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Longer read capabilities with more output for immune repertoire, shotgun metagenomics and more
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Integrated secondary analysis onboard the NovaSeq X System simplifies operations, accelerates the sequencing workflow turnaround
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Deeper studies, more samples, more modalities. The NovaSeq X and 25B flow cell make ultra-high depth multiomics more accessible.
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A new algorithm trained by natural selection can pinpoint disease-causing variants in humans
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The Cancer Methods Guide is a 40+ page comprehensive resource covering cancer research topics, sequencing methods, and solutions
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On the heels of three new RSV vaccines, an Arizona State University viromics lab identifies many variants
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The Mining Microbiome Analytics Platform is finding tiny solutions to some of our biggest environmental challenges
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Understanding cardiovascular diseases through genomic sequencing
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TBD
The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab
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Illumina Complete Long Read technology enables both long and short reads on the same NovaSeq instrument
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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.
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.
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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.
