Genomics Medicine Centre

Integrating precision diagnostics, clinical genomics, bioinformatics, and advanced multi-omics technologies to enhance patient care. Our multidisciplinary teams combine deep clinical expertise with state-of-the-art laboratory platforms to diagnose rare diseases, guide personalized treatments, and support national genomic healthcare initiatives.

The Bioinformatics Department uses advanced computational analysis, AI-powered tools, and high-performance data systems to interpret complex genomic and clinical information. The team supports critical areas like rare disease diagnosis, cancer genomics, and transplant medicine, while ensuring genomic data flows seamlessly into hospital systems. Beyond clinical support, the department drives digital automation across the hospital and trains healthcare professionals nationwide in scientific computing and bioinformatics.

The Translational Genomics Department turns cutting-edge research into real treatments for patients. The team takes discoveries from the lab—advanced sequencing techniques, biomarker research, and multi-omics data—and transforms them into practical diagnostic tools and therapies. Through close collaboration with researchers and clinicians, the department supports clinical trials, advances precision medicine, and brings next-generation genomic technologies directly to patient care.

Specialized care for inherited and metabolic disorders starts with comprehensive clinical evaluation, genetic counseling, and advanced genomic testing. The department's programs—prenatal genomics, cardiovascular genetics, expanded carrier screening, metabolic genetics, and virtual clinics—enable early detection, precision prevention, and personalized treatment plans that improve long-term outcomes for patients and their families.