Odelberg S J, Plaetke R, Eldridge J R, Ballard L, O'Connell P, Nakamura Y, Leppert M, Lalouel J M, White R
Department of Human Genetics, University of Utah Medical Center, Salt Lake City, 84132.
Genomics. 1989 Nov;5(4):915-24. doi: 10.1016/0888-7543(89)90134-1.
Allelic frequencies and their confidence intervals were obtained for eight independent VNTR loci from a sample of more than 75 Utah Caucasians. Using high-resolution agarose gel electrophoresis, we were able to resolve alleles at the D17S5 locus that differed by only one repeating unit; it was therefore possible to name the alleles according to the number of repeating units each contained. Two a priori probabilities were calculated for each VNTR locus separately and for all eight loci jointly: (i) the "power of exclusion" for an alleged father/mother/child trio and for an alleged parent/child duo, and (ii) the "probability of matching" when two unrelated individuals or two siblings are genotyped.
从75名以上犹他州白种人的样本中,获取了8个独立的VNTR基因座的等位基因频率及其置信区间。使用高分辨率琼脂糖凝胶电泳,我们能够分辨出D17S5基因座上仅相差一个重复单元的等位基因;因此,可以根据每个等位基因所含重复单元的数量来命名。分别为每个VNTR基因座以及联合所有8个基因座计算了两个先验概率:(i) 对于假定的父亲/母亲/孩子三人组和假定的父母/孩子二人组的“排除能力”,以及 (ii) 对两个无关个体或两个兄弟姐妹进行基因分型时的“匹配概率”。