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At Illumina, the faster we can innovate, the more lives we can help save.  As a genomics pioneer, we have proven through focused and continued innovation how unlocking the power of the genome can exponentially improve the human condition. Our ability to drive patient outcomes has made us a trusted partner in healthcare. Today, we’re providing tools that enable the next generation of researchers and clinicians to usher in the future of personalized medicine. Innovating at the intersection of technology, biology, and health, we are re-imagining what’s possible for clinicians, transforming how they detect, diagnose, and treat cancer, and rare, infectious, and genetic diseases.

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Content from this campaign

Health & Healthcare

The Growing Case for Whole-Genome Sequencing in All Blood Cancers
The Leukemia & Lymphoma Society estimates that by year end, 2024 will have seen 187,740 Americans diagnosed with a blood cancer—or about one person every three minutes.

Innovation & Technology

Independent Testing Proves Dragen Provides a Vastly More Comprehensive Genome
Illumina Vice President of Bioinformatics James Han has been in the industry for decades—so he’s witnessed every stride the company has made in that time. “Illumina has worked tirelessly for the last 20 years to improve sequencing,” he says.

Health & Healthcare

Trailblazing Study Shows Early CGP Leads to Better Precision Treatments
A large, multiyear study conducted by Illumina, Providence, and Microsoft Research has shown that a comprehensive genomic profiling (CGP) panel, which can assess more than 500 genetic variations in tumors, is a powerful tool to direct patients to advanced precision therapy.

Health & Healthcare

Why More Clinical Labs Are Turning to Whole-Genome Sequencing for Cancer
Whole-genome sequencing (WGS) use is more established for rare and pediatric disease, but next-generation sequencing in clinical use for cancer consists of various approaches.

Health & Healthcare

Finding the Needle in the Genomic Haystack With DRAGEN
When scientists want to sequence a DNA sample on an Illumina system, they don’t try to read all 4 billion base pairs of the genome at once. Instead, they slice the DNA into short fragments of about 500 base pairs that are easier to work with and faster to read.

Health & Healthcare

Nucleus Genomics Wants To Make Personalized Health Care a Reality
Nucleus Genomics is realizing the dream set into motion long ago by the Human Genome Project: to use the power of genomics to help people live lives that are as healthy and long as possible.

Health & Healthcare

Why Pathogen Surveillance Is Critical During a “Tripledemic”
The 2022–23 “tripledemic” season—in which influenza, SARS-CoV-2, and respiratory syncytial virus (RSV) all surged at the same time—was especially bad for Arizona, says Efrem Lim, an Arizona State University (ASU) virologist with the Center for Fundamental and Applied Microbiomics

Innovation & Technology

Highlights From Glasgow: Educating and Promoting the Impact of WGS
The Illumina NovaSeq X Plus took center stage at this year's European Society of Human Genetics (ESHG) conference in Glasgow, Scotland, considered Europe’s premier genomics event.

Innovation & Technology

What Our Primate Relatives Can Teach Us About Our Own Genomes
Each person’s genetic code harbors millions of variants that differ from one individual to the next, and account for differences in health and disease risk. The more human genomes are sequenced, the more data researchers have to compare and predict which variants are most likely.

Sustainable Finance & Socially Responsible Investment

Sequencing at Sea – Unlocking the Power of the Genome With eDNA and NextSeq™ 2000
In 2022, Illumina and Minderoo Foundation announced a $40M AUD partnership to leverage the power of genomics to accelerate scientific understanding of marine systems and help marine conservationists make informed decisions.
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