State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing 210023, China.
State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing 210023, China; Chemistry and Biomedicine Innovation Center (ChemBIC), Nanjing University, Nanjing 210023, China.
J Mol Biol. 2023 Jul 15;435(14):168142. doi: 10.1016/j.jmb.2023.168142. Epub 2023 May 5.
Although nascent RNA profiling data are widely used in transcriptional regulation studies, the development and standardization of data processing pipeline lags far behind RNA-seq. We are filling this gap by establishing the nASAP web server (https://grobase.top/nasap/) to provide practical quality evaluation and comprehensive analysis of nascent RNA datasets. In nASAP, four customized analysis modules are provided, including i) quality assessment, which summarizes the sequencing statistics, mapping ratio, and evaluates RNA integrity and mRNA contamination; ii) quantification analysis for mRNAs, lncRNAs and eRNAs; iii) pausing analysis across the whole genome based on sequencing reads distribution; and iv) network analysis to better understand the gene regulatory mechanism by obtaining annotated enhancer-promoter interactomes. The nASAP is user-friendly and outperforms the existing pipeline for quality control of nascent RNA profiling data. We anticipate that nASAP, which eases both basic and advanced analysis of nascent RNA data, will be extremely useful in various fields.
尽管新生 RNA 分析数据在转录调控研究中得到了广泛应用,但数据处理管道的开发和标准化远远落后于 RNA-seq。我们通过建立 nASAP 网络服务器(https://grobase.top/nasap/)来填补这一空白,该服务器为新生 RNA 数据集提供实用的质量评估和全面的分析。在 nASAP 中,提供了四个定制的分析模块,包括:i)质量评估,总结测序统计信息、映射比率,并评估 RNA 完整性和 mRNA 污染;ii)mRNA、lncRNA 和 eRNA 的定量分析;iii)基于测序reads 分布的全基因组暂停分析;以及 iv)网络分析,通过获取注释的增强子-启动子互作组来更好地理解基因调控机制。nASAP 用户友好,在新生 RNA 分析数据的质量控制方面优于现有的管道。我们预计,nASAP 将极大地帮助各种领域对新生 RNA 数据进行基础和高级分析。