Structure of a typical back-propagated multilayered perceptron used in this study. Structure of a typical back-propagated multilayered perceptron used.

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Structure of a typical back-propagated multilayered perceptron used in this study. Structure of a typical back-propagated multilayered perceptron used in this study. The predictive efficacy of a group of input parameters, such as expression levels of IL-1β, IL-6, IL-8, IL-10, TNF-α, CCL2, and FasL, was tested through the construction of a simple two-output neural network. Input parameters from a random 70% of the patient data were used to train the model to indicate what cytokine levels looked like in those patients that went on to develop sepsis and in those that did not. Each input parameter was assigned an arbitrary weighting during the training phase of model construction, and this was adjusted by an algorithm hidden layer that gave a prediction as to whether the group of input parameters had come from a patient that went on to develop sepsis (S) or had come from a patient that did not develop sepsis (C). The model then compared this prediction with the actual patient classification. It then adjusted the weightings and bias used to generate the initial classification and repeated the classification process (back propagation). This process was repeated until there was no significant improvement in classification output. Once the network was optimally trained, its predictive accuracy was tested using the remaining, unseen 30% of patient data. R. A. Lukaszewski et al. Clin. Vaccine Immunol. 2008; doi:10.1128/CVI.00486-07