公开(公告)号：US12062372B2

公开(公告)日：2024-08-13

申请号：US18338747

申请日：2023-06-21

申请人： Tempus AI, Inc.

发明人： Eric Lefkofsky ,  Jonathan Ozeran

IPC分类号： G10L15/22 ,  G06F3/0481 ,  G06F3/16 ,  G06F16/632 ,  G16H10/60 ,  G16H40/20 ,  G16H50/20 ,  G16H50/50 ,  G16H70/20 ,  G16H70/60 ,  H04B1/3827

CPC分类号： G10L15/22 ,  G06F3/0481 ,  G06F3/167 ,  G06F16/634 ,  G16H10/60 ,  G16H40/20 ,  G16H50/20 ,  G16H50/50 ,  G16H70/20 ,  G16H70/60 ,  H04B1/3827 ,  G10L2015/223

摘要： A method and system of audibly broadcasting responses to a user based on user queries about a specific patient report, the method comprising receiving an audible query from the user to a microphone coupled to a collaboration device, identifying at least one intent associated with the audible query, identifying at least one data operation associated with the at least one intent, associating each of the at least one data operations with a first set of data presented on the report, executing each of the at least one data operations on a second set of data to generate response data, generating an audible response file associated with the response data and providing the audible response file for broadcasting via a speaker coupled to the collaboration device.

公开(公告)号：US20240312581A1

公开(公告)日：2024-09-19

申请号：US18660213

申请日：2024-05-09

申请人： Tempus AI, Inc.

发明人： Christopher Shane Colley ,  Isaiah Simpson ,  Brian Reuter ,  Robert Tell ,  Hailey Lefkofsky ,  Hunter Lane ,  Kevin White ,  Nike Beaubier ,  Stephen Bush ,  Aly Khan ,  Denise Lau ,  Kaanan Shah ,  Eric Lefkofsky

IPC分类号： G16H10/60 ,  G16B30/00 ,  G16B40/20 ,  G16H15/00 ,  G16H20/10 ,  G16H20/40 ,  G16H50/20 ,  G16H50/30 ,  G16H50/50 ,  G16H50/70

CPC分类号： G16H10/60 ,  G16B30/00 ,  G16B40/20 ,  G16H15/00 ,  G16H20/10 ,  G16H20/40 ,  G16H50/20 ,  G16H50/30 ,  G16H50/50 ,  G16H50/70

摘要： A method for identifying actionable care events includes receiving data sources relating to a subject; storing data from them in a first database; generating a database comprising structured data fields and metadata fields from the sources; generating output data related to fields within the data or metadata fields; populating the database with the output data; generating criteria sets corresponding to respective actionable care events; evaluating the generated database using the criteria sets; identifying whether any of the criteria sets are not sufficiently satisfied by the database, wherein an underlying error or an indication of missing or incomplete information within the database with respect to a criteria set indicates a corresponding actionable care event; determining that other data sources within the collection do not sufficiently satisfy any of the identified criteria sets; and generating, based on the identifying and determining, a notification that at least one actionable care event applies.

公开(公告)号：US12112839B2

公开(公告)日：2024-10-08

申请号：US18188443

申请日：2023-03-22

申请人： Tempus AI, Inc.

发明人： Christopher Shane Colley ,  Isaiah Simpson ,  Brian Reuter ,  Robert Tell ,  Hailey Lefkofsky ,  Hunter Lane ,  Kevin White ,  Nike Beaubier ,  Stephen Bush ,  Aly Khan ,  Denise Lau ,  Kaanan Shah ,  Eric Lefkofsky

IPC分类号： G16H10/60 ,  G16B30/00 ,  G16B40/20 ,  G16H15/00 ,  G16H20/10 ,  G16H20/40 ,  G16H50/20 ,  G16H50/30 ,  G16H50/50 ,  G16H50/70

CPC分类号： G16H10/60 ,  G16B30/00 ,  G16B40/20 ,  G16H15/00 ,  G16H20/10 ,  G16H20/40 ,  G16H50/20 ,  G16H50/30 ,  G16H50/50 ,  G16H50/70

摘要： A method and system comprising storing a set of user application programs each requiring an application specific subset of data to perform application processes and generate a respective genomic variant characterization for each of a plurality of patients with cancerous cells and receiving cancer treatment. The method including, obtaining clinical records data including cancer related information, generating genomic sequencing data for the patient's cancerous cells and normal cells, shaping at least a subset of the genomic sequencing data to generate system structured data. Storing the system structured data in a first database, selecting the application specific data from the first database, storing the application specific data in a second database for application program interfacing, receiving the respective genomic variant characterization from the user application program, and storing the genomic variant characterization from the user application program in a third database.