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For PCR-based community analysis, the quantity of DNA is not the key factor because trace DNA (> 500 ng) is adequate for PCR amplification and subsequent sequencing.
In reliability analysis the quantity of interest is the time to failure, T (often called mission time) and the probability of failure, p f, for dynamic and static systems, respectively.
In order to present the relative changes in gene expression measured in qRT-PCR in the same scale as that found in microarray analysis the quantity of a transcript in one biological sample or state relative to that in a calibrating sample was expressed as log2 (fold change) in gene expression.
The comparative Ct method was used for analysis: the quantity of the PCR products was determined based on the threshold PCR cycle-values, and it was normalized with the quantities of the endogenous control PCR product, samples were analysed in triplets [ 17, 18].
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One of the main outputs of this analysis is the quantity of renewable energy feedstocks produced under the conditions of the various sub-scenarios.
Sensitivity analysis on the quantity of initial samples to estimate for in-control process mean vector and covariance matrix is also presented.
We illustrate the method on an example of fire safety analysis, where the quantity of interest is the probability of exceeding a tenability threshold in a building on fire.
This result was supported by flow cytometry analysis determining the quantity of DsRed positive cells.
Calculation was performed by second derivative maximum analysis and the quantity of each transcript was expressed as ct values.
The comparison applies to; a set of regional-scale sample survey questionnaires, a representative sample survey on drug use among drivers and an analysis of the quantity of cocaine-related metabolites in sewage.
This analysis models the quantity of excess pesticide residues that might be imported into the U.S. assuming exporters comply with originating country tolerances but not U.S. MRLs.
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