SOLVE: A Structured Orthogonal Latent Variable Framework for Disentangling Confounding in Matrix Data

Accepted by Biology Methods & Protocols on Dec 02, 2025. Corresponding author: Jialai She Abstract: Latent factor models are valuable in bioinformatics for accounting for unmeasured variation alongside observed covariates. Yet many methods struggle to separate known effects from latent structure and to handle losses beyond standard regression. We present a unified framework that augments row and column predictors with a low-rank latent component, jointly modeling measured effects and residual variation. To remove ambiguity in estimating observed and latent effects, we impose a carefully designed set of orthogonality constraints on the coefficient and latent factor matrices, relative to the spans of the predictor matrices. These constraints ensure identifiability, yield a decomposition in which the latent term captures only variation unexplained by the covariates, and improve interpretability. An efficient algorithm handles general non-quadratic losses via surrogates with monotone descent. Each iteration updates the latent term by truncated singular value decomposition of a doubly projected residual and refines coefficients by projections. The number of latent factors is selected by applying an elbow rule to a degrees-of-freedom-adjusted information criterion. A parametric bootstrap provides valid inference on feature-outcome associations under the regularized low-rank structure. Applied to real pharmacogenomic data, the method recovers biologically coherent gene-drug associations missed by standard factor models, such as the EGFR-inhibitor link, highlights novel candidates with plausible mechanisms, and reveals gene programs aligned with compound modes of action, including a latent unfolded-protein-response module affecting drug sensitivity. These results support the framework's utility for precision oncology, yielding stronger biomarkers for patient stratification and deeper insight into drug resistance mechanisms.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-12-02
DOI
https://doi.org/10.5281/zenodo.17861446
Primary Topic
Statistical Methods and Inference
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

SOLVE: A Structured Orthogonal Latent Variable Framework for Disentangling Confounding in Matrix Data

Zenodo (CERN European Organization for Nuclear Research)
Statistical Methods and Inference
article

SOLVE: A Structured Orthogonal Latent Variable Framework for Disentangling Confounding in Matrix Data

article en

Abstract

Accepted by Biology Methods & Protocols on Dec 02, 2025. Corresponding author: Jialai She Abstract: Latent factor models are valuable in bioinformatics for accounting for unmeasured variation alongside observed covariates. Yet many methods struggle to separate known effects from latent structure and to handle losses beyond standard regression. We present a unified framework that augments row and column predictors with a low-rank latent component, jointly modeling measured effects and residual variation. To remove ambiguity in estimating observed and latent effects, we impose a carefully designed set of orthogonality constraints on the coefficient and latent factor matrices, relative to the spans of the predictor matrices. These constraints ensure identifiability, yield a decomposition in which the latent term captures only variation unexplained by the covariates, and improve interpretability. An efficient algorithm handles general non-quadratic losses via surrogates with monotone descent. Each iteration updates the latent term by truncated singular value decomposition of a doubly projected residual and refines coefficients by projections. The number of latent factors is selected by applying an elbow rule to a degrees-of-freedom-adjusted information criterion. A parametric bootstrap provides valid inference on feature-outcome associations under the regularized low-rank structure. Applied to real pharmacogenomic data, the method recovers biologically coherent gene-drug associations missed by standard factor models, such as the EGFR-inhibitor link, highlights novel candidates with plausible mechanisms, and reveals gene programs aligned with compound modes of action, including a latent unfolded-protein-response module affecting drug sensitivity. These results support the framework's utility for precision oncology, yielding stronger biomarkers for patient stratification and deeper insight into drug resistance mechanisms.

Zenodo (CERN European Organization for Nuclear Research)
Peace, Justice and strong institutions
Openalex Percentile: Top 31%
Statistical Methods and Inference
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.