Dense SNP-based analyses complement forensic anthropology biogeographical ancestry assessments

IF 3.2 2区 医学 Q2 GENETICS & HEREDITY
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引用次数: 0

Abstract

Identification of unidentified human remains (UHRs) is crucial yet challenging, especially with traditional forensic techniques. Forensic anthropological examinations can yield ancestry estimations; however, the utility of these estimates is limited by the data points that can be collected from partial remains, complexities of admixture, and variation of phenotypic expression due to environmental effects. While it is generally known that anthropological estimates can be imprecise, the performance of these methods has not been studied at scale. Genome-wide SNP testing is an orthogonal approach for estimating ancestry and offers a unique opportunity to measure the magnitude of anthropological ancestry misattribution. Genomic ancestry inference leverages principal component analysis (PCA) and model-based clustering approaches. This study compares anthropologically determined ancestry with those estimated using genome-wide SNP markers. A dataset of 611 UHR samples with publicly available ancestry assessments from National Missing and Unidentified Persons System (NamUs) was analyzed. The genetic ancestry approach, validated against reference population samples, offers robust ancestry calculations for major population groups. Inconsistency between anthropological and genomic ancestry assignments were observed, particularly for admixed populations. Although forensic anthropological examinations remain valuable, their limitations emphasize the need for refinement and enhancement through the augmentation of SNP-based analyses. Further validation studies are crucial to define the uncertainty associated with both anthropological and genome-based ancestry estimates to resolve cases and aid law enforcement investigations. Additionally, current policy and practices for reporting ancestry for UHRs should be revisited to reduce potential misinformation.

基于 SNP 的密集分析是对法医人类学生物地理祖先评估的补充
身份不明人类遗骸(UHR)的鉴定至关重要,但也极具挑战性,尤其是使用传统的法医技术。法医人类学检查可以得出祖先估计值;但是,这些估计值的实用性受到以下因素的限制:从部分遗骸中收集到的数据点、混杂的复杂性以及环境影响导致的表型表达变化。众所周知,人类学估算可能并不精确,但这些方法的性能尚未得到大规模研究。全基因组 SNP 检测是估算祖先的一种正交方法,为测量人类学祖先错误归属的程度提供了一个独特的机会。基因组祖先推断利用了主成分分析(PCA)和基于模型的聚类方法。本研究将人类学确定的祖先与使用全基因组 SNP 标记估计的祖先进行了比较。研究分析了由 611 个 UHR 样本组成的数据集,这些样本的祖先评估结果可从国家失踪与身份不明人员系统(NamUs)中公开获取。根据参考人群样本验证的遗传祖先方法为主要人群提供了可靠的祖先计算。人类学和基因组祖先分配之间存在不一致,特别是在混血人群中。尽管法医人类学检查仍然很有价值,但其局限性强调了通过基于 SNP 的分析进行改进和提高的必要性。进一步的验证研究对于确定与人类学和基于基因组的祖先估计相关的不确定性以解决案件和协助执法调查至关重要。此外,应重新审视当前报告 UHR 血统的政策和做法,以减少潜在的错误信息。
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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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