Evidence map›Paper›PMID 40862236›Full record

ArticleInterface focus2025

Identification of models describing gene expression data leveraging machine learning methods.

Lucas F Jansen Klomp, Elena Queirolo, Janine N Post, Hil G E Meijer, Christoph Brune

Abstract read
In one paragraph

Article in Interface focus, 2025. 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

5 authors.

Lucas F Jansen KlompMathematics of Imaging & AI, Department of Applied Mathematics, University of Twente, Enschede, The Netherlands.ORCID https://orcid.org/0009-0003-8831-9330
Elena QueiroloIRMAR, University of Rennes, Rennes, France.ORCID https://orcid.org/0000-0002-1614-5621
Janine N PostDevelopmental BioEngineering, University of Twente, Enschede, The Netherlands.ORCID https://orcid.org/0000-0002-6645-6583
Hil G E MeijerMathematics of Imaging & AI, Department of Applied Mathematics, University of Twente, Enschede, The Netherlands.ORCID https://orcid.org/0000-0003-1526-3762
Christoph BruneMathematics of Imaging & AI, Department of Applied Mathematics, University of Twente, Enschede, The Netherlands.ORCID https://orcid.org/0000-0003-0145-5069

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanistic ordinary differential equation models of gene regulatory networks are a valuable tool for understanding biological processes that occur inside a cell, and they allow for the formulation of novel hypotheses on the mechanisms underlying these processes. Although data-driven methods for inferring these mechanistic models are becoming more prevalent, it is often unclear how recent advances in machine learning can be used effectively without jeopardi zing the interpretability of the resulting models. In this work, we present a framework to leverage neural networks for the identification of data-driven models for time-dependent intracellular processes, such as cell differentiation. In particular, we use a graph autoencoder model to suggest novel connections in a gene regulatory network. We show how the improvement of the graph suggested using this neural network leads to the generation of hypotheses on the dynamics of the resulting identified dynamical system.

Indexed as

gene regulatory networkgraph neural networkODE modellingscRNA-seq

Identifiers

PMID40862236
PMCPMC12371343

What OpenQuestion holds

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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.