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Conference Paper: A multiple regression approach for building genetic networks

TitleA multiple regression approach for building genetic networks
Authors
Issue Date2008
Citation
Biomedical Engineering And Informatics: New Development And The Future - Proceedings Of The 1St International Conference On Biomedical Engineering And Informatics, Bmei 2008, 2008, v. 1, p. 18-23 How to Cite?
AbstractThe construction of genetic regulatory networks from time series gene expression data is an important research topic in bioinformatics as large amounts of quantitative gene expression data can be routinely generated nowadays. One of the main difficulties in building such genetic networks is that the data set has huge number of genes but small number of time points. In this paper, we propose a linear regression model for uncovering the relations among the genes by using multiple regression method with filtering. The model takes into account of the fact that real biological networks have the scale-free property. Based on this property and the statistical tests, a filter can be constructed and the interactions among the genes can be inferred by minimizing the distance between the observed data and the predicted data. Numerical examples based on yeast gene expression data are given to demonstrate our method. © 2008 IEEE.
Persistent Identifierhttp://hdl.handle.net/10722/100316
References

 

DC FieldValueLanguage
dc.contributor.authorZhang, SQen_HK
dc.contributor.authorChing, WKen_HK
dc.contributor.authorTsing, NKen_HK
dc.contributor.authorLeung, HYen_HK
dc.contributor.authorGuo, DDen_HK
dc.date.accessioned2010-09-25T19:05:12Z-
dc.date.available2010-09-25T19:05:12Z-
dc.date.issued2008en_HK
dc.identifier.citationBiomedical Engineering And Informatics: New Development And The Future - Proceedings Of The 1St International Conference On Biomedical Engineering And Informatics, Bmei 2008, 2008, v. 1, p. 18-23en_HK
dc.identifier.urihttp://hdl.handle.net/10722/100316-
dc.description.abstractThe construction of genetic regulatory networks from time series gene expression data is an important research topic in bioinformatics as large amounts of quantitative gene expression data can be routinely generated nowadays. One of the main difficulties in building such genetic networks is that the data set has huge number of genes but small number of time points. In this paper, we propose a linear regression model for uncovering the relations among the genes by using multiple regression method with filtering. The model takes into account of the fact that real biological networks have the scale-free property. Based on this property and the statistical tests, a filter can be constructed and the interactions among the genes can be inferred by minimizing the distance between the observed data and the predicted data. Numerical examples based on yeast gene expression data are given to demonstrate our method. © 2008 IEEE.en_HK
dc.languageengen_HK
dc.relation.ispartofBioMedical Engineering and Informatics: New Development and the Future - Proceedings of the 1st International Conference on BioMedical Engineering and Informatics, BMEI 2008en_HK
dc.titleA multiple regression approach for building genetic networksen_HK
dc.typeConference_Paperen_HK
dc.identifier.emailChing, WK:wching@hku.hken_HK
dc.identifier.emailTsing, NK:nktsing@hku.hken_HK
dc.identifier.authorityChing, WK=rp00679en_HK
dc.identifier.authorityTsing, NK=rp00794en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1109/BMEI.2008.43en_HK
dc.identifier.scopuseid_2-s2.0-51649083296en_HK
dc.identifier.hkuros142637en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-51649083296&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume1en_HK
dc.identifier.spage18en_HK
dc.identifier.epage23en_HK
dc.identifier.scopusauthoridZhang, SQ=10143093600en_HK
dc.identifier.scopusauthoridChing, WK=13310265500en_HK
dc.identifier.scopusauthoridTsing, NK=6602663351en_HK
dc.identifier.scopusauthoridLeung, HY=24780941800en_HK
dc.identifier.scopusauthoridGuo, DD=24780473500en_HK

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