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  license: mit
 
 
 
 
 
 
 
 
 
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  license: mit
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+ library_name: pytorch
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+ pipeline_tag: other
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+ tags:
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+ - genomics
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+ - gene-expression
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+ - transcriptional-regulation
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+ language:
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+ - en
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+ pretty_name: RegFM
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  ---
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+
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+ # RegFM
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+
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+ **RegFM** is a context-aware foundation model for human transcriptional regulation.
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+ It treats regulation as a dialogue between **cis-regulatory sequences (CREs)** and **trans-acting regulators** (transcription factors and chromatin regulators), coupling long-range CRE representations with TF/CR activity.
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+
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+ Trained on large-scale ENCODE and CELLxGENE transcriptomic profiles, RegFM learns gene-centered regulatory representations that generalize across unseen cellular contexts.
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+
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+ [![GitHub](https://img.shields.io/badge/GitHub-ZjGaothu%2FRegFM-181717?logo=github)](https://github.com/ZjGaothu/RegFM)
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+
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+ <p align="center">
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+ <img src="init/model.jpg" width="85%" alt="RegFM overview">
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+ </p>
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+
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+ ## Model description
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+
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+ - **Inputs**: long-range cis-DNA sequence features + cell-context TF/CR and expression signals
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+ - **Outputs**: gene expression predictions and regulatory representations usable for downstream tasks
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+ - **Framework**: PyTorch
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+
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+ ## Intended uses
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+
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+ - Gene expression prediction in unseen cellular contexts
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+ - Cis-regulatory element annotation
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+ - Bivalent promoter / dosage-sensitivity related analyses
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+ - Perturbation-response prediction
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+ - Interpretable analysis of cis–trans regulatory interactions
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+
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+
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+ ## Code & demo
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+
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+ Code, training/prediction scripts, and a PBMC leave-one-out demo (predict on held-out **CD8 TEM 1**) live on GitHub:
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+
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+ **https://github.com/ZjGaothu/RegFM**
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+
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+ ```bash
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+ pip install git+https://github.com/ZjGaothu/RegFM.git
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+ # or clone and: pip install -e .
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+ ```
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+
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+ ## Citation
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+
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+ If you use RegFM, please cite:
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+
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+ Zijing Gao, et al. RegFM: an interpretable context-aware foundation model for human transcriptional regulation. bioRxiv, (2026).
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+ *(DOI will be added upon public release.)*
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+
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+ ## Contact
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+
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+ `gzj21@mails.tsinghua.edu.cn`
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+
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+ ## License
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+
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+ MIT