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Furthermore, the prevalence and the locations of sites where such conditions may have existed in the relevant time frame are identified.
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Where no frame was identified, however, we found that Jackson's problem diagrams did couch the requirements in their right context, and thus application of the problem frames approach was useful.
The corresponding block in the (t – 1) frame is identified by finding minimum NSAD t 1 with only an interpolated square block enclosing the interpolated region in the (t – 1/2) frame.
A single 3' end to the open reading frame was identified in ε-toxin-sensitive ACHN cells, corresponding to the canonical HAVCR1 protein (HAVCR1a, Figure 5A).
Two distinct 3' ends to the open reading frame were identified in ε-toxin-resistant 769-P cells; one transcript (HAVCR1a) corresponded to the canonical sequence whereas the second, shorter transcript (HAVCR1b) expresses a previously un-described, truncated protein [42], [43].
Alternatives confirmed by protein sequences and read in a single frame were identified in 3079 genes.
The LOC_Os01 g68850 open-reading frame was identified using FGENESH and contained a high amount of repetitive elements.
Candidate coding regions were sequenced within this interval, and a single C-to-T substitution at codon 236 of the ztf-16 open reading frame was identified.
Cell nuclei in each frame were identified automatically based on the CFP nuclear fluorescence, and the total fluorescence from each channel in each cell nuclei was recorded.
The azimuthal orientation of the crystals with respect to the AFM image frame was identified using an optical microscope above the AFM cell.
This extended 555 bp open reading frame was identified in sequences isolated from 27 independent samples of human genomic DNA, providing 54 unique alleles for analysis.
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