ArticleBioinformatics (Oxford, England)2011
Prognostic transcriptional association networks: a new supervised approach based on regression trees.
Article in Bioinformatics (Oxford, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Diagnostic biases in translational bioinformatics.BMC medical genomics · 2015Article
- Development and use of the Cytoscape app GFD-Net for measuring semantic dissimilarity of gene networks.F1000Research · 2014Article
- Interplay of microRNAs, transcription factors and target genes: linking dynamic expression changes to function.Nucleic acids research · 2013Article
- Transforming growth factor β receptor 1 is a new candidate prognostic biomarker after acute myocardial infarction.BMC medical genomics · 2011Article
- Information encoded in a network of inflammation proteins predicts clinical outcome after myocardial infarction.BMC medical genomics · 2011Article
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Authors and funding
7 authors.
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Abstract
motivationThe application of information encoded in molecular networks for prognostic purposes is a crucial objective of systems biomedicine. This approach has not been widely investigated in the cardiovascular research area. Within this area, the prediction of clinical outcomes after suffering a heart attack would represent a significant step forward. We developed a new quantitative prediction-based method for this prognostic problem based on the discovery of clinically relevant transcriptional association networks. This method integrates regression trees and clinical class-specific networks, and can be applied to other clinical domains.
resultsBefore analyzing our cardiovascular disease dataset, we tested the usefulness of our approach on a benchmark dataset with control and disease patients. We also compared it to several algorithms to infer transcriptional association networks and classification models. Comparative results provided evidence of the prediction power of our approach. Next, we discovered new models for predicting good and bad outcomes after myocardial infarction. Using blood-derived gene expression data, our models reported areas under the receiver operating characteristic curve above 0.70. Our model could also outperform different techniques based on co-expressed gene modules. We also predicted processes that may represent novel therapeutic targets for heart disease, such as the synthesis of leucine and isoleucine. AVAILABILITY: The SATuRNo software is freely available at http://www.lsi.us.es/isanepo/toolsSaturno/.
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