Academic literature on the topic 'Artificial Neural Networking (ANN)'

Tire-pavement interaction is a dominant noise source for passenger cars and trucks above 25 mph (40 km/h) and 43 mph (70 km/h), respectively. For the same pavement, tires with different tread pattern and construction generate noise of different levels and frequencies. In the present study, forty-two different tires were tested over a range of speeds (45-65 mph, i.e., 72-105 km/h) on a non-porous asphalt pavement (a section of U.S. Route 460, both eastbound and westbound). An On-Board Sound Intensity (OBSI) system was instrumented on the test vehicle to collect the tire noise data at both the leading and trailing edge of the tire contact patch. An optical sensor recording the once-per-revolution signal of the wheel was also installed to monitor the vehicle speed and, more importantly, to provide the data needed to perform the order tracking analysis in order to break down the tire noise into two components. These two components are: the tread pattern and the non-tread pattern noise. Based on the experimental noise data collected, two artificial neural networks (ANN) were developed to predict the tread pattern (ANN1) and the non-tread pattern noise (ANN2) components, separately. The inputs of ANN1 are the coherent tread profile spectrum and the air volume velocity spectrum calculated from the digitized 3D tread pattern. The inputs of ANN2 are the tire size and tread rubber hardness. The vehicle speed is also included as input for the two ANN's. The optimized ANN's are able to predict the tire-pavement interaction noise well for different tires on the pavement tested. Another outcome of this work is the complete literature review on Tire-Pavement Interaction Noise (TPIN), as an appendix of this dissertation and covering ~1000 references, which might be the most comprehensive compilation of this topic.<br>PHD

Artificial Neural Networks (ANNs) have been established as one of the most important algorithmic tools in the Machine Learning (ML) toolbox over the past few decades. ANNs' recent rise to widespread acceptance can be attributed to two developments: (1) the availability of large-scale training and testing datasets; and (2) the availability of new computer architectures for which ANN implementations are orders of magnitude more efficient. In this thesis, I present research on two aspects of the second development. First, I present a portable, open source implementation of ANNs in OpenCL and MPI. Second, I present performance and scaling models for ANN algorithms on state-of-the-art Graphics Processing Unit (GPU) based parallel compute clusters.<br>Master of Science

<p>This thesis is concerned with the prediction of protein mutations using artificial neural networks. From the biological perspective it is of interest to investigate weather it is possible to find rules of mutation between evolutionary adjacent (or closely related) proteins. Techniques from computer science are used in order to see if it is possible to predict protein mutations i.e. using artificial neural networks. The computer science perspective of this work would be to try optimizing the results from the neural networks. However, the focus of this thesis is primarily on the biological perspective and the performance of the computer science methods are secondary objective i.e. the primary interest is to show the existence of rules for protein mutations.</p><p>The method used in this thesis consists two neural networks. One network is used to predict the actual protein mutations and the other network is used to make a compressed representation of each amino acid. By using a compression network it is possible to make the prediction network much smaller (each amino acid is represented by 3 nodes instead of 22 nodes). The compression network is an auto associative network and the prediction network is a standard feed-forward network. The prediction network predicts a block of amino acids at a time and for comparison a sliding window technique has also been tested.</p><p>It is my belief that the results in this thesis indicate that there exists rules for protein mutations. However, the tests done in this thesis is only performed on a small portion of all proteins. Some protein families tested show really good results while other families are not as good. I believe that extended work using optimized neural networks would improve the predictions further.</p>

With the growing interest in the Marcellus Shale and its natural gas deposits, there are opportunities to purchase and hold land for investment purposes. A robust decision tool is needed to help guide investors towards the most profitable properties. Artificial neural networks have many unique benefits that make them an ideal candidate for this purpose. The artificial neural networks created in this study had nine independent variables. Combinations of these nine variables were created to describe 300 theoretical properties available for purchase. Each of these properties were then evaluated by an expert in the field and given a score from one to five to rate its investment potential, which was the dependent variable. Sixteen different network architectures were used to create over 200 neural networks. However, none of these networks met the criteria established to determine success. This is likely due to the unreliability in the data used to train the network, evidenced by the expert’s inability to reproduce previously assigned scores.

Colorectal cancer is the second cause of cancer death in the world. Aiming to early detect and prevent this type of cancer, clinicians perform screenings through the colon searching for polyps (colorectal cancer precursor lesions).If found, these lesions are susceptible of being removed in order to further ana-lyze their malignancy degree. Automatic polyp segmentation is of primary impor-tance when it comes to computer-aided medical diagnosis using images obtained in colonoscopy screenings. These results allow for more precise medical diagnosis which can lead to earlier detection.This project proposed a neural network based solution for semantic segmenta-tion, using the U-net architecture.Combining different data augmentation techniques to alleviate the problem of data scarcity and conducting experiments on the different hyperparameters of the network, the U-net scored a mean Intersection over Union (IoU) of 0,6814. A final approach that combines prediction maps of different models scored a mean IoU of 0,7236.

Last few decades have witnessed the use of artificial neural networks (ANN) in many real-world applications and have offered an attractive paradigm for a broad range of adaptive complex systems. In recent years ANN have enjoyed a great deal of success and have proven useful in wide variety pattern recognition or feature extraction tasks. Examples include optical character recognition, speech recognition and adaptive control to name a few. To keep the pace with its huge demand in diversified application areas, many different kinds of ANN architecture and learning types have been proposed by the researchers to meet varying needs. A novel hybrid learning approach for the training of a feed-forward ANN has been proposed in this thesis. The approach combines evolutionary algorithms with matrix solution methods such as singular value decomposition, Gram-Schmidt etc., to achieve optimum weights for hidden and output layers. The proposed hybrid method is to apply evolutionary algorithm in the first layer and least square method (LS) in the second layer of the ANN. The methodology also finds optimum number of hidden neurons using a hierarchical combination methodology structure for weights and architecture. A learning algorithm has many facets that can make a learning algorithm good for a particular application area. Often there are trade offs between classification accuracy and time complexity, nevertheless, the problem of memory complexity remains. This research explores all the different facets of the proposed new algorithm in terms of classification accuracy, convergence property, generalization ability, time and memory complexity.

The evaluation of structural performance of existing concrete buildings, built according to standards and materials quite different to those available today, requires procedures and methods able to cover lack of data about mechanical material properties and reinforcement detailing. To this end detailed inspections and test on materials are required. As a consequence tests on drilled cores are required; on the other end, it is stated that non-destructive testing (NDT) cannot be used as the only mean to get structural information, but can be used in conjunction with destructive testing (DT) by a representative correlation between DT and NDT. The aim of this study is to verify the accuracy of some formulas of correlation available in literature between measured parameters, i.e. rebound index, ultrasonic pulse velocity and compressive strength (SonReb Method). To this end a relevant number of DT and NDT tests has been performed on many school buildings located in Cesena (Italy). The above relationships have been assessed on site correlating NDT results to strength of core drilled in adjacent locations. Nevertheless, concrete compressive strength assessed by means of NDT methods and evaluated with correlation formulas has the advantage of being able to be implemented and used for future applications in a much more simple way than other methods, even if its accuracy is strictly limited to the analysis of concretes having the same characteristics as those used for their calibration. This limitation warranted a search for a different evaluation method for the non-destructive parameters obtained on site. To this aim, the methodology of neural identification of compressive strength is presented. Artificial Neural Network (ANN) suitable for the specific analysis were chosen taking into account the development presented in the literature in this field. The networks were trained and tested in order to detect a more reliable strength identification methodology.

Drug development is a long and expensive process. It is often not until potential drug candidates are administered to humans that accurate quantification of their pharmacokinetic characteristics is achieved. The goal of developing quantitative structure-pharmacokinetic relationships (QSPkRs) is to relate the molecular structure of a chemical entity with its pharmacokinetic characteristics. In this thesis artificial neural networks (ANNs) were used to construct in silico predictive QSPkRs for various pharmacokinetic parameters using different drug data sets. Drug pharmacokinetic data for all studies were taken from the literature. Information for model construction was extracted from drug molecular structure. Numerous theoretical descriptors were generated from drug structure ranging from simple constitutional and functional group counts to complex 3D quantum chemical numbers. Subsets of descriptors were selected which best modeled the target pharmacokinetic parameter(s). Using manual selective pruning, QSPkRs for physiological clearances, volumes of distribution, and fraction bound to plasma proteins were developed for a series of beta-adrenoceptor antagonists. All optimum ANN models had training and cross-validation correlations close to unity, while testing was performed with an independent set of compounds. In most cases the ANN models developed performed better than other published ANN models for the same drug data set. The ability of ANNs to develop QSPkRs with multiple target outputs was investigated for a series of cephalosporins. Multilayer perceptron ANN models were constructed for prediction of half life, volume of distribution, clearances (whole body and renal), fraction excreted in the urine, and fraction bound to plasma proteins. The optimum model was well able to differentiate compounds in a qualitative manner while quantitative predictions were mostly in agreement with observed literature values. The ability to make simultaneous predictions of important pharmacokinetic properties of a compound made this a valuable model. A radial-basis function ANN was employed to construct a quantitative structure-bioavailability relationship for a large, structurally diverse series of compounds. The optimum model contained descriptors encoding constitutional through to conformation dependent solubility characteristics. Prediction of bioavailability for the independent testing set were generally close to observed values. Furthermore, the optimum model provided a good qualitative tool for differentiating between drugs with either low or high experimental bioavailability. QSPkR models constructed with ANNs were compared with multilinear regression models. ANN models were shown to be more effective at selecting a suitable subset of descriptors to model a given pharmacokinetic parameter. They also gave more accurate predictions than multilinear regression equations. This thesis presents work which supports the use of ANNs in pharmacokinetic modeling. Successful QSPkRs were constructed using different combinations of theoretically-derived descriptors and model optimisation techniques. The results demonstrate that ANNs provide a valuable modeling tool that may be useful in drug discovery and development.

Thesis (M.A.)--Kent State University, 2009.<br>Title from PDF t.p. (viewed Mar. 11, 2010). Advisor: Mandy Munro-Stasiuk. Keywords: Remote Sensing Image; Cloud-free; Artificial Neural Networks. Includes bibliographical references (p. 57-59).