Abstract

Next-Generation Sequencing (NGS) has revolutionized the landscape of genetic research, enabling high p h throughput, cost-effective, and accurate sequencing of entire genomes. NGS technologies allow for the rapid analysis of DNA, providing unprecedented insights into the genetic makeup of organisms, from humans to microbes. This transformation has accelerated advancements in fields such as personalized medicine, disease diagnostics, evolutionary biology, and genetic disorders. By offering the ability to sequence large quantities of genetic material in a fraction of the time and cost of traditional methods, NGS is enabling researchers and clinicians to uncover genetic variants that influence health, development, and disease. With its vast potential, NGS is poised to redefine future genetic research and improve clinical outcomes by enabling more precise, tailored treatments and preventive measures.