Profile-based string kernels for remote homology detection and motif extraction.
Identifieur interne : 000400 ( Ncbi/Curation ); précédent : 000399; suivant : 000401Profile-based string kernels for remote homology detection and motif extraction.
Auteurs : Rui Kuang [États-Unis] ; Eugene Ie ; Ke Wang ; Kai Wang ; Mahira Siddiqi ; Yoav Freund ; Christina LeslieSource :
- Proceedings. IEEE Computational Systems Bioinformatics Conference [ 1551-7497 ] ; 2004.
Descripteurs français
- KwdFr :
- Algorithmes, Alignement de séquences (), Analyse de profil d'expression de gènes (), Analyse de regroupements, Analyse de séquence de protéine (), Expression des gènes (génétique), Intelligence artificielle, Motifs d'acides aminés, Reconnaissance automatique des formes (), Similitude de séquences d'acides aminés.
- MESH :
- génétique : Expression des gènes.
- Algorithmes, Alignement de séquences, Analyse de profil d'expression de gènes, Analyse de regroupements, Analyse de séquence de protéine, Intelligence artificielle, Motifs d'acides aminés, Reconnaissance automatique des formes, Similitude de séquences d'acides aminés.
English descriptors
- KwdEn :
- MESH :
Abstract
We introduce novel profile-based string kernels for use with support vector machines (SVMs) for the problems of protein classification and remote homology detection. These kernels use probabilistic profiles, such as those produced by the PSI-BLAST algorithm, to define position-dependent mutation neighborhoods along protein sequences for inexact matching of k-length subsequences ("k-mers") in the data. By use of an efficient data structure, the kernels are fast to compute once the profiles have been obtained. For example, the time needed to run PSI-BLAST in order to build the pro- files is significantly longer than both the kernel computation time and the SVM training time. We present remote homology detection experiments based on the SCOP database where we show that profile-based string kernels used with SVM classifiers strongly outperform all recently presented supervised SVM methods. We also show how we can use the learned SVM classifier to extract "discriminative sequence motifs" -- short regions of the original profile that contribute almost all the weight of the SVM classification score -- and show that these discriminative motifs correspond to meaningful structural features in the protein data. The use of PSI-BLAST profiles can be seen as a semi-supervised learning technique, since PSI-BLAST leverages unlabeled data from a large sequence database to build more informative profiles. Recently presented "cluster kernels" give general semi-supervised methods for improving SVM protein classification performance. We show that our profile kernel results are comparable to cluster kernels while providing much better scalability to large datasets.
DOI: 10.1109/csb.2004.1332428
PubMed: 16448009
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pubmed:16448009Le document en format XML
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<term>Gene Expression Profiling (methods)</term>
<term>Pattern Recognition, Automated (methods)</term>
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<term>Sequence Analysis, Protein (methods)</term>
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<term>Analyse de regroupements</term>
<term>Analyse de séquence de protéine</term>
<term>Intelligence artificielle</term>
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<front><div type="abstract" xml:lang="en">We introduce novel profile-based string kernels for use with support vector machines (SVMs) for the problems of protein classification and remote homology detection. These kernels use probabilistic profiles, such as those produced by the PSI-BLAST algorithm, to define position-dependent mutation neighborhoods along protein sequences for inexact matching of k-length subsequences ("k-mers") in the data. By use of an efficient data structure, the kernels are fast to compute once the profiles have been obtained. For example, the time needed to run PSI-BLAST in order to build the pro- files is significantly longer than both the kernel computation time and the SVM training time. We present remote homology detection experiments based on the SCOP database where we show that profile-based string kernels used with SVM classifiers strongly outperform all recently presented supervised SVM methods. We also show how we can use the learned SVM classifier to extract "discriminative sequence motifs" -- short regions of the original profile that contribute almost all the weight of the SVM classification score -- and show that these discriminative motifs correspond to meaningful structural features in the protein data. The use of PSI-BLAST profiles can be seen as a semi-supervised learning technique, since PSI-BLAST leverages unlabeled data from a large sequence database to build more informative profiles. Recently presented "cluster kernels" give general semi-supervised methods for improving SVM protein classification performance. We show that our profile kernel results are comparable to cluster kernels while providing much better scalability to large datasets.</div>
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