News
Feb 21, 2022: ncRNAvar updated these days after a period of data collection. More than 200 new variants were inserted into the database..
Sep 10, 2019: The variant mapping application was developed to prioritize and identify disease phenotype related ncRNA variants. The variant analysis allows users to input a set of ncRNA variants with disease phenotype, and to interpret the disease phenotype related ncRNA variants.
Aug 20, 2019: The network visualization application was developed to illustrate the connections between the ncRNA variant-disease associations in a network.
Jul 28, 2019: The word-cloud visualization application was developed to depict a word-cloud diagram for the prioritized ncRNA variant-disease associations.
Jun 20, 2019: The association prioritization application was developed to prioritize the ncRNA variant-disease associations.
May 25, 2019: Variants were annotated with chromosome position, alleles frequencies in 1000Genomes and TOPMED by using the dbSNP database. Variants were annotated with functional impacts and SNP positions in genes by using the CADD and GWAVA tools.
Mar 10, 2019: The ncRNAVar version1.0 was released.
Jun 1, 2018: Startup of the ncRNAVar project.
