Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/41643
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dc.titleDe novo peptide sequencing for mass spectra based on multi-charge strong tags
dc.contributor.authorNing, K.
dc.contributor.authorChong, K.F.
dc.contributor.authorLeong, H.W.
dc.date.accessioned2013-07-04T08:32:18Z
dc.date.available2013-07-04T08:32:18Z
dc.date.issued2007
dc.identifier.citationNing, K.,Chong, K.F.,Leong, H.W. (2007). De novo peptide sequencing for mass spectra based on multi-charge strong tags. Series on Advances in Bioinformatics and Computational Biology 5 : 287-296. ScholarBank@NUS Repository.
dc.identifier.isbn9781860947834
dc.identifier.issn17516404
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/41643
dc.description.abstractThis paper presents an improved algorithm for de novo sequencing of multi-charge mass spectra. Recent work based on the analysis of multi-charge mass spectra showed that taking advantage of multi-charge information can lead to higher accuracy (sensitivity and specificity) in peptide sequencing. A simple de novo algorithm, called GBST (Greedy algorithm with Best Strong Tag) was proposed and was shown to produce good results for spectra with charge > 2. In this paper, we analyze some of the shortcomings of GBST. We then present a new algorithm GST-SPC, by extending the GBST algorithm in two directions. First, we use a larger set of multi-charge strong tags and show that this improves the theoretical upper bound on performance. Second, we give an algorithm that computes a peptide sequence that is optimal with respect to shared peaks count from among all sequences that are derived from multi-charge strong tags. Experimental results demonstrate the improvement of GST-SPC over GBST.
dc.sourceScopus
dc.typeConference Paper
dc.contributor.departmentCOMPUTER SCIENCE
dc.description.sourcetitleSeries on Advances in Bioinformatics and Computational Biology
dc.description.volume5
dc.description.page287-296
dc.identifier.isiutNOT_IN_WOS
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