bioRxivGenomicsPreprint
scWeave: A deep learning model that bidirectionally translates between gene expression and chromatin structure at single cell resolution
Ghulam MurtazaiD, Shengqi HangiD, Xumeng ZhangiD, Shuhua XuiD, Tangqi FangiD, Doudou YuiD, Anupama JhaiD, Ritambhara SinghiD, Sheng WangiD, William Stafford NobleiD
Abstract
Chromatin structure and gene expression are intimately linked, yet characterizing how the two covary has proven challenging, primarily because the two modalities are rarely measured in the same cells. Recently, single-cell co-assay protocols have enabled simultaneous profiling of both modalities within the same cells, but these experiments remain costly and technically challenging. To better characterize the relationship between 3D chromatin architecture and gene expression and to enable cross-modality inference from single-modality measurements, we developed a model called scWeave that bidirectionally translates between gene expression (scRNA-seq) and 3D chromatin architecture (scHi-C) at single-cell resolution. The scWeave model employs dual autoencoders to extract separate cell-level latent representations and learns to translate between these representations using dedicated translation modules. We evaluate scWeave on six publicly available co-assay datasets spanning mouse embryonic development, mouse cortex, mouse olfactory epithelium, and human bone marrow. On held-out mouse cells, scWeave outperforms a nearest-neighbor baseline and existing methods adapted to single-cell resolution, achieving a 57% improvement in median Spearman correlation when predicting gene expression from chromatin structure and an 18.8% improvement in median HiCRep similarity in the reverse direction relative to the next-best baseline. We further show that scWeave learns cross-modally aligned latent representations at single-cell resolution, enabling cells profiled in one modality to be matched to their counterparts in the other. Finally, scWeave generalizes to entirely held-out developmental timepoints in mouse olfactory epithelium and performs well on held-out human bone marrow cells despite limited human training data. By predicting the unmeasured chromatin architecture or transcriptional state from a single measured modality, scWeave offers a route to extend the benefits of costly co-assays to the many cell types, developmental stages, and species that are currently profiled with only one modality.
- organism: mouse
- organism: human
- assay: scRNA-seq
- assay: scATAC-seq
- assay: Hi-C
- research focus: dimensionality reduction
- research focus: benchmarking
- approach: deep learning
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- scHiR learns joint cellular representations from paired single-cell transcriptome and 3D genome data
Yichao Zhao, Pengzhen Jia, … Min Li·bioRxiv·Nov 9, 2026
- scMultiNODE: Recovering Developmental Dynamics in Weakly Resolved Modalities through Multi-Modal Integration
Jiaqi Zhang, Manav Chakravarthy, Ritambhara Singh·bioRxiv·Oct 27, 2024
- Deep generative modeling and clustering of single cell Hi-C data
Qiao Liu, Wanwen Zeng, … Shaoting Zhang·Briefings in BioinformaticsPeer-reviewed·Oct 25, 2022
- Single-cell multiome regression models identify functional and disease-associated enhancers and enable chromatin potential analysis
Sneha Mitra, Rohan Malik, … Christina S. Leslie·bioRxiv·Jun 13, 2023
- scGAD: single-cell gene associating domain scores for exploratory analysis of scHi-C data
Siqi Shen, Ye Zheng, Sündüz Keleş·BioinformaticsPeer-reviewed·Jun 2, 2022
- Unveiling multi-scale architectural features in single-cell Hi-C data using scCAFE
Fuzhou Wang, Jiecong Lin, … Xiangtao Li·Advanced SciencePeer-reviewed·Apr 24, 2025