Literature DB >> 15867473

Expectation maximization algorithm based haplotype relative risk (EM-HRR): test of linkage disequilibrium using incomplete case-parents trios.

Chao-Yu Guo1, Anita L DeStefano, Kathryn L Lunetta, Josée Dupuis, L Adrienne Cupples.   

Abstract

The Haplotype Relative Risk (HRR) was first proposed [Falk et al., Ann Hum Genet 1987] to test for Linkage Disequilibrium (LD) between a marker and a putative disease locus using case-parent trios. Spurious association does not appear in such family-based studies under population admixture. In this paper, we extend the HRR to accommodate incomplete trios via the Expectation-Maximization (EM) algorithm [Dempster et al., J R Stat Soc Ser B, 1977]. In addition to triads and dyads (parent-offspring pair), the EM-HRR easily incorporates individuals with no parental genotype information available, which is excluded from the one parent Transmission/Disequilibrium Test (1-TDT) [Sun et al., Am J Epidemiol 1999]. Due to the data structure of EM-HRR, transmitted alleles are always available regardless of the number of missing parental genotypes. As a result of having a larger sample size, computer simulations reveal that the EM-HRR is more powerful in detecting LD than the 1-TDT in a population under Hardy-Weinberg Equilibirum (HWE). If admixture is not extreme, the EM-HRR remains more powerful. When a large degree of admixture exists, the EM-HRR performs better the 1-TDT when the association is strong, though not as well when the association is weak. We illustrate the proposed method with an application to the Framingham Heart Study. Copyright (c) 2005 S. Karger AG, Basel.

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Year:  2005        PMID: 15867473     DOI: 10.1159/000085571

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  5 in total

1.  Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls.

Authors:  Chao-Yu Guo; Kathryn L Lunetta; Anita L DeStefano; L Adrienne Cupples
Journal:  Genet Epidemiol       Date:  2009-01       Impact factor: 2.135

2.  Impact of non-ignorable missingness on genetic tests of linkage and/or association using case-parent trios.

Authors:  Chao-Yu Guo; Jing Cui; L Adrienne Cupples
Journal:  BMC Genet       Date:  2005-12-30       Impact factor: 2.797

3.  The impact of complex informative missingness on the validity of the transmission/disequilibrium test (TDT).

Authors:  Chao-Yu Guo
Journal:  BMC Proc       Date:  2007-12-18

4.  A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.

Authors:  David Burgner; Sonia Davila; Willemijn B Breunis; Sarah B Ng; Yi Li; Carine Bonnard; Ling Ling; Victoria J Wright; Anbupalam Thalamuthu; Miranda Odam; Chisato Shimizu; Jane C Burns; Michael Levin; Taco W Kuijpers; Martin L Hibberd
Journal:  PLoS Genet       Date:  2009-01-09       Impact factor: 5.917

5.  Dosage transmission disequilibrium test (dTDT) for linkage and association detection.

Authors:  Zhehao Zhang; Jen-Chyong Wang; William Howells; Peng Lin; Arpana Agrawal; Howard J Edenberg; Jay A Tischfield; Marc A Schuckit; Laura J Bierut; Alison Goate; John P Rice
Journal:  PLoS One       Date:  2013-05-14       Impact factor: 3.240

  5 in total

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