Merge branch 'master' into tool/elprep-merge

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("**.{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} ${prefix}.${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"

tests/config/pytest_modules.yml

@@ -599,6 +599,10 @@ ectyper:
   - modules/ectyper/**
   - tests/modules/ectyper/**
 
+elprep/filter:
+  - modules/elprep/filter/**
+  - tests/modules/elprep/filter/**
+
 elprep/merge:
   - modules/elprep/merge/**
   - tests/modules/elprep/merge/**

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"

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/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