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NovaSeq 6000 Sequencing System is by far our most powerful instrument, designed to adapt to your needs.
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P1 reagents are now available for NextSeq 1000/NextSeq 2000 Systems, offering added flexibility to meet your project's needs
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A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
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DRAGEN v3.9 release now available with multi-cloud support, accuracy improvements and more
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Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
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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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Illumina and the San Diego Zoo Wildlife Alliance try to preserve the species with the help of genomic data
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Upgrade your MiSeqDx instrument from Windows 7 to Windows 10
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Multiomics methods can better connect genotype to phenotype
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Learn about methods for SARS-CoV-2 surveillance, including requirements, workflow, and analysis
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Array-based SNP genotyping platforms have low genotype error rates compared to genotyping-by-sequencing
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Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation
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TBD
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Prof. Dr. Bernd Eiben discusses his experience with VeriSeq NIPT Solution v2
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Illumina supports the release of a landmark consensus on whole-genome sequencing in the diagnosis of genetic diseases in newborns
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Explore the latest genomics discoveries and data analysis innovations by Illumina scientists.
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.
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.
Discuss best practices, troubleshoot, and learn about how others are using Illumina products.
Learn from expert Illumina instructors with online courses and in-lab training options to help you make the most of your instrument.
We offer genomic solutions for diverse research areas and clinical applications, including reproductive and genetic health, cancer research, microbiology, and more.
Watch product demonstrations, interviews, and inspiring genomics stories from around the world.
Leading scientists describe their latest discoveries and discuss the impact of genomics with the Illumina Scientific Affairs team.
View on-demand educational 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 research.
We are dedicated to supporting medical genetics education through resources, grants, and clinical research.
