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Open AccessJournal ArticleDOI

Topaz-Denoise: general deep denoising models for cryoEM and cryoET.

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TLDR
It is shown that low dose collection, enabled by Topaz-Denoise, improves downstream analysis in addition to reducing data collection time, and a general 3D denoising model for cryoET is presented, able to denoise new datasets without additional training.
Abstract
Cryo-electron microscopy (cryoEM) is becoming the preferred method for resolving protein structures. Low signal-to-noise ratio (SNR) in cryoEM images reduces the confidence and throughput of structure determination during several steps of data processing, resulting in impediments such as missing particle orientations. Denoising cryoEM images can not only improve downstream analysis but also accelerate the time-consuming data collection process by allowing lower electron dose micrographs to be used for analysis. Here, we present Topaz-Denoise, a deep learning method for reliably and rapidly increasing the SNR of cryoEM images and cryoET tomograms. By training on a dataset composed of thousands of micrographs collected across a wide range of imaging conditions, we are able to learn models capturing the complexity of the cryoEM image formation process. The general model we present is able to denoise new datasets without additional training. Denoising with this model improves micrograph interpretability and allows us to solve 3D single particle structures of clustered protocadherin, an elongated particle with previously elusive views. We then show that low dose collection, enabled by Topaz-Denoise, improves downstream analysis in addition to reducing data collection time. We also present a general 3D denoising model for cryoET. Topaz-Denoise and pre-trained general models are now included in Topaz. We expect that Topaz-Denoise will be of broad utility to the cryoEM community for improving micrograph and tomogram interpretability and accelerating analysis. The low signal-to-noise ratio (SNR) in cryoEM images can make the first steps in cryoEM structure determination challenging, particularly for non-globular and small proteins. Here, the authors present Topaz-Denoise, a deep learning based method for micrograph denoising that significantly increases the SNR of cryoEM images and cryoET tomograms, which helps to accelerate the cryoEM pipeline.

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Journal ArticleDOI

Non-uniform refinement: adaptive regularization improves single-particle cryo-EM reconstruction.

TL;DR: Non-uniform refinement, an algorithm based on cross-validation optimization, is introduced, which automatically regularizes 3D density maps during refinement to account for spatial variability and yields dramatically improved resolution and 3D map quality in many cases.
References
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Book ChapterDOI

U-Net: Convolutional Networks for Biomedical Image Segmentation

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UCSF Chimera--a visualization system for exploratory research and analysis.

TL;DR: Two unusual extensions are presented: Multiscale, which adds the ability to visualize large‐scale molecular assemblies such as viral coats, and Collaboratory, which allows researchers to share a Chimera session interactively despite being at separate locales.
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U-Net: Convolutional Networks for Biomedical Image Segmentation

TL;DR: It is shown that such a network can be trained end-to-end from very few images and outperforms the prior best method (a sliding-window convolutional network) on the ISBI challenge for segmentation of neuronal structures in electron microscopic stacks.

Automatic differentiation in PyTorch

TL;DR: An automatic differentiation module of PyTorch is described — a library designed to enable rapid research on machine learning models that focuses on differentiation of purely imperative programs, with a focus on extensibility and low overhead.
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