Open kkarbasi opened 4 years ago
Thanks for the issue! Yes, I think a multi-sample VCF could be constructed from merged files. To do this, I'm envisioning the SNPs
object maintaining the results of each merge (e.g., RSIDs in common, discrepant SNPs) and building the VCF from that summary information.
Related, the fix for this issue should also operate in reverse to read a multi-sample VCF, identifying discrepant SNPs in the process.
Merging snps from different samples and saving them as a multi-sample VCF. Hi, would that be possible?
Thanks!