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In this source analysis, we assume that the hypocenter estimated by the back-projection method is located near the large slips.
At an angle of attack of α = 6.5° (Fig. 6a), the separation point predicted by the current method is located at x/c = 0.62, or in other words, the separation region covers 38%% chordwise of the upper surface.
The mutation cluster detected by our method is located in the substrate entry-loop between β-sheet F (βF) and α-helix G (αG), which tightens on the substrate upon its entry into the active site providing additional substrate-specific interactions [52] [55].
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The boundaries detected by the proposed method were located within 5 seconds of the actual boundaries.
Eg values obtained by this method are located in the range of 2.88 3.09 eV (Table 1).
The silicon (100) substrate patterned with Au using conventional photolithographic method was located downstream of the source powders.
It means that most of the facial point candidates in our method are located near the true facial point and thus with the increase of ROI size, the FP does not increased very much.
The three genes not identified from our method are located in conserved synteny blocks restricted to fewer species including those of the Lachancea clade (Figure 5A and Supplementary Figure 3).
The SNPs discovered by use of the in silico SNP mining method were located both in exons, introns and in 3'UTRs while the few SNPs discovered by use of the EPIC method were located in introns.
All polymorphisms discovered by the UTR-primed method were located within the 3'UTRs of the target genes.
The few outlier loci identified by the Bayesian method were located in different linkage groups in the R. Burrishoole and R. Saint John salmon comparisons.
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