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
Statistical methods for studying two...
~
Biernacka, Joanna Monika.
FindBook
Google Book
Amazon
博客來
Statistical methods for studying two linked disease genes.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Statistical methods for studying two linked disease genes./
作者:
Biernacka, Joanna Monika.
面頁冊數:
193 p.
附註:
Source: Dissertation Abstracts International, Volume: 66-06, Section: B, page: 3088.
Contained By:
Dissertation Abstracts International66-06B.
標題:
Health Sciences, Public Health. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=NR02643
ISBN:
049402643X
Statistical methods for studying two linked disease genes.
Biernacka, Joanna Monika.
Statistical methods for studying two linked disease genes.
- 193 p.
Source: Dissertation Abstracts International, Volume: 66-06, Section: B, page: 3088.
Thesis (Ph.D.)--University of Toronto (Canada), 2005.
Assuming there is exactly one disease gene in a chromosomal region, a generalized estimating equations (GEE) approach can be used to estimate the location of the gene (Liang et al., 2001, Human Heredity 51: 64--78) using marker identical-by-descent (IBD) sharing data at multiple markers in a sample of affected sib pairs (ASPs). For diseases with complex genetic etiology, more than one susceptibility gene may exist in one chromosomal region. In such situations, linkage methods designed to detect a single locus may not successfully localize either of these two genes. We derived an expression for expected allele sharing in affected sib pairs at each point across a chromosomal segment containing two susceptibility genes, and proposed a GEE approach for localizing both disease genes simultaneously. We developed an algorithm that uses marker IBD sharing for a sample of ASPS to estimate the locations of the two genes and the expected ASP IBD sharing at these two loci. We also proposed methods to evaluate the evidence for two linked disease loci, in this GEE estimation framework, based on approximate quasi-likelihood ratio and generalized Wald and score test statistics. We evaluated the proposed estimation and testing methods by simulation, and found that the proposed estimation method can improve disease gene localization and aid in resolving large peaks when two disease genes are present in one chromosomal region. The performance of the estimation method for localizing two linked disease genes, and the power to detect the presence of two linked genes, improve with increased excess allele sharing at the disease gene loci, increased distance between the disease genes, and increased number of affected sib pairs. We applied the described methods to data from a genome scan for type 1 diabetes (Mein et al., 1998, Nature Genetics 19: 297--300) and obtained estimates of two putative disease gene locations on chromosome 6, approximately 20 cM apart.
ISBN: 049402643XSubjects--Topical Terms:
1017659
Health Sciences, Public Health.
Statistical methods for studying two linked disease genes.
LDR
:02800nmm 2200277 4500
001
1812992
005
20060427132650.5
008
130610s2005 eng d
020
$a
049402643X
035
$a
(UnM)AAINR02643
035
$a
AAINR02643
040
$a
UnM
$c
UnM
100
1
$a
Biernacka, Joanna Monika.
$3
1902522
245
1 0
$a
Statistical methods for studying two linked disease genes.
300
$a
193 p.
500
$a
Source: Dissertation Abstracts International, Volume: 66-06, Section: B, page: 3088.
502
$a
Thesis (Ph.D.)--University of Toronto (Canada), 2005.
520
$a
Assuming there is exactly one disease gene in a chromosomal region, a generalized estimating equations (GEE) approach can be used to estimate the location of the gene (Liang et al., 2001, Human Heredity 51: 64--78) using marker identical-by-descent (IBD) sharing data at multiple markers in a sample of affected sib pairs (ASPs). For diseases with complex genetic etiology, more than one susceptibility gene may exist in one chromosomal region. In such situations, linkage methods designed to detect a single locus may not successfully localize either of these two genes. We derived an expression for expected allele sharing in affected sib pairs at each point across a chromosomal segment containing two susceptibility genes, and proposed a GEE approach for localizing both disease genes simultaneously. We developed an algorithm that uses marker IBD sharing for a sample of ASPS to estimate the locations of the two genes and the expected ASP IBD sharing at these two loci. We also proposed methods to evaluate the evidence for two linked disease loci, in this GEE estimation framework, based on approximate quasi-likelihood ratio and generalized Wald and score test statistics. We evaluated the proposed estimation and testing methods by simulation, and found that the proposed estimation method can improve disease gene localization and aid in resolving large peaks when two disease genes are present in one chromosomal region. The performance of the estimation method for localizing two linked disease genes, and the power to detect the presence of two linked genes, improve with increased excess allele sharing at the disease gene loci, increased distance between the disease genes, and increased number of affected sib pairs. We applied the described methods to data from a genome scan for type 1 diabetes (Mein et al., 1998, Nature Genetics 19: 297--300) and obtained estimates of two putative disease gene locations on chromosome 6, approximately 20 cM apart.
590
$a
School code: 0779.
650
4
$a
Health Sciences, Public Health.
$3
1017659
650
4
$a
Health Sciences, Pathology.
$3
1017854
650
4
$a
Biology, Biostatistics.
$3
1018416
650
4
$a
Biology, Genetics.
$3
1017730
690
$a
0573
690
$a
0571
690
$a
0308
690
$a
0369
710
2 0
$a
University of Toronto (Canada).
$3
1017674
773
0
$t
Dissertation Abstracts International
$g
66-06B.
790
$a
0779
791
$a
Ph.D.
792
$a
2005
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=NR02643
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
W9203863
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