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Merge branch 'master' into gatk_filter
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38
modules/mash/screen/main.nf
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38
modules/mash/screen/main.nf
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process MASH_SCREEN {
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tag "$meta.id"
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label 'process_medium'
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conda (params.enable_conda ? "bioconda::mash=2.3" : null)
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container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
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'https://depot.galaxyproject.org/singularity/mash:2.3--he348c14_1':
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'quay.io/biocontainers/mash:2.3--he348c14_1' }"
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input:
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tuple val(meta), path(query_sketch)
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path fastx_db
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output:
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tuple val(meta), path("*.screen"), emit: screen
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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 ?: "${meta.id}"
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"""
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mash \\
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screen \\
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$args \\
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-p $task.cpus \\
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$query_sketch \\
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$fastx_db \\
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> ${prefix}.screen
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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mash: \$( mash --version )
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END_VERSIONS
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"""
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}
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47
modules/mash/screen/meta.yml
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47
modules/mash/screen/meta.yml
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name: "mash_screen"
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description: Screens query sequences against large sequence databases
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keywords:
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- screen
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- containment
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- contamination
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- taxonomic assignment
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tools:
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- "mash":
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description: Fast sequence distance estimator that uses MinHash
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homepage: https://github.com/marbl/Mash
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documentation: https://mash.readthedocs.io/en/latest/sketches.html
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tool_dev_url: https://github.com/marbl/Mash
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doi: "10.1186/s13059-016-0997-x"
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licence: ["https://github.com/marbl/Mash/blob/master/LICENSE.txt"]
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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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- query_sketch:
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type: file
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description: MinHash sketch of query sequences
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pattern: "*.msh"
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- fastx_db:
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type: file
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description: Sequence files to match against
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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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- 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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- screen:
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type: file
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description: List of sequences from fastx_db similar to query sequences
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pattern: "*.screen"
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authors:
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- "@mahesh-panchal"
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@ -1218,6 +1218,10 @@ mash/dist:
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- modules/mash/dist/**
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- modules/mash/dist/**
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- tests/modules/mash/dist/**
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- tests/modules/mash/dist/**
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mash/screen:
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- modules/mash/screen/**
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- tests/modules/mash/screen/**
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mash/sketch:
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mash/sketch:
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- modules/mash/sketch/**
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- modules/mash/sketch/**
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- tests/modules/mash/sketch/**
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- tests/modules/mash/sketch/**
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21
tests/modules/mash/screen/main.nf
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21
tests/modules/mash/screen/main.nf
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#!/usr/bin/env nextflow
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nextflow.enable.dsl = 2
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include { MASH_SKETCH } from '../../../../modules/mash/sketch/main.nf'
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include { MASH_SCREEN } from '../../../../modules/mash/screen/main.nf'
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workflow test_mash_screen {
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input = [
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[ id:'test', single_end:false], // meta map
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[
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file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true),
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file(params.test_data['sarscov2']['illumina']['test_2_fastq_gz'], checkIfExists: true)
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]
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]
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fastx_db = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
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MASH_SKETCH ( input )
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MASH_SCREEN ( MASH_SKETCH.out.mash, fastx_db )
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}
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5
tests/modules/mash/screen/nextflow.config
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5
tests/modules/mash/screen/nextflow.config
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process {
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publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
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}
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12
tests/modules/mash/screen/test.yml
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12
tests/modules/mash/screen/test.yml
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- name: mash screen test_mash_screen
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command: nextflow run ./tests/modules/mash/screen -entry test_mash_screen -c ./tests/config/nextflow.config -c ./tests/modules/mash/screen/nextflow.config
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tags:
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- mash
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- mash/screen
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files:
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- path: output/mash/test.mash_stats
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md5sum: 2a6f297d8e69a5e4160243bc6c89129c
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- path: output/mash/test.msh
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md5sum: d747145a43dad5f82342036f8f5d9133
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- path: output/mash/test.screen
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md5sum: d3c871dccd5cd57ab54781fa5c5d7278
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