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Seven reports of six comparative studies which examined the validity of post-discharge surveillance methods were located; these involved different comparisons and some had methodological limitations, making it difficult to identify an optimal method.
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The errors for these methods are located in Table 1.
Supplementary Methods are located at http://bidmcgenomics.org/MIND_BODY_RR/(Login: benson) (Password: test1).
52 Most of the sRNAs identified through sequence homology and structure consensus methods are located in the specific intergenic regions showing phylogenetic conservation.
As is evident from Figures 1, B and C, the approximate transition distributions obtained with these methods are located too far to the right, a direct consequence of the assumption that s = O(N−1) (see Methods).
The strongest association for direct calving difficulty detected with both methods was located in a region around position 5.73 Mb (Bonferroni corrected p = 9.57 × 10−6; q = 4.65 × 10−6; BF = 3310.78).
The boundaries detected by the proposed method were located within 5 seconds of the actual boundaries.
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.
In the group of target genes tested by the in silico method 88% of all putative SNPs were located in coding sequences and 95% of putative SNPs that failed in the initial amplification step when applying this method were located in coding sequences.
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