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baredSC: Bayesian approach to retrieve expression distribution of single-cell data
BACKGROUND: The number of studies using single-cell RNA sequencing (scRNA-seq) is constantly growing. This powerful technique provides a sampling of the whole transcriptome of a cell. However, sparsity of the data can be a major hurdle when studying the distribution of the expression of a specific g...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756634/ https://www.ncbi.nlm.nih.gov/pubmed/35021985 http://dx.doi.org/10.1186/s12859-021-04507-8 |
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author | Lopez-Delisle, Lucille Delisle, Jean-Baptiste |
author_facet | Lopez-Delisle, Lucille Delisle, Jean-Baptiste |
author_sort | Lopez-Delisle, Lucille |
collection | PubMed |
description | BACKGROUND: The number of studies using single-cell RNA sequencing (scRNA-seq) is constantly growing. This powerful technique provides a sampling of the whole transcriptome of a cell. However, sparsity of the data can be a major hurdle when studying the distribution of the expression of a specific gene or the correlation between the expressions of two genes. RESULTS: We show that the main technical noise associated with these scRNA-seq experiments is due to the sampling, i.e., Poisson noise. We present a new tool named baredSC, for Bayesian Approach to Retrieve Expression Distribution of Single-Cell data, which infers the intrinsic expression distribution in scRNA-seq data using a Gaussian mixture model. baredSC can be used to obtain the distribution in one dimension for individual genes and in two dimensions for pairs of genes, in particular to estimate the correlation in the two genes’ expressions. We apply baredSC to simulated scRNA-seq data and show that the algorithm is able to uncover the expression distribution used to simulate the data, even in multi-modal cases with very sparse data. We also apply baredSC to two real biological data sets. First, we use it to measure the anti-correlation between Hoxd13 and Hoxa11, two genes with known genetic interaction in embryonic limb. Then, we study the expression of Pitx1 in embryonic hindlimb, for which a trimodal distribution has been identified through flow cytometry. While other methods to analyze scRNA-seq are too sensitive to sampling noise, baredSC reveals this trimodal distribution. CONCLUSION: baredSC is a powerful tool which aims at retrieving the expression distribution of few genes of interest from scRNA-seq data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04507-8. |
format | Online Article Text |
id | pubmed-8756634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87566342022-01-18 baredSC: Bayesian approach to retrieve expression distribution of single-cell data Lopez-Delisle, Lucille Delisle, Jean-Baptiste BMC Bioinformatics Research Article BACKGROUND: The number of studies using single-cell RNA sequencing (scRNA-seq) is constantly growing. This powerful technique provides a sampling of the whole transcriptome of a cell. However, sparsity of the data can be a major hurdle when studying the distribution of the expression of a specific gene or the correlation between the expressions of two genes. RESULTS: We show that the main technical noise associated with these scRNA-seq experiments is due to the sampling, i.e., Poisson noise. We present a new tool named baredSC, for Bayesian Approach to Retrieve Expression Distribution of Single-Cell data, which infers the intrinsic expression distribution in scRNA-seq data using a Gaussian mixture model. baredSC can be used to obtain the distribution in one dimension for individual genes and in two dimensions for pairs of genes, in particular to estimate the correlation in the two genes’ expressions. We apply baredSC to simulated scRNA-seq data and show that the algorithm is able to uncover the expression distribution used to simulate the data, even in multi-modal cases with very sparse data. We also apply baredSC to two real biological data sets. First, we use it to measure the anti-correlation between Hoxd13 and Hoxa11, two genes with known genetic interaction in embryonic limb. Then, we study the expression of Pitx1 in embryonic hindlimb, for which a trimodal distribution has been identified through flow cytometry. While other methods to analyze scRNA-seq are too sensitive to sampling noise, baredSC reveals this trimodal distribution. CONCLUSION: baredSC is a powerful tool which aims at retrieving the expression distribution of few genes of interest from scRNA-seq data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04507-8. BioMed Central 2022-01-12 /pmc/articles/PMC8756634/ /pubmed/35021985 http://dx.doi.org/10.1186/s12859-021-04507-8 Text en © The Author(s) 2022 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 Article Lopez-Delisle, Lucille Delisle, Jean-Baptiste baredSC: Bayesian approach to retrieve expression distribution of single-cell data |
title | baredSC: Bayesian approach to retrieve expression distribution of single-cell data |
title_full | baredSC: Bayesian approach to retrieve expression distribution of single-cell data |
title_fullStr | baredSC: Bayesian approach to retrieve expression distribution of single-cell data |
title_full_unstemmed | baredSC: Bayesian approach to retrieve expression distribution of single-cell data |
title_short | baredSC: Bayesian approach to retrieve expression distribution of single-cell data |
title_sort | baredsc: bayesian approach to retrieve expression distribution of single-cell data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756634/ https://www.ncbi.nlm.nih.gov/pubmed/35021985 http://dx.doi.org/10.1186/s12859-021-04507-8 |
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