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On the Representability of Complete Genomes by Multiple Competing Finite-Context (Markov) Models
A finite-context (Markov) model of order [Image: see text] yields the probability distribution of the next symbol in a sequence of symbols, given the recent past up to depth [Image: see text]. Markov modeling has long been applied to DNA sequences, for example to find gene-coding regions. With the f...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128062/ https://www.ncbi.nlm.nih.gov/pubmed/21738720 http://dx.doi.org/10.1371/journal.pone.0021588 |
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author | Pinho, Armando J. Ferreira, Paulo J. S. G. Neves, António J. R. Bastos, Carlos A. C. |
author_facet | Pinho, Armando J. Ferreira, Paulo J. S. G. Neves, António J. R. Bastos, Carlos A. C. |
author_sort | Pinho, Armando J. |
collection | PubMed |
description | A finite-context (Markov) model of order [Image: see text] yields the probability distribution of the next symbol in a sequence of symbols, given the recent past up to depth [Image: see text]. Markov modeling has long been applied to DNA sequences, for example to find gene-coding regions. With the first studies came the discovery that DNA sequences are non-stationary: distinct regions require distinct model orders. Since then, Markov and hidden Markov models have been extensively used to describe the gene structure of prokaryotes and eukaryotes. However, to our knowledge, a comprehensive study about the potential of Markov models to describe complete genomes is still lacking. We address this gap in this paper. Our approach relies on (i) multiple competing Markov models of different orders (ii) careful programming techniques that allow orders as large as sixteen (iii) adequate inverted repeat handling (iv) probability estimates suited to the wide range of context depths used. To measure how well a model fits the data at a particular position in the sequence we use the negative logarithm of the probability estimate at that position. The measure yields information profiles of the sequence, which are of independent interest. The average over the entire sequence, which amounts to the average number of bits per base needed to describe the sequence, is used as a global performance measure. Our main conclusion is that, from the probabilistic or information theoretic point of view and according to this performance measure, multiple competing Markov models explain entire genomes almost as well or even better than state-of-the-art DNA compression methods, such as XM, which rely on very different statistical models. This is surprising, because Markov models are local (short-range), contrasting with the statistical models underlying other methods, where the extensive data repetitions in DNA sequences is explored, and therefore have a non-local character. |
format | Online Article Text |
id | pubmed-3128062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31280622011-07-07 On the Representability of Complete Genomes by Multiple Competing Finite-Context (Markov) Models Pinho, Armando J. Ferreira, Paulo J. S. G. Neves, António J. R. Bastos, Carlos A. C. PLoS One Research Article A finite-context (Markov) model of order [Image: see text] yields the probability distribution of the next symbol in a sequence of symbols, given the recent past up to depth [Image: see text]. Markov modeling has long been applied to DNA sequences, for example to find gene-coding regions. With the first studies came the discovery that DNA sequences are non-stationary: distinct regions require distinct model orders. Since then, Markov and hidden Markov models have been extensively used to describe the gene structure of prokaryotes and eukaryotes. However, to our knowledge, a comprehensive study about the potential of Markov models to describe complete genomes is still lacking. We address this gap in this paper. Our approach relies on (i) multiple competing Markov models of different orders (ii) careful programming techniques that allow orders as large as sixteen (iii) adequate inverted repeat handling (iv) probability estimates suited to the wide range of context depths used. To measure how well a model fits the data at a particular position in the sequence we use the negative logarithm of the probability estimate at that position. The measure yields information profiles of the sequence, which are of independent interest. The average over the entire sequence, which amounts to the average number of bits per base needed to describe the sequence, is used as a global performance measure. Our main conclusion is that, from the probabilistic or information theoretic point of view and according to this performance measure, multiple competing Markov models explain entire genomes almost as well or even better than state-of-the-art DNA compression methods, such as XM, which rely on very different statistical models. This is surprising, because Markov models are local (short-range), contrasting with the statistical models underlying other methods, where the extensive data repetitions in DNA sequences is explored, and therefore have a non-local character. Public Library of Science 2011-06-30 /pmc/articles/PMC3128062/ /pubmed/21738720 http://dx.doi.org/10.1371/journal.pone.0021588 Text en Pinho et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Pinho, Armando J. Ferreira, Paulo J. S. G. Neves, António J. R. Bastos, Carlos A. C. On the Representability of Complete Genomes by Multiple Competing Finite-Context (Markov) Models |
title | On the Representability of Complete Genomes by Multiple Competing Finite-Context (Markov) Models |
title_full | On the Representability of Complete Genomes by Multiple Competing Finite-Context (Markov) Models |
title_fullStr | On the Representability of Complete Genomes by Multiple Competing Finite-Context (Markov) Models |
title_full_unstemmed | On the Representability of Complete Genomes by Multiple Competing Finite-Context (Markov) Models |
title_short | On the Representability of Complete Genomes by Multiple Competing Finite-Context (Markov) Models |
title_sort | on the representability of complete genomes by multiple competing finite-context (markov) models |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3128062/ https://www.ncbi.nlm.nih.gov/pubmed/21738720 http://dx.doi.org/10.1371/journal.pone.0021588 |
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