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The concordance between RNA-seq and microarray data depends on chemical treatment and transcript abundance

Title: The concordance between RNA-seq and microarray data depends on chemical treatment and transcript abundance
Authors: Wang, C.; Gong, B.; Bushel, P. R.; Thierry Mieg, J.; Thierry Mieg, D.; Xu, J.; Fang, H.; Hong, H.; Shen, J.; Su, Z.; Meehan, J.; Li, X.; Yang, L.; Li, H.; Łabaj, P. P.; Kreil, D. P.; Megherbi, D.; Gaj, S.; Caiment, F.; van Delft, J.; Kleinjans, J.; Scherer, A.; Devanarayan, V.; Wang, J.; Yang, Y.; Qian, H. R.; Lancashire, L. J.; Bessarabova, M.; Nikolsky, Y.; Furlanello, C.; Chierici, M.; Jurman, G.; Filosi, M.; Visintainer, R.; Zhang, K. K.; Li, J.; Hsieh, J. H.; Svoboda, D. L.; Fuscoe, J. C.; Deng, Y.; Shi, L.; Paules, R. S.; Auerbach, S. S.; Tong, W.; Albanese, Davide; Riccadonna, Samantha
Contributors: Wang, C.; Gong, B.; Bushel, P.R.; Thierry Mieg, J.; Thierry Mieg, D.; Xu, J.; Fang, H.; Hong, H.; Shen, J.; Su, Z.; Meehan, J.; Li, X.; Yang, L.; Li, H.; Łabaj, P.P.; Kreil, D.P.; Megherbi, D.; Gaj, S.; Caiment, F.; van Delft, J.; Kleinjans, J.; Scherer, A.; Devanarayan, V.; Wang, J.; Yang, Y.; Qian, H.R.; Lancashire, L.J.; Bessarabova, M.; Nikolsky, Y.; Furlanello, C.; Chierici, M.; Albanese, D.; Jurman, G.; Riccadonna, S.; Filosi, M.; Visintainer, R.; Zhang, K.K.; Li, J.; Hsieh, J.H.; Svoboda, D.L.; Fuscoe, J.C.; Deng, Y.; Shi, L.; Paules, R.S.; Auerbach, S.S.; Tong, W.
Publisher Information: Nature Publishing Group
Publication Year: 2014
Collection: Fondazione Edmund Mach: IRIS-OpenPub
Subject Terms: Settore BIO/18 - GENETICA
Description: RNA-seq facilitates unbiased genome-wide gene-expression profiling. However, its concordance with the well-established microarray platform must be rigorously assessed for confident uses in clinical and regulatory application. Here we use a comprehensive study design to generate Illumina RNA-seq and Affymetrix microarray data from the same set of liver samples of rats under varying degrees of perturbation by 27 chemicals representing multiple modes of action (MOA). The cross-platform concordance in terms of differentially expressed genes (DEGs) or enriched pathways is highly correlated with treatment effect size, gene-expression abundance and the biological complexity of the MOA. RNA-seq outperforms microarray (90% versus 76%) in DEG verification by quantitative PCR and the main gain is its improved accuracy for low expressed genes. Nonetheless, predictive classifiers derived from both platforms performed similarly. Therefore, the endpoint studied and its biological complexity, transcript abundance, and intended application are important factors in transcriptomic research and for decision-making
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000342600300032; volume:32; issue:9; firstpage:926; lastpage:932; journal:NATURE BIOTECHNOLOGY; https://hdl.handle.net/10449/24750
DOI: 10.1038/nbt.3001
Availability: https://hdl.handle.net/10449/24750; https://doi.org/10.1038/nbt.3001
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.D4145D0B
Database: BASE