Identification of Tamil handwritten calligraphies at different levels such as character, word and paragraph is complicated when compared to other western language scripts. None of the existing methods provides efficient Tamil handwriting writer identification (THWI). Also offline Tamil handwritten identification at different levels still offers many motivating challenges to researchers. This paper employs a deep learning algorithm for handwriting image classification. Deep learning has its own dimensions to generate new features from a limited set of training dataset. Convolutional Neural Networks (CNNs) is one of deep, feed-forward artificial neural network is applied to THWI. The dataset collection and classification phase of CNN enables data access and automatic feature generation. Since the number of parameters is significantly reduced, training time to THWI is proportionally reduced. Understandably, the CNNs produced much higher identification rate compared with traditional ANN at different levels of handwriting.
The autonomous driving aims at ensuring the vehicle to effectively sense the environment and use proper strategies to navigate the vehicle without the interventions of humans. Hence, there exist a prediction of the background scenes and that leads to discontinuity between the predicted and planned outputs. An optimal prediction engine is required that suitably reads the background objects and make optimal decisions. In this paper, the author(s) develop an autonomous model for vehicle driving using ensemble model for large Sport Utility Vehicles (SUVs) that uses three different modules involving (a) recognition model, (b) planning model and (c) prediction model. The study develops a direct realization method for an autonomous vehicle driving. The direct realization method is designed as a behavioral model that incorporates three different modules to ensure optimal autonomous driving. The behavioral model includes recognition, planning and prediction modules that regulates the input trajectory processing of input video datasets. A deep learning algorithm is used in the proposed approach that helps in the classification of known or unknown objects along the line of sight. This model is compared with conventional deep learning classifiers in terms of recall rate and root mean square error (RMSE) to estimate its efficacy. Simulation results on different traffic environment shows that the Ensemble Convolutional Network Reinforcement Learning (E-CNN-RL) offers increased accuracy of 95.45%, reduced RMSE and increased recall rate than existing Ensemble Convolutional Neural Networks (CNN) and Ensemble Stacked CNN.
Principal Component Regression (PCR) is a regression analysis technique based on Principal Component Analysis (PCA) which enables the identification of the principal components that can be used in a linear kernel and Support Vector Machine (SVM) as a classifier. In PCR, instead of regressing the dependent variable on the explanatory variables directly, the principal components of the explanatory variables are used as regresseors. Only a subset of all the principal components is made use of for regression, thus making PCR a kind of regularized procedure. The principal components with higher variances are selected as regressors and used in SVM linear kernel to estimate the coefficients of the kernel and the linear kernel is specified as Principal Component Kernel-Support Vector Machine (PCK-SVM). Writer Identification in Tamil handwriting is implemented by employing PCK-SVM and the results of the PCK-SVM are compared with our Weighted Least Square regression Kernel based Support Vector Machine (WLK-SVM) and Bayesian linear regression Kernel based Support Vector Machine (BLK-SVM)models. These methods are evaluated on several text images of handwriting at character, word and paragraph levels. The results show that modified linear kernel performs very well with minimum time taken to classify the writer. Performance comparison results of three kernels achieved highest performance of 94.9% accuracy in PCK-SVM than in WLK of 90.8% and BLK of 92.3% accuracy.
Purpose Diagnosing genetic neuromuscular disorder such as muscular dystrophy is complicated when the imperfection occurs while splicing. This paper aims in predicting the type of muscular dystrophy from the gene sequences by extracting the well-defined descriptors related to splicing mutations. An automatic model is built to classify the disease through pattern recognition techniques coded in python using scikit-learn framework. Design/methodology/approach In this paper, the cloned gene sequences are synthesized based on the mutation position and its location on the chromosome by using the positional cloning approach. For instance, in the human gene mutational database (HGMD), the mutational information for splicing mutation is specified as IVS1-5 T > G indicates (IVS - intervening sequence or introns), first intron and five nucleotides before the consensus intron site AG, where the variant occurs in nucleotide G altered to T. IVS (+ve) denotes forward strand 3′– positive numbers from G of donor site invariant and IVS (−ve) denotes backward strand 5′ – negative numbers starting from G of acceptor site. The key idea in this paper is to spot out discriminative descriptors from diseased gene sequences based on splicing variants and to provide an effective machine learning solution for predicting the type of muscular dystrophy disease with the splicing mutations. Multi-class classification is worked out through data modeling of gene sequences. The synthetic mutational gene sequences are created, as the diseased gene sequences are not readily obtainable for this intricate disease. Positional cloning approach supports in generating disease gene sequences based on mutational information acquired from HGMD. SNP-, gene- and exon-based discriminative features are identified and used to train the model. An eminent muscular dystrophy disease prediction model is built using supervised learning techniques in scikit-learn environment. The data frame is built with the extracted features as numpy array. The data are normalized by transforming the feature values into the range between 0 and 1 aid in scaling the input attributes for a model. Naïve Bayes, decision tree, K-nearest neighbor and SVM learned models are developed using python library framework in scikit-learn. Findings To the best knowledge of authors, this is the foremost pattern recognition model, to classify muscular dystrophy disease pertaining to splicing mutations. Certain essential SNP-, gene- and exon-based descriptors related to splicing mutations are proposed and extracted from the cloned gene sequences. An eminent model is built using statistical learning technique through scikit-learn in the anaconda framework. This paper also deliberates the results of statistical learning carried out with the same set of gene sequences with synonymous and non-synonymous mutational descriptors. Research limitations/implications The data frame is built with the Numpy array. Normalizing the data by transforming the feature values into the range between 0 and 1 aid in scaling the input attributes for a model. Naïve Bayes, decision tree, K-nearest neighbor and SVM learned models are developed using python library framework in scikit-learn. While learning the SVM model, the cost, gamma and kernel parameters are tuned to attain good results. Scoring parameters of the classifiers are evaluated using tenfold cross-validation using metric functions of scikit-learn library. Results of the disease identification model based on non-synonymous, synonymous and splicing mutations were analyzed. Practical implications Certain essential SNP-, gene- and exon-based descriptors related to splicing mutations are proposed and extracted from the cloned gene sequences. An eminent model is built using statistical learning technique through scikit-learn in the anaconda framework. The performance of the classifiers are increased by using different estimators from the scikit-learn library. Several types of mutations such as missense, non-sense and silent mutations are also considered to build models through statistical learning technique and their results are analyzed. Originality/value To the best knowledge of authors, this is the foremost pattern recognition model, to classify muscular dystrophy disease pertaining to splicing mutations.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.