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The H2-TPR analysis was executed by increasing gradually the sample temperature to 800 °C with the rate of 5 °C min−1 under Ar (4.95 %-mol H2 in Ar).
Statistical analysis was executed by the Statistical Programme R version 2.8.0.
Reconciliation analysis was executed by NOTUNG 2.1 [ 52], using default event costs.
The cost-effectiveness analysis was executed by the comparison of the ICER values of different screening strategies.
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A factorial map of principal component analysis was executed on the whole expressed data by the program Qlucore [ 68] on the differentially expressed (fold change >2).
State sensitivity analysis was executed with respect to design variables considered by the pantograph system.
Gene enrichment analysis was executed using DAVID [ 34, 35] with the genes represented by the microarray as background.
Then sensitivity analysis was executed.
The physicochemical parameter analysis was executed based on standard method.
The analysis was executed using the DMU Package [26], [27].
Confirmatory factor analysis was executed to determine factorial/construct validity.
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