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Multi-level cellular and functional annotation of single-cell transcriptomes using scPipeline

Single-cell RNA-sequencing (scRNA-seq) offers functional insight into complex biology, allowing for the interrogation of cellular populations and gene expression programs at single-cell resolution. Here, we introduce scPipeline, a single-cell data analysis toolbox that builds on existing methods and...

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Autores principales: Mikolajewicz, Nicholas, Gacesa, Rafael, Aguilera-Uribe, Magali, Brown, Kevin R., Moffat, Jason, Han, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616830/
https://www.ncbi.nlm.nih.gov/pubmed/36307536
http://dx.doi.org/10.1038/s42003-022-04093-2
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author Mikolajewicz, Nicholas
Gacesa, Rafael
Aguilera-Uribe, Magali
Brown, Kevin R.
Moffat, Jason
Han, Hong
author_facet Mikolajewicz, Nicholas
Gacesa, Rafael
Aguilera-Uribe, Magali
Brown, Kevin R.
Moffat, Jason
Han, Hong
author_sort Mikolajewicz, Nicholas
collection PubMed
description Single-cell RNA-sequencing (scRNA-seq) offers functional insight into complex biology, allowing for the interrogation of cellular populations and gene expression programs at single-cell resolution. Here, we introduce scPipeline, a single-cell data analysis toolbox that builds on existing methods and offers modular workflows for multi-level cellular annotation and user-friendly analysis reports. Advances to scRNA-seq annotation include: (i) co-dependency index (CDI)-based differential expression, (ii) cluster resolution optimization using a marker-specificity criterion, (iii) marker-based cell-type annotation with Miko scoring, and (iv) gene program discovery using scale-free shared nearest neighbor network (SSN) analysis. Both unsupervised and supervised procedures were validated using a diverse collection of scRNA-seq datasets and illustrative examples of cellular transcriptomic annotation of developmental and immunological scRNA-seq atlases are provided herein. Overall, scPipeline offers a flexible computational framework for in-depth scRNA-seq analysis.
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spelling pubmed-96168302022-10-30 Multi-level cellular and functional annotation of single-cell transcriptomes using scPipeline Mikolajewicz, Nicholas Gacesa, Rafael Aguilera-Uribe, Magali Brown, Kevin R. Moffat, Jason Han, Hong Commun Biol Article Single-cell RNA-sequencing (scRNA-seq) offers functional insight into complex biology, allowing for the interrogation of cellular populations and gene expression programs at single-cell resolution. Here, we introduce scPipeline, a single-cell data analysis toolbox that builds on existing methods and offers modular workflows for multi-level cellular annotation and user-friendly analysis reports. Advances to scRNA-seq annotation include: (i) co-dependency index (CDI)-based differential expression, (ii) cluster resolution optimization using a marker-specificity criterion, (iii) marker-based cell-type annotation with Miko scoring, and (iv) gene program discovery using scale-free shared nearest neighbor network (SSN) analysis. Both unsupervised and supervised procedures were validated using a diverse collection of scRNA-seq datasets and illustrative examples of cellular transcriptomic annotation of developmental and immunological scRNA-seq atlases are provided herein. Overall, scPipeline offers a flexible computational framework for in-depth scRNA-seq analysis. Nature Publishing Group UK 2022-10-28 /pmc/articles/PMC9616830/ /pubmed/36307536 http://dx.doi.org/10.1038/s42003-022-04093-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mikolajewicz, Nicholas
Gacesa, Rafael
Aguilera-Uribe, Magali
Brown, Kevin R.
Moffat, Jason
Han, Hong
Multi-level cellular and functional annotation of single-cell transcriptomes using scPipeline
title Multi-level cellular and functional annotation of single-cell transcriptomes using scPipeline
title_full Multi-level cellular and functional annotation of single-cell transcriptomes using scPipeline
title_fullStr Multi-level cellular and functional annotation of single-cell transcriptomes using scPipeline
title_full_unstemmed Multi-level cellular and functional annotation of single-cell transcriptomes using scPipeline
title_short Multi-level cellular and functional annotation of single-cell transcriptomes using scPipeline
title_sort multi-level cellular and functional annotation of single-cell transcriptomes using scpipeline
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616830/
https://www.ncbi.nlm.nih.gov/pubmed/36307536
http://dx.doi.org/10.1038/s42003-022-04093-2
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