Xi Chen

Ali Zafari, Xi Chen, Shirin Jalali

Zero-shot denoising aims to denoise observations without access to training samples or clean reference images. This setting is particularly relevant in practical imaging scenarios involving specialized domains such as medical imaging or biology. In this work, we propose the Zero-Shot Neural Compression Denoiser (ZS-NCD), a novel denoising framework based on neural compression. ZS-NCD treats a neural compression network as an untrained model, optimized directly on patches extracted from a single noisy image. The final reconstruction is then obtained by aggregating the outputs of the trained model over overlapping patches. Thanks to the built-in entropy constraints of compression architectures, our method naturally avoids overfitting and does not require manual regularization or early stopping. Through extensive experiments, we show that ZS-NCD achieves state-of-the-art performance among zero-shot denoisers for both Gaussian and Poisson noise, and generalizes well to both natural and non-natural images. Additionally, we provide new finite-sample theoretical results that characterize upper bounds on the achievable reconstruction error of general maximum-likelihood compression-based denoisers. These results further establish the theoretical foundations of compression-based denoising. Our code is available at: github.com/Computational-Imaging-RU/ZS-NCDenoiser.

Mengyu Zhao, Xi Chen, Xin Yuan et al.

Snapshot compressive imaging (SCI) recovers high-dimensional (3D) data cubes from a single 2D measurement, enabling diverse applications like video and hyperspectral imaging to go beyond standard techniques in terms of acquisition speed and efficiency. In this paper, we focus on SCI recovery algorithms that employ untrained neural networks (UNNs), such as deep image prior (DIP), to model source structure. Such UNN-based methods are appealing as they have the potential of avoiding the computationally intensive retraining required for different source models and different measurement scenarios. We first develop a theoretical framework for characterizing the performance of such UNN-based methods. The theoretical framework, on the one hand, enables us to optimize the parameters of data-modulating masks, and on the other hand, provides a fundamental connection between the number of data frames that can be recovered from a single measurement to the parameters of the untrained NN. We also employ the recently proposed bagged-deep-image-prior (bagged-DIP) idea to develop SCI Bagged Deep Video Prior (SCI-BDVP) algorithms that address the common challenges faced by standard UNN solutions. Our experimental results show that in video SCI our proposed solution achieves state-of-the-art among UNN methods, and in the case of noisy measurements, it even outperforms supervised solutions.

Xi Chen, Xingda Li

Diffuse correlation spectroscopy (DCS) is an emerging noninvasive technique that measures the tissue blood flow, by using near-infrared coherent point-source illumination to detect spectral changes. While machine learning has demonstrated significant potential for measuring blood flow index (BFi), an open question concerning the success of this approach pertains to its robustness in scenarios involving deviations between datasets with varying Signal-to-Noise Ratios (SNRs) originating from diverse clinical applications and various setups. This study proposes a transfer learning approach, aims to assess the influence of SNRs on the generalization ability of learned features, and demonstrate the robustness for transfer learning. A synthetic dataset with varying levels of added noise is utilized to simulate different SNRs. The proposed network takes a 1x64 autocorrelation curve as input and generates BFi and the correlation parameter beta. The proposed model demonstrates excellent performance across different SNRs, exhibiting enhanced fitting accuracy, particularly for low SNR datasets when compared with other fitting methods. This highlights its potential for clinical diagnosis and treatment across various scenarios under different clinical setups.