We present a simplified view of those parts of the human immune system which can be used to provide the basis for a data analysis tool. The motivation for and reasoning behind such a model is given and the desire for a 'transparent' model and meaningful visualization and interpretation techniques is noted. A minimalist formulation of an artificial immune system and some of its behaviour is described. A simple implementation and a suitable visualization technique are demonstrated using some trivial data and the famous 'iris' data set.
This paper describes an artificial immune system algorithm which implements a fairly close analogue of the memory mechanism proposed by Jerne(1) (usually known as the Immune Network Theory). The algorithm demonstrates the ability of these types of network to produce meta-stable structures representing populated regions of the antigen space. The networks produced retain their structure indefinitely and capture inherent structure within the sets of antigens used to train them. Results from running the algorithm on a variety of data sets are presented and shown to be stable over long time periods and wide ranges of parameters. The potential of the algorithm as a tool for multivariate data analysis is also explored.
Abstract. Many researchers are developing frameworks inspired by natural, especially biological, systems to solve complex real-world problems. This work extends previous work in the field of biologically inspired computing, proposing an artificial endocrine system for autonomous robot navigation. Having intrinsic self-organizing behaviour, the novel artificial endocrine system can be applied to a wide range of problems, particularly those that involve decision making under changing environmental conditions, such as autonomous robot navigation. This work draws on "embodied cognitive science", including the study of intelligence, adaptivity, homeostasis, and the dynamic aspects of cognition, in order to help lay down fundamental principles and techniques for a novel approach to more biologically plausible artificial homeostatic systems. Results from using the artificial endocrine system to control a simulated robot are presented.
Binary mixtures of model systems consisting of the antibiotic ampicillin with either Escherichia coli or Staphylococcus aureus were subjected to pyrolysis mass spectrometry (PyMS). To deconvolute the pyrolysis mass spectra, so as to obtain quantitative information on the concentration of ampicillin in the mixtures, partial least squares regression (PLS), principal components regression (PCR), and fully interconnected feedforward artificial neural networks (ANNs) were studied. In the latter case, the weights were modified using the standard backpropagation algorithm, and the nodes used a sigmoidal squashing function. It was found that each of the methods could be used to provide calibration models which gave excellent predictions for the concentrations of ampicillin in samples on which they had not been trained. Furthermore, ANNs trained to predict the amount of ampicillin in E. coli were able to generalise so as to predict the concentration of ampicillin in a S. aureus background, illustrating the robustness of ANNs to rather substantial variations in the biological background. The PyMS of the complex mixture of ampicillin in bacteria could not be expressed simply in terms of additive combinations of the spectra describing the pure components of the mixtures and their relative concentrations. Intermolecular reactions took place in the pyrolysate, leading to a lack of superposition of the spectral components and to a dependence of the normalized mass spectrum on sample size. Samples from fermentations of a single organism in a complex production medium were also analyzed quantitatively for a drug of commercial interest. The drug could also be quantified in a variety of mutant-producing strains cultivated in the same medium. The combination of PyMS and ANNs constitutes a novel, rapid, and convenient method for exploitation in strain improvement screening programs. 0 1994John Wiley & Sons, Inc.
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