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NGS panel for detection of germline mutations (SNV, InDel) for diagnosis of various hereditary cancer syndromes, which includes 62 genes.
Library preparation from buccal swabs or blood 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.
VEGA bioinformatics software can be used for data evaluation.
List of included genes:
APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, DDB2, DICER1, EPCAM, ERCC1, ERCC2, ERCC3, ERCC4, ERCC5, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FANCM, GREM1, HOXB13, MEN1, MLH1, MRE11, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, POLD1, POLE, POLH, PTEN, RAD50, RAD51C, RAD51D, RB1, RET, SDHAF2, SDHB, SDHC, SDHD, SLX4, SMAD4, SMARCA4, STK11, TP53, VHL, XPA, XPC
NEW! Medicover Genetics has obtained their certification under the new In Vitro Diagnostic Regulation (IVDR; 2017/746) for all NGS reagents incl. TarCET IVD kits:
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