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Fastest DNA sequencing technique helps undiagnosed patients find answers in mere hours

A new ultra-rapid genome sequencing approach developed by Stanford Medicine scientists and their collaborators was used to diagnose rare genetic diseases in an average of eight hours -- a feat thats nearly unheard of in standard clinical care.
John Gorzynski Sneha Goenka Euan Ashley National Institute Of Science Stanford School Of Medicine Precision Health

Biontech, Instadeep Develop and Successfully Test Early Warning System to Detect Potential High-Risk SARS-CoV-2 Variants

BioNTech SE and Tunisian InstaDeep Ltd announced on Tuesday the development of a new computational method that analyses worldwide available sequencing data and predicts high-risk variants of... | January 12, 2022
Instadeep Karim Beguir Instadeep Deepchain Ugur Sahin Tunisian Instadeep Ltd World Health Organization News Service English

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