Journal article

Improved heritability estimation from genome-wide SNPs

D Speed, G Hemani, MR Johnson, DJ Balding

American Journal of Human Genetics | Published : 2012

Open access

Abstract

Estimation of narrow-sense heritability, h2, from genome-wide SNPs genotyped in unrelated individuals has recently attracted interest and offers several advantages over traditional pedigree-based methods. With the use of this approach, it has been estimated that over half the heritability of human height can be attributed to the ∼300,000 SNPs on a genome-wide genotyping array. In comparison, only 5%-10% can be explained by SNPs reaching genome-wide significance. We investigated via simulation the validity of several key assumptions underpinning the mixed-model analysis used in SNP-based h 2 estimation. Although we found that the method is reasonably robust to violations of four key assumptio..

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University of Melbourne Researchers

Grants

Awarded by Medical Research Council


Funding Acknowledgements

We thank Will Astle and Vincent Plagnol for fruitful discussions, as well as the two anonymous reviewers for helpful comments. Access to Wellcome Trust data was authorized as work related to the project "Genome-wide association study of susceptibility and clinical phenotypes in epilepsy." This work is funded by the UK Medical Research Council under grant G0901388.