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

Three-Dimensional Microscopy in Microbiology01:28

Three-Dimensional Microscopy in Microbiology

374
Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...
374
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

8.3K
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...
8.3K
Phase Contrast and Differential Interference Contrast Microscopy01:26

Phase Contrast and Differential Interference Contrast Microscopy

11.0K
Phase-Contrast Microscopes
In-phase-contrast microscopes, interference between light directly passing through a cell and light refracted by cellular components is used to create high-contrast, high-resolution images without staining. It is the oldest and simplest type of microscope that creates an image by altering the wavelengths of light rays passing through the specimen. Altered wavelength paths are created using an annular stop in the condenser. The annular stop produces a hollow cone of...
11.0K

You might also read

Related Articles

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

Sort by
Same author

Flexible, multimodal, electrical-sensing-optical-transmission μfiber-sensors via an on-fiber printed electronics strategy.

National science review·2026
Same author

Re: Safety and Efficacy of Tranexamic Acid in Urologic Surgery: Results from the International, Randomized, Placebo-Controlled POISE-3 Trial.

European urology·2026
Same author

Adherence to Chinese Dietary Guidelines Is Associated with Better Bone Status in School-Aged Children and Adolescents.

Nutrients·2026
Same author

Plant viruses hijack and stabilize host ubiquitin-specific protease 14 to prevent viral protein degradation for efficient infection.

Molecular plant·2026
Same author

Serum matrix metalloproteinase-7 as a diagnostic and prognostic biomarker in primary biliary cholangitis.

Frontiers in medicine·2026
Same author

Ultra-dispersive metasurfaces enabled by convergence-phase design using simplified nanopillar arrays.

Nature communications·2026
Same journal

Label-free multimodal nonlinear microscopy enabled by an optical parametric generator.

APL photonics·2026
Same journal

Radial polarization imaging of entangled biphoton state.

APL photonics·2026
Same journal

Three-dimensional forward-scattering imaging flow cytometry system for single-cell analysis.

APL photonics·2025
Same journal

On the importance of simultaneous label-free multimodal nonlinear optical imaging for biomedical applications.

APL photonics·2025
Same journal

Mid-infrared hyperspectral microscopy with broadband 1-GHz dual frequency combs.

APL photonics·2025
Same journal

Fast and efficient Sb-based type-II phototransistors integrated on silicon.

APL photonics·2025
See all related articles

Related Experiment Video

Updated: Sep 29, 2025

Automation of the Micronucleus Assay Using Imaging Flow Cytometry and Artificial Intelligence
09:11

Automation of the Micronucleus Assay Using Imaging Flow Cytometry and Artificial Intelligence

Published on: January 27, 2023

2.3K

Computational interference microscopy enabled by deep learning.

Yuheng Jiao1,2, Yuchen R He1, Mikhail E Kandel1

  • 1Quantitative Light Imaging Laboratory, Department of Electrical and Computer Engineering, Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.

APL Photonics
|March 21, 2022
PubMed
Summary
This summary is machine-generated.

Deep learning generates high-sensitivity phase maps from diffraction phase microscopy (DPM) images, overcoming noise issues. This computational approach enables real-time, low-noise imaging for cell and tissue characterization.

More Related Videos

High-Speed Ultraviolet Photoacoustic Microscopy for Histological Imaging with Virtual-Staining assisted by Deep Learning
09:31

High-Speed Ultraviolet Photoacoustic Microscopy for Histological Imaging with Virtual-Staining assisted by Deep Learning

Published on: April 28, 2022

3.2K
Whole-Brain Single-Cell Imaging and Analysis of Intact Neonatal Mouse Brains Using MRI, Tissue Clearing, and Light-Sheet Microscopy
08:49

Whole-Brain Single-Cell Imaging and Analysis of Intact Neonatal Mouse Brains Using MRI, Tissue Clearing, and Light-Sheet Microscopy

Published on: August 1, 2022

3.8K

Related Experiment Videos

Last Updated: Sep 29, 2025

Automation of the Micronucleus Assay Using Imaging Flow Cytometry and Artificial Intelligence
09:11

Automation of the Micronucleus Assay Using Imaging Flow Cytometry and Artificial Intelligence

Published on: January 27, 2023

2.3K
High-Speed Ultraviolet Photoacoustic Microscopy for Histological Imaging with Virtual-Staining assisted by Deep Learning
09:31

High-Speed Ultraviolet Photoacoustic Microscopy for Histological Imaging with Virtual-Staining assisted by Deep Learning

Published on: April 28, 2022

3.2K
Whole-Brain Single-Cell Imaging and Analysis of Intact Neonatal Mouse Brains Using MRI, Tissue Clearing, and Light-Sheet Microscopy
08:49

Whole-Brain Single-Cell Imaging and Analysis of Intact Neonatal Mouse Brains Using MRI, Tissue Clearing, and Light-Sheet Microscopy

Published on: August 1, 2022

3.8K

Area of Science:

  • Biomedical Optics
  • Quantitative Phase Imaging
  • Computational Microscopy

Background:

  • Quantitative phase imaging (QPI) is crucial for cell and tissue characterization.
  • Spatial light interference microscopy (SLIM) offers high sensitivity but slow acquisition.
  • Diffraction phase microscopy (DPM) provides single-shot imaging but suffers from noise.

Purpose of the Study:

  • To develop a deep learning method for generating SLIM-quality phase maps from single-shot DPM images.
  • To overcome the limitations of DPM's noise and SLIM's slow acquisition rate.
  • To enable real-time, high-sensitivity phase imaging using computational methods.

Main Methods:

  • A U-net based deep learning model was trained on over 1000 paired DPM and SLIM images.
  • The DPM and SLIM modules were integrated onto an inverted microscope for simultaneous data acquisition.
  • Neural network inference was implemented into live acquisition software for real-time processing.

Main Results:

  • The deep learning model successfully removed speckles and background noise from DPM images.
  • Quantitative metrics showed high fidelity: SNR of 29.97, PCC of 0.79, and SSIM of 0.82.
  • Real-time, low-noise phase images were generated from DPM, enhancing image quality significantly.

Conclusions:

  • Deep learning effectively translates noisy single-shot DPM images into high-quality, SLIM-equivalent phase maps.
  • This computational approach significantly improves phase imaging capabilities for biological samples.
  • The method offers a promising pathway for real-time, noise-free quantitative phase imaging in microscopy.