Open aureliendejode opened 3 years ago
Yes
Ok good. My next question is there a recommend depth of coverage for polishing ? More precisely a maximum depth of coverage because I have close to 500X of Illumina raw reads, but I guess there is no need to use all of it ?
Question or Expected behavior I have a reference genome obtained after CANU assembly, purge_dups and long reads polishing with arrow. I'd like to polish with short reads using Next_polish. Should I use raw Illumina reads or do some pre-processing (e.g. reads trimming, remove low quality reads ...) of the short reads before using them for polishing ?
Thank you