Genomewide Rapid Association Using Mixed Model and Regression: A Fast and Simple Method For Genomewide Pedigree-Based Quantitative Trait Loci Association Analysis
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- 1 September 2007
- journal article
- Published by Oxford University Press (OUP) in Genetics
- Vol. 177 (1), 577-585
- https://doi.org/10.1534/genetics.107.075614
Abstract
For pedigree-based quantitative trait loci (QTL) association analysis, a range of methods utilizing within-family variation such as transmission-disequilibrium test (TDT)-based methods have been developed. In scenarios where stratification is not a concern, methods exploiting between-family variation in addition to within-family variation, such as the measured genotype (MG) approach, have greater power. Application of MG methods can be computationally demanding (especially for large pedigrees), making genomewide scans practically infeasible. Here we suggest a novel approach for genomewide pedigree-based quantitative trait loci (QTL) association analysis: genomewide rapid association using mixed model and regression (GRAMMAR). The method first obtains residuals adjusted for family effects and subsequently analyzes the association between these residuals and genetic polymorphisms using rapid least-squares methods. At the final step, the selected polymorphisms may be followed up with the full measured genotype (MG) analysis. In a simulation study, we compared type 1 error, power, and operational characteristics of the proposed method with those of MG and TDT-based approaches. For moderately heritable (30%) traits in human pedigrees the power of the GRAMMAR and the MG approaches is similar and is much higher than that of TDT-based approaches. When using tabulated thresholds, the proposed method is less powerful than MG for very high heritabilities and pedigrees including large sibships like those observed in livestock pedigrees. However, there is little or no difference in empirical power of MG and the proposed method. In any scenario, GRAMMAR is much faster than MG and enables rapid analysis of hundreds of thousands of markers.Keywords
This publication has 27 references indexed in Scilit:
- A novel missense mutation in ADRB3 increases risk for type 2 diabetes in a Mexican American familyDiabetes/Metabolism Research and Reviews, 2006
- The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratificationBMC Genomic Data, 2005
- A unified mixed-model method for association mapping that accounts for multiple levels of relatednessNature Genetics, 2005
- Linkage to 10q22 for Maximum Intraocular Pressure and 1p32 for Maximum Cup-to-Disc Ratio in an Extended Primary Open-Angle Glaucoma PedigreeInvestigative Opthalmology & Visual Science, 2005
- The Effect of Genetic Drift in a Young Genetically Isolated PopulationAnnals of Human Genetics, 2005
- Association testing with MendelGenetic Epidemiology, 2005
- Complex trait mapping in isolated populations: Are specific statistical methods required?European Journal of Human Genetics, 2005
- Coalescent-Based Association Mapping and Fine Mapping of Complex Trait LociGenetics, 2005
- Power of QTL detection using association tests with family controlsEuropean Journal of Human Genetics, 2003
- Score Tests for Association between Traits and Haplotypes when Linkage Phase Is AmbiguousAmerican Journal of Human Genetics, 2002