Since the human genome was first sequenced, life sciences researchers have sought to use this information to improve health. But they soon discovered that DNA sequence data alone has limited value when trying to understand the effects of genetic variation on health.
Today, researchers are increasingly linking genomic data to rich, longitudinal clinical information — a practice that yields clinicogenomics data. The field of clinicogenomics is unlocking novel insights to better understand diseases and to guide drug discovery, development and commercialization.
The study of clinicogenomics across large, diverse populations can help researchers:
- Better understand disease pathways
- Discover novel therapeutic targets
- Identify variation in disease onset and progression
- Evaluate drug safety and efficacy
Our latest white paper details the foundations of genomics-driven research and the sources of clinicogenomics data. It also highlights the ways clinicogenomics data can enhance clinical trials and fuel discovery and development of safer, more effective drugs.