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Those profiles were processed by the notorious Cambridge Analytica, and seemingly by its parent company, SCL.
RNAseq data from the half-cell profiles were processed using GenePattern (v3) software.
For experimental validation, 10 mm, 20 mm and 30 mm thick extruded profiles were processed and welded to correspond to the numerical method.
The topography of polymeric fracture surfaces was obtained using atomic force microscopy, AFM, and the corresponding height profiles were processed using the variable bandwidth method (standard deviation criteria) to obtain the roughness exponent of the surfaces.
T-RFLP profiles were processed by Peak Scanner software (Applied Biosystems).
For decomposition of the 10-A peak profile, the samples were rescanned in step scan mode for 4 s every 0.02°2θ step, and obtained profiles were processed by DECOMPXR (Lanson 1997).
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The deviations of the on-line measurements from a reference profile are processed by a multi-scale wavelet in order to determine the singularities of the transients and to reduce the dimensionality of the data.
Data were acquired by Flow Cytometry and cell cycle profile was processed by FlowJo software (Tree Star Inc, Ashland, OR, USA).
Samples for microRNA profiling studies were processed by Filgen, Inc. (Filgen, Inc., Japan), according to the company's standard operating procedures.
Metabolomics profiling data were processed as described previously (Lu et al. 2012).
For the 16S rRNA gene profiling, data were processed using mothur [ 67].
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