Find microarray and sequencing products for immunology research, neuroscience research, autoimmune disease research, and beyond.
49 Results
Targeted custom research panels optimized for sequencing specific targets or genomic content of interest.
Targeted RNA research panel to investigate T cell diversity and clonal expansion by sequencing T cell receptor beta chain rearrangements.
Tailor panel designs for human disease research efficiently and conveniently by selecting from a catalog of over 5,000 pretested genes.
FFPE-compatible panel for measuring T cell diversity and clonal expansion in tumor samples by sequencing T cell receptor beta chain rearrangements.
Targeted panel that measures expression levels of >20,000 human RefSeq genes.
An interactive omics knowledge base and data search engine that puts private data into biological context with highly curated public omics data.
DRAGEN Array provides accurate, comprehensive and efficient secondary analysis 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.
Accessible and highly scalable single-cell RNA-Seq solution for mRNA capture, barcoding, and library prep without complex workflows or microfluidics
Streamlined RNA-Seq solution for clear and comprehensive analysis across the coding and non-coding transcriptome with exceptional study flexibility.
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.