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Popular Genomics Applications

Illumina offers industry-leading technologies designed to make genomic analysis accessible to everyone. Using powerful, proven Illumina next-generation sequencing (NGS) and microarray solutions, researchers can now read and understand genetic variations at new depths, more easily and quickly than before, enabling a wide variety of genomics applications. As a result, discoveries that were unimaginable even a few years ago are now becoming routine.

Enabling genetic analysis
Genotyping

Genotyping is a popular and effective way to screen for SNPs and structural variations across the genome. Illumina technology provides the accuracy, reproducibility, and flexibility with content selection that is critical to the success of your genomics research.

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Gene Expression and Transcriptome Analysis

Illumina technologies enable characterization of all transcriptional activity (coding and non-coding), or focusing on a select subset of RNA transcripts within a given sample for high-quality gene expression and transcriptome analysis for a broad range of sample types.

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Epigenetics

Illumina offers a broad portfolio of simple-to-use, cost-efficient epigenetic analysis tools for studying epigenetic modifications and their impact on gene regulation. By working with leading epigenomics experts, Illumina ensures its solutions meet the field's rapidly evolving needs.

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Cytogenomics

Chromosome aberrations play a role in constitutional disorders and cancer. Cytogenetic analysis using proven Illumina sequencing and high-quality cytogenomic arrays can be performed on a single platform.

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NGS Technology
Next-Generation Sequencing

With its unprecedented throughput, scalability, and speed, NGS enables researchers to study biological systems at a level never before possible. Learn more about next-generation sequencing.

Microarray Technology
BeadArray Microarray Technology

BeadArray high-density microarray technology increases genomic coverage for whole-genome genotyping; resolution for cytogenetics and CNV detection; and sample throughput for gene expression, DNA methylation, and focused genotyping. Learn more about BeadArray microarray technology.

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Uncovering a New CNV Linked to Schizophrenia
Uncovering a New CNV Linked to Schizophrenia

Dr. Frank Middleton uses arrays, whole-genome sequencing, and gene expression analysis to screen for alterations in schizophrenia.

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