Matthew Kunzman News Today

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 that's nearly unheard of in standard clinical care.

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 that's nearly unheard of in standard clinical care.

A new ultra-rapid genome sequencing approach developed by scientists has been used to diagnose rare genetic diseases in an average of eight hours.

Stanford researchers reported that they had sequenced 12 seriously ill patients and successfully diagnosed five of them in record time.