| Literature DB >> 17038345 |
Guillaume Achaz1, Frédéric Boyer, Eduardo P C Rocha, Alain Viari, Eric Coissac.
Abstract
UNLABELLED: Chromosomes or other long DNA sequences contain many highly similar repeated sub-sequences. While there are efficient methods for detecting strict repeats or detecting already characterized repeats, there is no software available for detecting approximate repeats in large DNA sequences allowing for weighted substitutions and indels in a coherent statistical framework. Here, we present an implementation of a two-steps method (seed detection followed by their extension) that detects those approximate repeats. Our method is computationally efficient enough to handle large sequences and is flexible enough to account for influencing factors, such as sequence-composition biases both at the seed detection and alignment levels. AVAILABILITY: http://wwwabi.snv.jussieu.fr/public/RepSeek/Mesh:
Substances:
Year: 2006 PMID: 17038345 DOI: 10.1093/bioinformatics/btl519
Source DB: PubMed Journal: Bioinformatics ISSN: 1367-4803 Impact factor: 6.937