scholarly journals Metabolic Networks, Elementary Flux Modes, and Polyhedral Cones

2021 ◽  
Author(s):  
Isaac Klapper ◽  
Daniel B. Szyld ◽  
Kai Zhao
2020 ◽  
Vol 36 (14) ◽  
pp. 4163-4170
Author(s):  
Francisco Guil ◽  
José F Hidalgo ◽  
José M García

Abstract Motivation Elementary flux modes (EFMs) are a key tool for analyzing genome-scale metabolic networks, and several methods have been proposed to compute them. Among them, those based on solving linear programming (LP) problems are known to be very efficient if the main interest lies in computing large enough sets of EFMs. Results Here, we propose a new method called EFM-Ta that boosts the efficiency rate by analyzing the information provided by the LP solver. We base our method on a further study of the final tableau of the simplex method. By performing additional elementary steps and avoiding trivial solutions consisting of two cycles, we obtain many more EFMs for each LP problem posed, improving the efficiency rate of previously proposed methods by more than one order of magnitude. Availability and implementation Software is freely available at https://github.com/biogacop/Boost_LP_EFM. Contact [email protected] Supplementary information Supplementary data are available at Bioinformatics online.


2015 ◽  
Vol 31 (13) ◽  
pp. 2232-2234 ◽  
Author(s):  
Matthias P. Gerstl ◽  
Christian Jungreuthmayer ◽  
Jürgen Zanghellini

2009 ◽  
Vol 25 (23) ◽  
pp. 3158-3165 ◽  
Author(s):  
Luis F. de Figueiredo ◽  
Adam Podhorski ◽  
Angel Rubio ◽  
Christoph Kaleta ◽  
John E. Beasley ◽  
...  

2007 ◽  
Vol 97 (6) ◽  
pp. 1535-1549 ◽  
Author(s):  
Intawat Nookaew ◽  
Asawin Meechai ◽  
Chinae Thammarongtham ◽  
Kobkul Laoteng ◽  
Vasimon Ruanglek ◽  
...  

2019 ◽  
Author(s):  
Annika Röhl ◽  
Alexander Bockmayr

AbstractMetabolic network reconstructions are widely used in computational systems biology for in silico studies of cellular metabolism. A common approach to analyse these models are elementary flux modes (EFMs), which correspond to minimal functional units in the network. Already for medium-sized networks, it is often impossible to compute the set of all EFMs, due to their huge number. From a practical point of view, this might also not be necessary because a subset of EFMs may already be sufficient to answer relevant biological questions. In this article, we study MEMos or minimum sets of EFMs that can generate all possible steady-state behaviours of a metabolic network. The number of EFMs in a MEMo may be by several orders of magnitude smaller than the total number of EFMs. Using MEMos, we can compute generating sets of EFMs in metabolic networks where the whole set of EFMs is too large to be enumerated.


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