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Qoku, A.

Publications and source records attributed to Qoku, A..

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PACMON: Pathway-guided Multi-Omics data integration for interpreting large-scale perturbation screens

High-throughput perturbation screens coupled with single-cell molecular profiling enable systematic interrogation of gene function, yet interpreting the resulting data in terms of biological pathways remains challenging. Existing approaches either identify latent gene modules without linking them to perturbations, or model perturbation effects without incorporating prior biological knowledge, limiting interpretability and scalability. Here, we introduce PACMON (Pathwayguided Multi-Omics data integration for interpreting large-scale perturbation screens), a Bayesian latent factor model that jointly infers pathway-level programs and their modulation by experimental perturbations. PACMON decomposes multimodal molecular measurements into shared latent factors aligned with known biological pathways through structured sparsity priors, while simultaneously estimating how each perturbation activates or represses these pathway programs. The framework naturally accommodates multiple data modalities and employs stochastic variational inference for scalable application to large datasets. We evaluate PACMON in three settings of increasing complexity. On synthetic data with known ground truth, PACMON achieves near-perfect recovery of pathway structure and perturbation effects, outperforming existing methods in both accuracy and computational scalability. Applied to a multimodal Perturb-CITE-seq screen of melanoma cells, PACMON recovers coherent interferon-signaling and cell-cycle programs spanning RNA and surface-protein modalities and identifies interpretable perturbation-pathway associations consistent with known immune-evasion mechanisms. Finally, we apply PACMON to the Tahoe-100M perturbation atlas -- approximately 100 million cells and over 1,000 drug-dose combinations -- producing the first pathway-level latent factor analysis at this scale and revealing biologically meaningful drug-response landscapes across Hallmark pathway programs. PACMON provides a unified, scalable and interpretable framework for mapping perturbation effects onto biological pathways in modern large-scale perturbation experiments.

bioinformatics↗

MOFA-FLEX: A Factor Model Framework for Integrating Omics Data with Prior Knowledge

Latent factor models are first-line analysis approaches for single- and multi-omics data, essential for data integration, alignment, and biological signal discovery. To cater for new technologies and experimental designs, bespoke extensions of factor models have been proposed, incorporating spatial structure, temporal dynamics and the noise characteristics of single-cell assays. However, the development of tailored methods and software for individual use cases is laborious and requires advanced statistical and domain expertise, posing a significant barrier to users. To address this, we here propose MOFA-FLEX, a flexible and modular factor analysis framework designed for customisable modelling across diverse multi-omics data scenarios. Built on probabilistic programming, MOFA-FLEX unifies previously isolated extensions of factor analysis - including flexible priors, non-negativity constraints, supervision signals, and alternative data likelihoods - allowing models to be configured declaratively without requiring manual engineering. Additionally, MOFA-FLEX features a novel domain knowledge module to inform and connect latent factors to gene programs. We demonstrate MOFA-FLEX across multiple applications, showing (i) improved robustness in recovering gene programs from noisy prior knowledge in scRNA-seq data; (ii) effective disentanglement of technical and biological variation in multi-omic CITE-seq; and (iii) tailored spatial modelling that reveals spatially organised disease-associated gene programs in breast cancer.

bioinformatics↗