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Longer read capabilities with more output for immune repertoire, shotgun metagenomics and more
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New features include increased SNV and SV calling accuracy, improvements in small CNV calling accuracy, and new targeted callers
Our instrument performance service helps reduce unplanned downtime and minimize instrument requalification
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Combining the power of XLEAP-SBS chemistry with efficient workflows to enable transformational science at scale
A new algorithm trained by natural selection can pinpoint disease-causing variants in humans
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Our mission is to improve human health by unlocking the power of the genome
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Get instructions for using DRAGEN Secondary Analysis v4.2
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Lung cancer patients in Wales are about to get answers faster—and potentially find out if they’re a match for targeted therapies
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Rapid library prep from a broad range of sample types for studying the coding and non-coding transcriptome
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More than just a sweet treat, sugarcane can also be a source of greener energy
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Understanding cardiovascular diseases through genomic sequencing
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The NovaSeq 6000Dx is our first IVD-compliant high-throughput sequencing instrument for the clinical lab
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Illumina Complete Long Read technology enables both long and short reads on the same NovaSeq instrument
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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.