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构建两个荧光标记的非组合 DNA 指数系统 miniSTR 多重扩增系统,用于分析中国汉族人群中降解的 DNA 样本。

Construction of two fluorescence-labeled non-combined DNA index system miniSTR multiplex systems to analyze degraded DNA samples in the Chinese Han Population.

机构信息

Hebei Key Laboratory of Forensic Medicine, Department of Forensic Medicine, Hebei Medical University, No. 361 Zhong Shan east Road, Shijiazhuang, Hebei, P. R. China.

出版信息

Electrophoresis. 2010 Sep;31(17):2944-8. doi: 10.1002/elps.201000163.

Abstract

MiniSTR loci have been demonstrated to be an effective approach in recovering genetic information from degraded specimens, because of the reduced PCR amplicon sizes which improved the PCR efficiency. Eight non-combined DNA index system miniSTR loci suitable for the Chinese Han Population were analyzed in 300 unrelated Chinese Han individuals using two novel five fluorescence-labeled miniSTR multiplex systems(multiplex I: D10S1248, D2S441, D1S1677 and D9S2157; multiplex II: D9S1122, D10S1435, D12ATA63, D2S1776 and Amelogenin). The allele frequency distribution and forensic parameters in the Chinese Han Population were reported in this article. The Exact Test demonstrated that all loci surveyed here were found to be no deviation from Hardy-Weinberg equilibrium. The accumulated power of discrimination and power of exclusion for the eight loci were 0.999999992 and 0.98, respectively. The highly degraded DNA from artificially degraded samples and the degraded forensic case work samples was assessed with the two miniSTR multiplex systems, and the results showed that the systems were quite effective.

摘要

MiniSTR 基因座已被证明是从降解样本中恢复遗传信息的有效方法,因为减少的 PCR 扩增片段大小提高了 PCR 效率。使用两种新型五荧光标记 miniSTR 多重扩增系统(多重扩增 I:D10S1248、D2S441、D1S1677 和 D9S2157;多重扩增 II:D9S1122、D10S1435、D12ATA63、D2S1776 和 Amelogenin),对 300 名无关中国汉族个体的 8 个非组合 DNA 指数系统 miniSTR 基因座进行了分析。本文报道了中国汉族人群中的等位基因频率分布和法医学参数。确切检验表明,所有调查的基因座均未偏离哈迪-温伯格平衡。8 个基因座的累积鉴别力和排除力分别为 0.999999992 和 0.98。使用两种 miniSTR 多重扩增系统对人工降解样本和降解法医工作样本中的高度降解 DNA 进行了评估,结果表明该系统非常有效。

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