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- Nikos Perdikopanis
- Hellenic Pasteur Institute, Athens 11521, Greece
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- Georgios K Georgakilas
- Central European Institute of Technology, Masaryk University, Kamenice 735/5, 62500 Brno, Czech Republic
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- Dimitris Grigoriadis
- Hellenic Pasteur Institute, Athens 11521, Greece
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- Vasilis Pierros
- Hellenic Pasteur Institute, Athens 11521, Greece
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- Ioannis Kavakiotis
- Department of Computer Science and Biomedical Informatics, University of Thessaly, Greece
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- Panagiotis Alexiou
- Central European Institute of Technology, Masaryk University, Kamenice 735/5, 62500 Brno, Czech Republic
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- Artemis Hatzigeorgiou
- Hellenic Pasteur Institute, Athens 11521, Greece
説明
<jats:title>Abstract</jats:title> <jats:p>Deregulation of microRNA (miRNA) expression plays a critical role in the transition from a physiological to a pathological state. The accurate miRNA promoter identification in multiple cell types is a fundamental endeavor towards understanding and characterizing the underlying mechanisms of both physiological as well as pathological conditions. DIANA-miRGen v4 (www.microrna.gr/mirgenv4) provides cell type specific miRNA transcription start sites (TSSs) for over 1500 miRNAs retrieved from the analysis of >1000 cap analysis of gene expression (CAGE) samples corresponding to 133 tissues, cell lines and primary cells available in FANTOM repository. MiRNA TSS locations were associated with transcription factor binding site (TFBSs) annotation, for >280 TFs, derived from analyzing the majority of ENCODE ChIP-Seq datasets. For the first time, clusters of cell types having common miRNA TSSs are characterized and provided through a user friendly interface with multiple layers of customization. DIANA-miRGen v4 significantly improves our understanding of miRNA biogenesis regulation at the transcriptional level by providing a unique integration of high-quality annotations for hundreds of cell specific miRNA promoters with experimentally derived TFBSs.</jats:p>
収録刊行物
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- Nucleic Acids Research
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Nucleic Acids Research 49 (D1), D151-D159, 2020-11-27
Oxford University Press (OUP)