Search for products, methods, support...
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.
NGS technology can be used in rare disease research to discover causative variants of inherited disorders by assessing many genes at the same time.
We empower research into cardiomyopathy gene variant identification. Most variants associated with inherited cardiac conditions are unique familial variants.
Our cytogenetic microarrays reliably detect chromosomal imbalances of copy number and allelic contribution associated with constitutional disorders.
This is the international website for Illumina. If you are looking for information specific to your region, please select your location and we will redirect you.