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Cell type identification from single-cell transcriptomes in melanoma
BACKGROUND: Single-cell sequencing approaches allow gene expression to be measured at the single-cell level, providing opportunities and challenges to study the aetiology of complex diseases, including cancer. METHODS: Based on single-cell gene and lncRNA expression levels, we proposed a computation...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596920/ https://www.ncbi.nlm.nih.gov/pubmed/34784909 http://dx.doi.org/10.1186/s12920-021-01118-3 |
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author | Huo, Qiuyan Yin, Yu Liu, Fangfang Ma, Yuying Wang, Liming Qin, Guimin |
author_facet | Huo, Qiuyan Yin, Yu Liu, Fangfang Ma, Yuying Wang, Liming Qin, Guimin |
author_sort | Huo, Qiuyan |
collection | PubMed |
description | BACKGROUND: Single-cell sequencing approaches allow gene expression to be measured at the single-cell level, providing opportunities and challenges to study the aetiology of complex diseases, including cancer. METHODS: Based on single-cell gene and lncRNA expression levels, we proposed a computational framework for cell type identification that fully considers cell dropout characteristics. First, we defined the dropout features of the cells and identified the dropout clusters. Second, we constructed a differential co-expression network and identified differential modules. Finally, we identified cell types based on the differential modules. RESULTS: The method was applied to single-cell melanoma data, and eight cell types were identified. Enrichment analysis of the candidate cell marker genes for the two key cell types showed that both key cell types were closely related to the physiological activities of the major histocompatibility complex (MHC); one key cell type was associated with mitosis-related activities, and the other with pathways related to ten diseases. CONCLUSIONS: Through identification and analysis of key melanoma-related cell types, we explored the molecular mechanism of melanoma, providing insight into melanoma research. Moreover, the candidate cell markers for the two key cell types are potential therapeutic targets for melanoma. |
format | Online Article Text |
id | pubmed-8596920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85969202021-11-17 Cell type identification from single-cell transcriptomes in melanoma Huo, Qiuyan Yin, Yu Liu, Fangfang Ma, Yuying Wang, Liming Qin, Guimin BMC Med Genomics Research BACKGROUND: Single-cell sequencing approaches allow gene expression to be measured at the single-cell level, providing opportunities and challenges to study the aetiology of complex diseases, including cancer. METHODS: Based on single-cell gene and lncRNA expression levels, we proposed a computational framework for cell type identification that fully considers cell dropout characteristics. First, we defined the dropout features of the cells and identified the dropout clusters. Second, we constructed a differential co-expression network and identified differential modules. Finally, we identified cell types based on the differential modules. RESULTS: The method was applied to single-cell melanoma data, and eight cell types were identified. Enrichment analysis of the candidate cell marker genes for the two key cell types showed that both key cell types were closely related to the physiological activities of the major histocompatibility complex (MHC); one key cell type was associated with mitosis-related activities, and the other with pathways related to ten diseases. CONCLUSIONS: Through identification and analysis of key melanoma-related cell types, we explored the molecular mechanism of melanoma, providing insight into melanoma research. Moreover, the candidate cell markers for the two key cell types are potential therapeutic targets for melanoma. BioMed Central 2021-11-17 /pmc/articles/PMC8596920/ /pubmed/34784909 http://dx.doi.org/10.1186/s12920-021-01118-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Huo, Qiuyan Yin, Yu Liu, Fangfang Ma, Yuying Wang, Liming Qin, Guimin Cell type identification from single-cell transcriptomes in melanoma |
title | Cell type identification from single-cell transcriptomes in melanoma |
title_full | Cell type identification from single-cell transcriptomes in melanoma |
title_fullStr | Cell type identification from single-cell transcriptomes in melanoma |
title_full_unstemmed | Cell type identification from single-cell transcriptomes in melanoma |
title_short | Cell type identification from single-cell transcriptomes in melanoma |
title_sort | cell type identification from single-cell transcriptomes in melanoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8596920/ https://www.ncbi.nlm.nih.gov/pubmed/34784909 http://dx.doi.org/10.1186/s12920-021-01118-3 |
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