Stringham H M, Boehnke M
Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor 48109-2029, USA.
Am J Hum Genet. 1996 Oct;59(4):946-50.
A common problem encountered in linkage analyses is that execution of the computer program is halted because of genotypes in the data that are inconsistent with Mendelian inheritance. Such inconsistencies may arise because of pedigree errors or errors in typing. In some cases, the source of the inconsistencies is easily identified by examining the pedigree. In others, the error is not obvious, and substantial time and effort are required to identify the responsible genotypes. We have developed two methods for automatically identifying those individuals whose genotypes are most likely the cause of the inconsistencies. First, we calculate the posterior probability of genotyping error for each member of the pedigree, given the marker data on all pedigree members and allowing anyone in the pedigree to have an error. Second, we identify those individuals whose genotypes could be solely responsible for the inconsistency in the pedigree. We illustrate these methods with two examples: one a pedigree error, the second a genotyping error. These methods have been implemented as a module of the pedigree analysis program package MENDEL.
连锁分析中常见的一个问题是,由于数据中的基因型与孟德尔遗传不一致,计算机程序的执行会停止。这种不一致可能是由于系谱错误或分型错误引起的。在某些情况下,通过检查系谱很容易确定不一致的来源。在其他情况下,错误并不明显,需要大量的时间和精力来确定有问题的基因型。我们开发了两种方法来自动识别那些其基因型最有可能是不一致原因的个体。首先,在给定所有系谱成员的标记数据并允许系谱中的任何人出现错误的情况下,我们计算系谱中每个成员基因分型错误的后验概率。其次,我们识别那些其基因型可能是系谱不一致唯一原因的个体。我们用两个例子来说明这些方法:一个是系谱错误,另一个是基因分型错误。这些方法已作为系谱分析程序包MENDEL的一个模块实现。