SWAT4LS2009 – Matthias Loebe: TIM A semantic web application for the specification of metadata items in clinical research
November 20, 2009 1 Comment
(Again, these are live notes as bullet points.)
Problems with the Specification of Clinical Trials
- Development of trial protocol
- Preparation of study centres
- Registration of patients etc…..
- Case report Forms capture data at different time points (lab results, therapy outcomes, treatment history etc..) relevant for answering clinical questions
- Misconceptions and misinterpretations of data occur frequently either through underspecification or lack of metadata
Benefits of Detailing and Reusing Items
- Efficiency
- Data Quality
- Metaanalysis
Requirements for an Item Data Model
- Expressiveness – Items consist of subitems
- Adaptable system of rules – validity and consistency checking
- Supporting context
- Providing views – facests. Different information requirements for different types ofusers.
- Exploiting conceptual relations
- Mapping to terminologies
Architecture of Trial Item Manager
- Application behaviour is ontology driven…
- working data stored as rdf in separate model
- multiple rdf models (combined, raw, inferred)
Showing the specification of various trial items in rdf…..and examples of the ontology driving the app…
Advantage of th Semantic Approach
- open linked data, referencability
- extensible rules
- user guidence using semantics but invisible to user
- rapid response to change
- import external item sets
- personalisation on a per-user/user type basis
- navigation
- semantic search
Caveats:
- Open world reasoning sometimes gives unexpected results…..;-)
- No unique name assumption
- Performance
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