Thank you very much for this excellent tool. I was wondering how exactly the algorithm accounts for differences in repeat regions (ie IR-1) across various EBV genomes? For example, does the scaffolding specifically look for varied lengths of the repeat regions? If so, how? Thank you so much!
Thank you very much for this excellent tool. I was wondering how exactly the algorithm accounts for differences in repeat regions (ie IR-1) across various EBV genomes? For example, does the scaffolding specifically look for varied lengths of the repeat regions? If so, how? Thank you so much!