Evidence map›Paper›PMID 41890116›Full record

ArticlebioRxiv : the preprint server for biology2026

SynAPSeg: A novel dataset and image analysis framework for deep learning-based synapse detection and quantification.

Pascal Schamber, Sahana Darbhamulla, Molly Boyer, Madison Pelletier, Helene Hartman, Olivia Friedman, Shiyu Zhang, Allison Blais, Seyun Oh, Haining Zhong and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for 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.

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0cells of the map it votes in
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

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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

5 · Who and what money

Authors and funding

11 authors.

Pascal SchamberDepartment of Neuroscience, Tufts University, Boston, MA, USA.ORCID 0009-0001-7415-1325
Sahana DarbhamullaDepartment of Neuroscience, Tufts University, Boston, MA, USA.
Molly BoyerDepartment of Neuroscience, Tufts University, Boston, MA, USA.ORCID 0000-0003-2022-6042
Madison PelletierDepartment of Neuroscience, Tufts University, Boston, MA, USA.
Helene HartmanDepartment of Neuroscience, Tufts University, Boston, MA, USA.
Olivia FriedmanDepartment of Neuroscience, Tufts University, Boston, MA, USA.
Shiyu ZhangDepartment of Neuroscience, Tufts University, Boston, MA, USA.ORCID 0009-0004-0176-4798
Allison BlaisDepartment of Neuroscience, Tufts University, Boston, MA, USA.ORCID 0009-0001-0045-2758
Seyun OhDepartment of Neuroscience, Tufts University, Boston, MA, USA.ORCID 0009-0003-2673-765X
Haining ZhongVollum Institute, Oregon Health and Science University, Portland, OR, USA.ORCID 0000-0002-7109-4724
Alexei M BygraveDepartment of Neuroscience, Tufts University, Boston, MA, USA.ORCID 0000-0003-2291-923X

Funding

Cell-Specific Visualization of Endogenous ProteinsRF1MH120119 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI MAO, TIANYI, ZHONG, HAINING · 2019 to 2019
$2.8M
Sensing and manipulating neuromodulatory signaling in vivoRF1MH130784 · NIMH · OREGON HEALTH & SCIENCE UNIVERSITY · PI ZHONG, HAINING · 2023 to 2023
$2.6M
Molecular basis of glutamatergic synapse function in inhibitory interneuronsR00MH124920 · NIMH · TUFTS UNIVERSITY BOSTON · PI BYGRAVE, ALEXEI MANSFIELD · 2022 to 2024
$735k
NIMH NIH HHS R00 MH124920NIMH NIH HHS RF1 MH120119NIMH NIH HHS RF1 MH130784
6 · The paper itself

Abstract

Synapses are the fundamental units of neural computation, yet quantifying their organization across circuit-level scales remains a critical bottleneck in neuroscience. While advances in fluorescent labeling and imaging can generate vast datasets, analysis is often the limiting factor. Several deep learning-based tools have been proposed to ameliorate these issues. However, existing applications primarily focus on dendritic spines and lack robust solutions for segmenting synaptic puncta in dense tissue preparations. To address this, we introduce SynAPSeg, which encompasses an open-source framework for deep learning-based analysis and, to the best of our knowledge, the first large-scale, publicly available instance segmentation dataset specifically curated for synaptic puncta. We use this dataset to train deep learning models that reach the performance of human experts across a unique benchmark dataset. SynAPSeg integrates these models into an interactive interface, with support for multi-dimensional data, enabling fully automated segmentation and quantification pipelines alongside an annotation module for refinement and validation. We demonstrate the framework's scalability by performing the first comprehensive mapping of nearly 4 million excitatory postsynaptic PSD95 puncta within inhibitory interneurons across the dorsal hippocampus, revealing regional differences in synapse properties. Finally, we show SynAPSeg's utility for 3D quantification by applying these models to study aging-associated synaptic changes in CA1 parvalbumin (PV)-positive inhibitory neurons. Through this approach, we uncover a reduction in PSD95 density along PV dendrites in the aged CA1, indicating reduced glutamatergic recruitment of PV neurons which could contribute to age-related cognitive decline. Collectively, these results demonstrate that SynAPSeg provides a scalable solution for comprehensively studying synaptic architecture in health and disease.

Identifiers

PMID41890116
PMCPMC13015510

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LicenceCC BY-NC-ND
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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.