Merge branch 'master' into antismashlite

This commit is contained in:
Jasmin F 2022-05-16 10:38:01 +02:00 committed by GitHub
commit adcfae6cd4
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17 changed files with 460 additions and 23 deletions

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@ -11,6 +11,7 @@ process BOWTIE2_ALIGN {
tuple val(meta), path(reads)
path index
val save_unaligned
val sort_bam
output:
tuple val(meta), path("*.bam") , emit: bam
@ -36,8 +37,7 @@ process BOWTIE2_ALIGN {
reads_args = "-1 ${reads[0]} -2 ${reads[1]}"
}
def samtools_command = "samtools view -@ $task.cpus --bam --with-header ${args2} > ${prefix}.bam"
def samtools_command = sort_bam ? 'sort' : 'view'
"""
INDEX=`find -L ./ -name "*.rev.1.bt2" | sed "s/.rev.1.bt2//"`
@ -51,7 +51,7 @@ process BOWTIE2_ALIGN {
$unaligned \\
$args \\
2> ${prefix}.bowtie2.log \\
| $samtools_command
| samtools $samtools_command $args2 --threads $task.cpus -o ${prefix}.bam -
if [ -f ${prefix}.unmapped.fastq.1.gz ]; then
mv ${prefix}.unmapped.fastq.1.gz ${prefix}.unmapped_1.fastq.gz
@ -69,4 +69,3 @@ process BOWTIE2_ALIGN {
END_VERSIONS
"""
}

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@ -29,6 +29,15 @@ input:
type: file
description: Bowtie2 genome index files
pattern: "*.ebwt"
- save_unaligned:
type: boolean
description: |
Save reads that do not map to the reference (true) or discard them (false)
(default: false)
- sort_bam:
type: boolean
description: use samtools sort (true) or samtools view (false)
pattern: "true or false"
output:
- bam:
type: file

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@ -0,0 +1,48 @@
process GATK4_SPLITINTERVALS {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::gatk4=4.2.6.1" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/gatk4:4.2.6.1--hdfd78af_0':
'quay.io/biocontainers/gatk4:4.2.6.1--hdfd78af_0' }"
input:
tuple val(meta), path(intervals)
path(fasta)
path(fasta_fai)
path(dict)
output:
tuple val(meta), path("**.interval_list"), emit: split_intervals
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 reference = fasta ? "--reference $fasta" : ""
def avail_mem = 3
if (!task.memory) {
log.info '[GATK SplitIntervals] Available memory not known - defaulting to 3GB. Specify process memory requirements to change this.'
} else {
avail_mem = task.memory.giga
}
"""
gatk --java-options "-Xmx${avail_mem}g" SplitIntervals \\
--output ${prefix} \\
--intervals $intervals \\
$reference \\
--tmp-dir . \\
$args
cat <<-END_VERSIONS > versions.yml
"${task.process}":
gatk4: \$(echo \$(gatk --version 2>&1) | sed 's/^.*(GATK) v//; s/ .*\$//')
END_VERSIONS
"""
}

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@ -0,0 +1,53 @@
name: gatk4_splitintervals
keywords:
- interval
- bed
tools:
- gatk4:
description: Genome Analysis Toolkit (GATK4)
homepage: https://gatk.broadinstitute.org/hc/en-us
documentation: https://gatk.broadinstitute.org/hc/en-us/categories/360002369672s
tool_dev_url: https://github.com/broadinstitute/gatk
doi: "10.1158/1538-7445.AM2017-3590"
licence: ["BSD-3-clause"]
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test' ]
- interval:
type: file
description: Interval list or BED
pattern: "*.{interval,interval_list,bed}"
- fasta:
type: file
description: Reference FASTA
pattern: "*.{fa,fasta}"
- fasta_fai:
type: file
description: Reference FASTA index
pattern: "*.fai"
- dict:
type: file
description: Reference sequence dictionary
pattern: "*.dict"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test' ]
- bed:
type: file
description: A list of scattered interval lists
pattern: "*.interval_list"
- versions:
type: file
description: File containing software versions
pattern: "versions.yml"
authors:
- "@nvnieuwk"

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@ -0,0 +1,40 @@
process GENOMESCOPE2 {
tag "$meta.id"
label 'process_low'
conda (params.enable_conda ? "bioconda::genomescope2=2.0" : null)
container "${ workflow.containerEngine == 'singularity' && !task.ext.singularity_pull_docker_container ?
'https://depot.galaxyproject.org/singularity/genomescope2:2.0--py310r41hdfd78af_5':
'quay.io/biocontainers/genomescope2:2.0--py310r41hdfd78af_5' }"
input:
tuple val(meta), path(histogram)
output:
tuple val(meta), path("*_linear_plot.png") , emit: linear_plot_png
tuple val(meta), path("*_transformed_linear_plot.png"), emit: transformed_linear_plot_png
tuple val(meta), path("*_log_plot.png") , emit: log_plot_png
tuple val(meta), path("*_transformed_log_plot.png") , emit: transformed_log_plot_png
tuple val(meta), path("*_model.txt") , emit: model
tuple val(meta), path("*_summary.txt") , emit: summary
path "versions.yml" , emit: versions
when:
task.ext.when == null || task.ext.when
script:
def args = task.ext.args ?: ''
prefix = task.ext.prefix ?: "${meta.id}"
"""
genomescope2 \\
--input $histogram \\
$args \\
--output . \\
--name_prefix $prefix
cat <<-END_VERSIONS > versions.yml
'${task.process}':
genomescope2: \$( genomescope2 -v | sed 's/GenomeScope //' )
END_VERSIONS
"""
}

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@ -0,0 +1,67 @@
name: "genomescope2"
description: Estimate genome heterozygosity, repeat content, and size from sequencing reads using a kmer-based statistical approach
keywords:
- "genome size"
- "genome heterozygosity"
- "repeat content"
tools:
- "genomescope2":
description: "Reference-free profiling of polyploid genomes"
homepage: "http://qb.cshl.edu/genomescope/genomescope2.0/"
documentation: "https://github.com/tbenavi1/genomescope2.0/blob/master/README.md"
tool_dev_url: "https://github.com/tbenavi1/genomescope2.0"
doi: "https://doi.org/10.1038/s41467-020-14998-3"
licence: "['Apache License, Version 2.0 (Apache-2.0)']"
input:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- histogram:
type: file
description: A K-mer histogram file
pattern: "*.hist"
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"
- linear_plot_png:
type: file
description: A genomescope2 linear plot in PNG format
pattern: "*_linear_plot.png"
- linear_plot_png:
type: file
description: A genomescope2 linear plot in PNG format
pattern: "*_linear_plot.png"
- transformed_linear_plot_png:
type: file
description: A genomescope2 transformed linear plot in PNG format
pattern: "*_transformed_linear_plot.png"
- log_plot_png:
type: file
description: A genomescope2 log plot in PNG format
pattern: "*_log_plot.png"
- transformed_log_plot_png:
type: file
description: A genomescope2 transformed log plot in PNG format
pattern: "*_transformed_log_plot.png"
- model:
type: file
description: Genomescope2 model fit summary
pattern: "*_model.txt"
- summary:
type: file
description: Genomescope2 histogram summary
pattern: "*_summary.txt"
authors:
- "@mahesh-panchal"

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@ -35,12 +35,13 @@ process RTGTOOLS_VCFEVAL {
def eval_regions = evaluation_regions ? "--evaluation-regions=$evaluation_regions" : ""
def truth_index = truth_vcf_tbi ? "" : "rtg index $truth_vcf"
def query_index = query_vcf_tbi ? "" : "rtg index $query_vcf"
def avail_mem = task.memory.toGiga() + "G"
"""
$truth_index
$query_index
rtg vcfeval \\
rtg RTG_MEM=$avail_mem vcfeval \\
$args \\
--baseline=$truth_vcf \\
$bed_regions \\

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@ -823,6 +823,10 @@ gatk4/selectvariants:
- modules/gatk4/selectvariants/**
- tests/modules/gatk4/selectvariants/**
gatk4/splitintervals:
- modules/gatk4/splitintervals/**
- tests/modules/gatk4/splitintervals/**
gatk4/splitncigarreads:
- modules/gatk4/splitncigarreads/**
- tests/modules/gatk4/splitncigarreads/**
@ -843,6 +847,10 @@ genmap/mappability:
- modules/genmap/mappability/**
- tests/modules/genmap/mappability/**
genomescope2:
- modules/genomescope2/**
- tests/modules/genomescope2/**
genrich:
- modules/genrich/**
- tests/modules/genrich/**
@ -1651,14 +1659,14 @@ samtools/bam2fq:
- modules/samtools/bam2fq/**
- tests/modules/samtools/bam2fq/**
samtools/convert:
- modules/samtools/convert/**
- tests/modules/samtools/convert/**
samtools/collatefastq:
- modules/samtools/collatefastq/**
- tests/modules/samtools/collatefastq/**
samtools/convert:
- modules/samtools/convert/**
- tests/modules/samtools/convert/**
samtools/depth:
- modules/samtools/depth/**
- tests/modules/samtools/depth/**

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@ -14,9 +14,25 @@ workflow test_bowtie2_align_single_end {
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = false
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_single_end_sorted {
input = [
[ id:'test', single_end:true ], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true)
]
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = true
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_paired_end {
@ -29,7 +45,55 @@ workflow test_bowtie2_align_paired_end {
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = false
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_paired_end_sorted {
input = [
[ id:'test', single_end:false ], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true),
file(params.test_data['sarscov2']['illumina']['test_2_fastq_gz'], checkIfExists: true)
]
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = true
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_single_end_large_index {
input = [
[ id:'test', single_end:true ], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true)
]
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = false
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}
workflow test_bowtie2_align_paired_end_large_index {
input = [
[ id:'test', single_end:false ], // meta map
[
file(params.test_data['sarscov2']['illumina']['test_1_fastq_gz'], checkIfExists: true),
file(params.test_data['sarscov2']['illumina']['test_2_fastq_gz'], checkIfExists: true)
]
]
fasta = file(params.test_data['sarscov2']['genome']['genome_fasta'], checkIfExists: true)
save_unaligned = false
sort = false
BOWTIE2_BUILD ( fasta )
BOWTIE2_ALIGN ( input, BOWTIE2_BUILD.out.index, save_unaligned, sort )
}

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@ -5,6 +5,7 @@ params {
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
}
if (params.force_large_index) {

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@ -1,21 +1,49 @@
- name: bowtie2 align test_bowtie2_align_single_end
command: nextflow run ./tests/modules/bowtie2/align -entry test_bowtie2_align_single_end -c ./tests/config/nextflow.config -c ./tests/modules/bowtie2/align/nextflow.config
tags:
- bowtie2/align
- bowtie2
- bowtie2/align
files:
- path: output/bowtie2/test.bam
- path: output/bowtie2/test.bowtie2.log
md5sum: 7b8a9e61b7646da1089b041333c41a87
- path: output/bowtie2/versions.yml
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml
- name: bowtie2 align test_bowtie2_align_single_end_sorted
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
tags:
- bowtie2
- bowtie2/align
files:
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml
- name: bowtie2 align test_bowtie2_align_paired_end
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
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
tags:
- bowtie2/align
- bowtie2
- bowtie2/align
files:
- path: output/bowtie2/test.bam
- path: output/bowtie2/test.bowtie2.log
md5sum: bd89ce1b28c93bf822bae391ffcedd19
- path: output/bowtie2/versions.yml
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml
- name: bowtie2 align test_bowtie2_align_single_end_large_index
command: nextflow run tests/modules/bowtie2/align -entry test_bowtie2_align_single_end_large_index -c tests/config/nextflow.config -c tests/modules/bowtie2/align/nextflow.config --force_large_index
tags:
- bowtie2
- bowtie2/align
files:
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml
- name: bowtie2 align test_bowtie2_align_paired_end_large_index
command: nextflow run tests/modules/bowtie2/align -entry test_bowtie2_align_paired_end_large_index -c tests/config/nextflow.config -c tests/modules/bowtie2/align/nextflow.config --force_large_index
tags:
- bowtie2
- bowtie2/align
files:
- path: ./output/bowtie2/test.bam
- path: ./output/bowtie2/test.bowtie2.log
- path: ./output/bowtie2/versions.yml

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@ -0,0 +1,33 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { GATK4_SPLITINTERVALS } from '../../../../modules/gatk4/splitintervals/main.nf'
workflow test_gatk4_splitintervals_bed {
input = [
[ id:'test' ], // meta map
file(params.test_data['homo_sapiens']['genome']['genome_multi_interval_bed'], checkIfExists: true)
]
fasta = file(params.test_data['homo_sapiens']['genome']['genome_fasta'], checkIfExists: true)
fasta_fai = file(params.test_data['homo_sapiens']['genome']['genome_fasta_fai'], checkIfExists: true)
fasta_dict = file(params.test_data['homo_sapiens']['genome']['genome_dict'], checkIfExists: true)
GATK4_SPLITINTERVALS ( input, fasta, fasta_fai, fasta_dict)
}
workflow test_gatk4_splitintervals_intervals {
input = [
[ id:'test' ], // meta map
file(params.test_data['homo_sapiens']['genome']['genome_interval_list'], checkIfExists: true)
]
fasta = file(params.test_data['homo_sapiens']['genome']['genome_fasta'], checkIfExists: true)
fasta_fai = file(params.test_data['homo_sapiens']['genome']['genome_fasta_fai'], checkIfExists: true)
fasta_dict = file(params.test_data['homo_sapiens']['genome']['genome_dict'], checkIfExists: true)
GATK4_SPLITINTERVALS ( input, fasta, fasta_fai, fasta_dict)
}

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@ -0,0 +1,9 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
withName: GATK4_SPLITINTERVALS {
ext.args = "--scatter-count 2"
}
}

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@ -0,0 +1,23 @@
- name: gatk4 splitintervals test_gatk4_splitintervals_bed
command: nextflow run tests/modules/gatk4/splitintervals -entry test_gatk4_splitintervals_bed -c tests/config/nextflow.config
tags:
- gatk4/splitintervals
- gatk4
files:
- path: output/gatk4/test/0000-scattered.interval_list
md5sum: c8d6b19e7a92535b6ce9608eae558faa
- path: output/gatk4/test/0001-scattered.interval_list
md5sum: b1877ad96aec308906594c50ebbe3ded
- path: output/gatk4/versions.yml
- name: gatk4 splitintervals test_gatk4_splitintervals_intervals
command: nextflow run tests/modules/gatk4/splitintervals -entry test_gatk4_splitintervals_intervals -c tests/config/nextflow.config
tags:
- gatk4/splitintervals
- gatk4
files:
- path: output/gatk4/test/0000-scattered.interval_list
md5sum: ebd6b34a335efc6732ff541936c6d2d5
- path: output/gatk4/test/0001-scattered.interval_list
md5sum: 9459b0e124fa84ec1e64ac4615bc9af7
- path: output/gatk4/versions.yml

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@ -0,0 +1,19 @@
#!/usr/bin/env nextflow
nextflow.enable.dsl = 2
include { MERYL_COUNT } from '../../../modules/meryl/count/main.nf'
include { MERYL_HISTOGRAM } from '../../../modules/meryl/histogram/main.nf'
include { GENOMESCOPE2 } from '../../../modules/genomescope2/main.nf'
workflow test_genomescope2 {
input = [
[ id:'test', single_end:false ], // meta map
file(params.test_data['bacteroides_fragilis']['illumina']['test1_1_fastq_gz'], checkIfExists: true)
]
MERYL_COUNT ( input )
MERYL_HISTOGRAM ( MERYL_COUNT.out.meryl_db )
GENOMESCOPE2 ( MERYL_HISTOGRAM.out.hist )
}

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@ -0,0 +1,13 @@
process {
publishDir = { "${params.outdir}/${task.process.tokenize(':')[-1].tokenize('_')[0].toLowerCase()}" }
withName: 'MERYL.*' {
ext.args = 'k=21'
}
withName: 'GENOMESCOPE2' {
ext.args = '-k 21 -p 1'
}
}

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@ -0,0 +1,22 @@
- name: genomescope2 test_genomescope2
command: nextflow run tests/modules/genomescope2 -entry test_genomescope2 -c tests/config/nextflow.config
tags:
- genomescope2
files:
- path: output/genomescope2/test_linear_plot.png
md5sum: 94c165c5028156299a1d4d05766cac51
- path: output/genomescope2/test_log_plot.png
md5sum: 9d25ca463d92a0c73a893da7fd3979ba
- path: output/genomescope2/test_model.txt
md5sum: 3caf62f715f64a2f2b8fdff5d079cb84
- path: output/genomescope2/test_summary.txt
md5sum: 7452860e2cea99b85f3ff60daeac77f5
- path: output/genomescope2/test_transformed_linear_plot.png
md5sum: 99a64c1c18d8670f64cb863d4334abbb
- path: output/genomescope2/test_transformed_log_plot.png
md5sum: b4e029c9fb9987ca33b17392a691c1b4
- path: output/genomescope2/versions.yml
md5sum: 18afeb26f62a47f680b2bb3e27da9cbc
- path: output/meryl/test.hist
md5sum: f75362ab9cd70d96621b3690e952085f
- path: output/meryl/versions.yml