Constrained mixture estimation for analysis and robust classification of clinical time series
1Center of Informatics, Federal University of Pernambuco, Recife, Brazil, 2School of Computing Science, Simon Fraser University, Burnaby, BC, Canada and 3Department of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin, Germany
*To whom correspondence should be addressed.
 |
Abstract |
|---|
Motivation: 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-β (IFNβ) treatment response in Multiple Sclerosis (MS) patients which has attracted substantial attention in the recent past. Half of the patients remain unaffected by IFNβ treatment, which is still the standard. For them the treatment should be timely ceased to mitigate the side effects.
Results: We propose constrained estimation of mixtures of hidden Markov models as a methodology to classify patient response to IFNβ 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.
Availability: 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/
igcf/MSConst
Contact: igcf{at}cin.ufpe.br
Supplementary information: Supplementary data are available at Bioinformatics online.
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  T. Aittokallio Dealing with missing values in large-scale studies: microarray data imputation and beyond Brief Bioinform, December 4, 2009; (2009) bbp059v1. [Abstract] [Full Text] [PDF]
|
|