美国人群亲属关系检测用74个微单倍型的研究

IF 0.5 Q4 GENETICS & HEREDITY
Fabio Oldoni , Chiara Della Rocca , Daniele Podini
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引用次数: 1

摘要

微单倍型是由SNPs的单倍型块组成的标记,可以通过大规模平行测序技术进行分析。这允许通过对每个DNA链进行克隆测序来确定每个基因座的单倍型阶段。MHs是多态性位点,具有相同大小的等位基因,没有口吃,突变率低于STR。它们可以提供与STR试剂盒相同的辨别能力,因此可用于混合反卷积,但比STR更准确的祖先预测。在这项研究中,我们研究了最近开发的74plex MH面板使用Familias软件进行亲属关系测试的潜力。从美国四个主要群体的家族中收集样本,并使用74plex MH面板进行基因分型。将347名个体的MH等位基因频率数据与1036名个体的29个位点的STR等位基因数据(NIST数据集)一起导入Familias软件。对不同的家庭场景进行了测试,其中包括不相关与亲子、不相关与完全兄弟姐妹、不相关和同父异母兄弟姐妹以及不相关与表亲配对。四个感兴趣群体的亲属关系预测报告为似然比(LR)的Log10。总体而言,74MHs和29STR在预测测试的正确亲属关系场景方面表现出相似的性能。对于亲子、完全兄弟姐妹和半兄弟姐妹的情况,报告了正确的预测,但对于表亲对的情况则没有。由74个MHs组成的小组显示出比29个STR测定更大的Log10LR值,从而证明了该生物标志物作为亲属关系测试工具以及混合去卷积和祖先预测的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of 74 microhaplotypes for kinship testing in US populations

Microhaplotypes are markers that consist of haplotype blocks of SNPs, which can be analyzed by massively parallel sequencing technologies. These allow determining the haplotype phase at every locus by clonal sequencing each DNA strand. MHs are polymorphic loci with same size alleles, no stutter, and lower mutation rate than STRs. They can provide the same power of discrimination of STR-kits, thus useful for mixture deconvolution, but more accurate ancestry prediction than STRs. In this study we investigated the potential of a recently developed 74plex-MH panel for kinship testing using the Familias software.

Samples from families of four major US population groups were collected and genotyped using the 74plex-MH panel. MH allele frequency data from 347 individuals were imported into Familias software along with STR allele frequency data of 29 loci (NIST dataset) from 1036 individuals. Different family scenarios were tested and these included unrelated vs parent-child, unrelated vs full siblings, unrelated vs half siblings, unrelated vs cousin pairs. The prediction of the kinship relation for the four populations of interest was reported as Log10 of the likelihood ratio (LR).

Overall, the panel of 74MHs and 29STRs showed similar performance in predicting the correct kinship scenarios tested. Correct prediction was reported for parent-child, full siblings, and half sibling scenarios, but not for the cousin pairs scenario. The panel of 74 MHs showed larger Log10LR values than the 29 STR-assay, thus demonstrating the effectiveness of this biomarker as a tool for kinship testing in addition to mixture deconvolution and ancestry prediction.

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来源期刊
Forensic Science International: Genetics Supplement Series
Forensic Science International: Genetics Supplement Series Medicine-Pathology and Forensic Medicine
CiteScore
0.40
自引率
0.00%
发文量
122
审稿时长
25 days
期刊介绍: The Journal of Forensic Science International Genetics Supplement Series is the perfect publication vehicle for the proceedings of a scientific symposium, commissioned thematic issues, or for disseminating a selection of invited articles. The Forensic Science International Genetics Supplement Series is part of a duo of publications on forensic genetics, published by Elsevier on behalf of the International Society for Forensic Genetics.
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