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nextflow.config
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nextflow.config
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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
version = false
fastq = null
bam = null
out_dir = "output"
sample_sheet = null
sample = null
single_cell_sample_sheet = null
aws_image_prefix = null
aws_queue = null
disable_ping = false
kit_config = null
threads = 8
full_length_only = true
fastq_chunk = 1000000
ref_genome_dir = null
barcode_adapter1_suff_length = 10
barcode_min_quality = 15
barcode_max_ed = 2
barcode_min_ed_diff = 2
gene_assigns_minqv = 30
matrix_min_genes = 200
matrix_min_cells = 3
matrix_max_mito = 20
matrix_norm_count = 10000
genes_of_interest = null
umap_n_repeats = 3
kit = "3prime:v3"
expected_cells = 500
mito_prefix = "MT-"
stringtie_opts = "-c 2"
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,wf'
wf {
example_cmd = [
"--expected_cells 100",
"--fastq 'wf-single-cell-demo/chr17.fq.gz'",
"--kit '3prime:v3'",
"--ref_genome_dir 'wf-single-cell-demo'",
"--genes_of_interest 'wf-single-cell-demo/umap_plot_genes.csv'",
]
container_sha = "sha0fcdf10929fbef2d426bb985e16b81153a88c6f4"
common_sha = "shad28e55140f75a68f59bbecc74e880aeab16ab158"
}
}
manifest {
name = 'epi2me-labs/wf-single-cell'
author = 'Oxford Nanopore Technologies'
homePage = 'https://github.com/epi2me-labs/wf-single-cell'
description = 'Identification of cell- and UMI barcodes from single-cell sequencing.'
mainScript = 'main.nf'
nextflowVersion = '>=23.04.2'
version = '2.3.0'
}
epi2melabs {
tags = 'transcriptomics'
icon = 'faCircle'
}
env {
PYTHONNOUSERSITE = 1
}
// used by default for "standard" (docker) and singularity profiles,
// other profiles may override.
process {
withLabel:singlecell {
container = "ontresearch/wf-single-cell:${params.wf.container_sha}"
}
withLabel:wf_common {
container = "ontresearch/wf-common:${params.wf.common_sha}"
}
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
}
}
conda {
conda.enabled = true
}
// Using AWS batch.
// May need to set aws.region and aws.batch.cliPath
awsbatch {
process {
executor = 'awsbatch'
queue = "${params.aws_queue}"
memory = '8G'
withLabel:singlecell {
container = "${params.aws_image_prefix}-wf-single-cell:${params.wf.container_sha}"
}
withLabel:wf_common {
container = "${params.aws_image_prefix}-wf-common:${params.wf.common_sha}"
}
shell = ['/bin/bash', '-euo', 'pipefail']
}
}
// local profile for simplified development testing
local {
process.executor = 'local'
}
}
timeline {
enabled = true
overwrite = true
file = "${params.out_dir}/execution/timeline.html"
}
report {
enabled = true
overwrite = true
file = "${params.out_dir}/execution/report.html"
}
trace {
enabled = true
overwrite = true
file = "${params.out_dir}/execution/trace.txt"
}
env {
PYTHONNOUSERSITE = 1
JAVA_TOOL_OPTIONS = "-Xlog:disable -Xlog:all=warning:stderr"
}