23
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Pattern matching through Chaos Game Representation: bridging numerical and discrete data structures for biological sequence analysis

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Chaos Game Representation (CGR) is an iterated function that bijectively maps discrete sequences into a continuous domain. As a result, discrete sequences can be object of statistical and topological analyses otherwise reserved to numerical systems. Characteristically, CGR coordinates of substrings sharing an L-long suffix will be located within 2 -L distance of each other. In the two decades since its original proposal, CGR has been generalized beyond its original focus on genomic sequences and has been successfully applied to a wide range of problems in bioinformatics. This report explores the possibility that it can be further extended to approach algorithms that rely on discrete, graph-based representations.

          Results

          The exploratory analysis described here consisted of selecting foundational string problems and refactoring them using CGR-based algorithms. We found that CGR can take the role of suffix trees and emulate sophisticated string algorithms, efficiently solving exact and approximate string matching problems such as finding all palindromes and tandem repeats, and matching with mismatches. The common feature of these problems is that they use longest common extension (LCE) queries as subtasks of their procedures, which we show to have a constant time solution with CGR. Additionally, we show that CGR can be used as a rolling hash function within the Rabin-Karp algorithm.

          Conclusions

          The analysis of biological sequences relies on algorithmic foundations facing mounting challenges, both logistic (performance) and analytical (lack of unifying mathematical framework). CGR is found to provide the latter and to promise the former: graph-based data structures for sequence analysis operations are entailed by numerical-based data structures produced by CGR maps, providing a unifying analytical framework for a diversity of pattern matching problems.

          Related collections

          Most cited references26

          • Record: found
          • Abstract: found
          • Article: not found

          Alignment-free sequence comparison-a review.

          Genetic recombination and, in particular, genetic shuffling are at odds with sequence comparison by alignment, which assumes conservation of contiguity between homologous segments. A variety of theoretical foundations are being used to derive alignment-free methods that overcome this limitation. The formulation of alternative metrics for dissimilarity between sequences and their algorithmic implementations are reviewed. The overwhelming majority of work on alignment-free sequence has taken place in the past two decades, with most reports published in the past 5 years. Two main categories of methods have been proposed-methods based on word (oligomer) frequency, and methods that do not require resolving the sequence with fixed word length segments. The first category is based on the statistics of word frequency, on the distances defined in a Cartesian space defined by the frequency vectors, and on the information content of frequency distribution. The second category includes the use of Kolmogorov complexity and Chaos Theory. Despite their low visibility, alignment-free metrics are in fact already widely used as pre-selection filters for alignment-based querying of large applications. Recent work is furthering their usage as a scale-independent methodology that is capable of recognizing homology when loss of contiguity is beyond the possibility of alignment. Most of the alignment-free algorithms reviewed were implemented in MATLAB code and are available at http://bioinformatics.musc.edu/resources.html
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Dinucleotide relative abundance extremes: a genomic signature.

            Early biochemical experiments established that the set of dinucleotide odds ratios or 'general design' is a remarkably stable property of the DNA of an organism, which is essentially the same in protein-coding DNA, bulk genomic DNA, and in different renaturation rate and density gradient fractions of genomic DNA in many organisms. Analysis of currently available genomic sequence data has extended these earlier results, showing that the general designs of disjoint samples of a genome are substantially more similar to each other than to those of sequences from other organisms and that closely related organisms have similar general designs. From this perspective, the set of dinucleotide odds ratio (relative abundance) values constitute a signature of each DNA genome, which can discriminate between sequences from different organisms. Dinucleotide-odds ratio values appear to reflect not only the chemistry of dinucleotide stacking energies and base-step conformational preferences, but also the species-specific properties of DNA modification, replication and repair mechanisms.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              On-line construction of suffix trees

              E Ukkonen (1995)
                Bookmark

                Author and article information

                Journal
                Algorithms Mol Biol
                Algorithms Mol Biol
                Algorithms for Molecular Biology : AMB
                BioMed Central
                1748-7188
                2012
                2 May 2012
                : 7
                : 10
                Affiliations
                [1 ]Instituto de Engenharia de Sistemas e Computadores: Investigação e Desenvolvimento (INESC-ID), R. Alves Redol 9, 1000-029 Lisboa, Portugal
                [2 ]Dept Bioestatística e Informática, Faculdade de Ciências Médicas - Universidade Nova de Lisboa (FCM/UNL), C. Mártires Pátria 130, 1169-056 Lisboa, Portugal
                [3 ]Instituto de Telecomunicações (IT), Av. Rovisco Pais 1, Torre Norte, Piso 10, 1049-001 Lisboa, Portugal
                [4 ]Instituto Superior Técnico, Universidade Técnica de Lisboa (IST/UTL), Av. Rovisco Pais 1, 1049-001 Lisboa, Portugal
                [5 ]Div Informatics, Dept Pathology, University of Alabama at Birmingham, USA
                Article
                1748-7188-7-10
                10.1186/1748-7188-7-10
                3402988
                22551152
                48ccbd9b-822e-4d0a-967d-f481a63afcbd
                Copyright ©2012 Vinga et al.; licensee BioMed Central Ltd.

                This is an open access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 25 January 2012
                : 2 May 2012
                Categories
                Research

                Molecular biology
                Molecular biology

                Comments

                Comment on this article