Skip Navigation


Bioinformatics Advance Access originally published online on July 12, 2006
Bioinformatics 2006 22(18):2249-2253; doi:10.1093/bioinformatics/btl378
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (Print PDF) Freely available
Right arrowOA All Versions of this Article:
22/18/2249    most recent
btl378v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (5)
Google Scholar
Right arrow Articles by Nam, D.
Right arrow Articles by Chu, I.-S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nam, D.
Right arrow Articles by Chu, I.-S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2006 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (
http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

ADGO: analysis of differentially expressed gene sets using composite GO annotation

Dougu Nam 1, Sang-Bae Kim 1, Seon-Kyu Kim 1, Sungjin Yang 1, Seon-Young Kim 2 and In-Sun Chu 1,*

1 Korean BioInformation Center, Korea Research Institute of Bioscience and Biotechnology, 52 Eoun-dong Yuseong-gu, Daejeon 305-333, Korea
2 Human Genome Laboratory, Genome Research Center, Korea Research Institute of Bioscience and Biotechnology, 52 Eoun-dong Yuseong-gu, Daejeon 305-333, Korea

*To whom correspondence should be addressed.

Motivation: Genes are typically expressed in modular manners in biological processes. Recent studies reflect such features in analyzing gene expression patterns by directly scoring gene sets. Gene annotations have been used to define the gene sets, which have served to reveal specific biological themes from expression data. However, current annotations have limited analytical power, because they are classified by single categories providing only unary information for the gene sets.

Results: Here we propose a method for discovering composite biological themes from expression data. We intersected two annotated gene sets from different categories of Gene Ontology (GO). We then scored the expression changes of all the single and intersected sets. In this way, we were able to uncover, for example, a gene set with the molecular function F and the cellular component C that showed significant expression change, while the changes in individual gene sets were not significant. We provided an exemplary analysis for HIV-1 immune response. In addition, we tested the method on 20 public datasets where we found many ‘filtered’ composite terms the number of which reached ~34% (a strong criterion, 5% significance) of the number of significant unary terms on average. By using composite annotation, we can derive new and improved information about disease and biological processes from expression data.

Availability: We provide a web application (ADGO: http://array.kobic.re.kr/ADGO) for the analysis of differentially expressed gene sets with composite GO annotations. The user can analyze Affymetrix and dual channel array (spotted cDNA and spotted oligo microarray) data for four species: human, mouse, rat and yeast.

Contact: chu{at}kribb.re.kr

Supplementary information: http://array.kobic.re.kr/ADGO


Received on April 18, 2006; revised on July 5, 2006; accepted on July 5, 2006

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
D. W. Huang, B. T. Sherman, and R. A. Lempicki
Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists
Nucleic Acids Res., January 1, 2009; 37(1): 1 - 13.
[Abstract] [Full Text] [PDF]


Home page
Stem CellsHome page
J. M. Doherty, M. J. Geske, T. S. Stappenbeck, and J. C. Mills
Diverse Adult Stem Cells Share Specific Higher-Order Patterns of Gene Expression
Stem Cells, August 1, 2008; 26(8): 2124 - 2130.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
F. Al-Shahrour, J. Carbonell, P. Minguez, S. Goetz, A. Conesa, J. Tarraga, I. Medina, E. Alloza, D. Montaner, and J. Dopazo
Babelomics: advanced functional profiling of transcriptomics, proteomics and genomics experiments
Nucleic Acids Res., July 1, 2008; 36(suppl_2): W341 - W346.
[Abstract] [Full Text] [PDF]


Home page
Brief BioinformHome page
D. Nam and S.-Y. Kim
Gene-set approach for expression pattern analysis
Brief Bioinform, May 1, 2008; 9(3): 189 - 197.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
D. Shriner, T. M. Baye, M. A. Padilla, S. Zhang, L. K. Vaughan, and A. E. Loraine
Commonality of functional annotation: a method for prioritization of candidate genes from genome-wide linkage studies
Nucleic Acids Res., March 27, 2008; 36(4): e26 - e26.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
J. Liu, J. M. Hughes-Oliver, and J. A. Menius Jr
Domain-enhanced analysis of microarray data using GO annotations
Bioinformatics, May 15, 2007; 23(10): 1225 - 1234.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.