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      <image:title>News - Check out our latest pre-print!</image:title>
      <image:caption>If you are interested in high-throughput microfluidic droplet screening, check out our latest pre-print “Continuous FACS sorting of double emulsion picoreactors with a 3D printed vertical mixer.“ This project was led by postdocs Samuel Thompson &amp; Zijian (ZJ) Yang's (from the Soh lab) and demonstrates successful FACS sorting double emulsions at rates of 1,000,000/hour!</image:caption>
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      <image:title>News - CONGRATULATIONS NICOLE! - Make it stand out</image:title>
      <image:caption>Whatever it is, the way you tell your story online can make all the difference.</image:caption>
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    <lastmod>2024-06-04</lastmod>
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    <lastmod>2024-06-04</lastmod>
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    <lastmod>2021-10-15</lastmod>
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    <lastmod>2021-09-21</lastmod>
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    <loc>http://www.fordycelab.com/blog/2021/9/14/welcome-gaeun</loc>
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    <lastmod>2021-09-14</lastmod>
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    <loc>http://www.fordycelab.com/blog/2021/9/1/welcome-daria</loc>
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    <lastmod>2021-09-01</lastmod>
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    <loc>http://www.fordycelab.com/blog/2021/4/8/welcome-micah</loc>
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    <lastmod>2021-04-08</lastmod>
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    <loc>http://www.fordycelab.com/blog/2021/4/2/welcome-minsung</loc>
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    <lastmod>2021-04-02</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2021/3/23/congratulations-michael</loc>
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    <priority>0.5</priority>
    <lastmod>2021-03-24</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2021/3/1/welcome-to-the-world-rex</loc>
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    <lastmod>2021-03-01</lastmod>
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      <image:title>News - Welcome to the world, Rex!</image:title>
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    <loc>http://www.fordycelab.com/blog/2021/2/19/congratulations-conor</loc>
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    <lastmod>2021-02-19</lastmod>
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    <lastmod>2021-01-20</lastmod>
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    <loc>http://www.fordycelab.com/blog/2020/9/22/congratulations-peter</loc>
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    <lastmod>2020-09-22</lastmod>
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    <loc>http://www.fordycelab.com/blog/2020/9/22/congratulations-to-andy-and-the-beads-team</loc>
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    <lastmod>2020-09-22</lastmod>
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    <loc>http://www.fordycelab.com/blog/2020/9/22/welcome-renee</loc>
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    <lastmod>2020-09-22</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2020/9/15/farewell-to-gauen-and-jamin</loc>
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    <lastmod>2020-09-15</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2020/9/15/welcome-samuel</loc>
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    <lastmod>2020-09-15</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2020/9/15/congrats-bea</loc>
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    <lastmod>2020-09-15</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2020/9/15/welcome-michael</loc>
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    <lastmod>2020-09-15</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2020/6/30/arjun-aditham-publishes-a-paper</loc>
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    <lastmod>2020-07-02</lastmod>
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      <image:title>News - Arjun Aditham publishes a paper!</image:title>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2020/6/30/andy-publishes-paper</loc>
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    <lastmod>2020-06-30</lastmod>
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      <image:title>News - Congratulations to Yinnian (Andy) Feng on his new manuscript!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2020/6/30/kara-brower</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2020-07-02</lastmod>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1593714108811-8R4QOLJJX57JCSJ1BCTG/Screen+Shot+2020-06-30+at+10.17.43+AM.png</image:loc>
      <image:title>News - Kara Brower publishes paper!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2020/5/29/nicole-delrosso-passes-her-quals</loc>
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    <lastmod>2020-05-29</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2019/10/2/fordyce-lab-tours-our-new-lab-space</loc>
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    <priority>0.5</priority>
    <lastmod>2019-10-03</lastmod>
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      <image:title>News - Fordyce Lab Tours Our New Lab Space!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2019/4/19/polly-is-the-speaker-of-lets-have-an-awesome-time-doing-science-may-1-2019</loc>
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    <priority>0.5</priority>
    <lastmod>2019-04-19</lastmod>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1555713019397-4QLFYMBJVWAZUA1VHVTJ/LHAATDS_flyer_2019.jpg</image:loc>
      <image:title>News - Polly is the speaker of "Let's Have an Awesome Time Doing Science" - May 1, 2019</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2019/4/12/congratulate-gaeun-for-receiving-75k-on-an-reu-fellowship</loc>
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    <priority>0.5</priority>
    <lastmod>2019-04-12</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1555111038553-O8ZALICSHNQVBO6SF4ZH/image-2.jpg</image:loc>
      <image:title>News - congratulate Gaeun for receiving $7.5k on an REU Fellowship!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/8/31/polly-named-scialog-fellow-kdddg</loc>
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    <priority>0.5</priority>
    <lastmod>2019-04-12</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1555096090931-DZDUR6GFM7Z9NKKZZIFU/birthday.jpg</image:loc>
      <image:title>News - Hooray! Happy Birthday to Adam and Mason!</image:title>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1555096175937-MWO4S20XWMV904RMPFXK/birthday%2B2.jpg</image:loc>
      <image:title>News - Hooray! Happy Birthday to Adam and Mason!</image:title>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2019/3/14/professor-polly-fordyce-to-give-her-vision-talk-this-friday</loc>
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    <priority>0.5</priority>
    <lastmod>2019-04-12</lastmod>
    <image:image>
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      <image:title>News - Professor Polly Fordyce to give her Vision Talk this Friday</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2019/4/12/craig-and-daniels-poster-at-biophysical-society-conference-was-popular</loc>
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    <priority>0.5</priority>
    <lastmod>2019-04-12</lastmod>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1555111444955-7UO1UTZIS6CA7YN3YZEJ/Image%2Bfrom%2BiOS%2B%25281%2529.jpg</image:loc>
      <image:title>News - Craig and Daniel’s Poster at Biophysical Society Conference was popular.</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/8/31/polly-named-scialog-fellow</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2019-04-02</lastmod>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1504211714306-X7Z0IPA9J9Q0JQP1JHTZ/rescorp_logo.png</image:loc>
      <image:title>News - Polly named Scialog Fellow</image:title>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1504212053925-KUP7TH0XV7JBP1I7FXCW/gordon+betty+moore.jpeg</image:loc>
      <image:title>News - Polly named Scialog Fellow</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/8/31/bianca-cruz-joins-the-lab</loc>
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    <priority>0.5</priority>
    <lastmod>2017-09-01</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1504211381487-EXNIFAS9L7LHBA6EP78Z/bianca+cruz.png</image:loc>
      <image:title>News - Bianca Cruz joins the lab for the summer!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2018/9/5/kara-and-craig-present-at-the-gordon-research-conference</loc>
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    <priority>0.5</priority>
    <lastmod>2018-09-06</lastmod>
    <image:image>
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      <image:title>News - Polly, Kara &amp; Craig attend the GRC Microfluidic Conference in Italy</image:title>
    </image:image>
    <image:image>
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      <image:title>News - Polly, Kara &amp; Craig attend the GRC Microfluidic Conference in Italy</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/8/13/karas-paper-describing-an-open-source-pneumatics-build-for-microfluidic-control-is-posted-in-biorxiv</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2019-04-02</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/6/6/kara-earns-a-centennial-teaching-award</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2019-04-02</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/5/10/pollys-microfluidics-work-covered-in-stanford-alumni-1</loc>
    <changefreq>monthly</changefreq>
    <priority>0.5</priority>
    <lastmod>2017-05-10</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1494457911490-OF52RQTEMDTPX71ZDSFV/image-asset.jpeg</image:loc>
      <image:title>News - Polly's course covered in Stanford Alumni Magazine!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/3/9/polly-in-the-news</loc>
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    <priority>0.5</priority>
    <lastmod>2017-03-10</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1489114383465-GOL631DGYIQP4RMT6Y93/image-asset.jpeg</image:loc>
      <image:title>News - Polly profiled for Stanford Medicine News</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/2/27/alli-keyes-joins-the-lab</loc>
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    <priority>0.5</priority>
    <lastmod>2017-03-10</lastmod>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1488225506912-45VIPPN0WTXRS3EBEN0O/image-asset.png</image:loc>
      <image:title>News - Alli Keys joins the lab!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/2/23/polly-is-named-a-2017-sloan-fellow</loc>
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    <priority>0.5</priority>
    <lastmod>2017-02-24</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1487894496354-HM62JNKRDDTA099EU6X8/image-asset.jpeg</image:loc>
      <image:title>News - Polly is named a 2017 Sloan Fellow!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/2/21/polly-is-named-a-chan-zuckerberg-investigator</loc>
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    <priority>0.5</priority>
    <lastmod>2017-02-22</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1487743554539-71TQTNT5F0W0GHG8M3PT/image-asset.png</image:loc>
      <image:title>News - Polly is named a Chan Zuckerberg Investigator!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2017/2/21/alex-sockell-joins-the-lab</loc>
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    <priority>0.5</priority>
    <lastmod>2017-02-22</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/11/29/film-crew-visits-the-lab-for-our-upcoming-jove-article</loc>
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    <lastmod>2016-11-30</lastmod>
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      <image:title>News - Film crew visits the lab for our upcoming JoVE article!</image:title>
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    <image:image>
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      <image:title>News - Film crew visits the lab for our upcoming JoVE article!</image:title>
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    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1480466673856-PUO9ZBZIIZKT2EMCZH12/File_002.jpeg</image:loc>
      <image:title>News - Film crew visits the lab for our upcoming JoVE article!</image:title>
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    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1480466674803-9A4LJBMJ7T47REU6UK1B/File_003.jpeg</image:loc>
      <image:title>News - Film crew visits the lab for our upcoming JoVE article!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/11/29/tyler-officially-becomes-a-phd-candidate</loc>
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    <priority>0.5</priority>
    <lastmod>2016-11-30</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/10/18/our-new-paper-describing-spectrally-encoded-beads-with-1000-codes-is-out</loc>
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    <priority>0.5</priority>
    <lastmod>2016-10-18</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/10/4/the-fordyce-lab-is-awarded-an-nih-new-innovator-award</loc>
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    <priority>0.5</priority>
    <lastmod>2016-10-04</lastmod>
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      <image:title>News - The Fordyce Lab is awarded an NIH New Innovator Award!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/9/27/the-fordyce-lab-is-awarded-2-bio-x-seed-grants</loc>
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    <priority>0.5</priority>
    <lastmod>2016-09-28</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/7/27/welcome-huy-quoc-nguyen-and-congratulations</loc>
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    <priority>0.5</priority>
    <lastmod>2016-07-27</lastmod>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1469647163543-A3GMMCYY3OCATV13K9KT/image-asset.jpeg</image:loc>
      <image:title>News - Welcome Huy Quoc Nguyen and congratulations!</image:title>
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  <url>
    <loc>http://www.fordycelab.com/blog/2016/7/6/welcome-rebecca-varun-and-alex</loc>
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    <priority>0.5</priority>
    <lastmod>2016-07-06</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2018/9/5/craig-is-awarded-a-cihr-postdoctoral-fellowship</loc>
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    <priority>0.5</priority>
    <lastmod>2018-09-06</lastmod>
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      <image:title>News - Craig is awarded a CIHR Postdoctoral Fellowship!</image:title>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/6/22/adam-white-is-awarded-a-stanford-deans-postdoctoral-fellowship</loc>
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    <priority>0.5</priority>
    <lastmod>2016-06-23</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/6/22/welcome-arjun-aditham-and-scott-longwell</loc>
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    <lastmod>2016-06-23</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/6/16/fordyce-lab-wins-a-nist-jimb-seed-grant</loc>
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    <priority>0.5</priority>
    <lastmod>2016-06-17</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2016/6/13/welcome-tyler-shimko</loc>
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    <lastmod>2016-06-13</lastmod>
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      <image:title>News - Welcome Tyler Shimko!</image:title>
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  <url>
    <loc>http://www.fordycelab.com/blog/2016/4/18/bioengineering-retreat-2016</loc>
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    <lastmod>2016-04-18</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2016/4/18/fordyce-lab-awarded-a-beckman-technology-development-grant</loc>
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    <lastmod>2016-04-18</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2016/2/18/welcome-to-tyler-dave-and-scott-1</loc>
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    <lastmod>2016-02-19</lastmod>
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    <loc>http://www.fordycelab.com/blog/2015/10/1/welcome-linfeng-and-theo</loc>
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    <lastmod>2015-10-02</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2015/8/5/congratulations-to-kara-on-her-seed-grant</loc>
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    <lastmod>2015-08-06</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2015/8/5/welcome-craig-markin-1</loc>
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    <lastmod>2015-08-06</lastmod>
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      <image:title>News - Welcome Craig Markin!</image:title>
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  <url>
    <loc>http://www.fordycelab.com/blog/2015/6/30/welcome-chantal-guegler</loc>
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    <lastmod>2015-07-01</lastmod>
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      <image:title>News - Welcome Chantal Guegler!</image:title>
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  <url>
    <loc>http://www.fordycelab.com/blog/2015/5/14/seeking-applicants-for-joint-postdoctoral-position-with-novartis-and-nistabms</loc>
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    <lastmod>2015-05-15</lastmod>
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    <loc>http://www.fordycelab.com/blog/2015/4/20/kara-presents-the-first-fordyce-lab-poster</loc>
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    <lastmod>2015-04-21</lastmod>
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      <image:title>News - Kara presents the first Fordyce Lab poster!</image:title>
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  <url>
    <loc>http://www.fordycelab.com/blog/2015/3/31/congratulations-to-kara-eli-and-naomi</loc>
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    <priority>0.5</priority>
    <lastmod>2015-03-31</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2015/3/31/welcome-to-naomi-and-chris</loc>
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    <lastmod>2015-04-20</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/blog/2015/2/24/kara-brower-joins-the-fordyce-lab</loc>
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    <priority>0.5</priority>
    <lastmod>2015-04-20</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2015/2/24/more-lab-firsts</loc>
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    <lastmod>2015-02-25</lastmod>
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      <image:title>News - More lab firsts!</image:title>
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      <image:title>News - More lab firsts!</image:title>
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  <url>
    <loc>http://www.fordycelab.com/blog/2015/1/23/a-series-of-lab-firsts</loc>
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    <priority>0.5</priority>
    <lastmod>2015-01-23</lastmod>
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      <image:title>News - A series of lab firsts</image:title>
      <image:caption>First lab gel!</image:caption>
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    <image:image>
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      <image:title>News - A series of lab firsts</image:title>
      <image:caption>First wafer fabrication!</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2014/11/12/robert-puccinelli-joins-the-fordyce-lab</loc>
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    <priority>0.5</priority>
    <lastmod>2014-11-13</lastmod>
  </url>
  <url>
    <loc>http://www.fordycelab.com/blog/2014/6/27/fordyce-lab-opens-for-business-at-stanford</loc>
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    <lastmod>2014-06-30</lastmod>
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  <url>
    <loc>http://www.fordycelab.com/people-gallery</loc>
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      <image:title>People Gallery - Polly Fordyce</image:title>
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      <image:caption>Principal Investigator. She/Her Click here for CV. Click here for bio. Hobbies: Running, climbing, hiking, and spending time with my family</image:caption>
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      <image:caption>Graduate Student Chemical Engineering She/They Hobbies: Baking, cooking, painting, swimming, playing computer games and ttrpg, learning fun facts about octopus.</image:caption>
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      <image:caption>Principal Investigator. She/Her Click here for CV. Click here for bio. Hobbies: Running, climbing, hiking, and spending time with my family</image:caption>
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      <image:caption>Postdoctoral Fellow (joint with Herschlag Lab) He/Him Hobbies: Reading, crafting, rewatching The West Wing</image:caption>
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      <image:caption>Graduate Student Chemical Engineering He/Him Hobbies: Running, hiking, tossing frisbee, and solving the Monday NYT crossword puzzle</image:caption>
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      <image:caption>Postdoctoral Fellow Genetics Hobbies: biking, baking, sewing, thinking about stories.</image:caption>
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      <image:caption>Graduate Student Genetics He/Him Hobbies: Drumming, hiking with my dog, cooking</image:caption>
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      <image:caption>Graduate Student Bioengineering (Joint w/Dror Lab) she/her Hobbies: Hiking, skiing, eating any and all sweets</image:caption>
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      <image:caption>Postdoctoral Fellow (joint with Herschlag lab) He/Him Hobbies: Rock climbing, baseball, snowboarding</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1690304697814-MM3C1NPENVC25GVM6784/IMG_0268.jpg</image:loc>
      <image:title>People Gallery - Conor McClune</image:title>
      <image:caption>Postdoctoral Fellow (joint with Sattely Lab) He/Him Hobbies: Trail running, gardening, sparring with the HOA</image:caption>
    </image:image>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1732563806416-MVCVJVUGNB5Q6JEQI5Y9/foto+perfil.jpg</image:loc>
      <image:title>People Gallery - Ana Morzan</image:title>
      <image:caption>Lab Administrator Hobbies: Running, backpacking, climbing, and crocheting</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1719347030632-W5TRA1721AUZN0NRHHEA/IMG_0066.jpeg</image:loc>
      <image:title>People Gallery - Micah Olivas</image:title>
      <image:caption>Graduate Student Genetics He/Him Personal Site Hobbies: Live music, cooking, playing guitar, crashing weddings</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1633110809590-WM8C4B7UKCJVOO5YYUOF/Screen+Shot+2021-10-01+at+10.52.42+AM.png</image:loc>
      <image:title>People Gallery - Jennifer Ortiz Cárdenas</image:title>
      <image:caption>Microfluidics Foundry Director &amp; Outreach Coordinator She\Her Hobbies: Discovering new restaurants and wine bars, taking my dogs to the beach in Half Moon Bay, cooking new recipes, and watching reality TV.</image:caption>
    </image:image>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1724890300226-OGNUDCL7IEH8O7EU6F2P/image-asset.jpeg</image:loc>
      <image:title>People Gallery - Daria Passow</image:title>
      <image:caption>Graduate Student Biophysics She/Her Hobbies: listening to audiobooks, walking and cycling, reading MotorTrend magazine</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1755638326650-8BI15PF0T1N3LLD4F6WP/2025_professional_headshot_lowres.jpg</image:loc>
      <image:title>People Gallery - Lillian Petersen</image:title>
      <image:caption>Graduate Student Genetics (joint with Bintu Lab) Hobbies: Running, hiking, cycling, skiing, reading, violin, exploring art museums</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1690305635891-X0A7NSLUMIDTP7PO1ZXW/IMG_7644+-+Maya+Sheth.jpeg</image:loc>
      <image:title>People Gallery - Maya Sheth</image:title>
      <image:caption>Graduate Student Bioengineering She/Her Hobbies: Hiking, dogs, crossword puzzles</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1724890412813-QG1LMVUIIS8Y1S2FQT3W/F73BE9BB-58AB-4647-8989-23B728F5AAFD_1_105_c.jpeg</image:loc>
      <image:title>People Gallery - Alan Su</image:title>
      <image:caption>Graduate Student (joint w/ Petrov Lab) Chemical &amp; Systems Biology He/Him Hobbies: Basking in the glorious sun, squash, Formula 1, MTV's The Challenge, soup.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1536714108204-IQ2E6J446TPT9269JOHM/office-wall.jpg</image:loc>
      <image:title>People Gallery - Polly Fordyce</image:title>
      <image:caption>Principal Investigator. Click here for CV. Click here for bio.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1690309760758-8UOS46JQ8C8538BMZLQF/photo.jpg</image:loc>
      <image:title>People Gallery - Peter Suzuki</image:title>
      <image:caption>Graduate Student (joint with Bintu Lab) Bioengineering He/Him (LinkedIn) Hobbies: Music of all sorts (guitar + violin, from Silvio Rodriguez to the Strokes), baseball, policy/politics podcasts</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1415832767158-N1DL6IWPZTPDPXCJCUY2/RobertPuccinelli_2p5inchestall.jpg</image:loc>
      <image:title>People Gallery - Robert Puccinelli</image:title>
      <image:caption>Research Associate.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1690305994248-Y707FEBJ62M19G4Q536I/23_crop.jpg</image:loc>
      <image:title>People Gallery - Samuel (Channel) Thompson</image:title>
      <image:caption>Postdoctoral Fellow (joint with Baker Lab) He/She/They LinkedIn Hobbies: Baking, drawing, writing, listening to lots of audiobooks</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/research-summary-gallery</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2019-11-20</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474958399717-T0OY8IZ0MA8NSFMOCSA0/devicefromend_wlightbox_01_cropped_SMALL.jpg</image:loc>
      <image:title>Research Summary Gallery</image:title>
      <image:caption>MITOMI (Mechanically-Induced Trapping of Molecular Interactions) relies on spatial multiplexing to keep track of analytes throughout an experiment.  We are currently using these devices to better understand how transcription factors find and bind their genomic targets to regulate gene expression, as well as to understand how enzymes achieve their extraordinary catalytic efficiency and substrate specificity.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474958399717-T0OY8IZ0MA8NSFMOCSA0/devicefromend_wlightbox_01_cropped_SMALL.jpg</image:loc>
      <image:title>Research Summary Gallery</image:title>
      <image:caption>MITOMI (Mechanically-Induced Trapping of Molecular Interactions) relies on spatial multiplexing to keep track of analytes throughout an experiment.  We are currently using these devices to better understand how transcription factors find and bind their genomic targets to regulate gene expression, as well as to understand how enzymes achieve their extraordinary catalytic efficiency and substrate specificity.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474958323594-MD9YVQSRCZGTG18BZUYK/CoverArt_Option2.jpg</image:loc>
      <image:title>Research Summary Gallery</image:title>
      <image:caption>MRBLEs (Microspheres with Ratiometric Barcode Lanthanide Encoding) rely on spectral multiplexing to track analytes throughout an experiment.  In these assays, we can create microspheres containing &gt; 1,000 unique ratios of lanthanide nanophosphors that can be uniquely identified via imaging alone.  We are currently developing new assays that use these microspheres to understand how signaling proteins recognize their peptide substrates and to improve our ability to extract information from single cells.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474913093720-O4IEAAV2C1P5E6E3XG2P/devicefromend_wlightbox_01_cropped_SMALL.jpg</image:loc>
      <image:title>Research Summary Gallery - MITOMI</image:title>
      <image:caption>MITOMI (Mechanically-Induced Trapping of Molecular Interactions) relies on spatial multiplexing to keep track of analytes throughout an experiment.  We are currently using these devices to better understand how transcription factors find and bind their genomic targets to regulate gene expression, as well as to understand how enzymes achieve their extraordinary catalytic efficiency and substrate specificity.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474958296928-MMGXAY22CY9BP5SG654J/devicefromend_wlightbox_01_cropped_SMALL.jpg</image:loc>
      <image:title>Research Summary Gallery</image:title>
      <image:caption>MITOMI (Mechanically-Induced Trapping of Molecular Interactions) relies on spatial multiplexing to keep track of analytes throughout an experiment.  We are currently using these devices to better understand how transcription factors find and bind their genomic targets to regulate gene expression, as well as to understand how enzymes achieve their extraordinary catalytic efficiency and substrate specificity.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2016-11-04</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1475094955982-1LYKCV0AVE9M3O7P38AX/IconForWebsite.png</image:loc>
      <image:title>Publications Gallery 2016</image:title>
      <image:caption>Multi-step variable height photolithography for valved multilayer microfluidic devices. Brower, K.*, White, A.K.*, &amp; Fordyce, P.M. Journal of Visualized Experiments (in press). (* denotes equal authorship).</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1475094955982-1LYKCV0AVE9M3O7P38AX/IconForWebsite.png</image:loc>
      <image:title>Publications Gallery 2016</image:title>
      <image:caption>Multi-step variable height photolithography for valved multilayer microfluidic devices. Brower, K.*, White, A.K.*, &amp; Fordyce, P.M. Journal of Visualized Experiments (in press). (* denotes equal authorship).</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474961534820-B8VTGPUFQU6VFWP7PFD9/CoverArt_Option2.jpg</image:loc>
      <image:title>Publications Gallery 2016</image:title>
      <image:caption>Programmable microfluidic synthesis of over one thousand uniquely identifiable spectral codes. Nguyen, H.Q., Baxter, B.C., Brower, K., Diaz-Botia, C.A., DeRisi, J.L, Fordyce, P.M.*, and Thorn., K.S.* Advanced Optical Materials (2016). (* denotes co-corresponding authors). (pdf) (web)</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/research-project-gallery</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2016-09-27</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474958833280-37FBCEJCLQBJMDE4AUML/160919_MITOMI_DNA_Bound.jpg</image:loc>
      <image:title>MITOMI Project Gallery</image:title>
      <image:caption>Probing how transcription factors find and bind their genomic targets Gene expression is governed by binding of transcription factor proteins to regulatory sequences in the genome, where they either recruit or block transcriptional machinery to activate or repress expression.  Despite many years of research, we remain largely unable to predict where transcription factors bind in vivo, and current models cannot explain how closely related transcription factors often regulate very distinct sets of target genes.  We are combining the MITOMI platform with tools from chemical biology to precisely dissect the biophysical mechanisms by which transcription factors recognize DNA and improve our ability to predict these essential interactions.  </image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474958833280-37FBCEJCLQBJMDE4AUML/160919_MITOMI_DNA_Bound.jpg</image:loc>
      <image:title>MITOMI Project Gallery</image:title>
      <image:caption>Probing how transcription factors find and bind their genomic targets Gene expression is governed by binding of transcription factor proteins to regulatory sequences in the genome, where they either recruit or block transcriptional machinery to activate or repress expression.  Despite many years of research, we remain largely unable to predict where transcription factors bind in vivo, and current models cannot explain how closely related transcription factors often regulate very distinct sets of target genes.  We are combining the MITOMI platform with tools from chemical biology to precisely dissect the biophysical mechanisms by which transcription factors recognize DNA and improve our ability to predict these essential interactions.  </image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474958883719-LGMHY71MT9RGT2MT4KY3/Rplot.png</image:loc>
      <image:title>MITOMI Project Gallery</image:title>
      <image:caption>Revealing how kinetics of transcription factor binding affect occupancy and gene expression Recent evidence suggests that non-equilibrium binding dynamics may govern transcription factor activity at regulatory sites in the genome. Despite this fact, nearly all investigations of transcription factor binding in vitro measure only binding at equilibrium, without observing kinetics.  We are developing a high-throughput microfluidic assay that can measure the residency time of molecular interactions.  We expect this assay will be compatible with both extracted DNA and chromatin, allowing for investigations of the native epigenetic contexts that shape gene expression.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474958855217-QSDIVBY5GCOQH2M2H4S4/craig_AP_network_figure.jpg</image:loc>
      <image:title>MITOMI Project Gallery</image:title>
      <image:caption>Understanding how enzymes achieve their extraordinary catalytic efficiency and specificity Enzymes are the most efficient catalysts known, enhancing specific reaction rates by up to 17 orders of magnitude. However, we do not fully understand how they achieve this tremendous catalytic efficiency, which limits our ability to understand their biological function and design new enzymes with industrially or medically important applications.  In close collaboration with the Herschlag lab, we are using the MITOMI platform to enable high-throughput investigation of how individual residues throughout an enzyme contribute to catalysis.  This new platform allows detailed biochemical characterization of thousands of enzymes in parallel, enabling structure/function studies of enzymes at unprecedented scale.  </image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1475004169196-NY8C3JG8B5UC5KJ8E0L4/IMG_20160927_113332.jpg</image:loc>
      <image:title>MITOMI Project Gallery</image:title>
      <image:caption>Automating printing and image acquisition and analysis Uncovering the biophysical mechanisms that drive transcription factor binding requires the ability to efficiently and reproducibly collect and compare data from many proteins.  To streamline this process, we have been automating all asepcts of the experiments, from rebuilding old microarray printers to developing new software for valve automation and image processing.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/mrbles-project-gallery</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2016-09-27</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474960907065-PUCQH7LN3UVEVFQSBY4T/PxIxIT+Library+2+CN+WT+250+nM.jpg</image:loc>
      <image:title>MRBLEs Project Gallery</image:title>
      <image:caption>A high-throughput assay for profiling protein-peptide interactions While advances in deep sequencing have dramatically improved our ability to profile how DNA and RNA binding proteins interact with their substrates, we lack similar tools for quantitative, high-throughput investigation of protein-peptide interactions.  We have recently demonstrated that peptides can be synthesized directly on our encoded MRBLEs, laying the foundation for novel high-throughput on-bead assays to probe how proteins recognize their peptide substrates.  In collaboration with the Cyert Lab, we are using this platform to understand how calcineurin, a human phosphatase essential for the immune response and the target of several immunosuppresents, binds its targets.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474960907065-PUCQH7LN3UVEVFQSBY4T/PxIxIT+Library+2+CN+WT+250+nM.jpg</image:loc>
      <image:title>MRBLEs Project Gallery</image:title>
      <image:caption>A high-throughput assay for profiling protein-peptide interactions While advances in deep sequencing have dramatically improved our ability to profile how DNA and RNA binding proteins interact with their substrates, we lack similar tools for quantitative, high-throughput investigation of protein-peptide interactions.  We have recently demonstrated that peptides can be synthesized directly on our encoded MRBLEs, laying the foundation for novel high-throughput on-bead assays to probe how proteins recognize their peptide substrates.  In collaboration with the Cyert Lab, we are using this platform to understand how calcineurin, a human phosphatase essential for the immune response and the target of several immunosuppresents, binds its targets.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474960526618-2AJQNJY4FV0LY172J8PR/dmd_light_directed_synthesis_CROP.png</image:loc>
      <image:title>MRBLEs Project Gallery</image:title>
      <image:caption>A cheap and scalable way to synthesize custom peptide libraries on encoded beads The ability to flexible construct specific peptide libraries on spectrally encoded beads would provide a powerful proteomic tool.  Using a commercial video projector ($300, Amazon.com), we are developing a new system that uses patterned light to synthesize specific peptide sequences onto beads spatially arrayed within a microfluidic device.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474960538778-3WYXH6GDGDQBZZL1S89L/Composite+of+img0000s.png</image:loc>
      <image:title>MRBLEs Project Gallery</image:title>
      <image:caption>Using encoded beads to link genotype and phenotype for many single cells in parallel Recent developments in single-cell analysis have enabled the probing of phenotypes, transcriptomes, and genomes for individual cells, revealing previously hidden heterogeneity within cell populations of high significance for human health and disease.  The next great challenge is to understand both the cause and effect of this heterogeneity by linking changes in genetic information with their functional effects.  We are developing a new technologies that uses oligonucleotide arrays coupled to encoding beads to link different types of measurements for the same cell.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2014</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2016-09-27</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474992852121-XLI8IIL7V13UU9ISV3QN/LysNetworkDiagram_Small.jpg</image:loc>
      <image:title>Publications Gallery 2014</image:title>
      <image:caption>How duplicated transcription regulators can diversify to govern the expression of non overlapping sets of genes. Perez, J.C., Fordyce, P.M., Lohse, M.B., Hanson-Smith, V., DeRisi, J.L., &amp; Johnson, A.D. Genes &amp; Development (2014). (pdf) (web)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474992852121-XLI8IIL7V13UU9ISV3QN/LysNetworkDiagram_Small.jpg</image:loc>
      <image:title>Publications Gallery 2014</image:title>
      <image:caption>How duplicated transcription regulators can diversify to govern the expression of non overlapping sets of genes. Perez, J.C., Fordyce, P.M., Lohse, M.B., Hanson-Smith, V., DeRisi, J.L., &amp; Johnson, A.D. Genes &amp; Development (2014). (pdf) (web)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474993034967-9DSFEYSC8MHCRKZ9M7VF/larva02.JPG</image:loc>
      <image:title>Publications Gallery 2014</image:title>
      <image:caption>Hydraulic expulsion of tumbu fly larvae. Dybbro, E., Fordyce, P., Ponte, M., &amp; Arron, S.T. JAMA Derm. (2014). (pdf) (web)</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2013</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2016-09-27</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474993380123-OHI06THKBY6FK27RHG7A/WhiteOpaqueSwitching_Small.jpg</image:loc>
      <image:title>Publications Gallery 2013</image:title>
      <image:caption>Structure of the transcriptional network controlling white-opaque switching in Candida albicans. Hernday, A.D., Lohse, M.B.*, Fordyce, P.M.*, Nobile, C.J., DeRisi, J.L., &amp; Johnson, A.D. Molecular Microbiology (2013). (* denotes equal authorship). (pdf) (web)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474993380123-OHI06THKBY6FK27RHG7A/WhiteOpaqueSwitching_Small.jpg</image:loc>
      <image:title>Publications Gallery 2013</image:title>
      <image:caption>Structure of the transcriptional network controlling white-opaque switching in Candida albicans. Hernday, A.D., Lohse, M.B.*, Fordyce, P.M.*, Nobile, C.J., DeRisi, J.L., &amp; Johnson, A.D. Molecular Microbiology (2013). (* denotes equal authorship). (pdf) (web)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474993527561-4ABSESFQHQI67F8FFKS7/FOXP2Motif_HumanOnly.jpg</image:loc>
      <image:title>Publications Gallery 2013</image:title>
      <image:caption>Microfluidic affinity and ChIP-Seq analyses converge on a conserved FOXP2-binding motif in chimp and human, which enables the detection of evolutionarily novel targets.  Nelson, C.S., Fuller, C.K., Fordyce, P.M., Greninger, A.L., Li, H., &amp; DeRisi, J.L. Nucleic Acids Research (2013). (pdf) (web)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474993688964-BDGP4JY6BWGK3RC9W6H9/FinalWor3Motif.jpg</image:loc>
      <image:title>Publications Gallery 2013</image:title>
      <image:caption>Identification and characterization of a previously undescribed family of sequence-specific DNA-binding domains. Lohse, M.B., Hernday, A.D., Fordyce, P.M., Noiman, L., Sorrells, T.R., Hanson-Smith, V., Nobile, C., DeRisi, J.L., &amp; Johnson, A.D. PNAS (2013). (pdf) (web)</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2012</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2016-09-27</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474995136135-KFWYA24OT3TAQ2TQWYLH/Hac1Motifs_150PH.png</image:loc>
      <image:title>Publications Gallery 2012</image:title>
      <image:caption>Basic leucine zipper transcription factor Hac1 binds DNA in two distinct modes as revealed by microfluidic analyses. Fordyce, P.M., Pincus, D., Kimmig, P., Nelson, C.S., El-Samad, H., Walter, P., &amp; DeRisi, J.L. PNAS (2012). (pdf) (web)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474995136135-KFWYA24OT3TAQ2TQWYLH/Hac1Motifs_150PH.png</image:loc>
      <image:title>Publications Gallery 2012</image:title>
      <image:caption>Basic leucine zipper transcription factor Hac1 binds DNA in two distinct modes as revealed by microfluidic analyses. Fordyce, P.M., Pincus, D., Kimmig, P., Nelson, C.S., El-Samad, H., Walter, P., &amp; DeRisi, J.L. PNAS (2012). (pdf) (web)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1474995177657-OWXG1UQ3MPPQWDKLLLGA/BFBeadsInSerpentine_10x_0.7x_small.jpg</image:loc>
      <image:title>Publications Gallery 2012</image:title>
      <image:caption>Programmable microfluidic synthesis of spectrally encoded microspheres. Gerver, R.E.*, Gomez-Sjoberg, R.*, Baxter, B.C.*, Thorn, K.S.*, Fordyce, P.M.*, Diaz-Botia, C.A., Helms, B.A., &amp; DeRisi, J.L. Lab on a Chip (2012). (* denotes equal authorship, author order was determined by random draw). (pdf) (web)</image:caption>
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      <image:title>Publications Gallery 2012</image:title>
      <image:caption>Systematic characterization of feature dimensions and closing pressures for microfluidic valves produced via photoresist reflow. Fordyce, P.M., Diaz-Botia, C.A., DeRisi, J.L., &amp; Gomez-Sjoberg, R. Lab on a Chip (2012). (pdf) (web)</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2001</loc>
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    <lastmod>2016-09-27</lastmod>
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      <image:title>Publications Gallery 2001</image:title>
      <image:caption>Search for the decay KL -&gt; pi(0)e+e-. Alavi-Harati, A., et al. Physical Review Letters (2001). (web)</image:caption>
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      <image:title>Publications Gallery 2001</image:title>
      <image:caption>Search for the decay KL -&gt; pi(0)e+e-. Alavi-Harati, A., et al. Physical Review Letters (2001). (web)</image:caption>
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      <image:title>Publications Gallery 2001</image:title>
      <image:caption>Measurement of the branching ratio of the decay KL -&gt; e+e-gammagamma. Alavi-Harati, et al. Physical Review D (2001). (web)</image:caption>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2003</loc>
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    <lastmod>2016-09-27</lastmod>
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      <image:title>Publications Gallery 2003</image:title>
      <image:caption>Combined optical trapping and single-molecule fluorescence. Lang, M.J., Fordyce, P.M., &amp; Block, S.M. Journal of Biology (2003). (pdf) (web)</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1475016760145-FM13DZW7DLD3YXA3VCJE/KinesinRunLengths.jpg</image:loc>
      <image:title>Publications Gallery 2003</image:title>
      <image:caption>Stepping and stretching: how kinesis uses external strain to step processively. Rosenfeld, S.S., Fordyce, P.M., Jefferson, G.M., King, P.H., &amp; Block, S.M. Journal of Biological Chemistry (2003). (pdf) (web)</image:caption>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2011</loc>
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    <lastmod>2016-09-27</lastmod>
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      <image:title>Publications Gallery 2011</image:title>
      <image:caption>Integrating systems biology data to yield functional genomics insights. Fordyce, P., &amp; Ingolia, N. Genome Biology (2011). (pdf) (web)</image:caption>
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      <image:title>Publications Gallery 2011</image:title>
      <image:caption>Integrating systems biology data to yield functional genomics insights. Fordyce, P., &amp; Ingolia, N. Genome Biology (2011). (pdf) (web)</image:caption>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2008</loc>
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    <lastmod>2016-09-27</lastmod>
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      <image:title>Publications Gallery 2008</image:title>
      <image:caption>Advances in surface-based assays for single molecules. Fordyce, P.M.*, Valentine, M.T.*, &amp; Block, S.M. in "ingle-Molecule Techniques: A Laboratory Manual" (Cold Spring Harbor Monograph Series) (2008). (* denotes equal authorship) (pdf) (web)</image:caption>
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      <image:title>Publications Gallery 2008</image:title>
      <image:caption>Advances in surface-based assays for single molecules. Fordyce, P.M.*, Valentine, M.T.*, &amp; Block, S.M. in "ingle-Molecule Techniques: A Laboratory Manual" (Cold Spring Harbor Monograph Series) (2008). (* denotes equal authorship) (pdf) (web)</image:caption>
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      <image:title>Publications Gallery 2008</image:title>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2010</loc>
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    <lastmod>2016-09-27</lastmod>
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      <image:title>Publications Gallery 2010</image:title>
      <image:caption>De novo identification and biophysical characterization of transcription factor binding with microfluidic affinity analysis. Fordyce, P.M.*, Gerber, D.*, Tran, D., Zheng, J., Li, H., DeRisi, J.L., &amp; Quake, S.R. Nature Biotechnology (2010). (* denotes equal authorship) (pdf) (web)</image:caption>
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      <image:title>Publications Gallery 2010</image:title>
      <image:caption>De novo identification and biophysical characterization of transcription factor binding with microfluidic affinity analysis. Fordyce, P.M.*, Gerber, D.*, Tran, D., Zheng, J., Li, H., DeRisi, J.L., &amp; Quake, S.R. Nature Biotechnology (2010). (* denotes equal authorship) (pdf) (web)</image:caption>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2004</loc>
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    <lastmod>2016-09-27</lastmod>
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      <image:title>Publications Gallery 2004</image:title>
      <image:caption>Simultaneous, coincident optical trapping and single-molecule fluorescence. Lang, M.J.*, Fordyce, P.M.*, Engh, A.M., Neuman, K.C., &amp; Block, S.M. Nature Methods (2004). (* denotes equal authorship). (pdf) (web)</image:caption>
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      <image:title>Publications Gallery 2004</image:title>
      <image:caption>Simultaneous, coincident optical trapping and single-molecule fluorescence. Lang, M.J.*, Fordyce, P.M.*, Engh, A.M., Neuman, K.C., &amp; Block, S.M. Nature Methods (2004). (* denotes equal authorship). (pdf) (web)</image:caption>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2006</loc>
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    <lastmod>2016-09-27</lastmod>
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      <image:title>Publications Gallery 2006</image:title>
      <image:caption>Eg5 steps it up! Valentine, M.T., Fordyce, P.M., &amp; Block, S.M. Cell Division (2006). (pdf) (web)</image:caption>
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      <image:title>Publications Gallery 2006</image:title>
      <image:caption>Eg5 steps it up! Valentine, M.T., Fordyce, P.M., &amp; Block, S.M. Cell Division (2006). (pdf) (web)</image:caption>
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      <image:title>Publications Gallery 2006</image:title>
      <image:caption>Individual dimers of the mitotic kinetin Eg5 step processively and support substantial loads in vitro. Valentine, M.T.*, Fordyce, P.M.*, Krzysiak, T.C., Gilbert, S.P., &amp; Block, S.M. Nature Cell Biology (2006). (* denotes equal authorship) (pdf) (web)</image:caption>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2017</loc>
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    <priority>0.75</priority>
    <lastmod>2021-01-27</lastmod>
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      <image:title>Publications Gallery 2017</image:title>
      <image:caption>An open-Source, programmable pneumatic setup for operation and automated control of single-and multi-Layer microfluidic devices. Brower, K., Puccinelli, R., Markin, C., Shimko, T., Longwell, S., Cruz, B., Gomez-Sjoberg, R, Fordyce, P.; HardwareX (2017) (web); preprint on bioRXiv (2017) (web). OSF repository available here.</image:caption>
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      <image:title>Publications Gallery 2017</image:title>
      <image:caption>An open-Source, programmable pneumatic setup for operation and automated control of single-and multi-Layer microfluidic devices. Brower, K., Puccinelli, R., Markin, C., Shimko, T., Longwell, S., Cruz, B., Gomez-Sjoberg, R, Fordyce, P.; HardwareX (2017) (web); preprint on bioRXiv (2017) (web). OSF repository available here.</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1496951558151-AMFTJGJ9378B4RZZ8VU9/SPIE+logo.png</image:loc>
      <image:title>Publications Gallery 2017</image:title>
      <image:caption>Peptide library synthesis on spectrally encoded beads for multiplexed protein/peptide bioassays. Nguyen, H.Q., Brower, K., Harink, B., Baxter, B, Thorn, K., Fordyce, P. Proc. SPIE 10061, Microfluidics, BioMEMS, and Medical Microsystems XV, 100610Z (2017) (web).</image:caption>
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      <image:title>Publications Gallery 2017</image:title>
      <image:caption>Joker de Bruijn: Sequence libraries to cover all k-mers using joker characters. Ornenstein, Y., Puccinelli, R., Kim, R., Fordyce, P., and Berger, B.; Cell Systems (2017) (web).</image:caption>
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  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2018</loc>
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    <priority>0.75</priority>
    <lastmod>2019-10-19</lastmod>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1555103186057-DULUGYALXL94DAOW47EZ/Screen+Shot+2018-12-09+at+9.29.32+PM.png</image:loc>
      <image:title>Publications Gallery 2018</image:title>
      <image:caption>Diversification of DNA binding specificities enabled SREBP transcription regulators to expand the repertoire of cellular functions that they govern in fungi. Toledo, V. D. O., Puccinelli, R., Fordyce, P.M., and Perez, J.C. PLoS Genetics (in press). (PDF) (Web)</image:caption>
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      <image:title>Publications Gallery 2018</image:title>
      <image:caption>Diversification of DNA binding specificities enabled SREBP transcription regulators to expand the repertoire of cellular functions that they govern in fungi. Toledo, V. D. O., Puccinelli, R., Fordyce, P.M., and Perez, J.C. PLoS Genetics (in press). (PDF) (Web)</image:caption>
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      <image:title>Publications Gallery 2018</image:title>
      <image:caption>BET-seq: Binding energy topographies revealed by microfluidics and high-throughput sequencing. Aditham, A.K., Shimko, T.C., and Fordyce, P.M. Methods in Cell Biology - Microfluidics on a Molecular Scale (2018). (PDF) (web).</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541050796546-MW2LNRN0SO9XEXF9Y539/Screen+Shot+2018-10-31+at+10.38.50+PM.png</image:loc>
      <image:title>Publications Gallery 2018</image:title>
      <image:caption>Satb1 integrates DNA sequence, shape, motif density and torsional stress to differentially bind targets in nucleosome-dense regions. Ghosh, R.P., Shi, Q., Yang, L., Reddick, M.P., Nikitina, T., Zhurkin, V.B., Fordyce, P., Stasevich, T.J., Chang, H.Y., Greenleaf, W.J., and Liphardt, J.T., preprint on bioRXiv 10/2018; doi:10.1101/450262. (web)</image:caption>
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      <image:title>Publications Gallery 2018</image:title>
      <image:caption>High-throughput chromatin accessibility profiling at single-cell resolution. Mezger, A., Klemm, S., Mann, I., Brower, K., Mir, A., Bostick, M., Farmer, A., Fordyce, P., Linnarsson, S., &amp; Greenleaf, W.; Nat. Comm. (2018) (pdf) (web) (bioRXiv doi: 10.1101/310284)</image:caption>
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      <image:title>Publications Gallery 2018</image:title>
      <image:caption>Discovering epistatic feature interactions from neural network models of regulatory DNA sequences. Greenside, P.G., Shimko, T., Fordyce, P., &amp; Kundaje, A.; preprint on bioRXiv (04/17/2018); doi: 10.1101/302711 (web)</image:caption>
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      <image:title>Publications Gallery 2018</image:title>
      <image:caption>Comprehensive, high-resolution binding energy landscapes reveal context dependencies of transcription factor binding. Le, D.D., Shimko, T.C., Aditham, A.K., Keys, A.M., Orenstein, Y., and Fordyce, P.M. PNAS (3/27,8) (web) (pdf) (preprint in bioRXiv (9/26/17)</image:caption>
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      <image:title>Publications Gallery 2018</image:title>
      <image:caption>Diversification of DNA binding specificities enabled SREBP transcription regulators to expand the repertoire of cellular functions that they govern in fungi. del Olmo Toledo, V., Puccinelli, R., Fordyce, P.M., &amp; Perez, J.C. PLoS Genetics (in press).</image:caption>
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      <image:loc>https://static1.squarespace.com/static/53aa0662e4b0d4cbb80321fe/5ae90d5e70a6ad102dad9eda/5cb0fe01fa0d602643b99d55/1555103841002/</image:loc>
      <image:title>Publications Gallery 2018</image:title>
      <image:caption>BET-seq: Binding energy topographies revealed by microfluidics and high-throughput sequencing. Aditham, A.K., Shimko, T.C., and Fordyce, P.M. Methods in Cell Biology - Microfluidics on a Molecular Scale (2018). (web).</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2019</loc>
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    <priority>0.75</priority>
    <lastmod>2021-01-27</lastmod>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1571443304320-A3P8XTOX7177AMAA4UXO/Screen+Shot+2019-10-18+at+5.01.24+PM.png</image:loc>
      <image:title>Publications Gallery 2019</image:title>
      <image:caption>micrIO: An open-source autosampler and fraction collector for automated microfluidic input-output. Longwell, S.A., &amp; Fordyce, P.M. Lab on a Chip (2019). (PDF) (web)</image:caption>
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      <image:title>Publications Gallery 2019</image:title>
      <image:caption>micrIO: An open-source autosampler and fraction collector for automated microfluidic input-output. Longwell, S.A., &amp; Fordyce, P.M. Lab on a Chip (2019). (PDF) (web)</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1571443935137-LPURF960O1BFYTTOW41E/Screen+Shot+2019-10-18+at+5.11.42+PM.png</image:loc>
      <image:title>Publications Gallery 2019</image:title>
      <image:caption>Why do long zinc finger proteins have short motifs? Zuo, Z., Billings, T., Walker, M., Petkov, P., Fordyce, P., &amp; Stormo, G.D. bioRXiv (2019). (PDF) (web)</image:caption>
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      <image:title>Publications Gallery 2019</image:title>
      <image:caption>Quantitative mapping of protein-peptide affinity landscapes using spectrally encoded beads. Nguyen, H. Q., Roy, J., Harink, B., Damle, N. P., Latorraca, N. R., Baxter, B. C., Brower, K., Longwell, S., Kortemme, T., Thorn, K. S., Cyert, M. S., Fordyce, P.M eLife 8 (2019): e40499 (PDF) (Web) (OSF repository with all data)</image:caption>
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      <image:title>Publications Gallery 2019</image:title>
      <image:caption>Live imaging of Aiptasia larvae, a model system for coral and anemone bleaching, using a simple microfluidic device Treuren, W. V.*, Brower, K. K*., Labanieh, L., Hunt, D., Lensch, S., Cruz, B., Cartwright, H. N., Tran, C., Fordyce, P. M. Scientific reports 9 (2019). (PDF) (Web)</image:caption>
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      <image:title>Publications Gallery 2019</image:title>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1563556027171-11MA1ASOFSC947PA4YHQ/Capture.PNG</image:loc>
      <image:title>Publications Gallery 2019</image:title>
      <image:caption>An open-source software analysis package for Microspheres with Ratiometric Barcode Lanthanide Encoding (MRBLEs) Harink, B., Nguyen, H., Thorn, K., Fordyce, P. M. PLOS/ONE (PDF) (Web) (OSF Repository).</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/dropception-projects-gallery</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2020-03-17</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574145728146-ETW89ZYSFM1UMUU9BGG6/DECharacterization.png</image:loc>
      <image:title>Dropception Projects Gallery</image:title>
      <image:caption>Systematic characterization of DE droplets – By studying correlations between flow rates, droplet size, and device geometries, we are systematically optimizing DE droplet generation and testing fundamental droplet fluid physics and surfactant compatibility in complex interfaces.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574145728146-ETW89ZYSFM1UMUU9BGG6/DECharacterization.png</image:loc>
      <image:title>Dropception Projects Gallery</image:title>
      <image:caption>Systematic characterization of DE droplets – By studying correlations between flow rates, droplet size, and device geometries, we are systematically optimizing DE droplet generation and testing fundamental droplet fluid physics and surfactant compatibility in complex interfaces.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1584410966443-34HA3UB0YML16HI132N7/SingleCellMultiOmics.png</image:loc>
      <image:title>Dropception Projects Gallery</image:title>
      <image:caption>Multi-parameter single-cell analysis – Using sortable double emulsions, we are developing assays to simultaneously screen for rare cell populations and characterize downstream single cell gene expression (RNA-Seq) or epigenomic signatures (ATAC-Seq). The goal of these efforts is to enable new droplet-based techniques that allow tandem ‘omics measurements on the same single cell.</image:caption>
    </image:image>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574145744826-20RIV3KI8H9KWSBHN606/PlantCells.png</image:loc>
      <image:title>Dropception Projects Gallery</image:title>
      <image:caption>Characterization of individual plant cells at scale – The flexibility of double emulsion droplets permits us to bring single-cell analysis tools to new organisms and new assays. We are developing new ways to measure the transcriptomic profiles and phenotypes of individual rare plant cells of interest.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/mrbles-project-gallery-2019</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2020-01-29</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574147344290-C9LB81HPAWUQ7AZ6C055/MRBLE-path.png</image:loc>
      <image:title>MRBLEs Project Gallery 2019</image:title>
      <image:caption>MRBLE-path - In sepsis, the time to antibiotic treatment is critical for patient survival, and the choice of treatment depends on the pathogen responsible for infection. We are developing a new method to rapidly screen for the presence of multiple bacteria species in a single reaction using oligonucleotide hybridization probes conjugated to MRBLEs with a 1:1 relationship between probe sequence and embedded code, allowing multiplexed measurement of pathogens via imaging alone.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574147344290-C9LB81HPAWUQ7AZ6C055/MRBLE-path.png</image:loc>
      <image:title>MRBLEs Project Gallery 2019</image:title>
      <image:caption>MRBLE-path - In sepsis, the time to antibiotic treatment is critical for patient survival, and the choice of treatment depends on the pathogen responsible for infection. We are developing a new method to rapidly screen for the presence of multiple bacteria species in a single reaction using oligonucleotide hybridization probes conjugated to MRBLEs with a 1:1 relationship between probe sequence and embedded code, allowing multiplexed measurement of pathogens via imaging alone.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574148631026-2LTNA1VDYLFKG3ZRJNKI/Screen%2BShot%2B2019-11-18%2Bat%2B11.28.23%2BPM.jpg</image:loc>
      <image:title>MRBLEs Project Gallery 2019</image:title>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574148690705-M1ST7EHAD4VVPKS2QR8A/MRBLEPepHeatMap.png</image:loc>
      <image:title>MRBLEs Project Gallery 2019</image:title>
      <image:caption>MRBLE-pep - While advances in deep sequencing have dramatically improved our ability to profile how DNA and RNA binding proteins interact with their substrates, we lack similar tools for quantitative, high-throughput investigation of protein-peptide interactions. Here, we synthesize libraries of peptides directly on MRBLEs with a 1:1 linkage between embedded code and peptide sequence, allowing high-throughput measurement of 100 weak protein-peptide interactions in parallel using very little material. In collaboration with the Cyert lab, we are using this platform to understand how human signaling proteins recognize their downstream targets.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574147535101-M4KSF0EZSN6VYGHYJZF3/BATTLES.png</image:loc>
      <image:title>MRBLEs Project Gallery 2019</image:title>
      <image:caption>BATTLES - T cells can discriminate between self- and non-self-antigens with exquisite sensitivity and specificity: even a single non-self antigen in a sea of 100,000 self antigens. Despite the central importance of this process for immune surveillance, we do not yet understand the mechanisms involved or how to manipulate them to generate new therapies. We are using MRBLEs to allow high-throughput measurements of how T cell activation depends on presented antigen sequence and applied forces.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/mitomi-2019</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2019-11-20</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574281611840-G6FGHOQ8N4ILFUZ1TQTI/CACGTG.jpg</image:loc>
      <image:title>MITOMI 2019</image:title>
      <image:caption>Probing the dark matter of regulatory DNA - Though &gt; 90% of disease-causing variants in the human genome occur outside protein-coding regions, how these non-coding variants impact levels of gene expression remains largely unknown. To address this gap, we are leveraging the MITOMI platform to probe how sequence context outside transcription factor binding sites tunes binding kinetics and thermodynamics.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574281611840-G6FGHOQ8N4ILFUZ1TQTI/CACGTG.jpg</image:loc>
      <image:title>MITOMI 2019</image:title>
      <image:caption>Probing the dark matter of regulatory DNA - Though &gt; 90% of disease-causing variants in the human genome occur outside protein-coding regions, how these non-coding variants impact levels of gene expression remains largely unknown. To address this gap, we are leveraging the MITOMI platform to probe how sequence context outside transcription factor binding sites tunes binding kinetics and thermodynamics.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574281660902-C59YY8GVJBAYZD91HAGC/TFMutations.jpg</image:loc>
      <image:title>MITOMI 2019</image:title>
      <image:caption>Dissecting the functional effects of transcription factor mutations - Transcription Factor (TF) proteins bind regulatory DNA sequences to control the expression of downstream genes, and mutations to TFs can affect the affinity and specificity of DNA binding. We are using microfluidic devices to quantitatively measure DNA binding affinities and dissociation kinetics for 1000s of TF-DNA interactions in parallel. This approach provides critical experimental data needed to build computational models of effects of TF mutations required for precision medicine.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574281688495-I04ZXD715HG9SNFNX6FQ/HT-MEK.jpg</image:loc>
      <image:title>MITOMI 2019</image:title>
      <image:caption>HT-MEK: a new kind of enzymology - We have developed a new platform (HT-MEK, for high-throughput microfluidic enzyme kinetics) that enables, for the first time, the rapid and quantitative measurement of multiple parameters for designed enzyme libraries. To date, we have characterized over 1,100 enzyme mutants (measuring &gt;10,000 individual kinetic and thermodynamic parameters), and have identified structurally segregated regions controlling distinct biochemical properties within a model system phosphatase. Ultimately, these measurements will help yield next-generation predictive models of mutational effects required for rational enzyme design and precision medicine.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574281951115-U312ISGLMIZYP1JBGQ6O/HT-MES.jpg</image:loc>
      <image:title>MITOMI 2019</image:title>
      <image:caption>High-throughput and quantitative measurements of protein stability - Disease-associated protein mutations often act by destabilizing protein structure. In personalized medicine, the majority of disease-associated mutations are of unknown significance, preventing clinical action. We are developing parallel assays to quantify folding stability for thousands of proteins variants in parallel, using next-generation sequencing and fluorescence microscopy. With these approaches, we aim to characterize the protein stability landscape and better understand mechanisms of loss-of-function involved in disease.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574281929272-MVAD8K9T9HQVWE99U4JB/BET-seq.jpg</image:loc>
      <image:title>MITOMI 2019</image:title>
      <image:caption>BET-seq: ultra-high-throughput measurement of transcription factor-DNA binding affinities - The rapidly decreasing costs of next-generation sequencing (NGS) present an opportunity to sequence and identify millions of DNA molecules in parallel. Here, we paired MITOMI devices with NGS to quantitatively measure transcription factor binding energies for a million sequences in a single experiment. We are currently applying this platform to study how flanking nucleotides outside the canonical binding site can impact TF-DNA binding affinity.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/research-summary-gallery-2019</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2020-03-17</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574221655539-YBUBIIPUYAN3TWA2ZU04/devicefromend_wlightbox_01_cropped_SMALL.jpg</image:loc>
      <image:title>Research Summary Gallery 2019</image:title>
      <image:caption>Array-based multiplexing experiments (MITOMI and HT-MEK) employ microfluidic devices containing 1,568 valved reaction chambers aligned to printed DNA arrays. We are currently using these devices to better understand how transcription factors find and bind their genomic targets to regulate gene expression, as well as to understand how enzymes achieve their extraordinary catalytic efficiency and substrate specificity.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574221655539-YBUBIIPUYAN3TWA2ZU04/devicefromend_wlightbox_01_cropped_SMALL.jpg</image:loc>
      <image:title>Research Summary Gallery 2019</image:title>
      <image:caption>Array-based multiplexing experiments (MITOMI and HT-MEK) employ microfluidic devices containing 1,568 valved reaction chambers aligned to printed DNA arrays. We are currently using these devices to better understand how transcription factors find and bind their genomic targets to regulate gene expression, as well as to understand how enzymes achieve their extraordinary catalytic efficiency and substrate specificity.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574149041636-QH32F5IF9WOESJ9D6P19/CoverArt_Option2.jpg</image:loc>
      <image:title>Research Summary Gallery 2019</image:title>
      <image:caption>MRBLEs (Microspheres with Ratiometric Barcode Lanthanide Encoding) rely on spectral multiplexing to track analytes throughout an experiment. We can create microspheres containing &gt; 1,000 distinct ratios of lanthanide nanophosphors that can be uniquely identified via imaging alone, and are now using these MRBLEs in a variety of downstream assays.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1584410885816-YOMTSNNABPBUI5B46ERM/DEDroplets.jpg</image:loc>
      <image:title>Research Summary Gallery 2019</image:title>
      <image:caption>Dropception is a microfluidic platform for creating double emulsion (water-in-oil-in-water) droplets that can be sorted in high-throughput using standard flow cytometers (FACS machines). We recently demonstrated the ability to generate and sort double emulsion droplets without breakage, isolate individual rare droplets of interest in wells of a multiwell plate, and recover all encapsulated nucleic acids, enabling a wide range of novel single-cell multi-omic techniques.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/microwells-project-gallery-2019</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2019-11-20</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574224698379-JVB4XDOQGYNSVW8ATYWF/Screen+Shot+2019-11-19+at+8.31.09+PM.png</image:loc>
      <image:title>Microwells Project Gallery 2019</image:title>
      <image:caption>Organoid models of cancer have revolutionized our ability to recapitulate and observe in vivo cancer processes in a controlled in vitro environment. We are collaborating with Christina Curtis and Calvin Kuo to develop a microwell platform for performing high-throughput phenotyping of organoid heterogeneity across tumor development. This platform allows us to perform time-lapse imaging of thousands of organoids isolated in microwells, followed by computational reconstruction of growth trajectories for each organoid.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1574224698379-JVB4XDOQGYNSVW8ATYWF/Screen+Shot+2019-11-19+at+8.31.09+PM.png</image:loc>
      <image:title>Microwells Project Gallery 2019</image:title>
      <image:caption>Organoid models of cancer have revolutionized our ability to recapitulate and observe in vivo cancer processes in a controlled in vitro environment. We are collaborating with Christina Curtis and Calvin Kuo to develop a microwell platform for performing high-throughput phenotyping of organoid heterogeneity across tumor development. This platform allows us to perform time-lapse imaging of thousands of organoids isolated in microwells, followed by computational reconstruction of growth trajectories for each organoid.</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2020</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2021-08-12</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1606773488823-PUUEW2RDWR3UXLMGRGCN/Screen+Shot+2020-11-30+at+1.57.49+PM.png</image:loc>
      <image:title>Publications Gallery 2020</image:title>
      <image:caption>Revealing enzyme functional architecture via high-throughput microfluidic enzyme kinetics. Markin, C.J.*, Mokhtari, D.A.*, Sunden, F., Appel, M.J., Akiva, E., Longwell, S.A., Sabatti, C., Herschlag, D.‡, &amp; Fordyce, P.M.‡, Science (in press). (web) (pdf)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1593543248615-X7ZDNM3NUS1T0DPR1TVR/Screen+Shot+2020-06-30+at+11.48.06+AM.png</image:loc>
      <image:title>Publications Gallery 2020</image:title>
      <image:caption>MRBLES 2.0: High-throughput generation of chemically functionalized spectrally and magnetically-encoded hydrogel beads using a simple single-layer microfluidic device. Feng, Y., White, A.K., Hein, J.B., Appel, E.A., &amp; Fordyce, P.M., Microsystems &amp; Nanoengineering (2020). (web) (pdf) (OSF repository with all data and design files)</image:caption>
    </image:image>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1594182135604-933PFQK9TWYTYU1UV0GU/image-asset.jpeg</image:loc>
      <image:title>Publications Gallery 2020</image:title>
      <image:caption>High-throughput binding affinity measurements for mutations spanning a transcription factor-DNA interface reveal affinity and specificity determinants Aditham, A.K., Markin, C.J.*, Mokhtari, D.A.*, DelRosso, N.V., &amp; Fordyce, P.M. Cell Systems (2020). (pdf) (web)</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1594181421494-JSY3DF0988Q4O4K933VI/Screen+Shot+2020-07-07+at+9.09.52+PM.png</image:loc>
      <image:title>Publications Gallery 2020</image:title>
      <image:caption>Double emulsion picoreactors for high-throughput single-cell encapsulation and phenotyping via FACS. Brower, K.B.*, Khariton, M.*, Suzuki, P.H., Still, C., Kim, G., Calhoun, S.G.K., Qi, L.S., Wang, B.*, &amp; Fordyce, P.M.* Analytical Chemistry (2020). (web) (pdf) (OSF repository with all data and design files)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1588222370563-FT7J4CRFOXM3ON0HNQRM/Screen+Shot+2020-04-29+at+9.52.37+PM.png</image:loc>
      <image:title>Publications Gallery 2020</image:title>
      <image:caption>Protocol for peptide synthesis on spectrally encoded beads for MRBLE-pep assays. Hein, J.B., Nguyen, H.Q., Cyert, M., &amp; Fordyce, P.M. Bio-protocols (2020).</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1571443018570-2WLROYHPM4HXAFYY8H9F/Screen+Shot+2019-10-18+at+4.56.34+PM.png</image:loc>
      <image:title>Publications Gallery 2020</image:title>
      <image:caption>Optimized double emulsion flow cytometry with high-throughput single-droplet isolation. Brower, K.B., Carswell-Crumpton, C., Klemm, S., Cruz, B., Kim, G., Calhoun, S.G.K., Nichols, L, &amp; Fordyce, P.M. Lab on a Chip (2020). (PDF) (web) (OSF repository with all data and design files)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1588222544021-O3EQ8FZ4RTFL4AF2WMTO/Screen%2BShot%2B2019-10-18%2Bat%2B4.51.01%2BPM.jpg</image:loc>
      <image:title>Publications Gallery 2020</image:title>
      <image:caption>DeCoDe: degenerate codon design for complete protein-coding DNA libraries. Shimko, T.C., Fordyce, P.M., &amp; Orenstein, Y. Bioinformatics (2020). (PDF) (web)</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/publications-gallery-2021</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2021-08-23</lastmod>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1629739126729-AXMJY1GKIIK2L9D9O4NM/image-asset.png</image:loc>
      <image:title>Publications Gallery 2021</image:title>
      <image:caption>uPIC-M: efficient and scalable preparation of clonal single mutant libraries for high-throughput protein biochemistry. Appel, M.J., Longwell, S.A., Morri, M., Neff, N., Herschlag, D., &amp; Fordyce, P.M. bioRXiv (2021). (web) (pdf)</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1629739126729-AXMJY1GKIIK2L9D9O4NM/image-asset.png</image:loc>
      <image:title>Publications Gallery 2021</image:title>
      <image:caption>uPIC-M: efficient and scalable preparation of clonal single mutant libraries for high-throughput protein biochemistry. Appel, M.J., Longwell, S.A., Morri, M., Neff, N., Herschlag, D., &amp; Fordyce, P.M. bioRXiv (2021). (web) (pdf)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1606773488823-PUUEW2RDWR3UXLMGRGCN/Screen+Shot+2020-11-30+at+1.57.49+PM.png</image:loc>
      <image:title>Publications Gallery 2021</image:title>
      <image:caption>Revealing enzyme functional architecture via high-throughput microfluidic enzyme kinetics. Markin, C.J.*, Mokhtari, D.A.*, Sunden, F., Appel, M.J., Akiva, E., Longwell, S.A., Sabatti, C., Herschlag, D.‡, &amp; Fordyce, P.M.‡, Science (2021). (web) (pdf) • Science Perspective by Baumer &amp; Whitehead. • Discussion in Nature. • Stanford News article. • Chemical &amp; Engineering News article.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1619644202657-QVKPGIFKEEETI9I72H3B/Screen+Shot+2021-04-28+at+2.09.51+PM.png</image:loc>
      <image:title>Publications Gallery 2021</image:title>
      <image:caption>Structure-activity mapping of the peptide- and force-dependent landscape of T-cell activation Feng, Y., Zhao, X., White, A.K., Garcia, K.C., &amp; Fordyce, P.M., bioRxiv (2021). (web) (pdf)</image:caption>
    </image:image>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1619717115743-4B7NTD99R04KQYXROONT/Screen%2BShot%2B2021-04-29%2Bat%2B10.20.38%2BAM.jpg</image:loc>
      <image:title>Publications Gallery 2021</image:title>
      <image:caption>Fundamentals to function: quantitative and scalable approaches for measuring protein stability. Atsavapranee, B.*, Stark, C.D.*, Sunden, S., Thompson, S.‡, &amp; Fordyce, P.M.‡. Cell Systems (2021). (web) (pdf)</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1608267912266-33J4YSKY5JDXIRKXM4P3/Screen+Shot+2020-12-16+at+2.55.34+PM.png</image:loc>
      <image:title>Publications Gallery 2021</image:title>
      <image:caption>MRBLE-pep measurements reveal accurate binding affinities for B56, a PP2A regulatory subunit. Hein, J.B., Cyert, M.S., &amp; Fordyce, P.M. ACS Measurement Science (in press). (web) (pdf)</image:caption>
    </image:image>
  </url>
  <url>
    <loc>http://www.fordycelab.com/publications</loc>
    <changefreq>daily</changefreq>
    <priority>0.75</priority>
    <lastmod>2015-02-14</lastmod>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1403740741962-OG0T2R4JIXGZ62LZPS4R/Lys14NetworkStructure.jpg</image:loc>
      <image:title>Publications</image:title>
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      <image:title>Publications</image:title>
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      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>Co-encapsulation of double emulsion droplets (orange) and MRBLEs beads (blue) in single emulsions.</image:caption>
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      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>Encapsulated plant protoplasts engineered to constitutively express GFP from large Nicotiana benthamiana leaves in single emulsion droplets.</image:caption>
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      <image:caption>Schematic of trapping mechanism.</image:caption>
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      <image:caption>C. elegans at end of 10 µm trapping region.</image:caption>
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      <image:caption>Double emulsions trapped in U-trap device.</image:caption>
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      <image:caption>Double emulsions trapped in microwells device.</image:caption>
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      <image:caption>Flow and shear stress simulations of single and dual biofilm growth chambers.</image:caption>
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      <image:caption>Fluorescence signal immediately after the bacteria were injected (top, t = 0 hrs) and after overnight incubation (bottom, t = 24 hrs).</image:caption>
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      <image:caption>Encapsulating single B. braunii in water/oil droplets.</image:caption>
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      <image:caption>Growing B. braunii colonies within water/oil/water droplets.</image:caption>
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      <image:caption>BODIPY-stained water/oil/water droplets.</image:caption>
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      <image:caption>Photo showing device with generated gradient.</image:caption>
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      <image:caption>Composite image over 100 minutes showing stuck “sticker” caulobacter within the first chamber.</image:caption>
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      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>Composite image over 1.5 seconds showing highly motile “swimmer” caulobacter within the second chamber.</image:caption>
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      <image:caption>Photomask designs for design iteration Round 1 and 2.</image:caption>
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      <image:caption>Image of fabricated wafer with 15 µm separations between pillars.</image:caption>
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      <image:caption>Image of microscope with fabricated device and tubing.</image:caption>
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      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>Round 1: Main channel of cross-flow filtration device showing a large target cell remaining in the channel while a smaller cell gets pushed through pillars and lysed.</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/7bd6dc54-e20d-49ad-944d-67618895b79e/Screen+Shot+2022-10-26+at+4.01.32+PM.png</image:loc>
      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>Round 2: Target cells persisted in the main channel of the cross-flow filtration device without lysis after the between-pillar distance was reduced to 30 µm.</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/6130b099-d728-486e-b24a-654bd6ed594b/Screen+Shot+2022-10-26+at+4.32.46+PM.jpg</image:loc>
      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>Bonded glass device surrounding a thin membrane to facilitate co-culture.</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/e669c7d2-1dec-48d5-a158-4ff56755c3a0/Screen+Shot+2022-10-26+at+4.33.27+PM.png</image:loc>
      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>Human umbilical vein cells (HUVECs) growing on one side of the filter cell membrane within the glass device.</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/c92c824d-2939-4953-a55f-5819324354f8/Screen+Shot+2022-10-26+at+5.10.51+PM.jpg</image:loc>
      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>Image of red blood cells passing through small tapered channels to assess deformability.</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/e488a55c-192f-4e9d-b71d-a3d19711882a/Screen+Shot+2022-10-26+at+4.56.59+PM.png</image:loc>
      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>Example design for tapered channel trap devices.</image:caption>
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      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/063abf96-67a7-4bf1-a61c-2c654a95ba4f/Screen+Shot+2022-10-26+at+4.54.15+PM.jpg</image:loc>
      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>L2 worm immobilized in a 15 µm tall channel tapered from 20 µm to 5µm with an 0.5 mm extension.</image:caption>
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    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/3e3b538f-586d-4a77-8b60-56e90a0a4f58/Screen+Shot+2022-10-26+at+4.54.24+PM.jpg</image:loc>
      <image:title>Teaching - Make it stand out</image:title>
      <image:caption>L2 worm immobilized to allow tracking of fluorescently-labeled sex myoblast cells over 8 hours.</image:caption>
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    <image:image>
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      <image:title>Teaching</image:title>
      <image:caption>‘Horseshoe device’ cell loading: Day 1.</image:caption>
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    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1571086614028-OPL0Z1AYW91ZJN0G4XH9/Screen+Shot+2019-10-14+at+1.49.12+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Pneumatic and imaging setup for hydrodynamic breadboard.</image:caption>
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    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1571165852476-DBSRAIM8K4N8ZCNM58LL/Screen+Shot+2019-10-15+at+11.56.53+AM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Image of small (5 µm) features at device nozzle.</image:caption>
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    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1571165899653-BQU1L0WP55HY3E3WKGSX/Screen+Shot+2019-10-14+at+5.36.48+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Polydisperse double emulsion droplets with sizes ranging from 2 µm to 30 µm.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1571093262500-WH3Z8R8NCR72T24E43ED/image-asset.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Bright field image of 2 layer flow-focusing device.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1571093279209-12RX4LKI2IS15G9CTHVF/image-asset.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Bright field image showing co-axial flows.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541574827057-5UCX4CCFO2V8WVETIVY4/Screen+Shot+2018-11-06+at+11.13.16+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Figure 1. Schematic showing microfluidic planarian guillotines with varying channel widths after the guillotine blade.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541576966112-M6JM0ZREPTH2F7O5F6UX/Screen+Shot+2018-11-06+at+11.48.49+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Figure 1. Device design schematic.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541576585005-301QOTX0OKLE96BHZ3OC/image33.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Figure 1. Fluorescence image showing macrophages (green) and E. coli (red) within a chamber of the microfluidic device.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541623795423-6AJOZEWFMG3TEO7U1N36/Screen+Shot+2018-11-07+at+12.49.28+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Figure 1. Microfluidic droplet generator connected to syringe pumps on microscope illumination stage.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541623732761-ZZ3T9P0106HD1KYP8VIV/Screen+Shot+2018-11-07+at+12.48.12+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Figure 2. Droplets produced via T-junction (top) and flow focusing (bottom) devices at different flow rates.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541571724965-0N1Z2TZHE6CTRP9I897D/Screen+Shot+2018-11-06+at+10.20.15+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Figure 1 . Shear stress modeling results from COMSOL and particle image velocimetry.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541571974125-0UWFLIBFA02BVSY0HNMP/Screen+Shot+2018-11-06+at+10.25.11+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Figure 2. Example images showing overnight growth of cells.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541573752617-YA7NLLM6DXHZL6I8VMQY/Screen+Shot+2018-11-06+at+10.31.37+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>FIgure 1. Device schematic. (A) Each separation chamber has different pillar spacings to capture cells of different sizes. (B) Integrated valves allow selective retrieval of particular cell sizes.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541625611589-9RY3B6EAIVUU3CTMO1Z1/Screen+Shot+2018-11-07+at+1.19.41+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Figure 2. Image of the microfluidic device containing pillars with 50 µm gaps between them and 50 µm diameter beads successfully captured under constant pressure flow.</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/53aa0662e4b0d4cbb80321fe/1541573442219-QFEOCWBXP0WXRSXJ0GKE/Screen+Shot+2018-11-06+at+10.42.48+PM.png</image:loc>
      <image:title>Teaching</image:title>
      <image:caption>Figure 1. Image showing array of traps with Aiptasia larvae within them.</image:caption>
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      <image:title>Foundry - Make it stand out</image:title>
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