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<th align="RIGHT" nowrap="nowrap" valign="BASELINE">Sujet: </th>
<td>SYMPOSIUM : New genomics toward personalized medicine
LILLE - October 2013 10th</td>
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<th align="RIGHT" nowrap="nowrap" valign="BASELINE">Date: </th>
<td>Wed, 12 Jun 2013 17:00:49 +0200</td>
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<th align="RIGHT" nowrap="nowrap" valign="BASELINE">De: </th>
<td>Véronique Dhennin <a class="moz-txt-link-rfc2396E" href="mailto:veronique.dhennin@good.ibl.fr"><veronique.dhennin@good.ibl.fr></a></td>
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<th align="RIGHT" nowrap="nowrap" valign="BASELINE">Pour: </th>
<td>Veronique_Dhennin <a class="moz-txt-link-rfc2396E" href="mailto:vdhennin@good.ibl.fr"><vdhennin@good.ibl.fr></a></td>
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<p class="MsoTitle" style="margin-top:0cm;margin-right:-1.15pt;
margin-bottom:6.0pt;margin-left:0cm;mso-add-space:auto;text-align:center;
tab-stops:4.0cm;border:none;mso-padding-alt:0cm
0cm 0cm 0cm" align="center"><b style="mso-bidi-font-weight:normal"><span
style="font-size: 15pt;" lang="EN-US"><font color="#ff6600">We
are pleased to invite you to our next symposium related to
NGS : </font><br>
</span></b></p>
<p class="MsoTitle" style="margin-top:0cm;margin-right:-1.15pt;
margin-bottom:6.0pt;margin-left:0cm;mso-add-space:auto;text-align:center;
tab-stops:4.0cm;border:none;mso-padding-alt:0cm
0cm 0cm 0cm" align="center"><b style="mso-bidi-font-weight:normal"><span
style="font-size: 15pt;" lang="EN-US"><br>
<font color="#333399">New genomics toward personalized
medicine<o:p></o:p></font></span></b></p>
<font color="#333399"> </font>
<p class="MsoNormalCxSpFirst" style="margin-top:0cm;margin-right:
-1.15pt;margin-bottom:6.0pt;margin-left:0cm;mso-add-space:auto;text-align:center;
line-height:normal" align="center"><font color="#333399"><b
style="mso-bidi-font-weight:normal"><span style="font-size:
15pt;" lang="EN-US"><span style="mso-tab-count:1"> </span>Lille
Genomics
European symposium, 10th of October 2013<o:p></o:p></span></b></font></p>
<font color="#333399"> </font>
<p class="MsoNormalCxSpMiddle" style="margin-top:0cm;margin-right:
-1.15pt;margin-bottom:6.0pt;margin-left:0cm;mso-add-space:auto;text-align:center;
line-height:normal" align="center"><font color="#333399"><span
style="font-size: 14pt;">Institut de Biologie de Lille –
Campus Pasteur – Rue du Professeur Calmette - Lille<b
style="mso-bidi-font-weight:normal"><o:p></o:p></b></span></font></p>
<font color="#333399"> </font>
<p class="MsoNormal" style="margin-bottom:0cm;margin-bottom:.0001pt"><font
color="#333399"><b style="mso-bidi-font-weight:normal"><span
style="font-size: 14pt; line-height: 115%;"><o:p> <br>
</o:p></span></b></font></p>
<font color="#333399"> </font>
<p class="MsoNormal" style="text-align:center" align="center"><b
style="mso-bidi-font-weight: normal"><span
style="font-size:14.0pt;line-height:115%;color:#17365D;
mso-themecolor:text2;mso-themeshade:191;mso-ansi-language:EN-US"
lang="EN-US"><font color="#333399">Online Details &
Registration: <span style="mso-spacerun:yes"></span><a
moz-do-not-send="true" class="moz-txt-link-freetext"
href="http://www-good.ibl.fr/index.php/symposium-october2013">http://www-good.ibl.fr/index.php/symposium-october2013</a></font><br>
</span></b></p>
<p class="MsoNormal" style="text-align:center" align="center"><b
style="mso-bidi-font-weight:normal"><span
style="font-size:14.0pt;line-height:
115%;color:#17365D;mso-themecolor:text2;mso-themeshade:191"><br>
<font color="#ff6600">Registration FREE - Number of seats
limited !!!</font><br>
</span></b></p>
<p class="MsoNormal" style="text-align:center" align="center"><b
style="mso-bidi-font-weight:normal"><span
style="font-size:14.0pt;line-height:
115%;color:#17365D;mso-themecolor:text2;mso-themeshade:191"><br>
</span></b><font color="#ff6600"><b
style="mso-bidi-font-weight:normal"><span style="font-size:
14pt; line-height: 115%;">Please forward this message to
your contacts</span></b></font></p>
<p class="MsoNormal" style="text-align:center" align="center"><font
color="#ff6600"><b style="mso-bidi-font-weight:normal"><span
style="font-size: 14pt; line-height: 115%;">Program : see
below<br>
</span></b></font></p>
<p class="MsoNormal" style="text-align:center" align="center"><b
style="mso-bidi-font-weight:normal"><span
style="font-size:14.0pt;line-height:
115%;color:#17365D;mso-themecolor:text2;mso-themeshade:191"><font
color="#ff6600">Look forward to meet you there</font><br>
</span></b></p>
<p class="MsoNormal" style="text-align:center" align="center"><br>
<b style="mso-bidi-font-weight: normal"><span
style="font-size:14.0pt;line-height:115%;color:#17365D;
mso-themecolor:text2;mso-themeshade:191;mso-ansi-language:EN-US"
lang="EN-US"></span></b><span
style="font-size:14.0pt;line-height:115%;mso-ansi-language:EN-US"
lang="EN-US"><o:p></o:p></span></p>
<br>
<b style="mso-bidi-font-weight:normal"><span
style="font-size:14.0pt;mso-ansi-language:EN-US" lang="EN-US"><font
color="#333399">Program (subject to modifications)<br>
<br>
</font><o:p></o:p></span></b>
<p class="MsoNormal" style="tab-stops:70.9pt"><span
style="font-family: "Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US">8h45<span style="mso-tab-count:1">
</span>Registration / Posters installation<o:p></o:p></span></p>
<p class="MsoNormal" style="tab-stops:70.9pt"><span
style="font-family: "Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US">9h00<span style="mso-tab-count:1">
</span>Introduction of the day<o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">9h15</span><span
style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1">
</span>Keynote lecture 1: <b
style="mso-bidi-font-weight:normal">Joris Veltman</b> (N): <span
style="color:#548DD4;mso-themecolor:text2;mso-themetint:153">"Exome
sequencing
identifies disease causing de novo mutations"</span>. <span
class="st"><i style="mso-bidi-font-style:normal">Department of
Human Genetics. Radboud University Nijmegen Medical Centre.
Nijmegen, The Netherlands</i></span><o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">10h00
</span><span style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1"> </span><b
style="mso-bidi-font-weight: normal">Jean Muller</b> (F): <span
style="color:#548DD4;mso-themecolor:text2; mso-themetint:153">"Multi-gene
resequencing for molecular diagnosis of obesity"</span>. </span><i
style="mso-bidi-font-style:normal"><span
style="font-family:"Arial
Narrow","sans-serif";mso-bidi-font-family:
Arial;mso-ansi-language:EN-US" lang="EN-US">Integrative
Genomics and Bioinformatic Laboratory (IGBMC) - Genetic
Diagnostic Laboratory – Strasbourg, France</span></i><i
style="mso-bidi-font-style:normal"><span
style="font-family:"Arial
Narrow","sans-serif"; mso-ansi-language:EN-US"
lang="EN-US"><o:p></o:p></span></i></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US">10h30 <span style="mso-tab-count:1">
</span>Coffee break and poster viewing<o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">11h00
</span><span style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1"> </span><b
style="mso-bidi-font-weight: normal">Amélie Bonnefond</b> (F):
<span style="color:#548DD4;mso-themecolor:
text2;mso-themetint:153">"New technologies in gene
resequencing and in methylome analysis"</span>. <i
style="mso-bidi-font-style:normal">Department of Genomics and
Metabolic Diseases- CNRS UMR8199 & Institut de Biologie de
Lille - Institut Pasteur, Lille, France<o:p></o:p></i></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">11h30
</span><span style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1"> </span>Agilent R
& D: <span
style="color:#548DD4;mso-themecolor:text2;mso-themetint:153">Haloplex
a new method for resequencing</span> <o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">12h00
</span><span style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1"> </span>Illumina
R & D: <span
style="color:#548DD4;mso-themecolor:text2;mso-themetint:153">Perspectives
in genome sequencing</span><o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US">12h30<span style="mso-tab-count:1">
</span>Lunch<o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">13h45</span><span
style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1"> </span><b
style="mso-bidi-font-weight: normal">Ludovic Dupont</b>: <span
style="color:#548DD4;mso-themecolor:text2; mso-themetint:153">"Structure,
missions, achievements after one year of existence"</span>. <i
style="mso-bidi-font-style:normal">Plateforme maladies rares,
Paris, France</i><o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt"><span style="font-family:
"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:text2;mso-themetint:153;mso-ansi-language:EN-US"
lang="EN-US">14h00</span><span style="font-family: "Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count: 1">
</span>Keynote lecture 2<span style="mso-spacerun:yes"> </span><b
style="mso-bidi-font-weight:normal">Nicolas Lévy </b>(F): <span
style="color:#548DD4;mso-themecolor:text2;mso-themetint:153">"The
genomics and post genomics of rare diseases: the progeria
case"</span>. <i style="mso-bidi-font-style:normal">Department
of Medical and Development Genetics Inserm U910 <span
style="mso-spacerun:yes"> </span>Faculté de médecine de la
Timone & Department of Medical Genetics - Hôpital
d’enfants de la La Timone, Marseille, France<o:p></o:p></i></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">14h45</span><span
style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1"> </span><b
style="mso-bidi-font-weight: normal">Wim Van Criekinge</b>
(B): <span style="color:#548DD4;mso-themecolor:
text2;mso-themetint:153">"Next generation epigenetic
profiling"</span>. </span><i
style="mso-bidi-font-style:normal"><span style="font-family:
"Arial
Narrow","sans-serif";mso-fareast-font-family:"Times
New Roman"; mso-bidi-font-family:"Courier
New";mso-ansi-language:EN-US;mso-fareast-language: FR"
lang="EN-US">Center in Pharmaco(epi)genomics NXTGNT (</span></i><a
moz-do-not-send="true" href="http://www.nxtgnt.com"><i
style="mso-bidi-font-style:normal"><span
style="font-family:"Arial
Narrow","sans-serif";mso-fareast-font-family:
"Times New
Roman";mso-bidi-font-family:"Courier
New";color:windowtext;
mso-ansi-language:EN-US;mso-fareast-language:FR"
lang="EN-US">www.nxtgnt.com</span></i></a><i
style="mso-bidi-font-style:normal"><span
style="font-family:"Arial
Narrow","sans-serif";
mso-fareast-font-family:"Times New
Roman";mso-bidi-font-family:"Courier New";
mso-ansi-language:EN-US;mso-fareast-language:FR" lang="EN-US">),
Department of Mathematical Modelling, statistics and
Bioinformatics, Ghent University (UGent), Belgium</span></i><span
style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language: EN-US"
lang="EN-US"><o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">15h15</span><span
style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1"> </span>Fluidigm
R& D: <span
style="color:#548DD4;mso-themecolor:text2;mso-themetint:153">digital
PCR for rare even detection / single cell genomics</span><o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US">15h30<span style="mso-tab-count:1">
</span>Coffee break and poster viewing<o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">16h00</span><span
style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1"> </span>Keynote
lecture 3: <b style="mso-bidi-font-weight:normal">Jacques
Beckmann</b> (S): <span
style="color:#548DD4;mso-themecolor:text2;mso-themetint:153">"Copy
number Variants and their role in diseases"</span>. <i
style="mso-bidi-font-style: normal">Department of Clinical
Bioinformatics at Swiss Institute of Bioinformatics (SIB),
Lausanne, Swiss<o:p></o:p></i></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif";color:#548DD4;mso-themecolor:
text2;mso-themetint:153;mso-ansi-language:EN-US" lang="EN-US">16h45
</span><span style="font-family:"Arial
Narrow","sans-serif";mso-ansi-language:EN-US"
lang="EN-US"><span style="mso-tab-count:1"> </span><b
style="mso-bidi-font-weight: normal">Martin Maiden </b>(UK),
<i style="mso-bidi-font-style:normal"><span
style="color:#548DD4;mso-themecolor:text2;mso-themetint:153">title:
to be confirmed</span></i><o:p></o:p></span></p>
<p class="MsoNormal"
style="margin-top:0cm;margin-right:0cm;margin-bottom:8.0pt;
margin-left:70.9pt;text-indent:-70.9pt;tab-stops:70.9pt"><span
style="font-family:"Arial
Narrow","sans-serif"">17h30<span
style="mso-tab-count: 1"> </span>Conclusive
remarks <o:p></o:p></span></p>
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<pre class="moz-signature" cols="72">--
Save the date ! From 20 to 22 September 2013,
First Egid Fall School on "Modeling Diabetes".
Scientific program & informations:
<a moz-do-not-send="true" class="moz-txt-link-freetext" href="http://www-good.ibl.fr/index.php/ecole-egid">http://www-good.ibl.fr/index.php/ecole-egid</a>
Book your calendars on 10 October 2013!
New genomics toward personalized medicine
Lille Genomics European symposium
Details & registration:
<a moz-do-not-send="true" class="moz-txt-link-freetext" href="http://www-good.ibl.fr/index.php/symposium-october2013">http://www-good.ibl.fr/index.php/symposium-october2013</a>
Véronique DHENNIN - Responsable prestations
Génomique et Maladies Métaboliques-UMR 8199
Institut de Biologie de Lille
1 rue du Professeur Calmette
CS 50447
59021 LILLE CEDEX
Tel : + 33 (0)3 20 87 10 44
Fax : + 33 (0)3 20 87 10 31
<a moz-do-not-send="true" class="moz-txt-link-freetext" href="http://www-good.ibl.fr/index.php/services-prestations">http://www-good.ibl.fr/index.php/services-prestations</a>
<a moz-do-not-send="true" class="moz-txt-link-abbreviated" href="mailto:contact@good.ibl.fr">contact@good.ibl.fr</a></pre>
<br>
<pre class="moz-signature" cols="72">--
Olivier Sand, PhD
Responsable Bioinformatique
EGID FR3508 European Genomics Institute for Diabetes
CNRS UMR8199 Genomique et Maladies Metaboliques
Institut de Biologie de Lille
1, Rue du Professeur Calmette B.P. 245
CS 50447
59021 Lille Cedex
France
Tel: 33 (0)3 20 87 10 71
Fax: 33 (0)3 20 87 10 31
<a class="moz-txt-link-abbreviated" href="mailto:olivier.sand@good.ibl.fr">olivier.sand@good.ibl.fr</a>
<a class="moz-txt-link-freetext" href="http://www-good.ibl.fr/">http://www-good.ibl.fr/</a></pre>
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