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PMID: 26224250 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cafe Variome: general-purpose software for making genotype-phenotype data discoverable in restricted or open access contexts.

Human mutation ·Vol. 36 ·No. 10 ·2015-10-00 ·Pages 957-64

Lancaster O, Beck T, Atlan D, Swertz M, Thangavelu D, Veal C, Dalgleish R, Brookes AJ

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), "linkedAccess" (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.

Keywords
Cafe Variome Matchmaker Exchange data discovery genotype-phenotype rare disease software
MeSH Terms
Databases, Bibliographic Genetic Predisposition to Disease Genotype Humans Information Dissemination/methods Phenotype Rare Diseases/genetics Software User-Computer Interface Web Browser
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Lancaster Owen
Department of Genetics, University of Leicester, Leicester, UK.
Beck Tim
Department of Genetics, University of Leicester, Leicester, UK.
Atlan David
PhenoSystems SA, Belgium.
Swertz Morris
University Medical Center Groningen, The Netherlands.
Thangavelu Dhiwagaran
Department of Genetics, University of Leicester, Leicester, UK.
Veal Colin
Department of Genetics, University of Leicester, Leicester, UK.
Dalgleish Raymond
Department of Genetics, University of Leicester, Leicester, UK.
Brookes Anthony J
Department of Genetics, University of Leicester, Leicester, UK.
Article Info
Journal
Human mutation
Abbr.
Hum Mutat
ISSN
1098-1004
Published
2015-10-00
Epub
2015-00-25
Pages
957-64
Language
English
Region
United States
NLM ID
9215429
Subset
IM
Analysis Services
Analysis Services

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