The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.
The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.
Patent No.:
Date of Patent:
Oct. 08, 2024
Filed:
Mar. 22, 2023
Tempus Ai, Inc., Chicago, IL (US);
Christopher Shane Colley, Chicago, IL (US);
Isaiah Simpson, Chicago, IL (US);
Brian Reuter, Chicago, IL (US);
Robert Tell, Chicago, IL (US);
Hailey Lefkofsky, Chicago, IL (US);
Hunter Lane, Chicago, IL (US);
Kevin White, Chicago, IL (US);
Nike Beaubier, Chicago, IL (US);
Stephen Bush, Chicago, IL (US);
Aly Khan, Chicago, IL (US);
Denise Lau, Chicago, IL (US);
Kaanan Shah, Chicago, IL (US);
Eric Lefkofsky, Chicago, IL (US);
Tempus AI, Inc., Chicago, IL (US);
Abstract
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.