EWAS Open Platform 2026: a deeply integrated resource for epigenome-wide association studies

Fei Yang(Chinese Academy of Sciences), Zhuang Xiong(Fuzhou University), Wenting Zong(Chinese Academy of Sciences), Demian Kong(Chinese Academy of Sciences), Bixia Tang(Chinese Academy of Sciences), Xupeng Chen(Fuzhou University), Yaoke Wei(Chinese Academy of Sciences), Xiangyu Yu(Chinese Academy of Sciences), Yiran Zhang(Chinese Academy of Sciences), Dong Zou(Chinese Academy of Sciences), Zhang Zhang(Chinese Academy of Sciences), Yīmíng Bào(Chinese Academy of Sciences), Rujiao Li(Chinese Academy of Sciences)
Nucleic Acids Research
November 17, 2025
Cited by 1Open Access
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Abstract

Epigenome-wide association studies (EWAS) has become an indispensable approach for elucidating the epigenetic basis of complex traits. EWAS Open Platform (https://ngdc.cncb.ac.cn/ewas/) includes three main components: EWAS Atlas (curated associations from publications), EWAS Data Hub (normalized DNA methylation array data), and EWAS Toolkit (one-stop analysis services). Here, we present a new release of EWAS Open Platform with the following significant updates and enhancements: (i) Expanded information: EWAS Atlas houses over 800 000 associations and incorporates an additional 17 000 curated causal relationships. EWAS Data Hub contains >180 000 batch-corrected samples, which incorporate data from newly added Illumina MethylationEPIC v2.0 BeadChip (935K) as well as trait-specific methylation profiles. EWAS Toolkit now provides an online batch correction tool and an interactive epigenetic causal network. (ii) Enhanced interoperability: data, knowledge, and toolkit are fully interconnected through a unified retrieval, offering integrated summaries and visualization capabilities. (iii) Artificial intelligence (AI)-based service: the platform is newly equipped with an AI-assisted question-answering service, allowing users to interactively explore EWAS-related questions and generate tailored insights. Taken together, EWAS Open Platform has undergone a significant upgrade across data resources, analytical tools, and service functionalities, offering more advanced support for unraveling complex molecular mechanisms from an epigenomic perspective.


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