Our research entails the development and application of data integration approach to improve the ability to diagnose, treat, and prevent complex diseases. Our primary focus lies in integrating multi-omics data and biological knowledge to better translate genomic and biomedical data derived from electronic health records (EHR) into clinical products. Our past projects have been both theoretical and applied, and they include developing data integration methods that combine multi-omics data and biological knowledge, predicting clinical outcomes based on interactions between multi-omic features, integrating multi-modal neuroimaging and multi-omics data, and identifying gene-by-environment (GxE) interactions in several phenotypes/diseases. We plan to continue our work in these areas, focusing primarily on providing actionable clinical products based on inter-plays within/between different dimensional genomic data. In particular, our long-term research goal is to develop and evaluate sophisticated data integration methods that simultaneously combine peoples’ individual variations in genomic (‘omic) data, imaging data, phenotype data from EHR, and environment/lifelog data for advancing precision medicine.
Lecture - Translational research, via data integration
Why Data Integration?
A central problem in translational research is that it’s difficult to understand the genetic architecture of a complex disease. Many genome-wide association studies (GWAS) exist—but most of the genetic loci that have been identified have negligible effects: Heritability, in many cases, isn’t found. That’s why we need alternative strategies to find underlying disease causes, said Assistant Professor of Informatics Dokyoon Kim, PhD—and a systems genomics approach, using data integration, can get the job done.
One Math Model to Explain Disease Phenotype
With the traditional approach, you can analyze a beautiful multi-omics data set, Dr. Kim continued—but you must handle the associations one pair at a time. So he asked himself: Can I integrate everything into one mathematical model to predict outcome or explain disease phenotype?