Features generated for computational splice-site prediction correspond to functional elements

<p>Abstract</p> <p>Background</p> <p>Accurate selection of splice sites during the splicing of precursors to messenger RNA requires both relatively well-characterized signals at the splice sites and auxiliary signals in the adjacent exons and introns. We previously desc...

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Main Authors: Wilbur W John, Getoor Lise, Dogan Rezarta, Mount Stephen M
Format: Article
Language:English
Published: BMC 2007-10-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/8/410
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spelling doaj-9903897ff56f400999519d150ad233c92020-11-24T21:22:36ZengBMCBMC Bioinformatics1471-21052007-10-018141010.1186/1471-2105-8-410Features generated for computational splice-site prediction correspond to functional elementsWilbur W JohnGetoor LiseDogan RezartaMount Stephen M<p>Abstract</p> <p>Background</p> <p>Accurate selection of splice sites during the splicing of precursors to messenger RNA requires both relatively well-characterized signals at the splice sites and auxiliary signals in the adjacent exons and introns. We previously described a feature generation algorithm (FGA) that is capable of achieving high classification accuracy on human 3' splice sites. In this paper, we extend the splice-site prediction to 5' splice sites and explore the generated features for biologically meaningful splicing signals.</p> <p>Results</p> <p>We present examples from the observed features that correspond to known signals, both core signals (including the branch site and pyrimidine tract) and auxiliary signals (including GGG triplets and exon splicing enhancers). We present evidence that features identified by FGA include splicing signals not found by other methods.</p> <p>Conclusion</p> <p>Our generated features capture known biological signals in the expected sequence interval flanking splice sites. The method can be easily applied to other species and to similar classification problems, such as tissue-specific regulatory elements, polyadenylation sites, promoters, etc.</p> http://www.biomedcentral.com/1471-2105/8/410
collection DOAJ
language English
format Article
sources DOAJ
author Wilbur W John
Getoor Lise
Dogan Rezarta
Mount Stephen M
spellingShingle Wilbur W John
Getoor Lise
Dogan Rezarta
Mount Stephen M
Features generated for computational splice-site prediction correspond to functional elements
BMC Bioinformatics
author_facet Wilbur W John
Getoor Lise
Dogan Rezarta
Mount Stephen M
author_sort Wilbur W John
title Features generated for computational splice-site prediction correspond to functional elements
title_short Features generated for computational splice-site prediction correspond to functional elements
title_full Features generated for computational splice-site prediction correspond to functional elements
title_fullStr Features generated for computational splice-site prediction correspond to functional elements
title_full_unstemmed Features generated for computational splice-site prediction correspond to functional elements
title_sort features generated for computational splice-site prediction correspond to functional elements
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2007-10-01
description <p>Abstract</p> <p>Background</p> <p>Accurate selection of splice sites during the splicing of precursors to messenger RNA requires both relatively well-characterized signals at the splice sites and auxiliary signals in the adjacent exons and introns. We previously described a feature generation algorithm (FGA) that is capable of achieving high classification accuracy on human 3' splice sites. In this paper, we extend the splice-site prediction to 5' splice sites and explore the generated features for biologically meaningful splicing signals.</p> <p>Results</p> <p>We present examples from the observed features that correspond to known signals, both core signals (including the branch site and pyrimidine tract) and auxiliary signals (including GGG triplets and exon splicing enhancers). We present evidence that features identified by FGA include splicing signals not found by other methods.</p> <p>Conclusion</p> <p>Our generated features capture known biological signals in the expected sequence interval flanking splice sites. The method can be easily applied to other species and to similar classification problems, such as tissue-specific regulatory elements, polyadenylation sites, promoters, etc.</p>
url http://www.biomedcentral.com/1471-2105/8/410
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AT doganrezarta featuresgeneratedforcomputationalsplicesitepredictioncorrespondtofunctionalelements
AT mountstephenm featuresgeneratedforcomputationalsplicesitepredictioncorrespondtofunctionalelements
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