Exact(2)
Amongst the relevant records that were analysed, we identified 69 quality criteria that have distinct reporting characteristics (Table 1).
b) When the data were sampled and analysed, we identified a discrepancy in the performance of the Schober test, where Rater 1 had correctly been rounding up or down to the nearest half centimeter, while Rater 2 had only used whole centimeter measures.
Similar(58)
Using genome-wide analyses, we identified different pathways that are regulated by miR-34a in mammary progenitor cells.
Using pan-genome analyses, we identified more than 10,000 novel full-length protein-coding genes and a high number of presence absence variations.
By applying recently developed beta diversity analyses, we identified ecologically unique sites and distinguished between two beta diversity processes: species replacement and changes in species richness.
By retro-transcription polymerase chain reaction analyses we identified a new transcript with a shorter 5′-UTR region.
In both Drop-seq and PLISH analyses, we identified cells co-expressing Sftpc and Scgb1a1 (Supplementary Figure 7c, d, h); however, these cells were not found preferentially in bronchoalveolar duct junction regions.
Based on sequence homology analyses, we identified the Kunitz-type protease inhibitor (KPI) domain of human amyloid-β A4 precursor protein as being a potential candidate.
Using immunoprecipitation and Western blot analyses we identified a protein of about 260 kDa in size likely representing the shorter protein proposed here.
Using detailed in silico sequence analyses we identified AT-rich stretches in these integrin genes, which have high similarity to yeast mRNA 3′-end processing signals.
By means of tree regression analyses we identified the most important habitat structure variables affecting bird species richness and density in urban environments.
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