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Many more diseases could potentially be treated by controlling the expression of abnormal and normal genes
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.
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.
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Discuss best practices, troubleshoot, and learn about how others are using Illumina products.
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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.
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