S3^3R: Self-supervised Spectral Regression for Hyperspectral Histopathology Image Classification

Benefited from the rich and detailed spectral information in hyperspectral images (HSI), HSI offers great potential for a wide variety of medical applications such as computational pathology. But, the lack of adequate annotated data and the high spatiospectral dimensions of HSIs usually make classification networks prone to overfit. Thus, learning a general representation which can be transferred to the downstream tasks is imperative. To our knowledge, no appropriate self-supervised pre-training method has been designed for histopathology HSIs. In this paper, we introduce an efficient and effective Self-supervised Spectral Regression (S$^3$R) method, which exploits the low rank characteristic in the spectral domain of HSI. More concretely, we propose to learn a set of linear coefficients that can be used to represent one band by the remaining bands via masking out these bands. Then, the band is restored by using the learned coefficients to reweight the remaining bands. Two pre-text tasks are designed: (1)S$^3$R-CR, which regresses the linear coefficients, so that the pre-trained model understands the inherent structures of HSIs and the pathological characteristics of different morphologies; (2)S$^3$R-BR, which regresses the missing band, making the model to learn the holistic semantics of HSIs. Compared to prior arts i.e., contrastive learning methods, which focuses on natural images, S$^3$R converges at least 3 times faster, and achieves significant improvements up to 14% in accuracy when transferring to HSI classification tasks

Gene-induced Multimodal Pre-training for Image-omic Classification

Histology analysis of the tumor micro-environment integrated with genomic assays is the gold standard for most cancers in modern medicine. This paper proposes a Gene-induced Multimodal Pre-training (GiMP) framework, which jointly incorporates genomics and Whole Slide Images (WSIs) for classification tasks. Our work aims at dealing with the main challenges of multi-modality image-omic classification w.r.t. (1) the patient-level feature extraction difficulties from gigapixel WSIs and tens of thousands of genes, and (2) effective fusion considering high-order relevance modeling. Concretely, we first propose a group multi-head self-attention gene encoder to capture global structured features in gene expression cohorts. We design a masked patch modeling paradigm (MPM) to capture the latent pathological characteristics of different tissues. The mask strategy is randomly masking a fixed-length contiguous subsequence of patch embeddings of a WSI. Finally, we combine the classification tokens of paired modalities and propose a triplet learning module to learn high-order relevance and discriminative patient-level information.After pre-training, a simple fine-tuning can be adopted to obtain the classification results. Experimental results on the TCGA dataset show the superiority of our network architectures and our pre-training framework, achieving 99.47% in accuracy for image-omic classification. The code is publicly available at https://github.com/huangwudiduan/GIMP

SSDPT: Self-Supervised Dual-Path Transformer for Anomalous Sound Detection in Machine Condition Monitoring

Anomalous sound detection for machine condition monitoring has great potential in the development of Industry 4.0. However, these anomalous sounds of machines are usually unavailable in normal conditions. Therefore, the models employed have to learn acoustic representations with normal sounds for training, and detect anomalous sounds while testing. In this article, we propose a self-supervised dual-path Transformer (SSDPT) network to detect anomalous sounds in machine monitoring. The SSDPT network splits the acoustic features into segments and employs several DPT blocks for time and frequency modeling. DPT blocks use attention modules to alternately model the interactive information about the frequency and temporal components of the segmented acoustic features. To address the problem of lack of anomalous sound, we adopt a self-supervised learning approach to train the network with normal sound. Specifically, this approach randomly masks and reconstructs the acoustic features, and jointly classifies machine identity information to improve the performance of anomalous sound detection. We evaluated our method on the DCASE2021 task2 dataset. The experimental results show that the SSDPT network achieves a significant increase in the harmonic mean AUC score, in comparison to present state-of-the-art methods of anomalous sound detection

MagicNet: Semi-Supervised Multi-Organ Segmentation via Magic-Cube Partition and Recovery

We propose a novel teacher-student model for semi-supervised multi-organ segmentation. In teacher-student model, data augmentation is usually adopted on unlabeled data to regularize the consistent training between teacher and student. We start from a key perspective that fixed relative locations and variable sizes of different organs can provide distribution information where a multi-organ CT scan is drawn. Thus, we treat the prior anatomy as a strong tool to guide the data augmentation and reduce the mismatch between labeled and unlabeled images for semi-supervised learning. More specifically, we propose a data augmentation strategy based on partition-and-recovery N$^3$ cubes cross- and within- labeled and unlabeled images. Our strategy encourages unlabeled images to learn organ semantics in relative locations from the labeled images (cross-branch) and enhances the learning ability for small organs (within-branch). For within-branch, we further propose to refine the quality of pseudo labels by blending the learned representations from small cubes to incorporate local attributes. Our method is termed as MagicNet, since it treats the CT volume as a magic-cube and N$^3$-cube partition-and-recovery process matches with the rule of playing a magic-cube. Extensive experiments on two public CT multi-organ datasets demonstrate the effectiveness of MagicNet, and noticeably outperforms state-of-the-art semi-supervised medical image segmentation approaches, with +7% DSC improvement on MACT dataset with 10% labeled images. Code is available at https://github.com/DeepMed-Lab-ECNU/MagicNet.Comment: Accepted by CVPR 202

Intriguing Findings of Frequency Selection for Image Deblurring

Blur was naturally analyzed in the frequency domain, by estimating the latent sharp image and the blur kernel given a blurry image. Recent progress on image deblurring always designs end-to-end architectures and aims at learning the difference between blurry and sharp image pairs from pixel-level, which inevitably overlooks the importance of blur kernels. This paper reveals an intriguing phenomenon that simply applying ReLU operation on the frequency domain of a blur image followed by inverse Fourier transform, i.e., frequency selection, provides faithful information about the blur pattern (e.g., the blur direction and blur level, implicitly shows the kernel pattern). Based on this observation, we attempt to leverage kernel-level information for image deblurring networks by inserting Fourier transform, ReLU operation, and inverse Fourier transform to the standard ResBlock. 1x1 convolution is further added to let the network modulate flexible thresholds for frequency selection. We term our newly built block as Res FFT-ReLU Block, which takes advantages of both kernel-level and pixel-level features via learning frequency-spatial dual-domain representations. Extensive experiments are conducted to acquire a thorough analysis on the insights of the method. Moreover, after plugging the proposed block into NAFNet, we can achieve 33.85 dB in PSNR on GoPro dataset. Our method noticeably improves backbone architectures without introducing many parameters, while maintaining low computational complexity. Code is available at https://github.com/DeepMed-Lab/DeepRFT-AAAI2023.Comment: AAAI 202

Bcl-x Pre-mRNA splicing regulates brain injury after neonatal hypoxia-ischemia

The bcl-x gene appears to play a critical role in regulating apoptosis in the developing and mature central nervous system (CNS) and following CNS injury. Two isoforms of Bcl-x are produced as a result of alternative pre-mRNA splicing: Bcl-x(L) (the long form) is anti-apoptotic, while Bcl-x(S) (short form) is pro-apoptotic. Despite the antagonistic activities of these two isoforms, little is known about how regulation of alternative splicing of bcl-x may mediate neural cell apoptosis. Here, we report that apoptotic stimuli (staurosporine or C2-ceramide) reciprocally altered Bcl-x splicing in neural cells, decreasing Bcl-x(L) while increasing Bcl-x(S). Specific knockdown of Bcl-x(S) attenuated apoptosis. In order to further define regulatory elements that influenced Bcl-x splicing, a Bcl-x minigene was constructed. Deletional analysis revealed several consensus sequences within intron 2 that altered splicing. We found that the splicing factor, CUG-binding-protein-1 (CUGBP1), bound to a consensus sequence close to the Bcl-x(L) 5′ splice site, altering the Bcl-x(L)/Bcl-x(S) ratio and influencing cell death. In vivo, neonatal hypoxia-ischemia reciprocally altered Bcl-x pre-mRNA splicing, similar to the in vitro studies. Manipulation of the splice isoforms using viral gene transfer of Bcl-x(S) shRNA into the hippocampus of rats prior to neonatal hypoxia-ischemia decreased vulnerability to injury. Moreover, alterations in nuclear CUGBP1 preceded Bcl-x splicing changes. These results suggest that alternative pre-mRNA splicing may be an important regulatory mechanism for cell death after acute neurological injury, and may potentially provide novel targets for intervention