Meng Yang

Chengrui Wei, Meng Yang, Lei He et al.

It has long been an ill-posed problem to predict absolute depth maps from single images in real (unseen) indoor scenes. We observe that it is essentially due to not only the scale-ambiguous problem but also the focal-ambiguous problem that decreases the generalization ability of monocular depth estimation. That is, images may be captured by cameras of different focal lengths in scenes of different scales. In this paper, we develop a focal-and-scale depth estimation model to well learn absolute depth maps from single images in unseen indoor scenes. First, a relative depth estimation network is adopted to learn relative depths from single images with diverse scales/semantics. Second, multi-scale features are generated by mapping a single focal length value to focal length features and concatenating them with intermediate features of different scales in relative depth estimation. Finally, relative depths and multi-scale features are jointly fed into an absolute depth estimation network. In addition, a new pipeline is developed to augment the diversity of focal lengths of public datasets, which are often captured with cameras of the same or similar focal lengths. Our model is trained on augmented NYUDv2 and tested on three unseen datasets. Our model considerably improves the generalization ability of depth estimation by 41%/13% (RMSE) with/without data augmentation compared with five recent SOTAs and well alleviates the deformation problem in 3D reconstruction. Notably, our model well maintains the accuracy of depth estimation on original NYUDv2.

Ziqi Yang, Zhongyu Li, Chen Liu et al.

Convolutional neural networks excel in histopathological image classification, yet their pixel-level focus hampers explainability. Conversely, emerging graph convolutional networks spotlight cell-level features and medical implications. However, limited by their shallowness and suboptimal use of high-dimensional pixel data, GCNs underperform in multi-class histopathological image classification. To make full use of pixel-level and cell-level features dynamically, we propose an asymmetric co-training framework combining a deep graph convolutional network and a convolutional neural network for multi-class histopathological image classification. To improve the explainability of the entire framework by embedding morphological and topological distribution of cells, we build a 14-layer deep graph convolutional network to handle cell graph data. For the further utilization and dynamic interactions between pixel-level and cell-level information, we also design a co-training strategy to integrate the two asymmetric branches. Notably, we collect a private clinically acquired dataset termed LUAD7C, including seven subtypes of lung adenocarcinoma, which is rare and more challenging. We evaluated our approach on the private LUAD7C and public colorectal cancer datasets, showcasing its superior performance, explainability, and generalizability in multi-class histopathological image classification.