Alejandro Pazos

Epileptic seizure detection using multiwavelet transform based approximate entropy and artificial neural networks

Epilepsy is the most prevalent neurological disorder in humans after stroke. Recurrent seizure is the main characteristic of the epilepsy. Electroencephalogram (EEG) is the recording of brain electrical activity and it contains valuable information related to the different physiological states of the brain. Thus, EEG is considered an indispensable tool for diagnosing epilepsy in clinic applications. Since epileptic seizures occur irregularly and unpredictably, automatic seizure detection in EEG recordings is highly required. Multiwavelets, which contain several scaling and wavelet functions, offer orthogonality, symmetry and short support simultaneously, which is not possible for scalar wavelet. With these properties, recently multiwavelets have become promising in signal processing applications. Approximate entropy is a measure that quantifies the complexity or irregularity of the signal. This paper presents a novel method for automatic epileptic seizure detection, which uses approximate entropy features derived from multiwavelet transform and combines with an artificial neural network to classify the EEG signals regarding the existence or absence of seizure. To the best knowledge of the authors, there exists no similar work in the literature. A well-known public dataset was used to evaluate the proposed method. The high accuracy obtained for two different classification problems verified the success of the method.

Automatic epileptic seizure detection in EEGs based on line length feature and artificial neural networks

About 1% of the people in the world suffer from epilepsy. The main characteristic of epilepsy is the recurrent seizures. Careful analysis of the electroencephalogram (EEG) recordings can provide valuable information for understanding the mechanisms behind epileptic disorders. Since epileptic seizures occur irregularly and unpredictably, automatic seizure detection in EEG recordings is highly required. Wavelet transform (WT) is an effective analysis tool for non-stationary signals, such as EEGs. The line length feature reflects the waveform dimensionality changes and is a measure sensitive to variation of the signal amplitude and frequency. This paper presents a novel method for automatic epileptic seizure detection, which uses line length features based on wavelet transform multiresolution decomposition and combines with an artificial neural network (ANN) to classify the EEG signals regarding the existence of seizure or not. To the knowledge of the authors, there exists no similar work in the literature. A famous public dataset was used to evaluate the proposed method. The high accuracy obtained for three different classification problems testified the great success of the method.

Automatic feature extraction using genetic programming: An application to epileptic EEG classification

This paper applies genetic programming (GP) to perform automatic feature extraction from original feature database with the aim of improving the discriminatory performance of a classifier and reducing the input feature dimensionality at the same time. The tree structure of GP naturally represents the features, and a new function generated in this work automatically decides the number of the features extracted. In experiments on two common epileptic EEG detection problems, the classification accuracy on the GP-based features is significant higher than on the original features. Simultaneously, the dimension of the input features for the classifier is much smaller than that of the original features.

Classification of EEG signals using relative wavelet energy and artificial neural networks

Electroencephalographms (EEGs) are records of brain electrical activity. It is an indispensable tool for diagnosing neurological diseases, such as epilepsy. Wavelet transform (WT) is an effective tool for analysis of non-stationary signal, such as EEGs. Relative wavelet energy (RWE) provides information about the relative energy associated with different frequency bands present in EEG signals and their corresponding degree of importance. This paper deals with a novel method of analysis of EEG signals using relative wavelet energy, and classification using Artificial Neural Networks (ANNs). The obtained classification accuracy confirms that the proposed scheme has potential in classifying EEG signals.

Prediction and modeling of the rainfall-runoff transformation of a typical urban basin using ann and gp

This paper proposes an application of Genetic Programming (GP) and Artificial Neural Networks (ANN) in hydrology, showing how these two techniques can work together to solve a problem, namely for modeling the effect of rain on the runoff flow in a typical urban basin. The ultimate goal of this research is to design a real-time alarm system to warn of floods or subsidence in various types of urban basins. Results look promising and appear to offer some improvement for analyzing river basin systems over stochastic methods such as unitary hydrographs.

MIND-BEST: Web Server for Drugs and Target Discovery; Design, Synthesis, and Assay of MAO-B Inhibitors and Theoretical−Experimental Study of G3PDH Protein from Trichomonas gallinae

Many drugs with very different affinity to a large number of receptors are described. Thus, in this work, we selected drug-target pairs (DTPs/nDTPs) of drugs with high affinity/nonaffinity for different targets. Quantitative structure-activity relationship (QSAR) models become a very useful tool in this context because they substantially reduce time and resource-consuming experiments. Unfortunately, most QSAR models predict activity against only one protein target and/or they have not been implemented on a public Web server yet, freely available online to the scientific community. To solve this problem, we developed a multitarget QSAR (mt-QSAR) classifier combining the MARCH-INSIDE software for the calculation of the structural parameters of drug and target with the linear discriminant analysis (LDA) method in order to seek the best model. The accuracy of the best LDA model was 94.4% (3,859/4,086 cases) for training and 94.9% (1,909/2,012 cases) for the external validation series. In addition, we implemented the model into the Web portal Bio-AIMS as an online server entitled MARCH-INSIDE Nested Drug-Bank Exploration & Screening Tool (MIND-BEST), located at http://miaja.tic.udc.es/Bio-AIMS/MIND-BEST.php . This online tool is based on PHP/HTML/Python and MARCH-INSIDE routines. Finally, we illustrated two practical uses of this server with two different experiments. In experiment 1, we report for the first time a MIND-BEST prediction, synthesis, characterization, and MAO-A and MAO-B pharmacological assay of eight rasagiline derivatives, promising for anti-Parkinson drug design. In experiment 2, we report sampling, parasite culture, sample preparation, 2-DE, MALDI-TOF and -TOF/TOF MS, MASCOT search, 3D structure modeling with LOMETS, and MIND-BEST prediction for different peptides as new protein of the found in the proteome of the bird parasite Trichomonas gallinae, which is promising for antiparasite drug targets discovery.

Trypano-PPI: a web server for prediction of unique targets in trypanosome proteome by using electrostatic parameters of protein-protein interactions.

Trypanosoma brucei causes African trypanosomiasis in humans (HAT or African sleeping sickness) and Nagana in cattle. The disease threatens over 60 million people and uncounted numbers of cattle in 36 countries of sub-Saharan Africa and has a devastating impact on human health and the economy. On the other hand, Trypanosoma cruzi is responsible in South America for Chagas disease, which can cause acute illness and death, especially in young children. In this context, the discovery of novel drug targets in Trypanosome proteome is a major focus for the scientific community. Recently, many researchers have spent important efforts on the study of protein-protein interactions (PPIs) in pathogen Trypanosome species concluding that the low sequence identities between some parasite proteins and their human host render these PPIs as highly promising drug targets. To the best of our knowledge, there are no general models to predict Unique PPIs in Trypanosome (TPPIs). On the other hand, the 3D structure of an increasing number of Trypanosome proteins is reported in databases. In this regard, the introduction of a new model to predict TPPIs from the 3D structure of proteins involved in PPI is very important. For this purpose, we introduced new protein-protein complex invariants based on the Markov average electrostatic potential xi(k)(R(i)) for amino acids located in different regions (R(i)) of i-th protein and placed at a distance k one from each other. We calculated more than 30 different types of parameters for 7866 pairs of proteins (1023 TPPIs and 6823 non-TPPIs) from more than 20 organisms, including parasites and human or cattle hosts. We found a very simple linear model that predicts above 90% of TPPIs and non-TPPIs both in training and independent test subsets using only two parameters. The parameters were (d)xi(k)(s) = |xi(k)(s(1)) - xi(k)(s(2))|, the absolute difference between the xi(k)(s(i)) values on the surface of the two proteins of the pairs. We also tested nonlinear ANN models for comparison purposes but the linear model gives the best results. We implemented this predictor in the web server named TrypanoPPI freely available to public at http://miaja.tic.udc.es/Bio-AIMS/TrypanoPPI.php. This is the first model that predicts how unique a protein-protein complex in Trypanosome proteome is with respect to other parasites and hosts, opening new opportunities for antitrypanosome drug target discovery.

3D entropy and moments prediction of enzyme classes and experimental-theoretic study of peptide fingerprints in Leishmania parasites.

The number of protein 3D structures without function annotation in Protein Data Bank (PDB) has been steadily increased. This fact has led in turn to an increment of demand for theoretical models to give a quick characterization of these proteins. In this work, we present a new and fast Markov chain model (MCM) to predict the enzyme classification (EC) number. We used both linear discriminant analysis (LDA) and/or artificial neural networks (ANN) in order to compare linear vs. non-linear classifiers. The LDA model found is very simple (three variables) and at the same time is able to predict the first EC number with an overall accuracy of 79% for a data set of 4755 proteins (859 enzymes and 3896 non-enzymes) divided into both training and external validation series. In addition, the best non-linear ANN model is notably more complex but has an overall accuracy of 98.85%. It is important to emphasize that this method may help us to predict not only new enzyme proteins but also to select peptide candidates found on the peptide mass fingerprints (PMFs) of new proteins that may improve enzyme activity. In order to illustrate the use of the model in this regard, we first report the 2D electrophoresis (2DE) and MADLI-TOF mass spectra characterization of the PMF of a new possible malate dehydrogenase sequence from Leishmania infantum. Next, we used the models to predict the contribution to a specific enzyme action of 30 peptides found in the PMF of the new protein. We implemented the present model in a server at portal Bio-AIMS (http://miaja.tic.udc.es/Bio-AIMS/EnzClassPred.php). This free on-line tool is based on PHP/HTML/Python and MARCH-INSIDE routines. This combined strategy may be used to identify and predict peptides of prokaryote and eukaryote parasites and their hosts as well as other superior organisms, which may be of interest in drug development or target identification.

Artificial astrocytes improve neural network performance

Compelling evidence indicates the existence of bidirectional communication between astrocytes and neurons. Astrocytes, a type of glial cells classically considered to be passive supportive cells, have been recently demonstrated to be actively involved in the processing and regulation of synaptic information, suggesting that brain function arises from the activity of neuron-glia networks. However, the actual impact of astrocytes in neural network function is largely unknown and its application in artificial intelligence remains untested. We have investigated the consequences of including artificial astrocytes, which present the biologically defined properties involved in astrocyte-neuron communication, on artificial neural network performance. Using connectionist systems and evolutionary algorithms, we have compared the performance of artificial neural networks (NN) and artificial neuron-glia networks (NGN) to solve classification problems. We show that the degree of success of NGN is superior to NN. Analysis of performances of NN with different number of neurons or different architectures indicate that the effects of NGN cannot be accounted for an increased number of network elements, but rather they are specifically due to astrocytes. Furthermore, the relative efficacy of NGN vs. NN increases as the complexity of the network increases. These results indicate that artificial astrocytes improve neural network performance, and established the concept of Artificial Neuron-Glia Networks, which represents a novel concept in Artificial Intelligence with implications in computational science as well as in the understanding of brain function.

A new approach to the extraction of ANN rules and to their generalization capacity through GP

Various techniques for the extraction of ANN rules have been used, but most of them have focused on certain types of networks and their training. There are very few methods that deal with ANN rule extraction as systems that are independent of their architecture, training, and internal distribution of weights, connections, and activation functions. This article proposes a methodology for the extraction of ANN rules, regardless of their architecture, and based on genetic programming. The strategy is based on the previous algorithm and aims at achieving the generalization capacity that is characteristic of ANNs by means of symbolic rules that are understandable to human beings.