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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/26819


    Title: Gene network reconstruction from transcriptional dynamics under kinetic model uncertainty: a case for the second derivative
    Authors: Bickel,DR;Montazeri,Z;Hsieh,PC;Beatty,M;Lawit,SJ;Bate,NJ
    Contributors: 生物醫學工程研究所
    Keywords: BAYESIAN VARIABLE SELECTION;CYCLE-REGULATED GENES;MICROARRAY EXPERIMENTS;COMPOUND-MODE;EXPRESSION;CELL;IDENTIFICATION
    Date: 2009
    Issue Date: 2010-06-29 17:54:20 (UTC+8)
    Publisher: 中央大學
    Abstract: Motivation: Measurements of gene expression over time enable the reconstruction of transcriptional networks. However, Bayesian networks and many other current reconstruction methods rely on assumptions that conflict with the differential equations that describe transcriptional kinetics. Practical approximations of kinetic models would enable inferring causal relationships between genes from expression data of microarray, tag-based and conventional platforms, but conclusions are sensitive to the assumptions made. Results: The representation of a sufficiently large portion of genome enables computation of an upper bound on how much confidence one may place in influences between genes on the basis of expression data. Information about which genes encode transcription factors is not necessary but may be incorporated if available. The methodology is generalized to cover cases in which expression measurements are missing for many of the genes that might control the transcription of the genes of interest. The assumption that the gene expression level is roughly proportional to the rate of translation led to better empirical performance than did either the assumption that the gene expression level is roughly proportional to the protein level or the Bayesian model average of both assumptions.
    Relation: BIOINFORMATICS
    Appears in Collections:[Institute of Biomedical Engineering] journal & Dissertation

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