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New configurations will bring longer read capabilities with more output for immune repertoire, shotgun metagenomics and more
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Discover novel trait and disease associations with optimized tag SNPs and functional exonic content at an attractive price
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DRAGEN v4.0 release enables machine learning by default, providing increased accuracy out of the box
Our instrument performance service helps reduce unplanned downtime and minimize instrument requalification
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Robust methylation profiling microarray with extensive coverage of CpG islands, genes, and enhancers
Two DRAGENs help Cardio-CARE slay one petabyte of data to better understand heart disease in Hamburg
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Together, we’re finding answers to life’s biggest questions and broadening the positive impact of genomics around the world
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Get instructions for using Illumina DRAGEN Bio-IT Platform v4.0
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Enable comprehensive genomic profiling with accurate and comprehensive homologous recombination deficiency assessment
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Save on the Ribo-Zero Plus Microbiome rRNA Depletion Kit, restrictions apply
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A multi-species, low-cost, genome-wide genotyping platform to support molecular breeding in small grains
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A comprehensive, easy-to-implement, and versatile genomic analysis tool set for translational researchers
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The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab
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Delivers a range of ready-to-use and custom panels for simple, flexible targeted resequencing that provides high-quality data you can trust.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, user-friendly workflow for a wide range of target enrichment applications encompassing custom panels, fixed panels, and whole-exome sequencing.
Perform targeted genotyping on large numbers of samples. Scale up to more than 1 million samples per year.
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Affordable, fast, and accessible sequencing power for targeted or small genome sequencing in any lab.
Perform high-throughput, cost-effective genotyping for quality control, tracking, and stratification applications, including biobanking.
Purchase the TruSight Oncology 500 assay for the first time and receive an exclusive limited time offer.
Whole-genome sequencing library prep kits for small genomes (e.g. bacterial and viral genomes), amplicons, and plasmids.
Rapid library preparation from a broad range of sample types for studying the coding and non-coding transcriptome with unparalleled study flexibility.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
A simple, scalable, cost-effective, rapid single-day solution for analyzing the coding transcriptome leveraging as little as 25 ng input of standard (non-degraded) RNA.
This array offers an optimal and comprehensive set of both common and rare SNP content for diverse world populations.
Interrogate over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
Optimized chemistry to increase cluster density and read length, and improve sequencing quality scores, compared to earlier MiSeq reagent kit versions.
These sequencing reagent kits offer increased stability and robustness over the prior v2 kit version.