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dc.contributor.authorO'Sullivan, Declan
dc.contributor.authorLittle, Mark
dc.date.accessioned2025-02-16T15:09:03Z
dc.date.available2025-02-16T15:09:03Z
dc.date.issued2025
dc.date.submitted2025en
dc.identifier.citationPalacz W, Lichołai S, Musiał J, Wawrzycka-Adamczyk K, Ślusarczyk G, Strug B, Yaman B, Tesi M, Gisslander K, O'Sullivan D, Vaglio A, Emmi G, Little MA, Wójcik K. Ontology-based integration and querying of heterogeneous rare disease data sources - POLVAS perspective. Comput Biol Med. 2025 Feb;185:109452en
dc.identifier.otherY
dc.descriptionPUBLISHEDen
dc.description.abstractThe integration of rare disease medical databases belonging to different countries is an important problem, as a large number of observations are required for reliable statistical inference of patient data in order to facilitate clinical research. Such integration of national registry data, which requires harmonization of the heterogeneous data sets into a unified view, is facilitated in the European FAIRVASC project by developing a domain-specific ontology. The FAIRVASC project is dedicated to the rare disease of anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV). This paper focuses on the practical issues and challenges, encountered during the process of integrating the Polish national database POLVAS into the federated database within the FAIRVASC project. It discusses the use of ontology-based methods for data integration and the importance of ensuring patient privacy and data protection. It addresses the problem of missing information in POLVAS, which can be obtained by aggregating other data available within the database, incompatibility of data types and formats, and mapping polish data names into the common vocabulary. The modifications of mappings used to 'uplift' national data into the Resource Description Framework (RDF) triplestore are also proposed. The described methods allow for integrating the Polish national database into the European network over which federated queries are performed.en
dc.format.extent1en
dc.format.extent14en
dc.language.isoenen
dc.relation.ispartofseriesComputers in Biology and Medicine;
dc.relation.ispartofseries185;
dc.rightsYen
dc.subjectData integration, Federated queries, Ontologies, Rare diseasesen
dc.titleOntology-based integration and querying of heterogeneous rare disease data sources - POLVAS perspectiveen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/mlittle
dc.identifier.peoplefinderurlhttp://people.tcd.ie/osulldps
dc.identifier.rssinternalid273071
dc.identifier.doihttps://doi.org/10.1016/j.compbiomed.2024.109452
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeDigital Engagementen
dc.subject.TCDThemeImmunology, Inflammation & Infectionen
dc.subject.TCDTagDigital Healthen
dc.subject.TCDTagDigital Platformen
dc.subject.TCDTagKnowledge Graphsen
dc.subject.TCDTagRegistriesen
dc.subject.TCDTagVASCULITISen
dc.identifier.orcid_id0000-0001-6003-397X
dc.status.accessibleNen
dc.contributor.sponsorHealth Research Board (HRB)en
dc.contributor.sponsorEuropean Union (EU)en
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.identifier.urihttps://hdl.handle.net/2262/110899


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