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Computation of the full likelihood function for estimating variance at a quantitative trait locus.

S Xu
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Abstract

The proportion of alleles identical by descent (IBD) determines the genetic covariance between relatives, and thus is crucial in estimating genetic variances of quantitative trait loci (QTL). However, IBD proportions at QTL are unobservable and must be inferred from marker information. The conventional method of QTL variance analysis maximizes the likelihood function by replacing the missing IBDs by their conditional expectations (the expectation method), while in fact the full likelihood function should take into account the conditional distribution of IBDs (the distribution method). The distribution method for families of more than two sibs has not been obvious because there are n(n - 1)/2 IBD variables in a family of size n, forming an n x n symmetrical matrix. In this paper, I use four binary variables, where each indicates the event that an allele from one of the four grandparents has passed to the individual. The IBD proportion between any two sibs is then expressed as a function of the indicators. Subsequently, the joint distribution of the IBD matrix is derived from the distribution of the indicator variables. Given the joint distribution of the unknown IBDs, a method to compute the full likelihood function is developed for families of arbitrary sizes.

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AllelesAnimalsComputer SimulationGenetic MarkersGenetics, PopulationHumansModels, GeneticJournal ArticleResearch Support, U.S. Gov't, Non-P.H.S.

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S Xu. 1996. Computation of the full likelihood function for estimating variance at a quantitative trait locus.. https://doi.org/10.1093/genetics%2F144.4.1951

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