AIM 01Develop methods that predict disease risks for individuals with rare monogenic risk alleles.
AIM 02Integrate genetic and non-genetic factors for more accurate risk assessments.
AIM 03Analyze multi-omics data to uncover insights about disease biology.
AIM 04Leverage deep learning to improve the clinical utility of genetic information.
AIM 05Refine the accuracy of genetic diagnostics in predicting disease outcomes.