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		<title>WikiSysop: Created page with &quot;== Citation ==  Huang, Qinwen / Zhou, Ye / Liu, Hsuan-Fu / Bartesaghi, Alberto. Multiple-image super-resolution of cryo-electron micrographs based on deep internal learning. 2...&quot;</title>
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		<updated>2023-08-10T06:34:10Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Huang, Qinwen / Zhou, Ye / Liu, Hsuan-Fu / Bartesaghi, Alberto. Multiple-image super-resolution of cryo-electron micrographs based on deep internal learning. 2...&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;
Huang, Qinwen / Zhou, Ye / Liu, Hsuan-Fu / Bartesaghi, Alberto. Multiple-image super-resolution of cryo-electron micrographs based on deep internal learning. 2023. Biological Imaging, Vol. 3, p. e3 &lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
Single-particle cryo-electron microscopy (cryo-EM) is a powerful imaging modality capable of visualizing proteins&lt;br /&gt;
and macromolecular complexes at near-atomic resolution. The low electron-doses used to prevent radiation damage&lt;br /&gt;
to the biological samples, however, result in images where the power of the noise is 100 times greater than the power&lt;br /&gt;
of the signal. To overcome these low signal-to-noise ratios (SNRs), hundreds of thousands of particle projections are&lt;br /&gt;
averaged to determine the three-dimensional structure of the molecule of interest. The sampling requirements of highresolution&lt;br /&gt;
imaging impose limitations on the pixel sizes that can be used for acquisition, limiting the size of the field of&lt;br /&gt;
view and requiring data collection sessions of several days to accumulate sufficient numbers of particles. Meanwhile,&lt;br /&gt;
recent image super-resolution (SR) techniques based on neural networks have shown state-of-the-art performance on&lt;br /&gt;
natural images. Building on these advances, here, we present a multiple-image SR algorithm based on deep internal&lt;br /&gt;
learning designed specifically to work under low-SNR conditions. Our approach leverages the internal image&lt;br /&gt;
statistics of cryo-EM movies and does not require training on ground-truth data. When applied to single-particle&lt;br /&gt;
datasets of apoferritin and T20S proteasome, we show that the resolution of the 3D structure obtained from SR&lt;br /&gt;
micrographs can surpass the limits imposed by the imaging system. Our results indicate that the combination of low&lt;br /&gt;
magnification imaging with in silico image SR has the potential to accelerate cryo-EM data collection by virtue of&lt;br /&gt;
including more particles in each exposure and doing so without sacrificing resolution.&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
https://www.cambridge.org/core/journals/biological-imaging/article/multipleimage-superresolution-of-cryoem-micrographs-based-on-deep-internal-learning/69FF36A6FAA03343010F2F8E7A869DA0&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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