4.8 Article

SomamiR 2.0: a database of cancer somatic mutations altering microRNA-ceRNA interactions

Journal

NUCLEIC ACIDS RESEARCH
Volume 44, Issue D1, Pages D1005-D1010

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkv1220

Keywords

-

Funding

  1. Ramalingaswami Re-entry fellowship, Department of Biotechnology, India [BT/RLF/Re-entry/09/2013]

Ask authors/readers for more resources

SomamiR 2.0 (http://compbio.uthsc.edu/SomamiR) is a database of cancer somaticmutations in microRNAs (miRNA) and their target sites that potentially alter the interactions between miRNAs and competing endogenous RNAs (ceRNA) including mRNAs, circular RNAs (circRNA) and long noncoding RNAs (lncRNA). Here, we describe the recent major updates to the SomamiR database. We expanded the scope of the database by including somatic mutations that impact the interactions between miRNAs and two classes of non-coding RNAs, circRNAs and lncRNAs. Recently, a large number of miRNA target sites have been discovered by newly emerged high-throughput technologies for mapping the miRNA interactome. We have mapped 388 247 somatic mutations to the experimentally identified miRNA target sites. The updated database also includes a list of somaticmutations in the miRNA seed regions, which contain the most important guiding information for miRNA target recognition. A recently developed webserver, miR2GO, was integrated with the database to provide a seamless pipeline for assessing functional impacts of somatic mutations in miRNA seed regions. Data and functions from multiple sources including biological pathways and genome-wide association studies were updated and integrated with SomamiR 2.0 to make it a better platform for functional analysis of somaticmutations altering miRNAc-RNA interactions.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available