Comparison of three methods for obtaining principal components from family data in genetic analysis of complex disease

被引:8
作者
Moser, KL
Jedrey, CM
Conti, D
Schick, JH
Gray-McGuire, C
Nath, SK
Daley, D
Olson, JM
机构
[1] Case Western Reserve Univ, Metrohlth Med Ctr, Dept Epidemiol & Biostat, Rammelkamp Ctr Educ & Res, Cleveland, OH 44109 USA
[2] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA
关键词
Haseman-Elston method; multivariate analysis; principal components; quantitative traits;
D O I
10.1002/gepi.2001.21.s1.s726
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Three multivariate techniques used to derive principal components (PCs) from family data were compared for their ability to model family data and power to detect linkage. Using the simulated data from Genetic Analysis Workshop 12, the five quantitative traits were first adjusted for age, sex, and environmental factors 1 and 2. Then, standard PCs, PCs obtained from between-family covariance, and PCs obtained from within-family genetic covariance were derived and subjected to multivariate sib pair linkage analysis. The standard PCs obtained from the overall correlation matrix allowed identification of key features of the true genetic model more readily than did the other methods. For detection of linkage, standard PCs and PCs obtained from the between-family genetic covariance performed similarly in terms of both power and type I error, and both methods performed better than the PCs obtained from within-family genetic covariance. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:S726 / S731
页数:6
相关论文
共 9 条
[1]  
*CAS W RES U DEP E, 1998, SAGE STAT AN GEN EP
[2]  
Comuzzie AG, 1997, GENET EPIDEMIOL, V14, P975, DOI 10.1002/(SICI)1098-2272(1997)14:6<975::AID-GEPI69>3.0.CO
[3]  
2-I
[4]  
Elston RC, 2000, GENET EPIDEMIOL, V19, P1, DOI 10.1002/1098-2272(200007)19:1<1::AID-GEPI1>3.0.CO
[5]  
2-E
[6]  
Hasstedt SJ, 1994, PEDIGREE ANAL PACKAG
[7]  
Johnson R. A., 1999, APPL MULTIVARIATE ST
[8]  
Olson JM, 1999, GENET EPIDEMIOL, V17, pS271
[9]   A principal-components approach based on heritability for combining phenotype information [J].
Ott, J ;
Rabinowitz, D .
HUMAN HEREDITY, 1999, 49 (02) :106-111