Splooce: A new portal for the analysis of human splicing variants

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Abstract

Understanding alternative splicing is crucial to elucidate the mechanisms behind several biological phenomena, including diseases. The huge amount of expressed sequences available nowadays represents an opportunity and a challenge to catalog and display alternative splicing events (ASEs). Although several groups have faced this challenge with relative success, we still lack a computational tool that uses a simple and straightforward method to retrieve, name and present ASEs. Here we present SPLOOCE, a portal for the analysis of human splicing variants. SPLOOCE uses a method based on regular expressions for retrieval of ASEs. We propose a simple syntax that is able to capture the complexity of ASEs. © 2012 Landes Bioscience.

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Kroll, J. E., Galante, P. A. F., Ohara, D. T., Navarro, F. C. P., Ohno-Machado, L., & De Souza, S. J. (2012). Splooce: A new portal for the analysis of human splicing variants. RNA Biology, 9(11), 1339–1343. https://doi.org/10.4161/rna.22182

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