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Cardinality optimization in constraint-based modelling: application to human metabolism

MOTIVATION: Several applications in constraint-based modelling can be mathematically formulated as cardinality optimization problems involving the minimization or maximization of the number of nonzeros in a vector. These problems include testing for stoichiometric consistency, testing for flux consi...

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Autores principales: Fleming, Ronan M T, Haraldsdottir, Hulda S, Minh, Le Hoai, Vuong, Phan Tu, Hankemeier, Thomas, Thiele, Ines
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495685/
https://www.ncbi.nlm.nih.gov/pubmed/37697651
http://dx.doi.org/10.1093/bioinformatics/btad450
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author Fleming, Ronan M T
Haraldsdottir, Hulda S
Minh, Le Hoai
Vuong, Phan Tu
Hankemeier, Thomas
Thiele, Ines
author_facet Fleming, Ronan M T
Haraldsdottir, Hulda S
Minh, Le Hoai
Vuong, Phan Tu
Hankemeier, Thomas
Thiele, Ines
author_sort Fleming, Ronan M T
collection PubMed
description MOTIVATION: Several applications in constraint-based modelling can be mathematically formulated as cardinality optimization problems involving the minimization or maximization of the number of nonzeros in a vector. These problems include testing for stoichiometric consistency, testing for flux consistency, testing for thermodynamic flux consistency, computing sparse solutions to flux balance analysis problems and computing the minimum number of constraints to relax to render an infeasible flux balance analysis problem feasible. Such cardinality optimization problems are computationally complex, with no known polynomial time algorithms capable of returning an exact and globally optimal solution. RESULTS: By approximating the zero-norm with nonconvex continuous functions, we reformulate a set of cardinality optimization problems in constraint-based modelling into a difference of convex functions. We implemented and numerically tested novel algorithms that approximately solve the reformulated problems using a sequence of convex programs. We applied these algorithms to various biochemical networks and demonstrate that our algorithms match or outperform existing related approaches. In particular, we illustrate the efficiency and practical utility of our algorithms for cardinality optimization problems that arise when extracting a model ready for thermodynamic flux balance analysis given a human metabolic reconstruction. AVAILABILITY AND IMPLEMENTATION: Open source scripts to reproduce the results are here https://github.com/opencobra/COBRA.papers/2023_cardOpt with general purpose functions integrated within the COnstraint-Based Reconstruction and Analysis toolbox: https://github.com/opencobra/cobratoolbox.
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spelling pubmed-104956852023-09-13 Cardinality optimization in constraint-based modelling: application to human metabolism Fleming, Ronan M T Haraldsdottir, Hulda S Minh, Le Hoai Vuong, Phan Tu Hankemeier, Thomas Thiele, Ines Bioinformatics Original Paper MOTIVATION: Several applications in constraint-based modelling can be mathematically formulated as cardinality optimization problems involving the minimization or maximization of the number of nonzeros in a vector. These problems include testing for stoichiometric consistency, testing for flux consistency, testing for thermodynamic flux consistency, computing sparse solutions to flux balance analysis problems and computing the minimum number of constraints to relax to render an infeasible flux balance analysis problem feasible. Such cardinality optimization problems are computationally complex, with no known polynomial time algorithms capable of returning an exact and globally optimal solution. RESULTS: By approximating the zero-norm with nonconvex continuous functions, we reformulate a set of cardinality optimization problems in constraint-based modelling into a difference of convex functions. We implemented and numerically tested novel algorithms that approximately solve the reformulated problems using a sequence of convex programs. We applied these algorithms to various biochemical networks and demonstrate that our algorithms match or outperform existing related approaches. In particular, we illustrate the efficiency and practical utility of our algorithms for cardinality optimization problems that arise when extracting a model ready for thermodynamic flux balance analysis given a human metabolic reconstruction. AVAILABILITY AND IMPLEMENTATION: Open source scripts to reproduce the results are here https://github.com/opencobra/COBRA.papers/2023_cardOpt with general purpose functions integrated within the COnstraint-Based Reconstruction and Analysis toolbox: https://github.com/opencobra/cobratoolbox. Oxford University Press 2023-09-11 /pmc/articles/PMC10495685/ /pubmed/37697651 http://dx.doi.org/10.1093/bioinformatics/btad450 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Fleming, Ronan M T
Haraldsdottir, Hulda S
Minh, Le Hoai
Vuong, Phan Tu
Hankemeier, Thomas
Thiele, Ines
Cardinality optimization in constraint-based modelling: application to human metabolism
title Cardinality optimization in constraint-based modelling: application to human metabolism
title_full Cardinality optimization in constraint-based modelling: application to human metabolism
title_fullStr Cardinality optimization in constraint-based modelling: application to human metabolism
title_full_unstemmed Cardinality optimization in constraint-based modelling: application to human metabolism
title_short Cardinality optimization in constraint-based modelling: application to human metabolism
title_sort cardinality optimization in constraint-based modelling: application to human metabolism
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495685/
https://www.ncbi.nlm.nih.gov/pubmed/37697651
http://dx.doi.org/10.1093/bioinformatics/btad450
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