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A high-throughput framework to detect synapses in electron microscopy images
Motivation: Synaptic connections underlie learning and memory in the brain and are dynamically formed and eliminated during development and in response to stimuli. Quantifying changes in overall density and strength of synapses is an important pre-requisite for studying connectivity and plasticity i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694654/ https://www.ncbi.nlm.nih.gov/pubmed/23813014 http://dx.doi.org/10.1093/bioinformatics/btt222 |
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author | Navlakha, Saket Suhan, Joseph Barth, Alison L. Bar-Joseph, Ziv |
author_facet | Navlakha, Saket Suhan, Joseph Barth, Alison L. Bar-Joseph, Ziv |
author_sort | Navlakha, Saket |
collection | PubMed |
description | Motivation: Synaptic connections underlie learning and memory in the brain and are dynamically formed and eliminated during development and in response to stimuli. Quantifying changes in overall density and strength of synapses is an important pre-requisite for studying connectivity and plasticity in these cases or in diseased conditions. Unfortunately, most techniques to detect such changes are either low-throughput (e.g. electrophysiology), prone to error and difficult to automate (e.g. standard electron microscopy) or too coarse (e.g. magnetic resonance imaging) to provide accurate and large-scale measurements. Results: To facilitate high-throughput analyses, we used a 50-year-old experimental technique to selectively stain for synapses in electron microscopy images, and we developed a machine-learning framework to automatically detect synapses in these images. To validate our method, we experimentally imaged brain tissue of the somatosensory cortex in six mice. We detected thousands of synapses in these images and demonstrate the accuracy of our approach using cross-validation with manually labeled data and by comparing against existing algorithms and against tools that process standard electron microscopy images. We also used a semi-supervised algorithm that leverages unlabeled data to overcome sample heterogeneity and improve performance. Our algorithms are highly efficient and scalable and are freely available for others to use. Availability: Code is available at http://www.cs.cmu.edu/∼saketn/detect_synapses/ Contact: zivbj@cs.cmu.edu |
format | Online Article Text |
id | pubmed-3694654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36946542013-06-27 A high-throughput framework to detect synapses in electron microscopy images Navlakha, Saket Suhan, Joseph Barth, Alison L. Bar-Joseph, Ziv Bioinformatics Ismb/Eccb 2013 Proceedings Papers Committee July 21 to July 23, 2013, Berlin, Germany Motivation: Synaptic connections underlie learning and memory in the brain and are dynamically formed and eliminated during development and in response to stimuli. Quantifying changes in overall density and strength of synapses is an important pre-requisite for studying connectivity and plasticity in these cases or in diseased conditions. Unfortunately, most techniques to detect such changes are either low-throughput (e.g. electrophysiology), prone to error and difficult to automate (e.g. standard electron microscopy) or too coarse (e.g. magnetic resonance imaging) to provide accurate and large-scale measurements. Results: To facilitate high-throughput analyses, we used a 50-year-old experimental technique to selectively stain for synapses in electron microscopy images, and we developed a machine-learning framework to automatically detect synapses in these images. To validate our method, we experimentally imaged brain tissue of the somatosensory cortex in six mice. We detected thousands of synapses in these images and demonstrate the accuracy of our approach using cross-validation with manually labeled data and by comparing against existing algorithms and against tools that process standard electron microscopy images. We also used a semi-supervised algorithm that leverages unlabeled data to overcome sample heterogeneity and improve performance. Our algorithms are highly efficient and scalable and are freely available for others to use. Availability: Code is available at http://www.cs.cmu.edu/∼saketn/detect_synapses/ Contact: zivbj@cs.cmu.edu Oxford University Press 2013-07-01 2013-06-19 /pmc/articles/PMC3694654/ /pubmed/23813014 http://dx.doi.org/10.1093/bioinformatics/btt222 Text en © The Author 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Ismb/Eccb 2013 Proceedings Papers Committee July 21 to July 23, 2013, Berlin, Germany Navlakha, Saket Suhan, Joseph Barth, Alison L. Bar-Joseph, Ziv A high-throughput framework to detect synapses in electron microscopy images |
title | A high-throughput framework to detect synapses in electron microscopy images |
title_full | A high-throughput framework to detect synapses in electron microscopy images |
title_fullStr | A high-throughput framework to detect synapses in electron microscopy images |
title_full_unstemmed | A high-throughput framework to detect synapses in electron microscopy images |
title_short | A high-throughput framework to detect synapses in electron microscopy images |
title_sort | high-throughput framework to detect synapses in electron microscopy images |
topic | Ismb/Eccb 2013 Proceedings Papers Committee July 21 to July 23, 2013, Berlin, Germany |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694654/ https://www.ncbi.nlm.nih.gov/pubmed/23813014 http://dx.doi.org/10.1093/bioinformatics/btt222 |
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