You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
{{ message }}
This repository has been archived by the owner on Mar 16, 2022. It is now read-only.
Hi, here are my questions on running FALCON. I'm wondering if anyone has tested on these.
I’m assembling ONT reads using FALCON and FALCON unzip. Should I correct the raw ONT reads with CANU or some sort of correction program?
Do you have some suggestions for speeding up FALCON? We have three plant genomes, 350MB, 3GB, and 17GB. So far for 118x ONT reads of a 350 Mb genome, it took me two weeks to finish the 0-rawreads/las-merge-runs stage, which is way too slow.
What's an acceptable low coverage for diploids to adequately assemble primary contigs and haplotigs? I wonder if 50x coverage would just break the assembly down to small contigs or maybe lose some haplotigs while maintaining the assembled N50. Anyone has experience on this matter with lower coverage ONT reads using FALCON?
Here is what I’m planning to speed up the assembly:
a. Increase DBsplit_option -s from 100 to 200 to reduce the number of my tan-run jobs, 5461 jobs with -s 100 currently.
b. I want to play with njob and NPROC options. But I’m a little unsure about how they play out together. My local server has 48 cpus and 560 GB memory.
Thanks you in advance for any suggestion.
Here is my current run_falcon.cfg file for the 118x corrected-ONT reads for 350 Mb genome:
Hi, here are my questions on running FALCON. I'm wondering if anyone has tested on these.
I’m assembling ONT reads using FALCON and FALCON unzip. Should I correct the raw ONT reads with CANU or some sort of correction program?
Do you have some suggestions for speeding up FALCON? We have three plant genomes, 350MB, 3GB, and 17GB. So far for 118x ONT reads of a 350 Mb genome, it took me two weeks to finish the 0-rawreads/las-merge-runs stage, which is way too slow.
What's an acceptable low coverage for diploids to adequately assemble primary contigs and haplotigs? I wonder if 50x coverage would just break the assembly down to small contigs or maybe lose some haplotigs while maintaining the assembled N50. Anyone has experience on this matter with lower coverage ONT reads using FALCON?
Here is what I’m planning to speed up the assembly:
a. Increase DBsplit_option -s from 100 to 200 to reduce the number of my tan-run jobs, 5461 jobs with -s 100 currently.
b. I want to play with njob and NPROC options. But I’m a little unsure about how they play out together. My local server has 48 cpus and 560 GB memory.
Thanks you in advance for any suggestion.
Here is my current run_falcon.cfg file for the 118x corrected-ONT reads for 350 Mb genome:
The text was updated successfully, but these errors were encountered: