Successful design and conduct of genome-wide association studies

被引:47
作者
Amos, Christopher I.
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Epidemiol & Bioinformat, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Computat Biol, Houston, TX 77030 USA
关键词
D O I
10.1093/hmg/ddm161
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
Genome-wide association studies are becoming an increasingly effective tool for identifying genetic factors contributing to complex diseases. In this review, I discuss two sets of genome-wide association studies that identified novel genetic factors for age-related macular degeneration and genetic factors for type II diabetes. In reviewing these sets of studies, my goal is to identify factors that contributed to the success of these studies. Design-related factors include the selection of traits that show strong familiality, the selection of clinically homogeneous populations and the selection of cases that have a family history. Ethnic stratification within the study sample can lead to biases, and methods to control for stratification are briefly reviewed. Finally, the impact of single nucleotide polymorphism selection on the power of a study and procedures for improving power by inferring genotypes, by combining data across studies and by performing multistage analyses are discussed. The continuing success of genome-wide association studies depends on careful selection of populations for study and on collaborative analytical approaches.
引用
收藏
页码:R220 / R225
页数:6
相关论文
共 43 条
[1]   A haplotype map of the human genome [J].
Altshuler, D ;
Brooks, LD ;
Chakravarti, A ;
Collins, FS ;
Daly, MJ ;
Donnelly, P ;
Gibbs, RA ;
Belmont, JW ;
Boudreau, A ;
Leal, SM ;
Hardenbol, P ;
Pasternak, S ;
Wheeler, DA ;
Willis, TD ;
Yu, FL ;
Yang, HM ;
Zeng, CQ ;
Gao, Y ;
Hu, HR ;
Hu, WT ;
Li, CH ;
Lin, W ;
Liu, SQ ;
Pan, H ;
Tang, XL ;
Wang, J ;
Wang, W ;
Yu, J ;
Zhang, B ;
Zhang, QR ;
Zhao, HB ;
Zhao, H ;
Zhou, J ;
Gabriel, SB ;
Barry, R ;
Blumenstiel, B ;
Camargo, A ;
Defelice, M ;
Faggart, M ;
Goyette, M ;
Gupta, S ;
Moore, J ;
Nguyen, H ;
Onofrio, RC ;
Parkin, M ;
Roy, J ;
Stahl, E ;
Winchester, E ;
Ziaugra, L ;
Shen, Y .
NATURE, 2005, 437 (7063) :1299-1320
[2]   Cellular functions of the BRCA tumour-suppressor proteins [J].
Boulton, S. J. .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2006, 34 :633-645
[3]   Demonstrating stratification in a European American population [J].
Campbell, CD ;
Ogburn, EL ;
Lunetta, KL ;
Lyon, HN ;
Freedman, ML ;
Groop, LC ;
Altshuler, D ;
Ardlie, KG ;
Hirschhorn, JN .
NATURE GENETICS, 2005, 37 (08) :868-872
[4]   Efficiency and power in genetic association studies [J].
de Bakker, PIW ;
Yelensky, R ;
Pe'er, I ;
Gabriel, SB ;
Daly, MJ ;
Altshuler, D .
NATURE GENETICS, 2005, 37 (11) :1217-1223
[5]   A COMPARISON OF LINKAGE DISEQUILIBRIUM MEASURES FOR FINE-SCALE MAPPING [J].
DEVLIN, B ;
RISCH, N .
GENOMICS, 1995, 29 (02) :311-322
[6]  
DEVLIN B, BIOSTATISTICS, V14, P369
[7]   The prevalence of celiac disease in average-risk and at-risk Western European populations:: A systematic review [J].
Dubé, C ;
Rostom, A ;
Sy, R ;
Cranney, A ;
Saloojee, N ;
Garritty, C ;
Sampson, M ;
Zhang, L ;
Yazdi, F ;
Mamaladze, V ;
Pan, I ;
Macneil, J ;
Mack, D ;
Patel, D ;
Moher, D .
GASTROENTEROLOGY, 2005, 128 (04) :S57-S67
[8]  
EASTON DF, 2007, NATURE
[9]   Complement factor H polymorphism and age-related macular degeneration [J].
Edwards, AO ;
Ritter, R ;
Abel, KJ ;
Manning, A ;
Panhuysen, C ;
Farrer, LA .
SCIENCE, 2005, 308 (5720) :421-424
[10]   A simple and improved correction for population stratification in case-control studies [J].
Epstein, Michael P. ;
Allen, Andrew S. ;
Satten, Glen A. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2007, 80 (05) :921-930