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Published experimental data was utilised to validate the developed model.
An independent series of 101 bladder tumours (non-muscle invasive (n=56): pTa (n=24), pT1 (n=32); and muscle invasive (n=45): pT3 (n=16), pT4 (n=25), pT4 (n=4)) was utilised to validate the relevance of methylation candidates in bladder cancer progression (Sanchez-Carbayo et al, 2006).
An independent set of 10 pairs of bladder tumours and normal urothelium, similar to the set used for the discovery of explorative analyses, was utilised to validate the presence of cancer-specific methylation of SOX9 by an independent method, MS-PCR.
The performance measure, i.e. signal-to-noise ratio is utilised to validate by Monte Carlo simulations and to complement above study individual parameter tolerance sensitivity are investigated.
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A database of 205 experiments available from previous laboratory anchor tests was utilised to train, validate and test the developed neural network.
In this section, to validate the proposed model and also to evaluate the performance of the proposed hybrid CS-SA algorithm, design of experiment and benchmark methods are used as explained in the two following sub-sections: In this section, design of experiment method is utilised to verify and validate the proposed model and the hybrid CS-SA algorithm, which is proposed for solving the SDFLP.
Custom-made microarrays containing previously identified SCMV resistance candidate genes and resistance gene analogs were utilised to investigate and validate gene expression and expression patterns of isogenic lines under pathogen infection in order to obtain information about the molecular mechanisms involved in maize-potyvirus interactions.
Partheen et al (2008) utilised qPCR to validate a panel of seven genes identified via microarray analysis as prognostic factors in ovarian adenocarcinoma.
The model was validated and utilised to determine the optimal operating conditions for bench-scale batch lipid oil production.
38 Our study suggests that routinely collected clinical data concerning cumulative comorbidity may be utilised to quantify risk; however, further work would be required to validate this as a tool for use in clinical care.
Results of these tests are utilised to examine the barrier behaviour, in addition to being used to validate a couple FE/SPH model of the barrier system.
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