Schork N J
Department of Medicine, University of Michigan, Ann Arbor 48109-0500.
Genet Epidemiol. 1992;9(3):207-23. doi: 10.1002/gepi.1370090307.
Statistically characterizing factors responsible for quantitative phenotype expression (e.g., polygenes, major genes, shared household factors, etc.) through model selection strategies is a difficult task. A great deal of effort has been expended on refining mathematical and computational aspects of various segregation models used to characterize unique expressions of quantitative phenotypes in an effort to make these models easier to implement and evaluate for a given set of data. In this paper a slightly different angle is emphasized: namely, the explicit modeling of the potentially numerous heterogeneous genetic and environmental processes (i.e., segregation patterns, household aggregations, etiologic processes, etc.) that could contribute to the overall variation of a quantitative trait. As such, this paper describes tools for detecting quantitative trait heterogeneity that are meant to answer such questions as "are there pedigrees among a great many that show a pattern consistent with a possibly very specific single locus segregation pattern while the rest show compatibility with a polygenic or purely environmental pattern?" Methods for determining the significance of such heterogeneity are also discussed, as are the results of numerous examples and simulation studies carried out in an effort to validate and further elaborate aspects of the proposed techniques.
通过模型选择策略对负责定量表型表达的因素(如多基因、主基因、家庭共享因素等)进行统计学特征描述是一项艰巨的任务。人们在完善用于描述定量表型独特表达的各种分离模型的数学和计算方面投入了大量精力,以使这些模型在给定数据集下更易于实施和评估。本文强调了一个稍有不同的角度:即对可能众多的异质遗传和环境过程(即分离模式、家庭聚集、病因过程等)进行显式建模,这些过程可能导致定量性状的总体变异。因此,本文描述了用于检测定量性状异质性的工具,旨在回答诸如“在众多谱系中,是否存在一些谱系显示出与可能非常特定的单基因座分离模式一致的模式,而其余谱系则与多基因或纯环境模式兼容?”等问题。还讨论了确定这种异质性显著性的方法,以及为验证和进一步阐述所提出技术的各个方面而进行的大量实例和模拟研究的结果。