Narrow-sense heritability estimation of complex traits using identity-by-descent information

Haplotype Reference Consortium

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Heritability is a fundamental parameter in genetics. Traditional estimates based on family or twin studies can be biased due to shared environmental or non-additive genetic variance. Alternatively, those based on genotyped or imputed variants typically underestimate narrow-sense heritability contributed by rare or otherwise poorly tagged causal variants. Identical-by-descent (IBD) segments of the genome share all variants between pairs of chromosomes except new mutations that have arisen since the last common ancestor. Therefore, relating phenotypic similarity to degree of IBD sharing among classically unrelated individuals is an appealing approach to estimating the near full additive genetic variance while possibly avoiding biases that can occur when modeling close relatives. We applied an IBD-based approach (GREML-IBD) to estimate heritability in unrelated individuals using phenotypic simulation with thousands of whole-genome sequences across a range of stratification, polygenicity levels, and the minor allele frequencies of causal variants (CVs). In simulations, the IBD-based approach produced unbiased heritability estimates, even when CVs were extremely rare, although precision was low. However, population stratification and non-genetic familial environmental effects shared across generations led to strong biases in IBD-based heritability. We used data on two traits in ~120,000 people from the UK Biobank to demonstrate that, depending on the trait and possible confounding environmental effects, GREML-IBD can be applied to very large genetic datasets to infer the contribution of very rare variants lost using other methods. However, we observed apparent biases in these real data, suggesting that more work may be required to understand and mitigate factors that influence IBD-based heritability estimates.

Original languageEnglish (US)
Pages (from-to)616-630
Number of pages15
JournalHeredity
Volume121
Issue number6
DOIs
StatePublished - Dec 1 2018

Bibliographical note

Funding Information:
WHI Acknowledgment: The WHI program is funded by the National Heart, Lung, and Blood Institute, National Institutes of Health, U.S. Department of Health and Human Services through contracts HHSN268201600018C, HHSN268201600001C, HHSN268201600002C, HHSN268201600003C, and HHSN268201600004C. We thank the WHI investigators and staff for their dedication, and the study participants for making the program possible. A full listing of WHI investigators can be found at: http://www.whi.org/researchers/Documents%20%20Write%20a% 20Paper/WHI%20Investigator%20Long%20List.pdf

Funding Information:
Acknowledgements This work utilized the Janus supercomputer, which is supported by the National Science Foundation (award number CNS-0821794), the University of Colorado Boulder, the University of Colorado Denver, and the National Center for Atmospheric Research, and is operated by the University of Colorado Boulder. This research has been conducted using the UK Biobank Resource. We thank the participants of the individual HRC cohorts and the UK Biobank. We thank the Keller and Vrieze lab groups, the Institute for Behavioral Genetics, and Sean Caron. This study was funded by NIH R01MH100141 (MCK), NIH R01DA037904 and R01HG008983 (SV), NHMRC grants 1078037 (PMV) and 1113400 (PMV and JY), and Sylvia & Charles Viertel Charitable Foundation Senior Medical Research Fellowship (JY).

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