Comparison of computational methods for the identification of cell cycle-regulated genes

被引:149
作者
de Lichtenberg, U
Jensen, LJ
Fausboll, A
Jensen, TS
Bork, P
Brunak, S [1 ]
机构
[1] Tech Univ Denmark, Ctr Biol Sequence Anal, DK-2800 Lyngby, Denmark
[2] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词
D O I
10.1093/bioinformatics/bti093
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: DNA microarrays have been used extensively to study the cell cycle transcription programme in a number of model organisms. The Saccharomyces cerevisiae data in particular have been subjected to a wide range of bioinformatics analysis methods, aimed at identifying the correct and complete set of periodically expressed genes. Results: Here, we provide the first thorough benchmark of such methods, surprisingly revealing that most new and more mathematically advanced methods actually perform worse than the analysis published with the original microarray data sets. We show that this loss of accuracy specifically affects methods that only model the shape of the expression profile without taking into account the magnitude of regulation. We present a simple permutation-based method that performs better than most existing methods.
引用
收藏
页码:1164 / 1171
页数:8
相关论文
共 22 条
[1]   A genome-wide transcriptional analysis of the mitotic cell cycle [J].
Cho, RJ ;
Campbell, MJ ;
Winzeler, EA ;
Steinmetz, L ;
Conway, A ;
Wodicka, L ;
Wolfsberg, TG ;
Gabrielian, AE ;
Landsman, D ;
Lockhart, DJ ;
Davis, RW .
MOLECULAR CELL, 1998, 2 (01) :65-73
[2]   Transcriptional regulation and function during the human cell cycle [J].
Cho, RJ ;
Huang, MX ;
Campbell, MJ ;
Dong, HL ;
Steinmetz, L ;
Sapinoso, L ;
Hampton, G ;
Elledge, SJ ;
Davis, RW ;
Lockhart, DJ .
NATURE GENETICS, 2001, 27 (01) :48-54
[3]   Is whole-culture synchronization biology's 'perpetual-motion machine'? [J].
Cooper, S .
TRENDS IN BIOTECHNOLOGY, 2004, 22 (06) :266-269
[4]   Rejoinder: whole-culture synchronization cannot, and does not, synchronize cells [J].
Cooper, S .
TRENDS IN BIOTECHNOLOGY, 2004, 22 (06) :274-276
[5]   Protein feature based identification of cell cycle regulated proteins in yeast [J].
de Lichtenberg, U ;
Jensen, TS ;
Jensen, LJ ;
Brunak, S .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 329 (04) :663-674
[6]   The Stanford Microarray Database: data access and quality assessment tools [J].
Gollub, J ;
Ball, CA ;
Binkley, G ;
Demeter, J ;
Finkelstein, DB ;
Hebert, JM ;
Hernandez-Boussard, T ;
Jin, H ;
Kaloper, M ;
Matese, JC ;
Schroeder, M ;
Brown, PO ;
Botstein, D ;
Sherlock, G .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :94-96
[7]   A multivariate approach applied to microarray data for identification of genes with cell cycle-coupled transcription [J].
Johansson, D ;
Lindgren, P ;
Berglund, A .
BIOINFORMATICS, 2003, 19 (04) :467-473
[8]   Transcriptional regulatory networks in Saccharomyces cerevisiae [J].
Lee, TI ;
Rinaldi, NJ ;
Robert, F ;
Odom, DT ;
Bar-Joseph, Z ;
Gerber, GK ;
Hannett, NM ;
Harbison, CT ;
Thompson, CM ;
Simon, I ;
Zeitlinger, J ;
Jennings, EG ;
Murray, HL ;
Gordon, DB ;
Ren, B ;
Wyrick, JJ ;
Tagne, JB ;
Volkert, TL ;
Fraenkel, E ;
Gifford, DK ;
Young, RA .
SCIENCE, 2002, 298 (5594) :799-804
[9]   Statistical resynchronization and Bayesian detection of periodically expressed genes [J].
Lu, X ;
Zhang, W ;
Qin, ZHS ;
Kwast, KE ;
Liu, JS .
NUCLEIC ACIDS RESEARCH, 2004, 32 (02) :447-455
[10]   Model-based methods for identifying periodically expressed genes based on time course microarray gene expression data [J].
Luan, Y ;
Li, H .
BIOINFORMATICS, 2004, 20 (03) :332-339