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Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree

A wealth of clustering algorithms are available for single-cell RNA sequencing (scRNA-seq) data to enable the identification of functionally distinct subpopulations that each possess a different pattern of gene expression activity. Implementation of these methods requires a choice of resolution para...

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Autores principales: Peng, Minshi, Wamsley, Brie, Elkins, Andrew G, Geschwind, Daniel H, Wei, Yuting, Roeder, Kathryn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450107/
https://www.ncbi.nlm.nih.gov/pubmed/34125905
http://dx.doi.org/10.1093/nar/gkab481
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author Peng, Minshi
Wamsley, Brie
Elkins, Andrew G
Geschwind, Daniel H
Wei, Yuting
Roeder, Kathryn
author_facet Peng, Minshi
Wamsley, Brie
Elkins, Andrew G
Geschwind, Daniel H
Wei, Yuting
Roeder, Kathryn
author_sort Peng, Minshi
collection PubMed
description A wealth of clustering algorithms are available for single-cell RNA sequencing (scRNA-seq) data to enable the identification of functionally distinct subpopulations that each possess a different pattern of gene expression activity. Implementation of these methods requires a choice of resolution parameter to determine the number of clusters, and critical judgment from the researchers is required to determine the desired resolution. This supervised process takes significant time and effort. Moreover, it can be difficult to compare and characterize the evolution of cell clusters from results obtained at one single resolution. To overcome these challenges, we built Multi-resolution Reconciled Tree (MRtree), a highly flexible tree-construction algorithm that generates a cluster hierarchy from flat clustering results attained for a range of resolutions. Because MRtree can be coupled with most scRNA-seq clustering algorithms, it inherits the robustness and versatility of a flat clustering approach, while maintaining the hierarchical structure of cells. The constructed trees from multiple scRNA-seq datasets effectively reflect the extent of transcriptional distinctions among cell groups and align well with levels of functional specializations among cells. Importantly, application to fetal brain cells identified subtypes of cells determined mainly by maturation states, spatial location and terminal specification.
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spelling pubmed-84501072021-09-20 Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree Peng, Minshi Wamsley, Brie Elkins, Andrew G Geschwind, Daniel H Wei, Yuting Roeder, Kathryn Nucleic Acids Res Methods Online A wealth of clustering algorithms are available for single-cell RNA sequencing (scRNA-seq) data to enable the identification of functionally distinct subpopulations that each possess a different pattern of gene expression activity. Implementation of these methods requires a choice of resolution parameter to determine the number of clusters, and critical judgment from the researchers is required to determine the desired resolution. This supervised process takes significant time and effort. Moreover, it can be difficult to compare and characterize the evolution of cell clusters from results obtained at one single resolution. To overcome these challenges, we built Multi-resolution Reconciled Tree (MRtree), a highly flexible tree-construction algorithm that generates a cluster hierarchy from flat clustering results attained for a range of resolutions. Because MRtree can be coupled with most scRNA-seq clustering algorithms, it inherits the robustness and versatility of a flat clustering approach, while maintaining the hierarchical structure of cells. The constructed trees from multiple scRNA-seq datasets effectively reflect the extent of transcriptional distinctions among cell groups and align well with levels of functional specializations among cells. Importantly, application to fetal brain cells identified subtypes of cells determined mainly by maturation states, spatial location and terminal specification. Oxford University Press 2021-06-14 /pmc/articles/PMC8450107/ /pubmed/34125905 http://dx.doi.org/10.1093/nar/gkab481 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods Online
Peng, Minshi
Wamsley, Brie
Elkins, Andrew G
Geschwind, Daniel H
Wei, Yuting
Roeder, Kathryn
Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree
title Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree
title_full Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree
title_fullStr Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree
title_full_unstemmed Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree
title_short Cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree
title_sort cell type hierarchy reconstruction via reconciliation of multi-resolution cluster tree
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8450107/
https://www.ncbi.nlm.nih.gov/pubmed/34125905
http://dx.doi.org/10.1093/nar/gkab481
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