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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.

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Autors principals: Stitziel, Nathan O, Kiezun, Adam, Sunyaev, Shamil
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2011
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3308043/
https://ncbi.nlm.nih.gov/pubmed/21920052
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2011-12-9-227
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