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Multimodal network diffusion predicts future disease-gene-chemical associations.
Lin, Chih-Hsu; Konecki, Daniel M; Liu, Meng; Wilson, Stephen J; Nassar, Huda; Wilkins, Angela D; Gleich, David F; Lichtarge, Olivier.
Afiliação
  • Lin CH; Graduate Program in Quantitative and Computational Biosciences, Baylor College of Medicine, Houston, TX, USA.
  • Konecki DM; Graduate Program in Quantitative and Computational Biosciences, Baylor College of Medicine, Houston, TX, USA.
  • Liu M; Department of Computer Science, Purdue University, West Lafayette, IN, USA.
  • Wilson SJ; Department of Biochemistry and Molecular Biology, Houston, TX, USA.
  • Nassar H; Department of Computer Science, Purdue University, West Lafayette, IN, USA.
  • Wilkins AD; Departments of Molecular and Human Genetics, and Pharmacology, Houston, TX, USA.
  • Gleich DF; Computational and Integrative Biomedical Research Center, Baylor College of Medicine, Houston, TX, USA.
  • Lichtarge O; Department of Computer Science, Purdue University, West Lafayette, IN, USA.
Bioinformatics ; 35(9): 1536-1543, 2019 05 01.
Article em En | MEDLINE | ID: mdl-30304494
ABSTRACT
MOTIVATION Precision medicine is an emerging field with hopes to improve patient treatment and reduce morbidity and mortality. To these ends, computational approaches have predicted associations among genes, chemicals and diseases. Such efforts, however, were often limited to using just some available association types. This lowers prediction coverage and, since prior evidence shows that integrating heterogeneous data is likely beneficial, it may limit accuracy. Therefore, we systematically tested whether using more association types improves prediction.

RESULTS:

We study multimodal networks linking diseases, genes and chemicals (drugs) by applying three diffusion algorithms and varying information content. Ten-fold cross-validation shows that these networks are internally consistent, both within and across association types. Also, diffusion methods recovered missing edges, even if all the edges from an entire mode of association were removed. This suggests that information is transferable between these association types. As a realistic validation, time-stamped experiments simulated the predictions of future associations based solely on information known prior to a given date. The results show that many future published results are predictable from current associations. Moreover, in most cases, using more association types increases prediction coverage without significantly decreasing sensitivity and specificity. In case studies, literature-supported validation shows that these predictions mimic human-formulated hypotheses. Overall, this study suggests that diffusion over a more comprehensive multimodal network will generate more useful hypotheses of associations among diseases, genes and chemicals, which may guide the development of precision therapies. AVAILABILITY AND IMPLEMENTATION Code and data are available at https//github.com/LichtargeLab/multimodal-network-diffusion. SUPPLEMENTARY INFORMATION Supplementary data are available at Bioinformatics online.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Biologia Computacional Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Algoritmos / Biologia Computacional Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article