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Improved forensic DNA analysis through the use of alternative DNA polymerases and statistical modeling of DNA profiles.

机译:通过使用其他DNA聚合酶和DNA概况的统计模型,改进了法医DNA分析。

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摘要

DNA evidence, linking perpetrators to crime scenes, is central to many legal proceedings. However, DNA samples from crime scenes often contain PCR-inhibitory substances, which may generate blank or incomplete DNA profiles. Extensive DNA purification can be required to rid the sample of these inhibitors, although these procedures increase the risk of DNA loss. Most forensic laboratories use commercial DNA amplification kits (e.g., AmpFlSTR SGM Plus) with the DNA polymerase AmpliTaq Gold as the gold standard. Here, we show that alternative DNA polymerase-buffer systems can improve the quality of forensic DNA analysis and efficiently circumvent PCR inhibition in crime scene samples, without additional sample preparation. DNA profiles from 20 of 32 totally or partially inhibited crime scene saliva samples were significantly improved using Bio-X-Act Short, ExTaq Hot Start, or PicoMaxx High Fidelity instead of AmpliTaq Gold. A statistical model for unbiased quality control of forensic DNA profiles was developed to quantify the results. Our study demonstrates the importance of adjusting the chemistry of the PCR to enhance forensic DNA analysis and diagnostic PCR, providing an alternative to laborious sample preparation protocols.
机译:将犯罪者与犯罪现场联系起来的脱氧核糖核酸证据对于许多法律诉讼至关重要。但是,犯罪现场的DNA样品通常含有抑制PCR的物质,可能会产生空白或不完整的DNA谱图。尽管去除这些抑制剂的样品会增加DNA丢失的风险,但可能需要进行大量的DNA纯化以去除这些抑制剂的样品。大多数法医实验室使用以DNA聚合酶AmpliTaq Gold为金标准的商业DNA扩增试剂盒(例如AmpFlSTR SGM Plus)。在这里,我们表明替代性DNA聚合酶-缓冲液系统可以提高法医DNA分析的质量,并有效地绕过犯罪现场样本中的PCR抑制,而无需进行额外的样本制备。使用Bio-X-Act Short,ExTaq Hot Start或PicoMaxx High Fidelity代替AmpliTaq Gold,可显着改善32种完全或部分受抑制的犯罪现场唾液样本中20种的DNA谱。建立了一个统计模型,用于法医DNA配置文件的无偏质量控制,以量化结果。我们的研究表明,调整PCR化学结构以增强法医DNA分析和诊断PCR的重要性,为费力的样品制备方案提供了替代方案。

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