Closed kendaida closed 2 years ago
Hi, I would like to use plink2 pfiles including multialleclic variants. I installed pgenlib but it could not run at 'genotypeio.PlinkReader".
pr = genotypeio.PlinkReader(pfile_prefix_path)
I think plink bfile can not include multiallelic variants. Would you tell me how to solove it?
Hi, Multi-allelic variants are not fully supported in the API. I recommend splitting multiallelic sites instead, using bcftools norm for example.
bcftools norm
I got it. I appreciate you.
Hi, I would like to use plink2 pfiles including multialleclic variants. I installed pgenlib but it could not run at 'genotypeio.PlinkReader".
pr = genotypeio.PlinkReader(pfile_prefix_path)
I think plink bfile can not include multiallelic variants. Would you tell me how to solove it?