Closed azrasid closed 3 years ago
Hello Azra,
There are a number of ways. In short it really depends on the data available: do you have paired end reads, long reads etc?
The setting of parameters, in particular the hash length and coverage cutoff can also be adjusted to improve results. More information here: https://currentprotocols.onlinelibrary.wiley.com/doi/full/10.1002/0471250953.bi1105s31?casa_token=oFVJez9KtigAAAAA%3Af6Fi2dJ6rBASq8xikrW7wUjhYj85BEUlLOsVqon3CgZ_ifMcoXU63pCsn-A9XQW74-3WRhXrhh3cKkvV
Hope this helps,
Daniel
Yes it is helpful. Thanks and best wishes.
Hi, I am using velvet to de novo assemble a gene. I got contigs and scaffolds. Is there any way to improve the quality of contigs- a good length of contig.
Your suggestions will be highly appreciated.
Thanks, Azra