NovaSeq 6000 Sequencing System is by far our most powerful instrument, designed to adapt to your needs.
Kits & Reagents
Study the coding and non-coding transcriptome with unparalleled flexibility
Selection & Planning Tools
A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
Software & Informatics Products
Scalable multi-omics data management, analysis, and exploration
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
RNA library preparation with highly accurate results
Our leaders are pioneers of genetic research and clinical applications. They are deeply committed to scientific accessibility, data, and community.
Our 2021 CSR Report documents a year of positive impact
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Windows 10 upgrades and Windows 7 ESU licenses available for Illumina systems
All Support Tools
Product Support Services
Simultaneously assess multiple biomarkers in numerous tumor types with a single NGS assay
Cancer Research Products
Microbial Genomics Research
NGS supports effective infectious disease surveillance strategies to reduce transmission and infection
Microbial Genomics Products
A highly sensitive and accurate tool for measuring expression across the transcriptome
Although Africa is the continent with the highest amount of genetic diversity, it is underrepresented in global genomic databases
Complex Disease Research Products
Study gene expression changes in cancer, RNA biomarkers of drug response, and more
Deciding on an NIPT technology for your lab
Reproductive Health Products
Genomic luminaries Drs. Marc Lalande and Kamran Shazand establish the Genomics Institute
Genetic Health Products
Delivers a range of ready-to-use and custom panels for simple, flexible targeted resequencing that provides high-quality data you can trust.
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, user-friendly workflow for a wide range of target enrichment applications encompassing custom panels, fixed panels, and whole-exome sequencing.
Perform targeted genotyping on large numbers of samples. Scale up to more than 1 million samples per year.
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
Perform high-throughput, cost-effective genotyping for quality control, tracking, and stratification applications, including biobanking.
Purchase the TruSight Oncology 500 assay for the first time and receive an exclusive limited time offer.
Whole-genome sequencing library prep kits for small genomes (e.g. bacterial and viral genomes), amplicons, and plasmids.
Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
A simple, scalable, cost-effective, rapid single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
This array offers an optimal and comprehensive set of both common and rare SNP content for diverse world populations.
Interrogate over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
Optimized chemistry to increase cluster density and read length, and improve sequencing quality scores, compared to earlier MiSeq reagent kit versions.
These sequencing reagent kits offer increased stability and robustness over the prior v2 kit version.