The NovaSeq 6000 Sequencing System is designed to adapt to your needs. This robust, scalable system has been adopted by leading research centers and featured in countless publications. Impactful discoveries are within reach.
Scalable throughput for dynamic study sizes
So many ways to sequence. Scale up and down with a tunable output of up to 6 Tb and 20B single reads in < 2 days.
Broad, deep sequencing for clear answers
Accelerate your science with reliable sequencing breadth and depth for every project.
Tunable output for mix and match options
Do what you want. Mix and match flow cell types, and run one or two flow cells at a time. Choose between multiple read lengths, workflows, and more.
Advanced applications. Impactful discoveries.
The NovaSeq 6000 system offers deep and broad coverage through advanced applications for a comprehensive view of the genome. Unlock a full spectrum of genetic variation and biological function with high-throughput sequencing
The NovaSeq 6000 system performs whole-genome sequencing efficiently and cost-effectively. Its tunable output generates up to 6 Tb and 20B single reads in dual flow cell mode with streamlined workflows. Configure the system to sequence up to 48 genomes in ~2 days with comprehensive coverage.
Representing less than 2% of the genome, WES is a cost-effective alternative to WGS. The NovaSeq 6000 System offers sequencing of up to 500 exomes in a single run using a dual S4 flow cell.
Detect coding and multiple forms of noncoding RNA in normal or low-quality samples. With the NovaSeq 6000 System, you can sequence up to 400 transcriptomes in a single run using a dual S4 flow cell.