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

Maxam-Gilbert Sequencing01:05

Maxam-Gilbert Sequencing

11.2K
In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
11.2K
Next-generation Sequencing03:00

Next-generation Sequencing

88.9K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
88.9K
RNA-seq03:21

RNA-seq

10.0K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
10.0K

You might also read

Related Articles

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

Sort by
Same author

ToxiTaRGET: a multi-omics database for toxicant-responsive molecular targets.

Nature communications·2026
Same author

Benchmarking genome choice in functional genomics analyses.

Nature communications·2026
Same author

TaRGET II Data Portal: a multi-omics resource for environmental toxicant studies in mice.

Nature communications·2026
Same author

A Multimodal Single-Cell Epigenomic and 3D Genome Atlas of the Human Basal Ganglia.

bioRxiv : the preprint server for biology·2026
Same author

Single-cell Multiome Analysis of Chromatin State and Transcriptome in the Human Basal Ganglia.

bioRxiv : the preprint server for biology·2026
Same author

Single-Cell Atlas of Transcription and Chromatin States Reveals Regulatory Programs in the Human Brain.

bioRxiv : the preprint server for biology·2026

Related Experiment Video

Updated: Jul 8, 2025

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution
13:47

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution

Published on: February 24, 2015

25.6K

Modbed track: Visualization of modified bases in single-molecule sequencing.

Daofeng Li1, Xiaoyu Zhuo1, Jessica K Harrison1

  • 1Department of Genetics, The Edison Family Center for Genome Sciences & Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.

Cell Genomics
|December 20, 2023
PubMed
Summary

New visualization tools enable researchers to explore epigenome data from long-read sequencing. The modbed track type in the WashU Epigenome Browser displays chemical modifications on DNA bases within individual reads.

Keywords:
WashU Epigenome Browserlong-read sequencingmethylationvisualization

More Related Videos

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
09:10

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes

Published on: May 22, 2018

9.2K
Visualizing Protein-DNA Interactions in Live Bacterial Cells Using Photoactivated Single-molecule Tracking
16:21

Visualizing Protein-DNA Interactions in Live Bacterial Cells Using Photoactivated Single-molecule Tracking

Published on: March 10, 2014

17.8K

Related Experiment Videos

Last Updated: Jul 8, 2025

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution
13:47

Enhanced Reduced Representation Bisulfite Sequencing for Assessment of DNA Methylation at Base Pair Resolution

Published on: February 24, 2015

25.6K
A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes
09:10

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes

Published on: May 22, 2018

9.2K
Visualizing Protein-DNA Interactions in Live Bacterial Cells Using Photoactivated Single-molecule Tracking
16:21

Visualizing Protein-DNA Interactions in Live Bacterial Cells Using Photoactivated Single-molecule Tracking

Published on: March 10, 2014

17.8K

Area of Science:

  • Genomics and Epigenetics
  • Bioinformatics and Computational Biology

Background:

  • Long-read sequencing technologies have advanced significantly, improving read length and accuracy in detecting DNA base modifications.
  • Investigating the epigenome is crucial for understanding gene regulation, but visualization of modified bases in genome browsers remains a challenge.

Purpose of the Study:

  • To address the limitations in visualizing modified bases from long-read sequencing data.
  • To introduce a novel track type for enhanced exploration of epigenomic information.

Main Methods:

  • Development and implementation of the 'modbed' track type within the WashU Epigenome Browser.
  • The modbed track visualizes modification details at single-read and aggregated molecule levels across various resolutions.
  • Support for local file uploads and accessible URLs for seamless data integration.

Main Results:

  • The modbed track type successfully enables visualization of chemical modifications on canonical nucleotide bases from long-read sequencing data.
  • Users can now explore detailed modification patterns within individual sequencing reads and across multiple molecules.
  • The WashU Epigenome Browser provides a platform for dynamic and high-resolution epigenomic data visualization.

Conclusions:

  • The modbed track type significantly enhances the ability to visualize and analyze epigenomic data generated by long-read sequencing.
  • This advancement facilitates a more comprehensive exploration of the epigenome, opening new avenues for biological discovery.
  • The WashU Epigenome Browser offers a free and accessible tool for researchers studying DNA modifications.