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The next era in sequencing starts now
Kits & Reagents
Use these components in ATAC-Seq experiments to analyze chromatin accessibility
Selection & Planning Tools
Take your research further with the right sequencing panels or microarrays for your project
Software & Informatics Products
Provides accurate, ultra-rapid secondary analysis of sequencing data
Hands-on training with expert instructors or online courses to fit your schedule
Find popular product groupings designed for your research focus and instrument
RNA-Seq and HLA typing are increasing the power and efficiency of a target discovery platform
Helping Students Nationwide Learn the Real-World Impacts of Genomics
All Investor Information
Upgrade solution for Illumina systems
All Support Tools
Product Support Services
Illumina to collaborate with the Frederick National Laboratory for Cancer Research
Cancer Genomics Products
Microbial Genomics Research
A fast, integrated workflow for a wide range of applications
Microbial Genomics Products
Deadline for 2020 Agricultural Greater Good Initiative grant applications is December 6
Discover how genetic variants and PRS could enable more effective treatment of genetic conditions.
Complex Disease Research Products
Assay targeting multiple somatic variant types from plasma, including TMB and MSI
Learn how noninvasive prenatal testing (NIPT) is making an impact around the world.
Consortium aims to expand access to clinical whole-genome sequencing for genetic diseases
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.
Delivers a range of ready-to-use and custom panels for simple, flexible targeted resequencing that provides high-quality data you can trust.
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.
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.
Sequencing library prep kits with rRNA reduction chemistry for whole-transcriptome analysis.
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.
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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