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Age Estimation with DNA: From Forensic DNA Fingerprinting to Forensic (Epi) Genomics: A Mini-Review

机译:使用DNA的年龄估计:从法医DNA指纹识别到法医(EPI)基因组学:迷你审查

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Forensic genetics developed from protein-based techniques a quarter of a century ago and became famous as "DNA fingerprinting," this being based on restriction fragment length polymorphisms (RFLPs) of high-molecular-weight DNA. The amplification of much smaller short tandem repeat (STR) sequences using the polymerase chain reaction soon replaced RFLP analysis and advanced to become the gold standard in genetic identification. Meanwhile, STR multiplexes have been developed and made commercially available which simultaneously amplify up to 30 STR loci from as little as 15 cells or fewer. The enormous information content that comes with the large variety of observed STR genotypes allows for genetic individualisation (with the exception of identical twins). Carefully selected core STR loci form the basis of intelligence- led DNA databases that provide investigative leads by linking unsolved crime scenes and criminals through their matched STR profiles. Nevertheless, the success of modern DNA fingerprinting depends on the availability of reference material from suspects. In order to provide new investigative leads in cases where such reference samples are absent, forensic scientists started to explore the prediction of phenotypic traits from the DNA of the evidentiary sample. This paradigm change now uses DNA and epigenetic markers to forecast characteristics that are useful to triage further investigative work. So far, the best investigated externally visible characteristics are eye, hair and skin colour, as well as geographic ancestry and age. Information on the chronological age of a stain donor (or any sample donor) is elemental for forensic investigations in a number of aspects and has, therefore, been explored by researchers in some detail. Among different methodological approaches tested to date, the methylation-sensitive analysis of carefully selected DNA markers (CpG sites) has brought the most promising results by providing prediction accuracies of +/- 3-4 years, which can be comparable to, or even surpass those from, eyewitness reports. This mini-review puts recent developments in age estimation via (epi) genetic methods in the context of the requirements and goals of forensic genetics and highlights paths to follow in the future of forensic genomics. (C) 2018 S. Karger AG, Basel
机译:从蛋白质的技术开发的法医遗传学在一个世纪前的四分之一的技术中,众所周知的是“DNA指纹”,这是基于高分子量DNA的限制性片段长度多态性(RFLP)。使用聚合酶链反应的扩增更小的短串联重复(STR)序列很近替代RFLP分析并进入成为遗传鉴定中的黄金标准。同时,已经开发并制造了STR多路复用,可商购和制造,其同时扩增至多30个STR基因座,或者较少。随着各种观察到的STR基因型的巨大信息含量允许遗传个性(除了相同的双胞胎外)。精心挑选的核心STR基因座为智能导向DNA数据库的基础,通过将未解决的犯罪场景和犯罪分子通过其匹配的STR档案将未解决的犯罪场景和犯罪分子联系起来,提供调查潜力。尽管如此,现代DNA指纹识别的成功取决于嫌疑人的参考资料的可用性。为了提供新的调查导致,其中不存在此类参考样品,法医科学家开始探讨了避免了证据样本的DNA的表型性状的预测。此范例改变现在使用DNA和表观遗传标记来预测对进一步调查工作有用的特征。到目前为止,最好的调查的外部可见特征是眼睛,头发和肤色,以及地理血统和年龄。有关污渍供体(或任何样本供体)的时间年龄的信息是关于许多方面的法医调查的元素,因此研究人员已经详细探讨了。在测试到迄今为止测试的不同方法方法中,通过提供+/- 3-4岁的预测精度,致密地选择的DNA标记物(CPG位点)的甲基化敏感性分析带来了最有前途的结果,这可以与甚至超越甚至超越来自目击者的报告。该迷你审查在法医遗传学要求和目标的背景下,通过(EPI)遗传方法来提高近期估计的发展,并突出了在法医基因组学的未来遵循的路径。 (c)2018年S. Karger AG,巴塞尔

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