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10.1007/978-1-4939-4035-6_9

http://scihub22266oqcxt.onion/10.1007/978-1-4939-4035-6_9
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C5880289!5880289!27662873
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suck abstract from ncbi

pmid27662873      Methods+Mol+Biol 2017 ; 1468 (ä): 111-20
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  • Global Run-On sequencing (GRO-seq) #MMPMID27662873
  • Gardini A
  • Methods Mol Biol 2017[]; 1468 (ä): 111-20 PMID27662873show ga
  • Transcription occurring at gene loci results in accumulation of mature RNA molecules (i.e. mRNAs) that can be easily assayed by RT-PCR or RNA-sequencing. However, the steady-state level of RNA does not accurately mirror transcriptional activity per se. In fact, RNA stability plays a major role in determining the relative abundance of any given RNA molecule. Here, I describe a protocol of Nuclear Run-On assay coupled to deep sequencing to assess real-time transcription from engaged RNA polymerase. Mapping nascent transcripts at the genome-wide scale provides a reliable measure of transcriptional activity in mammalian cells and delivers a high-resolution map of coding and noncoding transcripts that is especially useful for annotation and quantification of short-lived RNA molecules.
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