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微单倍型面板在 DNA 混合分析中的评估。

Evaluation of the Microhaplotypes panel for DNA mixture analyses.

机构信息

Department of Forensic Medicine, Nanjing Medical University, Nanjing, Jiangsu, 211166, PR China.

Department of Forensic Medicine, Nanjing Medical University, Nanjing, Jiangsu, 211166, PR China.

出版信息

Forensic Sci Int Genet. 2018 Jul;35:149-155. doi: 10.1016/j.fsigen.2018.05.003. Epub 2018 May 12.

Abstract

The identification of a suspect in a DNA mixture typed with the standard short tandem repeat polymorphism (STR) kits has faced challenges. Several improved methods or technologies have been introduced to address this issue. However, some complex situations in the process remain elusive. In the present study, we presented a panel of 26 tiny microhaplotypes, each generating a relatively high (>3.0) effective number of alleles (A) and possessing low (<50 bp) sequence lengths. The average A and heterozygosity values among the 9 populations of 26 microhaps were in ranges from 2.60 to 4.54 and 0.59 to 0.96, respectively. Power of discrimination and power of exclusion values were ranged from 0.49 to 0.87 and 0.29 to 0.94, respectively. Significant positive correlations have been found between A values and heterozygosity (r = 0.43, p = 0.02) or power of discrimination values (r = 0.55, p = 0.003), respectively. The cumulative probability of detecting a mixture of two unrelated individuals could reach 0.9999998 when using a panel of 26 microhaps with A = 3. We further tested the panel by using massively parallel sequencing, and 14 out of 26 microhaps were successfully genotyped in a single multiplex system. 60 unrelated Chinese Han individuals and 2 artificially prepared samples mixed by two unrelated contributors (in duplicate, ie. 4 mixtures) were sequenced. Approximately 32.14% of the 14 loci presented three or four alleles in the two mixtures. The likelihood ratio values to cognizance the mixtures' contributor were in a range from 1.95 × 10 to 1.10 × 10. The results demonstrated that the present panel could offer a valuable complementary tool in forensic applications.

摘要

在使用标准短串联重复序列(STR)试剂盒进行 DNA 混合分型时,鉴定嫌疑人面临挑战。已经引入了几种改进的方法或技术来解决这个问题。然而,在这个过程中,一些复杂的情况仍然难以捉摸。在本研究中,我们提出了一组 26 个微小微单倍型,每个微单倍型产生相对较高(>3.0)的有效等位基因(A),并且具有较低(<50 bp)的序列长度。在 9 个人群的 26 个微单倍型中,A 和杂合度的平均值分别在 2.60 到 4.54 和 0.59 到 0.96 之间。鉴别力和排除力的值分别在 0.49 到 0.87 和 0.29 到 0.94 之间。A 值与杂合度(r=0.43,p=0.02)或鉴别力值(r=0.55,p=0.003)之间存在显著的正相关。当使用一组 A 值为 3 的 26 个微单倍型时,检测两个无关个体混合物的累积概率可达 0.9999998。我们进一步使用大规模平行测序对该面板进行了测试,在单个多重系统中成功地对 26 个微单倍型中的 14 个进行了基因分型。对 60 名无关汉族个体和 2 名由两个无关供体混合而成的人工制备样本(一式两份,即 4 个混合物)进行了测序。在两个混合物中,大约 32.14%的 14 个位点呈现出三个或四个等位基因。用于识别混合物供体的似然比数值在 1.95×10 到 1.10×10 之间。结果表明,本研究中的面板可为法医学应用提供有价值的补充工具。

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