Highly tunable data output to run virtually any genome, sequencing method, and scale of project
Kits & Reagents
A rapid, single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
Selection & Planning Tools
Cloud-based variant interpretation
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
Whole-genome shotgun sequencing and transcriptomics provide data to refine drug discovery and development
TruSight Software Suite accelerates identification of genetic diseases
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
A culture-free method for studying complex microbiomes or environments
Microbial Genomics Products
A highly sensitive and accurate tool for measuring expression across the transcriptome
TruSight Software Suite accelerates the identification of genetic diseases
Complex Disease Research Products
Study gene expression changes in cancer, RNA biomarkers of drug response, and more
Considerations for your lab
Reproductive Health Products
Genetic Health Products
Find tools to help you choose the right products for your needs and plan your experiments. Identify the right library prep kit or microarray, calculate sequencing coverage, explore methods compiled from publications, design custom assays, and more.
Find the system guide, site prep guide, indexed sequencing guide, and other supporting documentation.
Online Illumina sequencing courses are free, interactive, and available any time.
Don’t let your budget hold you back. Explore different buying options to find which best fits your needs.
Generate your own customized documentation, specifically tailored to your experiment.
Additional information about sequencing quality scores, how they are calculated, and the relationship between sequencing quality score and base call accuracy.
Learn how to estimate and achieve the necessary sequencing coverage for your experiment.
See our best practices for generating high-quality data from human whole-genome sequencing on the NovaSeq 6000 System.
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