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Moreover, the corresponding loci of the linkage map were mapped on most of linkage groups of the '273-7'-specific '273-7'-specific '273-7'-specific between the linkage group and chromapomes of M. truncandla.
As previously reported (Bennetzen et al. 2012), significant segregation distortion was observed on most of linkage group II, and several sections of linkage groups III, IV, V, VII, and IX, because of an excess of the S. italica alleles in those regions.
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Additionally, most assessments of linkage quality have concentrated on the capture of a single event, such as death or cancer registration [ 5- 7].
This error was because one of the 16 linkage groups of the 'T17-349'-specific data consisted of an extremely larger number of marker loci (32.4% of the total number of marker loci) than the other 15 groups, and corresponding marker loci classified to the largest linkage group were found on most of the linkage groups of the '273-7'-specific '273-7'-specific '273-7'-specific
Small effective population sizes eliminate most of the linkage combinations in each region such that they are in perfect linkage disequilibrium.
Clusters of RGH-SSRs were observed on most of the linkage groups of common bean and in positions associated with R-genes and QTL.
The order of those markers was conserved in most of the linkage groups.
Most of the linkage groups were consistent with those described previously [ 13].
Most of the linkage groups were determined at LOD scores >6.
Most of the linkage groups, except LG6a and LG6b, showed colinearity to eight chromosomes of M. truncatula (data not shown).
It was noteworthy that the observed expansion ranges were much larger than the estimated expansion ranges on most of the linkage groups (Table 2).
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