Evidence map›Paper›PMID 40462903›Full record

ArticlebioRxiv : the preprint server for biology2025

Developing a general AI model for integrating diverse genomic modalities and comprehensive genomic knowledge.

Zhenhao Zhang, Xinyu Bao, Linghua Jiang, Xin Luo, Yichun Wang, Annelise Comai, Joerg Waldhaus, Anders S Hansen, Wenbo Li, Jie Liu

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

10 authors.

Zhenhao ZhangDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA.
Xinyu BaoDepartment of Computer Science and Engineering, University of Michigan, Ann Arbor, MI, USA.
Linghua JiangDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA.
Xin LuoDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA.
Yichun WangDepartment of Biochemistry and Molecular Biology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Annelise ComaiDepartment of Biochemistry and Molecular Biology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Joerg WaldhausDepartment of Otolaryngology-Head and Neck Surgery, Kresge Hearing Research Institute, University of Michigan, Ann Arbor, MI, USA.
Anders S HansenDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Wenbo LiDepartment of Biochemistry and Molecular Biology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Jie LiuDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, USA.

Funding

PanKbase: a community hub for integrated pancreas knowledgeU24DK138515 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Marcela Brissova, Jean-Philippe Cartailler · 2024 to 2026
$11.3M
Predicting the Impact of Genomic Variation on Cellular StatesU01HG011952 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alan P Boyle · 2021 to 2026
$3.8M
Integrative analysis of multi-omic signatures and cellular function in human pancreas across developmental timeline at single-cell spatial resolutionU01DK135017 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BRISSOVA, MARCELA, CAICEDO, ALEJANDRO · 2022 to 2025
$3.8M
Multi-omic genetic regulatory signatures underlying tissue complexity of diabetes in the pancreas at single-cell spatial resolutionR01DK129469 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BRISSOVA, MARCELA, LIU, JIE · 2022 to 2025
$2.6M
Joint analysis of 3D chromatin organization and 1D epigenomeR35HG011279 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LIU, JIE · 2020 to 2024
$2.1M
Ultra-high resolution 3D genome maps for multiple human tissuesR03OD038390 · OD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HANSEN, ANDERS SEJR, LIU, JIE · 2024 to 2024
$309k
NHGRI NIH HHS R35 HG011279NHGRI NIH HHS U01 HG011952NIDDK NIH HHS R01 DK129469NIDDK NIH HHS U01 DK135017NIDDK NIH HHS U24 DK138515NIH HHS R03 OD038390
6 · The paper itself

Abstract

Advances in next-generation sequencing technologies have vastly expanded the availability of diverse genomic, epigenomic and transcriptomic data, presenting the opportunity to develop a general AI model that integrates comprehensive genomic knowledge into a unified model. Unlike previous predictive models, which are typically specialized to certain tasks, our general AI model unifies a wide range of genomic modalities, such as nascent RNA and ultra-high-resolution chromatin organization, within a multi-task architecture. Using ATAC-seq and DNA sequences as inputs, we incorporated diverse genomic modalities as output, and the model exhibits strong generalizability across different cell types and tissues in all tasks we trained. It accurately predicts gene-level transcription measured by various nascent RNA assays, and effectively captures enhancer-associated transcription. Additionally, it also accurately captures the potential functions of non-coding genetic variants and regulatory elements. Additionally, we extended the model trained on human data to a mouse general model, achieving accurate predictions of genomic modalities, such as high resolution chromatin contact maps with limited data availability, which are further validated using an established mouse inner-ear study. This comprehensive approach offers a powerful tool for understanding genome regulation in both human and mouse species.

Identifiers

PMID40462903
PMCPMC12132192

What OpenQuestion holds

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LicenceCC BY
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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.