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Dear All,
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<div class="">I am passing on this message on behalf of Mike Zody and members of the working group who have been discussing long read sequencing opportunities. <span style="font-family: Calibri, sans-serif;" class="">As a follow up to our discussions from the
last two CCG meetings, we would like to hear from people about their experiences with and thinking about long read and long range technologies including nanopore, PacBio, and 10X, but also non-sequencing long range techniques like optical mapping [e.g. BioNano]
and Hi-C [e.g., Dovetail]. Could you please let us know whether you or your colleagues</span></div>
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have any current projects using any of these technologies. Would you be willing to discuss at future meetings?<o:p class=""></o:p></li><li class="MsoListParagraph" style="margin: 0in 0in 0.0001pt; font-family: Calibri, sans-serif;">
have specific projects you would like to do that could be done with NYGC if we had the resources<o:p class=""></o:p></li><li class="MsoListParagraph" style="margin: 0in 0in 0.0001pt; font-family: Calibri, sans-serif;">
have bigger picture questions about cancer biology that could be addressed with these technologies, but you don’t know exactly which technologies or whether current technologies are suited to addressing your questions</li></ol>
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<div class=""><font face="Calibri, sans-serif" class="">Many thanks,</font></div>
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<div class=""><font face="Calibri, sans-serif" class="">Simon</font></div>
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Professor Simon Tavaré </div>
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Senior Associate Core Member </div>
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New York Genome Center</div>
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Rm 618</div>
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O: 1 646 977 7032</div>
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