NGS testing in clinical practice - what to expect
We help laboratories focus on what matters most to patients – correct and fast diagnosis every time. Our genetic test kits with integrated software set new standards in DNA diagnostic testing.
Screening for early detection of graft rejection and minimal residual disease in bone marrow and stem cell transplant patients. Learn more
Complete sequencing of the CFTR gene to detect all mutations. Learn more
Tests to evaluate multiple blood conditions and guide personalized treatment and family planning. Learn more
Rapid diagnosis of prenatal aneuploidies and male infertility. Learn more
Targeted cancer gene sequencing to identify clinically significant variants. Learn more
Fast diagnosis and cascade screening for monogenic and polygenic familial hypercholesterolemia. Learn more
“Early treatment made possible by more sensitive diagnostic methods is expected to improve patient survival and significantly reduce the costs for management of transplant patients.”
Dan Hauzenberger, MD., Ph.D., Karolinska University Hospital, Stockholm, Sweden
Webinar | February 16, 2023
Post-transplant monitoring: The future of chimerism testing.
Join our webinar featuring Dr. Helena Devos, MD, Clinical Biologist and Freidel Nollet, PhD, Molecular Biologist at AZ Sint-Jan in Bruges, Belgium. Where we will talk about the implementation of an NGS solution for chimerism testing and the clinical perspectives.Register now
News | January 25-26, 2023We are attending the Festival of Genomics & Biodata!
Podcast | December 6, 2022Collaborations and homebrew assays by Dan Hauzenberger & Turid Sundin Carlsson
News | November 10, 2022Devyser Diagnostics AB publishes Interim Report for the period, January to September 2022
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