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Showing papers by "Albert-László Barabási published in 2009"


Journal ArticleDOI
06 Feb 2009-Science
TL;DR: In this article, a field is emerging that leverages the capacity to collect and analyze data at a scale that may reveal patterns of individual and group behaviors at a large scale, such as behavior patterns.
Abstract: A field is emerging that leverages the capacity to collect and analyze data at a scale that may reveal patterns of individual and group behaviors.

2,619 citations


Journal ArticleDOI
24 Jul 2009-Science
TL;DR: An avalanche of research has shown that many real networks, independent of their age, function, and scope, converge to similar architectures, a universality that allowed researchers from different disciplines to embrace network theory as a common paradigm.
Abstract: For decades, we tacitly assumed that the components of such complex systems as the cell, the society, or the Internet are randomly wired together. In the past decade, an avalanche of research has shown that many real networks, independent of their age, function, and scope, converge to similar architectures, a universality that allowed researchers from different disciplines to embrace network theory as a common paradigm. The decade-old discovery of scale-free networks was one of those events that had helped catalyze the emergence of network science, a new research field with its distinct set of challenges and accomplishments.

1,865 citations


Journal ArticleDOI
TL;DR: The results indicate that high-throughput yeast two-hybrid interactions for human proteins are more precise than literature-curated interactions supported by a single publication, suggesting that HT-Y2H is suitable to map a significant portion of the human interactome.
Abstract: Several attempts have been made to systematically map protein-protein interaction, or 'interactome', networks. However, it remains difficult to assess the quality and coverage of existing data sets. Here we describe a framework that uses an empirically-based approach to rigorously dissect quality parameters of currently available human interactome maps. Our results indicate that high-throughput yeast two-hybrid (HT-Y2H) interactions for human proteins are more precise than literature-curated interactions supported by a single publication, suggesting that HT-Y2H is suitable to map a significant portion of the human interactome. We estimate that the human interactome contains approximately 130,000 binary interactions, most of which remain to be mapped. Similar to estimates of DNA sequence data quality and genome size early in the Human Genome Project, estimates of protein interaction data quality and interactome size are crucial to establish the magnitude of the task of comprehensive human interactome mapping and to elucidate a path toward this goal.

862 citations



Journal ArticleDOI
TL;DR: A new phenotypic database summarizing correlations obtained from the disease history of more than 30 million patients in a Phenotypic Disease Network (PDN) is introduced, offering the potential to enhance the understanding of the origin and evolution of human diseases.
Abstract: The use of networks to integrate different genetic, proteomic, and metabolic datasets has been proposed as a viable path toward elucidating the origins of specific diseases. Here we introduce a new phenotypic database summarizing correlations obtained from the disease history of more than 30 million patients in a Phenotypic Disease Network (PDN). We present evidence that the structure of the PDN is relevant to the understanding of illness progression by showing that (1) patients develop diseases close in the network to those they already have; (2) the progression of disease along the links of the network is different for patients of different genders and ethnicities; (3) patients diagnosed with diseases which are more highly connected in the PDN tend to die sooner than those affected by less connected diseases; and (4) diseases that tend to be preceded by others in the PDN tend to be more connected than diseases that precede other illnesses, and are associated with higher degrees of mortality. Our findings show that disease progression can be represented and studied using network methods, offering the potential to enhance our understanding of the origin and evolution of human diseases. The dataset introduced here, released concurrently with this publication, represents the largest relational phenotypic resource publicly available to the research community.

577 citations


Journal ArticleDOI
22 May 2009-Science
TL;DR: The mobility of mobile phone users is modeled in order to study the fundamental spreading patterns that characterize a mobile virus outbreak and it is found that although Bluetooth viruses can reach all susceptible handsets with time, they spread slowly because of human mobility, offering ample opportunities to deploy antiviral software.
Abstract: We modeled the mobility of mobile phone users in order to study the fundamental spreading patterns that characterize a mobile virus outbreak. We find that although Bluetooth viruses can reach all susceptible handsets with time, they spread slowly because of human mobility, offering ample opportunities to deploy antiviral software. In contrast, viruses using multimedia messaging services could infect all users in hours, but currently a phase transition on the underlying call graph limits them to only a small fraction of the susceptible users. These results explain the lack of a major mobile virus breakout so far and predict that once a mobile operating system's market share reaches the phase transition point, viruses will pose a serious threat to mobile communications.

516 citations


Journal ArticleDOI
TL;DR: By combining information on cellular interactions, disease‐‐gene associations, and population‐level disease patterns extracted from Medicare data, statistically significant correlations between the underlying structure of cellular networks and disease comorbidity patterns in the human population are found.
Abstract: The impact of disease-causing defects is often not limited to the products of a mutated gene but, thanks to interactions between the molecular components, may also affect other cellular functions, resulting in potential comorbidity effects. By combining information on cellular interactions, disease--gene associations, and population-level disease patterns extracted from Medicare data, we find statistically significant correlations between the underlying structure of cellular networks and disease comorbidity patterns in the human population. Our results indicate that such a combination of population-level data and cellular network information could help build novel hypotheses about disease mechanisms.

221 citations


Journal ArticleDOI
TL;DR: It is concluded that metabolic reconstruction and in silico analyses of multiple strains of the same bacterial species provide a novel approach for potential antibiotic target identification.
Abstract: Mortality due to multidrug-resistant Staphylococcus aureus infection is predicted to surpass that of human immunodeficiency virus/AIDS in the United States. Despite the various treatment options for S. aureus infections, it remains a major hospital- and community-acquired opportunistic pathogen. With the emergence of multidrug-resistant S. aureus strains, there is an urgent need for the discovery of new antimicrobial drug targets in the organism. To this end, we reconstructed the metabolic networks of multidrug-resistant S. aureus strains using genome annotation, functional-pathway analysis, and comparative genomic approaches, followed by flux balance analysis-based in silico single and double gene deletion experiments. We identified 70 single enzymes and 54 pairs of enzymes whose corresponding metabolic reactions are predicted to be unconditionally essential for growth. Of these, 44 single enzymes and 10 enzyme pairs proved to be common to all 13 S. aureus strains, including many that had not been previously identified as being essential for growth by gene deletion experiments in S. aureus. We thus conclude that metabolic reconstruction and in silico analyses of multiple strains of the same bacterial species provide a novel approach for potential antibiotic target identification.

159 citations


Book ChapterDOI
01 Jan 2009
TL;DR: In this article, a new algorithm based on a clique percolation technique was proposed to investigate in detail the time dependence of communities on a large scale and uncover basic relationships of the statistical features of community evolution.
Abstract: The rich set of interactions between individuals in the society results in complex community structure, capturing highly connected circles of friends, families, or professional cliques in a social network. Due to the frequent changes in the activity and communication patterns of individuals, the associated social and communication network is subject to constant evolution. The cohesive groups of people in such networks can grow by recruiting new members, or contract by loosing members; two (or more) groups may merge into a single community, while a large enough social group can split into several smaller ones; new communities are born and old ones may disappear. We discuss a new algorithm based on a clique percolation technique, that allows to investigate in detail the time dependence of communities on a large scale and as such, to uncover basic relationships of the statistical features of community evolution. According to the results, the behaviour of smaller collaborative or friendship circles and larger communities, e.g., institutions show significant differences. Social groups containing only a few members persist longer on average when the fluctuations of the members is small. In contrast, we find that the condition for stability for large communities is continuous changes in their membership, allowing for the possibility that after some time practically all members are exchanged.

53 citations


Journal Article
TL;DR: In this article, the authors modeled the mobility of mobile phone users in order to study the fundamental spreading patterns that characterize a mobile virus outbreak and found that although Bluetooth viruses can reach all susceptible handsets with time, they spread slowly because of human mobility, offering ample opportunities to deploy antiviral software.
Abstract: We modeled the mobility of mobile phone users in order to study the fundamental spreading patterns that characterize a mobile virus outbreak. We find that although Bluetooth viruses can reach all susceptible handsets with time, they spread slowly because of human mobility, offering ample opportunities to deploy antiviral software. In contrast, viruses using multimedia messaging services could infect all users in hours, but currently a phase transition on the underlying call graph limits them to only a small fraction of the susceptible users. These results explain the lack of a major mobile virus breakout so far and predict that once a mobile operating system's market share reaches the phase transition point, viruses will pose a serious threat to mobile communications.

19 citations


Proceedings ArticleDOI
19 Jul 2009
TL;DR: This work uses communication and web browsing data to show that there is deep order in the temporal domain of human dynamics, and discusses the different ways to understand and model the emerging patterns.
Abstract: Highly interconnected networks with amazingly complex topology describe systems as diverse as the World Wide Web, our cells, social systems or the economy. Recent studies indicate that these networks are the result of self-organizing processes governed by simple but generic laws, resulting in architectural features that makes them much more similar to each other than one would have expected by chance. I will discuss the amazing order characterizing our interconnected world and its implications to network robustness and spreading processes. Finally, most of these networks are driven by the temporal patterns characterizing human activity. I will use communication and web browsing data to show that there is deep order in the temporal domain of human dynamics, and discuss the different ways to understand and model the emerging patterns.

Book Chapter
01 Jan 2009
TL;DR: In this article, the reception of ancient Roman monuments in Western Renaissance documents (left), placed next to the the very same monuments as they appear in modern scholarly literature (right) is illustrated.
Abstract: the increasing availability of massive amounts of quantitative data is fundamentally changing our perspective and research. Understanding impressive amounts of data – including bibliographies, inventory and research databases, Flickr images of historic sites, scanned books, click-streams of literature downloads, and other linked data is just as transformative for humanities, as the ideas of quantum mechanics were for physics in the beginning of the twentieth century. In our hunt for general patterns and laws that characterize complex systems we find overarching themes, such as the one illustrated in figure 1, showing the reception of ancient Roman monuments in Western Renaissance documents (left), placed next to the the very same monuments as they appear in modern scholarly literature (right). The overall similarity between these two maps is obvious and rather amazing. Both show that most documents (represented as brown nodes) depict or mention only a small number of monuments (given in blue), whereas a few documents point to a disproportionally large number of monuments, representing reviews or large catalogues. That is the reference patterns of art historians appear to follow the same hub dominated scale-free topology as the one characterizing the www, scientific citations, or the human cell. Another common feature is the fact that most nodes of the network are reachable from every other node with a very few hops. Obviously, these maps are driven by the interests, judgements and actions of each author who placed themselves on the map by referring to a shared core set of monuments, which allows for communication with peers, without a central control. Human Activity From the Renaissance to the 21st Century 86