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Announcing NextSeq 1000 and NextSeq 2000.
Kits & Reagents
The power of high-throughput sequencing on a benchtop system with the v2.5 flow cell for greater stability and robustness
Selection & Planning Tools
Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in as little as 90 minutes
Software & Informatics Products
Accurate, rapid analysis for germline and somatic exome experiments
Verify instrument installation and operation, obtain an audit-ready report
Find popular product groupings designed for your workflow
Generating RNA libraries from ultra-low-input samples
By Dr Phil Febbo, Chief Medical Officer at Illumina
All Investor Information
Upgrade solution for Illumina systems
All Support Tools
Product Support Services
Cancer Genomics Products
Microbial Genomics Research
Microbial Genomics Products
Complex Disease Research Products
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Cost-efficient flexibility for new and emerging applications.
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.
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.
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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