TY - GEN
T1 - Nonlinear bionetwork structure inference using the random sampling-high dimensional model representation (RS-HDMR) algorithm
AU - Miller, Miles
AU - Feng, Xiaojiang
AU - Li, Genyuan
AU - Rabitz, Herschel
PY - 2009
Y1 - 2009
N2 - This work presents the random sampling - high dimensional model representation (RS-HDMR) algorithm for identifying complex bionetwork structures from multivariate data. RS-HDMR describes network interactions through a hierarchy of input-output (IO) functions of increasing dimensionality. Sensitivity analysis based on the calculated RS-HDMR component functions provides a statistically interpretable measure of network interaction strength, and can be used to efficiently infer network structure. Advantages of RS-HDMR include the ability to capture nonlinear and cooperative realtionships among network components, the ability to handle both continuous and discrete relationships, the ability to be used as a high-dimensional IO model for quantitative property prediction, and favorable scalability with respect to the number of variables. To demonstrate, RS-HDMR was applied to experimental data measuring the single-cell response of a protein-protein signaling network to various perturbations. The resultant analysis identified the network structure comparable to that reported in the literature and to the results from a previous Bayesian network (BN) analysis. The IO model also revealed several nonlinear feedback and cooperative mechanisms that were unidentified through BN analysis.
AB - This work presents the random sampling - high dimensional model representation (RS-HDMR) algorithm for identifying complex bionetwork structures from multivariate data. RS-HDMR describes network interactions through a hierarchy of input-output (IO) functions of increasing dimensionality. Sensitivity analysis based on the calculated RS-HDMR component functions provides a statistically interpretable measure of network interaction strength, and can be used to efficiently infer network structure. Advantages of RS-HDMR include the ability to capture nonlinear and cooperative realtionships among network components, the ability to handle both continuous and discrete relationships, the ability to be used as a high-dimensional IO model for quantitative property prediction, and favorable scalability with respect to the number of variables. To demonstrate, RS-HDMR was applied to experimental data measuring the single-cell response of a protein-protein signaling network to various perturbations. The resultant analysis identified the network structure comparable to that reported in the literature and to the results from a previous Bayesian network (BN) analysis. The IO model also revealed several nonlinear feedback and cooperative mechanisms that were unidentified through BN analysis.
UR - http://www.scopus.com/inward/record.url?scp=77951002678&partnerID=8YFLogxK
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U2 - 10.1109/IEMBS.2009.5333798
DO - 10.1109/IEMBS.2009.5333798
M3 - Conference contribution
C2 - 19964421
AN - SCOPUS:77951002678
SN - 9781424432967
T3 - Proceedings of the 31st Annual International Conference of the IEEE Engineering in Medicine and Biology Society: Engineering the Future of Biomedicine, EMBC 2009
SP - 6412
EP - 6415
BT - Proceedings of the 31st Annual International Conference of the IEEE Engineering in Medicine and Biology Society
PB - IEEE Computer Society
T2 - 31st Annual International Conference of the IEEE Engineering in Medicine and Biology Society: Engineering the Future of Biomedicine, EMBC 2009
Y2 - 2 September 2009 through 6 September 2009
ER -