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Developmental validation of an Improved Multiplex Assay for use in forensic casework: The simultaneous gender-typing and quantification of total human and male-only DNA within forensic samples.

机译:用于法医案件的改进的多重检测的开发验证:法医样品中同时进行性别分型和总人类和仅男性DNA定量。

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摘要

Scope and Method of Study. An end-point PCR-based multiplex assay was developmentally validated for use in forensic DNA casework that could simultaneously gender-type and quantify total human and male-only DNA. The developmental validation included the studies that are required by the Revised Validation Guidelines set forth by the Scientific Working Group on DNA Analysis Methods. DNA was extracted by an organic extraction method, or the Hair Extraction Kit. The samples were purified and de-salted using DNA IQ(TM) System with Differex(TM) or CentriconsRTM. The NIST SRM 2372 quantitation standards were purchased from the National Institute of Standards and Technology. Samples were amplified using an ABI 9700 thermal cycler and analyzed using an ABI Prism 310 Genetic Analyzer. The peak height and sizing of alleles was determined using the GeneScanRTM Analysis version 3.1.2 software and the alleles were labeled using a Genotyper RTM version 2.5.2 software macro developed for this research.;Findings and Conclusions. The Improved Multiplex Assay (IMA) has been developmentally validated as a valid quantitation method for use in criminal casework in CODIS participating forensic labs and meets or exceeds national standards. Based on a one to one relationship between the amount of amplified product from a known quantity of input DNA to a sample pre-amplification, a standard curve can be generated by serially diluting the NIST SRM 2372 Standards, amplifying, analyzing, generating a standard curve, and then comparing unknown samples to the standard curve to estimate the concentration of total human and male-only DNA in the unknown sample pre-amplification. The IMA is sensitive enough and can perform at a level that allows it to be used to screen evidence to determine what type of profiling test would provide optimal results. Because the IMA relies on the current equipment already used in DNA testing labs, it is cost effective to implement in an existing DNA testing lab. Any forensic laboratory can implement a low cost and DNA Advisory Board (DAB) and ASCLAD/LAB compliant DNA quantitation method based on this developmental validation.
机译:研究范围和方法。一种基于终点PCR的多重测定法经过开发验证,可用于法医DNA案例研究,该案例研究可同时进行性别分型并量化人类和仅男性的总DNA。发展性验证包括DNA分析方法科学工作组制定的《修订的验证指南》所要求的研究。通过有机提取方法或Hair Extraction Kit提取DNA。使用具有DifferexTM或CentriconsRTM的DNA IQTM系统对样品进行纯化和脱盐。 NIST SRM 2372定量标准品购自美国国家标准技术研究院。使用ABI 9700热循环仪扩增样品,并使用ABI Prism 310遗传分析仪进行分析。使用GeneScanRTM Analysis 3.1.2版软件确定等位基因的峰高和大小,并使用针对该研究开发的Genotyper RTM 2.5.2版软件宏对等位基因进行标记。改进的多重检测(IMA)已被开发验证为在CODIS参与的法医实验室中用于刑事案件的有效定量方法,并且达到或超过了国家标准。根据从已知数量的输入DNA到样品预扩增的扩增产物量之间的一对一关系,可以通过依次稀释NIST SRM 2372标准品,进行扩增,分析和生成标准曲线来生成标准曲线,然后将未知样品与标准曲线进行比较,以估算未知样品预扩增中人和男性的总DNA浓度。 IMA足够灵敏,可以在一定水平上执行,以使其能够用于筛选证据以确定哪种类型的性能分析测试将提供最佳结果。由于IMA依赖于DNA测试实验室中已经使用的当前设备,因此在现有DNA测试实验室中实施具有成本效益。任何法医实验室都可以根据这种发展验证来实施低成本且符合DNA咨询委员会(DAB)和ASCLAD / LAB要求的DNA定量方法。

著录项

  • 作者

    Wilson, Jonathan Price.;

  • 作者单位

    Oklahoma State University.;

  • 授予单位 Oklahoma State University.;
  • 学科 Biology Genetics.;Anthropology Medical and Forensic.;Biology Cell.
  • 学位 M.S.
  • 年度 2008
  • 页码 104 p.
  • 总页数 104
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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