Mouse Phenotype Database Integration Consortium: integration [corrected] of mouse phenome data resources.
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Authors
Hancock, John MAdams, Niels C
Aidinis, Vassilis
Blake, Andrew
Bogue, Molly
Brown, Steve D M
Chesler, Elissa J
Davidson, Duncan
Duran, Christopher
Eppig, Janan T
Gailus-Durner, Valérie
Gates, Hilary
Gkoutos, Georgios V
Greenaway, Simon
Hrabé de Angelis, Martin
Kollias, George
Leblanc, Sophie
Lee, Kirsty
Lengger, Christoph
Maier, Holger
Mallon, Ann-Marie
Masuya, Hiroshi
Melvin, David G
Müller, Werner
Parkinson, Helen
Proctor, Glenn
Reuveni, Eli
Schofield, Paul
Shukla, Aadya
Smith, Cynthia
Toyoda, Tetsuro
Vasseur, Laurent
Wakana, Shigeharu
Walling, Alison
White, Jacqui
Wood, Joe
Zouberakis, Michalis
Issue Date
2007-03
Metadata
Show full item recordAbstract
Understanding the functions encoded in the mouse genome will be central to an understanding of the genetic basis of human disease. To achieve this it will be essential to be able to characterize the phenotypic consequences of variation and alterations in individual genes. Data on the phenotypes of mouse strains are currently held in a number of different forms (detailed descriptions of mouse lines, first-line phenotyping data on novel mutations, data on the normal features of inbred lines) at many sites worldwide. For the most efficient use of these data sets, we have initiated a process to develop standards for the description of phenotypes (using ontologies) and file formats for the description of phenotyping protocols and phenotype data sets. This process is ongoing and needs to be supported by the wider mouse genetics and phenotyping communities to succeed. We invite interested parties to contact us as we develop this process further.Citation
Mouse Phenotype Database Integration Consortium: integration [corrected] of mouse phenome data resources. 2007, 18 (3):157-63 Mamm. GenomePubMed ID
17436037Type
ArticleLanguage
enISSN
0938-8990ae974a485f413a2113503eed53cd6c53
10.1007/s00335-007-9004-x
Scopus Count
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