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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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Study the coding and non-coding transcriptome with unparalleled flexibility
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Although Africa is the continent with the highest amount of genetic diversity, it is underrepresented in global genomic databases
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TBD
Study gene expression changes in cancer, RNA biomarkers of drug response, and more
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Deciding on an NIPT technology for your lab
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Genomic luminaries Drs. Marc Lalande and Kamran Shazand establish the Genomics Institute
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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.
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.
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.
