Entering edit mode
6.8 years ago
valopes
▴
30
Hi all,
I was wondering if I could use GBS data of some genotypes and ChiSeq of other genotypes or resequencing data to do the SNP calling and so GWA for all?
If so, how can I do that? Which parameters should I be careful using to try to sort of normalize all this data?
I know it may be a wide question, but I need to start from something.
Thanks in advance.