Identification of transcription factor–target gene interactions and construction of the gene regulatory networks (GRNs) are essential for understanding the molecular mechanisms underlying transcriptional gene regulation. Large-scale single-cell transcriptomics across different tissues offers unprecedented resolution of cellular diversity and regulatory dynamics by capturing gene expression heterogeneity. However, existing methods often lack effective multimodal integration and fail to fully exploit the hierarchical structure in Gene Ontology (GO) and gene sequence level representations, which limits their ability for predictive performance and biological interpretability. We present scMGFGRN, a multi-model deep learning framework that integrates single-cell transcriptomic profiles with gene functional hierarchical relationships, gene sequences by leveraging denoising auto-encoders, graph attention feature extraction and pertained DNA language model to capture multi-source dependencies within multi-model biological knowledge, while its gated multi-head attention module effectively identifies informative regulatory signatures and integrate complementary features from different sources to predict accurate gene regulatory networks. Benchmarking on the seven datasets of human and mouse demonstrates that scMGFGRN out-performs state-of-the-art methods in identifying GRNs. Further analyses reveal that scMGFGRN effectively identifies novel TF– gene interactions (TGIs) and reconstructs cell-type-specific GRNs. Interpretability analysis reveals the contribution patterns of heterogeneous biological sources, demonstrating the ability of scMGFGRN to integrate transcriptomic profiles with multi-model structure information.
Abstract Accurately inferring cell-type-specific gene regulatory networks (GRNs) is crucial for understanding cellular heterogeneity, lineage determination, and disease progression mechanisms. Although single-cell RNA sequencing (scRNA-seq) enables high-resolution expression profiling, its inherent sparsity and high no...
Yu-Ke Xie, Bo-Wen Fu, Lai-Jun Zhong et al.· Briefings in Bioinformatics· 0 citations
This chapter explores the integration of AI-driven approaches in gene expression analysis, focusing on differential expression analysis, clustering techniques, and gene regulatory network (GRN) inference, and discusses the role of dimensionality reduction and unsupervised learning in identifying disease subtypes and pa...
Yi Cong, Toshinori Endo· Methods in molecular biology· 0 citations
Sequence-to-function (S2F) deep learning models have become an important aid to decipher the genomic cis-regulatory code. However, current S2F models do not take the cellular trans-environment of transcription factors (TF) into account. Conversely, methods for gene regulatory network (GRN) inference often rely on heuri...
Gabriele Partel, Seppe De Winter, Vasilis Konstantakos et al.· bioRxiv· 0 citations
GB.GeneUnet, an 837M-parameter transformer-based U-Net pretrained on 6 trillion tokens from multi-species genomes in OpenGenome2 is introduced, extending genomic context to 1 Mb with up to 100× inference speedup over GeneMoE, a preliminary MoE transformer baseline of similar model size pretrained on the same data.
Ning Sun, William de Vazelhes, Pan Li et al.· bioRxiv· 0 citations
This review compares convolutional, Transformer-based and graph architectures used to represent local sequence features, chromatin state and three-dimensional genome organisation to their applications to transcription-factor binding, chromatin accessibility, gene expression, non-coding variant prioritisation and regula...