Author(s): Stitziel NO, Kiezun A, Sunyaev S, Stitziel NO, Kiezun A, Sunyaev S
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Abstract 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.
This article was published in Genome Biol
and referenced in Clinical & Medical Biochemistry