An effective algorithm for the peptide de novo sequencing from MS/MS spectrum
CPM'03 Proceedings of the 14th annual conference on Combinatorial pattern matching
Identification of Post-Translational Modifications via Blind Search of Mass-Spectra
CSB '05 Proceedings of the 2005 IEEE Computational Systems Bioinformatics Conference
Classifying b and y ions in peptide tandem mass spectra
FSKD'09 Proceedings of the 6th international conference on Fuzzy systems and knowledge discovery - Volume 5
BioDM'06 Proceedings of the 2006 international conference on Data Mining for Biomedical Applications
EigenMS: de novo analysis of peptide tandem mass spectra by spectral graph partitioning
RECOMB'05 Proceedings of the 9th Annual international conference on Research in Computational Molecular Biology
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For the identification of novel proteins using MS/MS, de novo sequencing software computes one or several possible amino acid sequences (called sequence tags) for each MS/MS spectrum. Those tags are then used to match, accounting amino acid mutations, the sequences in a protein database. If the de novo sequencing gives correct tags, the homologs of the proteins can be identified by this approach and software such as MS-BLAST is available for the matching. However, de novo sequencing very often gives only partially correct tags. The most common error is that a segment of amino acids is replaced by another segment with approximately the same masses. We developed a new efficient algorithm to match sequence tags with errors to database sequences for the purpose of protein and peptide identification. A software package, SPIDER, was developed and made available on Internet for free public use. This paper describes the algorithms and features of the SPIDER software.