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An improved algorithm for flux variability analysis
Flux balance analysis (FBA) is an optimization based approach to find the optimal steady state of a metabolic network, commonly of microorganisms such as yeast strains and Escherichia coli. However, the resulting solution from an FBA is typically not unique, as the optimization problem is, more ofte...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761963/ https://www.ncbi.nlm.nih.gov/pubmed/36536290 http://dx.doi.org/10.1186/s12859-022-05089-9 |
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author | Kenefake, Dustin Armingol, Erick Lewis, Nathan E. Pistikopoulos, Efstratios N. |
author_facet | Kenefake, Dustin Armingol, Erick Lewis, Nathan E. Pistikopoulos, Efstratios N. |
author_sort | Kenefake, Dustin |
collection | PubMed |
description | Flux balance analysis (FBA) is an optimization based approach to find the optimal steady state of a metabolic network, commonly of microorganisms such as yeast strains and Escherichia coli. However, the resulting solution from an FBA is typically not unique, as the optimization problem is, more often than not, degenerate. Flux variability analysis (FVA) is a method to determine the range of possible reaction fluxes that still satisfy, within some optimality factor, the original FBA problem. The resulting range of reaction fluxes can be utilized to determine metabolic reactions of high importance, amongst other analyses. In the literature, this has been done by solving [Formula: see text] linear programs (LPs), with n being the number of reactions in the metabolic network. However, FVA can be solved with less than [Formula: see text] LPs by utilizing the basic feasible solution property of bounded LPs to reduce the number of LPs that are needed to be solved. In this work, a new algorithm is proposed to solve FVA that requires less than [Formula: see text] LPs. The proposed algorithm is benchmarked on a problem set of 112 metabolic network models ranging from single cell organisms (iMM904, ect) to a human metabolic system (Recon3D). Showing a reduction in the number of LPs required to solve the FVA problem and thus the time to solve an FVA problem. |
format | Online Article Text |
id | pubmed-9761963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97619632022-12-20 An improved algorithm for flux variability analysis Kenefake, Dustin Armingol, Erick Lewis, Nathan E. Pistikopoulos, Efstratios N. BMC Bioinformatics Research Flux balance analysis (FBA) is an optimization based approach to find the optimal steady state of a metabolic network, commonly of microorganisms such as yeast strains and Escherichia coli. However, the resulting solution from an FBA is typically not unique, as the optimization problem is, more often than not, degenerate. Flux variability analysis (FVA) is a method to determine the range of possible reaction fluxes that still satisfy, within some optimality factor, the original FBA problem. The resulting range of reaction fluxes can be utilized to determine metabolic reactions of high importance, amongst other analyses. In the literature, this has been done by solving [Formula: see text] linear programs (LPs), with n being the number of reactions in the metabolic network. However, FVA can be solved with less than [Formula: see text] LPs by utilizing the basic feasible solution property of bounded LPs to reduce the number of LPs that are needed to be solved. In this work, a new algorithm is proposed to solve FVA that requires less than [Formula: see text] LPs. The proposed algorithm is benchmarked on a problem set of 112 metabolic network models ranging from single cell organisms (iMM904, ect) to a human metabolic system (Recon3D). Showing a reduction in the number of LPs required to solve the FVA problem and thus the time to solve an FVA problem. BioMed Central 2022-12-19 /pmc/articles/PMC9761963/ /pubmed/36536290 http://dx.doi.org/10.1186/s12859-022-05089-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kenefake, Dustin Armingol, Erick Lewis, Nathan E. Pistikopoulos, Efstratios N. An improved algorithm for flux variability analysis |
title | An improved algorithm for flux variability analysis |
title_full | An improved algorithm for flux variability analysis |
title_fullStr | An improved algorithm for flux variability analysis |
title_full_unstemmed | An improved algorithm for flux variability analysis |
title_short | An improved algorithm for flux variability analysis |
title_sort | improved algorithm for flux variability analysis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761963/ https://www.ncbi.nlm.nih.gov/pubmed/36536290 http://dx.doi.org/10.1186/s12859-022-05089-9 |
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