We are pleased to invite you to our next symposium related to NGS :

New genomics toward personalized medicine

         Lille Genomics European symposium, 10th of October 2013

Institut de Biologie de Lille – Campus Pasteur – Rue du Professeur Calmette - Lille

Online Details & Registration: http://www-good.ibl.fr/index.php/symposium-october2013

  Registration FREE - Number of seats limited !!!

Please forward this message to your contacts

Program : see below

Look forward to meet you there

8h45                      Registration / Posters installation

9h00                      Introduction of the day

9h15                      Keynote lecture 1: Joris Veltman (N): "Exome sequencing identifies disease causing de novo mutations". Department of Human Genetics. Radboud University Nijmegen Medical Centre. Nijmegen, The Netherlands

10h00                    Jean Muller (F): "Multi-gene resequencing for molecular diagnosis of obesity". Integrative Genomics and Bioinformatic Laboratory (IGBMC) - Genetic Diagnostic Laboratory – Strasbourg, France

10h30                    Coffee break and poster viewing

11h00                    Amélie Bonnefond (F): "New technologies in gene resequencing and in methylome analysis". Department of Genomics and Metabolic Diseases- CNRS UMR8199 & Institut de Biologie de Lille - Institut Pasteur, Lille, France

11h30                    Agilent R & D: Haloplex a new method for resequencing

12h00                    Illumina R & D: Perspectives in genome sequencing

12h30                    Lunch

13h45                    Ludovic Dupont: "Structure, missions, achievements after one year of existence". Plateforme maladies rares, Paris, France

14h00                    Keynote lecture 2  Nicolas Lévy (F): "The genomics and post genomics of rare diseases: the progeria case". Department of Medical and Development Genetics Inserm U910  Faculté de médecine de la Timone & Department of Medical Genetics - Hôpital d’enfants de la La Timone, Marseille, France

14h45                    Wim Van Criekinge (B): "Next generation epigenetic profiling". Center in Pharmaco(epi)genomics NXTGNT (www.nxtgnt.com), Department of Mathematical Modelling, statistics and Bioinformatics, Ghent University (UGent), Belgium

15h15                    Fluidigm R& D: digital PCR for rare even detection / single cell genomics

15h30                    Coffee break and poster viewing

16h00                    Keynote lecture 3: Jacques Beckmann (S): "Copy number Variants and their role in diseases". Department of Clinical Bioinformatics at Swiss Institute of Bioinformatics (SIB), Lausanne, Swiss

16h45                    Martin Maiden (UK), title: to be confirmed

17h30                    Conclusive remarks

-- 
Save the date ! From 20 to 22 September 2013,
First Egid Fall School on "Modeling Diabetes".
Scientific program & informations:
http://www-good.ibl.fr/index.php/ecole-egid 

Book your calendars on 10 October 2013!
New genomics toward personalized medicine
Lille Genomics European symposium
Details & registration: 
http://www-good.ibl.fr/index.php/symposium-october2013

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
http://www-good.ibl.fr/index.php/services-prestations
contact@good.ibl.fr

-- 
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
olivier.sand@good.ibl.fr
http://www-good.ibl.fr/