Grant Details
Grant Number: |
5R01CA052862-14 Interpret this number |
Primary Investigator: |
Thomas, Duncan |
Organization: |
University Of Southern California |
Project Title: |
Survival Models for Genetic Epidemiology |
Fiscal Year: |
2006 |
Abstract
DESCRIPTION (provided by applicant): This project is primarily concerned with
gene characterization for censored age-at-onset disease traits like cancer.
During previous cycles, we have investigated a number of design issues for
family-based studies, such as those arising in the context of our work on the
NCI's Cooperative Family Registries for Breast and Colorectal Cancer Studies
(CFRBCCS) as well as methods for modeling penetrance in relation to age and
multiple genetic and environmental factors. The present proposal represents a
continuation of work on these major themes. We propose to continue our efforts
on methodologic issues in gene characterization, with the following aims:
(i) Development of a unified likelihood framework for family-based association
studies, including creation of a likelihood for segregation, linkage, direct
association, and linkage disequilibrium for candidate genes, non-random
ascertainment of families, censored age-at-onset phenotypes, estimation of
penetrance from ascertained families with only some members genotyped, robust
tests and variance estimators allowing for residual familial aggregation,
multistage sampling of pedigrees, uncertainties in reported phenotype
information in genetic analyses, implementation of these methods in the
research version of the Genetic Analysis Package (GAP-A), and investigation of
the relative efficiency of alternative study designs;
(ii) Approaches to modeling complex disease traits, including methods for
analysis of multiple phenotypes (e.g., multiple sites of cancer, such as the
HNPCC syndrome), toxicokinetic models for complex metabolic pathways involving
multiple genes and environmental exposures, and penetrance models incorporating
genomic instability;
(iii) Methods for characterizing the phenotypic effect of highly polymorphic
genes;
(iv) Methods for allowing for population stratification in case-control and
cohort gene-association studies of unrelated individuals.
To illustrate our methodologic work, we will draw examples from the CFRBCCS and
other studies the genetic epidemiology of cancer in the USC Department of
Preventive Medicine.
Publications
None