Interpretation of simultaneous linkage and family-based association tests in genome screens

被引:13
作者
Chung, Ren-Hua
Hauser, Elizabeth R.
Martin, Eden R. [1 ]
机构
[1] N Carolina State Univ, Bioinformat Res Ctr, Raleigh, NC 27695 USA
[2] Duke Univ, Ctr Med, Ctr Human Genet, Durham, NC 27706 USA
关键词
linkage analysis; family-based association analysis; correlation;
D O I
10.1002/gepi.20196
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Linkage and association analyses have played important roles in identifying susceptibility genes for complex diseases. Linkage tests and family-based tests of association are often applied in the same data to help fine-map disease loci or validate results. This paradigm increases efficiency by making maximal use of family data sets. However, it is not intuitively clear under what conditions association and linkage tests performed in the same data set may be correlated. Understanding this relationship is important for interpreting the combined results of both tests. We used computer simulations and theoretical statements to estimate the correlation between linkage statistics (affected sib pair maximum LOD scores) and family-based association statistics (pedigree disequilibrium test (PDT) and association in the pressure of linkage (APL)) under various hypotheses. Different types of pedigrees were studied: nuclear families with affected sib pairs, extended pedigrees and incomplete pedigrees. Both simulation and theoretical results showed that when there is no linkage or no association, the linkage and association tests are not correlated. When there is linkage and association in the data, the two tests have a positive correlation. We concluded that when linkage and association tests are applied in the same data, the type I error rate of neither test will be affected and that power can be increased by applying tests conditionally. Genet. Epidemiol. 31:134-142, 2007. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:134 / 142
页数:9
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