当前位置: X-MOL 学术ACS Pharmacol. Transl. Sci. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Data Sharing Advances Rare and Neglected Disease Clinical Research and Treatments.
ACS Pharmacology & Translational Science Pub Date : 2019-08-22 , DOI: 10.1021/acsptsci.9b00034
Rachelle J Bienstock 1
Affiliation  

Because of the decreased cost and increased ease of whole genome analysis, the diagnosis of rare, orphan diseases has entered a new era. This new technological advance, combined with the worldwide web connections, now permits sharing, searching, and linking genotype, phenotype, and other information to facilitate diagnosis. Databases currently accessible and searchable by researchers, clinicians, and patients will be presented and discussed.

中文翻译:

数据共享促进了罕见病和被忽视疾病的临床研究和治疗。

由于降低了成本并提高了全基因组分析的简便性,罕见的孤儿疾病的诊断进入了一个新时代。这项新技术进步与全球网络连接相结合,现在允许共享,搜索和链接基因型,表型和其他信息,以方便诊断。将介绍和讨论研究人员,临床医生和患者当前可访问和搜索的数据库。
更新日期:2019-08-22
down
wechat
bug