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Computational Methods for Single-cell DNA Methylome Analysis

Dissecting intercellular epigenetic differences is key to understanding tissue heterogeneity. Recent advances in single-cell DNA methylome profiling have presented opportunities to resolve this heterogeneity at the maximum resolution. While these advances enable us to explore frontiers of chromatin...

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Detalles Bibliográficos
Autores principales: Iqbal, Waleed, Zhou, Wanding
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372927/
https://www.ncbi.nlm.nih.gov/pubmed/35718270
http://dx.doi.org/10.1016/j.gpb.2022.05.007
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author Iqbal, Waleed
Zhou, Wanding
author_facet Iqbal, Waleed
Zhou, Wanding
author_sort Iqbal, Waleed
collection PubMed
description Dissecting intercellular epigenetic differences is key to understanding tissue heterogeneity. Recent advances in single-cell DNA methylome profiling have presented opportunities to resolve this heterogeneity at the maximum resolution. While these advances enable us to explore frontiers of chromatin biology and better understand cell lineage relationships, they pose new challenges in data processing and interpretation. This review surveys the current state of computational tools developed for single-cell DNA methylome data analysis. We discuss critical components of single-cell DNA methylome data analysis, including data preprocessing, quality control, imputation, dimensionality reduction, cell clustering, supervised cell annotation, cell lineage reconstruction, gene activity scoring, and integration with transcriptome data. We also highlight unique aspects of single-cell DNA methylome data analysis and discuss how techniques common to other single-cell omics data analyses can be adapted to analyze DNA methylomes. Finally, we discuss existing challenges and opportunities for future development.
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spelling pubmed-103729272023-07-28 Computational Methods for Single-cell DNA Methylome Analysis Iqbal, Waleed Zhou, Wanding Genomics Proteomics Bioinformatics Review Dissecting intercellular epigenetic differences is key to understanding tissue heterogeneity. Recent advances in single-cell DNA methylome profiling have presented opportunities to resolve this heterogeneity at the maximum resolution. While these advances enable us to explore frontiers of chromatin biology and better understand cell lineage relationships, they pose new challenges in data processing and interpretation. This review surveys the current state of computational tools developed for single-cell DNA methylome data analysis. We discuss critical components of single-cell DNA methylome data analysis, including data preprocessing, quality control, imputation, dimensionality reduction, cell clustering, supervised cell annotation, cell lineage reconstruction, gene activity scoring, and integration with transcriptome data. We also highlight unique aspects of single-cell DNA methylome data analysis and discuss how techniques common to other single-cell omics data analyses can be adapted to analyze DNA methylomes. Finally, we discuss existing challenges and opportunities for future development. Elsevier 2023-02 2022-06-17 /pmc/articles/PMC10372927/ /pubmed/35718270 http://dx.doi.org/10.1016/j.gpb.2022.05.007 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Iqbal, Waleed
Zhou, Wanding
Computational Methods for Single-cell DNA Methylome Analysis
title Computational Methods for Single-cell DNA Methylome Analysis
title_full Computational Methods for Single-cell DNA Methylome Analysis
title_fullStr Computational Methods for Single-cell DNA Methylome Analysis
title_full_unstemmed Computational Methods for Single-cell DNA Methylome Analysis
title_short Computational Methods for Single-cell DNA Methylome Analysis
title_sort computational methods for single-cell dna methylome analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372927/
https://www.ncbi.nlm.nih.gov/pubmed/35718270
http://dx.doi.org/10.1016/j.gpb.2022.05.007
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