Flux Variability Analysis (FVA) is an important method to analyze the range of fluxes of a metabolic network. FVA consists in performing a large number of independent optimization problems, to obtain the maximum and minimum flux through each reaction in the network. Although several strategies to make the computation more efficient have been proposed, the computation time of an FVA can still be limiting. We present a two-step procedure to accelerate the FVA computational time that exploits the large presence within metabolic networks of sets of reactions that necessarily have an identical optimal flux value or only differ by a multiplication constant. The first step identifies such sets of reactions. The second step computes the maximum and minimum flux value for just one element of each of set, reducing the total number of optimization problems compared to the classical FVA. We show that, when applied to any metabolic network model included in the BiGG database, our FVA algorithm reduces the total number of optimization problems of about 35 %, and the computation time of FVA of about 30%.
Galuzzi, B., Damiani, C. (2023). An Efficient Implementation of Flux Variability Analysis for Metabolic Networks. In Artificial Life and Evolutionary Computation - 16th Italian Workshop, WIVACE 2022, Gaeta, Italy, September 14–16, 2022, Revised Selected Papers (pp.58-69). Springer [10.1007/978-3-031-31183-3_5].
An Efficient Implementation of Flux Variability Analysis for Metabolic Networks
Galuzzi, BG;Damiani, C
2023
Abstract
Flux Variability Analysis (FVA) is an important method to analyze the range of fluxes of a metabolic network. FVA consists in performing a large number of independent optimization problems, to obtain the maximum and minimum flux through each reaction in the network. Although several strategies to make the computation more efficient have been proposed, the computation time of an FVA can still be limiting. We present a two-step procedure to accelerate the FVA computational time that exploits the large presence within metabolic networks of sets of reactions that necessarily have an identical optimal flux value or only differ by a multiplication constant. The first step identifies such sets of reactions. The second step computes the maximum and minimum flux value for just one element of each of set, reducing the total number of optimization problems compared to the classical FVA. We show that, when applied to any metabolic network model included in the BiGG database, our FVA algorithm reduces the total number of optimization problems of about 35 %, and the computation time of FVA of about 30%.File | Dimensione | Formato | |
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