Evidence map›Paper›PMID 39897103›Full record

ArticleNAR genomics and bioinformatics2025

GEMCAT-a new algorithm for gene expression-based prediction of metabolic alterations.

Suraj Sharma, Roland Sauter, Madlen Hotze, Aaron Marcellus Paul Prowatke, Marc Niere, Tobias Kipura, Anna-Sophia Egger, Kathrin Thedieck, Marcel Kwiatkowski, Mathias Ziegler and 1 more

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

11 authors.

Suraj SharmaDepartment of Biomedicine, University of Bergen, 5020 Bergen, Norway.
Roland SauterDepartment of Arctic and Marine Biology, UiT The Arctic University of Norway, 9019 Tromsø, Norway.
Madlen HotzeInstitute of Biochemistry and Center for Molecular Biosciences Innsbruck, University of Innsbruck, A-6020 Innsbruck, Austria.
Aaron Marcellus Paul ProwatkeInstitute of Biochemistry and Center for Molecular Biosciences Innsbruck, University of Innsbruck, A-6020 Innsbruck, Austria.
Marc NiereDepartment of Biomedicine, University of Bergen, 5020 Bergen, Norway.
Tobias KipuraInstitute of Biochemistry and Center for Molecular Biosciences Innsbruck, University of Innsbruck, A-6020 Innsbruck, Austria.
Anna-Sophia EggerInstitute of Biochemistry and Center for Molecular Biosciences Innsbruck, University of Innsbruck, A-6020 Innsbruck, Austria.
Kathrin ThedieckInstitute of Biochemistry and Center for Molecular Biosciences Innsbruck, University of Innsbruck, A-6020 Innsbruck, Austria.
Marcel KwiatkowskiInstitute of Biochemistry and Center for Molecular Biosciences Innsbruck, University of Innsbruck, A-6020 Innsbruck, Austria.
Mathias ZieglerDepartment of Biomedicine, University of Bergen, 5020 Bergen, Norway.
Ines HeilandNeuro-SysMed, Department of Neurology, Haukeland University Hospital, 5021 Bergen, Norway.ORCID 0000-0002-9124-5112

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The interpretation of multi-omics datasets obtained from high-throughput approaches is important to understand disease-related physiological changes and to predict biomarkers in body fluids. We present a new metabolite-centred genome-scale metabolic modelling algorithm, the Gene Expression-based Metabolite Centrality Analysis Tool (GEMCAT). GEMCAT enables integration of transcriptomics or proteomics data to predict changes in metabolite concentrations, which can be verified by targeted metabolomics. In addition, GEMCAT allows to trace measured and predicted metabolic changes back to the underlying alterations in gene expression or proteomics and thus enables functional interpretation and integration of multi-omics data. We demonstrate the predictive capacity of GEMCAT on three datasets and genome-scale metabolic networks from two different organisms: (i) we integrated transcriptomics and metabolomics data from an engineered human cell line with a functional deletion of the mitochondrial NAD transporter; (ii) we used a large multi-tissue multi-omics dataset from rats for transcriptome- and proteome-based prediction and verification of training-induced metabolic changes and achieved an average prediction accuracy of 70%; and (iii) we used proteomics measurements from patients with inflammatory bowel disease and verified the predicted changes using metabolomics data from the same patients. For this dataset, the prediction accuracy achieved by GEMCAT was 79%.

Indexed as

AlgorithmsGene Expression ProfilingMetabolomicsSoftwareAnimalsHumansInflammatory Bowel DiseasesMetabolic Networks and PathwaysProteomicsRatsTranscriptome

Identifiers

PMID39897103
PMCPMC11783570

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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.