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Remote homology detection based on oligomer distances.

Identifieur interne : 002099 ( PubMed/Checkpoint ); précédent : 002098; suivant : 002100

Remote homology detection based on oligomer distances.

Auteurs : Thomas Lingner [Allemagne] ; Peter Meinicke

Source :

RBID : pubmed:16837522

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English descriptors

Abstract

Remote homology detection is among the most intensively researched problems in bioinformatics. Currently discriminative approaches, especially kernel-based methods, provide the most accurate results. However, kernel methods also show several drawbacks: in many cases prediction of new sequences is computationally expensive, often kernels lack an interpretable model for analysis of characteristic sequence features, and finally most approaches make use of so-called hyperparameters which complicate the application of methods across different datasets.

DOI: 10.1093/bioinformatics/btl376
PubMed: 16837522


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pubmed:16837522

Le document en format XML

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<name sortKey="Lingner, Thomas" sort="Lingner, Thomas" uniqKey="Lingner T" first="Thomas" last="Lingner">Thomas Lingner</name>
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<nlm:affiliation>Abteilung Bioinformatik, Institut für Mikrobiologie und Genetik, Georg-August-Universität Göttingen Goldschmidtstr. 1, 37077 Göttingen, Germany. thomas@gobics.de</nlm:affiliation>
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Abteilung Bioinformatik, Institut für Mikrobiologie und Genetik, Georg-August-Universität Göttingen Goldschmidtstr. 1, 37077 Göttingen</wicri:regionArea>
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<name sortKey="Meinicke, Peter" sort="Meinicke, Peter" uniqKey="Meinicke P" first="Peter" last="Meinicke">Peter Meinicke</name>
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<term>Algorithms</term>
<term>Amino Acid Sequence</term>
<term>Artificial Intelligence</term>
<term>Dimerization</term>
<term>Molecular Sequence Data</term>
<term>Pattern Recognition, Automated</term>
<term>Proteins (chemistry)</term>
<term>Sequence Alignment (methods)</term>
<term>Sequence Analysis, Protein (methods)</term>
<term>Sequence Homology, Amino Acid</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Algorithmes</term>
<term>Alignement de séquences ()</term>
<term>Analyse de séquence de protéine ()</term>
<term>Dimérisation</term>
<term>Données de séquences moléculaires</term>
<term>Intelligence artificielle</term>
<term>Protéines ()</term>
<term>Reconnaissance automatique des formes</term>
<term>Similitude de séquences d'acides aminés</term>
<term>Séquence d'acides aminés</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en">
<term>Sequence Alignment</term>
<term>Sequence Analysis, Protein</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Algorithms</term>
<term>Amino Acid Sequence</term>
<term>Artificial Intelligence</term>
<term>Dimerization</term>
<term>Molecular Sequence Data</term>
<term>Pattern Recognition, Automated</term>
<term>Sequence Homology, Amino Acid</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Algorithmes</term>
<term>Alignement de séquences</term>
<term>Analyse de séquence de protéine</term>
<term>Dimérisation</term>
<term>Données de séquences moléculaires</term>
<term>Intelligence artificielle</term>
<term>Protéines</term>
<term>Reconnaissance automatique des formes</term>
<term>Similitude de séquences d'acides aminés</term>
<term>Séquence d'acides aminés</term>
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<div type="abstract" xml:lang="en">Remote homology detection is among the most intensively researched problems in bioinformatics. Currently discriminative approaches, especially kernel-based methods, provide the most accurate results. However, kernel methods also show several drawbacks: in many cases prediction of new sequences is computationally expensive, often kernels lack an interpretable model for analysis of characteristic sequence features, and finally most approaches make use of so-called hyperparameters which complicate the application of methods across different datasets.</div>
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<Year>2009</Year>
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<ISSN IssnType="Electronic">1367-4811</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>22</Volume>
<Issue>18</Issue>
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<Year>2006</Year>
<Month>Sep</Month>
<Day>15</Day>
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<Title>Bioinformatics (Oxford, England)</Title>
<ISOAbbreviation>Bioinformatics</ISOAbbreviation>
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<ArticleTitle>Remote homology detection based on oligomer distances.</ArticleTitle>
<Pagination>
<MedlinePgn>2224-31</MedlinePgn>
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<AbstractText Label="MOTIVATION" NlmCategory="BACKGROUND">Remote homology detection is among the most intensively researched problems in bioinformatics. Currently discriminative approaches, especially kernel-based methods, provide the most accurate results. However, kernel methods also show several drawbacks: in many cases prediction of new sequences is computationally expensive, often kernels lack an interpretable model for analysis of characteristic sequence features, and finally most approaches make use of so-called hyperparameters which complicate the application of methods across different datasets.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">We introduce a feature vector representation for protein sequences based on distances between short oligomers. The corresponding feature space arises from distance histograms for any possible pair of K-mers. Our distance-based approach shows important advantages in terms of computational speed while on common test data the prediction performance is highly competitive with state-of-the-art methods for protein remote homology detection. Furthermore the learnt model can easily be analyzed in terms of discriminative features and in contrast to other methods our representation does not require any tuning of kernel hyperparameters.</AbstractText>
<AbstractText Label="AVAILABILITY" NlmCategory="BACKGROUND">Normalized kernel matrices for the experimental setup can be downloaded at www.gobics.de/thomas. Matlab code for computing the kernel matrices is available upon request.</AbstractText>
<AbstractText Label="CONTACT" NlmCategory="BACKGROUND">thomas@gobics.de, peter@gobics.de.</AbstractText>
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