Evidence map›Paper›PMID 31510702›Full record

ArticleBioinformatics (Oxford, England)2019

MCS2: minimal coordinated supports for fast enumeration of minimal cut sets in metabolic networks.

Reza Miraskarshahi, Hooman Zabeti, Tamon Stephen, Leonid Chindelevitch

Open access · hybridAbstract read
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Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Reza MiraskarshahiSchool of Computing Science, Simon Fraser University, Burnaby, BC, Canada.
Hooman ZabetiSchool of Computing Science, Simon Fraser University, Burnaby, BC, Canada.
Tamon StephenDepartment of Mathematics, Simon Fraser University, Burnaby, BC, Canada.
Leonid ChindelevitchSchool of Computing Science, Simon Fraser University, Burnaby, BC, Canada.
Simon Fraser University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationConstraint-based modeling of metabolic networks helps researchers gain insight into the metabolic processes of many organisms, both prokaryotic and eukaryotic. Minimal cut sets (MCSs) are minimal sets of reactions whose inhibition blocks a target reaction in a metabolic network. Most approaches for finding the MCSs in constrained-based models require, either as an intermediate step or as a byproduct of the calculation, the computation of the set of elementary flux modes (EFMs), a convex basis for the valid flux vectors in the network. Recently, Ballerstein et al. proposed a method for computing the MCSs of a network without first computing its EFMs, by creating a dual network whose EFMs are a superset of the MCSs of the original network. However, their dual network is always larger than the original network and depends on the target reaction. Here we propose the construction of a different dual network, which is typically smaller than the original network and is independent of the target reaction, for the same purpose. We prove the correctness of our approach, minimal coordinated support (MCS2), and describe how it can be modified to compute the few smallest MCSs for a given target reaction.

resultsWe compare MCS2 to the method of Ballerstein et al. and two other existing methods. We show that MCS2 succeeds in calculating the full set of MCSs in many models where other approaches cannot finish within a reasonable amount of time. Thus, in addition to its theoretical novelty, our approach provides a practical advantage over existing methods. AVAILABILITY AND IMPLEMENTATION: MCS2 is freely available at https://github.com/RezaMash/MCS under the GNU 3.0 license. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsMetabolic Networks and PathwaysModels, Biological

Identifiers

PMID31510702
PMCPMC6612898
OpenAlexW2956622428

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.