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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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A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
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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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Our 2021 Corporate Social Responsibility Report documents a year of positive impact
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New page replaces MyIllumina Technical Updates email
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Study gene expression changes in cancer, RNA biomarkers of drug response, and more
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NGS supports effective infectious disease surveillance strategies to reduce transmission and infection
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NGS in agriculture will allow for development of more productive and sustainable practices
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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
Simultaneously assess multiple biomarkers from numerous tumor types in a single NGS assay
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Weighing the benefits of whole-genome sequencing vs targeted approaches
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Genomic Answers for Kids project will use NGS to bring hope to families who have undergone multitudes of tests without progress
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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.
