JP2004348749A - Medical information system, system and method for providing medical information, and gene analysis system - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide medical information for registering gene information and providing necessary information related to the gene information. <P>SOLUTION: A medical information system has a storage means for storing personal SNP (Single Nucleotide Polymorphism) gene information linked to ID number and medical information, which is related to risk factors related to diseases, effects to medicines, allergy analysis for medicine ingredients and infection risks to viruses, linked to SNP gene information, which indicates base pairs that a base sequence of DNA that includes gene information is replaced with another base. In addition, the system also has a retrieval means for retrieving personal SNP gene information corresponding to ID number, a retrieval means for further retrieving medical information corresponding to personal SNP gene information, and a means for displaying SNP gene information and medical information for the ID number. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

  The present invention relates to a method for providing medical treatment information by a gene that registers genetic information and provides necessary information related thereto.

  Human genetic analysis is being performed worldwide on the basis of the Human Genome Project. These pieces of human genetic information are composed of DNA base sequences.

  Human base pairs are vast, with about 3 billion base pairs. Various applications such as gene diagnosis, gene therapy and powerful drugs are expected using such information.

  In particular, analysis of expressed proteins from genetic information, cloning of cDNA and protein expression, elucidation of the relationship between expressed protein functions and diseases, elucidation of functional protein structures, analysis of diseases and disease-related genes, progress of bioinformatics Etc. are expected. Furthermore, preventive medicine, tailor-made medicine, etc. are also declared.

  To collect and analyze human genetic information, a huge amount of information must be handled, and the existence of a computer capable of high-speed processing is indispensable. It is not an exaggeration.

  On the other hand, there is SNP (sing1e Nuc1eotide Polymorphism) information. The SNP is called a single-base mutation pair, and is a base pair in which the base sequence of DNA that carries genetic information is replaced by another base by one. It is said that these base pairs cause congenital genetic diseases, and that acquired factors such as living environment and SNP factors are involved, thereby causing diseases such as cancer and diabetes.

  It is said that humans have 3 to 10 million SNPs. Methods for analyzing where in a gene sequence SNPs are located using an information network have already begun to be implemented.

  At present, several innovative technologies are progressing toward genomic drug discovery, representative of which are as follows.

・ Search for drug targets based on genome: DNA chip targeting all genes
・ HTS (High-Throughtput Screening) for all proteins: DNA / protein chip
・ Evaluation laboratory aiming to streamline clinical development and shorten the period: * DNA / protein chip (pharmacogenomics)
・ SNP (Sing1e Nuc1eotide Po1ymorphism)
In other words, in the context of the gene industry, elucidation of human genetic information is currently the largest objective, and in order to achieve this, the development of new DNA chips, efficient analysis methods, and genomic informatics are flourishing. Researched and developed, showing progress to business.

  However, clinically meaningful genetic information has not been elucidated, and further research is desired. The clinical value of genetic diagnosis is expected to start with taking multiple samples and comparing them. In other words, it is necessary to associate a lot of genetic information with the disease.

  As described above, genetic information is still in the elucidation stage, and it is expected that diagnosis using this information is still far ahead. Even at that stage, it is necessary to register all data of a great deal of genetic information, and it is difficult to register them. Furthermore, even if they can be registered, it is very difficult and impractical to associate them with a disease and further search.

  An object of the present invention is to improve the confidentiality of genetic information.

  The present invention is a genetic medical information system including a medical information receiving system and a medical information providing system connected to a network, wherein the medical information receiving system includes an input unit for inputting an ID number of a subject; First storage means for storing an ID number in association with the name of the subject, and SNP gene information of the subject having the ID number from the second storage means of the medical care information providing system; From the second storage means of the information providing system, medical information relating to at least one of a risk factor for a disease associated with the SNP gene information of the ID number, an effect on a therapeutic drug, an allergy analysis for a drug component, and a risk of infection with a virus is stored. , Obtained through the network, and stored in the first storage unit corresponding to the ID number. Display means for displaying medical information related to the SNP gene information of the subject name by reading the name of the body, wherein the medical information providing system converts the SNP gene information of the individual subject into the ID number. A base sequence of DNA carrying genetic information, the second storage means for associating and storing medical information on at least one of a risk factor for the disease, an effect on a therapeutic drug, an analysis of allergy to a drug component, and a risk of infection with a virus; A third storage means for storing in association with SNP gene information representing a base pair in which one base is replaced by another base, a means for receiving an information provision request including an ID number from the medical information receiving terminal, The SNP gene information of the subject corresponding to the received ID number is searched from the second storage means, and the search is performed. Means for searching the third storage means for medical information corresponding to the SNP gene information of the individual subject, and transmitting the searched SNP gene information and medical information of the ID number to the display means of the medical information receiving system. And means for performing the operation.

  According to the present invention, the confidentiality of genetic information can be improved.

  Hereinafter, the best embodiment of the present invention will be described. FIG. 1 shows a general flow up to registration of information on SNP, and FIG. 2 shows a configuration of a system of this embodiment. FIG. 19 shows a detailed processing flow. As shown in FIG. 2A, a genetic analysis system 10 in a hospital genetic test room includes a display unit 11, a comparison unit 12, a storage unit 13, a data transmission / reception unit 14, a gene acquisition unit 15, a gene database 17 The data transmission / reception unit 14 is connected to an external network 18.

  Further, as shown in FIG. 2 (b), the gene analysis system 20 provided in the service center includes a display unit 21, an order monitor unit 22, a charging unit 23, an information amount counting unit 24, a first database 25, an individual SNP registration database 26, a medication and SNP database 27, a disease and SNP database 28, and a data transmission / reception unit 29. The data transmission / reception unit 29 is connected to the external network 18.

  First, in a genetic test room of a hospital, for example, general tests such as a blood test and a biochemical test necessary for diagnosing a patient are performed in step S1 in FIG. At this time, the doctor in charge determines whether or not there is a genetic test in step S12 as an optional test. If it is not necessary, the test is terminated. However, if it is determined that the genetic test is necessary, the consent of the patient is obtained in step S13 to obtain genetic information on the SNP of the patient (S91).

  Specifically, the necessary blood is collected in the genetic test room, and the blood is used as a sample to obtain the genetic information on the SNP using the genetic diagnosis heel 12a, that is, the entire gene base sequence or the gene base of the designated portion. Create an array.

  Generating personal genetic information using blood obtained from an individual. Individual gene information is acquired by a gene acquisition unit 15 such as a gene probe. The acquired individual genetic information is temporarily stored in the storage unit 13. At this time, for example, in the case of a diabetic patient, only DNA having genetic information related to diabetes is extracted.

  Next, in step S14, the standard gene sequence DB25 of the gene analysis system 20 of the service center is accessed, and the standard gene is extracted (S92).

  The extracted standard gene is stored in the storage unit 13 or the gene DB 17 via the data transmission / reception unit 14 of the hospital gene analysis system 10. At this time, a part of the genetic information necessary for analyzing the genetic information obtained in the previous individual gene obtaining step is stored.

  In the gene analysis system 20 of the service center, the type and amount of the extracted genetic information are counted by the information amount counting unit 24, and charging information is created by the charging unit 23 according to the information amount and type. The charging unit has a charging database in advance, and generates charging information by referring to the database.

  Thereafter, in step S15, the comparing unit 12 compares the gene of the patient stored in the storage unit 13 with the standard gene obtained from the service center (S93).

  As a result of the comparison, if a location where the gene base sequence of the patient is different from the downloaded general gene base sequence is found, a diagnosis result is advised to the patient based on the difference in step S16.

  On the other hand, in step S17, the gene information of the different place, that is, the SNP gene information is registered with the consent of the patient.

  The SNP information obtained by comparing both genes is stored in the gene DB 17 with an in-hospital examination number (temporary ID number) and the like. At the time of storage, the temporary ID number is registered in association with the SNP information (S93).

  At the same time that the SNP information is provisionally registered, the service center is notified of the provisional registration of the SNP information, the number thereof, and the like (S94). The main registration is urged and confirmed based on the notified information (S95). Doctors and patients make a formal registration. If it is not necessary, it becomes information sharing data in the hospital using the temporary ID. Registration is possible at any time.

  The procedure for registering the SNP gene information will be described in more detail with reference to the drawings. FIG. 3 shows the flow of this registration procedure.

  In step S21, for example, a patient name or the like is registered by inputting a registrant name and a health insurance card number on an input surface as shown in FIG. When the input is completed, the "next" button 41 is clicked, and the screen shifts to the screen shown in FIG. 5, and it is known that the temporary ID number has been issued (step S22).

  Next, the screen shifts to the screen shown in FIG. 6, and a confirmation is made as to whether to register the SNP information of the patient (step S23). When the “No” button 61 is clicked on the screen in FIG. 6, the SNP information is not registered.

  On the other hand, if the "Yes" button 62 is clicked, the process moves to step S24, and the authentication of the patient is requested. The doctor or the patient performs authentication using, for example, an authentication card such as an insurance card IC card, a registered insurance card number and a password, or a fingerprint or an eye glow. By inputting predetermined authentication information, "Authentication" is displayed as shown in FIG. 7, and when it is completed, the "OK" button 71 is clicked, and in step S25 of FIG. Enter genetic information.

  When the input is completed, the process proceeds to step S26, where the information is registered in the personal SNP registration DB 26 of the gene analysis system 20 of the service center (S98). Thereafter, the process proceeds to step S27, for example, a screen as shown in FIG. 8 appears, and it is known that the real ID has been issued. This ID number is required later for performing a diagnosis or the like, and is displayed together with a word for calling attention so as not to forget the information and a reference address for when the information is forgotten.

  Thus, the SNP gene information corresponding to the ID number is stored in the personal SNP registration DB 26 of the service center.

  As described above, the gene registration is completed, and after that, necessary information related to the SNP information can be received by transmitting the real ID and the menu information.

  When referring to SNP information or obtaining other information, doctors and patients use this ID number to contact the service center. This ID number may be input to an IC card, and when making an inquiry, the ID number may be input using the IC card, or the ID number may be input using a numeric keypad.

  As described above, the registration in the personal SNP registration DB 26 of the service center is registered not with the patient name but with a multi-digit ID number. By doing so, patients and physicians can know the genetic information from the ID number, but if anyone knows the SNP gene information, it cannot know who belongs to it. Service centers also cannot know who the SNP genetic information belongs to.

  In addition, a table for converting ID numbers into patient names is stored in the gene DB of each hospital, and necessary doctors can be introduced and known in hospitals, but other hospitals and service centers Cannot be seen from In this way, the SNP genetic information of the patient is kept secret.

  Next, a method for making a diagnosis based on the SNP gene information registered in the personal SNP gene DB 26 of the service center as described above will be described. FIG. 9 shows the procedure of diagnosis.

  First, the ID number previously given in step S31 is input (S101). FIG. 10 shows an example of the input screen in this case. That is, "Please enter your ID number." Is displayed. If you enter your ID number and click on the "OK" button 101, "Searching for the applicable person" is displayed below it.

  In step S32, it is checked whether the SNP gene information of the person corresponding to the input ID number exists in the personal SNP registration DB 26 of the service center (S102). If there is, the process proceeds to step S33, for example, a screen as shown in FIG. 11 is displayed. On this screen, all menus known from SNP gene information are displayed, such as disease risk analysis, therapeutic drug effect analysis, drug component allergy analysis, and virus infection risk analysis. In addition, it is possible to inform the patient of advice information on health management, advice of meals, and the like. These information are stored in the medication and SNPDB27, and the disease and SNPDB28.

  The user selects desired information from the information (S105). When desired information is selected in step S34, the process proceeds to step S35, where the selected information is analyzed and a result is created (S106).

  For example, if “1. Risk analysis of disease” is selected on the screen of FIG. 11, information as shown in FIG. 12 is obtained. It represents the risk for each factor of risk of getting the disease. That is, SNP gene information is A, B, C, D, E, F, A * B, A * C, A * D, A * for A disease, B disease, U disease, D syndrome, E syndrome. The risk for each of E, A * B * C, ... is displayed as a percentage.

  As a result of referring to the patient's ID number, it is assumed that the SNP gene information of this patient is A * B. A * B means that there are two SNPs, A and B. When the SNP gene information is A * B, the risk of developing A disease is 10%, the risk of developing A disease is 60%, the risk of acquiring U disease is 10%, and the risk of developing E syndrome is 20% from Fig. 12. It is understood that. The results are put together and notified to the person who entered the ID number in step S36. This notification may be arranged in descending order of risk, or may be displayed from a disease of interest to the patient (eg, heart disease).

  The patient or doctor can display the obtained result on a screen or print it. It can also be added as medical information such as an electronic medical record.

  The relationship between the disease risk factor and the SNP gene information as shown in FIG. 12 is stored in the disease and SNP DB28 of the gene analysis system 20 of the service center. This information is created based on drug information, epidemiological information, and disease risk information known up to that date.

  In the screen of FIG. 11, when “2. Analysis of effects on therapeutic agents” is selected, as shown in FIG. 13, for example, therapeutic agents, 1-drugs, 2-drugs, 3-drugs, 4-drugs, 5-drugs , Whereas the SNP gene information is A, B, C, D, E, F, A * B, A * C, A * D, A * E, A * B * C, The measured value is displayed as a percentage.

  Similarly, assuming that “3. Allergy analysis for drug components” is selected on the screen of FIG. 11, as shown in FIG. 14, the SNP gene is assigned to the drug components a, b, c, d, and e. If the information is A, B, C, D, E, F, A * B, A * C, A * D, A * E, A * B * C, etc., the risk is displayed as a percentage.

  Assuming that "4. Virus infection risk analysis" is selected on the screen of FIG. 11, as shown in FIG. 15, the SNP gene information for the viruses A, B, C, D, and E is A, B , C, D, E, F, A * B, A * C, A * D, A * E, A * B * C,.

  The tables shown in FIGS. 13 to 15 are also created based on various information up to that date, and are stored and accumulated in the personal SNP registration DB 16 of the service center.

  In the above embodiment, information on the standard gene was obtained at each hospital from the genetic analysis center of the service center, and the genetic information of each individual at each hospital was compared and analyzed. However, it is also possible to send all the individual's genetic information obtained at each hospital to a service center for analysis there.

  FIG. 16 shows the entire configuration in this case. In FIG. 16, numbers 130 to 149 except for number 132 correspond to numbers 10 to 29 in FIG. The analysis unit 132 is different from the comparison unit 12 in FIG. 2 in that it analyzes genes in each hospital. Reference numeral 150 denotes a comparison unit, and 151 denotes a storage unit.

  After the confirmation of the main registration and the reminder, it is the same as in the above embodiment.

  Generating personal genetic information using blood obtained from an individual. At each hospital, individual gene information is acquired by gene acquisition means such as a gene probe. The acquired individual's genetic information is temporarily stored in the gene acquiring unit 135. At this time, for example, in the case of a diabetic patient, only DNA having genetic information related to diabetes is extracted. Next, the obtained personal gene information is transmitted to the gene analysis system 140 of the service center through the data transmission / reception unit 134.

  The transmitted personal gene information is temporarily stored in the storage unit 151 of the gene analysis system 140. The standard gene is acquired using the stored gene information and the transmitted related information (for example, the position of the acquired gene information and the vicinity of DNA No. 22). The comparing unit 150 compares the standard gene acquired from the standard gene sequence DB 145 with the personal gene information to obtain SNP information. The obtained SNP information is stored in the storage unit 151.

  When the analysis and acquisition of the SNP information is completed, the comparison is completed and the fact that the SNP information has been obtained is notified to the hospital system. The hospital system tells you where the SNP is in the gene. The tree registration is urged and confirmed based on the notified information. Doctors and patients perform the main registration if necessary for the disease risk search and the medication risk search accompanying the main registration. If it is not necessary, it becomes information sharing data in the hospital using the temporary ID. Registration is possible at any time.

  When a doctor or patient makes a formal registration application at the hospital, the service center system 140 starts a patient approval procedure. The doctor or patient performs authentication using, for example, an insurance card IC card, a registered insurance card number and password, or personal authentication such as a fingerprint or glow of eyes. Upon completion of the patient authentication, the system 140 issues a registration ID number.

  Register the SNP information after this ID number is issued. The SNP information based on the temporary ID number is read out, and the SNP information is stored and registered in the personal SNP registration DB 146 of the system 140.

  As described above, the gene registration is completed, and after that, by transmitting the real ID and the menu information, necessary information related to the SNP information can be received.

  The real ID is transmitted from the system 130 of each hospital or the personal terminal 139 to the system 140 of the service center. When sent, menu information is displayed, and you can search for necessary SNP-related information.

  For example, for information on medication allergy related to the SNP information, the personal terminal 139 first searches for personal SNP information from the personal SNP registration DB 146. Based on the extracted personal SNP information, the registered data is searched in the medication at the service center and the SNP DB147. Alternatively, a search is made according to the sickness or disease information requested from the personal terminal 139 and the SNP information. The relationship between the SNP found as a result of the search and the medication allergy information is transmitted, and the result is displayed on the screen of the personal terminal 139.

  By setting up a specialized registration agency for SNP gene information separately from hospitals, various services can be provided. Another embodiment of this type will be described.

  FIG. 17 shows the configuration of this overall system. Reference numeral 160 denotes an SNP gene health information service provider that registers SNP gene information and provides health information based on the information. Reference numerals 161a and 161b denote hospitals, and reference numeral 162 denotes a pharmaceutical research laboratory. At the hospital 161a, the doctor 164 accesses the SNP gene health information service provider hider 160 from the terminal 165 of the hospital and registers the SNP gene information of the patient after obtaining approval (authentication) of the patient 163 (S41).

  The SNP gene information of the patient is registered with the SNP gene health information service provider 160 from another hospital 161b (S42), or information such as medicine is provided from the pharmaceutical research laboratory 162 to the SNP gene health information service provider 160 (S43). . In return, a predetermined reward is paid to the hospital 161b and the pharmaceutical laboratory 162 (S44).

  The SNP gene health information service provider 160 constantly investigates the correlation between the SNP gene and various risks, health, etc. from the above information and various publications, and creates a table as shown in FIGS. 12 to 15 are doing.

  Therefore, when the doctor 164 receives the treatment information of the patient from the SNP gene health information service provider 160 (S45), or when the patient 163 acquires the health information from the SNP gene health information service provider 160 (S46) A predetermined fee is paid to the provider 160 (S47).

  In this way, providing SNP gene information and earning a fee will enable management.

  As shown in FIG. 18, an insurance union or insurance company 171 is interposed between the patient and the SNP gene health information service prohibitor 160, collects a membership fee from the patient (S51), and collectively contracts with this provider to set a predetermined amount. Payment (S52), and health information based on the SNP gene may be provided to enrolled patients (S53).

FIG. 4 is a diagram for explaining a method according to an embodiment of the present invention. FIG. 1 is a diagram illustrating a configuration of a system according to an embodiment of the present invention. FIG. 4 is a diagram for explaining ID number issuance in one embodiment of the present invention. FIG. 4 is a diagram showing an example of an input screen for a patient name and the like in the embodiment of FIG. FIG. 4 is a diagram showing an example of a temporary ID number issuance screen in the embodiment of FIG. FIG. 4 is a diagram showing an example of a SNP information registration screen in the embodiment of FIG. FIG. 4 is a diagram showing an example of a screen of an authentication mark in the embodiment of FIG. FIG. 4 is a diagram showing an example of an ID number issuance screen in the embodiment of FIG. FIG. 5 is a diagram for explaining a process of obtaining desired information results from registered SNP gene information in the present invention. FIG. 10 is a diagram showing an example of an ID number input screen in the embodiment of FIG. FIG. 10 is a diagram showing an example of a menu display of desired information in the embodiment of FIG. FIG. 10 is a diagram showing an example of a table showing a relationship between SNP gene information and a risk of getting a disease in the embodiment of FIG. 9. FIG. 10 is a diagram showing an example of a table showing a relationship between SNP gene information and an effect on a therapeutic agent in the embodiment of FIG. 9. FIG. 10 is a diagram showing an example of a table showing a relationship between SNP gene information and a risk of occurrence of allergy to a drug component in the embodiment of FIG. 9. FIG. 10 is a diagram showing an example of a table showing a relationship between SNP gene information and susceptibility to virus infection in the embodiment of FIG. 9. FIG. 11 is a diagram for describing a configuration of a system according to another embodiment of the present invention. FIG. 2 is a diagram for explaining the relationship between a SNP gene health information service provider and a hospital. FIG. 2 is a diagram for explaining the relationship between a SNP gene health information service provider, a hospital, an insurance union, and the like. FIG. 3 is a diagram illustrating a detailed procedure of a process according to the exemplary embodiment illustrated in FIG. 2;

Explanation of reference numerals

  Reference Signs List 10: Gene analysis system, 11: Display unit, 12: Comparison unit, 13: Storage unit, 14: Data transmission / reception unit, 15: Gene acquisition unit 15, 17: Gene database, 18: Network, 20: Gene analysis system, 21 ... display unit, 22 ... order monitor unit, 24 ... information amount counting unit, 25 ... first database, 26 ... personal SNP registration database, 27 ... medication SNP database, 28 ... disease SNP database, 29 ... data transmission / reception unit.

Claims (10)

A medical information system based on a gene comprising a medical information receiving system and a medical information providing system connected to a network,
The medical information receiving system,
Input means for inputting the ID number of the subject;
First storage means for storing the ID number in association with the name of the subject;
The SNP gene information of the subject with the ID number is obtained from the second storage unit of the medical care information providing system via the network, and the name of the subject corresponding to the ID number is obtained from the first storage unit. Display means for displaying the SNP gene information of the subject name by reading the
The medical treatment information providing system
Second storage means for storing the SNP gene information of the subject individual in association with the ID number,
Means for receiving an information provision request including an ID number from the medical information receiving terminal;
Means for searching the second storage means for SNP gene information of the subject corresponding to the received ID number;
Means for transmitting the searched SNP gene information of the ID number to the display means of the medical information receiving system;
A medical information system comprising: The medical information providing system,
The base sequence of DNA carrying genetic information replaces one base with another base for medical information on at least one of risk factors for disease, effects on therapeutic drugs, allergy analysis for drug components, and risk of infection with viruses. Further comprising a third storage means for storing in association with the SNP gene information representing the base pair,
The search unit of the medical care information providing system searches the second storage unit for SNP gene information of the subject corresponding to the received ID number, and searches for the SNP gene information of the searched subject. Medical information to be retrieved from the third storage means,
The transmitting means of the medical information providing system transmits the SNP gene information and the medical information of the searched ID number to the display means of the medical information receiving system,
The display unit of the medical information receiving system is configured to transmit the SNP gene information of the subject having the ID number from the second storage unit of the medical information providing system and the medical information from the third storage unit via the network. The medical information related to the SNP gene information of the subject name is displayed by acquiring and reading out the name of the subject corresponding to an ID number from the first storage means. Medical information system. In a medical information providing system connected to a medical information receiving terminal via a network,
First storage means for storing SNP gene information of a subject individual in association with a subject-specific ID number;
Means for receiving an information provision request including an ID number from the medical information receiving terminal;
Means for searching the first storage means for SNP gene information of the subject corresponding to the received ID number;
Means for transmitting the searched individual SNP gene information to the medical information receiving terminal connected to second storage means for storing the ID number and the subject name in association with each other. Medical information providing system. The base sequence of DNA carrying genetic information replaces one base with another base for medical information on at least one of risk factors for disease, effects on therapeutic drugs, allergy analysis for drug components, and risk of infection with viruses. Further comprising a third storage means for storing in association with the SNP gene information representing the base pair,
The search means searches the first storage means for SNP gene information of the subject corresponding to the ID number received by the receiving means, and retrieves medical information corresponding to the searched SNP gene information of the subject. Searching from the third storage means,
4. The medical information providing system according to claim 3, wherein the transmitting unit transmits the searched medical information to the medical information receiving terminal. In a method for providing medical information to a medical information receiving terminal via a network,
Receiving an information provision request including a subject-specific ID number from the medical information receiving terminal;
A first storage unit for storing, in association with an ID number, SNP gene information of a subject representing a base pair in which the base sequence of DNA carrying genetic information has been replaced by another base by one, the received ID number; Obtaining the SNP gene information of the subject individual corresponding to the received ID number by searching for
A second storage unit for storing medical information relating to at least one of a risk factor for a disease, an effect on a therapeutic drug, an allergy analysis for a drug component, and a risk of infection with a virus in association with SNP gene information; Acquiring medical information corresponding to the obtained individual SNP gene information of the subject by searching with the SNP gene information;
Transmitting the medical information corresponding to the acquired individual SNP information of the subject to a medical information receiving terminal connected to a third storage unit that stores the ID number and the subject name in association with each other. Characteristic medical information providing method. A medical information system based on a gene comprising a medical information receiving system and a medical information providing system connected to a network,
The medical information receiving system,
Obtaining means for obtaining genetic information of the subject;
A first storage unit that stores DNA having genetic information related to a specific disease among the genetic information of the subject obtained by the obtaining unit;
Access to a first database of the medical information providing system, and store a base sequence of a part of standard genes necessary for analyzing genetic information of a subject stored in the first storage unit. Two storage units,
The base sequence of a part of the standard gene stored in the second storage unit is compared with the gene information of the subject stored in the first storage unit, and the base sequence of DNA carrying the gene information is compared. Comparison means for obtaining SNP information of a subject representing a base pair in which a part of the base is replaced by another base;
From various SNP information stored in the second database of the medical information providing center, medical information of the SNP gene information related to the SNP gene information of the subject is obtained and displayed via the network. Display means;
With
The medical information providing system,
A first database storing a base sequence of the standard gene;
First supply means for supplying the standard gene information from the first database to the medical information receiving system via a network in response to a request from the medical information receiving system;
A second database that stores medical information associated with various SNP gene information;
Obtaining means for obtaining the SNP gene information of the subject via a network, obtained by the comparing means of the medical information receiving system,
A second supply unit that reads medical information associated with the acquired SNP gene information of the subject from the second database and supplies the medical information to the medical receiving system via a network. Medical information system. A genetic analysis system connected by a network to a medical information providing terminal of a medical information providing center that provides medical information based on genetic information of a subject,
Obtaining means for obtaining genetic information of the subject;
A first storage unit for storing the gene information of the subject acquired by the acquisition unit;
A second storage unit for storing a base sequence of a part of standard genes necessary for analyzing the genetic information of the subject acquired by the acquiring means which has accessed and retrieved the first database of the medical information providing center; When,
The base sequence of a part of the standard gene stored in the second storage unit is compared with the gene information of the subject stored in the first storage unit, and the base sequence of DNA carrying the gene information is compared. Comparison means for obtaining SNP information of a subject representing a base pair in which a part of the base is replaced by another base;
From the medical information of various SNP gene information accumulated in the second database of the medical information providing center, the medical information of the SNP gene information related to the SNP gene information of the subject is obtained via the network. Display means for displaying
A gene analysis system comprising: A genetic analysis system connected by a network to a medical information providing terminal of a medical information providing center that provides medical information based on genetic information of a subject,
Obtaining means for obtaining genetic information of the subject;
An analysis unit that extracts DNA having genetic information related to a specific disease from the genetic information of the subject obtained by the obtaining unit;
A data transmitting / receiving unit that transmits the personal gene information of the subject extracted by the analyzing unit,
From the medical information of various SNP gene information stored in the database of the medical information providing center received by the data transmitting / receiving unit, the medical information of the SNP gene information related to the SNP gene information of the subject, Display means for acquiring and displaying via the network,
A gene analysis system comprising: 9. The gene according to claim 7, wherein the medical information is at least one of a risk factor for a disease, an effect on a therapeutic drug, an allergy analysis for a drug component, and a risk of infection with a virus. Analysis system. The data transmitting / receiving unit transmits the personal gene information to register the personal gene information of the subject in the database of the medical information providing center, to the data transmitting / receiving unit of the medical information providing center via the network. The gene analysis system according to any one of claims 7 to 10, wherein:

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