Closed licheng0921 closed 3 years ago
Yes, if you need more corrected data. Try to set correction_options = -b -p 10
and remove file workdir/02.cns_align/01.seed_cns.sh.done
and work/02.cns_align/01.seed_cns.sh.work/seed_cns*/nextDenovo.sh.done
, and rerun your main script. It will skip corrected seeds and only correct filtered seeds.
Thank you very much. I will do it as you advised.
Sorry to bother you again.
I checked others comments about correction_options = -b -p 10
.
I do not know whether my understanding right or not.
If I continue assemble using nextdenovo, I have no need to add -b
to rerun?
If I assemble the genome using other assembler, like: wtdbg2 or flye, I should rerun the main script with correction_options = -b -p 10
?
many thank!
yes, but you can not use the currently released NextDenovo to do the assembly, because your genome size is over the limit.
yes, I will try correct subreads using nextdenovo. thanks to remined me.
Hi, I tried to correct pacbio raw date with nextdenovo. I find that only ~20x reads left, it is normal? whether should I set seed cutoff shorter?
ps: the genome is ~7.4g, raw subreads = 590g(~80x) seed cutoff is calculated by seq_stat.