Application of Next Generation Sequencing in Molecular Diagnosis and a Tentative Analysis on its Standardization Management
The next generation sequencing (NGS) brings technological revolution to clinical molecular diagnosis (CMD) thanks to its low cost, high efficiency and high throughput. This paper comprehensively introduces the advantages of NGS in non-invasive prenatal testing, hereditary diseases diagnosis, early warning and prevention for cancer, then concludes and analyzes the problems that may handicap the development of CMD, finally propose some practical solutions for those issues from the perspective standardization.