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We used the common approach to randomly under-sample the data set by removing samples from the over-represented class.
Cell growth was monitored by removing samples from the bioreactors and measuring OD600 using a Beckman Coulter DU720 spectrophotometer (1.3 mm slit width) (Beckman Coulter, Inc., Brea, CA, USA) in a 1-mL cuvette.
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We manually curated them by removing samples that were not really from RNA-seq (but contained the keyword 'RNA-seq' in the initial downloaded files) or contained data only from other species.
The structures of counterflow non-premixed flames were measured by removing gas samples from the flame and analyzing the samples using a gas chromatograph.
The structures of these flames were measured by removing gas samples from the flame and analyzing them using a gas chromatograph.
Hair density was determined by removing hair samples from a determined area and counting the number of hair present in that area.
The specific activity of Av1 in the reaction vial was monitored by removing liquid samples from the assay mixture at specified time points, for immediate transfer into a pH 7.8 standard assay solution containing excess additional Av2 (CR of ∼60).
Bio-specimen biomarkers are obtained by removing a sample from a patient.
RNA was extracted by removing RNAlater from samples and adding Trizol reagent (Sigma-Aldrich) to each sample.
We can increase this likelihood somewhat by removing from the sample individuals originating from Poland.
The manual CEK count was performed by removing the enumerated samples from the 'MagNest' cartridges, processing them as cytospin preparations and counting them manually.
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