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CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data
Quantifying cell-type proportions and their corresponding gene expression profiles in tissue samples would enhance understanding of the contributions of individual cell types to the physiological states of the tissue. Current approaches that address tissue heterogeneity have drawbacks. Experimental...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907860/ https://www.ncbi.nlm.nih.gov/pubmed/31790389 http://dx.doi.org/10.1371/journal.pcbi.1007510 |
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author | Kang, Kai Meng, Qian Shats, Igor Umbach, David M. Li, Melissa Li, Yuanyuan Li, Xiaoling Li, Leping |
author_facet | Kang, Kai Meng, Qian Shats, Igor Umbach, David M. Li, Melissa Li, Yuanyuan Li, Xiaoling Li, Leping |
author_sort | Kang, Kai |
collection | PubMed |
description | Quantifying cell-type proportions and their corresponding gene expression profiles in tissue samples would enhance understanding of the contributions of individual cell types to the physiological states of the tissue. Current approaches that address tissue heterogeneity have drawbacks. Experimental techniques, such as fluorescence-activated cell sorting, and single cell RNA sequencing are expensive. Computational approaches that use expression data from heterogeneous samples are promising, but most of the current methods estimate either cell-type proportions or cell-type-specific expression profiles by requiring the other as input. Although such partial deconvolution methods have been successfully applied to tumor samples, the additional input required may be unavailable. We introduce a novel complete deconvolution method, CDSeq, that uses only RNA-Seq data from bulk tissue samples to simultaneously estimate both cell-type proportions and cell-type-specific expression profiles. Using several synthetic and real experimental datasets with known cell-type composition and cell-type-specific expression profiles, we compared CDSeq’s complete deconvolution performance with seven other established deconvolution methods. Complete deconvolution using CDSeq represents a substantial technical advance over partial deconvolution approaches and will be useful for studying cell mixtures in tissue samples. CDSeq is available at GitHub repository (MATLAB and Octave code): https://github.com/kkang7/CDSeq. |
format | Online Article Text |
id | pubmed-6907860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69078602019-12-27 CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data Kang, Kai Meng, Qian Shats, Igor Umbach, David M. Li, Melissa Li, Yuanyuan Li, Xiaoling Li, Leping PLoS Comput Biol Research Article Quantifying cell-type proportions and their corresponding gene expression profiles in tissue samples would enhance understanding of the contributions of individual cell types to the physiological states of the tissue. Current approaches that address tissue heterogeneity have drawbacks. Experimental techniques, such as fluorescence-activated cell sorting, and single cell RNA sequencing are expensive. Computational approaches that use expression data from heterogeneous samples are promising, but most of the current methods estimate either cell-type proportions or cell-type-specific expression profiles by requiring the other as input. Although such partial deconvolution methods have been successfully applied to tumor samples, the additional input required may be unavailable. We introduce a novel complete deconvolution method, CDSeq, that uses only RNA-Seq data from bulk tissue samples to simultaneously estimate both cell-type proportions and cell-type-specific expression profiles. Using several synthetic and real experimental datasets with known cell-type composition and cell-type-specific expression profiles, we compared CDSeq’s complete deconvolution performance with seven other established deconvolution methods. Complete deconvolution using CDSeq represents a substantial technical advance over partial deconvolution approaches and will be useful for studying cell mixtures in tissue samples. CDSeq is available at GitHub repository (MATLAB and Octave code): https://github.com/kkang7/CDSeq. Public Library of Science 2019-12-02 /pmc/articles/PMC6907860/ /pubmed/31790389 http://dx.doi.org/10.1371/journal.pcbi.1007510 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Kang, Kai Meng, Qian Shats, Igor Umbach, David M. Li, Melissa Li, Yuanyuan Li, Xiaoling Li, Leping CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data |
title | CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data |
title_full | CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data |
title_fullStr | CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data |
title_full_unstemmed | CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data |
title_short | CDSeq: A novel complete deconvolution method for dissecting heterogeneous samples using gene expression data |
title_sort | cdseq: a novel complete deconvolution method for dissecting heterogeneous samples using gene expression data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907860/ https://www.ncbi.nlm.nih.gov/pubmed/31790389 http://dx.doi.org/10.1371/journal.pcbi.1007510 |
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