Explore genomic variation analysis products designed to inform drug target discovery, validation, and development.
32 Results
Tailor panel designs for human disease research efficiently and conveniently by selecting from a catalog of over 5,000 pretested genes.
An interactive omics knowledge base that analyzes private omics data with highly curated public data to help researchers put their data into biological context.
DRAGEN Array provides accurate, comprehensive, and efficient genotyping, PGx CNV calling, and star allele annotation for Infinium microarrays.
A study design tool that combines private data with public data sets for rapidly building and exploring cohorts.
Operationalize informatics and drive scientific insights with Illumina Connected Analytics. Contact us for information on pricing, subscriptions, and more.
Targeted custom enrichment panels, providing simple and efficient solutions for multiple targeted sequencing applications.
An efficient, fast, and integrated library preparation workflow that yields highly accurate data for sensitive sequencing applications.
A fast, integrated workflow for preparing libraries for use in a wide range of sequencing applications.
Maximize genomic insights with DRAGEN secondary analysis, learn about the latest updates, read FAQs, and find product support.
Illumina Protein Prep combines trusted Illumina chemistry, SOMAmer technology, and DRAGEN data analysis for a comprehensive, automated NGS-based proteomics solution.
A fast, integrated workflow for producing enriched and indexed sequencing libraries from a broad range of sample types and RNA input quantities.
A standalone kit allowing for ribosomal RNA and human globin mRNA removal in human, mouse, rat, and bacterial samples.
Streamlined RNA-Seq solution for clear and comprehensive analysis across the coding and non-coding transcriptome with exceptional study flexibility.
A rapid, cost-effective workflow for accurate, unbiased detection of the protein-coding transcriptome with precise measurement of strand information.
A powerful, cost-effective genotyping microarray for large-scale genetic studies and pharmacogenomics in East Asian populations.
Fully customizable methylation microarray for large, targeted epigenetic applications.
The Global Clinical Research Array offers exceptional coverage of key genome-wide clinical content with a highly scalable workflow.
The Global Clinical Research Array offers exceptional coverage of key genome-wide clinical content with a highly scalable workflow.
Infinium Global Diversity Array (GDA) with Enhanced PGx is the most comprehensive genotyping microarray on the market for pharmacogenomics research.
BeadChip combining exceptional coverage of clinical research variants with optimized multiethnic, genome-wide content for genotype screening.
Illumina provides an innovative portfolio of NGS systems, products, and services for many phases of the drug development pipeline.
Pharmacogenomics, the study of how variations in the human genome affect our response to medications, may help reduce adverse drug reactions and medical costs.
Genomics in drug discovery & development
Explore innovative genomic analysis solutions designed to inform drug discovery efforts and support development of targeted therapeutics.