Efficient Approach to Unique Single-Nucleotide Polymorphism Discovery

Single-nucleotide polymorphisms (SNPs) are the most frequently found DNA sequence variations in the human genome. It has been argued that a dense set of SNP markers can be used to identify genetic factors associated with complex disease traits. Because all high-throughput genotyping methods require...

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Detaylı Bibliyografya
Asıl Yazarlar: Taillon-Miller, Patricia, Piernot, Ellen E., Kwok, Pui-Yan
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Cold Spring Harbor Laboratory Press 1999
Konular:
Methods
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC310784/
https://ncbi.nlm.nih.gov/pubmed/10330130
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