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

Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

Two-dimensional (2D) microscopy encompasses a range of optical techniques that capture images within a single focal plane, offering detailed representations of microscopic structures. These techniques are essential in biological and medical research, enabling the visualization of cellular and subcellular structures with different levels of contrast and specificity.There are several major types of 2D microscopy, each with strengths and applications.Bright-Field MicroscopyBright-field microscopy...

You might also read

Related Articles

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

Sort by
Same author

Correction: Mitochondrial impairment, decreased Sirtuin activity and protein acetylation in dorsal root ganglia in Friedreich ataxia models.

Cellular and molecular life sciences : CMLS·2025
Same author

4D mitochondrial network assumes distinct and predictive phenotypes through human lung and intestinal epithelial development.

bioRxiv : the preprint server for biology·2025
Same author

LiveLattice: Real-time visualisation of tilted light-sheet microscopy data using a memory-efficient transformation algorithm.

Journal of microscopy·2024
Same author

Phospho-KNL-1 recognition by a TPR domain targets the BUB-1-BUB-3 complex to C. elegans kinetochores.

The Journal of cell biology·2024
Same author

Phospho-KNL-1 recognition by a TPR domain targets the BUB-1-BUB-3 complex to <i>C. elegans</i> kinetochores.

bioRxiv : the preprint server for biology·2024
Same author

Far-red chemigenetic biosensors for multi-dimensional and super-resolved kinase activity imaging.

bioRxiv : the preprint server for biology·2024
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: Jun 8, 2026

Light-sheet Microscopy for Three-dimensional Visualization of Human Immune Cells
09:44

Light-sheet Microscopy for Three-dimensional Visualization of Human Immune Cells

Published on: June 13, 2018

8.1K

LiveLattice: Real-time visualization of tilted light-sheet microscopy data using a memory-efficient transformation

Zichen Wang1,2, Hiroyuki Hakozaki1,2, Gillian McMahon1,2

  • 1Department of Pharmacology, University of California, San Diego, San Diego, CA, 92093.

Biorxiv : the Preprint Server for Biology
|June 10, 2024
PubMed
Summary
This summary is machine-generated.

A new GPU-accelerated algorithm, WH-Transform, enables rapid, memory-efficient deskewing and rotation for light-sheet microscopy data. This allows real-time visualization of large 4D biological samples, overcoming computational challenges.

Keywords:
algorithm developmentfluorescence microscopylattice light-sheet microscopylight-sheet microscopymicroscopy data processingmicroscopy visualization

More Related Videos

Simultaneous Live Imaging of Multiple Insect Embryos in Sample Chamber-Based Light Sheet Fluorescence Microscopes
08:29

Simultaneous Live Imaging of Multiple Insect Embryos in Sample Chamber-Based Light Sheet Fluorescence Microscopes

Published on: September 9, 2020

3.0K
Author Spotlight: Advancing Knowledge in Far-From-Equilibrium Materials Through Light-Sheet Microscopy
08:32

Author Spotlight: Advancing Knowledge in Far-From-Equilibrium Materials Through Light-Sheet Microscopy

Published on: January 26, 2024

2.0K

Related Experiment Videos

Last Updated: Jun 8, 2026

Light-sheet Microscopy for Three-dimensional Visualization of Human Immune Cells
09:44

Light-sheet Microscopy for Three-dimensional Visualization of Human Immune Cells

Published on: June 13, 2018

8.1K
Simultaneous Live Imaging of Multiple Insect Embryos in Sample Chamber-Based Light Sheet Fluorescence Microscopes
08:29

Simultaneous Live Imaging of Multiple Insect Embryos in Sample Chamber-Based Light Sheet Fluorescence Microscopes

Published on: September 9, 2020

3.0K
Author Spotlight: Advancing Knowledge in Far-From-Equilibrium Materials Through Light-Sheet Microscopy
08:32

Author Spotlight: Advancing Knowledge in Far-From-Equilibrium Materials Through Light-Sheet Microscopy

Published on: January 26, 2024

2.0K

Area of Science:

  • Biophysics
  • Computational Biology
  • Microscopy

Background:

  • Light-sheet fluorescence microscopy (LSFM) provides 4D imaging capabilities.
  • Tilted-sample-plane LSFM techniques like iSPIM and LLSM simplify sample preparation but require complex post-processing.
  • Current deskewing and rotation methods for LSFM data are computationally intensive, limiting real-time analysis.

Purpose of the Study:

  • To develop a novel, memory-efficient algorithm for fast preprocessing of tilted-sample-plane LSFM data.
  • To enable real-time visualization and analysis of large 4D microscopy datasets.
  • To reduce the computational burden and hardware requirements for LSFM data processing.

Main Methods:

  • Developed WH-Transform, a GPU-accelerated algorithm integrating deskewing and rotation into a single transformation.
  • Implemented a memory-efficient approach to handle large image stacks.
  • Benchmarked WH-Transform against conventional methods using large 3D and 4D datasets.

Main Results:

  • WH-Transform reduces preprocessing run time by at least 10-fold compared to existing methods.
  • The algorithm demonstrates linear scalability, processing 15 GB 3D stacks in under a minute on a single GPU.
  • Real-time preprocessing was achieved for 4D datasets of human hepatocytes, lung, and brain organoids.

Conclusions:

  • WH-Transform significantly accelerates LSFM data preprocessing, overcoming memory and computational limitations.
  • The algorithm enables real-time, on-the-fly data processing and visualization on standard workstations.
  • This advancement revolutionizes biological imaging applications by improving the usability of LSFM, SPIM, and similar microscopes.