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

13.0K
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...
13.0K

You might also read

Related Articles

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

Sort by
Same author

Epigenetic landscape, key transcriptional regulators, and in vivo identification of human Tr1 cells.

Science advances·2026
Same author

XIST RNA-protein complex in female-biased autoimmunity: From molecular scaffolds to new clinical biomarkers.

The Journal of investigative dermatology·2026
Same author

Somatic mutations reveal the ontogeny of human microglia.

bioRxiv : the preprint server for biology·2026
Same author

Correction: Annotation of nuclear lncRNAs based on chromatin interactions.

PloS one·2026
Same author

Fast and accurate resolution of ecDNA sequence using Cycle-Extractor.

bioRxiv : the preprint server for biology·2026
Same author

A recipe for chaos: Extrachromosomal DNA and the hallmarks of cancer.

Cell·2026

Related Experiment Video

Updated: Apr 19, 2026

Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq
09:08

Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq

Published on: November 13, 2017

18.7K

ATAC-seq: A Method for Assaying Chromatin Accessibility Genome-Wide.

Jason D Buenrostro1,2, Beijing Wu1, Howard Y Chang2

  • 1Department of Genetics, Stanford University School of Medicine, Stanford, California.

Current Protocols in Molecular Biology
|January 7, 2015
PubMed
Summary

Assay for Transposase-Accessible Chromatin with high-throughput sequencing (ATAC-seq) maps genome-wide chromatin accessibility. This method uses Tn5 transposase to identify accessible DNA regions for downstream analyses like transcription factor binding and nucleosome positioning.

Keywords:
ATAC-seqchromatin accessibilitytransposase

More Related Videos

ATAC-Seq Optimization for Cancer Epigenetics Research
07:13

ATAC-Seq Optimization for Cancer Epigenetics Research

Published on: June 30, 2022

5.7K
ATAC-seq Assay with Low Mitochondrial DNA Contamination from Primary Human CD4+ T Lymphocytes
08:36

ATAC-seq Assay with Low Mitochondrial DNA Contamination from Primary Human CD4+ T Lymphocytes

Published on: March 22, 2019

13.3K

Related Experiment Videos

Last Updated: Apr 19, 2026

Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq
09:08

Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq

Published on: November 13, 2017

18.7K
ATAC-Seq Optimization for Cancer Epigenetics Research
07:13

ATAC-Seq Optimization for Cancer Epigenetics Research

Published on: June 30, 2022

5.7K
ATAC-seq Assay with Low Mitochondrial DNA Contamination from Primary Human CD4+ T Lymphocytes
08:36

ATAC-seq Assay with Low Mitochondrial DNA Contamination from Primary Human CD4+ T Lymphocytes

Published on: March 22, 2019

13.3K

Area of Science:

  • Genomics
  • Molecular Biology
  • Epigenetics

Background:

  • Chromatin accessibility is crucial for gene regulation.
  • Existing methods for genome-wide chromatin accessibility mapping have limitations.
  • Understanding nucleosome positioning and transcription factor binding requires precise genomic tools.

Purpose of the Study:

  • To describe the Assay for Transposase-Accessible Chromatin with high-throughput sequencing (ATAC-seq) method.
  • To highlight ATAC-seq as a tool for mapping genome-wide chromatin accessibility.
  • To present ATAC-seq as an efficient alternative to other established techniques.

Main Methods:

  • Utilizes hyperactive Tn5 transposase to probe DNA accessibility.
  • Tn5 transposase inserts sequencing adapters into accessible chromatin regions.
  • High-throughput sequencing of adapter-inserted DNA fragments.

Main Results:

  • Enables genome-wide mapping of accessible chromatin regions.
  • Facilitates inference of transcription-factor binding sites.
  • Allows for the determination of nucleosome positions within accessible regions.

Conclusions:

  • ATAC-seq is a fast and sensitive method for assaying chromatin accessibility.
  • The technique provides a comprehensive view of the accessible genome.
  • ATAC-seq offers advantages over DNase-seq and MNase-seq for specific applications.