Genomic VA,T,C,G RIATION disturbing ceRNA regulations

Get Started Help & FAQs
Cat 1
Cat 2
Cat 3

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

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-Fucntion

A tool to identify dysregulated fucntions of variation-ceRNA events.

LnCeVar-Hallmark

A tool to identify dysregulated cancer hallmarks of variation-ceRNA events.

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.

LnCeVar-Cluster

A tool to provide cluster profiles between different lncRNAs and ceRNAs.

LnCeVar-BodyMap

A global view of LnCeVar statistics based on the human body map.

Our works