Dataset Information

CDAE: A Cascade of Denoising Autoencoders for Noise Reduction in the Clustering of Single-Particle Cryo-EM Images.

ABSTRACT: As an emerging technology, cryo-electron microscopy (cryo-EM) has attracted more and more research interests from both structural biology and computer science, because many challenging computational tasks are involved in the processing of cryo-EM images. An important image processing step is to cluster the 2D cryo-EM images according to their projection angles, then the cluster mean images are used for the subsequent 3D reconstruction. However, cryo-EM images are quite noisy and denoising them is not easy, because the noise is a complicated mixture from samples and hardware. In this study, we design an effective cryo-EM image denoising model, CDAE, i.e., a cascade of denoising autoencoders. The new model comprises stacked blocks of deep neural networks to reduce noise in a progressive manner. Each block contains a convolutional autoencoder, pre-trained by simulated data of different SNRs and fine-tuned by target data set. We assess this new model on three simulated test sets and a real data set. CDAE achieves very competitive PSNR (peak signal-to-noise ratio) in the comparison of the state-of-the-art image denoising methods. Moreover, the denoised images have significantly enhanced clustering results compared to original image features or high-level abstraction features obtained by other deep neural networks. Both quantitative and visualized results demonstrate the good performance of CDAE for the noise reduction in clustering single-particle cryo-EM images.

SUBMITTER: Lei H

PROVIDER: S-EPMC7854571 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

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Publications

CDAE: A Cascade of Denoising Autoencoders for Noise Reduction in the Clustering of Single-Particle Cryo-EM Images.

Lei Houchao H Yang Yang Y

Frontiers in genetics 20210120

As an emerging technology, cryo-electron microscopy (cryo-EM) has attracted more and more research interests from both structural biology and computer science, because many challenging computational tasks are involved in the processing of cryo-EM images. An important image processing step is to cluster the 2D cryo-EM images according to their projection angles, then the cluster mean images are used for the subsequent 3D reconstruction. However, cryo-EM images are quite noisy and denoising them i ...[more]

PMID: 33552141

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Project description:MotivationCryo-electron microscopy (cryo-EM) is a widely used technology for ultrastructure determination, which constructs the 3D structures of protein and macromolecular complex from a set of 2D micrographs. However, limited by the electron beam dose, the micrographs in cryo-EM generally suffer from the extremely low signal-to-noise ratio (SNR), which hampers the efficiency and effectiveness of downstream analysis. Especially, the noise in cryo-EM is not simple additive or multiplicative noise whose statistical characteristics are quite different from the ones in natural image, extremely shackling the performance of conventional denoising methods.ResultsHere, we introduce the Noise-Transfer2Clean (NT2C), a denoising deep neural network (DNN) for cryo-EM to enhance image contrast and restore specimen signal, whose main idea is to improve the denoising performance by correctly learning the noise distribution of cryo-EM images and transferring the statistical nature of noise into the denoiser. Especially, to cope with the complex noise model in cryo-EM, we design a contrast-guided noise and signal re-weighted algorithm to achieve clean-noisy data synthesis and data augmentation, making our method authentically achieve signal restoration based on noise's true properties. Our work verifies the feasibility of denoising based on mining the complex cryo-EM noise patterns directly from the noise patches. Comprehensive experimental results on simulated datasets and real datasets show that NT2C achieved a notable improvement in image denoising, especially in background noise removal, compared with the commonly used methods. Moreover, a case study on the real dataset demonstrates that NT2C can greatly alleviate the obstacles caused by the SNR to particle picking and simplify the identifying of particles.Availabilityand implementationThe code is available at https://github.com/Lihongjia-ict/NoiseTransfer2Clean/.Supplementary informationSupplementary data are available at Bioinformatics online.

Project description:BackgroundAn important task of macromolecular structure determination by cryo-electron microscopy (cryo-EM) is the identification of single particles in micrographs (particle picking). Due to the necessity of human involvement in the process, current particle picking techniques are time consuming and often result in many false positives and negatives. Adjusting the parameters to eliminate false positives often excludes true particles in certain orientations. The supervised machine learning (e.g. deep learning) methods for particle picking often need a large training dataset, which requires extensive manual annotation. Other reference-dependent methods rely on low-resolution templates for particle detection, matching and picking, and therefore, are not fully automated. These issues motivate us to develop a fully automated, unbiased framework for particle picking.ResultsWe design a fully automated, unsupervised approach for single particle picking in cryo-EM micrographs. Our approach consists of three stages: image preprocessing, particle clustering, and particle picking. The image preprocessing is based on multiple techniques including: image averaging, normalization, cryo-EM image contrast enhancement correction (CEC), histogram equalization, restoration, adaptive histogram equalization, guided image filtering, and morphological operations. Image preprocessing significantly improves the quality of original cryo-EM images. Our particle clustering method is based on an intensity distribution model which is much faster and more accurate than traditional K-means and Fuzzy C-Means (FCM) algorithms for single particle clustering. Our particle picking method, based on image cleaning and shape detection with a modified Circular Hough Transform algorithm, effectively detects the shape and the center of each particle and creates a bounding box encapsulating the particles.ConclusionsAutoCryoPicker can automatically and effectively recognize particle-like objects from noisy cryo-EM micrographs without the need of labeled training data or human intervention making it a useful tool for cryo-EM protein structure determination.

Dataset Information

CDAE: A Cascade of Denoising Autoencoders for Noise Reduction in the Clustering of Single-Particle Cryo-EM Images.

Publications

CDAE: A Cascade of Denoising Autoencoders for Noise Reduction in the Clustering of Single-Particle Cryo-EM Images.

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