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In analytical method development, method attributes are generally defined as the steps the method must have, such as sample preparation, sample introduction, sample analysis, and data analysis.
As proteins are not released from the electrodes during the different functionalization steps, the method presented here could be used to construct protein arrays containing very large protein libraries, where the only constraint is the number of electrodes.
Among these steps, the method for immunoprecipitating the BrU-labeled nascent RNAs was based on a method described previously and optimized for DNA microarray analysis in the following manner.
Presently divided into five broad steps, the method seeks to identify RD and ET facets based on their inability to occupy a unique part of the target construct's variance.
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At the first step, the method decides whether a bearing fault exists or not.
At each time step, the method consists of two stages to update the new solution.
In the first step, the method builds the hierarchical tree without using the prior knowledge.
In this validation step, the method is examined using the datasets applied to ComPhy.
This is done in two steps: in the first step, the method learns a measure of similarity between pairs of genes; in the second step, the method reweights the network's edges using the similarity measure it just learned.
Clarify the steps in the method, copyedit for spelling, punctuation, style and grammar, and reformat steps when needed.
Fig. 1 Flow chart showing the steps in the method.
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