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	<title>2023Balyschew TomoBEAR - Revision history</title>
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	<updated>2026-05-24T20:17:59Z</updated>
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		<id>https://3demmethods.i2pc.es/index.php?title=2023Balyschew_TomoBEAR&amp;diff=4517&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  Balyschew, Nikita / Yushkevich, Artsemi / Mikirtumov, Vasilii / Sanchez, Ricardo M. / Sprink, Thiemo / Kudryashev, Mikhail. Streamlined structure determination...&quot;</title>
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		<updated>2024-01-09T08:33:34Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Balyschew, Nikita / Yushkevich, Artsemi / Mikirtumov, Vasilii / Sanchez, Ricardo M. / Sprink, Thiemo / Kudryashev, Mikhail. Streamlined structure determination...&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;
Balyschew, Nikita / Yushkevich, Artsemi / Mikirtumov, Vasilii / Sanchez, Ricardo M. / Sprink, Thiemo / Kudryashev, Mikhail. Streamlined structure determination by cryo-electron tomography and subtomogram averaging using TomoBEAR. 2023. Nature Communications, Vol. 14, No. 1, p. 6543 &lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
Structures of macromolecules in their native state provide unique unambiguous&lt;br /&gt;
insights into their functions. Cryo-electron tomography combined with&lt;br /&gt;
subtomogram averaging demonstrated the power to solve such structures in&lt;br /&gt;
situ at resolutions in the range of 3 Angstrom for some macromolecules. In&lt;br /&gt;
order to be applicable to the structural determination of the majority of&lt;br /&gt;
macromolecules observable in cells in limited amounts, processing of tomographic&lt;br /&gt;
data has to be performed in a high-throughput manner. Here we&lt;br /&gt;
present TomoBEAR—a modular configurable workflow engine for streamlined&lt;br /&gt;
processing of cryo-electron tomographic data for subtomogram averaging.&lt;br /&gt;
TomoBEAR combines commonly used cryo-EM packages with reasonable&lt;br /&gt;
presets to provide a transparent (“white box”) approach for datamanagement&lt;br /&gt;
and processing. We demonstrate applications of TomoBEAR to two data sets&lt;br /&gt;
of purified macromolecular targets, to an ion channel RyR1 in amembrane, and&lt;br /&gt;
the tomograms of plasma FIB-milled lamellae and demonstrate the ability to&lt;br /&gt;
produce high-resolution structures. TomoBEAR speeds up data processing,&lt;br /&gt;
minimizes human interventions, andwill help accelerate the adoption of in situ&lt;br /&gt;
structural biology by cryo-ET. The source code and the documentation are&lt;br /&gt;
freely available.&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
https://www.nature.com/articles/s41467-023-42085-w&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>
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