Closed koujiaodahan closed 7 months ago
And I noticed that the 1000genome LD panel in the directory is also GRCh37?
Yes they are in GRCh37. But note that PRS-CS/x uses rs ID, A1 and A2 to match SNPs; the base pair position is for reference only and is not used in any calculation. As a result genome build usually has a minimal impact on the result.
Yes they are in GRCh37. But note that PRS-CS/x uses rs ID, A1 and A2 to match SNPs; the base pair position is for reference only and is not used in any calculation. As a result genome build usually has a minimal impact on the result.
Thanks for your reply, and I will not liftover the position, and just guarantee the rsID, A1, A2.
Yes they are in GRCh37. But note that PRS-CS/x uses rs ID, A1 and A2 to match SNPs; the base pair position is for reference only and is not used in any calculation. As a result genome build usually has a minimal impact on the result.
Hi, would you recommend the dbsnp version for annotating rsID? I noticed that a specific position is named by different rsID in different dbsnp version
Hi - I think you can either use the version that is consistent with the reference panel or the latest version. A small number of SNPs may have inconsistent mapping between versions but in the vast majority of cases this should be minimal impact of the predictive power of the final score.
The UKB Reference is GRCh37?