Whole Genome Sequencing (WGS) is a diagnostic tool that comprehensively maps an individual's entire genetic makeup, offering unparalleled insights into genetic predispositions, potential inherited conditions, and personalized medicine opportunities. By examining the complete DNA sequence, WGS can identify genetic variations and mutations that may impact health, enabling early detection, targeted treatment plans, and informed family planning decisions. This powerful technology represents a significant step forward in personalized healthcare, empowering individuals and healthcare professionals with detailed genetic information to make informed health and lifestyle choices.