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Devyser BRCA NGS is a fast and robust NGS solution designed for the detection of genetic variants in the BRCA1 and BRCA2 genes. It offers comprehensive and uniform coverage of all coding exons and exon/intron junctions of both genes. In addition, it includes the detection of single nucleotide variants (SNVs), insertions/deletions (Indels), and copy number variations (CNVs), in both germline and somatic contexts.

Key Features

Comprehensive variant detection: Identifies relevant genetic variants in the BRCA1 and BRCA2 genes.
Fast workflow: optimized for rapid results with same-day library preparation and less than 45 minutes of hands-on time.
Identification of germline and somatic variants, including CNV detection.
Dedicated software: Provides automated, user-friendly analysis, with options for batch export and efficient variant analysis without the need for bioinformatics expertise.
Devyser BRCA NGS

Clinical Applications

It is intended for the comprehensive screening and characterization of BRCA1 and BRCA2, including SNV and CNV detection.

Intended Audience / User

Ideal for laboratories focused on the comprehensive screening and characterization of the BRCA1 and BRCA2 genes, including the detection of both SNVs and CNVs.

Benefits

Streamlined workflow: easy to implement and suitable for laboratories with varying sample volume needs. Ready-to-use reagents, ensuring a reproducible process and reducing the risk of sample mix-ups or contamination. Intuitive software: facilitates the interpretation of obtained data, reducing the need for bioinformatics intervention.

Technical Specifications

Starting material: Human genomic DNA extracted from whole blood or FFPE tissue.

Ordering Information

CE-IVD Kits
8-A100-8 8 tests
8-A100-24 24 tests
8-A100-96 96 tests
Accessories
8-A204 Devyser Library Clean
8-A200 Devyser Index Plate A

Other references: RUO version with references 8-A102-8, 8-A102-24, and 8-A102-96.

Area:

Digestive System, Hereditary cancer, Molecular Genetics, Reproductive System, Skin, Solid tumor, Targeted study of specific pathologies

Brand:

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