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	<title>CISMM</title>
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	<link>http://cismm.cs.unc.edu</link>
	<description>Computer Integrated Systems for Microscopy and Manipulation</description>
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		<title>Panoptes exploded-view</title>
		<link>http://cismm.cs.unc.edu/2013/03/panoptes-exploded-view/</link>
		<comments>http://cismm.cs.unc.edu/2013/03/panoptes-exploded-view/#comments</comments>
		<pubDate>Sat, 16 Mar 2013 15:29:16 +0000</pubDate>
		<dc:creator>rmtaylor@unc.edu</dc:creator>
				<category><![CDATA[Media Gallery]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=6270</guid>
		<description><![CDATA[This video shows a computer rendering of the Panoptes system, made by Christian Stith using the CAD models from Leandra Vicci.  It starts with the entire system, then shows how the light moves through the varioptic lens element and causes fluorescence in a single channel.  It then shows the second fluorescence channel.  It then reassembles [...]]]></description>
			<content:encoded><![CDATA[<p>This video shows a computer rendering of the Panoptes system, made by Christian Stith using the CAD models from Leandra Vicci.  It starts with the entire system, then shows how the light moves through the varioptic lens element and causes fluorescence in a single channel.  It then shows the second fluorescence channel.  It then reassembles the entire system and shows how it works, translating to each new position and exposing the two fluorescence channels to grab two images for each channel.</p>
<p><a href="http://cismm.cs.unc.edu/wp-content/uploads/2013/03/Panoptes.mp4"><img class="size-full wp-image-6274 alignnone" title="panoptes_crop" src="http://cismm.cs.unc.edu/wp-content/uploads/2013/03/panoptes_crop.jpg" alt="" width="377" height="333" /></a></p>
<p><a href="http://cismm.cs.unc.edu/wp-content/uploads/2013/03/Panoptes.mp4">Panoptes</a></p>
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		</item>
		<item>
		<title>Mitotic Spindle under Brownian Motion</title>
		<link>http://cismm.cs.unc.edu/2012/08/mitotic-spindle-under-brownian-motion/</link>
		<comments>http://cismm.cs.unc.edu/2012/08/mitotic-spindle-under-brownian-motion/#comments</comments>
		<pubDate>Fri, 24 Aug 2012 12:10:47 +0000</pubDate>
		<dc:creator>rmtaylor@unc.edu</dc:creator>
				<category><![CDATA[Cell mechanics]]></category>
		<category><![CDATA[Collaborations]]></category>
		<category><![CDATA[Kerry Bloom]]></category>
		<category><![CDATA[Media Gallery]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=5930</guid>
		<description><![CDATA[A model of the yeast mitotic spindle in metaphase was constructed based on a looping model of DNA distribution, where the loops are tied together at their base by condensin and they are linked by slip-rings of cohesin.    This model was created in collaboration between Kerry Bloom and his group and CISMM personnel.  The [...]]]></description>
			<content:encoded><![CDATA[<p>A model of the yeast mitotic spindle in metaphase was constructed based on a looping model of DNA distribution, where the loops are tied together at their base by condensin and they are linked by slip-rings of cohesin.    This model was created in collaboration between Kerry Bloom and his group and CISMM personnel.  The geometry of the model at its initial state is shown below.</p>
<p><a href="http://cismm.cs.unc.edu/wp-content/uploads/2012/08/brownian_yeast_initial_condition.png"><img class="size-full wp-image-5933 alignnone" title="brownian_yeast_initial_condition" src="http://cismm.cs.unc.edu/wp-content/uploads/2012/08/brownian_yeast_initial_condition.png" alt="" width="548" height="302" /></a></p>
<p>The code was developed by Belinda Johnson.  A coarse-grained simulation was run, based on the SOFA platform with the addition of Brownian forces and stiffness forces, to understand what the addition of Brownian forces on the structure would do to the distribution of DNA.  The parameters of the simulation included a random force of 1228, a mass_damping of 10, a mass_radius of 0.0045, a spring constant of 628000, a hinge force of 0.548, and an object mass of 33.3 (see simulation code for the units).  We believe that this model matches the expected behavior except for: (1) the viscosity is much lower than in reality so that the simulation will run in reasonable time (we expect the behavior to be the same).  (2) The cohesin rings are too large by about a factor of two (this was a mistake in the model set up, which we think will only serve to make the rings more mobile).  (3) There is no torsional restoring force on the DNA, so there will be no impact due to twisting of the DNA strands.</p>
<p>The resulting movie of the simulation is available here: <a href="http://cismm.cs.unc.edu/wp-content/uploads/2012/08/0001-0167.mov">0001-0167</a>.  It shows a snapshot of the simulation every 0.1 nanoseconds up to 17.6 nanoseconds.</p>
<p>The simulation showed the outside of the rings pulling in and the inside of the spindle pushing out.  There was not a large net offset to the cohesin rings from their initial position (each moves, but they seem to maintain their approximate position).  The ends of the DNA are pinned in space as if to stable microtubules.  Some images of the resulting configuration are shown below.<a href="http://cismm.cs.unc.edu/wp-content/uploads/2012/08/OUTFILE3_v2_endview.png"><img class="size-full wp-image-5938 alignnone" title="OUTFILE3_v2_endview" src="http://cismm.cs.unc.edu/wp-content/uploads/2012/08/OUTFILE3_v2_endview.png" alt="" width="538" height="538" /></a><a href="http://cismm.cs.unc.edu/wp-content/uploads/2012/08/OUTFILE3_v2_side_four_sisters.png"><img class="size-full wp-image-5937 alignnone" title="OUTFILE3_v2_side_four_sisters" src="http://cismm.cs.unc.edu/wp-content/uploads/2012/08/OUTFILE3_v2_side_four_sisters.png" alt="" width="538" height="538" /></a></p>
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		</item>
		<item>
		<title>Fungipod</title>
		<link>http://cismm.cs.unc.edu/2012/04/fungipod/</link>
		<comments>http://cismm.cs.unc.edu/2012/04/fungipod/#comments</comments>
		<pubDate>Sun, 01 Apr 2012 19:02:25 +0000</pubDate>
		<dc:creator>rmtaylor@unc.edu</dc:creator>
				<category><![CDATA[Aaron Neumann]]></category>
		<category><![CDATA[Cell mechanics]]></category>
		<category><![CDATA[Collaborations]]></category>
		<category><![CDATA[ImageSurfer]]></category>
		<category><![CDATA[Media Gallery]]></category>
		<category><![CDATA[Software]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=5455</guid>
		<description><![CDATA[Collaborator Aaron Neumann from the University of New Mexico is studying fungipods from human dendritic cells that attach to yeast.  The image above shows a combination of three different fluorophores that together show the behavior.  A green yeast is sitting on top of the cell membrane (transparent red) with three fungipods attached to it.  The [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: center;">
<div id="attachment_5456" class="wp-caption aligncenter" style="width: 546px"><a href="http://cismm.cs.unc.edu/wp-content/uploads/2012/04/larger_yeast.png"><img class="size-full wp-image-5456  " title="larger_yeast" src="http://cismm.cs.unc.edu/wp-content/uploads/2012/04/larger_yeast.png" alt="" width="536" height="361" /></a><p class="wp-caption-text">Actin-rich fungipods attack a yeast attached to a cell membrane</p></div>
<p>Collaborator Aaron Neumann from the University of New Mexico is studying fungipods from human dendritic cells that attach to yeast.  The image above shows a combination of three different fluorophores that together show the behavior.  A green yeast is sitting on top of the cell membrane (transparent red) with three fungipods attached to it.  The fungipods are very dense in actin (blue).</p>
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		</item>
		<item>
		<title>Limitations of modeling on Chimera</title>
		<link>http://cismm.cs.unc.edu/2011/11/limitations-of-modeling-on-chimera/</link>
		<comments>http://cismm.cs.unc.edu/2011/11/limitations-of-modeling-on-chimera/#comments</comments>
		<pubDate>Fri, 18 Nov 2011 21:10:24 +0000</pubDate>
		<dc:creator>phsiao@unc.edu</dc:creator>
				<category><![CDATA[Collaborations]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=5231</guid>
		<description><![CDATA[While working on generating protofibrils in Chimera, I thought it&#8217;d be great if the software can do: 1. Rotate and orientate the models but with certain points fixed. That would require the models becoming flexible. 2. Preview replicated monomers in real-time. So users don&#8217;t have to change one of the monomers, replicate more to see [...]]]></description>
			<content:encoded><![CDATA[<p>While working on generating protofibrils in Chimera, I thought it&#8217;d be great if the software can do:</p>
<p>1. Rotate and orientate the models but with certain points fixed. That would require the models becoming flexible.</p>
<p>2. Preview replicated monomers in real-time. So users don&#8217;t have to change one of the monomers, replicate more to see the structure, change the monomer again, and re-do the replication again to see how the structure looks like.</p>
]]></content:encoded>
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		</item>
		<item>
		<title>Yeast Mitotic Spindle</title>
		<link>http://cismm.cs.unc.edu/2011/05/yeast-mitotic-spindle/</link>
		<comments>http://cismm.cs.unc.edu/2011/05/yeast-mitotic-spindle/#comments</comments>
		<pubDate>Wed, 11 May 2011 18:58:27 +0000</pubDate>
		<dc:creator>rmtaylor@unc.edu</dc:creator>
				<category><![CDATA[Collaborations]]></category>
		<category><![CDATA[Kerry Bloom]]></category>
		<category><![CDATA[Media Gallery]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=4472</guid>
		<description><![CDATA[The image below is a proposed structure for the mitotic spindle of yeast during metaphase that was produced in a collaboration between Russell M. Taylor II, Andrew Stephens, Kerry Bloom, Leandra Vicci, Jolien Verdaasdonk, Steven Nedrud, Matt Larson, and Michael Falvo. Others participated in the earlier development of the model, including Kendall McKenzie and Callie [...]]]></description>
			<content:encoded><![CDATA[<p>The image below is a proposed structure for the mitotic spindle of yeast  during metaphase that was produced in a collaboration between Russell  M. Taylor II, Andrew Stephens, Kerry Bloom, Leandra Vicci, Jolien  Verdaasdonk, Steven Nedrud, Matt Larson, and Michael Falvo.</p>
<p style="text-align: center;">
<div id="attachment_4433" class="wp-caption aligncenter" style="width: 425px"><a href="http://cismm.cs.unc.edu/wp-content/uploads/2011/03/cismm_entry_science_contest_brighter.png"><img class="size-full wp-image-4433  " title="cismm_entry_science_contest_brighter" src="http://cismm.cs.unc.edu/wp-content/uploads/2011/03/cismm_entry_science_contest_brighter.png" alt="" width="415" height="233" /></a><p class="wp-caption-text">NSF/Science Honorable Mention Image</p></div>
<p>Others participated in the earlier development of the model, including Kendall McKenzie and Callie Holderman.</p>
<p>A high-resolution poster version of this image is available for download <a href="http://cismm.cs.unc.edu/wp-content/uploads/2011/05/cismm_entry_science_contest_poster.2.tif">here</a><a href="http://cismm.cs.unc.edu/wp-content/uploads/2011/05/cismm_entry_science_contest_poster.tif"><img class="alignright size-full wp-image-4477" title="cismm_entry_science_contest_poster" src="http://cismm.cs.unc.edu/wp-content/uploads/2011/05/cismm_entry_science_contest_poster.tif" alt="" /></a><a href="http://cismm.cs.unc.edu/wp-content/uploads/2011/05/cismm_entry_science_contest_poster.tif"><img class="alignright size-full wp-image-4477" title="cismm_entry_science_contest_poster" src="http://cismm.cs.unc.edu/wp-content/uploads/2011/05/cismm_entry_science_contest_poster.tif" alt="" /></a>.  Save the image by right-clicking on the link and then take it to your local copy center for printing onto glossy paper.</p>
<p>This model of the yeast mitoric spindle shows the spindle-pole bodies  as blue spheres, the kinetochore microtubules as green cylinders, the  DNA as yellow tubes, cohesin as linked red rings, and condensin linking  molecules in purple.  The translucent gray shell around the spindle  shows the center of the region that contains cohesin as seen in  fluorescence microscopy images taken of the spindle.  The DNA and other  structures are too small to be resolved in the microscope.  This is the  twentieth version of the model, which has been developed over a two-year  period of intense collaboration between cell biologists, computer  scientists, physicists, and artists.  This was developed as part of the  Computer-Integrates Systems for Microsopy and Manipulation NIH/NIBIB  National Research Resource.</p>
<p>It is a geometric model of a hyopthetical structure that has evolved  to be consistent with a number of experiments performed in the  department of Biology.  Its purpose is to display, in a consistent 3D  space, a model, all known aspects of the structure.  This forms a basis  for discussion, which then results in new planned experiments and in  changes to the model.</p>
<p>This image was an <a href="http://www.nsf.gov/news/special_reports/scivis/winners_2010.jsp#illustration">honorable mention</a> in the <em>illustration</em> category of the <em>NSF/Science visualization challenge 2010</em>.</p>
<p><em>About the yeast:</em> The yeast is Saccharomyces cerevisiae<strong> </strong>as  used for baking and brewing. The strains we use are science based  versions not commonly used for brewing or baking, but they are the same  species.  S cerevisiae is one of the most commonly used eukaryotic model  systems in biology.</p>
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		<item>
		<title>Fungipods</title>
		<link>http://cismm.cs.unc.edu/2011/03/4391/</link>
		<comments>http://cismm.cs.unc.edu/2011/03/4391/#comments</comments>
		<pubDate>Wed, 02 Mar 2011 18:48:13 +0000</pubDate>
		<dc:creator>cakici@cs.unc.edu</dc:creator>
				<category><![CDATA[Media Gallery]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=4391</guid>
		<description><![CDATA[Aaron Neumann and his colleagues from Cell and Developmental Biology found novel dorsal pseudopodial protrusions, the &#8220;fungipods&#8221;, formed by dendritic cells (red objects in the upper image)  after contact with yeast cells (i.e. green blobs in the upper image). Fungipods have a convoluted cell-proximal end and a smooth distal end. They persist for hours, and exhibit noticeable [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: center;">
<p style="text-align: center;"><a href="http://cismm.cs.unc.edu/wp-content/uploads/2011/03/1600_all_lined1.png"><img class="size-full wp-image-4408 aligncenter" title="Fungipods formed by immature dendritic cells after contact with yeast cells" src="http://cismm.cs.unc.edu/wp-content/uploads/2011/03/1600_all_lined1.png" alt="" width="492" height="492" /></a></p>
<p>Aaron Neumann and his colleagues from Cell and Developmental Biology found novel dorsal pseudopodial protrusions, the &#8220;fungipods&#8221;, formed by dendritic cells (red objects in the upper image)  after contact with yeast cells (i.e. green blobs in the upper image).</p>
<p>Fungipods have a convoluted cell-proximal end and a smooth distal end. They persist for hours, and exhibit noticeable growth at the contact. Aaron Neumann et al. think that fungipods may promote yeast particle phagocytosis (i.e. process of surrounding and consuming solid particles) by dendritic cells.</p>
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		<item>
		<title>Protected: Setting up a simple stereo system</title>
		<link>http://cismm.cs.unc.edu/2010/09/setting-up-a-simple-stereo-system/</link>
		<comments>http://cismm.cs.unc.edu/2010/09/setting-up-a-simple-stereo-system/#comments</comments>
		<pubDate>Thu, 23 Sep 2010 05:27:02 +0000</pubDate>
		<dc:creator>alexisc</dc:creator>
				<category><![CDATA[Uncategorized]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=3774</guid>
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		<item>
		<title>nDive Movie: Sparse Data-driven Spheres</title>
		<link>http://cismm.cs.unc.edu/2010/04/ndive-movie-sparse-data-driven-spheres/</link>
		<comments>http://cismm.cs.unc.edu/2010/04/ndive-movie-sparse-data-driven-spheres/#comments</comments>
		<pubDate>Fri, 23 Apr 2010 19:29:52 +0000</pubDate>
		<dc:creator>dfeng@unc.edu</dc:creator>
				<category><![CDATA[Advanced Analysis and vis (Core 3)]]></category>
		<category><![CDATA[Media Gallery]]></category>
		<category><![CDATA[Medical]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=3401</guid>
		<description><![CDATA[3D visualization of magnetic resonance spectroscopy (MRS) data. The background anatomical image is a T1 MRI image containing a bright outline that roughly corresponds to the location of a tumor. The colored spheres are a sphere-based representation of concentrations of different metabolites, which are functional markers. How it works: red spheres = choline green spheres [...]]]></description>
			<content:encoded><![CDATA[<p><object classid="clsid:d27cdb6e-ae6d-11cf-96b8-444553540000" width="480" height="385" codebase="http://download.macromedia.com/pub/shockwave/cabs/flash/swflash.cab#version=6,0,40,0"><param name="allowFullScreen" value="true" /><param name="allowscriptaccess" value="always" /><param name="src" value="http://www.youtube.com/v/YgBxcB9QyHY&amp;hl=en_US&amp;fs=1&#038;loop=1&amp;autoplay=0&amp;&#038;playlist=YgBxcB9QyHY" /><param name="allowfullscreen" value="true" /><embed type="application/x-shockwave-flash" width="480" height="385" src="http://www.youtube.com/v/YgBxcB9QyHY&amp;hl=en_US&amp;fs=1&#038;loop=1&amp;autoplay=0&amp;playlist=YgBxcB9QyHY" allowscriptaccess="always" allowfullscreen="true"></embed></object></p>
<p>3D visualization of magnetic resonance spectroscopy (MRS) data. The background anatomical image is a T1 MRI image containing a bright outline that roughly corresponds to the location of a tumor. The colored spheres are a sphere-based representation of concentrations of different metabolites, which are functional markers.  How it works:</p>
<ul>
<li> red spheres = choline</li>
<li> green spheres = creatine</li>
<li> blue spheres = glutamin</li>
<li> yellow spheres = n-acetylaspartate</li>
<li> sphere size corresponds to magnitude of the metabolite.</li>
</ul>
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		<item>
		<title>Vesicle and protein segmentation.</title>
		<link>http://cismm.cs.unc.edu/2009/10/vesicle-and-protein-segmentation/</link>
		<comments>http://cismm.cs.unc.edu/2009/10/vesicle-and-protein-segmentation/#comments</comments>
		<pubDate>Mon, 12 Oct 2009 20:33:32 +0000</pubDate>
		<dc:creator>rmtaylor@unc.edu</dc:creator>
				<category><![CDATA[Advanced Analysis and vis (Core 3)]]></category>
		<category><![CDATA[Analysis]]></category>
		<category><![CDATA[Core]]></category>
		<category><![CDATA[ImageSurfer]]></category>
		<category><![CDATA[Media Gallery]]></category>
		<category><![CDATA[Software]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=2945</guid>
		<description><![CDATA[vesicleProteinsLiberalThresholdSomeRemoved This image (and linked movie) shows a rotating 3D view of a vesicle that was semi-automatically segmented from a 3D TEM image reconstructed from a tilt series.  A handful of seed points were placed in one slice of the image and the 3D vesicle was automatically extracted.  The image also shows a very preliminary [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://cismm.cs.unc.edu/wp-content/uploads/2009/11/vesicleProteinsLiberalThresholdSomeRemoved.avi">vesicleProteinsLiberalThresholdSomeRemoved</a></p>
<div id="attachment_2953" class="wp-caption alignright" style="width: 319px"><a href="http://cismm.cs.unc.edu/wp-content/uploads/2009/11/Vesicle.png"><img class="size-full wp-image-2953 " title="Vesicle" src="http://cismm.cs.unc.edu/wp-content/uploads/2009/11/Vesicle.png" alt="Segmented vesicle witih proteins" width="309" height="264" /></a><p class="wp-caption-text">Segmented vesicle witih proteins</p></div>
<p>This image (and linked movie) shows a rotating 3D view of a vesicle that was semi-automatically segmented from a 3D TEM image reconstructed from a tilt series.  A handful of seed points were placed in one slice of the image and the 3D vesicle was automatically extracted.  The image also shows a very preliminary automatic segmentation of proteins extending through the vesicle wall; the extent of these proteins is currently clipped by an arbitrary global parameter setting.</p>
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		<item>
		<title>Virtual Lung Video: Mucus River, Scene 2</title>
		<link>http://cismm.cs.unc.edu/2009/09/virtual-lung-video-mucus-river-scene-2/</link>
		<comments>http://cismm.cs.unc.edu/2009/09/virtual-lung-video-mucus-river-scene-2/#comments</comments>
		<pubDate>Sat, 19 Sep 2009 20:12:55 +0000</pubDate>
		<dc:creator>rmtaylor@unc.edu</dc:creator>
				<category><![CDATA[Collaborations]]></category>
		<category><![CDATA[Lung]]></category>
		<category><![CDATA[Media Gallery]]></category>
		<category><![CDATA[Virtual Lung Project]]></category>

		<guid isPermaLink="false">http://cismm.cs.unc.edu/?p=2939</guid>
		<description><![CDATA[Clearance2.mov The second in a series of animated videos depicting the inner workings of the human lung on a microscopic scale. &#8220;Scene 2: Clearance: A Journey&#8221; asks questions about how clearance can possibly work when the volume through which the mucus flows decreases as it moves up from the depths of the lung to the [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://cismm.cs.unc.edu/wp-content/uploads/2009/11/Clearance2.mov">Clearance2.mov</a></p>
<p><span>The second in a series of animated videos depicting the inner workings of the human lung on a microscopic scale. &#8220;Scene 2: Clearance: A Journey&#8221; asks questions about how clearance can possibly work when the volume through which the mucus flows decreases as it moves up from the depths of the lung to the throat. </span></p>
<p><span>This video can also be <a href="http://www.youtube.com/watch?v=GJ0A-L_67hs">seen on YouTube</a>.<br />
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