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Identifying communities from multiplex biological networks by randomized optimization of modularity.
Didier, Gilles; Valdeolivas, Alberto; Baudot, Anaïs.
Affiliation
  • Didier G; Aix Marseille Univ, CNRS, Centrale Marseille, I2M, Marseille, France.
  • Valdeolivas A; Aix Marseille Univ, CNRS, Centrale Marseille, I2M, Marseille, France.
  • Baudot A; ProGeLife, Marseille, France.
F1000Res ; 7: 1042, 2018.
Article in En | MEDLINE | ID: mdl-30210790
ABSTRACT
The identification of communities, or modules, is a common operation in the analysis of large biological networks. The Disease Module Identification DREAM challenge established a framework to evaluate clustering approaches in a biomedical context, by testing the association of communities with GWAS-derived common trait and disease genes. We implemented here several extensions of the MolTi software that detects communities by optimizing multiplex (and monoplex) network modularity. In particular, MolTi now runs a randomized version of the Louvain algorithm, can consider edge and layer weights, and performs recursive clustering. On simulated networks, the randomization procedure clearly improves the detection of communities. On the DREAM challenge benchmark, the results strongly depend on the selected GWAS dataset and enrichment p -value threshold. However, the randomization procedure, as well as the consideration of weighted edges and layers generally increases the number of trait and disease community detected. The new version of MolTi and the scripts used for the DMI DREAM challenge are available at https//github.com/gilles-didier/MolTi-DREAM.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Algorithms / Software / Communicable Diseases / Quantitative Trait, Heritable Type of study: Clinical_trials / Prognostic_studies Limits: Humans Language: En Journal: F1000Res Year: 2018 Document type: Article Affiliation country: France

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Algorithms / Software / Communicable Diseases / Quantitative Trait, Heritable Type of study: Clinical_trials / Prognostic_studies Limits: Humans Language: En Journal: F1000Res Year: 2018 Document type: Article Affiliation country: France