Cafe Variome: General-Purpose Software for Making Genotype-Phenotype Data Discoverable in Restricted or Open Access Contexts

Owen Lancaster, Tim Beck, David Atlan, Morris Swertz, Dhiwagaran Thangavelu, Colin Veal, Raymond Dalgleish, Anthony J. Brookes*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

26 Citations (Scopus)

Abstract

Biomedical data sharing is desirable, but problematic. Data "discovery" approaches-which establish the existence rather than the substance of data-precisely connect data owners with data seekers, and thereby promote data sharing. Cafe Variome (http://www.cafevariome.org) was therefore designed to provide a general-purpose, Web-based, data discovery tool that can be quickly installed by any genotype-phenotype data owner, or network of data owners, to make safe or sensitive content appropriately discoverable. Data fields or content of any type can be accommodated, from simple ID and label fields through to extensive genotype and phenotype details based on ontologies. The system provides a "shop window" in front of data, with main interfaces being a simple search box and a powerful "query-builder" that enable very elaborate queries to be formulated. After a successful search, counts of records are reported grouped by "openAccess" (data may be directly accessed), "linked-Access" (a source link is provided), and "restrictedAccess" (facilitated data requests and subsequent provision of approved records). An administrator interface provides a wide range of options for system configuration, enabling highly customized single-site or federated networks to be established. Current uses include rare disease data discovery, patient matchmaking, and a Beacon Web service. (C) 2015 Wiley Periodicals, Inc.

Original languageEnglish
Pages (from-to)957-964
Number of pages8
JournalHuman Mutation
Volume36
Issue number10
DOIs
Publication statusPublished - Oct-2015

Keywords

  • Cafe Variome
  • genotype-phenotype
  • data discovery
  • software
  • rare disease
  • Matchmaker Exchange

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