Complete enumeration of elementary flux modes through scalable demand-based subnetwork definition. (3rd February 2014)
- Record Type:
- Journal Article
- Title:
- Complete enumeration of elementary flux modes through scalable demand-based subnetwork definition. (3rd February 2014)
- Main Title:
- Complete enumeration of elementary flux modes through scalable demand-based subnetwork definition
- Authors:
- Hunt, Kristopher A.
Folsom, James P.
Taffs, Reed L.
Carlson, Ross P. - Abstract:
- Abstract : Motivation: Elementary flux mode analysis (EFMA) decomposes complex metabolic network models into tractable biochemical pathways, which have been used for rational design and analysis of metabolic and regulatory networks. However, application of EFMA has often been limited to targeted or simplified metabolic network representations due to computational demands of the method. Results: Division of biological networks into subnetworks enables the complete enumeration of elementary flux modes (EFMs) for metabolic models of a broad range of complexities, including genome-scale. Here, subnetworks are defined using serial dichotomous suppression and enforcement of flux through model reactions. Rules for selecting appropriate reactions to generate subnetworks are proposed and tested; three test cases, including both prokaryotic and eukaryotic network models, verify the efficacy of these rules and demonstrate completeness and reproducibility of EFM enumeration. Division of models into subnetworks is demand-based and automated; computationally intractable subnetworks are further divided until the entire solution space is enumerated. To demonstrate the strategy's scalability, the splitting algorithm was implemented using an EFMA software package (EFMTool) and Windows PowerShell on a 50 node Microsoft high performance computing cluster. Enumeration of the EFMs in a genome-scale metabolic model of a diatom, Phaeodactylum tricornutum, identified ∼2 billion EFMs. The outputAbstract : Motivation: Elementary flux mode analysis (EFMA) decomposes complex metabolic network models into tractable biochemical pathways, which have been used for rational design and analysis of metabolic and regulatory networks. However, application of EFMA has often been limited to targeted or simplified metabolic network representations due to computational demands of the method. Results: Division of biological networks into subnetworks enables the complete enumeration of elementary flux modes (EFMs) for metabolic models of a broad range of complexities, including genome-scale. Here, subnetworks are defined using serial dichotomous suppression and enforcement of flux through model reactions. Rules for selecting appropriate reactions to generate subnetworks are proposed and tested; three test cases, including both prokaryotic and eukaryotic network models, verify the efficacy of these rules and demonstrate completeness and reproducibility of EFM enumeration. Division of models into subnetworks is demand-based and automated; computationally intractable subnetworks are further divided until the entire solution space is enumerated. To demonstrate the strategy's scalability, the splitting algorithm was implemented using an EFMA software package (EFMTool) and Windows PowerShell on a 50 node Microsoft high performance computing cluster. Enumeration of the EFMs in a genome-scale metabolic model of a diatom, Phaeodactylum tricornutum, identified ∼2 billion EFMs. The output represents an order of magnitude increase in EFMs computed compared with other published algorithms and demonstrates a scalable framework for EFMA of most systems. Availability and implementation: http://www.chbe.montana.edu/RossC . Contact: rossc@erc.montana.edu or kristopher.hunt@erc.montana.edu Supplementary Information: Supplemental materials are available at Bioinformatics online. … (more)
- Is Part Of:
- Bioinformatics. Volume 30:Number 11(2014)
- Journal:
- Bioinformatics
- Issue:
- Volume 30:Number 11(2014)
- Issue Display:
- Volume 30, Issue 11 (2014)
- Year:
- 2014
- Volume:
- 30
- Issue:
- 11
- Issue Sort Value:
- 2014-0030-0011-0000
- Page Start:
- 1569
- Page End:
- 1578
- Publication Date:
- 2014-02-03
- Subjects:
- Bioinformatics -- Periodicals
Genomics -- Data processing -- Periodicals
Computational biology -- Periodicals
572.80285 - Journal URLs:
- http://bioinformatics.oxfordjournals.org ↗
http://firstsearch.oclc.org ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/bioinformatics/btu021 ↗
- Languages:
- English
- ISSNs:
- 1367-4803
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2072.348000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12388.xml