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config.yaml
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config.yaml
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work_dir: "/mnt/md0/ontrapid"
database_dir: "/mnt/md0/Database/anvio"
threads:
normal: 2
large: 6
memory:
normal_gb: 4
large_gb: 50
# rasusa params (subsampling for speed)
rasusa:
subsampling: True
coverage: 30
genome_size: 2.4mb
use_porchop: False
# nanofilt params
nanofilt:
l: 500
q: 10
headcrop: 0
tailcrop: 0
assembler_opts: flye # default, canu, flye
# by default, canu and flye assemblies will be merged
# For single assembler i.e., canu and flye, # only polishment is applied.
# Skip quickmerge and circulator
# assembler params
flye:
mode: --nano-raw
ex_args:
canu:
size: 5m # estimated genomesize
usegrid: False
grid_opts: ''
stopOnLowCoverage: 10
minInputCoverage: 10
ex_args: 'cnsThreads=2 cnsMemory=32'
# quickmerge params (conseverative merge of lathe)
quickmerge:
# choose assembly as query and ref for quickmerge
# select a folder containing "assembly.fasta"
query: flye2polish
ref: canu2polish
# flye: flye assembly as query, canu as ref
# canu: vice versa
ml: 10000
c: 5
hco: 10
# circlator params
circlator:
assembler: spades
data_type: nanopore-corrected
bwa_opts: "'-x ont2d'" # escape single quotes
merge_min_id: 85
merge_breaklen: 1000
# minimap2 params
minimap2:
x: map-ont
# racon params (recommended by medaka)
racon:
iter: 2
m: 8
x: -6
g: -8
w: 500
# medaka params:
medaka:
iter: 1
m: r1041_e82_400bps_hac_v4.2.0
cudnn: False
# assembly qc
busco:
l: bacteria_odb10
m: genome
opts: ''
# pangenome
update_assembly: False
updated_assembly_dir: /mnt/md0/proferment/results/assembly_rename
import_from_gbk: False # overide update_assembly
external_gbk_dir: /mnt/md0/proferment/results/gbk
# variants:
variants:
ref: /mnt/md0/nano_snp/ref/ecoli_dh5a.fna #/mnt/md0/nano_snp/ref/ecoli_mg1655.fna
medaka:
model: r941_prom_hac_variant_g507
clair:
platform: ont
model: r941_prom_sup_g506
mode: --haploid_sensitive
snpEff:
g_version: Escherichia_coli_str_dh5a # Escherichia_coli_str_k_12_substr_mg1655
chr_exist: "CP017100\\.1" # "U00096\\.3"
chr_replace: Chromosome