Large-area cell-tracking cytometry for biophysical measurements of single cells

Thesis: Ph. D., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, May, 2020 === Cataloged from the official PDF of thesis. === Includes bibliographical references (pages 96-106). === Utility of single-cell biophysical markers is often limited due to th...

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Main Author: Apichitsopa, Nicha.
Other Authors: Joel Voldman.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2020
Subjects:
Online Access:https://hdl.handle.net/1721.1/127012
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-1270122020-09-06T06:48:49Z Large-area cell-tracking cytometry for biophysical measurements of single cells Apichitsopa, Nicha. Joel Voldman. Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science. Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science Electrical Engineering and Computer Science. Thesis: Ph. D., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, May, 2020 Cataloged from the official PDF of thesis. Includes bibliographical references (pages 96-106). Utility of single-cell biophysical markers is often limited due to the low-specificity nature of biophysical markers and lack of existing techniques which can test multiple biophysical characteristics for single cells. To address this challenge, I developed a multiparameter intrinsic cytometry approach which integrates multiple label-free biophysical measurements into a versatile (can combine techniques across domains) and readily extensible (to measure more than two biophysical markers) platform for single cell analysis. The proposed multiparameter cell-tracking intrinsic cytometry utilizes label-free microfluidic techniques to manipulate cells such that information regarding their biophysical properties can be extracted from their spatiotemporal positions. Furthermore, this technique utilizes cell tracking to extract and associate the biophysical markers for single cells. The specific instantiation of the cytometry platform can measure up to five intrinsic markers of cells, and has facilitated the quantitative investigation of label-free cell profiles and classification of cell types and functional states. The applications of this approach were extended by leveraging digital holographic microscopy and deep learning technologies to monitor cells in a large field of view, enabling rapid and high-throughput assessment of biophysical phenotypes. by Nicha Apichitsopa. Ph. D. Ph.D. Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science 2020-09-03T17:41:49Z 2020-09-03T17:41:49Z 2020 2020 Thesis https://hdl.handle.net/1721.1/127012 1191624346 eng MIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided. http://dspace.mit.edu/handle/1721.1/7582 106 pages application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Electrical Engineering and Computer Science.
spellingShingle Electrical Engineering and Computer Science.
Apichitsopa, Nicha.
Large-area cell-tracking cytometry for biophysical measurements of single cells
description Thesis: Ph. D., Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science, May, 2020 === Cataloged from the official PDF of thesis. === Includes bibliographical references (pages 96-106). === Utility of single-cell biophysical markers is often limited due to the low-specificity nature of biophysical markers and lack of existing techniques which can test multiple biophysical characteristics for single cells. To address this challenge, I developed a multiparameter intrinsic cytometry approach which integrates multiple label-free biophysical measurements into a versatile (can combine techniques across domains) and readily extensible (to measure more than two biophysical markers) platform for single cell analysis. The proposed multiparameter cell-tracking intrinsic cytometry utilizes label-free microfluidic techniques to manipulate cells such that information regarding their biophysical properties can be extracted from their spatiotemporal positions. Furthermore, this technique utilizes cell tracking to extract and associate the biophysical markers for single cells. The specific instantiation of the cytometry platform can measure up to five intrinsic markers of cells, and has facilitated the quantitative investigation of label-free cell profiles and classification of cell types and functional states. The applications of this approach were extended by leveraging digital holographic microscopy and deep learning technologies to monitor cells in a large field of view, enabling rapid and high-throughput assessment of biophysical phenotypes. === by Nicha Apichitsopa. === Ph. D. === Ph.D. Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science
author2 Joel Voldman.
author_facet Joel Voldman.
Apichitsopa, Nicha.
author Apichitsopa, Nicha.
author_sort Apichitsopa, Nicha.
title Large-area cell-tracking cytometry for biophysical measurements of single cells
title_short Large-area cell-tracking cytometry for biophysical measurements of single cells
title_full Large-area cell-tracking cytometry for biophysical measurements of single cells
title_fullStr Large-area cell-tracking cytometry for biophysical measurements of single cells
title_full_unstemmed Large-area cell-tracking cytometry for biophysical measurements of single cells
title_sort large-area cell-tracking cytometry for biophysical measurements of single cells
publisher Massachusetts Institute of Technology
publishDate 2020
url https://hdl.handle.net/1721.1/127012
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