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Optimal marker gene selection for cell type discrimination in single cell analyses
Single-cell technologies characterize complex cell populations across multiple data modalities at unprecedented scale and resolution. Multi-omic data for single cell gene expression, in situ hybridization, or single cell chromatin states are increasingly available across diverse tissue types. When i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895823/ https://www.ncbi.nlm.nih.gov/pubmed/33608535 http://dx.doi.org/10.1038/s41467-021-21453-4 |
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author | Dumitrascu, Bianca Villar, Soledad Mixon, Dustin G. Engelhardt, Barbara E. |
author_facet | Dumitrascu, Bianca Villar, Soledad Mixon, Dustin G. Engelhardt, Barbara E. |
author_sort | Dumitrascu, Bianca |
collection | PubMed |
description | Single-cell technologies characterize complex cell populations across multiple data modalities at unprecedented scale and resolution. Multi-omic data for single cell gene expression, in situ hybridization, or single cell chromatin states are increasingly available across diverse tissue types. When isolating specific cell types from a sample of disassociated cells or performing in situ sequencing in collections of heterogeneous cells, one challenging task is to select a small set of informative markers that robustly enable the identification and discrimination of specific cell types or cell states as precisely as possible. Given single cell RNA-seq data and a set of cellular labels to discriminate, scGeneFit selects gene markers that jointly optimize cell label recovery using label-aware compressive classification methods. This results in a substantially more robust and less redundant set of markers than existing methods, most of which identify markers that separate each cell label from the rest. When applied to a data set given a hierarchy of cell types as labels, the markers found by our method improves the recovery of the cell type hierarchy with fewer markers than existing methods using a computationally efficient and principled optimization. |
format | Online Article Text |
id | pubmed-7895823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78958232021-03-03 Optimal marker gene selection for cell type discrimination in single cell analyses Dumitrascu, Bianca Villar, Soledad Mixon, Dustin G. Engelhardt, Barbara E. Nat Commun Article Single-cell technologies characterize complex cell populations across multiple data modalities at unprecedented scale and resolution. Multi-omic data for single cell gene expression, in situ hybridization, or single cell chromatin states are increasingly available across diverse tissue types. When isolating specific cell types from a sample of disassociated cells or performing in situ sequencing in collections of heterogeneous cells, one challenging task is to select a small set of informative markers that robustly enable the identification and discrimination of specific cell types or cell states as precisely as possible. Given single cell RNA-seq data and a set of cellular labels to discriminate, scGeneFit selects gene markers that jointly optimize cell label recovery using label-aware compressive classification methods. This results in a substantially more robust and less redundant set of markers than existing methods, most of which identify markers that separate each cell label from the rest. When applied to a data set given a hierarchy of cell types as labels, the markers found by our method improves the recovery of the cell type hierarchy with fewer markers than existing methods using a computationally efficient and principled optimization. Nature Publishing Group UK 2021-02-19 /pmc/articles/PMC7895823/ /pubmed/33608535 http://dx.doi.org/10.1038/s41467-021-21453-4 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Dumitrascu, Bianca Villar, Soledad Mixon, Dustin G. Engelhardt, Barbara E. Optimal marker gene selection for cell type discrimination in single cell analyses |
title | Optimal marker gene selection for cell type discrimination in single cell analyses |
title_full | Optimal marker gene selection for cell type discrimination in single cell analyses |
title_fullStr | Optimal marker gene selection for cell type discrimination in single cell analyses |
title_full_unstemmed | Optimal marker gene selection for cell type discrimination in single cell analyses |
title_short | Optimal marker gene selection for cell type discrimination in single cell analyses |
title_sort | optimal marker gene selection for cell type discrimination in single cell analyses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895823/ https://www.ncbi.nlm.nih.gov/pubmed/33608535 http://dx.doi.org/10.1038/s41467-021-21453-4 |
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