Integration of mouse phenome data resources

被引:33
作者
Hancock, John M. [1 ]
Adams, Niels C.
Aidinis, Vassilis
Blake, Andrew
Blake, Judith A.
Bogue, Molly
Brown, Steve D. M.
Chesler, Elissa
Davidson, Duncan
Duran, Christopher
Eppig, Janan T.
Gailus-Durner, Valerie
Gates, Hilary
Gkoutos, Georgios V.
Greenaway, Simon
De Angelis, Martin Hrabe
Kollias, George
Leblanc, Sophie
Lee, Kirsty
Lengger, Christoph
Maier, Holger
Mallon, Ann-Marie
Masuya, Hiroshi
Melvin, David G.
Mueller, 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
机构
[1] MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England
[2] Wellcome Trust Sanger Inst, Cambridge CB10 1SA, England
[3] BSRC Fleming, Athens 16672, Greece
[4] Jackson Lab, Bar Harbor, ME 04609 USA
[5] Oak Ridge Natl Lab, Mammalian Genet & Genom Grp, Biosci Div, Oak Ridge, TN 37831 USA
[6] MRC Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[7] GSF Natl Res Ctr Environm & Hlth, Inst Expt Genet, D-85764 Neuherberg, Germany
[8] Univ Cambridge, Dept Genet, Cambridge CB2 3EH, England
[9] Inst Clin Souris, F-67404 Illkirch Graffenstaden, France
[10] RIKEN, Genom Sci Ctr, Tsukuba, Ibaraki, Japan
[11] Helmholtz Zentrum Infektionsforsch GmbH, D-38124 Braunschweig, Germany
[12] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
[13] European Bioinformat Inst, Cambridge CB10 1SD, England
[14] EMBL Monterotondo Outstn, Mouse Biol Unit, I-00016 Monterotondo, Italy
[15] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3DY, England
[16] Univ Oxford, Comp Lab, Oxford OX1 3QD, England
[17] MRC, Mary Lyon Ctr, Didcot OX11 0RD, Oxon, England
关键词
D O I
10.1007/s00335-007-9004-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:157 / 163
页数:7
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