NEXT-GENERATION SEQUENCING IN CLINICAL PRACTICE: IMPLICATIONS FOR DISEASE DIAGNOSIS AND MANAGEMENT

The main aim of this research is to identify the impact of next-generation sequencing in clinical practice for disease diagnosis and management. This process also has the capability to identify the response of individuals to using the drugs. Moreover, this information has the potential to optimize drug selection and dosages. Literature Review: Accuracy of the diagnosis has to be fostered by this process. Moreover, with the aid of this process, genetic disorders become identified and diagnosed. Trust of the patients in the treatment process becomes fostered, and it helps to develop the diagnosis process. The personalized medicine process becomes facilitated by this process. Methodology: This research study is based on the “theoretical analysis”, therefore, researchers are capable of collecting data from different online sources. This data collection process helps to get a deep conceptual understanding. After that, better knowledge about this study has to be collected with the aid of this data collection process Findings: Next-generation sequencing allows for the sequencing of the entire genome of an individual. Therefore, this has revolutionized precision medicine for personalized treatment. Better disease diagnosis, as well as genetic profile of patients is detected carefully with the aid of this process. Moreover, rare genetic diseases are also identified critically with the aid of this NGS process. Discussion: Overall knowledge about this study has to be identified by this study. This study helps to understand that, “Next-generation sequencing has a significant impact on clinical practices. Therefore, it has a remarkable impact on disease diagnosis and management Conclusion:  Genetic mutation is an important factor that has to be facilitated by this process. Moreover, different types of heredity disease and infectious diseases are detected carefully with the aid of this advanced disease diagnosis proces