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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
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