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    <meta name="description" content="New Results - Model-based clustering for pharmacovigilance data"/>
    <meta name="dc.title" content="New Results - Model-based clustering for pharmacovigilance data"/>
    <meta name="dc.creator" content="Gilles Celeux"/>
    <meta name="dc.creator" content="Christine Keribin"/>
    <meta name="dc.creator" content="Valérie Robert"/>
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    <meta name="dc.date" content="(SCHEME=ISO8601) 2017-01"/>
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      <div class="TdmEntry">Overall Objectives<ul><li><a href="./uid3.html">Model selection in Statistics</a></li></ul></div>
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	    Raweb 
	    2017</a> | <a href="http://www.inria.fr/en/teams/select">Presentation of the Project-Team SELECT</a> | <a href="http://www.math.u-psud.fr/select/">SELECT Web Site
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        <h2>Section: 
      New Results</h2>
        <h3 class="titre3">Model-based clustering for pharmacovigilance data</h3>
        <p class="participants"><span class="part">Participants</span> :
	Gilles Celeux, Christine Keribin, Valérie Robert.</p>
        <p>In collaboration with Pascale Tubert-Bitter, Ismael Ahmed and Mohamed Sedki, Gilles Celeux and Christine Keribin
worked on the detection of associations between drugs and adverse events in the framework
of the PhD of Valerie Robert, which was defended this year. At first, this team developed model-based clustering inspired by latent block models (LBMs),
which consists of co-clustering rows and columns of two binary tables, imposing the same row ranking. This enabled it
to highlight subgroups of individuals sharing the same drug profile, and subgroups of adverse effects and drugs with
strong interactions.
Furthermore, some sufficient conditions are provided to obtain identifiability of the model, and some results
are shown for simulated data.
The exact ICL criterion has been extended to this double block latent model.
Through computer experiments, Valérie Robert demonstrated the interest of the proposed model, compared with standard
contingency table analysis, to detect co-prescription and masking effects.</p>
        <p>Futhermore, with V. Robert, C. Kerebin and G. Celeux showed that it can be useful to use an LBM model on a contingency table of drugs and adverse effects to do cluster initialization for dealing with individual's data.
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