JSM 2005 - Toronto

Abstract #304696

This is the preliminary program for the 2005 Joint Statistical Meetings in Minneapolis, Minnesota. Currently included in this program is the "technical" program, schedule of invited, topic contributed, regular contributed and poster sessions; Continuing Education courses (August 7-10, 2005); and Committee and Business Meetings. This on-line program will be updated frequently to reflect the most current revisions.

To View the Program:
You may choose to view all activities of the program or just parts of it at any one time. All activities are arranged by date and time.



The views expressed here are those of the individual authors
and not necessarily those of the ASA or its board, officers, or staff.


The Program has labeled the meeting rooms with "letters" preceding the name of the room, designating in which facility the room is located:

Minneapolis Convention Center = “MCC” Hilton Minneapolis Hotel = “H” Hyatt Regency Minneapolis = “HY”

Back to main JSM 2005 Program page



Legend: = Applied Session, = Theme Session, = Presenter
Activity Number: 33
Type: Contributed
Date/Time: Sunday, August 7, 2005 : 2:00 PM to 3:50 PM
Sponsor: Biometrics Section
Abstract - #304696
Title: Genome Scans with Gene-Covariate Interaction
Author(s): Jie Peng*+ and Hsiu-Khuern Tang and David Siegmund
Companies: University of California, Davis and Hewlett-Packard Company and Stanford University
Address: Department of Statistics, Davis, CA, 95616, United States
Keywords: gene mapping ; linkage analysis ; gene-environment/covariate interaction ; score statistics ; quantitative traits
Abstract:

Genetic control of a complex trait is widely thought to involve a number of loci, which may interact with one another and/or with environmental covariates. Standard genome scanning methods usually ignore these possibilities, presumably because they involve larger, more complex models and/or because of difficulties in formulating a suitable model. In this paper, genetic models for gene-covariate interaction are described. Methods of linkage analysis that utilize special features of these models and the corresponding score statistics are derived. Their power is compared with that of simple genome scans that ignore these features, and substantial gains in power are observed when the gene-covariate interaction is strong. Quantitative trait mapping and affected sibpair mapping are discussed. For the latter case, a simpler statistic is proposed that has similar performance to the score statistic, but does not require the estimation of nuisance parameters. Because the nuisance parameters are not estimable solely from affected sibpair data, this statistic is much easier to apply in practice. Approximations for the P-value and power are derived under the framework of local alternatives.


  • The address information is for the authors that have a + after their name.
  • Authors who are presenting talks have a * after their name.

Back to the full JSM 2005 program

JSM 2005 For information, contact jsm@amstat.org or phone (888) 231-3473. If you have questions about the Continuing Education program, please contact the Education Department.
Revised March 2005