Entering edit mode
2.2 years ago
BioGeek
▴
170
I'm now working on a metagenome assembly project. There, I want to segregate and assemble all of the reads with stringent parameters: they should not overlap segments even if they have a single mutation in the sequence. Is there any software/tools or flags that can assist me in accomplishing this...
Note: At the moment I don't care about N50.