Clinical Genomics

Clinical genomics is the study of a person's genes and their relationship to health and disease. It involves analyzing DNA to identify genetic mutations that may cause or increase the risk of certain conditions. This information helps healthcare providers tailor treatments and prevention strategies for individuals based on their genetic makeup. By understanding a patient’s unique genetic profile, clinicians can make more informed decisions, leading to personalized medicine that aims to improve outcomes and reduce the trial-and-error approach often associated with traditional treatments. In essence, clinical genomics bridges genetics and medical care for better health management.