Identification of critical genes in microarray experiments by a Neuro-Fuzzy approach

被引:9
作者
Chen, Chin-Fu
Feng, Xin
Szeto, Jack
机构
[1] Clemson Univ, Dept Genet & Biochem, Clemson, SC 29634 USA
[2] Marquette Univ, Dept Elect & Comp Engn, Milwaukee, WI 53233 USA
关键词
gene expression; microarray; gene ontology; artificial networks; fuzzy logic;
D O I
10.1016/j.compbiolchem.2006.08.004
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gene expression profiling by microarray technology is usually difficult to interpret into a simpler pattern. One approach to resolve the complexity of gene expression profiles is the application of artificial neural networks (ANNs). A potential difficulty in this strategy, however, is that the non-linear nature of ANN makes it essentially a 'black-box' computation process. Addition of a fuzzy logic approach is useful because it can complement ANN by explicitly specifying membership function during computation. We employed a hybrid approach of neural network and fuzzy logic to further analyze a published microarray study of gene responses to eight bacteria in human macrophages. The original analysis by hierarchical clustering found common gene responses to all bacteria but did not address individual responses. Our method allowed exploration of the gene response of the host to individual bacterium. We implemented a two-layer, feed-forward neural network containing the principle of 'competitive learning' (i.e. 'winner-take-all'). The weights of the trained neural network were fed into a fuzzy logic inference system. A new measurement, called the impact rating (IR) was also introduced to explore the degree of importance of each gene. To assess the reliability of the IR value, a bootstrap re-sampling method was applied to the dataset and a confidence level for each IR was obtained. Our approach has successfully uncovered the unique features of host response to individual bacterium. Further, application of gene ontology (GO) annotation to the genes of high IR values in each response has suggested new biological pathways for individual host-pathogen interactions. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:372 / 381
页数:10
相关论文
共 33 条
[1]   FatiGO:: a web tool for finding significant associations of Gene Ontology terms with groups of genes [J].
Al-Shahrour, F ;
Díaz-Uriarte, R ;
Dopazo, J .
BIOINFORMATICS, 2004, 20 (04) :578-580
[2]  
[Anonymous], 1998, INTRO BOOTSTRAP
[3]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[4]  
Bose N.K., 1996, Neural Network Fundamentals with Graphs, Algorithms, and Applications
[5]   Exploring the new world of the genome with DNA microarrays [J].
Brown, PO ;
Botstein, D .
NATURE GENETICS, 1999, 21 (Suppl 1) :33-37
[6]   Chips with everything: DNA microarrays in infectious diseases [J].
Bryant, PA ;
Venter, D ;
Robins-Browne, R ;
Curtis, N .
LANCET INFECTIOUS DISEASES, 2004, 4 (02) :100-111
[7]  
Catto JWF, 2003, CLIN CANCER RES, V9, P4172
[8]   Protein motif extraction with neuro-fuzzy optimization [J].
Chang, BCH ;
Halgamuge, SK .
BIOINFORMATICS, 2002, 18 (08) :1084-1090
[9]  
CLINKENBEARD RA, 1992, P 1992 INT JOINT C N, V2, P1223
[10]  
Davidson AC, 1997, BOOTSTRAP METHODS TH