arXiv subjects

Suvojit Hazra

Publications and source records attributed to Suvojit Hazra.

3 recordsLinked to original sources

arXiv2026

MERLIN-SUITE: Probabilistic modular GRN inference from multi-omics data integrating regulatory priors and transcription factor activity

Accurately reconstructing gene regulatory networks (GRNs) is essential for understanding transcriptional processes in development and disease. MERLIN-SUITE (https://github.com/Roy-lab/MERLIN-SUITE) represents a collection of algorithmic extensions based on MERLIN (Modular regulatory network learning with per gene information) a probabilistic framework that infers gene-specific and module-specific regulatory programs of co-regulated modules, capturing both detailed and modular aspects of transcriptional networks. While expression-based inference is effective, it often aligns poorly with experimentally validated regulatory interactions. MERLIN-P addresses this by integrating external regulatory priors, such as motif, ChIP, and perturbation data, to enhance biological relevance and predictive accuracy. MERLIN-P-TFA further advances the framework by incorporating regularized estimation of latent transcription factor activity (TFA), overcoming the limitation that TF mRNA levels may not represent protein activity. By integrating expression data, prior knowledge, and activity-aware modeling, this unified approach supports robust GRN reconstruction in both bulk and single-cell datasets. This chapter presents the MERLIN-SUITE with a focus on MERLIN-P-TFA and demonstrates its use on a single-cell, multi-modal dataset of mouse cellular reprogramming to infer GRNs and identify key regulators.

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arXiv2026

scMTNI: Leveraging cellular trajectory and context to infer dynamic GRNs from single-cell multi-omics data

Transcriptional gene regulatory networks (GRNs) depict the directed relationships between regulators and target genes, determining gene expression patterns in a cell-type-specific manner. Single-cell multi-omics technologies, such as single-cell RNA sequencing (scRNA-seq) and single-cell Assay for Transposase-Accessible Chromatin using sequencing (scATAC-seq), enable high-resolution measurement of cell-type-specific gene expression and regulation in an unprecedented way. However, tools for inferring cell-type-specific GRNs and modeling their dynamics remain scarce. To facilitate the inference and analysis of cell-type-specific GRNs in contexts such as cellular development or disease progression, where cell lineage structure and dynamics are important, we developed a multi-task learning framework, single-cell Multi-Task Network Inference (scMTNI). scMTNI and its associated network analyses tools offer a comprehensive package to define cell-type-specific GRNs and examine their dynamics. This book chapter describes the scMTNI tool and demonstrates its application to an existing cellular reprogramming single cell multi-modal dataset to infer cell-type-specific GRNs and identify key regulators of cellular fate transitions during cellular reprogramming.

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arXiv2026

Modeling Dynamics, Cell Type Specificity, and Perturbations in Gene Regulatory Networks

Gene regulatory networks (GRNs) define the regulatory relationships among molecules such as transcription factors, chromatin remodelers, and target genes. GRNs play a critical role in diverse biological processes, including development, disease manifestation, and evolution. However, fully characterizing these networks across multiple cell types and states remains a significant challenge. Recent advances in single-cell omics have dramatically enhanced our ability to measure biological systems at unprecedented resolution. These technologies have opened new avenues for computational methods to infer GRNs, offering deeper insights into cell type-specific mechanisms, causality, and dynamic regulatory processes. This review summarizes the current state of GRN inference from single cell omic datasets, with a particular focus on dynamics and perturbations, and outlines key open challenges that must be addressed to advance the field.

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