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 Experiment Video

Updated: Jun 28, 2026

Ultralow Input Genome Sequencing Library Preparation from a Single Tardigrade Specimen
10:28

Ultralow Input Genome Sequencing Library Preparation from a Single Tardigrade Specimen

Published on: July 15, 2018

Genome-scale validation of deep-sequencing libraries.

Dominic Schmidt1, Rory Stark, Michael D Wilson

  • 1Cancer Research UK, Cambridge Research Institute, Li Ka Shing Centre, Cambridge, UK.

Plos One
|November 13, 2008
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

The prebiotic inulin affects virulence factor expression in <i>Candida albicans</i>.

mBio·2026
Same author

Short-term antagonism between bacteriophages and macrophages decreases with bacteria-phage coevolution.

The ISME journal·2026
Same author

Closing the gap on antifungal resistance.

Nature medicine·2026
Same author

Flipping sides in NETosis.

Nature immunology·2026
Same author

Activated ATF6α is a hepatic tumour driver restricting immunosurveillance.

Nature·2026
Same author

Mycobacterial α-glucans hijack dectin-1 to facilitate intracellular bacterial survival.

Science immunology·2026
Same journal

Analysis of strength degradation of coal and rock masses and stability of mined areas under long term immersion environment.

PloS one·2026
Same journal

Biogenic Silver-Selenium nanocomposite with anticancer activity and potent efficacy against vancomycin-resistant Staphylococcus aureus.

PloS one·2026
Same journal

Preparation and physicochemical characterization of a biodegradable chitosan/carboxymethyl cellulose hydrogel synthesized in NaOH/urea medium.

PloS one·2026
Same journal

Action-guilt, survivor-guilt, and depression in combat-related PTSD.

PloS one·2026
Same journal

Explainable machine learning for predicting activities of daily living at discharge in stroke patients: A retrospective study using SHAP interpretability.

PloS one·2026
Same journal

Deep learning based two-way feature depiction model for brain tumor detection.

PloS one·2026
See all related articles

Mab-seq uses genomic microarrays for quality control of sequencing libraries, enabling efficient genome-wide protein-DNA interaction analysis before deep sequencing. This method provides reliable preliminary data and complements high-throughput sequencing results.

Area of Science:

  • Genomics
  • Molecular Biology
  • Bioinformatics

Background:

  • Chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq) is crucial for mapping protein-DNA interactions genome-wide.
  • Limited access to sequencing technology hinders the widespread application of ChIP-seq.
  • Developing cost-effective and accessible methods for preliminary data generation is essential.

Purpose of the Study:

  • To introduce Mab-seq, a novel protocol for genome-scale quality evaluation of nucleic acid libraries for deep sequencing.
  • To demonstrate the utility of commercially available genomic microarrays in maximizing library creation efficiency.
  • To enable rapid generation of reliable preliminary data on a chromosomal scale prior to deep sequencing.

Main Methods:

  • Development and implementation of the Mab-seq protocol.

More Related Videos

Automated Gel Size Selection to Improve the Quality of Next-generation Sequencing Libraries Prepared from Environmental Water Samples
13:26

Automated Gel Size Selection to Improve the Quality of Next-generation Sequencing Libraries Prepared from Environmental Water Samples

Published on: April 17, 2015

Competitive Genomic Screens of Barcoded Yeast Libraries
11:59

Competitive Genomic Screens of Barcoded Yeast Libraries

Published on: August 11, 2011

Related Experiment Videos

Last Updated: Jun 28, 2026

Ultralow Input Genome Sequencing Library Preparation from a Single Tardigrade Specimen
10:28

Ultralow Input Genome Sequencing Library Preparation from a Single Tardigrade Specimen

Published on: July 15, 2018

Automated Gel Size Selection to Improve the Quality of Next-generation Sequencing Libraries Prepared from Environmental Water Samples
13:26

Automated Gel Size Selection to Improve the Quality of Next-generation Sequencing Libraries Prepared from Environmental Water Samples

Published on: April 17, 2015

Competitive Genomic Screens of Barcoded Yeast Libraries
11:59

Competitive Genomic Screens of Barcoded Yeast Libraries

Published on: August 11, 2011

  • Utilizing commercially available genomic microarrays for library quality assessment.
  • Comparison of enriched regions identified by microarray analysis versus high-throughput sequencing.
  • Main Results:

    • Mab-seq effectively generates genome-scale quality evaluations for sequencing libraries.
    • Genomic microarrays can be used to efficiently create libraries and obtain preliminary chromosomal-scale data.
    • Mab-seq results show agreement with high-throughput sequencing for core enriched regions.
    • The study characterizes additional enriched regions identifiable by high-throughput sequencing.

    Conclusions:

    • Mab-seq offers a valuable approach for preliminary assessment of ChIP-seq libraries, improving efficiency and accessibility.
    • The integration of microarrays provides a cost-effective method for initial data generation and quality control.
    • Mab-seq complements HTP sequencing by validating core findings and identifying additional regions of interest.