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使用不一致相对对的基因型关联分析。

Genotypic association analysis using discordant-relative-pairs.

作者信息

Yan T, Yang Y-N, Cheng X, DeAngelis M M, Hoh J, Zhang H

机构信息

Department of Statistics and Finance, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China.

出版信息

Ann Hum Genet. 2009 Jan;73(1):84-94. doi: 10.1111/j.1469-1809.2008.00488.x. Epub 2008 Nov 21.

DOI:10.1111/j.1469-1809.2008.00488.x
PMID:19040657
Abstract

In practice, family-based design has been widely used in disease-gene association analysis. The major advantage of such design is that it is not subject to spurious association due to population structure such as population stratification (PS) and admixture. A disadvantage is that parental genotypes are hard to obtain if the disease is late onset for which a discordant-relative-pair design is useful. Designs of such kind include full-sib-pair, half-sib-pair, first-cousin-pair, and so on. The closer the relatedness of the pair, the less possible that they are subject to population stratification. On the other hand, the association test using close relative-pairs may be less powerful due to over-matching. Trade-off between these two factors (population structure and over-matching) is the major concern of this study. Some tests, namely McNemar's test, matched Cochran-Armitage trend tests (CATTs), matched maximum efficient robust test (MERT), and Bhapkar's test, are used for testing disease-gene association based on relative-pair designs. These tests are shown to be valid in the presence of PS but not admixture. Numerical studies show that the McNemar's test, additive CATT, MERT, and Bhapkar's test are robust in power, but none of them is uniformly more powerful than the others. In most simulations, the power of any of the tests increases as the pair is more distant. The proposed methods are applied to two real examples.

摘要

在实际应用中,基于家系的设计已广泛用于疾病基因关联分析。这种设计的主要优点是它不会因群体结构(如群体分层(PS)和混合)而受到虚假关联的影响。一个缺点是,如果疾病是晚发性的,很难获得父母的基因型,而不一致亲属对设计对此很有用。这类设计包括全同胞对、半同胞对、一级表亲对等。亲属对的亲缘关系越近,他们受到群体分层影响的可能性就越小。另一方面,由于过度匹配,使用近亲对的关联检验可能效力较低。这两个因素(群体结构和过度匹配)之间的权衡是本研究的主要关注点。一些检验方法,即麦克尼马尔检验、匹配的 Cochr an - Armitage 趋势检验(CATTs)、匹配的最大有效稳健检验(MERT)和巴普卡尔检验,用于基于亲属对设计检验疾病基因关联。这些检验方法在存在群体分层的情况下是有效的,但在存在混合的情况下无效。数值研究表明,麦克尼马尔检验、加性 CATT、MERT 和巴普卡尔检验在效力方面是稳健的,但没有一种检验方法在所有情况下都比其他方法更具效力。在大多数模拟中,任何一种检验的效力都会随着亲属对关系的疏远而增加。所提出的方法应用于两个实际例子。

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