Turn-level dialogue evaluation models (TDEMs), using self-supervised learning (SSL) framework, have achieved state-of-the-art performance in open-domain dialogue evaluation. However, these models inevitably face two potential problems. First, they have low correlations with humans on medium coherence samples as the SSL framework often brings training data with unbalanced coherence distribution. Second, the SSL framework leads TDEM to nonuniform score distribution. There is a danger that the nonuniform score distribution will weaken the robustness of TDEM through our theoretical analysis.

Video self-supervised learning (VSSL) has made significant progress in recent years. However, the exact behavior and dynamics of these models under different forms of distribution shift are not yet known. In this paper, we comprehensively study the behavior of six popular self-supervised methods (v-SimCLR, v-MoCo, v-BYOL, v-SimSiam, v-DINO, v-MAE) in response to various forms of natural distribution shift, i.e., (i) context shift, (ii) viewpoint shift, (iii) actor shift, (iv) source shift, (v) generalizability to unknown classes (zero-shot), and (vi) open-set recognition. To perform this extensive study, we carefully craft a test bed consisting of 17 in-distribution and out-of-distribution benchmark pairs using available public datasets and a series of evaluation protocols to stress-test the different methods under the intended shifts. For instance, we observe that while video models generally struggle with context shifts, v-MAE and supervised learning exhibit more robustness.

Webly supervised learning has attracted increasing attention for its effectiveness in exploring publicly accessible data at scale without manual annotation. However, most existing methods of learning with web datasets are faced with challenges from label noise, and they have limited assumptions on clean samples under various noise. For instance, web images retrieved with queries of "tiger cat" (a cat species) and "drumstick" (a musical instrument) are almost dominated by images of tigers and chickens, which exacerbates the challenge of fine-grained visual concept learning. In this case, exploiting both web images and their associated texts is a requisite solution to combat real-world noise. In this paper, we propose Cross-modality Aligned Prototypes (CAPro), a unified prototypical contrastive learning framework to learn visual representations with correct semantics.

We propose a scheme for auditing differentially private machine learning systems with a single training run. This exploits the parallelism of being able to add or remove multiple training examples independently. We analyze this using the connection between differential privacy and statistical generalization, which avoids the cost of group privacy. Our auditing scheme requires minimal assumptions about the algorithm and can be applied in the black-box or white-box setting. We demonstrate the effectiveness of our framework by applying it to DP-SGD, where we can achieve meaningful empirical privacy lower bounds by training only one model.

We present an extensive study of surrogate losses for structured prediction supported by * H -consistency bounds*. These are recently introduced guarantees that are more relevant to learning than Bayes-consistency, since they are not asymptotic and since they take into account the hypothesis set H used. We first show that no non-trivial H -consistency bound can be derived for widely used surrogate structured prediction losses. We then define several new families of surrogate losses, including *structured comp-sum losses* and *structured constrained losses*, for which we prove H -consistency bounds and thus Bayes-consistency. These loss functions readily lead to new structured prediction algorithms with stronger theoretical guarantees, based on their minimization.

As annotations of data can be scarce in large-scale practical problems, leveraging unlabelled examples is one of the most important aspects of machine learning. This is the aim of semi-supervised learning. To benefit from the access to unlabelled data, it is natural to diffuse smoothly knowledge of labelled data to unlabelled one. This induces to the use of Laplacian regularization. Yet, current implementations of Laplacian regularization suffer from several drawbacks, notably the well-known curse of dimensionality.

Despite recent advances in its theoretical understanding, there still remains a significant gap in the ability of existing PAC-Bayesian theories on meta-learning to explain performance improvements in the few-shot learning setting, where the number of training examples in the target tasks is severely limited. This gap originates from an assumption in the existing theories which supposes that the number of training examples in the observed tasks and the number of training examples in the target tasks follow the same distribution, an assumption that rarely holds in practice. By relaxing this assumption, we develop two PAC-Bayesian bounds tailored for the few-shot learning setting and show that two existing meta-learning algorithms (MAML and Reptile) can be derived from our bounds, thereby bridging the gap between practice and PAC-Bayesian theories. Furthermore, we derive a new computationally-efficient PACMAML algorithm, and show it outperforms existing meta-learning algorithms on several few-shot benchmark datasets.

Virtual screening, which identifies potential drugs from vast compound databases to bind with a particular protein pocket, is a critical step in AI-assisted drug discovery. Traditional docking methods are highly time-consuming, and can only work with a restricted search library in real-life applications. Recent supervised learning approaches using scoring functions for binding-affinity prediction, although promising, have not yet surpassed docking methods due to their strong dependency on limited data with reliable binding-affinity labels. In this paper, we propose a novel contrastive learning framework, DrugCLIP, by reformulating virtual screening as a dense retrieval task and employing contrastive learning to align representations of binding protein pockets and molecules from a large quantity of pairwise data without explicit binding-affinity scores. We also introduce a biological-knowledge inspired data augmentation strategy to learn better protein-molecule representations.

We explore task-free continual learning (CL), in which a model is trained to avoid catastrophic forgetting in the absence of explicit task boundaries or identities. Among many efforts on task-free CL, a notable family of approaches are memory-based that store and replay a subset of training examples. However, the utility of stored seen examples may diminish over time since CL models are continually updated. Here, we propose Gradient based Memory EDiting (GMED), a framework for editing stored examples in continuous input space via gradient updates, in order to create more "challenging" examples for replay. GMED-edited examples remain similar to their unedited forms, but can yield increased loss in the upcoming model updates, thereby making the future replays more effective in overcoming catastrophic forgetting. By construction, GMED can be seamlessly applied in conjunction with other memory-based CL algorithms to bring further improvement.

Large language models have demonstrated surprising ability to perform in-context learning, i.e., these models can be directly applied to solve numerous downstream tasks by conditioning on a prompt constructed by a few input-output examples. However, prior research has shown that in-context learning can suffer from high instability due to variations in training examples, example order, and prompt formats. Therefore, the construction of an appropriate prompt is essential for improving the performance of in-context learning. In this paper, we revisit this problem from the view of predictive bias. Specifically, we introduce a metric to evaluate the predictive bias of a fixed prompt against labels or a given attributes. Then we empirically show that prompts with higher bias always lead to unsatisfactory predictive quality.