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Alexei Vazquez

Publications and source records attributed to Alexei Vazquez.

3 recordsLinked to original sources

Epidemic outbreaks on structured populations.

Our chances to halt epidemic outbreaks rely on how accurately we represent the population structure underlying the disease spread. When analysing global epidemics this force us to consider metapopulation models taking into account intra- and inter-community interactions. Here I introduce and analyze a metapopulation model which accounts for several features observed in real outbreaks. First, I demonstrate that depending on the intra-community expected outbreak size and the fraction of social bridges the epidemic outbreaks die out or there is a finite probability to observe a global epidemics. Second, I show that the global scenario is characterized by resurgent epidemics, their number increasing with increasing the intra-community average distance between individuals. Finally, I present empirical data for the AIDS epidemics supporting the model predictions.

Acquired Immunodeficiency Syndrome↗

Polynomial growth in branching processes with diverging reproductive number.

We study the spreading dynamics on graphs with a power law degree distribution pk approximately k-gamma, with 2<gamma<3, as an example of a branching process with a diverging reproductive number. We provide evidence that the divergence of the second moment of the degree distribution carries as a consequence a qualitative change in the growth pattern, deviating from the standard exponential growth. First, the population growth is extensive, meaning that the average number of vertices reached by the spreading process becomes of the order of the graph size in a time scale that vanishes in the large graph size limit. Second, the temporal evolution is governed by a polynomial growth, with a degree determined by the characteristic distance between vertices in the graph. These results open a path to further investigation on the dynamics on networks.

Animals↗

Global protein function prediction from protein-protein interaction networks.

Determining protein function is one of the most challenging problems of the post-genomic era. The availability of entire genome sequences and of high-throughput capabilities to determine gene coexpression patterns has shifted the research focus from the study of single proteins or small complexes to that of the entire proteome. In this context, the search for reliable methods for assigning protein function is of primary importance. There are various approaches available for deducing the function of proteins of unknown function using information derived from sequence similarity or clustering patterns of co-regulated genes, phylogenetic profiles, protein-protein interactions (refs. 5-8 and Samanta, M.P. and Liang, S., unpublished data), and protein complexes. Here we propose the assignment of proteins to functional classes on the basis of their network of physical interactions as determined by minimizing the number of protein interactions among different functional categories. Function assignment is proteome-wide and is determined by the global connectivity pattern of the protein network. The approach results in multiple functional assignments, a consequence of the existence of multiple equivalent solutions. We apply the method to analyze the yeast Saccharomyces cerevisiae protein-protein interaction network. The robustness of the approach is tested in a system containing a high percentage of unclassified proteins and also in cases of deletion and insertion of specific protein interactions.

Algorithms↗