Utilizing mutual learning can effectively enhance the performance of peer BNNs.

Under this setting, previous SSL methods tend to predict wrong pseudo-labels with the model fitted on labeled data, resulting in noise accumulation.

Did you specify all the training details (e.g., data splits, hyperparameters, how they

Q1: ...the claim that the algorithm really manages to align the latent distributions of real and simulated data... We will revise the inappropriate statements in the final version. Q2: In the model adaptation phase, are state-action pairs simply sampled randomly from their respective buffers? Do you have results for a single, monolithic model? Q4: Did you investigate the reasons for the slow learning in the 500 steps on InvertedPendulum compared to PETS? Q1: The experiments shown in Figure 2 do not outperform MBPO beyond the confidence bounds.

Such failure can be caused by distribution shift (also known as dataset shift) between the training and test datasets. For this reason, distribution shift and domain adaptation (a notion comprising techniques for tackling distribution shift) has been a major research topic in machine learning for some time. This paper takes the perspective of Kouw and Loog (2021) and studies the case where feature observations from the test dataset are available for analysis but observations of labels are missing. Under these circumstances, without any assumptions on the nature of the distribution shift between the training and test datasets meaningful prediction of the labels in the test dataset or of their distribution is not feasible. See Kouw and Loog (2021) for a survey of approaches to domain adaptation and their related assumptions. Arguably, covariate shift (also known as population drift) and label shift (also known as prior probability shift or target shift) are the most popular specific distribution shift assumptions, both for their intuiveness as well as their computational manageability. However, exclusive covariate and label shift assumptions have been criticised for being insufficient for common domain adaptation tasks (e.g.

Traditional semi-supervised learning (SSL) assumes that the feature distributions of labeled and unlabeled data are consistent which rarely holds in realistic scenarios. In this paper, we propose a novel SSL setting, where unlabeled samples are drawn from a mixed distribution that deviates from the feature distribution of labeled samples.Under this setting, previous SSL methods tend to predict wrong pseudo-labels with the model fitted on labeled data, resulting in noise accumulation. To tackle this issue, we propose \emph{Self-Supervised Feature Adaptation} (SSFA), a generic framework for improving SSL performance when labeled and unlabeled data come from different distributions. SSFA decouples the prediction of pseudo-labels from the current model to improve the quality of pseudo-labels. Particularly, SSFA incorporates a self-supervised task into the SSL framework and uses it to adapt the feature extractor of the model to the unlabeled data. In this way, the extracted features better fit the distribution of unlabeled data, thereby generating high-quality pseudo-labels. Extensive experiments show that our proposed SSFA is applicable to various pseudo-label-based SSL learners and significantly improves performance in labeled, unlabeled, and even unseen distributions.

Federated learning (FL) is a distributed learning framework that leverages commonalities between distributed client datasets to train a global model. Under heterogeneous clients, however, FL can fail to produce stable training results. Personalized federated learning (PFL) seeks to address this by learning individual models tailored to each client. One approach is to decompose model training into shared representation learning and personalized classifier training. Nonetheless, previous works struggle to navigate the bias-variance trade-off in classifier learning, relying solely on limited local datasets or introducing costly techniques to improve generalization.In this work, we frame representation learning as a generative modeling task, where representations are trained with a classifier based on the global feature distribution. We then propose an algorithm, pFedFDA, that efficiently generates personalized models by adapting global generative classifiers to their local feature distributions. Through extensive computer vision benchmarks, we demonstrate that our method can adjust to complex distribution shifts with significant improvements over current state-of-the-art in data-scarce settings.

Disease grading is a crucial task in medical image analysis. Due to the continuous progression of diseases, i.e., the variability within the same level and the similarity between adjacent stages, accurate grading is highly challenging.Furthermore, in real-world scenarios, models trained on limited source domain datasets should also be capable of handling data from unseen target domains.Due to the cross-domain variants, the feature distribution between source and unseen target domains can be dramatically different, leading to a substantial decrease in model performance.To address these challenges in cross-domain disease grading, we propose a Severity-aware Recurrent Modeling (Samba) method in this paper.As the core objective of most staging tasks is to identify the most severe lesions, which may only occupy a small portion of the image, we propose to encode image patches in a sequential and recurrent manner.Specifically, a state space model is tailored to store and transport the severity information by hidden states.Moreover, to mitigate the impact of cross-domain variants, an Expectation-Maximization (EM) based state recalibration mechanism is designed to map the patch embeddings into a more compact space.We model the feature distributions of different lesions through the Gaussian Mixture Model (GMM) and reconstruct the intermediate features based on learnable severity bases.Extensive experiments show the proposed Samba outperforms the VMamba baseline by an average accuracy of 23.5\%, 5.6\% and 4.1\% on the cross-domain grading of fatigue fracture, breast cancer and diabetic retinopathy, respectively. Source code is available at \url{https://github.com/BiQiWHU/Samba}.