摘要:
Method, system, and computer program product are provided for predicting diagnosis of a patient performed by a computerized device. The method may include: modeling data from a group of successfully diagnosed patients, wherein the data is modeled as treatment paths of patients including referrals to medical practitioners; and predicting diagnosis for a current patient by comparing a treatment path of the current patient with the modeled treatment paths of successfully diagnosed patients, including calculating a probability of a given diagnosis from the modeled treatment paths. The method may include: defining a set of medical entities including medical practitioners to which a patient has been referred; and gathering treatment paths of successfully diagnosed patients, wherein the treatment path links medical entities in a directional route. Predicting diagnosis for a current patient may use the modeled data to calculate the probability of each model instance for each diagnosis and choosing the model instance of the diagnosis that maximizes the treatment path probability.
摘要:
Novel splice variant nucleic acid sequences. The novel splice variants and their nucleic acid sequences according to the present invention may optionally be used for diagnosis of a variant-detectable disease as described herein.
摘要:
A method and system for querying a Health Level 7 (HL7) data repository which stores entries in HL7 Reference Information Model (RIM) terminology across multiple HL7 domains. The method includes: receiving a query input to retrieve data from the repository, wherein the query input is in a query language, converting the query input to a RIM query, and retrieving data from the repository using the RIM query. The RIM query expresses the query input using RIM physical classes and RIM codes. The method also includes converting retrieved RIM instances from the repository to a domain readable format. Providing the data repository includes receiving data for input in the data repository, wherein the data for input is defined at a domain level as a domain instance, and converting a domain instance to a RIM instance and inputting the RIM instance in the data repository.
摘要:
Novel splice variant nucleic acid sequences. The novel splice variants and their nucleic acid sequences according to the present invention may optionally be used for diagnosis of a variant-detectable disease as described herein.