NovaSeq 6000 Sequencing System is by far our most powerful instrument, designed to adapt to your needs.
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Improved Q30 score, support for UMIs, extended shelf life, and support for Illumina DNA PCR-Free Library Prep
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A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
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Scalable multi-omics data management, analysis, and exploration
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
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Our leaders are pioneers of genetic research and clinical applications. They are deeply committed to scientific accessibility, data, and community.
Two University of Cambridge chemists receive one of the world’s highest honors in science and technology
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Maximize identification of molecularly matched therapies with one biopsy, one test, one report
Cancer Research Products
Microbial Genomics Research
Partnership allows researchers to sequence hundreds of organisms and process data faster
Microbial Genomics Products
Dr. Bertram Brenig uses genomics grant to help save the bees
The continent with the highest amount of genetic diversity is underrepresented in global genomic databases
Complex Disease Research Products
The collaboration will introduce VeriSeq NIPT Solution v2 in Southeast Asia
Reproductive Health Products
Genomic Answers for Kids project will use NGS for families who have undergone many tests without progress
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.