Highly tunable data output to run virtually any genome, sequencing method, and scale of project
Kits & Reagents
Easy adoption with superior support across the entire workflow. Fast, simple library prep and enrichment workflow from Illumina.
Selection & Planning Tools
A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
Software & Informatics Products
Bringing efficiency and high confidence to case management, variant analysis, and interpretation in rare disease
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
Find popular product groupings for your workflow
Enables and accelerates research leveraging BaseSpace Correlation Engine
Environmentally friendly packaging reduces waste from landfills and carbon emissions
All Investor Information
Three approaches to help researchers with sequencing
All Support Tools
Product Support Services
Expanded portfolio enables comprehensive genomic profiling from blood and tissue
Cancer Research Products
Microbial Genomics Research
This high-throughput NGS test detects SARS-CoV-2 in nasopharyngeal, oropharyngeal, and mid-turbinate nasal swabs
Microbial Genomics Products
A transformational approach to biodiversity monitoring
New library prep kits enhance research in rare genetic diseases
Complex Disease Research Products
Why he believes CGP is poised to become a standard of care in oncology
Find out why laboratories In Europe have implemented VeriSeq NIPT
Reproductive Health Products
Genetic Health Products
Comprehensive array and next-generation sequencing solutions to accelerate research on various complex diseases.
Our targeted gene panels and microarrays can support genetic disease research by identifying causative genetic variants and chromosomal aberrations.
Learn how to analyze transcriptome changes or profile genome-wide gene expression levels in a single experiment with next-generation sequencing methods.
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