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
Model-based gene expression analysis.
~
Liu, Yunlong.
FindBook
Google Book
Amazon
博客來
Model-based gene expression analysis.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Model-based gene expression analysis./
作者:
Liu, Yunlong.
面頁冊數:
130 p.
附註:
Source: Dissertation Abstracts International, Volume: 65-11, Section: B, page: 5861.
Contained By:
Dissertation Abstracts International65-11B.
標題:
Engineering, Biomedical. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3154683
ISBN:
0496152300
Model-based gene expression analysis.
Liu, Yunlong.
Model-based gene expression analysis.
- 130 p.
Source: Dissertation Abstracts International, Volume: 65-11, Section: B, page: 5861.
Thesis (Ph.D.)--Purdue University, 2004.
Systems biology is a rapidly emerging branch of modern biology, aiming at elucidating the complex regulatory mechanisms using an ever-growing amount of molecular data and advanced mathematical, computational tools. To understand the genome-wide complexity of transcription regulation, my research objective was to develop a model-based approach to predict critical transcription-factor binding motifs (TFBMs) using microarray-derived mRNA expression levels and genomic DNA sequences. By defining an activation level of TFBMs as a unique state variable, the mathematical model was built to establish a quantitative relationship between the observed mRNA expression level and frequencies of TFBMs in regulatory DNA regions. Identification of the critical set of TFBMs was formulated as a combinatorial optimization problem using three biological systems including the shear-stress responses in synovial cells, the interleukin-1 responses in chondrocyte cells, and the differentiation processes in human chondrogenesis. Mathematical manipulations such as singular value decomposition, genetic algorithm, particle swarm optimization, and ant algorithm were employed to predict the critical set of TFBMs, whose number was estimated from Akaike information criterion. First, the results show that the described model is useful to predict and evaluate the critical set of TFBMs from high-throughput gene expression data and regulatory DNA sequences. Second, a genome-wide transcription network can be built by evaluating generality and specificity of the critical TFBMs in different biological model systems. Lastly, it is important to validate the predicted TFBMs using experimental assays because of uncertainties in existing knowledge, particularly definition of regulatory DNA regions. In conclusion, the described mathematical and computational approach can help biologists to raise testable hypotheses in transcription regulation. Combined with the biochemical assays such as a promoter competition assay, the model-based approach is expected to contribute to the understanding of system-wide regulatory processes and elucidating functional significance of TFBMs.
ISBN: 0496152300Subjects--Topical Terms:
1017684
Engineering, Biomedical.
Model-based gene expression analysis.
LDR
:03075nmm 2200289 4500
001
1841255
005
20050825081238.5
008
130614s2004 eng d
020
$a
0496152300
035
$a
(UnM)AAI3154683
035
$a
AAI3154683
040
$a
UnM
$c
UnM
100
1
$a
Liu, Yunlong.
$3
1929562
245
1 0
$a
Model-based gene expression analysis.
300
$a
130 p.
500
$a
Source: Dissertation Abstracts International, Volume: 65-11, Section: B, page: 5861.
500
$a
Major Professors: Hiroki Yokota; Peter C. Doerschuk.
502
$a
Thesis (Ph.D.)--Purdue University, 2004.
520
$a
Systems biology is a rapidly emerging branch of modern biology, aiming at elucidating the complex regulatory mechanisms using an ever-growing amount of molecular data and advanced mathematical, computational tools. To understand the genome-wide complexity of transcription regulation, my research objective was to develop a model-based approach to predict critical transcription-factor binding motifs (TFBMs) using microarray-derived mRNA expression levels and genomic DNA sequences. By defining an activation level of TFBMs as a unique state variable, the mathematical model was built to establish a quantitative relationship between the observed mRNA expression level and frequencies of TFBMs in regulatory DNA regions. Identification of the critical set of TFBMs was formulated as a combinatorial optimization problem using three biological systems including the shear-stress responses in synovial cells, the interleukin-1 responses in chondrocyte cells, and the differentiation processes in human chondrogenesis. Mathematical manipulations such as singular value decomposition, genetic algorithm, particle swarm optimization, and ant algorithm were employed to predict the critical set of TFBMs, whose number was estimated from Akaike information criterion. First, the results show that the described model is useful to predict and evaluate the critical set of TFBMs from high-throughput gene expression data and regulatory DNA sequences. Second, a genome-wide transcription network can be built by evaluating generality and specificity of the critical TFBMs in different biological model systems. Lastly, it is important to validate the predicted TFBMs using experimental assays because of uncertainties in existing knowledge, particularly definition of regulatory DNA regions. In conclusion, the described mathematical and computational approach can help biologists to raise testable hypotheses in transcription regulation. Combined with the biochemical assays such as a promoter competition assay, the model-based approach is expected to contribute to the understanding of system-wide regulatory processes and elucidating functional significance of TFBMs.
590
$a
School code: 0183.
650
4
$a
Engineering, Biomedical.
$3
1017684
650
4
$a
Biology, Genetics.
$3
1017730
690
$a
0541
690
$a
0369
710
2 0
$a
Purdue University.
$3
1017663
773
0
$t
Dissertation Abstracts International
$g
65-11B.
790
1 0
$a
Yokota, Hiroki,
$e
advisor
790
1 0
$a
Doerschuk, Peter C.,
$e
advisor
790
$a
0183
791
$a
Ph.D.
792
$a
2004
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3154683
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
W9190769
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