Development and validation of YARN: A novel SE-400 MPS kit for East Asian paternal lineage analysis

IF 3.2 2区 医学 Q2 GENETICS & HEREDITY Forensic Science International-Genetics Pub Date : 2024-03-05 DOI:10.1016/j.fsigen.2024.103029
Haoliang Fan , Yiran Xu , Yutao Zhao , Kai Feng , Liuxi Hong , Qiancheng Zhao , Xiaoyu Lu , Meisen Shi , Haiyan Li , Lingxiang Wang , Shaoqing Wen
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Abstract

Y-chromosomal short tandem repeat polymorphisms (Y-STRs) and Y-chromosomal single nucleotide polymorphisms (Y-SNPs) are valuable genetic markers used in paternal lineage identification and population genetics. Currently, there is a lack of an effective panel that integrates Y-STRs and Y-SNPs for studying paternal lineages, particularly in East Asian populations. Hence, we developed a novel Y-chromosomal targeted panel called YARN (Y-chromosome Ancestry and Region Network) based on multiplex PCR and a single-end 400 massive parallel sequencing (MPS) strategy, consisting of 44 patrilineage Y-STRs and 260 evolutionary Y-SNPs. A total of 386 reactions were validated for the effectiveness and applicability of YARN according to SWGDAM validation guidelines, including sensitivity (with a minimum input gDNA of 0.125 ng), mixture identification (ranging from 1:1–1:10), PCR inhibitor testing (using substances such as 50 μM hematin, 100 μM hemoglobin, 100 μM humic acid, and 2.5 mM indigo dye), species specificity (successfully distinguishing humans from other animals), repeatability study (achieved 100% accuracy), and concordance study (with 99.91% accuracy for 1121 Y-STR alleles). Furthermore, we conducted a pilot study using YARN in a cohort of 484 Han Chinese males from Huaiji County, Zhaoqing City, Guangdong, China (GDZQHJ cohort). In this cohort, we identified 52 different Y-haplogroups and 73 different surnames. We found weak to moderate correlations between the Y-haplogroups, Chinese surnames, and geographical locations of the GDZQHJ cohort (with λ values ranging from 0.050 to 0.340). However, when we combined two different categories into a new independent variable, we observed stronger correlations (with λ values ranging from 0.617 to 0.754). Overall, the YARN panel, which combines Y-STR and Y-SNP genetic markers, meets forensic DNA quality assurance guidelines and holds potential for East Asian geographical origin inference and paternal lineage analysis.

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开发和验证 YARN:用于东亚父系血统分析的新型 SE-400 MPS 套件
Y 染色体短串联重复多态性(Y-STR)和 Y 染色体单核苷酸多态性(Y-SNP)是用于父系鉴定和群体遗传学的重要遗传标记。目前,在研究父系血统,尤其是东亚人群的父系血统时,还缺乏一个整合了 Y-STR 和 Y-SNPs 的有效面板。因此,我们基于多重 PCR 和单端 400 大规模并行测序(MPS)策略,开发了一种名为 YARN(Y-染色体祖先和区域网络)的新型 Y 染色体靶向面板,由 44 个父系 Y-STR 和 260 个进化 Y-SNP 组成。根据 SWGDAM 验证指南,共对 386 个反应进行了验证,以确定 YARN 的有效性和适用性,包括灵敏度(最小输入 gDNA 为 0.125ng)、混合物鉴定(1:1-1:10)、PCR 抑制剂测试(使用 50μM 血蛋白、100μM 血红蛋白、100μM 腐殖酸和 2.5mM 靛蓝染料)、物种特异性(成功区分人类和其他动物)、重复性研究(准确率达到 100%)和一致性研究(1121 个 Y-STR 等位基因的准确率达到 99.91%)。此外,我们还利用 YARN 对中国广东省肇庆市怀集县的 484 名汉族男性进行了试点研究(GDZQHJ 队列)。在这个队列中,我们发现了 52 个不同的 Y 单倍群和 73 个不同的姓氏。我们发现,广东肇庆人队列中的 Yaplogroups、中国姓氏和地理位置之间存在微弱至中等程度的相关性(λ值在 0.050 至 0.340 之间)。然而,当我们将两个不同的类别合并为一个新的自变量时,我们观察到了更强的相关性(λ值在 0.617 到 0.754 之间)。总之,YARN 面板结合了 Y-STR 和 Y-SNP 遗传标记,符合法医 DNA 质量保证准则,具有推断东亚地理来源和分析父系血统的潜力。
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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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