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nextflow.config
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432 lines (400 loc) · 18.1 KB
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/*
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
nf-core/rnadnavar Nextflow config file
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Dbam_laign.configefault config options for all compute environments
----------------------------------------------------------------------------------------
*/
// Global default params, used in configs
params {
// Input options - mandatory
input = null // sample sheet
input_restart = null
step = 'mapping' // Starts with mapping
skip_tools = null // All tools (markduplicates + baserecalibrator + QC) are 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
rna = true
dna = true
// Genome and reference options
genome = 'GRCh38'
igenomes_base = 's3://ngi-igenomes/igenomes/'
igenomes_ignore = false
save_reference = false
build_only_index = false // Only build the reference indexes
download_cache = false // Do not download annotation cache
fasta_fai = null
dict = null
// Sequence read information
read_length = 76 // Required for STAR to build index and align reads TODO: automate
wes = false // Set to true, if data is exome/targeted sequencing data. Used to use correct models in various variant callers
// Alignment
bwa = null
bwamem2 = null
star_index = null
aligner = 'bwa-mem'
star_twopass = true
star_ignore_sjdbgtf = false // Ignore GTF file while creating index or alignment by STAR
star_max_memory_bamsort = 0 // STAR parameter limitBAMsortRAM to specify maximum RAM for sorting BAM
star_bins_bamsort = 50 // STAR parameter outBAMsortingBinsN to specify number of bins for sorting BAM
star_max_collapsed_junc = 1000000 // STAR parameter limitOutSJcollapsed to specify max number of collapsed junctions
seq_center = null
seq_platform = 'ILLUMINA' // Required for preparing for BAM headers for GATK to work
bam_csi_index = false
save_unaligned = false
save_align_intermeds = false
hisat2_build_memory = "200.GB"
splicesites = null
remove_duplicates = false
save_mapped = false // Mapped BAMs not saved
hisat2_index = null
dragmap = null
gff = null
// 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
split_fastq = 50000000 // FASTQ files will not be split by default by FASTP
save_trimmed = false
save_split_fastqs = false
// Variant calling
defaultvariantcallers = "sage,strelka,mutect2" // Default variant callers
no_intervals = false
intervals = null
nucleotides_per_second = 200000 // Default interval size
germline_resource = null
germline_resource_tbi = null
dbsnp = null
dbsnp_tbi = null
known_indels = null
known_indels_tbi = null
known_snps = null
known_snps_tbi = null
pon = null
pon_tbi = null
sage_actionablepanel = null
sage_highconfidence = null
sage_knownhotspots = null
sage_custom_args = "-validation_stringency LENIENT"
sage_resource_dir = null
sage_ensembl_dir = null
joint_mutect2 = false // if true, enables patient-wise multi-sample somatic variant calling
// GATK intervallist parameters
gatk_interval_scatter_count = 25
ignore_soft_clipped_bases = true
// Variant annotation
tools = null // No default Variant_Calling or Annotation tools
genesplicer = null // genesplicer disabled within VEP
dbnsfp = null // No dbnsfp processed file
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
dbnsfp_tbi = null // No dbnsfp processed file index
spliceai_indel = null // No spliceai_indel file
spliceai_indel_tbi = null // No spliceai_indel file index
spliceai_snv = null // No spliceai_snv file
spliceai_snv_tbi = null // No spliceai_snv file index
vep_custom_args = "--no_progress --offline --shift_hgvs 1 --check_existing --tsl --domains --total_length --allele_number --no_escape --xref_refseq --failed 1 --flag_pick_allele --pick_order canonical,tsl,biotype,rank,ccds,length --format vcf --biotype --force_overwrite --sift p --polyphen p --variant_class --regulatory --allele_number --af_gnomad --af_gnomadg --gene_phenotype --hgvs --hgvsg --max_af"
vep_cache = null // No directory for VEP cache
vep_include_fasta = true // Don't use fasta file for annotation with VEP
vep_dbnsfp = null
vep_loftee = null
vep_spliceai = null
vep_spliceregion = null
vep_out_format = 'vcf'
vep_cache_version = 110
vep_species = 'homo_sapiens'
vep_genome = null
outdir_cache = null // No default outdir cache
//filtering
whitelist = null
blacklist = null
rnaedits = null
chain = null
rna_pon = null
rna_pon2 = null
fasta2 = null
refname2 = null
refname = null
// MultiQC options
multiqc_config = null
multiqc_title = null
multiqc_logo = null
max_multiqc_email_size = '25.MB'
multiqc_methods_description = null
// Boilerplate options
outdir = null
publish_dir_mode = 'copy'
email = null
email_on_fail = null
plaintext_email = false
monochrome_logs = false
hook_url = System.getenv('HOOK_URL')
help = false
help_full = false
show_hidden = false
version = false
modules_testdata_base_path = 'https://raw.githubusercontent.com/nf-core/test-datasets/modules/data/'
pipelines_testdata_base_path = 'https://raw.githubusercontent.com/nf-core/test-datasets/rnadnavar/'
trace_report_suffix = new java.util.Date().format( 'yyyy-MM-dd_HH-mm-ss')// Config options
config_profile_name = null
config_profile_description = null
custom_config_version = 'master'
custom_config_base = "https://raw.githubusercontent.com/nf-core/configs/${params.custom_config_version}"
config_profile_contact = null
config_profile_url = null
// Schema validation default options
validate_params = true
}
// Load base.config by default for all pipelines
includeConfig 'conf/base.config'
profiles {
debug {
dumpHashes = true
process.beforeScript = 'echo $HOSTNAME'
cleanup = false
nextflow.enable.configProcessNamesValidation = true
}
conda {
conda.enabled = true
docker.enabled = false
singularity.enabled = false
podman.enabled = false
shifter.enabled = false
charliecloud.enabled = false
conda.channels = ['conda-forge', 'bioconda']
apptainer.enabled = false
}
mamba {
conda.enabled = true
conda.useMamba = true
docker.enabled = false
singularity.enabled = false
podman.enabled = false
shifter.enabled = false
charliecloud.enabled = false
apptainer.enabled = false
}
docker {
docker.enabled = true
conda.enabled = false
singularity.enabled = false
podman.enabled = false
shifter.enabled = false
charliecloud.enabled = false
apptainer.enabled = false
docker.runOptions = '-u $(id -u):$(id -g)'
}
arm64 {
process.arch = 'arm64'
// TODO https://github.com/nf-core/modules/issues/6694
// For now if you're using arm64 you have to use wave for the sake of the maintainers
// wave profile
apptainer.ociAutoPull = true
singularity.ociAutoPull = true
wave.enabled = true
wave.freeze = true
wave.strategy = 'conda,container'
}
emulate_amd64 {
docker.runOptions = '-u $(id -u):$(id -g) --platform=linux/amd64'
}
singularity {
singularity.enabled = true
singularity.autoMounts = true
conda.enabled = false
docker.enabled = false
podman.enabled = false
shifter.enabled = false
charliecloud.enabled = false
apptainer.enabled = false
}
podman {
podman.enabled = true
conda.enabled = false
docker.enabled = false
singularity.enabled = false
shifter.enabled = false
charliecloud.enabled = false
apptainer.enabled = false
}
shifter {
shifter.enabled = true
conda.enabled = false
docker.enabled = false
singularity.enabled = false
podman.enabled = false
charliecloud.enabled = false
apptainer.enabled = false
}
charliecloud {
charliecloud.enabled = true
conda.enabled = false
docker.enabled = false
singularity.enabled = false
podman.enabled = false
shifter.enabled = false
apptainer.enabled = false
}
apptainer {
apptainer.enabled = true
apptainer.autoMounts = true
conda.enabled = false
docker.enabled = false
singularity.enabled = false
podman.enabled = false
shifter.enabled = false
charliecloud.enabled = false
}
wave {
apptainer.ociAutoPull = true
singularity.ociAutoPull = true
wave.enabled = true
wave.freeze = true
wave.strategy = 'conda,container'
}
gitpod {
executor.name = 'local'
executor.cpus = 4
executor.memory = 8.GB
process {
resourceLimits = [
memory: 8.GB,
cpus : 4,
time : 1.h
]
}
}
gpu {
docker.runOptions = '-u $(id -u):$(id -g) --gpus all'
apptainer.runOptions = '--nv'
singularity.runOptions = '--nv'
}
// Basic test profile for CI
test { includeConfig 'conf/test.config' }
test_full { includeConfig 'conf/test_full.config' }
}
// Load nf-core custom profiles from different institutions
// If params.custom_config_base is set AND either the NXF_OFFLINE environment variable is not set or params.custom_config_base is a local path, the nfcore_custom.config file from the specified base path is included.
// Load nf-core/rnadnavar custom profiles from different institutions.
includeConfig params.custom_config_base && (!System.getenv('NXF_OFFLINE') || !params.custom_config_base.startsWith('http')) ? "${params.custom_config_base}/nfcore_custom.config" : "/dev/null"
// Load nf-core/rnadnavar custom profiles from different institutions.
includeConfig params.custom_config_base && (!System.getenv('NXF_OFFLINE') || !params.custom_config_base.startsWith('http')) ? "${params.custom_config_base}/pipeline/rnadnavar.config" : "/dev/null"
// Set default registry for Apptainer, Docker, Podman, Charliecloud and Singularity independent of -profile
// Will not be used unless Apptainer / Docker / Podman / Charliecloud / Singularity are enabled
// Set to your registry if you have a mirror of containers
apptainer.registry = 'quay.io'
docker.registry = 'quay.io'
podman.registry = 'quay.io'
singularity.registry = 'quay.io'
charliecloud.registry = 'quay.io'
// Load igenomes.config if required
includeConfig !params.igenomes_ignore ? 'conf/igenomes.config' : 'conf/igenomes_ignored.config'
// 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"
}
// Set bash options
process.shell = [
"bash",
"-C", // No clobber - prevent output redirection from overwriting files.
"-e", // Exit if a tool returns a non-zero status/exit code
"-u", // Treat unset variables and parameters as an error
"-o", // Returns the status of the last command to exit..
"pipefail" // ..with a non-zero status or zero if all successfully execute
]
// Disable process selector warnings by default. Use debug profile to enable warnings.
nextflow.enable.configProcessNamesValidation = false
timeline {
enabled = true
file = "${params.outdir}/pipeline_info/execution_timeline_${params.trace_report_suffix}.html"
}
report {
enabled = true
file = "${params.outdir}/pipeline_info/execution_report_${params.trace_report_suffix}.html"
}
trace {
enabled = true
file = "${params.outdir}/pipeline_info/execution_trace_${params.trace_report_suffix}.txt"
}
dag {
enabled = true
file = "${params.outdir}/pipeline_info/pipeline_dag_${params.trace_report_suffix}.html"
}
// Nextflow plugins
plugins {
id 'nf-schema@2.5.1' // Validation of pipeline parameters and creation of an input channel from a sample sheet
}
validation {
defaultIgnoreParams = ["genomes"]
monochromeLogs = params.monochrome_logs
help {
enabled = true
}
}
manifest {
name = 'nf-core/rnadnavar'
contributors = [
[
name: 'Raquel Manzano Garcia',
affiliation: 'Cancer Research UK',
email: 'Raquel.ManzanoGarcia@cruk.cam.ac.uk',
github: '@RaqManzano',
contribution: ['author', 'maintainer'],
orcid: '0000-0002-5124-8992'
],[
name: 'Maxime U Garcia',
affiliation: 'Seqera',
email: 'maxime.garcia@seqera.io',
github: '@maxulysse',
contribution: ['contributor'],
orcid: '0000-0003-2827-9261'
]
]
homePage = 'https://github.com/nf-core/rnadnavar'
description = """Pipeline for RNA and DNA integrated analysis for somatic mutation detection"""
mainScript = 'main.nf'
defaultBranch = 'master'
nextflowVersion = '!>=25.04.0'
version = '1.0'
doi = ''
}
// Load modules.config for DSL2 module specific options
includeConfig 'conf/modules/modules.config'
// prepare reference
includeConfig 'conf/modules/prepare_resources/prepare_cache.config'
includeConfig 'conf/modules/prepare_resources/prepare_genome.config'
includeConfig 'conf/modules/prepare_resources/prepare_intervals.config'
// quality control
includeConfig 'conf/modules/quality_control/quality_control.config'
includeConfig 'conf/modules/quality_control/trimming.config'
// alignment
includeConfig 'conf/modules/alignment/bam_align.config'
includeConfig 'conf/modules/alignment/alignment_to_fastq.config'
// preprocessing
includeConfig 'conf/modules/gatk4_preprocessing/markduplicates.config'
includeConfig 'conf/modules/gatk4_preprocessing/splitncigarreads.config'
includeConfig 'conf/modules/gatk4_preprocessing/prepare_recalibration.config'
includeConfig 'conf/modules/gatk4_preprocessing/recalibrate.config'
// variant calling
includeConfig 'conf/modules/variant_calling/strelka.config'
includeConfig 'conf/modules/variant_calling/mutect2.config'
includeConfig 'conf/modules/variant_calling/sage.config'
// normalization
includeConfig 'conf/modules/normalize/vt.config'
// annotate
includeConfig 'conf/modules/annotate/annotate.config'
// consensus
includeConfig 'conf/modules/consensus/vcf_consensus.config'
// filtering
includeConfig 'conf/modules/filtering/maf_filtering.config'
// prepare second run
includeConfig 'conf/modules/prepare_realignment/filtersamreads.config'
includeConfig 'conf/modules/prepare_realignment/extract_reads_id.config'