INSTITUTE
OF GENETICS & CYTOLOGY

Whole exome sequencing allows examining all exomes, i.e. all exome regions of the human genome. The exome makes up only about 1-2% of the total genome, but contains most of the protein-encoding genes that play an important role in the functioning of our body. This means that using whole exome sequencing, you will receive information about key genes associated with hereditary or acquired diseases.

One of the main advantages of whole exome sequencing is its ability to detect rare and novel gene variants that may be associated with specific diseases. This allows you to gain a deep understanding of the genetic basis for various conditions and helps doctors make accurate diagnoses, predict disease progression and choose the most effective therapy.