Evidence map›Paper›PMID 41277691›Full record

ArticleNucleic acids research2025

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

Zhenhao Zhang, Xinyu Bao, Linghua Jiang, Xin Luo, Zheyu Zhang, Jing Yin, Meiqi Zhao, Yichun Wang, Annelise Comai, Joerg Waldhaus and 3 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Zhenhao ZhangGilbert S. Omenn Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109, United States.
Xinyu BaoDepartment of Computer Science and Engineering, University of Michigan, Ann Arbor, MI 48109, United States.
Linghua JiangGilbert S. Omenn Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109, United States.
Xin LuoGilbert S. Omenn Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109, United States.
Zheyu ZhangDepartment of Computer Science and Engineering, University of Michigan, Ann Arbor, MI 48109, United States.
Jing YinGilbert S. Omenn Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109, United States.
Meiqi ZhaoGilbert S. Omenn Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109, United States.
Yichun WangDepartment of Biochemistry and Molecular Biology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Annelise ComaiDepartment of Biochemistry and Molecular Biology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Joerg WaldhausDepartment of Otolaryngology-Head and Neck Surgery, Kresge Hearing Research Institute, University of Michigan, Ann Arbor, MI 48109, United States.
Anders S HansenDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, United States.
Wenbo LiDepartment of Biochemistry and Molecular Biology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Jie LiuGilbert S. Omenn Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109, United States.ORCID 0000-0002-9504-0587

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
Enhancer RNAs in brain gene regulation and Alzheimer's diseaseR01AG082132 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Wenbo Li · 2023 to 2026
$3.0M
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
Mechanisms Underlying Enhancer Rnp Mediated Gene Regulation And Genome OrganizationR01GM136922 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LI, WENBO · 2020 to 2024
$2.0M
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 R35HG011279NHGRI NIH HHS U01 HG011952NIA NIH HHS R01 AG082132NIDDK NIH HHS R01 DK129469NIDDK NIH HHS U01 DK135017NIDDK NIH HHS U24 DK138515NIGMS NIH HHS R01 GM136922NIH 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 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.

Indexed as

GenomicsModels, GeneticAnimalsChromatinChromatin Immunoprecipitation SequencingHigh-Throughput Nucleotide SequencingHumansMiceChromatin

Identifiers

PMID41277691
PMCPMC12641268

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.