A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data

<p>Abstract</p> <p>Background</p> <p>Alternative splicing is an important gene regulation mechanism. It is estimated that about 74% of multi-exon human genes have alternative splicing. High throughput tandem (MS/MS) mass spectrometry provides valuable information for ra...

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Main Authors: Omenn Gilbert S, Wang Jun, Du Lin, Gao Feng, Hong Xu, Mo Fan, Lin Biaoyang
Format: Article
Language:English
Published: BMC 2008-12-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/9/537
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spelling doaj-5b69a9f8ac3546b2ad30ac220510ccbe2020-11-25T00:38:56ZengBMCBMC Bioinformatics1471-21052008-12-019153710.1186/1471-2105-9-537A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum dataOmenn Gilbert SWang JunDu LinGao FengHong XuMo FanLin Biaoyang<p>Abstract</p> <p>Background</p> <p>Alternative splicing is an important gene regulation mechanism. It is estimated that about 74% of multi-exon human genes have alternative splicing. High throughput tandem (MS/MS) mass spectrometry provides valuable information for rapidly identifying potentially novel alternatively-spliced protein products from experimental datasets. However, the ability to identify alternative splicing events through tandem mass spectrometry depends on the database against which the spectra are searched.</p> <p>Results</p> <p>We wrote scripts in perl, Bioperl, mysql and Ensembl API and built a theoretical exon-exon junction protein database to account for all possible combinations of exons for a gene while keeping the frame of translation (i.e., keeping only in-phase exon-exon combinations) from the Ensembl Core Database. Using our liver cancer MS/MS dataset, we identified a total of 488 non-redundant peptides that represent putative exon skipping events.</p> <p>Conclusion</p> <p>Our exon-exon junction database provides the scientific community with an efficient means to identify novel alternatively spliced (exon skipping) protein isoforms using mass spectrometry data. This database will be useful in annotating genome structures using rapidly accumulating proteomics data.</p> http://www.biomedcentral.com/1471-2105/9/537
collection DOAJ
language English
format Article
sources DOAJ
author Omenn Gilbert S
Wang Jun
Du Lin
Gao Feng
Hong Xu
Mo Fan
Lin Biaoyang
spellingShingle Omenn Gilbert S
Wang Jun
Du Lin
Gao Feng
Hong Xu
Mo Fan
Lin Biaoyang
A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data
BMC Bioinformatics
author_facet Omenn Gilbert S
Wang Jun
Du Lin
Gao Feng
Hong Xu
Mo Fan
Lin Biaoyang
author_sort Omenn Gilbert S
title A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data
title_short A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data
title_full A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data
title_fullStr A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data
title_full_unstemmed A compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data
title_sort compatible exon-exon junction database for the identification of exon skipping events using tandem mass spectrum data
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2008-12-01
description <p>Abstract</p> <p>Background</p> <p>Alternative splicing is an important gene regulation mechanism. It is estimated that about 74% of multi-exon human genes have alternative splicing. High throughput tandem (MS/MS) mass spectrometry provides valuable information for rapidly identifying potentially novel alternatively-spliced protein products from experimental datasets. However, the ability to identify alternative splicing events through tandem mass spectrometry depends on the database against which the spectra are searched.</p> <p>Results</p> <p>We wrote scripts in perl, Bioperl, mysql and Ensembl API and built a theoretical exon-exon junction protein database to account for all possible combinations of exons for a gene while keeping the frame of translation (i.e., keeping only in-phase exon-exon combinations) from the Ensembl Core Database. Using our liver cancer MS/MS dataset, we identified a total of 488 non-redundant peptides that represent putative exon skipping events.</p> <p>Conclusion</p> <p>Our exon-exon junction database provides the scientific community with an efficient means to identify novel alternatively spliced (exon skipping) protein isoforms using mass spectrometry data. This database will be useful in annotating genome structures using rapidly accumulating proteomics data.</p>
url http://www.biomedcentral.com/1471-2105/9/537
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