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PMID: 17924336 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Haplotype-based association analysis via variance-components score test.

American journal of human genetics ·Vol. 81 ·No. 5 ·2007-11-00 ·Pages 927-38

Tzeng JY, Zhang D

Abstract

Haplotypes provide a more informative format of polymorphisms for genetic association analysis than do individual single-nucleotide polymorphisms. However, the practical efficacy of haplotype-based association analysis is challenged by a trade-off between the benefits of modeling abundant variation and the cost of the extra degrees of freedom. To reduce the degrees of freedom, several strategies have been considered in the literature. They include (1) clustering evolutionarily close haplotypes, (2) modeling the level of haplotype sharing, and (3) smoothing haplotype effects by introducing a correlation structure for haplotype effects and studying the variance components (VC) for association. Although the first two strategies enjoy a fair extent of power gain, empirical evidence showed that VC methods may exhibit only similar or less power than the standard haplotype regression method, even in cases of many haplotypes. In this study, we report possible reasons that cause the underpowered phenomenon and show how the power of the VC strategy can be improved. We construct a score test based on the restricted maximum likelihood or the marginal likelihood function of the VC and identify its nontypical limiting distribution. Through simulation, we demonstrate the validity of the test and investigate the power performance of the VC approach and that of the standard haplotype regression approach. With suitable choices for the correlation structure, the proposed method can be directly applied to unphased genotypic data. Our method is applicable to a wide-ranging class of models and is computationally efficient and easy to implement. The broad coverage and the fast and easy implementation of this method make the VC strategy an effective tool for haplotype analysis, even in modern genomewide association studies.

MeSH Terms
Amyotrophic Lateral Sclerosis/genetics Computer Simulation Databases, Genetic Genetic Predisposition to Disease Haplotypes Humans Likelihood Functions Models, Genetic Polymorphism, Single Nucleotide/genetics Quantitative Trait, Heritable
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tzeng Jung-Ying
Department of Statistics, North Carolina State University, Raleigh, NC 27695, USA. [email protected]
Zhang Daowen
References (22)
22 references, click to expand
  1. Evolutionary-based association analysis using haplotype data.
    Genet Epidemiol. 2003 Jul;25(1):48-58 PMID: 12813726
  2. Estimation and tests of haplotype-environment interaction when linkage phase is ambiguous.
    Hum Hered. 2003;55(1):56-65 PMID: 12890927
  3. Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals.
    Hum Mol Genet. 2007 Jan 1;16(1):1-14 PMID: 17116639
  4. Assessment of linkage disequilibrium by the decay of haplotype sharing, with application to fine-scale genetic mapping.
    Am J Hum Genet. 1999 Sep;65(3):858-75 PMID: 10445904
  5. Evolutionary-based grouping of haplotypes in association analysis.
    Genet Epidemiol. 2005 Apr;28(3):220-31 PMID: 15726584
  6. Application of Bayesian spatial statistical methods to analysis of haplotypes effects and gene mapping.
    Genet Epidemiol. 2003 Sep;25(2):95-105 PMID: 12916018
  7. Evaluating and improving power in whole-genome association studies using fixed marker sets.
    Nat Genet. 2006 Jun;38(6):663-7 PMID: 16715096
  8. Haplotypes vs single marker linkage disequilibrium tests: what do we gain?
    Eur J Hum Genet. 2001 Apr;9(4):291-300 PMID: 11313774
  9. Evaluating associations of haplotypes with traits.
    Genet Epidemiol. 2004 Dec;27(4):348-64 PMID: 15543638
  10. The International HapMap Project.
    Nature. 2003 Dec 18;426(6968):789-96 PMID: 14685227
  11. Hypothesis testing in semiparametric additive mixed models.
    Biostatistics. 2003 Jan;4(1):57-74 PMID: 12925330
  12. Score tests for association between traits and haplotypes when linkage phase is ambiguous.
    Am J Hum Genet. 2002 Feb;70(2):425-34 PMID: 11791212
  13. Analysis of single-locus tests to detect gene/disease associations.
    Genet Epidemiol. 2005 Apr;28(3):207-19 PMID: 15637715
  14. Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.
    Lancet Neurol. 2007 Apr;6(4):322-8 PMID: 17362836
  15. Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes.
    Am J Hum Genet. 2004 Jul;75(1):35-43 PMID: 15148658
  16. Haplotype sharing analysis in affected individuals from nuclear families with at least one affected offspring.
    Genet Epidemiol. 1997;14(6):915-20 PMID: 9433600
  17. Regression-based association analysis with clustered haplotypes through use of genotypes.
    Am J Hum Genet. 2006 Feb;78(2):231-42 PMID: 16365833
  18. On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.
    Am J Hum Genet. 2003 Apr;72(4):891-902 PMID: 12610778
  19. Bayes estimates of haplotype effects.
    Genet Epidemiol. 2001;21 Suppl 1:S712-7 PMID: 11793766
  20. Statistical models for haplotype sharing in case-parent trio data.
    Hum Hered. 2007;64(1):35-44 PMID: 17483595
  21. Assessing the performance of the haplotype block model of linkage disequilibrium.
    Am J Hum Genet. 2003 Sep;73(3):502-15 PMID: 12916017
  22. Leveraging the HapMap correlation structure in association studies.
    Am J Hum Genet. 2007 Apr;80(4):683-91 PMID: 17357074
Article Info
Journal
American journal of human genetics
Abbr.
Am J Hum Genet
ISSN
0002-9297
Published
2007-11-00
Epub
2007-00-03
Pages
927-38
Language
English
Region
United States
NLM ID
0370475
PMCID
PMC2265651
Subset
IM
Grants
NCI NIH HHS · R01 CA085848 · United States
NIMH NIH HHS · R01 MH074027 · United States
NCI NIH HHS · R01 CA85848-04 · United States
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