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URL: http://research.nhgri.nih.gov/skippy/index.shtml
Proper Citation: SKIPPY (RRID:SCR_005430)
Description: A Web-based tool that allows users to input a set of exonic variants to score them for a number of features (such as changes in splicing regulatory elements) that have been shown to be predictive of known genome variations that cause exon skipping or activation of ectopic splice sites. In this way, variants can be either prioritized for further splicing-based functional analysis or the results can be used as further genomic evidence in cases in which the causative variant is already known.
Abbreviations: SKIPPY
Synonyms: SKIPPY - A Tool for the Detection of Exonic Variants that Modulate Splicing
Resource Type: service resource, analysis service resource, production service resource, data analysis service
Defining Citation: PMID:20158892
Keywords: exonic variant, splicing, genome variation, coding variant
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