NVE: A Separability and Coverage-Aware Internal Validation Metric for Biclustering

Biclustering, or co-clustering, aims to discover coherent submatrices by grouping rows and columns of a data matrix simultaneously. This local two-dimensional structure makes validation more difficult than in ordinary clustering, where internal indices usually rely on compactness and separation in a single shared feature space. Existing popular internal biclustering measures such as Mean Squared Residue (MSR), and Virtual Error (VE) mainly evaluate within-bicluster coherence. Although useful, these measures do not directly assess whether the extracted biclusters are mutually distinct or whether they explain a meaningful portion of the data matrix. This paper investigates Normalised Virtual Error (NVE), an internal validation metric that extends VE using a super-bicluster normalization strategy. By comparing the VE of each bicluster with the VE obtained after merging it with other biclusters, NVE introduces a relative notion of separability and redundancy. We also study a coverage-adjusted variant, NVE\textsubscript{cov}, which penalizes solutions that obtain low error by selecting only very small submatrices. Through controlled synthetic benchmarks and yeast gene-expression datasets, we examine whether NVE and NVE\textsubscript{cov} provide information beyond standard coherence-based metrics. The results show that NVE is sensitive to redundant and poorly separated biclusters, while NVE\textsubscript{cov} changes solution rankings when low-error biclusters cover only a negligible part of the matrix. These findings suggest that NVE-based measures are useful complementary criteria for internal co-clustering validation, especially when coherence, separability, and coverage must be considered jointly.

Sparse Functional Singular Value Decomposition for Biclustering and Triclustering Longitudinal Data

Identifying subtypes of complex conditions, such as Inflammatory Bowel Disease (IBD), often requires capturing latent patterns in longitudinal omics data. However, these data are typically high-dimensional, sparsely sampled, and irregularly observed over time, posing substantial challenges for conventional (bi)clustering and functional data analysis methods. We propose Tri-SfSVD, a unified sparse functional Singular Value Decomposition framework for discovering biclusters and triclusters in longitudinal data. Unlike existing functional biclustering methods that rely on ad hoc imputation or enforce restrictive shape-homogeneity assumptions, Tri-SfSVD integrates continuous trajectory estimation with simultaneous subject, feature, and temporal selection within a single optimization framework. By imposing sparse penalties across subjects, variables, and temporal subregions, the proposed method works directly on observed data to uncover localized structures at the subject, subject-feature, and subject-feature-time levels. Extensive simulations demonstrate that Tri-SfSVD outperforms existing approaches in high-dimensional settings. Applied to IBD multi-omics data, the method identified three biclusters linking sample clusters with distinct IBD-related clinical characteristics to microbial pathway groups associated with specific bacterial taxa, providing interpretable subject-pathway associations for characterizing disease heterogeneity. Applied to multi-channel EEG data, the method identified three triclusters linking sample clusters with distinct alcohol-related phenotypes to localized brain activity patterns, including subgroup differences separated by temporal subregions within the same spatial region.