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Add GATK UnifiedGenotyper
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4 changed files with 37 additions and 31 deletions
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@ -12,10 +12,9 @@ process GATK_UNIFIEDGENOTYPER {
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path(fasta)
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path(fai)
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path(dict)
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path(known_vcf)
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path(intervals)
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path(contamination)
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path(dbsnps)
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path(dbsnp)
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path(comp)
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output:
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@ -29,7 +28,7 @@ process GATK_UNIFIEDGENOTYPER {
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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 contamination_file = contamination ? "-contaminationFile ${contamination}" : ""
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def dbsnps_file = dbsnps ? "--dbsnp ${dbsnps}" : ""
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def dbsnp_file = dbsnp ? "--dbsnp ${dbsnp}" : ""
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def comp_file = comp ? "--comp ${comp}" : ""
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def intervals_file = intervals ? "--intervals ${intervals}" : ""
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@ -48,9 +47,9 @@ process GATK_UNIFIEDGENOTYPER {
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-I ${input} \\
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-R ${fasta} \\
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${contamination_file} \\
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${dbsnps_file} \\
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${dbsnp_file} \\
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${comp_file} \\
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${intervals_file}
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${intervals_file} \\
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-o ${prefix}.vcf \\
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$args
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@ -58,7 +57,7 @@ process GATK_UNIFIEDGENOTYPER {
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cat <<-END_VERSIONS > versions.yml
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"${task.process}":
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gatk: \$(echo \$(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*\$//' ))
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gatk: \$(echo \$(gatk3 --version))
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END_VERSIONS
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"""
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}
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@ -3,9 +3,6 @@ keywords:
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- bam
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- vcf
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- variant calling
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- indel
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- realignment
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- targets
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tools:
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- "gatk":
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description: "The full Genome Analysis Toolkit (GATK) framework, license restricted."
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@ -39,10 +36,22 @@ input:
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type: file
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description: GATK dict file for reference
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pattern: ".dict"
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- known_vcf:
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- intervals:
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type: file
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description: Optional input VCF file(s) with known indels
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pattern: ".vcf"
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description: Bed file with the genomic regions included in the library (optional)
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pattern: "*.intervals"
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- contamination:
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type: file
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description: Tab-separated file containing fraction of contamination in sequencing data (per sample) to aggressively remove
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pattern: "*"
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- dbsnps:
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type: file
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description: VCF file containing known sites (optional)
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pattern: "*"
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- comp:
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type: file
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description: Comparison VCF file (optional)
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pattern: "*"
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output:
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- meta:
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@ -6,10 +6,13 @@ include { GATK_UNIFIEDGENOTYPER } from '../../../../modules/gatk/unifiedgenotype
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workflow test_gatk_unifiedgenotyper {
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input = [
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[ id:'test', single_end:false ], // meta map
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file(params.test_data['sarscov2']['illumina']['test_paired_end_bam'], checkIfExists: true)
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input = [ [ id:'test' ], // meta map
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file(params.test_data['sarscov2']['illumina']['test_paired_end_sorted_bam'], checkIfExists: true),
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file(params.test_data['sarscov2']['illumina']['test_paired_end_sorted_bam_bai'], checkIfExists: true),
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]
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fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
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fai = file(params.test_data['sarscov2']['genome']['genome_fasta_fai'], checkIfExists: true)
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dict = file(params.test_data['sarscov2']['genome']['genome_dict'], checkIfExists: true)
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GATK_UNIFIEDGENOTYPER ( input )
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GATK_UNIFIEDGENOTYPER ( input, fasta, fai, dict, [], [], [], [])
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}
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@ -1,14 +1,9 @@
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## TODO nf-core: Please run the following command to build this file:
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# nf-core modules create-test-yml gatk/unifiedgenotyper
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- name: "gatk unifiedgenotyper"
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- name: gatk unifiedgenotyper test_gatk_unifiedgenotyper
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command: nextflow run ./tests/modules/gatk/unifiedgenotyper -entry test_gatk_unifiedgenotyper -c ./tests/config/nextflow.config -c ./tests/modules/gatk/unifiedgenotyper/nextflow.config
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tags:
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- "gatk"
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#
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- "gatk/unifiedgenotyper"
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#
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- gatk
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- gatk/unifiedgenotyper
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files:
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- path: "output/gatk/test.bam"
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md5sum: e667c7caad0bc4b7ac383fd023c654fc
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- path: output/gatk/versions.yml
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md5sum: a01fe51bc4c6a3a6226fbf77b2c7cf3b
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- path: output/gatk/test.vcf.gz
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contains:
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- "#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT test"
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