康芬1号万人坑中二战受害者的经典桑格和下一代测序有丝分裂型的比较。

IF 2.3 3区 医学 Q1 MEDICINE, LEGAL
Marcel Obal, Irena Zupanič Pajnič
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引用次数: 0

摘要

快速的技术进步极大地增强了DNA分析。一个关键的创新是下一代测序(NGS),也被称为大规模平行测序(MPS),它遵循了经典的桑格测序(CS)。与CS相比,NGS具有更高的灵敏度,分辨率和通量,使其在线粒体DNA (mtDNA)分析中特别有价值。mtDNA的高拷贝数、母系遗传和非重组性质,特别是其高变区(HV),使其在法医调查中具有高度相关性。NGS在mtDNA测序中引入了简化的方案和改进的低水平异质性检测。然而,对于任何新技术,其信息量和真实性都必须与传统方法进行比较。这项研究比较了从斯洛文尼亚乱葬坑中回收的退化的二战骨骼遗骸的有丝分裂型,使用相同的DNA提取方法来最小化测序前的差异。用机械和化学方法对股骨进行清洗、粉碎和完全脱矿。使用EZ1 Advanced XL提取和纯化DNA,并使用内部协议进行定量。CS测序采用BigDye Terminator Kit v1.1和ABI PRISM™3130遗传分析仪,NGS采用Precision ID mtDNA控制区面板和Ion GeneStudio™S5系统。有丝分裂型的比较表明,NGS鉴定出CS无法检测到的低水平异质性,特别是长度异质性。然而,由于离子激流™套件5.10.1容易出错,某些NGS变体不得不被忽略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of classic Sanger and next generation sequencing mitotypes of second world war victims from Konfin I mass grave.

Rapid technological advancements have significantly enhanced DNA analysis. A key innovation is Next-Generation Sequencing (NGS), also known as Massively Parallel Sequencing (MPS), which followed classic Sanger (CS) sequencing. Compared to CS, NGS offers higher sensitivity, resolution, and throughput, making it particularly valuable for mitochondrial DNA (mtDNA) analysis. The high copy number, matrilineal inheritance, and non-recombining nature of mtDNA, especially its hypervariable regions (HV), make it highly relevant in forensic investigations. NGS has introduced streamlined protocols and improved low-level heteroplasmy detection in mtDNA sequencing. However, with any new technology, its informativeness and authenticity must be evaluated against traditional methods. This study compared mitotypes from degraded WWII skeletal remains recovered from a Slovenian mass grave, using the same DNA extraction method to minimize pre-sequencing variability. Femurs were mechanically and chemically cleaned, pulverized, and fully demineralized. DNA was extracted and purified using EZ1 Advanced XL and quantified with an in-house protocol. CS sequencing was performed using BigDye Terminator Kit v1.1 and ABI PRISM™ 3130 Genetic Analyzer, while NGS was conducted with the Precision ID mtDNA Control Region Panel and Ion GeneStudio™ S5 System. Comparison of mitotypes revealed that NGS identified low-level heteroplasmies undetectable by CS, particularly in length heteroplasmy. However, since Ion Torrent™ Suite 5.10.1 is prone to errors, certain NGS variants had to be disregarded.

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来源期刊
CiteScore
5.80
自引率
9.50%
发文量
165
审稿时长
1 months
期刊介绍: The International Journal of Legal Medicine aims to improve the scientific resources used in the elucidation of crime and related forensic applications at a high level of evidential proof. The journal offers review articles tracing development in specific areas, with up-to-date analysis; original articles discussing significant recent research results; case reports describing interesting and exceptional examples; population data; letters to the editors; and technical notes, which appear in a section originally created for rapid publication of data in the dynamic field of DNA analysis.
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