LnCeVar: a comprehensive database of genomic variations that disturb ceRNA network regulation
LnCeVar: a comprehensive database of genomic variations that disturb ceRNA network regulation
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LnCeVar:干扰 ceRNA 网络调控的基因组变异综合数据库
DOI:
10.1093/nar/gkz887
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发表时间:
2020-01-08
影响因子:
14.9
通讯作者:
Li, Xia
中科院分区:
文献类型:
--
作者:
Wang, Peng;Li, Xin;Li, Xia
LnCeVar (http://www.bio-bigdata.net/LnCeVar/) is a comprehensive database that aims to provide genomic variations that disturb lncRNA-associated competing endogenous RNA (ceRNA) network regulation curated from the published literature and high-throughput data sets. LnCeVar curated 119 501 variation-ceRNA events from thousands of samples and cell lines, including: (i) more than 2000 experimentally supported circulating, drug-resistant and prognosis-related lncRNA biomarkers; (ii) 11 418 somatic mutation-ceRNA events from TCGA and COSMIC; (iii) 112 674 CNV-ceRNA events from TCGA; (iv) 67 066 SNP-ceRNA events from the 1000 Genomes Project. LnCeVar provides a user-friendly searching and browsing interface. In addition, as an important supplement of the database, several flexible tools have been developed to aid retrieval and analysis of the data. The LnCeVar-BLAST interface is a convenient way for users to search ceRNAs by interesting sequences. LnCeVar-Function is a tool for performing functional enrichment analysis. LnCeVar-Hallmark identifies dysregulated cancer hallmarks of variation-ceRNA events. LnCeVar-Survival performs COX regression analyses and produces survival curves for variation-ceRNA events. LnCeVar-Network identifies and creates a visualization of dysregulated variation-ceRNA networks. Collectively, LnCeVar will serve as an important resource for in vestigatingthe functions and mechanisms of personalized genomic variations that disturb ceRNA network regulation in human diseases.