Next generation sequencing to promote the diagnosis and treatment of rare genetic diseases
10.3760/cma.j.issn.1009-9158.2017.07.002
- VernacularTitle:下一代测序技术促进罕见遗传病的诊治和咨询
- Author:
Yiping SHEN
;
Jian WANG
- Keywords:
Genetic Diseases;
inborn;
High-throughput nucleotide sequencing;
Genetic counseling
- From:
Chinese Journal of Laboratory Medicine
2017;40(7):486-488
- CountryChina
- Language:Chinese
-
Abstract:
Next generation sequencing (NGS) based test provided us an unprecedented power for the molecular diagnosis of rare diseases with genetic etiology, thus enabling the practice of precision medicine.In order to maximize the clinical utilities of NGS-based test, attention should be paid to the improvement of the sequencing technology, data quality and the accuracy of data interpretation, as well as the clinical correlations and pre-and post-test genetic counseling services.In doing so, it is believed practice of NGS-based test can bring expected benefit to many patients and families.
