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Incorporating Covariates into Multipoint Association Mapping in the Case-Parent Design
被引:2
|作者:
Chiu, Yen-Feng
[1
]
Liang, Kung-Yee
[1
,2
]
Pan, Wen-Harn
[3
]
机构:
[1] Natl Hlth Res Inst, Inst Populat Hlth Sci, Div Biostat & Bioinformat, Zhunan 350, Miaoli, Taiwan
[2] Johns Hopkins Univ, Dept Biostat, Bloomberg Sch Publ Hlth, Baltimore, MD 21205 USA
[3] Acad Sinica, Inst Biomed Sci, Taipei, Taiwan
基金:
美国国家卫生研究院;
关键词:
Case-parent designs;
Gene-gene interactions;
Gene-environment interactions;
Gene-covariate interactions;
Relative efficiency;
Parametric;
Non-parametric;
GENE-ENVIRONMENT INTERACTION;
LINKAGE-DISEQUILIBRIUM;
UNIFIED FRAMEWORK;
GENOTYPE;
TRIADS;
TESTS;
HYPERTENSION;
REGRESSION;
TRAIT;
ONSET;
D O I:
10.1159/000291986
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Background/Aims: To improve the efficiency of disease locus localization in association mapping using case-parent designs and to assess or account for the main covariate effects and gene-covariate interaction effects, while localizing the disease locus. Methods: The present study extends a multipoint fine-mapping approach to incorporate covariates into the association mapping of case-parent designs through parametric and non-parametric modeling. This approach is based on the expected preferential-allele-transmission statistics for transmission from either parent to an affected child. Results: Simulation studies indicate that the efficiency in estimating the disease locus increases considerably when incorporating a covariate associated with the disease. This is especially true when the genetic effect of the disease locus is small. The proposed approach was applied to a young-onset hypertension data sample. The relative efficiency of estimating the locus of young-onset hypertension increases 110-fold after incorporating triglyceride into the association mapping while localizing the disease variant in the lipoprotein lipase gene in the non-parametric model. By incorporating the information of SNP variants into the fine-mapping, the proposed method further assesses the gene-gene interactions between the SNP and the disease locus. Conclusion: With the incorporation of covariates, the proposed method cannot only improve efficiency in estimating disease loci, but can also elucidate the etiology of a complex disease. Copyright (C) 2010 S. Karger AG, Basel
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页码:229 / 241
页数:13
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