<?xml version="1.0" encoding="utf-8"?>
<!DOCTYPE raweb PUBLIC "-//INRIA//DTD " "raweb2.dtd">
<raweb xml:lang="en" year="2006">
  <identification id="visages" isproject="true">
    <shortname>VisAGeS</shortname>
    <projectName><b>Vi</b>sion 
    <b>A</b>ction et 
    <b>Ge</b>stion d'informations en 
    <b>S</b>anté</projectName>
    <theme>BIO</theme>
    <team id="uid1">
      <participants category="Head_of_project-team">
        <person key="visages-2006-idm410090442464">
          <firstname>Christian</firstname>
          <lastname>Barillot</lastname>
          <affiliation>CNRS</affiliation>
          <categoryPro>Chercheur</categoryPro>
          <moreinfo>DR Cnrs</moreinfo>
          <hdr>oui</hdr>
        </person>
      </participants>
      <participants category="Administrative_assistant">
        <person key="adept-2006-idm317581853008">
          <firstname>Céline</firstname>
          <lastname>Ammoniaux</lastname>
          <affiliation>CNRS</affiliation>
          <categoryPro>Assistant</categoryPro>
          <moreinfo>TR Cnrs, shared with Espresso, R2D2 and Lagadic projects</moreinfo>
        </person>
        <person key="visages-2006-idm410090436016">
          <firstname>Aline</firstname>
          <lastname>Grosset</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Assistant</categoryPro>
          <moreinfo>AGT University of Rennes 1, 50% from medical faculty</moreinfo>
        </person>
      </participants>
      <participants category="Inria_research_scientists">
        <person key="visages-2006-idm410090432640">
          <firstname>Pierre</firstname>
          <lastname>Hellier</lastname>
          <affiliation>INRIA</affiliation>
          <categoryPro>Chercheur</categoryPro>
          <moreinfo>CR, on sabbatical at The McGill University, Montreal from 01/01/2006 till 18/12/2006</moreinfo>
        </person>
        <person key="visages-2006-idm410090429920">
          <firstname>Sylvain</firstname>
          <lastname>Prima</lastname>
          <affiliation>INRIA</affiliation>
          <categoryPro>Chercheur</categoryPro>
          <moreinfo>CR</moreinfo>
        </person>
        <person key="visages-2006-idm410090427296">
          <firstname>Clément</firstname>
          <lastname>De Guibert</lastname>
          <affiliation>AutreEtablissementPublic</affiliation>
          <categoryPro>Chercheur</categoryPro>
          <moreinfo>University of Rennes 2 Associate professor, on Inria secondment (délégation)</moreinfo>
        </person>
      </participants>
      <participants category="Inserm_research_scientists">
        <person key="visages-2006-idm410090423824">
          <firstname>Bernard</firstname>
          <lastname>Gibaud</lastname>
          <affiliation>AutreEtablissementPublic</affiliation>
          <categoryPro>Chercheur</categoryPro>
          <moreinfo>CR</moreinfo>
          <hdr>oui</hdr>
        </person>
        <person key="visages-2006-idm410090420800">
          <firstname>Pierre</firstname>
          <lastname>Jannin</lastname>
          <affiliation>AutreEtablissementPublic</affiliation>
          <categoryPro>Chercheur</categoryPro>
          <moreinfo>CR</moreinfo>
          <hdr>oui</hdr>
        </person>
      </participants>
      <participants category="University_of_Rennes_1_research_scientists">
        <person key="visages-2006-idm410090417120">
          <firstname>Xavier</firstname>
          <lastname>Morandi</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Enseignant</categoryPro>
          <moreinfo>PU-PH, Medical Faculty, University of Rennes 1 and University Hospital of Rennes, Neurosurgery Department</moreinfo>
          <hdr>oui</hdr>
        </person>
      </participants>
      <participants category="University_Hospital_of_Rennes_research_scientists">
        <person key="visages-2006-idm410090413168">
          <firstname>Sean-Patrick</firstname>
          <lastname>Morrissey</lastname>
          <affiliation>AutreEtablissementPublic</affiliation>
          <categoryPro>Chercheur</categoryPro>
          <moreinfo>PH, University Hospital of Rennes, Neurology Department</moreinfo>
        </person>
      </participants>
      <participants category="Inria_project_technical_staff">
        <person key="visages-2006-idm410090409824">
          <firstname>Eric</firstname>
          <lastname>Poiseau</lastname>
          <affiliation>INRIA</affiliation>
          <categoryPro>Technique</categoryPro>
          <moreinfo>IR, IHE project, until 01/07/2006</moreinfo>
        </person>
      </participants>
      <participants category="Inria_Junior_technical_staff">
        <person key="visages-2006-idm410090406560">
          <firstname>Alban</firstname>
          <lastname>Gaignard</lastname>
          <affiliation>INRIA</affiliation>
          <categoryPro>Technique</categoryPro>
          <moreinfo>IA, until 30/11/2006</moreinfo>
        </person>
      </participants>
      <participants category="Teaching_assistant">
        <person key="visages-2006-idm410090403264">
          <firstname>Cybèle</firstname>
          <lastname>Ciofolo</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Enseignant</categoryPro>
          <moreinfo>Lecturer Ifsic, University of Rennes 1, to 28/02/2006</moreinfo>
        </person>
        <person key="visages-2006-idm410090400480">
          <firstname>Laure</firstname>
          <lastname>Aït-Ali</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Enseignant</categoryPro>
          <moreinfo>Lecturer Ifsic, University of Rennes 1, from 01/09/2006</moreinfo>
        </person>
      </participants>
      <participants category="Invited_Researcher">
        <person key="visages-2006-idm410090397072">
          <firstname>Duygu</firstname>
          <lastname>Tosun</lastname>
          <affiliation>UnivEtrangere</affiliation>
          <categoryPro>Chercheur</categoryPro>
          <moreinfo>Invited Researcher, INRIA, from 01/10/2006 to 28/12/2006</moreinfo>
        </person>
      </participants>
      <participants category="Inria_Post-doctoral_fellows">
        <person key="visages-2006-idm410090393744">
          <firstname>Simon</firstname>
          <lastname>Duchesne</lastname>
          <affiliation>AutreEtablissementPublic</affiliation>
          <categoryPro>PostDoc</categoryPro>
        </person>
        <person key="visages-2006-idm410090391488">
          <firstname>Mathieu</firstname>
          <lastname>Monziol</lastname>
          <affiliation>INRIA</affiliation>
          <categoryPro>PostDoc</categoryPro>
          <moreinfo>from 01/09/2006</moreinfo>
        </person>
      </participants>
      <participants category="University_of_Rennes 1_technical_staff">
        <person key="visages-2006-idm410090388128">
          <firstname>Vincent</firstname>
          <lastname>Gratsac</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Technique</categoryPro>
          <moreinfo>IE, PlogICI project</moreinfo>
        </person>
        <person key="visages-2006-idm410090385472">
          <firstname>Daniel</firstname>
          <lastname>Garcia-Lorenzo</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Technique</categoryPro>
          <moreinfo>IE, PlogICI project, until 30/11/2006</moreinfo>
        </person>
      </participants>
      <participants category="Ph-D_students">
        <person key="visages-2006-idm410090400480">
          <firstname>Laure</firstname>
          <lastname>Aït-Ali</lastname>
          <affiliation>INRIA</affiliation>
          <categoryPro>PhD</categoryPro>
          <moreinfo>Inria-Brittany council grant, until 31/08/2006</moreinfo>
        </person>
        <person key="visages-2006-idm410090379552">
          <firstname>Pierrick</firstname>
          <lastname>Coupé</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>PhD</categoryPro>
          <moreinfo>Research Ministry grant</moreinfo>
        </person>
        <person key="visages-2006-idm410090376976">
          <firstname>Perrine</firstname>
          <lastname>Paul</lastname>
          <affiliation>EtablissementPrive</affiliation>
          <categoryPro>PhD</categoryPro>
          <moreinfo>Cifre, Medtronic Inc. grant, until 08/12/2006</moreinfo>
        </person>
        <person key="visages-2006-idm410090374304">
          <firstname>Lynda</firstname>
          <lastname>Temal</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>PhD</categoryPro>
          <moreinfo>University of Rennes 1-Brittany council grant</moreinfo>
        </person>
        <person key="visages-2006-idm410090371568">
          <firstname>Omar</firstname>
          <lastname>El Ganaoui</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>PhD</categoryPro>
          <moreinfo>Research Ministry grant</moreinfo>
        </person>
        <person key="visages-2006-idm410090368944">
          <firstname>Ammar</firstname>
          <lastname>Mechouche</lastname>
          <affiliation>AutreEtablissementPublic</affiliation>
          <categoryPro>PhD</categoryPro>
          <moreinfo>Inserm-Brittany council grant</moreinfo>
        </person>
        <person key="visages-2006-idm410090366288">
          <firstname>Nicolas</firstname>
          <lastname>Wiest-Daesslé</lastname>
          <affiliation>INRIA</affiliation>
          <categoryPro>PhD</categoryPro>
          <moreinfo>Inria grant</moreinfo>
        </person>
        <person key="visages-2006-idm410090363648">
          <firstname>Jérémy</firstname>
          <lastname>Lecoeur</lastname>
          <affiliation>INRIA</affiliation>
          <categoryPro>PhD</categoryPro>
          <moreinfo>Inria-Brittany council grant, from 01/11/2006</moreinfo>
        </person>
        <person key="visages-2006-idm410090385472">
          <firstname>Daniel</firstname>
          <lastname>Garcia-Lorenzo</lastname>
          <affiliation>INRIA</affiliation>
          <categoryPro>PhD</categoryPro>
          <moreinfo>Inria grant, from 01/12/2006</moreinfo>
        </person>
      </participants>
      <participants category="Associated_Faculty">
        <person key="visages-2006-idm410090357696">
          <firstname>Alain</firstname>
          <lastname>Bouliou</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Enseignant</categoryPro>
          <moreinfo>Assistant Professor, University of Rennes 1</moreinfo>
        </person>
        <person key="visages-2006-idm410090354928">
          <firstname>Arnaud</firstname>
          <lastname>Biraben</lastname>
          <affiliation>AutreEtablissementPublic</affiliation>
          <categoryPro>AutreCategorie</categoryPro>
          <moreinfo>PH, University Hospital of Rennes, Neurology Department</moreinfo>
        </person>
        <person key="visages-2006-idm410090352224">
          <firstname>Béatrice</firstname>
          <lastname>Carsin-Nicol</lastname>
          <affiliation>AutreEtablissementPublic</affiliation>
          <categoryPro>AutreCategorie</categoryPro>
          <moreinfo>PH, University Hospital of Rennes, Radiology Department</moreinfo>
        </person>
        <person key="visages-2006-idm410090349552">
          <firstname>Pierre</firstname>
          <lastname>Darnault</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Enseignant</categoryPro>
          <moreinfo>PU-PH, Medical Faculty, University of Rennes 1 and University Hospital of Rennes, Radiology Department</moreinfo>
        </person>
        <person key="visages-2006-idm410090346672">
          <firstname>Gilles</firstname>
          <lastname>Edan</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Enseignant</categoryPro>
          <moreinfo>PU-PH, Medical Faculty, University of Rennes 1 and University Hospital of Rennes, Neurology Department</moreinfo>
        </person>
        <person key="visages-2006-idm410090343840">
          <firstname>Benoît</firstname>
          <lastname>Godey</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Enseignant</categoryPro>
          <moreinfo>PU-PH, Medical Faculty, University of Rennes 1 and University Hospital of Rennes, Ear Nose and Throat Department</moreinfo>
        </person>
        <person key="visages-2006-idm410090340976">
          <firstname>Anne-Marie</firstname>
          <lastname>Bernard</lastname>
          <affiliation>UnivFr</affiliation>
          <categoryPro>Enseignant</categoryPro>
          <moreinfo>MCU-PH, Assistant Professor, Medical Faculty, University of Rennes 1</moreinfo>
        </person>
      </participants>
    </team>
    <UR name="Rennes"/>
  </identification>
  <presentation id="uid3">
    <bodyTitle>Overall Objectives</bodyTitle>
    <subsection level="1" id="uid4">
      <bodyTitle>Overall objectives</bodyTitle>
      <keyword><KW controle="MEDICAL IMAGING"/>medical imaging</keyword>
      <keyword><KW controle="REGISTRATION"/>registration</keyword>
      <keyword><KW controle="IMAGE SEGMENTATION"/><KW controle="IMAGE ANALYSIS"/>image segmentation and analysis</keyword>
      <keyword><KW controle="NEUROIMAGING"/>neuroimaging</keyword>
      <keyword><KW controle="STATISTICAL ANALYSIS IN MEDICAL IMAGING"/>statistical analysis in medical imaging</keyword>
      <keyword><KW controle="MANAGEMENT OF INFORMATION IN MEDICAL IMAGING"/>management of information in medical imaging</keyword>
      <keyword><KW controle="3D FREE-HAND ULTRASOUND"/>3D free-hand ultrasound</keyword>
      <keyword><KW controle="IMAGE-GUIDED INTERVENTION"/>image-guided intervention</keyword>
      <keyword><KW controle="CLINICAL NEUROSCIENCES"/>clinical neurosciences</keyword>
      <p>Since 1970s, medical imaging is a very rapidly growing research domain; the last three decades have shown a rapid evolution of the dimension and quantity of data physicians have to work
      with. The next decade will follow this evolution by adding not only new spatio-temporal dimensions to the image data produced and used in a clinical environment but also new scales of analysis
      (nano or micro biological and molecular images to macro medical images). Another evolution will also consist in adding new effectors during image-guided interventional procedures (surgery,
      interventional radiology...). The classical way of making use of these images, mostly based on human interpretation, becomes less and less feasible. In addition, the societal pressure for a
      cost effective use of the equipments on the one hand, and a better traceability and quality insurance of the decision making process on the other hand, makes the development of advanced
      computer-assisted medical imaging systems more and more essential. According to this context, our research team is devoted to the development of new processing algorithms in the context of
      medical image computing and computer-assisted interventions: image fusion (registration and visualization), image segmentation and analysis, management of image-related information ... In this
      very large domain, our work is primarily focused on clinical applications and for the most part on head and brain related diseases.</p>
      <p>Research activities of the 
      <span class="smallcap" align="left">VisAGeS</span>team are concerned with the development of new processing algorithms in the field of medical image computing and computer assisted
      interventions: image fusion (registration and visualization), image segmentation and analysis, management of image related information ... Since this is a very large domain, for seek of
      efficiency, the application of our work will be primarily focused on clinical aspects and for the most part on head and neck related diseases. Our research efforts mainly concern:</p>
      <simplelist>
        <li id="uid5">
          <p>The field of image fusion and image registration (rigid and deformable transformations) with a special emphasis on new challenging registration issues especially when statistical
          approaches based on joint histogram cannot be used or when the registration stage has to cope with loss or appearance of material (like in surgery or in tumor imaging for instance).</p>
        </li>
        <li id="uid6">
          <p>The field of image segmentation and structure recognition, with a special emphasis on the difficult problems of 
          <hi rend="italic">i</hi>) image restoration for new imaging sequences (new Magnetic Resonance Imaging protocols, 3D ultrasound sequences ...), and 
          <i>ii</i>) structure segmentation and labelling based on shape and statistical information.</p>
        </li>
        <li id="uid7">
          <p>The field of image analysis and statistical modelling with a new focus on Voxel Based Analysis (VBA) and group analysis problems. A special attention will be given also to the
          development of advanced frameworks for the construction of probabilistic atlases since this complicated problem is still only partially solved.</p>
        </li>
        <li id="uid8">
          <p>The field of information management in neuroimaging following the Neurobase project, for the development of distributed and heterogeneous medical image processing systems 
          <footnote id="uid9" place="foot" anchored="yes">( 
          <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://www.irisa.fr/visages/neurobase" location="extern" xyref="1952468020016" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest">
          http://www.irisa.fr/visages/neurobase</ref>)</footnote>.</p>
        </li>
      </simplelist>
      <p>Concerning the application domains, we emphasize our research efforts on the neuroimaging domain with two up-front priorities: Image Guided Neurosurgery and Image Analysis in Multiple
      Sclerosis, while developing new ones especially in the interventional aspects (per-operative imagery, robotics...).</p>
    </subsection>
  </presentation>
  <fondements id="uid10">
    <bodyTitle>Scientific Foundations</bodyTitle>
    <subsection level="1" id="uid11">
      <bodyTitle>Introduction</bodyTitle>
      <p>The scientific objectives of our team, concern the development of new medical image computing methods, dealing with image fusion (registration and visualization), image segmentation and
      analysis, and management of image-related information.</p>
      <p>In addition, since these methods are devoted (but not specific) to solve actual medical applications, a constant concern is to build an evaluation framework at each stage of the
      methodological development process. Therefore, this topic is present as a transversal concern among the generic developments and the applications.</p>
    </subsection>
    <subsection level="1" id="uid12">
      <bodyTitle>Registration</bodyTitle>
      <keyword><KW controle="RIGID REGISTRATION"/>Rigid registration</keyword>
      <keyword><KW controle="DEFORMABLE REGISTRATION"/>deformable registration</keyword>
      <keyword><KW controle="SIMILARITY MEASURES"/>similarity measures</keyword>
      <p>Image registration consists in finding a geometrical transformation in order to match 
      <i>n</i>sets of images. Our objective is to work both, on rigid registration methods in order to develop new similarity measures for new imaging modalities, and on deformable registration to
      address the problem of tissue dissipation.</p>
      <p>The registration between two images can be summarized by the expression  
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid0" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>:</p>
      <p>
        <formula type="display">
          <img align="middle" width="158" height="26" src="math_image_1.png" xylemeAttach="1" border="0" alt="Im1 $\mover {\#952 \#8712 \#920 ~}\mstyle {{arg~min}_\#936 ^{}\#916 \mfenced o=( c=) {\#934 _\#952 \mfenced o=( c=) \#937 _s-\#937 _t}}$"/>
        </formula>
      </p>
      <p>where 
      <span class="math" align="left"><img width="13" height="13" align="bottom" border="0" src="../../images/img_upper_omega.png" alt="$ \upper_omega$"/><sub><hi rend="it">s</hi></sub></span>and 
      <span class="math" align="left"><img width="13" height="13" align="bottom" border="0" src="../../images/img_upper_omega.png" alt="$ \upper_omega$"/><sub><hi rend="it">t</hi></sub></span>are respectively the two homologous sets of features respectively extracted from the source and the target images. These sets represent the two images in the registration process. They
      can be very different in nature, and can be deduced from a segmentation process (points, contours, crest lines ...) or directly from the image intensities (e.g. the joint histogram). 
      <span class="math" align="left"><img align="middle" width="14" height="12" src="math_image_2.png" xylemeAttach="2" border="0" alt="Im2 $\#934 _\#952 $"/></span>is the transformation, ( 
      <i><span class="math" align="left"><img width="12" height="13" align="bottom" border="0" src="../../images/img_theta.png" alt="$ \theta$"/></span></i>
      <span class="math" align="left"><img width="13" height="24" align="middle" border="0" src="../../images/img_other_in.png" alt="$ \in$"/><img width="14" height="13" align="bottom" border="0" src="../../images/img_upper_theta.png" alt="$ \upper_theta$"/></span>being the set of parameters for this transformation), 
      <span class="math" align="left"><img width="15" height="13" align="bottom" border="0" src="../../images/img_upper_delta.png" alt="$ \upper_delta$"/></span>is the cost (or similarity) function, and 
      <span class="math" align="left"><img width="14" height="13" align="bottom" border="0" src="../../images/img_upper_psi.png" alt="$ \upper_psi$"/></span>is the optimization method. { 
      <span class="math" align="left"><img width="13" height="13" align="bottom" border="0" src="../../images/img_upper_omega.png" alt="$ \upper_omega$"/>, 
      <img width="13" height="13" align="bottom" border="0" src="../../images/img_upper_phi.png" alt="$ \upper_phi$"/>, 
      <img width="15" height="13" align="bottom" border="0" src="../../images/img_upper_delta.png" alt="$ \upper_delta$"/>, 
      <img width="14" height="13" align="bottom" border="0" src="../../images/img_upper_psi.png" alt="$ \upper_psi$"/></span>} are the four major decisive factors in a registration procedure, the
      set 
      <span class="math" align="left"><img width="14" height="13" align="bottom" border="0" src="../../images/img_upper_theta.png" alt="$ \upper_theta$"/></span>being a priori defined. In addition to new evolutions of these factors, a constant concern is to propose a methodology for validating this registration procedure. We already have been
      largely involved in these aspects in the past and will maintain this effort  
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid1" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid2" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>.</p>
      <p>In the domain of 
      <b>rigid registration</b>, our research is more focused on new problems coming from the applications. For instance, the mono and multimodal registration of ultrasound images is still an open
      problem. In this context we are working in looking at new similarity measures to better take into account the nature of the echographic signal. Similarly, in the interventional theatre, new
      matching procedures are required between for instance video, optical or biological images and the pre-operative images (CT, MRI, SPECT/PET, Angiography ...). Some of these problems can be very
      challenging. For a number of new applications, there are no existing solutions to solve these problems (e.g. fusion of biological images with interventional images and images coming from the
      planning).</p>
      <p>In many contexts, a rigid transformation cannot account for the underlying phenomena. This is for instance true when observing evolving biological and physiological phenomena. Therefore, 
      <b>deformable registration</b>methods (also called non-rigid registration) are needed  
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid3" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>. In this domain, we are working in the
      following three directions:</p>
      <simplelist>
        <li id="uid13">
          <p>Non-rigid registration algorithms benefit from the incorporation of statistical priors. These statistical priors can be expressed locally (for instance through a statistical analysis of
          segmented shapes) or globally (by learning statistics about deformation fields directly). Statistical priors (local and global) are useful to capture probable or relevant deformations.</p>
        </li>
        <li id="uid14">
          <p>Non-rigid registration methods can be broadly sorted in two classes: geometric methods that rely on the extraction and matching of sparse anatomical structures and photometric methods
          that rely on image intensities directly. These two kinds of methods have their advantages and drawbacks. We are working on further cooperative approaches where information of different
          nature (global, hybrid and local) could be mixed in an elegant mathematical way.</p>
        </li>
        <li id="uid15">
          <p>Finally, our research is focused on a better modeling of the problems, mainly in two directions: firstly the relationship between the observed data (image intensities) and the variables
          (registration field) should be better understood. This leads to more adapted similarity measures in specific application contexts (for instance when registering ultrasound images).
          Secondly, specific modeling of the deformation field is useful in specific contexts (for instance when matter is disappearing, fluid mechanics models will be more adapted than classical
          regularized deformation fields).</p>
        </li>
      </simplelist>
    </subsection>
    <subsection level="1" id="uid16">
      <bodyTitle>Image segmentation and analysis</bodyTitle>
      <keyword><KW controle="IMAGE RESTORATION"/>image restoration</keyword>
      <keyword><KW controle="DEFORMABLE SHAPE MODELS"/>deformable shape models</keyword>
      <keyword><KW controle="LEVEL SETS"/>level sets</keyword>
      <keyword><KW controle="3D ULTRASOUND"/>3D ultrasound</keyword>
      <keyword><KW controle="MRI"/>MRI</keyword>
      <p>This topic is very classical in computer vision. For the concern of medical image computing, we are focusing on the development of new tools devoted to the restoration of corrupted images
      coming from the sources and to the segmentation of anatomical structures based on deformable shape models.</p>
      <p><b>Statistical methods for image restoration:</b>New applications of medical imaging systems are parallel to the development or the evolution of new machinery which come with specific artifacts
      that are still only partially understood. This is the case for instance with high field MRI, 3D ultrasound imaging or other modalities. With regards to the images to process and analyze, these
      artifacts translate into geometric or intensity distortions that drastically affect not only the visual interpretation, but also most of the segmentation or registration algorithms, and the
      quantitative measures that follow. A better comprehension of these artifacts necessitates an increased dialogue between the physicists (who make the images), the computer scientists (who
      process the images) and the clinicians (who interpret the images). This should lead to define new, specifically-designed algorithms, based on statistical models taking into account the physics
      of the acquisition.</p>
      <p><b>Segmentation using deformable shapes:</b>We aim at proposing a generic framework to build probabilistic shape models in a 3D 
      <span class="math" align="left">+ 
      <hi rend="it">t</hi></span>space applied to biomedical images with a particular emphasis on the problem of modeling anatomical and functional structures in neuroimaging (functional
      delineations, cortical or deep brain structures). Based on our previous contributions in this domain  
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid4" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid5" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid6" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, we work on a methodological framework to
      segment 3D shapes and to model, in space and time, shape descriptors which can be applied to new extracted shapes; this with the aim of proposing new quantification tools in biomedical
      imaging.</p>
    </subsection>
    <subsection level="1" id="uid17">
      <bodyTitle>Statistical analysis in medical imaging</bodyTitle>
      <keyword><KW controle="VOXEL BASED ANALYSIS"/>voxel based analysis</keyword>
      <keyword><KW controle="PROBABILISTIC BRAIN ATLAS"/>probabilistic brain atlas</keyword>
      <keyword><KW controle="IMAGE CLASSIFICATION"/>image classification</keyword>
      <keyword><KW controle="GROUP ANALYSIS"/>group analysis</keyword>
      <p>Nowadays, statistical analysis occupies a central place for the study of brain anatomy and function in medical imaging. It is indeed a question of exploiting huge image data bases, on which
      we look to reveal the relevant information: measure the anatomical variability to discover better what deviates from it, to measure the noise to discover an activation, etc., in brief, to
      distinguish what is statistically significant of what is not.</p>
      <p><b>Statistical methods for voxel-based analysis:</b>Statistical analysis tools play a key role in the study of the anatomy and functions of the brain. Typically, statisticians aim at extracting
      the significant information hidden below the noise and/or the natural variability. Some specific tools exist for the comparison of vector fields or geometrical landmarks. Some others have been
      developed for the analysis of functional data (PET, fMRI...). Thus, statistics are generally either spatial, or temporal. There is an increasing need for the development of statistics that
      consider time and space simultaneously. Applications include the follow-up of multiple sclerosis in MR images or the tracking of a deformable structure in an ultrasound image sequence.</p>
      <p><b>Probabilistic atlases:</b>One of the major problems in medical image analysis is to assist the clinician to interpret and exploit the high dimensionality of the images especially when he/she
      needs to confront his/her interpretation with "classical" cases (previous or reference cases). A solution to deal with this problem is to go through the use of an atlas which can represent a
      relevant 
      <i>a priori</i>knowledge. Probabilistic atlases have been studied to tackle this problem but most of the time they rely on global references which are not always relevant or precise enough, to
      solve some very complex problems like the interpretation of inter-individual variations of brain anatomy and functions. Based on our previous work proposing a cooperation between global and
      local references to build such probabilistic atlases  
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid7" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid1" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, we are working to develop a probabilistic
      atlas capable of labelling highly variable structure (anatomical and functional ones), or for defining relevant indexes for using with data bases systems.</p>
      <p><b>Classification and group analysis:</b>One of the major problems in quantitative image analysis is to be able to perform clustering based on descriptors extracted from images. This can be
      done either by using supervised or unsupervised algorithms. Our objectives is to develop statistical analysis methods in order to discriminate groups of data for clinical and medical research
      purposes (e.g. pathologic 
      <i>vs</i>. normal feature, male 
      <i>vs.</i>female, right-handed 
      <i>vs.</i>left-handed, etc.), these data may come from descriptors extracted by using image analysis procedures (e.g. shapes, measurements, volumes, etc.).</p>
    </subsection>
    <subsection level="1" id="uid18">
      <bodyTitle>Management of information in medical imaging</bodyTitle>
      <keyword><KW controle="MEDIATION"/>mediation</keyword>
      <keyword><KW controle="WRAPPER"/>wrapper</keyword>
      <keyword><KW controle="WORKFLOW"/>workflows</keyword>
      <keyword><KW controle="ONTOLOGY"/>ontology</keyword>
      <keyword><KW controle="WEB SERVICE"/>web services</keyword>
      <p>There is a strong need of a better sharing and a broader re-use of medical data and knowledge in the neuroimaging field. One of the most difficult problems is to represent this information
      in such a way that the structure and semantics are shared between the cognitive agents involved (i.e. programs and humans). This issue is not new, but the recent evolution of computer and
      networking technology (most notably, the Internet) increases information and processing tools sharing possibilities, and therefore makes this issue prevailing. The notion of ``semantic web''
      denotes a major change in the way computer applications will share information semantics in the future, with a great impact on available infrastructures and tools. In coherence with the rest of
      our research topics, we are focussing on brain imaging. This deals with accessing, referring to, and using knowledge in the field of brain imaging, whatever the kind of knowledge - either
      general knowledge (e.g. models of anatomical structures, ``know-how'' knowledge such as image processing tools), or related to individuals (such as a database of healthy subjects' images). This
      covers both information of a numerical nature (i.e. derived from measurements such as images or 3D surfaces depicting anatomical features), of a symbolic nature (such as salient properties,
      names - referring to common knowledge - and relationships between entities), as well as processing tools available in a shared environment. Two major aspects are considered: (1) representing
      anatomical or anatomo-functional data and knowledge and (2) sharing neuroimaging data and processing tools.</p>
    </subsection>
  </fondements>
  <domaine id="uid19">
    <bodyTitle>Application Domains</bodyTitle>
    <subsection level="1" id="uid20">
      <bodyTitle>Neuroimaging</bodyTitle>
      <keyword><KW controle="NEUROIMAGING"/>neuroimaging</keyword>
      <keyword><KW controle="CLINICAL NEUROSCIENCES"/>clinical neuroscience</keyword>
      <keyword><KW controle="IMAGE-GUIDED SURGERY"/>image-guided surgery</keyword>
      <keyword><KW controle="MULTIPLE SCLEROSIS"/>multiple sclerosis</keyword>
      <keyword><KW controle="PREOPERATIVE IMAGING"/>preoperative imaging</keyword>
      <keyword><KW controle="3D ULTRASOUND"/>3D ultrasound</keyword>
      <keyword><KW controle="MULTISPECTRAL MRI"/>multispectral MRI</keyword>
      <keyword><KW controle="BRAIN ATLAS"/>brain atlas</keyword>
      <p>One research objective in neuroimaging is the construction of anatomical and functional cerebral maps under normal and pathological conditions.</p>
      <p>Many researches are currently performed to find correlations between anatomical structures, essentially sulci and gyri, where neuronal activation takes place, and cerebral functions, as
      assessed by recordings obtained by the means of various neuroimaging modalities, such as PET (Positron Emission Tomography), fMRI (Functional Magnetic Resonance Imaging), EEG
      (Electro-EncephaloGraphy) and MEG (Magneto-EncephaloGraphy). Then, a central problem inherent to the formation of such maps is to put together recordings obtained from different modalities and
      from different subjects. This mapping can be greatly facilitated by the use of MR anatomical brain scans with high spatial resolution that allows a proper visualization of fine anatomical
      structures (sulci and gyri). Recent improvements in image processing techniques, such as segmentation, registration, delineation of the cortical ribbon, modeling of anatomical structures and
      multi-modality fusion, make possible this ambitious goal in neuroimaging. This problem is very rich in terms of applications since both clinical and neuroscience applications share similar
      problems. Since this domain is very generic by nature, our major contributions are directed towards clinical needs even though our work can address some specific aspects related to the
      neuroscience domain.</p>
      <p><b>Multiple sclerosis:</b>Over the past years, a discrepancy became apparent between clinical Multiple sclerosis (MS) classification describing on the one hand MS according to four different
      disease courses and, on the other hand, the description of two different disease stages (an early inflammatory and a subsequently neurodegenerative phase). It is to be expected that
      neuroimaging will play a critical role to define 
      <i>in vivo</i>those four different MS lesion patterns. An 
      <i>in vivo</i>distinction between the four MS lesion patterns, and also between early and late stages of MS will have an important impact in the future for a better understanding of the natural
      history of MS and even more for the appropriate selection and monitoring of drug treatment in MS patients. Since MRI has a low specificity for defining in more detail the pathological changes
      which could discriminate between the different lesion types, but a high sensitivity to detect focal and also widespread, diffuse pathology of the normal appearing white and grey matter, our
      major objective within this application domain is to define new neuroimaging markers for tracking the evolution of the pathology from high dimensional data (e.g. nD+t MRI). In addition, in
      order to complement MR neuroimaging data, we ambition to perform also cell labeling neuroimaging (e.g. MRI or PET) and to compare MR and PET data using standard and experimental MR contrast
      agents and radiolabeled PET tracers for activated microglia (e.g. USPIO or PK 11195). The goal is to define and develop, for routine purposes, cell specific and also quantitative imaging
      markers for the improved 
      <i>in vivo</i>characterization of MS pathology.</p>
      <p><b>Modeling of anatomical and anatomo-functional neurological patterns:</b>The major objective within this application domain is to build anatomical and functional brain atlases in the context
      of functional mapping for pre-surgical planning and for the study of neurodegenerative brain diseases (Multiple sclerosis, Epilepsy, Parkinson or even Alzheimer). This is a very competitive
      research domain; our contribution is based on our previous works in this field  
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid6" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid7" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid8" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid1" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>,and by continuing our local and wider
      collaborations ....</p>
      <p>An additional objective within this application domain is to find new descriptors to study the brain anatomy and/or function (e.g. variation of brain perfusion, evolution in shape and size
      of an anatomical structure in relation with pathology or functional patterns, computation of asymmetries ...). This is also a very critical research domain, especially for many
      neurodegenerative brain diseases (Epilepsy or Alzheimer for instance).</p>
      <p><b>Epilepsy:</b>The principle of epilepsy surgery is to remove the Epileptic Zone (EZ) (area of the brain where epileptic seizures are originating). The anatomical determination of this EZ is
      individualized, and surgery will be therefore individually tailored. To delineate this EZ, different sources of information are used and a congruence of several explorations is needed. Some are
      static, such as MRI and PET, and some may reflect the spatio-temporal dynamics of the seizures. Integration of multimodal information about brain perfusion (ictal and interictal SPECT),
      metabolism (PET-F18FDG), anatomy (MRI, DTI), as well as direct recording of electrical activity (MEG/EEG) may improve significantly on its own the way epileptic patients are explored and
      treated. Although none of these modalities added a significant contribution to this area, SPECT/PET and MEG/EEG could help localizing the EZ in temporal lobe epilepsy and limit the use of depth
      electrodes recordings, especially when focussing more specifically on the particular role of sub-cortical structures (such as thalamus, caudate nucleus, pallidum, etc.). From this standpoint,
      our goal is to tackle several of these questions? such as:</p>
      <simplelist>
        <li id="uid21">
          <p>What is the role of sub-cortical structures in temporal and frontal epilepsy? How do these observations correlate with depth electrodes recordings? How could this knowledge impact on
          treatment decisions (chemically on basal ganglia, or surgically with deep brain stimulations ?</p>
        </li>
        <li id="uid22">
          <p>What is the optimum use of the various imaging techniques available, in order to examine the various parts of an epileptic network, before performing a decision)?</p>
        </li>
      </simplelist>
    </subsection>
    <subsection level="1" id="uid23">
      <bodyTitle>Image guided intervention</bodyTitle>
      <p>Image-guided neurosurgical procedures rely on complex preoperative planning and intraoperative environment. This includes various multimodal examinations: anatomical, vascular, functional
      explorations for brain surgery and an increasing number of computer-assisted systems taking place in the Operating Room (OR). Hereto, using an image-guided surgery system, a rigid fusion
      between the patient's head and the preoperative data is determined. With an optical tracking system and Light Emitting Diodes (LED), it is possible to track the patient's head, the microscope
      and the surgical instruments in real time. The preoperative data can then be merged with the surgical field of view displayed in the microscope. This fusion is called ``augmented reality''.</p>
      <p>Unfortunately, the assumption of a rigid registration between the patient's head and the preoperative images only holds at the beginning of the procedure. This is because soft tissues tend
      to deform during the intervention. This is a common problem in many image-guided interventions, the particular case of neurosurgical procedures can be considered as a representative case. Brain
      shift is one manifestation of this problem but other tissue deformations can occur and must be taken into account for a more realistic predictive work.</p>
      <p>Within this application domain, we aim at developing systems using surgical guidance tools and real-time imagery in the interventional theatre. This imagery can come from video (using
      augmented reality procedures), echography or even interventional MRI, biological images or thermal imagery in the future.</p>
      <p><b>Per-operative imaging in neurosurgery:</b>Our major objective within this application domain is to correct for brain deformations that occur during surgery. Neuronavigation systems make it
      now possible to superimpose preoperative images with the surgical field under the assumption of a rigid transformation. Nevertheless, non-rigid brain deformations, as well as brain resection,
      drastically limit the efficiency of such systems. The major objective here is to estimate brain deformations using 3D ultrasound and video information.</p>
      <p><b>Modeling of surgical gesture expertise:</b>Our objective is to show how the formalization of the medical expertise could improve both the planning and the surgery itself. One way is to rely
      on previously defined generic model describing surgical procedures. From a data base of surgical cases described by the generic model and from a limited set of parameters related to the patient
      (i.e. extrinsic parameters), the closest surgical case can be retrieved in order to assist the surgical planning. Similarly, global surgical scenarii representing main categories of surgical
      procedures could be classified according to extrinsic parameters (coming from the current case) and retrieved from the database. New experiences based on this procedure could then feed the
      surgical modelling. Another issue would be to use the knowledge extracted from the data base to pre-fetch the image processing procedures (to speed up or tune processing workflows
      parameters).</p>
      <p><b>Robotics for 3D echography:</b>This project is conducted jointly with the Lagadic project-team. The goal is to use active vision concepts in order to control the trajectory of a robot based
      on the contents of echographic images and video frames (taken from the acquisition theatre). Possible applications are the acquisition of echographic data between two remote sites (the patient
      is away from the referent clinician) or the monitoring of interventional procedure like biopsy or selective catheterisms.</p>
      <p><b>3D free-hand ultrasound</b>: Our major objective within this application domain is to develop efficient and automatic procedures to allow the clinician to use conventional echography to
      acquire 3D ultrasound and to propose calibrated quantification tools for quantitative analysis and fusion procedures. This will be used to extend the scope of view of an examination.</p>
    </subsection>
  </domaine>
  <logiciels id="uid24">
    <bodyTitle>Software</bodyTitle>
    <subsection level="1" id="uid25">
      <bodyTitle>Introduction</bodyTitle>
      <p>Our objectives concerning the software development and dissemination are directed to the set-up of a software platform at the University Hospital in order to deploy new research advances and
      to validate them in the clinical context with our local partners. We intend to disseminate our results via a free software distribution. Complying with both objectives requires software
      engineering resources, which could be partially covered in the short term by a current PRIR application "PlogICI", but a longer term alternative already needs to be foreseen.</p>
    </subsection>
    <subsection level="1" id="uid26">
      <bodyTitle>VistaL</bodyTitle>
      <p>VistaL is a software platform of 3D and 3D+t image analysis allowing the development of generic algorithms used in different contexts (rigid and non-rigid registration, segmentation,
      statistical modelling, calibration of free-hand 3D ultrasound system and so on). This software platform is composed of generic C++ template classes (Image3D, Image4D, Lattice and so on) and a
      set of 3D/3D+t image processing libraries. VistaL is a multi-operating system environment (Windows, Linux/Unix...). VistaL APP registration number is: IDDN.FR.001.200014.S.P.2000.000.21000.</p>
    </subsection>
    <subsection level="1" id="uid27">
      <bodyTitle>Romeo</bodyTitle>
      <p>Romeo ( 
      <b>RO</b>bust 
      <b>M</b>ultigrid 
      <b>E</b>lastic registration based on 
      <b>O</b>ptical flow) is a non-rigid registration algorithm based on optical-flow. Romeo is developed using Vistal (C++ template classes described above). Romeo estimates a regularized
      deformation field between two volumes in a robust way: two robust estimators are used for both the data term (optical flow) and the regularization term (smoothness of the field). An efficient
      multiresolution and multigrid minimization scheme is implemented so as to estimate large deformations, to increase the accuracy and to speed up the algorithm  
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid9" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>. Romeo has been registered at APP with number:
      IDDN.FR.001.200014.SP.2000.000.21000.</p>
    </subsection>
    <subsection level="1" id="uid28">
      <bodyTitle>Juliet</bodyTitle>
      <p>Juliet ( 
      <b>J</b>oint 
      <b>U</b>se of 
      <b>L</b>andmarks and 
      <b>I</b>ntensity for 
      <b>E</b>lastic regis 
      <b>T</b>ration) is a non-rigid registration algorithm that is built on the Romeo software. Juliet makes it possible to incorporate sparse constraints deduced from the matching of anatomical
      structures such as cortical sulci for instance. A sparse deformation field is introduced as a soft constraint in the minimization to drive the registration process. A robust estimator is used
      so as to limit segmentation errors and false matching  
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid10" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>. Juliet has been registered at APP with
      number: IDDN.FR.001.45001.001.S.A.2001.000.21000.</p>
    </subsection>
    <subsection level="1" id="uid29">
      <bodyTitle>Tulipe</bodyTitle>
      <p>TULIPE ( 
      <b>T</b>hree dimensional 
      <b>UL</b>trasound reconstructioin 
      <b>I</b>ncorporating Prob 
      <b>E</b>trajectory) was developed using Vistal and is a registered at APP under IDDN.FR.001.120034.S.A.2006.000.21000. 3D freehand ultrasound is a technique based on the acquisition of B-scans,
      which can be parallel or not, whose position in 3D space is known by a 3D localizer (optic or magnetic) attached to the probe. From these irregularly distributed B-scans and their positions, a
      regular 3D lattice volume can be reconstructed. This reconstruction step is needed to apply conventional 3D computer vision algorithms like volumetric registration and segmentation, but is
      still an acute problem with regards to computation time and reconstruction quality. Tulipe explicitly takes into account the 3D probe trajectory. In the classical distance weighted
      interpolation, the interpolation kernel is composed of the orthogonal projections of the current point on the closest B-scans. In Tulipe, the interpolation kernel is composed of intersections
      between the probe trajectory (passing through the current point) and the closest B-scans  
      <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid11" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>.</p>
    </subsection>
  </logiciels>
  <resultats id="uid30">
    <bodyTitle>New Results</bodyTitle>
    <subsection level="1" id="uid31">
      <bodyTitle>Image Segmentation, Registration and Analysis</bodyTitle>
      <subsection level="2" id="uid32">
        <bodyTitle>Non-local means for image restoration</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Pierrick</firstname>
            <lastname>Coupé</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Yger</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Hellier</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>A critical issue in the context of image restoration is the problem of noise removal while keeping the integrity of relevant image information. Denoising is a crucial step to increase
        image conspicuity and to improve the performances of all the processings needed for quantitative imaging analysis. The method we have proposed is based on an optimized blockwise version of
        the Non Local (NL) Means fillter  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid12" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>. This approach uses the natural redundancy
        of information in image to remove the noise. If the performances of the NL-means filter have been already shown for 2D image, the critical aspect of extending the method to 3D images is the
        computational burden. To overcome this problem, we propose improvements to reduce the computational complexity. These different improvements allow us to divide by a factor of 350 the
        computational time. A fully-automated version of the blockwise NL-means filter has been performed, exhibiting good denoising results without expensive computational burden and without
        external parameter tuning. Tests were carried out on synthetic datasets and on real MR images from two specific sequences T1-w and T2-w. The quantitative results show that the blockwise
        approach outperforms the classical implementation of the NL-means filter, and also other classical denoising methods, such as Anisotropic Diffusion Filter  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid13" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>and Total Variation minimization
        process  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid14" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>. We have performed large scale
        experimentations to get qualitative results on real 3T T1-w MR images and T2-w images with Multiple Sclerosis (MS) lesions  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid15" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>.</p>
      </subsection>
      <subsection level="2" id="uid33">
        <bodyTitle>A new optimisation algorithm for medical image registration</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Nicolas</firstname>
            <lastname>Wiest-Daesslé</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Yger</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>In this work, we proposed to use a recently introduced optimisation method (termed NEWUOA, for NEW Unconstrained Optimization Algorithm) in the context of rigid registration of medical
        images. This optimisation method was compared with two other widely used algorithms, the Powell's direction set and Nelder-Mead's downhill simplex methods. We evaluated the performances of
        these three algorithms to optimise different image similarity measures for different mono- and multimodal problems. Images from the BrainWeb project were used as a gold standard for
        validation purposes. We showed that the proposed optimisation algorithm is more robust, more accurate and faster than the two other methods  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid16" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>.</p>
      </subsection>
      <subsection level="2" id="uid34">
        <bodyTitle>Shape analysis and level sets for segmentation of brain structures</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Cybèle</firstname>
            <lastname>Ciofolo</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>We have proposed a new method to segment 3D structures with competitive level sets driven by a shape model and fuzzy control. To this end, several contours evolve simultaneously towards
        previously defined targets. The main contribution of this work is the original introduction of a priori information provided by a shape model, which is used as an anatomical atlas, into a
        fuzzy decision system. The shape information is combined with the intensity distribution of the image and the relative position of the contours. This combination automatically determines the
        directional term of the evolution equation of each level set. This leads to a local expansion or contraction of the contours, in order to match the borders of their respective targets. The
        shape model is produced with a principal component analysis, and the resulting mean shape and variations are used to estimate the target location and the fuzzy states corresponding to the
        distance between the current contour and the target. By combining shape analysis and fuzzy control, we take advantage of both approaches to improve the level set segmentation process with a
        priori information. Experiments have been done for the 3D segmentation of deep brain structures from MRI, and a quantitative valuation was performed on a 18 volumes dataset  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid17" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>.</p>
      </subsection>
    </subsection>
    <subsection level="1" id="uid35">
      <bodyTitle>Image processing on Diffusion Weighted Magnetic Resonance Imaging</bodyTitle>
      <subsection level="2" id="uid36">
        <bodyTitle>Computation of the mid-sagittal plane in diffusion tensor MR brain images</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Nicolas</firstname>
            <lastname>Wiest-Daesslé</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>We proposed a method for the automated computation of the mid-sagittal plane of the brain in diffusion tensor MR images. We proposed to estimate this plane as the one that best matches the
        two hemispheres of the brain by reflection symmetry. This is done via the automated minimisation of a correlation-type global criterion over the tensor image. The minimisation is performed
        using the NEWUOA algorithm in a multiresolution framework. We validated our algorithm on synthetic diffusion tensor MR images. We quantitatively compared this computed plane with similar
        planes obtained from scalar diffusion images (such as FA and ADC maps) and from the B0 image (that is, without diffusion sensitisation). Finally, we showed some results on real diffusion
        tensor MR images  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid18" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>.</p>
      </subsection>
      <subsection level="2" id="uid37">
        <bodyTitle>Basic methods for processing and representation of diffusion tensor MRI data</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Nicolas</firstname>
            <lastname>Wiest-Daesslé</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Naman</firstname>
            <lastname>Singhal</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>We developed a general purpose application implementing most of the state-of-the-art methods for the pre- and post-processing of diffusion-weighted (DW) MRI data obtained from different
        MRI scanners. Tests were performed on the two MRI scanners of the Rennes university hospital: 1.5T Siemens Symphony and 3T Philips Achieva MRI scanners. The application includes import/export
        routines for DW-MRI raw data, low-level algorithms for retrospective correction of image artefacts (noise, distortions) and higher-level algorithms for image processing and analysis (tensor
        algebra, registration, visualisation). Preliminary experiments have been performed on DW-MRI data from individual MS patients. As expected from the literature, changes in the diffusion
        parameters computed from the tensor field were revealed, and additional studies are currently under investigation to validate these outcomes.</p>
      </subsection>
    </subsection>
    <subsection level="1" id="uid38">
      <bodyTitle>Management of Information in Neuroimaging</bodyTitle>
      <subsection level="2" id="uid39">
        <bodyTitle>Federation of Heterogenous and Distributed Information in Neuroimaging</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Lynda</firstname>
            <lastname>Temal</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Alban</firstname>
            <lastname>Gaignard</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Bernard</firstname>
            <lastname>Gibaud</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>In this topic we have continued our work with the Neurobase project in order to develop a demonstration environment to exhibit the way neuroimaging information (data and image processing
        tools) can be shared. Our goal was to elaborate a demonstrator based on some existing modules like Le Select 
        <footnote id="uid40" place="foot" anchored="yes"><ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://www-caravel.inria.fr/Fprototype_LeSelect.html" location="extern" xyref="1922911539029" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest">
          http://www-caravel.inria.fr/Fprototype_LeSelect.html</ref></footnote>, BrainVISA/Anatomist 
        <footnote id="uid41" place="foot" anchored="yes"><ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://brainvisa.info/" location="extern" xyref="89409499015" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest">http://brainvisa.info/</ref></footnote>, BALC (from our Grenoble partners) or VIsTAL 
        <footnote id="uid42" place="foot" anchored="yes"><ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://www.irisa.fr/visages/software-fra.html" location="extern" xyref="4192960121018" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest">
          http://www.irisa.fr/visages/software-fra.html</ref></footnote>. Several functionalities are being implemented such as data wrappers and mediators, medical image processing methods (data access, image processing, segmentation, visualization,
        ...) through a data flow model approach (see Figure 2 of  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid19" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>). In the Neurobase demonstrator, we have
        proposed architecture with a generic server model based on the LeSelect with a PostGres/SQL data base for managing the storage of temporary image data computed from Data Flow process. The
        data flow processes for image processing workflow procedures can be executed from a Tomcat server. We are actually implementing data flows being able to process image denoising, brain
        segmentation, brain tissue classification (white matter, grey matter, CSF). The computation mapping implemented in the current version (i.e. where data meet the image processing codes) can be
        in principle performed everywhere in the collaborative network. In practice, because we haven't set up efficient processing servers on each collaborative site, in current experiments, codes
        are executed were the data are located. At the present time, security aspects are just addressed by using a SSH tunnelling for the transactions between the servers and the clients.
        Confidentiality of the data including anonymization has to be performed by the publisher. This issue should be addressed in future versions, especially within the scope of the new "ANR:
        Technologies Logielles" Project called NeuroLOG which has been accepted this year.</p>
      </subsection>
      <subsection level="2" id="uid43">
        <bodyTitle>Ontologies for modelling brain structures in neuroimaging applications</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Ammar</firstname>
            <lastname>Mechouche</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Bernard</firstname>
            <lastname>Gibaud</lastname>
          </person>
        </participants>
        <p>The general objective of this work is to model and represent knowledge about brain anatomical structures in ways that facilitate sharing and re-use for various purposes. Based on first
        results obtained during Olivier Dameron's PhD thesis, our current objective is to represent symbolic knowledge about cortical structures (gyri and sulci) and to demonstrate the added value of
        this knowledge for the interpretation and annotation of MRI images. For example we are interested in showing how such information can complement other kinds of priors such as statistical
        probability maps. Therefore, our recent works have explored the feasibility of the joint use of an OWL ontology of brain cortical structures (focusing of the representation of part-of and
        topology relationships) and of rules (represented in SWRL), modelling complex dependencies between those relationships. Merging these two kinds of knowledge is made using the KAON2 reasoner 
        <footnote id="uid44" place="foot" anchored="yes"><ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://www.aifb.uni-karlsruhe.de/Projekte/viewProjekt?id_db=62" location="extern" xyref="1328754254031" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest">
          http://www.aifb.uni-karlsruhe.de/Projekte/viewProjekt?id_db=62</ref></footnote>.</p>
        <p>This work has been done in collaboration with Pr Christine Golbreich (LIM, UPRES 3888, Rennes), who is co-supervisor of Ammar Mechouche's PhD thesis  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid20" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid21" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>.</p>
      </subsection>
      <subsection level="2" id="uid45">
        <bodyTitle>Ontology of Datasets and Image processing tools in neuroimaging</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Lynda</firstname>
            <lastname>Temal</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Bernard</firstname>
            <lastname>Gibaud</lastname>
          </person>
        </participants>
        <p>Based on the work done during the exploratory phase of the Neurobase project, we have refined the Neurobase ontology towards a more formal and more modular ontology, called OntoNeurobase.
        Therefore, we adopted a specific, multi-layered, modular approach to ontology design, and we used DOLCE (Descriptive Ontology for Linguistic and Cognitive Engineering) as a foundational
        ontology together with three core ontologies, namely I&amp;DA (Information and Discourse Acts) for modelling documents (texts and images), COPS (Core Ontology of Programs and Software) for
        modelling programs and software, and OntoKADS for modelling problem solving activities. Our original contribution concerns Datasets and Image processing tools in the field of
        neuroimaging  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid22" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>. This work has been done in collaboration
        with Michel Dojat (INSERM U594) and Gilles Kassel and his colleagues from LaRIA (CNRS FRE 2733) in Amiens.</p>
      </subsection>
    </subsection>
    <subsection level="1" id="uid46">
      <bodyTitle>Image Guided Neurosurgery</bodyTitle>
      <subsection level="2" id="uid47">
        <bodyTitle>Intraoperative 3D Free-Hand Ultrasound</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Pierrick</firstname>
            <lastname>Coupé</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Hellier</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Xavier</firstname>
            <lastname>Morandi</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>We have continued our efforts in using ultrasound images during neurosurgical procedures. More specifically, we have adressed the problem of rigid registration of 
        <span class="math" align="left">3 
        <hi rend="it">D</hi></span>intraoperative ultrasond data to preoperative MR images. This is still a challenging problem due to the difference of information contained in each image modality.
        To overcome this difficulty, we introduce a new probabilistic function for similarity measurements based on the mean curvature of MR isophots and US hyperchogenic structures. Experiments were
        carried out on 3 patients and compared with three other registration approaches. The results show that the proposed method converges robustly compared to the standard registration techniques,
        with a computational time compatible with intraoperative use.</p>
      </subsection>
      <subsection level="2" id="uid48">
        <bodyTitle>Ultrasound shadows detection</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Hellier</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierrick</firstname>
            <lastname>Coupé</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Xavier</firstname>
            <lastname>Morandi</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>Acoustic shadows appear in ultrasound images as regions of low signal intensity after boundaries with very high acoustic impedance differences. Acoustic shadows can be viewed as
        informative features to detect lesions, calcifications, gallstones; or can be considered as damageable artifacts for image processing tasks such as segmentation, registration or 
        <span class="math" align="left">3 
        <hi rend="it">D</hi></span>reconstruction. In both cases, the detection of these acoustic shadows is useful. We have proposed a new geometrical method to detect the shadows based on
        statistical analysis of intensity profiles along the lines that compose the B-scan image. Results demonstrate that this detection improves the accuracy of 
        <span class="math" align="left">3 
        <hi rend="it">D</hi></span>reconstruction of intraoperative ultrasound.</p>
      </subsection>
      <subsection level="2" id="uid49">
        <bodyTitle>Multimodal and deformable validation phantom</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Hellier</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Xavier</firstname>
            <lastname>Morandi</lastname>
          </person>
        </participants>
        <p>The validation of registration processes is difficult when no ground truth is available. In the context of image-guided neurosurgery, the validation of non-rigid registration of ultrasound
        images is particularly needed and yet very challenging. We have designed a polyvinyl-alcohol (PVA) phantom to mimic the elastic properties of the human tissues. The phantom can be
        mechanically deformed and imaged with ultrasound and magnetic resonance imaging modalities. So as to provide a ground truth to validate the estimaion of deformations, fiducials were
        introduced. The use of chemical contrast agents makes it possible to change the 
        <span class="math" align="left"><hi rend="it">T</hi>1</span>value of the fiducials (thus changing the contrast in the MR images) without changing the echogeneicity of the fiducial. This phantom is also intended to be used
        for other validation purposes such as segmentation, reconstruction and enoising methods. Further work is needed to disseminate the validation phantom and the evaluation platform.</p>
      </subsection>
      <subsection level="2" id="uid50">
        <bodyTitle>Surface-based intraoperative imagery in neurosurgery</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Perrine</firstname>
            <lastname>Paul</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Jannin</lastname>
          </person>
        </participants>
        <p>Research on intra operative anatomical brain deformations focused on detection, quantification and tracking of surface brain deformations. The objective was to provide the surgeon with
        cheap, robust and reliable quantitative information about anatomical surface deformations during surgery. Following the development of brain operative surface acquisition system using
        stereovision from images of surgical microscope, we introduced a method for anatomical features video tracking from surgical microscope video flow. From this video tracking method, we
        introduced a new surface registration method. This method includes 3 terms: one is related to image intensity similarities, one is related to geometrical distance and the third one is related
        to the anatomical features tracked in video. This surface registration method is adapted to the 3D reconstructed surface from stereoscopic images. It allows precise and robust computation of
        deformation fields between brain surfaces. Performance evaluation showed high improvement of accuracy in comparison with usual registration methods, such as ICP. The method for brain surface
        acquisition was published in  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid23" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>and preliminary results for the registration
        method in  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid24" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>. This approach is limited to cortical
        surface deformations quantification. However it provides an interesting real-time constraint for volumetric approach. Video tracking in surgical microscope images is also a new challenging
        area.</p>
      </subsection>
      <subsection level="2" id="uid51">
        <bodyTitle>Surgical Workflows and Integration of pre- and intra-operative information for neurosurgical procedure</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Omar</firstname>
            <lastname>El Ganaoui</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Jannin</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Xavier</firstname>
            <lastname>Morandi</lastname>
          </person>
        </participants>
        <p>Research on modelling surgical procedures focused on understanding of complexity and extent of the surgical work domain to be modelled. The main long term objective consists in defining a
        global methodology for surgical modelling as well as for the identification of the different surgical aspects to be modelled. Collaborations were set up with the ICCAS research institute
        (International Center of Computer Assisted Surgery) from Leipzig University (Germany) and the GRESICO (Groupe de REcherche en Sciences de l'Information et de la COgnition) laboratory from the
        Université de Bretagne Sud in Vannes (France). With the german ICCAS group, we refined and adapted a methodology previously defined in the lab for surgical modelling  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid25" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>. We have demonstrated the importance of
        using upper level ontology for surgical ontology [2]. Then, we identified the different phases for data acquisition, analysis, treatment and visualization adapted to surgical models [3]. With
        the GRESICO lab, we are starting discussions for defining a methodology for specifying different surgical aspects to be modelled. A method based on abstraction hierarchy is under development.
        Two publications were accepted in international conferences which served as a basis for a PROCOPE funding proposal submitted in May 2006 (result expected in December 2006). Discussions and
        works with the ICCAS group started in November 2004 were used as a basis for the creation of a new DICOM group (WG 24: "DICOM in Surgery"). P. Jannin is a co-chair of one of the 10 project
        groups constituting the WG 24. Finally, these topics are an important part of the ITEA proposal submitted in September 2006 which gathers major European actors in computer assisted radiology
        and surgery. Complexity of this project requires an international collaborative work involving different surgical disciplines. This conceptual approach has to be used in a clinical context
        for identifying added values and for publications. The initial investment is heavy but the issue is directly proportional. Resulting applications may impact surgical planning, surgical
        performance as well as surgical education.</p>
      </subsection>
    </subsection>
    <subsection level="1" id="uid52">
      <bodyTitle>Medical Image Computing in Multiple Sclerosis</bodyTitle>
      <subsection level="2" id="uid53">
        <bodyTitle>Spatio-temporal segmentation of evolving 3D structures, application to segmentation of Multiple Sclerosis lesions</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Laure</firstname>
            <lastname>Aït-Ali</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sean</firstname>
            <lastname>Morrissey</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Béatrice</firstname>
            <lastname>Carsin-Nicol</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Gilles</firstname>
            <lastname>Edan</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>Multiple sclerosis (MS) is a prototype inflammatory autoimmune disorder of the central nervous system. Today, clinical markers are used for the diagnosis as well as for drugs assessment.
        However, these markers are subjective and show poor inter- and intra-rater reliability. Magnetic resonance imaging (MRI) becomes a mandatory surrogate exam for a better understanding of the
        disease. To make the lesions detection less fastidious and error prone, we have proposed to automatically segment MS lesions over time in longitudinal MR multi-sequences.</p>
        <p>We use a robust algorithm that allows the spatio-temporal segmentation of the abnormalities and propose an original rejection scheme for outliers. Our approach comes from a parametric
        clustering segmentation method, which uses multi-sequence intensities coming from the processed MR volumes. The parameters are robustly computed using a new estimator: the Trimmed Likelihood
        Estimator. Three MS lesions subtypes are then extracted among the outliers: enhancing lesions, T1 ``black holes'' and T2 hyper-intense lesions.</p>
        <p>Our algorithm is calibrated on simulated data for various artifacts. Our main results for this year was to extensively calibrate the method in order to quantitatively validate it on MS
        patients scans  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid26" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid27" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, 
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid28" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>.</p>
      </subsection>
      <subsection level="2" id="uid54">
        <bodyTitle>Automatic Characterisation of the Normal Appearing White Matter (NAWM) in Multiple Sclerosis</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Mathieu</firstname>
            <lastname>Monziol</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sean</firstname>
            <lastname>Morrissey</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>The purpose of this work is to propose an automatic approach to analyse the variations of the intensities of brain tissues in Magnetic Resonance Images, variations which are not visible by
        human inspection but which nevertheless characterise a pathological evolution of the subject's brain tissues. The problem can be regarded either in term of variation of MRI intensities with
        regard to a "normal" model (differentiation of a subject in a study of group), or in term of a non visible variation of intensities in longitudinal MRI sequences on the same patient. The
        application of this concerns Multiple Sclerosis where it was recently shown that variations of intensities not visible by human inspection are relevant and give quantitative indicators of the
        evolution of the Multiple Sclerosis pathology.</p>
      </subsection>
    </subsection>
    <subsection level="1" id="uid55">
      <bodyTitle>Computational morphometry in Parkinsonian disorders</bodyTitle>
      <subsection level="2" id="uid56">
        <bodyTitle>Voxel based Morphometry in parkinsonian disorders</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Simon</firstname>
            <lastname>Duchesne</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Bernard</firstname>
            <lastname>Gibaud</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>Reported error rates for initial clinical diagnosis in Parkinsonian disorders can reach up to 35%. Reducing this initial error rate is an important research goal. The objective of this
        work is to evaluate the ability of automated MR-based classification techniques in the differential diagnosis of Parkinson's disease (PD), multiple systems atrophy (MSA) and progressive
        supranuclear palsy (PSP) patients.</p>
        <p>The Neuroprotection and Natural history in Parkinsonian Plus Syndromes (NNIPPS) is a European-funded randomized, multi-centric clinical trial of MSA and PSP that aims to assess the
        neuroprotective effect of riluzole. The imaging component of the NNIPPS study has collected over 630 MRI scans at baseline. Additionally, the Movement Disorders clinic at the Centre
        Hospitalier Universitaire de Rennes has performed over 100 scans of subjects with either probable MSA/PSP or PD. All of these scans are or will be used in our analyses.</p>
        <p>A preliminary study  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid29" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>was conducted on 10 probable PD patients and
        10 patients with diagnostic of either probable MSA or PSP. T1-weighted (T1w) MR images were processed using an appearance-based technique built on extracted patterns of tissue transformations
        and deformations. Classification accuracy (agreement with long-term clinical follow-up) reached 85%, demonstrating the potential of such an approach. In parallel, an MRI-based atlas of the
        pons and a specific brainstem segmentation protocol were developed to perform three-dimensional pontine volumetry in young adults  
        <ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="#visages-2006-bid30" location="biblio" xyref="1262475508006" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest"/>, aging and Parkinsonian diseases.</p>
      </subsection>
      <subsection level="2" id="uid57">
        <bodyTitle>Surface-based Morphometry in Parkinsonian disorders</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Duygu</firstname>
            <lastname>Tosun</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Simon</firstname>
            <lastname>Duchesne</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>MR imaging had played an important role in diagnosis of numerous neurodegenerative disorders. It was recently that MRI was considered useful in establishing a differential diagnosis in
        Parkinson's Plus Disorder (PPD) patients. The objective of this project is to develop a cortical morphometry analysis framework to better understand the alteration on the brain structure due
        to PPD and propose a diagnosis framework differentiating Multiple System Atrophy (MSA) and Progressive supranuclear palsy (PSP) complementary to intensity-based MRI analysis. Affects (e.g.,
        atrophy, disturbance) on the cortical geometry will be quantified using the local and regional cortical complexity measures (i.e., shape index, curvedness, and regional bending energy),
        measures on sulcal depth and width, and gray matter tissue density (i.e., cortical thickness). A statistical analysis on these cortical features will be carried out to test for population
        related (MSA versus PSP versus PD) shape differences.</p>
      </subsection>
    </subsection>
    <subsection level="1" id="uid58">
      <bodyTitle>Anatomical and functionnal imaging in dysphasia</bodyTitle>
      <participants>
        <person key="PASUSERID">
          <firstname>Clément</firstname>
          <lastname>De Guibert</lastname>
        </person>
        <person key="PASUSERID">
          <firstname>Simon</firstname>
          <lastname>Duchesne</lastname>
        </person>
        <person key="PASUSERID">
          <firstname>Pierre</firstname>
          <lastname>Jannin</lastname>
        </person>
        <person key="PASUSERID">
          <firstname>Christian</firstname>
          <lastname>Barillot</lastname>
        </person>
      </participants>
      <p>Dysphasia is a developmental language-structural disorder in children that have currently received no neurobiological explanation. Morphometric (MRI) and functional (SPECT) neuroimaging have
      previously provided a few but inconstant results, implicating in some cases the language-related cerebral regions, although without clear localization and lateralisation. In the present
      research, we study with functional (fMRI) and diffusion-weighted MRI (DW-MRI) a population of dysphasic children from 7 to 14 years old, compared with paired normal children, with the aim to
      better figure out the localization and the lateralisation of anatomical and functional cerebral abnormalities in this disorder, by means of actual neuroimaging techniques and image processing.
      The project takes place in the context of a delegation of Clément De Guibert from the University of Rennes II Linguistics Department (Assistant Professor at UHB Rennes II) to INRIA (Project /
      Unit Visages, U746), and is achieved with the collaboration of the Radiology and Medical Imagery Department and the Reference Center of developmental language disorders of the University
      Hospital of Rennes (CHU, Pontchaillou).</p>
    </subsection>
  </resultats>
  <contrats id="uid59">
    <bodyTitle>Contracts and Grants with Industry</bodyTitle>
    <subsection level="1" id="uid60">
      <bodyTitle>Contracts and Grants with Industry</bodyTitle>
      <subsection level="2" id="uid61">
        <bodyTitle>contrats</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Eric</firstname>
            <lastname>Poiseau</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Bernard</firstname>
            <lastname>Gibaud</lastname>
          </person>
        </participants>
        <p>IHE</p>
        <p>Since 2001, the IDM Laboratory has been involved with IHE since its beginning in Europe. It organized the European connect-a-thons and contributed to the development of the European part
        of IHE. In order to better manage the IHE Connect-a-thon, a web tool known as Kudu was developed within the laboratory. Kudu consists of a database and a set of PHP scripts. The role of Kudu
        is to manage "the registration of companies to the connect-a-thon", "the configuration of the systems", and "the test to be performed by system before and during the connect-a-thon". The Kudu
        tool is now used for the management of the North American and Japanese connect-a-thons.</p>
        <p>Following the merging of the IDM laboratory and the Visages Unit/Project, IHE became a development project of INRIA hosted by IRISA. The new project is lead by Eric Poiseau, hosts an
        associate engineer and will soon recruit 2 expert engineers. This new project will still organize the European connect-a-thon, manage at the European level the development of tools for the
        evaluation of the implementation of IHE within companies product. Aside those activities, IHE Development will try to provide connections between INRIA research project and industry in the
        field of healthcare IT</p>
      </subsection>
      <subsection level="2" id="uid62">
        <bodyTitle>contrats</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Perrine</firstname>
            <lastname>Paul</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Jannin</lastname>
          </person>
        </participants>
        <p>Medtronic: Cifre convention</p>
        <p>
          <i>duration : 36 months, until 31/12/2006</i>
        </p>
        <p>This contract is dedicated to support the Cifre convention between Medtronic and Irisa/University of Rennes 1 regarding Perrine Paul's Ph.D. The goal of the Ph.D. is to enable
        augmented reality in the surgical room by using the outputs of the surgical microscope cameras for the development of brain operative surface acquisition using stereovision from images of
        surgical microscope.</p>
      </subsection>
    </subsection>
  </contrats>
  <international id="uid63">
    <bodyTitle>Other Grants and Activities</bodyTitle>
    <subsection level="1" id="uid64">
      <bodyTitle>Regional initiatives</bodyTitle>
      <subsection level="2" id="uid65">
        <bodyTitle>PRIR contract of Brittany region council PlogICI</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Alban</firstname>
            <lastname>Gaignard</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Daniel</firstname>
            <lastname>Garcia-Lorenzo</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Vincent</firstname>
            <lastname>Gratsac</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Bernard</firstname>
            <lastname>Gibaud</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Hellier</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Jannin</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>
          <i>duration : 36 months, until 31/12/2006</i>
        </p>
        <p>This two-year project is devoted to the development of a software platform dedicated to clinical neuroimaging and image guided neurosurgery applications. The objective is to build a
        software core made of proprietary libraries (e.g. Vistal) and public libraries available in the domain of 3D medical imaging or 3D rendering (e.g. VTK, ITK ...).</p>
      </subsection>
      <subsection level="2" id="uid66">
        <bodyTitle>AMStrIC project</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Laure</firstname>
            <lastname>Aït-Ali</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>
          <i>duration : 36 months, until 31/12/2006</i>
        </p>
        <p>This three-year project is devoted to the development of a solution for processing MRI data for the purpose of detecting MS lesions from spatiotemporal observations. This grant is being
        used for partially funding the position of Laure Aït-Ali.</p>
      </subsection>
      <subsection level="2" id="uid67">
        <bodyTitle>SIMUPACE project</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Jérémy</firstname>
            <lastname>Lecoeur</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>
          <i>duration : 36 months, from 01/11/2006</i>
        </p>
        <p>This three years project is devoted to the development of a solution for processing medical images from multi-dimensional signatures in order to study brain pathologies and to segment
        brain structures with complex image representation. This grant is being used for founding the position of Jérémy Lecoeur.</p>
      </subsection>
    </subsection>
    <subsection level="1" id="uid68">
      <bodyTitle>National initiatives</bodyTitle>
      <subsection level="2" id="uid69">
        <bodyTitle>ANR ``Technologies Logicielles'', NeuroLOG Project</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Lynda</firstname>
            <lastname>Temal</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sean-Patrick</firstname>
            <lastname>Morrissey</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Gilles</firstname>
            <lastname>Edan</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Bernard</firstname>
            <lastname>Gibaud</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>
          <i>duration : 36 months, from 01/10/2006</i>
        </p>
        <p>The NeuroLOG project has for objective to build a software environment in an open environment for the integration of resources in medical imaging (data, images and also image processing
        tools) and to confront this environment to target applications coming mainly from the neuroimaging and the oncology domains. This project intends to address problems related to:</p>
        <simplelist>
          <li id="uid70">
            <p>The management and the access to semi-structured heterogenous and distributed data in an open environment;</p>
          </li>
          <li id="uid71">
            <p>The control and the security of the access of the sensitive medical data;</p>
          </li>
          <li id="uid72">
            <p>The control of data and computing workflows involved in high demanding processing procedures by accessing grid computing infrastructures;</p>
          </li>
          <li id="uid73">
            <p>The extraction and the quantification of parameters for relevant application such as multiple sclerosis, strokes and brain tumours.</p>
          </li>
        </simplelist>
        <p>In addition to our Unit/Project and the Paris project from IRISA, this grant is conducted by CNRS/I3S at Sophia-Antipolis and is performed in collaboration with INRIA team Asclepios
        (Sophia-Antipolis), INSERM unit U594 from Grenoble, IFR 49 "Functional Neuroimagery" (Paris La Pitié Salpêtrière), the CNRS/LARIA at Amiens and Business Objects and Visioscopie for the
        industrial part.</p>
      </subsection>
    </subsection>
    <subsection level="1" id="uid74">
      <bodyTitle>International initiatives</bodyTitle>
      <subsection level="2" id="uid75">
        <bodyTitle>INRIA Associated Project NeurOMIMe</bodyTitle>
        <participants>
          <person key="PASUSERID">
            <firstname>Pierre</firstname>
            <lastname>Hellier</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sylvain</firstname>
            <lastname>Prima</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Sean-Patrick</firstname>
            <lastname>Morrissey</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Xavier</firstname>
            <lastname>Morandi</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Simon</firstname>
            <lastname>Duchesne</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Pierrick</firstname>
            <lastname>Coupe</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Laure</firstname>
            <lastname>Aït-Ali</lastname>
          </person>
          <person key="PASUSERID">
            <firstname>Christian</firstname>
            <lastname>Barillot</lastname>
          </person>
        </participants>
        <p>
          <i>duration : 24 months, from 01/01/2006</i>
        </p>
        <p>NeurOMIMe 
        <footnote id="uid76" place="foot" anchored="yes"><ref xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://www.irisa.fr/visages/documents/FormulaireNeurOMIMe.html" location="extern" xyref="2562613652031" xlink:show="replace" xlink:type="simple" xlink:actuate="onRequest">
          http://www.irisa.fr/visages/documents/FormulaireNeurOMIMe.html</ref></footnote>stands for "Objective Medical Image Methods Evaluation for Neurological and Neurosurgical Procedures". This International INRIA action is coordinated by Christian Barillot
        (Visages) and Louis Collins (IPL, Univ. McGill) and relates research dealing with medical image processing in clinical neurosciences performed in both collaborative sites: IRISA/Visages on
        one part and the Image Processing Laboratory of the McConnell Brain Imaging Centre at the Montreal Neurological Institute (Univ. Mc Gill, Montreal, Canada) on the other part.</p>
        <p>One important research objective in neuroimaging is to create anatomical and functional cerebral maps under normal and pathological conditions. The goal of this INRIA associated
        project-team is to combine the respective research efforts in clinical neuroinformatics of the VisAGeS and IPL teams, and thus benefit from the resulting cross-fertilization. We aim at
        addressing specific aspects of medical image processing for the purpose of neurological diseases analysis and their treatment through surgery. Both teams have significant experience in
        developing medical imaging software aimed at:</p>
        <simplelist>
          <li id="uid77">
            <p>improving neurosurgical practice through pre-operative planning, intra-operative guidance and imaging of brain deformations;</p>
          </li>
          <li id="uid78">
            <p>improving neurological exploitation of the spatio-temporal and multiparametric MRI data produced in the context of brain diseases (e.g. multiple sclerosis -MS- lesions); and</p>
          </li>
          <li id="uid79">
            <p>improving basic understanding of brain anatomy and cerebral function by using computerized procedures to model their relationship, especially in the context of the effect of pathology
            on brain structures (e.g. epilepsy, dementia, neurodegenerative diseases).</p>
          </li>
        </simplelist>
        <p>Through this project, the two teams will share their own, but complementary, expertise by distributing algorithms and data dealing within the clinical needs described above, in order to
        compare and cross-validate the different procedures developed at each site; then improve on the excellence and efficiency of these procedures.</p>
      </subsection>
    </subsection>
  </international>
  <diffusion id="uid80">
    <bodyTitle>Dissemination</bodyTitle>
    <subsection level="1" id="uid81">
      <bodyTitle>Leadership within the scientific community</bodyTitle>
      <subsection level="2" id="uid82">
        <bodyTitle>Editorial board of journals</bodyTitle>
        <simplelist>
          <li id="uid83">
            <p>C. Barillot is Associate Editor of IEEE Transactions on Medical Imaging (IEEE-TMI).</p>
          </li>
          <li id="uid84">
            <p>C. Barillot is Associate Editor of Medical Image Analysis (MedIA).</p>
          </li>
          <li id="uid85">
            <p>C. Barillot serves in the peer review committee of the Journal of Computer Assisted Tomography.</p>
          </li>
          <li id="uid86">
            <p>C. Barillot serves in the peer review committee of Neuroimage.</p>
          </li>
        </simplelist>
      </subsection>
      <subsection level="2" id="uid87">
        <bodyTitle>Peer Reviews of journals</bodyTitle>
        <simplelist>
          <li id="uid88">
            <p>Reviewing process for IEEE TMI (CB, PH, SP, PJ, BG), Medical Image Analysis (CB, PH, SP)</p>
          </li>
        </simplelist>
      </subsection>
      <subsection level="2" id="uid89">
        <bodyTitle>Conference board organization</bodyTitle>
        <simplelist>
          <li id="uid90">
            <p>C. Barillot was scientific chair of the Inria-Industries meeting co-sponsored by INSERM and dedicated on "Information, Communication and Sciences Technologies to assist Medicine ",
            Rocquencourt, jan. 2006</p>
          </li>
        </simplelist>
      </subsection>
      <subsection level="2" id="uid91">
        <bodyTitle>Technical Program Committees (TPC) of conferences</bodyTitle>
        <simplelist>
          <li id="uid92">
            <p>C. Barillot was area chair for SPIE Medical Imaging 2006, and TPC member for ECEH'06, ECCV/CVAMIA'06, JETIM'06, MIAR'06, MICCAI'06, MMBIA'06, WBIR'06</p>
          </li>
          <li id="uid93">
            <p>B. Gibaud was TPC member for CARS 2006</p>
          </li>
          <li id="uid94">
            <p>P. Jannin was TPC member for SPIE Medical Imaging 2006, CARS 2006</p>
          </li>
          <li id="uid95">
            <p>P. Hellier was TPC member of MICCAI 2006, RFIA 2006, IEEE ISBI 2006, MMBIA 2006</p>
          </li>
          <li id="uid96">
            <p>S. Prima was TPC member of MICCAI 2006, IEEE ISBI 2006</p>
          </li>
        </simplelist>
      </subsection>
      <subsection level="2" id="uid97">
        <bodyTitle>Scientific societies</bodyTitle>
        <simplelist>
          <li id="uid98">
            <p>P. Jannin is General Secretary of ISCAS</p>
          </li>
          <li id="uid99">
            <p>B. Gibaud is member of the AIM</p>
          </li>
          <li id="uid100">
            <p>C. Barillot, S. Duchesne and P. Jannin are members of IEEE EMBS</p>
          </li>
          <li id="uid101">
            <p>C. Barillot, S. Duchesne, P. Hellier, P. Jannin, S. Prima are members of the MICCAI society</p>
          </li>
        </simplelist>
      </subsection>
    </subsection>
    <subsection level="1" id="uid102">
      <bodyTitle>Teaching</bodyTitle>
      <p>Teaching on 3D Medical Imaging (visualization, segmentation, fusion, management, normalization) in the following tracks:</p>
      <simplelist>
        <li id="uid103">
          <p>DIIC-INC, IFSIC, University of Rennes I : 2h ( 
          <i>C. Barillot</i>), 2h ( 
          <i>P. Hellier</i>), 2h ( 
          <i>P. Jannin</i>), 2h ( 
          <i>S. Prima</i>)</p>
        </li>
        <li id="uid104">
          <p>Master 2 SIBM, University of Angers-Brest-Rennes : 26h ( 
          <i>C. Barillot, S. Prima, B. Gibaud, P. Jannin, X. Morandi, S.P. Morrissey</i>), C. Barillot, B. Gibaud and P. Jannin are responsible for three different semesters.</p>
        </li>
        <li id="uid105">
          <p>Master "Rayonnements ionisants et application ", Univ. de Nantes: 4h ( 
          <i>C. Barillot</i>)</p>
        </li>
        <li id="uid106">
          <p>Master "Méthodes de traitement de l'information biomédicale", University of Rennes I : 6h ( 
          <i>B. Gibaud</i>)</p>
        </li>
        <li id="uid107">
          <p>Master "Equipements biomédicaux", UTC Compiègne: 3h ( 
          <i>B. Gibaud</i>)</p>
        </li>
        <li id="uid108">
          <p>Master " Signaux et Images en Médecine ", University Paris XII Val de Marne: 3h ( 
          <i>B. Gibaud</i>)</p>
        </li>
        <li id="uid109">
          <p>European School for Medical Physics:3h ( 
          <i>P. Jannin</i>)</p>
        </li>
      </simplelist>
    </subsection>
    <subsection level="1" id="uid110">
      <bodyTitle>Participation to seminars, scientific evaluations, awards</bodyTitle>
      <simplelist>
        <li id="uid111">
          <p>B. Gibaud is member of the CSS 7 evaluation committee of INSERM</p>
        </li>
        <li id="uid112">
          <p>C. Barillot was member of the INSERM admission jury for CR2 and CR1 positions</p>
        </li>
        <li id="uid113">
          <p>B. Gibaud served as expert for ANR (TecSan and Masse de données)</p>
        </li>
        <li id="uid114">
          <p>C. Barillot served as external reviewer of an FP6 IST integrated Project</p>
        </li>
        <li id="uid115">
          <p>C. Barillot served as expert for ANR "Programme Blanc"</p>
        </li>
        <li id="uid116">
          <p>P. Hellier served as expert for PAI "France-Israel"</p>
        </li>
      </simplelist>
    </subsection>
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    </biblStruct>
  </biblio>
</raweb>
