<node id="290111">
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  <created>1397223522</created>
  <changed>1492118562</changed>
  <title><![CDATA[Bioengineering Seminar Series]]></title>
  <body><![CDATA[<p><strong>“Interrogating Cell-to-Cell Heterogeneity by Stochastic Profiling”<br /><br />Kevin Janes, PhD</strong><br /><strong>Assistant Professor</strong><br /><strong>Department of Biomedical Engineering</strong><br /><strong>University of Virginia<br /><br /></strong>Regulated changes in gene expression underlie many biological processes, but globally profiling cell-to-cell variations in transcriptional regulation is problematic when measuring single cells.&nbsp; The Janes lab has developed an approach, called stochastic profiling, that applies probability theory to transcriptome-wide measurements of small pools of cells to identify single-cell regulatory heterogeneities (Nat Methods 7:311-7 [2010]).&nbsp; In the first half of the talk, Janes will discuss a two-state regulatory circuit that was identified by stochastic profiling (Nat Cell Biol 16:345-56 [2014]).&nbsp; The circuit involves TGFb-family signaling and the junD transcription factor, which are asynchronously activated in 3D breast epithelial cultures to coordinate normal morphogenesis.&nbsp; The circuit also appears to be re-initiated during the early stages of basal-like breast cancer, contributing to the mosaicked expression patterns observed clinically by histology.&nbsp; In the second half of the talk, Janes will talk about work in progress that applies stochastic profiling as a tool for uncovering the mechanistic basis of phenotypes that are incompletely penetrant.&nbsp; Regulatory-state frequencies are matched to downstream phenotype frequencies to converge upon a tractable set of candidate states worthy of follow-up experimentation.&nbsp; Using the ErbB2 oncoprotein as a model trigger for an incompletely penetrant phenotype, they identify a handful of surprising candidates that significantly affect penetrance when perturbed.&nbsp; Stochastic profiling remains the only method compatible with cells microdissected in situ and thereby opens exciting opportunities in the areas of tissue morphogenesis and cancer<strong>.</strong></p>]]></body>
  <field_summary_sentence>
    <item>
      <value><![CDATA[“Interrogating Cell-to-Cell Heterogeneity by Stochastic Profiling” - Kevin Janes, PhD - University of Virginia]]></value>
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  </field_summary_sentence>
  <field_summary>
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      <value><![CDATA[<p>The Bioengineering Seminar Series is a joint seminar series between the Petit Institute and the Biomedical Engineering department. Seminars are held on Tuesdays or Thursdays between 11am-12pm in Petit Institute, room 1128, unless otherwise indicated.</p>]]></value>
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  <field_time>
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      <value><![CDATA[2014-09-23T16:00:00-04:00]]></value>
      <value2><![CDATA[2014-09-23T17:00:00-04:00]]></value2>
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      <timezone><![CDATA[America/New_York]]></timezone>
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      <value><![CDATA[]]></value>
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        <value><![CDATA[Undergraduate students]]></value>
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        <value><![CDATA[Faculty/Staff]]></value>
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        <value><![CDATA[Graduate students]]></value>
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  <field_contact>
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      <value><![CDATA[<p>Faculty host: <a href="%20melissa.kemp@bme.gatech.edu">Melissa Kemp, PhD</a></p>]]></value>
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  <field_phone>
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      <value><![CDATA[(404) 894-6228]]></value>
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      <url><![CDATA[http://www.ibb.gatech.edu]]></url>
      <title><![CDATA[]]></title>
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        <url>http://bme.virginia.edu/janes/index.html</url>
        <link_title><![CDATA[Janes lab website]]></link_title>
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          <item><![CDATA[Parker H. Petit Institute for Bioengineering and Bioscience (IBB)]]></item>
          <item><![CDATA[Bioengineering Graduate Program]]></item>
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        <tid>1795</tid>
        <value><![CDATA[Seminar/Lecture/Colloquium]]></value>
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        <tid>11877</tid>
        <value><![CDATA[BioE Seminar]]></value>
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        <tid>248</tid>
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