Illumina next-generation sequencing (NGS) and microarray technologies represent the gold standard in quality worldwide—and account for ~90% of the world’s sequencing data.* Innovative, intuitive, and completely integrated, our sample-to-data solutions empower your lab to keep ahead of the curve in the rapidly evolving genomics revolution. So you’ll be better able to perform the world-class research you strive for—with the goal of uncovering new insights into the biology of cancer that can lead to meaningful advances in personalized medicine.
Our comprehensive product offerings support multiple cancer research applications, including studies of DNA, RNA, epigenetics, and more. Our range of sequencers can be scaled to meet your needs—from powerful, yet personal, desktop models to versatile, high-throughput systems. With intuitive data analysis and management capabilities and unsurpassed customer support, we can deliver the answers you seek—quickly, accurately, and cost-effectively.
Explore genomics-based approaches to investigating cancer using NGS and microarrays.
The MiniSeq System delivers cost-efficient, reliable sequencing for low-throughput cancer research labs. Targeted sequencing on the MiniSeq System enables accurate identification of variants and gene fusions, with streamlined sample-to-results workflow and onboard data analysis.View System
A reproducible, economical method for sequencing coding RNA from FFPE and other low-quality samples. Learn MoreSee all sequencing kits
Flexible desktop sequencing systems that support various applications, from targeted panels to whole-genome sequencing. Learn MoreSee all sequencers
*Data on file based on a 2013 study.