whitepaper

Easily identify BRCA1 and BRCA2 genetic mutations

With cancer identified as the leading cause of death in high-income countries, early identification and treatment of cancer, and potential cancer-causing genetic variants, is essential. As the second most common cancer worldwide, and the most frequently diagnosed cancer among women, breast cancer nonetheless has a high survival rate if diagnosed and treated. Read more about …

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New Whitepaper: Familial Hypercholesterolemia

Devyser is pleased to announce the publication of a new whitepaper Familial Hypercholesterolemia: Genetic Diagnosis and Cascade Testing Using NGS. The 6th in our Expert Review series, this paper is co-authored by Peter Benedek and Kristina Duvefelt, of Karolinska University  Hospital, Stockholm. The paper is a guide to conducting testing using NGS, and the benefits of …

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