@ -33,28 +30,10 @@ process GATK4_MUTECT2 {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def panels_command = ''
def normals_command = ''
def inputs_command = '-I ' + input.join( ' -I ')
def interval = intervals ? "-L ${intervals}" : ""
if(run_pon) {
panels_command = ''
normals_command = ''
} else if(run_single) {
panels_command = " --germline-resource $germline_resource --panel-of-normals $panel_of_normals"
normals_command = ''
} else if(run_mito){
panels_command = "-L ${intervals} --mitochondria-mode"
normals_command = ''
} else {
panels_command = " --germline-resource $germline_resource --panel-of-normals $panel_of_normals --f1r2-tar-gz ${prefix}.f1r2.tar.gz"
normals_command = '-normal ' + which_norm.join( ' -normal ')
}
def inputs = input.collect{ "--input $it"}.join(" ")
def interval_command = intervals ? "--intervals $intervals" : ""
def pon_command = panel_of_normals ? "--panel-of-normals $panel_of_normals" : ""
def gr_command = germline_resource ? "--germline-resource $germline_resource" : ""
def avail_mem = 3
if (!task.memory) {
@ -64,12 +43,13 @@ process GATK4_MUTECT2 {
}
"""
gatk --java-options "-Xmx${avail_mem}g" Mutect2 \\
-R ${fasta} \\
${inputs_command} \\
${normals_command} \\
${panels_command} \\
${interval} \\
-O ${prefix}.vcf.gz \\
$inputs \\
--output ${prefix}.vcf.gz \\
--reference $fasta \\
$pon_command \\
$gr_command \\
$interval_command \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

16
modules/gatk4/mutect2/meta.yml
View file

@ -34,22 +34,6 @@ input:
type: File/string
description: Specify region the tools is run on.
pattern: ".{bed,interval_list}/chrM"
- which_norm:
type: list
description: optional list of sample headers contained in the normal sample bam files (these are required for tumor_normal_pair mode)
pattern: "testN"
- run_single:
type: boolean
description: Specify whether or not to run in tumor_single mode instead of tumor_normal_pair mode (will be ignored if run_pon is also true)
pattern: "true/false"
- run_pon:
type: boolean
description: Specify whether or not to run in panel_of_normal mode instead of tumor_normal_pair mode
pattern: "true/false"
- run_mito:
type: boolean
description: Specify whether or not to run in mitochondria-mode instead of tumor_normal_pair mode
pattern: "true/false"
- fasta:
type: file
description: The reference fasta file

6
modules/gatk4/revertsam/main.nf
View file

@ -20,6 +20,7 @@ process GATK4_REVERTSAM {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK RevertSam] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -28,8 +29,9 @@ process GATK4_REVERTSAM {
}
"""
gatk --java-options "-Xmx${avail_mem}g" RevertSam \\
I=$bam \\
O=${prefix}.reverted.bam \\
--INPUT $bam \\
--OUTPUT ${prefix}.reverted.bam \\
--TMP_DIR . \\
$args
cat <<-END_VERSIONS > versions.yml

6
modules/gatk4/samtofastq/main.nf
View file

@ -20,7 +20,8 @@ process GATK4_SAMTOFASTQ {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def output = meta.single_end ? "FASTQ=${prefix}.fastq.gz" : "FASTQ=${prefix}_1.fastq.gz SECOND_END_FASTQ=${prefix}_2.fastq.gz"
def output = meta.single_end ? "--FASTQ ${prefix}.fastq.gz" : "--FASTQ ${prefix}_1.fastq.gz --SECOND_END_FASTQ ${prefix}_2.fastq.gz"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK SamToFastq] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -29,8 +30,9 @@ process GATK4_SAMTOFASTQ {
}
"""
gatk --java-options "-Xmx${avail_mem}g" SamToFastq \\
I=$bam \\
--INPUT $bam \\
$output \\
--TMP_DIR . \\
$args
cat <<-END_VERSIONS > versions.yml

6
modules/gatk4/selectvariants/main.nf
View file

@ -21,6 +21,7 @@ process GATK4_SELECTVARIANTS {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK VariantFiltration] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -29,8 +30,9 @@ process GATK4_SELECTVARIANTS {
}
"""
gatk --java-options "-Xmx${avail_mem}G" SelectVariants \\
-V $vcf \\
-O ${prefix}.selectvariants.vcf.gz \\
--variant $vcf \\
--output ${prefix}.selectvariants.vcf.gz \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

8
modules/gatk4/splitncigarreads/main.nf
View file

@ -23,6 +23,7 @@ process GATK4_SPLITNCIGARREADS {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK SplitNCigarReads] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -31,9 +32,10 @@ process GATK4_SPLITNCIGARREADS {
}
"""
gatk --java-options "-Xmx${avail_mem}g" SplitNCigarReads \\
-R $fasta \\
-I $bam \\
-O ${prefix}.bam \\
--input $bam \\
--output ${prefix}.bam \\
--reference $fasta \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

10
modules/gatk4/variantfiltration/main.nf
View file

@ -8,7 +8,7 @@ process GATK4_VARIANTFILTRATION {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(vcf), path(vcf_tbi)
tuple val(meta), path(vcf), path(tbi)
path fasta
path fai
path dict
@ -24,6 +24,7 @@ process GATK4_VARIANTFILTRATION {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
def avail_mem = 3
if (!task.memory) {
log.info '[GATK VariantFiltration] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
@ -32,9 +33,10 @@ process GATK4_VARIANTFILTRATION {
}
"""
gatk --java-options "-Xmx${avail_mem}G" VariantFiltration \\
-R $fasta \\
-V $vcf \\
-O ${prefix}.vcf.gz \\
--variant $vcf \\
--output ${prefix}.vcf.gz \\
--reference $fasta \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

23
modules/gatk4/variantrecalibrator/main.nf
View file

@ -8,11 +8,11 @@ process GATK4_VARIANTRECALIBRATOR {
'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
input:
tuple val(meta), path(vcf) , path(tbi)
path fasta
path fai
path dict
tuple path(resvcfs), path(restbis), val(reslabels)
tuple val(meta), path(vcf), path(tbi)
tuple path(vcfs), path(tbis), val(labels)
path fasta
path fai
path dict
output:
tuple val(meta), path("*.recal") , emit: recal
@ -27,8 +27,8 @@ process GATK4_VARIANTRECALIBRATOR {
script:
def args = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
refCommand = fasta ? "-R ${fasta} " : ''
resourceCommand = '--resource:' + reslabels.join( ' --resource:')
def reference_command = fasta ? "--reference $fasta " : ''
def resource_command = labels.collect{"--resource:$it"}.join(' ')
def avail_mem = 3
if (!task.memory) {
@ -38,11 +38,12 @@ process GATK4_VARIANTRECALIBRATOR {
}
"""
gatk --java-options "-Xmx${avail_mem}g" VariantRecalibrator \\
${refCommand} \\
-V ${vcf} \\
-O ${prefix}.recal \\
--variant $vcf \\
--output ${prefix}.recal \\
--tranches-file ${prefix}.tranches \\
${resourceCommand} \\
$reference_command \\
$resource_command \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml

6
modules/hisat2/align/main.nf
View file

@ -4,10 +4,10 @@ process HISAT2_ALIGN {
tag "$meta.id"
label 'process_high'
conda (params.enable_conda ? "bioconda::hisat2=2.2.0 bioconda::samtools=1.10" : null)
conda (params.enable_conda ? "bioconda::hisat2=2.2.0 bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-a97e90b3b802d1da3d6958e0867610c718cb5eb1:2880dd9d8ad0a7b221d4eacda9a818e92983128d-0' :
'quay.io/biocontainers/mulled-v2-a97e90b3b802d1da3d6958e0867610c718cb5eb1:2880dd9d8ad0a7b221d4eacda9a818e92983128d-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-a97e90b3b802d1da3d6958e0867610c718cb5eb1:0e773bb207600fcb4d38202226eb20a33c7909b6-0' :
'quay.io/biocontainers/mulled-v2-a97e90b3b802d1da3d6958e0867610c718cb5eb1:0e773bb207600fcb4d38202226eb20a33c7909b6-0' }"
input:
tuple val(meta), path(reads)

10
modules/kaiju/kaiju/main.nf
View file

@ -9,11 +9,11 @@ process KAIJU_KAIJU {
input:
tuple val(meta), path(reads)
tuple path(db), path(dbnodes)
path(db)
output:
tuple val(meta), path('*.tsv'), emit: results
path "versions.yml" , emit: versions
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -23,11 +23,13 @@ process KAIJU_KAIJU {
def prefix = task.ext.prefix ?: "${meta.id}"
def input = meta.single_end ? "-i ${reads}" : "-i ${reads[0]} -j ${reads[1]}"
"""
dbnodes=`find -L ${db} -name "*nodes.dmp"`
dbname=`find -L ${db} -name "*.fmi" -not -name "._*"`
kaiju \\
$args \\
-z $task.cpus \\
-t ${dbnodes} \\
-f ${db} \\
-t \$dbnodes \\
-f \$dbname \\
-o ${prefix}.tsv \\
$input

1
modules/kaiju/kaiju/meta.yml
View file

@ -50,3 +50,4 @@ output:
authors:
- "@talnor"
- "@sofstam"
- "@jfy133"

40
modules/kaiju/kaiju2table/main.nf Normal file
View file

@ -0,0 +1,40 @@
process KAIJU_KAIJU2TABLE {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::kaiju=1.8.2" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/kaiju:1.8.2--h5b5514e_1':
'quay.io/biocontainers/kaiju:1.8.2--h2e03b76_0' }"
input:
tuple val(meta), path(results)
path db
val taxon_rank
output:
tuple val(meta), path('*.txt'), emit: summary
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}"
"""
dbnodes=`find -L ${db} -name "*nodes.dmp"`
dbname=`find -L ${db} -name "*.fmi" -not -name "._*"`
kaiju2table $args \\
-t \$dbnodes \\
-n \$dbname \\
-r ${taxon_rank} \\
-o ${prefix}.txt \\
${results}
cat <<-END_VERSIONS > versions.yml
"${task.process}":
kaiju: \$(echo \$( kaiju -h 2>&1 | sed -n 1p | sed 's/^.*Kaiju //' ))
END_VERSIONS
"""
}

50
modules/kaiju/kaiju2table/meta.yml Normal file
View file

@ -0,0 +1,50 @@
name: "kaiju_kaiju2table"
description: write your description here
keywords:
- classify
- metagenomics
tools:
- kaiju:
description: Fast and sensitive taxonomic classification for metagenomics
homepage: https://kaiju.binf.ku.dk/
documentation: https://github.com/bioinformatics-centre/kaiju/blob/master/README.md
tool_dev_url: https://github.com/bioinformatics-centre/kaiju
doi: "10.1038/ncomms11257"
licence: ["GNU GPL v3"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- results:
type: file
description: File containing the kaiju classification results
pattern: "*.{txt}"
- taxon_rank:
type: string
description: |
Taxonomic rank to display in report
pattern: "phylum|class|order|family|genus|species"
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"
- results:
type: file
description: |
Summary table for a given taxonomic rank
pattern: "*.{tsv}"
authors:
- "@sofstam"
- "@talnor"
- "@jfy133"

23
modules/kraken2/kraken2/main.nf
View file

@ -10,12 +10,15 @@ process KRAKEN2_KRAKEN2 {
input:
tuple val(meta), path(reads)
path db
val save_output_fastqs
val save_reads_assignment
output:
tuple val(meta), path('*classified*') , emit: classified
tuple val(meta), path('*unclassified*'), emit: unclassified
tuple val(meta), path('*report.txt') , emit: txt
path "versions.yml" , emit: versions
tuple val(meta), path('*classified*') , optional:true, emit: classified_reads_fastq
tuple val(meta), path('*unclassified*') , optional:true, emit: unclassified_reads_fastq
tuple val(meta), path('*classifiedreads*'), optional:true, emit: classified_reads_assignment
tuple val(meta), path('*report.txt') , emit: report
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -26,19 +29,25 @@ process KRAKEN2_KRAKEN2 {
def paired = meta.single_end ? "" : "--paired"
def classified = meta.single_end ? "${prefix}.classified.fastq" : "${prefix}.classified#.fastq"
def unclassified = meta.single_end ? "${prefix}.unclassified.fastq" : "${prefix}.unclassified#.fastq"
def classified_command = save_output_fastqs ? "--classified-out ${classified}" : ""
def unclassified_command = save_output_fastqs ? "--unclassified-out ${unclassified}" : ""
def readclassification_command = save_reads_assignment ? "--output ${prefix}.kraken2.classifiedreads.txt" : ""
def compress_reads_command = save_output_fastqs ? "pigz -p $task.cpus *.fastq" : ""
"""
kraken2 \\
--db $db \\
--threads $task.cpus \\
--unclassified-out $unclassified \\
--classified-out $classified \\
--report ${prefix}.kraken2.report.txt \\
--gzip-compressed \\
$unclassified_command \\
$classified_command \\
$readclassification_command \\
$paired \\
$args \\
$reads
pigz -p $task.cpus *.fastq
$compress_reads_command
cat <<-END_VERSIONS > versions.yml
"${task.process}":

25
modules/kraken2/kraken2/meta.yml
View file

@ -27,25 +27,40 @@ input:
- db:
type: directory
description: Kraken2 database
- save_output_fastqs:
type: boolean
description: |
If true, optional commands are added to save classified and unclassified reads
as fastq files
- save_reads_assignment:
type: boolean
description: |
If true, an optional command is added to save a file reporting the taxonomic
classification of each input read
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- classified:
- classified_reads_fastq:
type: file
description: |
Reads classified to belong to any of the taxa
Reads classified as belonging to any of the taxa
on the Kraken2 database.
pattern: "*{fastq.gz}"
- unclassified:
- unclassified_reads_fastq:
type: file
description: |
Reads not classified to belong to any of the taxa
Reads not classified to any of the taxa
on the Kraken2 database.
pattern: "*{fastq.gz}"
- txt:
- classified_reads_assignment:
type: file
description: |
Kraken2 output file indicating the taxonomic assignment of
each input read
- report:
type: file
description: |
Kraken2 report containing stats about classified

5
modules/manta/germline/main.nf
View file

@ -8,11 +8,10 @@ process MANTA_GERMLINE {
'quay.io/biocontainers/manta:1.6.0--h9ee0642_1' }"
input:
tuple val(meta), path(input), path(index)
//Matching the target bed with the input sample allows to parallelize the same sample run across different intervals or a single bed file
tuple val(meta), path(input), path(index), path(target_bed), path(target_bed_tbi)
path fasta
path fasta_fai
tuple path(target_bed), path(target_bed_tbi)
output:
tuple val(meta), path("*candidate_small_indels.vcf.gz") , emit: candidate_small_indels_vcf

38
modules/megan/rma2info/main.nf Normal file
View file

@ -0,0 +1,38 @@
process MEGAN_RMA2INFO {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::megan=6.21.7" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/megan:6.21.7--h9ee0642_0':
'quay.io/biocontainers/megan:6.21.7--h9ee0642_0' }"
input:
tuple val(meta), path(rma6)
val(megan_summary)
output:
tuple val(meta), path("*.txt.gz") , emit: txt
tuple val(meta), path("*.megan"), optional: true, emit: megan_summary
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 summary = megan_summary ? "-es ${prefix}.megan" : ""
"""
rma2info \\
-i ${rma6} \\
-o ${prefix}.txt.gz \\
${summary} \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
megan: \$(echo \$(rma2info 2>&1) | grep version | sed 's/.*version //g;s/, built.*//g')
END_VERSIONS
"""
}

51
modules/megan/rma2info/meta.yml Normal file
View file

@ -0,0 +1,51 @@
name: "megan_rma2info"
description: Analyses an RMA file and exports information in text format
keywords:
- megan
- rma6
- classification
- conversion
tools:
- "megan":
description: "A tool for studying the taxonomic content of a set of DNA reads"
homepage: "https://uni-tuebingen.de/fakultaeten/mathematisch-naturwissenschaftliche-fakultaet/fachbereiche/informatik/lehrstuehle/algorithms-in-bioinformatics/software/megan6/"
documentation: "https://software-ab.informatik.uni-tuebingen.de/download/megan6/welcome.html"
tool_dev_url: "https://github.com/husonlab/megan-ce"
doi: "10.1371/journal.pcbi.1004957"
licence: "['GPL >=3']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- rma6:
type: file
description: RMA6 file from MEGAN or MALT
pattern: "*.rma6"
- megan_summary:
type: boolean
description: Specify whether to generate an MEGAN summary file
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"
- txt:
type: file
description: Compressed text file
pattern: "*.txt.gz"
- megan_summary:
type: file
description: Optionally generated MEGAN summary file
pattern: "*.megan"
authors:
- "@jfy133"

9
modules/picard/collecthsmetrics/main.nf
View file

@ -15,8 +15,8 @@ process PICARD_COLLECTHSMETRICS {
path target_intervals
output:
tuple val(meta), path("*collecthsmetrics.txt"), emit: hs_metrics
path "versions.yml" , emit: versions
tuple val(meta), path("*_metrics") , emit: metrics
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
@ -41,7 +41,8 @@ process PICARD_COLLECTHSMETRICS {
-BAIT_INTERVALS $bait_intervals \\
-TARGET_INTERVALS $target_intervals \\
-INPUT $bam \\
-OUTPUT ${prefix}_collecthsmetrics.txt
-OUTPUT ${prefix}.CollectHsMetrics.coverage_metrics
cat <<-END_VERSIONS > versions.yml
"${task.process}":
@ -52,7 +53,7 @@ process PICARD_COLLECTHSMETRICS {
stub:
def prefix = task.ext.prefix ?: "${meta.id}"
"""
touch ${prefix}_collecthsmetrics.txt
touch ${prefix}.CollectHsMetrics.coverage_metrics
cat <<-END_VERSIONS > versions.yml
"${task.process}":

7
modules/picard/collecthsmetrics/meta.yml
View file

@ -57,10 +57,11 @@ output:
type: file
description: File containing software versions
pattern: "versions.yml"
- hs_metrics:
- metrics:
type: file
description: The metrics file.
pattern: "*_collecthsmetrics.txt"
description: Alignment metrics files generated by picard
pattern: "*_{metrics}"
authors:
- "@projectoriented"
- "@matthdsm"

6
modules/qualimap/bamqccram/main.nf
View file

@ -2,10 +2,10 @@ process QUALIMAP_BAMQCCRAM {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::qualimap=2.2.2d bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::qualimap=2.2.2d bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-d3934ca6bb4e61334891ffa2e9a4c87a530e3188:9838874d42d4477d5042782ee019cec9854da7d5-0' :
'quay.io/biocontainers/mulled-v2-d3934ca6bb4e61334891ffa2e9a4c87a530e3188:9838874d42d4477d5042782ee019cec9854da7d5-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-d3934ca6bb4e61334891ffa2e9a4c87a530e3188:61f6d4658ac88635fc37623af50bba77561988ab-0' :
'quay.io/biocontainers/mulled-v2-d3934ca6bb4e61334891ffa2e9a4c87a530e3188:61f6d4658ac88635fc37623af50bba77561988ab-0' }"
input:
tuple val(meta), path(cram), path(crai)

6
modules/samblaster/main.nf
View file

@ -2,10 +2,10 @@ process SAMBLASTER {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::samblaster=0.1.26 bioconda::samtools=1.14" : null)
conda (params.enable_conda ? "bioconda::samblaster=0.1.26 bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/mulled-v2-19fa9f1a5c3966b63a24166365e81da35738c5ab:ba4a02b56f3e524a6e006bcd99fe8cc1d7fe09eb-0' :
'quay.io/biocontainers/mulled-v2-19fa9f1a5c3966b63a24166365e81da35738c5ab:ba4a02b56f3e524a6e006bcd99fe8cc1d7fe09eb-0' }"
'https://depot.galaxyproject.org/singularity/mulled-v2-19fa9f1a5c3966b63a24166365e81da35738c5ab:fff03944e664bbf9a139f7b174b9cb2d4163271a-0' :
'quay.io/biocontainers/mulled-v2-19fa9f1a5c3966b63a24166365e81da35738c5ab:fff03944e664bbf9a139f7b174b9cb2d4163271a-0' }"
input:
tuple val(meta), path(bam)

6
modules/samtools/ampliconclip/main.nf
View file

@ -2,10 +2,10 @@ process SAMTOOLS_AMPLICONCLIP {
tag "$meta.id"
label 'process_medium'
conda (params.enable_conda ? "bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/samtools:1.15--h1170115_1' :
'quay.io/biocontainers/samtools:1.15--h1170115_1' }"
'https://depot.galaxyproject.org/singularity/samtools:1.15.1--h1170115_0' :
'quay.io/biocontainers/samtools:1.15.1--h1170115_0' }"
input:
tuple val(meta), path(bam)

6
modules/samtools/bam2fq/main.nf
View file

@ -2,10 +2,10 @@ process SAMTOOLS_BAM2FQ {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/samtools:1.15--h1170115_1' :
'quay.io/biocontainers/samtools:1.15--h1170115_1' }"
'https://depot.galaxyproject.org/singularity/samtools:1.15.1--h1170115_0' :
'quay.io/biocontainers/samtools:1.15.1--h1170115_0' }"
input:
tuple val(meta), path(inputbam)

47
modules/samtools/collatefastq/main.nf Normal file
View file

@ -0,0 +1,47 @@
process SAMTOOLS_COLLATEFASTQ {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/samtools:1.15.1--h1170115_0' :
'quay.io/biocontainers/samtools:1.15.1--h1170115_0' }"
input:
tuple val(meta), path(input)
output:
//TODO might be good to have ordered output of the fastq files, so we can
// make sure the we get the right files
tuple val(meta), path("*_{1,2}.fq.gz"), path("*_other.fq.gz"), path("*_singleton.fq.gz"), emit: reads
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
def args2 = task.ext.args ?: ''
def prefix = task.ext.prefix ?: "${meta.id}"
"""
samtools collate \\
$args \\
--threads $task.cpus \\
-O \\
$input \\
. |
samtools fastq \\
$args2 \\
--threads $task.cpus \\
-1 ${prefix}_1.fq.gz \\
-2 ${prefix}_2.fq.gz \\
-0 ${prefix}_other.fq.gz \\
-s ${prefix}_singleton.fq.gz
cat <<-END_VERSIONS > versions.yml
"${task.process}":
samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
END_VERSIONS
"""
}

48
modules/samtools/collatefastq/meta.yml Normal file
View file

@ -0,0 +1,48 @@
name: samtools_collatefastq
description: |
The module uses collate and then fastq methods from samtools to
convert a SAM, BAM or CRAM file to FASTQ format
keywords:
- bam2fq
- samtools
- fastq
tools:
- samtools:
description: Tools for dealing with SAM, BAM and CRAM files
homepage: None
documentation: http://www.htslib.org/doc/1.1/samtools.html
tool_dev_url: None
doi: ""
licence: ["MIT"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- input:
type: file
description: BAM/CRAM/SAM file
pattern: "*.{bam,cram,sam}"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- reads:
type: file
description: |
FASTQ files, which will be either a group of 4 files (read_1, read_2, other and singleton)
or a single interleaved .fq.gz file if the user chooses not to split the reads.
pattern: "*.fq.gz"
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
authors:
- "@lescai"
- "@maxulysse"

6
modules/samtools/depth/main.nf
View file

@ -2,10 +2,10 @@ process SAMTOOLS_DEPTH {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/samtools:1.15--h1170115_1' :
'quay.io/biocontainers/samtools:1.15--h1170115_1' }"
'https://depot.galaxyproject.org/singularity/samtools:1.15.1--h1170115_0' :
'quay.io/biocontainers/samtools:1.15.1--h1170115_0' }"
input:
tuple val(meta), path(bam)

6
modules/samtools/faidx/main.nf
View file

@ -2,10 +2,10 @@ process SAMTOOLS_FAIDX {
tag "$fasta"
label 'process_low'
conda (params.enable_conda ? "bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/samtools:1.15--h1170115_1' :
'quay.io/biocontainers/samtools:1.15--h1170115_1' }"
'https://depot.galaxyproject.org/singularity/samtools:1.15.1--h1170115_0' :
'quay.io/biocontainers/samtools:1.15.1--h1170115_0' }"
input:
tuple val(meta), path(fasta)

6
modules/samtools/fastq/main.nf
View file

@ -2,10 +2,10 @@ process SAMTOOLS_FASTQ {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::samtools=1.15" : null)
conda (params.enable_conda ? "bioconda::samtools=1.15.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/samtools:1.15--h1170115_1' :
'quay.io/biocontainers/samtools:1.15--h1170115_1' }"
'https://depot.galaxyproject.org/singularity/samtools:1.15.1--h1170115_0' :
'quay.io/biocontainers/samtools:1.15.1--h1170115_0' }"
input:
tuple val(meta), path(bam)

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