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Dear all, <br>
<p> We are pleased to announce the SIB course: <br>
<br>
<b> </b><b>"NGS - Genome variant analysis</b><b>"</b><b>, 30 - 31
May 2017, in Bern.</b><br>
<br>
The detection of genetic changes using diverse next generation
sequencing technologies e.g. whole genome, whole exome, RNA and
target sequencing has several applications in genomics and other
omics fields. The unbiased reliable detection of variants remains
a challenge for many.<br>
This two-days course targets biologists and computational
biologists. We will mainly introduce and practice the methodology
for detecting germline mutations by validating mapping data,
realigning regions of interest to reduce false discovery and
calling for known variants as well as de novo discoveries.<br>
<br>
Further detailed information, prerequisites and application form
are available from <a
href="http://www.sib.swiss/training/upcoming-training-events/2017-05-ngs2-variant">here</a>.<br>
Any question? Don't hesitate to contact us at <a
class="moz-txt-link-abbreviated"
href="mailto:training@sib.swiss">training@sib.swiss</a>.<br>
<br>
Best wishes,<br>
Patricia Palagi</p>
<br>
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