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

Nucleotide sequence-based multitarget identification.

T Vinayagamoorthy1, Kirk Mulatz, Roger Hodkinson

  • 1Bio-ID Diagnostic, Inc., Saskatoon, Saskatchewan S7N 4N1, Canada. moorthy@innovationplace.com

Journal of Clinical Microbiology
|July 5, 2003
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

StereoPylot: An open-source Raspberry PI-based stereotaxic apparatus controller with 3D printed components for fully motorized control, digital display, and customizable features.

eNeuro·2026
Same author

Withdrawn: A systematic review of autopsy findings in deaths after COVID-19 vaccination.

Forensic science international·2024
Same author

Response to: Szuster-Ciesielska, letter to the editor regarding 'Autopsy findings in cases of fatal COVID-19 vaccine-induced myocarditis'.

ESC heart failure·2024
Same author

Response to: Van Wyk et al. letter to the editor regarding 'Autopsy findings in cases of fatal COVID-19 vaccine-induced myocarditis'.

ESC heart failure·2024
Same author

Autopsy findings in cases of fatal COVID-19 vaccine-induced myocarditis.

ESC heart failure·2024
Same author

Expansion microscopy-based imaging of nuclear structures in cultured cells.

STAR protocols·2021
Same journal

Ebola laboratory preparedness at frontline hospitals: can we or can't we?

Journal of clinical microbiology·2026
Same journal

Reporting macrolide-resistant <i>Mycoplasma pneumoniae</i>: a diagnostic obligation?

Journal of clinical microbiology·2026
Same journal

Diagnostic value of HHV-6A/B genotyping in immunocompromised adults.

Journal of clinical microbiology·2026
Same journal

Multicenter performance evaluation of the Simplexa <i>C. auris</i> Direct assay for the detection of <i>Candida auris</i> colonization in bilateral axilla/groin swabs.

Journal of clinical microbiology·2026
Same journal

Comparison of blood culture contamination rates with standard practice versus two blood diversion devices at a single institution.

Journal of clinical microbiology·2026
Same journal

Risk assessment and mitigation of hepatitis C virus RNA carryover contamination in a reflex testing algorithm.

Journal of clinical microbiology·2026
See all related articles

MULTIGEN technology enables simultaneous DNA sequencing from multiple targets in a single electropherogram. This novel approach uses differentially weighted sequencing primers for effective separation and analysis of various DNA sequences.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biotechnology

Background:

  • Conventional sequencing methods can be time-consuming and complex when analyzing multiple DNA targets.
  • Existing technologies may face challenges in multiplexing DNA analysis efficiently.
  • There is a need for streamlined methods to analyze diverse DNA targets simultaneously.

Purpose of the Study:

  • To introduce and explain the MULTIGEN technology for simultaneous DNA sequencing.
  • To demonstrate the versatility of MULTIGEN technology through diverse applications.
  • To highlight the advantages of MULTIGEN over conventional sequencing approaches.

Main Methods:

  • MULTIGEN technology modifies conventional sequencing by generating a single electropherogram from a mixture of known DNA targets.

Related Experiment Videos

  • Sequencing primers with progressively higher molecular weights are utilized.
  • Electrophoretic separation is based on the molecular weights of truncated DNA molecules, ensuring distinct signal separation.
  • Main Results:

    • The technology allows for the effective separation of truncated DNA molecules from multiple targets in a single lane without sequence overlap.
    • Successful applications demonstrated include pathogen detection (Neisseria gonorrhoeae, Chlamydia trachomatis, Ureaplasma urealyticum), contaminant identification in meat (coliforms, E. coli O157:H7), and SNP detection (NAT1 gene).

    Conclusions:

    • MULTIGEN technology offers a powerful and efficient method for multiplex DNA sequencing.
    • Its applications span diagnostics, food safety, and genetic research.
    • The method provides a significant advancement in analyzing multiple DNA targets simultaneously.