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Assessment of network module identification across complex diseases.
Choobdar, Sarvenaz; Ahsen, Mehmet E; Crawford, Jake; Tomasoni, Mattia; Fang, Tao; Lamparter, David; Lin, Junyuan; Hescott, Benjamin; Hu, Xiaozhe; Mercer, Johnathan; Natoli, Ted; Narayan, Rajiv; Subramanian, Aravind; Zhang, Jitao D; Stolovitzky, Gustavo; Kutalik, Zoltán; Lage, Kasper; Slonim, Donna K; Saez-Rodriguez, Julio; Cowen, Lenore J; Bergmann, Sven; Marbach, Daniel.
Afiliação
  • Choobdar S; Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.
  • Ahsen ME; Swiss Institute of Bioinformatics, Lausanne, Switzerland.
  • Crawford J; Icahn Institute for Genomics and Multiscale Biology and Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Tomasoni M; Department of Computer Science, Tufts University, Medford, MA, USA.
  • Fang T; Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.
  • Lamparter D; Swiss Institute of Bioinformatics, Lausanne, Switzerland.
  • Lin J; Roche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Hescott B; Department of Computational Biology, University of Lausanne, Lausanne, Switzerland.
  • Hu X; Swiss Institute of Bioinformatics, Lausanne, Switzerland.
  • Mercer J; Verge Genomics, San Francisco, CA, USA.
  • Natoli T; Department of Mathematics, Tufts University, Medford, MA, USA.
  • Narayan R; College of Computer and Information Science, Northeastern University, Boston, MA, USA.
  • Subramanian A; Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Zhang JD; Stanley Center at the Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Stolovitzky G; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Kutalik Z; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Slonim DK; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Saez-Rodriguez J; Roche Pharma Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
  • Cowen LJ; Icahn Institute for Genomics and Multiscale Biology and Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Bergmann S; IBM T.J. Watson Research Center, Yorktown Heights, NY, USA.
  • Marbach D; Swiss Institute of Bioinformatics, Lausanne, Switzerland.
Nat Methods ; 16(9): 843-852, 2019 09.
Article em En | MEDLINE | ID: mdl-31471613
ABSTRACT
Many bioinformatics methods have been proposed for reducing the complexity of large gene or protein networks into relevant subnetworks or modules. Yet, how such methods compare to each other in terms of their ability to identify disease-relevant modules in different types of network remains poorly understood. We launched the 'Disease Module Identification DREAM Challenge', an open competition to comprehensively assess module identification methods across diverse protein-protein interaction, signaling, gene co-expression, homology and cancer-gene networks. Predicted network modules were tested for association with complex traits and diseases using a unique collection of 180 genome-wide association studies. Our robust assessment of 75 module identification methods reveals top-performing algorithms, which recover complementary trait-associated modules. We find that most of these modules correspond to core disease-relevant pathways, which often comprise therapeutic targets. This community challenge establishes biologically interpretable benchmarks, tools and guidelines for molecular network analysis to study human disease biology.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença / Biologia Computacional / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas / Redes Reguladoras de Genes / Estudo de Associação Genômica Ampla / Modelos Biológicos Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: Nat Methods Assunto da revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença / Biologia Computacional / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas / Redes Reguladoras de Genes / Estudo de Associação Genômica Ampla / Modelos Biológicos Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: Nat Methods Assunto da revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Suíça
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