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In the last few years, this imaging technique has progressively evolved from the simple staining of the common samples used in pathology for HC/IHC to the direct application on tissues that can be stained without additional procedures.
First, a matrix A0 is generated by identifying common samples with somatic mutations and CNVs and merging their genes over the common samples.
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More importantly, users can determine the appropriate sampling rate by analyzing the common sampling rate, at which features imply high utility information and low privacy information.
When applying the common sampling theorem to signals non-bandlimited in the FT domain may lead to wrong (or at least suboptimal) conclusions [5].
Moreover, calculate the common sample variance-covariance matrix (hat{Sigma }_{pool} = sum ^K_{k=1}frac{n_k}{n}hat{Sigma }_k) and (mathbf {z}_{ik} = hat{Sigma }^{-1/2}_{pool}(mathbf {x}_{ik} - bar{mathbf {x}}_{k}),) (i=1,ldots,n_k).
Therefore, none of the common sample collection and processing artifacts account for the reported results.
Tissues are among the common sample types known to contain inhibitors like collagen [ 30].
For vertebrates, the common sample of choice is generally blood or blood clots, as the cells are often still living and the DNA is usually of high quality.
For aminoglycosides, the common sampling times for the peak are 30 min after a 30-min infusion or 15 min after a 60-min infusion.
To obtain a proper comparison, we also log10 transformed the values of the available expression data coming from [ 4], considering all the 24 common samples shared between the two datasets.
Based on the previous observation of the effect of the additional 100 control samples on the transferability between AFX and AGL, we decided to conduct another analysis using the 318 common samples.
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CEO of Professional Science Editing for Scientists @ prosciediting.com