Since the launch of our first Infinium BeadChip in 2005, Illumina has innovated robust, economical, and scalable microarray solutions for an ever increasing range of applications. Powered by industry-leading BeadArray and Infinium assay technologies, our comprehensive suite of microarrays delivers exceptional data quality and genomic coverage to accelerate both targeted and whole genome studies.
Through collaboration with key opinion leaders and institutions around the world, we develop products and workflow solutions that help propel scientific progress. We listen to our customers and seek to understand how we can help empower their research pursuits across the genomic continuum, from arrays to next-generation sequencing (NGS).
Choose from ready-to-use BeadChip arrays with expert-developed content, or design custom iSelect or semicustom arrays to suit specific research and analysis needs.
Our latest array solution introduces a new Infinium array format, workflow and software to support production-scale genotyping throughput levels.
Introducing the Infinium XT Production-Scale Genotyping Solution
Microarrays are ideal for processing thousands of samples cost-effectively to identify mutations and structural variants or changes in gene expression and methylation. Additional advantages include:
Perform whole-genome or targeted genotyping of human samples with BeadChip microarrays for genome-wide association studies (GWAS), population studies and biobanking, or tailor research studies to detect common variants, CNVs, and more.Learn More
Carry out whole-genome selection studies, DNA fingerprinting, net merit, and marker-assisted breeding with species-specific catalog and consortia-developed BeadChip microarrays, or genotype species of interest with custom arrays.Learn More
Analyze and quantify methylation across the genome quickly and accurately with BeadChip methylation arrays.Learn More
Visualize and analyze data from any BeadChip array with efficient software tools. See a comprehensive view of the genome, gene expression, and gene regulation with GenomeStudio Software, calculate statistics and interrogate clusters with Beeline Software, and develop custom and semi-custom arrays to fit specific research needs using the Assay Design Tool.Learn More
Our high-resolution array scanners are designed and optimized to deliver high-quality data for a broad range of applications, with the flexibility to meet a variety of throughput needs. These systems enable rapid, sensitive, and accurate imaging of Illumina microarrays. Learn more about our microarray scanners.
Find genotyping solutions that enable researchers to leverage biobank samples for translational and pharmacogenomic research, population studies, and more. Learn more about biobank sample genotyping.
Study cancer predisposition and risk with Illumina microarrays, sequencing systems, and data analysis software. Learn more about cancer germline mutation analysis.
High-resolution cytogenomic arrays enable detection of low-level mosaics, CNVs, LOH, and AOH across the genome. Learn more about cytogenomics.
Cytogenetics researchers can use complementary microarray and sequencing technologies for thorough analysis of chromosomal changes in cancer. Learn more about cancer cytogenetics.
High-throughput sequencing and array technologies enable researchers to screen large sample numbers quickly to find disease-related causal variants. Learn more about causal variant discovery.
Cost-effectively identify common genetic variations among populations using high-performance, population-scale sequencing systems. Learn more about the HiSeq X Ten and HiSeq X Five Systems.
As the cost of NGS continues to decline, sequencing becomes a powerful tool for performing genotyping studies. GBS is an efficient, cost-effective tool to discover and genotype SNPs in large populations. Learn more about GBS.
Genotyping studies in plants and animals can uncover the relationship between genotype and phenotype, informing breeding decisions and the genetic selection of valued traits. Learn more about plant and animal genotyping.