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PMID: 15619965 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Visualizing the laboratory mouse: capturing phenotype information.

Genetica ·Vol. 122 ·No. 1 ·2004-09-00 ·Pages 89-97

Strivens M, Eppig JT

Abstract

A concerted effort to develop myriad new phenotypic alleles through mutagenesis programs presents new challenges for the biomedical community and for the informatics infrastructure needed to support this work. To handle and co-ordinate large programs of treatment, breeding, and sequential or longitudinal testing for a variety of obvious and subtle traits requires sophisticated data management software. Further, trait analyses, heritability testing, and animal availability and status must be captured and disseminated to the wider community. The Mouse Genome Database (MGD) will serve as the central integration point for the various mutagenesis programs, registering new alleles, providing accession identifiers, and capturing phenotypic descriptions. In addition, MGD will provide public access to unified searches over all alleles with links to the centres of origin for detailed testing data.

MeSH Terms
Animals Databases, Genetic Genome Mice/genetics Phenotype Terminology as Topic
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Strivens Mark
Informatics Group, Mammalian Genetics Unit, UK Mouse Genome Centre, Harwell, Oxfordshire, OX11 ORD, UK.
Eppig Janan T
Article Info
Journal
Genetica
Abbr.
Genetica
ISSN
0016-6707
Published
2004-09-00
Pages
89-97
Language
English
Region
Netherlands
NLM ID
0370740
Subset
IM
Grants
NHGRI NIH HHS · HG00330 · United States
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