Myeongjang Pyeon

Insu Jeon, Wonkwang Lee, Myeongjang Pyeon et al.

We propose a new GAN-based unsupervised model for disentangled representation learning. The new model is discovered in an attempt to utilize the Information Bottleneck (IB) framework to the optimization of GAN, thereby named IB-GAN. The architecture of IB-GAN is partially similar to that of InfoGAN but has a critical difference; an intermediate layer of the generator is leveraged to constrain the mutual information between the input and the generated output. The intermediate stochastic layer can serve as a learnable latent distribution that is trained with the generator jointly in an end-to-end fashion. As a result, the generator of IB-GAN can harness the latent space in a disentangled and interpretable manner. With the experiments on dSprites and Color-dSprites dataset, we demonstrate that IB-GAN achieves competitive disentanglement scores to those of state-of-the-art \b{eta}-VAEs and outperforms InfoGAN. Moreover, the visual quality and the diversity of samples generated by IB-GAN are often better than those by \b{eta}-VAEs and Info-GAN in terms of FID score on CelebA and 3D Chairs dataset.

Myeongjang Pyeon, Janghyeon Lee, Minsoo Lee et al.

In digital pathology, whole-slide images (WSIs) are often difficult to handle due to their gigapixel scale, so most approaches train patch encoders via self-supervised learning (SSL) and then aggregate the patch-level embeddings via multiple instance learning (MIL) or slide encoders for downstream tasks. However, patch-level SSL may overlook complex domain-specific features that are essential for biomarker prediction, such as mutation status and molecular characteristics, as SSL methods rely only on basic augmentations selected for natural image domains on small patch-level area. Moreover, SSL methods remain less data efficient than fully supervised approaches, requiring extensive computational resources and datasets to achieve competitive performance. To address these limitations, we present EXAONE Path 2.0, a pathology foundation model that learns patch-level representations under direct slide-level supervision. Using only 37k WSIs for training, EXAONE Path 2.0 achieves state-of-the-art average performance across 10 biomarker prediction tasks, demonstrating remarkable data efficiency.