The views expressed here are those of the individual authors and not necessarily those of the JSM sponsors, their officers, or their staff.
Online Program Home
Abstract Details
Activity Number:
|
628
|
Type:
|
Contributed
|
Date/Time:
|
Thursday, August 2, 2012 : 8:30 AM to 10:20 AM
|
Sponsor:
|
Biometrics Section
|
Abstract - #306694 |
Title:
|
Analytical Methods for RRBS Methylation Data
|
Author(s):
|
Michelle Lacey*+
|
Companies:
|
Tulane University
|
Address:
|
6823 St. Charles Ave, New Orleans, LA, 70118-5665, United States
|
Keywords:
|
epigenomics ;
methylation ;
bisulfite sequencing
|
Abstract:
|
Reduced representation bisulfite sequencing (RRBS) provides measurements of DNA methylation in sequencing experiments, thereby enabling single-nucleotide analyses on a genomic scale. Datasets consist of counts of methylated and unmethylated reads at millions of measured sites, and the detection of differentially methylated regions (DMRs) between sets of samples is a popular application of this technology. However, existing methods for the statistical analysis of RRBS datasets require that regions of interest be specified a priori and do not appropriately account for the considerable variation in read coverage that is observed when sets of samples are analyzed jointly. Through a study of methylation associated with myogenesis in both normal tissues and in FSHD patients, a new approach is presented to analyze RRBS data at the chromosomal level.
|
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 2012 program
|
2012 JSM Online Program Home
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.