CREATE: cell-type-specific cis-regulatory element identification via discrete embedding

Cis-regulatory elements (CREs), including enhancers, silencers, promoters and insulators, play pivotal roles in orchestrating gene regulatory mechanisms that drive complex biological traits. However, current approaches for CRE identification are predominantly sequence-based and typically focus on individual CRE types, limiting insights into their cell-type-specific functions and regulatory dynamics. Here, we present CREATE, a multimodal deep learning framework based on Vector Quantized Variational AutoEncoder, tailored for comprehensive CRE identification and characterization. CREATE integrates genomic sequences, chromatin accessibility, and chromatin interaction data to generate discrete CRE embeddings, enabling accurate multi-class classification and robust characterization of CREs. CREATE excels in identifying cell-type-specific CREs, and provides quantitative and interpretable insights into CRE-specific features, uncovering the underlying regulatory codes. By facilitating large-scale prediction of CREs in specific cell types, CREATE enhances the recognition of disease- or phenotype-associated biological variabilities of CREs, thus advancing our understanding of gene regulatory landscapes and their roles in health and disease.

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Publication Details

Journal
Nature Communications
Published
2025-05-17
DOI
https://doi.org/10.1038/s41467-025-59780-5
Citations
5
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
4.03
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article

CREATE: cell-type-specific cis-regulatory element identification via discrete embedding

Qijin Yin, Xuejian Cui, Shengquan Chen, Hairong Lv et al.
5 citations
Nature Communications
Genomics and Chromatin Dynamics
4.03
article

CREATE: cell-type-specific cis-regulatory element identification via discrete embedding

Qijin Yin, Xuejian Cui, Shengquan Chen, Hairong Lv, Wanwen Zeng, Zijing Gao, Zhen Li, Qiao Liu, Xiaoyang Chen, Rui Jiang
article en
5 citations

Abstract

Cis-regulatory elements (CREs), including enhancers, silencers, promoters and insulators, play pivotal roles in orchestrating gene regulatory mechanisms that drive complex biological traits. However, current approaches for CRE identification are predominantly sequence-based and typically focus on individual CRE types, limiting insights into their cell-type-specific functions and regulatory dynamics. Here, we present CREATE, a multimodal deep learning framework based on Vector Quantized Variational AutoEncoder, tailored for comprehensive CRE identification and characterization. CREATE integrates genomic sequences, chromatin accessibility, and chromatin interaction data to generate discrete CRE embeddings, enabling accurate multi-class classification and robust characterization of CREs. CREATE excels in identifying cell-type-specific CREs, and provides quantitative and interpretable insights into CRE-specific features, uncovering the underlying regulatory codes. By facilitating large-scale prediction of CREs in specific cell types, CREATE enhances the recognition of disease- or phenotype-associated biological variabilities of CREs, thus advancing our understanding of gene regulatory landscapes and their roles in health and disease.

Nature CommunicationsVol. 16(1)
Nankai University (CN), Stanford Medicine (US), Laboratoire de physique de la matière condensée (FR), Stanford University (US), Tsinghua University (CN)
Openalex Percentile: Top 6%
Genomics and Chromatin Dynamics
4.03
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