mirror of
https://github.com/MillironX/taxprofiler.git
synced 2024-11-10 21:53:09 +00:00
Add modules
This commit is contained in:
parent
2bae9d58ee
commit
a821f748ee
13 changed files with 554 additions and 2 deletions
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@ -164,6 +164,47 @@ process {
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]
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}
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withName: MINIMAP2_INDEX {
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ext.args = '-x map-ont'
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publishDir = [
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path: { "${params.outdir}/minimap2/index" },
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mode: params.publish_dir_mode,
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enabled: params.save_minimap2_hostremoval_index,
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pattern: 'minimap2'
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]
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}
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withName: MINIMAP2_ALIGN {
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ext.prefix = { "${meta.id}_${meta.run_accession}" }
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publishDir = [
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path: { "${params.outdir}/minimap2/align" },
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mode: params.publish_dir_mode,
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enabled: params.save_minimap2_hostremoval_mapped,
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pattern: '*.bam'
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]
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}
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withName: SAMTOOLS_VIEW {
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ext.args = '-f 4'
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ext.prefix = { "${meta.id}.mapped.sorted" }
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publishDir = [
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path: { "${params.outdir}/samtools/view" },
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mode: params.publish_dir_mode,
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enabled: params.save_samtools_unmapped_bam,
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pattern: '*.bam'
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]
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}
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withName: SAMTOOLS_BAM2FQ {
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ext.prefix = { "${meta.id}_${meta.run_accession}" }
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publishDir = [
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path: { "${params.outdir}/samtools/bam2fq" },
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mode: params.publish_dir_mode,
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enabled: params.save_minimap2_unmapped_fq,
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pattern: '*.fq.gz'
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]
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}
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withName: BBMAP_BBDUK {
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ext.args = [
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"entropy=${params.shortread_complexityfilter_entropy}",
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14
modules.json
14
modules.json
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@ -52,6 +52,12 @@
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"git_sha": "2d38566eca4cc15142b2ffa7c11837569b39aece"
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},
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"metaphlan3": {
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"git_sha": "ed4dd1a928ebf4308efb720de878045f7773f8e2"
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},
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"minimap2/align": {
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"git_sha": "1a5a9e7b4009dcf34e6867dd1a5a1d9a718b027b"
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},
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"minimap2/index": {
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"git_sha": "e745e167c1020928ef20ea1397b6b4d230681b4d"
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},
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"multiqc": {
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@ -63,9 +69,15 @@
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"prinseqplusplus": {
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"git_sha": "f1c5384c31e985591716afdd732cf8c2ae29d05b"
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},
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"samtools/bam2fq": {
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"git_sha": "897c33d5da084b61109500ee44c01da2d3e4e773"
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},
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"samtools/view": {
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"git_sha": "12afb6b0faf3cabf769c9a2a7dd477e3f066eac0"
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},
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"untar": {
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"git_sha": "e080f4c8acf5760039ed12ec1f206170f3f9a918"
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}
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}
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}
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}
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}
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2
modules/nf-core/modules/metaphlan3/main.nf
generated
2
modules/nf-core/modules/metaphlan3/main.nf
generated
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@ -23,7 +23,7 @@ process METAPHLAN3 {
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script:
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def args = task.ext.args ?: ''
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def prefix = task.ext.prefix ?: "${meta.id}"
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def input_type = ("$input".endsWith(".fastq.gz")) ? "--input_type fastq" : ("$input".contains(".fasta")) ? "--input_type fasta" : ("$input".endsWith(".bowtie2out.txt")) ? "--input_type bowtie2out" : "--input_type sam"
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def input_type = ("$input".endsWith(".fastq.gz") || "$input".endsWith(".fq.gz")) ? "--input_type fastq" : ("$input".contains(".fasta")) ? "--input_type fasta" : ("$input".endsWith(".bowtie2out.txt")) ? "--input_type bowtie2out" : "--input_type sam"
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def input_data = ("$input_type".contains("fastq")) && !meta.single_end ? "${input[0]},${input[1]}" : "$input"
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def bowtie2_out = "$input_type" == "--input_type bowtie2out" || "$input_type" == "--input_type sam" ? '' : "--bowtie2out ${prefix}.bowtie2out.txt"
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48
modules/nf-core/modules/minimap2/align/main.nf
generated
Normal file
48
modules/nf-core/modules/minimap2/align/main.nf
generated
Normal file
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@ -0,0 +1,48 @@
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process MINIMAP2_ALIGN {
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tag "$meta.id"
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label 'process_medium'
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conda (params.enable_conda ? 'bioconda::minimap2=2.21 bioconda::samtools=1.12' : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/mulled-v2-66534bcbb7031a148b13e2ad42583020b9cd25c4:1679e915ddb9d6b4abda91880c4b48857d471bd8-0' :
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'quay.io/biocontainers/mulled-v2-66534bcbb7031a148b13e2ad42583020b9cd25c4:1679e915ddb9d6b4abda91880c4b48857d471bd8-0' }"
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input:
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tuple val(meta), path(reads)
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path reference
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val bam_format
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val cigar_paf_format
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val cigar_bam
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output:
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tuple val(meta), path("*.paf"), optional: true, emit: paf
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tuple val(meta), path("*.bam"), optional: true, emit: bam
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path "versions.yml" , emit: versions
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when:
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task.ext.when == null || task.ext.when
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script:
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def args = task.ext.args ?: ''
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def prefix = task.ext.prefix ?: "${meta.id}"
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def input_reads = meta.single_end ? "$reads" : "${reads[0]} ${reads[1]}"
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def bam_output = bam_format ? "-a | samtools sort | samtools view -@ ${task.cpus} -b -h -o ${prefix}.bam" : "-o ${prefix}.paf"
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def cigar_paf = cigar_paf_format && !bam_format ? "-c" : ''
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def set_cigar_bam = cigar_bam && bam_format ? "-L" : ''
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"""
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minimap2 \\
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$args \\
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-t $task.cpus \\
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$reference \\
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$input_reads \\
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$cigar_paf \\
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$set_cigar_bam \\
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$bam_output
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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minimap2: \$(minimap2 --version 2>&1)
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END_VERSIONS
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"""
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}
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65
modules/nf-core/modules/minimap2/align/meta.yml
generated
Normal file
65
modules/nf-core/modules/minimap2/align/meta.yml
generated
Normal file
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@ -0,0 +1,65 @@
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name: minimap2_align
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description: A versatile pairwise aligner for genomic and spliced nucleotide sequences
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keywords:
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- align
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- fasta
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- fastq
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- genome
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- paf
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- reference
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tools:
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- minimap2:
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description: |
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A versatile pairwise aligner for genomic and spliced nucleotide sequences.
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homepage: https://github.com/lh3/minimap2
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documentation: https://github.com/lh3/minimap2#uguide
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licence: ["MIT"]
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input:
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- meta:
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type: map
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description: |
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Groovy Map containing sample information
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e.g. [ id:'test', single_end:false ]
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- reads:
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type: file
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description: |
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List of input FASTA or FASTQ files of size 1 and 2 for single-end
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and paired-end data, respectively.
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- reference:
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type: file
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description: |
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Reference database in FASTA format.
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- bam_format:
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type: boolean
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description: Specify that output should be in BAM format
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- cigar_paf_format:
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type: boolean
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description: Specify that output CIGAR should be in PAF format
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- cigar_bam:
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type: boolean
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description: |
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Write CIGAR with >65535 ops at the CG tag. This is recommended when
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doing XYZ (https://github.com/lh3/minimap2#working-with-65535-cigar-operations)
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output:
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- meta:
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type: map
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description: |
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Groovy Map containing sample information
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e.g. [ id:'test', single_end:false ]
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- paf:
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type: file
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description: Alignment in PAF format
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pattern: "*.paf"
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- bam:
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type: file
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description: Alignment in BAM format
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pattern: "*.bam"
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- versions:
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type: file
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description: File containing software versions
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pattern: "versions.yml"
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authors:
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- "@heuermh"
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- "@sofstam"
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- "@sateeshperi"
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- "@jfy133"
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33
modules/nf-core/modules/minimap2/index/main.nf
generated
Normal file
33
modules/nf-core/modules/minimap2/index/main.nf
generated
Normal file
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@ -0,0 +1,33 @@
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process MINIMAP2_INDEX {
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label 'process_medium'
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conda (params.enable_conda ? 'bioconda::minimap2=2.21' : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/minimap2:2.21--h5bf99c6_0' :
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'quay.io/biocontainers/minimap2:2.21--h5bf99c6_0' }"
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input:
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path fasta
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output:
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path "*.mmi" , emit: index
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path "versions.yml" , emit: versions
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when:
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task.ext.when == null || task.ext.when
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script:
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def args = task.ext.args ?: ''
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"""
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minimap2 \\
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-t $task.cpus \\
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-d ${fasta.baseName}.mmi \\
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$args \\
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$fasta
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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minimap2: \$(minimap2 --version 2>&1)
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END_VERSIONS
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"""
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}
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30
modules/nf-core/modules/minimap2/index/meta.yml
generated
Normal file
30
modules/nf-core/modules/minimap2/index/meta.yml
generated
Normal file
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@ -0,0 +1,30 @@
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name: minimap2_index
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description: Provides fasta index required by minimap2 alignment.
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keywords:
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- index
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- fasta
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- reference
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tools:
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- minimap2:
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description: |
|
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A versatile pairwise aligner for genomic and spliced nucleotide sequences.
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homepage: https://github.com/lh3/minimap2
|
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documentation: https://github.com/lh3/minimap2#uguide
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licence: ["MIT"]
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input:
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- fasta:
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type: file
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description: |
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Reference database in FASTA format.
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output:
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- mmi:
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type: file
|
||||
description: Minimap2 fasta index.
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pattern: "*.mmi"
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||||
- versions:
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type: file
|
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description: File containing software versions
|
||||
pattern: "versions.yml"
|
||||
authors:
|
||||
- "@yuukiiwa"
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- "@drpatelh"
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56
modules/nf-core/modules/samtools/bam2fq/main.nf
generated
Normal file
56
modules/nf-core/modules/samtools/bam2fq/main.nf
generated
Normal file
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@ -0,0 +1,56 @@
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process SAMTOOLS_BAM2FQ {
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tag "$meta.id"
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label 'process_low'
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||||
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||||
conda (params.enable_conda ? "bioconda::samtools=1.15.1" : null)
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container "${ 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(inputbam)
|
||||
val split
|
||||
|
||||
output:
|
||||
tuple val(meta), path("*.fq.gz"), emit: reads
|
||||
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 (split){
|
||||
"""
|
||||
samtools \\
|
||||
bam2fq \\
|
||||
$args \\
|
||||
-@ $task.cpus \\
|
||||
-1 ${prefix}_1.fq.gz \\
|
||||
-2 ${prefix}_2.fq.gz \\
|
||||
-0 ${prefix}_other.fq.gz \\
|
||||
-s ${prefix}_singleton.fq.gz \\
|
||||
$inputbam
|
||||
|
||||
cat <<-END_VERSIONS > versions.yml
|
||||
"${task.process}":
|
||||
samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
|
||||
END_VERSIONS
|
||||
"""
|
||||
} else {
|
||||
"""
|
||||
samtools \\
|
||||
bam2fq \\
|
||||
$args \\
|
||||
-@ $task.cpus \\
|
||||
$inputbam | gzip > ${prefix}_interleaved.fq.gz
|
||||
|
||||
cat <<-END_VERSIONS > versions.yml
|
||||
"${task.process}":
|
||||
samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
|
||||
END_VERSIONS
|
||||
"""
|
||||
}
|
||||
}
|
55
modules/nf-core/modules/samtools/bam2fq/meta.yml
generated
Normal file
55
modules/nf-core/modules/samtools/bam2fq/meta.yml
generated
Normal file
|
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|
|||
name: samtools_bam2fq
|
||||
description: |
|
||||
The module uses bam2fq method 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 ]
|
||||
- inputbam:
|
||||
type: file
|
||||
description: BAM/CRAM/SAM file
|
||||
pattern: "*.{bam,cram,sam}"
|
||||
- split:
|
||||
type: boolean
|
||||
description: |
|
||||
TRUE/FALSE value to indicate if reads should be separated into
|
||||
/1, /2 and if present other, or singleton.
|
||||
Note: choosing TRUE will generate 4 different files.
|
||||
Choosing FALSE will produce a single file, which will be interleaved in case
|
||||
the input contains paired reads.
|
||||
|
||||
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"
|
||||
- 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"
|
||||
|
||||
authors:
|
||||
- "@lescai"
|
44
modules/nf-core/modules/samtools/view/main.nf
generated
Normal file
44
modules/nf-core/modules/samtools/view/main.nf
generated
Normal file
|
@ -0,0 +1,44 @@
|
|||
process SAMTOOLS_VIEW {
|
||||
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
|
||||
|
||||
output:
|
||||
tuple val(meta), path("*.bam") , emit: bam , optional: true
|
||||
tuple val(meta), path("*.cram"), emit: cram, optional: true
|
||||
path "versions.yml" , emit: versions
|
||||
|
||||
when:
|
||||
task.ext.when == null || task.ext.when
|
||||
|
||||
script:
|
||||
def args = task.ext.args ?: ''
|
||||
def args2 = task.ext.args2 ?: ''
|
||||
def prefix = task.ext.prefix ?: "${meta.id}"
|
||||
def reference = fasta ? "--reference ${fasta} -C" : ""
|
||||
def file_type = input.getExtension()
|
||||
if ("$input" == "${prefix}.${file_type}") error "Input and output names are the same, use \"task.ext.prefix\" to disambiguate!"
|
||||
"""
|
||||
samtools \\
|
||||
view \\
|
||||
--threads ${task.cpus-1} \\
|
||||
${reference} \\
|
||||
$args \\
|
||||
$input \\
|
||||
$args2 \\
|
||||
> ${prefix}.${file_type}
|
||||
|
||||
cat <<-END_VERSIONS > versions.yml
|
||||
"${task.process}":
|
||||
samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
|
||||
END_VERSIONS
|
||||
"""
|
||||
}
|
57
modules/nf-core/modules/samtools/view/meta.yml
generated
Normal file
57
modules/nf-core/modules/samtools/view/meta.yml
generated
Normal file
|
@ -0,0 +1,57 @@
|
|||
name: samtools_view
|
||||
description: filter/convert SAM/BAM/CRAM file
|
||||
keywords:
|
||||
- view
|
||||
- bam
|
||||
- sam
|
||||
- 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/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
|
||||
pattern: "*.{fasta,fa}"
|
||||
output:
|
||||
- meta:
|
||||
type: map
|
||||
description: |
|
||||
Groovy Map containing sample information
|
||||
e.g. [ id:'test', single_end:false ]
|
||||
- bam:
|
||||
type: file
|
||||
description: filtered/converted BAM/SAM file
|
||||
pattern: "*.{bam,sam}"
|
||||
- cram:
|
||||
type: file
|
||||
description: filtered/converted CRAM file
|
||||
pattern: "*.cram"
|
||||
- versions:
|
||||
type: file
|
||||
description: File containing software versions
|
||||
pattern: "versions.yml"
|
||||
authors:
|
||||
- "@drpatelh"
|
||||
- "@joseespinosa"
|
||||
- "@FriederikeHanssen"
|
56
nf-core/modules/samtools/bam2fq/main.nf
Normal file
56
nf-core/modules/samtools/bam2fq/main.nf
Normal file
|
@ -0,0 +1,56 @@
|
|||
process SAMTOOLS_BAM2FQ {
|
||||
tag "$meta.id"
|
||||
label 'process_low'
|
||||
|
||||
conda (params.enable_conda ? "bioconda::samtools=1.15.1" : null)
|
||||
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
|
||||
'https://depot.galaxyproject.org/singularity/samtools:1.15.1--h1170115_0' :
|
||||
'quay.io/biocontainers/samtools:1.15.1--h1170115_0' }"
|
||||
|
||||
input:
|
||||
tuple val(meta), path(inputbam)
|
||||
val split
|
||||
|
||||
output:
|
||||
tuple val(meta), path("*.fq.gz"), emit: reads
|
||||
path "versions.yml" , emit: versions
|
||||
|
||||
when:
|
||||
task.ext.when == null || task.ext.when
|
||||
|
||||
script:
|
||||
def args = task.ext.args ?: ''
|
||||
def prefix = task.ext.prefix ?: "${meta.id}"
|
||||
|
||||
if (split){
|
||||
"""
|
||||
samtools \\
|
||||
bam2fq \\
|
||||
$args \\
|
||||
-@ $task.cpus \\
|
||||
-1 ${prefix}_1.fq.gz \\
|
||||
-2 ${prefix}_2.fq.gz \\
|
||||
-0 ${prefix}_other.fq.gz \\
|
||||
-s ${prefix}_singleton.fq.gz \\
|
||||
$inputbam
|
||||
|
||||
cat <<-END_VERSIONS > versions.yml
|
||||
"${task.process}":
|
||||
samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
|
||||
END_VERSIONS
|
||||
"""
|
||||
} else {
|
||||
"""
|
||||
samtools \\
|
||||
bam2fq \\
|
||||
$args \\
|
||||
-@ $task.cpus \\
|
||||
$inputbam >${prefix}_interleaved.fq.gz
|
||||
|
||||
cat <<-END_VERSIONS > versions.yml
|
||||
"${task.process}":
|
||||
samtools: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//')
|
||||
END_VERSIONS
|
||||
"""
|
||||
}
|
||||
}
|
55
nf-core/modules/samtools/bam2fq/meta.yml
Normal file
55
nf-core/modules/samtools/bam2fq/meta.yml
Normal file
|
@ -0,0 +1,55 @@
|
|||
name: samtools_bam2fq
|
||||
description: |
|
||||
The module uses bam2fq method 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 ]
|
||||
- inputbam:
|
||||
type: file
|
||||
description: BAM/CRAM/SAM file
|
||||
pattern: "*.{bam,cram,sam}"
|
||||
- split:
|
||||
type: boolean
|
||||
description: |
|
||||
TRUE/FALSE value to indicate if reads should be separated into
|
||||
/1, /2 and if present other, or singleton.
|
||||
Note: choosing TRUE will generate 4 different files.
|
||||
Choosing FALSE will produce a single file, which will be interleaved in case
|
||||
the input contains paired reads.
|
||||
|
||||
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"
|
||||
- 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"
|
||||
|
||||
authors:
|
||||
- "@lescai"
|
Loading…
Reference in a new issue