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基于非二元单核苷酸多态性的新型短微单倍型组用于法医疑难样本分析

A novel set of short microhaplotypes based on non-binary SNPs for forensic challenging samples.

作者信息

Zhao Xingchun, Fan Yang, Zeye Moutanou Modeste Judes, He Wei, Wen Dan, Wang Chudong, Li Jienan, Hua Zichun

机构信息

School of Biopharmacy, China Pharmaceutical University, Nanjing, 211198, China.

National Engineering Laboratory for Forensic Science, Beijing, 100038, China.

出版信息

Int J Legal Med. 2022 Jan;136(1):43-53. doi: 10.1007/s00414-021-02719-4. Epub 2021 Oct 15.

Abstract

Short tandem repeats (STRs) are the most widely used genetic markers in forensic application, but they are not ideal genetic markers for the analysis of forensic challenging samples such as highly degraded or unbalanced mixed samples because of their relatively large amplicons and stutter peaks. In this study, we developed a set of short microhaplotypes based on non-binary SNPs with molecular extent sizes no longer than 60 bases and genotyped 100 unrelated individuals from northern Han groups. Our results showed this panel has similar discrimination power to STR kits, as the combined random match probability (CMP) reached 1.396 × 10 and mean effective number of alleles (Ae) was 3.59. The cumulative probability of exclusion for duos (CPE-duos) was 0.999919 and the cumulative probability of exclusion for trios (CPE-trios) was 0.9999999987, suggesting this panel could be applied for forensic personal identification and parentage testing independently. Population differentiation in 26 populations from the 1000 Genomes Project indicated this panel could distinguish populations from Africa, East Asia, South Asia, America, and Europe. These microhaplotypes based on non-binary SNPs have short amplicons, good discrimination power, no stutter artifacts, and have great potential in detection of highly degraded and unbalanced mixtures for personal identification, paternity testing, and ancestry inference.

摘要

短串联重复序列(STRs)是法医应用中使用最广泛的遗传标记,但由于其扩增子相对较大且存在拖尾峰,对于分析高度降解或不平衡混合样本等具有挑战性的法医样本而言,它们并非理想的遗传标记。在本研究中,我们基于分子长度不超过60个碱基的非二元单核苷酸多态性(SNP)开发了一组短微单倍型,并对100名来自北方汉族群体的无关个体进行了基因分型。我们的结果表明,该面板具有与STR试剂盒相似的鉴别能力,因为其组合随机匹配概率(CMP)达到1.396×10,平均有效等位基因数(Ae)为3.59。二人组累计排除概率(CPE - duos)为0.999919,三人组累计排除概率(CPE - trios)为0.9999999987,这表明该面板可独立应用于法医个人识别和亲子鉴定。来自千人基因组计划的26个群体的群体分化表明,该面板能够区分来自非洲、东亚、南亚、美洲和欧洲的群体。这些基于非二元SNP的微单倍型具有短扩增子、良好的鉴别能力、无拖尾假象,在检测高度降解和不平衡混合物用于个人识别、亲子鉴定和血统推断方面具有巨大潜力。

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