| Literature DB >> 23631825 |
Frank S Ong1, Jimmy C Lin, Kingshuk Das, Daniel S Grosu, Jian-Bing Fan.
Abstract
The development of next-generation sequencing (NGS) technology has made DNA sequencing not only rapid and cost-effective, but also highly accurate and reproducible. The translational utility of genomic sequencing is clear, from understanding of human genetic variation and its association with disease risk and individual response to treatment, to the interpretation and translation of the data for clinical decision making. It will be a critical technology for disease characterization and monitoring in molecular pathology and is expected to become a central piece of routine healthcare management which will result in accurate and reliable reporting, a prerequisite for physicians to practice genomic medicine.Entities:
Keywords: Cancer genome sequencing; Clinical sequencing; NGS; NIPT; Next-generation sequencing; Non-invasive diagnosis
Mesh:
Year: 2013 PMID: 23631825 DOI: 10.1016/j.ygeno.2013.04.012
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736