Clinical exome sequencing is a genetic test optimized to simultaneously sequence 4813 clinically relevant genes. This genetic test is based on the next generation sequencing approach and has superior diagnostic performance in comparison to Sanger sequencing. Therefore, the method is especially suitable for diagnostics of rare inherited diseases.

Clinical exome sequencing could be applied to:

  • Analyze several genes at the same time
  • Analyze a large gene (with large number of exons)
  • Urgently analyze any clinically relevant gene

It is necessary to deliver 2.5 ml of peripheral blood using 3.8% sodium citrate as anticoagulant. It is possible to deliver a blood sample that has already been frozen. The samples are accepted every day from 10 to 13h. There is possibility to deliver the sample via post express service. The patient’s referral diagnosis is needed for accurate interpretation of the obtained results. The analysis is performed within 40 working days. The results and the bill are sent to the patient's home address, or can be collected personally at the Institute from 10 to 16h every day.

For payment instructions, please contact us.



dr Maja Stojiljković

dr Sonja Pavlović

Tel: +381 11 3976 445

Mob: +381 65 3976 445

Fax: +381 11 3975 808


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