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	<id>https://www.na-mic.org/w/index.php?action=history&amp;feed=atom&amp;title=MBIRN%3A_Reproducibility_of_T2</id>
	<title>MBIRN: Reproducibility of T2 - Revision history</title>
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	<updated>2026-05-19T09:07:16Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://www.na-mic.org/w/index.php?title=MBIRN:_Reproducibility_of_T2&amp;diff=4191&amp;oldid=prev</id>
		<title>Andy: Update from Wiki</title>
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		<updated>2006-12-18T13:37:43Z</updated>

		<summary type="html">&lt;p&gt;Update from Wiki&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;'''UPDATES'''&lt;br /&gt;
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* '''May 17, 2005''' (J. MacFall, J. Jovicich)&lt;br /&gt;
** Reproducibility of white matter lesions with T2/PD/FLAIR/T1: controls and depressed subjects with white matter lesions are being recruited for acquisition of test-retest data on three platforms: GE 1.5T, Siemens 3T, GE 4T. Expect to scan first subject within a month. Although nice, it's unlikely that we can fit an additional DTI scan in this 1-hour protocol. Analysis plan is to start using Guido Gerig's lesion detection tool. We could use the NAMIC drive to push the distribution of this tool. '''NEED:''' recommendation for T1 protocol, and RF coils.&lt;br /&gt;
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* '''Feb 11, 2005''' (J. MacFall, J. Jovicich)&lt;br /&gt;
** James &amp;amp; Jorge met over the phone for updates&lt;br /&gt;
** The Duke scanners that will be used for lesion reproducibility are: GE 1.5T, GE 4T, Siemens 3T&lt;br /&gt;
** Subjects: (number?) subjects will be scanned at each of the three scanners twice in a 6-month period. I expect to begin recruitment soon and imaging in late March or early April. That means that by early October we should have the whole data acquired.&lt;br /&gt;
** Acquisition Protocols:&lt;br /&gt;
*** 3D T1: FLASH 30deg/5deg for 1.5T. Needs feedback from Anders re 3T &amp;amp; Allen re 4T&lt;br /&gt;
*** 2D FSE T2/PD&lt;br /&gt;
*** 2D FLAIR&lt;br /&gt;
** Analysis: G. Gerig's multi-spectral segmentation tool (lesion, CSF, WM, GM) will be used to look at reproducibility across platforms. Who will be responsible for running this analyses and pushing for a publication?&lt;br /&gt;
** Tests: wouldn't it be prudent to have a normal control be scanned at least on the high field systems to make sure that the acquisition protocols have some preliminary tuning before the subjects with lesions come in?&lt;br /&gt;
** T2 goals for Oct 2005: Presumably we should be able to have acquired all data (two time-points per subject on the three platforms). We should have also completed the segmentations for all first-time lesion brains and completed across-platform reproducibility analysis of these.&lt;br /&gt;
** We have been focusing on the administrative matters of getting the contract finalized. This could not be done without the calibration IRB being finalized and I am happy to report that we now have the IRB in place (Biomedical Informatics Research Network (BIRN) Imaging Reproducibility Study, Duke IRB # 6789-05-2R0). This now allows the Duke contract to be finalized.&lt;br /&gt;
** We reviewed Duke's [[Active_Collaborations|Active Collaborations]]&lt;br /&gt;
** We also reviewed [[MIRIAD|MIRIAD]] progress&lt;br /&gt;
** It was clarified that the Morph BIRN grant 'cuts' reflect simply the new grant cycle that NCRR made for us, so that the budget period is from 09/30/2004 - 05/31/2005 (8 months instead of 12, so it looks like a 33% cut if you think that it corresponds to a full calendar year).&lt;br /&gt;
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* '''Jan 6, 2005''' (J. MacFall)&lt;br /&gt;
** Budget cut is being discussed and we are meeting Friday to figure out how to modify Duke's objectives&lt;br /&gt;
** IRB used for the grant submission is not suitable for grant so we have submitted a new one that will require full board review. It may be approved in February 2005.&lt;br /&gt;
** We have a large group of suitable subjects but we have to get permission from the IRB to use the list generated for another study.&lt;br /&gt;
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		<author><name>Andy</name></author>
		
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