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GMDS 2012: 57. Jahrestagung der Deutschen Gesellschaft für Medizinische Informatik, Biometrie und Epidemiologie e. V. (GMDS)

Deutsche Gesellschaft für Medizinische Informatik, Biometrie und Epidemiologie

16. - 20.09.2012, Braunschweig

On the possibility of a holistic class model for the clinical bioinformatics domain

Meeting Abstract

Suche in Medline nach

  • Markus Gumbel - Hochschule Mannheim, Institut für Medizinische Informatik, Mannheim, Deutschland
  • Patrick Sturm - Hochschule Mannheim, Institut für Medizinische Informatik, Mannheim, Deutschland
  • Florian Meyerer - Hochschule Mannheim, Institut für Medizinische Informatik, Mannheim, Deutschland
  • Amelie Bauer - Hochschule Mannheim, Institut für Medizinische Informatik, Mannheim, Deutschland

GMDS 2012. 57. Jahrestagung der Deutschen Gesellschaft für Medizinische Informatik, Biometrie und Epidemiologie e.V. (GMDS). Braunschweig, 16.-20.09.2012. Düsseldorf: German Medical Science GMS Publishing House; 2012. Doc12gmds091

DOI: 10.3205/12gmds091, URN: urn:nbn:de:0183-12gmds0919

Veröffentlicht: 13. September 2012

© 2012 Gumbel et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen ( Er darf vervielfältigt, verbreitet und öffentlich zugänglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.



Introduction: Gene-technology-based methods along with their bioinformatics methods are more and more applied in clinical medicine. Examples are the support for diagnoses or pharmacogenomics including personalized medicine [1]. Many databases with molecular-biological content are available. However, databases that additionally consider individual patients are rare. Thus, a universal data model, which could be used as a template for a biomedical information system, is not available. Instead, molecular entities are modeled with ontologies, markup languages, terminologies, or with HL7v3 ([2], [3] and below). However, if different data sources need to be integrated there are interoperability issues [4] which only could be solved if the entities, their relationships and thus their semantics are known and specified globally. We have analyzed the possibility of modeling such a holistic data model by means of UML [5].

Material and Methods: Data integration methods in life science have a long history. We have analyzed, a) which solutions for data integration already exist, b) which public databases could be integrated, c) which existing sources for a (new) domain model could be used and d) which techniques could be useful to develop a de-novo model. Based on the outcome of this analysis, a UML prototype was created. The class-diagram was also influenced by an object-oriented database which was created in another project to demonstrate that biomedical data can naturally be stored in object-oriented databases [6].

Results: a) BioMart [7] and BioRS [8] were evaluated as tools for data integration. Apparently, data integration postpones the creation of a domain model until it is needed in concrete use-case dependent scenarios at a customer/organization. Thus, public and reusable domain models are not available. b) Public APIs of 30 key data sources from a list of about 1,300 databases [9] were examined. It turned out that many APIs are difficult to locate and to use. Their data structures are often text-based and mostly semi-structured. c) The gene ontology GO [10], the markup languages SBML [11] and GSVML [12], HL7's "Clinical Genomics" model [2] and to some extend the terminology UMLS [13] were considered as input for a domain model. We found that markup languages and HL7 are less suitable because of their hierarchical data-structures. Ontologies, in contrast, are a good source but a framework like GO is much too complex to be converted into UML directly. d) UML, like other modeling concepts, has the constraint of only having two meta levels [14].) Nevertheless, we never encountered a scenario where UML appeared to be inappropriate. Overall, our prototype model consists of 30 classes.

Discussion: Surprisingly, there are not many methods available for developing a domain model from scratch - modeling still seems to be an art. Methods for the transformation of ontologies to UML and back should be further investigated ([15], [16]). We believe it is possible to formulate a holistic domain model for clinical bioinformatics in UML. It could be used for the integration of data from different data sources, for querying them, for message exchange and as a template for information systems.


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