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By this method, single nucleotide variants (SNV), insertions and deletions and copy-number changes can be identified.
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One of the novel features of this study is the measure of %FGV assessed by the method single-energy X-ray absorptiometry (SXA) [ 17– 20].
By this method, a single crystal is indented, and the material input to a FE model of the experiment is iteratively changed until agreement is achieved.
Quantitative PCR revealed that strains generated by this method contain single- or low-copy transgenes.
A range of compounds were prepared by using this method and single crystal X-ray diffraction study was performed using a representative compound.
So far, most of the studies on ZnO prepared by this method mainly employed single liquid (such as water, methanol, ethanol, and acetone) as solvent.
One specific advantage of the method is that when ensemble mean value is considered as a forecast, the peak flows are predicted with improved accuracy by this method compared to traditional single point forecasted ANNs.
All screened EZ-Tn5 mutants obtained by this method contained only a single transposon insertion and were stable over at least 10 sequential overnight culturings.
These results suggest that viral protein translation rates are too low to be detected by this method in VSV-LUC single infections but are detectable (and surprisingly similar) in co-infections with VACV-WR or ΔA51R strains.
The greater scattering of the R2 region in cell suspensions obtained by this method suggests that not single cells but groups of them, typically enterocytes, were present, as corroborated in the semithin sections.
By this method, each species yielded a single flagellin gene sequence.
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