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Benchtop sequencer ease-of-use with production-scale power in a single platform
Kits & Reagents
Assay targeting multiple somatic variant types from plasma, including TMB and MSI
Selection & Planning Tools
Fast library prep, optimized for small genomes, PCR amplicons, and plasmids
Software & Informatics Products
CNV analysis on somatic samples, population-level cohort analysis
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
Popular product groupings for your workflow
NGS offers a universal, hypothesis-free research method for use with viruses, bacteria, or parasites
One mother’s quest for a diagnosis
All Investor Information
Procedures for extended lab closures
All Support Tools
Product Support Services
Expanded portfolio enables comprehensive genomic profiling from blood and tissue
Cancer Research Products
Microbial Genomics Research
Sequence virtually any small genome and make new discoveries with scalable throughput
Microbial Genomics Products
Contributing to a sustainable environment and food supply
An economical tool for genetic screening of large global populations
Complex Disease Research Products
In-lab aneuploidy screening solution for accurate NIPT results in 26 hours
Reproductive Health Products
Many more diseases could potentially be treated by controlling the expression of abnormal and normal genes
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.
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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