Lindblom B, Holmlund G, Stennek A
Avdelningsföreståndare, RiLuniversitetssjukhuset i Linköping.
Lakartidningen. 1991 May 29;88(22):2055-9.
Variable number of tandem repeat (VNTR) polymorphisms are used as genetic markers in paternity testing and forensic investigation. The blot patterns obtained with single locus probes are easily interpreted, and the fragment sizes can be calculated for further statistical evaluation. Fragments cleaved with Hinf I and analysed with the probe YNH 24 were found to vary in estimated size within +/- 1.5 per cent of the number of base pairs. In paternity testing, a window of +2.5 per cent will yield a risk of false exclusion of less than 1 in 10(6), with an estimated exclusion rate of about 90 per cent. In paternity testing, electrophoresis of mixed DNA samples from the child and the suspected father yields significant information irrespective of exclusion. The mean calculated paternity index for non-excluded men obtained with the YNH 24 probe was 8.4 (range, 2.6-19.2).
可变串联重复序列(VNTR)多态性在亲子鉴定和法医调查中用作遗传标记。用单基因座探针获得的印迹模式易于解读,并且可以计算片段大小以进行进一步的统计评估。发现用Hinf I切割并用探针YNH 24分析的片段,其估计大小在碱基对数量的±1.5%范围内变化。在亲子鉴定中,2.5%的窗口将产生小于十万分之一的错误排除风险,估计排除率约为90%。在亲子鉴定中,来自孩子和疑似父亲的混合DNA样本的电泳,无论是否排除,都会产生重要信息。用YNH 24探针获得的未被排除的男性的平均计算父权指数为8.4(范围为2.6 - 19.2)。