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dc.contributor.authorLu, Y.
dc.contributor.authorChen, Q.M.
dc.contributor.authorAn, L.
dc.date.accessioned2024-04-01T22:53:44Z
dc.date.available2024-04-01T22:53:44Z
dc.date.issued2023-12-23
dc.identifier.citationYingying Lu, Qin M Chen, Lingling An, Semi-reference based cell type deconvolution with application to human metastatic cancers, NAR Genomics and Bioinformatics, Volume 5, Issue 4, December 2023, lqad109, https://doi.org/10.1093/nargab/lqad109
dc.identifier.issn2631-9268
dc.identifier.doi10.1093/nargab/lqad109
dc.identifier.urihttp://hdl.handle.net/10150/672047
dc.description.abstractBulk RNA-seq experiments, commonly used to discern gene expression changes across conditions, often neglect critical cell type-specific information due to their focus on average transcript abundance. Recognizing cell type contribution is crucial to understanding phenotype and disease variations. The advent of single-cell RNA sequencing has allowed detailed examination of cellular heterogeneity; however, the cost and analytic caveat prohibits such sequencing for a large number of samples. We introduce a novel deconvolution approach, SECRET, that employs cell type-specific gene expression profiles from single-cell RNA-seq to accurately estimate cell type proportions from bulk RNA-seq data. Notably, SECRET can adapt to scenarios where the cell type present in the bulk data is unrepresented in the reference, thereby offering increased flexibility in reference selection. SECRET has demonstrated superior accuracy compared to existing methods using synthetic data and has identified unknown tissue-specific cell types in real human metastatic cancers. Its versatility makes it broadly applicable across various human cancer studies. © The Author(s) 2023. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics.
dc.language.isoen
dc.publisherOxford University Press
dc.rights© The Author(s) 2023. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/).
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/)
dc.titleSemi-reference based cell type deconvolution with application to human metastatic cancers
dc.typeArticle
dc.typetext
dc.contributor.departmentInterdisciplinary Program in Statistics and Data Science, University of Arizona
dc.contributor.departmentCollege of Pharmacy, University of Arizona
dc.contributor.departmentCancer Biology Program, University of Arizona
dc.contributor.departmentInterdisciplinary Program in Statistics and Data Science, University of Arizona
dc.contributor.departmentDepartment of Biosystems Engineering, University of Arizona
dc.contributor.departmentDepartment of Epidemiology and Biostatistics, University of Arizona
dc.identifier.journalNAR Genomics and Bioinformatics
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal Published Version
dc.source.journaltitleNAR Genomics and Bioinformatics
refterms.dateFOA2024-04-01T22:53:44Z


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© The Author(s) 2023. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/).
Except where otherwise noted, this item's license is described as © The Author(s) 2023. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/).