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
Confocal Fluorescence Microscopy01:16

Confocal Fluorescence Microscopy

20.0K
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,...
20.0K
Immunofluorescence Microscopy01:12

Immunofluorescence Microscopy

12.9K
A fluorescence microscope uses fluorescent chromophores called fluorochromes, which can absorb energy from a light source and then emit this energy as visible light. Fluorochromes include naturally fluorescent substances (such as chlorophylls) and fluorescent stains that are added to the specimen to create contrast. Dyes such as Texas red and FITC are examples of fluorochromes. Other examples include the nucleic acid dyes 4’,6’-diamidino-2-phenylindole (DAPI), and acridine orange.
12.9K

You might also read

Related Articles

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

Sort by
Same author

Minimal <i>N</i>-methylated and stapled peptide inhibitors of the autophagy protein GABARAP.

RSC chemical biology·2026
Same author

Inhibition of Chikungunya virus nsP2 protease in vitro by scorpion venom peptide pantinin-1.

PloS one·2026
Same author

Transthyretin stabilizer therapy increases naturally-occurring antibodies in ATTR cardiomyopathy.

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis·2026
Same author

Minimal <i>N</i> -methylated and stapled peptide inhibitors of the autophagy protein GABARAP.

bioRxiv : the preprint server for biology·2026
Same author

The Proteome of Human Amyloid Beta Oligomers.

Biochemistry·2026
Same author

Drug Development.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2025

Related Experiment Video

Updated: Jan 18, 2026

Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy
09:30

Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy

Published on: January 18, 2017

12.4K

Artifact detection in fluorescence microscopy using convolutional autoencoder.

Fabian Rehn1,2,3, Marlene Pils3, Tuyen Bujnicki2

  • 1Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, Universitätsstr. 1, 40225, Düsseldorf, Germany.

Scientific Reports
|September 12, 2025
PubMed
Summary
This summary is machine-generated.

This study introduces an automated method for detecting artifacts in microscopy images without prior training. The convolutional autoencoder model accurately identifies unseen artifacts, improving image analysis accuracy and reproducibility.

More Related Videos

DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning
04:17

DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning

Published on: May 10, 2024

1.5K
Excitation-Scanning Hyperspectral Imaging Microscopy to Efficiently Discriminate Fluorescence Signals
07:34

Excitation-Scanning Hyperspectral Imaging Microscopy to Efficiently Discriminate Fluorescence Signals

Published on: August 22, 2019

8.4K

Related Experiment Videos

Last Updated: Jan 18, 2026

Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy
09:30

Open Source High Content Analysis Utilizing Automated Fluorescence Lifetime Imaging Microscopy

Published on: January 18, 2017

12.4K
DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning
04:17

DNA Virus Detection System Based on RPA-CRISPR/Cas12a-SPM and Deep Learning

Published on: May 10, 2024

1.5K
Excitation-Scanning Hyperspectral Imaging Microscopy to Efficiently Discriminate Fluorescence Signals
07:34

Excitation-Scanning Hyperspectral Imaging Microscopy to Efficiently Discriminate Fluorescence Signals

Published on: August 22, 2019

8.4K

Area of Science:

  • Microscopy
  • Image Analysis
  • Artificial Intelligence

Background:

  • Robust artifact detection is crucial for accurate fluorescence microscopy image analysis.
  • Automated methods reduce time, cost, and bias while enhancing reproducibility.
  • Current AI methods often require large training datasets for known artifact types.

Purpose of the Study:

  • To develop an automated method for detecting previously unseen artifacts in microscopy images.
  • To eliminate the need for training sets of artifact-laden images.
  • To improve the reliability of image analysis in large or time-sensitive datasets.

Main Methods:

  • Trained a convolutional autoencoder on artifact-free images using surface-based intensity distribution analysis (sFIDA) technology.
  • Detected artifacts by measuring discrepancies between input and reconstructed images.
  • Validated the model across multiple datasets and artifact types.

Main Results:

  • Achieved an average accuracy of 95.5% in classifying artifacts across different datasets.
  • Successfully detected novel artifacts with variations in cause, structure, size, and intensity.
  • Demonstrated the model's effectiveness without requiring a specific artifact training set.

Conclusions:

  • Convolutional autoencoders offer a lightweight yet effective solution for automated artifact detection in microscopy.
  • The proposed method's independence from artifact-specific training enables broad applicability across various microscopy techniques.
  • This approach enhances analytical accuracy and reproducibility in fluorescence microscopy image analysis.