| Literature DB >> 26304412 |
Sander Willems1, Marie-Alice Fraiture2, Dieter Deforce3, Sigrid C J De Keersmaecker4, Marc De Loose5, Tom Ruttink6, Philippe Herman7, Filip Van Nieuwerburgh3, Nancy Roosens8.
Abstract
Because the number and diversity of genetically modified (GM) crops has significantly increased, their analysis based on real-time PCR (qPCR) methods is becoming increasingly complex and laborious. While several pioneers already investigated Next Generation Sequencing (NGS) as an alternative to qPCR, its practical use has not been assessed for routine analysis. In this study a statistical framework was developed to predict the number of NGS reads needed to detect transgene sequences, to prove their integration into the host genome and to identify the specific transgene event in a sample with known composition. This framework was validated by applying it to experimental data from food matrices composed of pure GM rice, processed GM rice (noodles) or a 10% GM/non-GM rice mixture, revealing some influential factors. Finally, feasibility of NGS for routine analysis of GM crops was investigated by applying the framework to samples commonly encountered in routine analysis of GM crops.Entities:
Keywords: Bioinformatics; GM rice; GMO detection; NGS; Processed food; Statistical framework
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Year: 2015 PMID: 26304412 DOI: 10.1016/j.foodchem.2015.07.074
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514