BMC Bioinformatics

official impact factor 3.03

Open Access Highly Access Methodology article

SynTReN: a generator of synthetic gene expression data for design and analysis of structure learning algorithms

Tim Van den Bulcke1, Koenraad Van Leemput2, Bart Naudts2, Piet van Remortel2, Hongwu Ma3, Alain Verschoren2, Bart De Moor1 and Kathleen Marchal1,4*

Author Affiliations

1 ESAT-SCD, K.U.Leuven, Kasteelpark Arenberg 10, B-3001 Heverlee, Belgium

2 ISLab, Dept. Math. and Comp. Sc., University of Antwerp, Middelheimlaan 1, B-2020 Antwerpen, Belgium

3 Dept. of Genome Analysis, German Research Center for Biotechnology, Mascheroder Weg 1, D-38124 Braunschweig, Germany

4 CMPG, Dept. Microbial and Molecular Systems, K.U.Leuven, Kasteelpark Arenberg 20, B-3001 Heverlee, Belgium

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BMC Bioinformatics 2006, 7:43 doi:10.1186/1471-2105-7-43

Published: 26 January 2006

Abstract

Background

The development of algorithms to infer the structure of gene regulatory networks based on expression data is an important subject in bioinformatics research. Validation of these algorithms requires benchmark data sets for which the underlying network is known. Since experimental data sets of the appropriate size and design are usually not available, there is a clear need to generate well-characterized synthetic data sets that allow thorough testing of learning algorithms in a fast and reproducible manner.

Results

In this paper we describe a network generator that creates synthetic transcriptional regulatory networks and produces simulated gene expression data that approximates experimental data. Network topologies are generated by selecting subnetworks from previously described regulatory networks. Interaction kinetics are modeled by equations based on Michaelis-Menten and Hill kinetics. Our results show that the statistical properties of these topologies more closely approximate those of genuine biological networks than do those of different types of random graph models. Several user-definable parameters adjust the complexity of the resulting data set with respect to the structure learning algorithms.

Conclusion

This network generation technique offers a valid alternative to existing methods. The topological characteristics of the generated networks more closely resemble the characteristics of real transcriptional networks. Simulation of the network scales well to large networks. The generator models different types of biological interactions and produces biologically plausible synthetic gene expression data.