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The peak HGB concentrations were extracted and plotted against KDA and CLA.
Results from albumin, total protein, C-reactive protein (CRP), and haemoglobin concentrations were extracted from the patient records.
Initial substrate concentrations were extracted from [ 36] (Additional file 3) and we performed a RSA and a FBA with maximization of the biomass (Fig. 4).
The calibration, measurements and limits of detection were based on the areas of the Kα x-ray peaks as assessed by the software package GUPIX Elemental, and concentrations were extracted from PIXE spectra using GUPIX software ([email protected]).
Depending on the author, data for serum 25(OH D concentrations were extracted as both nanograms per milliliter and nanomoles per liter, with results converted to the SI unit of nanomoles per liter for this review.
The calibration, measurements, and limits of detection were based on the areas of the Kα x-ray peaks as measured by the software package GUPIX Elemental, and concentrations were extracted from PIXE spectra using GUPIX software (University of Guelph, ON, Canada), as previously described [ 10, 46].
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The experimental condition (cytokine concentrations) was extracted from publications as inputs of supervised learning models.
Results for hemoglobin level, hematocrit, RBC count, mean corpuscular volume, mean corpuscular hemoglobin, and mean corpuscular hemoglobin concentration were extracted from the EMR from January 1994 to September 2009.
Total RNA from constructs (n = 3 per concentration) were extracted using Trizol reagent (Invitrogen, Carlsbad, California) and the isolated RNA concentration and quality was determined using a spectrophotometer.
The energy band and hole concentration is extracted at the 3 nm below the gate oxide.
The carrier concentration is extracted to be 2.25 × 1017 cm-3 from the Raman line shape analysis.
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