Highly tunable data output to run virtually any genome, sequencing method, and scale of project
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A rapid, single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
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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
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Whole-genome shotgun sequencing and transcriptomics provide data to refine drug discovery and development
TruSight Software Suite accelerates identification of genetic diseases
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Three approaches to help researchers with sequencing
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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
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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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