Learning Representations from Persian Handwriting for Offline Signature Verification, a Deep Transfer Learning Approach

Offline Signature Verification (OSV) is a challenging pattern recognition task, especially when it is expected to generalize well on the skilled forgeries that are not available during the training. Its challenges also include small training sample and large intra-class variations. Considering the limitations, we suggest a novel transfer learning approach from Persian handwriting domain to multi-language OSV domain. We train two Residual CNNs on the source domain separately based on two different tasks of word classification and writer identification. Since identifying a person signature resembles identifying ones handwriting, it seems perfectly convenient to use handwriting for the feature learning phase. The learned representation on the more varied and plentiful handwriting dataset can compensate for the lack of training data in the original task, i.e. OSV, without sacrificing the generalizability. Our proposed OSV system includes two steps: learning representation and verification of the input signature. For the first step, the signature images are fed into the trained Residual CNNs. The output representations are then used to train SVMs for the verification. We test our OSV system on three different signature datasets, including MCYT (a Spanish signature dataset), UTSig (a Persian one) and GPDS-Synthetic (an artificial dataset). On UT-SIG, we achieved 9.80% Equal Error Rate (EER) which showed substantial improvement over the best EER in the literature, 17.45%. Our proposed method surpassed state-of-the-arts by 6% on GPDS-Synthetic, achieving 6.81%. On MCYT, EER of 3.98% was obtained which is comparable to the best previously reported results

Neurogenesis Deep Learning

Neural machine learning methods, such as deep neural networks (DNN), have achieved remarkable success in a number of complex data processing tasks. These methods have arguably had their strongest impact on tasks such as image and audio processing - data processing domains in which humans have long held clear advantages over conventional algorithms. In contrast to biological neural systems, which are capable of learning continuously, deep artificial networks have a limited ability for incorporating new information in an already trained network. As a result, methods for continuous learning are potentially highly impactful in enabling the application of deep networks to dynamic data sets. Here, inspired by the process of adult neurogenesis in the hippocampus, we explore the potential for adding new neurons to deep layers of artificial neural networks in order to facilitate their acquisition of novel information while preserving previously trained data representations. Our results on the MNIST handwritten digit dataset and the NIST SD 19 dataset, which includes lower and upper case letters and digits, demonstrate that neurogenesis is well suited for addressing the stability-plasticity dilemma that has long challenged adaptive machine learning algorithms.Comment: 8 pages, 8 figures, Accepted to 2017 International Joint Conference on Neural Networks (IJCNN 2017

Transfer learning in hierarchical feature spaces

© 2015 IEEE. Transfer learning provides an approach to solve target tasks more quickly and effectively by using previously acquired knowledge learned from source tasks. As one category of transfer learning approaches, feature-based transfer learning approaches aim to find a latent feature space shared between source and target domains. The issue is that the sole feature space can't exploit the relationship of source domain and target domain fully. To deal with this issue, this paper proposes a transfer learning method that uses deep learning to extract hierarchical feature spaces, so knowledge of source domain can be exploited and transferred in multiple feature spaces with different levels of abstraction. In the experiment, the effectiveness of transfer learning in multiple feature spaces is compared and this can help us find the optimal feature space for transfer learning

A Novel Deep Convolutional Neural Network Architecture Based on Transfer Learning for Handwritten Urdu Character Recognition

Deep convolutional neural networks (CNN) have made a huge impact on computer vision and set the state-of-the-art in providing extremely definite classification results. For character recognition, where the training images are usually inadequate, mostly transfer learning of pre-trained CNN is often utilized. In this paper, we propose a novel deep convolutional neural network for handwritten Urdu character recognition by transfer learning three pre-trained CNN models. We fine-tuned the layers of these pre-trained CNNs so as to extract features considering both global and local details of the Urdu character structure. The extracted features from the three CNN models are concatenated to train with two fully connected layers for classification. The experiment is conducted on UNHD, EMILLE, DBAHCL, and CDB/Farsi dataset, and we achieve 97.18% average recognition accuracy which outperforms the individual CNNs and numerous conventional classification methods

Generating Focussed Molecule Libraries for Drug Discovery with Recurrent Neural Networks

In de novo drug design, computational strategies are used to generate novel molecules with good affinity to the desired biological target. In this work, we show that recurrent neural networks can be trained as generative models for molecular structures, similar to statistical language models in natural language processing. We demonstrate that the properties of the generated molecules correlate very well with the properties of the molecules used to train the model. In order to enrich libraries with molecules active towards a given biological target, we propose to fine-tune the model with small sets of molecules, which are known to be active against that target. Against Staphylococcus aureus, the model reproduced 14% of 6051 hold-out test molecules that medicinal chemists designed, whereas against Plasmodium falciparum (Malaria) it reproduced 28% of 1240 test molecules. When coupled with a scoring function, our model can perform the complete de novo drug design cycle to generate large sets of novel molecules for drug discovery.Comment: 17 pages, 17 figure