Researchers from Harbin Medical University describe LincSNP 2.0, an updated database that is used specifically to store and annotate disease-associated single nucleotide polymorphisms (SNPs) in human long non-coding RNAs (lncRNAs) and their transcription factor binding sites (TFBSs).
In LincSNP 2.0, the researchers have updated the database with more data and several new features, including:
- expanding disease-associated SNPs in human lncRNAs;
- identifying disease-associated SNPs in lncRNA TFBSs;
- updating LD-SNPs from the 1000 Genomes Project; and
- collecting more experimentally supported SNP-lncRNA-disease associations.
Furthermore, the researchers developed three flexible online tools to retrieve and analyze the data. Linc-Mart is a convenient way for users to customize their own data. Linc-Browse is a tool for all data visualization. Linc-Score predicts the associations between lncRNA and disease. In addition, they provided users a newly designed, user-friendly interface to search and download all the data in LincSNP 2.0 and they also provided an interface to submit novel data into the database. LincSNP 2.0 is a continually updated database and will serve as an important resource for investigating the functions and mechanisms of lncRNAs in human diseases.
Architecture of LincSNP 2.0
Availability – LincSNP 2.0 is available at: http://bioinfo.hrbmu.edu.cn/LincSNP