2015
DOI: 10.1093/nar/gkv1254
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DIANA-miRGen v3.0: accurate characterization of microRNA promoters and their regulators

Abstract: microRNAs (miRNAs) are small non-coding RNAs that actively fine-tune gene expression. The accurate characterization of the mechanisms underlying miRNA transcription regulation will further expand our knowledge regarding their implication in homeostatic and pathobiological networks. Aim of DIANA-miRGen v3.0 (http://www.microrna.gr/mirgen) is to provide for the first time accurate cell-line-specific miRNA gene transcription start sites (TSSs), coupled with genome-wide maps of transcription factor (TF) binding si… Show more

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Cited by 55 publications
(50 citation statements)
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“…Manual curation furthermore identified the promoter for an additional 196, mostly intergenic, pre-miRNAs, thereby generating the—to our knowledge—largest miRNA promoter collection to date (Table S17, Figure S20a). Across the human robust set, an associated ENCODE RAMPAGE (RNA Annotation and Mapping of Promoters for the Analysis of Gene Expression 32 ) 5′ end was found within 300 base pairs of more than 75% of the FANTOM5 curated promoters both for intergenic and intronic miRNAs, outperforming the miRGen 33 , Chang et al 14 , miRStart 34 , and TSmiR 35 collections of miRNA promoter annotations (Figure S20b). The median distance between the FANTOM5 annotated miRNA promoter and the associated RAMPAGE 5′ end was 1 nucleotide, and was thereby closer than any of the existing miRNA promoter annotations (Figure S20c).…”
Section: Resultsmentioning
confidence: 99%
“…Manual curation furthermore identified the promoter for an additional 196, mostly intergenic, pre-miRNAs, thereby generating the—to our knowledge—largest miRNA promoter collection to date (Table S17, Figure S20a). Across the human robust set, an associated ENCODE RAMPAGE (RNA Annotation and Mapping of Promoters for the Analysis of Gene Expression 32 ) 5′ end was found within 300 base pairs of more than 75% of the FANTOM5 curated promoters both for intergenic and intronic miRNAs, outperforming the miRGen 33 , Chang et al 14 , miRStart 34 , and TSmiR 35 collections of miRNA promoter annotations (Figure S20b). The median distance between the FANTOM5 annotated miRNA promoter and the associated RAMPAGE 5′ end was 1 nucleotide, and was thereby closer than any of the existing miRNA promoter annotations (Figure S20c).…”
Section: Resultsmentioning
confidence: 99%
“…In order to identify the regulation mechanism of miRNAs in Homo sapiens and Mus musculus (Georgakilas et al 2015), the DIANA-miRGen v3.0 using accurate cellline-specific miRNA gene transcription start sites (TSSs) and genome-wide maps of transcription factor binding sites were combined. GeneNetworkBuilder facilitates identification of the complex coregulatory network including TFs, miRNAs and mRNAs by combining binding site identifying and gene expression technologies such as chip-seq, chip-chip, microarray, and RNA-Seq (Ou and Zhu 2016).…”
Section: Discussionmentioning
confidence: 99%
“…Colors are used to mark interactions also predicted by other algorithms ( 5 ). The MRE panel can be expanded for each interaction ( 6 ). This panel provides access to tools and metadata for the interacting miRNA and mRNA ( 7 ), as well as extensive information regarding the identifi ed binding sites ( 8 ).…”
Section: Selecting Candidate Mirnas For Downstream Studies From Ngs Dmentioning
confidence: 99%
“…Available utilities cover a very large scope of different needs and research scenarios, rendering DIANA website a one-stop-shop for miRNA analyses. The most commonly utilized databases and algorithms , include DIANA-microT-CDS [ 4 ], DIANA-TarBase v7.0 [ 3 ], DIANA-lncBase v2.0 [ 5 ], DIANAmiRGen v3.0 [ 6 ], DIANA-miRPath v3.0 [ 7 ], and DIANAmirExTra v2.0. A brief introduction to each tool is presented below:…”
Section: Introductionmentioning
confidence: 99%
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