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Titlebook: Comparative Genomics; 16th International C Mathieu Blanchette,Aïda Ouangraoua Conference proceedings 2018 Springer Nature Switzerland AG 20

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Designgewichte in komplexen Stichproben,nvolves integrating sequence divergence and gene pair loss through fractionation, using a birth-and-death process and a mutational model. We account not only for the timing of these events in terms of local modes, but also the amplitude and variance of the component distributions. This model is then
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https://doi.org/10.1007/978-3-531-94185-1s of phylogenetic incongruence, using either statistical tests based on expected phylogenetic patterns in small phylogenies or probabilistic modeling in a phylogenetic network context. Introgression leaves a phylogenetic signal similar to horizontal gene transfer, and it has been suggested that its
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Designgewichte in komplexen Stichproben,independent evolution for each family. While this assumption is reasonable for genes that are far apart in the genome, it is clearly not suited for genes grouped in syntenic blocks, which are more plausibly the result of a concerted evolution. Here, we introduce the . model, that extends the traditi
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https://doi.org/10.1007/978-3-658-34396-5 first problem arises when comparing two trees where the leaf set of one tree is a proper subset of the other. The second problem arises when the two trees to be compared have only partially overlapping leaf sets. The traditional approach to handling these problems is to first restrict the two trees
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Silke L. Schneider,Verena Ortmannsxtent is the Tree of Life not truly a tree reflecting strict “vertical” divergence, but rather a more general graph structure known as a phylogenetic network which also captures “horizontal” gene flow? The answer to this fundamental question not only depends upon densely sampled and divergent genomi
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