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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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DRAGEN v3.10 release now available, setting new standards for accuracy and increased genome coverage.
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Mapping genetic diversity to identify where confiscated gorillas come from and boost survival rates
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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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Comprehensive, IVD, in-lab aneuploidy screening solution for accurate NIPT results in 26 hours
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Whole-genome sequencing (WGS) for rare disease offers key advantages over other genetic testing methods
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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.
