Reduce hands-on time from days to minutes with Devyser’s CE-IVD single tube, next-generation sequencing (NGS) library prep kit for fast and complete characterisation of BRCA1 and BRCA2.

Discover the advantages of Devyser’s NGS workflow

•   Detect all mutations in BRCA1 and BRCA2
•   One tube per sample means no need for sample splitting
•   Reduce hands-on time from days to under 45 minutes
• One kit for both germline and somatic mutations
• Choice of several validated software options, including CNV analysis

NGS has never been easier

The Devyser BRCA kit is easy to implement and highly cost-effective, making it a good match for laboratories of any size. With ready-to-use reagents and a user-friendly workflow, it suites both manual and automated workflows. Devyser’s unique single-tube approach simplifies the workflow, reduces hands-on time and minimizes the risk of sample mix-up and contamination.

Watch full video to see how it is done

Whitepaper

NGS: Full Gene Sequencing of BRCA1 and BRCA2

With the increasing use of NGS, the number of detected variants in BRCA1 and BRCA2 are increasing fast. As a consequence, the absolute numbers of Variants of Uncertain Significance (VUS) are also increasing. This paper describes current initiatives to classify and interpret VUS in BRCA1 and BRCA2, and how laboratories can contribute to these efforts and ultimately improve the counseling of tested patients.