4.4 Article

sgDI-tector: defective interfering viral genome bioinformatics for detection of coronavirus subgenomic RNAs

期刊

RNA
卷 28, 期 3, 页码 277-289

出版社

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1261/rna.078969.121

关键词

subgenomic RNA; SARS-CoV-2; defective viral genomes; user-friendly bioinformatics

资金

  1. National Reference Center (CNR) for Respiratory Viruses at the Institut Pasteur
  2. ANR (Agence Nationale de la Recherche)
  3. FRM (Fondation de la Recherche Medicale)
  4. ANR [ANR-LBX-62 IBEID CoV-2SENSING/COVID 19]
  5. France Genomique [ANR10-INBS-09-09]

向作者/读者索取更多资源

It is crucial to study the production of sgRNA in the vast amount of NGS data of SARS-CoV-2, and a user-friendly bioinformatic tool called sgDI-tector is introduced to identify and quantify these sgRNAs. Researchers successfully detected the nested set of sgRNAs in SARS-CoV-2 using this tool, and compared their production level with other types of viral RNA products.
Coronavirus RNA-dependent RNA polymerases produce subgenomic RNAs (sgRNAs) that encode viral structural and accessory proteins. User-friendly bioinformatic tools to detect and quantify sgRNA production are urgently needed to study the growing number of next-generation sequencing (NGS) data of SARS-CoV-2. We introduced sgDI-tector to identify and quantify sgRNA in SARS-CoV-2 NGS data. sgDI-tector allowed detection of sgRNA without initial knowledge of the transcription-regulatory sequences. We produced NGS data and successfully detected the nested set of sgRNAs with the ranking M > ORF3a > N>ORF6 > ORF7a > ORF8 > S > E>ORF7b. We also compared the level of sgRNA production with other types of viral RNA products such as defective interfering viral genomes.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据