Closed wez078 closed 7 months ago
The threshold in HiFi is very high so single-base differences would disallow reads to overlap. Thus, the bubbles likely contain both alternate haplotypes and noise/systematic errors in the reads. I would suggest setting some filters based on length (50kb or so) and number of reads (reported in the fasta header line, 5-10 would make sense I think) to see how many bubbles remain.
Dear Skoren, Thanks for your comments, I will give it a try to see Cheers'wentao
Idle
**
report_Cabu.pdf
Dears,
I survey the genome, and hetero is close to zero, and after I assembled with hiCanu, I still get some bubble contigs, wonder they are alternative or sequencing error, I used Pcabio hifi reads . Canu report as below
Thanks wentao