A Mismatch EndoNuclease Array-Based Methodology (MENA) for Identifying Known SNPs or Novel Point Mutations

Accurate and rapid identification or confirmation of single nucleotide polymorphisms (SNPs), point mutations and other human genomic variation facilitates understanding the genetic basis of disease. We have developed a new methodology (called MENA (Mismatch EndoNuclease Array)) pairing DNA mismatch...

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Detalles Bibliográficos
Autores principales: Comeron, Josep M., Reed, Jordan, Christie, Matthew, Jacobs, Julia S., Dierdorff, Jason, Eberl, Daniel F., Manak, J. Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003483/
https://www.ncbi.nlm.nih.gov/pubmed/27600073
http://dx.doi.org/10.3390/microarrays5020007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003483/
https://www.ncbi.nlm.nih.gov/pubmed/27600073
http://dx.doi.org/10.3390/microarrays5020007

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