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Development and validation of InnoQuant~(TM), a sensitive human DNA quantitation and degradation assessment method for forensic samples using high copy number mobile elements Alu and SVA

机译:InnoQuant〜(TM)的开发和验证,这是一种使用高拷贝数移动元素Alu和SVA对法医样品进行敏感的人类DNA定量和降解评估的方法

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摘要

There is a constant need in forensic casework laboratories for an improved way to increase the first-pass success rate of forensic samples. The recent advances in mini STR analysis, SNP, and Alu marker systems have now made it possible to analyze highly compromised samples, yet few tools are available that can simultaneously provide an assessment of quantity, inhibition, and degradation in a sample prior to genotyping. Currently there are several different approaches used for fluorescence-based quantification assays which provide a measure of quantity and inhibition. However, a system which can also assess the extent of degradation in a forensic sample will be a useful tool for DNA analysts. Possessing this information prior to genotyping will allow an analyst to more informatively make downstream decisions for the successful typing of a forensic sample without unnecessarily consuming DNA extract. Real-time PCR provides a reliable method for determining the amount and quality of amplifiable DNA in a biological sample.
机译:法医案例研究实验室一直需要一种改进的方法来提高法医样品的首次通过成功率。微型STR分析,SNP和Alu标记系统的最新进展现已使分析高度受损的样品成为可能,但是很少有工具可以在进行基因分型之前同时提供样品的数量,抑制和降解的评估。当前,有几种不同的方法可用于基于荧光的定量分析,这些方法可提供数量和抑制作用的量度。但是,一个可以评估法医样品降解程度的系统将是DNA分析人员的有用工具。在进行基因分型之前拥有此信息将使分析人员能够在进行不必要的DNA提取物消耗的情况下,为成功地鉴定法医样品做出更明智的下游决策。实时PCR提供了一种可靠的方法来确定生物样品中可扩增DNA的数量和质量。

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