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From battlefield to burial: Complex casualty identification using rapid DNA analysis in 21st century warfare 从战场到埋葬:21世纪战争中使用快速DNA分析的复杂伤亡鉴定
Q3 Medicine Pub Date : 2025-12-01 DOI: 10.1016/j.fsir.2025.100439
Dan M. Weinthal , Amit Blumberg , Elisha Ziv , Hillel Shuman , Danielle Waingrod , Reouven Berdugo , David Shore , Noam Shomron , Alon Oz
On October 7, 2023, terror organizations launched a large-scale surprise attack on Israel, resulting in the deadliest mass fatality incident in the nation’s history. The assault left 1438 Israelis dead, 255 taken hostage, and over 1600 assailants killed in defensive operations. In the immediate aftermath, the Israel Defense Forces (IDF) Genomic Center for Casualties Identification rapidly expanded its capacity by integrating rapid DNA technology and implementing refined sample prioritization protocols to accelerate the identification process. This mass fatality incident unfolded under unprecedented circumstances. Thousands of human remains, often fragmented, burned, or intermingled with those of perpetrators, were recovered across multiple sites. Conventional identification methods such as dental or fingerprint analysis were frequently unavailable, leaving DNA profiling the primary method of identification. The extreme scale and severity of the event meant that each case presented unique combination of sample types, often requiring repeated extractions and multiple testing approaches to obtain viable genetic profiles. These challenges, though described here in scientific terms, reflected the reality of a brutal attack that left families anxiously awaiting for closure, and forensic teams working around the clock in conditions rarely seen in civilian laboratories. Our findings indicate that while rapid DNA profiling enabled identifications in under three hours, the key determinant of timely results was precise sample triage and prioritization. We therefore propose a combined approach integrating strategic triage with fast-track DNA profiling to manage complex casualty events effectively. Using this approach, all casualties within our ground operations were identified within 2–3 h. Beyond the technical achievements, this experience underscores the dual mission of forensic science during national crisis: to uphold the highest standard of accuracy and integrity, while performing this work with humanity and respect amidst profound loss. The lessons learned from October 7th, much like those drawn from 9/11 and the long-term work of the International Commission on Missing Persons (ICMP), which investigates mass graves and missing persons from conflicts and disasters, provide valuable guidance for forensic agencies worldwide, offering strategies to strengthen preparedness and resilience for future mass fatality incidents.
2023年10月7日,恐怖组织对以色列发动大规模突然袭击,造成以色列历史上最严重的集体死亡事件。这次袭击造成1438名以色列人死亡,255人被劫持为人质,1600多名袭击者在防御行动中丧生。在事故发生后不久,以色列国防军(IDF)伤亡鉴定基因组中心通过整合快速DNA技术和实施精细的样本优先排序协议,迅速扩大了其能力,以加速鉴定过程。这起大规模死亡事件是在前所未有的情况下发生的。在多个地点发现了数千具人类遗骸,这些遗骸通常是破碎的、烧毁的,或者与肇事者的遗骸混在一起。传统的鉴定方法,如牙齿或指纹分析,往往是不可用的,留下DNA分析的主要鉴定方法。该事件的极端规模和严重性意味着每个病例都呈现出独特的样本类型组合,通常需要反复提取和多种测试方法才能获得可行的基因图谱。尽管本文用科学术语描述了这些挑战,但它们反映了残酷袭击的现实,让家属焦急地等待结束,法医小组在民用实验室罕见的条件下夜以继日地工作。我们的研究结果表明,虽然快速DNA分析能够在三小时内进行鉴定,但及时结果的关键决定因素是精确的样本分类和优先排序。因此,我们提出了一种结合战略分诊和快速DNA分析的综合方法,以有效地管理复杂的伤亡事件。使用这种方法,我们地面行动中的所有伤亡都在2-3 小时内确定。除了技术成就之外,这一经历还强调了法医学在国家危机期间的双重使命:在遭受重大损失的情况下,保持最高标准的准确性和完整性,同时以人道和尊重的态度开展这项工作。从10月7日事件中吸取的教训,就像从9/11事件中吸取的教训,以及调查冲突和灾害中万人坑和失踪人员的国际失踪人员委员会(ICMP)的长期工作一样,为世界各地的法医机构提供了宝贵的指导,提供了加强对未来大规模死亡事件的准备和复原力的战略。
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引用次数: 0
Internal validation of probabilistic genotyping software STRmix™ V2.8 for GlobalFiler™ profiles generated from Japanese individuals 概率基因分型软件STRmix™V2.8对日本个体生成的GlobalFiler™档案进行内部验证
Q3 Medicine Pub Date : 2025-11-19 DOI: 10.1016/j.fsir.2025.100437
Takashi Fukagawa, Haruhiko Watahiki, Yusuke Mita, Tetsushi Kitayama, Koji Fujii, Natsuko Mizuno
The interpretation of mixed DNA profiles originating from multiple individuals can be very challenging. Probabilistic genotyping software is used to interpret such mixed DNA profiles, and it assigns a likelihood ratio based on the evidence given two hypotheses: a prosecution hypothesis and a defense hypothesis. For proper utilization of probabilistic genotyping software, internal validation is required. In this study, we performed internal validation of the probabilistic genotyping software STRmix™. Our internal validation studies complied with the Scientific Working Group on DNA Analysis Methods guidelines for the validation of probabilistic genotyping systems, and was performed using GlobalFiler™ profiles generated from Japanese individuals to study the sensitivity, specificity, and precision of STRmix™, and the effects of the addition of a known contributor and incorrect assumption of the number of contributors were also assessed. The results of our internal validation studies suggest that STRmix™ using our laboratory-specific parameters is suitable for the purpose of interpreting mixed DNA profiles and statistical evaluation in our experimental and analytical environment. In addition, there were a few rare cases in which STRmix™ interpreted the results as exclusion (likelihood ratio = 0), despite the person of interest being a true contributor, due to extreme heterozygote imbalance and/or significant differences in the mixture ratio between loci due to the stochastic effects of PCR amplification. Therefore, we report these rare cases along with the results of our internal validation studies.
对来自多个个体的混合DNA图谱的解释可能非常具有挑战性。概率基因分型软件被用来解释这种混合的DNA图谱,它根据两个假设的证据分配一个可能性比:起诉假设和辩护假设。为了正确利用概率基因分型软件,需要进行内部验证。在本研究中,我们对概率基因分型软件STRmix™进行了内部验证。我们的内部验证研究遵循了DNA分析方法科学工作组关于概率基因分型系统验证的指南,并使用从日本个体生成的GlobalFiler™档案来研究STRmix™的敏感性、特异性和精度,并评估了添加已知贡献者和错误假设贡献者数量的影响。我们的内部验证研究结果表明,使用我们实验室特定参数的STRmix™适用于在我们的实验和分析环境中解释混合DNA图谱和统计评估。此外,在少数罕见的情况下,STRmix™将结果解释为排除(可能性比= 0),尽管感兴趣的人是一个真正的贡献者,由于极端杂合子不平衡和/或由于PCR扩增的随机效应,位点之间的混合比例存在显着差异。因此,我们报告了这些罕见的病例以及我们内部验证研究的结果。
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引用次数: 0
Population and forensic genetic data of 27 Y-STR and 12 X-STR loci in four British Isles populations 4个不列颠群岛人群27个Y-STR位点和12个X-STR位点的群体和法医遗传资料
Q3 Medicine Pub Date : 2025-11-19 DOI: 10.1016/j.fsir.2025.100438
Sasitaran Iyavoo
This study presents population data for 27 Y-chromosomal STR (Y-STR) loci and 12 X-chromosomal STR (X-STR) loci from 888 unrelated males representing four populations of the British Isles (English, Irish, Scottish, and Welsh). Genotyping was performed using the Yfiler Plus and Investigator Argus X-12 QS kits under ISFG-aligned quality control procedures. All four populations exhibited 100 % haplotype diversity for both marker systems, confirming strong discriminatory capacity. Several rare allelic variants were identified, including deletions, insertions, and a tri-allelic pattern among Y-STRs, as well as insertion events at X-STR loci. Linkage disequilibrium (LD) analysis revealed patterns consistent with the physical arrangement of X-STR loci, with marginally significant LD detected within several linkage groups in the English and Irish populations. Based on these results, haplotype-based analyses were conducted using all 886 valid male profiles across the four linkage groups, showing that LG1 and LG4 exhibited the highest discriminatory capacities. Phylogenetic and multidimensional scaling analyses incorporating global reference datasets revealed clear and interpretable patterns of population structure. Y-STR data positioned the British Isles populations within a north-western European paternal cluster, with Irish and Welsh forming a distinct Celtic subgroup. X-STR results showed a close maternal-line relationship between English and German populations consistent with Anglo-Saxon migrations, and a separate Celtic cluster comprising Irish and Welsh, with the Scottish population showing intermediate affinity. Overall, this study provides a robust and forensically relevant dataset reflecting both paternal and maternal genetic diversity across the British Isles, improving the accuracy of forensic identification and kinship analysis.
本研究提供了来自不列颠群岛(英格兰、爱尔兰、苏格兰和威尔士)四个种群的888名无亲缘关系男性的27个y染色体STR (Y-STR)位点和12个x染色体STR (X-STR)位点的种群数据。使用Yfiler Plus和调查员Argus X-12 QS试剂盒在符合isfg的质量控制程序下进行基因分型。所有4个群体在两种标记系统中均表现出100% %的单倍型多样性,证实了强烈的歧视能力。发现了几个罕见的等位基因变异,包括y - str位点的缺失、插入和三等位基因模式,以及X-STR位点的插入事件。连锁不平衡(LD)分析揭示了与X-STR位点的物理排列一致的模式,在英国和爱尔兰人群的几个连锁群体中检测到边缘显著的LD。在此基础上,对4个连锁群体的886份有效男性基因进行了单倍型分析,结果表明LG1和LG4表现出最高的歧视能力。结合全球参考数据集的系统发育和多维尺度分析揭示了清晰和可解释的种群结构模式。Y-STR数据将不列颠群岛人口定位在西北欧父系群中,爱尔兰人和威尔士人形成了一个独特的凯尔特亚群。X-STR结果显示,与盎格鲁-撒克逊移民一致的英格兰和德国人口之间存在密切的母系关系,以及一个由爱尔兰人和威尔士人组成的独立凯尔特集群,苏格兰人口表现出中间亲缘关系。总体而言,本研究提供了一个强大的法医相关数据集,反映了整个不列颠群岛的父系和母系遗传多样性,提高了法医鉴定和亲属关系分析的准确性。
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引用次数: 0
A 3-year retrospective review of fatal carbon monoxide toxicity in the Western Cape, South Africa (2022–2024) 南非西开普省致命一氧化碳毒性的3年回顾性分析(2022-2024)
Q3 Medicine Pub Date : 2025-11-17 DOI: 10.1016/j.fsir.2025.100434
Carl Grevel , Marie Belle Kathrina Mendoza Hlela , Domonica Dos Reis , Chanté du Toit , Bronwen Davies
Charcoal burning (CB) in enclosed spaces has emerged as a recognised method of suicide due to the inhalation of lethal levels of carbon monoxide (CO). While this has been widely documented globally, CB is also implicated in accidental CO poisoning deaths, particularly in densely populated, low-income communities where limited access to safer heating, cooking, and lighting alternatives increases vulnerability and contributes to preventable fatalities. This retrospective study examined CO toxicity deaths unrelated to fire-burns in the Western Cape province of South Africa over a three-year period, from 2022 to 2024, focusing on prevalence, characteristics, and circumstantial patterns. A total of 68 postmortem cases were included from routine submissions to the Forensic Toxicology Unit in Cape Town. Of these, 50 % were suspected accidents, 30.9 % alleged suicides, and 19.1 % remained under investigation. Most victims were male (69.1 %), middle-aged (44.1 %), and deaths peaked in winter (p < 0.001), primarily driven by accidental exposures. CB was the most frequently identified source of CO, followed by vehicle exhaust and gullies/imbawulas (makeshift metal drums of combustible wood, coals, or refuse). The source of CO exposure was significantly associated with the suspected manner of death (p < 0.001). The mean carboxyhaemoglobin (COHb) level was 60.7 % (range: 31.4–78.4 %) with significantly higher levels in suicides (p < 0.001), while the mean blood alcohol concentration (BAC) was 0.07 g/100 mL (range: 0.01–0.26 g/100 mL). Most fatalities occurred in congested domestic settings within socio-economically disadvantaged areas, highlighting non-fire CO poisoning as an underrecognised public health concern. Prevention should include public education, housing safety improvements, warning labels, and greater access to safer energy sources.
由于吸入致命水平的一氧化碳(CO),在封闭空间中燃烧木炭(CB)已成为公认的自杀方法。虽然这在全球范围内得到了广泛的记录,但炭黑也与CO中毒意外死亡有关,特别是在人口密集的低收入社区,这些社区获得更安全的取暖、烹饪和照明替代品的机会有限,增加了脆弱性,并导致了可预防的死亡。这项回顾性研究调查了南非西开普省从2022年到2024年三年期间与火灾无关的CO毒性死亡,重点关注患病率、特征和间接模式。从例行提交给开普敦法医毒理学股的报告中,共纳入了68个死后病例。其中,50. %疑似事故,30.9 %疑似自杀,19.1 %仍在调查中。大多数受害者为男性(69.1 %)和中年人(44.1% %),死亡高峰出现在冬季(p <; 0.001),主要由意外暴露所致。炭黑是最常见的CO来源,其次是汽车尾气和沟渠/imbawulas(由可燃木材、煤炭或垃圾制成的临时金属桶)。一氧化碳暴露源与疑似死亡方式显著相关(p <; 0.001)。平均血氧血红蛋白(COHb)水平为60.7 %(范围:31.4-78.4 %),自杀者的血氧血红蛋白水平显著高于自杀者(p <; 0.001),平均血酒精浓度(BAC)为0.07 g/100 mL(范围:0.01-0.26 g/100 mL)。大多数死亡发生在社会经济不利地区拥挤的家庭环境中,突出表明非火灾一氧化碳中毒是一个未得到充分认识的公共卫生问题。预防措施应包括公共教育、住房安全改进、警告标签以及更容易获得更安全的能源。
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引用次数: 0
Non-fatal overdose following ingestion of encapsulated pure bromazolam powder: A case report 服用包封的纯溴唑仑粉末后非致死性过量:一例报告
Q3 Medicine Pub Date : 2025-10-26 DOI: 10.1016/j.fsir.2025.100432
Adam Bauer , Elva Eir Gretarsdottir , Valthor Asgrimsson , Sigurbergur Karason
Bromazolam is a potent designer benzodiazepine increasingly encountered in forensic and clinical toxicology. Here, a case of non-fatal intoxication involving the ingestion of encapsulated pure bromazolam powder is reported, and, to our knowledge, it resulted in the highest documented bromazolam serum concentration to date. A healthy 20-year-old male was found unresponsive at home and admitted to intensive care. Toxicology confirmed bromazolam as the primary intoxicant, with an initial serum concentration exceeding 5800 ng/mL. The patient required prolonged intubation, and sedation persisted for over ten days despite supportive care and flumazenil administration. Five serum samples collected over 204 h showed declining bromazolam concentrations with an estimated half-life of 31 h. Analytical testing of seized powder at the scene confirmed pure bromazolam content, supporting the conclusion of high-dose exposure. Serum samples were diluted to fit within the method’s linear range, and dilution integrity testing demonstrated accurate bromazolam quantification at these levels. This case underscores the severe toxicological effects of ingesting pure bromazolam, the importance of timely toxicological confirmation in clinical decision-making, and the need for methods to identify novel substances and quantify high-concentration samples.
溴唑仑是一种有效的设计苯二氮卓类药物越来越多地遇到法医和临床毒理学。在这里,报告了一例涉及摄入包封的纯溴唑仑粉末的非致命中毒,据我们所知,它导致了迄今为止最高的溴唑仑血清浓度。一名20岁的健康男性在家中被发现没有反应,并被送入重症监护室。毒理学证实溴唑仑为主要毒物,初始血清浓度超过5800 ng/mL。患者需要延长插管时间,尽管给予支持治疗和氟马西尼,镇静仍持续了十多天。在204 h以上收集的5份血清样品显示溴唑仑浓度下降,估计半衰期为31 h。对现场缴获的粉末进行分析测试,证实其含有纯溴唑仑,支持高剂量暴露的结论。对血清样品进行稀释,使其符合该方法的线性范围,稀释完整性测试证明在这些水平上可以准确地定量溴唑仑。该病例强调了摄入纯溴唑仑的严重毒理学影响,及时进行毒理学确认在临床决策中的重要性,以及鉴定新物质和定量高浓度样品的方法的必要性。
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引用次数: 0
First documented cases of heteropaternal superfecundation in dizygotic twins from the Dominican Republic: A case report 多米尼加共和国异卵双胞胎异父超受精的首例记录病例:一例报告
Q3 Medicine Pub Date : 2025-10-24 DOI: 10.1016/j.fsir.2025.100433
Thais Reyes, Rosneld Rivero, Santa Jiménez, Karla Figueroa, Eileen Riego
Heteropaternal superfecundation (HSF) is a rare reproductive event where two ova from the same menstrual cycle are fertilized by sperm from different men. This phenomenon challenges conventional assumptions in paternity testing, particularly for dizygotic (DZ) twins. This report describes the first two documented cases of HSF in the Dominican Republic, identified from a review of 61 DZ twin pairs undergoing kinship analysis. Genetic analysis using autosomal (aSTR) and Y-chromosome (Y-STR) markers confirmed that in both cases—one involving opposite-sex twins and the other same-sex male twins—the twins shared a mother but had different biological fathers. These findings underscore the critical importance of testing both DZ twins individually in all paternity disputes to prevent erroneous legal and social outcomes. This report serves as a guide for forensic and medical professionals facing similar complex kinship scenarios.
异父超受精(HSF)是一种罕见的生殖事件,即来自同一月经周期的两个卵子与来自不同男性的精子受精。这一现象挑战了亲子鉴定的传统假设,特别是对异卵双胞胎(DZ)。本报告描述了多米尼加共和国前两例有记录的HSF病例,它们是在对61对DZ双胞胎进行亲属关系分析后发现的。利用常染色体(aSTR)和y染色体(Y-STR)标记进行的遗传分析证实,在这两种情况下——一个涉及异性双胞胎,另一个涉及同性男性双胞胎——双胞胎共享一个母亲,但有不同的生父。这些发现强调了在所有父权纠纷中对DZ双胞胎进行单独测试的重要性,以防止错误的法律和社会结果。这份报告为面临类似复杂亲属关系情况的法医和医疗专业人员提供了指南。
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引用次数: 0
Hidden ballistic injury and fall from height: An unusual complex suicide and review of the literature 隐藏的弹道伤害和高空坠落:一种不寻常的复杂自杀和文献综述
Q3 Medicine Pub Date : 2025-10-08 DOI: 10.1016/j.fsir.2025.100431
A. Fort , J. Borges , F. Chiron , F. Paysant , T. Willeman , M. Peoc’h , V. Scolan
In France, firearm suicide is the second most common method among men, after hanging. Complex suicides, which involve multiple methods, are rare but significant. Forensic investigations are essential for determining the sequence of events and whether methods were used simultaneously or if one followed the failure of another. Ballistic suicides are frequently associated with hanging. This case report details a rare unplanned complex suicide involving a cranioencephalic ballistic injury followed by fall from height in a 56-year-old man. He was discovered deceased beneath his building. Autopsy revealed a non-fatal and non-incapacitating ballistic injury, confirmed by X-ray, in contrast to the severe traumatic injuries sustained from the fall, which were lethal. This specific combination of methods is rarely reported in literature. Analyzing the sequence and vitality of each injury is essential to rule out potential criminal acts.
在法国,枪支自杀是男性中第二常见的自杀方式,仅次于上吊。涉及多种自杀方式的复杂自杀很少见,但意义重大。法医调查对于确定事件的顺序以及是否同时使用了两种方法,还是一种方法是在另一种方法失败之后使用的至关重要。弹道自杀通常与上吊有关。本病例报告详细介绍了一个罕见的意外复杂自杀,涉及颅脑弹道伤,随后从高处坠落的56岁男子。他被发现死在他的楼房下面。尸检显示,经x光检查证实,这是一种非致命和非致残的弹道伤害,与坠落造成的严重创伤形成鲜明对比,后者是致命的。这种特殊的方法组合在文献中很少报道。分析每一种伤害的顺序和生命力对于排除潜在的犯罪行为至关重要。
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引用次数: 0
The aggrandizement of scientific data in the media: The Shroud of Turin blood marks as a case example 媒体对科学数据的夸大:以都灵裹尸布的血迹为例
Q3 Medicine Pub Date : 2025-09-17 DOI: 10.1016/j.fsir.2025.100430
Kelly P. Kearse
The Shroud of Turin is a fourteen-foot-long cloth bearing the life size image of a man with blood marks and has been heralded as the most scientifically studied archaeological artifact in human history. The Shroud has been proclaimed to be either the actual burial cloth of the historical Jesus of Nazareth or a cunning medieval forgery. In several recent television programs that received widespread international media attention, a “Shroud expert” made the claims that the blood on the Shroud has been demonstrated to be human, male, and type AB, and was identified as Semitic. Additionally, it was reported that high levels of ferritin and creatine, indicative of polytrauma, had been found on the cloth and that premortem and postmortem blood had been identified. Discussed below is a scientific fact check about such characteristics of the blood on the Shroud of Turin and the capabilities and limitations of the techniques used in these investigations.
都灵裹尸布是一块14英尺长的布,上面有一个真人大小的血迹,被誉为人类历史上研究最科学的考古文物。裹尸布被宣称要么是历史上拿撒勒人耶稣的真正埋葬布,要么是一个狡猾的中世纪伪造品。在最近几个受到国际媒体广泛关注的电视节目中,一位“裹尸布专家”声称裹尸布上的血液已被证明是人类,男性,AB型血,并被确定为闪米特人。此外,据报道,在布上发现了高水平的铁蛋白和肌酸,表明有多处创伤,并鉴定了死前和死后的血液。下面讨论的是对都灵裹尸布上的这些血液特征的科学事实核查,以及在这些调查中使用的技术的能力和局限性。
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引用次数: 0
Internal quality assessment and genotyping error investigation in SNP microarray testing: Lessons from the ESWG-ISFG forensic proficiency trial SNP微阵列检测的内部质量评估和基因分型错误调查:来自ESWG-ISFG法医熟练度试验的教训
Q3 Medicine Pub Date : 2025-09-15 DOI: 10.1016/j.fsir.2025.100429
Sasitaran Iyavoo , Sharlize Pedroza Matute , Kiera Turvey , Stephen Cummings , Thomas Haizel
In 2024, the English Speaking Working Group of the International Society for Forensic Genetics (ESWG-ISFG) introduced single nucleotide polymorphism (SNP) genotyping into its annual proficiency trial, providing DNA testing laboratories with their first opportunity to evaluate performance in this area. Twelve laboratories participated using a range of sequencing and microarray platforms. AttoLife Limited, a UKAS-accredited laboratory, contributed results using the Infinium HTS iSelect custom ‘Rita’ microarray containing 4366 SNP markers. Blood samples from a child and alleged father were supplied on FTA cards, extracted with the QIAamp DNA Mini Kit, quantified using the Quantifiler Trio kit, and genotyped following the Infinium HTS protocol with GenomeStudio analysis. SNP call rates exceeded 99 % (excluding Y-SNPs in the female child), confirming high-quality data. Three discrepancies were identified, rs10108270 in both samples and rs10513300 in the child, which subsequent Sanger sequencing attributed to probe-binding site variation and potential copy number imbalance. These findings illustrate the value of proficiency testing in detecting locus-specific challenges, reinforce the need for cautious interpretation of uncertain results, and highlight the importance of cross-platform comparison to strengthen confidence in forensic SNP genotyping.
2024年,国际法医遗传学学会英语工作组(ESWG-ISFG)将单核苷酸多态性(SNP)基因分型引入其年度熟练度试验,为DNA测试实验室提供了第一次评估该领域表现的机会。12个实验室使用一系列测序和微阵列平台参与了这项研究。AttoLife有限公司是ukas认可的实验室,使用Infinium HTS iSelect定制“Rita”微阵列提供了包含4366个SNP标记的结果。儿童和疑似父亲的血液样本放在FTA卡上,用QIAamp DNA Mini Kit提取,使用Quantifiler Trio试剂盒定量,并根据Infinium HTS协议与GenomeStudio分析进行基因分型。SNP呼叫率超过99% %(不包括女性儿童的y -SNP),证实了高质量的数据。发现了三个差异,两个样本中的rs10108270和孩子中的rs10513300,随后的Sanger测序将其归因于探针结合位点变异和潜在的拷贝数失衡。这些发现说明了熟练程度测试在检测基因座特异性挑战方面的价值,强调了对不确定结果谨慎解释的必要性,并强调了跨平台比较对增强法医SNP基因分型信心的重要性。
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引用次数: 0
Anthropometric analysis of facial dimensions using 3D imaging for forensic identification and ethnicity-specific reference models 使用3D成像进行面部尺寸的人体测量分析,用于法医鉴定和特定种族的参考模型
Q3 Medicine Pub Date : 2025-09-09 DOI: 10.1016/j.fsir.2025.100428
Saurjya Ranjan Das , Sreepreeti Champatyray , Dhiren Kumar Panda

Background

Facial morphology plays a crucial role in forensic identification, anthropological research, and reconstructive surgery. However, forensic reference databases often lack ethnicity-specific 3D anthropometric data, limiting the accuracy of forensic facial reconstruction and automated facial recognition systems. This study integrates 3D imaging technology and multivariate statistical analyses to enhance forensic facial identification models by providing ethnicity-specific facial measurements.

Methods

A cross-sectional study was conducted with 500 participants (250 males and 250 females) from seven Indian ethnic groups (Odia, Bengali, Tamil, Punjabi, Maratha, Telugu, and Gujarati). High-resolution 3D facial scans were obtained using the Artec Eva 3D scanner and analyzed using landmark-based anthropometry. Multivariate Analysis of Variance (MANOVA) assessed sex and ethnic differences in upper facial height (UFH), lower facial height (LFH), intercanthal distance (ICD), and face width (FW). Principal Component Analysis (PCA) and Structural Equation Modeling (SEM) were used to evaluate the interdependencies among facial dimensions.

Results

Males exhibited significantly larger UFH and ICD, while females had greater LFH (p < 0.001). Significant ethnic differences were observed (p < 0.01), with the Odia group having the widest face and the Bengali group showing the smallest ICD. PCA revealed two major components that explained 81.4 % of the total variance, with UFH and FW being the primary contributors. SEM demonstrated a strong correlation between UFH and FW (β = 0.72, p < 0.001) and an inverse relationship between LFH and ICD (β = −0.48, p = 0.002).

Conclusion

This study provides forensically relevant, ethnicity-specific 3D anthropometric data for facial reconstruction and forensic identification. These findings support the integration of 3D morphometric databases into forensic facial analysis software, enhancing population-specific identification accuracy. Future research should consider including Body Mass Index (BMI) as a variable to account for the potential impact of soft tissue distribution on facial morphology.
面部形态学在法医鉴定、人类学研究和重建手术中起着至关重要的作用。然而,法医参考数据库往往缺乏特定种族的3D人体测量数据,限制了法医面部重建和自动面部识别系统的准确性。本研究将3D影像技术与多元统计分析相结合,通过提供特定种族的面部测量来增强法医面部识别模型。方法对来自印度7个民族(奥迪亚族、孟加拉族、泰米尔族、旁遮普族、马拉地族、泰卢固族和古吉拉特族)的500名参与者(250男250女)进行横断面研究。使用Artec Eva 3D扫描仪获得高分辨率3D面部扫描,并使用基于地标的人体测量学进行分析。多变量方差分析(MANOVA)评估了上面部高度(UFH)、下面部高度(LFH)、颊间距离(ICD)和面部宽度(FW)的性别和种族差异。采用主成分分析(PCA)和结构方程模型(SEM)来评估面部维度之间的相互依赖性。结果男性有较大的UFH和ICD,女性有较大的LFH (p <; 0.001)。观察到显著的种族差异(p <; 0.01),Odia组的面部最宽,孟加拉组的ICD最小。PCA揭示了两个主要成分,解释了81.4 %的总方差,其中UFH和FW是主要贡献者。扫描电镜显示UFH和FW之间有很强的相关性(β = 0.72, p <; 0.001),LFH和ICD之间呈负相关(β = - 0.48, p = 0.002)。结论本研究为面部重建和法医鉴定提供了与法医相关的、种族特异性的三维人体测量数据。这些发现支持将3D形态测量数据库集成到法医面部分析软件中,从而提高特定人群识别的准确性。未来的研究应考虑将身体质量指数(BMI)作为一个变量,以解释软组织分布对面部形态的潜在影响。
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Forensic Science International: Reports
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