基于扩散模型的半监督脑肿瘤分割内含数据集和环境说明.zip

# Semi-supervised Brain Tumor Segmentation using Diffusion Models We provide the official PyTorch implementation of the paper titled [Semi-supervised Brain Tumor Segmentation Using Diffusion Models](https://link.springer.com/chapter/10.1007/978-3-031-34111-3_27) by Ahmed Alshenoudy, Bertram Sabrowsky-Hirsch, Stefan Thumfart, Michael Giretzlehner and Erich Kobler. Our implementation is based on [Label-Efficient Semantic Segmentation with Diffusion Models](https://github.com/yandex-research/ddpm-segmentation), where we also employ [Improved Denoising Diffusion Probabilistic Models](https://github.com/openai/improved-diffusion). Various core functions were heavily influenced from [nnUNet V1](https://github.com/MIC-DKFZ/nnUNet/tree/nnunetv1/nnunet/training/network_training) as well. ## Overview In this paper, we leverage learned visual representations from diffusion models for the challenging task of brain tumor segmentation. We compare the segmentation performance against a supervised baseline over a varying degree of training samples. For the downstream segmentation task, we used pixel-level classifiers and additionally proposed the fine-tuning of the noise predictor network of the diffusion model. Our results show that, with less than 20 training samples, all methods outperform the supervised baseline across all tumor regions. We also provide a practical use-case where we automatically annotate tumor regions across different axial slices within the same patient, with very limited supervision. ## Data We evaluate the presented approach on the Brain Tumor Segmentation (BraTS) 2021 data. Axial slices were extracted from the original 3D MR sequences, while stratifying longitudinal slicing locations to increase the proportion of slices containing a segmented tumor. All slices were normalized and down-sampled to (128, 128). This resulted in a dataset consisting of 8,757 slices, of which 8,000 were used for testing and the 757 remaining slices were used as a training pool to sample various training datasets from for our experiments. ## Results - Our trained diffusion model and a small batch of generated samples can be found [here](https://www.dropbox.com/sh/78x8aamupsidxax/AABmtL06uEh6CGwWWvP3fcCMa?dl=0). We visualize a batch of generated mpMRI samples from the fully trained model in the figure below. This is to visually assess how well the model is able to approximate the dataset distribution. <figure> <img src="https://raw.githubusercontent.com/risc-mi/braintumor-ddpm/main/docs/assets/generated_samples.png" alt="Generated 128 x 128 BraTS samples" style="width:100%"> <figcaption><b>Fig. 1: Generated (128, 128) BraTS samples.</b></figcaption> </figure> &nbsp; - Extracted visual representations for sample inputs are visualized in Fig. 2, our results align with the original paper, where earlier layer capture high-level features and later layers capture more detailed features while also becoming noisier. <figure> <img src="https://raw.githubusercontent.com/risc-mi/braintumor-ddpm/main/docs/assets/representations.png" alt="Generated 128 x 128 BraTS samples" style="width:100%"> <figcaption><b>Fig. 2: Extracted visual representations for different samples across different layers and time steps.</b></figcaption> </figure> &nbsp; - Sample predictions of different tumor regions are visualized in Fig. 3, a comparison between two pixel-level classifier architectures, the fine-tuned noise predictor network and the nnU-Net supervised baseline. <figure> <img src="https://raw.githubusercontent.com/risc-mi/braintumor-ddpm/main/docs/assets/sample_predictions.png" alt="Generated 128 x 128 BraTS samples" style="width:100%"> <figcaption><b>Fig. 3: Sample predictions for multiple input scans.</b></figcaption> </figure> &nbsp; - A sample practical use-case, where a few tumor containing axial slices from the same patient are used to train the downstream pixel-level classifier to produce segmentation maps for the remaining slices within the same volume. Performance is very good for slices that contain larger sections of the tumor, while a significant drop in performance is observed for out of distribution slices that were not used for training the downstream model or the diffusion model itself. <figure> <img src="https://raw.githubusercontent.com/risc-mi/braintumor-ddpm/main/docs/assets/usecase.png" alt="Generated 128 x 128 BraTS samples" style="width:100%"> <figcaption><b>Fig. 4: Practical use-case for patient-level segmentation.</b></figcaption> </figure> ### Citation If you find this codebase useful for your research, we would appreciate citing the following conference paper: ``` @InProceedings{braintumor_ddpm2023, author={Alshenoudy, Ahmed and Sabrowsky-Hirsch, Bertram and Thumfart, Stefan and Giretzlehner, Michael and Kobler, Erich}, editor={Maglogiannis, Ilias and Iliadis, Lazaros and MacIntyre, John and Dominguez, Manuel}, title={Semi-supervised Brain Tumor Segmentation Using Diffusion Models}, booktitle={Artificial Intelligence Applications and Innovations}, year={2023}, publisher={Springer Nature Switzerland}, address={Cham}, pages={314--325}, isbn={978-3-031-34111-3}. doi={10.1007/978-3-031-34111-3_27} } ``` ### Acknowledgements This project is financed by research subsidies granted by the government of Upper Austria. RISC Software GmbH is Member of UAR (Upper Austrian Research) Innovation Network. ### TODO: - [ ] Tutorial notebook on how to use the pipeline for segmentation - [ ] Addition of Deep/Wide MLP architecture and normal initialization - [ ] Requirements file notes: - [ ] Numpy (< 1.24.0) due to conflict with MedPy (used for HD95 metric) - [ ] Introduced anti-alias parameter in torchvision - [ ] MPI, used for `dist_utils` in improved diffusion