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Francisco Guil 0002

dblp:160/8041 · also Francisco De Asís Guil Asensio · DBLP profile ↗
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2ranked-venue papers
2as first author
1since 2021 · last 2023
0000-0002-6846-1888ORCID · verified

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 2 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 100%
Theoretical computer science
1 paper
Mathematical optimization · 100%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › systems biology
metabolic network analysis
1.122023
On the representativeness and stability of a set of EFMs · Bioinform. 2023
Boosting the extraction of elementary flux modes in genome-scale metabolic networks using the linear programming approach · Bioinform. 2020
Bioinformatics and computational biology › systems biology › metabolic network analysis
elementary flux modes
0.712023
On the representativeness and stability of a set of EFMs · Bioinform. 2023
Bioinformatics and computational biology › systems biology › metabolic network analysis
elementary flux mode computation
0.412020
Boosting the extraction of elementary flux modes in genome-scale metabolic networks using the linear programming approach · Bioinform. 2020
Mathematical optimization
linear programming
0.412020
Boosting the extraction of elementary flux modes in genome-scale metabolic networks using the linear programming approach · Bioinform. 2020
Bioinformatics and computational biology › systems biology › metabolic network analysis
genome-scale metabolic model analysis
0.112020
Boosting the extraction of elementary flux modes in genome-scale metabolic networks using the linear programming approach · Bioinform. 2020

Methods — techniques the papers use, named apart from their topics

simplex method · 0.9linear programming · 0.9elementary flux modes · 0.9elementary flux mode computation · 0.7
YearPublicationVenuePosition
2023 On the representativeness and stability of a set of EFMs
abstract
MOTIVATION: Elementary flux modes are a well-known tool for analyzing metabolic networks. The whole set of elementary flux modes (EFMs) cannot be computed in most genome-scale networks due to their large cardinality. Therefore, different methods have been proposed to compute a smaller subset of EFMs that can be used for studying the structure of the network. These latter methods pose the problem of studying the representativeness of the calculated subset. In this article, we present a methodology to tackle this problem. RESULTS: We have introduced the concept of stability for a particular network parameter and its relation to the representativeness of the EFM extraction method studied. We have also defined several metrics to study and compare the EFM biases. We have applied these techniques to compare the relative behavior of previously proposed methods in two case studies. Furthermore, we have presented a new method for the EFM computation (PiEFM), which is more stable (less biased) than previous ones, has suitable representativeness measures, and exhibits better variability in the extracted EFMs. AVAILABILITY AND IMPLEMENTATION: Software and additional material are freely available at https://github.com/biogacop/PiEFM.
Francisco Guil 0002, José F. Hidalgo, José M. García 0001
Bioinform.1
2020 Boosting the extraction of elementary flux modes in genome-scale metabolic networks using the linear programming approach
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.
Francisco Guil 0002, José F. Hidalgo, José M. García 0001
Bioinform.1