Skip Navigation



Bioinformatics Advance Access published online on December 19, 2008

Bioinformatics, doi:10.1093/bioinformatics/btn653
This Article
Right arrow Advance Access manuscript (PDF) Freely available
Right arrowOA All Versions of this Article:
25/5/655    most recent
btn653v1
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
Google Scholar
Right arrow Articles by Chelala, C.
Right arrow Articles by Lemoine, N. R
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chelala, C.
Right arrow Articles by Lemoine, N. R
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

SNPnexus: A web database for functional annotation of newly discovered and public domain Single Nucleotide Polymorphisms

Claude Chelala 1,*, Arshad Khan 1 and Nicholas R Lemoine 1

1 Centre for Molecular Oncology and Imaging, Institute of Cancer & CR-UK Clinical Centre, Barts & The London School of Medicine (QMUL), Charterhouse Square London EC1M 6BQ, United Kingdom

*To whom correspondence should be addressed. Dr. Claude Chelala, E-mail: Claude.Chelala{at}cancer.org.uk


   Abstract

Motivation: Design a new computational tool allowing scientists to functionally annotate newly discovered and public domain Single Nucleotide Polymorphisms in order to help in prioritising targets in further disease studies and large-scale genotyping projects.

Summary: SNPnexus database provides functional annotation for both novel and public SNPs. Possible effects on the transcriptome and proteome levels are characterised and reported from five major annotation systems providing the most extensive information on alternative splicing. Additional information on HapMap genotype and allele frequency, overlaps with potential regulatory elements or structural variations as well as related genetic diseases can be also retrieved. The SNPnexus database has a user-friendly web inter-face, providing single or batch query options using SNP identifiers from dbSNP as well as genomic location on clones, contigs or chromosomes. Therefore, SNPnexus is the only database currently providing a complete set of functional annotations of SNPs in public databases and newly detected from sequencing projects. Hence, we describe SNPnexus, provide details of the query options, the anno-tation categories as well as biological examples of use.

Availability: The SNPnexus database is freely available at http://www.snp-nexus.org.

Contact: Claude.Chelala{at}cancer.org.uk

Associate Editor: Dr. Alex Bateman


Received on September 29, 2008; revised on November 25, 2008; accepted on December 17, 2008

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




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.