Fast image and data processing methods for novel neuroscience technologies

The nematode C. elegans, a transparent animal with 302 neurons, is a suitable model organism for whole-brain measurement of nervous activity. However, under panneuronal labeling, it is difficult to resolve the identity of the neurons by shape or location alone. We propose a fluorescent in situ hybri...

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Bibliographic Details
Main Author: Çeliker, Orhan Tunç
Other Authors: Boyden, Edward S.
Format: Thesis
Published: Massachusetts Institute of Technology 2022
Online Access:https://hdl.handle.net/1721.1/143327
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author Çeliker, Orhan Tunç
author2 Boyden, Edward S.
author_facet Boyden, Edward S.
Çeliker, Orhan Tunç
author_sort Çeliker, Orhan Tunç
collection MIT
description The nematode C. elegans, a transparent animal with 302 neurons, is a suitable model organism for whole-brain measurement of nervous activity. However, under panneuronal labeling, it is difficult to resolve the identity of the neurons by shape or location alone. We propose a fluorescent in situ hybridization (FISH) based pipeline for reading out gene expression from neurons. Using optimization methods, we select a compact set of genes that provide enough information to distinguish every neighboring pair of neurons in the nervous system. We show that we can process volumetric images of live and fixed C. elegans to read out the gene expression patterns of each observed neuron and match it to their calcium indicator data. Separately, we also outline computational approaches to processing fluorescence data from novel fluorescent sensors.
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spelling mit-1721.1/1433272022-06-16T03:36:10Z Fast image and data processing methods for novel neuroscience technologies Çeliker, Orhan Tunç Boyden, Edward S. Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science The nematode C. elegans, a transparent animal with 302 neurons, is a suitable model organism for whole-brain measurement of nervous activity. However, under panneuronal labeling, it is difficult to resolve the identity of the neurons by shape or location alone. We propose a fluorescent in situ hybridization (FISH) based pipeline for reading out gene expression from neurons. Using optimization methods, we select a compact set of genes that provide enough information to distinguish every neighboring pair of neurons in the nervous system. We show that we can process volumetric images of live and fixed C. elegans to read out the gene expression patterns of each observed neuron and match it to their calcium indicator data. Separately, we also outline computational approaches to processing fluorescence data from novel fluorescent sensors. Ph.D. 2022-06-15T13:12:49Z 2022-06-15T13:12:49Z 2022-02 2022-03-04T20:47:40.841Z Thesis https://hdl.handle.net/1721.1/143327 In Copyright - Educational Use Permitted Copyright MIT http://rightsstatements.org/page/InC-EDU/1.0/ application/pdf Massachusetts Institute of Technology
spellingShingle Çeliker, Orhan Tunç
Fast image and data processing methods for novel neuroscience technologies
title Fast image and data processing methods for novel neuroscience technologies
title_full Fast image and data processing methods for novel neuroscience technologies
title_fullStr Fast image and data processing methods for novel neuroscience technologies
title_full_unstemmed Fast image and data processing methods for novel neuroscience technologies
title_short Fast image and data processing methods for novel neuroscience technologies
title_sort fast image and data processing methods for novel neuroscience technologies
url https://hdl.handle.net/1721.1/143327
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