64 research outputs found
Modeling the impact of white-plague coral disease in climate change scenarios
Coral reefs are in global decline, with coral diseases increasing both in prevalence and in space, a situation that is expected only to worsen as future thermal stressors increase. Through intense surveillance, we have collected a unique and highly resolved dataset from the coral reef of Eilat (Israel, Red Sea), that documents the spatiotemporal dynamics of a White Plague Disease (WPD) outbreak over the course of a full season. Based on modern statistical methodologies, we develop a novel spatial epidemiological model that uses a maximum-likelihood procedure to fit the data and assess the transmission pattern of WPD. We link the model to sea surface temperature (SST) and test the possible effect of increasing temperatures on disease dynamics. Our results reveal that the likelihood of a susceptible coral to become infected is governed both by SST and by its spatial location relative to nearby infected corals. The model shows that the magnitude of WPD epidemics strongly depends on demographic circumstances; under one extreme, when recruitment is free-space regulated and coral density remains relatively constant, even an increase of only 0.5 degrees C in SST can cause epidemics to double in magnitude. In reality, however, the spatial nature of transmission can effectively protect the community, restricting the magnitude of annual epidemics. This is because the probability of susceptible corals to become infected is negatively associated with coral density. Based on our findings, we expect that infectious diseases having a significant spatial component, such as Red-Sea WPD, will never lead to a complete destruction of the coral community under increased thermal stress
Upper bounds for number of removed edges in the Erased Configuration Model
Models for generating simple graphs are important in the study of real-world
complex networks. A well established example of such a model is the erased
configuration model, where each node receives a number of half-edges that are
connected to half-edges of other nodes at random, and then self-loops are
removed and multiple edges are concatenated to make the graph simple. Although
asymptotic results for many properties of this model, such as the limiting
degree distribution, are known, the exact speed of convergence in terms of the
graph sizes remains an open question. We provide a first answer by analyzing
the size dependence of the average number of removed edges in the erased
configuration model. By combining known upper bounds with a Tauberian Theorem
we obtain upper bounds for the number of removed edges, in terms of the size of
the graph. Remarkably, when the degree distribution follows a power-law, we
observe three scaling regimes, depending on the power law exponent. Our results
provide a strong theoretical basis for evaluating finite-size effects in
networks
The interplay of microscopic and mesoscopic structure in complex networks
Not all nodes in a network are created equal. Differences and similarities
exist at both individual node and group levels. Disentangling single node from
group properties is crucial for network modeling and structural inference.
Based on unbiased generative probabilistic exponential random graph models and
employing distributive message passing techniques, we present an efficient
algorithm that allows one to separate the contributions of individual nodes and
groups of nodes to the network structure. This leads to improved detection
accuracy of latent class structure in real world data sets compared to models
that focus on group structure alone. Furthermore, the inclusion of hitherto
neglected group specific effects in models used to assess the statistical
significance of small subgraph (motif) distributions in networks may be
sufficient to explain most of the observed statistics. We show the predictive
power of such generative models in forecasting putative gene-disease
associations in the Online Mendelian Inheritance in Man (OMIM) database. The
approach is suitable for both directed and undirected uni-partite as well as
for bipartite networks
Discovering universal statistical laws of complex networks
Different network models have been suggested for the topology underlying
complex interactions in natural systems. These models are aimed at replicating
specific statistical features encountered in real-world networks. However, it
is rarely considered to which degree the results obtained for one particular
network class can be extrapolated to real-world networks. We address this issue
by comparing different classical and more recently developed network models
with respect to their generalisation power, which we identify with large
structural variability and absence of constraints imposed by the construction
scheme. After having identified the most variable networks, we address the
issue of which constraints are common to all network classes and are thus
suitable candidates for being generic statistical laws of complex networks. In
fact, we find that generic, not model-related dependencies between different
network characteristics do exist. This allows, for instance, to infer global
features from local ones using regression models trained on networks with high
generalisation power. Our results confirm and extend previous findings
regarding the synchronisation properties of neural networks. Our method seems
especially relevant for large networks, which are difficult to map completely,
like the neural networks in the brain. The structure of such large networks
cannot be fully sampled with the present technology. Our approach provides a
method to estimate global properties of under-sampled networks with good
approximation. Finally, we demonstrate on three different data sets (C.
elegans' neuronal network, R. prowazekii's metabolic network, and a network of
synonyms extracted from Roget's Thesaurus) that real-world networks have
statistical relations compatible with those obtained using regression models
Evolving Clustered Random Networks
We propose a Markov chain simulation method to generate simple connected
random graphs with a specified degree sequence and level of clustering. The
networks generated by our algorithm are random in all other respects and can
thus serve as generic models for studying the impacts of degree distributions
and clustering on dynamical processes as well as null models for detecting
other structural properties in empirical networks
Neighbor Overlap Is Enriched in the Yeast Interaction Network: Analysis and Implications
The yeast protein-protein interaction network has been shown to have distinct topological features such as a scale free degree distribution and a high level of clustering. Here we analyze an additional feature which is called Neighbor Overlap. This feature reflects the number of shared neighbors between a pair of proteins. We show that Neighbor Overlap is enriched in the yeast protein-protein interaction network compared with control networks carefully designed to match the characteristics of the yeast network in terms of degree distribution and clustering coefficient. Our analysis also reveals that pairs of proteins with high Neighbor Overlap have higher sequence similarity, more similar GO annotations and stronger genetic interactions than pairs with low ones. Finally, we demonstrate that pairs of proteins with redundant functions tend to have high Neighbor Overlap. We suggest that a combination of three mechanisms is the basis for this feature: The abundance of protein complexes, selection for backup of function, and the need to allow functional variation
Simultaneous Genome-Wide Inference of Physical, Genetic, Regulatory, and Functional Pathway Components
Biomolecular pathways are built from diverse types of pairwise interactions, ranging from physical protein-protein interactions and modifications to indirect regulatory relationships. One goal of systems biology is to bridge three aspects of this complexity: the growing body of high-throughput data assaying these interactions; the specific interactions in which individual genes participate; and the genome-wide patterns of interactions in a system of interest. Here, we describe methodology for simultaneously predicting specific types of biomolecular interactions using high-throughput genomic data. This results in a comprehensive compendium of whole-genome networks for yeast, derived from ∼3,500 experimental conditions and describing 30 interaction types, which range from general (e.g. physical or regulatory) to specific (e.g. phosphorylation or transcriptional regulation). We used these networks to investigate molecular pathways in carbon metabolism and cellular transport, proposing a novel connection between glycogen breakdown and glucose utilization supported by recent publications. Additionally, 14 specific predicted interactions in DNA topological change and protein biosynthesis were experimentally validated. We analyzed the systems-level network features within all interactomes, verifying the presence of small-world properties and enrichment for recurring network motifs. This compendium of physical, synthetic, regulatory, and functional interaction networks has been made publicly available through an interactive web interface for investigators to utilize in future research at http://function.princeton.edu/bioweaver/
Identification and Classification of Hubs in Brain Networks
Brain regions in the mammalian cerebral cortex are linked by a complex network of fiber bundles. These inter-regional networks have previously been analyzed in terms of their node degree, structural motif, path length and clustering coefficient distributions. In this paper we focus on the identification and classification of hub regions, which are thought to play pivotal roles in the coordination of information flow. We identify hubs and characterize their network contributions by examining motif fingerprints and centrality indices for all regions within the cerebral cortices of both the cat and the macaque. Motif fingerprints capture the statistics of local connection patterns, while measures of centrality identify regions that lie on many of the shortest paths between parts of the network. Within both cat and macaque networks, we find that a combination of degree, motif participation, betweenness centrality and closeness centrality allows for reliable identification of hub regions, many of which have previously been functionally classified as polysensory or multimodal. We then classify hubs as either provincial (intra-cluster) hubs or connector (inter-cluster) hubs, and proceed to show that lesioning hubs of each type from the network produces opposite effects on the small-world index. Our study presents an approach to the identification and classification of putative hub regions in brain networks on the basis of multiple network attributes and charts potential links between the structural embedding of such regions and their functional roles
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