Neural Information Processing Systems http://nips.cc/

Weobtain them directly from the low-rank Gaussian distribution for the logits in the network head of SSNs, based on a previously unconsidered view of this distribution as a factor model.

Exhaustively evaluating many large language models (LLMs) on a large suite of benchmarks is expensive. We cast benchmarking as finite-population inference and, under a fixed query budget, seek tight confidence intervals (CIs) for model accuracy with valid frequentist coverage. We propose Factorized Active Querying (FAQ), which (a) leverages historical information through a Bayesian factor model; (b) adaptively selects questions using a hybrid variance-reduction/active-learning sampling policy; and (c) maintains validity through Proactive Active Inference -- a finite-population extension of active inference (Zrnic & Candès, 2024) that enables direct question selection while preserving coverage. With negligible overhead cost, FAQ delivers up to $5\times$ effective sample size gains over strong baselines on two benchmark suites, across varying historical-data missingness levels: this means that it matches the CI width of uniform sampling while using up to $5\times$ fewer queries. We release our source code and our curated datasets to support reproducible evaluation and future research.

High-dimensional data often exhibit variation that can be captured by lower dimensional factors. For high-dimensional data from multiple studies or environments, one goal is to understand which underlying factors are common to all studies, and which factors are study or environment-specific. As a particular example, we consider platelet gene expression data from patients in different disease groups. In this data, factors correspond to clusters of genes which are co-expressed; we may expect some clusters (or biological pathways) to be active for all diseases, while some clusters are only active for a specific disease. To learn these factors, we consider a nonlinear multi-study factor model, which allows for both shared and specific factors. To fit this model, we propose a multi-study sparse variational autoencoder. The underlying model is sparse in that each observed feature (i.e. each dimension of the data) depends on a small subset of the latent factors. In the genomics example, this means each gene is active in only a few biological processes. Further, the model implicitly induces a penalty on the number of latent factors, which helps separate the shared factors from the group-specific factors. We prove that the latent factors are identified, and demonstrate our method recovers meaningful factors in the platelet gene expression data.

In this paper, we propose a distributed framework for reducing the dimensionality of high-dimensional, large-scale, heterogeneous matrix-variate time series data using a factor model. The data are first partitioned column-wise (or row-wise) and allocated to node servers, where each node estimates the row (or column) loading matrix via two-dimensional tensor PCA. These local estimates are then transmitted to a central server and aggregated, followed by a final PCA step to obtain the global row (or column) loading matrix estimator. Given the estimated loading matrices, the corresponding factor matrices are subsequently computed. Unlike existing distributed approaches, our framework preserves the latent matrix structure, thereby improving computational efficiency and enhancing information utilization. We also discuss row- and column-wise clustering procedures for settings in which the group memberships are unknown. Furthermore, we extend the analysis to unit-root nonstationary matrix-variate time series. Asymptotic properties of the proposed method are derived for the diverging dimension of the data in each computing unit and the sample size $T$. Simulation results assess the computational efficiency and estimation accuracy of the proposed framework, and real data applications further validate its predictive performance.

High-dimensional, simultaneous recordings of neural spiking activity are often explored, analyzed and visualized with the help of latent variable or factor models. Such models are however ill-equipped to extract structure beyond shared, distributed aspects of firing activity across multiple cells. Here, we extend unstructured factor models by proposing a model that discovers subpopulations or groups of cells from the pool of recorded neurons. The model combines aspects of mixture of factor analyzer models for capturing clustering structure, and aspects of latent dynamical system models for capturing temporal dependencies. In the resulting model, we infer the subpopulations and the latent factors from data using variational inference and model parameters are estimated by Expectation Maximization (EM). We also address the crucial problem of initializing parameters for EM by extending a sparse subspace clustering algorithm to integer-valued spike count observations. We illustrate the merits of the proposed model by applying it to calcium-imaging data from spinal cord neurons, and we show that it uncovers meaningful clustering structure in the data.

We address the challenge of forecasting counterfactual outcomes in a panel data with missing entries and temporally dependent latent factors -- a common scenario in causal inference, where estimating unobserved potential outcomes ahead of time is essential. We propose Forecasting Counterfactuals under Stochastic Dynamics (Focus), a method that extends traditional matrix completion methods by leveraging time series dynamics of the factors, thereby enhancing the prediction accuracy of future counterfactuals. Building upon a PCA estimator, our method accommodates both stochastic and deterministic components within the factors, and provides a flexible framework for various applications. In case of stationary autoregressive factors and under standard conditions, we derive error bounds and establish asymptotic normality of our estimator. Empirical evaluations demonstrate that our method outperforms existing benchmarks when the latent factors have an autoregressive component. We illustrate Focus results on HeartSteps, a mobile health study, illustrating its effectiveness in forecasting step counts for users receiving activity prompts, thereby leveraging temporal patterns in user behavior.

The intricate dynamics of stock markets have led to extensive research on models that are able to effectively explain their inherent complexities. This study leverages the econometrics literature to explore the dynamic factor model as an interpretable model with sufficient predictive capabilities for capturing essential market phenomena. Although the model has been extensively applied for predictive purposes, this study focuses on analyzing the extracted loadings and common factors as an alternative framework for understanding stock price dynamics. The results reveal novel insights into traditional market theories when applied to the Philippine Stock Exchange using the Kalman method and maximum likelihood estimation, with subsequent validation against the capital asset pricing model. Notably, a one-factor model extracts a common factor representing systematic or market dynamics similar to the composite index, whereas a two-factor model extracts common factors representing market trends and volatility. Furthermore, an application of the model for nowcasting the growth rates of the Philippine gross domestic product highlights the potential of the extracted common factors as viable real-time market indicators, yielding over a 34% decrease in the out-of-sample prediction error. Overall, the results underscore the value of dynamic factor analysis in gaining a deeper understanding of market price movement dynamics.