Interpretation of ANOVA models for microarray data using PCA

被引:52
作者
de Haan, J. R.
Wehrens, R.
Bauerschmidt, S.
Piek, E.
van Schaik, R. C.
Buydens, L. M. C.
机构
[1] Radboud Univ Nijmegen, Inst Mol & Mat, NL-6525 ED Nijmegen, Netherlands
[2] NV Organon, NL-5340 BH Oss, Netherlands
[3] Radboud Univ Nijmegen, Dept Appl Biol, NL-6525 ED Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Ctr Mol & Biomol Informat, Nijmegen Ctr Mol Life Sci, NL-6525 ED Nijmegen, Netherlands
关键词
D O I
10.1093/bioinformatics/btl572
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: ANOVA is a technique, which is frequently used in the analysis of microarray data, e.g. to assess the significance of treatment effects, and to select interesting genes based on P-values. However, it does not give information about what exactly is causing the effect. Our purpose is to improve the interpretation of the results from ANOVA on large microarray datasets, by applying PCA on the individual variance components. Interaction effects can be visualized by biplots, showing genes and variables in one plot, providing insight in the effect of e.g. treatment or time on gene expression. Because ANOVA has removed uninteresting sources of variance, the results are much more interpretable than without ANOVA. Moreover, the combination of ANOVA and PCA provides a simple way to select genes, based on the interactions of interest. Results: It is shown that the components from an ANOVA model can be summarized and visualized with PCA, which improves the interpretability of the models. The method is applied to a real time-course gene expression dataset of mesenchymal stem cells. The dataset was designed to investigate the effect of different treatments on osteogenesis. The biplots generated with the algorithm give specific information about the effects of specific treatments on genes over time. These results are in agreement with the literature. The biological validation with GO annotation from the genes present in the selections shows that biologically relevant groups of genes are selected.
引用
收藏
页码:184 / 190
页数:7
相关论文
共 30 条
[11]   Effective dimensionality for principal component analysis of time series expression data [J].
Hörnquist, M ;
Hertz, J ;
Wahde, M .
BIOSYSTEMS, 2003, 71 (03) :311-317
[12]  
Jackson JE, 1991, A user's guide to principal components
[13]   Dexamethasone, BMP-2, and 1,25-dihydroxyvitamin D enhance a more differentiated osteoblast phenotype: validation of an in vitro model for human bone marrow-derived primary osteoblasts [J].
Jorgensen, NR ;
Henriksen, Z ;
Sorensen, OH ;
Civitelli, R .
STEROIDS, 2004, 69 (04) :219-226
[14]   Natural genetic variation in whole-genome expression in Arabidopsis thaliana:: the impact of physiological QTL introgression [J].
Juenger, TE ;
Wayne, T ;
Boles, S ;
Symonds, VV ;
Mckay, J ;
Coughlan, SJ .
MOLECULAR ECOLOGY, 2006, 15 (05) :1351-1365
[15]  
Kerr M K, 2001, Biostatistics, V2, P183, DOI 10.1093/biostatistics/2.2.183
[16]  
Kerr MK, 2002, STAT SINICA, V12, P203
[17]   Analysis of variance for gene expression microarray data [J].
Kerr, MK ;
Martin, M ;
Churchill, GA .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2000, 7 (06) :819-837
[18]   BMP-2-induced Osterix expression is mediated by Dlx5 but is independent of Runx2 [J].
Lee, MH ;
Kwon, TG ;
Park, HS ;
Wozney, JM ;
Ryoo, HM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 309 (03) :689-694
[19]   High density synthetic oligonucleotide arrays [J].
Lipshutz, RJ ;
Fodor, SPA ;
Gingeras, TR ;
Lockhart, DJ .
NATURE GENETICS, 1999, 21 (Suppl 1) :20-24
[20]   Interactive exploration of microarray gene expression patterns in a reduced dimensional space [J].
Misra, J ;
Schmitt, W ;
Hwang, D ;
Hsiao, LL ;
Gullans, S ;
Stephanopoulos, G ;
Stephanopoulos, G .
GENOME RESEARCH, 2002, 12 (07) :1112-1120