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Population genetics of insertion-deletion polymorphisms in South Koreans using Investigator DIPplex kit

机译:使用Investigator DIPplex试剂盒对韩国人进行插入删除多态性的群体遗传学

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摘要

We assessed the applicability of 30 insertion-deletion polymorphisms (INDELs) in forensic use and the level of genetic diversity in South Korea (n = 373) using the Investigator DIPplex? kit (Qiagen). Allele frequencies, heterozygocities, and forensic efficacy parameters were determined. No deviation from Hardy-Weinberg equilibrium was observed for any of the INDEL markers. A high level of discrimination power was observed (combined power of discrimination: 0.99999999995). The combined match probability value was 2.84 × 10-11 and the mean typical paternity indices were 0.878. Furthermore, we found one microvariant allele at HLD93 (rs2307570) that has not been reported. We expect that these 30 loci of INDEL markers will be useful for forensic identification and paternity testing in the South Korean population.
机译:我们使用Investigator DIPplex评估了30种插入删除多态性(INDEL)在法医学中的适用性以及韩国(n = 373)的遗传多样性水平。套件(恰根)。确定了等位基因频率,杂合性和法医功效参数。对于任何INDEL标记,均未观察到与Hardy-Weinberg平衡的偏差。观察到较高的辨别力(辨别力合计:0.99999999995)。组合匹配概率值为2.84×10-11,平均典型父子指数为0.878。此外,我们在HLD93(rs2307570)上发现了一个微变等位基因,尚未报道。我们预计,这30个INDEL标记位点将可用于韩国人群的法医鉴定和亲子鉴定。

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