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1.
BMC Med Inform Decis Mak ; 19(Suppl 7): 276, 2019 12 23.
Artigo em Inglês | MEDLINE | ID: mdl-31865899

RESUMO

BACKGROUND: The medical community uses a variety of data standards for both clinical and research reporting needs. ISO 11179 Common Data Elements (CDEs) represent one such standard that provides robust data point definitions. Another standard is the Biomedical Research Integrated Domain Group (BRIDG) model, which is a domain analysis model that provides a contextual framework for biomedical and clinical research data. Mapping the CDEs to the BRIDG model is important; in particular, it can facilitate mapping the CDEs to other standards. Unfortunately, manual mapping, which is the current method for creating the CDE mappings, is error-prone and time-consuming; this creates a significant barrier for researchers who utilize CDEs. METHODS: In this work, we developed a semi-automated algorithm to map CDEs to likely BRIDG classes. First, we extended and improved our previously developed artificial neural network (ANN) alignment algorithm. We then used a collection of 1284 CDEs with robust mappings to BRIDG classes as the gold standard to train and obtain the appropriate weights of six attributes in CDEs. Afterward, we calculated the similarity between a CDE and each BRIDG class. Finally, the algorithm produces a list of candidate BRIDG classes to which the CDE of interest may belong. RESULTS: For CDEs semantically similar to those used in training, a match rate of over 90% was achieved. For those partially similar, a match rate of 80% was obtained and for those with drastically different semantics, a match rate of up to 70% was achieved. DISCUSSION: Our semi-automated mapping process reduces the burden of domain experts. The weights are all significant in six attributes. Experimental results indicate that the availability of training data is more important than the semantic similarity of the testing data to the training data. We address the overfitting problem by selecting CDEs randomly and adjusting the ratio of training and verification samples. CONCLUSIONS: Experimental results on real-world use cases have proven the effectiveness and efficiency of our proposed methodology in mapping CDEs with BRIDG classes, both those CDEs seen before as well as new, unseen CDEs. In addition, it reduces the mapping burden and improves the mapping quality.


Assuntos
Pesquisa Biomédica , Elementos de Dados Comuns , Neoplasias , Redes Neurais de Computação , Algoritmos , Humanos , Projetos de Pesquisa , Semântica
2.
Cancer Res ; 84(9): 1384-1387, 2024 May 02.
Artigo em Inglês | MEDLINE | ID: mdl-38488505

RESUMO

The NCI Cancer Research Data Commons (CRDC) is a collection of data commons, analysis platforms, and tools that make existing cancer data more findable and accessible by the cancer research community. In practice, the two biggest hurdles to finding and using data for discovery are the wide variety of models and ontologies used to describe data, and the dispersed storage of that data. Here, we outline core CRDC services to aggregate descriptive information from multiple studies for findability via a single interface and to provide a single access method that spans multiple data commons. See related articles by Wang et al., p. 1388, Pot et al., p. 1396, and Kim et al., p. 1404.


Assuntos
National Cancer Institute (U.S.) , Neoplasias , Humanos , Estados Unidos , Neoplasias/terapia , Pesquisa Biomédica/normas , Bases de Dados Factuais
3.
AMIA Jt Summits Transl Sci Proc ; 2020: 517-526, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32477673

RESUMO

While using data standards can facilitate research by making it easier to share data, manually mapping to data standards creates an obstacle to their adoption. Semi-automated mapping strategies can reduce the manual mapping burden. Machine learning approaches, such as artificial neural networks, can predict mappings between clinical data standards but are limited by the need for training data. We developed a graph database that incorporates the Biomedical Research Integrated Domain Group (BRIDG) model, Common Data Elements (CDEs) from the National Cancer Institute's (NCI) cancer Data Standards Registry and Repository, and the NCI Thesaurus. We then used a shortest path algorithm to predict mappings from CDEs to classes in the BRIDG model. The resulting graph database provides a robust semantic framework for analysis and quality assurance testing. Using the graph database to predict CDE to BRIDG class mappings was limited by the subjective nature of mapping and data quality issues.

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