Evidence map›Paper›PMID 42174433›Full record

ArticleBMC bioinformatics2026

Selecting methods for draft GEM generation in multicellular eukaryotes: a comparative analysis.

Natalia E Jiménez, Mikael Espinoza, Sebastián Mejías, Sebastián N Mendoza, Ignacia Segovia, J Cristian Salgado, Carlos Conca, Ziomara P Gerdtzen

Abstract readComparative Study
In one paragraph

Article in BMC bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Natalia E JiménezInstitute for Biological and Medical Engineering, Pontificia Universidad Católica de Chile, Santiago, Chile. natalia.jimenez@uc.cl.ORCID http://orcid.org/0000-0003-2084-1256
Mikael EspinozaDepartment of Chemical Engineering, Biotechnology and Materials, Faculty of Physical and Mathematical Sciences (DIQBM), University of Chile, Santiago, Chile.
Sebastián MejíasDepartment of Chemical Engineering, Biotechnology and Materials, Faculty of Physical and Mathematical Sciences (DIQBM), University of Chile, Santiago, Chile.
Sebastián N MendozaCenter for Mathematical Modeling (CMM), University of Chile, Santiago, Chile.ORCID http://orcid.org/0000-0002-2192-5569
Ignacia SegoviaDepartment of Chemical Engineering, Biotechnology and Materials, Faculty of Physical and Mathematical Sciences (DIQBM), University of Chile, Santiago, Chile.
J Cristian SalgadoDepartment of Chemical Engineering, Biotechnology and Materials, Faculty of Physical and Mathematical Sciences (DIQBM), University of Chile, Santiago, Chile.
Carlos ConcaCentre for Biotechnology and Bioengineering (CeBiB), University of Chile, Santiago, Chile.
Ziomara P GerdtzenDepartment of Chemical Engineering, Biotechnology and Materials, Faculty of Physical and Mathematical Sciences (DIQBM), University of Chile, Santiago, Chile.ORCID http://orcid.org/0000-0002-7486-8537

Funding

Agencia Nacional de Investigación y Desarrollo CMM FB210005Agencia Nacional de Investigación y Desarrollo NCN2021033Agencia Nacional de Investigación y Desarrollo STIC190013
6 · The paper itself

Abstract

Motivated by the applications of genome-scale metabolic models (GEMs) for biological discovery and metabolic engineering, several approaches have been developed for automatic generation of draft GEMs. However, most of these methods are not optimized for their use in multicellular eukaryotes and their performance for this task is unclear. In this work we present a comparative analysis of seven automated reconstruction tools (AuReMe, CarveMe, merlin, ModelSEED, Pathway Tools, RAVEN and Reconstructor) applied to three multicellular eukaryotes: the mosquito Aedes aegypti, the CHO (Chinese Hamster Ovary) cell line from Cricetulus griseus and the brown algae Ectocarpus siliculosus. Evaluation of these tools was based on metrics for network size, functionality, consistency, representation of organelle-specific functions and organism-specific metabolites, annotation quality and execution time. We find that methods differ strongly in a trade-off between model functionality and representation of eukaryotic features such as compartmentalization and organism-specific metabolism, with no single approach excelling at both. Our work aims at providing a practical resource to guide researchers in selecting methods for draft generation tailored to organism characteristics and research goals.

Indexed as

Models, BiologicalAnimalsCHO CellsCricetinaeCricetulusGenomeMetabolic Networks and PathwaysPhaeophyceaeAutomated reconstructionGenome-scale modelsMetabolic modelsMulticellular eukaryotes

Identifiers

PMID42174433
PMCPMC13390297

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