Bridging the diagnosis gap for Canada’s Indigenous children
The Silent Genomes Project is building a first-of-its-kind variant library for First Nations, Inuit, and Métis populations
The Silent Genomes Project is building a first-of-its-kind variant library for First Nations, Inuit, and Métis populations
The Welsh government launches a program aimed at accelerating diagnosis and improving clinical outcomes
At ESHG 2023, researchers, clinicians, and industry leaders gathered to discuss the practice of genomics
With limited space in the curricula for genomics, residents and physicians are turning to other sources for training
Taiwanese study shows 500-gene panel detects actionable mutations and other critical biomarkers to open doors to advanced treatments
Date | Publication | Title |
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Jun 12, 2023 | GenomeWeb | ESHG: German Study Shows Utility of Rapid Whole-Genome Trio Sequencing in Critically Ill Children |
Jun 3, 2023 | Fierce Biotech | ASCO: Illumina's oncology exec on the need to 'democratize genomic profiling in cancer' |
Jun 1, 2023 | Science | Hundreds of new primate genomes offer window into human health—and our past |
Jun 1, 2023 | The Washington Post | New AI tool searches genetic haystacks to find disease-causing variants |
May 12, 2023 | CNBC | Leaders Speak: Illumina Asia-Pac medical head on the expanded scope of precision medicine in AI era |
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