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

8.2K
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...
8.2K
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

15.0K
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,...
15.0K

You might also read

Related Articles

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

Sort by
Same author

Phthalazine-based quaternary ammonium salts: synthesis, biological evaluation and membrane-targeting mechanism against <i>Staphylococcus aureus</i>.

Frontiers in microbiology·2026
Same author

Exposure to multiple metallic elements and risk of thyroid tumors: insights from elemental profiling, diet, and molecular characteristics plasma levels of metallic elements.

Frontiers in oncology·2026
Same author

Novel Perspective for Prognostic Stratification and Personalized Therapy in Breast Cancer Patients: Development of Cancer Stem Cells and Metabolism-Associated Prognostic Model.

International journal of women's health·2026
Same author

Rare <i>BRCA1</i> c.3418_3419insTGACTACT:p.S1140Mfs*18 germline mutation in a family with breast and ovarian cancer.

Oncology letters·2026
Same author

Discovery of Potent 1,3-Cyclobutane-Containing Dual A<sub>2A</sub>/A<sub>2B</sub> Receptor Antagonists with Low Projected Human Dose for the Treatment of Cancer.

ACS medicinal chemistry letters·2026
Same author

CIRCADIAN CLOCK-ASSOCIATED 1 represses thermotolerance by inhibiting <i>HEAT SHOCK FACTOR A2</i> expression in nonheading Chinese cabbage.

Horticulture research·2026
Same journal

Denoising algorithm of Φ-OTDR systems based on adaptive fractional wavelet transform denoising.

Optics express·2026
Same journal

Millisecond photon-to-photon latency and high-speed volumetric projection system for optogenetics.

Optics express·2026
Same journal

Polarization-encoded coaxial structured light for high-precision 3D surface profilometry.

Optics express·2026
Same journal

Discrete freeform optical design based on collaborative optimization of point cloud and local normals.

Optics express·2026
Same journal

Ultrafast ghost imaging with 25 GHz speckle switching and wavelength-division multiplexing.

Optics express·2026
Same journal

Atomic vapor cells fabricated by femtosecond laser welding of standard-optical-quality glass.

Optics express·2026
See all related articles

Related Experiment Video

Updated: Sep 25, 2025

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
12:51

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy

Published on: December 9, 2013

9.0K

Spatial resolution improved fluorescence lifetime imaging via deep learning.

Dong Xiao, Zhenya Zang, Wujun Xie

    Optics Express
    |April 27, 2022
    PubMed
    Summary
    This summary is machine-generated.

    This study introduces a deep learning method to enhance low-resolution fluorescence lifetime imaging (FLIM) data, achieving high-resolution results. The novel approach improves spatial resolution in FLIM, enabling faster acquisition of detailed cellular images.

    More Related Videos

    Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells
    09:45

    Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells

    Published on: February 9, 2012

    25.5K
    Fluorescence Imaging with One-nanometer Accuracy FIONA
    11:56

    Fluorescence Imaging with One-nanometer Accuracy FIONA

    Published on: September 26, 2014

    17.8K

    Related Experiment Videos

    Last Updated: Sep 25, 2025

    Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
    12:51

    Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy

    Published on: December 9, 2013

    9.0K
    Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells
    09:45

    Fluorescence Lifetime Imaging of Molecular Rotors in Living Cells

    Published on: February 9, 2012

    25.5K
    Fluorescence Imaging with One-nanometer Accuracy FIONA
    11:56

    Fluorescence Imaging with One-nanometer Accuracy FIONA

    Published on: September 26, 2014

    17.8K

    Area of Science:

    • Biomedical Imaging
    • Computational Biology
    • Deep Learning

    Background:

    • Fluorescence Lifetime Imaging (FLIM) systems often produce low-resolution images, limiting detailed cellular analysis.
    • Acquiring high-resolution FLIM data can be time-consuming and technically challenging.
    • Existing methods struggle to reconstruct fine spatial details from limited pixel resolution in FLIM.

    Purpose of the Study:

    • To develop a deep learning approach for generating high-resolution (HR) fluorescence lifetime images from low-resolution (LR) FLIM data.
    • To create a robust method for generating semi-synthetic FLIM data suitable for neural network training.
    • To introduce a novel hybrid neural network, SRI-FLIMnet, for simultaneous lifetime estimation and LR-to-HR image transformation.

    Main Methods:

    • Proposed a theoretical framework for training neural networks using semi-synthetic FLIM data with diverse cellular features and lifetime characteristics.
    • Developed a degrading model to generate paired LR-HR FLIM images for supervised learning.
    • Designed and implemented the spatial resolution improved FLIM net (SRI-FLIMnet), a hybrid neural network for enhanced FLIM reconstruction.

    Main Results:

    • SRI-FLIMnet demonstrated superior performance in reconstructing spatial information from LR FLIM images.
    • Evaluated performance using semi-synthetic data and experimental images of bacterial-infected mouse macrophage cells.
    • The proposed data generation method and SRI-FLIMnet successfully achieved superior spatial resolution in FLIM applications.

    Conclusions:

    • The developed deep learning approach and SRI-FLIMnet provide an effective solution for obtaining HR FLIM images.
    • The method enables faster acquisition of high-resolution FLIM data, crucial for detailed biological studies.
    • This work advances FLIM capabilities by improving spatial resolution and image quality.