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疾病的双基因座模型:似然法与非参数连锁法的比较

Two-locus models of disease: comparison of likelihood and nonparametric linkage methods.

作者信息

Goldin L R, Weeks D E

机构信息

Clinical Neurogenetics Branch, National Institute of Mental Health, Bethesda, MD 20892.

出版信息

Am J Hum Genet. 1993 Oct;53(4):908-15.

Abstract

The power to detect linkage for likelihood and nonparametric (Haseman-Elston, affected-sib-pair, and affected-pedigree-member) methods is compared for the case of a common, dichotomous trait resulting from the segregation of two loci. Pedigree data for several two-locus epistatic and heterogeneity models have been simulated, with one of the loci linked to a marker locus. Replicate samples of 20 three-generation pedigrees (16 individuals/pedigree) were simulated and then ascertained for having at least 6 affected individuals. The power of linkage detection calculated under the correct two-locus model is only slightly higher than that under a single locus model with reduced penetrance. As expected, the nonparametric linkage methods have somewhat lower power than does the lod-score method, the difference depending on the mode of transmission of the linked locus. Thus, for many pedigree linkage studies, the lod-score method will have the best power. However, this conclusion depends on how many times the lod score will be calculated for a given marker. The Haseman-Elston method would likely be preferable to calculating lod scores under a large number of genetic models (i.e., varying both the mode of transmission and the penetrances), since such an analysis requires an increase in the critical value of the lod criterion. The power of the affected-pedigree-member method is lower than the other methods, which can be shown to be largely due to the fact that marker genotypes for unaffected individuals are not used.

摘要

针对由两个基因座分离产生的常见二分性状的情况,比较了似然法和非参数法(哈斯曼 - 埃尔斯顿法、患病同胞对法和患病家系成员法)检测连锁的效能。对几个两基因座上位性和异质性模型的家系数据进行了模拟,其中一个基因座与一个标记基因座连锁。模拟了20个三代家系(每个家系16人)的重复样本,然后确定至少有6个患病个体。在正确的两基因座模型下计算的连锁检测效能仅略高于在具有降低外显率的单基因座模型下的效能。正如预期的那样,非参数连锁法的效能略低于对数计分法,差异取决于连锁基因座的传递模式。因此,对于许多家系连锁研究,对数计分法将具有最佳效能。然而,这一结论取决于对于给定标记将计算多少次对数计分。在大量遗传模型(即同时改变传递模式和外显率)下,哈斯曼 - 埃尔斯顿法可能比计算对数计分更可取,因为这样的分析需要提高对数计分标准的临界值。患病家系成员法的效能低于其他方法,这在很大程度上可以证明是由于未使用未患病个体的标记基因型。

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