Increasing mapping precision of genome-wide association studies: to genotype and impute, sequence, or both?
Abstract Fine-mapping to identify causal variants in genome-wide association studies remains challenging. A recent study provides guidance for future research.
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2017-06-01
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| Series: | Genome Biology |
| Online Access: | http://link.springer.com/article/10.1186/s13059-017-1255-6 |