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NCJRS Abstract

The document referenced below is part of the NCJRS Library collection. To conduct further searches of the collection, visit the NCJRS Abstracts Database. See the Obtain Documents page for direction on how to access resources online, via mail, through interlibrary loans, or in a local library.

 
  NCJ Number: NCJ 241201     Find in a Library
  Title: Quantitative PCR Assay for the Assessment of DNA Degradation in Forensic Samples
  Author(s): Katie L. Swango ; Mark D. Timken ; Mavis Date Chong ; Martin R. Buoncristiani
  Journal: Forensic Science International  Volume:158  Issue:1  Dated:2006  Pages:14 to 26
  Date Published: 2005
  Page Count: 13
  Annotation: This article describes the results of a study to develop a quantitative PCR assay for the assessment of DNA degradation in forensic samples.
  Abstract: The study found that for highly degraded DNA samples, the rate of genotyping success improved when an appropriately long qPCR target was used for determining the amount of template needed for amplification for STR (short tandem repeat) analysis. The study also found that a degradation ratio was able to be calculated from quantitation results obtained with the nuTH01-nuCSF-IPC triplex qPCR assay, and that this ratio proved to be a good estimate of the quality of the DNA extracted from the degraded sample. The primary objective of the study was to develop a quantitative PCR (qPCR) assay for use in assessing the degradation of DNA in forensic samples. Data for the study were obtained from analyses of both non-degraded and highly degraded DNA samples. The nuTH01 and nuCSF qPCR assays were tested on the samples in order to ensure that equivalent results could be obtained in both singleplex and duplex reactions. The IPC assay was then added to the nuTH01-nuCSF duplex assay. This triplex assay was then tested on the DNA samples and found to be highly successful at quantifying DNA in the degraded samples. This finding indicates that the nutH01-nuCSF-IPC triplex assay can be a useful tool for simultaneously assessing the quantity and quality of DNA, thereby minimizing the need for large of amounts of extracted DNA and maximizing the throughput and efficiency of DNA analysis. Tables, figures, and references
  Main Term(s): Forensics/Forensic Sciences
  Index Term(s): Evidence identification and analysis ; Evidence ; Forensic pathology ; DNA fingerprinting ; Forensic engineering ; NIJ grant-related documents
  Sponsoring Agency: National Institute of Justice (NIJ)
US Department of Justice
Office of Justice Programs
United States of America
  Grant Number: 2002-IJ-CX-K008
  Type: Research (Applied/Empirical)
  Country: United States of America
  Language: English
   
  To cite this abstract, use the following link:
https://www.ncjrs.gov/App/Publications/abstract.aspx?ID=263291

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