Computational and statistical approaches to analyzing variants identified by exome sequencing

New sequencing technology has enabled the identification of thousands of single nucleotide polymorphisms in the exome, and many computational and statistical approaches to identify disease-association signals have emerged.

Detalles Bibliográficos
Autores principales: Stitziel, Nathan O, Kiezun, Adam, Sunyaev, Shamil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308043/
https://www.ncbi.nlm.nih.gov/pubmed/21920052
http://dx.doi.org/10.1186/gb-2011-12-9-227

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3308043/
https://www.ncbi.nlm.nih.gov/pubmed/21920052
http://dx.doi.org/10.1186/gb-2011-12-9-227

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