Skip Navigation


Bioinformatics Advance Access first published online on November 5, 2004
This version published online on November 16, 2004

Bioinformatics, doi:10.1093/bioinformatics/bti103
Bioinformatics © Oxford University Press 2004; all rights reserved
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrow All Versions of this Article:
21/8/1644    most recent
bti103v2
bti103v1
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
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 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 arrowRequest Permissions
Google Scholar
Right arrow Articles by Kemmeren, P.
Right arrow Articles by Holstege, F. C. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kemmeren, P.
Right arrow Articles by Holstege, F. C. P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Received August 27, 2004
Revised October 1, 2004
Accepted October 15, 2004

Article

Predicting gene function through systematic analysis and quality assessment of high-throughput data

Patrick Kemmeren 1, Thessa T. J. P. Kockelkorn 1, Theo Bijma 1, Rogier Donders 2, and Frank C. P. Holstege 1*

1 Department of Physiological Chemistry, University Medical Center Utrecht, P.O. box 85060, 3508 AB Utrecht, the Netherlands
2 Department of Innovation Studies, Copernicus Institute, Utrecht University, Utrecht, the Netherlands

* To whom correspondence should be addressed.
Frank C. P. Holstege, E-mail: f.c.p.holstege{at}med.uu.nl


   Abstract

Motivation: Determining gene function is an important challenge arising from the availability of whole genome sequences. Until recently, approaches based on sequence homology were the only high-throughput method for predicting gene function. Use of high-throughput generated experimental datasets for determining gene function has been limited for several reasons.

Results: Here a new approach is presented for integration of high-throughput datasets, leading to prediction of function based on relationships supported by multiple types and sources of data. This is achieved with a database containing 125 different high-throughput datasets describing phenotypes, cellular localizations, protein interactions and mRNA expression levels from S. cerevisiae, using a bit-vector representation and information content based ranking. The approach takes characteristic and qualitative differences between the datasets into account, is highly flexible, efficient and scalable. Database queries result in predictions for 543 uncharacterized genes, based on multiple functional relationships each supported by at least three types of experimental data. Some of these are experimentally verified, further demonstrating their reliability. The results also generate insights into the relative merits of different data types and provide a coherent framework for functional genomic datamining.

Availability: Free availability over the internet.

Supplementary Information: http://www.genomics.med.uu.nl/pub/pk/comb_gen_network.


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
BioinformaticsHome page
Y. Tao, L. Sam, J. Li, C. Friedman, and Y. A. Lussier
Information theory applied to the sparse gene ontology annotation network to predict novel gene function
Bioinformatics, July 1, 2007; 23(13): i529 - i538.
[Abstract] [Full Text] [PDF]


Home page
Phil Trans R Soc BHome page
T. Schlitt and A. Brazma
Modelling in molecular biology: describing transcription regulatory networks at different scales
Phil Trans R Soc B, March 29, 2006; 361(1467): 483 - 494.
[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.