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Asynchrony was also analyzed using a standardized automated method over the same period, to prevent interobserver variability and to avoid observer subjectivity [19].
Importantly, the ACT tool uses NASC/GARNet data sets that were labeled, hybridized and analyzed using a standardized procedure thus providing a homogeneous and readily comparable data set.
To validate the method, the viability of our corticostriatal organotypic slice cultures was analyzed using a standardized protocol for PI uptake.
Subsequently, the results were analyzed using a standardized consensus tool, and the recommendations were rated as valid if they matched three of our criteria.
Articles were analyzed using a standardized grid based on four items: 1) terminology used; 2) factors that influenced transferability; 3) capacity of the research and evaluation designs to assess transferability; and 4) tools and criteria available to assess transferability.
Individual functional data were analyzed using a standardized evaluation routine with a dynamic statistical threshold [ 30– 33]: A minimum cluster size of 36 mm was preset as the standard for data evaluation to achieve a precise determination of the anatomical correlates of the different functional activations and also to eliminate very small clusters in the activation maps.
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ALP levels were standardized to protein content, which was analyzed using a Micro BCA Protein Assay Kit (Pierce, Rockford, USA) according to manufacturers' instructions.
Cells were analyzed using a BD FACSCalibur.
Data were analyzed using a Matlab program.
In order to standardize the HLA designation of prior low-resolution typings with the more advanced DNA based typings, all HLA-A, −B and -DR were analyzed using a low resolution serologic equivalent.
In order to standardize the HPLC profile, crude extracts were analyzed using an established method [ 6].
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