EasySeq™ BRCA1/2 + CHEK2 HS is specifically developed to assist in the identification of genetic mutations associated with an increased risk of breast cancer.


The purpose of the RC-PCR driven NGS library preparation is to sequence again the coding exons of the human BRCA1 and BRCA2 genes. This includes a minimum of 20 bases before and after each exon. The test additionally incorporates the CHEK2 1100del C mutation (NM_001005735) hotspot.


Intended for research purposes exclusively. Not intended for utilisation in diagnostic procedures.