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Sökning: (WFRF:(Schliep Alexander 1967)) srt2:(2005-2009) > (2009)

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1.
  • Costa, Ivan G, et al. (författare)
  • Constrained mixture estimation for analysis and robust classification of clinical time series.
  • 2009
  • Ingår i: Bioinformatics (Oxford, England). - : Oxford University Press (OUP). - 1367-4811 .- 1367-4803. ; 25:12
  • Tidskriftsartikel (refereegranskat)abstract
    • Personalized medicine based on molecular aspects of diseases, such as gene expression profiling, has become increasingly popular. However, one faces multiple challenges when analyzing clinical gene expression data; most of the well-known theoretical issues such as high dimension of feature spaces versus few examples, noise and missing data apply. Special care is needed when designing classification procedures that support personalized diagnosis and choice of treatment. Here, we particularly focus on classification of interferon-beta (IFNbeta) treatment response in Multiple Sclerosis (MS) patients which has attracted substantial attention in the recent past. Half of the patients remain unaffected by IFNbeta treatment, which is still the standard. For them the treatment should be timely ceased to mitigate the side effects.We propose constrained estimation of mixtures of hidden Markov models as a methodology to classify patient response to IFNbeta treatment. The advantages of our approach are that it takes the temporal nature of the data into account and its robustness with respect to noise, missing data and mislabeled samples. Moreover, mixture estimation enables to explore the presence of response sub-groups of patients on the transcriptional level. We clearly outperformed all prior approaches in terms of prediction accuracy, raising it, for the first time, >90%. Additionally, we were able to identify potentially mislabeled samples and to sub-divide the good responders into two sub-groups that exhibited different transcriptional response programs. This is supported by recent findings on MS pathology and therefore may raise interesting clinical follow-up questions.The method is implemented in the GQL framework and is available at http://www.ghmm.org/gql. Datasets are available at http://www.cin.ufpe.br/ approximately igcf/MSConst.Supplementary data are available at Bioinformatics online.
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2.
  • Georgi, Benjamin, et al. (författare)
  • Partially-supervised protein subclass discovery with simultaneous annotation of functional residues.
  • 2009
  • Ingår i: BMC structural biology. - : Springer Science and Business Media LLC. - 1472-6807. ; 9
  • Tidskriftsartikel (refereegranskat)abstract
    • The study of functional subfamilies of protein domain families and the identification of the residues which determine substrate specificity is an important question in the analysis of protein domains. One way to address this question is the use of clustering methods for protein sequence data and approaches to predict functional residues based on such clusterings. The locations of putative functional residues in known protein structures provide insights into how different substrate specificities are reflected on the protein structure level.We have developed an extension of the context-specific independence mixture model clustering framework which allows for the integration of experimental data. As these are usually known only for a few proteins, our algorithm implements a partially-supervised learning approach. We discover domain subfamilies and predict functional residues for four protein domain families: phosphatases, pyridoxal dependent decarboxylases, WW and SH3 domains to demonstrate the usefulness of our approach.The partially-supervised clustering revealed biologically meaningful subfamilies even for highly heterogeneous domains and the predicted functional residues provide insights into the basis of the different substrate specificities.
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  • Resultat 1-3 av 3

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