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

Mutations01:39

Mutations

94.5K
Overview
94.5K
Mutations01:35

Mutations

44.6K
Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
44.6K
Viral Mutations00:36

Viral Mutations

39.9K
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
39.9K
Adaptive Mechanisms in Cancer Cells02:53

Adaptive Mechanisms in Cancer Cells

7.1K
Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
7.1K
Cells of the Adaptive Immune Response01:23

Cells of the Adaptive Immune Response

8.9K
The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
8.9K
Mutation, Gene Flow, and Genetic Drift01:09

Mutation, Gene Flow, and Genetic Drift

64.4K
In a population that is not at Hardy-Weinberg equilibrium, the frequency of alleles changes over time. Therefore, any deviations from the five conditions of Hardy-Weinberg equilibrium can alter the genetic variation of a given population. Conditions that change the genetic variability of a population include mutations, natural selection, non-random mating, gene flow, and genetic drift (small population size).
64.4K

You might also read

Related Articles

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

Sort by
Same author

Bio-inspired fiber-optic-neural network enabled multi-physical sensing for tissue-safe robotic adhesion.

Biosensors & bioelectronics·2026
Same author

In Vivo Mapping of Vasculature and Mechanics for Skin Tumor Using Optical Coherence Tomography.

Journal of biophotonics·2026
Same author

Fabrication of low-damage, high-strength FBG using a weak-reflection femtosecond point-by-point technique.

Optics express·2026
Same author

Intracavity spectral control and full temperature range stability optimization of a superfluorescent fiber source for the high-precision fiber optic gyroscope.

Applied optics·2026
Same author

Gold metasurfaces on GaSb for compressively sensed mid-wave infrared spectral reconstruction.

Applied optics·2026
Same author

Strain and temperature cross-sensitivity decoupling method via a single glass fiber-reinforced polymer encapsulated chirped fiber Bragg grating.

Optics express·2026
Same journal

RETRACTED: Bakshi et al. Crocin Inhibits Angiogenesis and Metastasis in Colon Cancer via TNF-α/NF-kB/VEGF Pathways. <i>Cells</i> 2022, <i>11</i>, 1502.

Cells·2026
Same journal

Correction: Verde et al. Molecular Mechanisms of Protein Aggregation in ALS-FTD: Focus on TDP-43 and Cellular Protective Responses. <i>Cells</i> 2025, <i>14</i>, 680.

Cells·2026
Same journal

Inflammation in Cardiomyopathies: Cellular Mechanisms Across Cardiac Phenotype.

Cells·2026
Same journal

IL-4/IL-13-Driven Dysregulation of Epidermal Lipid Metabolism in Atopic Dermatitis: An Immunometabolic Link Between Type 2 Inflammation and Barrier Dysfunction.

Cells·2026
Same journal

Activity of DNA- and RNA-Guided Prokaryotic Argonautes in Human Mitochondria.

Cells·2026
Same journal

Placental Pathophysiology in Maternal Psychoactive Substance Use: Biological, Clinical, and Forensic Perspectives.

Cells·2026
See all related articles

Related Experiment Video

Updated: Feb 5, 2026

Author Spotlight: Efficient Image Recognition Using Directional Gradient Histogram Technique and Support Vector Machines
08:27

Author Spotlight: Efficient Image Recognition Using Directional Gradient Histogram Technique and Support Vector Machines

Published on: January 5, 2024

1.6K

Cell Group Recognition Method Based on Adaptive Mutation PSO-SVM.

Yue Wang1, Xiaochen Meng2, Lianqing Zhu3

  • 1Beijing Key Laboratory for Optoelectronic Measurement Technology, Beijing Information Science and Technology University, Beijing 100192, China. wangyue_1231@sina.com.

Cells
|September 15, 2018
PubMed
Summary
This summary is machine-generated.

This study introduces an adaptive mutation particle swarm optimization-support vector machine (PSO-SVM) model to enhance flow cytometry (FCM) data analysis. The novel method significantly improves cell clustering accuracy and overcomes limitations of traditional algorithms.

Keywords:
adaptive mutation PSO-SVMbiomedicinecell clusteringflow cytometryfluorescent reagentsupervised clustering

More Related Videos

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
12:40

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors

Published on: December 7, 2014

15.3K
Quantification of Colonic Stem Cell Mutations
07:53

Quantification of Colonic Stem Cell Mutations

Published on: September 25, 2015

7.0K

Related Experiment Videos

Last Updated: Feb 5, 2026

Author Spotlight: Efficient Image Recognition Using Directional Gradient Histogram Technique and Support Vector Machines
08:27

Author Spotlight: Efficient Image Recognition Using Directional Gradient Histogram Technique and Support Vector Machines

Published on: January 5, 2024

1.6K
A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
12:40

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors

Published on: December 7, 2014

15.3K
Quantification of Colonic Stem Cell Mutations
07:53

Quantification of Colonic Stem Cell Mutations

Published on: September 25, 2015

7.0K

Area of Science:

  • Biomedical Detection Technology
  • Computational Biology
  • Statistical Analysis

Background:

  • High-throughput flow cytometry (FCM) generates large, complex multidimensional data, increasing demand for robust statistical analysis methods.
  • Support Vector Machines (SVM) are effective for classification, but their clustering accuracy heavily depends on optimal selection of penalty factor (c) and kernel parameter (g).
  • Traditional Particle Swarm Optimization (PSO) can struggle with local optima and poor convergence for large datasets.

Purpose of the Study:

  • To develop an optimized SVM algorithm for improved FCM data clustering.
  • To address the parameter optimization challenges in SVM for accurate cell identification.
  • To enhance the reliability and efficiency of multidimensional FCM data analysis.

Main Methods:

  • Proposed an adaptive mutation particle swarm optimization (PSO) algorithm integrated with SVM (PSO-SVM) for parameter optimization.
  • Selected an appropriate kernel function for the FCM sample data.
  • Applied the adaptive mutation PSO algorithm to optimize SVM parameters for cell clustering.
  • Validated the method using extensive FCM experimental data.

Main Results:

  • The proposed PSO-SVM method significantly improved clustering correctness by 19.38% compared to traditional SVM.
  • Achieved a high clustering correctness rate of 99.79% for FCM data.
  • Demonstrated superior performance over cross-validation and standard PSO algorithms in FCM data clustering.
  • Showcased lower time complexity and reduced need for manual intervention.

Conclusions:

  • The adaptive mutation PSO-SVM algorithm offers a highly accurate and efficient solution for analyzing complex FCM data.
  • This method effectively overcomes the limitations of traditional SVM and PSO, particularly for large-scale biological datasets.
  • The developed approach advances cell group identification in biomedical detection technology.