Skip Navigation

Nucleic Acids Research 2006 34(Web Server issue):W555-W559; doi:10.1093/nar/gkl224
This Article
Right arrow Full Text Freely available
Right arrow Print PDF (871K) Freely available
Right arrow Screen PDF (219K) Freely available
Right arrow Alert me when this article is cited
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 arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Sinha, S.
Right arrow Articles by Siggia, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sinha, S.
Right arrow Articles by Siggia, E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2006. Published by Oxford University Press. All rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org


Article

Stubb: a program for discovery and analysis of cis-regulatory modules

Saurabh Sinha*, Yupu Liang1 and Eric Siggia1

Department of Computer Science, University of Illinois, Urbana-Champaign NY, USA 1 Center for Studies in Physics and Biology, The Rockefeller University NY, USA

*To whom correspondence should be addressed. Tel: +1 217 333 3233; Fax: +1 217 244 6500; Email: sinhas{at}cs.uiuc.edu

Received February 14, 2006. Revised March 6, 2006. Accepted March 27, 2006.

Given the DNA-binding specificities (motifs) of one or more transcription factors, an important bioinformatics problem is to discover significant clusters of binding sites for the transcription factors(s). Such clusters often correspond to cis-regulatory modules mediating regulation of an adjacent gene. In earlier work, we developed the Stubb program that uses a probabilistic model and a maximum likelihood approach to efficiently detect cis-regulatory modules over genomic scales. It may optionally exploit a second related genome to improve module prediction accuracy. We describe here the use of a web-based interface for the Stubb program. The interface is equipped with a special post-processing step for in-depth analysis of specific modules, in order to reveal individual binding sites predicted in the module. The web server may be accessed at the URL http://stubb.rockefeller.edu/.


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
Nucleic Acids ResHome page
R. Alazard, L. Mourey, C. Ebel, P. V. Konarev, M. V. Petoukhov, D. I. Svergun, and M. Erard
Fine-tuning of intrinsic N-Oct-3 POU domain allostery by regulatory DNA targets
Nucleic Acids Res., July 26, 2007; 35(13): 4420 - 4432.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
D. Papatsenko
ClusterDraw web server: a tool to identify and visualize clusters of binding motifs for transcription factors
Bioinformatics, April 15, 2007; 23(8): 1032 - 1034.
[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.