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 cancer genomics 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 genomics 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.
Explore genomics-based approaches to investigating cancer using NGS and microarrays.
During this webinar, our expert speakers provide background information on next-generation sequencing (NGS), discuss the achievements and challenges associated with NGS, and discuss how an integrated multiomics approach can be used in cancer diagnosis and treatment.
View WebinarA new exome-based test will help determine the genetic variants—germline and somatic—driving these rare cancers
Read ArticleDeveloping and automating workflows for analyzing, processing, and sharing genomic data among researchers and clinicians.
Read InterviewOn World Cancer Day, Illumina celebrates the nonprofits and institutions working hard to increase access to care
Read ArticleUnify single-cell gene expression and chromatin accessibility to help reveal cellular mechanisms driving gene regulation.
Read Tech NoteLearn how to incorporate protein detection into bulk RNA-Seq and develop a workflow for BEN-Seq, providing a holistic approach to cell analysis.
Read Application NoteIn this podcast episode, Drs. Obi and Malachi Griffith, Professors of Medicine at Washington University in St. Louis, MO, discuss their work in improving interpretations of sequence variants in cancer and enhancing bioinformatics education.
Listen NowAn overview of recent cancer genomics research publications featuring Illumina technology.
Munich Leukemia Laboratory is using NGS to gain a better understanding of leukemia and lymphoma subtypes and discover new therapeutic pathways.
Explore a variety of webinars on topics ranging from cancer research to NGS data analysis, microbiome studies, and more.
This updated guide provides an overview of NGS-based and microarray workflows for a broad range of cancer research applications.
A researcher from Massachusetts General Hospital compares sequencing results from FFPE and fresh-frozen tumor samples.
*Data on file based on a 2013 study.