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系谱数据方差分量模型的拟合优度及确定方法

Ascertainment and goodness of fit of variance component models for pedigree data.

作者信息

Boehnke M, Lange K

出版信息

Prog Clin Biol Res. 1984;147:173-92.

PMID:6547532
Abstract

The multivariate normal parameterization of the polygenic model (Lange et al., 1976) provides a great deal of flexibility for analyzing quantitative data on pedigrees. The likelihood approach employed ensures statistical efficiency and allows for hypothesis testing using the likelihood ratio criterion. The parameterization also facilitates ascertainment correction and goodness-of-fit testing (Spence et al., 1977; Ott, 1979; Hopper and Mathews, 1982; Boehnke, 1983). We reviewed these results and then described a simulation study undertaken to determine their utility when applied to data. Pedigree data were generated under polygenic and mixed models and sampled either randomly or via probands. We found that the variance components of the model were accurately estimated for random sampling, but less so for ascertained data analyzed by conditioning on probands. Goodness-of-fit tests employing test statistics corresponding to individual phenotypes and entire pedigrees were conservative, but pedigree tests did demonstrate reasonable power to reject a variety of mixed model alternatives. In addition, we found that the pedigree test statistics could be used to enrich a sample of pedigrees for those pedigrees segregating at a major locus, providing an objective criterion for choosing pedigrees to be included in a linkage analysis.

摘要

多基因模型的多元正态参数化(兰格等人,1976年)为分析系谱中的定量数据提供了很大的灵活性。所采用的似然方法确保了统计效率,并允许使用似然比准则进行假设检验。这种参数化还便于进行确定校正和拟合优度检验(斯彭斯等人,1977年;奥特,1979年;霍珀和马修斯,1982年;博恩克,1983年)。我们回顾了这些结果,然后描述了一项模拟研究,以确定它们应用于数据时的效用。系谱数据是在多基因模型和混合模型下生成的,并通过随机抽样或先证者抽样。我们发现,对于随机抽样,模型的方差成分能被准确估计,但对于通过先证者条件分析的确定数据,估计效果较差。使用对应于个体表型和整个系谱的检验统计量进行的拟合优度检验是保守的,但系谱检验确实显示出有合理的能力来拒绝各种混合模型备选方案。此外,我们发现系谱检验统计量可用于富集在主要位点发生分离的系谱样本,为选择纳入连锁分析的系谱提供一个客观标准。

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