David B. Allison, Bonnie Thiel, Pamela St. Jean, Robert C

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Multiple Phenotype Modeling in Gene-Mapping Studies of Quantitative Traits: Power Advantages  David B. Allison, Bonnie Thiel, Pamela St. Jean, Robert C. Elston, Ming C. Infante, Nicholas J. Schork  The American Journal of Human Genetics  Volume 63, Issue 4, Pages 1190-1201 (October 1998) DOI: 10.1086/302038 Copyright © 1998 The American Society of Human Genetics Terms and Conditions

Figure 1 Simulation results examining the effect of the residual correlation between two traits on the power to detect a major locus (allele frequency = .20) with pleiotropic effects on two traits. A fully informative marker at distance of 1 cM from the trait locus was assumed. Figure 1 depicts the power of the proposed bivariate mapping method as a function of the residual correlation with the locus accounting for 50% or 25% of the variance of each trait. The American Journal of Human Genetics 1998 63, 1190-1201DOI: (10.1086/302038) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

Figure 2 depicts power of the proposed bivariate mapping method as a function of the effect of a locus on two traits (i.e., the locus was assumed to influence the two traits in an equivalent manner). Three scenarios were investigated, each assuming a different residual correlation between the two traits. The American Journal of Human Genetics 1998 63, 1190-1201DOI: (10.1086/302038) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

Figure 3 The effect of a second trait and marker distance on the power to detect linkage. The diagram depicts the power of proposed bivariate mapping method to detect linkage as a function of the effect of a relevant locus on the second of two traits (the locus was assumed to explain 25% of the variation of the first trait for all simulations). An allele frequency of 0.2 was assumed for all simulations. The residual correlation between the traits was assumed to be 0.0, 0.5, or −0.5. A fully informative marker at distance of 1 cM from the trait locus was assumed. The American Journal of Human Genetics 1998 63, 1190-1201DOI: (10.1086/302038) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

Figure 4 depicts the power of the proposed bivariate mapping method as a function of the distance (in cMs) between the marker locus and the trait locus. The trait locus was assumed to explain 33% of each of the two traits' variance. An allele frequency of 0.5 was assumed for all simulations. Fully informative markers were also assumed. The American Journal of Human Genetics 1998 63, 1190-1201DOI: (10.1086/302038) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

Figure 5 depicts a “Mosaic” pleiotropy relationship among a QTL and phenotypes X1 and X2. The American Journal of Human Genetics 1998 63, 1190-1201DOI: (10.1086/302038) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

Figure 6 depicts a “Relational” pleiotropy relationship among a QTL and phenotypes X1 and X2. The American Journal of Human Genetics 1998 63, 1190-1201DOI: (10.1086/302038) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

Figure 7 depicts a relationship among a QTL and phenotypes X1 and X2 with exogenous phenotype. The American Journal of Human Genetics 1998 63, 1190-1201DOI: (10.1086/302038) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

Figure 8 depicts a relationship among a QTL and phenotypes X1 and X2 with correlated phenotype. The American Journal of Human Genetics 1998 63, 1190-1201DOI: (10.1086/302038) Copyright © 1998 The American Society of Human Genetics Terms and Conditions

Figure 9 depicts a relationship among a QTL and phenotypes X1 and X2. With intermediate phenotype. The American Journal of Human Genetics 1998 63, 1190-1201DOI: (10.1086/302038) Copyright © 1998 The American Society of Human Genetics Terms and Conditions