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Computing distribution of scale independent motifs in biological sequences

Jonas S Almeida1 email and Susana Vinga2,3 email

Dept Biostatistics and Applied Mathematics, Univ. Texas MDAnderson Cancer Center, 1515 Holcombe Blvd, Houston TX 77030-4009, USA

Instituto de Engenharia de Sistemas e Computadores: Investigação e Desenvolvimento (INESC-ID), R. Alves Redol 9, 1000-029 Lisboa, Portugal

Departamento de Bioestatística e Informática, Faculdade de Ciências Médicas – Universidade Nova de Lisboa (FCM/UNL), Campo dos Mártires da Pátria 130, 1169-056 Lisboa, Portugal

author email corresponding author email

Algorithms for Molecular Biology 2006, 1:18doi:10.1186/1748-7188-1-18

Published: 18 October 2006

Abstract

The use of Chaos Game Representation (CGR) or its generalization, Universal Sequence Maps (USM), to describe the distribution of biological sequences has been found objectionable because of the fractal structure of that coordinate system. Consequently, the investigation of distribution of symbolic motifs at multiple scales is hampered by an inexact association between distance and sequence dissimilarity. A solution to this problem could unleash the use of iterative maps as phase-state representation of sequences where its statistical properties can be conveniently investigated. In this study a family of kernel density functions is described that accommodates the fractal nature of iterative function representations of symbolic sequences and, consequently, enables the exact investigation of sequence motifs of arbitrary lengths in that scale-independent representation. Furthermore, the proposed kernel density includes both Markovian succession and currently used alignment-free sequence dissimilarity metrics as special solutions. Therefore, the fractal kernel described is in fact a generalization that provides a common framework for a diverse suite of sequence analysis techniques.


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