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A scalable and modular automated pipeline for stitching of large electron microscopy datasets
Serial-section electron microscopy (ssEM) is the method of choice for studying macroscopic biological samples at extremely high resolution in three dimensions. In the nervous system, nanometer-scale images are necessary to reconstruct dense neural wiring diagrams in the brain, so -called connectomes...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427110/ https://www.ncbi.nlm.nih.gov/pubmed/35880860 http://dx.doi.org/10.7554/eLife.76534 |
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author | Mahalingam, Gayathri Torres, Russel Kapner, Daniel Trautman, Eric T Fliss, Tim Seshamani, Shamishtaa Perlman, Eric Young, Rob Kinn, Samuel Buchanan, JoAnn Takeno, Marc M Yin, Wenjing Bumbarger, Daniel J Gwinn, Ryder P Nyhus, Julie Lein, Ed Smith, Steven J Reid, R Clay Khairy, Khaled A Saalfeld, Stephan Collman, Forrest Macarico da Costa, Nuno |
author_facet | Mahalingam, Gayathri Torres, Russel Kapner, Daniel Trautman, Eric T Fliss, Tim Seshamani, Shamishtaa Perlman, Eric Young, Rob Kinn, Samuel Buchanan, JoAnn Takeno, Marc M Yin, Wenjing Bumbarger, Daniel J Gwinn, Ryder P Nyhus, Julie Lein, Ed Smith, Steven J Reid, R Clay Khairy, Khaled A Saalfeld, Stephan Collman, Forrest Macarico da Costa, Nuno |
author_sort | Mahalingam, Gayathri |
collection | PubMed |
description | Serial-section electron microscopy (ssEM) is the method of choice for studying macroscopic biological samples at extremely high resolution in three dimensions. In the nervous system, nanometer-scale images are necessary to reconstruct dense neural wiring diagrams in the brain, so -called connectomes. The data that can comprise of up to 10(8) individual EM images must be assembled into a volume, requiring seamless 2D registration from physical section followed by 3D alignment of the stitched sections. The high throughput of ssEM necessitates 2D stitching to be done at the pace of imaging, which currently produces tens of terabytes per day. To achieve this, we present a modular volume assembly software pipeline ASAP (Assembly Stitching and Alignment Pipeline) that is scalable to datasets containing petabytes of data and parallelized to work in a distributed computational environment. The pipeline is built on top of the Render Trautman and Saalfeld (2019) services used in the volume assembly of the brain of adult Drosophila melanogaster (Zheng et al. 2018). It achieves high throughput by operating only on image meta-data and transformations. ASAP is modular, allowing for easy incorporation of new algorithms without significant changes in the workflow. The entire software pipeline includes a complete set of tools for stitching, automated quality control, 3D section alignment, and final rendering of the assembled volume to disk. ASAP has been deployed for continuous stitching of several large-scale datasets of the mouse visual cortex and human brain samples including one cubic millimeter of mouse visual cortex (Yin et al. 2020); Microns Consortium et al. (2021) at speeds that exceed imaging. The pipeline also has multi-channel processing capabilities and can be applied to fluorescence and multi-modal datasets like array tomography. |
format | Online Article Text |
id | pubmed-9427110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-94271102022-08-31 A scalable and modular automated pipeline for stitching of large electron microscopy datasets Mahalingam, Gayathri Torres, Russel Kapner, Daniel Trautman, Eric T Fliss, Tim Seshamani, Shamishtaa Perlman, Eric Young, Rob Kinn, Samuel Buchanan, JoAnn Takeno, Marc M Yin, Wenjing Bumbarger, Daniel J Gwinn, Ryder P Nyhus, Julie Lein, Ed Smith, Steven J Reid, R Clay Khairy, Khaled A Saalfeld, Stephan Collman, Forrest Macarico da Costa, Nuno eLife Cell Biology Serial-section electron microscopy (ssEM) is the method of choice for studying macroscopic biological samples at extremely high resolution in three dimensions. In the nervous system, nanometer-scale images are necessary to reconstruct dense neural wiring diagrams in the brain, so -called connectomes. The data that can comprise of up to 10(8) individual EM images must be assembled into a volume, requiring seamless 2D registration from physical section followed by 3D alignment of the stitched sections. The high throughput of ssEM necessitates 2D stitching to be done at the pace of imaging, which currently produces tens of terabytes per day. To achieve this, we present a modular volume assembly software pipeline ASAP (Assembly Stitching and Alignment Pipeline) that is scalable to datasets containing petabytes of data and parallelized to work in a distributed computational environment. The pipeline is built on top of the Render Trautman and Saalfeld (2019) services used in the volume assembly of the brain of adult Drosophila melanogaster (Zheng et al. 2018). It achieves high throughput by operating only on image meta-data and transformations. ASAP is modular, allowing for easy incorporation of new algorithms without significant changes in the workflow. The entire software pipeline includes a complete set of tools for stitching, automated quality control, 3D section alignment, and final rendering of the assembled volume to disk. ASAP has been deployed for continuous stitching of several large-scale datasets of the mouse visual cortex and human brain samples including one cubic millimeter of mouse visual cortex (Yin et al. 2020); Microns Consortium et al. (2021) at speeds that exceed imaging. The pipeline also has multi-channel processing capabilities and can be applied to fluorescence and multi-modal datasets like array tomography. eLife Sciences Publications, Ltd 2022-07-26 /pmc/articles/PMC9427110/ /pubmed/35880860 http://dx.doi.org/10.7554/eLife.76534 Text en © 2022, Mahalingam, Torres et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Mahalingam, Gayathri Torres, Russel Kapner, Daniel Trautman, Eric T Fliss, Tim Seshamani, Shamishtaa Perlman, Eric Young, Rob Kinn, Samuel Buchanan, JoAnn Takeno, Marc M Yin, Wenjing Bumbarger, Daniel J Gwinn, Ryder P Nyhus, Julie Lein, Ed Smith, Steven J Reid, R Clay Khairy, Khaled A Saalfeld, Stephan Collman, Forrest Macarico da Costa, Nuno A scalable and modular automated pipeline for stitching of large electron microscopy datasets |
title | A scalable and modular automated pipeline for stitching of large electron microscopy datasets |
title_full | A scalable and modular automated pipeline for stitching of large electron microscopy datasets |
title_fullStr | A scalable and modular automated pipeline for stitching of large electron microscopy datasets |
title_full_unstemmed | A scalable and modular automated pipeline for stitching of large electron microscopy datasets |
title_short | A scalable and modular automated pipeline for stitching of large electron microscopy datasets |
title_sort | scalable and modular automated pipeline for stitching of large electron microscopy datasets |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9427110/ https://www.ncbi.nlm.nih.gov/pubmed/35880860 http://dx.doi.org/10.7554/eLife.76534 |
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