CellPolaris: Decoding Cell Fate through Generalization Transfer Learning of Gene Regulatory Networks
Feng, G.; Qin, X.; Zhang, J.; Huang, W.; Zhang, Y.; Cui, W.; Li, S.; Chen, Y.; Liu, W.; Tian, Y.; Liu, Y.; Dong, J.; Xu, P.; Man, Z.; Liu, G.; Liang, Z.; Jiang, X.; Yang, X.; Wang, P.; Yang, G.; Wang, H.; Wang, X.; Tong, M.-H.; Zhou, Y.; Zhang, S.; Chen, Y.; Wang, Y.; Li, X.
Show abstract
Cell fate changes are determined by gene regulatory network (GRN), a sophisticated system regulating gene expression in precise spatial and temporal patterns. However, existing methods for reconstructing GRNs suffer from inherent limitations, leading to compromised accuracy and application generalizability. In this study, we introduce CellPolaris, a computational system that leverages transfer learning algorithms to generate high-quality, cell-type-specific GRNs. Diverging from conventional GRN inference models, which heavily rely on integrating epigenomic data with transcriptomic information or adopt causal strategies through gene co-expression networks, CellPolaris employs high-confidence GRN sources for model training, relying exclusively on transcriptomic data to generate previously unknown cell-type-specific GRNs. Applications of CellPolaris demonstrate remarkable efficacy in predicting master regulatory factors and simulating in-silico perturbations of transcription factors during cell fate transition, attaining state-of-the-art performance in accurately predicting candidate key factors and outcomes in cell reprogramming and spermatogenesis with validated datasets. It is worth noting that, with a transfer learning framework, CellPolaris can perform GRN based predictions in all cell types even across species. Together, CellPolaris represents a significant advancement in deciphering the mechanisms of cell fate regulation, thereby enhancing the precision and efficiency of cell fate manipulation at high resolution.
Matching journals
The top 7 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- LineageVAE: Reconstructing Historical Cell States and Transcriptomes toward Unobserved Progenitors 96%
- SAILER: Scalable and Accurate Invariant Representation Learning for Single-Cell ATAC-Seq Processing and Integration 96%
- scNODE: Generative Model for Temporal Single Cell Transcriptomic Data Prediction 95%
Similar papers in this journal
- scGCN: a Graph Convolutional Networks Algorithm for Knowledge Transfer in Single Cell Omics 96%
- mcRigor: a statistical method to enhance the rigor of metacell partitioning in single-cell data analysis 96%
- CellFM: a large-scale foundation model pre-trained on transcriptomics of 100 million human cells 96%
Similar papers in this journal
- A scalable computational framework for predicting gene expression from candidate cis-regulatory elements 97%
- Cross-species cell-type assignment of single-cell RNA-seq by a heterogeneous graph neural network 96%
- Highly accurate reference and method selection for universal cross-dataset cell type annotation with CAMUS 95%
Similar papers in this journal
- Inferring cell trajectories of spatial transcriptomics via optimal transport analysis 96%
- scTrace+: enhance the cell fate inference by integrating the lineage-tracing and multi-faceted transcriptomic similarity information 94%
- Ultrafast and interpretable single-cell 3D genome analysis with Fast-Higashi 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.