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

MuPlex: multi-objective multiplex PCR assay design.

John Rachlin1, Chunming Ding, Charles Cantor

  • 1Bioinformatics Program, Boston University, Boston, MA 02215, USA. rachlin@bu.edu

Nucleic Acids Research
|June 28, 2005
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

Earlier postoperative ctDNA detection predicts recurrence and adjuvant therapy benefit in stage II-III colorectal cancer.

NPJ precision oncology·2026
Same author

A simplified multitarget stool test for colorectal cancer and advanced precancerous lesion detection.

Clinical chemistry and laboratory medicine·2026
Same author

Provenance Tracing in Network Diffusion Algorithms.

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing·2026
Same author

Highly specific multiplex DNA methylation detection for liquid biopsy of colorectal cancer.

Clinica chimica acta; international journal of clinical chemistry·2024
Same author

SPIDER: constructing cell-type-specific protein-protein interaction networks.

Bioinformatics advances·2024
Same author

Injectable platelet-rich fibrin promotes proliferation and trichogenic inductivity of dermal papilla cells through activating TGF-β/Smad signaling pathway.

Cellular and molecular biology (Noisy-le-Grand, France)·2024
Same journal

Correction to 'scSuperAnnotator: A platform for benchmarking comparison and visualizing automated cellular annotation methods for scRNA-seq data'.

Nucleic acids research·2026
Same journal

Correction to 'Differentiable partition function calculation for RNA'.

Nucleic acids research·2026
Same journal

Deployment of non-canonical splicing in tunicate genomes is mediated by divergent U2AF function and changing m6A modification in U1 and U6 snRNA.

Nucleic acids research·2026
Same journal

Bacillus subtilis DnaB forms multiple protein-protein interactions essential for DNA replication initiation.

Nucleic acids research·2026
Same journal

Multiple forms of protein-protein and DNA binding are exhibited by BrxC from the BREX phage restriction system.

Nucleic acids research·2026
Same journal

Biosynthesis of glycosylated 5-hydroxycytosine in the DNA of diverse viruses.

Nucleic acids research·2026
See all related articles

Researchers can now design multiplex PCR assays more efficiently using MuPlex. This web-enabled system aids in selecting primers and optimizing assay design for applications like genotyping and pathogen detection.

Area of Science:

  • Genomics
  • Molecular Biology
  • Bioinformatics

Background:

  • Multiplex PCR is crucial for applications like pathogen detection, whole-genome sequencing, and forensic analysis.
  • Designing multiplex PCR assays is computationally complex due to competing objectives and primer interactions.
  • Existing methods struggle with large-scale assay design requiring high coverage of numerous targets.

Purpose of the Study:

  • To develop a web-enabled system, MuPlex, for automated multiplex PCR assay design.
  • To facilitate the design of multiplex PCR assays covering a maximum number of input DNA sequences.
  • To provide researchers with multiple design alternatives highlighting objective tradeoffs.

Main Methods:

  • MuPlex accepts DNA sequences, primer selection criteria, interaction parameters, and multiplexing level as input.

Related Experiment Videos

  • The system computationally analyzes primer-pair interactions to screen for cross-reactivity.
  • MuPlex generates multiplex PCR assay designs optimized for coverage and efficiency.
  • Main Results:

    • MuPlex successfully designs multiplex PCR assays for large-scale applications.
    • The system provides multiple solution alternatives, illustrating tradeoffs between competing design objectives.
    • MuPlex is suitable for high-throughput environments requiring coverage of thousands of single nucleotide polymorphisms.

    Conclusions:

    • MuPlex offers an automated and efficient solution for multiplex PCR assay design.
    • The system addresses the computational challenges associated with complex multiplex PCR design.
    • MuPlex supports large-scale genomic applications by enabling high-throughput assay development.