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

Chromatin Immunoprecipitation- ChIP02:36

Chromatin Immunoprecipitation- ChIP

11.6K
Chromatin immunoprecipitation, or ChIP, is an antibody-based technique used to identify sites on DNA that bind to transcription factors of interest or histone proteins. It also helps determine the type of histone modifications such as acetylation, phosphorylation, or methylation.
Types of ChIP
ChIP can be divided into two types - X-ChIP and N-ChIP. X-ChIP involves in vivo cross-linking of histones and regulatory proteins to DNA, fragmenting the DNA by sonication, and isolating the protein-DNA...
11.6K
Histone Modification02:32

Histone Modification

14.9K
The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
14.9K
Duplication of Chromatin Structure02:05

Duplication of Chromatin Structure

6.7K
The process of chromosome duplication during cell division requires genome-wide disruption and re-assembly of chromatin. The chromatin structure must be accurately inherited, reassembled, and maintained in the daughter cells to ensure lineage propagation.
The basic unit of the chromatin is the nucleosome, consisting of DNA wrapped around octameric histone proteins and short stretches of linker DNA separating individual nucleosomes. The histone proteins within the nucleosome have their...
6.7K

You might also read

Related Articles

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

Sort by
Same author

Caregiver-Associated Physical Activity Patterns, Dietary Behaviors and Interventional Beliefs in Individuals with Down Syndrome: Insights from a Large European Survey.

Nutrients·2026
Same author

Understanding Obesity in Individuals with Down Syndrome: Caregiver Perceptions, Awareness, and Motivation.

Nutrients·2026
Same author

De novo design of RNA pseudoknots with deep learning.

bioRxiv : the preprint server for biology·2026
Same author

Ex vivo expansion of hematopoietic stem and progenitor cells from human mobilized peripheral blood for gene therapy applications.

Molecular therapy : the journal of the American Society of Gene Therapy·2026
Same author

Simultaneous orthogonal cell engineering by a single CRISPR-Cas9 polyfunctional editor.

Nature communications·2026
Same author

A Systematic Survey and Benchmark of Deep Learning for Molecular Property Prediction in the Foundation Model Era.

Journal of chemical theory and computation·2026

Related Experiment Video

Updated: Nov 8, 2025

Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C
09:32

Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C

Published on: October 14, 2022

3.9K

Advantages of using graph databases to explore chromatin conformation capture experiments.

Daniele D'Agostino1, Pietro Liò2, Marco Aldinucci3

  • 1Institute of Electronics, Computer and Telecommunication Engineering, National Research Council of Italy, Genoa, Italy. dagostino@ieiit.cnr.it.

BMC Bioinformatics
|April 27, 2021
PubMed
Summary

This study introduces NeoHiC, a graph database application for analyzing chromosome conformation capture (Hi-C) data. NeoHiC enables efficient visualization and comparison of 3D genome folding patterns across experiments.

Keywords:
Chromatin captureGraph databasesGraph visualisationHi-C

More Related Videos

Adaptation of Hybridization Capture of Chromatin-associated Proteins for Proteomics to Mammalian Cells
09:27

Adaptation of Hybridization Capture of Chromatin-associated Proteins for Proteomics to Mammalian Cells

Published on: June 1, 2018

6.4K
Generation of Genome-wide Chromatin Conformation Capture Libraries from Tightly Staged Early Drosophila Embryos
10:35

Generation of Genome-wide Chromatin Conformation Capture Libraries from Tightly Staged Early Drosophila Embryos

Published on: October 3, 2018

20.9K

Related Experiment Videos

Last Updated: Nov 8, 2025

Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C
09:32

Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C

Published on: October 14, 2022

3.9K
Adaptation of Hybridization Capture of Chromatin-associated Proteins for Proteomics to Mammalian Cells
09:27

Adaptation of Hybridization Capture of Chromatin-associated Proteins for Proteomics to Mammalian Cells

Published on: June 1, 2018

6.4K
Generation of Genome-wide Chromatin Conformation Capture Libraries from Tightly Staged Early Drosophila Embryos
10:35

Generation of Genome-wide Chromatin Conformation Capture Libraries from Tightly Staged Early Drosophila Embryos

Published on: October 3, 2018

20.9K

Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • High-throughput Chromosome Conformation Capture (Hi-C) generates genome-wide DNA interaction data, typically in matrix format.
  • Matrix representations struggle to capture the complex 3D topology of DNA in eukaryotic cells.
  • Graph-based representations offer advantages for describing intricate DNA spatial organization.

Purpose of the Study:

  • To explore the utility of graph databases for storing and analyzing large-scale Hi-C data.
  • To address the limitations of existing visualization tools in managing the vast number of contacts in graph representations of Hi-C data.
  • To leverage graph databases for efficient spatial pattern analysis and comparison of Hi-C experiments.

Main Methods:

  • Utilizing a graph database to store and analyze Hi-C experimental data.
  • Implementing strategies to manage a large number of edges (contacts) connecting nodes (genes).
  • Employing graph database capabilities for both analysis and visualization of spatial patterns in Hi-C data.

Main Results:

  • Developed NeoHiC, an open-source web application for visualizing and analyzing Hi-C networks.
  • NeoHiC is based on the Neo4j graph database.
  • The application facilitates progressive visualization and analysis of Hi-C data.

Conclusions:

  • NeoHiC provides a user-friendly platform for analyzing Hi-C data.
  • Future accumulation of experiments will enhance its utility for comparing gene neighbors and functional domains.
  • The tool aids in identifying changes in genomic compartments and co-organization across different conditions.