easyEWAS: a flexible and user-friendly R package for epigenome-wide association study.

IF 2.4 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY Bioinformatics advances Pub Date : 2025-02-13 eCollection Date: 2025-01-01 DOI:10.1093/bioadv/vbaf026
Yuting Wang, Meijie Jiang, Siyuan Niu, Xu Gao
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Abstract

Motivation: Rapid advancements in high-throughput sequencing technologies especially the Illumina DNA methylation Beadchip greatly fuelled the surge in epigenome-wide association study (EWAS), providing crucial insights into intrinsic DNA methylation modifications associated with environmental exposure, diseases, and health traits. However, current tools are complex and less user-friendly to accommodate appropriate EWAS designs and make downstream analyses and result interpretations complicated, especially for clinicians and public health professionals with limited bioinformatic skills.

Results: We integrated the current state-of-the-art EWAS analysis methods and tools to develop a flexible and user-friendly R package easyEWAS for conducting DNA methylation-based research using Illumina DNA methylation Beadchips. With easyEWAS, we provide a battery of statistical methods to support differential methylation position analysis across various scenarios, as well as differential methylation region analysis based on the DMRcate method. To facilitate result interpretation, we provide comprehensive functional annotation and result visualization functionalities. Additionally, a bootstrap-based internal validation was incorporated into easyEWAS to ensure the robustness of EWAS results. Evaluation in asthma patients as the example demonstrated that easyEWAS could simplify and streamline the conduction of EWAS and corresponding downstream analyses, thus effectively advancing DNA methylation research in public health and clinical settings.

Availability and implementation: easyEWAS is implemented as an R package and is available at https://github.com/ytwangZero/easyEWAS.

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easyEWAS:用于全表观基因组关联研究的灵活且用户友好的 R 软件包。
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