Skip Navigation

Bioinformatics 2005 21(Suppl 2):ii204-ii205; doi:10.1093/bioinformatics/bti1132
This Article
Right arrow FREE Full Text (Print PDF) Freely available
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 (1)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Schwartz, J.-M.
Right arrow Articles by Kanehisa, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schwartz, J.-M.
Right arrow Articles by Kanehisa, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2005. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions{at}oxfordjournals.org

A quadratic programming approach for decomposing steady-state metabolic flux distributions onto elementary modes

Jean-Marc Schwartz * and Minoru Kanehisa

Bioinformatics Center, Institute for Chemical Research, Kyoto University Uji, Kyoto 611-0011, Japan

*To whom correspondence should be addressed.

Motivation: It is known that steady-state flux distributions in metabolic networks can be expressed as non-negative combinations of elementary modes. However, little understanding has been achieved so far in how individual elementary modes contribute to the reconstruction of actual physiological flux distributions.

Results: We introduce an approach for decomposing steady-state flux distributions onto elementary modes based on quadratic programming. The decomposition is performed so as to favour modes that are closest to the actual state of the system, i.e. most relevant for biological interpretation. As an illustration, an application of this approach to a model of yeast glycolysis is presented.

Availability: Software is available upon request from the authors.

Contact: jean{at}kuicr.kyoto-u.ac.jp



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




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.