• 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

EuSplice:用于分析真核基因剪接信号和可变剪接的统一资源。

EuSplice: a unified resource for the analysis of splice signals and alternative splicing in eukaryotic genes.

作者信息

Bhasi Ashwini, Pandey Ram Vinay, Utharasamy Suriya Prabha, Senapathy Periannan

机构信息

Department of Human Genetics, Genome Technologies, Inc., 8000 Excelsior Drive, Madison, WI 53717, USA.

出版信息

Bioinformatics. 2007 Jul 15;23(14):1815-23. doi: 10.1093/bioinformatics/btm084. Epub 2007 Mar 7.

DOI:10.1093/bioinformatics/btm084
PMID:17344236
Abstract

MOTIVATION

Despite increased availability of genome annotation data, a comprehensive resource for in-depth analysis of splice signal distributions and alternative splicing (AS) patterns in eukaryote genomes is still lacking. To meet this need, we have developed EuSplice--a unique splice-centric database which provides reliable splice signal and AS information for 23 eukaryotes.

RESULTS

The EuSplice database contains 95,822 AS events and 2.1 million splice signals associated with over 270,000 protein-coding genes. The intuitive, user-friendly EuSplice web interface has powerful data mining and graphics capabilities for inter-genomic comparative analysis of splice signals, putative cryptic splice sites and AS events. Moreover, the seamless integration of splicing data to extensive gene-specific annotations, such as homolog annotations, functional information, mutations and sequence details makes EuSplice a powerful one-stop information resource for investigating the molecular mechanisms of complex splicing events, disease associations and the evolution of splicing in eukaryotes.

AVAILABILITY

http://66.170.16.154/EuSplice.

SUPPLEMENTARY INFORMATION

Supplementary tables and figures at Bioinfo online.

摘要

动机

尽管基因组注释数据的可用性有所提高,但仍缺乏一个用于深入分析真核生物基因组中剪接信号分布和可变剪接(AS)模式的综合资源。为满足这一需求,我们开发了EuSplice——一个独特的以剪接为中心的数据库,它为23种真核生物提供了可靠的剪接信号和AS信息。

结果

EuSplice数据库包含95,822个AS事件以及与超过270,000个蛋白质编码基因相关的210万个剪接信号。直观、用户友好的EuSplice网络界面具有强大的数据挖掘和图形功能,可用于剪接信号、潜在隐蔽剪接位点和AS事件的基因组间比较分析。此外,剪接数据与广泛的基因特异性注释(如同源物注释、功能信息、突变和序列细节)的无缝整合,使EuSplice成为一个强大的一站式信息资源,用于研究复杂剪接事件的分子机制、疾病关联以及真核生物中剪接的进化。

可用性

http://66.170.16.154/EuSplice。

补充信息

Bioinfo在线的补充表格和图。

相似文献

1
EuSplice: a unified resource for the analysis of splice signals and alternative splicing in eukaryotic genes.EuSplice:用于分析真核基因剪接信号和可变剪接的统一资源。
Bioinformatics. 2007 Jul 15;23(14):1815-23. doi: 10.1093/bioinformatics/btm084. Epub 2007 Mar 7.
2
AspAlt: A tool for inter-database, inter-genomic and user-specific comparative analysis of alternative transcription and alternative splicing in 46 eukaryotes.AspAlt:一种用于46种真核生物中可变转录和可变剪接的跨数据库、跨基因组及用户特定比较分析的工具。
Genomics. 2009 Jul;94(1):48-54. doi: 10.1016/j.ygeno.2009.02.006. Epub 2009 Mar 11.
3
ASTALAVISTA: dynamic and flexible analysis of alternative splicing events in custom gene datasets.ASTALAVISTA:对定制基因数据集中的可变剪接事件进行动态灵活分析。
Nucleic Acids Res. 2007 Jul;35(Web Server issue):W297-9. doi: 10.1093/nar/gkm311. Epub 2007 May 7.
4
ASPIC: a web resource for alternative splicing prediction and transcript isoforms characterization.ASPIC:一个用于可变剪接预测和转录本异构体表征的网络资源。
Nucleic Acids Res. 2006 Jul 1;34(Web Server issue):W440-3. doi: 10.1093/nar/gkl324.
5
ANOSVA: a statistical method for detecting splice variation from expression data.ANOSVA:一种从表达数据中检测剪接变异的统计方法。
Bioinformatics. 2005 Jun;21 Suppl 1:i107-15. doi: 10.1093/bioinformatics/bti1010.
6
ECgene: genome annotation for alternative splicing.ECgene:可变剪接的基因组注释
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D75-9. doi: 10.1093/nar/gki118.
7
Automated splicing mutation analysis by information theory.基于信息论的自动剪接突变分析
Hum Mutat. 2005 Apr;25(4):334-42. doi: 10.1002/humu.20151.
8
Exon Array Analyzer: a web interface for Affymetrix exon array analysis.外显子数组分析器:一个用于 Affymetrix 外显子数组分析的网络界面。
Bioinformatics. 2009 Dec 15;25(24):3323-4. doi: 10.1093/bioinformatics/btp577. Epub 2009 Oct 6.
9
Detection, annotation and visualization of alternative splicing from RNA-Seq data with SplicingViewer.利用 SplicingViewer 从 RNA-Seq 数据中检测、注释和可视化可变剪接。
Genomics. 2012 Mar;99(3):178-82. doi: 10.1016/j.ygeno.2011.12.003. Epub 2011 Dec 28.
10
PPD - Proteome Profile Database.PPD - 蛋白质组图谱数据库。
In Silico Biol. 2004;4(2):219-23.

引用本文的文献

1
PlantSPEAD: a web resource towards comparatively analysing stress-responsive expression of splicing-related proteins in plant.植物剪接相关蛋白应激反应表达的比较分析网络资源:PlantSPEAD
Plant Biotechnol J. 2021 Feb;19(2):227-229. doi: 10.1111/pbi.13486. Epub 2020 Oct 25.
2
Architecture and Distribution of Introns in Core Genes of Four Species.四种物种核心基因中内含子的结构与分布
G3 (Bethesda). 2017 Nov 6;7(11):3809-3820. doi: 10.1534/g3.117.300344.
3
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.
来自德国多中心队列的335例斯塔加特病患者ABCA4基因的突变谱——特定内含子深层变异和常见单核苷酸多态性的影响
Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):394-403. doi: 10.1167/iovs.16-19936.
4
Genome sequence of the plant growth promoting endophytic yeast Rhodotorula graminis WP1.促进植物生长的内生酵母禾本科红酵母WP1的基因组序列
Front Microbiol. 2015 Sep 17;6:978. doi: 10.3389/fmicb.2015.00978. eCollection 2015.
5
DBATE: database of alternative transcripts expression.DBATE:替代转录本表达数据库。
Database (Oxford). 2013 Jul 9;2013:bat050. doi: 10.1093/database/bat050. Print 2013.
6
Alternative splicing for diseases, cancers, drugs, and databases.疾病、癌症、药物及数据库的可变剪接
ScientificWorldJournal. 2013 May 22;2013:703568. doi: 10.1155/2013/703568. Print 2013.
7
A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis.先天性鱼鳞病新型鼠模型中 Fatp4/Scl27a4 剪接位点的自发突变。
PLoS One. 2012;7(11):e50634. doi: 10.1371/journal.pone.0050634. Epub 2012 Nov 30.
8
Function of alternative splicing.可变剪接的功能。
Gene. 2013 Feb 1;514(1):1-30. doi: 10.1016/j.gene.2012.07.083. Epub 2012 Aug 15.
9
SpliceDisease database: linking RNA splicing and disease.SpliceDisease 数据库:连接 RNA 剪接与疾病。
Nucleic Acids Res. 2012 Jan;40(Database issue):D1055-9. doi: 10.1093/nar/gkr1171. Epub 2011 Dec 1.
10
Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome.由 hERG 剪接位点突变 2592+1G>A 引起的多种剪接缺陷与长 QT 综合征相关。
Am J Physiol Heart Circ Physiol. 2011 Jan;300(1):H312-8. doi: 10.1152/ajpheart.00818.2010. Epub 2010 Nov 5.