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Data in Freyer and Sutherland17 were taken with spheroids obtained from EMT6/Ro cells grown under standard oxygen and glucose concentrations (the original data are shown in the top panel of figure 3 in17).
Data in Kunz-Schughart et al.18 were taken with single spheroids of a given size obtained from both Rat1-T1 and MR1 cells (the original data are shown in panel C of figure 2 in ref. 18).
The original data are shown on the left.
Original data are shown, as run-plots, in Additional file 1: Figure S9.
The original data are shown in the first column, the BF-filtered data in the middle and the MAF-filtered data on the right.
45 Results from original data are shown.
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The proposed method, which utilizes genetic algorithm to learn and merge multiple FCM models that are computed from subsets of the original data, is shown to be faster than other genetic algorithm-based designs while resulting in the FCMs of comparable quality.
The algorithms of denoising and recognition are being made field experiment in north China oilfield; the field experiment instrument is showed in Figure12, and part of the intercepted original data is shown below.
The reviewers requested that more of the original data is shown with separate fluorescence channels.
A ML tree based on the original data is shown in [Additional file 3].
The spectra representing all phosphopeptides and the original data were shown in Additional file 2. Of the 1,592 non-redundant phosphosites, 89.4% were phosphorylated at serine, 9.5% at threonine, and 1.1% at tyrosine residues.
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