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

Why FRET over genomics?

D A De Angelis1

  • 1Cellular Biochemistry and Biophysics Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA. d-deangelis@ski.mskcc.org

Physiological Genomics
|October 4, 2000
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

Nitric oxide attenuates signal transduction: possible role in dissociating caveolin-1 scaffold.

Circulation research·2001
Same author

PRIM: proximity imaging of green fluorescent protein-tagged polypeptides.

Proceedings of the National Academy of Sciences of the United States of America·1998
Same author

Visualizing secretion and synaptic transmission with pH-sensitive green fluorescent proteins.

Nature·1998
Same author

2',3'-Cyclic nucleotide 3'-phosphodiesterase binds to actin-based cytoskeletal elements in an isoprenylation-independent manner.

Journal of neurochemistry·1996
Same author

Binding of 2',3'-cyclic nucleotide 3'-phosphodiesterase to myelin: an in vitro study.

Journal of neurochemistry·1996
Same author

Isoprenylation of brain 2',3'-cyclic nucleotide 3'-phosphodiesterase modulates cell morphology.

Journal of neuroscience research·1994
Same journal

Regulation of RGS2 is an important piece to the puzzle of syncytiotrophoblast dysfunction in preeclampsia.

Physiological genomics·2026
Same journal

Maternal Estradiol Impacts Fetal HPA Axis and Pulmonary Transcriptomes in Sheep.

Physiological genomics·2026
Same journal

OBESITY AS AN EPIGENETIC CONTINUUM: DEVELOPMENTAL ROOTS, ADIPOSE REMODELING, AND THE LIMITS OF REVERSIBILITY.

Physiological genomics·2026
Same journal

<i>Akkermansia muciniphila</i>: a member of the gut microbiota that modulates intestinal stem cell function.

Physiological genomics·2026
Same journal

Differential gene transcription following intravenous injection of air bubbles in rats with varying resistance to decompression sickness.

Physiological genomics·2026
Same journal

Genomic informational field theory to identify genetic associations of a complex trait using a small sample size.

Physiological genomics·2026
See all related articles

Fluorescence resonance energy transfer (FRET) offers high-throughput solutions for genomics challenges. This technique aids in identifying gene functions, expression factors, and complex traits by analyzing genetic variants.

Area of Science:

  • Genomics
  • Molecular Biology
  • Biotechnology

Background:

  • Vast amounts of genetic information are rapidly generated through automated genome sequencing.
  • Key challenges include assigning functions to gene products, identifying expression regulators, and characterizing complex traits influenced by genetic variants.
  • High-throughput methods are crucial for analyzing large-scale genomic data.

Purpose of the Study:

  • To provide an overview of fluorescence resonance energy transfer (FRET) applications in genomics.
  • To highlight FRET's potential in addressing major genomics challenges.
  • To showcase FRET's utility in high-throughput genetic analysis.

Main Methods:

  • Fluorescence resonance energy transfer (FRET) as a detection method.

Related Experiment Videos

  • Application of FRET in identifying single-nucleotide polymorphisms (SNPs).
  • Utilizing FRET for detecting protein-protein interactions.
  • Employing FRET for genomewide analysis of regulatory sequences.
  • Main Results:

    • FRET enables rapid and high-capacity detection of molecular interactions and genetic variations.
    • Demonstrated success of FRET in SNP identification, protein interaction studies, and regulatory sequence analysis.
    • Fluorescence-based readouts are advantageous for automating genomic processes.

    Conclusions:

    • FRET is a powerful and versatile tool for advancing genomics research.
    • The technique streamlines and automates critical genomic analyses, accelerating discovery.
    • FRET holds significant potential for future high-throughput genomic applications.