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Sample features such as lumen diameters and cell wall thickness were manually measured using the program Axio Vision 4.8 (Carl Zeiss, Oberkochen, Germany).
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Investigation of genomic variants between whole-genome sequencing and transcriptome sequencing for matched samples revealed features such as gene-expression levels, allele-specific gene expression and transcriptional base modifications (TBMs) or RNA editing.
Petrographically, all analysed samples exhibit common features such as dominant quartz and low groundmass birefringence; this unique petrographic fabric could be subdivided, however, into the following four sub-fabrics characterized by different groundmass and grain size features.
In addition, MMP15, a metalloproteinase that was found over expressed in our samples, is also over expressed in samples with important clinical features such as higher grades, positive lymph nodes, and poor prognosis (Table 2).
The surface of the modified sample does not exhibit features such as superhydrophobicity, low roughness or low surface energy, which can give properties of adhesion-repellent to the surface [47].
The fluorescent structures therefore appear out of context of the sample's anatomy and features such as the growth or migration of fluorescent tissue through the surrounding tissue may therefore be hard to interpret.
A study of the distribution of results in each frequency band with the same sampling shows some interesting features, such as bimodal repartitions in some ranges.
The significant genetic structure and observed in C. pica has some commonalities in pattern with more commonly sampled taxa, but presents features, such as the differentiation of Bonaire, that appear unique.
The second one (blue, "general" or "serous") containing the serous and other tumor samples, comprises more general features such as no pain, no weight loss, and pT stage zero (no primary tumor identified, [ 25]) that apply to a wider area in transcription space.
Features such as disposable sample tips, sample and reagent delivery verification, and clog and clog detection have been incorporated in the design for assay robustness.
In addition, features such as sample size, homogeneity of units under study, ratio between sample size and number of input and output variables, and input/output returns-to-scale orientation also affect the estimated efficiency scores [ 6, 10- 16].
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