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复杂信息缺失对传递/不平衡检验(TDT)有效性的影响。

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

作者信息

Guo Chao-Yu

机构信息

Department of Mathematics and Statistics, Boston University, Boston, Massachusetts and National Heart, Lung and Blood Institute, Framingham Heart Study, Framingham, Massachusetts 01702, USA.

出版信息

BMC Proc. 2007;1 Suppl 1(Suppl 1):S26. doi: 10.1186/1753-6561-1-s1-s26. Epub 2007 Dec 18.

Abstract

The transmission/disequilibrium test was introduced to test for linkage and association between a marker and a putative disease locus using case-parent triads. Several extensions have been proposed to accommodate incomplete triads. Some strategies assumed that parental genotypes were missing completely at random and some methods allowed informative missingness for parental genotypes. However, the above tests assumed that offspring genotypes were missing completely at random and concluded that the transmission/disequilibrium test remained a valid test by excluding incomplete triads from the analysis. In this article, the conditional distribution of ascertained triads allowing informative missingness for offspring genotypes, as well as their parental genotypes, was derived and several tests under such scenarios were evaluated. In simulations, independent triads from the Genetic Analysis Workshop 15 simulated data (Problem 3) was ascertained. When offspring genotypes were missing informatively, simulation results revealed inflated type I error and/or reduced power for the transmission/disequilibrium test excluding incomplete triads.

摘要

传递/不平衡检验被引入,用于使用病例-父母三联体来检验一个标记与一个假定的疾病位点之间的连锁和关联。已经提出了几种扩展方法来处理不完全三联体。一些策略假定父母基因型完全随机缺失,一些方法允许父母基因型存在信息性缺失。然而,上述检验假定后代基因型完全随机缺失,并通过在分析中排除不完全三联体得出传递/不平衡检验仍然是有效的检验。在本文中,推导了允许后代基因型及其父母基因型存在信息性缺失的确定三联体的条件分布,并评估了在这种情况下的几种检验。在模拟中,确定了来自遗传分析研讨会15模拟数据(问题3)的独立三联体。当后代基因型存在信息性缺失时,模拟结果显示,排除不完全三联体的传递/不平衡检验的I型错误率膨胀和/或检验效能降低。

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引用本文的文献

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PLoS One. 2013 May 14;8(5):e63526. doi: 10.1371/journal.pone.0063526. Print 2013.

本文引用的文献

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