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	<title>2023Liu NextPYP - Revision history</title>
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	<updated>2026-05-24T22:00:59Z</updated>
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		<id>https://3demmethods.i2pc.es/index.php?title=2023Liu_NextPYP&amp;diff=4533&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  Liu, Hsuan-Fu / Zhou, Ye / Huang, Qinwen / Piland, Jonathan / Jin, Weisheng / Mandel, Justin / Du, Xiaochen / Martin, Jeffrey / Bartesaghi, Alberto. nextPYP: a...&quot;</title>
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		<updated>2024-01-12T08:11:59Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Liu, Hsuan-Fu / Zhou, Ye / Huang, Qinwen / Piland, Jonathan / Jin, Weisheng / Mandel, Justin / Du, Xiaochen / Martin, Jeffrey / Bartesaghi, Alberto. nextPYP: a...&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;
Liu, Hsuan-Fu / Zhou, Ye / Huang, Qinwen / Piland, Jonathan / Jin, Weisheng / Mandel, Justin / Du, Xiaochen / Martin, Jeffrey / Bartesaghi, Alberto. nextPYP: a comprehensive and scalable platform for characterizing protein variability in situ using single-particle cryo-electron tomography. 2023. Nature Methods, 20, p. 1909-1919&lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
Single-particle cryo-electron tomography is an emerging technique capable&lt;br /&gt;
of determining the structure of proteins imaged within the native context of&lt;br /&gt;
cells at molecular resolution. While high-throughput techniques for sample&lt;br /&gt;
preparation and tilt-series acquisition are beginning to provide sufficient&lt;br /&gt;
data to allow structural studies of proteins at physiological concentrations,&lt;br /&gt;
the complex data analysis pipeline and the demanding storage and&lt;br /&gt;
computational requirements pose major barriers for the development and&lt;br /&gt;
broader adoption of this technology. Here, we present a scalable, end-to-end&lt;br /&gt;
framework for single-particle cryo-electron tomography data analysis from&lt;br /&gt;
on-the-fly pre-processing of tilt series to high-resolution refinement and&lt;br /&gt;
classification, which allows efficient analysis and visualization of datasets&lt;br /&gt;
with hundreds of tilt series and hundreds of thousands of particles. We&lt;br /&gt;
validate our approach using in vitro and cellular datasets, demonstrating&lt;br /&gt;
its effectiveness at achieving high-resolution and revealing conformational&lt;br /&gt;
heterogeneity in situ. The framework is made available through an intuitive&lt;br /&gt;
and easy-to-use computer application, nextPYP (http://nextpyp.app).&lt;br /&gt;
&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/s41592-023-02045-0&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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