Illumina creates tools and services to take your studies of the genome and all of its variations further. Whether your studies require a broad review of the genome or in-depth, base-by-base interrogation of a particular loci, Illumina offers solutions designed to help you generate more complete answers, as efficiently and effectively as possible. Have confidence in your data, knowing that Illumina sequencing by synthesis (SBS) technology has been used to generate >90% of the world’s sequencing data.* Illumina BeadChip microarrays offer ease of use, robust performance, and reproducibility for a diverse range of studies.
Today, researchers around the world rely on our next-generation sequencing (NGS) and array solutions to analyze tens of thousands of genomes each year. From disease research to agrigenomics to microbiology, the applications are as diverse as life itself.
With platforms for every scale, Illumina provides a comprehensive range of NGS solutions to accommodate a wide variety of study designs.
DNA SequencingOffering flexible content and scalable multiplexing, Illumina high-density BeadArray technology enables diverse applications.
Human Genotyping with ArraysUsing powerful, proven Illumina NGS and microarray solutions, researchers can now understand genetic variations at new depths.
GenotypingUltra-high throughput, scalability, and speed enable biological understanding never before possible.
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Find out how researchers are using Illumina technology to further scientific research.
All the information you need, from BeadChip arrays to library prep to sequencer selection and analysis. Select the best tools for your lab.
*Data calculations on file. Illumina, Inc., 2015