Evidence map›Paper›PMID 41708728›Full record

ArticleScientific reports2026

LUMIN: an automated graphical analysis toolbox for high-throughput calcium imaging of in vitro neuronal cultures.

Erno Hänninen, Anika K Mueller, Jonas Viswalingam Bagge, Lucía Sena Trujillo, Lorenzo Fedrizzi, Agnete Kirkeby, Janko Kajtez

Abstract read
In one paragraph

Article in Scientific reports, 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.

Erno HänninenDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, 2200, Copenhagen, Denmark. erno.hanninen@sund.ku.dk.
Anika K MuellerDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, 2200, Copenhagen, Denmark.
Jonas Viswalingam BaggeDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, 2200, Copenhagen, Denmark.
Lucía Sena TrujilloDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, 2200, Copenhagen, Denmark.
Lorenzo FedrizziDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, 2200, Copenhagen, Denmark.
Agnete KirkebyDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, 2200, Copenhagen, Denmark.
Janko KajtezDepartment of Biomedical Sciences, Faculty of Health and Medical Sciences, Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, 2200, Copenhagen, Denmark. janko.kajtez@sund.ku.dk.

Funding

Danmarks Frie Forskningsfond 0169-00073BInnovation office at University of Copenhagen 521-0949/23-7000Innovationsfonden 2078-00002BLundbeck Foundation R336-2019-2927Lundbeck Foundation R380-2021-1267Novo Nordisk Fonden NNF21CC0073729
6 · The paper itself

Abstract

Human pluripotent stem cell-derived in vitro models, combined with advances in high-content live-cell calcium imaging, provide a powerful platform for disease modeling and drug screening. However, most calcium imaging analysis tools have been developed for in vivo applications with suboptimal features for processing data from cultured neurons. Here, we present LUMIN (Live-cell User Module for Imaging and analysis of Neuronal activity), a scalable and broadly applicable software that integrates a graphical user interface with automated data analysis encompassing single-cell segmentation, signal extraction, and activity quantification. Two analysis modules for transiently active or quiescent stimuli-evoked neurons make it broadly applicable for cultures with distinct functional properties. Its efficient data processing and linear time complexity enable processing thousands of cells within hours (~ 7000 cells from ~ 70 recordings per 30 min) on a standard laptop. We demonstrate LUMIN’s performance on human stem cell-derived ventral midbrain neurons through two applications: (1) modulation of spontaneous activity with well-characterized pharmacological compounds, and (2) evoking responses in quiescent neurons upon compound stimulation.

Indexed as

CalciumHigh-Throughput Screening AssaysImage Processing, Computer-AssistedNeuronsSoftwareCalcium SignalingCells, CulturedHumansCalcium

Identifiers

PMID41708728
PMCPMC13004900

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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.