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

Cluster Sampling Method01:20

Cluster Sampling Method

14.9K
Appropriate sampling methods ensure that samples are drawn without bias and accurately represent the population. Because measuring the entire population in a study is not practical, researchers use samples to represent the population of interest.
To choose a cluster sample, divide the population into clusters (groups) and then randomly select some of the clusters. All the members from these clusters are in the cluster sample. For example, if you randomly sample four departments from your...
14.9K
Protein Networks02:26

Protein Networks

4.6K
An organism can have thousands of different proteins, and these proteins must cooperate to ensure the health of an organism. Proteins bind to other proteins and form complexes to carry out their functions. Many proteins interact with multiple other proteins creating a complex network of protein interactions.
These interactions can be represented through maps depicting protein-protein interaction networks, represented as nodes and edges. Nodes are circles that are representative of a protein,...
4.6K
Analysis of Population Pharmacokinetic Data01:12

Analysis of Population Pharmacokinetic Data

821
Analysis of population pharmacokinetic data involves studying the behavior of drugs within diverse populations to understand their pharmacokinetic parameters. Traditional pharmacokinetic methods typically involve collecting samples from a few individuals and estimating these parameters. While these methods are commonly used, they have limitations in capturing the variability in drug response among individuals or heterogeneous populations. Population pharmacokinetics is employed to address these...
821
Network Covalent Solids02:18

Network Covalent Solids

16.3K
Network covalent solids contain a three-dimensional network of covalently bonded atoms as found in the crystal structures of nonmetals like diamond, graphite, silicon, and some covalent compounds, such as silicon dioxide (sand) and silicon carbide (carborundum, the abrasive on sandpaper). Many minerals have networks of covalent bonds.
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
16.3K
Bioavailability Study Design: Single Versus Multiple Dose Studies01:11

Bioavailability Study Design: Single Versus Multiple Dose Studies

255
Bioavailability studies are essential for understanding how a drug is absorbed, distributed, metabolized, and excreted in the body. These studies assess the extent and rate at which the active pharmaceutical agent becomes available at the site of action. The design of bioavailability studies can involve single-dose or multiple-dose regimens, each with distinct advantages and limitations.Single-dose studies are the preferred approach due to their simplicity and reduced drug exposure for...
255
Extraction: Partition and Distribution Coefficients01:14

Extraction: Partition and Distribution Coefficients

5.0K
The distribution law or Nernst's distribution law is the law that governs the distribution of a solute between two immiscible solvents. This law, also known as the partition law, states that if a solute is added to the mixture of two immiscible solvents at a constant temperature, the solute is distributed between the two solvents in such a way that the ratio of solute concentrations in the solvents remains constant at equilibrium.
For extracting a solute from an aqueous phase into an...
5.0K

You might also read

Related Articles

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

Sort by
Same author

An AI-powered Bayesian Generative Modeling Approach for Causal Inference in Observational Studies.

Journal of the American Statistical Association·2026
Same author

Fault-tolerant 3D reconstruction from 2D spatial proteomics sections.

bioRxiv : the preprint server for biology·2026
Same author

Coordinated immune-epithelial dynamics in the nasal epithelium protect against respiratory virus infection.

bioRxiv : the preprint server for biology·2026
Same author

Robust semi-supervised scRNA-seq integration from virtual adversarial learning.

bioRxiv : the preprint server for biology·2026
Same author

MIXPRS enables multi-population and multi-method polygenic risk scores using summary statistics.

Nature genetics·2026
Same author

Analysis Of Salivary Herpesviruses Reveals Associations Between HHV-6 And Long COVID Severity.

medRxiv : the preprint server for health sciences·2026

Related Experiment Video

Updated: Feb 16, 2026

CRISPR Gene Editing Tool for MicroRNA Cluster Network Analysis
10:40

CRISPR Gene Editing Tool for MicroRNA Cluster Network Analysis

Published on: April 25, 2022

2.9K

Scalable multi-sample single-cell data analysis by Partition-Assisted Clustering and Multiple Alignments of Networks.

Ye Henry Li1, Dangna Li2, Nikolay Samusik3

  • 1Structural Biology Department and Public Policy Program, Stanford University, Stanford, United States of America.

Plos Computational Biology
|December 28, 2017
PubMed
Summary
This summary is machine-generated.

Partition-Assisted Clustering and Multiple Alignments of Networks (PAC-MAN) offers automated cell population discovery in mass cytometry (CyTOF) data. This method efficiently aligns subpopulations across multiple samples for comprehensive cellular state analysis.

More Related Videos

JUMPn: A Streamlined Application for Protein Co-Expression Clustering and Network Analysis in Proteomics
07:28

JUMPn: A Streamlined Application for Protein Co-Expression Clustering and Network Analysis in Proteomics

Published on: October 19, 2021

3.7K
Author Spotlight: Emerging Technologies and Advanced Tools for Decoding Metabolomics Data Analysis
07:11

Author Spotlight: Emerging Technologies and Advanced Tools for Decoding Metabolomics Data Analysis

Published on: November 10, 2023

3.3K

Related Experiment Videos

Last Updated: Feb 16, 2026

CRISPR Gene Editing Tool for MicroRNA Cluster Network Analysis
10:40

CRISPR Gene Editing Tool for MicroRNA Cluster Network Analysis

Published on: April 25, 2022

2.9K
JUMPn: A Streamlined Application for Protein Co-Expression Clustering and Network Analysis in Proteomics
07:28

JUMPn: A Streamlined Application for Protein Co-Expression Clustering and Network Analysis in Proteomics

Published on: October 19, 2021

3.7K
Author Spotlight: Emerging Technologies and Advanced Tools for Decoding Metabolomics Data Analysis
07:11

Author Spotlight: Emerging Technologies and Advanced Tools for Decoding Metabolomics Data Analysis

Published on: November 10, 2023

3.3K

Area of Science:

  • Immunology
  • Computational Biology
  • Biotechnology

Background:

  • Mass cytometry (CyTOF) enables high-dimensional single-cell analysis with numerous markers.
  • Generating and analyzing multiple CyTOF samples presents challenges for subpopulation discovery and cross-sample alignment.
  • Existing computational methods struggle with the scalability and complexity of large, multi-sample CyTOF datasets.

Purpose of the Study:

  • To develop a computational method for automated cell population identification in mass cytometry data.
  • To enable accurate alignment of cell subpopulations across multiple CyTOF samples.
  • To facilitate the definition of dataset-level cellular states from large-scale CyTOF experiments.

Main Methods:

  • Developed Partition-Assisted Clustering and Multiple Alignments of Networks (PAC-MAN) algorithm.
  • PAC-MAN performs fast, automatic identification of cell populations.
  • The method aligns subpopulations across samples to define dataset-level cellular states.

Main Results:

  • PAC-MAN achieves automated cell population discovery comparable to expert manual analysis.
  • The algorithm is computationally efficient, handling large-scale CyTOF datasets.
  • Enables robust alignment of cellular states across multiple samples.

Conclusions:

  • PAC-MAN overcomes limitations in analyzing multi-sample CyTOF data.
  • Provides a scalable solution for subpopulation discovery and cross-sample analysis.
  • Accelerates insights from large CyTOF datasets in clinical and cancer research.