Library and Information Science Commons^™

Strategic Planning For Sustaining User-Generated Content In Digital Collections, Cory K. Lampert, Su Kim Chung

Library Faculty Presentations

• Should there be an overarching philosophy for user-generated content in the organization?

• Who in the management or leadership determines this philosophy or guides the organization to come up with a shared vision?

•What technical considerations are there for these projects? Are there staff that need to be consulted for software choices and technical customization?

•Is there are point person for the project and does this person have the authority and appropriate expertise to moderate content and respond to user’s contributions?

•Should there be appropriate guidelines for communicating an institutions’ brand or message in these new venues?

•And ultimately, …

Skos And The Semantic Web: Knowledge Organization, Metadata, And Interoperability, Eric A. Robinson

Other Topics

The Simplified Knowledge Organization System (SKOS) is a Semantic Web framework, based on the Resource Description Framework (RDF) for thesauri, classification schemes and simple ontologies. It allows for machine-actionable description of the structure of these knowledge organization systems (KOS) and provides an excellent tool for addressing interoperability and vocabulary control problems inherent to the rapidly expanding information environment of the Web. This paper discusses the foundations of the SKOS framework and reviews the literature on a variety of SKOS implementations. The limitations of SKOS that have been revealed through its broad application are addressed with brief attention to the proposed …

[Rd] Prism Library: Patient Registry Item Specifications And Metadata For Rare Diseases, Rachel L. Richesson, Denise Shereff, James E. Andrews

School of Information Faculty Publications

Patient registries are important for understanding the causes and origins of rare diseases and estimating their impact; and they may prove critical developing new diagnostics and therapeutics. This paper introduces the [RD] PRISM resource , an NIH-funded project to develop a library of standardized question and answer sets to support rare disease research. The paper presents a project case-driven plan for creating a new registry using questions from an existing related registry, revising and expanding an existing registry, and showing interoperability of data collected from different registries and data sources. Each of the use cases involves the retrieval of indexed …