Devyser HBOC NGS

Product code: 8-A111

Producer: Devyser AB

Detection of germline mutations in 12 genes associated with breast and ovarian tumor syndromes by amplicon sequencing.

More detailed product information

A simple and rapid diagnostic test for the detection of SNV, InDel and CNV germline mutations in 12 genes associated with breast and ovarian cancer. Preparation of a single patient library in a single PCR reaction.

Results can be evaluated using AmpliconSuite (SmartSeq), SexNext (JSI), Sophia DDM (Sophia Genetics).

The kit is validated for Illumina NGS sequencers and is CE IVD certified.

List of genes involved: ATM, BARD1, BRIP1, CDH1, CHEK2, NBN, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53

A simple online tool can be used to make the most of the cartridge capacity: https://calculator.devyser.com/

For more information, please contact us by e-mail: diagnostika@pentagen.cz