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 Concept Videos

PCR - Polymerase Chain Reaction01:32

PCR - Polymerase Chain Reaction

Overview
PCR01:32

PCR

Overview

You might also read

Related Articles

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

Sort by
Same author

Uniform bacterial genetic diversity along the gut.

Nature communications·2026
Same author

Microplastics and nanoplastics in the human gut: from signals to standards.

Nature reviews. Gastroenterology & hepatology·2026
Same author

Microbial regulation of stress-associated signaling molecules and its role in health and disease.

NPJ biofilms and microbiomes·2026
Same author

A Bacteroides synthetic biology toolkit to build an in vivo malabsorption biosensor.

Cell·2026
Same author

In mouse and in vitro models, bowel preparation promotes pathogen colonization, translocation, and exacerbation of inflammation.

Cell reports. Medicine·2025
Same author

WEE1 inhibitors trigger GCN2-mediated activation of the integrated stress response.

Nature communications·2025
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
Same journal

Deep molecular profiling in three dimensions.

Nature methods·2026
See all related articles

Related Experiment Video

Updated: May 31, 2026

Simple Bulk Readout of Digital Nucleic Acid Quantification Assays
06:55

Simple Bulk Readout of Digital Nucleic Acid Quantification Assays

Published on: September 24, 2015

Megapixel digital PCR.

Kevin A Heyries1, Carolina Tropini, Michael Vaninsberghe

  • 1Centre for High-Throughput Biology, University of British Columbia, Vancouver, British Columbia, Canada.

Nature Methods
|July 5, 2011
PubMed
Summary
This summary is machine-generated.

This study introduces a microfluidic digital PCR device with one million reactors for precise DNA analysis. The technology enables highly sensitive detection of genetic variations and copy number differences.

More Related Videos

Detection of Live Escherichia coli O157:H7 Cells by PMA-qPCR
08:16

Detection of Live Escherichia coli O157:H7 Cells by PMA-qPCR

Published on: February 1, 2014

Particle Templated Emulsification enables Microfluidic-Free Droplet Assays
11:03

Particle Templated Emulsification enables Microfluidic-Free Droplet Assays

Published on: March 9, 2021

Related Experiment Videos

Last Updated: May 31, 2026

Simple Bulk Readout of Digital Nucleic Acid Quantification Assays
06:55

Simple Bulk Readout of Digital Nucleic Acid Quantification Assays

Published on: September 24, 2015

Detection of Live Escherichia coli O157:H7 Cells by PMA-qPCR
08:16

Detection of Live Escherichia coli O157:H7 Cells by PMA-qPCR

Published on: February 1, 2014

Particle Templated Emulsification enables Microfluidic-Free Droplet Assays
11:03

Particle Templated Emulsification enables Microfluidic-Free Droplet Assays

Published on: March 9, 2021

Area of Science:

  • Biotechnology
  • Molecular Biology
  • Microfluidics

Background:

  • Digital PCR (dPCR) offers high precision for nucleic acid quantification.
  • Existing dPCR platforms face limitations in reactor density and dynamic range.
  • Advancements in microfluidic technologies are crucial for improving dPCR capabilities.

Purpose of the Study:

  • To develop a high-throughput microfluidic digital PCR device with a 'megapixel' capacity.
  • To achieve high-fidelity single DNA molecule amplification in a large number of reactors.
  • To enhance the dynamic range and sensitivity of digital PCR for genetic analysis.

Main Methods:

  • Utilized a microfluidic platform with surface tension-based sample partitioning.
  • Implemented precise dehydration control for consistent amplification.
  • Engineered picoliter-volume reactors with densities up to 440,000 reactors cm(-2).

Main Results:

  • Successfully amplified single DNA molecules in 1,000,000 reactors.
  • Achieved a dynamic range of 10^7 for quantitative analysis.
  • Demonstrated single-nucleotide-variant detection below one copy per 100,000 wild-type sequences.
  • Showcased discrimination of a 1% difference in chromosome copy number.

Conclusions:

  • The developed microfluidic dPCR device significantly advances high-throughput genetic analysis.
  • This technology enables unprecedented sensitivity for detecting rare variants and copy number variations.
  • The 'megapixel' dPCR platform holds potential for applications in diagnostics and research.