Skip Navigation



Bioinformatics Advance Access published online on September 9, 2004
Bioinformatics, doi:10.1093/bioinformatics/bti017
Bioinformatics © Oxford University Press 2004; all rights reserved
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrow All Versions of this Article:
21/3/408    most recent
bti017v1
Right arrow Comments: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Comments are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Bradford, I.
Right arrow Articles by Bard, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bradford, I.
Right arrow Articles by Bard, J.
Social Bookmarking
Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Received June 29, 2004
Revised August 23, 2004
Accepted September 2, 2004

Article

Human-mouse gene searcher: a tool to assist discovery of malformation-associated genes by using phenotype databases

Ian Bradford 1*, Robin Winter** 1, Carl Evans 2, and Jonathan Bard 3

1 Institute of Child Health, 30 Guilford Street, London, WC1N 1EH, UK
2 School of Computing Science, Middlesex University, EH8 9XD, UK
3 Bioinformatics, Medical School, University of Edinburgh, EH8 9XD, UK

* To whom correspondence should be addressed. E-mail: i.bradford{at}ich.ucl.ac.uk.


  Abstract

An open-access World Wide Web application has been developed that enables the cross-linking of anatomical data on the phenotypic manifestations of human and mouse malformation syndromes to data on gene function and/or expression patterns in the mouse GXD database. Ultimately, the system has been designed to assist biologists in the process of discovering hitherto unidentified malformation genes. More specifically, it facilitates search from the phenotypic level. The application and further information is available at http://genetics.ich.ucl.ac.uk/linksearchtool.

** Deceased


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
 Brief Funct Genomic ProteomicHome page
J. M. Hancock and A.-M. Mallon
Phenobabelomics mouse phenotype data resources
Brief Funct Genomic Proteomic, January 11, 2008; (2008) elm033v1.
[Abstract] [Full Text] [PDF]


Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.