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Full DNA sequencing

Interpretation of the results by bioinformatics and medical geneticist. The patient's DNA is compared with databases of known mutations

The results of the whole genome sequencing study provide information broken down into the following sections:

Carrying genetic diseases

is important for determining the risk in offspring, since in a “healthy person” carriage of latent mutations can be detected that can manifest themselves in offspring.

Hereditary tumor syndromes and the risks of cancer

is vital for determining a hereditary predisposition to cancer which, when the carriage of a pathogenic polymorphism is detected, makes it possible to develop an individual plan with screening tests to detect the disease early and effectively treat it, as well as to put together recommendations to decrease the risk that the disease will develop further

Multifactorial diseases

  • cardiovascular diseases
  • endocrine system diseases
  • central nervous system diseases
  • respiratory system diseases
  • musculoskeletal system diseases
  • visual organ diseases
  • urogenital system diseases
  • digestive tract diseases
  • skin diseases

Population genetics

analyzes the subject’s origin, where his or her ancestors came from (determining haplogroups). The results are shown on a map of how the haplogroup spread around the world, with the frequency, it is encountered.


is dedicated to individual sensitivity to medicinal products.


helps determine individual recommendations in terms of diet.

Beauty and Genetics in Fitness

gives recommendations on how to take care of the skin and choose the most effective workout regimen.