Kühnau W, Böhm I, Krawczak M, Schmidtke J
Institut für Humangenetik, Medizinische Hochschule Hannover, Germany.
Electrophoresis. 1997 Aug;18(9):1598-601. doi: 10.1002/elps.1150180919.
A paternity case is presented in which DNA typing with thirteen variable number of tandem repeat (VNTR) systems was in apparent conflict with an initial multilocus DNA analysis using oligonucleotide probe (CAC)5. A dual approach was necessary, because the multilocus analysis yielded a proportion of aberrant nonmaternal offspring bands far too small and level of band-sharing too high for non-paternity. The case could finally be solved by reference to the joint likelihood ratio combining both approaches. Arguments are presented that summation of log likelihoods is indeed valid even if no information is available regarding linkage between the VNTR loci and the loci contributing to a multilocus DNA fingerprint.
本文介绍了一个亲子鉴定案例,其中使用13个串联重复可变数目(VNTR)系统进行的DNA分型与最初使用寡核苷酸探针(CAC)5进行的多位点DNA分析明显冲突。需要采用双重方法,因为多位点分析产生的异常非母系后代条带比例过小,且条带共享水平过高,不符合非父系的情况。最终通过参考结合两种方法的联合似然比解决了该案例。文中提出,即使没有关于VNTR位点与构成多位点DNA指纹的位点之间连锁关系的信息,对数似然值的求和确实是有效的。