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Enable comprehensive genomic profiling with accurate and comprehensive homologous recombination deficiency assessment
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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
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
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Whole-exome sequencing kit with library prep, hybridization reagents, exome probe panel, size selection beads, and indexes
See what is possible through the latest advances in high-throughput sequencing technology
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View the unveiling of our newest technologies and products on-demand, recorded live at the Illumina Genomics Forum
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Get instructions for using Illumina DRAGEN Bio-IT Platform v4.0
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Monitor SARS-CoV-2 variants and other respiratory viruses in the community
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Mapping genetic diversity to identify where confiscated gorillas come from and boost survival rates
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Explore the advantages of NGS for analysis of gene expression, gene regulation, and methylation
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Comprehensive, IVD, in-lab aneuploidy screening solution for accurate NIPT results in 26 hours
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Whole-genome sequencing (WGS) for rare disease offers key advantages over other genetic testing methods
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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.