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The variable m describes the number of the samples; then, we can deduce the post probability of the decision j, that the ith classifier make decision k, defined by Eq. 14: begin{aligned} P {D}_{i}=k|R=j)=frac{P(R=j|{D}_{i}=k)}{sum_{l=1}^{n}P(R=j|{D}_{i}=l)}.
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If one peptide labeled with QDs has stronger antigenicity, more molecules of this peptide bind to its antibody in the standard serum sample; then, we can measure a higher FP value using the fluorescence polarization analyzer.
We considered that this was unlikely because if the contaminating molecules of such misfolded amyloid intermediates were substantially present in the sample, then we would expect the A11-reactive proteins, especially non-chaperone proteins like toxins, not to suppress β aggregation (Figure 4D, E).
At first, we selected three towns by random sampling; then, we randomly sampled three to five villages for each town, and eventually we selected 13 villages.
We first determine what proportion of each source will compose the tumor sample, then we generate the sequence reads that are observed in the sample.
If this is applicable to our study sample then we are likely to have understated the strength of the association between carer education and mental health.
If 0.8 is significantly higher than the average probability for this exposure category in the whole sample, then we can interpret group 1 as characterized by subjects who are, on the whole, exposed to a relatively high level of PM10.
If the number of quantitatively correct registrations is a large percentage of the images in the sample, then we will conclude that automatic registration is as good as manual registration.
If cold regions are purely artifacts of sampling, then we would expect their location to be random, such that they should not be replicated in independent experiments and that their number and size should decrease as an increasing number of meioses are sampled.
To identify tissue/cell markers in independent AF samples at different pregnancy stages, we first filtered genes with expression level >90 percentile of all samples, and then we compared the abundantly expressed genes in AF from preterm, late preterm and full term samples to identify common vs unique expressed genes.
We gently vortexed each volume collected to homogenize the sample and then we stored the samples at 4 °C until NGS analysis.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com