wf-transcriptomes-v202/nextflow.config
2021-12-08 14:34:07 +00:00

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//
// Notes to End Users.
//
// The workflow should run without editing this configuration file,
// however there may be instances in which you wish to edit this
// file for compute performance or other reasons. Please see:
//
// https://nextflow.io/docs/latest/config.html#configuration
//
// for further help editing this file.
params {
help = false
fastq = null
ref_genome = null
ref_annotation = null
// Process cDNA reads using pychopper, turn off for direct RNA:
use_pychopper = true
threads = 4
out_dir = null
sample = null
sample_sheet = null
sanitize_fastq = false
wfversion = "v0.0.1"
aws_image_prefix = null
aws_queue = null
report_name = "report"
monochrome_logs = false
validate_params = true
show_hidden_params = false
schema_ignore_params = 'show_hidden_params,validate_params,monochrome_logs,aws_queue,aws_image_prefix,wfversion'
// Options passed to pychopper:
pychopper_opts = ""
// Extra option passed to minimap2 when generating index
minimap_index_opts = "-k14"
// Extra options passed to minimap2
minimap2_opts = "-uf"
// Add this for SIRV data:
// "--splice-flank=no"
// Minmum mapping quality
minimum_mapping_quality = 40
// Internal priming filter context size:
poly_context = 24
// Maximum allowed poly(A) length in the genome near the 3' end of mapping:
max_poly_run = 8
// Minimium number of reads in BAM bundles:
bundle_min_reads = 50000
// Options passed to stringtie:
stringtie_opts = " --conservative "
// Options passed to gffcompare:
gffcompare_opts = " -R "
// Plot gffcompare results:
plot_gffcmp_stats = true
disable_ping = false
}
manifest {
name = 'epi2me-labs/wf-isoforms'
author = 'Oxford Nanopore Technologies'
homePage = 'https://github.com/epi2me-labs/wf-isoforms'
description = 'RNA/cDNA isoform analysis workflow'
mainScript = 'main.nf'
nextflowVersion = '>=20.10.0'
//version = 'v0.0.7' // TODO: do switch to this?
}
executor {
$local {
cpus = 4
memory = "8 GB"
}
}
// used by default for "standard" (docker) and singularity profiles,
// other profiles may override.
process {
withLabel:isoforms {
container = "ontresearch/wf-isoforms:${params.wfversion}"
}
shell = ['/bin/bash', '-euo', 'pipefail']
}
profiles {
// the "standard" profile is used implicitely by nextflow
// if no other profile is given on the CLI
standard {
docker {
enabled = true
// this ensures container is run as host user and group, but
// also adds host user to the within-container group
runOptions = "--user \$(id -u):\$(id -g) --group-add 100"
}
}
// using singularity instead of docker
singularity {
singularity {
enabled = true
autoMounts = true
}
}
// profile using conda environments
conda {
docker.enabled = false
process {
withLabel:isoforms {
conda = "${projectDir}/environment.yaml"
}
shell = ['/bin/bash', '-euo', 'pipefail']
}
conda {
cacheDir = ""
useMamba = true
}
}
// Using AWS batch.
// May need to set aws.region and aws.batch.cliPath
awsbatch {
process {
executor = 'awsbatch'
queue = "${params.aws_queue}"
memory = '8G'
withLabel:isoforms {
container = "${params.aws_image_prefix}-wf-isoforms:${params.wfversion}"
}
shell = ['/bin/bash', '-euo', 'pipefail']
}
}
// local profile for simplified development testing
local {
process.executor = 'local'
}
}
timeline {
enabled = true
file = "${params.out_dir}/execution/timeline.html"
}
report {
enabled = true
file = "${params.out_dir}/execution/report.html"
}
trace {
enabled = true
file = "${params.out_dir}/execution/trace.txt"
}
dag {
enabled = true
file = "${params.out_dir}/execution/pipeline.svg"
}