Entering edit mode
7.7 years ago
michael.nagle
▴
100
I amplified genes in E. grandis x urophylla and had them sequenced by Sanger. I have .ab1 files showing double peaks that clearly look like SNPs in the grandis and urophylla alleles. I also have the published grandis .fa for these genes.
Without scrolling through, clicking and editing for every double peak, how can I get a .fa for the urophylla allele?
