Use

Genomic Unity® Whole Genome Analysis is a comprehensive diagnostic test designed to identify genetic variants correlating with a patient's phenotype. It uses a whole genome sequencing platform to detect major clinically relevant variant types from a single sample. The analysis is performed jointly with parental DNA if family samples are included, providing a unified clinical report that can replace multiple traditional tests, making it suitable when symptoms suggest multiple genetic issues, specific diagnostic tests are unavailable, or prior tests were nondiagnostic.