Liyun Tu

CV
h-index9
3papers
8citations
Novelty53%
AI Score29

3 Papers

IVAug 7, 2024Code
Distillation Learning Guided by Image Reconstruction for One-Shot Medical Image Segmentation

Feng Zhou, Yanjie Zhou, Longjie Wang et al.

Traditional one-shot medical image segmentation (MIS) methods use registration networks to propagate labels from a reference atlas or rely on comprehensive sampling strategies to generate synthetic labeled data for training. However, these methods often struggle with registration errors and low-quality synthetic images, leading to poor performance and generalization. To overcome this, we introduce a novel one-shot MIS framework based on knowledge distillation, which allows the network to directly 'see' real images through a distillation process guided by image reconstruction. It focuses on anatomical structures in a single labeled image and a few unlabeled ones. A registration-based data augmentation network creates realistic, labeled samples, while a feature distillation module helps the student network learn segmentation from these samples, guided by the teacher network. During inference, the streamlined student network accurately segments new images. Evaluations on three public datasets (OASIS for T1 brain MRI, BCV for abdomen CT, and VerSe for vertebrae CT) show superior segmentation performance and generalization across different medical image datasets and modalities compared to leading methods. Our code is available at https://github.com/NoviceFodder/OS-MedSeg.

CVFeb 23, 2024
Label-efficient multi-organ segmentation with a diffusion model

Yongzhi Huang, Fengjun Xi, Liyun Tu et al.

Accurate segmentation of multiple organs in Computed Tomography (CT) images plays a vital role in computer-aided diagnosis systems. While various supervised learning approaches have been proposed recently, these methods heavily depend on a large amount of high-quality labeled data, which are expensive to obtain in practice. To address this challenge, we propose a label-efficient framework using knowledge transfer from a pre-trained diffusion model for CT multi-organ segmentation. Specifically, we first pre-train a denoising diffusion model on 207,029 unlabeled 2D CT slices to capture anatomical patterns. Then, the model backbone is transferred to the downstream multi-organ segmentation task, followed by fine-tuning with few labeled data. In fine-tuning, two fine-tuning strategies, linear classification and fine-tuning decoder, are employed to enhance segmentation performance while preserving learned representations. Quantitative results show that the pre-trained diffusion model is capable of generating diverse and realistic 256x256 CT images (Fréchet inception distance (FID): 11.32, spatial Fréchet inception distance (sFID): 46.93, F1-score: 73.1%). Compared to state-of-the-art methods for multi-organ segmentation, our method achieves competitive performance on the FLARE 2022 dataset, particularly in limited labeled data scenarios. After fine-tuning with 1% and 10% labeled data, our method achieves dice similarity coefficients (DSCs) of 71.56% and 78.51%, respectively. Remarkably, the method achieves a DSC score of 51.81% using only four labeled CT slices. These results demonstrate the efficacy of our approach in overcoming the limitations of supervised learning approaches that is highly dependent on large-scale labeled data.

MLSep 9, 2021
Supervising the Decoder of Variational Autoencoders to Improve Scientific Utility

Liyun Tu, Austin Talbot, Neil Gallagher et al.

Probabilistic generative models are attractive for scientific modeling because their inferred parameters can be used to generate hypotheses and design experiments. This requires that the learned model provide an accurate representation of the input data and yield a latent space that effectively predicts outcomes relevant to the scientific question. Supervised Variational Autoencoders (SVAEs) have previously been used for this purpose, where a carefully designed decoder can be used as an interpretable generative model while the supervised objective ensures a predictive latent representation. Unfortunately, the supervised objective forces the encoder to learn a biased approximation to the generative posterior distribution, which renders the generative parameters unreliable when used in scientific models. This issue has remained undetected as reconstruction losses commonly used to evaluate model performance do not detect bias in the encoder. We address this previously-unreported issue by developing a second order supervision framework (SOS-VAE) that influences the decoder to induce a predictive latent representation. This ensures that the associated encoder maintains a reliable generative interpretation. We extend this technique to allow the user to trade-off some bias in the generative parameters for improved predictive performance, acting as an intermediate option between SVAEs and our new SOS-VAE. We also use this methodology to address missing data issues that often arise when combining recordings from multiple scientific experiments. We demonstrate the effectiveness of these developments using synthetic data and electrophysiological recordings with an emphasis on how our learned representations can be used to design scientific experiments.