The birth and death of human single-nucleotide polymorphisms: new experimental evidence and implications for human history and medicine

被引：32

作者：

Miller, RD ^{[1
]}

Kwok, PY ^{[1
]}

机构：

[1] Washington Univ, Sch Med, Div Dermatol, St Louis, MO 63110 USA

来源：

HUMAN MOLECULAR GENETICS | 2001年 / 10卷 / 20期

关键词：

D O I：

10.1093/hmg/10.20.2195

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Extensive, new databases of single-nucleotide polymorphisms (SNPs) provide a powerful resource for disease gene discovery, and they will be even more useful as more frequency data become available. Interesting observed genomic, patterns include SNP deserts (regions of low SNP incidence) and lengthy regions of linkage disequilibrium containing only a few haplotypes. A variety of genetic studies will benefit from SNP resources.

引用

页码：2195 / 2198

页数：4

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