最新特色文章
Illuminating Rare Disease
Bringing to light the challenges and hopes for the rare disease community
特色文章
Shriners医院启动大型测序项目
基因组学杰出人物Marc Lalande博士和Kamran Shazand博士利用Trusight软件套装建立了基因组学研究所，这个美国的标志性医疗系统将推动从墨西哥城到蒙特利尔等更多地区的研究和个性化医疗。
访谈：Illumina最多产的女性发明家Jenn Foley
聊一聊检测历程、毅力及如何克服失败
COVID监测先驱：犹他州公共卫生实验室
在模范公共卫生实验室中为基因组测序铺平道路
视频： 推动癌症治疗选择的全球发展
日本和比利时的研究试图推进肿瘤精准医疗
新闻发布
In the News
| 日期 | 发表 | 标题 |
|---|---|---|
| 2021-2-25 | Kaiser Health News | Have a Case of a Covid Variant? No One Is Going to Tell You |
| 2021-2-25 | BioPharma Reporter | German program using whole genome sequencing to diagnose rare diseases and cancer risk |
| 2021-2-17 | Cambridge Independent | Illumina Accelerator Cambridge announces four chosen genomics start-ups and £20m match-funding pledge |
| 2021-2-17 | Associated Press | Government rushes virus gene-mapping as mutations spread |
| 2021-2-17 | Bloomberg Technology | Illumina's deSouza on Tech Growth and Need for a Bio Force |
