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It provides research base and ideas for building of seismic loading quality control and Digital seismic exploration.
The copy number of each unknown sample for each gene was standardized to that of Gapdh gene to control for differences in RNA loading, quality and cDNA synthesis.
Results were normalized to a geometric mean of beta-actin (Actb), glyceraldehydes-6-phosphate dehydrogenase (Gapd) and hypoxanthine guanine phosphoribosyl transferase (Hprt) mRNA levels to control for differences in RNA loading, quality and cDNA synthesis.
The copy number of each unknown sample for each gene was standardized to the geometric mean of house-keeping gene, Rpl7 to control for differences in RNA loading, quality and cDNA synthesis.
The gene expression level of each sample for each gene was standardized to the house-keeping gene, Actb, to control for differences in RNA loading, quality and cDNA synthesis using the ΔΔCt method.
The expression level of each sample for each miRNA was standardized to U6 small nuclear RNA (snRNA), to control for differences in RNA loading, quality, and complementary DNA (cDNA) synthesis using the ΔΔCt method.
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By synthesizing the coupling matrix, the coupling coefficients between the resonators and the input/output singly loaded quality factor Q are determined.
The total (loaded) quality factor of a resonance is defined as Q_{l}= bigglvert frac{f_{p}'}{2f_{p}"} biggrvert.
Qf load quality factor.
Here, the load quality factor is generally less than the oscillator quality factor which ensures that transmission efficiency is always over zero.
The coefficient of friction depends on factors such as the microstructure of materials, load, quality levels and how it is the measured.
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