Identifying marker typing incompatibilities in linkage analysis.

HM Stringham, M Boehnke - American journal of human genetics, 1996 - ncbi.nlm.nih.gov
American journal of human genetics, 1996ncbi.nlm.nih.gov
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 …
Abstract
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.
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