全球人口中非 CODIS STRs 的全面情况为了解具有挑战性的 DNA 图谱提供了新的视角

IF 3.2 2区 医学 Q2 GENETICS & HEREDITY
Yuguo Huang , Mengge Wang , Chao Liu , Guanglin He
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引用次数: 0

摘要

法医遗传学在全球范围内使用短串联重复序列(STR)图谱,因此有必要建立和扩大 CODIS 核心基因位点集,以促进有效的数据管理和交换。目前,大多数通用的法医工具包都采用了 CODIS 的主要 STR。然而,在生物地理祖先推断、复杂 DNA 混合图谱解释和远缘关系分析等具有挑战性的任务中,仅依靠这些基因位点无法获得令人满意的结果。在这种情况下,非 CODIS STR 是增强系统分辨能力的有力补充,尤其是在与高通量下一代测序(NGS)技术相结合时。然而,在不同人群中对非 CODIS STRs 的全面评估还很少,这阻碍了它们在常规病例中的进一步应用。为了填补这一空白,我们调查了 178 种历史上可用的非 CODIS STRs 的遗传变异,这些 STRs 来自世界各地不同的民族语言人群,并通过高覆盖率的全基因组测序(WGS)数据研究了它们的特征和法医潜力。起初,我们通过序列搜索、重复结构扫描和人工检测来确定这些非 CODIS 标记的基因组特性。随后的群体遗传学分析表明,这些非 CODIS STR 具有与 CODIS STR 相当的多态性水平和法医效力。此外,我们还构建了一个由 108 条 STR(20 条 CODIS STR 和 88 条非 CODIS STR)组成的理论下一代测序(NGS)面板,并使用真实和模拟数据集评估了其在推断生物地理祖先起源、分解复杂 DNA 混合物和区分远亲关系方面的性能。我们的研究结果表明,加入补充的非 CODIS STR 可以从单一 STR 图谱中推断出多维信息,从而为分析具有挑战性的法医任务提供便利。总之,本研究展示了全球人群中法医非 CODIS STR 的广泛基因组图谱,并强调了在未来基于 NGS 的法医系统中纳入更多多态非 CODIS STR 的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive landscape of non-CODIS STRs in global populations provides new insights into challenging DNA profiles

The worldwide implementation of short tandem repeats (STR) profiles in forensic genetics necessitated establishing and expanding the CODIS core loci set to facilitated efficient data management and exchange. Currently, the mainstay CODIS STRs are adopted in most general-purpose forensic kits. However, relying solely on these loci failed to yield satisfactory results for challenging tasks, such as bio-geographical ancestry inference, complex DNA mixture profile interpretation, and distant kinship analysis. In this context, non-CODIS STRs are potent supplements to enhance the systematic discriminating power, particularly when combined with the high-throughput next-generation sequencing (NGS) technique. Nevertheless, comprehensive evaluation on non-CODIS STRs in diverse populations was scarce, hindering their further application in routine caseworks. To address this gap, we investigated genetic variations of 178 historically available non-CODIS STRs from ethnolinguistically different worldwide populations and studied their characteristics and forensic potentials via high-coverage whole genome sequencing (WGS) data. Initially, we delineated the genomic properties of these non-CODIS markers through sequence searching, repeat structure scanning, and manual inspection. Subsequent population genetics analysis suggested that these non-CODIS STRs had comparable polymorphism levels and forensic utility to CODIS STRs. Furthermore, we constructed a theoretical next-generation sequencing (NGS) panel comprising 108 STRs (20 CODIS STRs and 88 non-CODIS STRs), and evaluated its performance in inferring bio-geographical ancestry origins, deconvoluting complex DNA mixtures, and differentiating distant kinships using real and simulated datasets. Our findings demonstrated that incorporating supplementary non-CODIS STRs enabled the extrapolation of multidimensional information from a single STR profile, thereby facilitating the analysis of challenging forensic tasks. In conclusion, this study presents an extensive genomic landscape of forensic non-CODIS STRs among global populations, and emphasized the imperative inclusion of additional polymorphic non-CODIS STRs in future NGS-based forensic systems.

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来源期刊
CiteScore
7.50
自引率
32.30%
发文量
132
审稿时长
11.3 weeks
期刊介绍: Forensic Science International: Genetics is the premier journal in the field of Forensic Genetics. This branch of Forensic Science can be defined as the application of genetics to human and non-human material (in the sense of a science with the purpose of studying inherited characteristics for the analysis of inter- and intra-specific variations in populations) for the resolution of legal conflicts. The scope of the journal includes: Forensic applications of human polymorphism. Testing of paternity and other family relationships, immigration cases, typing of biological stains and tissues from criminal casework, identification of human remains by DNA testing methodologies. Description of human polymorphisms of forensic interest, with special interest in DNA polymorphisms. Autosomal DNA polymorphisms, mini- and microsatellites (or short tandem repeats, STRs), single nucleotide polymorphisms (SNPs), X and Y chromosome polymorphisms, mtDNA polymorphisms, and any other type of DNA variation with potential forensic applications. Non-human DNA polymorphisms for crime scene investigation. Population genetics of human polymorphisms of forensic interest. Population data, especially from DNA polymorphisms of interest for the solution of forensic problems. DNA typing methodologies and strategies. Biostatistical methods in forensic genetics. Evaluation of DNA evidence in forensic problems (such as paternity or immigration cases, criminal casework, identification), classical and new statistical approaches. Standards in forensic genetics. Recommendations of regulatory bodies concerning methods, markers, interpretation or strategies or proposals for procedural or technical standards. Quality control. Quality control and quality assurance strategies, proficiency testing for DNA typing methodologies. Criminal DNA databases. Technical, legal and statistical issues. General ethical and legal issues related to forensic genetics.
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