Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

6.8K
Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
6.8K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Versatile and Scalable Reflective Micromirrors for Single-Objective Light Sheet Microscopy.

Nano letters·2026
Same author

Increased Telomere Mobility in Progeria is Restored by Isoprenylcysteine Carboxyl Methyltransferase Inhibition.

bioRxiv : the preprint server for biology·2026
Same author

Quantitative Mapping of Nanoscale EGFR-Grb2 Assemblies by DNA-PAINT.

Chemphyschem : a European journal of chemical physics and physical chemistry·2026
Same author

Versatile and Scalable Reflective Micromirrors for Single-Objective Light Sheet Microscopy.

bioRxiv : the preprint server for biology·2026
Same author

Wash-Free Multi-Target Super-Resolution Microscopy With Photocaged DNA Labels.

Angewandte Chemie (International ed. in English)·2026
Same author

Compact Spectral Encoding Microscopy by Terrace Grating Optics.

ACS photonics·2026
Same journal

Layered social competition coordinates reproductive hierarchy formation in ants.

bioRxiv : the preprint server for biology·2026
Same journal

Combination epigenetic-targeted therapy increases the immunogenicity of poorly immunogenic sarcomas.

bioRxiv : the preprint server for biology·2026
Same journal

Loss of LanC-like proteins delays post-injury regeneration of aging skeletal muscles.

bioRxiv : the preprint server for biology·2026
Same journal

Integrative Transfer Network: Deep Transfer Learning Across Populations and Prediction Targets.

bioRxiv : the preprint server for biology·2026
Same journal

Confidence-supported label-free metabolic imaging with FPhaS phase autofluorescence microscopy.

bioRxiv : the preprint server for biology·2026
Same journal

Sequence-encoded autoinhibition couples mRNA decapping activity to phase separation.

bioRxiv : the preprint server for biology·2026
See all related articles

Related Experiment Video

Updated: May 17, 2025

Deep Learning-Based Segmentation of Cryo-Electron Tomograms
10:25

Deep Learning-Based Segmentation of Cryo-Electron Tomograms

Published on: November 11, 2022

8.4K

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

Alon Saguy1, Dafei Xiao2, Kaarjel K Narayanasamy3

  • 1Faculty of Biomedical Engineering, Technion - Israel Institute of Technology, Haifa, Israel.

Biorxiv : the Preprint Server for Biology
|May 16, 2025
PubMed
Summary
This summary is machine-generated.

New software, AutoDS and AutoDS3D, automates single-molecule super-resolution microscopy analysis. These tools reduce manual labor and computation time, improving imaging throughput and reducing the need for user expertise in deep learning models.

More Related Videos

Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells
11:06

Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells

Published on: June 30, 2018

8.4K
Super-resolution Imaging of the Bacterial Division Machinery
08:47

Super-resolution Imaging of the Bacterial Division Machinery

Published on: January 21, 2013

11.7K

Related Experiment Videos

Last Updated: May 17, 2025

Deep Learning-Based Segmentation of Cryo-Electron Tomograms
10:25

Deep Learning-Based Segmentation of Cryo-Electron Tomograms

Published on: November 11, 2022

8.4K
Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells
11:06

Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells

Published on: June 30, 2018

8.4K
Super-resolution Imaging of the Bacterial Division Machinery
08:47

Super-resolution Imaging of the Bacterial Division Machinery

Published on: January 21, 2013

11.7K

Area of Science:

  • Biophysics
  • Microscopy
  • Computational Biology

Background:

  • Deep neural networks advance microscopy image analysis, particularly in single-molecule localization super-resolution microscopy.
  • Current methods require extensive manual parameter tuning and expertise, limiting model generalization and requiring retraining for new experimental conditions.

Purpose of the Study:

  • To introduce AutoDS and AutoDS3D, software programs that automate single-molecule super-resolution microscopy data reconstruction.
  • To significantly reduce human intervention and computational expertise needed for analyzing microscopy data.

Main Methods:

  • AutoDS automatically extracts experimental parameters from raw imaging data for optimal model selection in 2D.
  • AutoDS3D improves computational efficiency and integrates a graphical user interface for single-click 3D image reconstruction.
  • Both methods are based on Deep-STORM and DeepSTORM3D, respectively.

Main Results:

  • AutoDS removes user supervision by selecting optimal pre-trained models for 2D analysis.
  • AutoDS3D offers improved computational efficiency and a streamlined workflow for 3D reconstruction.
  • Both pipelines demonstrate superior performance compared to Deep-STORM and DeepSTORM3D on complex biological samples.

Conclusions:

  • AutoDS and AutoDS3D significantly reduce manual labor and computation time in single-molecule super-resolution microscopy.
  • These automated tools enhance the accessibility and efficiency of advanced microscopy data analysis.
  • The software enables robust analysis of complex biological samples with minimal user intervention.