Exact(1)
Absorbance at 492 nm for each sample was read using a plate reader, with increased absorbance corresponding to increased amounts of DNA damage.
Similar(59)
Following incubation for 30 min–3 h, luminescence of each sample was read using a plate-reading luminometer as directed by the manufacturer.
Samples were read using a Stago coagulation analyser.
Samples were read using an Ilab-600 automatic system.
After Illumina standard quality control filtering, read quality for each sample was visualized using FastQC version 0.10.0 (Andrews 2010).
The pH reading for each sample was recorded using pH meter (HI 8424 microcomputer HANNA instruments).
Samples were read for 10 seconds.
The initial fluorescence reading for each sample was used to identify compounds contributing high background fluorescence.
Aligned reads for each sample were assembled using Cufflinks version 2.0.2.
Gene fusion candidates for each sample were determined using defuse by McPherson et al. (2011) on the RNA reads.
reads for each sample were retained and used for further analysis.
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