Evidence map›Paper›PMID 42608578›Full record

ArticleMolecular systems biology2026

Integrated metabolomics data analysis to generate mechanistic hypotheses with MetaProViz.

Christina Schmidt, Jannik Franken, Denes Turei, Dimitrios Prymidis, Macabe Daley, Christian Frezza, Julio Saez-Rodriguez

Abstract read
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In one paragraph

Article in Molecular systems biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Christina SchmidtHeidelberg University, Faculty of Medicine, and Heidelberg University Hospital, Institute for Computational Biomedicine, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-3867-0881
Jannik FrankenHeidelberg University, Faculty of Medicine, and Heidelberg University Hospital, Institute for Computational Biomedicine, Heidelberg, Germany.ORCID http://orcid.org/0009-0006-2460-2841
Denes TureiHeidelberg University, Faculty of Medicine, and Heidelberg University Hospital, Institute for Computational Biomedicine, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-7249-9379
Dimitrios PrymidisUniversity of Cologne, Faculty of Medicine and University Hospital Cologne, Institute for Metabolomics in Ageing, Cluster of Excellence Cellular Stress Responses in Aging-associated Diseases (CECAD), Cologne, Germany.
Macabe DaleyHeidelberg University, Faculty of Medicine, and Heidelberg University Hospital, Institute for Computational Biomedicine, Heidelberg, Germany.
Christian FrezzaUniversity of Cologne, Faculty of Medicine and University Hospital Cologne, Institute for Metabolomics in Ageing, Cluster of Excellence Cellular Stress Responses in Aging-associated Diseases (CECAD), Cologne, Germany. christian.frezza@uni-koeln.de.ORCID http://orcid.org/0000-0002-3293-7397
Julio Saez-RodriguezHeidelberg University, Faculty of Medicine, and Heidelberg University Hospital, Institute for Computational Biomedicine, Heidelberg, Germany. saezlab@ebi.ac.uk.ORCID http://orcid.org/0000-0002-8552-8976

Funding

Bundesministerium für Forschung, Technologie und Raumfahrt (BMBF) 03LW0233KCancer Research UK Programme Foundation C51061/A27453
6 · The paper itself

Abstract

The lack of standardised workflows and ambiguous metabolite annotations hampers metabolomics integration with prior knowledge, thus limiting the extraction of meaningful biological insights. We present MetaProViz (Metabolomics Processing, functional analysis and Visualization), an open-source Bioconductor R package for metabolomics data analysis that integrates prior knowledge to generate mechanistic hypotheses ( https://saezlab.github.io/MetaProViz/ ). MetaProViz operates on annotated intensity values and offers a flexible framework consisting of five modules: processing, differential analysis, prior knowledge integration, functional analysis and visualisation, applicable to intracellular and exometabolomics experiments. To improve functional analysis, we created the Metabolism Signature Database (MetSigDB), a collection of annotated metabolite sets. MetSigDB includes pathway-metabolite, metabolite-receptor, metabolite-transporter sets, and chemical class-metabolite sets. MetaProViz enables the conversion of gene sets to metabolite sets, metabolite identifier expansion and analyses mapping ambiguities. The MetaProViz functional analysis toolkit includes sample metadata analysis, enrichment analysis and biologically informed clustering. By applying MetaProViz to kidney cancer metabolomics data, we identified increased methionine usage in line with decreased methionine levels in tumour samples. In summary, MetaProViz facilitates and improves the analysis and interpretation of metabolomics data.

Identifiers

PMID42608578

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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.