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Kits & Reagents
These additional kits are most commonly purchased with the MiSeq Reagent v3 kits.
Find the system that's right for your application needs
Software & Informatics Products
Simplify your bioinformatics with an economical and powerful computing environment to manage, analyze, and share data
Complimentary and secure instrument monitoring can help you avoid unplanned downtime
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI)
Learn the basics of next-generation sequencing and find tips for getting started
A snapshot of the company, its markets, its portfolio and more
All Investor Information
Resources for planning RNA-Seq experiments
All Support Tools
Product Support Services
How to calculate the right read length for your sequencing run
Cancer Genomics Products
Microbial Genomics Research
Microbial Genomics Products
Sequencing directly on a CMOS chip can reduce instrument cost and simplify NGS
Episode 46: How NGS can unravel interactions that regulate antibody response and autoimmunity
Complex Disease Research Products
AnchorDx to focus on early cancer detection and clinical management panels
Researchers at Newcastle University are looking into genetic factors of male infertility
Consortium aims to expand access to clinical whole-genome sequencing for genetic diseases
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
See our sequencing and array technologies in action. Learn about how they work and what they can do for you.
Explore popular genomics techniques—such as RNA-Seq, exome sequencing, methylation arrays, and more—and find relevant products for each workflow step.
Compare published sequencing methods and find the best approach for your project.
We offer genomic solutions for diverse research areas and clinical applications, including reproductive and genetic health, cancer research, microbiology, and more.
These summaries of peer-reviewed publications highlight some key ways Illumina technology is powering modern science.
Find out what our customers are saying about our products and the future of genomics with these in-depth interviews.
We help connect researchers who share similar goals, so they can reduce costs and make discoveries together.
In this open forum, researchers can come together to support one another, ask questions, and collaborate on great science.
Learn from expert Illumina instructors with online courses and in-lab training options to help you make the most of your instrument.
Watch product demonstrations, interviews, and inspiring genomics stories from around the world.
Leading scientists discuss how their work in genomics is shaping the way we think about the world around us.
View on-demand webinars about Illumina products and popular topics in genomics.
Transform complex genomic data into biological insight with our intuitive software tools.
Learn about the science behind our sequencing and array technologies and find out how to use them in your study.
We are dedicated to supporting medical genetics education through resources, grants, and clinical research.
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