Evidence map›Paper›PMID 42443492›Full record

ArticleNature biotechnology2026

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

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

Abstract read
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In one paragraph

Article in Nature biotechnology, 2026. 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, USA.ORCID http://orcid.org/0000-0003-2827-8824
Sagar R ShahWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0003-4869-4104
Abdullah OzerDepartment of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0001-6861-2853
Yutong ZhuDepartment of Computational Biology, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0001-7493-1463
Xiuqi PanWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY, USA.
Tianyu XiaDepartment of Computational Biology, Cornell University, Ithaca, NY, USA.
Junke ZhangDepartment of Computational Biology, Cornell University, Ithaca, NY, USA.ORCID http://orcid.org/0000-0002-2178-1307
Alden King-Yung LeungDepartment of Computational Biology, Cornell University, Ithaca, NY, USA.
Meihan WeiDepartment of Computational Biology, Cornell University, Ithaca, NY, USA.
John T LisDepartment of Computational Biology, Cornell University, Ithaca, NY, USA.
Haiyuan YuDepartment of Computational Biology, Cornell University, Ithaca, NY, USA. haiyuan.yu@cornell.edu.ORCID http://orcid.org/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
U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AG077899U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01HG012970
6 · The paper itself

Abstract

Single-cell sequencing methods such as scRNA-seq and scATAC-seq have advanced our understanding of individual cellular functions but experimentally adapting genome-wide assays measuring other genomic features to achieve single-cell resolution remains a technical challenge. Here we introduce deep-learning-based deconvolution of tissue profiles with accurate interpretation of locus-specific signals (DeepDETAILS), a quasisupervised framework performing cross-modality deconvolution using scATAC-seq reference libraries for other bulk datasets. DeepDETAILS enables base-pair-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. Using DeepDETAILS, we generated a 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, a progressive cholestatic liver disorder, and revealed a potential etiology of the disease.

Identifiers

PMID42443492

What OpenQuestion holds

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Registered trials

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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.