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

Comeron, Josep M; Reed, Jordan; Christie, Matthew; Jacobs, Julia S; Dierdorff, Jason; Eberl, Daniel F; Manak, J Robert

Comeron, Josep M; Reed, Jordan; Christie, Matthew; Jacobs, Julia S; Dierdorff, Jason; Eberl, Daniel F; Manak, J Robert.

Afiliação

Comeron JM; Department of Biology, University of Iowa, Iowa City, IA 52242, USA. josep-comeron@uiowa.edu.
Reed J; Graduate Program in Genetics, University of Iowa, Iowa City, IA 52242, USA. josep-comeron@uiowa.edu.
Christie M; Department of Biology, University of Iowa, Iowa City, IA 52242, USA. jordanreed.uiowa@gmail.com.
Jacobs JS; Department of Biology, University of Iowa, Iowa City, IA 52242, USA. matthew.c.christie@gmail.com.
Dierdorff J; Department of Biology, University of Iowa, Iowa City, IA 52242, USA. julie-jacobs@uiowa.edu.
Eberl DF; Department of Biology, University of Iowa, Iowa City, IA 52242, USA. jason-dierdorff@uiowa.edu.
Manak JR; Department of Biology, University of Iowa, Iowa City, IA 52242, USA. daniel-eberl@uiowa.edu.

Microarrays (Basel) ; 5(2)2016 Apr 05.

Article em En | MEDLINE | ID: mdl-27600073

Palavras-chave

SNP detection; disease mutation; endonuclease; genetic variation; microarray; mismatch

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Microarrays (Basel) Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

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