Supporting a broad range of targeted DNA and RNA applications for examining single genes or entire pathways, the system features an intuitive user interface, load-and-go operation, and onboard data analysis. The integrated workflow from library to results simplifies sequencing so it’s easy to learn and easy to use. Now you can perform NGS in your own lab on your own schedule.
At Illumina, we help make the extraordinary happen daily. Through collaborative scientific innovation, we are improving human health by unlocking the power of the genome. From cancer research to prenatal screening and agriculture to forensics, the applications of our technologies are as universal as life itself. Join us as we transform the future.