Targeted Sequencing Approach and Its Clinical Applications for the Molecular Diagnosis of Human Diseases

卷:12

Review

关键词: POLYCYSTIC KIDNEY-DISEASE;    CELL-FREE DNA;    BACTERIAL IDENTIFICATION;    INTELLECTUAL DISABILITY;    GENE;    GENOME;    CANCER;    RARE;    MICROBIOLOGY;    VALIDATION;   

DOI  :  10.3390/cells12030493

来源: SCIE

【 摘 要 】

The outbreak of COVID-19 has positively impacted the NGS market recently. Targeted sequencing (TS) has become an important routine technique in both clinical and research settings, with advantages including high confidence and accuracy, a reasonable turnaround time, relatively low cost, and fewer data burdens with the level of bioinformatics or computational demand. Since there are no clear consensus guidelines on the wide range of next-generation sequencing (NGS) platforms and techniques, there is a vital need for researchers and clinicians to develop efficient approaches, especially for the molecular diagnosis of diseases in the emergency of the disease and the global pandemic outbreak of COVID-19. In this review, we aim to summarize different methods of TS, demonstrate parameters for TS assay designs, illustrate different TS panels, discuss their limitations, and present the challenges of TS concerning their clinical application for the molecular diagnosis of human diseases.