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nextflow.config
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nextflow.config
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/*
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
nf-core/sarek Nextflow config file
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Default config options for all compute environments
----------------------------------------------------------------------------------------
*/
params {
// Workflow flags:
// Mandatory arguments
input = null // No default input
step = 'mapping' // Starts with mapping
// Genome and references options
genome = 'GATK.GRCh38'
igenomes_base = 's3://ngi-igenomes/igenomes/'
igenomes_ignore = false
save_reference = false // Built references not saved
// Main options
no_intervals = false // Intervals will be built from the fasta file
nucleotides_per_second = 1000 // Default interval size
tools = null // No default Variant_Calling or Annotation tools
skip_tools = null // All tools (markduplicates + baserecalibrator + QC) are used by default
split_fastq = 50000000 // FASTQ files will not be split by default by FASTP
// Modify fastqs (trim/split) with FASTP
trim_fastq = false // No trimming
clip_r1 = 0
clip_r2 = 0
three_prime_clip_r1 = 0
three_prime_clip_r2 = 0
trim_nextseq = 0
save_trimmed = false
save_split_fastqs = false
// UMI tagged reads
umi_read_structure = null // no UMI
group_by_umi_strategy = 'Adjacency' // default strategy when running with UMI for GROUPREADSBYUMI
// Preprocessing
aligner = 'bwa-mem' // Default is bwa-mem, bwa-mem2 and dragmap can be used too
use_gatk_spark = null // GATK Spark implementation of their tools in local mode not used by default
save_bam_mapped = false // Mapped BAMs not saved
save_output_as_bam = false //Output files from preprocessing are saved as bam and not as cram files
seq_center = null // No sequencing center to be written in read group CN field by aligner
seq_platform = 'ILLUMINA' // Default platform written in read group PL field by aligner
// Variant Calling
only_paired_variant_calling = false //if true, skips germline variant calling for normal-paired samples
ascat_ploidy = null // default value for ASCAT
ascat_min_base_qual = 20 // default value for ASCAT
ascat_min_counts = 10 // default value for ASCAT
ascat_min_map_qual = 35 // default value for ASCAT
ascat_purity = null // default value for ASCAT
cf_ploidy = 2 // default value for Control-FREEC
cf_coeff = 0.05 // default value for Control-FREEC
cf_contamination = 0 // default value for Control-FREEC
cf_contamination_adjustment = false // by default we are not using this in Control-FREEC
cf_mincov = 0 // ControlFreec default values
cf_minqual = 0 // ControlFreec default values
cf_window = null // by default we are not using this in Control-FREEC
ignore_soft_clipped_bases = false // no --dont-use-soft-clipped-bases for GATK Mutect2
wes = false // Set to true, if data is exome/targeted sequencing data. Used to use correct models in various variant callers
joint_germline = false // g.vcf & joint germline calling are not run by default if HaplotypeCaller is selected
// Annotation
vep_out_format = 'vcf'
vep_dbnsfp = null // dbnsfp plugin disabled within VEP
dbnsfp = null // No dbnsfp processed file
dbnsfp_tbi = null // No dbnsfp processed file index
dbnsfp_consequence = null // No default consequence for dbnsfp plugin
dbnsfp_fields = "rs_dbSNP,HGVSc_VEP,HGVSp_VEP,1000Gp3_EAS_AF,1000Gp3_AMR_AF,LRT_score,GERP++_RS,gnomAD_exomes_AF" // Default fields for dbnsfp plugin
vep_loftee = null // loftee plugin disabled within VEP
vep_spliceai = null // spliceai plugin disabled within VEP
spliceai_snv = null // No spliceai_snv file
spliceai_snv_tbi = null // No spliceai_snv file index
spliceai_indel = null // No spliceai_indel file
spliceai_indel_tbi = null // No spliceai_indel file index
vep_spliceregion = null // spliceregion plugin disabled within VEP
snpeff_cache = null // No directory for snpEff cache
vep_cache = null // No directory for VEP cache
vep_include_fasta = false // Don't use fasta file for annotation with VEP
// MultiQC options
multiqc_config = null
multiqc_title = null
max_multiqc_email_size = '25.MB'
// Boilerplate options
outdir = 'results'
tracedir = "${params.outdir}/pipeline_info"
publish_dir_mode = 'copy'
email = null
email_on_fail = null
plaintext_email = false
monochrome_logs = false
help = false
validate_params = true
show_hidden_params = false
schema_ignore_params = 'genomes,snpeff_version,vep_version'
enable_conda = false
// Config options
custom_config_version = 'master'
custom_config_base = "https://raw.githubusercontent.com/nf-core/configs/${params.custom_config_version}"
config_profile_description = null
config_profile_contact = null
config_profile_url = null
config_profile_name = null
// Max resource options
// Defaults only, expecting to be overwritten
max_memory = '128.GB'
max_cpus = 16
max_time = '240.h'
}
// Load base.config by default for all pipelines
includeConfig 'conf/base.config'
// Load nf-core custom profiles from different Institutions
try {
includeConfig "${params.custom_config_base}/nfcore_custom.config"
} catch (Exception e) {
System.err.println("WARNING: Could not load nf-core/config profiles: ${params.custom_config_base}/nfcore_custom.config")
}
// Load nf-core/sarek custom profiles from different institutions.
try {
includeConfig "${params.custom_config_base}/pipeline/sarek.config"
} catch (Exception e) {
System.err.println("WARNING: Could not load nf-core/config/sarek profiles: ${params.custom_config_base}/pipeline/sarek.config")
}
profiles {
debug { process.beforeScript = 'echo $HOSTNAME' }
conda {
params.enable_conda = true
docker.enabled = false
singularity.enabled = false
podman.enabled = false
shifter.enabled = false
charliecloud.enabled = false
}
docker {
docker.enabled = true
docker.userEmulation = { params.use_gatk_spark ? false : true }.call()
singularity.enabled = false
podman.enabled = false
shifter.enabled = false
charliecloud.enabled = false
fixOwnership = true
}
singularity {
singularity.enabled = true
singularity.autoMounts = true
docker.enabled = false
podman.enabled = false
shifter.enabled = false
charliecloud.enabled = false
}
podman {
podman.enabled = true
docker.enabled = false
singularity.enabled = false
shifter.enabled = false
charliecloud.enabled = false
}
shifter {
shifter.enabled = true
docker.enabled = false
singularity.enabled = false
podman.enabled = false
charliecloud.enabled = false
}
charliecloud {
charliecloud.enabled = true
docker.enabled = false
singularity.enabled = false
podman.enabled = false
shifter.enabled = false
}
test { includeConfig 'conf/test.config' }
test_full { includeConfig 'conf/test_full.config' }
test_full_somatic { includeConfig 'conf/test_full_somatic.config' }
}
// Load igenomes.config if required
if (!params.igenomes_ignore) {
includeConfig 'conf/igenomes.config'
} else {
params.genomes = [:]
}
// Export these variables to prevent local Python/R libraries from conflicting with those in the container
// The JULIA depot path has been adjusted to a fixed path `/usr/local/share/julia` that needs to be used for packages in the container.
// See https://apeltzer.github.io/post/03-julia-lang-nextflow/ for details on that. Once we have a common agreement on where to keep Julia packages, this is adjustable.
env {
PYTHONNOUSERSITE = 1
R_PROFILE_USER = "/.Rprofile"
R_ENVIRON_USER = "/.Renviron"
JULIA_DEPOT_PATH = "/usr/local/share/julia"
}
// Capture exit codes from upstream processes when piping
process.shell = ['/bin/bash', '-euo', 'pipefail']
def trace_timestamp = new java.util.Date().format( 'yyyy-MM-dd_HH-mm-ss')
timeline {
enabled = true
file = "${params.tracedir}/execution_timeline_${trace_timestamp}.html"
}
report {
enabled = true
file = "${params.tracedir}/execution_report_${trace_timestamp}.html"
}
trace {
enabled = true
file = "${params.tracedir}/execution_trace_${trace_timestamp}.txt"
}
dag {
enabled = true
file = "${params.tracedir}/pipeline_dag_${trace_timestamp}.html"
}
manifest {
name = 'nf-core/sarek'
author = 'Maxime Garcia, Szilveszter Juhos, Friederike Hanssen'
homePage = 'https://github.com/nf-core/sarek'
description = 'An open-source analysis pipeline to detect germline or somatic variants from whole genome or targeted sequencing'
mainScript = 'main.nf'
nextflowVersion = '!>=21.10.3'
version = '3.0'
}
// Load modules.config for DSL2 module specific options
includeConfig 'conf/modules.config'
// Function to ensure that resource requirements don't go beyond
// a maximum limit
def check_max(obj, type) {
if (type == 'memory') {
try {
if (obj.compareTo(params.max_memory as nextflow.util.MemoryUnit) == 1)
return params.max_memory as nextflow.util.MemoryUnit
else
return obj
} catch (all) {
println " ### ERROR ### Max memory '${params.max_memory}' is not valid! Using default value: $obj"
return obj
}
} else if (type == 'time') {
try {
if (obj.compareTo(params.max_time as nextflow.util.Duration) == 1)
return params.max_time as nextflow.util.Duration
else
return obj
} catch (all) {
println " ### ERROR ### Max time '${params.max_time}' is not valid! Using default value: $obj"
return obj
}
} else if (type == 'cpus') {
try {
return Math.min( obj, params.max_cpus as int )
} catch (all) {
println " ### ERROR ### Max cpus '${params.max_cpus}' is not valid! Using default value: $obj"
return obj
}
}
}