Identifying significant temporal variation in time course microarray data without replicates

被引:12
作者
Billups, Stephen C. [1 ]
Neville, Margaret C. [2 ]
Rudolph, Michael [3 ]
Porter, Weston [4 ]
Schedin, Pepper [5 ]
机构
[1] Univ Colorado, Dept Math & Stat Sci, Denver, CO 80202 USA
[2] Univ Colorado, Dept Physiol, Aurora, CO USA
[3] Univ Colorado, Dept Pathol, Aurora, CO USA
[4] Texas A&M Univ, Dept Interact Biosci, College Stn, TX USA
[5] Univ Colorado, AMC Canc Res Ctr, Colorado Canc Ctr, Dept Med, Aurora, CO USA
来源
BMC BIOINFORMATICS | 2009年 / 10卷
关键词
GENE-EXPRESSION;
D O I
10.1186/1471-2105-10-96
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: An important component of time course microarray studies is the identification of genes that demonstrate significant time-dependent variation in their expression levels. Until recently, available methods for performing such significance tests required replicates of individual time points. This paper describes a replicate-free method that was developed as part of a study of the estrous cycle in the rat mammary gland in which no replicate data was collected. Results: A temporal test statistic is proposed that is based on the degree to which data are smoothed when fit by a spline function. An algorithm is presented that uses this test statistic together with a false discovery rate method to identify genes whose expression profiles exhibit significant temporal variation. The algorithm is tested on simulated data, and is compared with another recently published replicate-free method. The simulated data consists both of genes with known temporal dependencies, and genes from a null distribution. The proposed algorithm identifies a larger percentage of the time-dependent genes for a given false discovery rate. Use of the algorithm in a study of the estrous cycle in the rat mammary gland resulted in the identification of genes exhibiting distinct circadian variation. These results were confirmed in follow-up laboratory experiments. Conclusion: The proposed algorithm provides a new approach for identifying expression profiles with significant temporal variation without relying on replicates. When compared with a recently published algorithm on simulated data, the proposed algorithm appears to identify a larger percentage of time-dependent genes for a given false discovery rate. The development of the algorithm was instrumental in revealing the presence of circadian variation in the virgin rat mammary gland during the estrous cycle.
引用
收藏
页数:14
相关论文
共 7 条
[1]  
[Anonymous], 1983, Johns Hopkins Series in the Mathematical Sciences
[2]  
[Anonymous], 1978, PRACTICAL GUIDE SPLI
[3]   Analyzing time series gene expression data [J].
Bar-Joseph, Z .
BIOINFORMATICS, 2004, 20 (16) :2493-2503
[4]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[5]   Circadian clock and cell cycle gene expression in mouse mammary epithelial cells and in the developing mouse mammary gland [J].
Metz, RP ;
Qu, XY ;
Laffin, B ;
Earnest, D ;
Porter, WW .
DEVELOPMENTAL DYNAMICS, 2006, 235 (01) :263-271
[6]   Estrous cycle regulation of mammary epithelial cell proliferation, differentiation, and death in the Sprague-Dawley rat: A model for investigating the role of estrous cycling in mammary carcinogenesis [J].
Schedin, P ;
Mitrenga, T ;
Kaeck, M .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 2000, 5 (02) :211-225
[7]   Significance analysis of time course microarray experiments [J].
Storey, JD ;
Xiao, WZ ;
Leek, JT ;
Tompkins, RG ;
Davis, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (36) :12837-12842