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add sort option to bowtie2
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parent
919275103a
commit
cbc47767f7
4 changed files with 46 additions and 8 deletions
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@ -11,6 +11,7 @@ process BOWTIE2_ALIGN {
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tuple val(meta), path(reads)
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path index
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val save_unaligned
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val sort_bam
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output:
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tuple val(meta), path("*.bam") , emit: bam
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@ -36,8 +37,7 @@ process BOWTIE2_ALIGN {
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reads_args = "-1 ${reads[0]} -2 ${reads[1]}"
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}
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def samtools_command = "samtools view -@ $task.cpus --bam --with-header ${args2} > ${prefix}.bam"
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def samtools_command = sort_bam ? 'sort' : 'view'
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"""
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INDEX=`find -L ./ -name "*.rev.1.bt2" | sed "s/.rev.1.bt2//"`
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@ -51,7 +51,7 @@ process BOWTIE2_ALIGN {
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$unaligned \\
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$args \\
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2> ${prefix}.bowtie2.log \\
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| $samtools_command
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| samtools $samtools_command $args2 --threads $task.cpus -o ${prefix}.bam -
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if [ -f ${prefix}.unmapped.fastq.1.gz ]; then
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mv ${prefix}.unmapped.fastq.1.gz ${prefix}.unmapped_1.fastq.gz
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@ -29,6 +29,15 @@ input:
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type: file
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description: Bowtie2 genome index files
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pattern: "*.ebwt"
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- save_unaligned:
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type: boolean
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description: |
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Save reads that do not map to the reference (true) or discard them (false)
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(default: false)
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- sort_bam:
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type: boolean
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description: use samtools sort (true) or samtools view (false)
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pattern: "true or false"
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output:
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- bam:
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type: file
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@ -14,9 +14,25 @@ workflow test_bowtie2_align_single_end {
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]
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fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
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save_unaligned = false
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sort = false
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BOWTIE2_BUILD ( fasta )
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BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned )
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BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
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}
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workflow test_bowtie2_align_single_end_sorted {
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input = [
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[ id:'test', single_end:true ], // 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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]
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]
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fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
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save_unaligned = false
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sort = true
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BOWTIE2_BUILD ( fasta )
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BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
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}
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workflow test_bowtie2_align_paired_end {
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@ -29,9 +45,10 @@ workflow test_bowtie2_align_paired_end {
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]
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fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
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save_unaligned = false
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sort = false
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BOWTIE2_BUILD ( fasta )
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BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned )
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BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
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}
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workflow test_bowtie2_align_single_end_large_index {
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@ -43,9 +60,10 @@ workflow test_bowtie2_align_single_end_large_index {
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]
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fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
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save_unaligned = false
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sort = false
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BOWTIE2_BUILD ( fasta )
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BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned )
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BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
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}
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workflow test_bowtie2_align_paired_end_large_index {
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@ -58,7 +76,8 @@ workflow test_bowtie2_align_paired_end_large_index {
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]
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fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
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save_unaligned = false
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sort = false
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BOWTIE2_BUILD ( fasta )
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BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned )
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BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
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}
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@ -8,6 +8,16 @@
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- path: ./output/bowtie2/test.bowtie2.log
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- path: ./output/bowtie2/versions.yml
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- name: bowtie2 align test_bowtie2_align_single_end
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command: nextflow run ./tests/modules/bowtie2/align -entry test_bowtie2_align_single_end_sorted -c ./tests/config/nextflow.config -c ./tests/modules/bowtie2/align/nextflow.config
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tags:
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- bowtie2
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- bowtie2/align
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files:
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- path: ./output/bowtie2/test.bam
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- path: ./output/bowtie2/test.bowtie2.log
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- path: ./output/bowtie2/versions.yml
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- name: bowtie2 align test_bowtie2_align_paired_end
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command: nextflow run tests/modules/bowtie2/align -entry test_bowtie2_align_paired_end -c tests/config/nextflow.config -c tests/modules/bowtie2/align/nextflow.config
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tags:
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