How much genomic information can you get for $150?

If you're spending too much time and money identifying variants through Sanger sequencing or qPCR, download our guide to learn how targeted NGS can help you determine variants in less time and for less money.

Within a 2-week period, we get 24 700 kb data files that have been annotated and categorized on rareness and pathogenicity. 24 people every 2 weeks. It is just impossible to compare to a Sanger 1000-base-pair-at-a-time sequencing process.

– John Robinson, Ph.D at the Robarts Research Institute

Download Guide »

  • Why now is the time to consider targeted NGS?
  • When does targeted resequencing make the most sense?
  • Benefits of targeted resequencing vs qPCR and Sanger Sequencing
  • Introduction to Illumina targeted NGS solutions