Whole   genome      sequencing         (WGS)       is   a comprehensive      technique     that   analyzes     an individual's entire genome, including   both    coding and non-coding regions of    DNA.    Unlike     whole exome   sequencing,      which         only        targets  protein-coding    regions, WGS provides a complete view of the genetic blueprint.    This   method     can identify genetic mutations, structural  variants,   and other changes that may contribute to  diseases     or traits. WGS is particularly useful  for   understanding complex genetic conditions and uncovering  rare  or previously     unknown    mutations.       It    involves  high-throughput    sequencing    technologies    that generate vast amounts of data for analysis.   WGS is increasingly used in personalized medicine, genetic counseling, and research into  genetic      disorders. The information from WGS  can    guide    treatment plans,    risk    assessments,   and   family   planning decisions.