High-density single-nucleotide polymorphism maps of the human genome

被引:64
作者
Miller, RD
Phillips, MS
Jo, I
Donaldson, MA
Studebaker, JF
Addleman, N
Alfisi, SV
Ankener, WM
Bhatti, HA
Callahan, CE
Carey, BJ
Conley, CL
Cyr, JM
Derohannessian, V
Donaldson, RA
Elosua, C
Ford, SE
Forman, AM
Gelfand, CA
Grecco, NM
Gutendorf, SM
Hock, CR
Hozza, MJ
Hur, S
In, SM
Jackson, DL
Jo, SA
Jung, SC
Kim, S
Kimm, K
Kloss, EF
Koboldt, DC
Kuebler, JM
Kuo, FS
Lathrop, JA
Lee, JK [1 ]
Leis, KL
Livingston, SA
Lovins, EG
Lundy, ML
Maggan, S
Minton, M
Mockler, MA
Morris, DW
Nachtman, EP
Oh, B
Park, C
Park, CW
Pavelka, N
Perkins, AB
机构
[1] Washington Univ, Div Dermatol, St Louis, MO 63130 USA
[2] Orchid BioSci Inc, Princeton, NJ USA
[3] NIH, Dept Biomed Sci, Seoul, South Korea
[4] DNA Link Inc, Seoul, South Korea
[5] Natl Genome Res Inst, NIH, Seoul, South Korea
[6] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
关键词
SNP; human variation; the SNP consortium; pooled sequencing; single-base primer extension; Korean population; complex disease variation search;
D O I
10.1016/j.ygeno.2005.04.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Here we report a large, extensively characterized set of single-nucleotide polymorphisms (SNPs) covering the human genome. We determined the allele frequencies of 55,018 SNPs in African Americans, Asians (Japanese-Chinese), and European Americans as part of The SNP Consortium's Allele Frequency Project. A subset of 8333 SNPs was also characterized in Koreans. Because these SNPs were ascertained in the same way, the data set is particularly useful for modeling. Our results document that much genetic variation is shared among populations. For autosomes, some 44% of these SNPs have a minor allele frequency >= 10% in each population, and the average allele frequency differences between populations with different continental origins are less than 19%. However, the several percentage point allele frequency differences among the closely related Korean, Japanese, and Chinese populations suggest caution in using mixtures of well-established populations for case-control genetic studies of complex traits. We estimate that similar to 7% of these SNPs are private SNPs with minor allele frequencies < 1%. A useful set of characterized SNPs with large allele frequency differences between populations (> 60%) can be used for admixture studies. High-density maps of high-quality, characterized SNPs produced by this project are freely available. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:117 / 126
页数:10
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