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NGS panels for detection of germline mutations (SNV, InDel) for diagnosis of various hereditary diseases, preconception testing and PGT.
Library preparation from buccal swabs is based on hybridization capture technology. The solution includes Sirius Genetic Data Management, which can be used for sequencing run planning or maximizing cartridge capacity utilization.
The kit is validated for Illumina NGS sequencers.
Varsome Clinical can be used for data evaluation.
The kits are CE-IVD certified.
| TarCET PGT Kit | 23 chromosomal pairs |
| TarCET Metabolic Kit | 223 genes |
| TarCET Hereditary Cancer Kit | 62 genes |
| TarCET Carrier Screening Core Kit | 19 genes |
| TarCET Carrier Screening Comprehensive Kit | 228 genes |
| TarCET Neonatal Kit | 140 genes |
| TarCET Aortopathy Kit | 48 genes |
| TarCET Arrhythmia Kit | 42 genes |
| TarCET Cardiomyopathy Kit | 98 genes |
| TarCET Congenital Heart Defects Kit | 80 genes |
| TarCET FH, PH and RAS Kit | 11, 11 a 30 genes |
| TarCET Cardiac Comprehensive Kit | 292 genes |
| TarCET Infertility Kit | Female 54 genes, Male 39 genes |
For more information, please contact us by e-mail: diagnostika@pentagen.cz