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Accurate estimation of cell composition in bulk expression through robust integration of single-cell information
We present Bisque, a tool for estimating cell type proportions in bulk expression. Bisque implements a regression-based approach that utilizes single-cell RNA-seq (scRNA-seq) or single-nucleus RNA-seq (snRNA-seq) data to generate a reference expression profile and learn gene-specific bulk expression...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181686/ https://www.ncbi.nlm.nih.gov/pubmed/32332754 http://dx.doi.org/10.1038/s41467-020-15816-6 |
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author | Jew, Brandon Alvarez, Marcus Rahmani, Elior Miao, Zong Ko, Arthur Garske, Kristina M. Sul, Jae Hoon Pietiläinen, Kirsi H. Pajukanta, Päivi Halperin, Eran |
author_facet | Jew, Brandon Alvarez, Marcus Rahmani, Elior Miao, Zong Ko, Arthur Garske, Kristina M. Sul, Jae Hoon Pietiläinen, Kirsi H. Pajukanta, Päivi Halperin, Eran |
author_sort | Jew, Brandon |
collection | PubMed |
description | We present Bisque, a tool for estimating cell type proportions in bulk expression. Bisque implements a regression-based approach that utilizes single-cell RNA-seq (scRNA-seq) or single-nucleus RNA-seq (snRNA-seq) data to generate a reference expression profile and learn gene-specific bulk expression transformations to robustly decompose RNA-seq data. These transformations significantly improve decomposition performance compared to existing methods when there is significant technical variation in the generation of the reference profile and observed bulk expression. Importantly, compared to existing methods, our approach is extremely efficient, making it suitable for the analysis of large genomic datasets that are becoming ubiquitous. When applied to subcutaneous adipose and dorsolateral prefrontal cortex expression datasets with both bulk RNA-seq and snRNA-seq data, Bisque replicates previously reported associations between cell type proportions and measured phenotypes across abundant and rare cell types. We further propose an additional mode of operation that merely requires a set of known marker genes. |
format | Online Article Text |
id | pubmed-7181686 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71816862020-04-29 Accurate estimation of cell composition in bulk expression through robust integration of single-cell information Jew, Brandon Alvarez, Marcus Rahmani, Elior Miao, Zong Ko, Arthur Garske, Kristina M. Sul, Jae Hoon Pietiläinen, Kirsi H. Pajukanta, Päivi Halperin, Eran Nat Commun Article We present Bisque, a tool for estimating cell type proportions in bulk expression. Bisque implements a regression-based approach that utilizes single-cell RNA-seq (scRNA-seq) or single-nucleus RNA-seq (snRNA-seq) data to generate a reference expression profile and learn gene-specific bulk expression transformations to robustly decompose RNA-seq data. These transformations significantly improve decomposition performance compared to existing methods when there is significant technical variation in the generation of the reference profile and observed bulk expression. Importantly, compared to existing methods, our approach is extremely efficient, making it suitable for the analysis of large genomic datasets that are becoming ubiquitous. When applied to subcutaneous adipose and dorsolateral prefrontal cortex expression datasets with both bulk RNA-seq and snRNA-seq data, Bisque replicates previously reported associations between cell type proportions and measured phenotypes across abundant and rare cell types. We further propose an additional mode of operation that merely requires a set of known marker genes. Nature Publishing Group UK 2020-04-24 /pmc/articles/PMC7181686/ /pubmed/32332754 http://dx.doi.org/10.1038/s41467-020-15816-6 Text en © The Author(s) 2020 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 Jew, Brandon Alvarez, Marcus Rahmani, Elior Miao, Zong Ko, Arthur Garske, Kristina M. Sul, Jae Hoon Pietiläinen, Kirsi H. Pajukanta, Päivi Halperin, Eran Accurate estimation of cell composition in bulk expression through robust integration of single-cell information |
title | Accurate estimation of cell composition in bulk expression through robust integration of single-cell information |
title_full | Accurate estimation of cell composition in bulk expression through robust integration of single-cell information |
title_fullStr | Accurate estimation of cell composition in bulk expression through robust integration of single-cell information |
title_full_unstemmed | Accurate estimation of cell composition in bulk expression through robust integration of single-cell information |
title_short | Accurate estimation of cell composition in bulk expression through robust integration of single-cell information |
title_sort | accurate estimation of cell composition in bulk expression through robust integration of single-cell information |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181686/ https://www.ncbi.nlm.nih.gov/pubmed/32332754 http://dx.doi.org/10.1038/s41467-020-15816-6 |
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