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Manual cell selection in single cell transcriptomics using scSELpy supports the analysis of immune cell subsets
INTRODUCTION: Single cell RNA sequencing plays an increasing and indispensable role in immunological research such as in the field of inflammatory bowel diseases (IBD). Professional pipelines are complex, but tools for the manual selection and further downstream analysis of single cell populations a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166880/ https://www.ncbi.nlm.nih.gov/pubmed/37180117 http://dx.doi.org/10.3389/fimmu.2023.1027346 |
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author | Dedden, Mark Wiendl, Maximilian Müller, Tanja M. Neurath, Markus F. Zundler, Sebastian |
author_facet | Dedden, Mark Wiendl, Maximilian Müller, Tanja M. Neurath, Markus F. Zundler, Sebastian |
author_sort | Dedden, Mark |
collection | PubMed |
description | INTRODUCTION: Single cell RNA sequencing plays an increasing and indispensable role in immunological research such as in the field of inflammatory bowel diseases (IBD). Professional pipelines are complex, but tools for the manual selection and further downstream analysis of single cell populations are missing so far. METHODS: We developed a tool called scSELpy, which can easily be integrated into Scanpy-based pipelines, allowing the manual selection of cells on single cell transcriptomic datasets by drawing polygons on various data representations. The tool further supports the downstream analysis of the selected cells and the plotting of results. RESULTS: Taking advantage of two previously published single cell RNA sequencing datasets we show that this tool is useful for the positive and negative selection of T cell subsets implicated in IBD beyond standard clustering. We further demonstrate the feasibility for subphenotyping T cell subsets and use scSELpy to corroborate earlier conclusions drawn from the dataset. Moreover, we also show its usefulness in the context of T cell receptor sequencing. DISCUSSION: Collectively, scSELpy is a promising additive tool fulfilling a so far unmet need in the field of single cell transcriptomic analysis that might support future immunological research. |
format | Online Article Text |
id | pubmed-10166880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101668802023-05-10 Manual cell selection in single cell transcriptomics using scSELpy supports the analysis of immune cell subsets Dedden, Mark Wiendl, Maximilian Müller, Tanja M. Neurath, Markus F. Zundler, Sebastian Front Immunol Immunology INTRODUCTION: Single cell RNA sequencing plays an increasing and indispensable role in immunological research such as in the field of inflammatory bowel diseases (IBD). Professional pipelines are complex, but tools for the manual selection and further downstream analysis of single cell populations are missing so far. METHODS: We developed a tool called scSELpy, which can easily be integrated into Scanpy-based pipelines, allowing the manual selection of cells on single cell transcriptomic datasets by drawing polygons on various data representations. The tool further supports the downstream analysis of the selected cells and the plotting of results. RESULTS: Taking advantage of two previously published single cell RNA sequencing datasets we show that this tool is useful for the positive and negative selection of T cell subsets implicated in IBD beyond standard clustering. We further demonstrate the feasibility for subphenotyping T cell subsets and use scSELpy to corroborate earlier conclusions drawn from the dataset. Moreover, we also show its usefulness in the context of T cell receptor sequencing. DISCUSSION: Collectively, scSELpy is a promising additive tool fulfilling a so far unmet need in the field of single cell transcriptomic analysis that might support future immunological research. Frontiers Media S.A. 2023-04-25 /pmc/articles/PMC10166880/ /pubmed/37180117 http://dx.doi.org/10.3389/fimmu.2023.1027346 Text en Copyright © 2023 Dedden, Wiendl, Müller, Neurath and Zundler https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Dedden, Mark Wiendl, Maximilian Müller, Tanja M. Neurath, Markus F. Zundler, Sebastian Manual cell selection in single cell transcriptomics using scSELpy supports the analysis of immune cell subsets |
title | Manual cell selection in single cell transcriptomics using scSELpy supports the analysis of immune cell subsets |
title_full | Manual cell selection in single cell transcriptomics using scSELpy supports the analysis of immune cell subsets |
title_fullStr | Manual cell selection in single cell transcriptomics using scSELpy supports the analysis of immune cell subsets |
title_full_unstemmed | Manual cell selection in single cell transcriptomics using scSELpy supports the analysis of immune cell subsets |
title_short | Manual cell selection in single cell transcriptomics using scSELpy supports the analysis of immune cell subsets |
title_sort | manual cell selection in single cell transcriptomics using scselpy supports the analysis of immune cell subsets |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166880/ https://www.ncbi.nlm.nih.gov/pubmed/37180117 http://dx.doi.org/10.3389/fimmu.2023.1027346 |
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