DNA next-generation sequencer NovaSeq 6000

for RNAlaboratory

Since its launch, the NovaSeq 6000 Sequencing System has revolutionized genomics studies. Hear how the system has continued to evolve to meet customer demands and shape what’s possible in the future of genomics. 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. A flexible workflow designed to help you accelerate your research and maximize results 1 Manage workflow Manage your workflow seamlessly with Clarity LIMS software or your existing LIMS system. 2 Prepare libraries Prepare libraries with a broad range of high-performance library preparation kits. 3 Sequence Generate sequences with ready-to-use reagents featuring proven Illumina sequencing by synthesis chemistry. 4 Analyze data Leverage Illumina DRAGEN software or BaseSpace Sequence Hub for accurate, rapid secondary analysis. 5 Interpret results Gain insights and drive discovery with variant analysis and interpretation software. Advanced applications. Impactful discoveries. The NovaSeq 6000 System offers deep, 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.