Open Karenmagh opened 3 weeks ago
The primary.fasta
and alternate.fasta
files can be polished using Illumina data. It's best to concatenate them into a single file and polish them together. This method also applies to haplotype_1.fasta
and haplotype_2.fasta
.
Do you recommend any subsequent method for re-separation? I am considering using Hapo-G (https://github.com/institut-de-genomique/HAPO-G) for polishing.
I would greatly appreciate your response @lemene
The contig names are different between primary.fasta
and alternate.fasta
. After polishing, the contigs can be separated by their names. I have used Pilon but not Hapo-G, so I can't give useful advice on Hapo-G.
Thanks so much @lemene , you can close this issue.
Hello, I have a question, is possible polish the primary/alternate and haplo1/haplo2 with illumina reads?
Thanks so much.