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Kits & Reagents
Reagent kits for the NovaSeq 6000 System provide ready-to-use cartridge-based reagents for cluster generation and SBS
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A rapid, sensitive method for profiling accessible chromatin across the genome
By Dr. Phil Febbo, Chief Medical Officer at Illumina
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The Breast Cancer Atlas Project is sequencing more than a million breast cancer cells with the NovaSeq 6000 System
Cancer Genomics Products
Microbial Genomics Research
Learn about eDNA through sequencing the seas
Microbial Genomics Products
International Mungbean Improvement Network Wins Grant
Uncover how chromatin packaging and other factors affect gene expression
Complex Disease Research Products
Dr. Phil Febbo, SVP and Chief Medical Officer
Two next-generation sequencers now available for in vitro diagnostics
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
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.
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.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
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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