Closed Jung19911124 closed 4 months ago
Yes.
Thank you for your answer.
This animal is very small hence we could not yield enough HMW DNA for CLR and HiFi. CLR and HiFi data were obtained from different individuals.
In this situation (of course, we do not intend to complete phasing perfectly), will the HiFi data from different individual work correctly?
Is the sample of short-read data the same as the sample of HiFi?
No, short read data was from the same indivdual of CLR.
So I don't suggest to use NextPolish2
in this case, you can use NextPolish
Thanks. I will try NextPolish.
I am involved in a genome project for a wild animal species with a huge genome (6.5 Gb). We expect the genome to be highly heterozygous, and perhaps over half of it will be repetitive sequences.
Due to budget constraints, we could only obtain x80 coverage of CLR, x20 of Hifi data, and x150 of short-read data. I plan to use CLR to make draft assembly and then use HiFi. Would it be effective to use HiFi data in Nextpolish2 for policing against the draft assembly made with CLR?
Any suggestions would be appreciated.