Using whole-genome sequencing, a forward-looking organization is helping diagnose rare genetic diseases faster for more patients
Dr. Ranjana Bhattacharjee is using whole-genome sequencing to understand the crop’s evolution and generate improved varieties
A Brazilian sequencing program for EB patients brings access to more accurate diagnoses and better treatment
How genomics provided critical answers—and in record time—to transform outcomes for a newborn and his family
An Illumina iConserve project is mapping genetic diversity to identify where confiscated gorillas come from and boost survival rates
| 日付 | 論文 | タイトル |
|---|---|---|
| 2021/02/25 | Kaiser Health News | Have a Case of a Covid Variant? No One Is Going to Tell You |
| 2021/02/25 | BioPharma Reporter | German program using whole genome sequencing to diagnose rare diseases and cancer risk |
| 2021/02/17 | Cambridge Independent | Illumina Accelerator Cambridge announces four chosen genomics start-ups and £20m match-funding pledge |
| 2021/02/17 | Bloomberg Technology | Illumina's deSouza on Tech Growth and Need for a Bio Force |
| 2021/02/17 | Associated Press | Government rushes virus gene-mapping as mutations spread |
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