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To examine the selection pressure acting on the potentially fixed Rover copies, we evaluated the strength of purifying selection on their transposases in comparison with the 104 genes used for phylogenetic reconstructions.
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Using cDNA samples of known copy numbers, we evaluated the detection limit of our PCR method targeting nsp14.
Using data collected from 248 first and second grade students who had submitted copies of their vaccination records, we evaluated the effectiveness of DTaP vaccination in infancy against adult pertussis.
We evaluated the copy number of HER-2/neu sequences per cell using a dual-colour FISH assay which included the gene probe and the centromere probe as a control.
Finally, we evaluated the ERBB2 copy number averages by aCGH in 22 ER+, 25 ER-, 20 IBC and 31 NIBC cases.
To further analyse the relationship between LRIG1 and ERBB2 at the genomic level, we evaluated the ERBB2 gene copy numbers in 18 tumours with increased LRIG1 copy number using FISH analysis according to standard procedures.
Next, we evaluated the reproducibility of the copy numbers obtained by the three methods.
In this study, we evaluate the potential of low-copy nuclear genes as DNA barcodes in Clermontia and Cyrtandra, and discuss some of their advantages and disadvantages compared to frequently used plastid genes.
We further evaluated the DNA copy number (CN) of 14 MB of DNA sequence surrounding the PIK3CA locus.
We further evaluated the frequency of single copy integrations with the various tagging methods.
We evaluated copy numbers and transcript amounts of the mitochondrial genes rps3, rps10, and rps13 because they are part of the 3′-domain in the prokaryotic small subunit of the ribosome (Bunner et al. 2010).
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