Merge branch 'nf-core:master' into motus_profile

modules/amplify/predict/main.nf

@@ -0,0 +1,41 @@
+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
+    """
+}

modules/amplify/predict/meta.yml

@@ -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"

modules/antismash/antismashlitedownloaddatabases/main.nf

@@ -0,0 +1,50 @@
+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/created 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.
+    These files are also emitted as output channels in this module to enable the antismash-lite module to use them as mount volumes to the docker/singularity containers.
+    */
+
+    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("css"), emit: css_dir
+    path("detection"), emit: detection_dir
+    path("modules"), emit: modules_dir
+    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-lite: \$(antismash --version | sed 's/antiSMASH //')
+    END_VERSIONS
+    """
+}

modules/antismash/antismashlitedownloaddatabases/meta.yml

@@ -0,0 +1,70 @@
+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 user 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 user 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 user 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"
+  - css_dir:
+      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 user 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"
+  - detection_dir:
+      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 user 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"
+  - modules_dir:
+      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 user 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"
+
+authors:
+  - "@jasmezz"

modules/bclconvert/.gitignore

@@ -0,0 +1,2 @@
+bcl-convert
+*.rpm

modules/bclconvert/Dockerfile

@@ -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

modules/bclconvert/LICENSE

@@ -0,0 +1,30 @@
+ILLUMINA END-USER SOFTWARE LICENSE AGREEMENT
+
+IMPORTANT-READ CAREFULLY. THIS IS A LICENSE AGREEMENT THAT YOU ARE REQUIRED TO ACCEPT BEFORE, DOWNLOADING, INSTALLING AND USING ANY SOFTWARE MADE AVAILABLE FROM THE ILLUMINA SUPPORT CENTER (https://support.illumina.com).
+
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+
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+
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+License Restrictions. Except as expressly permitted in Section 1, Licensee may not make, have made, import, use, copy, reproduce, distribute, display, publish, sell, re-sell, lease, or sub-license the Software, in whole or in part, except as expressly provided for in this Agreement. Licensee may not modify, improve, translate, reverse engineer, decompile, disassemble, or create derivative works of the Software or otherwise attempt to (a) defeat, avoid, by-pass, remove, deactivate, or otherwise circumvent any software protection mechanisms in the Software including, without limitation, any such mechanism used to restrict or control the functionality of the Software, or (b) derive the source code or the underlying ideas, algorithms, structure, or organization form of the Software.  Licensee will not allow, at any time, including during and after the term of the license, the Software or any portions or copies thereof in any form to become available to any third parties.  Licensee may use the Software solely with genomic data that is generated using the Product; Licensee may not use the Software with any data generated from other products or instruments.  Licensee may not use the Software to perform any data analysis services for any third party.
+Ownership. The Software is protected by United States and international intellectual property laws. All right, title, and interest in and to the Software (including associated intellectual property rights) are and will remain vested in Illumina or Illumina’s affiliated companies or licensors. Licensee acknowledges that no rights, license or interest to any Illumina trademarks are granted hereunder. Licensee acknowledges that unauthorized reproduction or distribution of the Software, or any portion of it, may result in severe civil and criminal penalties.  Illumina reserves all rights in and to the Software not expressly granted to Licensee under this Agreement.
+Upgrades/Updates. Illumina may, at its sole discretion, provide updates or upgrades to the Software. In that case, Licensee WILL have the same rights and obligations under such updates or upgrades as it has for the versions of the Software initially provided to Licensee hereunder.  Licensee recognizes that Illumina is not obligated to provide any upgrades or updates to, or support for, the Software.
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+Term of License. This Agreement will be in effect from the time Licensee expressly accepts the terms and conditions of this license, or otherwise installs the Software, thereby accepting the terms and conditions contained herein, and will remain in effect until terminated. This license will otherwise terminate upon the conditions set forth in this Agreement, if revoked by Illumina, or if Licensee fails to comply with any term or condition of this Agreement including failure to pay any applicable license fee. Licensee agrees upon termination of this Agreement for any reason to immediately discontinue use of and un-install the Software and destroy all copies of the Software in its possession and/or under its control, and return or destroy, at Illumina’s option, any compact disks, floppy disks or other media provided by Illumina storing the Software thereon (together with any authorized copies thereof), as well as any documentation associated therewith
+Limited Warranty. Illumina warrants that, for a period of 6 months from the date of download or installation of the Software by Licensee, the Software will perform in all material respects in accordance with the accompanying documentation available on the Illumina Support Center. EXCEPT AND TO THE EXTENT EXPRESSLY PROVIDED IN THE FOREGOING, AND TO THE FULLEST EXTENT PERMITTED BY APPLICABLE LAW, THE SOFTWARE IS PROVIDED “AS IS” AND ILLUMINA EXPRESSLY DISCLAIMS ALL WARRANTIES AND CONDITIONS REGARDING THE SOFTWARE AND RESULTS GENERATED BY THE SOFTWARE, INCLUDING WITHOUT LIMITATION, TO THE FULLEST EXTENT PERMITTED BY APPLICABLE LAW, ALL OTHER EXPRESS OR IMPLIED WARRANTIES OR CONDITIONS OF MERCHANTABLE QUALITY, NON-INFRINGEMENT, AND FITNESS FOR A PARTICULAR PURPOSE, AND THOSE ARISING BY STATUTE OR OTHERWISE IN LAW OR FROM A COURSE OF DEALING OR USAGE OF TRADE.  ILLUMINA DOES NOT WARRANT THAT THE FUNCTIONS CONTAINED IN THE SOFTWARE WILL MEET LICENSEE"S REQUIREMENTS, OR THAT THE OPERATION OF THE SOFTWARE WILL BE ERROR FREE OR UNINTERRUPTED.
+Limitation of Liability.
+(a) ILLUMINA’S ENTIRE LIABILITY AND LICENSEE"S EXCLUSIVE REMEDY UNDER THE LIMITED WARRANTY PROVISION  OF SECTION 7 ABOVE WILL BE, AT ILLUMINA’S OPTION, EITHER (i) RETURN OF THE PRICE PAID FOR THE SOFTWARE, OR (ii) REPAIR OR REPLACEMENT OF THE PORTIONS OF THE SOFTWARE THAT DO NOT COMPLY WITH ILLUMINA’S LIMITED WARRANTY. THIS LIMITED WARRANTY IS VOID AND ILLUMINA WILL HAVE NO LIABILITY AT ALL IF FAILURE OF THE SOFTWARE TO COMPLY WITH ILLUMINA LIMITED WARRANTY HAS RESULTED FROM: (w) FAILURE TO USE THE SOFTWARE IN ACCORDANCE WITH ILLUMINA’S THEN CURRENT USER MANUAL OR THIS AGREEMENT; (x) ACCIDENT, ABUSE, OR MISAPPLICATION; (y) PRODUCTS OR EQUIPMENT NOT SPECIFIED BY ILLUMINA AS BEING COMPATIBLE WITH THE SOFTWARE; OR (z) IF LICENSEE HAS NOT NOTIFIED ILLUMINA IN WRITING OF THE DEFECT WITHIN THE ABOVE WARRANTY PERIOD.
+
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+
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+General. Licensee may not sublicense, assign, share, pledge, rent or transfer any of its rights under this Agreement in relation to the Software or any portion thereof including documentation. Illumina reserves the right to change this Agreement at any time. When Illumina makes any changes, Illumina will provide the updated Agreement, or a link to it, on Illumina’s website (www.illumina.com) and such updated Agreement WILL become effective immediately. Licensee’s continued access to or use of the Software represents Licensee’s agreement to any revised Agreement. If one or more provisions of this Agreement are found to be invalid or unenforceable, this Agreement WILL not be rendered inoperative but the remaining provisions WILL continue in full force and effect.  This Agreement constitutes the entire agreement between the parties with respect to the subject matter of this Agreement and merges all prior communications except that a “hard-copy” form of licensing agreement relating to the Software previously agreed to in writing by Illumina and Licensee WILL supersede and govern in the event of any conflicting provisions.
+Governing Law. This Agreement WILL be governed by and construed in accordance with the laws of the state of California, USA, without regard to its conflicts of laws principles, and independent of where a suit or action hereunder may be filed.
+U.S. Government End Users.  If Licensee is a branch agency or instrumentality of the United States Government, the following provision applies.  The Software is a “commercial item” as that term is defined at 48 C.F.R. 2.101, consisting of “commercial computer software” and “commercial computer software documentation,” as such terms are used in 48 C.F.R. 12.212 or 48 C.F.R. 227.7202 (as applicable).  Consistent with 48 C.F.R. 12.212 and 48 C.F.R. 227.7202-1 through 227.7202-4, all United States Government end users acquire the Software with only those rights set forth herein.
+Contact. Any questions regarding legal rights, duties, obligations, or restrictions associated with the software hereunder should be directed to Illumina, Inc., 5200 Illumina Way, San Diego, CA 92122, Attention: Legal Department, Phone: (858) 202-4500, Fax: (858) 202-4599, web site: www.illumina.com <http://www.illumina.com>.
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+END OF END-USER SOFTWARE LICENSE AGREEMENT.

modules/bclconvert/README.md

@@ -0,0 +1,17 @@
+# 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>
+   ```

modules/bclconvert/main.nf

@@ -0,0 +1,81 @@
+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
+    """
+}

modules/bclconvert/meta.yml

@@ -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"

modules/cat/fastq/main.nf

@@ -4,8 +4,8 @@ process CAT_FASTQ {
 
     conda (params.enable_conda ? "conda-forge::sed=4.7" : null)
     container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
-        'https://containers.biocontainers.pro/s3/SingImgsRepo/biocontainers/v1.2.0_cv1/biocontainers_v1.2.0_cv1.img' :
-        'biocontainers/biocontainers:v1.2.0_cv1' }"
+        'https://depot.galaxyproject.org/singularity/ubuntu:20.04' :
+        'ubuntu:20.04' }"
 
     input:
     tuple val(meta), path(reads, stageAs: "input*/*")

modules/custom/getchromsizes/main.nf

@@ -2,10 +2,10 @@ process CUSTOM_GETCHROMSIZES {
     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:
     path fasta

modules/elprep/filter/main.nf

@@ -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
+    """
+}

modules/elprep/filter/meta.yml

@@ -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"

modules/elprep/split/main.nf

@@ -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
+    """
+}

modules/elprep/split/meta.yml

@@ -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"

modules/gamma/main.nf

@@ -0,0 +1,41 @@
+def VERSION = '2.1' // Version information not provided by tool on CLI
+
+process GAMMA {
+    tag "$meta.id"
+    label 'process_low'
+
+    conda (params.enable_conda ? "bioconda::gamma=2.1" : null)
+    container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
+        'https://depot.galaxyproject.org/singularity/gamma%3A2.1--hdfd78af_0':
+        'quay.io/biocontainers/gamma:2.1--hdfd78af_0' }"
+
+    input:
+    tuple val(meta), path(fasta)
+    path(db)
+
+    output:
+    tuple val(meta), path("*.gamma")                , emit: gamma
+    tuple val(meta), path("*.psl")                  , emit: psl
+    tuple val(meta), path("*.gff")  , optional:true , emit: gff
+    tuple val(meta), path("*.fasta"), optional:true , emit: fasta
+    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}"
+    """
+    GAMMA.py \\
+        $args \\
+        $fasta \\
+        $db \\
+        $prefix
+
+    cat <<-END_VERSIONS > versions.yml
+    "${task.process}":
+        gamma: $VERSION
+    END_VERSIONS
+    """
+}

modules/gamma/meta.yml

@@ -0,0 +1,63 @@
+name: "gamma"
+description: Gene Allele Mutation Microbial Assessment
+keywords:
+  - gamma
+  - gene-calling
+tools:
+  - "gamma":
+      description: "Tool for Gene Allele Mutation Microbial Assessment"
+      homepage: "https://github.com/rastanton/GAMMA"
+      documentation: "https://github.com/rastanton/GAMMA"
+      tool_dev_url: "https://github.com/rastanton/GAMMA"
+      doi: "10.1093/bioinformatics/btab607"
+      licence: "['Apache License 2.0']"
+
+input:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - fasta:
+      type: file
+      description: FASTA file
+      pattern: "*.{fa,fasta}"
+  - db:
+      type: file
+      description: Database in FASTA format
+      pattern: "*.{fa,fasta}"
+
+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"
+
+  - gamma:
+      type: file
+      description: GAMMA file with annotated gene matches
+      pattern: "*.{gamma}"
+
+  - psl:
+      type: file
+      description: PSL file with all gene matches found
+      pattern: "*.{psl}"
+
+  - gff:
+      type: file
+      description: GFF file
+      pattern: "*.{gff}"
+
+  - fasta:
+      type: file
+      description: multifasta file of the gene matches
+      pattern: "*.{fasta}"
+
+authors:
+  - "@sateeshperi"
+  - "@rastanton"

modules/gatk4/haplotypecaller/main.nf

@@ -17,7 +17,7 @@ process GATK4_HAPLOTYPECALLER {
 
     output:
     tuple val(meta), path("*.vcf.gz"), emit: vcf
-    tuple val(meta), path("*.tbi")   , emit: tbi
+    tuple val(meta), path("*.tbi")   , optional:true, emit: tbi
     path "versions.yml"              , emit: versions
 
     when:

modules/gatk4/splitncigarreads/main.nf

@@ -8,7 +8,7 @@ process GATK4_SPLITNCIGARREADS {
         'quay.io/biocontainers/gatk4:4.2.5.0--hdfd78af_0' }"
 
     input:
-    tuple val(meta), path(bam)
+    tuple val(meta), path(bam), path(bai), path(intervals)
     path  fasta
     path  fai
     path  dict
@@ -23,6 +23,7 @@ process GATK4_SPLITNCIGARREADS {
     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) {
@@ -35,6 +36,7 @@ process GATK4_SPLITNCIGARREADS {
         --input $bam \\
         --output ${prefix}.bam \\
         --reference $fasta \\
+        $interval_command \\
         --tmp-dir . \\
         $args
 

modules/gatk4/splitncigarreads/meta.yml

@@ -23,6 +23,13 @@ input:
       type: list
       description: BAM/SAM/CRAM file containing reads
       pattern: "*.{bam,sam,cram}"
+  - bai:
+      type: list
+      description: BAI/SAI/CRAI index file (optional)
+      pattern: "*.{bai,sai,crai}"
+  - intervals:
+      type: file
+      description: Bed file with the genomic regions included in the library (optional)
   - fasta:
       type: file
       description: The reference fasta file

modules/gunzip/main.nf

@@ -4,8 +4,8 @@ process GUNZIP {
 
     conda (params.enable_conda ? "conda-forge::sed=4.7" : null)
     container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
-        'https://containers.biocontainers.pro/s3/SingImgsRepo/biocontainers/v1.2.0_cv1/biocontainers_v1.2.0_cv1.img' :
-        'biocontainers/biocontainers:v1.2.0_cv1' }"
+        'https://depot.galaxyproject.org/singularity/ubuntu:20.04' :
+        'ubuntu:20.04' }"
 
     input:
     tuple val(meta), path(archive)

modules/kaiju/kaiju2table/main.nf

@@ -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
+    """
+}

modules/kaiju/kaiju2table/meta.yml

@@ -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"

modules/kraken2/kraken2/main.nf

@@ -10,11 +10,14 @@ 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
+    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:
@@ -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}":

modules/kraken2/kraken2/meta.yml

@@ -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

modules/minimap2/align/main.nf

@@ -2,17 +2,21 @@ process MINIMAP2_ALIGN {
     tag "$meta.id"
     label 'process_medium'
 
-    conda (params.enable_conda ? 'bioconda::minimap2=2.21' : null)
+    conda (params.enable_conda ? 'bioconda::minimap2=2.21 bioconda::samtools=1.12' : null)
     container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
-        'https://depot.galaxyproject.org/singularity/minimap2:2.21--h5bf99c6_0' :
-        'quay.io/biocontainers/minimap2:2.21--h5bf99c6_0' }"
+        'https://depot.galaxyproject.org/singularity/mulled-v2-66534bcbb7031a148b13e2ad42583020b9cd25c4:1679e915ddb9d6b4abda91880c4b48857d471bd8-0' :
+        'quay.io/biocontainers/mulled-v2-66534bcbb7031a148b13e2ad42583020b9cd25c4:1679e915ddb9d6b4abda91880c4b48857d471bd8-0' }"
 
     input:
     tuple val(meta), path(reads)
     path reference
+    val bam_format
+    val cigar_paf_format
+    val cigar_bam
 
     output:
-    tuple val(meta), path("*.paf"), emit: paf
+    tuple val(meta), path("*.paf"), optional: true, emit: paf
+    tuple val(meta), path("*.bam"), optional: true, emit: bam
     path "versions.yml"           , emit: versions
 
     when:
@@ -22,13 +26,19 @@ process MINIMAP2_ALIGN {
     def args = task.ext.args ?: ''
     def prefix = task.ext.prefix ?: "${meta.id}"
     def input_reads = meta.single_end ? "$reads" : "${reads[0]} ${reads[1]}"
+    def bam_output = bam_format ? "-a | samtools sort | samtools view -@ ${task.cpus} -b -h -o ${prefix}.bam" : "-o ${prefix}.paf"
+    def cigar_paf = cigar_paf_format && !sam_format ? "-c" : ''
+    def set_cigar_bam = cigar_bam && sam_format ? "-L" : ''
     """
     minimap2 \\
         $args \\
         -t $task.cpus \\
         $reference \\
         $input_reads \\
-        > ${prefix}.paf
+        $cigar_paf \\
+        $set_cigar_bam \\
+        $bam_output
+
 
     cat <<-END_VERSIONS > versions.yml
     "${task.process}":

modules/minimap2/align/meta.yml

@@ -29,6 +29,17 @@ input:
       type: file
       description: |
         Reference database in FASTA format.
+  - bam_format:
+      type: boolean
+      description: Specify that output should be in BAM format
+  - cigar_paf_format:
+      type: boolean
+      description: Specify that output CIGAR should be in PAF format
+  - cigar_bam:
+      type: boolean
+      description: |
+        Write CIGAR with >65535 ops at the CG tag. This is recommended when
+        doing XYZ (https://github.com/lh3/minimap2#working-with-65535-cigar-operations)
 output:
   - meta:
       type: map
@@ -39,9 +50,16 @@ output:
       type: file
       description: Alignment in PAF format
       pattern: "*.paf"
+  - bam:
+      type: file
+      description: Alignment in BAM format
+      pattern: "*.bam"
   - versions:
       type: file
       description: File containing software versions
       pattern: "versions.yml"
 authors:
   - "@heuermh"
+  - "@sofstam"
+  - "@sateeshperi"
+  - "@jfy133"

modules/phantompeakqualtools/main.nf

@@ -23,10 +23,11 @@ process PHANTOMPEAKQUALTOOLS {
 
     script:
     def args   = task.ext.args ?: ''
+    def args2  = task.ext.args2 ?: ''
     def prefix = task.ext.prefix ?: "${meta.id}"
     """
     RUN_SPP=`which run_spp.R`
-    Rscript $args -e "library(caTools); source(\\"\$RUN_SPP\\")" -c="$bam" -savp="${prefix}.spp.pdf" -savd="${prefix}.spp.Rdata" -out="${prefix}.spp.out" -p=$task.cpus
+    Rscript $args -e "library(caTools); source(\\"\$RUN_SPP\\")" -c="$bam" -savp="${prefix}.spp.pdf" -savd="${prefix}.spp.Rdata" -out="${prefix}.spp.out" $args2
 
     cat <<-END_VERSIONS > versions.yml
     "${task.process}":

modules/picard/collecthsmetrics/main.nf

@@ -15,7 +15,7 @@ process PICARD_COLLECTHSMETRICS {
     path target_intervals
 
     output:
-    tuple val(meta), path("*collecthsmetrics.txt"), emit: hs_metrics
+    tuple val(meta), path("*_metrics")  , emit: metrics
     path "versions.yml"                 , emit: versions
 
     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}":

modules/picard/collecthsmetrics/meta.yml

@@ -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"

modules/rsem/calculateexpression/main.nf

@@ -2,10 +2,10 @@ process RSEM_CALCULATEEXPRESSION {
     tag "$meta.id"
     label 'process_high'
 
-    conda (params.enable_conda ? "bioconda::rsem=1.3.3 bioconda::star=2.7.6a" : null)
+    conda (params.enable_conda ? "bioconda::rsem=1.3.3 bioconda::star=2.7.10a" : null)
     container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
-        'https://depot.galaxyproject.org/singularity/mulled-v2-cf0123ef83b3c38c13e3b0696a3f285d3f20f15b:606b713ec440e799d53a2b51a6e79dbfd28ecf3e-0' :
-        'quay.io/biocontainers/mulled-v2-cf0123ef83b3c38c13e3b0696a3f285d3f20f15b:606b713ec440e799d53a2b51a6e79dbfd28ecf3e-0' }"
+        'https://depot.galaxyproject.org/singularity/mulled-v2-cf0123ef83b3c38c13e3b0696a3f285d3f20f15b:64aad4a4e144878400649e71f42105311be7ed87-0' :
+        'quay.io/biocontainers/mulled-v2-cf0123ef83b3c38c13e3b0696a3f285d3f20f15b:64aad4a4e144878400649e71f42105311be7ed87-0' }"
 
     input:
     tuple val(meta), path(reads)

modules/rsem/preparereference/main.nf

@@ -2,10 +2,10 @@ process RSEM_PREPAREREFERENCE {
     tag "$fasta"
     label 'process_high'
 
-    conda (params.enable_conda ? "bioconda::rsem=1.3.3 bioconda::star=2.7.6a" : null)
+    conda (params.enable_conda ? "bioconda::rsem=1.3.3 bioconda::star=2.7.10a" : null)
     container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
-        'https://depot.galaxyproject.org/singularity/mulled-v2-cf0123ef83b3c38c13e3b0696a3f285d3f20f15b:606b713ec440e799d53a2b51a6e79dbfd28ecf3e-0' :
-        'quay.io/biocontainers/mulled-v2-cf0123ef83b3c38c13e3b0696a3f285d3f20f15b:606b713ec440e799d53a2b51a6e79dbfd28ecf3e-0' }"
+        'https://depot.galaxyproject.org/singularity/mulled-v2-cf0123ef83b3c38c13e3b0696a3f285d3f20f15b:64aad4a4e144878400649e71f42105311be7ed87-0' :
+        'quay.io/biocontainers/mulled-v2-cf0123ef83b3c38c13e3b0696a3f285d3f20f15b:64aad4a4e144878400649e71f42105311be7ed87-0' }"
 
     input:
     path fasta, stageAs: "rsem/*"

modules/samtools/bamtocram/main.nf

@@ -0,0 +1,35 @@
+//There is a -L option to only output alignments in interval, might be an option for exons/panel data?
+process SAMTOOLS_BAMTOCRAM {
+    tag "$meta.id"
+    label 'process_medium'
+
+    conda (params.enable_conda ? "bioconda::samtools=1.15.1" : null)
+    container "${ 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), path(index)
+    path  fasta
+    path  fai
+
+    output:
+    tuple val(meta), path("*.cram"), path("*.crai"), emit: cram_crai
+    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}"
+    """
+    samtools view --threads ${task.cpus} --reference ${fasta} -C $args $input > ${prefix}.cram
+    samtools index -@${task.cpus} ${prefix}.cram
+
+    cat <<-END_VERSIONS > versions.yml
+    "${task.process}":
+        samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
+    END_VERSIONS
+    """
+}

modules/samtools/bamtocram/meta.yml

@@ -0,0 +1,52 @@
+name: samtools_bamtocram
+description: filter/convert and then index CRAM file
+keywords:
+  - view
+  - index
+  - bam
+  - cram
+tools:
+  - samtools:
+      description: |
+        SAMtools is a set of utilities for interacting with and post-processing
+        short DNA sequence read alignments in the SAM, BAM and CRAM formats, written by Heng Li.
+        These files are generated as output by short read aligners like BWA.
+      homepage: http://www.htslib.org/
+      documentation: hhttp://www.htslib.org/doc/samtools.html
+      doi: 10.1093/bioinformatics/btp352
+      licence: ["MIT"]
+input:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - input:
+      type: file
+      description: BAM/SAM file
+      pattern: "*.{bam,sam}"
+  - index:
+      type: file
+      description: BAM/SAM index file
+      pattern: "*.{bai,sai}"
+  - fasta:
+      type: file
+      description: Reference file to create the CRAM file
+      pattern: "*.{fasta,fa}"
+output:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - cram_crai:
+      type: file
+      description: filtered/converted CRAM file + index
+      pattern: "*{.cram,.crai}"
+  - version:
+      type: file
+      description: File containing software version
+      pattern: "*.{version.txt}"
+authors:
+  - "@FriederikeHanssen"
+  - "@maxulysse"

modules/samtools/collatefastq/main.nf

@@ -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
+    """
+}

modules/samtools/collatefastq/meta.yml

@@ -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"

modules/samtools/view/main.nf

@@ -8,7 +8,7 @@ process SAMTOOLS_VIEW {
         'quay.io/biocontainers/samtools:1.15.1--h1170115_0' }"
 
     input:
-    tuple val(meta), path(input)
+    tuple val(meta), path(input), path(index)
     path fasta
 
     output:

modules/samtools/view/meta.yml

@@ -25,6 +25,10 @@ input:
       type: file
       description: BAM/CRAM/SAM file
       pattern: "*.{bam,cram,sam}"
+  - index:
+      type: optional file
+      description: BAM.BAI/CRAM.CRAI file
+      pattern: "*.{.bai,.crai}"
   - fasta:
       type: optional file
       description: Reference file the CRAM was created with

modules/stranger/main.nf

@@ -9,6 +9,7 @@ process STRANGER {
 
     input:
     tuple val(meta), path(vcf)
+    path variant_catalog
 
     output:
     tuple val(meta), path("*.gz"), emit: vcf
@@ -20,10 +21,23 @@ process STRANGER {
     script:
     def args = task.ext.args ?: ''
     def prefix = task.ext.prefix ?: "${meta.id}"
+    def options_variant_catalog = variant_catalog ? "--repeats-file $variant_catalog" : ""
     """
     stranger \\
         $args \\
-        $vcf | gzip --no-name > ${prefix}.vcf.gz
+        $vcf \\
+        $options_variant_catalog | gzip --no-name > ${prefix}.vcf.gz
+
+    cat <<-END_VERSIONS > versions.yml
+    "${task.process}":
+        stranger: \$( stranger --version )
+    END_VERSIONS
+    """
+
+    stub:
+    def prefix = task.ext.prefix ?: "${meta.id}"
+    """
+    touch ${prefix}.vcf.gz
 
     cat <<-END_VERSIONS > versions.yml
     "${task.process}":

modules/stranger/meta.yml

@@ -24,6 +24,10 @@ input:
       type: file
       description: VCF with repeat expansions
       pattern: "*.{vcf.gz,vcf}"
+  - variant_catalog:
+      type: file
+      description: json file with repeat expansion sites to genotype
+      pattern: "*.{json}"
 
 output:
   - meta:

modules/stringtie/merge/main.nf

@@ -2,10 +2,10 @@ process STRINGTIE_MERGE {
     label 'process_medium'
 
     // Note: 2.7X indices incompatible with AWS iGenomes.
-    conda     (params.enable_conda ? "bioconda::stringtie=2.1.7" : null)
+    conda     (params.enable_conda ? "bioconda::stringtie=2.2.1" : null)
     container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
-        'https://depot.galaxyproject.org/singularity/stringtie:2.1.7--h978d192_0' :
-        'quay.io/biocontainers/stringtie:2.1.7--h978d192_0' }"
+        'https://depot.galaxyproject.org/singularity/stringtie:2.2.1--hecb563c_2' :
+        'quay.io/biocontainers/stringtie:2.2.1--hecb563c_2' }"
 
     input:
     path stringtie_gtf

modules/stringtie/stringtie/main.nf

@@ -1,11 +1,11 @@
-process STRINGTIE {
+process STRINGTIE_STRINGTIE {
     tag "$meta.id"
     label 'process_medium'
 
-    conda (params.enable_conda ? "bioconda::stringtie=2.1.7" : null)
+    conda (params.enable_conda ? "bioconda::stringtie=2.2.1" : null)
     container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
-        'https://depot.galaxyproject.org/singularity/stringtie:2.1.7--h978d192_0' :
-        'quay.io/biocontainers/stringtie:2.1.7--h978d192_0' }"
+        'https://depot.galaxyproject.org/singularity/stringtie:2.2.1--hecb563c_2' :
+        'quay.io/biocontainers/stringtie:2.2.1--hecb563c_2' }"
 
     input:
     tuple val(meta), path(bam)

modules/stringtie/stringtie/meta.yml

@@ -1,4 +1,4 @@
-name: stringtie
+name: stringtie_stringtie
 description: Transcript assembly and quantification for RNA-Se
 keywords:
   - transcript

modules/tabix/bgzip/main.nf

@@ -11,7 +11,7 @@ process TABIX_BGZIP {
     tuple val(meta), path(input)
 
     output:
-    tuple val(meta), path("*.gz"), emit: gz
+    tuple val(meta), path("${prefix}*"), emit: output
     path  "versions.yml"               , emit: versions
 
     when:
@@ -19,9 +19,12 @@ process TABIX_BGZIP {
 
     script:
     def args = task.ext.args ?: ''
-    def prefix = task.ext.prefix ?: "${meta.id}"
+    prefix   = task.ext.prefix ?: "${meta.id}"
+    in_bgzip = input.toString().endsWith(".gz")
+    command1 = in_bgzip ? '-d' : '-c'
+    command2 = in_bgzip ? ''   : " > ${prefix}.${input.getExtension()}.gz"
     """
-    bgzip -c $args $input > ${prefix}.${input.getExtension()}.gz
+    bgzip $command1 $args -@${task.cpus} $input $command2
 
     cat <<-END_VERSIONS > versions.yml
     "${task.process}":

modules/tabix/bgzip/meta.yml

@@ -1,13 +1,14 @@
 name: tabix_bgzip
-description: Compresses files
+description: Compresses/decompresses files
 keywords:
   - compress
+  - decompress
   - bgzip
   - tabix
 tools:
   - bgzip:
       description: |
-        Bgzip compresses files in a similar manner to, and compatible with, gzip.
+        Bgzip compresses or decompresses files in a similar manner to, and compatible with, gzip.
       homepage: https://www.htslib.org/doc/tabix.html
       documentation: http://www.htslib.org/doc/bgzip.html
       doi: 10.1093/bioinformatics/btp352
@@ -18,19 +19,19 @@ input:
       description: |
         Groovy Map containing sample information
         e.g. [ id:'test', single_end:false ]
-  - file:
+  - input:
       type: file
-      description: text file
+      description: file to compress or to decompress
 output:
   - meta:
       type: map
       description: |
         Groovy Map containing sample information
         e.g. [ id:'test', single_end:false ]
-  - file:
+  - output:
       type: file
-      description: Output compressed file
-      pattern: "*.{gz}"
+      description: Output compressed/decompressed file
+      pattern: "*."
   - versions:
       type: file
       description: File containing software versions

modules/tiddit/sv/main.nf

@@ -24,7 +24,7 @@ process TIDDIT_SV {
     script:
     def args = task.ext.args ?: ''
     def prefix = task.ext.prefix ?: "${meta.id}"
-    def reference = fasta == "dummy_file.txt" ? "--ref $fasta" : ""
+    def reference = fasta ? "--ref $fasta" : ""
     """
     tiddit \\
         --sv \\

modules/trimgalore/main.nf

@@ -11,12 +11,13 @@ process TRIMGALORE {
     tuple val(meta), path(reads)
 
     output:
-    tuple val(meta), path("*.fq.gz")    , emit: reads
-    tuple val(meta), path("*report.txt"), emit: log
+    tuple val(meta), path("*{trimmed,val}*.fq.gz"), emit: reads
+    tuple val(meta), path("*report.txt")          , emit: log
     path "versions.yml"                           , emit: versions
 
-    tuple val(meta), path("*.html"), emit: html optional true
-    tuple val(meta), path("*.zip") , emit: zip optional true
+    tuple val(meta), path("*unpaired*.fq.gz")     , emit: unpaired, optional: true
+    tuple val(meta), path("*.html")               , emit: html    , optional: true
+    tuple val(meta), path("*.zip")                , emit: zip     , optional: true
 
     when:
     task.ext.when == null || task.ext.when
@@ -52,6 +53,7 @@ process TRIMGALORE {
             $c_r1 \\
             $tpc_r1 \\
             ${prefix}.fastq.gz
+
         cat <<-END_VERSIONS > versions.yml
         "${task.process}":
             trimgalore: \$(echo \$(trim_galore --version 2>&1) | sed 's/^.*version //; s/Last.*\$//')
@@ -73,6 +75,7 @@ process TRIMGALORE {
             $tpc_r2 \\
             ${prefix}_1.fastq.gz \\
             ${prefix}_2.fastq.gz
+
         cat <<-END_VERSIONS > versions.yml
         "${task.process}":
             trimgalore: \$(echo \$(trim_galore --version 2>&1) | sed 's/^.*version //; s/Last.*\$//')

modules/trimgalore/meta.yml

@@ -37,6 +37,11 @@ output:
         List of input adapter trimmed FastQ files of size 1 and 2 for
         single-end and paired-end data, respectively.
       pattern: "*.{fq.gz}"
+  - unpaired:
+      type: file
+      description: |
+        FastQ files containing unpaired reads from read 1 or read 2
+      pattern: "*unpaired*.fq.gz"
   - html:
       type: file
       description: FastQC report (optional)

modules/untar/main.nf

@@ -2,10 +2,10 @@ process UNTAR {
     tag "$archive"
     label 'process_low'
 
-    conda (params.enable_conda ? "conda-forge::tar=1.34" : null)
+    conda (params.enable_conda ? "conda-forge::sed=4.7" : null)
     container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
-        'https://containers.biocontainers.pro/s3/SingImgsRepo/biocontainers/v1.2.0_cv2/biocontainers_v1.2.0_cv2.img' :
-        'biocontainers/biocontainers:v1.2.0_cv2' }"
+        'https://depot.galaxyproject.org/singularity/ubuntu:20.04' :
+        'ubuntu:20.04' }"
 
     input:
     tuple val(meta), path(archive)

tests/config/pytest_modules.yml

@@ -26,6 +26,10 @@ allelecounter:
   - modules/allelecounter/**
   - tests/modules/allelecounter/**
 
+amplify/predict:
+  - modules/amplify/predict/**
+  - tests/modules/amplify/predict/**
+
 amps:
   - modules/amps/**
   - tests/modules/amps/**
@@ -38,6 +42,10 @@ amrfinderplus/update:
   - modules/amrfinderplus/update/**
   - tests/modules/amrfinderplus/update/**
 
+antismash/antismashlitedownloaddatabases:
+  - modules/antismash/antismashlitedownloaddatabases/**
+  - tests/modules/antismash/antismashlitedownloaddatabases/**
+
 arriba:
   - modules/arriba/**
   - tests/modules/arriba/**
@@ -166,6 +174,10 @@ bcftools/view:
   - modules/bcftools/view/**
   - tests/modules/bcftools/view/**
 
+bclconvert:
+  - modules/bclconvert/**
+  - tests/modules/bclconvert/**
+
 bedtools/bamtobed:
   - modules/bedtools/bamtobed/**
   - tests/modules/bedtools/bamtobed/**
@@ -587,6 +599,14 @@ ectyper:
   - modules/ectyper/**
   - tests/modules/ectyper/**
 
+elprep/filter:
+  - modules/elprep/filter/**
+  - tests/modules/elprep/filter/**
+
+elprep/split:
+  - modules/elprep/split/**
+  - tests/modules/elprep/split/**
+
 emmtyper:
   - modules/emmtyper/**
   - tests/modules/emmtyper/**
@@ -655,10 +675,18 @@ freebayes:
   - modules/freebayes/**
   - tests/modules/freebayes/**
 
+gamma:
+  - modules/gamma/**
+  - tests/modules/gamma/**
+
 gatk4/applybqsr:
   - modules/gatk4/applybqsr/**
   - tests/modules/gatk4/applybqsr/**
 
+gatk4/applybqsrspark:
+  - modules/gatk4/applybqsrspark/**
+  - tests/modules/gatk4/applybqsrspark/**
+
 gatk4/applyvqsr:
   - modules/gatk4/applyvqsr/**
   - tests/modules/gatk4/applyvqsr/**
@@ -667,6 +695,10 @@ gatk4/baserecalibrator:
   - modules/gatk4/baserecalibrator/**
   - tests/modules/gatk4/baserecalibrator/**
 
+gatk4/baserecalibratorspark:
+  - modules/gatk4/baserecalibratorspark/**
+  - tests/modules/gatk4/baserecalibratorspark/**
+
 gatk4/bedtointervallist:
   - modules/gatk4/bedtointervallist/**
   - tests/modules/gatk4/bedtointervallist/**
@@ -743,6 +775,10 @@ gatk4/markduplicates:
   - modules/gatk4/markduplicates/**
   - tests/modules/gatk4/markduplicates/**
 
+gatk4/markduplicatesspark:
+  - modules/gatk4/markduplicatesspark/**
+  - tests/modules/gatk4/markduplicatesspark/**
+
 gatk4/mergebamalignment:
   - modules/gatk4/mergebamalignment/**
   - tests/modules/gatk4/mergebamalignment/**
@@ -977,6 +1013,10 @@ kaiju/kaiju:
   - modules/kaiju/kaiju/**
   - tests/modules/kaiju/kaiju/**
 
+kaiju/kaiju2table:
+  - modules/kaiju/kaiju2table/**
+  - tests/modules/kaiju/kaiju2table/**
+
 kallisto/index:
   - modules/kallisto/index/**
   - tests/modules/kallisto/index/**
@@ -1559,6 +1599,14 @@ samtools/bam2fq:
   - modules/samtools/bam2fq/**
   - tests/modules/samtools/bam2fq/**
 
+samtools/bamtocram:
+  - modules/samtools/bamtocram/**
+  - tests/modules/samtools/bamtocram/**
+
+samtools/collatefastq:
+  - modules/samtools/collatefastq/**
+  - tests/modules/samtools/collatefastq/**
+
 samtools/depth:
   - modules/samtools/depth/**
   - tests/modules/samtools/depth/**

tests/config/test_data.config

@@ -112,6 +112,7 @@ params {
         }
         'homo_sapiens' {
             'genome' {
+                genome_elfasta                                 = "${test_data_dir}/genomics/homo_sapiens/genome/genome.elfasta"
                 genome_fasta                                   = "${test_data_dir}/genomics/homo_sapiens/genome/genome.fasta"
                 genome_fasta_fai                               = "${test_data_dir}/genomics/homo_sapiens/genome/genome.fasta.fai"
                 genome_dict                                    = "${test_data_dir}/genomics/homo_sapiens/genome/genome.dict"
@@ -123,6 +124,7 @@ params {
                 genome_header                                  = "${test_data_dir}/genomics/homo_sapiens/genome/genome.header"
                 genome_bed_gz                                  = "${test_data_dir}/genomics/homo_sapiens/genome/genome.bed.gz"
                 genome_bed_gz_tbi                              = "${test_data_dir}/genomics/homo_sapiens/genome/genome.bed.gz.tbi"
+                genome_elsites                                 = "${test_data_dir}/genomics/homo_sapiens/genome/genome.elsites"
                 transcriptome_fasta                            = "${test_data_dir}/genomics/homo_sapiens/genome/transcriptome.fasta"
                 genome2_fasta                                  = "${test_data_dir}/genomics/homo_sapiens/genome/genome2.fasta"
                 genome_chain_gz                                = "${test_data_dir}/genomics/homo_sapiens/genome/genome.chain.gz"
@@ -136,6 +138,7 @@ params {
                 genome_21_multi_interval_bed_gz_tbi            = "${test_data_dir}/genomics/homo_sapiens/genome/chr21/sequence/multi_intervals.bed.gz.tbi"
                 genome_21_chromosomes_dir                      = "${test_data_dir}/genomics/homo_sapiens/genome/chr21/sequence/chromosomes.tar.gz"
 
+                dbsnp_146_hg38_elsites                         = "${test_data_dir}/genomics/homo_sapiens/genome/vcf/dbsnp_146.hg38.elsites"
                 dbsnp_146_hg38_vcf_gz                          = "${test_data_dir}/genomics/homo_sapiens/genome/vcf/dbsnp_146.hg38.vcf.gz"
                 dbsnp_146_hg38_vcf_gz_tbi                      = "${test_data_dir}/genomics/homo_sapiens/genome/vcf/dbsnp_146.hg38.vcf.gz.tbi"
                 gnomad_r2_1_1_vcf_gz                           = "${test_data_dir}/genomics/homo_sapiens/genome/vcf/gnomAD.r2.1.1.vcf.gz"
@@ -242,8 +245,8 @@ params {
                 test2_2_fastq_gz                               = "${test_data_dir}/genomics/homo_sapiens/illumina/fastq/test2_2.fastq.gz"
                 test2_umi_1_fastq_gz                           = "${test_data_dir}/genomics/homo_sapiens/illumina/fastq/test2.umi_1.fastq.gz"
                 test2_umi_2_fastq_gz                           = "${test_data_dir}/genomics/homo_sapiens/illumina/fastq/test2.umi_2.fastq.gz"
-                test_rnaseq_1_fastq_gz                         = "${test_data_dir}/genomics/homo_sapiens/illumina/fastq/test.rnaseq_1.fastq.gz"
-                test_rnaseq_2_fastq_gz                         = "${test_data_dir}/genomics/homo_sapiens/illumina/fastq/test.rnaseq_2.fastq.gz"
+                test_rnaseq_1_fastq_gz                         = "${test_data_dir}/genomics/homo_sapiens/illumina/fastq/test_rnaseq_1.fastq.gz"
+                test_rnaseq_2_fastq_gz                         = "${test_data_dir}/genomics/homo_sapiens/illumina/fastq/test_rnaseq_2.fastq.gz"
 
                 test_baserecalibrator_table                    = "${test_data_dir}/genomics/homo_sapiens/illumina/gatk/test.baserecalibrator.table"
                 test2_baserecalibrator_table                   = "${test_data_dir}/genomics/homo_sapiens/illumina/gatk/test2.baserecalibrator.table"
@@ -332,6 +335,7 @@ params {
         'bacteroides_fragilis' {
             'genome' {
                 genome_fna_gz                   = "${test_data_dir}/genomics/prokaryotes/bacteroides_fragilis/genome/genome.fna.gz"
+                genome_gbff_gz                  = "${test_data_dir}/genomics/prokaryotes/bacteroides_fragilis/genome/genome.gbff.gz"
                 genome_paf                      = "${test_data_dir}/genomics/prokaryotes/bacteroides_fragilis/genome/genome.paf"
                 genome_mapping_potential_arg    = "${test_data_dir}/genomics/prokaryotes/bacteroides_fragilis/genome/genome.mapping.potential.ARG"
 

tests/modules/amplify/predict/main.nf

@@ -0,0 +1,18 @@
+#!/usr/bin/env nextflow
+
+nextflow.enable.dsl = 2
+
+include { PRODIGAL } from '../../../modules/prodigal/main.nf' addParams( options: [:] )
+include { AMPLIFY_PREDICT } from '../../../../modules/amplify/predict/main.nf' addParams( options: [:] )
+
+workflow amplify_predict {
+    
+    input = [
+        [ id:'test', single_end:false ], // meta map
+        file(params.test_data['sarscov2']['illumina']['contigs_fasta'], checkIfExists: true)
+    ]
+    model_dir = []
+
+    PRODIGAL ( input, "gff" )
+    AMPLIFY_PREDICT ( PRODIGAL.out.amino_acid_fasta, model_dir)
+}

tests/modules/amplify/predict/nextflow.config

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

tests/modules/amplify/predict/test.yml

@@ -0,0 +1,9 @@
+- name: amplify predict amplify_predict
+  command: nextflow run tests/modules/amplify/predict -entry amplify_predict -c tests/config/nextflow.config
+  tags:
+    - amplify/predict
+    - amplify
+  files:
+    - path: output/amplify/test.tsv
+      md5sum: 1951084ce1d410028be86754997e5852
+    - path: output/amplify/versions.yml

tests/modules/antismash/antismashlitedownloaddatabases/main.nf

@@ -0,0 +1,29 @@
+#!/usr/bin/env nextflow
+
+nextflow.enable.dsl = 2
+
+include { UNTAR as UNTAR1 } from '../../../../modules/untar/main.nf'
+include { UNTAR as UNTAR2 } from '../../../../modules/untar/main.nf'
+include { UNTAR as UNTAR3 } from '../../../../modules/untar/main.nf'
+include { ANTISMASH_ANTISMASHLITEDOWNLOADDATABASES } from '../../../../modules/antismash/antismashlitedownloaddatabases/main.nf'
+
+workflow test_antismash_antismashlitedownloaddatabases {
+    input1 = [
+        [],
+        file('https://github.com/nf-core/test-datasets/raw/modules/data/delete_me/antismash/css.tar.gz', checkIfExists: true)
+    ]
+    input2 = [
+        [],
+        file('https://github.com/nf-core/test-datasets/raw/modules/data/delete_me/antismash/detection.tar.gz', checkIfExists: true)
+    ]
+    input3 = [
+        [],
+        file('https://github.com/nf-core/test-datasets/raw/modules/data/delete_me/antismash/modules.tar.gz', checkIfExists: true)
+    ]
+
+    UNTAR1 ( input1 )
+    UNTAR2 ( input2 )
+    UNTAR3 ( input3 )
+
+    ANTISMASH_ANTISMASHLITEDOWNLOADDATABASES ( UNTAR1.out.untar.map{ it[1] },  UNTAR2.out.untar.map{ it[1] }, UNTAR3.out.untar.map{ it[1] } )
+}

tests/modules/antismash/antismashlitedownloaddatabases/nextflow.config

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

tests/modules/antismash/antismashlitedownloaddatabases/test.yml

@@ -0,0 +1,17 @@
+- name: antismash antismashlitedownloaddatabases test_antismash_antismashlitedownloaddatabases
+  command: nextflow run tests/modules/antismash/antismashlitedownloaddatabases -entry test_antismash_antismashlitedownloaddatabases -c tests/config/nextflow.config
+  tags:
+    - antismash
+    - antismash/antismashlitedownloaddatabases
+  files:
+    - path: output/antismash/versions.yml
+      md5sum: 24859c67023abab99de295d3675a24b6
+    - path: output/antismash/antismash_db
+    - path: output/antismash/antismash_db/clusterblast
+    - path: output/antismash/antismash_db/clustercompare
+    - path: output/antismash/antismash_db/pfam
+    - path: output/antismash/antismash_db/resfam
+    - path: output/antismash/antismash_db/tigrfam
+    - path: output/antismash/css
+    - path: output/antismash/detection
+    - path: output/antismash/modules

tests/modules/bclconvert/main.nf

@@ -0,0 +1,22 @@
+#!/usr/bin/env nextflow
+
+nextflow.enable.dsl = 2
+
+include { BCLCONVERT } from '../../../modules/bclconvert/main.nf'
+
+process STUB_BCLCONVERT_INPUT {
+    output:
+    path "SampleSheet.csv"          ,emit: samplesheet
+    path "DDMMYY_SERIAL_FLOWCELL"   ,emit: run_dir
+
+    stub:
+    """
+    mkdir DDMMYY_SERIAL_FLOWCELL
+    echo "SampleSheet" > SampleSheet.csv
+    """
+}
+
+workflow test_bclconvert {
+    STUB_BCLCONVERT_INPUT ()
+    BCLCONVERT (STUB_BCLCONVERT_INPUT.out.samplesheet, STUB_BCLCONVERT_INPUT.out.run_dir)
+}

tests/modules/bclconvert/nextflow.config

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

tests/modules/bclconvert/test.yml

@@ -0,0 +1,52 @@
+- name: bclconvert test_bclconvert
+  command: nextflow run tests/modules/bclconvert -entry test_bclconvert -c tests/config/nextflow.config -stub-run
+  tags:
+    - bclconvert
+  files:
+    - path: output/bclconvert/InterOp/InterOp.bin
+      md5sum: d3dea0bb4ab1c8754af324f40b001481
+    - path: output/bclconvert/Logs/Errors.log
+      md5sum: 334645f09074b2597a692e395b716a9c
+    - path: output/bclconvert/Logs/FastqComplete.txt
+      md5sum: a4c4c6ce2d0de67d3b7ac7d1fcb512e4
+    - path: output/bclconvert/Logs/Info.log
+      md5sum: d238822d379f2277cac950ca986cb660
+    - path: output/bclconvert/Logs/Warnings.log
+      md5sum: aeefd2d631817e170f88f25ecaaf4664
+    - path: output/bclconvert/Reports/Adapter_Metrics.csv
+      md5sum: af62e9c7b44940cfd8ea11064a1f42ae
+    - path: output/bclconvert/Reports/Demultiplex_Stats.csv
+      md5sum: d11313931fcaabb5ce159462ad3dd1da
+    - path: output/bclconvert/Reports/IndexMetricsOut.bin
+      md5sum: 6bcee11c8145e3b1059ceaa91d2f5be7
+    - path: output/bclconvert/Reports/Index_Hopping_Counts.csv
+      md5sum: 697e40e0c0d48b4bd25f138ef60b0bde
+    - path: output/bclconvert/Reports/Quality_Metrics.csv
+      md5sum: 3902fd38f6b01f1ce0f0e8724238f8f2
+    - path: output/bclconvert/Reports/RunInfo.xml
+      md5sum: 5bef7c7e76360231b0c4afdfc915fd44
+    - path: output/bclconvert/Reports/SampleSheet.csv
+      md5sum: c579e7d2c9c917c4cfb875a0373c0936
+    - path: output/bclconvert/Reports/Top_Unknown_Barcodes.csv
+      md5sum: 39a5e7f6d21c12d6051afdc8261b6330
+    - path: output/bclconvert/Reports/fastq_list.csv
+      md5sum: 32c51ab10e013fd547928de57361ffcb
+    - path: output/bclconvert/sample1_S1_L001_R1_001.fastq.gz
+      md5sum: 9b831a39755935333f86f167527a094d
+    - path: output/bclconvert/sample1_S1_L001_R2_001.fastq.gz
+      md5sum: 082f4f767b7619f409ca7e752ef482bf
+    - path: output/bclconvert/sample1_S1_L002_R1_001.fastq.gz
+      md5sum: 837764c89db93dfb53cd663c4f26f3d7
+    - path: output/bclconvert/sample1_S1_L002_R2_001.fastq.gz
+      md5sum: 1a42cf6ba0bb8fc7770f278e6d1ab676
+    - path: output/bclconvert/sample2_S2_L001_R1_001.fastq.gz
+      md5sum: 475bc426b7cc48d0551d40e31457dc78
+    - path: output/bclconvert/sample2_S2_L001_R2_001.fastq.gz
+      md5sum: f670ccd7d9352e0e67fe1c1232429d94
+    - path: output/bclconvert/sample2_S2_L002_R1_001.fastq.gz
+      md5sum: ebd5ff6fa5603e7d704b5a10598de58c
+    - path: output/bclconvert/sample2_S2_L002_R2_001.fastq.gz
+      md5sum: 2f83b460f52620d2548c7ef8845b31d7
+    - path: output/stub/SampleSheet.csv
+      md5sum: c579e7d2c9c917c4cfb875a0373c0936
+    - path: output/bclconvert/versions.yml

tests/modules/elprep/filter/main.nf

@@ -0,0 +1,18 @@
+#!/usr/bin/env nextflow
+
+nextflow.enable.dsl = 2
+
+include { ELPREP_FILTER } from '../../../../modules/elprep/filter/main.nf'
+
+workflow test_elprep_filter {
+
+    input = [
+        [ id:'test', single_end:false ], // meta map
+        file(params.test_data['homo_sapiens']['illumina']['test_paired_end_sorted_bam'], checkIfExists: true)
+    ]
+    reference_elfasta = file(params.test_data['homo_sapiens']['genome']['genome_elfasta'], checkIfExists: true)
+    known_sites_elsites = file(params.test_data['homo_sapiens']['genome']['dbsnp_146_hg38_elsites'], checkIfExists: true)
+    target_regions_bed = file(params.test_data['homo_sapiens']['genome']['genome_bed'], checkIfExists: true)
+
+    ELPREP_FILTER ( input, true, true, [],  [], reference_elfasta, known_sites_elsites, target_regions_bed, [], [], true, true)
+}

tests/modules/elprep/filter/nextflow.config

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

tests/modules/elprep/filter/test.yml

@@ -0,0 +1,13 @@
+- name: elprep filter test_elprep_filter
+  command: nextflow run tests/modules/elprep/filter -entry test_elprep_filter -c tests/config/nextflow.config
+  tags:
+    - elprep
+    - elprep/filter
+  files:
+    - path: output/elprep/test.activity_profile.igv
+    - path: output/elprep/test.assembly_regions.igv
+    - path: output/elprep/output/test.bam
+    - path: output/elprep/test.g.vcf.gz
+    - path: output/elprep/test.metrics.txt
+    - path: output/elprep/test.recall
+    - path: output/elprep/versions.yml

tests/modules/elprep/split/main.nf

@@ -0,0 +1,15 @@
+#!/usr/bin/env nextflow
+
+nextflow.enable.dsl = 2
+
+include { ELPREP_SPLIT } from '../../../../modules/elprep/split/main.nf'
+
+workflow test_elprep_split {
+
+    input = [
+        [ id:'test', single_end:false ], // meta map
+        file(params.test_data['homo_sapiens']['illumina']['test_paired_end_sorted_bam'], checkIfExists: true)
+    ]
+
+    ELPREP_SPLIT ( input )
+}

tests/modules/elprep/split/nextflow.config

@@ -0,0 +1,9 @@
+process {
+
+    publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
+
+    withName : ELPREP_SPLIT {
+        ext.args = "--contig-group-size 1 --output-type bam"
+    }
+
+}

tests/modules/elprep/split/test.yml

@@ -0,0 +1,10 @@
+- name: elprep split test_elprep_split
+  command: nextflow run tests/modules/elprep/split -entry test_elprep_split -c tests/config/nextflow.config
+  tags:
+    - elprep
+    - elprep/split
+  files:
+    - path: output/elprep/output/splits/test-group00001.bam
+    - path: output/elprep/output/splits/test-unmapped.bam
+    - path: output/elprep/output/test-spread.bam
+    - path: output/elprep/versions.yml

tests/modules/gamma/main.nf

@@ -0,0 +1,17 @@
+#!/usr/bin/env nextflow
+
+nextflow.enable.dsl = 2
+
+include { GAMMA } from '../../../modules/gamma/main.nf'
+
+workflow test_gamma {
+    
+    input = [
+        [ id:'test', single_end:false ], // meta map
+        file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
+    ]
+
+    db = [ file(params.test_data['sarscov2']['genome']['transcriptome_fasta'], checkIfExists: true) ]
+
+    GAMMA ( input, db )
+}

tests/modules/gamma/nextflow.config

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

tests/modules/gamma/test.yml

@@ -0,0 +1,13 @@
+- name: gamma test_gamma
+  command: nextflow run tests/modules/gamma -entry test_gamma -c tests/config/nextflow.config
+  tags:
+    - gamma
+  files:
+    - path: output/gamma/test.fasta
+      md5sum: df37b48466181311e0a679f3c5878484
+    - path: output/gamma/test.gamma
+      md5sum: 3256708fa517a65ed01d99e0e3c762ae
+    - path: output/gamma/test.psl
+      md5sum: 162a2757ed3b167ae1e0cdb24213f940
+    - path: output/gamma/versions.yml
+      md5sum: 3fefb5b46c94993362243c5f9a472057

tests/modules/gatk4/splitncigarreads/main.nf

@@ -6,7 +6,23 @@ include { GATK4_SPLITNCIGARREADS } from '../../../../modules/gatk4/splitncigarre
 
 workflow test_gatk4_splitncigarreads {
     input = [ [ id:'test' ], // meta map
-              [ file(params.test_data['sarscov2']['illumina']['test_paired_end_bam'], checkIfExists: true) ] 
+                file(params.test_data['sarscov2']['illumina']['test_paired_end_bam'], checkIfExists: true),
+                [],
+                []
+            ]
+
+    fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
+    fai = file(params.test_data['sarscov2']['genome']['genome_fasta_fai'], checkIfExists: true)
+    dict = file(params.test_data['sarscov2']['genome']['genome_dict'], checkIfExists: true)
+
+    GATK4_SPLITNCIGARREADS ( input, fasta, fai, dict )
+}
+
+workflow test_gatk4_splitncigarreads_intervals {
+    input = [ [ id:'test' ], // meta map
+                file(params.test_data['sarscov2']['illumina']['test_paired_end_sorted_bam'], checkIfExists: true),
+                file(params.test_data['sarscov2']['illumina']['test_paired_end_sorted_bam_bai'], checkIfExists: true),
+                file(params.test_data['sarscov2']['genome']['test_bed'], checkIfExists: true)
             ]
     fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
     fai = file(params.test_data['sarscov2']['genome']['genome_fasta_fai'], checkIfExists: true)

tests/modules/gatk4/splitncigarreads/test.yml

@@ -5,5 +5,14 @@
     - gatk4/splitncigarreads
   files:
     - path: output/gatk4/test.bam
-      md5sum: ceed15c0bd64ff5c38d3816905933b0b
+      md5sum: 436d8e31285c6b588bdd1c7f1d07f6f2
+    - path: output/gatk4/versions.yml
+- name: gatk4 splitncigarreads test_gatk4_splitncigarreads_intervals
+  command: nextflow run tests/modules/gatk4/splitncigarreads -entry test_gatk4_splitncigarreads_intervals -c tests/config/nextflow.config
+  tags:
+    - gatk4
+    - gatk4/splitncigarreads
+  files:
+    - path: output/gatk4/test.bam
+      md5sum: cd56e3225950f519fd47164cca60a0bb
     - path: output/gatk4/versions.yml

tests/modules/kaiju/kaiju2table/main.nf

@@ -0,0 +1,21 @@
+#!/usr/bin/env nextflow
+
+nextflow.enable.dsl = 2
+
+include { UNTAR             } from '../../../../modules/untar/main.nf'
+include { KAIJU_KAIJU       } from '../../../../modules/kaiju/kaiju/main.nf'
+include { KAIJU_KAIJU2TABLE } from '../../../../modules/kaiju/kaiju2table/main.nf'
+
+workflow test_kaiju_kaiju_single_end {
+
+    input = [
+        [ id:'test', single_end:true ], // meta map
+        file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true)
+    ]
+    db    = [ [], file(params.test_data['sarscov2']['genome']['kaiju_tar_gz'], checkIfExists: true) ]
+    taxon_rank = "species"
+
+    ch_db = UNTAR ( db )
+    KAIJU_KAIJU ( input, ch_db.untar.map{ it[1] } )
+    KAIJU_KAIJU2TABLE ( KAIJU_KAIJU.out.results, ch_db.untar.map{ it[1] }, taxon_rank )
+}

tests/modules/kaiju/kaiju2table/nextflow.config

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

tests/modules/kaiju/kaiju2table/test.yml

@@ -0,0 +1,9 @@
+- name: kaiju kaiju2table test_kaiju_kaiju_single_end
+  command: nextflow run tests/modules/kaiju/kaiju2table -entry test_kaiju_kaiju_single_end -c tests/config/nextflow.config
+  tags:
+    - kaiju
+    - kaiju/kaiju2table
+  files:
+    - path: output/kaiju/test.txt
+      md5sum: 0d9f8fd36fcf2888296ae12632c5f0a8
+    - path: output/kaiju/versions.yml

tests/modules/kraken2/kraken2/main.nf

@@ -12,7 +12,7 @@ workflow test_kraken2_kraken2_single_end {
     db    = [ [], file(params.test_data['sarscov2']['genome']['kraken2_tar_gz'], checkIfExists: true) ]
 
     UNTAR ( db )
-    KRAKEN2_KRAKEN2 ( input, UNTAR.out.untar.map{ it[1] } )
+    KRAKEN2_KRAKEN2 ( input, UNTAR.out.untar.map{ it[1] }, true, false )
 }
 
 workflow test_kraken2_kraken2_paired_end {
@@ -23,5 +23,15 @@ workflow test_kraken2_kraken2_paired_end {
     db    = [ [], file(params.test_data['sarscov2']['genome']['kraken2_tar_gz'], checkIfExists: true) ]
 
     UNTAR ( db )
-    KRAKEN2_KRAKEN2 ( input, UNTAR.out.untar.map{ it[1] } )
+    KRAKEN2_KRAKEN2 ( input, UNTAR.out.untar.map{ it[1] }, true, false )
+}
+
+workflow test_kraken2_kraken2_classifyreads {
+    input = [ [ id:'test', single_end:true ], // meta map
+              [ file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true) ]
+            ]
+    db    = [ [], file(params.test_data['sarscov2']['genome']['kraken2_tar_gz'], checkIfExists: true) ]
+
+    UNTAR ( db )
+    KRAKEN2_KRAKEN2 ( input, UNTAR.out.untar.map{ it[1] }, false, true )
 }

tests/modules/kraken2/kraken2/test.yml

@@ -1,29 +1,43 @@
-- name: kraken2 kraken2 single-end
-  command: nextflow run ./tests/modules/kraken2/kraken2 -entry test_kraken2_kraken2_single_end -c ./tests/config/nextflow.config -c ./tests/modules/kraken2/kraken2/nextflow.config
+- name: kraken2 kraken2 test_kraken2_kraken2_single_end
+  command: nextflow run tests/modules/kraken2/kraken2 -entry test_kraken2_kraken2_single_end -c tests/config/nextflow.config
   tags:
     - kraken2
     - kraken2/kraken2
   files:
     - path: output/kraken2/test.classified.fastq.gz
-      should_exist: true
-    - path: output/kraken2/test.unclassified.fastq.gz
-      should_exist: true
     - path: output/kraken2/test.kraken2.report.txt
       md5sum: 4227755fe40478b8d7dc8634b489761e
+    - path: output/kraken2/test.unclassified.fastq.gz
+    - path: output/kraken2/versions.yml
+      md5sum: 6e3ad947ac8dee841a89216071c181cc
+    - path: output/untar/versions.yml
 
-- name: kraken2 kraken2 paired-end
-  command: nextflow run ./tests/modules/kraken2/kraken2 -entry test_kraken2_kraken2_paired_end -c ./tests/config/nextflow.config -c ./tests/modules/kraken2/kraken2/nextflow.config
+- name: kraken2 kraken2 test_kraken2_kraken2_paired_end
+  command: nextflow run tests/modules/kraken2/kraken2 -entry test_kraken2_kraken2_paired_end -c tests/config/nextflow.config
   tags:
     - kraken2
     - kraken2/kraken2
   files:
     - path: output/kraken2/test.classified_1.fastq.gz
-      should_exist: true
     - path: output/kraken2/test.classified_2.fastq.gz
-      should_exist: true
-    - path: output/kraken2/test.unclassified_1.fastq.gz
-      should_exist: true
-    - path: output/kraken2/test.unclassified_2.fastq.gz
-      should_exist: true
     - path: output/kraken2/test.kraken2.report.txt
       md5sum: 4227755fe40478b8d7dc8634b489761e
+    - path: output/kraken2/test.unclassified_1.fastq.gz
+    - path: output/kraken2/test.unclassified_2.fastq.gz
+    - path: output/kraken2/versions.yml
+      md5sum: 604482fe7a4519f890fae9c8beb1bd6e
+    - path: output/untar/versions.yml
+
+- name: kraken2 kraken2 test_kraken2_kraken2_classifyreads
+  command: nextflow run tests/modules/kraken2/kraken2 -entry test_kraken2_kraken2_classifyreads -c tests/config/nextflow.config
+  tags:
+    - kraken2
+    - kraken2/kraken2
+  files:
+    - path: output/kraken2/test.kraken2.classifiedreads.txt
+      md5sum: e7a90531f0d8d777316515c36fe4cae0
+    - path: output/kraken2/test.kraken2.report.txt
+      md5sum: 4227755fe40478b8d7dc8634b489761e
+    - path: output/kraken2/versions.yml
+      md5sum: 3488c304259e83c5bea573403293fce9
+    - path: output/untar/versions.yml

tests/modules/minimap2/align/main.nf

@@ -9,8 +9,11 @@ workflow test_minimap2_align_single_end {
               [ file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true)]
             ]
     fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
+    bam_format = true
+    cigar_paf_format = false
+    cigar_bam = false
 
-    MINIMAP2_ALIGN ( input, fasta )
+    MINIMAP2_ALIGN ( input, fasta, bam_format, cigar_paf_format, cigar_bam)
 }
 
 workflow test_minimap2_align_paired_end {
@@ -19,6 +22,9 @@ workflow test_minimap2_align_paired_end {
                 file(params.test_data['sarscov2']['illumina']['test_2_fastq_gz'], checkIfExists: true) ]
             ]
     fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
+    bam_format  = true
+    cigar_paf_format = false
+    cigar_bam = false
 
-    MINIMAP2_ALIGN ( input, fasta )
+    MINIMAP2_ALIGN ( input, fasta, bam_format, cigar_paf_format, cigar_bam )
 }

tests/modules/minimap2/align/test.yml

@@ -1,17 +1,17 @@
-- name: minimap2 align single-end
-  command: nextflow run ./tests/modules/minimap2/align -entry test_minimap2_align_single_end -c ./tests/config/nextflow.config -c ./tests/modules/minimap2/align/nextflow.config
+- name: minimap2 align test_minimap2_align_single_end
+  command: nextflow run tests/modules/minimap2/align -entry test_minimap2_align_single_end -c tests/config/nextflow.config
   tags:
     - minimap2
     - minimap2/align
   files:
-    - path: ./output/minimap2/test.paf
-      md5sum: 70e8cf299ee3ecd33e629d10c1f588ce
+    - path: output/minimap2/test.bam
+    - path: output/minimap2/versions.yml
 
-- name: minimap2 align paired-end
-  command: nextflow run ./tests/modules/minimap2/align -entry test_minimap2_align_paired_end -c ./tests/config/nextflow.config -c ./tests/modules/minimap2/align/nextflow.config
+- name: minimap2 align test_minimap2_align_paired_end
+  command: nextflow run tests/modules/minimap2/align -entry test_minimap2_align_paired_end -c tests/config/nextflow.config
   tags:
     - minimap2
     - minimap2/align
   files:
-    - path: ./output/minimap2/test.paf
-      md5sum: 5e7b55a26bf0ea3a2843423d3e0b9a28
+    - path: output/minimap2/test.bam
+    - path: output/minimap2/versions.yml

tests/modules/picard/collecthsmetrics/test.yml

@@ -5,4 +5,4 @@
     - picard/collecthsmetrics
   files:
     # The file can't be md5'd consistently
-    - path: output/picard/test_collecthsmetrics.txt
+    - path: output/picard/test.CollectHsMetrics.coverage_metrics

tests/modules/rsem/calculateexpression/test.yml

@@ -42,7 +42,7 @@
     - path: output/rsem/rsem/genome.transcripts.fa
       md5sum: 050c521a2719c2ae48267c1e65218f29
     - path: output/rsem/rsem/genomeParameters.txt
-      md5sum: 2fe3a030e1706c3e8cd4df3818e6dd2f
+      md5sum: df5a456e3242520cc36e0083a6a7d9dd
     - path: output/rsem/rsem/sjdbInfo.txt
       md5sum: 5690ea9d9f09f7ff85b7fd47bd234903
     - path: output/rsem/rsem/sjdbList.fromGTF.out.tab
@@ -63,4 +63,4 @@
     - path: output/rsem/test.stat/test.theta
       md5sum: de2e4490c98cc5383a86ae8225fd0a28
     - path: output/rsem/test.transcript.bam
-      md5sum: 7846491086c478858419667d60f18edd
+      md5sum: ed681d39f5700ffc74d6321525330d93

tests/modules/samtools/bamtocram/main.nf

@@ -0,0 +1,17 @@
+#!/usr/bin/env nextflow
+
+nextflow.enable.dsl = 2
+
+include { SAMTOOLS_BAMTOCRAM } from '../../../../modules/samtools/bamtocram/main.nf'
+
+workflow test_samtools_bamtocram {
+
+    input = [ [ id:'test', single_end:false ], // meta map
+                file(params.test_data['sarscov2']['illumina']['test_paired_end_sorted_bam'], checkIfExists: true),
+                file(params.test_data['sarscov2']['illumina']['test_paired_end_sorted_bam_bai'], checkIfExists: true)]
+
+    fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
+    fai   = file(params.test_data['sarscov2']['genome']['genome_fasta_fai'], checkIfExists: true)
+
+    SAMTOOLS_BAMTOCRAM ( input, fasta, fai )
+}

tests/modules/samtools/bamtocram/nextflow.config

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

tests/modules/samtools/bamtocram/test.yml

@@ -0,0 +1,9 @@
+- name: samtools bamtocram test_samtools_bamtocram
+  command: nextflow run ./tests/modules/samtools/bamtocram -entry test_samtools_bamtocram -c ./tests/config/nextflow.config -c ./tests/modules/samtools/bamtocram/nextflow.config
+  tags:
+    - samtools/bamtocram
+    - samtools
+  files:
+    - path: output/samtools/test.cram
+    - path: output/samtools/test.cram.crai
+    - path: output/samtools/versions.yml

tests/modules/samtools/collatefastq/main.nf

@@ -0,0 +1,13 @@
+#!/usr/bin/env nextflow
+
+nextflow.enable.dsl = 2
+
+include { SAMTOOLS_COLLATEFASTQ } from '../../../../modules/samtools/collatefastq/main.nf'
+
+workflow test_samtools_collatefastq {
+    input = [ [ id:'test', single_end:false ], // meta map
+                file(params.test_data['sarscov2']['illumina']['test_paired_end_bam'], checkIfExists: true)
+            ]
+
+    SAMTOOLS_COLLATEFASTQ ( input )
+}

tests/modules/samtools/collatefastq/nextflow.config

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

tests/modules/samtools/collatefastq/test.yml

@@ -0,0 +1,14 @@
+- name: samtools fastq test_samtools_collatefastq
+  command: nextflow run ./tests/modules/samtools/collatefastq -entry test_samtools_collatefastq -c ./tests/config/nextflow.config -c ./tests/modules/samtools/collatefastq/nextflow.config
+  tags:
+    - samtools
+    - samtools/collatefastq
+  files:
+    - path: output/samtools/test_1.fq.gz
+      md5sum: 829732de4e937edca90f27b07e5b501a
+    - path: output/samtools/test_2.fq.gz
+      md5sum: ef27d3809e495620fd93df894280c03a
+    - path: output/samtools/test_other.fq.gz
+      md5sum: 709872fc2910431b1e8b7074bfe38c67
+    - path: output/samtools/test_singleton.fq.gz
+      md5sum: 709872fc2910431b1e8b7074bfe38c67

tests/modules/samtools/view/main.nf

@@ -6,7 +6,8 @@ include { SAMTOOLS_VIEW } from '../../../../modules/samtools/view/main.nf'
 
 workflow test_samtools_view {
     input = [ [ id:'test', single_end:false ], // meta map
-                file(params.test_data['sarscov2']['illumina']['test_paired_end_bam'], checkIfExists: true)
+                file(params.test_data['sarscov2']['illumina']['test_paired_end_bam'], checkIfExists: true),
+                []
             ]
 
     SAMTOOLS_VIEW ( input, [] )

tests/modules/stranger/main.nf

@@ -5,15 +5,26 @@ nextflow.enable.dsl = 2
 include { EXPANSIONHUNTER } from '../../../modules/expansionhunter/main.nf'
 include { STRANGER } from '../../../modules/stranger/main.nf'
 
-workflow test_stranger {
 
-    input = [ [ id:'test', gender:'male' ], // meta map
+input = [ [ id:'test', gender:'male' ], // meta map
             file(params.test_data['homo_sapiens']['illumina']['test_paired_end_sorted_bam'], checkIfExists: true),
             file(params.test_data['homo_sapiens']['illumina']['test_paired_end_sorted_bam_bai'], checkIfExists: true),
         ]
-    fasta = file(params.test_data['homo_sapiens']['genome']['genome_fasta'], checkIfExists: true)
-    variant_catalog = file(params.test_data['homo_sapiens']['genome']['repeat_expansions'], checkIfExists: true)
+fasta = file(params.test_data['homo_sapiens']['genome']['genome_fasta'], checkIfExists: true)
+variant_catalog = file(params.test_data['homo_sapiens']['genome']['repeat_expansions'], checkIfExists: true)
 
+
+workflow test_stranger {
     EXPANSIONHUNTER ( input, fasta, variant_catalog )
-    STRANGER ( EXPANSIONHUNTER.out.vcf )
+    STRANGER ( EXPANSIONHUNTER.out.vcf, variant_catalog )
+}
+
+workflow test_stranger_without_optional_variant_catalog {
+    EXPANSIONHUNTER ( input, fasta, variant_catalog )
+    STRANGER ( EXPANSIONHUNTER.out.vcf, [] )
+}
+
+workflow test_stranger_without_optional_variant_catalog_stubs {
+    EXPANSIONHUNTER ( input, fasta, variant_catalog )
+    STRANGER ( EXPANSIONHUNTER.out.vcf, [] )
 }

tests/modules/stranger/test.yml

@@ -8,6 +8,30 @@
     - path: output/expansionhunter/versions.yml
       md5sum: f3962a6eecfddf9682414c0f605a885a
     - path: output/stranger/test.vcf.gz
-      md5sum: bbe15159195681d5c18596d3ad85c78f
+      md5sum: 68b0ca1319851134ffa8793a4704dc11
     - path: output/stranger/versions.yml
       md5sum: 5ec35fd835fb1be50bc3e7c004310fc0
+
+- name: stranger test_stranger_without_optional_variant_catalog
+  command: nextflow run tests/modules/stranger -entry test_stranger_without_optional_variant_catalog -c tests/config/nextflow.config
+  tags:
+    - stranger
+  files:
+    - path: output/expansionhunter/test.vcf
+      md5sum: cfd4a1d35c0e469b99eb6aaa6d22de76
+    - path: output/expansionhunter/versions.yml
+      md5sum: c95af9e6d8cd9bd2ce1090ca4e7a6020
+    - path: output/stranger/test.vcf.gz
+      md5sum: bbe15159195681d5c18596d3ad85c78f
+    - path: output/stranger/versions.yml
+      md5sum: 8558542a007e90ea5dcdceed3f12585d
+
+- name: stranger test_stranger_without_optional_variant_catalog_stubs
+  command: nextflow run tests/modules/stranger -entry test_stranger_without_optional_variant_catalog -c tests/config/nextflow.config -stub-run
+  tags:
+    - stranger
+  files:
+    - path: output/expansionhunter/test.vcf
+    - path: output/expansionhunter/versions.yml
+    - path: output/stranger/test.vcf.gz
+    - path: output/stranger/versions.yml

tests/modules/stringtie/merge/main.nf

@@ -2,7 +2,7 @@
 
 nextflow.enable.dsl = 2
 
-include { STRINGTIE       } from '../../../../modules/stringtie/stringtie/main.nf'
+include { STRINGTIE_STRINGTIE } from '../../../../modules/stringtie/stringtie/main.nf'
 include { STRINGTIE_MERGE     } from '../../../../modules/stringtie/merge/main.nf'
 
 /*
@@ -15,8 +15,8 @@ workflow test_stringtie_forward_merge {
     ]
     annotation_gtf = file(params.test_data['homo_sapiens']['genome']['genome_gtf'], checkIfExists: true)
 
-    STRINGTIE ( input, annotation_gtf )
-    STRINGTIE
+    STRINGTIE_STRINGTIE ( input, annotation_gtf )
+    STRINGTIE_STRINGTIE
         .out
         .transcript_gtf
         .map { it -> it[1] }
@@ -35,8 +35,8 @@ workflow test_stringtie_reverse_merge {
     ]
     annotation_gtf = file(params.test_data['homo_sapiens']['genome']['genome_gtf'], checkIfExists: true)
 
-    STRINGTIE ( input, annotation_gtf )
-    STRINGTIE
+    STRINGTIE_STRINGTIE ( input, annotation_gtf )
+    STRINGTIE_STRINGTIE
         .out
         .transcript_gtf
         .map { it -> it[1] }

tests/modules/stringtie/merge/test.yml

@@ -5,7 +5,7 @@
     - stringtie/merge
   files:
     - path: output/stringtie/stringtie.merged.gtf
-      md5sum: 9fab7049ef2eafdea246fc787d1def40
+      md5sum: d959eb2fab0db48ded7275e0a2e83c05
     - path: output/stringtie/test.ballgown/e2t.ctab
       md5sum: 9ae42e056c955a88a883e5e917840d77
     - path: output/stringtie/test.ballgown/e_data.ctab
@@ -17,11 +17,10 @@
     - path: output/stringtie/test.ballgown/t_data.ctab
       md5sum: 92a98902784e7406ffe054d2adbabc7c
     - path: output/stringtie/test.coverage.gtf
-      md5sum: d41d8cd98f00b204e9800998ecf8427e
     - path: output/stringtie/test.gene.abundance.txt
-      md5sum: 9708811bcefe0f6384293d6f419f3250
+      md5sum: 8bcd8e2730ed3337e2730186dbc184f3
     - path: output/stringtie/test.transcripts.gtf
-      md5sum: 0e42709bfe30c2c7f2574ba664f5fa9f
+      md5sum: a914bd55b68a4b5f607738b17861e362
 
 - name: stringtie merge test_stringtie_reverse_merge
   command: nextflow run ./tests/modules/stringtie/merge -entry test_stringtie_reverse_merge -c ./tests/config/nextflow.config -c ./tests/modules/stringtie/merge/nextflow.config
@@ -30,7 +29,7 @@
     - stringtie/merge
   files:
     - path: output/stringtie/stringtie.merged.gtf
-      md5sum: afc461bb3cbc368f268a7a45c1b54497
+      md5sum: 6da479298d73d5b3216d4e1576a2bdf4
     - path: output/stringtie/test.ballgown/e2t.ctab
       md5sum: 9ae42e056c955a88a883e5e917840d77
     - path: output/stringtie/test.ballgown/e_data.ctab
@@ -42,8 +41,7 @@
     - path: output/stringtie/test.ballgown/t_data.ctab
       md5sum: 92a98902784e7406ffe054d2adbabc7c
     - path: output/stringtie/test.coverage.gtf
-      md5sum: d41d8cd98f00b204e9800998ecf8427e
     - path: output/stringtie/test.gene.abundance.txt
-      md5sum: 94b85145d60ab1b80a7f0f6cf08418b0
+      md5sum: f289f41b3ba1b9f0aa05d14408f1a5da
     - path: output/stringtie/test.transcripts.gtf
-      md5sum: 3196e3d50fd461aae6408e0a70acae68
+      md5sum: 9dcdc9577c0fdbb25089eda210267546

tests/modules/stringtie/stringtie/main.nf

@@ -2,7 +2,7 @@
 
 nextflow.enable.dsl = 2
 
-include { STRINGTIE } from '../../../../modules/stringtie/stringtie/main.nf'
+include { STRINGTIE_STRINGTIE } from '../../../../modules/stringtie/stringtie/main.nf'
 //
 // Test with forward strandedness
 //
@@ -13,7 +13,7 @@ workflow test_stringtie_forward {
     ]
     annotation_gtf = file(params.test_data['sarscov2']['genome']['genome_gtf'], checkIfExists: true)
 
-    STRINGTIE ( input, annotation_gtf )
+    STRINGTIE_STRINGTIE ( input, annotation_gtf )
 }
 
 //
@@ -26,5 +26,5 @@ workflow test_stringtie_reverse {
     ]
     annotation_gtf = file(params.test_data['sarscov2']['genome']['genome_gtf'], checkIfExists: true)
 
-    STRINGTIE ( input, annotation_gtf )
+    STRINGTIE_STRINGTIE ( input, annotation_gtf )
 }

tests/modules/stringtie/stringtie/test.yml

@@ -8,7 +8,6 @@
     - path: ./output/stringtie/test.gene.abundance.txt
       md5sum: 7d8bce7f2a922e367cedccae7267c22e
     - path: ./output/stringtie/test.coverage.gtf
-      md5sum: d41d8cd98f00b204e9800998ecf8427e
     - path: ./output/stringtie/test.ballgown/e_data.ctab
       md5sum: 6b4cf69bc03f3f69890f972a0e8b7471
     - path: ./output/stringtie/test.ballgown/i_data.ctab
@@ -30,7 +29,6 @@
     - path: ./output/stringtie/test.gene.abundance.txt
       md5sum: 7385b870b955dae2c2ab78a70cf05cce
     - path: ./output/stringtie/test.coverage.gtf
-      md5sum: d41d8cd98f00b204e9800998ecf8427e
     - path: ./output/stringtie/test.ballgown/e_data.ctab
       md5sum: 879b6696029d19c4737b562e9d149218
     - path: ./output/stringtie/test.ballgown/i_data.ctab

tests/modules/tabix/bgzip/main.nf

@@ -4,10 +4,18 @@ nextflow.enable.dsl = 2
 
 include { TABIX_BGZIP } from '../../../../modules/tabix/bgzip/main.nf'
 
-workflow test_tabix_bgzip {
+workflow test_tabix_bgzip_compress {
     input = [ [ id:'test' ], // meta map
               [ file(params.test_data['sarscov2']['illumina']['test_vcf'], checkIfExists: true) ]
             ]
 
     TABIX_BGZIP ( input )
 }
+
+workflow test_tabix_bgzip_decompress {
+    input = [ [ id:'test' ], // meta map
+              [ file(params.test_data['sarscov2']['genome']['test_bed_gz'], checkIfExists: true) ]
+            ]
+
+    TABIX_BGZIP ( input )
+}

tests/modules/tabix/bgzip/test.yml

@@ -1,8 +1,16 @@
-- name: tabix bgzip
-  command: nextflow run ./tests/modules/tabix/bgzip -entry test_tabix_bgzip -c ./tests/config/nextflow.config -c ./tests/modules/tabix/bgzip/nextflow.config
+- name: tabix bgzip compress
+  command: nextflow run ./tests/modules/tabix/bgzip -entry test_tabix_bgzip_compress -c ./tests/config/nextflow.config -c ./tests/modules/tabix/bgzip/nextflow.config
   tags:
     - tabix
     - tabix/bgzip
   files:
     - path: ./output/tabix/test.vcf.gz
       md5sum: fc178eb342a91dc0d1d568601ad8f8e2
+- name: tabix bgzip decompress
+  command: nextflow run ./tests/modules/tabix/bgzip -entry test_tabix_bgzip_decompress -c ./tests/config/nextflow.config -c ./tests/modules/tabix/bgzip/nextflow.config
+  tags:
+    - tabix
+    - tabix/bgzip
+  files:
+    - path: ./output/tabix/test.bed
+      md5sum: fe4053cf4de3aebbdfc3be2efb125a74

tests/modules/tiddit/sv/test.yml

@@ -9,6 +9,7 @@
     - path: output/tiddit/test.signals.tab
       md5sum: dab4b2fec4ddf8eb1c23005b0770150e
     - path: output/tiddit/test.vcf
+      md5sum: bdce14ae8292bf3deb81f6f255baf859
 
 - name: tiddit sv no ref
   command: nextflow run ./tests/modules/tiddit/sv -entry test_tiddit_sv_no_ref -c ./tests/config/nextflow.config -c ./tests/modules/tiddit/sv/nextflow.config
@@ -21,3 +22,4 @@
     - path: output/tiddit/test.signals.tab
       md5sum: dab4b2fec4ddf8eb1c23005b0770150e
     - path: output/tiddit/test.vcf
+      md5sum: 3d0e83a8199b2bdb81cfe3e6b12bf64b