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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.

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Stitziel, Nathan O, Kiezun, Adam, Sunyaev, Shamil
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BioMed Central 2011
Pynciau:
Mynediad Ar-lein: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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