Department of Human Genetics, University of Pittsburgh, 130 Desoto St., Pittsburgh, PA 15261, USA.
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S144. doi: 10.1186/1471-2156-6-S1-S144.
Complex diseases are multifactorial in nature and can involve multiple loci with gene x gene and gene x environment interactions. Research on methods to uncover the interactions between those genes that confer susceptibility to disease has been extensive, but many of these methods have only been developed for sibling pairs or sibships. In this report, we assess the performance of two methods for finding gene x gene interactions that are applicable to arbitrarily sized pedigrees, one based on correlation in per-family nonparametric linkage scores and another that incorporates candidate loci genotypes as covariates into an affected relative pair linkage analysis. The power and type I error rate of both of these methods was addressed using the simulated Genetic Analysis Workshop 14 data. In general, we found detection of the interacting loci to be a difficult problem, and though we experienced some modest success there is a clear need to continue developing new methods and approaches to the problem.
复杂疾病本质上是多因素的,可能涉及多个具有基因 x 基因和基因 x 环境相互作用的基因座。研究发现易患疾病的这些基因之间相互作用的方法已经很广泛,但是其中许多方法仅适用于兄弟姐妹对或家系。在本报告中,我们评估了两种适用于任意大小家系的发现基因 x 基因相互作用的方法的性能,一种方法基于家族内非参数连锁分数的相关性,另一种方法将候选基因座基因型作为协变量纳入受影响的相对对连锁分析中。使用模拟的遗传分析研讨会 14 数据解决了这两种方法的功效和 I 型错误率问题。一般来说,我们发现检测相互作用的基因座是一个困难的问题,虽然我们取得了一些适度的成功,但显然需要继续开发新的方法和方法来解决这个问题。