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. © 2011 BioMed Central Ltd.
CITATION STYLE
Stitziel, N. O., Kiezun, A., & Sunyaev, S. (2011, September 14). Computational and statistical approaches to analyzing variants identified by exome sequencing. Genome Biology. https://doi.org/10.1186/gb-2011-12-9-227
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