Advances in cancer DNA methylation analysis with methPLIER: use of non-negative matrix factorization and knowledge-based constraints to enhance biological interpretability
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Published:2024-03-04
Issue:3
Volume:56
Page:646-655
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ISSN:2092-6413
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Container-title:Experimental & Molecular Medicine
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language:en
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Short-container-title:Exp Mol Med
Author:
Takasawa Ken, Asada Ken, Kaneko Syuzo, Shiraishi Kouya, Machino HidenoriORCID, Takahashi Satoshi, Shinkai Norio, Kouno Nobuji, Kobayashi Kazuma, Komatsu Masaaki, Mizuno Takaaki, Okubo Yu, Mukai Masami, Yoshida Tatsuya, Yoshida Yukihiro, Horinouchi Hidehito, Watanabe Shun-Ichi, Ohe Yuichiro, Yatabe YasushiORCID, Kohno Takashi, Hamamoto RyujiORCID
Abstract
AbstractDNA methylation is an epigenetic modification that results in dynamic changes during ontogenesis and cell differentiation. DNA methylation patterns regulate gene expression and have been widely researched. While tools for DNA methylation analysis have been developed, most of them have focused on intergroup comparative analysis within a dataset; therefore, it is difficult to conduct cross-dataset studies, such as rare disease studies or cross-institutional studies. This study describes a novel method for DNA methylation analysis, namely, methPLIER, which enables interdataset comparative analyses. methPLIER combines Pathway Level Information Extractor (PLIER), which is a non-negative matrix factorization (NMF) method, with regularization by a knowledge matrix and transfer learning. methPLIER can be used to perform intersample and interdataset comparative analysis based on latent feature matrices, which are obtained via matrix factorization of large-scale data, and factor-loading matrices, which are obtained through matrix factorization of the data to be analyzed. We used methPLIER to analyze a lung cancer dataset and confirmed that the data decomposition reflected sample characteristics for recurrence-free survival. Moreover, methPLIER can analyze data obtained via different preprocessing methods, thereby reducing distributional bias among datasets due to preprocessing. Furthermore, methPLIER can be employed for comparative analyses of methylation data obtained from different platforms, thereby reducing bias in data distribution due to platform differences. methPLIER is expected to facilitate cross-sectional DNA methylation data analysis and enhance DNA methylation data resources.
Funder
Japan Agency for Medical Research and Development MEXT | JST | Core Research for Evolutional Science and Technology MEXT | Japan Society for the Promotion of Science MEXT | Japan Science and Technology Agency
Publisher
Springer Science and Business Media LLC
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