Evidence map›Paper›PMID 42523313›Full record

ArticlebioRxiv : the preprint server for biology2026

scWeave: A deep learning model that bidirectionally translates between gene expression and chromatin structure at single-cell resolution.

Ghulam Murtaza, Shengqi Hang, Xumeng Zhang, Shuhua Xu, Tangqi Fang, Doudou Yu, Anupama Jha, Ritambhara Singh, Sheng Wang, William Stafford Noble

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Ghulam MurtazaDepartment of Genome Sciences, University of Washington.ORCID 0000-0002-1803-1134
Shengqi HangPaul G. Allen School of Computer Science and Engineering, University of Washington.ORCID 0000-0002-3279-2183
Xumeng ZhangDepartment of Genome Sciences, University of Washington.
Shuhua XuDepartment of Genome Sciences, University of Washington.
Tangqi FangPaul G. Allen School of Computer Science and Engineering, University of Washington.ORCID 0009-0007-8471-3890
Doudou YuDepartment of Genome Sciences, University of Washington.ORCID 0000-0002-5142-0406
Anupama JhaDepartment of Genetics, Yale University.ORCID 0000-0003-3029-2086
Ritambhara SinghDepartment of Computer Science, Brown University.
Sheng WangPaul G. Allen School of Computer Science and Engineering, University of Washington.ORCID 0000-0002-5718-7529
William Stafford NobleDepartment of Genome Sciences, University of Washington.ORCID 0000-0001-7283-4715

Funding

Deep integrative analysis of Hi-C dataR01HG013321 · NHGRI · UNIVERSITY OF WASHINGTON · PI Sheng Wang · 2024 to 2026
$1.5M
Selective vulnerability of cell types in brain aging and Alzheimer's diseaseK00AG083292 · NIA · UNIVERSITY OF WASHINGTON · PI Doudou Yu · 2025 to 2026
$143k
NHGRI NIH HHS R01 HG013321NIA NIH HHS K00 AG083292
6 · The paper itself

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.

Identifiers

PMID42523313
PMCPMC13404969

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.