Literature DB >> 8788027

Gain in efficiency from using generalized least squares in the Haseman-Elston test.

R M Single1, S J Finch.   

Abstract

Techniques that test for linkage between a marker and a trait locus based on the regression methods proposed by Haseman and Elston [1972] involve testing a null hypothesis of no linkage by examination of the regression coefficient. Modified Haseman-Elston methods accomplish this using ordinary least squares (OLS), weighted least squares (WLS), in which weights are reciprocals of estimated variances, and generalized estimating equations (GEE). Methods implementing the WLS and GEE currently use a diagonal covariance matrix, thus incorrectly treating the squared trait differences of two sib pairs within a family as uncorrelated. Correctly specifying the correlations between sib pairs in a family yields the best linear unbiased estimator of the regression coefficient [Scheffe, 1959]. This estimator will be referred to as the generalized least squares (GLS) estimator. We determined the null variance of the GLS estimator and the null variance of the WLS/OLS estimator. The correct null variance of the WLS/OLS estimate of the Haseman-Elston (H-E) regression coefficient may be either larger or smaller than the variance of the WLS/OLS estimate calculated assuming that the squared sib-pair differences are uncorrelated. For a fully informative marker locus, the gain in efficiency using GLS rather than WLS/OLS under the null hypothesis is approximately 11% in a large multifamily study with three siblings per family and 25% for families with four siblings each.

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Year:  1995        PMID: 8788027     DOI: 10.1002/gepi.1370120660

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  3 in total

1.  Haseman-Elston regression in ascertained samples: importance of dependent variable and mean correction factor selection.

Authors:  Ritwik Sinha; Courtney Gray-McGuire
Journal:  Hum Hered       Date:  2007-09-26       Impact factor: 0.444

2.  A rapid generalized least squares model for a genome-wide quantitative trait association analysis in families.

Authors:  Xiang Li; Saonli Basu; Michael B Miller; William G Iacono; Matt McGue
Journal:  Hum Hered       Date:  2011-04-08       Impact factor: 0.444

3.  An efficient method to handle the 'large p, small n' problem for genomewide association studies using Haseman-Elston regression.

Authors:  Bujun Mei; Zhihua Wang
Journal:  J Genet       Date:  2016-12       Impact factor: 1.166

  3 in total

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