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Taulant Koka

Publications and source records attributed to Taulant Koka.

4 recordsLinked to original sources

Virtual Dummies: Enabling Scalable FDR-Controlled Variable Selection via Sequential Sampling of Null Features

High-dimensional variable selection, particularly in genomics, requires error-controlling procedures that scale to millions of predictors. The Terminating-Random Experiments (T-Rex) selector achieves false discovery rate (FDR) control by aggregating results of early terminated random experiments, each combining original predictors with i.i.d. synthetic null variables (dummies). At biobank scales, however, explicit dummy augmentation requires terabytes of memory. We demonstrate that this bottleneck is not fundamental. Formalizing the information flow of forward selection through a filtration, we show that compatible selectors interact with unselected dummies solely through projections onto an adaptively evolving low-dimensional subspace. For rotationally invariant dummy distributions, we derive an adaptive stick-breaking construction sampling these projections from their exact conditional distribution given the selection history, thereby eliminating dummy matrix materialization. We prove a pathwise universality theorem: under mild delocalization conditions, selection paths driven by generic standardized i.i.d. dummies converge to the same Gaussian limit. We instantiate the theory through Virtual Dummy LARS (VD-LARS), reducing memory and runtime by several orders of magnitude while preserving the exact selection law and FDR guarantees of the T-Rex selector. Experiments on realistic genome-wide association study data confirm that VD-T-Rex controls FDR and achieves power at scales where all competing methods either fail or time out.

stat.ME

Cross-Channel Unlabeled Sensing over a Union of Signal Subspaces

Cross-channel unlabeled sensing addresses the problem of recovering a multi-channel signal from measurements that were shuffled across channels. This work expands the cross-channel unlabeled sensing framework to signals that lie in a union of subspaces. The extension allows for handling more complex signal structures and broadens the framework to tasks like compressed sensing. These mismatches between samples and channels often arise in applications such as whole-brain calcium imaging of freely moving organisms or multi-target tracking. We improve over previous models by deriving tighter bounds on the required number of samples for unique reconstruction, while supporting more general signal types. The approach is validated through an application in whole-brain calcium imaging, where organism movements disrupt sample-to-neuron mappings. This demonstrates the utility of our framework in real-world settings with imprecise sample-channel associations, achieving accurate signal reconstruction.

eess.SP

False Discovery Rate Control for Gaussian Graphical Models via Neighborhood Screening

Gaussian graphical models emerge in a wide range of fields. They model the statistical relationships between variables as a graph, where an edge between two variables indicates conditional dependence. Unfortunately, well-established estimators, such as the graphical lasso or neighborhood selection, are known to be susceptible to a high prevalence of false edge detections. False detections may encourage inaccurate or even incorrect scientific interpretations, with major implications in applications, such as biomedicine or healthcare. In this paper, we introduce a nodewise variable selection approach to graph learning and provably control the false discovery rate of the selected edge set at a self-estimated level. A novel fusion method of the individual neighborhoods outputs an undirected graph estimate. The proposed method is parameter-free and does not require tuning by the user. Benchmarks against competing false discovery rate controlling methods in numerical experiments considering different graph topologies show a significant gain in performance.

stat.ML

Shuffled Multi-Channel Sparse Signal Recovery

Mismatches between samples and their respective channel or target commonly arise in several real-world applications. For instance, whole-brain calcium imaging of freely moving organisms, multiple-target tracking or multi-person contactless vital sign monitoring may be severely affected by mismatched sample-channel assignments. To systematically address this fundamental problem, we pose it as a signal reconstruction problem where we have lost correspondences between the samples and their respective channels. Assuming that we have a sensing matrix for the underlying signals, we show that the problem is equivalent to a structured unlabeled sensing problem, and establish sufficient conditions for unique recovery. To the best of our knowledge, a sampling result for the reconstruction of shuffled multi-channel signals has not been considered in the literature and existing methods for unlabeled sensing cannot be directly applied. We extend our results to the case where the signals admit a sparse representation in an overcomplete dictionary (i.e., the sensing matrix is not precisely known), and derive sufficient conditions for the reconstruction of shuffled sparse signals. We propose a robust reconstruction method that combines sparse signal recovery with robust linear regression for the two-channel case. The performance and robustness of the proposed approach is illustrated in an application related to whole-brain calcium imaging. The proposed methodology can be generalized to sparse signal representations other than the ones considered in this work to be applied in a variety of real-world problems with imprecise measurement or channel assignment.

eess.SP