SNPs made routine

被引：4

作者：

Broman, KW ^{[1
]}

Feingold, E

机构：

[1] Johns Hopkins Univ, Dept Biostat, Baltimore, MD 21205 USA

[2] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA

[3] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Biostat, Pittsburgh, PA 15261 USA

来源：

NATURE METHODS | 2004年 / 1卷 / 02期

关键词：

D O I：

10.1038/nmeth1104-104

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

With the sequencing of the human genome, millions of single- nucleotide polymorphisms, or SNPs, have been discovered and can be used as markers to identify genes contributing to common human diseases. Two large sets of SNPs have now been organized in panels for high-throughput genotyping. © 2004 Nature Publishing Group.

引用

页码：104 / 105

页数：4

共 9 条

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