JSM 2005 - Toronto

Abstract #303571

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: 277
Type: Contributed
Date/Time: Tuesday, August 9, 2005 : 10:30 AM to 12:20 PM
Sponsor: Section on Bayesian Statistical Science
Abstract - #303571
Title: Modeling Correlated Structures in Sequence Motif Problems
Author(s): Qing Zhou*+ and Wing Hung Wong
Companies: Harvard University and Stanford University
Address: Dept of Statistics, Cambridge, MA, 02138, United States
Keywords: Motif discovery ; Cis-regulatory modules ; Transcription factor ; Comparative genomics
Abstract:

Cis-regulatory modules (CRMs) composed of multiple transcription factor binding sites (TFBSs) control gene expression in eukaryotic genomes. Comparative genomic studies show these regulatory elements are more conserved across species due to evolutionary constraints. We propose a coupling hidden Markov model that utilizes these two sorts of information from coregulated modules and from multiple genome conservation under a unified probabilistic framework. Based on the model, we perform Bayesian inference using the Gibbs sampling algorithm to de novo discover CRMs and their component motifs. We applied our algorithm to different genomes, and significant improvements were observed compared with other existing methods.


  • 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