NGS identification of both male and female cancer risks
Do you know a man who has participated at least once in “Movember”? Every year, thousands of men...
Oncology
Precise. Personalized. Preventive.
Genetic diagnostic testing for cancer is centerstage as oncology transitions to precision medicine and personalized treatment. Our fast, accurate DNA tests assist in detection and prevention – and help drive the development of individualized therapies. At a time when genetic oncology grows at unprecedented speed, we believe that, in some cases, less is more.
Less disease, longer lives
Cancer treatment is changing fast. The shift to precision medicine and personalized therapies is rapid and real. Genetic testing is a crucial enabler of this transformation..
At a time when genetic oncology is growing at unprecedented speed, we believe that less is sometimes more.
Increased preventive DNA cancer screening makes it possible to identify more individuals at risk. It can also help combat the rising incidence of some cancer types in an aging population.
Our diagnostic tests for breast, ovarian and other cancers identify clinically significant variants with unsurpassed accuracy. Their high user convenience and fast, actionable results support the drive towards individualized cancer diagnostics.
A single-tube format generates a simple workflow with short hands-on time. User-friendly analysis software ensures effective automation throughout the process.
The end-to-end procedure is fully CE IVD-certified in compliance with the EU’s In-Vitro Diagnostic Medical Device Directive, guaranteeing robust results in clinical use that you can trust.
One tube per patient sample - no sample splitting
45
Less than 45 minutes hands-on time
CE-IVD
CE-IVD certified solution – from sample to result
Breast cancer
Breast cancer is the leading cause of cancer-related death in women. An estimated one in eight will develop the disease in their lifetime, while ovarian cancer is responsible for more deaths than any other cancer of the female reproductive system. We provide diagnostic solutions to cover women along the whole way – from prevention to treatment. Our germline mutation analysis identifies those who are at risk of developing breast and ovarian cancer and detects individuals who may benefit from risk-reducing strategies. Our somatic mutation analysis identifies women who may benefit from targeted treatment using PARP inhibitor.
Webinar on-demand | February 16, 2023
Post-transplant monitoring: The future of chimerism testingNews | January 25-26, 2023
We are attending the Festival of Genomics & Biodata!Podcast | December 6, 2022
Collaborations and homebrew assays by Dan Hauzenberger & Turid Sundin Carlsson
CRISPR Helps BRCA1 Researchers Determine Functional And Non-Functional Mutations
BRCA1 variants may generally be divided into three categories: benign variants, which cause no...
New Devyser BRCA NGS study published
Check out a recent publication from Capone et al from the University of Florence!
Robust NGS workflow provides full BRCA1 & BRCA2 screening
The team at Devyser were excited to see our products put to use in a recent research project,...
What are the latest trends in genetic screening for breast and ovarian cancer, and what does the scientific research mean for you and your laboratory? 