<?xml version="1.0"?>
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	<id>https://www.slicer.org/w/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Irosen</id>
	<title>Slicer Wiki - User contributions [en]</title>
	<link rel="self" type="application/atom+xml" href="https://www.slicer.org/w/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Irosen"/>
	<link rel="alternate" type="text/html" href="https://www.slicer.org/wiki/Special:Contributions/Irosen"/>
	<updated>2026-04-12T14:36:19Z</updated>
	<subtitle>User contributions</subtitle>
	<generator>MediaWiki 1.33.0</generator>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42243</id>
		<title>Documentation/4.4/gif tutorial v3 4</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42243"/>
		<updated>2015-07-20T20:29:29Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; style=&amp;quot;border-spacing: 2px; border: 1px solid darkgray;&amp;quot;&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; | Table of Contents&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 1|1. Loading DTI and Baseline Data]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 2|2. Segmentation]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 3|3. Tractography exploration of peritumoral white matter fibers]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:l.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:m.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Click on the Modules menu and select the module &amp;quot;Tractography Interactive Seeding&amp;quot; after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.&lt;br /&gt;
|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it in the 3D viewer.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:n.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:o.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up..&lt;br /&gt;
|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 3|Previous Step]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42242</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42242"/>
		<updated>2015-07-20T20:28:41Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; style=&amp;quot;border-spacing: 2px; border: 1px solid darkgray;&amp;quot;&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; | Table of Contents&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 1|1. Loading DTI and Baseline Data]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 2|2. Segmentation]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 4|4. Tractography exploration of the ipsilateral and contralateral side]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Make sure the cystic part is selected and visible in the 3 slice views.   b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5.  a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;.   b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.  a) Under the Seed Placement Options: Check the Use Index Space.   b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 4|Next Step]]'''&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 2|Previous Step]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42241</id>
		<title>Documentation/4.4/gif tutorial v3 2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42241"/>
		<updated>2015-07-20T20:27:35Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; style=&amp;quot;border-spacing: 2px; border: 1px solid darkgray;&amp;quot;&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; | Table of Contents&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 1|1. Loading DTI and Baseline Data]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 3|3. Tractography exploration of peritumoral white matter fibers]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 4|4. Tractography exploration of the ipsilateral and contralateral side]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:5.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:6.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.&lt;br /&gt;
|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:7.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:8.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor&lt;br /&gt;
|4. Select the GrowCutEffect tool and then click Apply&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:9.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:10.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.&lt;br /&gt;
|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:11.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:12.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.&lt;br /&gt;
|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:13.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:14.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.&lt;br /&gt;
|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:15.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 3|Next Step]]'''&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 1|Previous Step]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42240</id>
		<title>Documentation/4.4/gif tutorial v3 1</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42240"/>
		<updated>2015-07-20T20:26:56Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; style=&amp;quot;border-spacing: 2px; border: 1px solid darkgray;&amp;quot;&lt;br /&gt;
! scope=&amp;quot;col&amp;quot; | Table of Contents&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 2|2. Segmentation]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 3|3. Tractography exploration of peritumoral white matter fibers]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 4|4. Tractography exploration of the ipsilateral and contralateral side]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 2|Next Step]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42239</id>
		<title>Documentation/4.4/gif tutorial v3 1</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42239"/>
		<updated>2015-07-20T20:25:22Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot; style=&amp;quot;border-spacing: 2px; border: 1px solid darkgray;&amp;quot;&lt;br /&gt;
|+ '''Table Of Contents'''&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 2|Segmentation]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 3|Tractography exploration of peritumoral white matter fibers]]&lt;br /&gt;
|-&lt;br /&gt;
|[[Documentation/4.4/gif tutorial v3 4|Tractography exploration of the ipsilateral and contralateral side]]&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 2|Next Step]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42238</id>
		<title>Documentation/4.4/gif tutorial v3 4</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42238"/>
		<updated>2015-07-20T19:39:44Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:l.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:m.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Click on the Modules menu and select the module &amp;quot;Tractography Interactive Seeding&amp;quot; after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.&lt;br /&gt;
|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it in the 3D viewer.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:n.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:o.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up..&lt;br /&gt;
|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 3|Previous Step]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42237</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42237"/>
		<updated>2015-07-20T19:39:26Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Make sure the cystic part is selected and visible in the 3 slice views.   b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5.  a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;.   b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.  a) Under the Seed Placement Options: Check the Use Index Space.   b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 4|Next Step]]'''&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 2|Previous Step]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42236</id>
		<title>Documentation/4.4/gif tutorial v3 2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42236"/>
		<updated>2015-07-20T19:35:35Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:5.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:6.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.&lt;br /&gt;
|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:7.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:8.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor&lt;br /&gt;
|4. Select the GrowCutEffect tool and then click Apply&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:9.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:10.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.&lt;br /&gt;
|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:11.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:12.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.&lt;br /&gt;
|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:13.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:14.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.&lt;br /&gt;
|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:15.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 3|Next Step]]'''&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 1|Previous Step]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42235</id>
		<title>Documentation/4.4/gif tutorial v3 1</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42235"/>
		<updated>2015-07-20T19:35:21Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 2|Next Step]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42234</id>
		<title>Documentation/4.4/gif tutorial v3 4</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42234"/>
		<updated>2015-07-20T19:34:30Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Tractography exploration of the ipsilateral and contralateral side===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:l.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:m.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Click on the Modules menu and select the module &amp;quot;Tractography Interactive Seeding&amp;quot; after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.&lt;br /&gt;
|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it in the 3D viewer.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:n.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:o.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up..&lt;br /&gt;
|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 3|Previous]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42233</id>
		<title>Documentation/4.4/gif tutorial v3 4</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42233"/>
		<updated>2015-07-20T19:33:09Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Tractography exploration of peritumoral white matter fibers */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Tractography exploration of the ipsilateral and contralateral side===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:l.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:m.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Click on the Modules menu and select the module &amp;quot;Tractography Interactive Seeding&amp;quot; after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.&lt;br /&gt;
|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it in the 3D viewer.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:n.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:o.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up..&lt;br /&gt;
|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42232</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42232"/>
		<updated>2015-07-20T19:28:48Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Make sure the cystic part is selected and visible in the 3 slice views.   b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5.  a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;.   b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.  a) Under the Seed Placement Options: Check the Use Index Space.   b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 4|Next]]'''&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 2|Previous]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42231</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42231"/>
		<updated>2015-07-20T19:28:27Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Make sure the cystic part is selected and visible in the 3 slice views.   b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5.  a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;.   b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.  a) Under the Seed Placement Options: Check the Use Index Space.   b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 4|Next]]'''&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 2|Previous]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42230</id>
		<title>Documentation/4.4/gif tutorial v3 4</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_4&amp;diff=42230"/>
		<updated>2015-07-20T19:16:57Z</updated>

		<summary type="html">&lt;p&gt;Irosen: Created page with '===Tractography exploration of peritumoral white matter fibers===  {| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot; |-align=&amp;quot;center&amp;quot; |style=&amp;quot;width:50%&amp;quot;|600px |style=…'&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Make sure the cystic part is selected and visible in the 3 slice views.   b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5.  a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;.   b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.  a) Under the Seed Placement Options: Check the Use Index Space.   b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42229</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42229"/>
		<updated>2015-07-20T19:13:05Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Loading DTI and Baseline Data */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Make sure the cystic part is selected and visible in the 3 slice views.   b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5.  a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;.   b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.  a) Under the Seed Placement Options: Check the Use Index Space.   b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42228</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42228"/>
		<updated>2015-07-20T19:09:28Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Loading DTI and Baseline Data */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1.  a) Make sure the cystic part is selected and visible in the 3 slice views.   b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5.  a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;.   b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.  a) Under the Seed Placement Options: Check the Use Index Space.   b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42227</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42227"/>
		<updated>2015-07-20T19:07:52Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Loading DTI and Baseline Data */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42226</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42226"/>
		<updated>2015-07-20T19:07:00Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Loading DTI and Baseline Data */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|      2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. a) For Output Fiber Bundle select &amp;quot;Create and&lt;br /&gt;
rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42225</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42225"/>
		<updated>2015-07-20T19:05:51Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Tractography exploration of peritumoral white matter fibers */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. a) For Output Fiber Bundle select &amp;quot;Create and&lt;br /&gt;
rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;.&lt;br /&gt;
|6.a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42224</id>
		<title>Documentation/4.4/gif tutorial v3 2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42224"/>
		<updated>2015-07-20T19:03:04Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:5.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:6.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.&lt;br /&gt;
|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:7.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:8.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor&lt;br /&gt;
|4. Select the GrowCutEffect tool and then click Apply&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:9.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:10.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.&lt;br /&gt;
|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:11.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:12.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.&lt;br /&gt;
|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:13.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:14.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.&lt;br /&gt;
|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:15.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 3|Next]]'''&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 1|Previous]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42223</id>
		<title>Documentation/4.4/gif tutorial v3 1</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42223"/>
		<updated>2015-07-20T19:02:30Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 2|Next]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42222</id>
		<title>Documentation/4.4/gif tutorial v3 2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42222"/>
		<updated>2015-07-20T19:02:24Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Segmentation===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:5.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:6.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.&lt;br /&gt;
|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:7.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:8.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor&lt;br /&gt;
|4. Select the GrowCutEffect tool and then click Apply&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:9.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:10.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.&lt;br /&gt;
|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:11.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:12.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.&lt;br /&gt;
|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:13.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:14.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.&lt;br /&gt;
|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:15.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 3|Next]]'''&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 1|Previous]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42221</id>
		<title>Documentation/4.4/gif tutorial v3 1</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42221"/>
		<updated>2015-07-20T19:01:19Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;text-align: center;&amp;quot;&amp;gt;'''[[Documentation/4.4/gif tutorial v3 2|Next]]'''&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42220</id>
		<title>Documentation/4.4/gif tutorial v3 3</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_3&amp;diff=42220"/>
		<updated>2015-07-20T18:49:04Z</updated>

		<summary type="html">&lt;p&gt;Irosen: Created page with '===Tractography exploration of peritumoral white matter fibers===  &amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt; {|sty…'&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on Apply 3 times to generate the peritumoral volume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|5. a) For Output Fiber Bundle select &amp;quot;Create and&lt;br /&gt;
rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|6. a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.  ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42219</id>
		<title>Documentation/4.4/gif tutorial v3 2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_2&amp;diff=42219"/>
		<updated>2015-07-20T18:26:28Z</updated>

		<summary type="html">&lt;p&gt;Irosen: Created page with '===Segmentation===  {| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot; |-align=&amp;quot;center&amp;quot; |style=&amp;quot;width:50%&amp;quot;|600px |style=&amp;quot;width:50%&amp;quot;|600px |-valig…'&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;===Segmentation===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:5.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:6.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.&lt;br /&gt;
|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:7.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:8.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor&lt;br /&gt;
|4. Select the GrowCutEffect tool and then click Apply&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:9.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:10.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.&lt;br /&gt;
|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:11.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:12.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.&lt;br /&gt;
|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:13.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:14.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.&lt;br /&gt;
|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:15.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42218</id>
		<title>Documentation/4.4/gif tutorial v3 1</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v3_1&amp;diff=42218"/>
		<updated>2015-07-20T18:26:05Z</updated>

		<summary type="html">&lt;p&gt;Irosen: Created page with '|center  ===Loading DTI and Baseline Data===  {| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot; |-align=&amp;quot;center&amp;quot; |style=&amp;quot;width:50%&amp;quot;|[[im…'&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42113</id>
		<title>Documentation/4.4/gif tutorial v2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42113"/>
		<updated>2015-07-10T19:45:15Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:5.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:6.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.&lt;br /&gt;
|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:7.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:8.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor&lt;br /&gt;
|4. Select the GrowCutEffect tool and then click Apply&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:9.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:10.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.&lt;br /&gt;
|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:11.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:12.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.&lt;br /&gt;
|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:13.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:14.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.&lt;br /&gt;
|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:15.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;&lt;br /&gt;
|6. a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:l.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:m.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Click on the Modules menu and select the moduleTractography Interactive Seeding after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.&lt;br /&gt;
|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it in the 3D viewer.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:n.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:o.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up.&lt;br /&gt;
|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15&lt;br /&gt;
|}&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42112</id>
		<title>Documentation/4.4/gif tutorial v2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42112"/>
		<updated>2015-07-10T19:41:26Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:5.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:6.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.&lt;br /&gt;
|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:7.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:8.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor&lt;br /&gt;
|4. Select the GrowCutEffect tool and then click Apply&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:9.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:10.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.&lt;br /&gt;
|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:11.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:12.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.&lt;br /&gt;
|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:13.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:14.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.&lt;br /&gt;
|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:15.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:x.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:y.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.&lt;br /&gt;
|2. Click on Apply 3 times to generate the peritumoral volume&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:z.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:c.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;&lt;br /&gt;
|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:a.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:b.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. a) For Output Fiber Bundle select &amp;quot;Create and rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;&lt;br /&gt;
|6. a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:d.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. a) Click on the Modules menu and select the module&lt;br /&gt;
Tractography Interactive Seeding after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it&lt;br /&gt;
in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15 ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42111</id>
		<title>Documentation/4.4/gif tutorial v2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42111"/>
		<updated>2015-07-10T19:33:40Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:5.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:6.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.&lt;br /&gt;
|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:7.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:8.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor&lt;br /&gt;
|4. Select the GrowCutEffect tool and then click Apply&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:9.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:10.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.&lt;br /&gt;
|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:11.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:12.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.&lt;br /&gt;
|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:13.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:14.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.&lt;br /&gt;
|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:15.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on Apply 3 times to generate the peritumoral volume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|5. a) For Output Fiber Bundle select &amp;quot;Create and&lt;br /&gt;
rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|6. a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.  ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. a) Click on the Modules menu and select the module&lt;br /&gt;
Tractography Interactive Seeding after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it&lt;br /&gt;
in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15 ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42110</id>
		<title>Documentation/4.4/gif tutorial v2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42110"/>
		<updated>2015-07-10T19:28:45Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:5.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:6.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:7.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:8.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:9.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:10.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:11.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:12.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on Apply 3 times to generate the peritumoral volume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|5. a) For Output Fiber Bundle select &amp;quot;Create and&lt;br /&gt;
rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|6. a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.  ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. a) Click on the Modules menu and select the module&lt;br /&gt;
Tractography Interactive Seeding after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it&lt;br /&gt;
in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15 ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42109</id>
		<title>Documentation/4.4/gif tutorial v2</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial_v2&amp;diff=42109"/>
		<updated>2015-07-10T19:23:44Z</updated>

		<summary type="html">&lt;p&gt;Irosen: Created page with '|center  {| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot; |-align=&amp;quot;center&amp;quot; |style=&amp;quot;width:50%&amp;quot;|600px |style=&amp;quot;width…'&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
{| class=&amp;quot;wikitable3&amp;quot; cellpadding=&amp;quot;5px&amp;quot;&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:1.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:2.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData&lt;br /&gt;
|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume.&lt;br /&gt;
|-align=&amp;quot;center&amp;quot;&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:3.gif|frame|600px]]&lt;br /&gt;
|style=&amp;quot;width:50%&amp;quot;|[[image:4.gif|frame|600px]]&lt;br /&gt;
|-valign=&amp;quot;top&amp;quot;&lt;br /&gt;
|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu&lt;br /&gt;
|4. Manually adjust the Window Level editor presets with the Volume module menu&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on Apply 3 times to generate the peritumoral volume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|5. a) For Output Fiber Bundle select &amp;quot;Create and&lt;br /&gt;
rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|6. a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.  ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. a) Click on the Modules menu and select the module&lt;br /&gt;
Tractography Interactive Seeding after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it&lt;br /&gt;
in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15 ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42108</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42108"/>
		<updated>2015-07-09T20:24:29Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Tractography exploration of the ipsilateral and contralateral side */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on Apply 3 times to generate the peritumoral volume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|5. a) For Output Fiber Bundle select &amp;quot;Create and&lt;br /&gt;
rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|6. a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.  ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. a) Click on the Modules menu and select the module&lt;br /&gt;
Tractography Interactive Seeding after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it&lt;br /&gt;
in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|4. Under the &amp;quot;Tractography Seeding Parameters&amp;quot; set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15 ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42107</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42107"/>
		<updated>2015-07-09T20:23:00Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Tractography exploration of the ipsilateral and contralateral side */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on Apply 3 times to generate the peritumoral volume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|5. a) For Output Fiber Bundle select &amp;quot;Create and&lt;br /&gt;
rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|6. a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.  ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. a) Click on the Modules menu and select the module&lt;br /&gt;
Tractography Interactive Seeding after selecting &amp;quot;Diffusion&amp;quot; then selecting &amp;quot;Diffusion Tensor Imaging&amp;quot;. b) For the Red Slice view position the mouse over the pin icon and change the volume to DTIVolume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Select the Fiducial icon located at the top, and position the F-1 point next to the cystic part of the tumor by clicking near it&lt;br /&gt;
in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. Under the &amp;quot;Tractography Seeding Parameters set the Minimum Path Length to 10.0 mm and the FA Stopping Value at 0.15 ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|4. Under IO set Input DTI Volume to &amp;quot;DTIVolume&amp;quot;, set Fiducial List or Model to &amp;quot;F&amp;quot;, set Output Fiber Bundle to &amp;quot;Create new Fiber Bundle&amp;quot;, then click ok for the pop-up.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42099</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42099"/>
		<updated>2015-07-09T19:58:14Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Tractography exploration of peritumoral white matter fibers */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. a) Make sure the cystic part is selected and visible in the 3 slice views. b) Click on the Dilate Effect tool then click on the cystic part of the tumor on the red slice view.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on Apply 3 times to generate the peritumoral volume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. Select the module &amp;quot;Tractography Label Map Seeding&amp;quot; by clicking &amp;quot;Editor&amp;quot; at the top, then &amp;quot;Diffusion&amp;quot;, then &amp;quot;Diffusion Tensor Imaging&amp;quot;.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|4. Make sure that &amp;quot;DTI Volume&amp;quot; is selected for Input DTI Volume and &amp;quot;BaselineVolumeregion_1-label&amp;quot; is selected for Input Label Map]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|5. a) For Output Fiber Bundle select &amp;quot;Create and&lt;br /&gt;
rename newFiberBundle&amp;quot;. b)When the pop-up appears rename the fiber bundle to to &amp;quot;newFiberBundle&amp;quot;. ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|6. a) Under the Seed Placement Options: Check the Use Index Space. b) Under Tractography Seeding parameter set the stopping value to &amp;quot;0.15&amp;quot; and make sure for Stopping Criteria that &amp;quot;Fractional Anisotropy&amp;quot; is selected.  ]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|7. Under Label Definition set the &amp;quot;Seeding Label&amp;quot; to 293, and Click on Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42098</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42098"/>
		<updated>2015-07-09T19:22:50Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Tractography */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of peritumoral white matter fibers===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42097</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42097"/>
		<updated>2015-07-09T18:36:35Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Tractography */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=File:O.gif&amp;diff=42096</id>
		<title>File:O.gif</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=File:O.gif&amp;diff=42096"/>
		<updated>2015-07-09T18:35:05Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=File:N.gif&amp;diff=42095</id>
		<title>File:N.gif</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=File:N.gif&amp;diff=42095"/>
		<updated>2015-07-09T18:34:26Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=File:M.gif&amp;diff=42094</id>
		<title>File:M.gif</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=File:M.gif&amp;diff=42094"/>
		<updated>2015-07-09T18:33:48Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=File:L.gif&amp;diff=42093</id>
		<title>File:L.gif</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=File:L.gif&amp;diff=42093"/>
		<updated>2015-07-09T18:32:53Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42092</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42092"/>
		<updated>2015-07-09T18:32:24Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Loading DTI and Baseline Data */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography exploration of the ipsilateral and contralateral side ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42091</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42091"/>
		<updated>2015-07-09T18:18:45Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:l.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:m.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:n.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:o.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=File:A.gif&amp;diff=42090</id>
		<title>File:A.gif</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=File:A.gif&amp;diff=42090"/>
		<updated>2015-07-09T18:12:39Z</updated>

		<summary type="html">&lt;p&gt;Irosen: uploaded a new version of &amp;quot;File:A.gif&amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=File:D.gif&amp;diff=42089</id>
		<title>File:D.gif</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=File:D.gif&amp;diff=42089"/>
		<updated>2015-07-09T18:11:57Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=File:B.gif&amp;diff=42088</id>
		<title>File:B.gif</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=File:B.gif&amp;diff=42088"/>
		<updated>2015-07-09T18:11:20Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=File:A.gif&amp;diff=42087</id>
		<title>File:A.gif</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=File:A.gif&amp;diff=42087"/>
		<updated>2015-07-09T18:06:24Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42086</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42086"/>
		<updated>2015-07-09T18:04:54Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Tractography */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42085</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42085"/>
		<updated>2015-07-09T18:04:05Z</updated>

		<summary type="html">&lt;p&gt;Irosen: /* Tractography */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:a.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:b.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:d.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42084</id>
		<title>Documentation/4.4/gif tutorial</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=Documentation/4.4/gif_tutorial&amp;diff=42084"/>
		<updated>2015-07-09T18:02:59Z</updated>

		<summary type="html">&lt;p&gt;Irosen: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;|[[image:Neurosurgical Planning tutorial.png|700px|center]]&lt;br /&gt;
&lt;br /&gt;
===Loading DTI and Baseline Data===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:1.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:2.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:3.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:4.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
===Segmentation===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:5.gif|600px|frame|1. a) Click on the Modules menu and select the module Editor. b)The ‘SlicerApp-real’ window appears. Select the label map GenericAnatomyColors and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:6.gif|600px|frame|2. a) Select the PaintEffect b) Scroll down the Editor module and choose color #293 for the region 1 label]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:7.gif|600px|frame|3. a) In a single motion, draw a short line in the cystic part of the tumor b) Select color #294 for the mass label and, again in a single motion, draw a short line in the solid part of the tumor c) Select color #295 for the region 3 and draw a circle around the tumor]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:8.gif|600px|frame|4. Select the GrowCutEffect tool and then click Apply]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:9.gif|600px|frame|5. Scroll up the Editor menu and select the tab Per-Structure Volumes. Then click Split Merge Volume.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:10.gif|600px|frame|6. a) Select the volume BaselineVolumeregion_3-label so that it is highlighted and that the yellow region is visible in the viewer b) Select the ThresholdEffect tool]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:11.gif|600px|frame|7. Scroll down the Editor module and set the lower Threshold Range to 1700 and click Apply.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:12.gif|600px|frame|8. a) Select the SaveIslandEffect in the Editor module b) With the SaveIslandEffect tool equipped, click in the occipital horn of the ventricle.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:13.gif|600px|frame|9. a) Scroll back up and click on Merge and Build to merge the different label maps, and generate the 3D models of the tumor and ventricles using a Marching Cubes algorithm. b) Click on the Layout menu and select Conventional.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:14.gif|600px|frame|10. Slicer displays the 3D surface reconstructions of the ventricles, and solid and cystic parts of the tumor.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:15.gif|600px|frame|11. Position the mouse over the pin icon, and select the eye icon to view the all the slices in the 3D viewer.]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
===Tractography===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:c.gif|600px|frame|Manually adjust the Window Level editor presets with the Volume module menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
&amp;lt;div style=&amp;quot;width: 62%; height:525px; overflow:auto; border: 2px solid #088; margin: 1em auto 1em auto;&amp;quot;&amp;gt;&lt;br /&gt;
{|style=&amp;quot;width: 62%; height: 200px;&amp;quot; border=&amp;quot;1&amp;quot;&lt;br /&gt;
|[[image:x.gif|600px|frame|1. Load the sample data by selecting &amp;quot;Load Data&amp;quot;, then &amp;quot;Choose Directory to Add&amp;quot; and finally going to wherever it is that you downloaded the sample data and selecting the folder WhiteMatterExplorationData]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:y.gif|600px|frame|2. Click on the pin icon to display the slice menu,then click on the link icon to link the 3 anatomical viewers. Then change the background so it is set to BaselineVolume]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|[[image:z.gif|600px|frame|3. a) Click on the Layout Menu and select Red Slice Only. b) Select the Volumes Module from the Modules menu]]&lt;br /&gt;
|- style=&amp;quot;height: 100px;&amp;quot;&lt;br /&gt;
|}&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
	<entry>
		<id>https://www.slicer.org/w/index.php?title=File:Y.gif&amp;diff=42083</id>
		<title>File:Y.gif</title>
		<link rel="alternate" type="text/html" href="https://www.slicer.org/w/index.php?title=File:Y.gif&amp;diff=42083"/>
		<updated>2015-07-09T17:57:24Z</updated>

		<summary type="html">&lt;p&gt;Irosen: uploaded a new version of &amp;quot;File:Y.gif&amp;quot;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;/div&gt;</summary>
		<author><name>Irosen</name></author>
		
	</entry>
</feed>