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Announcing NextSeq 1000 and NextSeq 2000.
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The power of high-throughput sequencing on a benchtop system with the v2.5 flow cell for greater stability and robustness
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Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in as little as 90 minutes
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Accurate, rapid analysis for germline and somatic exome experiments
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Generating RNA libraries from ultra-low-input samples
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Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Cost-efficient flexibility for new and emerging applications.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
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 discuss how their work in genomics is shaping the way we think about the world around us.
View on-demand 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 study.
We are dedicated to supporting medical genetics education through resources, grants, and clinical research.
