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Today’s genomic solutions for tomorrow’s cancer breakthroughs

Cancer Genomics Research

Illumina next-generation sequencing (NGS) and microarray technologies represent the gold standard in quality worldwide—and account for ~90% of the world’s sequencing data.* Innovative, intuitive, and completely integrated, our sample-to-data solutions empower your lab to keep ahead of the curve in the rapidly evolving genomics revolution. So you’ll be better able to perform the world-class research you strive for—with the goal of uncovering new insights into the biology of cancer that can lead to meaningful advances in personalized medicine.

Our comprehensive product offerings support multiple cancer research applications, including studies of DNA, RNA, epigenetics, and more. Our range of sequencers can be scaled to meet your needs—from powerful, yet personal, benchtop models to versatile, high-throughput systems. With intuitive data analysis and management capabilities and unsurpassed customer support, we can deliver the answers you seek—quickly, accurately, and cost-effectively.

Oncology

Cancer Genomics Research Stories

NGS Panels Demonstrate Value in Brain Tumor Studies
NGS Panels Demonstrate Value in Brain Tumor Studies

TruSight Tumor 170 accurately identifies diffuse glioma genetic markers, supporting use in tumor characterization for clinical research studies.

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Deciphering the Role of Long Non-Coding RNA in Cancer
Deciphering the Role of Long Non-Coding RNA in Cancer

Researchers are using RNA-Seq to reveal how lncRNAs could be used to identify, measure, and treat cancer.

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A New View of Cancer Pathways in Pediatric Leukemia
A New View of Cancer Pathways in Pediatric Leukemia

Researchers use targeted RNA sequencing to understand the role of fusion genes in pediatric leukemia.

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Genomic Technologies for Cancer Research

Learn the numerous ways that genomic technologies can be applied to tumor biology.

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Cancer Research Review

An overview of recent cancer genomics research publications featuring Illumina technology.

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Insights into Leukemia and Lymphoma

Munich Leukemia Laboratory is using NGS to gain a better understanding of leukemia and lymphoma subtypes and discover new therapeutic pathways.

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Exploring the Forgotten Genome of Cancer Research
Exploring the Forgotten Genome of Cancer Research

A Garvan Institute sarcoma study identifies rare cancer-associated variants in the germline.

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Methods Guide
Methods Guide

All the information you need, from BeadChips to library preparation to sequencer selection and analysis. Select the best tools for your lab.

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Sequencing Analysis of Tissue Samples: Fresh Frozen vs. FFPE

A researcher from Massachusetts General Hospital compares sequencing results from FFPE and fresh-frozen tumor samples.

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References

*Data on file based on a 2013 study.