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	<id>https://3demmethods.i2pc.es/index.php?action=history&amp;feed=atom&amp;title=2020Gupta_MultiCryoGAN</id>
	<title>2020Gupta MultiCryoGAN - Revision history</title>
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	<updated>2026-05-24T22:01:28Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2020Gupta_MultiCryoGAN&amp;diff=3959&amp;oldid=prev</id>
		<title>WikiSysop at 15:33, 15 April 2021</title>
		<link rel="alternate" type="text/html" href="https://3demmethods.i2pc.es/index.php?title=2020Gupta_MultiCryoGAN&amp;diff=3959&amp;oldid=prev"/>
		<updated>2021-04-15T15:33:45Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 15:33, 15 April 2021&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l5&quot;&gt;Line 5:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 5:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Abstract ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Abstract ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;We propose a deep-learning-based reconstruction method for&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;cryo-electron microscopy (Cryo-EM) that can model multiple conformations&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;of a nonrigid biomolecule in a standalone manner. Cryo-EM&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;produces many noisy projections from separate instances of the same&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;but randomly oriented biomolecule. Current methods rely on pose and&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;conformation estimation which are inefficient for the reconstruction of&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;continuous conformations that carry valuable information. We introduce&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;Multi-CryoGAN, which sidesteps the additional processing by casting&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;the volume reconstruction into the distribution matching problem. By&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;introducing a manifold mapping module, Multi-CryoGAN can learn continuous&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;structural heterogeneity without pose estimation nor clustering.&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;We also give a theoretical guarantee of recovery of the true conformations.&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;Our method can successfully reconstruct 3D protein complexes on&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;synthetic 2D Cryo-EM datasets for both continuous and discrete structural&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;variability scenarios. Multi-CryoGAN is the first model that can&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;reconstruct continuous conformations of a biomolecule from Cryo-EM&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;&amp;lt;br&amp;gt;&lt;/del&gt;images in a fully unsupervised and end-to-end manner.  &lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;We propose a deep-learning-based reconstruction method for cryo-electron microscopy (Cryo-EM) that can model multiple conformations of a nonrigid biomolecule in a standalone manner. Cryo-EM produces many noisy projections from separate instances of the same but randomly oriented biomolecule. Current methods rely on pose and conformation estimation which are inefficient for the reconstruction of continuous conformations that carry valuable information. We introduce Multi-CryoGAN, which sidesteps the additional processing by casting the volume reconstruction into the distribution matching problem. By introducing a manifold mapping module, Multi-CryoGAN can learn continuous structural heterogeneity without pose estimation nor clustering. We also give a theoretical guarantee of recovery of the true conformations. Our method can successfully reconstruct 3D protein complexes on synthetic 2D Cryo-EM datasets for both continuous and discrete structural variability scenarios. Multi-CryoGAN is the first model that can reconstruct continuous conformations of a biomolecule from Cryo-EM images in a fully unsupervised and end-to-end manner.  &lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Keywords ==&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;== Keywords ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>WikiSysop</name></author>
	</entry>
	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2020Gupta_MultiCryoGAN&amp;diff=3958&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  Gupta, H.; Phan, T. H.; Yoo, J. &amp;amp; Unser, M. Multi-CryoGAN: Reconstruction of Continuous Conformations in Cryo-EM Using Generative Adversarial Networks. Eur...&quot;</title>
		<link rel="alternate" type="text/html" href="https://3demmethods.i2pc.es/index.php?title=2020Gupta_MultiCryoGAN&amp;diff=3958&amp;oldid=prev"/>
		<updated>2021-04-15T15:32:18Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Gupta, H.; Phan, T. H.; Yoo, J. &amp;amp; Unser, M. Multi-CryoGAN: Reconstruction of Continuous Conformations in Cryo-EM Using Generative Adversarial Networks. Eur...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Citation ==&lt;br /&gt;
&lt;br /&gt;
Gupta, H.; Phan, T. H.; Yoo, J. &amp;amp;amp; Unser, M. Multi-CryoGAN: Reconstruction of Continuous Conformations in Cryo-EM Using Generative Adversarial Networks. European Conference on Computer Vision, 2020, 429-444 &lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
We propose a deep-learning-based reconstruction method for&amp;lt;br&amp;gt;cryo-electron microscopy (Cryo-EM) that can model multiple conformations&amp;lt;br&amp;gt;of a nonrigid biomolecule in a standalone manner. Cryo-EM&amp;lt;br&amp;gt;produces many noisy projections from separate instances of the same&amp;lt;br&amp;gt;but randomly oriented biomolecule. Current methods rely on pose and&amp;lt;br&amp;gt;conformation estimation which are inefficient for the reconstruction of&amp;lt;br&amp;gt;continuous conformations that carry valuable information. We introduce&amp;lt;br&amp;gt;Multi-CryoGAN, which sidesteps the additional processing by casting&amp;lt;br&amp;gt;the volume reconstruction into the distribution matching problem. By&amp;lt;br&amp;gt;introducing a manifold mapping module, Multi-CryoGAN can learn continuous&amp;lt;br&amp;gt;structural heterogeneity without pose estimation nor clustering.&amp;lt;br&amp;gt;We also give a theoretical guarantee of recovery of the true conformations.&amp;lt;br&amp;gt;Our method can successfully reconstruct 3D protein complexes on&amp;lt;br&amp;gt;synthetic 2D Cryo-EM datasets for both continuous and discrete structural&amp;lt;br&amp;gt;variability scenarios. Multi-CryoGAN is the first model that can&amp;lt;br&amp;gt;reconstruct continuous conformations of a biomolecule from Cryo-EM&amp;lt;br&amp;gt;images in a fully unsupervised and end-to-end manner. &lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
https://link.springer.com/chapter/10.1007/978-3-030-66415-2_28&lt;br /&gt;
&lt;br /&gt;
== Related software ==&lt;br /&gt;
&lt;br /&gt;
== Related methods ==&lt;br /&gt;
&lt;br /&gt;
== Comments ==&lt;/div&gt;</summary>
		<author><name>WikiSysop</name></author>
	</entry>
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