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1.
AMIA Annu Symp Proc ; 2019: 681-690, 2019.
Article in English | MEDLINE | ID: mdl-32308863

ABSTRACT

Developing promising treatments in biomedicine often requires aggregation and analysis of data from disparate sources across the healthcare and research spectrum. To facilitate these approaches, there is a growing focus on supporting interoperation of datasets by standardizing data-capture and reporting requirements. Common Data Elements (CDEs)-precise specifications of questions and the set of allowable answers to each question-are increasingly being adopted to help meet these standardization goals. While CDEs can provide a strong conceptual foundation for interoperation, there are no widely recognized serialization or interchange formats to describe and exchange their definitions. As a result, CDEs defined in one system cannot be easily be reused by other systems. An additional problem is that current CDE-based systems tend to be rather heavyweight and cannot be easily adopted and used by third-parties. To address these problems, we developed extensions to a metadata management system called the CEDAR Workbench to provide a platform to simplify the creation, exchange, and use of CDEs. We show how the resulting system allows users to quickly define and share CDEs and to immediately use these CDEs to build and deploy Web-based forms to acquire conforming metadata. We also show how we incorporated a large CDE library from the National Cancer Institute's caDSR system and made these CDEs publicly available for general use.


Subject(s)
Biomedical Research , Common Data Elements , Data Collection/standards , Data Management/methods , Common Data Elements/standards , Data Management/standards , Humans , Internet , Metadata , National Institutes of Health (U.S.) , Registries , United States , User-Computer Interface
3.
J Biomed Inform ; 41(1): 106-23, 2008 Feb.
Article in English | MEDLINE | ID: mdl-17512259

ABSTRACT

One of the requirements for a federated information system is interoperability, the ability of one computer system to access and use the resources of another system. This feature is particularly important in biomedical research systems, which need to coordinate a variety of disparate types of data. In order to meet this need, the National Cancer Institute Center for Bioinformatics (NCICB) has created the cancer Common Ontologic Representation Environment (caCORE), an interoperability infrastructure based on Model Driven Architecture. The caCORE infrastructure provides a mechanism to create interoperable biomedical information systems. Systems built using the caCORE paradigm address both aspects of interoperability: the ability to access data (syntactic interoperability) and understand the data once retrieved (semantic interoperability). This infrastructure consists of an integrated set of three major components: a controlled terminology service (Enterprise Vocabulary Services), a standards-based metadata repository (the cancer Data Standards Repository) and an information system with an Application Programming Interface (API) based on Domain Model Driven Architecture. This infrastructure is being leveraged to create a Semantic Service-Oriented Architecture (SSOA) for cancer research by the National Cancer Institute's cancer Biomedical Informatics Grid (caBIG).


Subject(s)
Computational Biology/methods , Database Management Systems , Databases, Factual , Information Storage and Retrieval/methods , Meta-Analysis as Topic , Models, Theoretical , Vocabulary, Controlled , Internet , National Cancer Institute (U.S.) , Semantics , United States
4.
BMC Med Inform Decis Mak ; 6: 25, 2006 Jun 20.
Article in English | MEDLINE | ID: mdl-16787533

ABSTRACT

BACKGROUND: The Cancer Biomedical Informatics Grid (caBIG) is a network of individuals and institutions, creating a world wide web of cancer research. An important aspect of this informatics effort is the development of consistent practices for data standards development, using a multi-tier approach that facilitates semantic interoperability of systems. The semantic tiers include (1) information models, (2) common data elements, and (3) controlled terminologies and ontologies. The College of American Pathologists (CAP) cancer protocols and checklists are an important reporting standard in pathology, for which no complete electronic data standard is currently available. METHODS: In this manuscript, we provide a case study of Cancer Common Ontologic Representation Environment (caCORE) data standard implementation of the CAP cancer protocols and checklists model--an existing and complex paper based standard. We illustrate the basic principles, goals and methodology for developing caBIG models. RESULTS: Using this example, we describe the process required to develop the model, the technologies and data standards on which the process and models are based, and the results of the modeling effort. We address difficulties we encountered and modifications to caCORE that will address these problems. In addition, we describe four ongoing development projects that will use the emerging CAP data standards to achieve integration of tissue banking and laboratory information systems. CONCLUSION: The CAP cancer checklists can be used as the basis for an electronic data standard in pathology using the caBIG semantic modeling methodology.


Subject(s)
Database Management Systems , Internet , Medical Informatics , Medical Oncology/standards , Neoplasms/pathology , Pathology, Clinical/standards , Clinical Protocols , Humans , National Institutes of Health (U.S.) , Natural Language Processing , Neoplasms/classification , Semantics , Systems Integration , United States , User-Computer Interface , Vocabulary, Controlled
5.
AMIA Annu Symp Proc ; 2003(2003): 1048, 2003.
Article in English | MEDLINE | ID: mdl-14728551

ABSTRACT

The NCI provides the cancer Data Standards Repository (caDSR) to support development and deployment of CDEs in cancer research. The caDSR, part of the NCI caCORE infrastructure, supports data management workflow requirements and adherence to ISO/IEC 11179 metadata standards. CDEs are developed using standard terminology from caCORE vocabulary services, and are then deployed to multi-site clinical trials data management systems. Here we describe the caDSR and how CDEs are managed and deployed in clinical research.


Subject(s)
Clinical Trials as Topic/standards , Biomedical Research/standards , Clinical Trials as Topic/statistics & numerical data , Humans , Terminology as Topic , Vocabulary, Controlled
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