Illumina to Acquire GRAIL Read More
Using NGS to Study Rare Undiagnosed Genetic Disease

Customer Interview

Using NGS to Study Rare Undiagnosed Genetic Disease

Whole-exome and transcriptome sequencing prove beneficial in uncovering mutations and pathways associated with rare disease.

Read Article
Using Analytics to Improve Cancer Diagnosis and Therapy Selection

Customer Interview

Using Analytics to Improve Cancer Diagnosis and Therapy Selection

Developing and automating best-practice workflows that make analyzing, processing, and disseminating genomic data accessible to researchers...

Read Article
Sandip Patel, MD: Comprehensive Genomic Profiling

Customer Video

Sandip Patel, MD: Comprehensive Genomic Profiling

Sandip Patel, MD, from UCSD Moores Cancer Center provides his point of view on Comprehensive Genomic Profiling (CGP), as an approach for assessing...

View Video
 

Core Technology

Sequencing

See what sequencing can do for you

Learn MoreCompare Sequencers
 

Core Technology

Microarrays

Analyze genetic variation on any scale

Learn MoreCompare Array Scanners
 

Depend on Our Sequencing

Enabling you with trusted next-generation sequencing technology

Learn More

Innovations in Library Prep

We keep you on the forefront of emerging applications through continued innovation. Fast, simple library prep and enrichment workflow from Illumina

Learn More

NovaSeq 6000 Reagent Kits v1.5

Improved Q30 score, support for UMIs, extended shelf life, and support for Illumina DNA PCR-Free Library Prep

Order Now

Training and Webinars

Illumina offers webinars and free online training courses to get the most out of your experiments and products

View WebinarsView CoursesOn Demand
 
Employee Story

Clinical lab manager Rita walks you through her day

View Video View More Stories