Explore Illumina Mobile Tools
Library Prep and Array Kit Selector
Gene Panel Finder
Sequencing Method Selector
Sequencing Platform Comparison Tool
Find Your Area of Interest
Molecular Biology Research Tools
Applied Genomics Solutions
Genomics in Drug Development
Complex Disease Genomics
Commercial Agricultural Applications
Infectious Disease Surveillance
Biobank Analysis Solutions
Illumina Clinical Services Laboratory
Reproductive & Genetic Health
Explore Research Techniques
Popular Genomics Applications
Sequencing Data Analysis
Explore Our Entire System Portfolio
Find the right system for your application needs.
Browse by Type:
Use Our Interactive Selection Tool:
Browse by System:
Explore Our Products
Browse by Product Type:
Clinical Research Products
Molecular Biology Reagents
Browse All Products
Browse by Area of Interest:
Find Products for Your System:
Additional Product Selection & Experiment Planning Tools:
See All Tools
Access Informatics Solutions
BaseSpace Informatics Suite
Scientific & Educational Content
Sequencing Method Explorer
Education for Researchers
Learn About Illumina
Doing Business with Illumina
See All Support Options
Support for popular kits
View All Sequencing Kits
View All Array Kits
Support for popular systems
Support for Your System
AutoLoader 2.x Support Links
View All AutoLoader 2.x Support
BeadArray Reader Support Links
View All BeadArray Reader Support
BeadXpress Reader Support Links
View All BeadXpress Reader Support
cBot Support Links
View All cBot Support
cBot 2 Support Links
View All cBot 2 Support
Cluster Station Support Links
View All Cluster Station Support
Popular Kits for Cluster Station
Genome Analyzer IIx Support Links
View All Genome Analyzer IIx Support
Popular Kits for Genome Analyzer IIx
View All Supported Kits
HiScan Support Links
View All HiScan Support
Popular Kits for HiScan
HiSeq 1000 Support Links
View All HiSeq 1000 Support
Popular Kits for HiSeq 1000
HiSeq 1500 Support Links
View All HiSeq 1500 Support
Popular Kits for HiSeq 1500
HiSeq 2000 Support Links
View All HiSeq 2000 Support
Popular Kits for HiSeq 2000
HiSeq 2500 Support Links
View All HiSeq 2500 Support
Popular Kits for HiSeq 2500
HiSeq 3000 Support Links
View All HiSeq 3000 Support
Popular Kits for HiSeq 3000
HiSeq 4000 Support Links
View All HiSeq 4000 Support
Popular Kits for HiSeq 4000
HiScanSQ Support Links
View All HiScanSQ Support
Popular Kits for HiScanSQ
HiSeq X Support Links
View All HiSeq X Support
Popular Kits for HiSeq X
iScan Support Links
View All iScan Support
Popular Kits for iScan
MiniSeq Support Links
View All MiniSeq Support
MiSeq Support Links
View All MiSeq Support
Popular Kits for MiSeq
MiSeqDx Support Links
View All MiSeqDx Support
Popular Kits for MiSeqDx
MiSeq FGx Support Links
View All MiSeq FGx Support
Popular Kits for MiSeq FGx
NextSeq 500 Support Links
View All NextSeq 500 Support
Popular Kits for NextSeq 500
NextSeq 550 Support Links
View All NextSeq 550 Support
Popular Kits for NextSeq 550
NeoPrep Library Prep System Support Links
View All NeoPrep Library Prep System Support
Popular Kits for NeoPrep Library Prep System
NovaSeq 6000 Support Links
View All NovaSeq 6000 Support
Support for Popular Kits
Support for your organization
Support for your workflow
Helpful tools and tips
Support for Your Workflow
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.
Identify coding variants up to 70% faster with this exome library prep and enrichment kit. Expanded kit sequences untranslated regions (UTRs) and miRNA.
This library prep kit delivers sensitive and specific amplicon sequencing results from both low-input and FFPE DNA samples.
Focus on key genomic regions of interest with this targeted resequencing solution, useful for very high plexity pools or longer amplicons.
Simple, all-inclusive whole-genome sequencing (WGS) library preparation that provides accurate and comprehensive coverage of complex genomes.
This kit provides a low-cost exome sequencing solution that delivers exceptional target coverage over a broad range of read depths.
Generate whole-genome sequencing libraries and efficiently interrogate samples with limited available DNA.
DNA library preparation for use with the NeoPrep System, providing comprehensive genomic coverage with low DNA input and minimal hands-on time.
The TruSeq RNA Library Preparation Kits provide a simple, cost-effective solution for analysis of the coding transcriptome.
This exome sequencing library prep kit uses a simple, one-day workflow to provide a fast path to greater understanding of the human exome.
A robust, highly scalable whole-transcriptome analysis (RNA-Seq) solution for a variety of species and sample types, including human, mouse, and FFPE.
Prepare whole-transcriptome sequencing libraries from blood-derived RNA with an efficient workflow that removes rRNA and globin mRNA in a single step.
Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information.
Complete view of the transcriptome with walk-away workflow, lower input requirement, and excellent reproducibility.
A targeted RNA sequencing panel to study cellular pathways affected by cardiotoxic compounds or stress. Assay targets cardiotoxic response markers.
A targeted RNA sequencing panel for studying the cell cycle. Assays target genes involved in all cell cycle phases as well as DNA replication.
A targeted RNA sequencing panel for studying cytochrome p450 (CYP) genes. Assays target CYP genes involved in drug and toxin metabolism.
Targeted RNA assays for gene expression studies: fixed or custom sequencing panels, with a simple workflow and automated data analysis.
A targeted RNA sequencing panel for studying neurodegenerative and neurotoxic pathways such as those implicated in Alzheimer’s Disease.
GSA is a next-generation genotyping array for population-scale genetics, variant screening, and precision medicine research.
A cost-effective array for understanding complex disease in diverse human populations, focused on Hispanic and African American populations.
A cost-effective array for understanding complex disease in diverse human populations, focused on European, East Asian, and South Asian populations.
A cost-effective array for understanding complex disease in diverse human populations.
Advance your Chinese population GWAS. This microarray provides coverage of common, intermediate, and rare variation specific to Chinese populations.
genotyping for quality control, tracking, and stratification applications including biobanking.
Infinium XT is a comprehensive microarray solution that enables production-scale genotyping of up to 50,000 single or multi-species custom variants.
Interrogate virtually any target across any species to create a fully-customized genotyping array tailored to your unique study needs.
Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.
This kit removes unwanted ribosomal RNA and globin mRNA from mammalian blood RNA samples before sequencing.
This kit removes both cytoplasmic and mitochondrial rRNA from human, mouse, and rat samples, including partially degraded samples.
This kit removes cytoplasmic ribosomal RNA from human, mouse, or rat samples, including partially degraded samples.
Leveraging innovative library prep, sequencing, and informatics solutions to enable powerful NGS-based biomarker analysis.
Illumina provides an innovative portfolio of NGS systems, products, and services for many phases of the drug development pipeline.
Leaders in translational genomics and computational biology designed an array to support earlier target selection and validation in drug development.