Using whole-genome sequencing, a forward-looking organization is helping diagnose rare genetic diseases faster for more patients
記事を読む日付 | 論文 | タイトル |
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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 |