Treffer: Using formal concept analysis for microarray data comparison.

Title:
Using formal concept analysis for microarray data comparison.
Authors:
Choi V; Department of Computer Science, Virginia Tech, 660 McBryde Hall, Blacksburg, VA 24061, USA. vchoi@cs.vt.edu, Huang Y, Lam V, Potter D, Laubenbacher R, Duca K
Source:
Journal of bioinformatics and computational biology [J Bioinform Comput Biol] 2008 Feb; Vol. 6 (1), pp. 65-75.
Publication Type:
Journal Article
Language:
English
Journal Info:
Publisher: World Scientific Publishing Europe Ltd Country of Publication: Singapore NLM ID: 101187344 Publication Model: Print Cited Medium: Print ISSN: 0219-7200 (Print) Linking ISSN: 02197200 NLM ISO Abbreviation: J Bioinform Comput Biol Subsets: MEDLINE
Imprint Name(s):
Publication: [Singapore] : World Scientific Publishing Europe Ltd.
Original Publication: London : Imperial College Press, c2003-
Entry Date(s):
Date Created: 20080308 Date Completed: 20080724 Latest Revision: 20191110
Update Code:
20250114
DOI:
10.1142/s021972000800328x
PMID:
18324746
Database:
MEDLINE

Weitere Informationen

Microarray technologies, which can measure tens of thousands of gene expression values simultaneously in a single experiment, have become a common research method for biomedical researchers. Computational tools to analyze microarray data for biological discovery are needed. In this paper, we investigate the feasibility of using formal concept analysis (FCA) as a tool for microarray data analysis. The method of FCA builds a (concept) lattice from the experimental data together with additional biological information. For microarray data, each vertex of the lattice corresponds to a subset of genes that are grouped together according to their expression values and some biological information related to gene function. The lattice structure of these gene sets might reflect biological relationships in the dataset. Similarities and differences between experiments can then be investigated by comparing their corresponding lattices according to various graph measures. We apply our method to microarray data derived from influenza-infected mouse lung tissue and healthy controls. Our preliminary results show the promise of our method as a tool for microarray data analysis.