Expanding Genomic Cancer Research
to Arab Populations
to Arab Populations
Cancer genomics research has historically focused on White European populations, creating a significant data gap for Arab communities. This limits the effectiveness of genetic screening and preventive care for these populations.
Analyse genomic data from Saudi Arabian patients with familial cancers and their immediate family members
Identify population-specific variants in known cancer genes which may be pathogenic
Characterise familial cancer patterns
Improve screening protocols within University hospitals
Empower patients and healthcare providers by enabling proactive healthcare management
Population-specific variant identification
Statistical modelling of genetic distributions
Comparative analysis with existing databases
Risk assessment modelling
Developed population-specific analysis pipelines
Applied variant classification system and researched variants
Presented statistics and evidenced novel associations with familial cancers
Address reviewer comments on a related existing manuscript and apply statistical changes to increase robustness
Healthcare provider guidance
Publication of data to inform healthcare policy
Identified key variants associated with prostate, colorectal and breast cancer unique to Arab populations
Mapped novel genetic patterns
Published Research
Clinical Benefits
More accurate risk assessment
Improved preventive care options
Better informed clinical decisions
Enhanced family health planning
"UMBIZO was amazing to work with, very responsive and readily available for consultations. Their statistical abilities are top notch, as well as their technical expertise. The team was professional, courteous and provided quick feedback. They exceeded our expectations in expanding genetic research for Arab populations."
Dr. Malak Adbelgathari, Chair, Genomics Research Department,
Saudi Human Genome Lab
Initial Analysis: 2 weeks
Implementation and manuscript submission: 1 month
Clinical Integration: 3 months
We have continued to work with this team on a second study. We look forward to expanding analysis to additional cancer types and developing more comprehensive screening protocols for diverse populations.