NovaSeq 6000 Sequencing System is by far our most powerful instrument, designed to adapt to your needs.
Kits & Reagents
Enabling comprehensive genomic profiling from FFPE samples.
Selection & Planning Tools
A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
Software & Informatics Products
DRAGEN v3.9 release now available with multi-cloud support, accuracy improvements and more
Find popular product groupings for your workflow
Our leaders are pioneers of genetic research and clinical applications. They are deeply committed to scientific accessibility, data, and community.
Next-generation sequencing is helping Native nations with sovereignty and genetic research
All Investor Information
New page replaces MyIllumina Technical Updates email
All Support Tools
Product Support Services
Maximize identification of molecularly matched therapies with one biopsy, one test, one report
Cancer Research Products
Microbial Genomics Research
With the debut of the COVIDSeq Assay, smaller labs are participating in surveillance
Microbial Genomics Products
Identifying variants could help select highly productive breeds that adapt to rapidly changing climates
The most comprehensive genotyping microarray on the market for pharmacogenomic research now at 25% off, restrictions apply
Complex Disease Research Products
Comprehensive genomic profiling is driving innovation across the 51-hospital system
The collaboration will introduce VeriSeq NIPT Solution v2 in Southeast Asia
Reproductive Health Products
Illumina supports the release of a landmark consensus on whole-genome sequencing in the diagnosis of genetic diseases in newborns
Genetic Health Products
Find tools to help you choose the right products for your needs and plan your experiments. Identify the right library prep kit or microarray, calculate sequencing coverage, explore methods compiled from publications, design custom assays, and more.
This guide contains an overview of instrument components and instructions for operating and maintaining the MiniSeq System.
This guide contains lab specifications and requirements for preparing the lab for the MiniSeq System.
Online Illumina sequencing courses are free, interactive, and available any time.
This tool will help you determine the best hands-on sequencing training for your needs based on your area of interest, application, library preparation kit, and platform.
Sequencing coverage describes the average number of NGS reads that align to known reference bases. Coverage requirements vary by application.
Additional information about sequencing quality scores, how they are calculated, and the relationship between quality score and base call accuracy.
Find system guides, related application and technical notes, and other supporting documentation for the MiniSeq System.
These short videos provide expert tips for common sequencing issues such as overclustering and inconsistent quantitation.
The Custom Protocol Selector enables you to generate your own customized documentation, specifically tailored to your experiment.
Discover how the simple, affordable MiniSeq System makes sequencing an everyday tool for labs of any size.
Mattia Prosperi, PhD, will use his MINI Cooper and MiniSeq to study the spread of mosquito-borne pathogens in Florida.
Hongmei Li-Byarlay, PhD, describes how she will use the MiniSeq to study the honeybee.
Una McVeigh discusses how the MiniSeq System will help her identify new genetic variants associated with breast cancer.
This webinar provides an introduction to the MiniSeq System and its simple, streamlined workflow.
Learn how comprehensive tumor profiling with NGS can help you avoid costly and time-consuming iterative testing.