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The percentage of erroneous responses for each emotional label was calculated as the rate of erroneously selected labels in all trials for that facial expression.
The intensity of fluorescence of nuclear DNA of neurons, 1s/2s cells and epithelial cells that retained label and those that did not retain label was calculated after subtracting background intensity.
For undirected graphs, the clustering coefficient of vertex v is defined as: C C v = 2 e j, t k v k v - 1 Generally, the clustering coefficient is defined as the percentage of neighboring proteins that interact with each other Enrichment of a population (for example, the top 20% of proteins in terms of betweenness) for a particular functional label was calculated using the hypergeometric test.
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Two classifiers are built for two newly constructed views for the target data (denoted as f 1 and f 2) where f 1 is initialized to the source prediction function h and f 2 is initialized to 0. The predicted label is calculated as a function of these two views thus creating an ensemble classifier.
Success rate of the model with respect to the GI data label is calculated as the classification error.
The percentage of label is calculated by dividing the intensity of the heavy mass by the intensity of the light mass and subtracting the natural C abundance calculated from the control.
Protein concentration and degree of labelling was calculated by measuring absorbances with a NanoDrop 2000/2000c Spectrophotometer (Thermo Fisher Scientific) using extinction coefficients provided by the dye manufacturer.
Degree of labeling was calculated to 3 mole dye per mole protein.
The degree of labeling was calculated and found to be 3.11 mole of Alexa Fluor® dye per mole of transferrin.
The density of pMAPK labeling was calculated as the ratio between the total number of pMAPK labeled neurons and the contour area (mm2) of each LA subnucleus.
After removal of free dye, and buffer exchange to 50 mM phosphate buffer pH 7.0, the efficiency of protein labeling was calculated as mole of dye per mole of protein according to manufacturer's protocols (Invitrogen).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com