Thesis Abstract

Abstract
This thesis explores the "Application of Next-Generation Sequencing (NGS) in the Diagnosis and Management of Genetic Disorders in Clinical Laboratory Settings." Next-Generation Sequencing has revolutionized genetic testing by enabling rapid, cost-effective, and high-throughput analysis of DNA sequences. This research aims to investigate the utility of NGS in diagnosing and managing genetic disorders within clinical laboratory settings. The introduction provides a comprehensive overview of the background of the study, highlighting the importance of genetic testing in precision medicine and the challenges associated with traditional diagnostic methods. The problem statement underscores the limitations of conventional genetic testing techniques and the need for more efficient and accurate approaches. The objectives of the study are to evaluate the effectiveness of NGS in diagnosing a wide range of genetic disorders, assess the impact of NGS on patient outcomes and treatment decisions, and explore the challenges and limitations of implementing NGS in clinical laboratories. The scope of the study focuses on the application of NGS in clinical settings, including its potential benefits and challenges. The literature review delves into ten key areas, including the principles of NGS technology, its applications in genetic testing, the impact of NGS on clinical practice, and the challenges associated with implementing NGS in laboratory settings. The research methodology section outlines the study design, sample selection criteria, data collection methods, and data analysis techniques employed in this research. The discussion of findings chapter presents a detailed analysis of the results obtained from the study, highlighting the diagnostic accuracy, turnaround time, and cost-effectiveness of NGS compared to traditional genetic testing methods. The chapter also discusses the challenges faced during the implementation of NGS in clinical laboratories and proposes recommendations for overcoming these obstacles. In conclusion, this thesis underscores the significance of NGS in transforming genetic testing practices and improving patient care in clinical laboratory settings. The findings of this study contribute to the growing body of evidence supporting the widespread adoption of NGS in the diagnosis and management of genetic disorders. This research provides valuable insights into the potential benefits and challenges of integrating NGS into routine clinical practice, paving the way for more personalized and precise healthcare interventions.

Thesis Overview