"Sequencing-grade" screening for BRCA1 variants by oligo-arrays

The need for fast, efficient, and less costly means to screen genetic variants associated with disease predisposition led us to develop an oligo-nucleotide array-based process for gene-specific single nucleotide polymorphism (SNP) genotyping. This cost-effective, high-throughput strategy has high se...

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Detalles Bibliográficos
Autores principales: Monaco, Alessandro, Menolascina, Filippo, Zhao, Yingdong, Tommasi, Stefania, Sabatino, Marianna, Fasano, Ross, Paradiso, Angelo, Marincola, Francesco M, Wang, Ena
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2583995/
https://www.ncbi.nlm.nih.gov/pubmed/18973698
http://dx.doi.org/10.1186/1479-5876-6-64

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2583995/
https://www.ncbi.nlm.nih.gov/pubmed/18973698
http://dx.doi.org/10.1186/1479-5876-6-64

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