Increasing mapping precision of genome-wide association studies: to genotype and impute, sequence, or both?
oleh: Zhaoming Wang, Nilanjan Chatterjee
| Format: | Article |
|---|---|
| Diterbitkan: | BMC 2017-06-01 |
Deskripsi
Abstract Fine-mapping to identify causal variants in genome-wide association studies remains challenging. A recent study provides guidance for future research.