DocumentCode
2401376
Title
The inferelator 2.0: A scalable framework for reconstruction of dynamic regulatory network models
Author
Madar, Aviv ; Greenfield, Alex ; Ostrer, Harry ; Vanden-Eijnden, Eric ; Bonneau, Richard
Author_Institution
Center for Genomics&Syst. Biol., New York Univ., New York, NY, USA
fYear
2009
fDate
3-6 Sept. 2009
Firstpage
5448
Lastpage
5451
Abstract
Current methods for reconstructing biological networks often learn either the topology of large networks or the kinetic parameters of smaller networks with a well-characterized topology. We have recently described a network reconstruction algorithm, the Inferelator 1.0, that given a set of genome-wide measurements as input, simultaneously learns both topology and kinetic-parameters. Specifically, it learns a system of ordinary differential equations (ODEs) that describe the rate of change in transcription of each gene or gene-cluster, as a function of environmental and transcription factors. In order to scale to large networks, in Inferelator 1.0 we have approximated the system of ODEs to be uncoupled, and have solved each ODE using a one-step finite difference approximation. Naturally, these approximations become crude as the simulated time-interval increases. Here we present, implement, and test a new Markov-Chain-Monte-Carlo (MCMC) dynamical modeling method, Inferelator 2.0, that works in tandem with Inferelator 1.0 and is designed to relax these approximations. We show results for the prokaryote Halobacterium that demonstrate a marked improvement in our predictive performance in modeling the regulatory dynamics of the system over longer time-scales.
Keywords
Markov processes; Monte Carlo methods; biology computing; complex networks; data analysis; differential equations; finite difference methods; genomics; microorganisms; network topology; pattern clustering; Inferelator 2.0; Markov-Chain-Monte-Carlo method; biological network learning algorithm; biological network reconstruction algorithm; dynamic regulatory network models; dynamical modeling method; environmental factors; gene-cluster analysis; genome-wide measurements; kinetic parameters; large network topology; one-step finite difference approximation; ordinary differential equations; prokaryote Halobacterium; scalable framework; transcription factors; Algorithms; Bacterial Proteins; Computer Simulation; Feedback, Physiological; Gene Expression Regulation, Bacterial; Halobacterium; Models, Biological; Signal Transduction; Software;
fLanguage
English
Publisher
ieee
Conference_Titel
Engineering in Medicine and Biology Society, 2009. EMBC 2009. Annual International Conference of the IEEE
Conference_Location
Minneapolis, MN
ISSN
1557-170X
Print_ISBN
978-1-4244-3296-7
Electronic_ISBN
1557-170X
Type
conf
DOI
10.1109/IEMBS.2009.5334018
Filename
5334018
Link To Document