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GenomeRNAi:一个基于细胞和体内 RNAi 表型的数据库,2013 年更新。

GenomeRNAi: a database for cell-based and in vivo RNAi phenotypes, 2013 update.

机构信息

Division Signaling and Functional Genomics, German Cancer Research Center (DKFZ), D-69120 Heidelberg, Germany.

出版信息

Nucleic Acids Res. 2013 Jan;41(Database issue):D1021-6. doi: 10.1093/nar/gks1170. Epub 2012 Nov 27.

DOI:10.1093/nar/gks1170
PMID:23193271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3531141/
Abstract

RNA interference (RNAi) represents a powerful method to systematically study loss-of-function phenotypes on a large scale with a wide variety of biological assays, constituting a rich source for the assignment of gene function. The GenomeRNAi database (http://www.genomernai.org) makes available RNAi phenotype data extracted from the literature for human and Drosophila. It also provides RNAi reagent information, along with an assessment as to their efficiency and specificity. This manuscript describes an update of the database previously featured in the NAR Database Issue. The new version has undergone a complete re-design of the user interface, providing an intuitive, flexible framework for additional functionalities. Screen information and gene-reagent-phenotype associations are now available for download. The integration with other resources has been improved by allowing in-links via GenomeRNAi screen IDs, or external gene or reagent identifiers. A distributed annotation system (DAS) server enables the visualization of the phenotypes and reagents in the context of a genome browser. We have added a page listing 'frequent hitters', i.e. genes that show a phenotype in many screens, which might guide on-going RNAi studies. Structured annotation guidelines have been established to facilitate consistent curation, and a submission template for direct submission by data producers is available for download.

摘要

RNA 干扰 (RNAi) 代表了一种强大的方法,可以在广泛的生物学测定中系统地研究大规模的功能丧失表型,为基因功能的分配提供了丰富的来源。GenomeRNAi 数据库 (http://www.genomernai.org) 提供了从文献中提取的人类和果蝇的 RNAi 表型数据。它还提供了 RNAi 试剂信息,并评估了它们的效率和特异性。本文描述了对以前在 NAR 数据库特刊中介绍的数据库的更新。新版本对用户界面进行了全面重新设计,为附加功能提供了直观、灵活的框架。屏幕信息和基因-试剂-表型关联现在可下载。通过允许通过 GenomeRNAi 屏幕 ID 或外部基因或试剂标识符进行内联,与其他资源的集成得到了改善。分布式注释系统 (DAS) 服务器可用于在基因组浏览器中可视化表型和试剂。我们添加了一个列出“常见命中者”的页面,即许多屏幕中出现表型的基因,这可能指导正在进行的 RNAi 研究。已经建立了结构化注释指南,以促进一致的策展,并提供了直接由数据生成者提交的提交模板供下载。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b7/3531141/de003acf8264/gks1170f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b7/3531141/de003acf8264/gks1170f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3b7/3531141/de003acf8264/gks1170f1p.jpg

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