Discovering gene expression patterns in time course microarray experiments by ANOVA-SCA

被引:62
作者
Nueda, Maria Jose [1 ]
Conesa, Ana
Westerhuis, Johan A.
Hoefsloot, Huub C. J.
Smilde, Age K.
Talon, Manuel
Ferrer, Alberto
机构
[1] Univ Alicante, Dept Estadist & Invest Operat, E-03080 Alicante, Spain
[2] Inst Valenciano Invest Agr, Ctr Gen, E-46113 Moncada, Spain
[3] Univ Amsterdam, NL-1018 WV Amsterdam, Netherlands
[4] TNO Qual Life, Zeist, Netherlands
[5] Univ Politecn Valencia, Dept Estadist & Invest Operat Aplicadas & Calidad, Apartado 46022, Spain
[6] Ctr Invest Principe Felipe, Bioinformat Dept, E-46013 Valencia, Spain
关键词
COMPONENT ANALYSIS; PROFILES; TOXICOGENOMICS; ASCA; TOOL;
D O I
10.1093/bioinformatics/btm251
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Designed microarray experiments are used to investigate the effects that controlled experimental factors have on gene expression and learn about the transcriptional responses associated with external variables. In these datasets, signals of interest coexist with varying sources of unwanted noise in a framework of (co)relation among the measured variables and with the different levels of the studied factors. Discovering experimentally relevant transcriptional changes require methodologies that take all these elements into account. Results: In this work, we develop the application of the Analysis of variance-simultaneous component analysis (ANOVA-SCA) Smilde et al, Bioinformatics, (2005) to the analysis of multiple series time course microarray data as an example of multifactorial gene expression profiling experiments. We denoted this implementation as ASCA-genes. We show how the combination of ANOVA-modeling and a dimension reduction technique is effective in extracting targeted signals from data by-passing structural noise. The methodology is valuable for identifying main and secondary responses associated with the experimental factors and spotting relevant experimental conditions. We additionally propose a novel approach for gene selection in the context of the relation of individual transcriptional patterns to global gene expression signals. We demonstrate the methodology on both real and synthetic datasets.
引用
收藏
页码:1792 / 1800
页数:9
相关论文
共 25 条
[1]   Comparing the continuous representation of time-series expression profiles to identify differentially expressed genes [J].
Bar-Joseph, Z ;
Gerber, G ;
Simon, L ;
Gifford, DK ;
Jaakkola, TS ;
Jaakkola, TS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (18) :10146-10151
[2]  
BOX GEP, 1951, AM MATH STAT, V25, P290
[3]   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
[4]   maSigPro:: a method to identify significantly differential expression profiles in time-course microarray experiments [J].
Conesa, A ;
Nueda, MJ ;
Ferrer, A ;
Talón, M .
BIOINFORMATICS, 2006, 22 (09) :1096-1102
[5]   Blast2GO:: a universal tool for annotation, visualization and analysis in functional genomics research [J].
Conesa, A ;
Götz, S ;
García-Gómez, JM ;
Terol, J ;
Talón, M ;
Robles, M .
BIOINFORMATICS, 2005, 21 (18) :3674-3676
[6]  
Dai JJ, 2006, STAT APPL GENET MOL, V5
[7]  
Hartigan J. A., 1979, Applied Statistics, V28, P100, DOI 10.2307/2346830
[8]   Toxicogenomics of bromobenzene hepatotoxicity: a combined transcriptomics and proteomics approach [J].
Heijne, WHM ;
Stierum, RH ;
Slijper, M ;
van Bladeren, PJ ;
van Ommen, B .
BIOCHEMICAL PHARMACOLOGY, 2003, 65 (05) :857-875
[9]   A hierarchical unsupervised growing neural network for clustering gene expression patterns [J].
Herrero, J ;
Valencia, A ;
Dopazo, J .
BIOINFORMATICS, 2001, 17 (02) :126-136
[10]   Statistical analysis of array expression data as applied to the problem of tamoxifen resistance [J].
Hilsenbeck, SG ;
Friedrichs, WE ;
Schiff, R ;
O'Connell, P ;
Hansen, RK ;
Osborne, CK ;
Fuqua, SAW .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (05) :453-459