Evidence map›Paper›PMID 31391098›Full record

ArticleGenome biology2019

A systematic assessment of current genome-scale metabolic reconstruction tools.

Sebastián N Mendoza, Brett G Olivier, Douwe Molenaar, Bas Teusink

Abstract readEvaluation Study
In one paragraph

Article in Genome biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed, 2 pooled it
–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

120 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  5. Nutrient control enables metabolic reconstruction ofbioRxiv : the preprint server for biology · 2026
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  19. Evaluating Metabolic Support in Pairwise Microbial Communities Using MetQuest.Methods in molecular biology (Clifton, N.J.) · 2026
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60 more citing papers are in PubMed but not listed here.

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

4 authors.

Sebastián N MendozaSystems Bioinformatics, AIMMS, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Brett G OlivierSystems Bioinformatics, AIMMS, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Douwe MolenaarSystems Bioinformatics, AIMMS, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Bas TeusinkSystems Bioinformatics, AIMMS, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands. b.teusink@vu.nl.ORCID 0000-0003-3929-0423

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral genome-scale metabolic reconstruction software platforms have been developed and are being continuously updated. These tools have been widely applied to reconstruct metabolic models for hundreds of microorganisms ranging from important human pathogens to species of industrial relevance. However, these platforms, as yet, have not been systematically evaluated with respect to software quality, best potential uses and intrinsic capacity to generate high-quality, genome-scale metabolic models. It is therefore unclear for potential users which tool best fits the purpose of their research.

resultsIn this work, we perform a systematic assessment of current genome-scale reconstruction software platforms. To meet our goal, we first define a list of features for assessing software quality related to genome-scale reconstruction. Subsequently, we use the feature list to evaluate the performance of each tool. To assess the similarity of the draft reconstructions to high-quality models, we compare each tool's output networks with that of the high-quality, manually curated, models of Lactobacillus plantarum and Bordetella pertussis, representatives of gram-positive and gram-negative bacteria, respectively. We additionally compare draft reconstructions with a model of Pseudomonas putida to further confirm our findings. We show that none of the tools outperforms the others in all the defined features.

conclusionsModel builders should carefully choose a tool (or combinations of tools) depending on the intended use of the metabolic model. They can use this benchmark study as a guide to select the best tool for their research. Finally, developers can also benefit from this evaluation by getting feedback to improve their software.

Indexed as

Genome, BacterialSoftwareBacteriaBordetella pertussisGenes, BacterialLactiplantibacillus plantarumMetabolic Networks and PathwaysPseudomonas putidaBordetella pertussisGenome-scale metabolic modelsGenome-scale metabolic reconstructionLactobacillus plantarumPseudomonas putidaSystematic evaluation

Identifiers

PMID31391098
PMCPMC6685185

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Textmetadata
LicenceCC BY
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Registered trials

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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.