• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

RED:一款使用基于规则和统计过滤器来识别和可视化RNA编辑位点的Java - MySQL软件。

RED: A Java-MySQL Software for Identifying and Visualizing RNA Editing Sites Using Rule-Based and Statistical Filters.

作者信息

Sun Yongmei, Li Xing, Wu Di, Pan Qi, Ji Yuefeng, Ren Hong, Ding Keyue

机构信息

School of Information and Communication Engineering, Beijing University of Posts & Telecommunications, Beijing, P. R. China.

Key Laboratory of Molecular Biology for Infectious Diseases (Ministry of Education), Institute for Viral Hepatitis, Department of Infectious Diseases, The Second Affiliated Hospital, Chongqing Medical University, Chongqing, China.

出版信息

PLoS One. 2016 Mar 1;11(3):e0150465. doi: 10.1371/journal.pone.0150465. eCollection 2016.

DOI:10.1371/journal.pone.0150465
PMID:26930599
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4773184/
Abstract

RNA editing is one of the post- or co-transcriptional processes that can lead to amino acid substitutions in protein sequences, alternative pre-mRNA splicing, and changes in gene expression levels. Although several methods have been suggested to identify RNA editing sites, there remains challenges to be addressed in distinguishing true RNA editing sites from its counterparts on genome and technical artifacts. In addition, there lacks a software framework to identify and visualize potential RNA editing sites. Here, we presented a software - 'RED' (RNA Editing sites Detector) - for the identification of RNA editing sites by integrating multiple rule-based and statistical filters. The potential RNA editing sites can be visualized at the genome and the site levels by graphical user interface (GUI). To improve performance, we used MySQL database management system (DBMS) for high-throughput data storage and query. We demonstrated the validity and utility of RED by identifying the presence and absence of C→U RNA-editing sites experimentally validated, in comparison with REDItools, a command line tool to perform high-throughput investigation of RNA editing. In an analysis of a sample data-set with 28 experimentally validated C→U RNA editing sites, RED had sensitivity and specificity of 0.64 and 0.5. In comparison, REDItools had a better sensitivity (0.75) but similar specificity (0.5). RED is an easy-to-use, platform-independent Java-based software, and can be applied to RNA-seq data without or with DNA sequencing data. The package is freely available under the GPLv3 license at http://github.com/REDetector/RED or https://sourceforge.net/projects/redetector.

摘要

RNA编辑是一种转录后或共转录过程,可导致蛋白质序列中的氨基酸替换、前体mRNA可变剪接以及基因表达水平的变化。尽管已经提出了几种方法来识别RNA编辑位点,但在区分真正的RNA编辑位点与基因组上的对应位点和技术假象方面仍存在挑战。此外,缺乏一个用于识别和可视化潜在RNA编辑位点的软件框架。在这里,我们展示了一款名为“RED”(RNA编辑位点检测器)的软件,它通过整合多个基于规则和统计的过滤器来识别RNA编辑位点。潜在的RNA编辑位点可以通过图形用户界面(GUI)在基因组和位点水平上进行可视化。为了提高性能,我们使用MySQL数据库管理系统(DBMS)进行高通量数据存储和查询。与REDItools(一种用于进行RNA编辑高通量研究的命令行工具)相比,我们通过实验验证了C→U RNA编辑位点的存在与否,从而证明了RED的有效性和实用性。在对一个包含28个经实验验证的C→U RNA编辑位点的样本数据集进行分析时,RED的灵敏度和特异性分别为0.64和0.5。相比之下,REDItools具有更好的灵敏度(0.75)但特异性相似(0.5)。RED是一款易于使用、基于Java且与平台无关的软件,可应用于有无DNA测序数据的RNA-seq数据。该软件包可在GPLv3许可下免费获取,网址为http://github.com/REDetector/RED或https://sourceforge.net/projects/redetector 。

相似文献

1
RED: A Java-MySQL Software for Identifying and Visualizing RNA Editing Sites Using Rule-Based and Statistical Filters.RED:一款使用基于规则和统计过滤器来识别和可视化RNA编辑位点的Java - MySQL软件。
PLoS One. 2016 Mar 1;11(3):e0150465. doi: 10.1371/journal.pone.0150465. eCollection 2016.
2
Using REDItools to Detect RNA Editing Events in NGS Datasets.使用REDItools在NGS数据集中检测RNA编辑事件。
Curr Protoc Bioinformatics. 2015 Mar 9;49:12.12.1-12.12.15. doi: 10.1002/0471250953.bi1212s49.
3
RES-Scanner: a software package for genome-wide identification of RNA-editing sites.RES-Scanner:一个用于全基因组识别 RNA 编辑位点的软件包。
Gigascience. 2016 Aug 18;5(1):37. doi: 10.1186/s13742-016-0143-4.
4
REDItools: high-throughput RNA editing detection made easy.REDItools:轻松实现高通量 RNA 编辑检测。
Bioinformatics. 2013 Jul 15;29(14):1813-4. doi: 10.1093/bioinformatics/btt287. Epub 2013 Jun 5.
5
Investigating RNA editing in deep transcriptome datasets with REDItools and REDIportal.使用 REDItools 和 REDIportal 研究深度转录组数据集的 RNA 编辑。
Nat Protoc. 2020 Mar;15(3):1098-1131. doi: 10.1038/s41596-019-0279-7. Epub 2020 Jan 29.
6
Read-Split-Run: an improved bioinformatics pipeline for identification of genome-wide non-canonical spliced regions using RNA-Seq data.读取-分割-运行:一种利用RNA测序数据识别全基因组非经典剪接区域的改进型生物信息学流程。
BMC Genomics. 2016 Aug 22;17 Suppl 7(Suppl 7):503. doi: 10.1186/s12864-016-2896-7.
7
REDO: RNA Editing Detection in Plant Organelles Based on Variant Calling Results.REDO:基于变异检测结果的植物细胞器RNA编辑检测
J Comput Biol. 2018 May;25(5):509-516. doi: 10.1089/cmb.2017.0214. Epub 2018 Apr 11.
8
HPC-REDItools: a novel HPC-aware tool for improved large scale RNA-editing analysis.HPC-REDItools:一种新型的 HPC 感知工具,可提高大规模 RNA 编辑分析的效率。
BMC Bioinformatics. 2020 Aug 21;21(Suppl 10):353. doi: 10.1186/s12859-020-03562-x.
9
ISVASE: identification of sequence variant associated with splicing event using RNA-seq data.
BMC Bioinformatics. 2017 Jun 28;18(1):320. doi: 10.1186/s12859-017-1732-7.
10
Analysis of RNA Editing Sites from RNA-Seq Data Using GIREMI.使用GIREMI从RNA测序数据中分析RNA编辑位点
Methods Mol Biol. 2018;1751:101-108. doi: 10.1007/978-1-4939-7710-9_7.

引用本文的文献

1
RNA Editing in Chloroplast: Advancements and Opportunities.叶绿体中的RNA编辑:进展与机遇
Curr Issues Mol Biol. 2022 Nov 12;44(11):5593-5604. doi: 10.3390/cimb44110379.
2
A-to-I RNA Editing in Cancer: From Evaluating the Editing Level to Exploring the Editing Effects.癌症中的A到I RNA编辑:从评估编辑水平到探索编辑效应
Front Oncol. 2021 Feb 11;10:632187. doi: 10.3389/fonc.2020.632187. eCollection 2020.
3
Long Non-coding RNAs in Endothelial Biology.内皮生物学中的长链非编码RNA

本文引用的文献

1
Leveraging a Multi-Omics Strategy for Prioritizing Personalized Candidate Mutation-Driver Genes: A Proof-of-Concept Study.利用多组学策略对个性化候选突变驱动基因进行优先级排序:一项概念验证研究。
Sci Rep. 2015 Dec 3;5:17564. doi: 10.1038/srep17564.
2
A Comparison of Variant Calling Pipelines Using Genome in a Bottle as a Reference.使用“瓶中基因组”作为参考的变异检测流程比较
Biomed Res Int. 2015;2015:456479. doi: 10.1155/2015/456479. Epub 2015 Oct 11.
3
RCARE: RNA Sequence Comparison and Annotation for RNA Editing.RCARE:用于RNA编辑的RNA序列比较与注释
Front Physiol. 2018 May 14;9:522. doi: 10.3389/fphys.2018.00522. eCollection 2018.
4
An Evolutionary Landscape of A-to-I RNA Editome across Metazoan Species.动物物种中 A-to-I RNA 编辑组的进化景观。
Genome Biol Evol. 2018 Feb 1;10(2):521-537. doi: 10.1093/gbe/evx277.
5
SPRINT: an SNP-free toolkit for identifying RNA editing sites.SPRINT:一个无 SNP 的 RNA 编辑位点识别工具包。
Bioinformatics. 2017 Nov 15;33(22):3538-3548. doi: 10.1093/bioinformatics/btx473.
BMC Med Genomics. 2015;8 Suppl 2(Suppl 2):S8. doi: 10.1186/1755-8794-8-S2-S8. Epub 2015 May 29.
4
APOBEC3A cytidine deaminase induces RNA editing in monocytes and macrophages.载脂蛋白B mRNA编辑酶催化多肽3A胞苷脱氨酶在单核细胞和巨噬细胞中诱导RNA编辑。
Nat Commun. 2015 Apr 21;6:6881. doi: 10.1038/ncomms7881.
5
Genome sequence-independent identification of RNA editing sites.不依赖基因组序列的RNA编辑位点鉴定
Nat Methods. 2015 Apr;12(4):347-50. doi: 10.1038/nmeth.3314. Epub 2015 Mar 2.
6
Adenosine-to-inosine RNA editing and human disease.腺苷到肌苷的RNA编辑与人类疾病
Genome Med. 2013 Nov 29;5(11):105. doi: 10.1186/gm508. eCollection 2013.
7
RADAR: a rigorously annotated database of A-to-I RNA editing.RADAR:一个经过严格注释的 A 到 I RNA 编辑数据库。
Nucleic Acids Res. 2014 Jan;42(Database issue):D109-13. doi: 10.1093/nar/gkt996. Epub 2013 Oct 25.
8
Reliable identification of genomic variants from RNA-seq data.从 RNA-seq 数据中可靠地识别基因组变异。
Am J Hum Genet. 2013 Oct 3;93(4):641-51. doi: 10.1016/j.ajhg.2013.08.008. Epub 2013 Sep 26.
9
VIRGO: visualization of A-to-I RNA editing sites in genomic sequences.VIRGO:基因组序列中 A 到 I RNA 编辑位点的可视化。
BMC Bioinformatics. 2013;14 Suppl 7(Suppl 7):S5. doi: 10.1186/1471-2105-14-S7-S5. Epub 2013 Apr 22.
10
REDItools: high-throughput RNA editing detection made easy.REDItools:轻松实现高通量 RNA 编辑检测。
Bioinformatics. 2013 Jul 15;29(14):1813-4. doi: 10.1093/bioinformatics/btt287. Epub 2013 Jun 5.