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Participating databases contain a representative sample of the respective populations based on age and sex.
For C1-pigs, exposure was assumed to start at the midpoint of the interval between the last HEV-negative and first HEV-positive faecal sample of the respective iv-pig.
For all PCR assays, Ct numbers were established by using SDS 1.1 RQ software (Applied Biosystems), and the copy number, normalized against a reference gene (RNase P), and the calibrator (normal sample of the respective pair) were determined by using the formula 2-ΔΔ C t.
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The system consisted of two microdialysis probes, each optimally constructed for sampling of the respective body fluids, inserted into the right jugular vein and striatum of male Sprague Dawley rats.
Tissue samples of the respective areas harvested from 6 consecutive brain sections were pooled and used for quantitative real-time PCR.
It is evident from the figure that the gene markers for each tumor subtypes have either high expression values (up-regulated) or low expression values (down-regulated) over all the samples of the respective tumor class.
Further, most of the samples of the respective genotype clustered within the same stimulation condition.
Lung tissue samples of the respective pigs were also highly positive.
The respective samples were randomly selected from collections of samples of the respective species and haplogroups used in an earlier analysis (Zinner et al., 2009).
A probe set is treated as present if p ≤ 0.01 in at least 75% of the samples of the respective pathology group (tumour or NAT).
Note that the ranking criterion weights the effect of tissues according to the number of samples of the respective tissue category.
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