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Roche and Broad Labs team up to use advanced genome sequencing to speed up diagnoses for sick newborns.
Roche and Broad Clinical Labs are collaborating to integrate Roche's fast and scalable SBX sequencing technology into clinical care, starting with whole genome sequencing for critically ill newborns and their parents.
This could lead to quicker, more precise diagnoses and better outcomes for genetic disorders.
The partnership also aims to explore RNA sequencing for deeper disease understanding and new treatments.
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Roche y Broad Labs se unen para usar secuenciación avanzada del genoma para acelerar los diagnósticos de recién nacidos enfermos.