NGS原理- small RNA检测方法-QsRNA-seq

image.png

Fig. 2
QsRNA-seq library preparation scheme. A general scheme for preparation of sRNA library for high-throughput sequencing. Low molecular weight (LMW) RNA fraction is ligated to 3′ adapter. Next, the 3′-ligated sRNA is separated first from longer RNA species (tRNA, mRNA, etc.) and then from the remaining free 3′ adapter. 3′-ligated sRNA is then ligated to 5′ adapter possessing UMI. In the next step, the 3′-5′-ligated sRNA is separated from free 5′ adapter and from 3′-5′ adapter dimer and subjected to reverse transcription and PCR amplification. All the separation steps of the protocol are performed by size selection using SPRI paramagnetic beads

原文链接:
https://genomebiology.biomedcentral.com/articles/10.1186/s13059-018-1495-0#MOESM2

你可能感兴趣的:(NGS原理- small RNA检测方法-QsRNA-seq)