Analysis and application of European genetic substructure using 300 KSNP information

被引:190
作者
Tian, Chao [1 ,2 ,3 ]
Plenge, Robert M. [4 ,5 ,6 ]
Ransom, Michael [1 ,2 ,3 ]
Lee, Annette [7 ]
Villoslada, Pablo [8 ]
Selmi, Carlo [3 ,12 ]
Klareskog, Lars [11 ]
Pulver, Ann E. [10 ]
Qi, Lihong [1 ,9 ]
Gregersen, Peter K. [7 ]
Seldin, Michael F. [1 ,2 ,3 ]
机构
[1] Univ Calif Davis, Rowe Program Human Genet, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Biochem, Davis, CA 95616 USA
[3] Univ Calif Davis, Dept Med, Davis, CA 95616 USA
[4] Broad Inst Harvard, Cambridge, MA USA
[5] MIT, Cambridge, MA 02139 USA
[6] Brigham & Womens Hosp, Div Rheumatol Allergy & Immunol, Boston, MA 02115 USA
[7] N Shore LIJ Hlth Syst, Feinstein Inst Med Res, Robert S Boas Ctr Genom & Human Genet, Manhasset, NY USA
[8] Univ Navarra, Ctr Appl Med Res, E-31080 Pamplona, Spain
[9] Univ Calif Davis, Dept Publ Hlth Sci, Davis, CA 95616 USA
[10] Johns Hopkins Sch Med, Dept Psychiat & Behav Sci, Baltimore, MD USA
[11] Karolinska Univ Hosp, Stockholm, Sweden
[12] Univ Milan, San Paolo Hosp Sch Med, Div Internal Med, Milan, Italy
来源
PLOS GENETICS | 2008年 / 4卷 / 01期
关键词
D O I
10.1371/journal.pgen.0040004
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
European population genetic substructure was examined in a diverse set of > 1,000 individuals of European descent, each genotyped with > 300 K SNPs. Both STRUCTURE and principal component analyses (PCA) showed the largest division/principal component (PC) differentiated northern from southern European ancestry. A second PC further separated Italian, Spanish, and Greek individuals from those of Ashkenazi Jewish ancestry as well as distinguishing among northern European populations. In separate analyses of northern European participants other substructure relationships were discerned showing a west to east gradient. Application of this substructure information was critical in examining a real dataset in whole genome association (WGA) analyses for rheumatoid arthritis in European Americans to reduce false positive signals. In addition, two sets of European substructure ancestry informative markers (ESAIMs) were identified that provide substantial substructure information. The results provide further insight into European population genetic substructure and show that this information can be used for improving error rates in association testing of candidate genes and in replication studies of WGA scans.
引用
收藏
页码:0029 / 0039
页数:11
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