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A simple and rapid diagnostic test for the detection of germline and somatic SNV, InDel and CNV mutations in the BRCA1, BRCA2 and PALB2 genes. Preparation of a single patient library in a single PCR reaction.
Results can be evaluated using AmpliconSuite (SmartSeq), SexNext (JSI).
The kit is validated for Illumina NGS sequencers.
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