Mapping And Analysis of Quantitative Trait Loci (QTL) for Binary Distributed Data

碩士 === 國立臺灣大學 === 農藝學系研究所 === 86 === Most quantitative traits are assumed to be continuously and normally distributed. Due to the nature of response, limitation of measurement or some other theoretical or practical considerat...

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Main Authors: Chiang, Chih-ming, 江志民
Other Authors: Ching Liu
Format: Others
Language:zh-TW
Published: 1998
Online Access:http://ndltd.ncl.edu.tw/handle/51486537381198249938
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spelling ndltd-TW-086NTU004170122016-06-29T04:13:46Z http://ndltd.ncl.edu.tw/handle/51486537381198249938 Mapping And Analysis of Quantitative Trait Loci (QTL) for Binary Distributed Data 數量性狀基因座定位法在二項分布資料上之應用 Chiang, Chih-ming 江志民 碩士 國立臺灣大學 農藝學系研究所 86 Most quantitative traits are assumed to be continuously and normally distributed. Due to the nature of response, limitation of measurement or some other theoretical or practical considerations, only the discrete binary data are available. Published statistical methods for mapping and analyzing quantitative trait loci(QTL) all center on the normal assumption and thus can not be directly applied for binary distributed data. This study proposes a logistic mixture regression model for binary distributed data based on simple interval mapping(SIM) and composite interval mapping(CIM) respectively. Iteratively reweighted least squares(IRLS) derived by expectation- maximization(EM) algorithm is used to obtain the maximum likelihood solutions of the effects and positions of QTLs. The methods presented in this paper are conceptually simple, easy to implement and fast in convergency. Results from simulated F2 intercross data indicate the proposed methods can effectively detect the putative QTLs. Method based on SIM has higher power than method based on CIM for the case of single QTL on each chromosome. Method based on SIM becomes less effective than method based on CIM when there are two or more QTLs on each chromosome, especially when QTLs are close together. In other words, method based on CIM has higher resolution than method based on SIM when there are two or more QTLs on each chromosome. However, interpretation of genetic parameters is more difficult for CIM model than for SIM model. Since number of QTLs on each chromosome is not known in practice, both CIM and SIM models should be tested and compared for any particular set of data. Two linked QTLs are not likely to be distinguished by both the methods studied if the distance between QTLs is less than about 20cM. Ching Liu 劉清 --- 1998 學位論文 ; thesis 70 zh-TW
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description 碩士 === 國立臺灣大學 === 農藝學系研究所 === 86 === Most quantitative traits are assumed to be continuously and normally distributed. Due to the nature of response, limitation of measurement or some other theoretical or practical considerations, only the discrete binary data are available. Published statistical methods for mapping and analyzing quantitative trait loci(QTL) all center on the normal assumption and thus can not be directly applied for binary distributed data. This study proposes a logistic mixture regression model for binary distributed data based on simple interval mapping(SIM) and composite interval mapping(CIM) respectively. Iteratively reweighted least squares(IRLS) derived by expectation- maximization(EM) algorithm is used to obtain the maximum likelihood solutions of the effects and positions of QTLs. The methods presented in this paper are conceptually simple, easy to implement and fast in convergency. Results from simulated F2 intercross data indicate the proposed methods can effectively detect the putative QTLs. Method based on SIM has higher power than method based on CIM for the case of single QTL on each chromosome. Method based on SIM becomes less effective than method based on CIM when there are two or more QTLs on each chromosome, especially when QTLs are close together. In other words, method based on CIM has higher resolution than method based on SIM when there are two or more QTLs on each chromosome. However, interpretation of genetic parameters is more difficult for CIM model than for SIM model. Since number of QTLs on each chromosome is not known in practice, both CIM and SIM models should be tested and compared for any particular set of data. Two linked QTLs are not likely to be distinguished by both the methods studied if the distance between QTLs is less than about 20cM.
author2 Ching Liu
author_facet Ching Liu
Chiang, Chih-ming
江志民
author Chiang, Chih-ming
江志民
spellingShingle Chiang, Chih-ming
江志民
Mapping And Analysis of Quantitative Trait Loci (QTL) for Binary Distributed Data
author_sort Chiang, Chih-ming
title Mapping And Analysis of Quantitative Trait Loci (QTL) for Binary Distributed Data
title_short Mapping And Analysis of Quantitative Trait Loci (QTL) for Binary Distributed Data
title_full Mapping And Analysis of Quantitative Trait Loci (QTL) for Binary Distributed Data
title_fullStr Mapping And Analysis of Quantitative Trait Loci (QTL) for Binary Distributed Data
title_full_unstemmed Mapping And Analysis of Quantitative Trait Loci (QTL) for Binary Distributed Data
title_sort mapping and analysis of quantitative trait loci (qtl) for binary distributed data
publishDate 1998
url http://ndltd.ncl.edu.tw/handle/51486537381198249938
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