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SPRQ-Nx on the Vega system. Supercharge your targeted sequencing with HiFi long reads. Download the guide.

Our latest targeted sequencing guide maps the complete Vega + SPRQ-Nx workflow to help you resolve challenging regions with a single approach that can replace single-gene Sanger or genotyping assays.

Your download includes information about:

  • PureTarget: for complex or repetitive regions with native methylation
  • Amplicon: for low-cost single-gene or small panels
  • Hybrid capture: for small- or large-gene panels, structural variants and phasing
Getting started with targeted long-read sequencing - guide cover

Getting started with HiFi for targeted gene sequencing

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More projects

Up to 90 Gb per run lets labs run more samples and tackle broader applications.

Lower cost

~40% lower cost per Gb brings HiFi within reach for more labs.

Smaller sample size

As low as 500 ng DNA input allows work with precious or limited samples.

Ready for tomorrow

Added support for regulated environments, designed to support customers’ 21 CFR Part 11 compliance efforts

What researchers are saying about Vega

 

Supercharge your targeted sequencing with HiFi

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