Literature DB >> 8839128

Assessing genetic linkage and association with robust components of variance approaches.

C I Amos1, D K Zhu, E Boerwinkle.   

Abstract

Simulation studies are used to explore the properties of procedures for estimating components of variance and constructing test statistics in genetic linkage studies of quantitative traits. We evaluated the bias and median squared error of estimates of the linked additive genetic variance obtained by regression, maximum likelihood and quasilikelihood estimation procedures. The quasilikelihood and regression procedures provided unbiased estimates of the additive component of variance. Maximum likelihood procedures that assumed multivariate normality were biased for most sample sizes considered but had more precision for most generating models than regression or quasilikelihood methods did. Wald tests derived from quasilikelihood procedures had similar or greater power than Wald tests based upon estimators from maximum likelihood analyses. Quasilikelihood estimation may therefore be preferable whenever there is uncertainty about the generating distribution for the error variance, but the robustness of this approach is offset by its required computational complexity.

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Year:  1996        PMID: 8839128     DOI: 10.1111/j.1469-1809.1996.tb01184.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  37 in total

1.  Assessment of parent-of-origin effects in linkage analysis of quantitative traits.

Authors:  R L Hanson; S Kobes; R S Lindsay; W C Knowler
Journal:  Am J Hum Genet       Date:  2001-03-13       Impact factor: 11.025

2.  Joint multipoint linkage analysis of multivariate qualitative and quantitative traits. I. Likelihood formulation and simulation results.

Authors:  J T Williams; P Van Eerdewegh; L Almasy; J Blangero
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

3.  Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure.

Authors:  D B Allison; M C Neale; R Zannolli; N J Schork; C I Amos; J Blangero
Journal:  Am J Hum Genet       Date:  1999-08       Impact factor: 11.025

4.  Estimation of variance components of quantitative traits in inbred populations.

Authors:  M Abney; M S McPeek; C Ober
Journal:  Am J Hum Genet       Date:  2000-02       Impact factor: 11.025

5.  A general test of association for quantitative traits in nuclear families.

Authors:  G R Abecasis; L R Cardon; W O Cookson
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

6.  A genomewide linkage scan for quantitative-trait loci for obesity phenotypes.

Authors:  Hong-Wen Deng; Hongyi Deng; Yong-Jun Liu; Yao-Zhong Liu; Fu-Hua Xu; Hui Shen; Theresa Conway; Jin-Long Li; Qing-Yang Huang; K M Davies; Robert R Recker
Journal:  Am J Hum Genet       Date:  2002-03-28       Impact factor: 11.025

7.  A unified Haseman-Elston method for testing linkage with quantitative traits.

Authors:  X Xu; S Weiss; X Xu; L J Wei
Journal:  Am J Hum Genet       Date:  2000-08-28       Impact factor: 11.025

8.  A tobit variance-component method for linkage analysis of censored trait data.

Authors:  Michael P Epstein; Xihong Lin; Michael Boehnke
Journal:  Am J Hum Genet       Date:  2003-02-13       Impact factor: 11.025

9.  Exact multipoint quantitative-trait linkage analysis in pedigrees by variance components.

Authors:  S C Pratt; M J Daly; L Kruglyak
Journal:  Am J Hum Genet       Date:  2000-03       Impact factor: 11.025

10.  Bias toward the null hypothesis in model-free linkage analysis is highly dependent on the test statistic used.

Authors:  Heather J Cordell
Journal:  Am J Hum Genet       Date:  2004-04-29       Impact factor: 11.025

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