Detection of rare point mutation via allele-specific amplification in emulsion PCR

It is essential to analyze rare mutations in many fields of biomedical research. However, the detection of rare mutations is usually failed due to the interference of predominant wild-type DNA surrounded. Herein we describe a sensitive and facile method of detecting rare point mutation on the basis...

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Detalles Bibliográficos
Autores principales: Cheng, Changming, Zhou, Yin, Yang, Chao, Chen, Juan, Wang, Jie, Zhang, Jie, Zhao, Guoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2013
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133893/
https://www.ncbi.nlm.nih.gov/pubmed/23710638
http://dx.doi.org/10.5483/BMBRep.2013.46.5.155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133893/
https://www.ncbi.nlm.nih.gov/pubmed/23710638
http://dx.doi.org/10.5483/BMBRep.2013.46.5.155

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