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- Publisher Website: 10.1142/S0219720008003825
- Scopus: eid_2-s2.0-54049115762
- PMID: 18942164
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Article: Finding alternative splicing patterns with strong support from expressed sequences on individual exons/introns
Title | Finding alternative splicing patterns with strong support from expressed sequences on individual exons/introns |
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Authors | |
Keywords | Alternative splicing pattern ESTs Expressed sequences |
Issue Date | 2008 |
Publisher | Imperial College Press. The Journal's web site is located at http://www.worldscinet.com/jbcb/jbcb.shtml |
Citation | Journal Of Bioinformatics And Computational Biology, 2008, v. 6 n. 5, p. 1021-1033 How to Cite? |
Abstract | We consider the problem of predicting alternative splicing patterns from a set of expressed sequences (cDNAs and ESTs). Some of these expressed sequences may be errorous, thus forming incorrect exons/introns. These incorrect exons/introns may cause a lot of false positives. For example, we examined a popular alternative splicing database, ECgene, which predicts alternate splicing patterns from expressed sequences. The result shows that about 81.3%-81.6% (sensitivity) of known patterns are found, but the specificity can be as low as 5.9%. Based on the idea that errorous sequences are usually not consistent with other sequences, in this paper we provide an alternative approach for finding alternative splicing patterns which ensures that individual exons/introns of the reported patterns have enough support from the expressed sequences. On the same dataset, our approach can achieve a much higher specificity and a slight increase in sensitivity (38.9% and 84.9%, respectively). Our approach also gives better results compared with popular alternative splicing databases (ASD, ECgene, SpliceNest) and the software ClusterMerge. © 2008 Imperial College Press. |
Persistent Identifier | http://hdl.handle.net/10722/60613 |
ISSN | 2023 Impact Factor: 0.9 2023 SCImago Journal Rankings: 0.270 |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wong, TKF | en_HK |
dc.contributor.author | Lam, TW | en_HK |
dc.contributor.author | Yang, W | en_HK |
dc.contributor.author | Yiu, SM | en_HK |
dc.date.accessioned | 2010-05-31T04:14:59Z | - |
dc.date.available | 2010-05-31T04:14:59Z | - |
dc.date.issued | 2008 | en_HK |
dc.identifier.citation | Journal Of Bioinformatics And Computational Biology, 2008, v. 6 n. 5, p. 1021-1033 | en_HK |
dc.identifier.issn | 0219-7200 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/60613 | - |
dc.description.abstract | We consider the problem of predicting alternative splicing patterns from a set of expressed sequences (cDNAs and ESTs). Some of these expressed sequences may be errorous, thus forming incorrect exons/introns. These incorrect exons/introns may cause a lot of false positives. For example, we examined a popular alternative splicing database, ECgene, which predicts alternate splicing patterns from expressed sequences. The result shows that about 81.3%-81.6% (sensitivity) of known patterns are found, but the specificity can be as low as 5.9%. Based on the idea that errorous sequences are usually not consistent with other sequences, in this paper we provide an alternative approach for finding alternative splicing patterns which ensures that individual exons/introns of the reported patterns have enough support from the expressed sequences. On the same dataset, our approach can achieve a much higher specificity and a slight increase in sensitivity (38.9% and 84.9%, respectively). Our approach also gives better results compared with popular alternative splicing databases (ASD, ECgene, SpliceNest) and the software ClusterMerge. © 2008 Imperial College Press. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Imperial College Press. The Journal's web site is located at http://www.worldscinet.com/jbcb/jbcb.shtml | en_HK |
dc.relation.ispartof | Journal of Bioinformatics and Computational Biology | en_HK |
dc.subject | Alternative splicing pattern | en_HK |
dc.subject | ESTs | en_HK |
dc.subject | Expressed sequences | en_HK |
dc.subject.mesh | Algorithms | en_HK |
dc.subject.mesh | Alternative Splicing - genetics | en_HK |
dc.subject.mesh | Base Sequence | en_HK |
dc.subject.mesh | Exons - genetics | en_HK |
dc.subject.mesh | Gene Expression - genetics | en_HK |
dc.subject.mesh | Introns - genetics | en_HK |
dc.subject.mesh | Molecular Sequence Data | en_HK |
dc.subject.mesh | RNA Splice Sites - genetics | en_HK |
dc.subject.mesh | Sequence Analysis, DNA - methods | en_HK |
dc.title | Finding alternative splicing patterns with strong support from expressed sequences on individual exons/introns | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0219-7200&volume=6&issue=5&spage=1021&epage=1033&date=2008&atitle=Finding+Alternative+Splicing+Patterns+with+Strong+Support+from+Expressed+Sequences+on+Individual+Exons/Introns | en_HK |
dc.identifier.email | Lam, TW:twlam@cs.hku.hk | en_HK |
dc.identifier.email | Yang, W:yangwl@hkucc.hku.hk | en_HK |
dc.identifier.email | Yiu, SM:smyiu@cs.hku.hk | en_HK |
dc.identifier.authority | Lam, TW=rp00135 | en_HK |
dc.identifier.authority | Yang, W=rp00524 | en_HK |
dc.identifier.authority | Yiu, SM=rp00207 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1142/S0219720008003825 | en_HK |
dc.identifier.pmid | 18942164 | - |
dc.identifier.scopus | eid_2-s2.0-54049115762 | en_HK |
dc.identifier.hkuros | 155950 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-54049115762&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 6 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.spage | 1021 | en_HK |
dc.identifier.epage | 1033 | en_HK |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Wong, TKF=25423289800 | en_HK |
dc.identifier.scopusauthorid | Lam, TW=7202523165 | en_HK |
dc.identifier.scopusauthorid | Yang, W=23101349500 | en_HK |
dc.identifier.scopusauthorid | Yiu, SM=7003282240 | en_HK |
dc.identifier.issnl | 0219-7200 | - |