Evidence map›Paper›PMID 40569855›Full record

ArticleBioinformatics (Oxford, England)2025

SpyDen: simplifying molecular and structural analysis across spines and dendrites.

Maximilian F Eggl, Surbhit Wagle, Jean P Filling, Thomas E Chater, Yukiko Goda, Tatjana Tchumatchenko

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. 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

6 authors.

Maximilian F EgglInstitute of Experimental Epileptology and Cognition Research, University of Bonn Medical Centre, Bonn 53127, Germany.ORCID 0000-0001-5815-1045
Surbhit WagleInstitute of Experimental Epileptology and Cognition Research, University of Bonn Medical Centre, Bonn 53127, Germany.ORCID 0000-0002-3825-6875
Jean P FillingInstitute of Physiological Chemistry, University of Mainz Medical Centre, Mainz 55128, Germany.
Thomas E ChaterLaboratory for Synaptic Plasticity and Connectivity, RIKEN Centre for Brain Science, Wako-Shi, Saitama 351-0198, Japan.
Yukiko GodaLaboratory for Synaptic Plasticity and Connectivity, RIKEN Centre for Brain Science, Wako-Shi, Saitama 351-0198, Japan.
Tatjana TchumatchenkoInstitute of Experimental Epileptology and Cognition Research, University of Bonn Medical Centre, Bonn 53127, Germany.ORCID 0000-0001-9137-809X

Funding

European Research CouncilEuropean Union's Horizon 2020 ResearchFundación La Caixa LCF/BQ/PI23/11970039Innovation Program
6 · The paper itself

Abstract

motivationInvestigating the molecular composition of different neural compartments such as axons, dendrites, or synapses is critical for understanding learning and memory. State-of-the-art microscopy techniques now resolve individual molecules and pinpoint their position with a micrometer or nanometre resolution across hundreds of micrometres, allowing the labelling of multiple structures of interest simultaneously. Algorithmically, tracking individual molecules across hundreds of micrometres and determining whether they are inside a particular cellular compartment can be challenging. Historically, microscopy images are annotated manually, often using multiple software packages to detect fluorescence puncta and quantify cellular compartments of interest. Advanced ANN-based automated tools, while powerful, often can only help with selected parts of the data analysis, may be optimized for specific spatial resolutions, cell preparations, and may not be fully open source and open access to be sufficiently customizable.

resultsThus, we developed SpyDen, a Python package based upon three principles: (i) ease of use for multi-task scenarios, (ii) open-source accessibility and data export to a standard, open data format, (iii) the ability to edit any software-generated annotation and generalize across spatial resolutions. SpyDen operates on 2D microscopy time-series data, offering robust temporal tracking and spatial analysis capabilities. Equipped with a graphical user interface and accompanied by video tutorials, SpyDen provides a collection of powerful algorithms that can be used for neurite and synapse detection, fluorescent puncta, and intensity analysis. We validated SpyDen using expert annotation across numerous use cases to prove a powerful, integrated platform for efficient and reproducible molecular imaging analysis. AVAILABILITY AND IMPLEMENTATION: SpyDen is available on https://github.com/meggl23/SpyDen while the compiled executables can be found at https://gin.g-node.org/CompNeuroNetworks/SpyDenTrainedNetwork.

Indexed as

DendritesDendritic SpinesImage Processing, Computer-AssistedSoftwareAlgorithmsAnimalsHumansMicroscopy, FluorescenceSynapses

Identifiers

PMID40569855
PMCPMC12233091

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.