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Bayesian implementation of a genetic model-free approach to the meta-analysis of genetic association studies.

机译:贝叶斯实施的无遗传模型方法对遗传关联研究进行荟萃分析。

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摘要

A genetic model-free method for the meta-analysis of genetic association studies is described that estimates the mode of inheritance from the data rather than assuming that it is known. For a bi-allelic polymorphism, with G as risk allele and g as wild-type, the genetic model depends on the ratio of the two log odds ratios, lambda = log OR(Gg)/log OR(GG), where OR(GG) compares GG with gg and OR(Gg) compares Gg with gg. Modelling log OR(GG) as a random effect creates a hierarchical model that can be implemented within a Bayesian framework.In Bayesian modelling, vague prior distributions have to be specified for all unknown parameters when no external information is available. When the data are sparse even supposedly vague prior distributions may have an influence on the posterior estimates. We investigate the impact of different vague prior distributions for the between-study standard deviation of log OR(GG) and for lambda, by considering three published meta-analyses and associated simulations. Our results show that depending on the characteristics of the meta-analysis the results may indeed be sensitive to the choice of vague prior distribution for either parameter.Genetic association studies usually use a case-control design that should be analysed by the corresponding retrospective likelihood. However, under some circumstances the prospective likelihood has been shown to produce identical results and it is usually preferred for its simplicity. In our meta-analyses the two likelihoods give very similar results.
机译:描述了一种用于遗传关联研究的荟萃分析的无遗传模型方法,该方法从数据中估计遗传模式,而不是假设已知遗传模式。对于双等位基因多态性,以G为风险等位基因且g为野生型,遗传模型取决于两个对数比值比的比率,λ= log OR(Gg)/ log OR(GG),其中OR( GG)将GG与gg进行比较,OR(Gg)将Gg与gg进行比较。将对数OR(GG)建模为随机效应会创建一个可在贝叶斯框架内实现的分层模型。在贝叶斯建模中,如果没有外部信息可用,则必须为所有未知参数指定模糊的先验分布。当数据稀疏时,据称模糊的先前分布也可能对后验估计产生影响。通过考虑三个已发表的荟萃分析和相关模拟,我们研究了不同模糊先验分布对log OR(GG)和lambda的研究之间标准差的影响。我们的研究结果表明,根据荟萃分析的特征,结果可能确实对每个参数的模糊先验分布选择敏感。遗传关联研究通常使用病例对照设计,应通过相应的回顾性可能性进行分析。但是,在某些情况下,预期可能性已显示出相同的结果,通常由于其简单性而被优先考虑。在我们的荟萃分析中,两种可能性得出的结果非常相似。

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