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Additionally, we validated the model output by comparing it with the observation data collected during the same period of the following year.
Additionally, we validated the proposed GRN models by testing if they also recovered gene configurations of experimentally characterized loss and gain of function mutants.
Additionally, we validated the use of AKAP-4 antigen to track tumor growth in vivo and to specifically identify MM cells in mouse tissues.
Additionally, we validated the expression of three genes of interest (cystatin c, NF1X, and purpurin) which were identified in our screen (see below).
Additionally, we validated the OWSQLI by relating its scores to those of instruments that measure social support (SIMSS), as well as physical and mental QofL (MOS SF-36).
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Additionally, we validate the decomposition results through a comparative study using empirical analysis.
Additionally, we validate the model for the case of 2D and 3D circular braiding processes run in the transitory stage.
Additionally, we validate the in vivo images with conventional confocal images collected with a bench top instrument.
Additionally, we validate this technique by means of simulations, considering one of the scenarios defined as part of the Winner Phase II Channel Models, specifically designed for high-speed train scenarios.
Additionally, we validated some of the microarray data by Western blot analysis of select genes.
Additionally, we validated inferences of absence from the OrthoMCL analyses by performing detailed sequence comparisons using BLAST+ [ 53] (Additional file 2).
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