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,...
Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

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...
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

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 developed.

You might also read

Related Articles

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

Sort by
Same author

Interfacial properties of plant protein-flavonoid hybrid particles: towards influencing in vitro gastric digestion of emulsions.

Food chemistry·2026
Same author

Computational modeling of immersed non-spherical bodies in viscous flows to study embolus-hemodynamics interactions in large-vessel occlusion stroke.

Engineering with computers·2026
Same author

Modeling Nonstationary Time Series Using Locally Stationary Basis Processes.

Journal of time series analysis·2026
Same author

Modeling Particle Transport In Biomedical Flows Using Implicit Geometry Representations.

bioRxiv : the preprint server for biology·2026
Same author

Unravelling the Role of Oat β-Glucan on the Surface Behavior of an Oat Protein-Rich Coextract: An Enzymatic Approach.

Biomacromolecules·2026
Same author

Integrating transcriptomics and gene-level interpretable probabilistic Tsetlin Machine reveals elevated pancreatic cancer risk in Type 2 diabetes.

Computational biology and chemistry·2026

Related Experiment Video

Updated: Jun 2, 2026

Lens-free Video Microscopy for the Dynamic and Quantitative Analysis of Adherent Cell Culture
09:04

Lens-free Video Microscopy for the Dynamic and Quantitative Analysis of Adherent Cell Culture

Published on: February 23, 2018

In-context adaptation of VLMs for few-shot cell detection in optical microscopy.

Shreyan Ganguly1, Angona Biswas1, Jaydeep Rade1

  • 1Iowa State University, Ames, IA, United States.

Frontiers in Artificial Intelligence
|June 1, 2026
PubMed
Summary

Foundation vision-language models (VLMs) show promise for biomedical microscopy object detection. Few-shot learning with the Micro-OD benchmark improves performance, highlighting in-context adaptation for cell type identification.

Keywords:
artificial intelligencebiomedical imagingfew-shot learningmicroscopymultimodal sensingobject detectionreasoning

More Related Videos

A Label-Free Segmentation Approach for Intravital Imaging of Mammary Tumor Microenvironment
10:39

A Label-Free Segmentation Approach for Intravital Imaging of Mammary Tumor Microenvironment

Published on: May 24, 2022

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
10:07

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers

Published on: April 9, 2014

Related Experiment Videos

Last Updated: Jun 2, 2026

Lens-free Video Microscopy for the Dynamic and Quantitative Analysis of Adherent Cell Culture
09:04

Lens-free Video Microscopy for the Dynamic and Quantitative Analysis of Adherent Cell Culture

Published on: February 23, 2018

A Label-Free Segmentation Approach for Intravital Imaging of Mammary Tumor Microenvironment
10:39

A Label-Free Segmentation Approach for Intravital Imaging of Mammary Tumor Microenvironment

Published on: May 24, 2022

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers
10:07

Highly Resolved Intravital Striped-illumination Microscopy of Germinal Centers

Published on: April 9, 2014

Area of Science:

  • Biomedical Imaging
  • Computer Vision
  • Artificial Intelligence

Background:

  • Foundation vision-language models (VLMs) excel with natural images but are underexplored in biomedical microscopy.
  • Large annotated datasets are often unavailable for microscopic image analysis, limiting traditional deep learning approaches.

Purpose of the Study:

  • Investigate the utility of in-context learning with state-of-the-art VLMs for few-shot object detection in microscopy.
  • Introduce and utilize the Micro-OD benchmark for evaluating VLM performance on cell type detection.

Main Methods:

  • Systematic evaluation of eight VLMs under few-shot conditions using the Micro-OD benchmark.
  • Comparison of VLM variants with and without implicit test-time reasoning tokens.
  • Implementation of a hybrid Few-Shot Object Detection (FSOD) pipeline combining a detection head with VLM-based classification.

Main Results:

  • Zero-shot performance was weak due to domain gap, but few-shot support consistently improved detection accuracy.
  • Marginal performance gains were observed after six shots.
  • Some reasoning variants showed task-specific gains, varying across models and settings.

Conclusions:

  • In-context adaptation is a promising direction for VLM development in microscopy.
  • The Micro-OD benchmark provides a reproducible testbed for advancing open-vocabulary detection in biomedical imaging.
  • Further research is needed to enhance VLM utility for microscopic image analysis.