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 genetic variants such as 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 copy number variation (CNV) data analysis tools can analyze results for 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.

Learn More
Targeted Genotyping

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

Learn More
Custom Genotyping

Perform studies on genome regions or organisms of interest for which standard products are not available.

Learn More
Copy Number Variation Analysis

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

Learn More
Production-Scale Genotyping Solution

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.

Learn More
Infinium BeadChip Arrays
Genotyping Plants and Animals
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 Mutation Studies
Cancer Germline Studies

Analyze germline mutations that predispose individuals to cancer using microarrays and NGS. Learn more about cancer germline mutation analysis.

Biobank Sample Genotyping
Biobank Sample Analysis

Leverage biobank samples for translational and pharmacogenomic research, epidemiology, population studies, and more. Learn more about biobank sample genotyping.

SNP Genotyping Data Analysis
GenomeStudio Genotyping Module

GenomeStudio Software enables efficient SNP genotype calling, data normalization, loss of heterozygosity (LOH) calculation, CNV analysis, and more. Learn more about GenomeStudio Software.

Interested in receiving newsletters, case studies, and information on genomic analysis techniques? Enter your email address.
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.

Find the Right Kit Find the Right Kit
Next-Generation Sequencing (NGS)
NGS Technology

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

Explore NGS
BeadArray Microarray Technology
BeadArray Microarray Technology

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

Learn More
Array Solutions
Array Solutions

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

Learn More
Genotyping Consortia
Genomics Consortia

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

Learn More