NovaSeq 6000 Sequencing System is by far our most powerful instrument, designed to adapt to your needs so groundbreaking discoveries are always within reach. It's flexible, scalable science on your terms.Contact an Illumina Representative
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, 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 our new reagent kits. Automated flow cell loading. Open platform for build-your-own applications. We're dedicated to helping you maximize efficiency at every turn.
Dr. Carolyn Hogg and Professor Kathy Belov are researchers from the University of Sydney, Australia who are using whole genome sequencing of rare and endangered species with aims to provide conservation plans for the species ongoing survival.View Video
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.
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.
Want more stories, case studies, and news about the topics you're interested in most? Sign up today.
Rady Children’s Institute for Genomic Medicine is using the DNA PCR-Free Prep kit for NovaSeq 6000 to make a potentially record-breaking time-to-diagnosis for children with rare genetic disordersRead More
Cole Trapnell, PhD is transforming the world of biology by making bioinformatics tools available to allRead More
OmniSeq, Inc. scaled up to process a large number of both tissue and blood plasma samples every week, batching from 16 to 192 samples in a single run on NovaSeq 6000 with the TruSight Oncology 500 suite of productsRead More
Genomics England’s human genome initiative (GenOMICC) is launching a new study aimed at uncovering genetic factors in susceptibility to COVID-19, furthering our understanding of the pandemic through genomicsRead More
The DRAGEN platform enables GeneDx to scale to whole-genome analysis and identify variants with precisionRead More
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