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

Two-Dimensional Microscopy in Microbiology01:29

Two-Dimensional Microscopy in Microbiology

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...

You might also read

Related Articles

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

Sort by
Same author

Reliable Molecular Retrieval from Mass Spectra Using Conformal Prediction.

Journal of chemical information and modeling·2026
Same author

Life strategies of bacterial taxa in rearing water microbiomes of whiteleg shrimp (Litopenaeus vannamei) larviculture.

World journal of microbiology & biotechnology·2026
Same author

Hidden threats: exploring biofilm communities in broiler houses and pig nursery units drinking water lines.

BMC microbiology·2026
Same author

How negative sampling shapes the performance of transcription factor binding site prediction models.

Bioinformatics (Oxford, England)·2026
Same author

Harnessing machine learning to predict antibiotic susceptibility in Pseudomonas aeruginosa biofilms.

NPJ biofilms and microbiomes·2025
Same author

Differential recovery of chain-elongating bacteria: comparing droplet, plating, and dilution-to-extinction methods.

mSystems·2025
Same journal

Cysteine-S-nitrosylation inhibits ROP5-mediated immune evasion in <i>Toxoplasma gondii</i>.

mSphere·2026
Same journal

Inheritance of four-membrane-bound structures in the "apicoplast-minus" <i>Plasmodium falciparum</i>.

mSphere·2026
Same journal

mSphere of Influence: The bacterial growth law-revisiting the old to discover the new.

mSphere·2026
Same journal

Preclinical characterization of immune responses induced by a candidate gonococcal native outer membrane vesicle vaccine.

mSphere·2026
Same journal

Auxotrophy from bioenergetic demand: the case of proline addiction in <i>Clostridioides difficile</i>.

mSphere·2026
Same journal

Applying PCR cycle autonormalization to PacBio full-length 16S rRNA library preparations: impacts on error rates and sequence distributions.

mSphere·2026
See all related articles

Related Experiment Video

Updated: Jun 23, 2026

Characterizing Microbiome Dynamics &#8211; Flow Cytometry Based Workflows from Pure Cultures to Natural Communities
09:57

Characterizing Microbiome Dynamics – Flow Cytometry Based Workflows from Pure Cultures to Natural Communities

Published on: July 12, 2018

12.3K

PhenoGMM: Gaussian Mixture Modeling of Cytometry Data Quantifies Changes in Microbial Community Structure.

Peter Rubbens1,2, Ruben Props3, Frederiek-Maarten Kerckhof3

  • 1KERMIT, Department of Data Analysis and Mathematical Modelling, Ghent University, Ghent, Belgium peter.rubbens@vliz.be.

Msphere
|February 4, 2021
PubMed
Summary
This summary is machine-generated.

We developed PhenoGMM, an automated method using Gaussian mixture models to analyze microbial flow cytometry data. This approach quantifies microbial community structure and dynamics rapidly and quantitatively.

Keywords:
diversityfingerprintflow cytometrymachine learningmicrobial communitiesmixture model

More Related Videos

Author Spotlight: Advancing Research in Microbial Autoaggregation Using Imaging Flow Cytometry
05:19

Author Spotlight: Advancing Research in Microbial Autoaggregation Using Imaging Flow Cytometry

Published on: September 29, 2023

1.0K
Assembly and Quantification of Co-Cultures Combining Heterotrophic Yeast with Phototrophic Sugar-Secreting Cyanobacteria
05:44

Assembly and Quantification of Co-Cultures Combining Heterotrophic Yeast with Phototrophic Sugar-Secreting Cyanobacteria

Published on: December 27, 2024

1.3K

Related Experiment Videos

Last Updated: Jun 23, 2026

Characterizing Microbiome Dynamics &#8211; Flow Cytometry Based Workflows from Pure Cultures to Natural Communities
09:57

Characterizing Microbiome Dynamics – Flow Cytometry Based Workflows from Pure Cultures to Natural Communities

Published on: July 12, 2018

12.3K
Author Spotlight: Advancing Research in Microbial Autoaggregation Using Imaging Flow Cytometry
05:19

Author Spotlight: Advancing Research in Microbial Autoaggregation Using Imaging Flow Cytometry

Published on: September 29, 2023

1.0K
Assembly and Quantification of Co-Cultures Combining Heterotrophic Yeast with Phototrophic Sugar-Secreting Cyanobacteria
05:44

Assembly and Quantification of Co-Cultures Combining Heterotrophic Yeast with Phototrophic Sugar-Secreting Cyanobacteria

Published on: December 27, 2024

1.3K

Area of Science:

  • Microbiology
  • Computational Biology
  • Ecology

Background:

  • Microbial communities are crucial in ecosystems.
  • Traditional 16S rRNA gene sequencing is time-consuming.
  • Flow cytometry offers rapid single-cell analysis of microbial communities.

Purpose of the Study:

  • To develop an automated fingerprinting method for microbial flow cytometry data.
  • To address limitations of manual annotation and multivariate data handling in existing methods.
  • To enable rapid and quantitative characterization of microbial community structure and dynamics.

Main Methods:

  • Development of PhenoGMM, a model-based fingerprinting approach using Gaussian mixture models.
  • Application of PhenoGMM to analyze flow cytometry data from synthetic and natural ecosystems.
  • Comparison of PhenoGMM performance against a generic binning fingerprinting approach.

Main Results:

  • PhenoGMM successfully quantifies changes in microbial community structure.
  • The method expresses community changes in terms of cytometric diversity.
  • PhenoGMM demonstrates general applicability across diverse ecosystem data.

Conclusions:

  • PhenoGMM provides a rapid and quantitative tool for screening microbial community structure.
  • The automated approach overcomes limitations of traditional cytometric fingerprinting methods.
  • PhenoGMM facilitates efficient analysis of microbial dynamics using flow cytometry.