Discovering Association between Alternative Splicing and Disease

碩士 === 臺中健康暨管理學院 === 資訊科技研究所 === 92 === Introduction: Alternative splicing is important because more proteins can be made from the relative few genes and. it is also an important mechanism regulating genetic expression. In this thesis, we will try to find out alternative splicing isoforms...

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Main Author: 古天雄
Other Authors: 許芳榮
Format: Others
Language:en_US
Published: 2004
Online Access:http://ndltd.ncl.edu.tw/handle/91171388752690808595
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spelling ndltd-TW-092THMU03960282016-06-15T04:17:29Z http://ndltd.ncl.edu.tw/handle/91171388752690808595 Discovering Association between Alternative Splicing and Disease 尋找選擇性剪裁與疾病之間的關聯 古天雄 碩士 臺中健康暨管理學院 資訊科技研究所 92 Introduction: Alternative splicing is important because more proteins can be made from the relative few genes and. it is also an important mechanism regulating genetic expression. In this thesis, we will try to find out alternative splicing isoforms specific to several cancers and schizophenia and different development stage. The integrated information about diseases, pathways, proteins, and alternative splicing will be present. Methods: Alternative splicing database were constructed by aligning EST to whole genomic sequence using multi-layer unique marker methods. Each splicing site will be queried for their EST expression frequency in specific disease or development stage by the specific splicing isoforms. Significance were tested with Fish’s exact test. Using the position in the contig, splicing site was link to their correlated pretein, gene. By linking the same gene, disease information in OMIM and pathway information in KEGG were integrated. Results: 1263 disease specific splicing sites were identified. 63 exon skipping sites and 231 intron retain sites were correlated with hepatoma. 17 sites were correlated with schizophrenia. 163 splicing site were specific to fetal and infantile development stage. Discussion: Further laboratory investigation will be needed for confirming the real significant splicing site clinically. 許芳榮 2004 學位論文 ; thesis 31 en_US
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language en_US
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description 碩士 === 臺中健康暨管理學院 === 資訊科技研究所 === 92 === Introduction: Alternative splicing is important because more proteins can be made from the relative few genes and. it is also an important mechanism regulating genetic expression. In this thesis, we will try to find out alternative splicing isoforms specific to several cancers and schizophenia and different development stage. The integrated information about diseases, pathways, proteins, and alternative splicing will be present. Methods: Alternative splicing database were constructed by aligning EST to whole genomic sequence using multi-layer unique marker methods. Each splicing site will be queried for their EST expression frequency in specific disease or development stage by the specific splicing isoforms. Significance were tested with Fish’s exact test. Using the position in the contig, splicing site was link to their correlated pretein, gene. By linking the same gene, disease information in OMIM and pathway information in KEGG were integrated. Results: 1263 disease specific splicing sites were identified. 63 exon skipping sites and 231 intron retain sites were correlated with hepatoma. 17 sites were correlated with schizophrenia. 163 splicing site were specific to fetal and infantile development stage. Discussion: Further laboratory investigation will be needed for confirming the real significant splicing site clinically.
author2 許芳榮
author_facet 許芳榮
古天雄
author 古天雄
spellingShingle 古天雄
Discovering Association between Alternative Splicing and Disease
author_sort 古天雄
title Discovering Association between Alternative Splicing and Disease
title_short Discovering Association between Alternative Splicing and Disease
title_full Discovering Association between Alternative Splicing and Disease
title_fullStr Discovering Association between Alternative Splicing and Disease
title_full_unstemmed Discovering Association between Alternative Splicing and Disease
title_sort discovering association between alternative splicing and disease
publishDate 2004
url http://ndltd.ncl.edu.tw/handle/91171388752690808595
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