Differential Expression Analysis in RNA-seq Data Using a Geometric Approach
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1089/cmb.2017.0244 http://hdl.handle.net/11449/185176 |
Resumo: | Although differential gene expression (DGE) profiling in RNA-seq is used by many researchers, new packages and pipelines are continuously being presented as a result of an ongoing investigation. In this work, a geometric approach based on Supervised Variational Relevance Learning (Suvrel) was compared with DEpackages (edgeR, DESEq, baySeq, PoissonSeq, and limma) in the DGE profiling. The Suvrel method seeks to determine the relevance of characteristics (e.g., gene or transcript) based on intraclass and interclass distances. The comparison was performed using technical and biological replicates. For technical replicates, we used receiver operating characteristic (ROC) analysis, while for the other ones, we used robustness analysis. From ROC analysis, we found that geometric approach had a better performance than the DEpackages. Particularly, for a reduced list of differentially expressed genes (DEG), we noticed that this method had a remarkable advantage in ranking of most DEG (with a specificity ranging from 1 to 0.8). From robustness analysis associated to biological replicates, we found that geometric approach has comparable performance to the DEpackages. We conclude that the geometric approach had a slight overall better performance than the other methods. Moreover, it is a simple method that does not make any assumption about the distribution associated with RNA-seq data set. From this perspective, the relevance of this study was to show that a simple method can provide as good performance as more complex methods. |
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Differential Expression Analysis in RNA-seq Data Using a Geometric Approachanalysisdifferential expression evaluationRNA-SeqAlthough differential gene expression (DGE) profiling in RNA-seq is used by many researchers, new packages and pipelines are continuously being presented as a result of an ongoing investigation. In this work, a geometric approach based on Supervised Variational Relevance Learning (Suvrel) was compared with DEpackages (edgeR, DESEq, baySeq, PoissonSeq, and limma) in the DGE profiling. The Suvrel method seeks to determine the relevance of characteristics (e.g., gene or transcript) based on intraclass and interclass distances. The comparison was performed using technical and biological replicates. For technical replicates, we used receiver operating characteristic (ROC) analysis, while for the other ones, we used robustness analysis. From ROC analysis, we found that geometric approach had a better performance than the DEpackages. Particularly, for a reduced list of differentially expressed genes (DEG), we noticed that this method had a remarkable advantage in ranking of most DEG (with a specificity ranging from 1 to 0.8). From robustness analysis associated to biological replicates, we found that geometric approach has comparable performance to the DEpackages. We conclude that the geometric approach had a slight overall better performance than the other methods. Moreover, it is a simple method that does not make any assumption about the distribution associated with RNA-seq data set. From this perspective, the relevance of this study was to show that a simple method can provide as good performance as more complex methods.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Univ Estadual Paulista, Inst Biociencias Letras & Ciencias Exatas, Dept Fis, BR-15054000 Sao Jose Do Rio Preto, BrazilSwiss Fed Inst Technol, Dept Biosyst Sci & Engn D BSSE, Basel, SwitzerlandUniv Estadual Paulista, Inst Biociencias Letras & Ciencias Exatas, Dept Fis, BR-15054000 Sao Jose Do Rio Preto, BrazilFAPESP: 2014/06862-7FAPESP: 2016/19766-1Mary Ann Liebert, IncUniversidade Estadual Paulista (Unesp)Swiss Fed Inst TechnolTambonis, Tiago [UNESP]Boareto, MarceloLeite, Vitor B. P. [UNESP]2019-10-04T12:33:12Z2019-10-04T12:33:12Z2018-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1257-1265http://dx.doi.org/10.1089/cmb.2017.0244Journal Of Computational Biology. New Rochelle: Mary Ann Liebert, Inc, v. 25, n. 11, p. 1257-1265, 2018.1066-5277http://hdl.handle.net/11449/18517610.1089/cmb.2017.0244WOS:000452242100008Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Computational Biologyinfo:eu-repo/semantics/openAccess2021-10-23T19:49:56Zoai:repositorio.unesp.br:11449/185176Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:06:23.223650Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Differential Expression Analysis in RNA-seq Data Using a Geometric Approach |
title |
Differential Expression Analysis in RNA-seq Data Using a Geometric Approach |
spellingShingle |
Differential Expression Analysis in RNA-seq Data Using a Geometric Approach Tambonis, Tiago [UNESP] analysis differential expression evaluation RNA-Seq |
title_short |
Differential Expression Analysis in RNA-seq Data Using a Geometric Approach |
title_full |
Differential Expression Analysis in RNA-seq Data Using a Geometric Approach |
title_fullStr |
Differential Expression Analysis in RNA-seq Data Using a Geometric Approach |
title_full_unstemmed |
Differential Expression Analysis in RNA-seq Data Using a Geometric Approach |
title_sort |
Differential Expression Analysis in RNA-seq Data Using a Geometric Approach |
author |
Tambonis, Tiago [UNESP] |
author_facet |
Tambonis, Tiago [UNESP] Boareto, Marcelo Leite, Vitor B. P. [UNESP] |
author_role |
author |
author2 |
Boareto, Marcelo Leite, Vitor B. P. [UNESP] |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Swiss Fed Inst Technol |
dc.contributor.author.fl_str_mv |
Tambonis, Tiago [UNESP] Boareto, Marcelo Leite, Vitor B. P. [UNESP] |
dc.subject.por.fl_str_mv |
analysis differential expression evaluation RNA-Seq |
topic |
analysis differential expression evaluation RNA-Seq |
description |
Although differential gene expression (DGE) profiling in RNA-seq is used by many researchers, new packages and pipelines are continuously being presented as a result of an ongoing investigation. In this work, a geometric approach based on Supervised Variational Relevance Learning (Suvrel) was compared with DEpackages (edgeR, DESEq, baySeq, PoissonSeq, and limma) in the DGE profiling. The Suvrel method seeks to determine the relevance of characteristics (e.g., gene or transcript) based on intraclass and interclass distances. The comparison was performed using technical and biological replicates. For technical replicates, we used receiver operating characteristic (ROC) analysis, while for the other ones, we used robustness analysis. From ROC analysis, we found that geometric approach had a better performance than the DEpackages. Particularly, for a reduced list of differentially expressed genes (DEG), we noticed that this method had a remarkable advantage in ranking of most DEG (with a specificity ranging from 1 to 0.8). From robustness analysis associated to biological replicates, we found that geometric approach has comparable performance to the DEpackages. We conclude that the geometric approach had a slight overall better performance than the other methods. Moreover, it is a simple method that does not make any assumption about the distribution associated with RNA-seq data set. From this perspective, the relevance of this study was to show that a simple method can provide as good performance as more complex methods. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-11-01 2019-10-04T12:33:12Z 2019-10-04T12:33:12Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1089/cmb.2017.0244 Journal Of Computational Biology. New Rochelle: Mary Ann Liebert, Inc, v. 25, n. 11, p. 1257-1265, 2018. 1066-5277 http://hdl.handle.net/11449/185176 10.1089/cmb.2017.0244 WOS:000452242100008 |
url |
http://dx.doi.org/10.1089/cmb.2017.0244 http://hdl.handle.net/11449/185176 |
identifier_str_mv |
Journal Of Computational Biology. New Rochelle: Mary Ann Liebert, Inc, v. 25, n. 11, p. 1257-1265, 2018. 1066-5277 10.1089/cmb.2017.0244 WOS:000452242100008 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal Of Computational Biology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1257-1265 |
dc.publisher.none.fl_str_mv |
Mary Ann Liebert, Inc |
publisher.none.fl_str_mv |
Mary Ann Liebert, Inc |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128895591907328 |