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

Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

8.8K
Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
In optical microscopy, the specimen to be viewed is placed on a glass slide and clipped on the stage...
8.8K
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
Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

1.0K
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...
1.0K

You might also read

Related Articles

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

Sort by
Same author

Real-Time Structural Illumination with Hyperspectral Images: A Tunable Projection-Capture Synchronizer for Three-Phase Demodulation on Embedded Heterogeneous Computing Platforms.

Sensors (Basel, Switzerland)·2026
Same author

Multimodal HSI-MRI system for tumor delineation in neurosurgical guidance.

International journal of computer assisted radiology and surgery·2026
Same author

Improving Brain Tumor Detection by Cortical Surface and Vessels Segmentation Through RGB-to-HSI Transfer Learning.

Cancers·2026
Same author

Comprehensive predictive modeling in subarachnoid hemorrhage: integrating radiomics and clinical variables.

Neurosurgical review·2025
Same author

Benchmarking commercial depth sensors for intraoperative markerless registration in neurosurgery applications.

International journal of computer assisted radiology and surgery·2025
Same author

Spectral analysis comparison of pushbroom and snapshot hyperspectral cameras for <i>in vivo</i> brain tissues and chromophore identification.

Journal of biomedical optics·2024

Related Experiment Video

Updated: Jan 13, 2026

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

Structure-from-motion in micro-image domain for uncalibrated plenoptic 2.0 cameras.

Sarah Dury1, Daniele Bonatto1, Jaime Sancho2

  • 1LISA, Université Libre de Bruxelles, Brussels, Belgium.

International Journal of Computer Vision
|January 9, 2026
PubMed
Summary

We developed a new structure-from-motion method for plenoptic cameras, overcoming limitations like scale ambiguity. This approach enables robust 3D scene reconstruction from multiple uncalibrated cameras without complex calibration.

Keywords:
CalibrationMicro-lensPlenoptic 2.0 camerasStructure-from-motion

More Related Videos

Determining 3D Flow Fields via Multi-camera Light Field Imaging
14:25

Determining 3D Flow Fields via Multi-camera Light Field Imaging

Published on: March 6, 2013

17.1K
A Field Primer for Monitoring Benthic Ecosystems Using Structure-From-Motion Photogrammetry
06:36

A Field Primer for Monitoring Benthic Ecosystems Using Structure-From-Motion Photogrammetry

Published on: April 15, 2021

4.2K

Related Experiment Videos

Last Updated: Jan 13, 2026

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
Determining 3D Flow Fields via Multi-camera Light Field Imaging
14:25

Determining 3D Flow Fields via Multi-camera Light Field Imaging

Published on: March 6, 2013

17.1K
A Field Primer for Monitoring Benthic Ecosystems Using Structure-From-Motion Photogrammetry
06:36

A Field Primer for Monitoring Benthic Ecosystems Using Structure-From-Motion Photogrammetry

Published on: April 15, 2021

4.2K

Area of Science:

  • Computer Vision
  • Photogrammetry
  • Computational Imaging

Background:

  • Plenoptic cameras capture depth information using a micro-lens array, offering advantages over traditional monocular cameras.
  • Classical structure-from-motion (SfM) methods face challenges with low angular disparity and scale ambiguity, especially with complex camera setups.

Purpose of the Study:

  • To introduce a novel structure-from-motion (SfM) method tailored for raw micro-images from plenoptic 2.0 cameras.
  • To address limitations of traditional SfM by leveraging inherent disparity information in plenoptic imaging.

Main Methods:

  • Developed a SfM pipeline that identifies pinhole camera constraints and utilizes plenoptic camera disparity.
  • Enabled robust initialization and reconstruction without calibration patterns or subaperture view extraction.
  • Reconstructed scenes from multiple uncalibrated plenoptic cameras.

Main Results:

  • Achieved 10% error accuracy in relative pose estimation on natural and synthetic datasets, comparable to calibration-based methods.
  • Demonstrated robustness to coarse initialization and ability to reconstruct scenes with parallel cameras.
  • Outperformed reconstruction methods based on pinhole camera conversion.

Conclusions:

  • The proposed SfM method effectively reconstructs 3D scenes from uncalibrated plenoptic cameras.
  • It overcomes key limitations of classical SfM, including scale and angular disparity ambiguity.
  • Offers a more accurate and versatile solution for 3D scene reconstruction using plenoptic imaging.