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Accessory genetic elements mainly consist of highly variable mobile elements of antibiotic genes or mobile-antibiotic gene mosaic structures.
A considerable part of exon 8 (h6/m7) is similar to mobile elements of different classes (SINEs, LINEs, and DNA transposons) (Fig. 1).
Part of exon 1, intron 3 and exons 5 to 7 are all remnants of Lnx3, whereas exons 2 to 4 and 8 to 10 originated from mobile elements of various classes (Fig. 3, Table 2).
Moreover we have found that many Xist exons originated from mobile elements of various classes, which gave rise to simple tandem repeats detectable in the structure of the gene.
As demonstrated previously, the main part of the Enox Jpx) exons, except for exon 1, evolved from mobile elements of various classes [2]; moreover, different types of dispersed repeats gave rise to the exons of the gene in different mammalian species.
In this way, we identified 22 mobile elements of diverse classes in the S. cephaloptera genomic sequences examined (table 2).
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The presence of these four ORFs indicates that the 7 kp region may be a mobile element of bacterial origin.
Remarkably, about two-thirds of these genomic rearrangements were associated with the presence of mobile genetic elements (IS, MITE, Tn, CTn, and a not well-defined large mobile element of W83).
Thus, we propose to define the region spanning from SLI0868 to SLI0957, which encode two identical InsA paralogs, as the SLP3 amplifiable and mobile element of S. lividans 66 (fig. 2).
DCW1 denotes the ratios of more-mobile to less-mobile elements of the weathered rock.
424: 788–793) using truly irreversible RGCs (insertions of mobile elements) for a relatively small number of species.
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