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<font face="Helvetica, Arial, sans-serif">Dear all, <br>
<br>
We are pleased to announce a course from SIB / Staromics doctoral
program entitled: <br>
<br>
<strong>"</strong><strong>Exploring common and rare diseases
genetics with GWAS and NGS"</strong>.<br>
<br>
This four-day course, which will be held in <b>Lausanne </b>during
the week of <b>16-19 March 2015</b>, will be dedicated to
genome-wide analysis of variation including GWAS, next generation
sequencing (NGS) and how to identify and interpret variants in
exomes. The course will also introduce techniques to extend GWAS
using NGS data. </font>
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<p> </p>
<p><font face="Helvetica, Arial, sans-serif"> Further information
and application form are available from <a
href="http://edu.isb-sib.ch/course/view.php?id=203">http://edu.isb-sib.ch/course/view.php?id=203</a><br>
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<font face="Helvetica, Arial, sans-serif"> <br>
For administrative questions, please contact <a
moz-do-not-send="true" href="mailto:staromics@cuso.ch">staromics@cuso.ch
</a><br>
For technical and scientific questions, please contact <a
moz-do-not-send="true" href="mailto:training@isb-sib.ch">training@isb-sib.ch</a><br>
<br>
Hope to see you there!<br>
<br>
For the organizers,<br>
Grégoire Rossier</font>
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