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Exhaustive Collection of Gene Modules that Changes Functions and Structures of Cells

Exhaustive Collection of Gene Modules that Changes Functions and Structures of Cells
详尽收集改变细胞功能和结构的基因模块
批准号:
18510178
负责人:
FUJIBUCHI Wataru
金额:
$1.16万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2006
资助国家:
日本
项目状态:
已结题
起止时间:
2006 至 2007

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中文摘要
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英文摘要
We performed a research to describe differences of shapes and works of cells by gene modules. First, as a data resource, we obtained expression data of 35,951 genes against 210 cells/tissues in total, from the collaborated researcher. And we obtained microscope images about 100 kinds of cells from the collaborator and others. Second, to measure the shapes of cells, we devised an image processing method that is robust against noise. Third, in order to extract combinatorial patterns of genes and cells exhaustively, we developed a fast biclustering method. With the two methods, we collected gene modules from gene expression data, while measuring parameters related to the contours of cells and nucleuses and the lining of cells. Analyzing the results, we obtained the whole set of gene modules that are commonly or reversely expressed among different cells. We found that this analysis allows us to perform digital differential display in more efficient way, for example, there was an extracted gene module that contained receptors, channels, transcription factors, etc., where genes were expressed reversely between brain and heart cells. Although it was not written in the proposal, to predict the shapes of cells from gene expression states, we performed the Support Vector Machine learning, and were able to predict the shapes of cells with 18 morphological parameters with 69.1 to 78.2% accuracies, against the test cells. We presented these results in two academic meetings, published three journal papers, and opened an Internet web service for retrieving and analyzing gene modules. Currently, we are writing a paper to summarize the whole study. Recognizing the values of the primary and the secondary datasets that we created in this project, our institute proceeded to support the development of the database from the fiscal year of 2008 to open it to public.
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A biclustering method for gene expression module discovery using closed itemset enumeration algorithm
使用闭项集枚举算法发现基因表达模块的双聚类方法
DOI: --
发表时间: 2007
期刊: IPSJ Transactions on Bioinformatics 48・SIG5
影响因子: --
作者: [岡田吉史, 藤渕 航, Paul Horton]
通讯作者: Paul Horton
DOI: --
发表时间: 2007
期刊:
影响因子: --
作者: [Yoshifumi Okada;W. Fujibuchi;P. Horton]
通讯作者: Yoshifumi Okada;W. Fujibuchi;P. Horton
細胞輪郭抽出装置、細胞輪郭抽出方法およびプログラム
细胞轮廓提取装置、细胞轮廓提取方法及程序
DOI: --
发表时间: 2006
期刊:
影响因子: --
作者: []
通讯作者:
Mming a Large-scale Microarray Database for Similar Gene Expression Modules to Find Distant Relationships between Down Syndrome andHuntingtonIs Disease
建立类似基因表达模块的大规模微阵列数据库来寻找唐氏综合症和亨廷顿舞蹈症之间的远距离关系
DOI: --
发表时间: 2007
期刊:
影响因子: --
作者: [Okada, Y.and Fujibuchi, W.]
通讯作者: W.
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