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The input tested was 'ECE 4760'ECE
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A linear relationship was established between TDIN uptake and loading over the range of inputs tested.
Of the 521 physical inputs tested, only 22 changed total cost by 0.1% or more and 411 inputs had a negligible effect (0.01% or less).
This robustness was observed for virtually all the metabolic intermediates, for all the label inputs tested, and under a broad range of metabolic states.
Of 219 non-drug/supply inputs tested, 157 had an impact of less than 0.05% on the total cost of PAC.
The percentage of variant reads/allele frequency remained consistent over all the DNA inputs tested and the overall percentage coverage at 100x depth was unaffected by the range of input DNA quantities used.
We next quantitated Ponceau and β-actin signals, and showed a strong correlation between both signals, for the range of protein inputs tested (20 to 140 μg, with 20 μg increments; R = 0.97 ± 0.007).
The test and input represented tested samples and input control samples, respectively.
Two independent stimulating electrodes were placed separately in the Schaffer collateral CA1 input (test pathway) and subiculum CA1 input (control pathway).
In Fig.2.4a, we see samples of the input test sinusoid overlaid with the continuous sinusoid represented by those samples.
Pseudo-random patterns generated by Linear Feedback Shift Register (LFSR) are used as input test patterns.
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