JUST LAUNCHED
The Prosigna Breast ROR Test Now Available for Providers to Order in the US*
Your ally in the race against cancer
Our high-performing molecular tests empower clinicians and their patients with important information that has helped guide care decisions for over 900,000 people.1
Our tests assess the unique biology of each patient’s tumor. This helps clinicians answer key questions and make confident decisions for thyroid, prostate, breast, bladder, and lung cancer. The important information from our tests helps enable personalized and effective patient care.
JUST LAUNCHED
The Prosigna Breast ROR Test Now Available for Providers to Order in the US*
Find the information most relevant to you.
Patients benefited from our genomic tests across multiple cancer types
Peer-reviewed publications validate our platform’s clinical utility
Phase 2 & 3 trials evaluating our tests
Did You Know?
is the only gene expression test included in the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for prostate cancer2
A powerful evidence-generation engine that delivers diagnostic innovation.
Transcriptomes, genomes, complementary data sources, and clinical outcomes
For current tests and new cancer applications
From the analysis of real-world data and clinical studies
From AI-assisted data mining, multimodal analysis, and bioinformatics analysis
Every breakthrough brings us closer to improved outcomes for those touched by cancer. Explore our latest updates, news, and insights.
We value a diverse, inclusive workplace where creativity, collaboration, and compassion thrive. Our team members are empowered to lead discoveries that are changing the future of cancer care, with positions in state-of-the-art labs, offices, field locations, and remote work.
* Prosigna testing is available in the United States as a laboratory developed test (LDT) service and has not been cleared or approved by the FDA. The test is not yet available in New York.
Decipher testing is available in the United States as part of Veracyte’s CLIA-validated laboratory developed test (LDT) service, and FDA clearance is not required.