The overall goal of this project is to evaluate statistical genetic methods for detecting, characterizing, and mapping the genes that influence complex diseases and their precursors and risk factors. We will pursue this goal by: (l) Continuing the organization of the Genetic Analysis Workshops (GAWs). The Genetic Analysis Workshops are a collaborative effort among genetic epidemiologists to evaluate and compare statistical genetic methods. For each GAW, topics are chosen for their relevance to current analytical issues in genetic epidemiology, and sets of computer-simulated or real data are distributed to investigators worldwide. Results of analyses are discussed and compared at a 2 1/2 day meeting. GAW10 will be held in 1996, and GAW11, in 1998. Planning and data distribution for GAW12 will be ongoing by the end of the requested period of support in 2000. (2) Conducting evaluations of methods of genetic analysis. Some issues concerning the strengths and limitations of statistical genetic methods can be more readily addressed outside a workshop setting. Using computer- simulated data, we will address questions of power or sensitivity, specificity, and robustness of various analytical methods. Because many current analytical problems in genetic epidemiology involve complex diseases with associated quantitative precursors and risk factors, we will focus on analysis of such quantitative traits. We will evaluate (l) the utility of multivariate linkage analysis for detecting loci that contribute to quantitative traits, and (2) the effects on statistical inference of including or disregarding genotype x environment (GxE) interaction. This research will complement the Workshops in the sense that many of the same simulation programs and data sets will be used, and special problems that are revealed in the Workshops will be pursued in greater detail. (3) Distributing simulation programs, simulated data, and programs for genetic analysis. As a result of our efforts in generating data for the GAWs and in evaluating methods of genetic analysis, we are developing computer programs and simulated data sets that are of potential value to other investigators. We will continue to document these programs and data sets and provide them to interested investigators.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM031575-15
Application #
2518913
Study Section
Epidemiology and Disease Control Subcommittee 2 (EDC)
Project Start
1983-04-01
Project End
1999-08-31
Budget Start
1997-09-01
Budget End
1998-08-31
Support Year
15
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Southwest Foundation for Biomedical Research
Department
Type
DUNS #
City
San Antonio
State
TX
Country
United States
Zip Code
78245
Lim, Elise; Xu, Hanfei; Wu, Peitao et al. (2018) Network analysis of drug effect on triglyceride-associated DNA methylation. BMC Proc 12:27
Li, Liming; Wang, Chan; Lu, Tianyuan et al. (2018) Indirect effect inference and application to GAW20 data. BMC Genet 19:67
Cherlin, Svetlana; Howey, Richard A J; Cordell, Heather J (2018) Using penalized regression to predict phenotype from SNP data. BMC Proc 12:38
de Andrade, Mariza; Warwick Daw, E; Kraja, Aldi T et al. (2018) The challenge of detecting genotype-by-methylation interaction: GAW20. BMC Genet 19:81
Kraja, Aldi T; An, Ping; Lenzini, Petra et al. (2018) Simulation of a medication and methylation effects on triglycerides in the Genetic Analysis Workshop 20. BMC Proc 12:25
Kulkarni, Hemant; Mukhopadhyay, Indranil; Ghosh, Saurabh (2018) Transmission-based association mapping of triglyceride levels in a longitudinal framework using quasi-likelihood. BMC Proc 12:39
Yasmeen, Summaira; Burger, Patricia; Friedrichs, Stefanie et al. (2018) Relating drug response to epigenetic and genetic markers using a region-based kernel score test. BMC Proc 12:47
Xu, Zheng; Duan, Qing; Cui, Juan et al. (2018) Analysis of genetic and nongenetic factors influencing triglycerides-lowering drug effects based on paired observations. BMC Proc 12:46
Nustad, Haakon E; Page, Christian M; Reiner, Andrew H et al. (2018) A Bayesian mixed modeling approach for estimating heritability. BMC Proc 12:31
Porto, Arthur; Peralta, Juan M; Blackburn, Nicholas B et al. (2018) Reliability of genomic predictions of complex human phenotypes. BMC Proc 12:51

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