Evidence map›Paper›PMID 41818641›Full record

ArticlePLoS computational biology2026

Fast and accessible morphology-free functional fluorescence imaging analysis.

Alejandro Estrada Berlanga, Gabrielle Y Kang, Amanda Kwok, Thomas Broggini, Jennifer Lawlor, Kishore V Kuchibhotla, David Kleinfeld, Gal Mishne, Adam S Charles

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. 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

9 authors.

Alejandro Estrada BerlangaDepartment of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
Gabrielle Y KangDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America.
Amanda KwokDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America.
Thomas BrogginiFrankfurt Cancer Institute (FCI), Goethe University Frankfurt, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0002-3733-486X
Jennifer LawlorDepartment of Psychological and Brain Sciences, Johns Hopkins University, Baltimore, Maryland, United States of America.
Kishore V KuchibhotlaDepartment of Psychological and Brain Sciences, Johns Hopkins University, Baltimore, Maryland, United States of America.
David KleinfeldDepartment of Physics, University of California San Diego, La Jolla, California, United States of America.
Gal MishneHalıcıoğlu Data Science Institute, University of California San Diego, La Jolla, California, United States of America.ORCID https://orcid.org/0000-0002-5287-3626
Adam S CharlesDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland, United States of America.ORCID https://orcid.org/0000-0002-9045-3489

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Optical calcium imaging is a powerful tool for recording neural activity across a wide range of spatial scales, from dendrites and spines to whole-brain imaging through two-photon and widefield microscopy. Traditional methods for analyzing functional calcium imaging data rely heavily on spatial features, such as the compact shapes of somas, to extract regions of interest and their associated temporal traces. This spatial dependency can introduce biases in time trace estimation and limit the applicability of these methods across different neuronal morphologies and imaging scales. To address these limitations, the Graph Filtered Temporal Dictionary Learning (GraFT) uses a graph-based approach to identify neural components based on shared temporal activity rather than spatial proximity, enhancing generalizability across diverse datasets. Here we present significant advancements to the GraFT algorithm, including the integration of a more efficient solver for the L1 least absolute shrinkage and selection operator (LASSO) problem and the application of compressive sensing techniques to reduce computational complexity. By employing random projections to reduce data dimensionality, we achieve substantial speedups while maintaining analytical accuracy. These advancements significantly accelerate the GraFT algorithm, making it more scalable for larger and more complex datasets. Moreover, to increase accessibility, we developed a graphical user interface to facilitate running and analyzing the outputs of GraFT. Finally, we demonstrate the utility of GraFT to imaging data beyond meso-scale imaging, including vascular and axonal imaging.

Indexed as

Image Processing, Computer-AssistedOptical ImagingAlgorithmsAnimalsBrainCalciumComputational BiologyNeuronsCalcium

Identifiers

PMID41818641
PMCPMC13038116

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.