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Almost all groups of three or more SNP markers listed in Table 3 were mapped to small chromosomal regions and could thus be defined as clusters, with the exception of only a few SNPs, dispersed along the chromosomes in different cultivars.
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Species should instead be defined as cluster concepts (Hull 1965) or recognized to be individuals (i.e. spatio-temporally restricted, historically contingent particulars) to which organisms belong as parts, and not classes, sets, or natural kinds at all (Ghiselin 1974; Hull 1978).
Haplotypes were defined as clusters of identical genotypes in a 10-kb window.
Lumens were defined as clusters of CD31 stained cells with a central lumen clearly visible (Figure 3B).
Profiles were defined as clusters of positive CD31 stained cells within the dermis with no central lumen visible (Figure 3B).
CGIs are defined as clusters of CpG dinucleotides above particular thresholds of length, CpG frequency (corrected for GC content) and GC content (Fig. 4B) [16].
Areas of functional activity were defined as clusters of 20 or more contiguous voxels which exceeded an uncorrected p-value of.0005.
The false-discovery-rate (FDR) [38] threshold of p<0.05 was adopted to deal with the problem of multiple comparisons by automatically defining a statistical significance threshold ensuring that the average rate of false positives among the voxels activated would be less than p. Activated brain regions were defined as clusters consisting of more than 10 contiguous voxels.
Genes were defined as clusters of known isoforms defined by the GNFAtlas2 table.
Genes were defined as clusters of known transcripts defined by the GNFAtlas2 table.
Colonies were defined as clusters consisting of 40 or more cells.
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