Shrinkage-based similarity metric for cluster analysis of microarray data

被引:24
作者
Cherepinsky, V
Feng, JW
Rejali, M
Mishra, B
机构
[1] NYU, Courant Inst Math Sci, New York, NY 10012 USA
[2] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
关键词
D O I
10.1073/pnas.1633770100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The current standard correlation coefficient used in the analysis of microarray data was introduced by M. B. Eisen, P. T. Spellman, P. O. Brown, and D. Botstein [(1998) Proc. Nati. Acad Sci. USA 95, 1486314868]. Its formulation is rather arbitrary. We give a mathematically rigorous correlation coefficient of two data vectors based on James-Stein shrinkage estimators. We use the assumptions described by Eisen et al., also using the fact that the data can be treated as transformed into normal distributions. While Eisen et A use zero as an estimator for the expression vector mean mu, we start with the assumption that for each gene, IL is itself a zero-mean normal random variable [with a priori distribution N(0, tau(2))], and use Bayesian analysis to obtain a posteriori distribution of mu in terms of the data. The shrunk estimator for mu differs from the mean of the data vectors and ultimately leads to a statistically robust estimator for correlation coefficients. To evaluate the effectiveness of shrinkage, we conducted in silico experiments and also compared similarity metrics on a biological example by using the data set from Eisen et A For the latter, we classified genes involved in the regulation of yeast cell-cycle functions by computing clusters based on various definitions of correlation coefficients and contrasting them against clusters based on the activators known in the literature. The estimated false positives and false negatives from this study indicate that using the shrinkage metric improves the accuracy of the analysis.
引用
收藏
页码:9668 / 9673
页数:6
相关论文
共 13 条
[1]  
CHEREPINSKY V, 2003, 2003845 NYU CS
[2]   The transcriptional program of sporulation in budding yeast [J].
Chu, S ;
DeRisi, J ;
Eisen, M ;
Mulholland, J ;
Botstein, D ;
Brown, PO ;
Herskowitz, I .
SCIENCE, 1998, 282 (5389) :699-705
[3]   Exploring the metabolic and genetic control of gene expression on a genomic scale [J].
DeRisi, JL ;
Iyer, VR ;
Brown, PO .
SCIENCE, 1997, 278 (5338) :680-686
[4]  
EGAN JP, 1975, SIGNAL DETECTION THE
[5]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[6]   Stein estimation - A review [J].
Hoffmann, K .
STATISTICAL PAPERS, 2000, 41 (02) :127-158
[7]  
JAMES W, 1961, 4TH P BERK S MATH ST, V1, P361
[8]   A PRACTICAL BAYESIAN FRAMEWORK FOR BACKPROPAGATION NETWORKS [J].
MACKAY, DJC .
NEURAL COMPUTATION, 1992, 4 (03) :448-472
[9]   Parallel human genome analysis: Microarray-based expression monitoring of 1000 genes [J].
Schena, M ;
Shalon, D ;
Heller, R ;
Chai, A ;
Brown, PO ;
Davis, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :10614-10619
[10]   Serial regulation of transcriptional regulators in the yeast cell cycle [J].
Simon, I ;
Barnett, J ;
Hannett, N ;
Harbison, CT ;
Rinaldi, NJ ;
Volkert, TL ;
Wyrick, JJ ;
Zeitlinger, J ;
Gifford, DK ;
Jaakkola, TS ;
Young, RA .
CELL, 2001, 106 (06) :697-708