- Products
- Reproduction
- Molecular diagnostics
- Careers
- About us
- Contacts
NGS panel for clinical exome sequencing, which enables the detection of SNV, InDel and CNV variants in 5500 genes using hybrid capture technology.
NGS panel for whole exome sequencing, which enables the detection of SNV, InDel and CNV variants in 19 425 genes using hybrid capture technology.