Evidence map›Paper›PMID 40291712›Full record

ArticlebioRxiv : the preprint server for biology2025

High-resolution reconstruction of cell-type specific transcriptional regulatory processes from bulk sequencing samples.

Li Yao, Sagar R Shah, Abdullah Ozer, Junke Zhang, Xiuqi Pan, Tianyu Xia, Vrushali D Fangal, Alden King-Yung Leung, Meihan Wei, John T Lis and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Li YaoDepartment of Computational Biology, Cornell University, Ithaca, NY 14853.ORCID 0000-0003-2827-8824
Sagar R ShahWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY 14853.
Abdullah OzerDepartment of Computational Biology, Cornell University, Ithaca, NY 14853.
Junke ZhangDepartment of Computational Biology, Cornell University, Ithaca, NY 14853.
Xiuqi PanWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY 14853.
Tianyu XiaDepartment of Computational Biology, Cornell University, Ithaca, NY 14853.
Vrushali D FangalDepartment of Computational Biology, Cornell University, Ithaca, NY 14853.
Alden King-Yung LeungDepartment of Computational Biology, Cornell University, Ithaca, NY 14853.
Meihan WeiDepartment of Computational Biology, Cornell University, Ithaca, NY 14853.
John T LisDepartment of Computational Biology, Cornell University, Ithaca, NY 14853.
Haiyuan YuDepartment of Computational Biology, Cornell University, Ithaca, NY 14853.ORCID 0000-0001-7597-6049

Funding

Genome-wide identification and characterization of Alzheimer's Disease-associated enhancersR01AG077899 · NIA · CORNELL UNIVERSITY · PI Li Gan, JOHN T LIS · 2022 to 2026
$4.0M
Functional Architecture and Interplay of Transcription Regulatory Elements of the Human GenomeR01HG012970 · NHGRI · CORNELL UNIVERSITY · PI JOHN T LIS, Haiyuan Yu · 2023 to 2026
$2.7M
NHGRI NIH HHS R01 HG012970NIA NIH HHS R01 AG077899
6 · The paper itself

Abstract

Biological systems exhibit remarkable heterogeneity, characterized by intricate interplay among diverse cell types. Resolving the regulatory processes of specific cell types is crucial for delineating developmental mechanisms and disease etiologies. While single-cell sequencing methods such as scRNA-seq and scATAC-seq have revolutionized our understanding of individual cellular functions, adapting bulk genome-wide assays to achieve single-cell resolution of other genomic features remains a significant technical challenge. Here, we introduce Deep-learning-based DEconvolution of Tissue profiles with Accurate Interpretation of Locus-specific Signals (DeepDETAILS), a novel quasi-supervised framework to reconstruct cell-type-specific genomic signals with base-pair precision. DeepDETAILS' core innovation lies in its ability to perform cross-modality deconvolution using scATAC-seq reference libraries for other bulk datasets, benefiting from the affordability and availability of scATAC-seq data. DeepDETAILS enables high-resolution mapping of genomic signals across diverse cell types, with great versatility for various omics datasets, including nascent transcript sequencing (such as PRO-cap and PRO-seq) and ChIP-seq for chromatin modifications. Our results demonstrate that DeepDETAILS significantly outperformed traditional statistical deconvolution methods. Using DeepDETAILS, we developed a comprehensive compendium of high-resolution nascent transcription and histone modification signals across 39 diverse human tissues and 86 distinct cell types. Furthermore, we applied our compendium to fine-map risk variants associated with Primary Sclerosing Cholangitis (PSC), a progressive cholestatic liver disorder, and revealed a potential etiology of the disease. Our tool and compendium provide invaluable insights into cellular complexity, opening new avenues for studying biological processes in various contexts.

Identifiers

PMID40291712
PMCPMC12026507

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.