4 research outputs found

    Sobre modelos de rearranjo de genomas

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    Orientador: João MeidanisTese (doutorado) - Universidade Estadual de Campinas, Instituto de ComputaçãoResumo: Rearranjo de genomas é o nome dado a eventos onde grandes blocos de DNA trocam de posição durante o processo evolutivo. Com a crescente disponibilidade de sequências completas de DNA, a análise desse tipo de eventos pode ser uma importante ferramenta para o entendimento da genômica evolutiva. Vários modelos matemáticos de rearranjo de genomas foram propostos ao longo dos últimos vinte anos. Nesta tese, desenvolvemos dois novos modelos. O primeiro foi proposto como uma definição alternativa ao conceito de distância de breakpoint. Essa distância é uma das mais simples medidas de rearranjo, mas ainda não há um consenso quanto à sua definição para o caso de genomas multi-cromossomais. Pevzner e Tesler deram uma definição em 2003 e Tannier et al. a definiram de forma diferente em 2008. Nesta tese, nós desenvolvemos uma outra alternativa, chamada de single-cut-or-join (SCJ). Nós mostramos que, no modelo SCJ, além da distância, vários problemas clássicos de rearranjo, como a mediana de rearranjo, genome halving e pequena parcimônia são fáceis, e apresentamos algoritmos polinomiais para eles. O segundo modelo que apresentamos é o formalismo algébrico por adjacências, uma extensão do formalismo algébrico proposto por Meidanis e Dias, que permite a modelagem de cromossomos lineares. Esta era a principal limitação do formalismo original, que só tratava de cromossomos circulares. Apresentamos algoritmos polinomiais para o cálculo da distância algébrica e também para encontrar cenários de rearranjo entre dois genomas. Também mostramos como calcular a distância algébrica através do grafo de adjacências, para facilitar a comparação com outras distâncias de rearranjo. Por fim, mostramos como modelar todas as operações clássicas de rearranjo de genomas utilizando o formalismo algébricoAbstract: Genome rearrangements are events where large blocks of DNA exchange places during evolution. With the growing availability of whole genome data, the analysis of these events can be a very important and promising tool for understanding evolutionary genomics. Several mathematical models of genome rearrangement have been proposed in the last 20 years. In this thesis, we propose two new rearrangement models. The first was introduced as an alternative definition of the breakpoint distance. The breakpoint distance is one of the most straightforward genome comparison measures, but when it comes to defining it precisely for multichromosomal genomes, there is more than one way to go about it. Pevzner and Tesler gave a definition in a 2003 paper, and Tannier et al. defined it differently in 2008. In this thesis we provide yet another alternative, calling it single-cut-or-join (SCJ). We show that several genome rearrangement problems, such as genome median, genome halving and small parsimony, become easy for SCJ, and provide polynomial time algorithms for them. The second model we introduce is the Adjacency Algebraic Theory, an extension of the Algebraic Formalism proposed by Meidanis and Dias that allows the modeling of linear chromosomes, the main limitation of the original formalism, which could deal with circular chromosomes only. We believe that the algebraic formalism is an interesting alternative for solving rearrangement problems, with a different perspective that could complement the more commonly used combinatorial graph-theoretic approach. We present polynomial time algorithms to compute the algebraic distance and find rearrangement scenarios between two genomes. We show how to compute the rearrangement distance from the adjacency graph, for an easier comparison with other rearrangement distances. Finally, we show how all classic rearrangement operations can be modeled using the algebraic theoryDoutoradoCiência da ComputaçãoDoutor em Ciência da Computaçã

    Models and Algorithms for Whole-Genome Evolution and their Use in Phylogenetic Inference

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    The rapid accumulation of sequenced genomes offers the chance to resolve longstanding questions about the evolutionary histories, or phylogenies, of groups of organisms. The relatively rare occurrence of large-scale evolutionary events in a whole genome, events such as genome rearrangements, duplications and losses, enables us to extract a strong and robust phylogenetic signal from whole-genome data. The work presented in this dissertation focuses on models and algorithms for whole-genome evolution and their use in phylogenetic inference. We designed algorithms to estimate pairwise genomic distances from large-scale genomic changes. We refined the evolutionary models on whole-genome evolution. We also made use of these results to provide fast and accurate methods for phylogenetic inference, that scales up, in both speed and accuracy, to modern high-resolution whole-genome data. We designed algorithms to estimate the true evolutionary distance between two genomes under genome rearrangements, and also under rearrangements, plus gains and losses. We refined the evolutionary model to be the first mathematical model to preserve the structural dichotomy in genomic organization between most prokaryotes and most eukaryotes. Those models and associated distance estimators provide a basis for studying facets of possible mechanisms of evolution through simulation and application to real genomes. Phylogenetic analyses from whole-genome data have been limited to small collections of genomes and low-resolution data; they have also lacked an effective assessment of robustness. We developed an approach that combines our distance estimator, any standard distance-based reconstruction algorithm, and a novel bootstrapping method based on resampling genomic adjacencies. The resulting tool overcomes a serious and long-standing impediment to the use of whole-genome data in phylogenetic inference and provides results comparable in accuracy and robustness to distance-based methods for sequence data. Maximum-likelihood approaches have been successfully applied to phylogenetic inferences for aligned sequences, but such applications remain primitive for whole-genome data. We developed a maximum-likelihood approach to phylogenetic analysis from whole-genome data. In combination with our bootstrap scheme, this new approach yields the first reliable phylogenetic tool for the analysis of whole-genome data at the level of syntenic blocks

    Rearrangement Models and Single-Cut Operations

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    Medvedev P, Stoye J. Rearrangement Models and Single-Cut Operations. In: Comparative Genomics : International Workshop, RECOMB-CG 2009, Budapest, Hungary, September 27-29, 2009. Proceedings. Lecture Notes in Computer Science. Vol 5817. Berlin, Heidelberg: Springer; 2009: 84-97

    Rearrangement Models and Single-Cut Operations

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    Bergeron A, Medvedev P, Stoye J. Rearrangement Models and Single-Cut Operations. Journal of Computational Biology. 2010;17(9):1213-1225
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