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Seminar on Complex Systems The Human Disease Network K.I. Goh, M. E. Cusick A.-L. Barabási et al. Cornelius Müller Berlin, 06/05/2015 1 Motivation • Before: disease-gene association pairs Studies focused on a single disease • Now: Disease-gene-relation at a higher level Linking all genetic disorders with all disease genes 2 The Data 3 Construction of the Bipartite Network 4 Construction of the Bipartite Network 5 Construction of the Bipartite Network 6 Human Disease Network 67 % of all disorders with at least one link to others Giant component: 516 of 1284 disorders (40%) 7 Human Disease Network 8 Disease Gene Network 9 Disease Gene Network 10 Functional Clustering • HDN: Average size of giant component: 516 genes; randomly 643 812 links between disorders; randomly 107 • DGN: Average size of giant component: 903 genes; randomly 1087 11 Functional Modules 12 Centrality and Peripherality Essential genes have high impact in early development Nonessential genes do not encode hubs 13 Further applications of bipartite networks • People that share preferences • Metabolites that share chemical reactions • Authors that share papers 14 Conclusion • Bipartite networks enable inductive networking • HDN and DGN create additional understanding about disease biology • Evaluation of networks can connect with further data 15 Discussion • Clustering of HDN includes a wide range • Database of HDN and DGN is not complete • Many diseases can not be linked to others 16 Literature • Goh, Cusick, Valle, Vidal, Barabasi: The Human Disease Network, PNAS 2007 • Supporting information text • http://rocs.hu-berlin.de/ complex_sys_2015/resources/Introduction-toNetworks.pdf 17