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      <title>Genomics Case 1 Question 1B by </title>
      <link>https://padlet.com/haspelr/4glpoa0ayh64fage</link>
      <description>You are considering genetic testing to aid in selecting chemotherapy. </description>
      <language>en-us</language>
      <pubDate>2021-09-16 14:46:40 UTC</pubDate>
      <lastBuildDate>2021-10-28 12:31:17 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>Which panel would you select? </title>
         <author>haspelr</author>
         <link>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1746207940</link>
         <description><![CDATA[<div><strong>There are 2 gene panels you are considering for your patient (workshop faculty do not endorse any specific laboratory):&nbsp;<br></strong><br></div><div>Laboratory 1: <a href="https://bit.ly/TRIGLab1"><strong>https://bit.ly/TRIGLab1</strong></a></div><div>Laboratory 2: <a href="https://bit.ly/TRIGLab2"><strong>https://bit.ly/TRIGLab2</strong></a>&nbsp;</div><div><br><strong>Which panel would you select?&nbsp; Explain your choice in up to three sentences. Review relevant guidelines.</strong>&nbsp;</div><div>_____________________________________________<strong><br></strong>To create a new post, double-click on a blank space or click the plus sign in the lower right-hand corner. You can ignore the&nbsp; Subject line if you prefer. In the body (under the icons), type your response.&nbsp; Click "Publish" when you are finished. You can resize your posts by dragging on the edges<strong><br><br></strong><a href="https://devryuniversity.padlet.org/eanderson90/genomics21"><strong>RETURN to Main Padlet here</strong></a><strong>.</strong></div>]]></description>
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         <pubDate>2021-09-16 14:46:40 UTC</pubDate>
         <guid>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1746207940</guid>
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         <title></title>
         <author></author>
         <link>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767687890</link>
         <description><![CDATA[<div>Lab 2; that select panel is all what is needed currently for targeted therapy of that tumor</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-09-25 19:04:16 UTC</pubDate>
         <guid>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767687890</guid>
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         <title></title>
         <author></author>
         <link>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767687906</link>
         <description><![CDATA[<div>Panel 1 as tumor may have acquired new mutations </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-09-25 19:04:17 UTC</pubDate>
         <guid>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767687906</guid>
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      <item>
         <title>2nd.  NCCN guidelines</title>
         <author></author>
         <link>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767687927</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-09-25 19:04:18 UTC</pubDate>
         <guid>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767687927</guid>
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         <title></title>
         <author></author>
         <link>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767687953</link>
         <description><![CDATA[<div>panel #2 because more clinically relevant and cost efficient</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-09-25 19:04:20 UTC</pubDate>
         <guid>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767687953</guid>
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      <item>
         <title>Foundation Medicine CDx for the following reasons:</title>
         <author></author>
         <link>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767688311</link>
         <description><![CDATA[<div>NTRK3 and 2 missing in targeted panel<br>NCCN recommends TMB which is missing in targeted panel<br>Improves options for clinical trials for patients to have larger panel</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-09-25 19:04:45 UTC</pubDate>
         <guid>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767688311</guid>
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      <item>
         <title></title>
         <author></author>
         <link>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767688389</link>
         <description><![CDATA[<div>Larger panel for a more comprehensive analysis. Would cast a wider net to identify what is driving patients disease. Limited panel might miss unusual alterations even in select genes. </div>]]></description>
         <enclosure url="" />
         <pubDate>2021-09-25 19:04:52 UTC</pubDate>
         <guid>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767688389</guid>
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      <item>
         <title>Panel #1, if still cost effective. Tests the most clinically relevant genes + more for opportunity for more individualized care</title>
         <author></author>
         <link>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767689008</link>
         <description><![CDATA[]]></description>
         <enclosure url="" />
         <pubDate>2021-09-25 19:05:41 UTC</pubDate>
         <guid>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767689008</guid>
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      <item>
         <title></title>
         <author></author>
         <link>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767690340</link>
         <description><![CDATA[<div>2</div>]]></description>
         <enclosure url="" />
         <pubDate>2021-09-25 19:07:17 UTC</pubDate>
         <guid>https://padlet.com/haspelr/4glpoa0ayh64fage/wish/1767690340</guid>
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