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Content owners and end users include NCI and its partners in clinical trials, academic institutions (including NCI Designated Cancer Centers, SPOREs and NCTN/ETCTN), other NIH institutes (including NICHD, NHLBI, NCATS and NIDCR), other federal agencies (in particular the FDA), pharmaceutical companies, standards development organizations (e.g. CDISC) and a range of international biomedical organizations. For more information see the caDSR Collaborations and Use.
Requirements from researchers and/or their supporting informatics groups drive the creation of metadata in the caDSR. Metadata content development usually starts with a request for assistance by a researcher planning clinical or research data collection. Metadata curators work with the user and EVS to identify appropriate vocabulary while identifying a mix of new and existing CDE content to support the scientific requirement. Curators always attempt to reuse existing metadata (where that content supports the scientific requirement) as a way to help scientists ensure the compatibility of their data with other data collected across the enterprise, and sometimes researchers request that their content be harmonized with specific existing projects.
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- caDSR Database and Tools
Provides access to caDSR tools and links to the tool summary page for current user documentation and technical information like release notes.caDSR for Application Developers
Focuses on the software interfaces to the caDSR available to programmers and software developers. The pages include details on the caDSR API, XML messages produced and consumed by the caDSR products and the caDSR UML Model.caDSR Installation and Implementation
Focuses on Open Source adoption of the
- caDSR Database and Tools. The pages include ISO 11179 implementation extensions, software implementation architectures and Downloads.
caDSR Future Requirements
We continually look at new requirements and have an initiative begun in 2014 to replace the aging software and infrastructure currently supporting caDSR end users. This is an opportunity to link our efforts more broadly with NIH wide CDE and metadata initiatives. Please see the caDSR Requirements pages for more information.
Documentation
For a complete list of current caDSR Tool user documentation, application guides, release notes, and FAQs, see the caDSR Documentation wiki page.
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List/Forum | Email address or URL | Description |
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For end user issues regarding the caDSR tools and content | ||
For developer issues regarding the caDSR APIs and use of caDSR Metadata | ||
Archive for content users such as Curators | ||
Archive for developers using caDSR Metadata, such as UML Model owners (subscription required) | ||
For adopters | ||
None | Index of all NIH mail lists | |
Application Support |
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Komatsoulis, G.A., Warzel, D.B., Hartel, F.W., Shanbhag, K, Chilukuri, R, Fragoso, G., de Coronado, S, Reeves, D.M., Hadfield, J.B., Ludet, C., and P.A. Covitz (2007) "caCORE version 3: Implementation of a model driven, service-oriented architecture for semantic interoperability." Journal of Biomed Informatics. 2008 February; 41(1): 106--123. Published online 2007 April 2. doi: 10.1016/j.jbi.2007.03.009.
To cite the caDSR Form Builder OneData general software, use the following reference.
NCI caDSR Form BuilderOneData. <https://formbuildercadsr.ncicancer.nih.gov/FormBuilderonedata/formSearchActionHome.dojsp> National Cancer Institute, Center for Biomedical Informatics and Information Technology, 01 Oct. 2010. Web. 17 Jan. 2013.
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"[Protocol or Classification Scheme Name]." [Context name], [Node name], NCI caDSR Form BuilderOneData. <https://formbuildercadsr.nci.nih.govcancer.gov/onedata/Home.jsp> National Cancer Institute, Center for Biomedical Informatics and Information Technology, 01 Oct. 2010. Web. 17 Jan. 2013
Example: " CALGB: 10603 Treatment Form ." CTEP, Protocol Forms, NCI caDSR Form BuilderOneData. <https://formbuildercadsr.nci.nih.govcancer.gov/onedata/Home.jsp> National Cancer Institute, Center for Biomedical Informatics and Information Technology, 01 Oct. 2010. Web. 17 Jan. 2013
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