Evidence map›Paper›PMID 41258300›Full record

ArticleNature communications2025

Omnireg-gpt: a high-efficiency foundation model for comprehensive genomic sequence understanding.

Aowen Wang, Jiaqi Li, Hongyu Dong, Bocheng Xu, Qingyu Yin, Yanchao Xu, Jie Fu, Junbo Zhao

Abstract read
In one paragraph

Article in Nature communications, 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. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Aowen Wang *College of Computer Science and Technology, Zhejiang University, Hangzhou, Zhejiang, China.
Jiaqi Li *Liangzhu Laboratory, Zhejiang University Medical Center, Hangzhou, Zhejiang, China. jiaqili@zju.edu.cn.ORCID http://orcid.org/0000-0002-4626-9000
Hongyu Dong *College of Computer Science and Technology, Zhejiang University, Hangzhou, Zhejiang, China.ORCID http://orcid.org/0009-0008-1858-3597
Bocheng XuZhejiang University, Hangzhou, Zhejiang, China.ORCID http://orcid.org/0000-0001-5403-0991
Qingyu YinZhejiang University, Hangzhou, Zhejiang, China.
Yanchao XuCollege of Computer Science and Technology, Zhejiang University, Hangzhou, Zhejiang, China.
Jie FuShanghai Artificial Intelligence Laboratory, Shanghai, China.
Junbo ZhaoCollege of Computer Science and Technology, Zhejiang University, Hangzhou, Zhejiang, China. j.zhao@zju.edu.cn.ORCID http://orcid.org/0000-0002-3637-2936

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32500539National Natural Science Foundation of China (National Science Foundation of China) U24A201401
6 · The paper itself

Abstract

The human genome contains a sophisticated array of elements that regulate gene activity and organismal functions. Developing a large window foundation model capable of efficiently processing long sequence inputs is essential yet challenging for decoding the multi-layered and complex landscape of the cis-regulatory elements. Here, we introduce OmniReg-GPT, a generative foundation model designed for the low-resource pretraining of long genomic sequences by optimized attention mechanism. During pretraining, OmniReg-GPT captures the complete distribution of regulatory elements across nucleotide to megabase scales with efficient training speed and memory usage. We demonstrate exceptional performance in downstream regulotary applications spanning the entire spectrum of genomic scales, including various cis-regulatory elements identification, context dependent gene expression prediction, single-cell chromatin accessibility analysis, and 3D chromatin contact modeling. As a generative model, OmniReg-GPT also holds the potential to generate candidate cell-type-specific enhancers through prompt engineering. Overall, OmniReg-GPT extends the boundaries of foundation models in the genomic field, and provides a valuable pretraining model resource which can be extensively applied for genomic researches.

Indexed as

Genome, HumanGenomicsModels, GeneticChromatinEnhancer Elements, GeneticHumansRegulatory Sequences, Nucleic AcidChromatin

Identifiers

PMID41258300
PMCPMC12630854

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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.