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It should be noted that false positive and false negative targets are expected when using an miRNA array.
Although, it should be noted that false negative results might occur in genomes with low sequencing coverage and few copies.
It should be noted that false negative results are relatively common in such urine samples with lower [Cr].
However, it should be noted that false positive peaks are likely to display low number of reads in each replicate experiment, and thus are unlikely to be called differentially bound across experiments.
It should be noted that false negatives (missed transferred genes) arise when genes have ameliorated due to the mutational processes affecting the recipient genome or the genes are closely related to the recipient genome in terms of context bias [ 50].
It should also be noted that false positive results might be apparent if, for example, core cuts were compared with sections of an excision biopsy in a short term 'window of opportunity' study: the apparent reduction in pAKT and pERK could, in these circumstances, be read as evidence of therapeutic efficacy.
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It should be noted that false-positive staining was noted on keratin both in keratin pearls and in the epithelium, but this staining was excluded from evaluation.
It should however be noted that false-positive amplification due to mutant primers binding to wild-type templates will not be differentiated from true positive amplification by means of HRM analysis.
However, it should be noted that false-positive FDG uptake from a wide variety of sources including infection, post-radiation inflammation in the immediate post-treatment period or in patients with fistulas can all make interpretation slightly more difficult.
However, it should be noted that the false positive rate (in the present case mostly in the Shape condition) remains unknown.
It should be noted that the false positive rate of 9.2% for the predicted miRNA target sites could weaken but not bias our results, because the selection pressure on the falsely predicted miRNA binding sites is expected to be same as that on their flanking regions Population genetics is a useful tool to detect the evolutionary selection on miRNA target loci [ 13].
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