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Genotyping was repeated in 10% of the study samples (with independent assessment) and for 99.98% of those samples there was exact agreement between the two.
What is clear is that in our tumour samples there was significantly higher total p53 protein.
Further, in several samples there was inadequate dermis within the punch skin biopsy specimens for review.
Thus, in several samples there was underreporting of As species concentrations, because some forms of As were not quantified.
However, in both the luminal A and B samples there was a range of Recurrence Score results (Fig. 3).
For all three resin samples there was minimal difference between the shape of the intra-particle binding profiles.
In diarrhea samples there was: four (5.0%) A. lumbricoides, three (3.75%) with the presence of E. nana and rotavirus and one (1.25%) with T. trichiura and G. lamblia.
In 2/33 culture negative infection samples there was identification of Enterococcus gallium (1) and Coliforms (1) from swabs which were regarded as non-pathogenic contamination.
For abomasal fluid samples there was a further extraction step using ethyl acetate before C18 cartridge extraction, as reported by Lanusse et al. [ 35].
For descriptive outcomes the intra-cluster correlations for year 2 and year 5 samples there was consistency in the patterns of ICCs across samples.
"When I gave those samples, there was not EPO in those samples.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com