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 Kernel Models for Statistic...
~
Crawford, Lorin.
FindBook
Google Book
Amazon
博客來
Bayesian Kernel Models for Statistical Genetics and Cancer Genomics.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Bayesian Kernel Models for Statistical Genetics and Cancer Genomics./
作者:
Crawford, Lorin.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2017,
面頁冊數:
245 p.
附註:
Source: Dissertation Abstracts International, Volume: 78-09(E), Section: B.
Contained By:
Dissertation Abstracts International78-09B(E).
標題:
Statistics. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10261357
ISBN:
9781369735420
Bayesian Kernel Models for Statistical Genetics and Cancer Genomics.
Crawford, Lorin.
Bayesian Kernel Models for Statistical Genetics and Cancer Genomics.
- Ann Arbor : ProQuest Dissertations & Theses, 2017 - 245 p.
Source: Dissertation Abstracts International, Volume: 78-09(E), Section: B.
Thesis (Ph.D.)--Duke University, 2017.
The main contribution of this thesis is to examine the utility of kernel regression approaches and variance component models for solving complex problems in statistical genetics and molecular biology. Many of these types of statistical methods have been developed specifically to be applied to solve similar biological problems. For example, kernel regression models have a long history in statistics, applied mathematics, and machine learning. More recently, variance component models have been extensively utilized as tools to broaden understanding of the genetic basis of phenotypic variation. However, because of large combinatorial search spaces and other confounding factors, many of these current methods face enormous computational challenges and often suffer from low statistical power --- particularly when phenotypic variation is driven by complicated underlying genetic architectures (e.g. the presence of epistatic effects involving higher order genetic interactions). This thesis highlights two novel methods which provide innovative solutions to better address the important statistical and computational hurdles faced within complex biological data sets. The first is a Bayesian non-parametric statistical framework that allows for efficient variable selection in nonlinear regression which we refer to as "Bayesian approximate kernel regression", or BAKR. The second is a novel algorithm for identifying genetic variants that are involved in epistasis without the need to identify the exact partners with which the variants interact. We refer to this method as the "MArginal ePIstasis Test", or MAPIT. Here, we develop the theory of these two approaches, and demonstrate their power, interpretability, and computational efficiency for analyzing complex phenotypes. We also illustrate their ability to facilitate novel biological discoveries in several real data sets, each of them representing a particular class of analyses: genome-wide association studies (GWASs), molecular trait quantitative trait loci (QTL) mapping studies, and cancer biology association studies. Lastly, we will also explore the potential of these approaches in radiogenomics, a brand new subfield of genetics and genomics that focuses on the study of correlations between imaging or network features and genetic variation.
ISBN: 9781369735420Subjects--Topical Terms:
517247
Statistics.
Bayesian Kernel Models for Statistical Genetics and Cancer Genomics.
LDR
:03245nmm a2200301 4500
001
2124078
005
20171023101707.5
008
180830s2017 ||||||||||||||||| ||eng d
020
$a
9781369735420
035
$a
(MiAaPQ)AAI10261357
035
$a
AAI10261357
040
$a
MiAaPQ
$c
MiAaPQ
100
1
$a
Crawford, Lorin.
$3
3286052
245
1 0
$a
Bayesian Kernel Models for Statistical Genetics and Cancer Genomics.
260
1
$a
Ann Arbor :
$b
ProQuest Dissertations & Theses,
$c
2017
300
$a
245 p.
500
$a
Source: Dissertation Abstracts International, Volume: 78-09(E), Section: B.
500
$a
Advisers: Sayan Mukherjee; Kris C. Wood.
502
$a
Thesis (Ph.D.)--Duke University, 2017.
520
$a
The main contribution of this thesis is to examine the utility of kernel regression approaches and variance component models for solving complex problems in statistical genetics and molecular biology. Many of these types of statistical methods have been developed specifically to be applied to solve similar biological problems. For example, kernel regression models have a long history in statistics, applied mathematics, and machine learning. More recently, variance component models have been extensively utilized as tools to broaden understanding of the genetic basis of phenotypic variation. However, because of large combinatorial search spaces and other confounding factors, many of these current methods face enormous computational challenges and often suffer from low statistical power --- particularly when phenotypic variation is driven by complicated underlying genetic architectures (e.g. the presence of epistatic effects involving higher order genetic interactions). This thesis highlights two novel methods which provide innovative solutions to better address the important statistical and computational hurdles faced within complex biological data sets. The first is a Bayesian non-parametric statistical framework that allows for efficient variable selection in nonlinear regression which we refer to as "Bayesian approximate kernel regression", or BAKR. The second is a novel algorithm for identifying genetic variants that are involved in epistasis without the need to identify the exact partners with which the variants interact. We refer to this method as the "MArginal ePIstasis Test", or MAPIT. Here, we develop the theory of these two approaches, and demonstrate their power, interpretability, and computational efficiency for analyzing complex phenotypes. We also illustrate their ability to facilitate novel biological discoveries in several real data sets, each of them representing a particular class of analyses: genome-wide association studies (GWASs), molecular trait quantitative trait loci (QTL) mapping studies, and cancer biology association studies. Lastly, we will also explore the potential of these approaches in radiogenomics, a brand new subfield of genetics and genomics that focuses on the study of correlations between imaging or network features and genetic variation.
590
$a
School code: 0066.
650
4
$a
Statistics.
$3
517247
650
4
$a
Biostatistics.
$3
1002712
650
4
$a
Genetics.
$3
530508
690
$a
0463
690
$a
0308
690
$a
0369
710
2
$a
Duke University.
$b
Statistical Science.
$3
1023903
773
0
$t
Dissertation Abstracts International
$g
78-09B(E).
790
$a
0066
791
$a
Ph.D.
792
$a
2017
793
$a
English
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10261357
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
W9334690
電子資源
01.外借(書)_YB
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