Closed termithorbor closed 2 years ago
Well. my initial answer is don't do that :smile: If the read sets are from different isolates, then I don't expect them to assemble well together!
But if you need to for some reason, I'd try both a short-read-first approach like Unicycler and a long-read-first approach like Trycycler+polishing. A Unicycler assembly will probably look more like the genome in the short-read set, and a Trycycler+polishing assembly may look more like the genome in the long-read set.
For either approach, the closer the two isolates are, the better I'd expect the assembly to work. Good luck!
Ryan
Hi,
what would be the best approach for assembling the genome when the short and long reads come from different isolates?
Thanks in advance :)