Next generation sequencing (NGS) allows you to read the entire genome sequence or certain sections of it.

NGS- tests are essential for:

• diagnosis of hereditary pathologies, especially in cases of hard-to-diagnose and heterogeneous diseases to confirm the diagnosis;
• clarification of genetic risks;
• detection of latent mutations when planning a pregnancy (to clarify the risk of having a diseased child), etc.

 We provide DNA and RNA sequencing services with the NGS technology including processing the research results:

• whole exome sequencing;
• targeted sequencing.