75 breakthrough innovations and our simplest workflow yet
Kits & Reagents
Streamlined high output single-cell sequencing on your benchtop
Selection & Planning Tools
A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
Software & Informatics Products
Bringing efficiency and high confidence to case management, variant analysis, and interpretation in rare disease
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
Find popular product groupings for your workflow
Highly sensitive sequencing approaches to detect SARS-CoV-2, track transmission, study viral genetics, and more
Bringing genetic testing to Hispanic breast cancer patients in Latin America
All Investor Information
Windows 10 upgrades and Windows 7 ESU licenses available for Illumina systems
All Support Tools
Product Support Services
Simultaneously assess multiple biomarkers from numerous tumor types in a single NGS assay
Cancer Research Products
Microbial Genomics Research
Microbial Genomics Products
2020 Agricultural Greater Good Initiative Winner shares how grant will improve crop yield and insect resistance
Powerful tools for studying the transcriptome in an unbiased manner from minimal input
Complex Disease Research Products
NIPT is now recommended for all pregnancies regardless of age or risk
Reproductive Health Products
New library prep kits enhance research in rare genetic diseases
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.
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