Guidelines for validation of qualitative real-time PCR methods

被引:340
作者
Broeders, S. [1 ]
Huber, I. [2 ]
Grohmann, L. [3 ]
Berben, G. [4 ]
Taverniers, I. [5 ]
Mazzara, M. [6 ]
Roosens, N. [1 ]
Morisset, D. [7 ]
机构
[1] Sci Inst Publ Hlth WIV ISP, B-1050 Brussels, Belgium
[2] Bavarian Hlth & Food Safety Author LGL, D-85764 Oberschleissheim, Germany
[3] Fed Off Consumer Protect & Food Safety BVL, D-10117 Berlin, Germany
[4] Walloon Agr Res Ctr CRA W, B-5030 Gembloux, Belgium
[5] Inst Agr & Fisheries Res EV ILVO, B-9820 Merelbeke, Belgium
[6] European Commiss, Directorate Gen Joint Res Ctr, Inst Hlth & Consumer Protect EC JRC IHCP, I-21027 Ispra, VA, Italy
[7] Natl Inst Biol, Ljubljana 1000, Slovenia
关键词
GENETICALLY-MODIFIED ORGANISMS; MINIMUM INFORMATION; SCREENING METHODS; REFERENCE GENE; PUBLICATION; DUPLEX; ASSAYS; FOOD;
D O I
10.1016/j.tifs.2014.03.008
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
As for many areas of molecular testing, detection of Genetically Modified Organisms (GMO) relies on the real-time Polymerase Chain Reaction (qPCR) technology. Due to the increasing number of GMO, a screening approach using qualitative screening methods has become an integrated part of GMO detection. However, specific guidelines for the validation of these methods are lacking. Here, a pragmatic approach to conduct in-house and inter-laboratory validation studies for GMO screening methods, is proposed. Such guidelines could be adapted to other areas where qualitative qPCR methods are used for molecular testing allowing to implement easily a more reliable screening phase where necessary.
引用
收藏
页码:115 / 126
页数:12
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