The goal of this project is to facilitate the development and evaluation of statistical methods for identifying and characterizing the genetic contribution to complex diseases and their precursors and risk factors. We propose to pursue this goal by continuing the organization of the Genetic Analysis Workshops (GAWs), which began in 1982. The Genetic Analysis Workshops are a collaborative effort among genetic epidemiologists and statistical geneticists to evaluate and compare genetic analysis methods. For each GAW, topics are chosen for their relevance to current analytical issues in genetic epidemiology, and sets of real and computer-simulated data are distributed to investigators worldwide. Participants submit the results of their analyses, which are discussed and compared at a 3 1/2 day meeting. Participation at GAWs has increased tremendously, from fewer than 30 at GAW1 in 1982 to 272 at GAW17. In the current grant period GAW16 (2008) and GAW17 (2010) were held. The GAW17 proceedings are currently in press with publication anticipated in December 2011 and planning for GAW18 has begun. During the proposed grant period, the GAW18 Proceedings will be published and two GAWs will be held: GAW19 (in 2014) and GAW20 (in 2016). Before the Workshops, participants devote months to data analysis, communicate with others who have done similar types of analyses, and plan integrated presentations. The GAW submissions invariably contain new ideas for methods to handle complex phenotypes and a number of widely used analytical techniques had their start at a GAW. Recent GAWs have included genome-wide association data and exome sequence data, giving participants an opportunity to try out new methods for localizing and characterizing variants influencing disease risk. Topics for future GAWs will be selected from among currently challenging analytical problems. Suggestions from GAW participants include methods for analyzing whole genome sequence;genome-wide methylation profiles;comparisons of study designs for next generation sequencing projects;analyzing sequence data in admixed populations;gene-environment and gene-gene interactions;and copy number variation. We also will continue to distribute real and simulated data from past GAWs with the permission of the data providers. Long after each GAW is over, investigators continue to use GAW data sets to evaluate new analytical methods and software, to estimate power and false positive rates, and to demonstrate the feasibility of statistical techniques for finding disease genes. GAW data are extensively used in grant proposals and in teaching and dissertation research.

Public Health Relevance

The goal of this project is to facilitate the development and evaluation of statistical methods for identifying genes contributing to risk of complex diseases and related risk factors. Continuing innovation in analytical methods is needed to keep pace with new study designs and new types of data made possible by advances in laboratory technologies and computing. Development of new statistical methods has the potential to significantly advance research in biomedical genetics because such methods can be applied in studies of many complex human diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM031575-29
Application #
8373431
Study Section
Genomics, Computational Biology and Technology Study Section (GCAT)
Program Officer
Krasnewich, Donna M
Project Start
1983-04-01
Project End
2017-07-31
Budget Start
2013-08-01
Budget End
2014-07-31
Support Year
29
Fiscal Year
2013
Total Cost
$627,619
Indirect Cost
$284,658
Name
Texas Biomedical Research Institute
Department
Type
DUNS #
007936834
City
San Antonio
State
TX
Country
United States
Zip Code
78245
Zhou, Wenda; Lo, Shaw-Hwa (2018) Analysis of genotype by methylation interactions through sparsity-inducing regularized regression. BMC Proc 12:40
Howey, Richard A J; Cordell, Heather J (2018) Application of Bayesian networks to GAW20 genetic and blood lipid data. BMC Proc 12:19
Veenstra, Jenna; Kalsbeek, Anya; Koster, Karissa et al. (2018) Epigenome wide association study of SNP-CpG interactions on changes in triglyceride levels after pharmaceutical intervention: a GAW20 analysis. BMC Proc 12:58
Jiang, Lai; Zhao, Kaiqiong; Klein, Kathleen et al. (2018) Investigating potential causal relationships between SNPs, DNA methylation and HDL. BMC Proc 12:20
Yang, Hsin-Chou; Chen, Chia-Wei (2018) Homozygosity disequilibrium associated with treatment response and its methylation regulation. BMC Proc 12:45
Tintle, Nathan L; Fardo, David W; de Andrade, Mariza et al. (2018) GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics. BMC Proc 12:26
Daw, E Warwick; Hicks, James; Lenzini, Petra et al. (2018) Methods for detecting methylation by SNP interaction in GAW20 simulation. BMC Proc 12:37
Chen, Lili; Wang, Yong; Zhou, Yajing (2018) Association analysis of rare and common variants with multiple traits based on variable reduction method. Genet Res (Camb) 100:e2
Konigorski, Stefan; Wang, Yuan; Cigsar, Candemir et al. (2018) Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations. Genet Epidemiol 42:174-186
Aslibekyan, Stella; Almasy, Laura; Province, Michael A et al. (2018) Data for GAW20: genome-wide DNA sequence variation and epigenome-wide DNA methylation before and after fenofibrate treatment in a family study of metabolic phenotypes. BMC Proc 12:35

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