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Merge pull request #157 from CBIIT/PODCAT-731
Merge Podcat 731 to dev branch
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public/User Guide for CCDC v1.2.0.pdf

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src/pages/glossaryPage/index.js

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<div className="r">
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<h2 className="glossaryItemHeader">Repository</h2>
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<span className="glossaryItemType">Resource Type</span>
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<p className="glossaryItemDescription">Biomedical data repositories accept submission of relevant data from the community to store, organize, validate, archive, preserve and distribute the data, in compliance with the FAIR Data Principles. A system for storing multiple research artifacts, provided at least some of the research artifacts contain Individual Research Data. A data repository often contains artifacts from multiple studies. Some data repositories accept research datasets irrespective of the structure of those datasets; other data repositories require all research datasets to conform to a standard reference model.</p>
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<p className="glossaryItemDescription">Biomedical data repositories store, organize, validate, archive, preserve, and distribute data, in compliance with the FAIR Data Principles. It is a system for storing multiple research artifacts, provided at least some of the research artifacts contain Individual Research Data. A data repository often contains artifacts from multiple studies. Some data repositories accept research datasets irrespective of the structure of those datasets; other data repositories require all research datasets to conform to a standard reference model.</p>
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<div className="r">

src/pages/participatingResourceDetailPage/ParticipatingResourceDetail.js

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}) => {
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const { id } = useParams();
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const tooltips = {
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Repository: "Biomedical data repositories accept submission of relevant data from the community to store, organize, validate, archive, preserve and distribute the data, in compliance with the FAIR Data Principles. A system for storing multiple research artifacts, provided at least some of the research artifacts contain Individual Research Data. A data repository often contains artifacts from multiple studies. Some data repositories accept research datasets irrespective of the structure of those datasets; other data repositories require all research datasets to conform to a standard reference model.",
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Repository: "Biomedical data repositories store, organize, validate, archive, preserve, and distribute data, in compliance with the FAIR Data Principles. It is a system for storing multiple research artifacts, provided at least some of the research artifacts contain Individual Research Data. A data repository often contains artifacts from multiple studies. Some data repositories accept research datasets irrespective of the structure of those datasets; other data repositories require all research datasets to conform to a standard reference model.",
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Catalog: "A data catalog is not a data repository but rather a place where data is described with an index to what is available. A collection of digests and references (e.g., URL or POC) to corresponding research artifacts. There is a consistent structure across the collection of digests to facilitate filtering and identifying research artifacts of interest. A catalog contains some combination of Summary Research Data, Summary Clinical Data, Data Overview, and Resource Metadata.",
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Collection: "A group of datasets collected together for any reason by an organization of researchers, stewards, or stakeholders either pertaining to a common theme or for a common purpose. For example, the Treehouse Childhood Cancer Initiative maintains a collection of cell line data as part of their repository of pediatric cancer genomic data.",
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Knowledgebase: "Biomedical knowledgebases extract, accumulate, organize, annotate, and link the growing body of information that is related to and relies on core datasets.",

src/pages/participatingResourcesPage/SearchResult/SearchResult.js

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resultList,
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const tooltips = {
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Repository: "Biomedical data repositories accept submission of relevant data from the community to store, organize, validate, archive, preserve and distribute the data, in compliance with the FAIR Data Principles. A system for storing multiple research artifacts, provided at least some of the research artifacts contain Individual Research Data. A data repository often contains artifacts from multiple studies. Some data repositories accept research datasets irrespective of the structure of those datasets; other data repositories require all research datasets to conform to a standard reference model.",
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Repository: "Biomedical data repositories store, organize, validate, archive, preserve, and distribute data, in compliance with the FAIR Data Principles. It is a system for storing multiple research artifacts, provided at least some of the research artifacts contain Individual Research Data. A data repository often contains artifacts from multiple studies. Some data repositories accept research datasets irrespective of the structure of those datasets; other data repositories require all research datasets to conform to a standard reference model.",
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Catalog: "A data catalog is not a data repository but rather a place where data is described with an index to what is available. A collection of digests and references (e.g., URL or POC) to corresponding research artifacts. There is a consistent structure across the collection of digests to facilitate filtering and identifying research artifacts of interest. A catalog contains some combination of Summary Research Data, Summary Clinical Data, Data Overview, and Resource Metadata.",
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Knowledgebase: "Biomedical knowledgebases extract, accumulate, organize, annotate, and link the growing body of information that is related to and relies on core datasets.",
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Registry: "A cancer registry is an information system designed for the collection, storage, and management of data on persons with cancer. An inventory of individuals or samples, usually focused on a specific diagnosis or condition. In some cases, public health laws require collecting information in registries about individuals who have a specific disease or condition. In other cases, individuals provide information about themselves to these registries voluntarily. Thus, a registry contains Individual Clinical Data, but not Individual Research Data.",

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