Evidence map›Paper›PMID 32316881›Full record

ArticleJournal of the Royal Society, Interface2020

Efficient manipulation and generation of Kirchhoff polynomials for the analysis of non-equilibrium biochemical reaction networks.

Pencho Yordanov, Jörg Stelling

Abstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2020. 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
–field-weighted citation impact
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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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Cycle Network Model of Prostaglandin H Synthase-1.Pharmaceuticals (Basel, Switzerland) · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Pencho YordanovDepartment of Biosystems Science and Engineering and SIB Swiss Institute of Bioinformatics, ETH Zurich, Basel, Switzerland.
Jörg StellingDepartment of Biosystems Science and Engineering and SIB Swiss Institute of Bioinformatics, ETH Zurich, Basel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kirchhoff polynomials are central for deriving symbolic steady-state expressions of models whose dynamics are governed by linear diffusion on graphs. In biology, such models have been unified under a common linear framework subsuming studies across areas such as enzyme kinetics, G-protein coupled receptors, ion channels and gene regulation. Due to 'history dependence' away from thermodynamic equilibrium, these models suffer from a (super) exponential growth in the size of their symbolic steady-state expressions and, respectively, Kirchhoff polynomials. This algebraic explosion has limited applications of the linear framework. However, recent results on the graph-based prime factorization of Kirchhoff polynomials may help subdue the combinatorial complexity. By prime decomposing the graphs contained in an expression of Kirchhoff polynomials and identifying the graphs giving rise to equal polynomials, we formulate a coarse-grained variant of the expression suitable for symbolic simplification. We devise criteria to efficiently test the equality of Kirchhoff polynomials and propose two heuristic algorithms to explicitly generate individual Kirchhoff polynomials in a compressed form; they are inspired by algebraic simplifications but operate on the corresponding graphs. We illustrate the practicality of the developed theory and algorithms for a diverse set of graphs of different sizes and for non-equilibrium gene regulation analyses.

Indexed as

AlgorithmsThermodynamicsgraph Laplacianlinear compartmental modelslinear nonnegative systemsMarkov process master equationmatrix-tree theoremsymbolic steady state

Identifiers

PMID32316881
PMCPMC7211475

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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.