ESFinder – Identification of Exon Skipping Events from High-Throughput RNA Sequencing Data

The emergence of next-generation high-throughput RNA sequencing (RNA-Seq) provides tremendous opportunities for researchers to analyze alternative splicing on a genome-wide scale. However, accurate identification of alternative splicing events from RNA-Seq data has remained an unresolved challenge in next-generation sequencing (NGS) studies. Identifying exon skipping (ES) events is an essential part in genome-wide alternative splicing event identification.

Researchers from the Harbin Institute of Technology have developed a novel method ESFinder, a random forest classifier to identify ES events from RNA-Seq data. ESFinder conducts thorough studies on predicting features and figures out proper features according to their relevance for ES event identification. Experimental results on real human skeletal muscle and brain RNA-Seq data show that ESFinder could effectively predict ES events with high predictive accuracy.


Availability – The codes of ESFinder are available at

Bai Y, Ji S, Jiang Q, Wang Y. (2015) Identification Exon Skipping Events From High-Throughput RNA Sequencing Data. IEEE Trans Nanobioscience [Epub ahead of print]. [abstract]

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