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Comprehensive genetic screening that analyzes more than 10,000 genetic variants in 164 genes and covers more than 170 hereditary diseases
Designed for individuals or couples planning a pregnancy who want to know their genetic risks and reduce the likelihood of passing on hereditary diseases to their child; for people who have experienced a miscarriage; people who want to confirm the results of high-risk prenatal screening.
Method: Next Generation Sequencing (NGS) – highly accurate analysis of DNA from peripheral blood.
Options: Mini Panel (11 diseases) Targeted Panel 2.0 (172 diseases)
Rozšírený Panel : 1200+ (viac ako 1200 ochorení)
99%
precision
99%
precision
Designed for individuals or couples planning a pregnancy who want to know their genetic risks and reduce the likelihood of passing hereditary diseases to their child; for people who have experienced a miscarriage; people who want to confirm the results of high-risk prenatal screening.
Method: Next Generation Sequencing (NGS) – high-precision DNA analysis from peripheral blood.
Options: Mini Panel (11 diseases) Targeted Panel 2.0 (172 diseases)
Extended Panel: 1200+ (more than 1200 diseases)
Nova
- Comprehensive newborn genetic screening aimed at identifying the risk of 50 hereditary disorders in newborns.
- The test is suitable for newborns and designed for early detection of genetic predispositions that may affect the child's health, while also providing personalized genetic information for further health decision-making.
- Method: Genetic analysis using sequencing and specific gene panels according to the range of disorders tested.
