Thesis Abstract

Abstract
Next-Generation Sequencing (NGS) has revolutionized the field of medical genetics by enabling rapid, accurate, and cost-effective sequencing of entire genomes. This thesis explores the implementation of NGS in the diagnosis of genetic disorders, with a focus on its potential to transform clinical practice and improve patient outcomes. The study begins with an introduction to the background and significance of NGS technology in medical laboratory science. It also addresses the problem statement of traditional genetic testing methods, highlighting the limitations and challenges faced in diagnosing genetic disorders. The objectives of this study are to evaluate the effectiveness of NGS in clinical settings, identify the scope of its application, and understand the significance of integrating NGS into routine diagnostic workflows. Chapter One provides an overview of the research context, outlining the structure of the thesis and defining key terms related to genetic sequencing technologies. Chapter Two comprises a comprehensive literature review that examines current research, methodologies, and applications of NGS in genetic disorder diagnosis. The review covers ten key aspects, including the evolution of NGS technologies, bioinformatics tools, data analysis pipelines, and challenges in variant interpretation. Chapter Three details the research methodology employed in this study, presenting eight components such as study design, sample collection, sequencing protocols, data analysis methods, and quality control measures. The chapter describes the process of implementing NGS in a clinical laboratory setting, highlighting the steps involved in sample preparation, library construction, sequencing, and data interpretation. Chapter Four presents the findings of the study, discussing the diagnostic accuracy, efficiency, and clinical utility of NGS in identifying genetic variants associated with different disorders. The chapter analyzes case studies and real-world examples to demonstrate the practical application of NGS in diagnosing genetic conditions, illustrating its potential to enhance personalized medicine and genetic counseling. In conclusion, Chapter Five summarizes the key findings of the study and provides insights into the implications of integrating NGS into routine clinical practice for the diagnosis of genetic disorders. The thesis concludes with recommendations for future research directions, policy implications, and considerations for the widespread adoption of NGS technology in medical laboratory science. In summary, this thesis explores the implementation of Next-Generation Sequencing in the diagnosis of genetic disorders, highlighting its potential to revolutionize clinical genomics and improve patient care outcomes. By leveraging the power of NGS technology, healthcare practitioners can enhance diagnostic accuracy, facilitate personalized treatment strategies, and advance our understanding of genetic diseases.

Thesis Overview