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We observed that 11 of the 34 unique SNPs identified through the MDR analyses were located in coding regions, with the remaining 23 being located in non-coding regions (Supplementary Table S7), supporting the notion that most associations exhibited pervasive epistatic effects and that it involves both non-coding and coding polymorphisms.
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The results of these analyses are located in Table 7.
The SNP at physical position 151,295,233 bp on chromosome 9, which was identified in both the North Carolina and combined analyses, is located in an intronic region of a cellulose synthase-like family A/mannan synthase gene (Table 3).
A secondary analysis was completed using waist circumference (WC) and MMW as independent variables and the complete results of these analyses are located in the supplemental information (see online supplementary figure S1).
The four SNPs within the GLUT9 gene region analysed in our study were located in intronic and intergenic regions.
All CTB+ astrocytes analysed for hemichannel studies were located in the striatum, where measurements were initiated at the brain abscess border and extended outward for a distance of up to 1 mm.
These species were analysed separately establishing where data points were located in transformed or pristine areas.
A total of 101 lesions selected according to the procedure outlined in the section Computed tomography were analysed (3 were primary lesions, 70 were located in the liver, 12 in the lungs, 9 in the peritoneum, and 7 at other various locations; Table 1).
The naturally infected field included in our analyses was located near an artificially infected field that was inoculated with strains from across Germany, hence we expect that some ascospore movement among fields would introduce inoculated strains into our sampled field, generating a significant degree of population admixture.
Using bioinformatic analyses, we found that the STAR elements were located in different genomic loci within each staphylococcal species.
The two corvettes were located in 2000.
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