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

12.2K
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...
12.2K

You might also read

Related Articles

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

Sort by
Same author

Foveated light-field compound imager.

Science advances·2026
Same author

Cell division timing shapes the morphology and size of nascent multicellular organisms.

bioRxiv : the preprint server for biology·2026
Same author

Evaluating age-dependent transmission and vaccination policy in Singapore's SARS-CoV-2 epidemic: A computational modelling approach.

Epidemics·2026
Same author

Host-Pathogen Network and Eco-Evolutionary Drivers of Avian Influenza Transmission in Wild Birds.

Ecology letters·2026
Same author

HYPER-Net: Physics-Conditioned Self-Supervised Reconstruction for Fourier Light-Field Microscopy.

bioRxiv : the preprint server for biology·2026
Same author

Volumetric Scattering Microscopy.

bioRxiv : the preprint server for biology·2026
Same journal

Plasmonic nanocomposite helices for weather-adaptive LiDAR function.

Nature communications·2026
Same journal

Multidirectional strain-insensitive stretchable RF electronics.

Nature communications·2026
Same journal

In-scanner thoughts contribute to resting-state functional connectivity.

Nature communications·2026
Same journal

Metal-center electron affinity modulates multicolor electrochromism in 2D conjugated metal-organic frameworks.

Nature communications·2026
Same journal

Hyperbranched dielectric polymer networks exhibiting giant energy storage density at 250 °C.

Nature communications·2026
Same journal

3D nanoprinting of metals by spatiotemporally confined hot electrons via multiple-electron excitations in nanocrystals.

Nature communications·2026
See all related articles
  1. Home
  2. Real-time, High-throughput Super-resolution Microscopy Via Panoramic Integration.
  1. Home
  2. Real-time, High-throughput Super-resolution Microscopy Via Panoramic Integration.

Related Experiment Video

Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy iPALM
11:57

Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy iPALM

Published on: December 1, 2016

11.1K

Real-time, high-throughput super-resolution microscopy via panoramic integration.

Kyungduck Yoon1,2,3,4, Hansol Yoon1,2,5, Kidan Tadesse1,2,3

  • 1Laboratory for Systems Biophotonics, Georgia Institute of Technology, Atlanta, GA, USA.

Nature Communications
|October 21, 2025

View abstract on PubMed

Summary
This summary is machine-generated.

We developed super-resolution panoramic integration (SPI), a microscopy method for instant, high-throughput imaging. SPI achieves subdiffractional resolution, enabling detailed biological analysis beyond current limitations.

More Related Videos

High-Throughput Total Internal Reflection Fluorescence and Direct Stochastic Optical Reconstruction Microscopy Using a Photonic Chip
14:09

High-Throughput Total Internal Reflection Fluorescence and Direct Stochastic Optical Reconstruction Microscopy Using a Photonic Chip

Published on: November 16, 2019

7.4K
Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform
06:25

Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform

Published on: February 12, 2014

8.8K

Related Experiment Videos

Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy iPALM
11:57

Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy iPALM

Published on: December 1, 2016

11.1K
High-Throughput Total Internal Reflection Fluorescence and Direct Stochastic Optical Reconstruction Microscopy Using a Photonic Chip
14:09

High-Throughput Total Internal Reflection Fluorescence and Direct Stochastic Optical Reconstruction Microscopy Using a Photonic Chip

Published on: November 16, 2019

7.4K
Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform
06:25

Time Multiplexing Super Resolving Technique for Imaging from a Moving Platform

Published on: February 12, 2014

8.8K

Area of Science:

  • Microscopy
  • Cell Biology
  • Biotechnology

Background:

  • Traditional microscopy faces limitations in resolution and throughput.
  • High-throughput screening requires efficient imaging techniques.

Purpose of the Study:

  • To introduce a novel microscopy technique, super-resolution panoramic integration (SPI).
  • To enable instantaneous generation of subdiffractional images for high-throughput screening.

Main Methods:

  • SPI utilizes multifocal optical rescaling and high-content sweeping.
  • Synchronized line-scan readout is employed with minimal post-processing.
  • The technique is compatible with standard epi-fluorescence microscopy settings.

Main Results:

  • Demonstrated SPI for analyzing subcellular and populational morphology.
  • Showcased SPI for assessing cellular function and heterogeneity.
  • Achieved subdiffractional image generation concurrently with screening.
  • Conclusions:

    • SPI is a versatile microscopy platform overcoming optical and computational constraints.
    • This technique offers a practical approach for advancing biological insights.
    • SPI facilitates scalable, high-throughput biological discovery.