一个整合了 STR 和 SNP 的 193 复式 MPS 面板凸显了法医遗传学在个体鉴定和亲子鉴定中的应用价值。

IF 3.8 2区 生物学 Q2 GENETICS & HEREDITY
Human Genetics Pub Date : 2024-03-01 Epub Date: 2024-03-18 DOI:10.1007/s00439-024-02658-1
Xueyuan Liu, Chengliang Yang, Xiaohui Chen, Xiaolong Han, Hong Liu, Xingkun Zhang, Quyi Xu, Xingyi Yang, Changhui Liu, Ling Chen, Chao Liu
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引用次数: 0

摘要

大规模平行测序(MPS)已成为法医遗传学中同时针对多个基因位点的一项前景广阔的技术。在本研究中,通过在 MGISEQ-2000™ 平台上采用单端 400 bp 测序策略,设计了一种新型的 193 复式测序板,以 28 个 A-STR、41 个 Y-STR、21 个 X-STR、3 个性别鉴定位点和 100 个 A-SNP 为目标。在本研究中,对 1642 个人群样本进行了一系列验证和测序,以评估基于 MPS 的面板的整体性能及其在 SWGDAM 指南下的法医应用中的实用性。总体而言,我们小组中的 193 个复合物标记在物种特异性、稳定性和可重复性方面表现良好。与商业化试剂盒相比,该小组在标准 gDNA 方面的一致性达到了 100%,在 14,560 个群体基因型方面的一致性达到了 99.87%。此外,该试剂盒还能从 0.5 纳克 DNA 模板中检测出 100% 的基因座,并能以 1:4 的 DNA 混合比(0.2 纳克次要贡献者)检测出所有独特的等位基因。此外,还在一项人群研究中计算了 STR 和 SNP 的几个法医参数。结果表明,CPE 和 CPD 值均大于 0.9999999,这些结果可作为应用该面板进行个体识别和亲子鉴定的有用参考。总之,该 193 复合物 MPS 面板已被证明是一种可靠、可重复、稳健、廉价且功能强大的工具,足以用于法医实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A novel 193-plex MPS panel integrating STRs and SNPs highlights the application value of forensic genetics in individual identification and paternity testing.

A novel 193-plex MPS panel integrating STRs and SNPs highlights the application value of forensic genetics in individual identification and paternity testing.

Massively parallel sequencing (MPS) has emerged as a promising technology for targeting multiple genetic loci simultaneously in forensic genetics. Here, a novel 193-plex panel was designed to target 28 A-STRs, 41 Y-STRs, 21 X-STRs, 3 sex-identified loci, and 100 A-SNPs by employing a single-end 400 bp sequencing strategy on the MGISEQ-2000™ platform. In the present study, a series of validations and sequencing of 1642 population samples were performed to evaluate the overall performance of the MPS-based panel and its practicality in forensic application according to the SWGDAM guidelines. In general, the 193-plex markers in our panel showed good performance in terms of species specificity, stability, and repeatability. Compared to commercial kits, this panel achieved 100% concordance for standard gDNA and 99.87% concordance for 14,560 population genotypes. Moreover, this panel detected 100% of the loci from 0.5 ng of DNA template and all unique alleles at a 1:4 DNA mixture ratio (0.2 ng minor contributor), and the applicability of the proposed approach for tracing and degrading DNA was further supported by case samples. In addition, several forensic parameters of STRs and SNPs were calculated in a population study. High CPE and CPD values greater than 0.9999999 were clearly demonstrated and these results could be useful references for the application of this panel in individual identification and paternity testing. Overall, this 193-plex MPS panel has been shown to be a reliable, repeatable, robust, inexpensive, and powerful tool sufficient for forensic practice.

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来源期刊
Human Genetics
Human Genetics 生物-遗传学
CiteScore
10.80
自引率
3.80%
发文量
94
审稿时长
1 months
期刊介绍: Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology. Unless reporting entirely novel and unusual aspects of a topic, clinical case reports, cytogenetic case reports, papers on descriptive population genetics, articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described, and papers that report meta-analyses of previously published datasets will normally not be accepted. The Journal typically will not consider for publication manuscripts that report merely the isolation, map position, structure, and tissue expression profile of a gene of unknown function unless the gene is of particular interest or is a candidate gene involved in a human trait or disorder.
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