Evaluation of experimental designs for two-color cDNA microarrays

被引:3
作者
Yang, CW
Hsiao, CF
Chou, CK [1 ]
机构
[1] Chang Gung Univ, Dept Life Sci, Taoyuan 333, Taiwan
[2] Natl Yang Ming Univ, Inst Biochem, Taipei 112, Taiwan
[3] Natl Hlth Res Inst, Div Biostat & Bioinformat, Zhunan Town 350, Taiwan
[4] Natl Hlth Res Inst, Div Mol & Genom Med, Zhunan Town 350, Taiwan
[5] Vet Gen Hosp Taipei, Dept Med Res & Educ, Taipei 112, Taiwan
[6] Natl Taipei Coll Nursing, Taipei 112, Taiwan
关键词
cDNA microarray; experimental design; gene expression profile;
D O I
10.1089/cmb.2005.12.1202
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The major goal of two-color cDNA microarray experiments is to measure the relative gene expression level (i.e., relative amount of mRNA) of each gene between samples in studies of gene expression. More specifically, given an N-sample experiment, we need all N(N-1)/2 relative expression levels of all sample pairs of each gene for identification of the differentially expressed genes and for clustering of gene expression patterns. However, the intensities observed from two-color cDNA microarray experiments do not simply represent the relative gene expression level. They are composed of signal (gene expression level), noise, and other factors. In discussions on the experimental design of two-color cDNA microarray experiments, little attention has been given to the fact that different combinations of test and control samples will produce microarray intensities data with varying intrinsic composition of factors. As a consequence, not all experimental designs for two-color cDNA microarray experiments are able to provide all possible relative gene expression levels. This phenomenon has never been addressed. To obtain all possible relative gene expression levels, a novel method for two-color cDNA microarray experimental design evaluation is necessary that will allow the making of an accurate choice. In this study, we propose a model-based approach to illustrate how the factor composition of microarray intensities changed with different experimental designs in two-color cDNA microarray experiments. By analyzing 12 experimental designs (including 5 general forms), we demonstrate that not all experimental designs are able to provide all possible relative gene expression levels due to the differences in factor composition. Our results indicate that whether an experimental design can provide all possible relative expression levels of all sample pairs for each gene should be the first criterion to be considered in an evaluation of experimental designs for two-color cDNA microarray experiments.
引用
收藏
页码:1202 / 1220
页数:19
相关论文
共 39 条
[11]   Cyclin F is degraded during G2-M by mechanisms fundamentally different from other cyclins [J].
Fung, TK ;
Sin, WY ;
Yam, CH ;
Lau, A ;
Poon, RYC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (38) :35140-35149
[12]   Diversity of gene expression in adenocarcinoma of the lung [J].
Garber, ME ;
Troyanskaya, OG ;
Schluens, K ;
Petersen, S ;
Thaesler, Z ;
Pacyna-Gengelbach, M ;
van de Rijn, M ;
Rosen, GD ;
Perou, CM ;
Whyte, RI ;
Altman, RB ;
Brown, PO ;
Botstein, D ;
Petersen, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13784-13789
[13]   Better therapeutics through microarrays [J].
Gerhold, DL ;
Jensen, RV ;
Gullans, SR .
NATURE GENETICS, 2002, 32 (Suppl 4) :547-552
[14]   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
[15]   Unfolding of microarray data [J].
Goryachev, AB ;
MacGregor, PF ;
Edwards, AM .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2001, 8 (04) :443-461
[16]   Cag pathogenicity island-specific responses of gastric epithelial cells to Helicobacter pylori infection [J].
Guillemin, K ;
Salama, NR ;
Tompkins, LS ;
Falkow, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (23) :15136-15141
[17]   Gene expression patterns in renal cell carcinoma assessed by complementary DNA microarray [J].
Higgins, JPT ;
Shinghal, R ;
Gill, H ;
Reese, JH ;
Terris, M ;
Cohen, RJ ;
Fero, M ;
Pollack, JR ;
van de Rijn, M ;
Brooks, JD .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (03) :925-932
[18]   Options available - from start to finish - for obtaining data from DNA microarrays [J].
Holloway, AJ ;
van Laar, RK ;
Tothill, RW ;
Bowtell, DDL .
NATURE GENETICS, 2002, 32 (Suppl 4) :481-489
[19]   The transcriptional program in the response of human fibroblasts to serum [J].
Iyer, VR ;
Eisen, MB ;
Ross, DT ;
Schuler, G ;
Moore, T ;
Lee, JCF ;
Trent, JM ;
Staudt, LM ;
Hudson, J ;
Boguski, MS ;
Lashkari, D ;
Shalon, D ;
Botstein, D ;
Brown, PO .
SCIENCE, 1999, 283 (5398) :83-87
[20]   Comprehensive analysis of the gene expression profiles in human gastric cancer cell lines [J].
Ji, JF ;
Chen, X ;
Leung, SY ;
Chi, JTA ;
Chu, KM ;
Yuen, ST ;
Li, R ;
Chan, ASY ;
Li, JY ;
Dunphy, N ;
So, S .
ONCOGENE, 2002, 21 (42) :6549-6556