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Elements of the Tc1-Mariner superfamily usually insert into TA sequences, while TEs of the Mutator superfamily have insertion sites that vary from 9 to 11 bp [ 15].
In addition, almost 80%% of highly expressed non-TE genes have insertion mutations, indicating that highly expressed genes in rice chromosomes are more likely to have mutations by mutagens such as T-DNA, Ds, dSpm and Tos17.
Also, if residues have insertion codes, the distance with neighboring residues is calculated and discarded if structurally equivalent.
In conclusion, minimal introns <87 nt in size are more likely to have insertion mutations, whereas those >87 nt in size are more likely to delete sequences.
Second, some mobile genetic elements, such as the D. melanogaster P transposable element (TE), have insertion site preferences related to the physical structure of candidate insertion sites rather than to a specific nucleotide sequence in the host DNA [4].
The switch's insertion loss compares favorably with that of 50/50 fiber couplers, which typically have insertion losses of 3.4 dB (excess loss of 0.4 dB).
Similar(49)
Most of the spontaneous mutants have insertions of a particular mobile element named "gypsy". This element affects the functions of sequences removed from the site of insertion.
Most of the spontaneous mutants have insertions of a particular mobile element named "gypsy".
These proteins also tend to have insertions between strands β1 and β2 and/or β4 and β5.
These P-element lines have insertions within or around genes including Tropomyosin 1 (Tm1), CG33129, UGP, and Glycerol 3 phosphate dehydrogenase (Gpdh) respectively.
Most of the TEI-derived deletions indeed have insertions as the ancestral state.
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