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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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Enabling comprehensive genomic profiling from FFPE samples.
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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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Our leaders are pioneers of genetic research and clinical applications. They are deeply committed to scientific accessibility, data, and community.
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Next-generation sequencing is helping Native nations with sovereignty and genetic research
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New page replaces MyIllumina Technical Updates email
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Maximize identification of molecularly matched therapies with one biopsy, one test, one report
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With the debut of the COVIDSeq Assay, smaller labs are participating in surveillance
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Identifying variants could help select highly productive breeds that adapt to rapidly changing climates
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The most comprehensive genotyping microarray on the market for pharmacogenomic research now at 25% off, restrictions apply
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TBD
Comprehensive genomic profiling is driving innovation across the 51-hospital system
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The collaboration will introduce VeriSeq NIPT Solution v2 in Southeast Asia
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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.
