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One of three extraction methods was used: an ammonium acetate method [ 61], a sodium acetate method [ 62] or an adapted phenol-chloroform method [ 63].
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The above two feature extraction methods are used to extract the curve eigenvectors of the experimental data (down-hole dynamometer cards) to structure the data set (different fault types of down-hole dynamometer cards with different data distribution).
This study found different outcomes when other DNA extraction methods were used and DNA extracts were quantified by UV and fluorescence.
The heat and cold extraction methods were used in the preparation of extracts from the prepared sample.
The following five DNA extraction methods were used in the study: DNA was extracted from 200 µl of the tested specimens using the DNeasy® Blood & Tissue Kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions using the protocol for animal blood or cells.
Ion-exchange and solvent extraction methods are used when high purity is desired.
For each modality, three feature extraction methods were used and four different classifiers were trained.
Four different DNA extraction methods were used to test the sensitivity of PCR with four different primer sets.
The sequential extraction methods were used to investigate the forms of P in the phosphate-adsorbed ZrMZ.
The protein precipitation and liquid liquid extraction methods were used for the pretreatment of plasma and brain homogenates, respectively.
For each modality, three feature extraction methods are used and four different classifiers (multilayer perceptron, decision tree, support vector machines, and probabilistic neural network) are trained by using two fusion methods which are matching score level and feature level fusion.
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