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.

Opis bibliograficzny
Główni autorzy: Stitziel, Nathan O., Kiezun, Adam, Sunyaev, Shamil R.
Kolejni autorzy: Harvard University--MIT Division of Health Sciences and Technology
Format: Artykuł
Język:en_US
Wydane: BioMed Central Ltd. 2012
Dostęp online:http://hdl.handle.net/1721.1/70548