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 Videos

Microarray-based genomic selection for high-throughput resequencing.

David T Okou1, Karyn Meltz Steinberg, Christina Middle

  • 1Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Suite 301, Atlanta, Georgia 30322, USA.

Nature Methods
|October 16, 2007
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

Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.

medRxiv : the preprint server for health sciences·2026
Same author

Heritability of Long-Term Complications in Classic Galactosemia.

Journal of inherited metabolic disease·2026
Same author

Sustainability of gap funding programs aimed at commercializing academic innovation.

Nature biotechnology·2026
Same author

H/ACA snoRNAs and snoRNPs Dysregulation Links rRNA Modification to Glioblastoma Progression.

Research square·2026
Same author

A powerful framework for differential co-expression analysis of general risk factors.

Bioinformatics (Oxford, England)·2025
Same author

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios.

American journal of human genetics·2025
Same journal

Efficient evidence-based genome annotation with EviAnn.

Nature methods·2026
Same journal

ClairS: a deep-learning method for long-read tumor-normal pair somatic small variant calling.

Nature methods·2026
Same journal

RNAbpFlow: base pair-augmented SE(3) flow matching for conditional RNA 3D structure generation.

Nature methods·2026
Same journal

Spatio-DARLIN enables robust and efficient in situ lineage tracing in mice at single-cell resolution.

Nature methods·2026
Same journal

EasyGrid: a versatile platform for automated cryo-EM sample preparation and quality control.

Nature methods·2026
Same journal

Cloud-based microscope enables live neuroimaging for 24 h and beyond with worldwide access.

Nature methods·2026
See all related articles

We developed microarray-based genomic selection (MGS) to enrich targeted DNA sequences from complex genomes. This method enables large-scale DNA resequencing, even in smaller labs.

Area of Science:

  • Genomics
  • Molecular Biology

Background:

  • Bacterial artificial chromosome (BAC)-based selection requires repeat blocking steps.
  • Targeting large genomic regions in eukaryotes is challenging.

Purpose of the Study:

  • To develop a general method for selecting and enriching targeted sequences from complex eukaryotic genomes.
  • To enable large-scale resequencing in single-investigator laboratories.

Main Methods:

  • Developed microarray-based genomic selection (MGS).
  • MGS bypasses repeat blocking steps.
  • Enriched large human genomic regions (hundreds of kilobases) using resequencing arrays.

Main Results:

  • Demonstrated successful enrichment of large human genomic regions.

Related Experiment Videos

  • MGS is effective without repeat blocking.
  • Combined MGS with next-generation resequencing technology.
  • Conclusions:

    • MGS is a versatile method for genomic selection.
    • MGS facilitates large-scale resequencing.
    • Enables advanced genomic studies in resource-limited settings.