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美国和加拿大26个法医实验室关于使用AmpliType PM PCR扩增和分型试剂盒的验证研究总结。

Summary of validation studies from twenty-six forensic laboratories in the United States and Canada on the use of the AmpliType PM PCR amplification and typing kit.

作者信息

Word C J, Sawosik T M, Bing D H

机构信息

Cellmark Diagnostics, Germantown, MD, USA.

出版信息

J Forensic Sci. 1997 Jan;42(1):39-48.

PMID:8988573
Abstract

A cooperative study was undertaken to collect and summarize the results of validation studies from forensic laboratories in the United States and Canada on the use of the AmpliType PM PCR amplification and typing kit for genetic typing of forensic biological evidence. This report compiles data from 26 laboratories on: 1) reproducibility studies on DNA extracted from various samples, 2) genetic typing of DNA extracted from a variety of biological samples on various substrates, 3) the effects of exogenous chemicals, materials, and environmental factors on test results, 4) sensitivity studies to determine the least detectable amount of extracted genomic DNA that can be reliably typed, 5) analysis of mixtures containing two sources of genomic DNA, 6) cross-hybridization with DNA extracted from various nonhuman species, and 7) evaluation of assay performance on parallel studies with other genetic typing systems on proficiency test panels, mock cases, and adjudicated/nonprobative casework. Equivalent results were obtained by each laboratory that supplied data, demonstrating the reliability and consistency of the test. Overall, it can be concluded from this study that the AmpliType PM PCR amplification and typing kit meets the guidelines of the Technical Working Group on DNA Analysis Methods (TWGDAM) and there is general scientific acceptability of this kit for forensic DNA testing.

摘要

开展了一项合作研究,以收集和总结美国和加拿大法医实验室对用于法医生物证据基因分型的AmpliType PM PCR扩增和分型试剂盒的验证研究结果。本报告汇编了26个实验室的数据,内容包括:1)对从各种样本中提取的DNA进行的重复性研究;2)对从各种底物上的多种生物样本中提取的DNA进行基因分型;3)外源化学物质、材料和环境因素对测试结果的影响;4)敏感性研究,以确定能够可靠分型的提取基因组DNA的最低可检测量;5)对含有两种基因组DNA来源的混合物进行分析;6)与从各种非人类物种中提取的DNA进行交叉杂交;7)在能力验证测试样本、模拟案例以及已判决/无证明力的实际案件中,与其他基因分型系统进行平行研究时对检测性能的评估。提供数据的每个实验室都获得了等效结果,证明了该测试的可靠性和一致性。总体而言,从这项研究可以得出结论,AmpliType PM PCR扩增和分型试剂盒符合DNA分析方法技术工作组(TWGDAM)的指导方针,并且该试剂盒在法医DNA检测方面具有普遍的科学可接受性。

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