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The quantity measures the effect size variance of gene g, measuring the sampling error for the i th study.
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Technical replicates were performed by measuring the sample three independent times.
The estimated systematic error in determining M is ~10% due to inaccuracy of measuring the sample mass that was typically several mg (this is difficult because of the extreme sensitivity of intercalated GLs to moisture and oxygen).
Furthermore, the method does not require measuring the sample mass.
Before measuring, the samples are degassed at 60 °C.
The time between the cleaning and measuring the sample with XPS was about 30 min.
This method consists of measuring the samples mass loss, surface S during the immersion in a corrosive solution.
We followed the degradation by measuring the sample mass that remained after each hydrolysis period.
They were trained in techniques for weighing and measuring the sample being studied.
Small 0.5% oscillatory strain was applied throughout the experiment while measuring the sample storage and loss modulus over time.
Most of the detailed laboratory work was done by S.G. who measured the samples and together with J.G.R., A.C.B. analyzed the data.
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