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奋进更新:一个用于多种物种基因优先级排序的网络资源。

ENDEAVOUR update: a web resource for gene prioritization in multiple species.

作者信息

Tranchevent Léon-Charles, Barriot Roland, Yu Shi, Van Vooren Steven, Van Loo Peter, Coessens Bert, De Moor Bart, Aerts Stein, Moreau Yves

机构信息

Department of Electrical Engineering ESAT-SCD, Katholieke Universiteit Leuven, Belgium.

出版信息

Nucleic Acids Res. 2008 Jul 1;36(Web Server issue):W377-84. doi: 10.1093/nar/gkn325. Epub 2008 May 28.

DOI:10.1093/nar/gkn325
PMID:18508807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2447805/
Abstract

Endeavour (http://www.esat.kuleuven.be/endeavourweb; this web site is free and open to all users and there is no login requirement) is a web resource for the prioritization of candidate genes. Using a training set of genes known to be involved in a biological process of interest, our approach consists of (i) inferring several models (based on various genomic data sources), (ii) applying each model to the candidate genes to rank those candidates against the profile of the known genes and (iii) merging the several rankings into a global ranking of the candidate genes. In the present article, we describe the latest developments of Endeavour. First, we provide a web-based user interface, besides our Java client, to make Endeavour more universally accessible. Second, we support multiple species: in addition to Homo sapiens, we now provide gene prioritization for three major model organisms: Mus musculus, Rattus norvegicus and Caenorhabditis elegans. Third, Endeavour makes use of additional data sources and is now including numerous databases: ontologies and annotations, protein-protein interactions, cis-regulatory information, gene expression data sets, sequence information and text-mining data. We tested the novel version of Endeavour on 32 recent disease gene associations from the literature. Additionally, we describe a number of recent independent studies that made use of Endeavour to prioritize candidate genes for obesity and Type II diabetes, cleft lip and cleft palate, and pulmonary fibrosis.

摘要

Endeavour(网址:http://www.esat.kuleuven.be/endeavourweb;该网站免费向所有用户开放,无需登录)是一个用于对候选基因进行优先级排序的网络资源。我们的方法是利用一组已知参与感兴趣的生物学过程的基因作为训练集,包括:(i)推断多个模型(基于各种基因组数据源);(ii)将每个模型应用于候选基因,根据已知基因的概况对这些候选基因进行排名;(iii)将多个排名合并为候选基因的全局排名。在本文中,我们描述了Endeavour的最新进展。首先,除了我们的Java客户端外,我们还提供了一个基于网络的用户界面,以使Endeavour更易于广泛使用。其次,我们支持多种物种:除了智人,我们现在还为三种主要模式生物提供基因优先级排序:小家鼠、褐家鼠和秀丽隐杆线虫。第三,Endeavour利用了更多的数据源,现在包括众多数据库:本体和注释、蛋白质-蛋白质相互作用、顺式调控信息、基因表达数据集、序列信息和文本挖掘数据。我们在文献中最近的32个疾病基因关联上测试了Endeavour的新版本。此外,我们还描述了一些最近的独立研究,这些研究利用Endeavour对肥胖症、II型糖尿病、唇腭裂和肺纤维化的候选基因进行优先级排序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/2447805/46780a27fbb7/gkn325f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/2447805/638ff184e910/gkn325f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/2447805/46780a27fbb7/gkn325f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/2447805/638ff184e910/gkn325f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5738/2447805/46780a27fbb7/gkn325f2.jpg

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2
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Nat Genet. 2008 Mar;40(3):281-3. doi: 10.1038/ng.89. Epub 2008 Feb 10.
3
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4
Biological Network Mining.生物网络挖掘。
Methods Mol Biol. 2021;2328:139-151. doi: 10.1007/978-1-0716-1534-8_8.
5
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Genes (Basel). 2019 Oct 23;10(11):836. doi: 10.3390/genes10110836.
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4
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