To meet different user needs, the NovaSeq Series is offered in 2 configurations. The NovaSeq 5000 System offers cost-effective high-throughput sequencing across a broad range of applications. The NovaSeq 6000 System delivers those applications with unprecedented throughput at the lowest cost per sample. No matter which system you choose, you’ll have throughput that matches your science.
The NovaSeq Series provides tremendous scalability and flexibility to accommodate diverse applications and project sizes, while achieving maximum operational efficiency. Users can run 1 or 2 flow cells at a time and choose between 4 flow cell types, easily adjusting output for each sequencing run. With highly tunable data output you can run virtually any genome, sequencing method, and scale of project.
The NovaSeq Series is compatible with a broad range of Illumina library preparation kits, from transcriptome sequencing to whole-genome sequencing and everything in between. High-quality, high-coverage sequencing offers a comprehensive view of the genome to detect variants accurately, characterize isoforms, and more. With increased throughput and reduced price per sample, the NovaSeq Series is ideal for data-intensive applications.
The NovaSeq Series combines the features that make our benchtop sequencers so easy to use with the power of a high-throughput sequencing platform. It offers fully automated, onboard cluster generation to minimize hands-on time. Integrated, ready-to-use reagent cartridges streamline run setup and prevent improper loading. RFID encoded consumables enable fully automated reagent traceability. In all, it takes only minutes to set up a run on the NovaSeq 5000 System or NovaSeq 6000 System, giving you increased lab efficiency.
Manage the workflow seamlessly with BaseSpace Clarity LIMS or your existing LIMS system.
Prepare libraries with a broad range of high performance library preparation kits from Illumina.
Generate sequences with proven sequencing by synthesis (SBS) chemistry more than a decade in the making.
Analyze data with seamless integration into BaseSpace Sequence Hub. Share your results in a secure cloud environment.
Interpret results, get insights, and drive discovery with BaseSpace Variant Interpreter (Beta) and BaseSpace Cohort Analyzer.
*Specifications based on a dual flow cell run of S4 flow cells which have not been released, therefore performance metrics are subject to change.
Aris Baras and John Overton of Regeneron discuss their latest work and overall mission to explore new variations in genomes that can help explain disease. Hear how they plan to utilize the NovaSeq 6000 System.View Video
Reagent kits for the NovaSeq 5000 and NovaSeq 6000 Systems provide ready-to-use cartridge-based reagents for cluster generation and SBS.
Simple, all-inclusive whole-genome sequencing (WGS) library preparation that provides accurate and comprehensive coverage of complex genomes.
A robust, highly scalable whole-transcriptome analysis (RNA-Seq) solution for a variety of species and sample types, including human, mouse, and FFPE.