Over-dependence on domain ontology and lack of knowledge sharing across domains are two practical and yet less studied problems of dialogue state tracking. Existing approaches generally fall short in tracking unknown slot values during inference and often have difficulties in adapting to new domains. In this paper, we propose a TRAnsferable Dialogue statE generator (TRADE) that generates dialogue states from utterances using a copy mechanism, facilitating knowledge transfer when predicting (domain, slot, value) triplets not encountered during training. Our model is composed of an utterance encoder, a slot gate, and a state generator, which are shared across domains. Empirical results demonstrate that TRADE achieves state-of-the-art joint goal accuracy of 48.62% for the five domains of Mul-tiWOZ, a human-human dialogue dataset. In addition, we show its transferring ability by simulating zero-shot and few-shot dialogue state tracking for unseen domains.
Early diagnosis, playing an important role in preventing progress and treating the Alzheimer's disease (AD), is based on classification of features extracted from brain images. The features have to accurately capture main AD-related variations of anatomical brain structures, such as, e.g., ventricles size, hippocampus shape, cortical thickness, and brain volume. This paper proposed to predict the AD with a deep 3D convolutional neural network (3D-CNN), which can learn generic features capturing AD biomarkers and adapt to different domain datasets. The 3D-CNN is built upon a 3D convolutional autoencoder, which is pre-trained to capture anatomical shape variations in structural brain MRI scans. Fully connected upper layers of the 3D-CNN are then fine-tuned for each task-specific AD classification. Experiments on the CADDementia MRI dataset with no skull-stripping preprocessing have shown our 3D-CNN outperforms several conventional classifiers by accuracy. Abilities of the 3D-CNN to generalize the features learnt and adapt to other domains have been validated on the ADNI dataset.Index Terms-Alzheimer's disease, deep learning, 3D convolutional neural network, autoencoder, brain MRI
Abstract-We demonstrate a new deep learning autoencoder network, trained by a nonnegativity constraint algorithm (NCAE), that learns features which show part-based representation of data. The learning algorithm is based on constraining negative weights. The performance of the algorithm is assessed based on decomposing data into parts and its prediction performance is tested on three standard image data sets and one text dataset. The results indicate that the nonnegativity constraint forces the autoencoder to learn features that amount to a part-based representation of data, while improving sparsity and reconstruction quality in comparison with the traditional sparse autoencoder and Nonnegative Matrix Factorization. It is also shown that this newly acquired representation improves the prediction performance of a deep neural network.
Task-oriented dialogue is often decomposed into three tasks: understanding user input, deciding actions, and generating a response. While such decomposition might suggest a dedicated model for each sub-task, we find a simple, unified approach leads to state-of-the-art performance on the MultiWOZ dataset. SimpleTOD is a simple approach to task-oriented dialogue that uses a single causal language model trained on all sub-tasks recast as a single sequence prediction problem. This allows SimpleTOD to fully leverage transfer learning from pre-trained, open domain, causal language models such as GPT-2. SimpleTOD improves over the prior state-of-the-art by 0.49 points in joint goal accuracy for dialogue state tracking. More impressively, SimpleTOD also improves the main metrics used to evaluate action decisions and response generation in an end-to-end setting for task-oriented dialog systems: inform rate by 8.1 points, success rate by 9.7 points, and combined score by 7.2 points.Preprint. Under review.
No abstract
Early diagnosis, playing an important role in preventing progress and treating the Alzheimer's disease (AD), is based on classification of features extracted from brain images. The features have to accurately capture main AD-related variations of anatomical brain structures, such as, e.g., ventricles size, hippocampus shape, cortical thickness, and brain volume. This paper proposes to predict the AD with a deep 3D convolutional neural network (3D-CNN), which can learn generic features capturing AD biomarkers and adapt to different domain datasets. The 3D-CNN is built upon a 3D convolutional autoencoder, which is pre-trained to capture anatomical shape variations in structural brain MRI scans. Fully connected upper layers of the 3D-CNN are then finetuned for each task-specific AD classification. Experiments on the ADNI MRI dataset with no skull-stripping preprocessing have shown our 3D-CNN outperforms several conventional classifiers by accuracy and robustness. Abilities of the 3D-CNN to generalize the features learnt and adapt to other domains have been validated on the CADDementia dataset.
No abstract
Domain adaptation plays an important role for speech recognition models, in particular, for domains that have low resources. We propose a novel generative model based on cyclicconsistent generative adversarial network (CycleGAN) for unsupervised non-parallel speech domain adaptation. The proposed model employs multiple independent discriminators on the power spectrogram, each in charge of different frequency bands. As a result we have 1) better discriminators that focus on fine-grained details of the frequency features, and 2) a generator that is capable of generating more realistic domainadapted spectrogram. We demonstrate the effectiveness of our method on speech recognition with gender adaptation, where the model only has access to supervised data from one gender during training, but is evaluated on the other at test time. Our model is able to achieve an average of 7.41% on phoneme error rate, and 11.10% word error rate relative performance improvement as compared to the baseline, on TIMIT and WSJ dataset, respectively. Qualitatively, our model also generates more natural sounding speech, when conditioned on data from the other domain.
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.