ArticleBioinformatics (Oxford, England)2009
Constrained mixture estimation for analysis and robust classification of clinical time series.
Article in Bioinformatics (Oxford, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- GeTeSEPdb: A comprehensive database and online tool for the identification and analysis of gene profiles with temporal-specific expression patterns.Computational and structural biotechnology journal · 2024Article
- Phenotype similarities in automatically grouped T2D patients by variation-based clustering of IL-1β gene expression.EJIFCC · 2023Article
- Time-frequency time-space LSTM for robust classification of physiological signals.Scientific reports · 2021Article
- Generalized Correlation Coefficient for Non-Parametric Analysis of Microarray Time-Course Data.Journal of integrative bioinformatics · 2017Article
- Article
- Classification of time series gene expression in clinical studies via integration of biological network.PloS one · 2013Article
- Early classification of multivariate temporal observations by extraction of interpretable shapelets.BMC bioinformatics · 2012Article
- Studying and modelling dynamic biological processes using time-series gene expression data.Nature reviews. Genetics · 2012Review
- Detection and interpretation of metabolite-transcript coresponses using combined profiling data.Bioinformatics (Oxford, England) · 2011Article
- A growth curve model with fractional polynomials for analysing incomplete time-course data in microarray gene expression studies.Advances in bioinformatics · 2011Article
- Introducing knowledge into differential expression analysis.Journal of computational biology : a journal of computational molecular cell biology · 2010Article
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Authors and funding
4 authors.
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Abstract
motivationPersonalized 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.
resultsWe 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. 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/ approximately igcf/MSConst. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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