So many ways to sequence. Scale up and down effortlessly with our improved economics and an output of up to 6 Tb and 20 B reads in < 2 days.
Go where discoveries are made. Accelerate your science with immense sequencing breadth and depth when you need it. All on one instrument.
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.
You're in control. Improved sequencing costs via the latest NovaSeq 6000 reagent kits. Automated flow cell loading. Open platform for build-your-own applications. We're dedicated to helping you maximize efficiency at every turn.
NovaSeq 6000 offers deeper and broader coverage through advanced applications for a comprehensive view of the genome. Unlock the full spectrum of genetic variation and biological function with high-throughput sequencing.See All Applications
Manage your workflow seamlessly with BaseSpace Clarity LIMS or your existing LIMS system.
Prepare libraries with a broad range of high-performance library preparation kits.
Generate sequences with ready-to-use reagents featuring proven Illumina sequencing by synthesis chemistry.
Leverage the Illumina DRAGEN Bio-IT Platform or BaseSpace Sequence Hub for accurate, rapid secondary analysis.
Interpret results, get insights, and drive discovery with BaseSpace Variant Interpreter, BaseSpace Cohort Analyzer, and TruSight Software Suite.
Probe deeper into a single sample for insights or process more samples to improve statistical signficance.
Perform transformative science with access to multiple emerging high-throughput omics applications.
New kits feature updated reagent formulations with 2x longer shelf life and improved sequencing costs to help power your most impactful studies.
The NovaSeq Xp workflow enables labs to load libraries directly into each lane of a NovaSeq 6000 System flow cell, without additional instrumentation.
Achieve rapid, targeted interrogation of an expansive number of target genes with exceptional capture efficiency and coverage uniformity.
A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing.
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Join a community of like-minded customers using Illumina sequencers, library preparation kits, and automated data analysis to fuel groundbreaking research. Discuss best practices, troubleshoot, and collaborate with Illumina scientists, developers, and each other.Learn More