Universal sequence map (USM) of arbitrary discrete sequences

被引:39
作者
Almeida, JS
Vinga, S
机构
[1] Med Univ S Carolina, Dept Epidemiol & Biometry, Charleston, SC 29425 USA
[2] Univ Nova Lisboa, Inst Tecnol Quim & Biol, P-2781901 Oeiras, Portugal
关键词
D O I
10.1186/1471-2105-3-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: For over a decade the idea of representing biological sequences in a continuous coordinate space has maintained its appeal but not been fully realized. The basic idea is that any sequence of symbols may define trajectories in the continuous space conserving all its statistical properties. Ideally, such a representation would allow scale independent sequence analysis without the context of fixed memory length. A simple example would consist on being able to infer the homology between two sequences solely by comparing the coordinates of any two homologous units. Results: We have successfully identified such an iterative function for bijective mappingpsi of discrete sequences into objects of continuous state space that enable scale-independent sequence analysis. The technique, named Universal Sequence Mapping (USM), is applicable to sequences with an arbitrary length and arbitrary number of unique units and generates a representation where map distance estimates sequence similarity. The novel USM procedure is based on earlier work by these and other authors on the properties of Chaos Game Representation (CGR). The latter enables the representation of 4 unit type sequences (like DNA) as an order free Markov Chain transition table. The properties of USM are illustrated with test data and can be verified for other data by using the accompanying web-based tool: [http://bioinformatics.musc.edu/-jonas/usm/]. Conclusions: USM is shown to enable a statistical mechanics approach to sequence analysis. The scale independent representation frees sequence analysis from the need to assume a memory length in the investigation of syntactic rules.
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页数:11
相关论文
共 23 条
[1]   Analysis of genomic sequences by Chaos Game Representation [J].
Almeida, JS ;
Carriço, JA ;
Maretzek, A ;
Noble, PA ;
Fletcher, M .
BIOINFORMATICS, 2001, 17 (05) :429-437
[2]  
Arnold B.C., 1992, WILEY SERIES PROBABI
[3]   Chaos game representation of proteins [J].
Basu, S ;
Pan, A ;
Dutta, C ;
Das, J .
JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 1997, 15 (05) :279-289
[4]  
COPE W, 1993, SERIOUS CONCERNS
[5]   Genomic signature: Characterization and classification of species assessed by chaos game representation of sequences [J].
Deschavanne, PJ ;
Giron, A ;
Vilain, J ;
Fagot, G ;
Fertil, B .
MOLECULAR BIOLOGY AND EVOLUTION, 1999, 16 (10) :1391-1399
[6]  
Durbin R., 1998, BIOL SEQUENCE ANAL P
[7]   Molecular typing of bacteria directly from cerebrospinal fluid [J].
Enright, MC ;
Knox, K ;
Griffiths, D ;
Crook, DWM ;
Spratt, BG .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2000, 19 (08) :627-630
[8]   CHAOS GAME REPRESENTATION OF PROTEIN STRUCTURES [J].
FISER, A ;
TUSNADY, GE ;
SIMON, I .
JOURNAL OF MOLECULAR GRAPHICS, 1994, 12 (04) :302-304
[9]   Chaos games for iterated function systems with grey level maps [J].
Forte, B ;
Mendivil, F ;
Vrscay, ER .
SIAM JOURNAL ON MATHEMATICAL ANALYSIS, 1998, 29 (04) :878-890
[10]   NUCLEOTIDE, DINUCLEOTIDE AND TRINUCLEOTIDE FREQUENCIES EXPLAIN PATTERNS OBSERVED IN CHAOS GAME REPRESENTATIONS OF DNA-SEQUENCES [J].
GOLDMAN, N .
NUCLEIC ACIDS RESEARCH, 1993, 21 (10) :2487-2491