| Literature DB >> 27382152 |
David Heckerman1, Deepti Gurdasani2, Carl Kadie3, Cristina Pomilla2, Tommy Carstensen2, Hilary Martin4, Kenneth Ekoru2, Rebecca N Nsubuga5, Gerald Ssenyomo5, Anatoli Kamali5, Pontiano Kaleebu5, Christian Widmer6, Manjinder S Sandhu2.
Abstract
The linear mixed model (LMM) is now routinely used to estimate heritability. Unfortunately, as we demonstrate, LMM estimates of heritability can be inflated when using a standard model. To help reduce this inflation, we used a more general LMM with two random effects-one based on genomic variants and one based on easily measured spatial location as a proxy for environmental effects. We investigated this approach with simulated data and with data from a Uganda cohort of 4,778 individuals for 34 phenotypes including anthropometric indices, blood factors, glycemic control, blood pressure, lipid tests, and liver function tests. For the genomic random effect, we used identity-by-descent estimates from accurately phased genome-wide data. For the environmental random effect, we constructed a covariance matrix based on a Gaussian radial basis function. Across the simulated and Ugandan data, narrow-sense heritability estimates were lower using the more general model. Thus, our approach addresses, in part, the issue of "missing heritability" in the sense that much of the heritability previously thought to be missing was fictional. Software is available at https://github.com/MicrosoftGenomics/FaST-LMM.Entities:
Keywords: Gaussian radial basis function; environment; heritability estimation; linear mixed model; model misspecification
Mesh:
Year: 2016 PMID: 27382152 PMCID: PMC4941438 DOI: 10.1073/pnas.1510497113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205