Check if PR works with centrifuge/centrifuge module

.github/workflows/ci.yml

@@ -29,8 +29,16 @@ jobs:
           - NXF_VER: ""
             NXF_EDGE: "1"
         parameters:
+          - "--longread_clip false"
+          - "--shortread_clip false"
           - "--shortread_clipmerge_tool fastp"
+          - "--shortread_clipmerge_tool fastp --shortread_clipmerge_mergepairs --shortread_clipmerge_excludeunmerged"
+          - "--shortread_clipmerge_tool fastp --shortread_clipmerge_mergepairs"
           - "--shortread_clipmerge_tool adapterremoval"
+          - "--shortread_clipmerge_tool adapterremoval --shortread_clipmerge_mergepairs --shortread_clipmerge_excludeunmerged"
+          - "--shortread_clipmerge_tool adapterremoval --shortread_clipmerge_mergepairs"
+          - "--shortread_complexityfilter_tool bbduk"
+          - "--shortread_complexityfilter_tool prinseq"
 
     steps:
       - name: Check out pipeline code

CITATIONS.md

@@ -18,21 +18,27 @@
 
 - [fastp](https://doi.org/10.1093/bioinformatics/bty560)
 
-  > Chen, Shifu, Yanqing Zhou, Yaru Chen, and Jia Gu. 2018. “Fastp: An Ultra-Fast All-in-One FASTQ Preprocessor.” Bioinformatics 34 (17): i884-90. 10.1093/bioinformatics/bty560.
+  > Chen, Shifu, Yanqing Zhou, Yaru Chen, and Jia Gu. 2018. Fastp: An Ultra-Fast All-in-One FASTQ Preprocessor. Bioinformatics 34 (17): i884-90. 10.1093/bioinformatics/bty560.
 
 - [AdapterRemoval2](https://doi.org/10.1186/s13104-016-1900-2)
 
-  > Schubert, Mikkel, Stinus Lindgreen, and Ludovic Orlando. 2016. “AdapterRemoval v2: Rapid Adapter Trimming, Identification, and Read Merging.” BMC Research Notes 9 (February): 88. doi:10.1186/s13104-016-1900-2.
+  > Schubert, Mikkel, Stinus Lindgreen, and Ludovic Orlando. 2016. AdapterRemoval v2: Rapid Adapter Trimming, Identification, and Read Merging. BMC Research Notes 9 (February): 88. doi:10.1186/s13104-016-1900-2.
 
 - [Porechop](https://github.com/rrwick/Porechop)
 
+- [BBTools](http://sourceforge.net/projects/bbmap/)
+
+- [PRINSEQ++](https://doi.org/10.7287/peerj.preprints.27553v1)
+
+  > Cantu, Vito Adrian, Jeffrey Sadural, and Robert Edwards. 2019. PRINSEQ++, a Multi-Threaded Tool for Fast and Efficient Quality Control and Preprocessing of Sequencing Datasets. e27553v1. PeerJ Preprints. doi: 10.7287/peerj.preprints.27553v1.
+
 - [Kraken2](https://doi.org/10.1186/s13059-019-1891-0)
 
-  > Wood, Derrick E., Jennifer Lu, and Ben Langmead. 2019. “Improved Metagenomic Analysis with Kraken 2.” Genome Biology 20 (1): 257. doi: 10.1186/s13059-019-1891-0.
+  > Wood, Derrick E., Jennifer Lu, and Ben Langmead. 2019. Improved Metagenomic Analysis with Kraken 2. Genome Biology 20 (1): 257. doi: 10.1186/s13059-019-1891-0.
 
 - [MALT](https://doi.org/10.1038/s41559-017-0446-6)
 
-  > Vågene, Åshild J., Alexander Herbig, Michael G. Campana, Nelly M. Robles García, Christina Warinner, Susanna Sabin, Maria A. Spyrou, et al. 2018. “Salmonella Enterica Genomes from Victims of a Major Sixteenth-Century Epidemic in Mexico.” Nature Ecology & Evolution 2 (3): 520-28. doi: 10.1038/s41559-017-0446-6.
+  > Vågene, Åshild J., Alexander Herbig, Michael G. Campana, Nelly M. Robles García, Christina Warinner, Susanna Sabin, Maria A. Spyrou, et al. 2018. Salmonella Enterica Genomes from Victims of a Major Sixteenth-Century Epidemic in Mexico. Nature Ecology & Evolution 2 (3): 520-28. doi: 10.1038/s41559-017-0446-6.
 
 - [MetaPhlAn3](https://doi.org/10.7554/eLife.65088)
 

conf/modules.config

@@ -12,12 +12,6 @@
 
 process {
 
-    publishDir = [
-        path: { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" },
-        mode: params.publish_dir_mode,
-        saveAs: { filename -> filename.equals('versions.yml') ? null : filename }
-    ]
-
     withName: SAMPLESHEET_CHECK {
         publishDir = [
             path: { "${params.outdir}/pipeline_info" },
@@ -34,20 +28,12 @@ process {
         ]
     }
 
-    withName: UNTAR {
-        publishDir = [
-            path: { "${params.outdir}/databases" },
-            mode: params.publish_dir_mode,
-            saveAs: { filename -> filename.equals('versions.yml') ? null : filename }
-        ]
-    }
-
     withName: FASTQC {
         ext.args = '--quiet'
         ext.prefix = { "${meta.id}_${meta.run_accession}_raw" }
         publishDir = [
             path: { "${params.outdir}/fastqc/raw" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
             pattern: '*.html'
         ]
     }
@@ -57,7 +43,7 @@ process {
         ext.prefix = { "${meta.id}_${meta.run_accession}_processed" }
         publishDir = [
             path: { "${params.outdir}/fastqc/processed" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
             pattern: '*.html'
         ]
     }
@@ -73,8 +59,9 @@ process {
         ext.prefix = { "${meta.id}_${meta.run_accession}" }
         publishDir = [
             path: { "${params.outdir}/fastp" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
-            pattern: '*.fastq.gz'
+            pattern: '*.fastq.gz',
+            enabled: params.save_preprocessed_reads
         ]
     }
 
@@ -92,8 +79,9 @@ process {
         ext.prefix = { "${meta.id}_${meta.run_accession}" }
         publishDir = [
             path: { "${params.outdir}/fastp" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
-            pattern: '*.fastq.gz'
+            pattern: '*.fastq.gz',
+            enabled: params.save_preprocessed_reads
         ]
     }
 
@@ -108,8 +96,9 @@ process {
         ext.prefix = { "${meta.id}_${meta.run_accession}" }
         publishDir = [
             path: { "${params.outdir}/adapterremoval" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
-            pattern: '*.fastq.gz'
+            pattern: '*.fastq.gz',
+            enabled: params.save_preprocessed_reads
         ]
     }
 
@@ -127,26 +116,48 @@ process {
         ext.prefix = { "${meta.id}_${meta.run_accession}" }
         publishDir = [
             path: { "${params.outdir}/adapterremoval" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
-            pattern: '*.fastq.gz'
+            pattern: '*.fastq.gz',
+            enabled: params.save_preprocessed_reads
         ]
     }
 
-
     withName: PORECHOP {
         ext.prefix = { "${meta.id}_${meta.run_accession}" }
         publishDir = [
             path: { "${params.outdir}/porechop" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
-            pattern: '*.fastq.gz'
+            pattern: '*.fastq.gz',
+            enabled: params.save_preprocessed_reads
         ]
     }
 
-    withName: CAT_FASTQ {
+    withName: BBMAP_BBDUK {
+        ext.args =  [
+                "entropy=${params.shortread_complexityfilter_entropy}",
+                "entropywindow=${params.shortread_complexityfilter_bbduk_windowsize}",
+                params.shortread_complexityfilter_bbduk_mask ?  "entropymask=t" : "entropymask=f"
+            ].join(' ').trim()
+        ext.prefix = { "${meta.id}-${meta.run_accession}" }
         publishDir = [
-            path: { "${params.outdir}/prepared_sequences" },
+            path: { "${params.outdir}/bbduk/" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
-            pattern: '*.fastq.gz'
+            pattern: '*.{fastq.gz,log}',
+            enabled: params.save_complexityfiltered_reads
+        ]
+    }
+
+    withName: PRINSEQPLUSPLUS {
+        ext.args =  [
+                params.shortread_complexityfilter_prinseqplusplus_mode == 'dust' ? "-lc_dust=${params.shortread_complexityfilter_prinseqplusplus_dustscore}" : "-lc_entropy=${params.shortread_complexityfilter_entropy}",
+                "-trim_qual_left=0 -trim_qual_left=0 -trim_qual_window=0 -trim_qual_step=0"
+            ].join(' ').trim()
+        ext.prefix = { "${meta.id}-${meta.run_accession}" }
+        publishDir = [
+            path: { "${params.outdir}/prinseqplusplus/" },
+            mode: params.publish_dir_mode,
+            pattern: '*{_good_out.fastq.gz,_good_out_R1.fastq.gz,_good_out_R2.fastq.gz,log}',
+            enabled: params.save_complexityfiltered_reads
         ]
     }
 
@@ -155,7 +166,7 @@ process {
         ext.prefix = { "${meta.id}-${meta.run_accession}-${meta.db_name}" }
         publishDir = [
             path: { "${params.outdir}/malt/${meta.db_name}" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
             pattern: '*.{rma6,tab,text,sam,log}'
         ]
     }
@@ -165,7 +176,7 @@ process {
         ext.prefix = { "${meta.id}-${meta.run_accession}-${meta.db_name}" }
         publishDir = [
             path: { "${params.outdir}/kraken2/${meta.db_name}" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
             pattern: '*.{fastq.gz,txt}'
         ]
     }
@@ -187,10 +198,10 @@ process {
         ]
     }
 
-    withName: CENTRIFUGE {
+    withName: CENTRIFUGE_CENTRIFUGE {
         publishDir = [
             path: { "${params.outdir}/centrifuge/${meta.db_name}" },
-            mode: 'copy',
+            mode: params.publish_dir_mode,
             pattern: '*.{fastq.gz,txt}'
         ]
         ext.args = { "${meta.db_params}" }

conf/test.config

@@ -22,12 +22,13 @@ params {
     // Input data
     // TODO nf-core: Specify the paths to your test data on nf-core/test-datasets
     // TODO nf-core: Give any required params for the test so that command line flags are not needed
-    input               = 'https://raw.githubusercontent.com/nf-core/test-datasets/taxprofiler/samplesheet.csv'
+    input                         = 'https://raw.githubusercontent.com/nf-core/test-datasets/taxprofiler/samplesheet.csv'
-    databases           = 'https://raw.githubusercontent.com/nf-core/test-datasets/taxprofiler/database.csv'
+    databases                     = 'https://raw.githubusercontent.com/nf-core/test-datasets/taxprofiler/database.csv'
-    run_kraken2         = true
+    run_kraken2                   = true
-    run_malt            = true
+    run_malt                      = true
-    run_metaphlan3      = true
+    run_metaphlan3                = true
-    shortread_clipmerge = true
+    run_centrifuge                = true
-    run_centrifuge      = true
+    shortread_clipmerge           = true
-
+    longread_clip                 = false
+    shortread_complexityfilter    = true
 }

modules.json

@@ -4,11 +4,17 @@
     "repos": {
         "nf-core/modules": {
             "adapterremoval": {
-                "git_sha": "f0800157544a82ae222931764483331a81812012"
+                "git_sha": "879d42c5e28661fe0a5e744c9e2c515868f9e08a"
+            },
+            "bbmap/bbduk": {
+                "git_sha": "e745e167c1020928ef20ea1397b6b4d230681b4d"
             },
             "cat/fastq": {
                 "git_sha": "e745e167c1020928ef20ea1397b6b4d230681b4d"
             },
+            "centrifuge/centrifuge": {
+                "git_sha": "d2726fcf75063960f06b36d2229a4c0966614108"
+            },
             "custom/dumpsoftwareversions": {
                 "git_sha": "e745e167c1020928ef20ea1397b6b4d230681b4d"
             },
@@ -33,12 +39,12 @@
             "porechop": {
                 "git_sha": "e20e57f90b6787ac9a010a980cf6ea98bd990046"
             },
-            "centrifuge": {
+            "prinseqplusplus": {
-                "git_sha": "ea41a8a6f761b9993d857570e872abaae3fea555"
+                "git_sha": "f1c5384c31e985591716afdd732cf8c2ae29d05b"
             },
             "untar": {
                 "git_sha": "e080f4c8acf5760039ed12ec1f206170f3f9a918"
             }
         }
     }
-}
+}

modules/nf-core/modules/adapterremoval/main.nf

@@ -12,15 +12,14 @@ process ADAPTERREMOVAL {
     path(adapterlist)
 
     output:
-    tuple val(meta), path("${prefix}.truncated.gz")            , optional: true, emit: singles_truncated
+    tuple val(meta), path("${prefix}.truncated.fastq.gz")            , optional: true, emit: singles_truncated
-    tuple val(meta), path("${prefix}.discarded.gz")            , optional: true, emit: discarded
+    tuple val(meta), path("${prefix}.discarded.fastq.gz")            , optional: true, emit: discarded
-    tuple val(meta), path("${prefix}.pair1.truncated.gz")      , optional: true, emit: pair1_truncated
+    tuple val(meta), path("${prefix}.pair{1,2}.truncated.fastq.gz")  , optional: true, emit: paired_truncated
-    tuple val(meta), path("${prefix}.pair2.truncated.gz")      , optional: true, emit: pair2_truncated
+    tuple val(meta), path("${prefix}.collapsed.fastq.gz")            , optional: true, emit: collapsed
-    tuple val(meta), path("${prefix}.collapsed.gz")            , optional: true, emit: collapsed
+    tuple val(meta), path("${prefix}.collapsed.truncated.fastq.gz")  , optional: true, emit: collapsed_truncated
-    tuple val(meta), path("${prefix}.collapsed.truncated.gz")  , optional: true, emit: collapsed_truncated
+    tuple val(meta), path("${prefix}.paired.fastq.gz")               , optional: true, emit: paired_interleaved
-    tuple val(meta), path("${prefix}.paired.gz")               , optional: true, emit: paired_interleaved
+    tuple val(meta), path('*.settings')                              , emit: settings
-    tuple val(meta), path('*.log')                             , emit: log
+    path "versions.yml"                                              , emit: versions
-    path "versions.yml"                                        , emit: versions
 
     when:
     task.ext.when == null || task.ext.when
@@ -38,10 +37,19 @@ process ADAPTERREMOVAL {
             $adapterlist \\
             --basename ${prefix} \\
             --threads ${task.cpus} \\
-            --settings ${prefix}.log \\
             --seed 42 \\
             --gzip
 
+        ensure_fastq() {
+            if [ -f "\${1}" ]; then
+                mv "\${1}" "\${1::-3}.fastq.gz"
+            fi
+
+        }
+
+        ensure_fastq '${prefix}.truncated.gz'
+        ensure_fastq '${prefix}.discarded.gz'
+
         cat <<-END_VERSIONS > versions.yml
         "${task.process}":
             adapterremoval: \$(AdapterRemoval --version 2>&1 | sed -e "s/AdapterRemoval ver. //g")
@@ -56,10 +64,24 @@ process ADAPTERREMOVAL {
             $adapterlist \\
             --basename ${prefix} \\
             --threads $task.cpus \\
-            --settings ${prefix}.log \\
             --seed 42 \\
             --gzip
 
+        ensure_fastq() {
+            if [ -f "\${1}" ]; then
+                mv "\${1}" "\${1::-3}.fastq.gz"
+            fi
+
+        }
+
+        ensure_fastq '${prefix}.truncated.gz'
+        ensure_fastq '${prefix}.discarded.gz'
+        ensure_fastq '${prefix}.pair1.truncated.gz'
+        ensure_fastq '${prefix}.pair2.truncated.gz'
+        ensure_fastq '${prefix}.collapsed.gz'
+        ensure_fastq '${prefix}.collapsed.truncated.gz'
+        ensure_fastq '${prefix}.paired.gz'
+
         cat <<-END_VERSIONS > versions.yml
         "${task.process}":
             adapterremoval: \$(AdapterRemoval --version 2>&1 | sed -e "s/AdapterRemoval ver. //g")

modules/nf-core/modules/adapterremoval/meta.yml

@@ -43,43 +43,43 @@ output:
         Adapter trimmed FastQ files of either single-end reads, or singleton
         'orphaned' reads from merging of paired-end data (i.e., one of the pair
         was lost due to filtering thresholds).
-      pattern: "*.truncated.gz"
+      pattern: "*.truncated.fastq.gz"
   - discarded:
       type: file
       description: |
         Adapter trimmed FastQ files of reads that did not pass filtering
         thresholds.
-      pattern: "*.discarded.gz"
+      pattern: "*.discarded.fastq.gz"
   - pair1_truncated:
       type: file
       description: |
         Adapter trimmed R1 FastQ files of paired-end reads that did not merge
         with their respective R2 pair due to long templates. The respective pair
         is stored in 'pair2_truncated'.
-      pattern: "*.pair1.truncated.gz"
+      pattern: "*.pair1.truncated.fastq.gz"
   - pair2_truncated:
       type: file
       description: |
         Adapter trimmed R2 FastQ files of paired-end reads that did not merge
         with their respective R1 pair due to long templates. The respective pair
         is stored in 'pair1_truncated'.
-      pattern: "*.pair2.truncated.gz"
+      pattern: "*.pair2.truncated.fastq.gz"
   - collapsed:
       type: file
       description: |
         Collapsed FastQ of paired-end reads that successfully merged with their
         respective R1 pair but were not trimmed.
-      pattern: "*.collapsed.gz"
+      pattern: "*.collapsed.fastq.gz"
   - collapsed_truncated:
       type: file
       description: |
         Collapsed FastQ of paired-end reads that successfully merged with their
         respective R1 pair and were trimmed of adapter due to sufficient overlap.
-      pattern: "*.collapsed.truncated.gz"
+      pattern: "*.collapsed.truncated.fastq.gz"
   - log:
       type: file
       description: AdapterRemoval log file
-      pattern: "*.log"
+      pattern: "*.settings"
   - versions:
       type: file
       description: File containing software versions

modules/nf-core/modules/bbmap/bbduk/main.nf

@@ -0,0 +1,43 @@
+process BBMAP_BBDUK {
+    tag "$meta.id"
+    label 'process_medium'
+
+    conda (params.enable_conda ? "bioconda::bbmap=38.90" : null)
+    container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
+        'https://depot.galaxyproject.org/singularity/bbmap:38.90--he522d1c_1' :
+        'quay.io/biocontainers/bbmap:38.90--he522d1c_1' }"
+
+    input:
+    tuple val(meta), path(reads)
+    path contaminants
+
+    output:
+    tuple val(meta), path('*.fastq.gz'), emit: reads
+    tuple val(meta), path('*.log')     , emit: log
+    path "versions.yml"                , emit: versions
+
+    when:
+    task.ext.when == null || task.ext.when
+
+    script:
+    def args = task.ext.args ?: ''
+    def prefix = task.ext.prefix ?: "${meta.id}"
+    def raw      = meta.single_end ? "in=${reads[0]}" : "in1=${reads[0]} in2=${reads[1]}"
+    def trimmed  = meta.single_end ? "out=${prefix}.fastq.gz" : "out1=${prefix}_1.fastq.gz out2=${prefix}_2.fastq.gz"
+    def contaminants_fa = contaminants ? "ref=$contaminants" : ''
+    """
+    maxmem=\$(echo \"$task.memory\"| sed 's/ GB/g/g')
+    bbduk.sh \\
+        -Xmx\$maxmem \\
+        $raw \\
+        $trimmed \\
+        threads=$task.cpus \\
+        $args \\
+        $contaminants_fa \\
+        &> ${prefix}.bbduk.log
+    cat <<-END_VERSIONS > versions.yml
+    "${task.process}":
+        bbmap: \$(bbversion.sh)
+    END_VERSIONS
+    """
+}

modules/nf-core/modules/bbmap/bbduk/meta.yml

@@ -0,0 +1,52 @@
+name: bbmap_bbduk
+description: Adapter and quality trimming of sequencing reads
+keywords:
+  - trimming
+  - adapter trimming
+  - quality trimming
+tools:
+  - bbmap:
+      description: BBMap is a short read aligner, as well as various other bioinformatic tools.
+      homepage: https://jgi.doe.gov/data-and-tools/bbtools/bb-tools-user-guide/
+      documentation: https://jgi.doe.gov/data-and-tools/bbtools/bb-tools-user-guide/
+      tool_dev_url: None
+      doi: ""
+      licence: ["UC-LBL license (see package)"]
+
+input:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - reads:
+      type: file
+      description: |
+        List of input FastQ files of size 1 and 2 for single-end and paired-end data,
+        respectively.
+  - contaminants:
+      type: file
+      description: |
+        Reference files containing adapter and/or contaminant sequences for sequence kmer matching
+
+output:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - reads:
+      type: file
+      description: The trimmed/modified fastq reads
+      pattern: "*fastq.gz"
+  - versions:
+      type: file
+      description: File containing software versions
+      pattern: "versions.yml"
+  - log:
+      type: file
+      description: Bbduk log file
+      pattern: "*bbduk.log"
+
+authors:
+  - "@MGordon09"

modules/nf-core/modules/centrifuge/centrifuge/main.nf

@@ -0,0 +1,61 @@
+process CENTRIFUGE_CENTRIFUGE {
+    tag "$meta.id"
+    label 'process_high'
+
+    conda (params.enable_conda ? "bioconda::centrifuge=1.0.4_beta" : null)
+    container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
+        'https://depot.galaxyproject.org/singularity/centrifuge:1.0.4_beta--h9a82719_6' :
+        'quay.io/biocontainers/centrifuge:1.0.4_beta--h9a82719_6' }"
+
+    input:
+    tuple val(meta), path(reads)
+    path db
+    val save_unaligned
+    val save_aligned
+    val sam_format
+
+    output:
+    tuple val(meta), path('*report.txt')                 , emit: report
+    tuple val(meta), path('*results.txt')                , emit: results
+    tuple val(meta), path('*.sam')                       , optional: true, emit: sam
+    tuple val(meta), path('*.mapped.fastq{,.1,.2}.gz')   , optional: true, emit: fastq_mapped
+    tuple val(meta), path('*.unmapped.fastq{,.1,.2}.gz') , optional: true, emit: fastq_unmapped
+    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 paired = meta.single_end ? "-U ${reads}" :  "-1 ${reads[0]} -2 ${reads[1]}"
+    def unaligned = ''
+    def aligned = ''
+    if (meta.single_end) {
+        unaligned = save_unaligned ? "--un-gz ${prefix}.unmapped.fastq.gz" : ''
+        aligned = save_aligned ? "--al-gz ${prefix}.mapped.fastq.gz" : ''
+    } else {
+        unaligned = save_unaligned ? "--un-conc-gz ${prefix}.unmapped.fastq.gz" : ''
+        aligned = save_aligned ? "--al-conc-gz ${prefix}.mapped.fastq.gz" : ''
+    }
+    def sam_output = sam_format ? "--out-fmt 'sam'" : ''
+    """
+    ## we add "-no-name ._" to ensure silly Mac OSX metafiles files aren't included
+    db_name=`find -L ${db} -name "*.1.cf" -not -name "._*"  | sed 's/.1.cf//'`
+    centrifuge \\
+        -x \$db_name \\
+        -p $task.cpus \\
+        $paired \\
+        --report-file ${prefix}.report.txt \\
+        -S ${prefix}.results.txt \\
+        $unaligned \\
+        $aligned \\
+        $sam_output \\
+        $args
+
+    cat <<-END_VERSIONS > versions.yml
+    "${task.process}":
+        centrifuge: \$( centrifuge --version  | sed -n 1p | sed 's/^.*centrifuge-class version //')
+    END_VERSIONS
+    """
+}

modules/nf-core/modules/centrifuge/centrifuge/meta.yml

@@ -0,0 +1,66 @@
+name: centrifuge_centrifuge
+description: Classifies metagenomic sequence data
+keywords:
+  - classify
+  - metagenomics
+  - fastq
+  - db
+tools:
+  - centrifuge:
+      description: Centrifuge is a classifier for metagenomic sequences.
+      homepage: https://ccb.jhu.edu/software/centrifuge/
+      documentation: https://ccb.jhu.edu/software/centrifuge/manual.shtml
+      doi: 10.1101/gr.210641.116
+      licence: ["GPL v3"]
+input:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - reads:
+      type: file
+      description: |
+        List of input FastQ files of size 1 and 2 for single-end and paired-end data,
+        respectively.
+  - db:
+      type: directory
+      description: Path to directory containing centrifuge database files
+  - save_unaligned:
+      type: value
+      description: If true unmapped fastq files are saved
+  - save_aligned:
+      type: value
+      description: If true mapped fastq files are saved
+output:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - report:
+      type: file
+      description: |
+        File containing a classification summary
+      pattern: "*.{report.txt}"
+  - results:
+      type: file
+      description: |
+        File containing classification results
+      pattern: "*.{results.txt}"
+  - fastq_unmapped:
+      type: file
+      description: Unmapped fastq files
+      pattern: "*.unmapped.fastq.gz"
+  - fastq_mapped:
+      type: file
+      description: Mapped fastq files
+      pattern: "*.mapped.fastq.gz"
+  - versions:
+      type: file
+      description: File containing software versions
+      pattern: "versions.yml"
+authors:
+  - "@sofstam"
+  - "@jfy133"
+  - "@sateeshperi"

modules/nf-core/modules/nf-core/modules/centrifuge/main.nf

@@ -10,7 +10,6 @@ process CENTRIFUGE {
     input:
     tuple val(meta), path(reads)
     path db
-    val db_name
     val save_unaligned
     val save_aligned
     val sam_format
@@ -43,8 +42,9 @@ process CENTRIFUGE {
     }
     def sam_output = sam_format ? "--out-fmt 'sam'" : ''
     """
+    tar -xf $db
     centrifuge \\
-        -x ${db}/${db_name} \\
+        -x $db_name \\
         -p $task.cpus \\
         $paired \\
         --report-file ${prefix}.report.txt \\

modules/nf-core/modules/nf-core/modules/centrifuge/meta.yml

@@ -27,9 +27,6 @@ input:
       type: directory
       description: Centrifuge database in .tar.gz format
       pattern: "*.tar.gz"
-  - db_name:
-      type: string
-      description: Centrifuge database filenames without the suffix ".cf"
   - save_unaligned:
       type: value
       description: If true unmapped fastq files are saved

modules/nf-core/modules/prinseqplusplus/main.nf

@@ -0,0 +1,61 @@
+process PRINSEQPLUSPLUS {
+    tag "$meta.id"
+    label 'process_low'
+
+    conda (params.enable_conda ? "bioconda::prinseq-plus-plus=1.2.3" : null)
+    container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
+        'https://depot.galaxyproject.org/singularity/prinseq-plus-plus:1.2.3--hc90279e_1':
+        'quay.io/biocontainers/prinseq-plus-plus:1.2.3--hc90279e_1' }"
+
+    input:
+    tuple val(meta), path(reads)
+
+    output:
+    tuple val(meta), path("*_good_out*.fastq.gz")                  , emit: good_reads
+    tuple val(meta), path("*_single_out*.fastq.gz"), optional: true, emit: single_reads
+    tuple val(meta), path("*_bad_out*.fastq.gz")   , optional: true, emit: bad_reads
+    tuple val(meta), path("*.log")                                 , emit: log
+    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}"
+
+    if (meta.single_end) {
+        """
+        prinseq++ \\
+            -threads $task.cpus \\
+            -fastq ${reads} \\
+            -out_name ${prefix} \\
+            -out_gz \\
+            -VERBOSE 1 \\
+            $args \\
+            | tee ${prefix}.log
+
+        cat <<-END_VERSIONS > versions.yml
+        "${task.process}":
+            prinseqplusplus: \$(echo \$(prinseq++ --version | cut -f 2 -d ' ' ))
+        END_VERSIONS
+        """
+    } else {
+        """
+        prinseq++ \\
+            -threads $task.cpus \\
+            -fastq ${reads[0]} \\
+            -fastq2 ${reads[1]} \\
+            -out_name ${prefix} \\
+            -out_gz \\
+            -VERBOSE 1 \\
+            $args \\
+            | tee ${prefix}.log
+
+        cat <<-END_VERSIONS > versions.yml
+        "${task.process}":
+            prinseqplusplus: \$(echo \$(prinseq++ --version | cut -f 2 -d ' ' ))
+        END_VERSIONS
+        """
+    }
+}

modules/nf-core/modules/prinseqplusplus/meta.yml

@@ -0,0 +1,60 @@
+name: "prinseqplusplus"
+description: PRINSEQ++ is a C++ implementation of the prinseq-lite.pl program. It can be used to filter, reformat or trim genomic and metagenomic sequence data
+keywords:
+  - fastq
+  - fasta
+  - filter
+  - trim
+tools:
+  - "prinseqplusplus":
+      description: "PRINSEQ++ - Multi-threaded C++ sequence cleaning"
+      homepage: "https://github.com/Adrian-Cantu/PRINSEQ-plus-plus"
+      documentation: "https://github.com/Adrian-Cantu/PRINSEQ-plus-plus"
+      tool_dev_url: "https://github.com/Adrian-Cantu/PRINSEQ-plus-plus"
+      doi: "10.7287/peerj.preprints.27553v1"
+      licence: "['GPL v2']"
+
+input:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - reads:
+      type: file
+      description: |
+        List of input FastQ files of size 1 and 2 for single-end and paired-end
+        data, respectively.
+
+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"
+  - good_reads:
+      type: file
+      description: Reads passing filter(s) in gzipped FASTQ format
+      pattern: "*_good_out_{R1,R2}.fastq.gz"
+  - single_reads:
+      type: file
+      description: |
+        Single reads without the pair passing filter(s) in gzipped FASTQ format
+      pattern: "*_single_out_{R1,R2}.fastq.gz"
+  - bad_reads:
+      type: file
+      description: |
+        Reads without not passing filter(s) in gzipped FASTQ format
+      pattern: "*_bad_out_{R1,R2}.fastq.gz"
+  - log:
+      type: file
+      description: |
+        Verbose level 2 STDOUT information in a log file
+      pattern: "*.log"
+
+authors:
+  - "@jfy133"

nextflow.config

@@ -51,7 +51,7 @@ params {
     max_cpus                   = 16
     max_time                   = '240.h'
 
-    // Databaess
+    // Databases
     databases = null
 
     // FASTQ preprocessing
@@ -64,6 +64,18 @@ params {
     shortread_clipmerge_adapter2            = null
     shortread_clipmerge_minlength           = 15
     longread_clip                           = false
+    save_preprocessed_reads                 = false
+
+    // Complexity filtering
+    shortread_complexityfilter                           = false
+    shortread_complexityfilter_tool                      = 'bbduk'
+    shortread_complexityfilter_entropy                   = 0.3
+    shortread_complexityfilter_bbduk_windowsize          = 50
+    shortread_complexityfilter_bbduk_mask                = false
+    shortread_complexityfilter_prinseqplusplus_mode      = 'entropy'
+    shortread_complexityfilter_prinseqplusplus_dustscore = 0.5
+    save_complexityfiltered_reads                        = false
+
 
     // MALT
     run_malt                   = false

nextflow_schema.json

@@ -276,8 +276,7 @@
             "type": "boolean"
         },
         "shortread_clipmerge_excludeunmerged": {
-            "type": "boolean",
+            "type": "boolean"
-            "default": false
         },
         "longread_clip": {
             "type": "boolean"
@@ -334,9 +333,40 @@
             "type": "integer",
             "default": 15
         },
-        "centrifuge_db_name": {
+        "save_preprocessed_reads": {
+            "type": "boolean",
+            "default": false
+        },
+        "shortread_complexityfilter_tool": {
             "type": "string",
-            "default": null
+            "default": "bbduk"
+        },
+        "shortread_complexityfilter_bbduk_windowsize": {
+            "type": "integer",
+            "default": 50
+        },
+        "shortread_complexityfilter_bbduk_mask": {
+            "type": "boolean"
+        },
+        "shortread_complexityfilter": {
+            "type": "boolean"
+        },
+        "shortread_complexityfilter_entropy": {
+            "type": "number",
+            "default": 0.3
+        },
+        "shortread_complexityfilter_prinseqplusplus_mode": {
+            "type": "string",
+            "default": "entropy",
+            "enum": ["entropy", "dust"]
+        },
+        "shortread_complexityfilter_prinseqplusplus_dustscore": {
+            "type": "number",
+            "default": 0.5
+        },
+        "save_complexityfiltered_reads": {
+            "type": "boolean",
+            "default": false
         }
     }
-}
+}

nf-core/modules/centrifuge/centrifuge/main.nf

@@ -0,0 +1,61 @@
+process CENTRIFUGE_CENTRIFUGE {
+    tag "$meta.id"
+    label 'process_high'
+
+    conda (params.enable_conda ? "bioconda::centrifuge=1.0.4_beta" : null)
+    container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
+        'https://depot.galaxyproject.org/singularity/centrifuge:1.0.4_beta--h9a82719_6' :
+        'quay.io/biocontainers/centrifuge:1.0.4_beta--h9a82719_6' }"
+
+    input:
+    tuple val(meta), path(reads)
+    path db
+    val save_unaligned
+    val save_aligned
+    val sam_format
+
+    output:
+    tuple val(meta), path('*report.txt')                 , emit: report
+    tuple val(meta), path('*results.txt')                , emit: results
+    tuple val(meta), path('*.sam')                       , optional: true, emit: sam
+    tuple val(meta), path('*.mapped.fastq{,.1,.2}.gz')   , optional: true, emit: fastq_mapped
+    tuple val(meta), path('*.unmapped.fastq{,.1,.2}.gz') , optional: true, emit: fastq_unmapped
+    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 paired = meta.single_end ? "-U ${reads}" :  "-1 ${reads[0]} -2 ${reads[1]}"
+    def unaligned = ''
+    def aligned = ''
+    if (meta.single_end) {
+        unaligned = save_unaligned ? "--un-gz ${prefix}.unmapped.fastq.gz" : ''
+        aligned = save_aligned ? "--al-gz ${prefix}.mapped.fastq.gz" : ''
+    } else {
+        unaligned = save_unaligned ? "--un-conc-gz ${prefix}.unmapped.fastq.gz" : ''
+        aligned = save_aligned ? "--al-conc-gz ${prefix}.mapped.fastq.gz" : ''
+    }
+    def sam_output = sam_format ? "--out-fmt 'sam'" : ''
+    """
+    ## we add "-no-name ._" to ensure silly Mac OSX metafiles files aren't included
+    db_name=`find -L ${db} -name "*.1.cf" -not -name "._*"  | sed 's/.1.cf//'`
+    centrifuge \\
+        -x \$db_name \\
+        -p $task.cpus \\
+        $paired \\
+        --report-file ${prefix}.report.txt \\
+        -S ${prefix}.results.txt \\
+        $unaligned \\
+        $aligned \\
+        $sam_output \\
+        $args
+
+    cat <<-END_VERSIONS > versions.yml
+    "${task.process}":
+        centrifuge: \$( centrifuge --version  | sed -n 1p | sed 's/^.*centrifuge-class version //')
+    END_VERSIONS
+    """
+}

nf-core/modules/centrifuge/centrifuge/meta.yml

@@ -0,0 +1,66 @@
+name: centrifuge_centrifuge
+description: Classifies metagenomic sequence data
+keywords:
+  - classify
+  - metagenomics
+  - fastq
+  - db
+tools:
+  - centrifuge:
+      description: Centrifuge is a classifier for metagenomic sequences.
+      homepage: https://ccb.jhu.edu/software/centrifuge/
+      documentation: https://ccb.jhu.edu/software/centrifuge/manual.shtml
+      doi: 10.1101/gr.210641.116
+      licence: ["GPL v3"]
+input:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - reads:
+      type: file
+      description: |
+        List of input FastQ files of size 1 and 2 for single-end and paired-end data,
+        respectively.
+  - db:
+      type: directory
+      description: Path to directory containing centrifuge database files
+  - save_unaligned:
+      type: value
+      description: If true unmapped fastq files are saved
+  - save_aligned:
+      type: value
+      description: If true mapped fastq files are saved
+output:
+  - meta:
+      type: map
+      description: |
+        Groovy Map containing sample information
+        e.g. [ id:'test', single_end:false ]
+  - report:
+      type: file
+      description: |
+        File containing a classification summary
+      pattern: "*.{report.txt}"
+  - results:
+      type: file
+      description: |
+        File containing classification results
+      pattern: "*.{results.txt}"
+  - fastq_unmapped:
+      type: file
+      description: Unmapped fastq files
+      pattern: "*.unmapped.fastq.gz"
+  - fastq_mapped:
+      type: file
+      description: Mapped fastq files
+      pattern: "*.mapped.fastq.gz"
+  - versions:
+      type: file
+      description: File containing software versions
+      pattern: "versions.yml"
+authors:
+  - "@sofstam"
+  - "@jfy133"
+  - "@sateeshperi"

subworkflows/local/longread_preprocessing.nf

@@ -1,6 +1,6 @@
-/*
+//
-Process long raw reads with porechop
+// Process long raw reads with porechop
-*/
+//
 
 include { FASTQC as FASTQC_PROCESSED } from '../../modules/nf-core/modules/fastqc/main'
 include { PORECHOP                   } from '../../modules/nf-core/modules/porechop/main'
@@ -25,7 +25,7 @@ workflow LONGREAD_PREPROCESSING {
 
     FASTQC_PROCESSED ( PORECHOP.out.reads )
     ch_versions = ch_versions.mix(PORECHOP.out.versions.first())
-    ch_multiqc_files = ch_multiqc_files.mix( FASTQC_PROCESSED.out.zip.collect{it[1]} )
+    ch_multiqc_files = ch_multiqc_files.mix( FASTQC_PROCESSED.out.zip )
 
 
     emit:

subworkflows/local/shortread_adapterremoval.nf

@@ -1,15 +1,10 @@
-/*
+//
-Process short raw reads with AdapterRemoval
+// Process short raw reads with AdapterRemoval
-*/
+//
 
 include { ADAPTERREMOVAL as ADAPTERREMOVAL_SINGLE       } from '../../modules/nf-core/modules/adapterremoval/main'
 include { ADAPTERREMOVAL as ADAPTERREMOVAL_PAIRED       } from '../../modules/nf-core/modules/adapterremoval/main'
 include { CAT_FASTQ                                     } from '../../modules/nf-core/modules/cat/fastq/main'
-include {
-    ENSURE_FASTQ_EXTENSION as ENSURE_FASTQ_EXTENSION1;
-    ENSURE_FASTQ_EXTENSION as ENSURE_FASTQ_EXTENSION2;
-    ENSURE_FASTQ_EXTENSION as ENSURE_FASTQ_EXTENSION3;
-} from '../../modules/local/ensure_fastq_extension'
 
 workflow SHORTREAD_ADAPTERREMOVAL {
 
@@ -36,89 +31,63 @@ workflow SHORTREAD_ADAPTERREMOVAL {
 
     if ( params.shortread_clipmerge_mergepairs && !params.shortread_clipmerge_excludeunmerged ) {
 
-        ENSURE_FASTQ_EXTENSION1(
+        ch_concat_fastq = Channel.empty()
-            Channel.empty().mix(
+            .mix(
                 ADAPTERREMOVAL_PAIRED.out.collapsed,
                 ADAPTERREMOVAL_PAIRED.out.collapsed_truncated,
                 ADAPTERREMOVAL_PAIRED.out.singles_truncated,
-                ADAPTERREMOVAL_PAIRED.out.pair1_truncated,
+                ADAPTERREMOVAL_PAIRED.out.paired_truncated
-                ADAPTERREMOVAL_PAIRED.out.pair2_truncated
             )
             .map { meta, reads ->
-                meta.single_end = true
+                def meta_new = meta.clone()
-                [meta, reads]
+                meta_new.single_end = true
+                [meta_new, reads]
             }
-        )
+            .groupTuple()
+            // Paired-end reads cause a nested tuple during grouping.
+            // We want to present a flat list of files to `CAT_FASTQ`.
+            .map { meta, fastq -> [meta, fastq.flatten()] }
 
-        CAT_FASTQ(
-            ENSURE_FASTQ_EXTENSION1.out.reads
-                .groupTuple()
-        )
 
-        ENSURE_FASTQ_EXTENSION2(ADAPTERREMOVAL_SINGLE.out.singles_truncated)
+        CAT_FASTQ(ch_concat_fastq)
 
         ch_adapterremoval_reads_prepped = CAT_FASTQ.out.reads
-            .mix(ENSURE_FASTQ_EXTENSION2.out.reads)
+            .mix(ADAPTERREMOVAL_SINGLE.out.singles_truncated)
 
     } else if ( params.shortread_clipmerge_mergepairs && params.shortread_clipmerge_excludeunmerged ) {
 
-        ENSURE_FASTQ_EXTENSION1(
+        ch_concat_fastq = Channel.empty()
-            Channel.empty().mix(
+            .mix(
                 ADAPTERREMOVAL_PAIRED.out.collapsed,
                 ADAPTERREMOVAL_PAIRED.out.collapsed_truncated
             )
             .map { meta, reads ->
-                meta.single_end = true
+                def meta_new = meta.clone()
-                [meta, reads]
+                meta_new.single_end = true
+                [meta_new, reads]
             }
-        )
+            .groupTuple()
+            .map { meta, fastq -> [meta, fastq.flatten()] }
 
-        CAT_FASTQ(
-            ENSURE_FASTQ_EXTENSION1.out.reads
-                .groupTuple()
-        )
 
-        ENSURE_FASTQ_EXTENSION2(ADAPTERREMOVAL_SINGLE.out.singles_truncated)
+        CAT_FASTQ(ch_concat_fastq)
 
         ch_adapterremoval_reads_prepped = CAT_FASTQ.out.reads
-            .mix(ENSURE_FASTQ_EXTENSION2.out.reads)
+            .mix(ADAPTERREMOVAL_SINGLE.out.singles_truncated)
 
     } else {
 
-        ENSURE_FASTQ_EXTENSION1(
+        ch_adapterremoval_reads_prepped = ADAPTERREMOVAL_PAIRED.out.paired_truncated
-            ADAPTERREMOVAL_PAIRED.out.pair1_truncated
+            .mix(ADAPTERREMOVAL_SINGLE.out.singles_truncated)
-            .map { meta, reads ->
-                meta.single_end = true
-                [meta, reads]
-            }
-        )
-
-        ENSURE_FASTQ_EXTENSION2(
-            ADAPTERREMOVAL_PAIRED.out.pair2_truncated
-            .map { meta, reads ->
-                meta.single_end = true
-                [meta, reads]
-            }
-        )
-
-        ENSURE_FASTQ_EXTENSION3(ADAPTERREMOVAL_SINGLE.out.singles_truncated)
-
-        ch_adapterremoval_reads_prepped = ENSURE_FASTQ_EXTENSION1.out.reads
-            .join(ENSURE_FASTQ_EXTENSION2.out.reads)
-            .groupTuple()
-            .map { meta, pair1, pair2 ->
-                meta.single_end = false
-                [ meta, [ pair1, pair2 ].flatten() ]
-            }
-            .mix(ENSURE_FASTQ_EXTENSION3.out.reads)
 
     }
 
     ch_versions = ch_versions.mix( ADAPTERREMOVAL_SINGLE.out.versions.first() )
     ch_versions = ch_versions.mix( ADAPTERREMOVAL_PAIRED.out.versions.first() )
+
     ch_multiqc_files = ch_multiqc_files.mix(
-        ADAPTERREMOVAL_PAIRED.out.log.collect{it[1]},
+        ADAPTERREMOVAL_PAIRED.out.settings,
-        ADAPTERREMOVAL_SINGLE.out.log.collect{it[1]}
+        ADAPTERREMOVAL_SINGLE.out.settings
     )
 
     emit:

subworkflows/local/shortread_complexityfiltering.nf

@@ -0,0 +1,32 @@
+//
+// Check input samplesheet and get read channels
+//
+
+include { BBMAP_BBDUK     } from '../../modules/nf-core/modules/bbmap/bbduk/main'
+include { PRINSEQPLUSPLUS } from '../../modules/nf-core/modules/prinseqplusplus/main'
+
+workflow SHORTREAD_COMPLEXITYFILTERING {
+    take:
+    reads // [ [ meta ], [ reads ] ]
+
+    main:
+    ch_versions       = Channel.empty()
+    ch_multiqc_files  = Channel.empty()
+
+    if ( params.shortread_complexityfilter_tool == 'bbduk' ) {
+        ch_filtered_reads = BBMAP_BBDUK ( reads, [] ).reads
+        ch_versions        =  ch_versions.mix( BBMAP_BBDUK.out.versions.first() )
+        ch_multiqc_files   =  ch_multiqc_files.mix( BBMAP_BBDUK.out.log )
+    } else if ( params.shortread_complexityfilter_tool == 'prinseqplusplus' ) {
+        ch_filtered_reads = PRINSEQPLUSPLUS ( reads ).good_reads
+        ch_versions        =  ch_versions.mix( PRINSEQPLUSPLUS.out.versions.first() )
+    } else {
+        ch_filtered_reads = reads
+    }
+
+    emit:
+    reads    = ch_filtered_reads    // channel: [ val(meta), [ reads ] ]
+    versions = ch_versions          // channel: [ versions.yml ]
+    mqc      = ch_multiqc_files
+}
+

subworkflows/local/shortread_fastp.nf

@@ -1,6 +1,6 @@
-/*
+//
-Process short raw reads with FastP
+// Process short raw reads with FastP
-*/
+//
 
 include { FASTP as FASTP_SINGLE       } from '../../modules/nf-core/modules/fastp/main'
 include { FASTP as FASTP_PAIRED       } from '../../modules/nf-core/modules/fastp/main'
@@ -44,8 +44,8 @@ workflow SHORTREAD_FASTP {
 
     ch_processed_reads = ch_fastp_reads_prepped
 
-    ch_multiqc_files = ch_multiqc_files.mix( FASTP_SINGLE.out.json.collect{it[1]} )
+    ch_multiqc_files = ch_multiqc_files.mix( FASTP_SINGLE.out.json )
-    ch_multiqc_files = ch_multiqc_files.mix( FASTP_PAIRED.out.json.collect{it[1]} )
+    ch_multiqc_files = ch_multiqc_files.mix( FASTP_PAIRED.out.json )
 
     emit:
     reads    = ch_processed_reads   // channel: [ val(meta), [ reads ] ]

subworkflows/local/shortread_preprocessing.nf

@@ -1,5 +1,5 @@
 //
-// Check input samplesheet and get read channels
+// Perform read trimming and merging
 //
 
 
@@ -9,7 +9,7 @@ include { FASTQC as FASTQC_PROCESSED       } from '../../modules/nf-core/modules
 
 workflow SHORTREAD_PREPROCESSING {
     take:
-    reads // file: /path/to/samplesheet.csv
+    reads //  [ [ meta ], [ reads ] ]
 
     main:
     ch_versions       = Channel.empty()
@@ -29,7 +29,7 @@ workflow SHORTREAD_PREPROCESSING {
 
     FASTQC_PROCESSED ( ch_processed_reads )
     ch_versions = ch_versions.mix( FASTQC_PROCESSED.out.versions )
-    ch_multiqc_files = ch_multiqc_files.mix( FASTQC_PROCESSED.out.zip.collect{it[1]} )
+    ch_multiqc_files = ch_multiqc_files.mix( FASTQC_PROCESSED.out.zip )
 
     emit:
     reads    = ch_processed_reads   // channel: [ val(meta), [ reads ] ]

workflows/taxprofiler.nf

@@ -17,7 +17,7 @@ for (param in checkPathParamList) { if (param) { file(param, checkIfExists: true
 // Check mandatory parameters
 if (params.input    ) { ch_input     = file(params.input)     } else { exit 1, 'Input samplesheet not specified!' }
 if (params.databases) { ch_databases = file(params.databases) } else { exit 1, 'Input database sheet not specified!' }
-if (params.shortread_clipmerge_mergepairs && params.run_malt ) log.warn "[nf-core/taxprofiler] warning: MALT does not except uncollapsed paired-reads. Pairs will be profiled as separate files."
+if (params.shortread_clipmerge_mergepairs && params.run_malt ) log.warn "[nf-core/taxprofiler] warning: MALT does not accept uncollapsed paired-reads. Pairs will be profiled as separate files."
 if (params.shortread_clipmerge_excludeunmerged && !params.shortread_clipmerge_mergepairs) exit 1, "[nf-core/taxprofiler] error: cannot include unmerged reads when merging not turned on. Please specify --shortread_clipmerge_mergepairs"
 
 /*
@@ -40,9 +40,10 @@ ch_multiqc_custom_config = params.multiqc_config ? Channel.fromPath(params.multi
 //
 include { INPUT_CHECK             } from '../subworkflows/local/input_check'
 
-include { DB_CHECK                } from '../subworkflows/local/db_check'
+include { DB_CHECK                      } from '../subworkflows/local/db_check'
-include { SHORTREAD_PREPROCESSING } from '../subworkflows/local/shortread_preprocessing'
+include { SHORTREAD_PREPROCESSING       } from '../subworkflows/local/shortread_preprocessing'
-include { LONGREAD_PREPROCESSING  } from '../subworkflows/local/longread_preprocessing'
+include { LONGREAD_PREPROCESSING        } from '../subworkflows/local/longread_preprocessing'
+include { SHORTREAD_COMPLEXITYFILTERING } from '../subworkflows/local/shortread_complexityfiltering'
 
 /*
 ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
@@ -60,7 +61,7 @@ include { CUSTOM_DUMPSOFTWAREVERSIONS } from '../modules/nf-core/modules/custom/
 include { CAT_FASTQ                   } from '../modules/nf-core/modules/cat/fastq/main'
 include { MALT_RUN                    } from '../modules/nf-core/modules/malt/run/main'
 include { KRAKEN2_KRAKEN2             } from '../modules/nf-core/modules/kraken2/kraken2/main'
-include { CENTRIFUGE                  } from '../modules/nf-core/modules/centrifuge/main'
+include { CENTRIFUGE_CENTRIFUGE       } from '../modules/nf-core/modules/centrifuge/centrifuge/main'
 include { METAPHLAN3                  } from '../modules/nf-core/modules/metaphlan3/main'
 
 /*
@@ -91,7 +92,7 @@ workflow TAXPROFILER {
     /*
         MODULE: Run FastQC
     */
-    ch_input_for_fastqc = INPUT_CHECK.out.fastq.mix( INPUT_CHECK.out.nanopore ).dump(tag: "input_to_fastq")
+    ch_input_for_fastqc = INPUT_CHECK.out.fastq.mix( INPUT_CHECK.out.nanopore )
 
     FASTQC (
         ch_input_for_fastqc
@@ -99,10 +100,6 @@ workflow TAXPROFILER {
 
     ch_versions = ch_versions.mix(FASTQC.out.versions.first())
 
-    CUSTOM_DUMPSOFTWAREVERSIONS (
-        ch_versions.unique().collectFile(name: 'collated_versions.yml')
-    )
-
     /*
         SUBWORKFLOW: PERFORM PREPROCESSING
     */
@@ -115,17 +112,26 @@ workflow TAXPROFILER {
     if ( params.longread_clip ) {
         ch_longreads_preprocessed = LONGREAD_PREPROCESSING ( INPUT_CHECK.out.nanopore ).reads
                                         .map { it -> [ it[0], [it[1]] ] }
-    ch_versions = ch_versions.mix(LONGREAD_PREPROCESSING.out.versions.first())
     } else {
         ch_longreads_preprocessed = INPUT_CHECK.out.nanopore
     }
 
+    /*
+        SUBWORKFLOW: COMPLEXITY FILTERING
+    */
+
+    if ( params.shortread_complexityfilter ) {
+        ch_shortreads_filtered = SHORTREAD_COMPLEXITYFILTERING ( ch_shortreads_preprocessed ).reads
+    } else {
+        ch_shortreads_filtered = ch_shortreads_preprocessed
+    }
+
     /*
         COMBINE READS WITH POSSIBLE DATABASES
     */
 
     // e.g. output [DUMP: reads_plus_db] [['id':'2612', 'run_accession':'combined', 'instrument_platform':'ILLUMINA', 'single_end':1], <reads_path>/2612.merged.fastq.gz, ['tool':'malt', 'db_name':'mal95', 'db_params':'"-id 90"'], <db_path>/malt90]
-    ch_input_for_profiling = ch_shortreads_preprocessed
+    ch_input_for_profiling = ch_shortreads_filtered
             .mix( ch_longreads_preprocessed )
             .combine(DB_CHECK.out.dbs)
             .branch {
@@ -179,7 +185,6 @@ workflow TAXPROFILER {
     // RUN PROFILING
     //
     ch_input_for_metaphlan3 = ch_input_for_profiling.metaphlan3
-                            .dump(tag: "input_metaphlan3")
                             .multiMap {
                                 it ->
                                     reads: [it[0] + it[2], it[1]]
@@ -198,7 +203,7 @@ workflow TAXPROFILER {
     }
 
     if ( params.run_centrifuge ) {
-        CENTRIFUGE ( ch_input_for_centrifuge.reads, ch_input_for_centrifuge.db, params.centrifuge_db_name, params.centrifuge_save_unaligned, params.centrifuge_save_aligned, params.centrifuge_sam_format  )
+        CENTRIFUGE_CENTRIFUGE ( ch_input_for_centrifuge.reads, ch_input_for_centrifuge.db, params.centrifuge_save_unaligned, params.centrifuge_save_aligned, params.centrifuge_sam_format  )
     }
 
     if ( params.run_metaphlan3 ) {
@@ -208,6 +213,12 @@ workflow TAXPROFILER {
     /*
         MODULE: MultiQC
     */
+
+    CUSTOM_DUMPSOFTWAREVERSIONS (
+        ch_versions.unique().collectFile(name: 'collated_versions.yml')
+    )
+
+
     workflow_summary    = WorkflowTaxprofiler.paramsSummaryMultiqc(workflow, summary_params)
     ch_workflow_summary = Channel.value(workflow_summary)
 
@@ -219,21 +230,30 @@ workflow TAXPROFILER {
     ch_multiqc_files = ch_multiqc_files.mix(FASTQC.out.zip.collect{it[1]}.ifEmpty([]))
 
     if (params.shortread_clipmerge) {
-        ch_multiqc_files = ch_multiqc_files.mix(SHORTREAD_PREPROCESSING.out.mqc)
+        ch_multiqc_files = ch_multiqc_files.mix( SHORTREAD_PREPROCESSING.out.mqc.collect{it[1]}.ifEmpty([]) )
-    }
+        ch_versions = ch_versions.mix( SHORTREAD_PREPROCESSING.out.versions )
-    if (params.longread_clip) {
+    }
-        ch_multiqc_files = ch_multiqc_files.mix(LONGREAD_PREPROCESSING.out.mqc)
+
-    }
+    if (params.longread_clip) {
-    if (params.run_kraken2) {
+        ch_multiqc_files = ch_multiqc_files.mix( LONGREAD_PREPROCESSING.out.mqc.collect{it[1]}.ifEmpty([]) )
-        ch_multiqc_files = ch_multiqc_files.mix(KRAKEN2_KRAKEN2.out.txt.collect{it[1]}.ifEmpty([]))
+        ch_versions = ch_versions.mix( LONGREAD_PREPROCESSING.out.versions )
-        ch_versions = ch_versions.mix(KRAKEN2_KRAKEN2.out.versions.first())
+    }
-    }
+
-    if (params.run_malt) {
+    if (params.shortread_complexityfilter){
-        ch_multiqc_files = ch_multiqc_files.mix(MALT_RUN.out.log.collect{it[1]}.ifEmpty([]))
+        ch_multiqc_files = ch_multiqc_files.mix( SHORTREAD_COMPLEXITYFILTERING.out.mqc.collect{it[1]}.ifEmpty([]) )
-        ch_versions = ch_versions.mix(MALT_RUN.out.versions.first())
+        ch_versions = ch_versions.mix( SHORTREAD_COMPLEXITYFILTERING.out.versions )
+    }
+
+    if (params.run_kraken2) {
+        ch_multiqc_files = ch_multiqc_files.mix( KRAKEN2_KRAKEN2.out.txt.collect{it[1]}.ifEmpty([])  )
+        ch_versions = ch_versions.mix( KRAKEN2_KRAKEN2.out.versions.first() )
+    }
+
+    if (params.run_malt) {
+        ch_multiqc_files = ch_multiqc_files.mix( MALT_RUN.out.log.collect{it[1]}.ifEmpty([])  )
+        ch_versions = ch_versions.mix( MALT_RUN.out.versions.first() )
     }
 
-    // TODO MALT results overwriting per database?
     // TODO Versions for Karken/MALT not report?
     // TODO create multiQC module for metaphlan
     MULTIQC (