Abstract

BackgroundMeasures of linkage disequilibrium (LD) play a key role in a wide range of applications from disease association to demographic history estimation. The true population LD cannot be measured directly and instead can only be inferred from genetic samples, which are unavoidably subject to measurement error. Previous studies of r2 (a measure of LD), such as the bias due to finite sample size and its variance, were based on the special case that the true population-wise LD is zero. These results generally do not hold for non-zero {r}_{true}^2 values, which are more common in real genetic data.ResultsThis work generalises the estimation of r2 to all levels of LD, and for both phased and unphased data. First, we provide new formulae for the effect of finite sample size on the observed r2 values. Second, we find a new empirical formula for the variance of the observed r2, equals to 2E[r2](1 − E[r2])/n, where n is the diploid sample size. Third, we propose a new routine, Constrained ML, a likelihood-based method to directly estimate haplotype frequencies and r2 from diploid genotypes under Hardy-Weinberg Equilibrium. While serving the same purpose as the pre-existing Expectation-Maximisation algorithm, the new routine can have better convergence and is simpler to use. A new likelihood-ratio test is also introduced to test for the absence of a particular haplotype. Extensive simulations are run to support these findings.ConclusionMost inferences on LD will benefit from our new findings, from point and interval estimation to hypothesis testing. Genetic analyses utilising r2 information will become more accurate as a result.

Highlights

  • Measures of linkage disequilibrium (LD) play a key role in a wide range of applications from disease association to demographic history estimation

  • The plots of r2phased versus r2true are shown in Fig. 1 for several sample sizes

  • The estimates of intercepts and slopes were very close to 1/2n and (1 − 1/2n), which agree to our derivation for r2 under finite sample size

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Summary

Introduction

Measures of linkage disequilibrium (LD) play a key role in a wide range of applications from disease association to demographic history estimation. Since that time there has been much research on the topic, some focused on how LD is quantified and defined [2,3,4,5,6,7], and a larger fraction on the connection between LD and various evolutionary forces that shape it, including genetic drift [8,9,10,11] and selection [12, 13] These investigations have extended to subdivided or structured populations [14,15,16,17]. These theoretical works allow one to infer features of the underlying processes from measures of LD [18, 19] Another application of LD includes association studies to identify genes for diseases, such as in the Human Haplotype Map project [20].

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