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

14.7K
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...
14.7K
Electron Microscope Tomography and Single-particle Reconstruction01:07

Electron Microscope Tomography and Single-particle Reconstruction

3.0K
Transmission electron microscopy (TEM) can be used to determine the 3D structure of biological samples with the help of techniques such as electron microscope tomography and single-particle reconstruction. While single-particle reconstruction can examine macromolecules and macromolecular complexes in vitro conditions only, tomography permits the study of cell components or small cells in vivo.
Electron Tomography
Electron tomography can be performed either in TEM or STEM (scanning transmission...
3.0K
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

21.6K
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,...
21.6K

You might also read

Related Articles

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

Sort by
Same author

Advances in Functional Near-Infrared Spectroscopy: Physical Principles and Expanding Applications in Neuroscience.

Journal of biophotonics·2025
Same author

Exploring the neural mechanisms of ADHD in children: a multifeature cross-task fNIRS analysis.

Cerebral cortex (New York, N.Y. : 1991)·2025
Same author

Improved strong tracking Sage-Husa adaptive algorithm for multi-MEMS IMU data fusion.

The Review of scientific instruments·2025
Same author

Self-Supervised Image Segmentation Using Meta-Learning and Multi-Backbone Feature Fusion.

International journal of neural systems·2025
Same author

Sparse-Laplace hybrid graph manifold method for fluorescence molecular tomography.

Physics in medicine and biology·2024
Same author

Enhanced model iteration algorithm with graph neural network for diffuse optical tomography.

Biomedical optics express·2024

Related Experiment Video

Updated: Mar 9, 2026

Computed Tomography-guided Time-domain Diffuse Fluorescence Tomography in Small Animals for Localization of Cancer Biomarkers
12:24

Computed Tomography-guided Time-domain Diffuse Fluorescence Tomography in Small Animals for Localization of Cancer Biomarkers

Published on: July 17, 2012

12.9K

Fast and Robust Reconstruction for Fluorescence Molecular Tomography via L1-2 Regularization.

Haibo Zhang1, Guohua Geng1, Xiaodong Wang1

  • 1School of Information Sciences and Technology, Northwest University, Xi'an, Shaanxi 710027, China.

Biomed Research International
|January 5, 2017
PubMed
Summary

This study introduces a new fluorescence molecular tomography (FMT) reconstruction method using L1-L2 norm minimization. It effectively addresses challenges posed by coherent system matrices, outperforming existing sparse reconstruction techniques.

More Related Videos

Born Normalization for Fluorescence Optical Projection Tomography for Whole Heart Imaging
16:44

Born Normalization for Fluorescence Optical Projection Tomography for Whole Heart Imaging

Published on: June 2, 2009

10.8K
Correlative Microscopy for 3D Structural Analysis of Dynamic Interactions
13:43

Correlative Microscopy for 3D Structural Analysis of Dynamic Interactions

Published on: June 24, 2013

14.6K

Related Experiment Videos

Last Updated: Mar 9, 2026

Computed Tomography-guided Time-domain Diffuse Fluorescence Tomography in Small Animals for Localization of Cancer Biomarkers
12:24

Computed Tomography-guided Time-domain Diffuse Fluorescence Tomography in Small Animals for Localization of Cancer Biomarkers

Published on: July 17, 2012

12.9K
Born Normalization for Fluorescence Optical Projection Tomography for Whole Heart Imaging
16:44

Born Normalization for Fluorescence Optical Projection Tomography for Whole Heart Imaging

Published on: June 2, 2009

10.8K
Correlative Microscopy for 3D Structural Analysis of Dynamic Interactions
13:43

Correlative Microscopy for 3D Structural Analysis of Dynamic Interactions

Published on: June 24, 2013

14.6K

Area of Science:

  • Biomedical Imaging
  • Medical Physics
  • Computational Imaging

Background:

  • Sparse reconstruction is crucial for fluorescence molecular tomography (FMT).
  • High coherence in FMT system matrices limits the effectiveness of standard L1 minimization for accurate reconstruction.
  • Existing methods struggle with sparsity when system matrices are highly coherent.

Purpose of the Study:

  • To develop a novel sparse reconstruction method for FMT that overcomes limitations of L1 minimization with coherent system matrices.
  • To introduce an L1-L2 norm minimization approach for improved FMT reconstruction.
  • To present an efficient algorithm for solving the proposed L1-L2 minimization problem.

Main Methods:

  • Proposed a novel reconstruction method minimizing the difference between L1 and L2 norms (L1-L2 minimization).
  • Developed an iterative Difference of Convex Algorithm (DCA) to solve the non-convex L1-L2 minimization problem.
  • Employed the alternating direction method of multipliers (ADMM) with an adaptive penalty to solve L1 minimization subproblems within each DCA iteration.

Main Results:

  • The proposed L1-L2 minimization method, solved via DCA, demonstrated superior performance compared to L1, L2, L1/2, and L0 minimization.
  • Outperformance was particularly evident when dealing with highly coherent system matrices common in FMT.
  • Validation was performed using both simulated and in vivo experimental FMT data.

Conclusions:

  • The DCA-based L1-L2 minimization offers a robust and effective solution for sparse reconstruction in FMT, especially under challenging conditions of high system matrix coherence.
  • This novel approach enhances reconstruction accuracy and sparsity compared to conventional methods.
  • The findings suggest a significant advancement in FMT reconstruction algorithms for biomedical applications.