語系:
繁體中文
English
說明(常見問題)
回圖書館首頁
手機版館藏查詢
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
FindBook
Google Book
Amazon
博客來
Machine Learning for Clinical Trials and Precision Medicine.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Machine Learning for Clinical Trials and Precision Medicine./
作者:
Liu, Ruishan.
面頁冊數:
1 online resource (134 pages)
附註:
Source: Dissertations Abstracts International, Volume: 84-04, Section: B.
Contained By:
Dissertations Abstracts International84-04B.
標題:
Patients. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=29342256click for full text (PQDT)
ISBN:
9798352603581
Machine Learning for Clinical Trials and Precision Medicine.
Liu, Ruishan.
Machine Learning for Clinical Trials and Precision Medicine.
- 1 online resource (134 pages)
Source: Dissertations Abstracts International, Volume: 84-04, Section: B.
Thesis (Ph.D.)--Stanford University, 2022.
Includes bibliographical references
Machine learning (ML) has been wildly applied in biomedicine and healthcare. The growing abundance of medical data and the advance of biological technologies (e.g. next-generation sequencing) have offered great opportunities for using ML in computational biology and health. In this thesis, I present my works contributing to this emerging field in three aspects --- using large-scale datasets to advance medical studies, developing algorithms to solve biological challenges, and building analysis tools for new technologies.In the first part, I present two works of applying ML on large-scale real-world data: one for clinical trial design and one for precision medicine. Overly restrictive eligibility criteria has been a key barrier for clinical trials. In the thesis, I introduce a powerful computational framework, Trial Pathfinder, which enables inclusive criteria and data valuation for clinical trials. A critical goal for precision medicine is to characterize how patients with specific genetic mutations respond to therapies. In the thesis, I present systematic pan-cancer analysis of mutation-treatment interactions using large real-world clinico-genomics data.In the second part, I introduce my work on developing algorithms to solve biological challenge --- aligning multiple datasets with subset correspondence information. In many biological and medical applications, we have multiple related datasets from different sources or domains, and learning efficient computational mappings between these datasets is an important problem. In the thesis, I present an end-to-end optimal transport framework that effectively leverages side information to align datasets.Finally, I present my work on developing analysis tools for new technologies --- spatial transcriptomics and RNA velocity. Recently high-throughput image-based transcriptomic methods were developed and enabled researchers to spatially resolve gene expression variation at the molecular level for the first time. In the thesis, I describe a general analysis tool to quantitatively study the spatial correlations of gene expression in fixed tissue sections. Recent development in inferring RNA velocity from single-cell RNA-seq opens up exciting new vista into developmental lineage and cellular dynamics. In the thesis, I introduce a principled computational framework that extends RNA velocity to quantify systems level dynamics and improve single-cell data analysis.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023
Mode of access: World Wide Web
ISBN: 9798352603581Subjects--Topical Terms:
1961957
Patients.
Index Terms--Genre/Form:
542853
Electronic books.
Machine Learning for Clinical Trials and Precision Medicine.
LDR
:03720nmm a2200361K 4500
001
2359814
005
20230917195254.5
006
m o d
007
cr mn ---uuuuu
008
241011s2022 xx obm 000 0 eng d
020
$a
9798352603581
035
$a
(MiAaPQ)AAI29342256
035
$a
(MiAaPQ)STANFORDyv799ny4496
035
$a
AAI29342256
040
$a
MiAaPQ
$b
eng
$c
MiAaPQ
$d
NTU
100
1
$a
Liu, Ruishan.
$3
3700428
245
1 0
$a
Machine Learning for Clinical Trials and Precision Medicine.
264
0
$c
2022
300
$a
1 online resource (134 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: 84-04, Section: B.
500
$a
Advisor: Zou, James ; Soh, H. Tom ; Tse, David.
502
$a
Thesis (Ph.D.)--Stanford University, 2022.
504
$a
Includes bibliographical references
520
$a
Machine learning (ML) has been wildly applied in biomedicine and healthcare. The growing abundance of medical data and the advance of biological technologies (e.g. next-generation sequencing) have offered great opportunities for using ML in computational biology and health. In this thesis, I present my works contributing to this emerging field in three aspects --- using large-scale datasets to advance medical studies, developing algorithms to solve biological challenges, and building analysis tools for new technologies.In the first part, I present two works of applying ML on large-scale real-world data: one for clinical trial design and one for precision medicine. Overly restrictive eligibility criteria has been a key barrier for clinical trials. In the thesis, I introduce a powerful computational framework, Trial Pathfinder, which enables inclusive criteria and data valuation for clinical trials. A critical goal for precision medicine is to characterize how patients with specific genetic mutations respond to therapies. In the thesis, I present systematic pan-cancer analysis of mutation-treatment interactions using large real-world clinico-genomics data.In the second part, I introduce my work on developing algorithms to solve biological challenge --- aligning multiple datasets with subset correspondence information. In many biological and medical applications, we have multiple related datasets from different sources or domains, and learning efficient computational mappings between these datasets is an important problem. In the thesis, I present an end-to-end optimal transport framework that effectively leverages side information to align datasets.Finally, I present my work on developing analysis tools for new technologies --- spatial transcriptomics and RNA velocity. Recently high-throughput image-based transcriptomic methods were developed and enabled researchers to spatially resolve gene expression variation at the molecular level for the first time. In the thesis, I describe a general analysis tool to quantitatively study the spatial correlations of gene expression in fixed tissue sections. Recent development in inferring RNA velocity from single-cell RNA-seq opens up exciting new vista into developmental lineage and cellular dynamics. In the thesis, I introduce a principled computational framework that extends RNA velocity to quantify systems level dynamics and improve single-cell data analysis.
533
$a
Electronic reproduction.
$b
Ann Arbor, Mich. :
$c
ProQuest,
$d
2023
538
$a
Mode of access: World Wide Web
650
4
$a
Patients.
$3
1961957
650
4
$a
Gene expression.
$3
643979
650
4
$a
Age.
$3
1486010
650
4
$a
Mutation.
$3
837917
650
4
$a
Clinical trials.
$3
724498
650
4
$a
Algorithms.
$3
536374
650
4
$a
Survival analysis.
$3
3566266
650
4
$a
Bioinformatics.
$3
553671
650
4
$a
Computer science.
$3
523869
650
4
$a
Genetics.
$3
530508
650
4
$a
Pharmaceutical sciences.
$3
3173021
655
7
$a
Electronic books.
$2
lcsh
$3
542853
690
$a
0715
690
$a
0984
690
$a
0369
690
$a
0572
710
2
$a
ProQuest Information and Learning Co.
$3
783688
710
2
$a
Stanford University.
$3
754827
773
0
$t
Dissertations Abstracts International
$g
84-04B.
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=29342256
$z
click for full text (PQDT)
筆 0 讀者評論
館藏地:
全部
電子資源
出版年:
卷號:
館藏
1 筆 • 頁數 1 •
1
條碼號
典藏地名稱
館藏流通類別
資料類型
索書號
使用類型
借閱狀態
預約狀態
備註欄
附件
W9482170
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
在架
0
1 筆 • 頁數 1 •
1
多媒體
評論
新增評論
分享你的心得
Export
取書館
處理中
...
變更密碼
登入