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Identification of an epigenetic signature in human induced pluripotent stem cells using a linear machine learning model

The use of human induced pluripotent stem cells (iPSCs), used as an alternative to human embryonic stem cells (ESCs), is a potential solution to challenges, such as immune rejection, and does not involve the ethical issues concerning the use of ESCs in regenerative medicine, thereby enabling develop...

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Autores principales: Nishino, Koichiro, Takasawa, Ken, Okamura, Kohji, Arai, Yoshikazu, Sekiya, Asato, Akutsu, Hidenori, Umezawa, Akihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788050/
https://www.ncbi.nlm.nih.gov/pubmed/33047283
http://dx.doi.org/10.1007/s13577-020-00446-3
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author Nishino, Koichiro
Takasawa, Ken
Okamura, Kohji
Arai, Yoshikazu
Sekiya, Asato
Akutsu, Hidenori
Umezawa, Akihiro
author_facet Nishino, Koichiro
Takasawa, Ken
Okamura, Kohji
Arai, Yoshikazu
Sekiya, Asato
Akutsu, Hidenori
Umezawa, Akihiro
author_sort Nishino, Koichiro
collection PubMed
description The use of human induced pluripotent stem cells (iPSCs), used as an alternative to human embryonic stem cells (ESCs), is a potential solution to challenges, such as immune rejection, and does not involve the ethical issues concerning the use of ESCs in regenerative medicine, thereby enabling developments in biological research. However, comparative analyses from previous studies have not indicated any specific feature that distinguishes iPSCs from ESCs. Therefore, in this study, we established a linear classification-based learning model to distinguish among ESCs, iPSCs, embryonal carcinoma cells (ECCs), and somatic cells on the basis of their DNA methylation profiles. The highest accuracy achieved by the learned models in identifying the cell type was 94.23%. In addition, the epigenetic signature of iPSCs, which is distinct from that of ESCs, was identified by component analysis of the learned models. The iPSC-specific regions with methylation fluctuations were abundant on chromosomes 7, 8, 12, and 22. The method developed in this study can be utilized with comprehensive data and widely applied to many aspects of molecular biology research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13577-020-00446-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-77880502021-01-14 Identification of an epigenetic signature in human induced pluripotent stem cells using a linear machine learning model Nishino, Koichiro Takasawa, Ken Okamura, Kohji Arai, Yoshikazu Sekiya, Asato Akutsu, Hidenori Umezawa, Akihiro Hum Cell Research Article The use of human induced pluripotent stem cells (iPSCs), used as an alternative to human embryonic stem cells (ESCs), is a potential solution to challenges, such as immune rejection, and does not involve the ethical issues concerning the use of ESCs in regenerative medicine, thereby enabling developments in biological research. However, comparative analyses from previous studies have not indicated any specific feature that distinguishes iPSCs from ESCs. Therefore, in this study, we established a linear classification-based learning model to distinguish among ESCs, iPSCs, embryonal carcinoma cells (ECCs), and somatic cells on the basis of their DNA methylation profiles. The highest accuracy achieved by the learned models in identifying the cell type was 94.23%. In addition, the epigenetic signature of iPSCs, which is distinct from that of ESCs, was identified by component analysis of the learned models. The iPSC-specific regions with methylation fluctuations were abundant on chromosomes 7, 8, 12, and 22. The method developed in this study can be utilized with comprehensive data and widely applied to many aspects of molecular biology research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s13577-020-00446-3) contains supplementary material, which is available to authorized users. Springer Singapore 2020-10-12 2021 /pmc/articles/PMC7788050/ /pubmed/33047283 http://dx.doi.org/10.1007/s13577-020-00446-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Nishino, Koichiro
Takasawa, Ken
Okamura, Kohji
Arai, Yoshikazu
Sekiya, Asato
Akutsu, Hidenori
Umezawa, Akihiro
Identification of an epigenetic signature in human induced pluripotent stem cells using a linear machine learning model
title Identification of an epigenetic signature in human induced pluripotent stem cells using a linear machine learning model
title_full Identification of an epigenetic signature in human induced pluripotent stem cells using a linear machine learning model
title_fullStr Identification of an epigenetic signature in human induced pluripotent stem cells using a linear machine learning model
title_full_unstemmed Identification of an epigenetic signature in human induced pluripotent stem cells using a linear machine learning model
title_short Identification of an epigenetic signature in human induced pluripotent stem cells using a linear machine learning model
title_sort identification of an epigenetic signature in human induced pluripotent stem cells using a linear machine learning model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788050/
https://www.ncbi.nlm.nih.gov/pubmed/33047283
http://dx.doi.org/10.1007/s13577-020-00446-3
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