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INSTITUTE OF MOLECULAR GENETICS
AND GENETIC ENGINEERING
University of Belgrade

Our Clinical Genomics Center is an expert center in molecular medicine for rare diseases and tumors, advancing personalized medicine through pharmacogenomic testing. Since 2021, the Republic Health Insurance Fund of Serbia (RFZO) has been supporting genetic testing for patients with suspected rare diseases through advanced diagnostic methods, including whole-exome sequencing. This approach enables the simultaneous analysis of 4,813 clinically relevant genes (CES) or entire set of human genes (around 20,000 genes) (WES), providing comprehensive genetic insights and more accurate diagnoses.

What We Offer

Molecular Diagnostics

Next-Generation Sequencing (NGS):

  • Clinical exome (CES)
  • Whole exome (WES)
  • Mitochondrial DNA (mtDNA)

Bioinformatics

  • Internal protocols (pipelines) for variant identification and annotation
  • Detection of mitochondrial variants
  • Machine learning models for data interpretation and predictive analysis

Innovation

  • Designing panels for pharmacogenomic testing

Science and Collaboration

  • Projects with global pharmaceutical companies
  • EU-funded projects
  • PhD theses in the field of molecular medicine
  • Physicians

Training

Organization of lectures and workshops for:

  • Physicians
  • Geneticists
  • Patient associations
  • Other interested stakeholders

Our Infrastructure

Why Partner With Us?

Connect with our Clinical Genomics Center to access cutting-edge NGS diagnostics, innovative pharmacogenomic platforms, and machine learning-driven insights for personalized medicine. We offer precise testing for rare diseases and tumors, foster collaborative research, and provide tailored educational training for stakeholders.

Contact our experts to explore collaboration opportunities:

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Head office / Mailing address: Vojvode Stepe 444a, 11042 Belgrade 152, Serbia / Web System By Emarket1ng.NET