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executable file
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nextflow.config
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executable file
·87 lines (76 loc) · 2.17 KB
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// EXECUTOR PARAMETERS
// Should edit, at least to change queueSize (number of parallel jobs
// submitted at the same time)
executor {
queueSize=2 // for running on local machine
}
//Parameters for the different steps in the pipeline
// grouped by relevant section
params {
// Run Options
trace_file_name = 'trace.txt'
run_valet = false
denovo = true
scaffolding = false
frc_curves = false
ref_info = false
// required
forward = ''
reverse = ''
unpaired = ''
output = ''
reference_db = ''
/**** reference selection ****/
// TODO: Remove local directory reference
filter_refs = false
// filter_refs
ms = 28
clean = 0.0
match = 0.01
masking = "-nomasking"
readlen = '300'
// cluster_refs
depth_of_coverage=1
breadth_of_coverage=0.9
percent_markers_covered = 75
/**** reference culling ****/
ref_culling_ms = 16 // kmer-size used for the culling step
num_matches = 2
stop = 0.01 //Parameter used to denote the lower bound of overlap when selecting reference genomes in culling
/**** reference-guided assembly ****/
// valet - Not used if run_valet set to 'false'
valet_path = "/fs/cbcb-lab/mpop/Valet/VALET/bin/valet.sh"
// pilon
flank = '5'
mindepth = '3'
ref_sel = 'tax'
ref_pick = 'breadth'
mincov = '1'
minctglen = '1'
de_novo = '1'
tracks = false
threads = '16' /* also for pilon in ref assembly */
memory = '20' /* also for pilon in ref assembly */
help = false
/**** scaffolding ****/
// Not used if scaffolding set to 'false'
metacarvel_path = "run.py"
/**** report generation ****/
// FRC - Not used if frc_curves set to 'false'
frc_path = "FRC/get_FRC_data"
// data properties for FRC
libsize_avg = 165
libsize_sdv = 92.8
orientation_a = '+'
orientation_b = '-'
// statistical parameters for FRC
mp_size_z_cutoff = 2.58
mp_edge_z_cutoff = 2.58
doc_logp_cutoff = 7
}
trace {
overwrite = true
enabled = true
file = params.trace_file_name
fields = 'task_id,name,status,exit,submit,start,duration,realtime,%cpu,%mem,read_bytes,write_bytes'
}