Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse

被引:315
作者
Lindblad-Toh, K [1 ]
Winchester, E
Daly, MJ
Wang, DG
Hirschhorn, JN
Laviolette, JP
Ardlie, K
Reich, DE
Robinson, E
Sklar, P
Shah, N
Thomas, D
Fan, JB
Gingeras, T
Warrington, J
Patil, N
Hudson, TJ
Lander, ES
机构
[1] MIT, Whitehead Inst Biomed Res, Ctr Genome Res, Cambridge, MA 02139 USA
[2] Bristol Myers Squibb, Princeton, NJ USA
[3] Childrens Hosp, Div Endocrinol, Boston, MA 02115 USA
[4] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[5] Affymetrix Inc, Santa Clara, CA USA
[6] McGill Univ, Ctr Hlth, Montreal Genome Ctr, Montreal, PQ H3A 2T5, Canada
[7] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
D O I
10.1038/74215
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Single-nucleotide polymorphisms (SNPs) have been the focus of much attention in human genetics because they are extremely abundant and well-suited for automated large-scale genotyping, Human SNPs, however, are less informative than other types of genetic markers (such as simple-sequence length polymorphisms or microsatellites) and thus more loci are required for mapping traits. SNPs offer similar advantages for experimental genetic organisms such as the mouse, but they entail no loss of informativeness because bi-allelic markers are fully informative in analysing crosses between inbred strains. Here we report a large-scale analysis of SNPs in the mouse genome. We characterized the rate of nucleotide polymorphism in eight mouse strains and identified a collection of 2,848 SNPs located in 1,755 sequence-tagged sites (STSs) using high-density oligonucleotide arrays. Three-quarters of these SNPs have been mapped on the mouse genome, providing a first-generation SNP map of the mouse. We have also developed a multiplex genotyping procedure by which a genome scan can be performed with only six genotyping reactions per animal.
引用
收藏
页码:381 / 386
页数:6
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