Evidence map›Paper›PMID 41638993›Full record

ArticleBioinformatics (Oxford, England)2026

VUScope: a mathematical model for evaluating image-based drug response measurements and predicting long-term incubation outcomes.

Nguyen Khoa Tran, My Ky Huynh, Alexander D Kotman, Martin Jürgens, Thomas Kurz, Sascha Dietrich, Gunnar W Klau, Nan Qin

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

Nguyen Khoa TranDepartment of Computer Science, Heinrich Heine University Düsseldorf, Düsseldorf, 40225, Germany.ORCID 0000-0002-4732-4294
My Ky HuynhDepartment of Computer Science, Heinrich Heine University Düsseldorf, Düsseldorf, 40225, Germany.
Alexander D KotmanClinic of Hematology, Oncology, and Clinical Immunology, University Hospital of Düsseldorf, Düsseldorf, 40225, Germany.
Martin JürgensDepartment of Computer Science, Heinrich Heine University Düsseldorf, Düsseldorf, 40225, Germany.
Thomas KurzInstitute of Pharmaceutical and Medicinal Chemistry, Heinrich Heine University Düsseldorf, Düsseldorf, 40225, Germany.
Sascha DietrichClinic of Hematology, Oncology, and Clinical Immunology, University Hospital of Düsseldorf, Düsseldorf, 40225, Germany.
Gunnar W KlauDepartment of Computer Science, Heinrich Heine University Düsseldorf, Düsseldorf, 40225, Germany.ORCID 0000-0002-6340-0090
Nan QinClinic of Hematology, Oncology, and Clinical Immunology, University Hospital of Düsseldorf, Düsseldorf, 40225, Germany.ORCID 0000-0002-3442-8043

Funding

German Childhood Cancer Foundation 3267German Childhood Cancer Foundation DKS 2021.20Research Committee of the Medical Faculty 2021-44Research Committee of the Medical Faculty 2024-64
6 · The paper itself

Abstract

motivationLive-cell imaging-based drug screening increases the likelihood of identifying effective and safe drugs by providing dynamic, high-content, and physiologically relevant data. As a result, it improves the success rate of drug development and facilitates the translation of benchside discoveries to bedside applications. Despite these advantages, no comprehensive metrics currently exist to evaluate dose-time-dependent drug responses. To address this gap, we established a systematic framework to assess drug effects across a range of concentrations and exposure durations simultaneously. This metric enables more accurate evaluation of drug responses measured by live-cell imaging.

resultsWe employed treatment concentrations ranging from 0 to 10 μM and performed live-cell imaging-based measurements over a 120-h incubation period. To analyze the experimental data, we developed VUScope, a new mathematical model combining the 4-parameter logistic curve and a logistic function to characterize dose-time-dependent responses. This enabled us to calculate the Growth Rate Inhibition Volume Under the dose-time-response Surface (GRIVUS), which serves as a critical metric for assessing dynamic drug responses. Furthermore, our mathematical model allowed us to predict long-term treatment responses based on short-term drug responses. We validated the predictive capabilities of our model using independent datasets and observed that VUScope enhances prediction accuracy and offers deeper insights into drug effects than previously possible. By integrating VUScope into high-throughput drug screening platforms, we can further improve the efficacy of drug development and treatment selection. AVAILABILITY AND IMPLEMENTATION: We have made VUScope more accessible to users conducting pharmacological studies by uploading a detailed description, example datasets, and the source code to vuscope.albi.hhu.de, https://github.com/AlBi-HHU/VUScope, and https://doi.org/10.5281/zenodo.17610533.

Indexed as

Models, TheoreticalSoftwareDose-Response Relationship, DrugDrug Evaluation, PreclinicalHumans

Identifiers

PMID41638993
PMCPMC12904834

What Socratic holds

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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 Socratic graph.