High throughput detection of nascent RNA is critical for studies of transcription and much more challenging than that of mRNA. Recently, several massively parallel nascent RNA sequencing methods were
*p-value for mean total RNA concentration between methods. Total RNA concentration and purity for Trizol LS and Qiagen miRNeasy with RNA yeast carrier.
This project contains RNA-seq data from 8 experimental groups in triplicate. This project attempted to elucidate the biological function of SrMasc and Sarmad.
To exploit the therapeutic mechanism of our proposed alkaline phosphatase-controllable and red light-activated RNA modification approach at the genetic level, we established an RNA-modified group (f-R