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To assess G-actin content of the input, the sample was subjected to ultracentrifugation to remove F-actin.
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The number of input data, the sample size.
The pump power is −83.8 dBm at the input of the sample box.
We input the training samples and test samples as mentioned in Section 3.3.
More precisely, we consider the output function that adds up all inputs of the sample.
(1) Input the next samples to the registers.
To selectively degrade the prokaryotic input DNA, the samples were treated for 1 h at 37°C with DpnI.
The corresponding input from the samples also exhibited comparable expression of VEGFR2 and HIF α as obtained from immunoprecipitation.
The enrichment of DNA was quantified as percentage of the amount in the input sample and the p-values for enrichment of FUS and EWS were calculated.
The DNA amount was quantified as percent of the amount measured in the input sample using the X0-method [ 78].
Fold enrichment was calculated as fold enrichment relative to the input sample, and the ΔCT was calculated using the average CT of the INPUT sample as the calibrating sample (sample CT CT of the INPUT sample).
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