Abel L, Müller-Myhsok B
INSERM U.436, Mathematical and Statistical Modeling in Biology and Medicine, Hôpital Pitié-Salpêtrière, Paris, France.
Am J Hum Genet. 1998 Aug;63(2):638-47. doi: 10.1086/301958.
The maximum-likelihood-binomial (MLB) method, based on the binomial distribution of parental marker alleles among affected offspring, recently was shown to provide promising results by two-point linkage analysis of affected-sibship data. In this article, we extend the MLB method to multipoint linkage analysis, using the general framework of hidden Markov models. Furthermore, we perform a large simulation study to investigate the robustness and power of the MLB method, compared with those of the maximum-likelihood-score (MLS) method as implemented in MAPMAKER/SIBS, in the multipoint analysis of different affected-sibship samples. Analyses of multiple-affected sibships by means of the MLS were conducted by consideration of all possible sib pairs, with (weighted MLS [MLSw]) or without (unweighted MLS [MLSu]) application of a classic weighting procedure. In simulations under the null hypothesis, the MLB provided very consistent type I errors regardless of the type of family sample (sib pairs or multiple-affected sibships), as did the MLS for samples with sib pairs only. When samples included multiple-affected sibships, the MLSu led to inflation of low type I errors, whereas the MLSw yielded very conservative tests. Power comparisons showed that the MLB generally was more powerful than the MLS, except in recessive models with allele frequencies <.3. Missing parental marker data did not strongly influence type I error and power results in these multipoint analyses. The MLB approach, which in a natural way accounts for multiple-affected sibships and which provides a simple likelihood-ratio test for linkage, is an interesting alternative for multipoint analysis of sibships.
基于患病后代中亲代标记等位基因的二项分布的最大似然二项式(MLB)方法,最近通过对患病同胞数据的两点连锁分析显示出了有前景的结果。在本文中,我们使用隐马尔可夫模型的通用框架将MLB方法扩展到多点连锁分析。此外,我们进行了一项大型模拟研究,以调查在不同患病同胞样本的多点分析中,与MAPMAKER/SIBS中实现的最大似然分数(MLS)方法相比,MLB方法的稳健性和效能。通过考虑所有可能的同胞对,使用(加权MLS [MLSw])或不使用(未加权MLS [MLSu])经典加权程序,对多个患病同胞进行MLS分析。在零假设下的模拟中,无论家庭样本类型(同胞对或多个患病同胞)如何,MLB都提供了非常一致的I型错误,仅包含同胞对的样本的MLS也是如此。当样本包括多个患病同胞时,MLSu导致低I型错误的膨胀,而MLSw产生非常保守的检验。效能比较表明,除了等位基因频率<.3的隐性模型外,MLB通常比MLS更具效能。缺失亲代标记数据在这些多点分析中对I型错误和效能结果没有强烈影响。MLB方法以自然的方式考虑了多个患病同胞,并提供了一种简单的连锁似然比检验,是同胞多点分析的一个有趣替代方法。