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
Bayesian Methods and Computation for...
~
Watts, Krista Leigh.
FindBook
Google Book
Amazon
博客來
Bayesian Methods and Computation for Large Observational Datasets.
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Bayesian Methods and Computation for Large Observational Datasets./
作者:
Watts, Krista Leigh.
面頁冊數:
110 p.
附註:
Source: Dissertation Abstracts International, Volume: 74-10(E), Section: B.
Contained By:
Dissertation Abstracts International74-10B(E).
標題:
Biology, Biostatistics. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3567120
ISBN:
9781303187582
Bayesian Methods and Computation for Large Observational Datasets.
Watts, Krista Leigh.
Bayesian Methods and Computation for Large Observational Datasets.
- 110 p.
Source: Dissertation Abstracts International, Volume: 74-10(E), Section: B.
Thesis (Ph.D.)--Harvard University, 2013.
Much health related research depends heavily on the analysis of a rapidly expanding universe of observational data. A challenge in analysis of such data is the lack of sound statistical methods and tools that can address multiple facets of estimating treatment or exposure effects in observational studies with a large number of covariates. We sought to advance methods to improve analysis of large observational datasets with an end goal of understanding the effect of treatments or exposures on health. First we compared existing methods for propensity score (PS) adjustment, specifically Bayesian propensity scores. This concept had previously been introduced (McCandless et al., 2009) but no rigorous evaluation had been done to evaluate the impact of feedback when fitting the joint likelihood for both the PS and outcome models. We determined that unless specific steps were taken to mitigate the impact of feedback, it has the potential to distort estimates of the treatment effect. Next, we developed a method for accounting for uncertainty in confounding adjustment in the context of multiple exposures. Our method allows us to select confounders based on their association with the joint exposure and the outcome while also accounting for the uncertainty in the confounding adjustment. Finally, we developed two methods to combine heterogenous sources of data for effect estimation, specifically information coming from a primary data source that provides information for treatments, outcomes, and a limited set of measured confounders on a large number of people and smaller supplementary data sources containing a much richer set of covariates. Our methods avoid the need to specify the full joint distribution of all covariates.
ISBN: 9781303187582Subjects--Topical Terms:
1018416
Biology, Biostatistics.
Bayesian Methods and Computation for Large Observational Datasets.
LDR
:02602nam a2200277 4500
001
1967870
005
20141121132933.5
008
150210s2013 ||||||||||||||||| ||eng d
020
$a
9781303187582
035
$a
(MiAaPQ)AAI3567120
035
$a
AAI3567120
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Watts, Krista Leigh.
$3
2104961
245
1 0
$a
Bayesian Methods and Computation for Large Observational Datasets.
300
$a
110 p.
500
$a
Source: Dissertation Abstracts International, Volume: 74-10(E), Section: B.
500
$a
Adviser: Francesca Dominici.
502
$a
Thesis (Ph.D.)--Harvard University, 2013.
520
$a
Much health related research depends heavily on the analysis of a rapidly expanding universe of observational data. A challenge in analysis of such data is the lack of sound statistical methods and tools that can address multiple facets of estimating treatment or exposure effects in observational studies with a large number of covariates. We sought to advance methods to improve analysis of large observational datasets with an end goal of understanding the effect of treatments or exposures on health. First we compared existing methods for propensity score (PS) adjustment, specifically Bayesian propensity scores. This concept had previously been introduced (McCandless et al., 2009) but no rigorous evaluation had been done to evaluate the impact of feedback when fitting the joint likelihood for both the PS and outcome models. We determined that unless specific steps were taken to mitigate the impact of feedback, it has the potential to distort estimates of the treatment effect. Next, we developed a method for accounting for uncertainty in confounding adjustment in the context of multiple exposures. Our method allows us to select confounders based on their association with the joint exposure and the outcome while also accounting for the uncertainty in the confounding adjustment. Finally, we developed two methods to combine heterogenous sources of data for effect estimation, specifically information coming from a primary data source that provides information for treatments, outcomes, and a limited set of measured confounders on a large number of people and smaller supplementary data sources containing a much richer set of covariates. Our methods avoid the need to specify the full joint distribution of all covariates.
590
$a
School code: 0084.
650
4
$a
Biology, Biostatistics.
$3
1018416
650
4
$a
Statistics.
$3
517247
690
$a
0308
690
$a
0463
710
2
$a
Harvard University.
$b
Biostatistics.
$3
2104931
773
0
$t
Dissertation Abstracts International
$g
74-10B(E).
790
$a
0084
791
$a
Ph.D.
792
$a
2013
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3567120
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
W9262876
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