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In the testing phase the performance of the generated classifier is evaluated by extracting standard accuracy measures for classifiers.
These temporal FLIM data cubes are denoted by I x, y, t; λ1), I x, y, t; λ2) and I x, y, t; λ3) in Fig. 3; where the process of extracting standard FLIM features is illustrated for the case of a 3 wavelength multispectral FLIM data cube.
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To identify the chemical constituents of plant extract standard procedures were followed.
Where trials reported the data using geometric means, we recorded this information and extracted standard deviations on the log scale.
Relative recoveries were determined by comparing the % of drug recovered from serum matrix against detector response for extracted standards.
Fifty-microliter extracts (standard and isolated bacteria) were loaded on SDS-PAGE.
Total RNA was extracted using standard Trizol extraction (Invitrogen, Carlsbad, California).
Genomic DNA was extracted using standard phenol-chloroform extraction.
DNA was extracted by standard phenol-chloroform extraction procedure and stored at −80°C.
Placenta genomic DNA was extracted using standard phenol-chloroform extraction methods.
Nascent RNA was then extracted using standard Trizol RNA extraction (Invitrogen, Carlsbad, California).
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