Evidence map›Paper›PMID 40376092›Full record

ArticlebioRxiv : the preprint server for biology2025

One-click image reconstruction in single-molecule localization microscopy via deep learning.

Alon Saguy, Dafei Xiao, Kaarjel K Narayanasamy, Yuya Nakatani, Anna-Karin Gustavsson, Mike Heilemann, Yoav Shechtman

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 · Who and what money

Authors and funding

7 authors.

Alon SaguyFaculty of Biomedical Engineering, Technion - Israel Institute of Technology, Haifa, Israel.ORCID 0000-0003-3852-7628
Dafei XiaoRussell Berrie Nanotechnology Institute, Technion-Israel Institute of Technology, Haifa, Israel.ORCID 0009-0001-5126-9742
Kaarjel K NarayanasamyEMBL Imaging Centre, European Molecular Biology Laboratory, Heidelberg, Germany.ORCID 0000-0001-9977-6500
Yuya NakataniDepartment of Chemistry, Rice University, Houston, TX, USA.ORCID 0000-0001-8909-360X
Anna-Karin GustavssonDepartment of Chemistry, Rice University, Houston, TX, USA.ORCID 0000-0002-0980-1168
Mike HeilemannInstitute of Physical and Theoretical Chemistry, Goethe-University Frankfurt, Germany.ORCID 0000-0002-9821-3578
Yoav ShechtmanFaculty of Biomedical Engineering, Technion - Israel Institute of Technology, Haifa, Israel.ORCID 0000-0001-8498-5203

Funding

Molecular mechanisms in the mammalian cell nucleusR35GM155365 · NIGMS · RICE UNIVERSITY · PI Anna Karin Eva Gustavsson · 2024 to 2026
$1.1M
NIGMS NIH HHS R35 GM155365
6 · The paper itself

Abstract

Deep neural networks have led to significant advancements in microscopy image generation and analysis. In single-molecule localization based super-resolution microscopy, neural networks are capable of predicting fluorophore positions from high-density emitter data, thus reducing acquisition time, and increasing imaging throughput. However, neural network-based solutions in localization microscopy require intensive human intervention and computation expertise to address the compromise between model performance and its generalization. For example, researchers manually tune parameters to generate training images that are similar to their experimental data; thus, for every change in the experimental conditions, a new training set should be manually tuned, and a new model should be trained. Here, we introduce AutoDS and AutoDS3D, two software programs for reconstruction of single-molecule super-resolution microscopy data that are based on Deep-STORM and DeepSTORM3D, that significantly reduce human intervention from the analysis process by automatically extracting the experimental parameters from the imaging raw data. In the 2D case, AutoDS selects the optimal model for the analysis out of a set of pre-trained models, hence, completely removing user supervision from the process. In the 3D case, we improve the computation efficiency of DeepSTORM3D and integrate the lengthy workflow into a graphic user interface that enables image reconstruction with a single click. Ultimately, we demonstrate superior performance of both pipelines compared to Deep-STORM and DeepSTORM3D for single-molecule imaging data of complex biological samples, while significantly reducing the manual labor and computation time.

Identifiers

PMID40376092
PMCPMC12080944

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.