Enabling Genetic Analysis
Illumina offers 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.
Explore Popular Genomics Applications
Genotyping
Genotyping is a popular and effective way to screen for SNPs and structural variations across the genome. Illumina technology offers accuracy, reproducibility, and flexibility with content selection.
Learn MoreGene 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.
Learn MoreEpigenetics
Illumina offers a broad portfolio of simple-to-use, cost-efficient epigenetic analysis tools for studying epigenetic modifications and their impact on gene regulation.
Learn MoreGenome Editing
NGS enables researchers to discover CRISPR genome editing off-target effects, confirm gene knockouts, and assess the functional impact of edits.
Learn MoreBeginner's Guide to Next-Generation Sequencing
Considering bringing next-generation sequencing to your lab, but unsure where to start? These resources cover key topics in NGS and are designed to help you plan your first experiment.
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Related Solutions
NGS Technology
With ultra-high throughput, scalability, and speed, NGS enables researchers to study biological systems at a level never before possible. Learn more about how NGS works.
Microarray Technology
Illumina offers a high-density microarray technology that increases genomic coverage for whole-genome genotyping; resolution for cytogenetics and CNV detection; and sample throughput for focused genotyping and DNA methylation. Learn more about microarray technology.
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Additional Resources
Uncovering a CNV Linked to Schizophrenia
Dr. Frank Middleton uses arrays, whole-genome sequencing, and gene expression analysis to screen for alterations in schizophrenia.
Illumina Methods Guide
All the information you need, from BeadChips to library preparation to sequencer selection and analysis. Select the best tools for your lab.
Video Hub
Gain insight with our webinars, scientific reviews, product introductions, and more.
Chan Zuckerberg Biohub and the NovaSeq System
The Chan Zuckerberg Biohub uses the NovaSeq System to conduct innovative experiments in genomics.