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Cell type discovery using single-cell transcriptomics: implications for ontological representation
Cells are fundamental function units of multicellular organisms, with different cell types playing distinct physiological roles in the body. The recent advent of single-cell transcriptional profiling using RNA sequencing is producing ‘big data’, enabling the identification of novel human cell types...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946857/ https://www.ncbi.nlm.nih.gov/pubmed/29590361 http://dx.doi.org/10.1093/hmg/ddy100 |
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author | Aevermann, Brian D Novotny, Mark Bakken, Trygve Miller, Jeremy A Diehl, Alexander D Osumi-Sutherland, David Lasken, Roger S Lein, Ed S Scheuermann, Richard H |
author_facet | Aevermann, Brian D Novotny, Mark Bakken, Trygve Miller, Jeremy A Diehl, Alexander D Osumi-Sutherland, David Lasken, Roger S Lein, Ed S Scheuermann, Richard H |
author_sort | Aevermann, Brian D |
collection | PubMed |
description | Cells are fundamental function units of multicellular organisms, with different cell types playing distinct physiological roles in the body. The recent advent of single-cell transcriptional profiling using RNA sequencing is producing ‘big data’, enabling the identification of novel human cell types at an unprecedented rate. In this review, we summarize recent work characterizing cell types in the human central nervous and immune systems using single-cell and single-nuclei RNA sequencing, and discuss the implications that these discoveries are having on the representation of cell types in the reference Cell Ontology (CL). We propose a method, based on random forest machine learning, for identifying sets of necessary and sufficient marker genes, which can be used to assemble consistent and reproducible cell type definitions for incorporation into the CL. The representation of defined cell type classes and their relationships in the CL using this strategy will make the cell type classes being identified by high-throughput/high-content technologies findable, accessible, interoperable and reusable (FAIR), allowing the CL to serve as a reference knowledgebase of information about the role that distinct cellular phenotypes play in human health and disease. |
format | Online Article Text |
id | pubmed-5946857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59468572018-05-16 Cell type discovery using single-cell transcriptomics: implications for ontological representation Aevermann, Brian D Novotny, Mark Bakken, Trygve Miller, Jeremy A Diehl, Alexander D Osumi-Sutherland, David Lasken, Roger S Lein, Ed S Scheuermann, Richard H Hum Mol Genet Invited Reviews Cells are fundamental function units of multicellular organisms, with different cell types playing distinct physiological roles in the body. The recent advent of single-cell transcriptional profiling using RNA sequencing is producing ‘big data’, enabling the identification of novel human cell types at an unprecedented rate. In this review, we summarize recent work characterizing cell types in the human central nervous and immune systems using single-cell and single-nuclei RNA sequencing, and discuss the implications that these discoveries are having on the representation of cell types in the reference Cell Ontology (CL). We propose a method, based on random forest machine learning, for identifying sets of necessary and sufficient marker genes, which can be used to assemble consistent and reproducible cell type definitions for incorporation into the CL. The representation of defined cell type classes and their relationships in the CL using this strategy will make the cell type classes being identified by high-throughput/high-content technologies findable, accessible, interoperable and reusable (FAIR), allowing the CL to serve as a reference knowledgebase of information about the role that distinct cellular phenotypes play in human health and disease. Oxford University Press 2018-05-01 2018-03-24 /pmc/articles/PMC5946857/ /pubmed/29590361 http://dx.doi.org/10.1093/hmg/ddy100 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Invited Reviews Aevermann, Brian D Novotny, Mark Bakken, Trygve Miller, Jeremy A Diehl, Alexander D Osumi-Sutherland, David Lasken, Roger S Lein, Ed S Scheuermann, Richard H Cell type discovery using single-cell transcriptomics: implications for ontological representation |
title | Cell type discovery using single-cell transcriptomics: implications for ontological representation |
title_full | Cell type discovery using single-cell transcriptomics: implications for ontological representation |
title_fullStr | Cell type discovery using single-cell transcriptomics: implications for ontological representation |
title_full_unstemmed | Cell type discovery using single-cell transcriptomics: implications for ontological representation |
title_short | Cell type discovery using single-cell transcriptomics: implications for ontological representation |
title_sort | cell type discovery using single-cell transcriptomics: implications for ontological representation |
topic | Invited Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946857/ https://www.ncbi.nlm.nih.gov/pubmed/29590361 http://dx.doi.org/10.1093/hmg/ddy100 |
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