Identification of functional genetic variation in exome sequence analysis

Recent technological advances have allowed us to study individual genomes at a base-pair resolution and have demonstrated that the average exome harbors more than 15,000 genetic variants. However, our ability to understand the biological significance of the identified variants and to connect these o...

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Detalles Bibliográficos
Autores principales: Jaffe, Andrew, Wojcik, Genevieve, Chu, Audrey, Golozar, Asieh, Maroo, Ankit, Duggal, Priya, Klein, Alison P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287847/
https://www.ncbi.nlm.nih.gov/pubmed/22373437
http://dx.doi.org/10.1186/1753-6561-5-S9-S13

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287847/
https://www.ncbi.nlm.nih.gov/pubmed/22373437
http://dx.doi.org/10.1186/1753-6561-5-S9-S13

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