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SEGMENT: identifying compositional domains in DNA sequences
DOI:10.1093/bioinformatics/15.12.974.png)
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Abstract
Motivation: DNA sequences are formed by patches or domains of different nucleotide composition. In a few simple sequences, domains can simply be identified by eye; however, most DNA sequences show a complex compositional heterogeneity (fractal structure), which cannot be properly detected by current methods. Recently, a computationally efficient segmentation method to analyse such nonstationary sequence structures, based on the Jensen–Shannon entropic divergence, has been described. Specific algorithms implementing this method are now needed.
Results: Here we describe a heuristic segmentation algorithm for DNA sequences, which was implemented on a Windows program (SEGMENT). The program divides a DNA sequence into compositionally homogeneous domains by iterating a local optimization procedure at a given statistical significance. Once a sequence is partitioned into domains, a global measure of sequence compositional complexity (SCC), accounting for both the sizes and compositional biases of all the domains in the sequence, is derived. SEGMENT computes SCC as a function of the significance level, which provides a multiscale view of sequence complexity.
Availability: SEGMENT is available on the Web at http://www.ugr.es/local/oliver/segment/
Contact: oliver@ugr.es
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