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Recently some evidence for differences in virulence gene regulation between these two sibling species has been published [28], [29].
According to the results of the identity test, niche diversification between these two sibling species must be considered highly significant.
According to this scenario, differences in transcription regulation between these two sibling species may be responsible for rapid adaptive evolution.
Detecting the gene expression difference in HGs between these two sibling species is important for understanding the mechanism of high royal jelly production.
Introgression of genes in autosomal chromosomes through rare hybridisation between these two sibling species has been demonstrated previously, particularly for chromosome 2L [ 21, 22].
However, very high F ST values were detected in all loci between these two sibling species and they were even higher for Rp49, RpS29 and RpS2 (0.8865, 0.8865 and 0.8502, respectively for the whole fragment) than for timeless, Clock and cycle (0.8150, 0.7088 and 0.5806, respectively for the whole fragment).
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Moreover, the distance between any two sibling nodes in a WSAN is no more than 2R c, because both of them are in the communication range of the parent node.
Finally, the solid box shows the difference in transposition rates between two sibling male seed mice, one hemizygous and one homozygous for the transposase transgene.
To eliminate the possibility that the glabrous allele was introduced from other pollen sources (which was very unlikely in the greenhouse), we genotyped RIL-46 M and RIL-46 W with 238 highly polymorphic SSRs that were used in polymorphic screening in genetic mapping of this gene (see below), and no polymorphism was found between the two sibling lines.
Number of siblings (Coding is 0 = no siblings, 1 = one sibling, 2 = two sibling and 3 = three or more siblings).
1a) two sibling female lures (60 replicates); exp.
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