Skip Navigation



Bioinformatics Advance Access published online on September 16, 2004

Bioinformatics, doi:10.1093/bioinformatics/bti039
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:
21/5/582    most recent
bti039v1
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 arrowRequest Permissions
Google Scholar
Right arrow Articles by Campagna, D.
Right arrow Articles by Valle, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Campagna, D.
Right arrow Articles by Valle, G.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Received May 4, 2004
Revised August 2, 2004
Accepted August 23, 2004

Article

RAP: a new computer program for de novo identification of repeated sequences in whole genomes

Davide Campagna 1, Chiara Romualdi 1, Nicola Vitulo 1, Micky Del Favero 1, Matej Lexa 1, Nicola Cannata 1, and Giorgio Valle 1*

1 CRIBI, Università degli Studi di Padova, via Ugo Bassi 58b, I-35121 Padova, Italy

* To whom correspondence should be addressed. E-mail: giorgio.valle{at}unipd.it.


   Abstract

Motivation: DNA repeats are a common feature of most genomic sequences. Their de novo identification is still difficult despite being a crucial step in genomic analysis and oligonucleotides design. Several efficient algorithms based on word counting are available, but too short words decrease specificity while long words decrease sensitivity, particularly in degenerated repeats.

Results: The Repeat Analysis Program (RAP) is based on a new word-counting algorithm optimized for high resolution repeat identification using gapped words. Many different overlapping gapped words can be counted at the same genomic position, thus producing a better signal than the single ungapped word. This results in better specificity both in terms of low-frequency detection, being able to identify sequences repeated only once, and highly divergent detection, producing a generally high score in most intron sequences.

Availability: The program is freely available for non-profit organization, upon request to the authors.

Supplementary information: The program has been tested on the C. elegans genome using word lengths of 12, 14 and 16 bases. The full analysis has been implemented in the UCSC Genome Browser and is accessible at http://genome.cribi.unipd.it.


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
BioinformaticsHome page
X. Li, T. Kahveci, and A. M. Settles
A novel genome-scale repeat finder geared towards transposons
Bioinformatics, February 15, 2008; 24(4): 468 - 476.
[Abstract] [Full Text] [PDF]


Home page
Brief BioinformHome page
C. M. Bergman and H. Quesneville
Discovering and detecting transposable elements in genome sequences
Brief Bioinform, November 1, 2007; 8(6): 382 - 392.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
M. Hou, P. Berman, C.-H. Hsu, and R. S. Harris
HomologMiner: looking for homologous genomic groups in whole genomes
Bioinformatics, April 15, 2007; 23(8): 917 - 925.
[Abstract] [Full Text] [PDF]


Home page
BioinformaticsHome page
A. Morgulis, E. M. Gertz, A. A. Schaffer, and R. Agarwala
WindowMasker: window-based masker for sequenced genomes
Bioinformatics, January 15, 2006; 22(2): 134 - 141.
[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.