Rogatko A, Zacks S
Fox Chase Cancer Center, Philadelphia, PA 19111.
Am J Hum Genet. 1993 May;52(5):947-57.
Determination of the relative gene order on chromosomes is of critical importance in the construction of human gene maps. In this paper we develop a sequential algorithm for gene ordering. We start by comparing three sequential procedures to order three genes on the basis of Bayesian posterior probabilities, maximum-likelihood ratio, and minimal recombinant class. In the second part of the paper we extend sequential procedure based on the posterior probabilities to the general case of g genes. We present a theorem that states that the predicted average probability of committing a decision error, associated with a Bayesian sequential procedure that accepts the hypothesis of a gene-order configuration with posterior probability equal to or greater than pi *, is smaller than 1 - pi *. This theorem holds irrespective of the number of genes, the genetic model, and the source of genetic information. The theorem is an extension of a classical result of Wald, concerning the sum of the actual and the nominal error probabilities in the sequential probability ratio test of two hypotheses. A stepwise strategy for ordering a large number of genes, with control over the decision-error probabilities, is discussed. An asymptotic approximation is provided, which facilitates the calculations with existing computer software for gene mapping, of the posterior probabilities of an order and the error probabilities. We illustrate with some simulations that the stepwise ordering is an efficient procedure.
确定染色体上基因的相对顺序在构建人类基因图谱中至关重要。在本文中,我们开发了一种用于基因排序的序列算法。我们首先比较三种基于贝叶斯后验概率、最大似然比和最小重组类来对三个基因进行排序的序列程序。在本文的第二部分,我们将基于后验概率的序列程序扩展到 g 个基因的一般情况。我们给出了一个定理,该定理指出,与接受后验概率等于或大于π的基因顺序配置假设的贝叶斯序列程序相关的预测平均决策错误概率小于 1 - π。无论基因数量、遗传模型和遗传信息来源如何,该定理都成立。该定理是 Wald 的一个经典结果的扩展,该结果涉及两个假设的序列概率比检验中的实际和名义错误概率之和。讨论了一种用于对大量基因进行排序的逐步策略,同时控制决策错误概率。提供了一种渐近近似,这便于使用现有的基因图谱计算机软件计算顺序的后验概率和错误概率。我们通过一些模拟说明了逐步排序是一种有效的程序。