Human Genomics
Our scientists combine advanced genomic and informatics technologies to understand the genetic causes and mechanisms of human disease.
Overview
Deciphering the human genome is enabling scientists to gain new insights into the drivers of health and disease.
We use the latest genomic tools coupled with machine learning to advance personalized interventions based on the unique health characteristics of individuals.
Genome sequencing has revolutionized our ability to predict disease risk, empowering patients with actionable information that can help them better manage their health.
Machine and deep learning prediction of disease risk
We develop artificial intelligence models that improve the rates of disease prediction and detection with the goal of advancing personalized interventions tailored to individual patients.
Genetic risk scores
The app-based MyGeneRank research program sought to understand how your genetic risk influences health decisions. Findings from the initial analysis, focusing on coronary artery disease, indicate increased statin initiation among high genetic risk individuals.
Healthy aging
The Wellderly study investigated the genetic secrets behind lifelong health. By analyzing genomic data from 1,400 people between the ages of 80 and 105 who have not developed any common chronic medical conditions or disease, researchers found a link between genes that protect against cognitive decline and healthy aging.
The Genomic Revolution: Using DNA to predict disease risk and individualize treatment
Your DNA contains an incredible amount of information about every aspect of your being, including your risk of developing certain diseases. But up until recently, it was nearly impossible for doctors to analyze that information for individual patients. Now, with the help of affordable genomic sequencing, artificial intelligence and machine learning, scientists are working towards personalizing medical care.
