• 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

DAVID:一个用于基因列表功能富集分析和功能注释的网络服务器(2021 更新)。

DAVID: a web server for functional enrichment analysis and functional annotation of gene lists (2021 update).

机构信息

Laboratory of Human Retrovirology and Immunoinformatics, Applied and Developmental Research Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.

Clinical Services Program, Applied and Developmental Research Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD21702, USA.

出版信息

Nucleic Acids Res. 2022 Jul 5;50(W1):W216-W221. doi: 10.1093/nar/gkac194.

DOI:10.1093/nar/gkac194
PMID:35325185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9252805/
Abstract

DAVID is a popular bioinformatics resource system including a web server and web service for functional annotation and enrichment analyses of gene lists. It consists of a comprehensive knowledgebase and a set of functional analysis tools. Here, we report all updates made in 2021. The DAVID Gene system was rebuilt to gain coverage of more organisms, which increased the taxonomy coverage from 17 399 to 55 464. All existing annotation types have been updated, if available, based on the new DAVID Gene system. Compared with the last version, the number of gene-term records for most annotation types within the updated Knowledgebase have significantly increased. Moreover, we have incorporated new annotations in the Knowledgebase including small molecule-gene interactions from PubChem, drug-gene interactions from DrugBank, tissue expression information from the Human Protein Atlas, disease information from DisGeNET, and pathways from WikiPathways and PathBank. Eight of ten subgroups split from Uniprot Keyword annotation were assigned to specific types. Finally, we added a species parameter for uploading a list of gene symbols to minimize the ambiguity between species, which increases the efficiency of the list upload and eliminates confusion for users. These current updates have significantly expanded the Knowledgebase and enhanced the discovery power of DAVID.

摘要

DAVID 是一个受欢迎的生物信息学资源系统,包括一个用于基因列表的功能注释和富集分析的网络服务器和网络服务。它由一个综合知识库和一组功能分析工具组成。在这里,我们报告了 2021 年的所有更新。DAVID Gene 系统进行了重建,以覆盖更多的生物体,将分类学覆盖率从 17399 增加到 55464。所有现有的注释类型都已根据新的 DAVID Gene 系统进行了更新(如果可用)。与上一个版本相比,更新后的知识库中大多数注释类型的基因-术语记录数量都显著增加。此外,我们还在知识库中纳入了新的注释,包括来自 PubChem 的小分子-基因相互作用、来自 DrugBank 的药物-基因相互作用、来自 Human Protein Atlas 的组织表达信息、来自 DisGeNET 的疾病信息以及来自 WikiPathways 和 PathBank 的途径。从 Uniprot Keyword 注释中拆分的十个亚组中的八个被分配到特定的类型。最后,我们添加了一个物种参数,用于上传基因符号列表,以最大限度地减少物种之间的歧义,这提高了列表上传的效率,并消除了用户的困惑。这些当前的更新显著扩展了知识库,并增强了 DAVID 的发现能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/9252805/da807bbeb7dc/gkac194figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/9252805/da807bbeb7dc/gkac194figgra1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df17/9252805/da807bbeb7dc/gkac194figgra1.jpg

相似文献

1
DAVID: a web server for functional enrichment analysis and functional annotation of gene lists (2021 update).DAVID:一个用于基因列表功能富集分析和功能注释的网络服务器(2021 更新)。
Nucleic Acids Res. 2022 Jul 5;50(W1):W216-W221. doi: 10.1093/nar/gkac194.
2
DAVID Knowledgebase: a gene-centered database integrating heterogeneous gene annotation resources to facilitate high-throughput gene functional analysis.大卫知识库:一个以基因为中心的数据库,整合了异构基因注释资源,以促进高通量基因功能分析。
BMC Bioinformatics. 2007 Nov 2;8:426. doi: 10.1186/1471-2105-8-426.
3
DAVID Bioinformatics Resources: expanded annotation database and novel algorithms to better extract biology from large gene lists.DAVID生物信息学资源:扩展注释数据库和新颖算法,以便从大型基因列表中更好地提取生物学信息。
Nucleic Acids Res. 2007 Jul;35(Web Server issue):W169-75. doi: 10.1093/nar/gkm415. Epub 2007 Jun 18.
4
DAVID-WS: a stateful web service to facilitate gene/protein list analysis.DAVID-WS:一个有状态的 Web 服务,用于方便基因/蛋白质列表分析。
Bioinformatics. 2012 Jul 1;28(13):1805-6. doi: 10.1093/bioinformatics/bts251. Epub 2012 Apr 27.
5
DAVID Ortholog: an integrative tool to enhance functional analysis through orthologs.DAVID 直系同源基因:通过直系同源基因增强功能分析的综合工具。
Bioinformatics. 2024 Oct 1;40(10). doi: 10.1093/bioinformatics/btae615.
6
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.利用DAVID生物信息学资源对大型基因列表进行系统和综合分析。
Nat Protoc. 2009;4(1):44-57. doi: 10.1038/nprot.2008.211.
7
BACA: bubble chArt to compare annotations.BACA:用于比较注释的气泡图。
BMC Bioinformatics. 2015 Feb 5;16(1):37. doi: 10.1186/s12859-015-0477-4.
8
Algal Functional Annotation Tool: a web-based analysis suite to functionally interpret large gene lists using integrated annotation and expression data.藻种功能注释工具:一个基于网络的分析套件,可使用集成注释和表达数据来对大型基因列表进行功能解释。
BMC Bioinformatics. 2011 Jul 12;12:282. doi: 10.1186/1471-2105-12-282.
9
Lists2Networks: integrated analysis of gene/protein lists.Lists2Networks:基因/蛋白质列表的综合分析。
BMC Bioinformatics. 2010 Feb 12;11:87. doi: 10.1186/1471-2105-11-87.
10
UniProt: the Universal Protein Knowledgebase in 2025.通用蛋白质知识库(UniProt):2025年的情况
Nucleic Acids Res. 2025 Jan 6;53(D1):D609-D617. doi: 10.1093/nar/gkae1010.

引用本文的文献

1
Differential phagocytosis induces diverse macrophage activation states in malignant gliomas.差异性吞噬作用在恶性胶质瘤中诱导多种巨噬细胞激活状态。
J Immunother Cancer. 2025 Sep 5;13(9):e012211. doi: 10.1136/jitc-2025-012211.
2
Nucleotide Metabolism and Immune Genes Can Predict the Prognostic Risk of Hepatocellular Carcinoma and the Immune Microenvironment.核苷酸代谢与免疫基因可预测肝细胞癌的预后风险及免疫微环境
Biology (Basel). 2025 Aug 18;14(8):1079. doi: 10.3390/biology14081079.
3
Mapping cancer heterogeneity: a consensus network approach to subtypes and pathways.
绘制癌症异质性图谱:一种针对亚型和通路的共识网络方法。
Brief Bioinform. 2025 Aug 31;26(5). doi: 10.1093/bib/bbaf452.
4
Silvestrol inhibits nasopharyngeal carcinoma cells and synergizes with CX-5461: Insights from a proteomics study.西维司特罗抑制鼻咽癌细胞并与CX-5461协同作用:蛋白质组学研究的见解
Mol Clin Oncol. 2025 Aug 19;23(5):95. doi: 10.3892/mco.2025.2890. eCollection 2025 Nov.
5
Development of an in vitro method to assess the immunogenicity of biologics in the prevention of infectious diseases.开发一种体外方法以评估生物制品在预防传染病中的免疫原性。
Immunol Res. 2025 Sep 3;73(1):126. doi: 10.1007/s12026-025-09681-y.
6
DNA methylation insulates genic regions from CTCF loops near nuclear speckles.DNA甲基化使基因区域与核斑附近的CTCF环绝缘。
Elife. 2025 Sep 3;13:RP102930. doi: 10.7554/eLife.102930.
7
BACH1 recruits STAT3 to enhance leukemia inhibitory factor receptor activity and augments the self-renewal capacity of mouse embryonic stem cells.BACH1招募信号转导和转录激活因子3(STAT3)以增强白血病抑制因子受体活性,并增强小鼠胚胎干细胞的自我更新能力。
Stem Cell Res Ther. 2025 Sep 2;16(1):483. doi: 10.1186/s13287-025-04578-x.
8
Integrative multi-omic analysis reveals a PAX8-driven gene network linking tumor stemness to therapy response in ovarian cancer.整合多组学分析揭示了一个由PAX8驱动的基因网络,该网络将卵巢癌中的肿瘤干性与治疗反应联系起来。
NAR Genom Bioinform. 2025 Aug 27;7(3):lqaf113. doi: 10.1093/nargab/lqaf113. eCollection 2025 Sep.
9
A comparative study of capacitation-mediated changes in whole mouse sperm proteome.小鼠精子整体蛋白质组中获能介导变化的比较研究。
Anim Cells Syst (Seoul). 2025 Aug 28;29(1):556-569. doi: 10.1080/19768354.2025.2548936. eCollection 2025.
10
Identification of progression-related genes and construction of prognostic model for chronic kidney disease by machine learning.通过机器学习识别慢性肾脏病进展相关基因并构建预后模型
Front Cell Dev Biol. 2025 Aug 15;13:1627355. doi: 10.3389/fcell.2025.1627355. eCollection 2025.