利用先进的基因组测序来加速诊断新生儿病人的病情。 Roche and Broad Labs team up to use advanced genome sequencing to speed up diagnoses for sick newborns.

Roche和大临床实验室正在合作,将Roche的快速和可扩展的SBX测序技术纳入临床护理,从重病新生儿及其父母的整个基因组测序开始。 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. 这可能导致更快、更准确的诊断和更好的遗传疾病结果。 This could lead to quicker, more precise diagnoses and better outcomes for genetic disorders. 伙伴关系还旨在探索RNA测序,以加深对疾病的了解和新的治疗方法。 The partnership also aims to explore RNA sequencing for deeper disease understanding and new treatments.