Welcome to LnCeVar
LnCeVar is a comprehensive database that aims to infer genomic variations that disturb lncRNA-associated ceRNA regulation.
- Manual curation of variation-ceRNA events from the published literature.
- Manual curation of more than 2,000 experimentally supported circulating, drug-resistant and prognosis-related lncRNA biomarkers.
- Identification of somatic mutation-ceRNA events occurring in 33 cancers from TCGA and mutation profiles of over 1,000 cell lines from Cosmic.
- Identification of CNV-ceRNA events in thousands of patients from TCGA.
- Identification of SNP-ceRNA events from the 1000-Genome project. More...
Services
SNPs-1000Genomes
CNVs-TCGA
Mutations-TCGA
Mutations-Cosmic
Manual curation
Search Genome
Search
Search the genomic variations including somatic mutations, SNPs, CNVs which disturbing ceRNA regulations.
Browse
Browse the LnCeVar database by genomic variations, diseases, lncRNAs, miRNAs, locations and etc.
LnCeVar-Survival
A tool to perform COX regression analysis and survival curves of variation-ceRNA events.
LnCeVar-Network
A tool to identify and perform visualization of dysregulated variation-ceRNA network.
Our works
