How to estimate heritability, a guide for epidemiologists
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Traditionally, heritability has been estimated using family-based methods such as twin studies. Advancements in molecular genomics have facilitated the development of alternative methods that utilise large samples of unrelated or related individuals. Yet, specific challenges persist in the estimation of heritability such as epistasis, assortative mating and indirect genetic effects. Here, we provide an overview of common methods applied in genetic epidemiology to estimate heritability i.e., the proportion of phenotypic variation explained by genetic variation. We provide a guide to key genetic concepts required to understand heritability estimation methods from family-based designs (twin and family studies), genomic designs based on unrelated individuals (LD score regression, GREML), and family-based genomic designs (Sibling regression, GREML-KIN, Trio-GCTA, MGCTA, RDR). For each method, we describe how heritability is estimated, the assumptions underlying its estimation, and discuss the implications when these assumptions are not met. We further discuss the benefits and limitations of estimating heritability within samples of unrelated individuals compared to samples of related individuals. Overall, this article is intended to help the reader determine the circumstances when each method would be appropriate and why.
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