Genomic Diagnostics

Genomic diagnostics involve analyzing a person’s DNA—their genetic blueprint—to identify variations that might cause or influence health conditions. By examining specific genes, scientists can detect genetic mutations linked to diseases, helping doctors make accurate diagnoses, determine the best treatments, or assess health risks. This approach provides detailed insights into an individual’s genetic makeup, enabling personalized medicine and proactive healthcare strategies. Essentially, genomic diagnostics translate complex genetic information into useful knowledge for managing and understanding health.