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The OncoFinder algorithm for minimizing the errors introduced by the high-throughput methods of transcriptome analysis

The diversity of the installed sequencing and microarray equipment make it increasingly difficult to compare and analyze the gene expression datasets obtained using the different methods. Many applications requiring high-quality and low error rates cannot make use of available data using traditional...

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Autores principales: Buzdin, Anton A., Zhavoronkov, Alex A., Korzinkin, Mikhail B., Roumiantsev, Sergey A., Aliper, Alexander M., Venkova, Larisa S., Smirnov, Philip Y., Borisov, Nikolay M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428387/
https://www.ncbi.nlm.nih.gov/pubmed/25988149
http://dx.doi.org/10.3389/fmolb.2014.00008
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author Buzdin, Anton A.
Zhavoronkov, Alex A.
Korzinkin, Mikhail B.
Roumiantsev, Sergey A.
Aliper, Alexander M.
Venkova, Larisa S.
Smirnov, Philip Y.
Borisov, Nikolay M.
author_facet Buzdin, Anton A.
Zhavoronkov, Alex A.
Korzinkin, Mikhail B.
Roumiantsev, Sergey A.
Aliper, Alexander M.
Venkova, Larisa S.
Smirnov, Philip Y.
Borisov, Nikolay M.
author_sort Buzdin, Anton A.
collection PubMed
description The diversity of the installed sequencing and microarray equipment make it increasingly difficult to compare and analyze the gene expression datasets obtained using the different methods. Many applications requiring high-quality and low error rates cannot make use of available data using traditional analytical approaches. Recently, we proposed a new concept of signalome-wide analysis of functional changes in the intracellular pathways termed OncoFinder, a bioinformatic tool for quantitative estimation of the signaling pathway activation (SPA). We also developed methods to compare the gene expression data obtained using multiple platforms and minimizing the error rates by mapping the gene expression data onto the known and custom signaling pathways. This technique for the first time makes it possible to analyze the functional features of intracellular regulation on a mathematical basis. In this study we show that the OncoFinder method significantly reduces the errors introduced by transcriptome-wide experimental techniques. We compared the gene expression data for the same biological samples obtained by both the next generation sequencing (NGS) and microarray methods. For these different techniques we demonstrate that there is virtually no correlation between the gene expression values for all datasets analyzed (R(2) < 0.1). In contrast, when the OncoFinder algorithm is applied to the data we observed clear-cut correlations between the NGS and microarray gene expression datasets. The SPA profiles obtained using NGS and microarray techniques were almost identical for the same biological samples allowing for the platform-agnostic analytical applications. We conclude that this feature of the OncoFinder enables to characterize the functional states of the transcriptomes and interactomes more accurately as before, which makes OncoFinder a method of choice for many applications including genetics, physiology, biomedicine, and molecular diagnostics.
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spelling pubmed-44283872015-05-18 The OncoFinder algorithm for minimizing the errors introduced by the high-throughput methods of transcriptome analysis Buzdin, Anton A. Zhavoronkov, Alex A. Korzinkin, Mikhail B. Roumiantsev, Sergey A. Aliper, Alexander M. Venkova, Larisa S. Smirnov, Philip Y. Borisov, Nikolay M. Front Mol Biosci Molecular Biosciences The diversity of the installed sequencing and microarray equipment make it increasingly difficult to compare and analyze the gene expression datasets obtained using the different methods. Many applications requiring high-quality and low error rates cannot make use of available data using traditional analytical approaches. Recently, we proposed a new concept of signalome-wide analysis of functional changes in the intracellular pathways termed OncoFinder, a bioinformatic tool for quantitative estimation of the signaling pathway activation (SPA). We also developed methods to compare the gene expression data obtained using multiple platforms and minimizing the error rates by mapping the gene expression data onto the known and custom signaling pathways. This technique for the first time makes it possible to analyze the functional features of intracellular regulation on a mathematical basis. In this study we show that the OncoFinder method significantly reduces the errors introduced by transcriptome-wide experimental techniques. We compared the gene expression data for the same biological samples obtained by both the next generation sequencing (NGS) and microarray methods. For these different techniques we demonstrate that there is virtually no correlation between the gene expression values for all datasets analyzed (R(2) < 0.1). In contrast, when the OncoFinder algorithm is applied to the data we observed clear-cut correlations between the NGS and microarray gene expression datasets. The SPA profiles obtained using NGS and microarray techniques were almost identical for the same biological samples allowing for the platform-agnostic analytical applications. We conclude that this feature of the OncoFinder enables to characterize the functional states of the transcriptomes and interactomes more accurately as before, which makes OncoFinder a method of choice for many applications including genetics, physiology, biomedicine, and molecular diagnostics. Frontiers Media S.A. 2014-08-26 /pmc/articles/PMC4428387/ /pubmed/25988149 http://dx.doi.org/10.3389/fmolb.2014.00008 Text en Copyright © 2014 Buzdin, Zhavoronkov, Korzinkin, Roumiantsev, Aliper, Venkova, Smirnov and Borisov. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Molecular Biosciences
Buzdin, Anton A.
Zhavoronkov, Alex A.
Korzinkin, Mikhail B.
Roumiantsev, Sergey A.
Aliper, Alexander M.
Venkova, Larisa S.
Smirnov, Philip Y.
Borisov, Nikolay M.
The OncoFinder algorithm for minimizing the errors introduced by the high-throughput methods of transcriptome analysis
title The OncoFinder algorithm for minimizing the errors introduced by the high-throughput methods of transcriptome analysis
title_full The OncoFinder algorithm for minimizing the errors introduced by the high-throughput methods of transcriptome analysis
title_fullStr The OncoFinder algorithm for minimizing the errors introduced by the high-throughput methods of transcriptome analysis
title_full_unstemmed The OncoFinder algorithm for minimizing the errors introduced by the high-throughput methods of transcriptome analysis
title_short The OncoFinder algorithm for minimizing the errors introduced by the high-throughput methods of transcriptome analysis
title_sort oncofinder algorithm for minimizing the errors introduced by the high-throughput methods of transcriptome analysis
topic Molecular Biosciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428387/
https://www.ncbi.nlm.nih.gov/pubmed/25988149
http://dx.doi.org/10.3389/fmolb.2014.00008
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