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Experience comprehensive genomics

Delivering valuable insights previously unavailable to the scientific community, the PacBio Sequel System provides an unmatched depth of genetic information through long-read sequencing and high consensus accuracy.

Sequel System: Superior accuracy, long reads, uniform coverage


The Sequel System is based on our proven Single Molecule, Real-Time (SMRT) Sequencing technology achieves:

  • 10 Gb with 20 kb average read lengths for whole genome sequencing projects
  • 20 Gb with 40 kb average read lengths for amplicon and RNA sequencing projects
  • >99.999% (QV50) consensus accuracy with data free of systematic errors
  • With an efficient <1 day workflow

 

 

Sequel System features

  • Automated consumable handling with integrated software
  • Intuitive run setup and monitoring
  • Run-time flexibility up to 20 hours per SMRT Cell
  • Walk away time up to 4 days

Watch this ~3 minute video to further explore the features and benefits of the Sequel System

 

High-quality sequencing for genomes, transcriptomes and epigenomes

Whole Genome Sequencing

For humans, plants, animals and microbes including de novo sequencing and structural variant detection

Complex Populations

Understand variants among bacterial, viral and cancer cell populations

 

RNA Sequencing

In-depth analysis of cDNA sequences across the entire transcriptome or targeted genes

Epigenetics

Detect DNA modifications in your samples while you sequence on the PacBio platform

Targeted Sequencing

Study relevant genome targets across any regions of interest

SMRT Sequencing Project Calculators

Tell us about your sequencing project and receive an estimate on the time and materials needed to perform it using the Sequel System, including:

Accelerate your research with the Sequel System

 

Human Biomedical
Research
Plant and Animal
Science
Microbiology and
Infectious Disease

To learn more about how the Sequel System can further your research efforts, contact us