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Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information
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Mine over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research
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Reagent kits for the NovaSeq 6000 System provide ready-to-use cartridge-based reagents for cluster generation and SBS
Low NovaSeq 6000 System sequencing costs spark new projects and customer growth
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Survey finds Americans unaware of DNA's power to improve lives
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Deep, comprehensive, and accessible sequencing power for detecting solid tumor biomarkers
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Local scientists analyze transmission patterns and trace origin of Ebola outbreak in the Democratic Republic of Congo
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A rapidly emerging method for studying biodiversity and monitoring ecosystem changes
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In podcast episode 41, Dr. Åke Borg discusses developing better biomarkers for risk stratification of individuals with breast cancer
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Rethink prenatal screenining. Think VeriSeq NIPT.
Families facing rare diseases often spend years pinpointing the problem in solitude – until now
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
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.
We help connect researchers who share similar goals, so they can reduce costs and make discoveries together.
In this open forum, researchers can come together to support one another, ask questions, and collaborate on great science.
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.
