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Genetic polymorphism of the 26 short tandem repeat loci in the Chinese Hebei Han population using two commercial forensic kits

机译:使用两个商业法医试剂盒对中国河北汉族人群中的26个短串联重复基因座进行遗传多态性分析

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We determined the allele frequencies and forensic parameters for the 26 short tandem repeat (STR) autosomal markers in two commercial kits (the Investigator HDplex and AmpFLSTR (R) Identifiler (R) systems) for 183 unrelated individuals from the Han population of the Hebei Province of China. The 26 STRs were all in Hardy-Weinberg equilibrium. No linkage disequilibrium was detected between any pair of loci. The combined power of discrimination and the combined power of exclusion for the 26 STR loci were 1-7.74E-31 and 1-1.21E-11, respectively. Six rare alleles of D10S2325 were identified and named 20, 21, 22, 23, 24, and 31. All the length of the six rare alleles were out of the range of allelic ladder. We calculated the population pairwise genetic distance based on the allele frequencies, using published population data including German, central Polish, south Dutch, northeastern Polish, south Brazilian, Korean, Sichuan Han of China, and Shanghai Han of China. Also we examined the population pairwise genetic distance of loci included in Identifiler system between Hebei Han and other ethnic population of China. These 26 autosomal STR loci could provide highly informative polymorphic data for paternity testing and forensic identification in the Hebei Han population in China. Because they are all in linkage equilibrium, they could be used together to solve deficient kinship cases or cases with mutations.
机译:我们确定了两个商业试剂盒(调查员HDplex和AmpFLSTR(R)标识符(R)系统)中来自河北省汉族的183个无关个体的26个短串联重复(STR)常染色体标记的等位基因频率和法医参数。中国。 26个STR均处于Hardy-Weinberg平衡状态。在任何一对基因座之间均未检测到连锁不平衡。 26个STR基因座的鉴别力和排斥力分别为1-7.74E-31和1-1.21E-11。鉴定出D10S2325的六个稀有等位基因,并将其命名为20、21、22、23、24和31。六个稀有等位基因的所有长度均不在等位基因阶梯的范围内。我们根据等位基因频率,使用已公布的人口数据,包括德国,中部波兰人,南荷兰人,东北波兰人,巴西南部,韩国人,中国四川人和中国上海人,计算了成对的遗传距离。我们还研究了河北汉族与中国其他民族之间身份识别系统中包括的基因座的成对遗传距离。这26个常染色体STR位点可以为中国河北汉族人群的亲子鉴定和法医鉴定提供高度信息化的多态性数据。由于它们都处于连锁平衡状态,因此可以一起使用它们来解决亲缘关系不足的案例或具有突变的案例。

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