Provides guidance on genetic risks, testing options, and inherited conditions to individuals and families.

Studies genes, inheritance, and molecular mechanisms to understand traits, diseases, and biological variation.

Analyses genomic datasets to identify variants, biological patterns, and disease-associated signals.

Investigates genomes and large-scale genetic data to understand biological function, disease mechanisms, and population variation.

Performs molecular tests to detect genetic mutations, pathogens, and biomarkers for clinical diagnosis and patient care.