Method for personalized selection of a drug for a subject
AssigneeCipherome, Inc.
InventorsJu Han KIM, Su Yeon BAIK, Soo Youn LEE
Life of this patent
Estimating the term…
Abstract
The present invention relates to a method and a system for selecting a drug customized on the basis of individual protein information by using individual genome sequences. The method and the system of the present invention can predict the individual side effects or danger of a certain drug by analyzing the sequence of the exon region of a gene encoding various proteins involved in the pharmacokinetics or pharmacodynamics of a predetermined drug or drug group, and have high reliability and are widely applicable and universal.
Claims21
A method for personalizing selection of a drug for a subject using individual genome sequence variations of the subject, comprising:
- obtaining, by a computer system, information regarding gene sequences of the subject for a set of genes involved in pharmacodynamics or pharmacokinetics of a drug group, wherein the drug group consists of a plurality of drugs;
- determining, by the computer system, gene sequence variation information indicating variations present in the gene sequences involved in the pharmacodynamics or pharmacokinetics of the group;
- for each gene of the set of genes:
- determining, by the computer system, a gene sequence variation score;
- for each protein encoded by a gene of the set of genes:
- calculating, by the computer system, an individual protein damage score for the protein by using [Equation 2], wherein [Equation 2] is:
- S
- g
-
- (
- v
- 1
- ,
- …
-
- ,
- v
- n
- )
- =
- (
- ∏
- i
- =
- 1
- n
-
-
- v
- i
- w
- i
- )
- 1
- /
- ∑
- i
- =
- 1
- n
-
-
- w
- i
- wherein Sg is the individual protein damage score of a protein encoded by a gene g, n is the number of target sequence variations for analysis among sequence variations of the gene g, vi is a gene sequence variation score of an ith gene sequence variation, and wi is a weighting assigned to the gene sequence variation score vi of the ith gene sequence variation;
- for each drug in the drug group:
- calculating, by the computer system, an individual drug score by using [Equation 4], wherein [Equation 4] is:
- S
- d
-
- (
- g
- 1
- ,
- …
-
- ,
- g
- n
- )
- =
- (
- ∏
- i
- =
- 1
- n
-
-
- g
- i
- w
- i
- )
- 1
- /
- ∑
- i
- =
- 1
- n
-
-
- w
- i
- wherein Sd is the individual drug score of a drug d, n is a number of proteins encoded by one or more genes involved in the pharmacodynamics or pharmacokinetics of the drug group d, gi is a protein damage score of a protein encoded by one or more genes involved in the pharmacodynamics or pharmacokinetics of the drug group d, and wi is a weighting assigned to the protein damage score gi of the protein encoded by one or more genes involved in the pharmacodynamics or pharmacokinetics of the drug group d;
- ranking, by the computer system, drugs in the drug group by comparing the individual drug scores for the drugs;
- and
- selecting a drug based on the ranking.
A computer-readable storage medium comprising stored instructions, wherein the instructions when executed by a processor cause the processor to perform steps comprising:
- obtaining information regarding gene sequences of a subject for a set of genes involved in pharmacodynamics or pharmacokinetics of a drug group, wherein the drug group consists of a plurality of drugs;
- determining gene sequence variation information indicating variations present in the gene sequences involved in the pharmacodynamics or pharmacokinetics of the drug group;
- for each gene of the set of genes:
- determining, by the computer system, a gene sequence variation score;
- for each protein encoded by a gene of the set of genes
- calculating an individual protein damage score for the protein by using [Equation 2], wherein [Equation 2] is:
- S
- g
-
- (
- v
- 1
- ,
- …
-
- ,
- v
- n
- )
- =
- (
- ∏
- i
- =
- 1
- n
-
-
- v
- i
- w
- i
- )
- 1
- /
- ∑
- i
- =
- 1
- n
-
-
- w
- i
- wherein Sg is the individual protein damage score of a protein encoded by a gene g, n is the number of target sequence variations for analysis among sequence variations of the gene g, vi is a gene sequence variation score of an ith gene sequence variation, and wi is a weighting assigned to the gene sequence variation score vi of the ith gene sequence variation;
- for each drug in the drug group:
- calculating an individual drug score by using [Equation 4], wherein [Equation 4] is:
- S
- d
-
- (
- g
- 1
- ,
- …
-
- ,
- g
- n
- )
- =
- (
- ∏
- i
- =
- 1
- n
-
-
- g
- i
- w
- i
- )
- 1
- /
- ∑
- i
- =
- 1
- n
-
-
- w
- i
- wherein Sd is the individual drug score of a drug d, n is a number of proteins encoded by one or more genes involved in the pharmacodynamics or pharmacokinetics of the drug group d, gi is a protein damage score of a protein encoded by one or more genes involved in the pharmacodynamics or pharmacokinetics of the drug group d, and wi is a weighting assigned to the protein damage score gi of the protein encoded by one or more genes involved in the pharmacodynamics or pharmacokinetics of the drug group d;
- ranking drugs in the drug group by comparing the individual drug scores for the drugs;
- and
- selecting a drug based on the ranking.
A system for providing information for personalizing drug selection using individual genome sequence variations, the system comprising:
- a processor;
- a computer readable storage medium comprising stored instructions, wherein the instructions when executed by a processor cause the processor to perform steps comprising:
- obtaining information regarding gene sequences of a subject for a set of genes involved in pharmacodynamics or pharmacokinetics of a drug group, wherein the drug group consists of a plurality of drugs;
- determining gene sequence variation information indicating variations present in the gene sequences involved in the pharmacodynamics or pharmacokinetics of the drug group;
- for each gene of the set of genes:
- determining, by the computer system, a gene sequence variation score;
- for each protein encoded by a gene of the set of genes
- calculating an individual protein damage score for the protein by using [Equation 2], wherein [Equation 2] is:
- S
- g
-
- (
- v
- 1
- ,
- …
-
- ,
- v
- n
- )
- =
- (
- ∏
- i
- =
- 1
- n
-
-
- v
- i
- w
- i
- )
- 1
- /
- ∑
- i
- =
- 1
- n
-
-
- w
- i
- wherein Sg is the individual protein damage score of a protein encoded by a gene g, n is the number of target sequence variations for analysis among sequence variations of the gene g, vi is a gene sequence variation score of an ith gene sequence variation, and wi is a weighting assigned to the gene sequence variation score vi of the ith gene sequence variation;
- for each drug in the drug group:
- calculating an individual drug score by using [Equation 4], wherein [Equation 4] is:
- S
- d
-
- (
- g
- 1
- ,
- …
-
- ,
- g
- n
- )
- =
- (
- ∏
- i
- =
- 1
- n
-
-
- g
- i
- w
- i
- )
- 1
- /
- ∑
- i
- =
- 1
- n
-
-
- w
- i
- wherein Sd is the individual drug score of a drug d, n is a number of proteins encoded by one or more genes involved in the pharmacodynamics or pharmacokinetics of the drug group d, gi is a protein damage score of a protein encoded by one or more genes involved in the pharmacodynamics or pharmacokinetics of the drug group d, and wi is a weighting assigned to the protein damage score gi of the protein encoded by one or more genes involved in the pharmacodynamics or pharmacokinetics of the drug group d;
- ranking drugs in the drug group by comparing the individual drug scores for the drugs;
- and
- selecting a drug based on the ranking.
Dependencies are inferred from the claim text.