Language:
English
繁體中文
Help
回圖書館首頁
手機版館藏查詢
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Linked to FindBook
Google Book
Amazon
博客來
Single-Cell Methods and Spatial Analysis for Highly Multiplexed Tissue Images.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Single-Cell Methods and Spatial Analysis for Highly Multiplexed Tissue Images./
Author:
Novikov, Edward.
Description:
1 online resource (225 pages)
Notes:
Source: Dissertations Abstracts International, Volume: 84-12, Section: B.
Contained By:
Dissertations Abstracts International84-12B.
Subject:
Applied mathematics. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30490084click for full text (PQDT)
ISBN:
9798379611163
Single-Cell Methods and Spatial Analysis for Highly Multiplexed Tissue Images.
Novikov, Edward.
Single-Cell Methods and Spatial Analysis for Highly Multiplexed Tissue Images.
- 1 online resource (225 pages)
Source: Dissertations Abstracts International, Volume: 84-12, Section: B.
Thesis (Ph.D.)--Harvard University, 2023.
Includes bibliographical references
A transformation is currently underway in the study of tissue biology from one in which deep characterization of cell types and states is possible only following the dissociation of tissues into single cells to one in which spatial relationships can be preserved. Recent breakthroughs in highly multiplexed imaging enable the measurement of tens to hundreds of bio-molecules at single-cell resolution in tissues of human biopsies. These technologies extract molecular information about single cells in situ, thereby preserving their spatial characteristics within a tissue context. The data they produce are essential for understanding the organization of multi-cellular populations in health and diseases at multiple spatial scales ranging from single cells to groups of hundreds of thousands of cells. It is well established that tissue structure influences the underlying physiology of organisms and thus will assist in deciphering spatial signatures of disease.However, the high dimensional nature of single-cell, spatially resolved data poses difficulties for computational and statistical analyses. In this thesis I begin by providing a mathematical background of spatial point patterns and lattice data in the context of spatial biology. Embedded throughout is a survey of spatial statistical approaches to modeling the spatial dependence and heterogeneity of single cells in tissue. I follow this introduction with contributions to three key challenges inherent in the analysis of multiplexed data. First, I propose a robust segmentation framework to automatically extract single cells from gigapixel images in a manner that generalizes to diverse tissue types. Second, I present a novel approach for identifying cell phenotypes that capitalizes on protein spatial distributions and cellular morphology. I show that unsupervised deep clustering has the ability to extract cell states as well as neighborhoods of complex tissue motifs, with the potential to uncover rare, and previously unrecognized, cell phenotypes. Furthermore, I show that morphological information identifies molecular features of distinct histological classes of tumors. Third, I developa statistical approach for performing differential spatial analysis between groups of cells in the same or different tissue that discriminates the most salient spatial features. In addition, I introduce a set of in-silico tissue generation models that are specified from a desired functional form of correlation structure. Realizations of these synthetic tissues are used to assess cell-cell interactions and overcome limitations in gene expression studies when there is no access to spatial information. Together these contributions will assist biologists and clinicians in understanding the key mechanisms and drivers of normal tissue structure and development as well as circumstances in which these go awry in human disease.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023
Mode of access: World Wide Web
ISBN: 9798379611163Subjects--Topical Terms:
2122814
Applied mathematics.
Subjects--Index Terms:
Generative modelingIndex Terms--Genre/Form:
542853
Electronic books.
Single-Cell Methods and Spatial Analysis for Highly Multiplexed Tissue Images.
LDR
:04321nmm a2200421K 4500
001
2363529
005
20231127093432.5
006
m o d
007
cr mn ---uuuuu
008
241011s2023 xx obm 000 0 eng d
020
$a
9798379611163
035
$a
(MiAaPQ)AAI30490084
035
$a
AAI30490084
040
$a
MiAaPQ
$b
eng
$c
MiAaPQ
$d
NTU
100
1
$a
Novikov, Edward.
$3
3704293
245
1 0
$a
Single-Cell Methods and Spatial Analysis for Highly Multiplexed Tissue Images.
264
0
$c
2023
300
$a
1 online resource (225 pages)
336
$a
text
$b
txt
$2
rdacontent
337
$a
computer
$b
c
$2
rdamedia
338
$a
online resource
$b
cr
$2
rdacarrier
500
$a
Source: Dissertations Abstracts International, Volume: 84-12, Section: B.
500
$a
Advisor: Sorger, P.
502
$a
Thesis (Ph.D.)--Harvard University, 2023.
504
$a
Includes bibliographical references
520
$a
A transformation is currently underway in the study of tissue biology from one in which deep characterization of cell types and states is possible only following the dissociation of tissues into single cells to one in which spatial relationships can be preserved. Recent breakthroughs in highly multiplexed imaging enable the measurement of tens to hundreds of bio-molecules at single-cell resolution in tissues of human biopsies. These technologies extract molecular information about single cells in situ, thereby preserving their spatial characteristics within a tissue context. The data they produce are essential for understanding the organization of multi-cellular populations in health and diseases at multiple spatial scales ranging from single cells to groups of hundreds of thousands of cells. It is well established that tissue structure influences the underlying physiology of organisms and thus will assist in deciphering spatial signatures of disease.However, the high dimensional nature of single-cell, spatially resolved data poses difficulties for computational and statistical analyses. In this thesis I begin by providing a mathematical background of spatial point patterns and lattice data in the context of spatial biology. Embedded throughout is a survey of spatial statistical approaches to modeling the spatial dependence and heterogeneity of single cells in tissue. I follow this introduction with contributions to three key challenges inherent in the analysis of multiplexed data. First, I propose a robust segmentation framework to automatically extract single cells from gigapixel images in a manner that generalizes to diverse tissue types. Second, I present a novel approach for identifying cell phenotypes that capitalizes on protein spatial distributions and cellular morphology. I show that unsupervised deep clustering has the ability to extract cell states as well as neighborhoods of complex tissue motifs, with the potential to uncover rare, and previously unrecognized, cell phenotypes. Furthermore, I show that morphological information identifies molecular features of distinct histological classes of tumors. Third, I developa statistical approach for performing differential spatial analysis between groups of cells in the same or different tissue that discriminates the most salient spatial features. In addition, I introduce a set of in-silico tissue generation models that are specified from a desired functional form of correlation structure. Realizations of these synthetic tissues are used to assess cell-cell interactions and overcome limitations in gene expression studies when there is no access to spatial information. Together these contributions will assist biologists and clinicians in understanding the key mechanisms and drivers of normal tissue structure and development as well as circumstances in which these go awry in human disease.
533
$a
Electronic reproduction.
$b
Ann Arbor, Mich. :
$c
ProQuest,
$d
2023
538
$a
Mode of access: World Wide Web
650
4
$a
Applied mathematics.
$3
2122814
650
4
$a
Statistics.
$3
517247
650
4
$a
Bioinformatics.
$3
553671
650
4
$a
Cellular biology.
$3
3172791
653
$a
Generative modeling
653
$a
Multiplexed imaging
653
$a
Segmentation
653
$a
Spatial biology
653
$a
Spatial statistics
653
$a
Tumor heterogeneity
655
7
$a
Electronic books.
$2
lcsh
$3
542853
690
$a
0364
690
$a
0463
690
$a
0715
690
$a
0379
710
2
$a
ProQuest Information and Learning Co.
$3
783688
710
2
$a
Harvard University.
$b
Engineering and Applied Sciences - Applied Math.
$3
3184332
773
0
$t
Dissertations Abstracts International
$g
84-12B.
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30490084
$z
click for full text (PQDT)
based on 0 review(s)
Location:
ALL
電子資源
Year:
Volume Number:
Items
1 records • Pages 1 •
1
Inventory Number
Location Name
Item Class
Material type
Call number
Usage Class
Loan Status
No. of reservations
Opac note
Attachments
W9485885
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
On shelf
0
1 records • Pages 1 •
1
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login