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<p class="MsoNormal">Hi All,<o:p></o:p></p>
<p class="MsoNormal">With the commissioning of our 4 new scopes we are debating if we should put SerialEM and Leginon on the same microscopes. I have heard from some people that there may be some problems that arise during the transition. We have mostly been
using Leginon so have a great deal of experience with it and use SerialEM for our limited tomography users. I cannot see any reason they should conflict but want to ask the 3DEM community if they have any specific experience where this has been a problem.
Thank you and I look forward to your advice.<o:p></o:p></p>
<p class="MsoNormal">Regards,<o:p></o:p></p>
<p class="MsoNormal">Bob<o:p></o:p></p>
<p class="MsoNormal"><o:p> </o:p></p>
<p class="MsoNormal"><o:p> </o:p></p>
<p class="MsoNormal">Robert Grassucci<o:p></o:p></p>
<p class="MsoNormal">Co Director CryoEM Core Facility<o:p></o:p></p>
<p class="MsoNormal">Columbia University Medical Center<o:p></o:p></p>
<p class="MsoNormal">Biochemistry and Molecular Biophysics Dept.<o:p></o:p></p>
<p class="MsoNormal">Black Building 2-221<o:p></o:p></p>
<p class="MsoNormal">650 W 168 Street<o:p></o:p></p>
<p class="MsoNormal">New York, NY 10032<o:p></o:p></p>
<p class="MsoNormal">Phone: 212-305-9520<o:p></o:p></p>
<p class="MsoNormal"><o:p> </o:p></p>
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