Data in non-small-cell lung cancer, presented at ASCO 2023, shows single-gene tests deplete biopsy material, reducing CGP's efficacy
In Indonesia, a former patient turns his efforts toward helping others beat the second-leading infectious disease killer worldwide
The Silent Genomes Project is building a first-of-its-kind variant library for First Nations, Inuit, and Métis populations
全ゲノムシーケンスを使用して、将来を見据えた組織が、より多くの患者の希少な遺伝性疾患の迅速な診断を支援しています
Two DRAGENs help Cardio-CARE slay one petabyte of data to better understand heart disease in Hamburg
| 日付 | 論文 | タイトル |
|---|---|---|
| 2023/07/26 | Medical Device Network | Illumina and Pillar collaborate to commercialise oncology assays |
| 2023/07/20 | Biocompare | Selecting the Right NGS Method |
| 2023/07/19 | Genetic Engineering and Biotechnology News | Alliance for Genomic Discovery Announces Five Founding Biopharma Members |
| 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 |
イルミナでは、限界に挑んでいます。従来の枠を超えて考えます。私たちは大きな夢を抱いています。非常に多くの明るく熟練した人々のエネルギーにより、機会は無限に広がります。
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