Evidence map›Paper›PMID 37402625›Full record

ArticleBioinformatics (Oxford, England)2023

COVRECON: automated integration of genome- and metabolome-scale network reconstruction and data-driven inverse modeling of metabolic interaction networks.

Jiahang Li, Steffen Waldherr, Wolfram Weckwerth

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Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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  6. Millets for a sustainable future.Journal of experimental botany · 2025
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jiahang LiMolecular Systems Biology Lab (MOSYS), Department of Functional and Evolutionary Ecology (FEE), University of Vienna, Djerassiplatz 1, 1030 Vienna, Austria.ORCID 0000-0001-9544-5544
Steffen WaldherrMolecular Systems Biology Lab (MOSYS), Department of Functional and Evolutionary Ecology (FEE), University of Vienna, Djerassiplatz 1, 1030 Vienna, Austria.ORCID 0000-0002-0936-579X
Wolfram WeckwerthMolecular Systems Biology Lab (MOSYS), Department of Functional and Evolutionary Ecology (FEE), University of Vienna, Djerassiplatz 1, 1030 Vienna, Austria.ORCID 0000-0002-9719-6358

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationOne central goal of systems biology is to infer biochemical regulations from large-scale OMICS data. Many aspects of cellular physiology and organismal phenotypes can be understood as results of metabolic interaction network dynamics. Previously, we have proposed a convenient mathematical method, which addresses this problem using metabolomics data for the inverse calculation of biochemical Jacobian matrices revealing regulatory checkpoints of biochemical regulations. The proposed algorithms for this inference are limited by two issues: they rely on structural network information that needs to be assembled manually, and they are numerically unstable due to ill-conditioned regression problems for large-scale metabolic networks.

resultsTo address these problems, we developed a novel regression loss-based inverse Jacobian algorithm, combining metabolomics COVariance and genome-scale metabolic RECONstruction, which allows for a fully automated, algorithmic implementation of the COVRECON workflow. It consists of two parts: (i) Sim-Network and (ii) inverse differential Jacobian evaluation. Sim-Network automatically generates an organism-specific enzyme and reaction dataset from Bigg and KEGG databases, which is then used to reconstruct the Jacobian's structure for a specific metabolomics dataset. Instead of directly solving a regression problem as in the previous workflow, the new inverse differential Jacobian is based on a substantially more robust approach and rates the biochemical interactions according to their relevance from large-scale metabolomics data. The approach is illustrated by in silico stochastic analysis with differently sized metabolic networks from the BioModels database and applied to a real-world example. The characteristics of the COVRECON implementation are that (i) it automatically reconstructs a data-driven superpathway model; (ii) more general network structures can be investigated, and (iii) the new inverse algorithm improves stability, decreases computation time, and extends to large-scale models. AVAILABILITY AND IMPLEMENTATION: The code is available in the website https://bitbucket.org/mosys-univie/covrecon.

Indexed as

Metabolic Networks and PathwaysMetabolomeAlgorithmsGenomeMetabolomics

Identifiers

PMID37402625
PMCPMC10356784

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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.