<?xml version="1.0"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en">
	<id>https://3demmethods.i2pc.es/index.php?action=history&amp;feed=atom&amp;title=2019Thompson_Protocol</id>
	<title>2019Thompson Protocol - Revision history</title>
	<link rel="self" type="application/atom+xml" href="https://3demmethods.i2pc.es/index.php?action=history&amp;feed=atom&amp;title=2019Thompson_Protocol"/>
	<link rel="alternate" type="text/html" href="https://3demmethods.i2pc.es/index.php?title=2019Thompson_Protocol&amp;action=history"/>
	<updated>2026-05-24T21:06:13Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
	<generator>MediaWiki 1.44.2</generator>
	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2019Thompson_Protocol&amp;diff=3425&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  Thompson, R. F.; Iadanza, M. G.; Hesketh, E. L.; Rawson, S. and Ranson, N. A. Collection, pre-processing and on-the-fly analysis of data for high-resolution, s...&quot;</title>
		<link rel="alternate" type="text/html" href="https://3demmethods.i2pc.es/index.php?title=2019Thompson_Protocol&amp;diff=3425&amp;oldid=prev"/>
		<updated>2019-01-17T08:11:53Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Thompson, R. F.; Iadanza, M. G.; Hesketh, E. L.; Rawson, S. and Ranson, N. A. Collection, pre-processing and on-the-fly analysis of data for high-resolution, s...&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;
Thompson, R. F.; Iadanza, M. G.; Hesketh, E. L.; Rawson, S. and Ranson, N. A. Collection, pre-processing and on-the-fly analysis of data for high-resolution, single-particle cryo-electron microscopy. Nature protocols, 2019, 14, 100-118 &lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
The dramatic growth in the use of cryo-electron microscopy (cryo-EM) to generate high-resolution structures of macromolecular complexes has changed the landscape of structural biology. The majority of structures deposited in the Electron Microscopy Data Bank (EMDB) at higher than 4-Å resolution were collected on Titan Krios microscopes. Although the pipeline for single-particle data collection is becoming routine, there is much variation in how sessions are set up. Furthermore, when collection is under way, there are a range of approaches for efficiently moving and pre-processing these data. Here, we present a standard operating procedure for single-particle data collection with Thermo Fisher Scientific EPU software, using the two most common direct electron detectors (the Thermo Fisher Scientific Falcon 3 (F3EC) and the Gatan K2), as well as a strategy for structuring these data to enable efficient pre-processing and on-the-fly monitoring of data collection. This protocol takes 3-6 h to set up a typical automated data collection session. &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/s41596-018-0084-8.pdf&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>
</feed>