Identification of methylated transcripts using the TRIBE approach

m6A is the most abundant internal modification on mRNA. Recent improvements of high-throughput sequencing techniques enables its detection at the transcriptome level, even at the nucleotide resolution. However most current techniques require large amounts of starting material to detect the modificat...

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Bibliographic Details
Main Authors: Worpenberg, Lina (Author) , Jakobi, Tobias (Author) , Dieterich, Christoph (Author)
Format: Chapter/Article
Language:English
Published: 2019
In: Epitranscriptomics
Year: 2018, Pages: 89-106
DOI:10.1007/978-1-4939-8808-2_7
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/978-1-4939-8808-2_7
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Author Notes:Lina Worpenberg, Tobias Jakobi, Christoph Dieterich, Jean-Yves Roignant
Description
Summary:m6A is the most abundant internal modification on mRNA. Recent improvements of high-throughput sequencing techniques enables its detection at the transcriptome level, even at the nucleotide resolution. However most current techniques require large amounts of starting material to detect the modification. Here, we describe a complementary technique of standard meRIP-seq/miCLIP-seq approaches to identify methylated RNA using a low amount of material. We believe this approach can be applied in vivo to identify methylated targets in specific tissues or subpopulations of cells.
Item Description:First online: 12 December 2018
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Physical Description:Online Resource
ISBN:9781493988082
DOI:10.1007/978-1-4939-8808-2_7