
A knowledge gap exists regarding the impact of organizational parameters of trauma centers and patient outcomes. This is partially due to such organizational parameters being understudied. The Ontology of Organizational Structures of Trauma Centers and Trauma Systems (OOSTT) provides a controlled vocabulary to study that specific area. It is used in tools created by the TIPTOE project to provide trauma stakeholders with novel insights on role of organizational parameters and patient outcomes. This paper reports the extension of OOSTT to cover relevant patient outcome measures.
Background: In radiation oncology, the data generated from preclinical trials serve as initial validation for treatment effectiveness and optimizing clinical approaches by unraveling molecular mechanisms underlying different treatment responses. Therefore, it is important to standardize the practice in managing preclinical trial data to ensure consistency and reproducibility across studies, promoting collaboration, and facilitating regulatory review. The primary goal of this work is to standardize the representation of data collected from preclinical radiobiology and radiation oncology studies as a way to facilitate knowledge discovery. To achieve this goal, we combined ontology with semantic Web techniques to publish mapped data and easily query them using SPARQL Protocol and RDF Query Language (SPARQL). Results: We expanded the Radiation Oncology Ontology (ROO) to include terminology related to the exposure of animal models to treatment, animal model’s demographic characteristics; as well as clinical information in live animals. The extended ROO contains 123 new entities (89 classes, 29 data properties and 5 object properties). We combined the extended ontology with Semantic Web technologies to demonstrate how to integrate and query data from different relational databases. Discussion: The use of ontologies and semantic web tools are a way to comply to the FAIR principles. FAIR preclinical data improve collaboration, transparency, and reproducibility in radiotherapy research.
BackgroundWithin the Open Biological and Biomedical Ontology (OBO) Foundry, many ontologies represent the execution of a plan specification as a process in which a realizable entity that concretizes the plan specification, a "realizable concretization" (RC), is realized. This representation, which we call the "RC-account", provides a straightforward way to relate a plan specification to the entity that bears the realizable concretization and the process that realizes the realizable concretization. However, the adequacy of the RC-account has not been evaluated in the scientific literature. In this manuscript, we provide this evaluation and, thereby, give ontology developers sound reasons to use or not use the RC-account pattern.ResultsAnalysis of the RC-account reveals that it is not adequate for representing failed plans. If the realizable concretization is flawed in some way, it is unclear what (if any) relation holds between the realizable entity and the plan specification. If the execution (i.e., realization) of the realizable concretization fails to carry out the actions given in the plan specification, it is unclear under the RC-account how to directly relate the failed execution to the entity carrying out the instructions given in the plan specification. These issues are exacerbated in the presence of changing plans.ConclusionsWe propose two solutions for representing failed plans. The first uses the Common Core Ontologies 'prescribed by' relation to connect a plan specification to the entity or process that utilizes the plan specification as a guide. The second, more complex, solution incorporates the process of creating a plan (in the sense of an intention to execute a plan specification) into the representation of executing plan specifications. We hypothesize that the first solution (i.e., use of 'prescribed by') is adequate for most situations. However, more research is needed to test this hypothesis as well as explore the other solutions presented in this manuscript.
BACKGROUND:The exploration of cancer vaccines has yielded a multitude of studies, resulting in a diverse collection of information. The heterogeneity of cancer vaccine data significantly impedes effective integration and analysis. While CanVaxKB serves as a pioneering database for over 670 manually annotated cancer vaccines, it is important to distinguish that a database, on its own, does not offer the structured relationships and standardized definitions found in an ontology. Recognizing this, we expanded the Vaccine Ontology (VO) to include those cancer vaccines present in CanVaxKB that were not initially covered, enhancing VO's capacity to systematically define and interrelate cancer vaccines. RESULTS:An ontology design pattern (ODP) was first developed and applied to semantically represent various cancer vaccines, capturing their associated entities and relations. By applying the ODP, we generated a cancer vaccine template in a tabular format and converted it into the RDF/OWL format for generation of cancer vaccine terms in the VO. '12MP vaccine' was used as an example of cancer vaccines to demonstrate the application of the ODP. VO also reuses reference ontology terms to represent entities such as cancer diseases and vaccine hosts. Description Logic (DL) and SPARQL query scripts were developed and used to query for cancer vaccines based on different vaccine's features and to demonstrate the versatility of the VO representation. Additionally, ontological modeling was applied to illustrate cancer vaccine related concepts and studies for in-depth cancer vaccine analysis. A cancer vaccine-specific VO view, referred to as "CVO," was generated, and it contains 928 classes including 704 cancer vaccines. The CVO OWL file is publicly available on: http://purl.obolibrary.org/obo/vo/cvo.owl , for sharing and applications. CONCLUSION:To facilitate the standardization, integration, and analysis of cancer vaccine data, we expanded the Vaccine Ontology (VO) to systematically model and represent cancer vaccines. We also developed a pipeline to automate the inclusion of cancer vaccines and associated terms in the VO. This not only enriches the data's standardization and integration, but also leverages ontological modeling to deepen the analysis of cancer vaccine information, maximizing benefits for researchers and clinicians. AVAILABILITY:The VO-cancer GitHub website is: https://github.com/vaccineontology/VO/tree/master/CVO .