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 will 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 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 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 345 at GAW15. In the current grant period, the proceedings of GAW13 (held in 2002) were published, and GAW14 (2004) and GAW15 (2006) were held. Preparation of the GAW15 proceedings is in progress and planning for GAW16 has begun. During the proposed grant period, three GAWs will be held: GAW 16 (in 2008), GAW17 (in 2010), and GAW18 (in 2012). Before the Workshops, participants 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. Recent GAWs have included genome scan data (microsatellites and SNPs), dense SNP data in specific chromosomal regions, simulated sequence data, as well as microarray expression data, giving participants an opportunity to try out new methods for localizing and characterizing disease-causing genes. For the first time in GAW13, longitudinal phenotypic data were distributed (from the Framingham Heart Study). Topics for future GAWs will be selected from among currently challenging analytical problems. Suggestions include methods for analyzing genotype W environment interaction;how to best use very high density marker maps;following up genome-wide localization with region-specific, gene-centric, and/or sequence-based analyses;analysis of transcriptomic (RNA expression phenotypes) and other types of -omics data;and issues involved in analysis of association-based genome-wide screening. We will continue to distribute real and simulated data from past GAWs with the permission of the data providers, as well as programs for genetic analysis. 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.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM031575-27
Application #
7763188
Study Section
Genomics, Computational Biology and Technology Study Section (GCAT)
Program Officer
Krasnewich, Donna M
Project Start
1983-04-01
Project End
2012-01-31
Budget Start
2010-02-01
Budget End
2011-01-31
Support Year
27
Fiscal Year
2010
Total Cost
$586,925
Indirect Cost
Name
Texas Biomedical Research Institute
Department
Type
DUNS #
007936834
City
San Antonio
State
TX
Country
United States
Zip Code
78245
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
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
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
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
Porto, Arthur; Peralta, Juan M; Blackburn, Nicholas B et al. (2018) Reliability of genomic predictions of complex human phenotypes. BMC Proc 12:51
Nustad, Haakon E; Page, Christian M; Reiner, Andrew H et al. (2018) A Bayesian mixed modeling approach for estimating heritability. BMC Proc 12:31
Cantor, Rita; Navarro, Linda; Pan, Calvin (2018) Identifying fenofibrate responsive CpG sites. BMC Proc 12:43
Hsu, Yayun; Auerbach, Jonathan; Zheng, Tian et al. (2018) Coping with family structure in genome-wide association studies: a comparative evaluation. BMC Proc 12:42
Zhou, Xiaofei; Wang, Meng; Zhang, Han et al. (2018) Logistic Bayesian LASSO for detecting association combining family and case-control data. BMC Proc 12:54
Sun, Rui; Weng, Haoyi; Men, Ruoting et al. (2018) Gene-methylation epistatic analyses via the W-test identifies enriched signals of neuronal genes in patients undergoing lipid-control treatment. BMC Proc 12:53

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