Show simple item record

dc.contributor.authorHancock, John M
dc.contributor.authorAdams, Niels C
dc.contributor.authorAidinis, Vassilis
dc.contributor.authorBlake, Andrew
dc.contributor.authorBogue, Molly
dc.contributor.authorBrown, Steve D M
dc.contributor.authorChesler, Elissa J
dc.contributor.authorDavidson, Duncan
dc.contributor.authorDuran, Christopher
dc.contributor.authorEppig, Janan T
dc.contributor.authorGailus-Durner, Valérie
dc.contributor.authorGates, Hilary
dc.contributor.authorGkoutos, Georgios V
dc.contributor.authorGreenaway, Simon
dc.contributor.authorHrabé de Angelis, Martin
dc.contributor.authorKollias, George
dc.contributor.authorLeblanc, Sophie
dc.contributor.authorLee, Kirsty
dc.contributor.authorLengger, Christoph
dc.contributor.authorMaier, Holger
dc.contributor.authorMallon, Ann-Marie
dc.contributor.authorMasuya, Hiroshi
dc.contributor.authorMelvin, David G
dc.contributor.authorMüller, Werner
dc.contributor.authorParkinson, Helen
dc.contributor.authorProctor, Glenn
dc.contributor.authorReuveni, Eli
dc.contributor.authorSchofield, Paul
dc.contributor.authorShukla, Aadya
dc.contributor.authorSmith, Cynthia
dc.contributor.authorToyoda, Tetsuro
dc.contributor.authorVasseur, Laurent
dc.contributor.authorWakana, Shigeharu
dc.contributor.authorWalling, Alison
dc.contributor.authorWhite, Jacqui
dc.contributor.authorWood, Joe
dc.contributor.authorZouberakis, Michalis
dc.date.accessioned2009-02-03T15:13:12Z
dc.date.available2009-02-03T15:13:12Z
dc.date.issued2007-03
dc.identifier.citationMouse Phenotype Database Integration Consortium: integration [corrected] of mouse phenome data resources. 2007, 18 (3):157-63 Mamm. Genomeen
dc.identifier.issn0938-8990
dc.identifier.pmid17436037
dc.identifier.doi10.1007/s00335-007-9004-x
dc.identifier.urihttp://hdl.handle.net/10033/48394
dc.description.abstractUnderstanding 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.
dc.language.isoenen
dc.subject.meshAnimalsen
dc.subject.meshDatabases, Geneticen
dc.subject.meshGenomicsen
dc.subject.meshMiceen
dc.subject.meshMice, Inbred Strainsen
dc.subject.meshMice, Mutant Strainsen
dc.subject.meshPhenotypeen
dc.titleMouse Phenotype Database Integration Consortium: integration [corrected] of mouse phenome data resources.en
dc.typeArticleen
dc.identifier.journalMammalian genome : official journal of the International Mammalian Genome Societyen
refterms.dateFOA2018-06-12T22:59:44Z
html.description.abstractUnderstanding 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.


Files in this item

Thumbnail
Name:
Hancock et al_final.pdf
Size:
413.2Kb
Format:
PDF
Description:
original manuscript

This item appears in the following Collection(s)

Show simple item record