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Article: Diffusion-based deep learning method for augmenting ultrastructural imaging and volume electron microscopy

TitleDiffusion-based deep learning method for augmenting ultrastructural imaging and volume electron microscopy
Authors
Issue Date1-Jun-2024
PublisherNature Portfolio
Citation
Nature Communications, 2024, v. 15, n. 1 How to Cite?
AbstractElectron microscopy (EM) revolutionized the way to visualize cellular ultrastructure. Volume EM (vEM) has further broadened its three-dimensional nanoscale imaging capacity. However, intrinsic trade-offs between imaging speed and quality of EM restrict the attainable imaging area and volume. Isotropic imaging with vEM for large biological volumes remains unachievable. Here, we developed EMDiffuse, a suite of algorithms designed to enhance EM and vEM capabilities, leveraging the cutting-edge image generation diffusion model. EMDiffuse generates realistic predictions with high resolution ultrastructural details and exhibits robust transferability by taking only one pair of images of 3 megapixels to fine-tune in denoising and super-resolution tasks. EMDiffuse also demonstrated proficiency in the isotropic vEM reconstruction task, generating isotropic volume even in the absence of isotropic training data. We demonstrated the robustness of EMDiffuse by generating isotropic volumes from seven public datasets obtained from different vEM techniques and instruments. The generated isotropic volume enables accurate three-dimensional nanoscale ultrastructure analysis. EMDiffuse also features self-assessment functionalities on predictions’ reliability. We envision EMDiffuse to pave the way for investigations of the intricate subcellular nanoscale ultrastructure within large volumes of biological systems.
Persistent Identifierhttp://hdl.handle.net/10722/348668

 

DC FieldValueLanguage
dc.contributor.authorLu, Chixiang-
dc.contributor.authorChen, Kai-
dc.contributor.authorQiu, Heng-
dc.contributor.authorChen, Xiaojun-
dc.contributor.authorChen, Gu-
dc.contributor.authorQi, Xiaojuan-
dc.contributor.authorJiang, Haibo-
dc.date.accessioned2024-10-11T00:31:22Z-
dc.date.available2024-10-11T00:31:22Z-
dc.date.issued2024-06-01-
dc.identifier.citationNature Communications, 2024, v. 15, n. 1-
dc.identifier.urihttp://hdl.handle.net/10722/348668-
dc.description.abstractElectron microscopy (EM) revolutionized the way to visualize cellular ultrastructure. Volume EM (vEM) has further broadened its three-dimensional nanoscale imaging capacity. However, intrinsic trade-offs between imaging speed and quality of EM restrict the attainable imaging area and volume. Isotropic imaging with vEM for large biological volumes remains unachievable. Here, we developed EMDiffuse, a suite of algorithms designed to enhance EM and vEM capabilities, leveraging the cutting-edge image generation diffusion model. EMDiffuse generates realistic predictions with high resolution ultrastructural details and exhibits robust transferability by taking only one pair of images of 3 megapixels to fine-tune in denoising and super-resolution tasks. EMDiffuse also demonstrated proficiency in the isotropic vEM reconstruction task, generating isotropic volume even in the absence of isotropic training data. We demonstrated the robustness of EMDiffuse by generating isotropic volumes from seven public datasets obtained from different vEM techniques and instruments. The generated isotropic volume enables accurate three-dimensional nanoscale ultrastructure analysis. EMDiffuse also features self-assessment functionalities on predictions’ reliability. We envision EMDiffuse to pave the way for investigations of the intricate subcellular nanoscale ultrastructure within large volumes of biological systems.-
dc.languageeng-
dc.publisherNature Portfolio-
dc.relation.ispartofNature Communications-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleDiffusion-based deep learning method for augmenting ultrastructural imaging and volume electron microscopy-
dc.typeArticle-
dc.identifier.doi10.1038/s41467-024-49125-z-
dc.identifier.pmid38824146-
dc.identifier.scopuseid_2-s2.0-85195008069-
dc.identifier.volume15-
dc.identifier.issue1-
dc.identifier.eissn2041-1723-
dc.identifier.issnl2041-1723-

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