Genetic analysis of complex traits is one of the major challenges facing biomedical researchers in the so-called """"""""'post-genomic era."""""""" Complex traits of particular interest include common diseases such as diabetes, asthma, hypertension, psychiatric illnesses, and cancer that together account for a large portion of the health care burden in the United States. They are familial, but do not have simple patterns of transmission and are likely to result from the actions and interactions of multiple genetic and environmental factors. The genetic architecture of such traits is complex and remains poorly characterized. Identifying and characterizing the genetic component to complex disorders should be useful in determining not only the primary defects for such disorders, but also in clarifying the role of environmental risk factors, which could also be targets of cost-effective treatment and prevention strategies. Study designs and methods of analysis that have worked well for simple Mendelian traits may not be sufficient for analysis of complex traits. The long-term objective of the proposed research is development of statistical methods for mapping and genetic analysis of human complex traits. The proposal is focused specifically on development of methods for linkage disequilibrium mapping of qualitative traits, with haplotype or multilocus genotype data. We propose to develop and test statistical models and methods and distribute software implementing new approaches in: (1) assessment of linkage disequilibrium in isolated founder populations with inbred pedigrees; 2) linkage disequilibrium mapping in isolated founder populations with inbred pedigrees; (3) assessment of high-resolution haplotype structure in outbred populations; and (4) methods for linkage disequilibrium mapping in outbred populations, that make use of information on high-resolution haplotype structure. Our preliminary studies indicate that these approaches can improve the ability to detect and localize genes for complex traits, thereby improving the odds for successful positional cloning.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Project (R01)
Project #
2R01HG001645-06
Application #
6576356
Study Section
Genome Study Section (GNM)
Program Officer
Brooks, Lisa
Project Start
1997-09-01
Project End
2008-01-31
Budget Start
2003-02-09
Budget End
2004-01-31
Support Year
6
Fiscal Year
2003
Total Cost
$298,879
Indirect Cost
Name
University of Chicago
Department
Biostatistics & Other Math Sci
Type
Schools of Arts and Sciences
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Wu, Xiaowei; McPeek, Mary Sara (2018) L-GATOR: Genetic Association Testing for a Longitudinally Measured Quantitative Trait in Samples with Related Individuals. Am J Hum Genet 102:574-591
Wang, Miaoyan; Roux, Fabrice; Bartoli, Claudia et al. (2018) Two-way mixed-effects methods for joint association analysis using both host and pathogen genomes. Proc Natl Acad Sci U S A 115:E5440-E5449
Zhong, Sheng; Jiang, Duo; McPeek, Mary Sara (2016) CERAMIC: Case-Control Association Testing in Samples with Related Individuals, Based on Retrospective Mixed Model Analysis with Adjustment for Covariates. PLoS Genet 12:e1006329
Jiang, Duo; Zhong, Sheng; McPeek, Mary Sara (2016) Retrospective Binary-Trait Association Test Elucidates Genetic Architecture of Crohn Disease. Am J Hum Genet 98:243-55
Wang, Miaoyan; Jakobsdottir, Johanna; Smith, Albert V et al. (2016) G-STRATEGY: Optimal Selection of Individuals for Sequencing in Genetic Association Studies. Genet Epidemiol 40:446-60
Jiang, Duo; Mbatchou, Joelle; McPeek, Mary Sara (2015) Retrospective Association Analysis of Binary Traits: Overcoming Some Limitations of the Additive Polygenic Model. Hum Hered 80:187-95
Jiang, Duo; McPeek, Mary Sara (2014) Robust rare variant association testing for quantitative traits in samples with related individuals. Genet Epidemiol 38:10-20
Jakobsdottir, Johanna; McPeek, Mary Sara (2013) MASTOR: mixed-model association mapping of quantitative traits in samples with related individuals. Am J Hum Genet 92:652-66
McPeek, Mary Sara (2012) BLUP genotype imputation for case-control association testing with related individuals and missing data. J Comput Biol 19:756-65
Thornton, Timothy; Zhang, Qian; Cai, Xiaochen et al. (2012) XM: association testing on the X-chromosome in case-control samples with related individuals. Genet Epidemiol 36:438-50

Showing the most recent 10 out of 15 publications