Illumina genotyping solutions

A complete range of advanced sequencing and microarray solutions for every need

Genotyping SNPs and Other Variants

Genotyping enables researchers to explore the underlying genetic variants, including single nucleotide polymorphisms (SNPs) and large structural changes in DNA. High-throughput genomic technologies such as next-generation sequencing (NGS) and microarrays enable a deeper understanding of disease etiology on a molecular level.

With multiple genomic targets potentially contributing to disease, analysis requires flexibility and accuracy. SNP genotyping and CNV genotyping data analysis tools can analyze data across millions of markers and probes and detect sample outliers, providing insight into the functional consequences of genetic variation.

Introduction to Genotyping
Whole-Genome Genotyping

Interrogate SNPs and other variants across the entire genome to obtain the most comprehensive view of genomic variation.

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Targeted Genotyping

Focus time, effort, and resources on analyzing SNPs and other variants in a specific genomic region of interest, often with higher coverage.

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Custom Genotyping

Focus on specific regions of the genome or perform studies on regions or organisms for which standard products are not available.

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Copy Number Variation Analysis

Detect DNA copy number changes, as well as aberrant chromosome amplifications and deletions, relative to a reference genome.

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Production-Scale Genotyping

Infinium XT optimizes the user experience as labs take production-scale genotyping studies to the next level of throughput. This 96-sample BeadChip array enables processing of 100,000 to > 1,000,000+ samples/year, for any species, with user-defined content.

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Infinium BeadChip Arrays
Plant and Animal Genotyping
Plant and Animal Genotyping

Enhance the value of crops and herds with screening and discovery tools that aid in breeding decisions. Learn more about plant and animal genotyping.

Cancer Germline Studies
Cancer Germline Studies

Analyze germline mutations that predispose individuals to cancer using microarrays and next-generation sequencing. Learn more about cancer germline mutation studies.

Biobank Sample Genotyping
Biobank Sample Analysis

Leverage biobank samples for translational, regenerative medicine, pharmacogenomic, clinical trial, epidemiology, and population studies. Learn more about biobank sample genotyping.

Causal Variant Discovery
Causal Variant Discovery

Screen large sample numbers quickly to find SNPs and other causal variants associated with complex diseases. Learn more about causal variant discovery.

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Library Prep and Array Kit Selector
Array and Library Prep Kit Selector

Easily identify the best array or sequencing library prep kit based on project type, starting material, and method.

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Next-Generation Sequencing (NGS)
NGS Technology

With unprecedented throughput, scalability, and speed, NGS enables study of biological systems at a level never before possible.

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BeadArray Microarray Technology
BeadArray Microarray Technology

BeadArray technology enables high-density BeadChip arrays to facilitate diverse applications, including SNP genotyping and more.

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Array Solutions
Array Solutions

Access a comprehensive range of microarray solutions for DNA, RNA, and epigenetic studies.

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Genotyping Consortia
Genomics Consortia

Illumina helps researchers who share similar goals join efforts to pool resources and create genomics tools.

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