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nextflow.config
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nextflow.config
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/*
* -------------------------------------------------
* nf-core/rnaseq Nextflow config file
* -------------------------------------------------
* Default config options for all environments.
*/
// Global default params, used in configs
params {
// Pipeline Options
// Workflow flags
genome = false
reads = "data/*{1,2}.fastq.gz"
singleEnd = false
// References
genome = false
salmon_index = false
transcript_fasta = false
splicesites = false
saveReference = false
gencode = false
compressedReference = false
// Strandedness
forwardStranded = false
reverseStranded = false
unStranded = false
// Trimming
skipTrimming = false
clip_r1 = 0
clip_r2 = 0
three_prime_clip_r1 = 0
three_prime_clip_r2 = 0
trim_nextseq = 0
pico = false
saveTrimmed = false
// Ribosomal RNA removal
removeRiboRNA = false
save_nonrRNA_reads = false
rRNA_database_manifest = false
// Alignment
aligner = 'star'
pseudo_aligner = false
stringTieIgnoreGTF = false
seq_center = false
saveAlignedIntermediates = false
skipAlignment = false
saveUnaligned = false
// Read Counting
fc_extra_attributes = 'gene_name'
fc_group_features = 'gene_id'
fc_count_type = 'exon'
fc_group_features_type = 'gene_biotype'
sampleLevel = false
skipBiotypeQC = false
// QC
skipQC = false
skipFastQC = false
skipPreseq = false
skipDupRadar = false
skipQualimap = false
skipRseQC = false
skipEdgeR = false
skipMultiQC = false
// Defaults
project = false
markdup_java_options = '"-Xms4000m -Xmx7g"' //Established values for markDuplicate memory consumption, see issue PR #689 (in Sarek) for details
hisat_build_memory = 200 // Required amount of memory in GB to build HISAT2 index with splice sites
readPaths = null
star_memory = false // Cluster specific param required for hebbe
rRNA_database_manifest = "$baseDir/assets/rrna-db-defaults.txt"
// Boilerplate options
clusterOptions = false
outdir = './results'
name = false
multiqc_config = "$baseDir/assets/multiqc_config.yaml"
email = false
email_on_fail = false
max_multiqc_email_size = 25.MB
plaintext_email = false
monochrome_logs = false
help = false
igenomes_base = "./iGenomes"
tracedir = "${params.outdir}/pipeline_info"
awsqueue = false
awsregion = 'eu-west-1'
igenomesIgnore = false
custom_config_version = 'master'
custom_config_base = "https://raw.githubusercontent.com/nf-core/configs/${params.custom_config_version}"
hostnames = false
config_profile_description = false
config_profile_contact = false
config_profile_url = false
}
// Container slug. Stable releases should specify release tag!
// Developmental code should specify :dev
process.container = 'nfcore/rnaseq:1.4.2'
// 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: ${params.custom_config_base}/nfcore_custom.config")
}
profiles {
awsbatch { includeConfig 'conf/awsbatch.config' }
conda { process.conda = "$baseDir/environment.yml" }
debug { process.beforeScript = 'echo $HOSTNAME' }
docker { docker.enabled = true }
singularity { singularity.enabled = true
singularity.autoMounts = true }
test { includeConfig 'conf/test.config' }
test_gz { includeConfig 'conf/test_gz.config' }
}
// Avoid this error:
// WARNING: Your kernel does not support swap limit capabilities or the cgroup is not mounted. Memory limited without swap.
// Testing this in nf-core after discussion here https://github.com/nf-core/tools/pull/351, once this is established and works well, nextflow might implement this behavior as new default.
docker.runOptions = '-u \$(id -u):\$(id -g)'
// Load igenomes.config if required
if (!params.igenomesIgnore) {
includeConfig 'conf/igenomes.config'
}
// Capture exit codes from upstream processes when piping
process.shell = ['/bin/bash', '-euo', 'pipefail']
timeline {
enabled = true
file = "${params.tracedir}/execution_timeline.html"
}
report {
enabled = true
file = "${params.tracedir}/execution_report.html"
}
trace {
enabled = true
file = "${params.tracedir}/execution_trace.txt"
}
dag {
enabled = true
file = "${params.tracedir}/pipeline_dag.svg"
}
manifest {
name = 'nf-core/rnaseq'
author = 'Phil Ewels, Rickard Hammarén'
homePage = 'https://github.com/nf-core/rnaseq'
description = 'Nextflow RNA-Seq analysis pipeline, part of the nf-core community.'
mainScript = 'main.nf'
nextflowVersion = '>=19.04.0'
version = '1.4.2'
}
// Function to ensure that resource requirements don't go beyond
// a maximum limit
def check_max(obj, type) {
if (type == 'memory') {
try {
if (obj.compareTo(params.max_memory as nextflow.util.MemoryUnit) == 1)
return params.max_memory as nextflow.util.MemoryUnit
else
return obj
} catch (all) {
println " ### ERROR ### Max memory '${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
}
}
}