Find microarray and sequencing products for immunology research, neuroscience research, autoimmune disease research, and beyond.
43 Results
Targeted custom research panels optimized for sequencing specific targets or genomic content of interest.
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 complete targeted resequencing solution for a wide range of applications, with fast integrated workflow and options for custom and fixed enrichment panels.
A high-performance, fast, and reliable human whole-exome sequencing solution that includes a comprehensive, up-to-date exome enrichment panel.
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.
A targeted NGS-based assay for sequencing mycobacterium, M. tuberculosis complex (MTBC) strains, and antimicrobial resistance markers.
Predesigned, optimized panel to provide enhanced coverage of challenging-to-map regions within protein-coding genes using Illumina Complete Long Reads with Enrichment library prep kit. Analyzed in combination with a required ≥ 30× standard short-read whole genome.
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.
Infinium Exome-24 Kit arrays deliver exceptional coverage of putative functional exonic variants representing diverse populations and a range of common conditions.
Complex and genetic disease research
Comprehensive array and next-generation sequencing solutions to accelerate research of various genetic complex diseases.
Genome-wide association studies
Genome-wide association studies enable the discovery and characterization of genetic variants associated with disease.
Learn how to profile gene expression changes for a deeper understanding of biology.