With the proliferation of digital communication, dialogue summarization has become increasingly important. However, it still faces a shortage of data. To address this issue, we developed **Gen**erative **D**ata Augmentation Strategy Leveraging **Ex**ternal Data for Abstractive Dialogue Summarization (**GENDEX**), which is based on the hypothetical foundation that texts containing people and their interpersonal interactions can potentially serve as summaries of corresponding dialogues. We filter short texts containing people and resolve coreferences for better contextual analysis. We then identify the semantic roles of words within the texts and filter them based on the patterns observed in the dialogue summarization datasets. Using these texts, we generate synthetic dialogues through a controlled generation method. To better leverage the augmented data, we utilize noise-tolerant training to fine-tune the summarization model. The experimental results demonstrate the effectiveness of our proposed method, showing its robust performance, generalizability, and scalability. Moreover, performance improvements by *GENDEX* were observed regardless of complexity of dialogues. The code is available at https://github.com/DMCB-GIST/GENDEX.

Early stopping, which is widely used to prevent overfitting, is generally based on a separate validation set. However, in low resource settings, validation-based stopping can be risky because a small validation set may not be sufficiently representative, and the reduction in the number of samples by validation split may result in insufficient samples for training. In this study, we propose an early stopping method that uses unlabeled samples. The proposed method is based on confidence and class distribution similarities. To further improve the performance, we present a calibration method to better estimate the class distribution of the unlabeled samples. The proposed method is advantageous because it does not require a separate validation set and provides a better stopping point by using a large unlabeled set. Extensive experiments are conducted on five text classification datasets and several stop-methods are compared. Our results show that the proposed model even performs better than using an additional validation set as well as the existing stop-methods, in both balanced and imbalanced data settings. Our code is available at https://github.com/DMCB-GIST/BUS-stop.

Since the development and wide use of pretrained language models (PLMs), several approaches have been applied to boost their performance on downstream tasks in specific domains, such as biomedical or scientific domains. Additional pre-training with in-domain texts is the most common approach for providing domain-specific knowledge to PLMs. However, these pre-training methods require considerable in-domain data and training resources and a longer training time. Moreover, the training must be re-performed whenever a new PLM emerges. In this study, we propose a domain knowledge transferring (DoKTra) framework for PLMs without additional in-domain pretraining. Specifically, we extract the domain knowledge from an existing in-domain pretrained language model and transfer it to other PLMs by applying knowledge distillation. In particular, we employ activation boundary distillation, which focuses on the activation of hidden neurons. We also apply an entropy regularization term in both teacher training and distillation to encourage the model to generate reliable output probabilities, and thus aid the distillation. By applying the proposed DoKTra framework to downstream tasks in the biomedical, clinical, and financial domains, our student models can retain a high percentage of teacher performance and even outperform the teachers in certain tasks. Our code is available at https://github.com/DMCB-GIST/DoKTra.

The extraction of interactions between chemicals and proteins from several biomedical articles is important in many fields of biomedical research such as drug development and prediction of drug side effects. Several natural language processing methods, including deep neural network (DNN) models, have been applied to address this problem. However, these methods were trained with hard-labeled data, which tend to become over-confident, leading to degradation of the model reliability. To estimate the data uncertainty and improve the reliability, “calibration” techniques have been applied to deep learning models. In this study, to extract chemical–protein interactions, we propose a DNN-based approach incorporating uncertainty information and calibration techniques. Our model first encodes the input sequence using a pre-trained language-understanding model, following which it is trained using two calibration methods: mixup training and addition of a confidence penalty loss. Finally, the model is re-trained with augmented data that are extracted using the estimated uncertainties. Our approach has achieved state-of-the-art performance with regard to the Biocreative VI ChemProt task, while preserving higher calibration abilities than those of previous approaches. Furthermore, our approach also presents the possibilities of using uncertainty estimation for performance improvement.